Temporal variation in glucocorticoid levels during the resting phase is associated in opposite way with maternal and paternal melanic coloration

Sex‐dependent selection can help maintain sexual dimorphism. When the magnitude of selection exerted on a heritable sex trait differs between the sexes, it may prevent each sex to reach its phenotypic optimum. As a consequence, the benefit of expressing a sex trait to a given value may differ between males and females favouring sex‐specific adaptations associated with different values of a sex trait. The level of metabolites regulated by genes that are under sex‐dependent selection may therefore covary with the degree of ornamentation differently in the two sexes. We investigated this prediction in the barn owl, a species in which females display on average larger black spots on the plumage than males, a heritable ornament. This melanin‐based colour trait is strongly selected in females and weakly counter‐selected in males indicating sex‐dependent selection. In nestling barn owls, we found that daily variation in baseline corticosterone levels, a key hormone that mediates life history trade‐offs, covaries with spot diameter displayed by their biological parents. When their mother displayed larger spots, nestlings had lower corticosterone levels in the morning and higher levels in the evening, whereas the opposite pattern was found with the size of paternal spots. Our study suggests a link between daily regulation of glucocorticoids and sex‐dependent selection exerted on sexually dimorphic melanin‐based ornaments.     

Sexual selection for white tail spots in the barn swallow in relation to habitat choice by feather lice

Many bird species have white spots in their tails or wing feathers, and such characters have been hypothesized to be either reliable signals (handicaps) or amplifiers that facilitate the message of a signal. In barn swallows, Hirundo rustica, the size of the white spots in the tail feathers is sexually dimorphic and positively correlated with feather length. We tested whether such spots act as handicaps or amplifiers. These white spots affect sexual selection in barn swallows, as shown by an experiment in which we randomly subjected males to (1) a considerable reduction of the size of all the spots by the use of a black permanent marker pen, (2) a small reduction of the size of the spots, or (3) no reduction. There was a positive association between spot size and the number of offspring produced per season. The white tail spots were preferred by feather-eating Mallophaga as a feeding site: holes made by Mallophaga were more abundant in the white spots than expected by chance. A habitat choice experiment with Mallophaga on barn swallow tail feathers revealed that they preferred white spots over black parts of the tail feathers. We therefore expected long-tailed male barn swallows to have more Mallophaga than short-tailed males. However, the opposite relationship was observed, indicating that long-tailed males may reliably signal their quality by the presence of large white tail spots without parasite damage. Thus white tail spots in barn swallows appear to be a reliable signal of phenotypic quality. Copyright 1999 The Association for the Study of Animal Behaviour.     

Evolutionary trade‐off between naturally‐ and sexually‐selected melanin‐based colour traits in worldwide barn owls and allies

Natural selection typically constrains the evolution of sexually‐selected characters. The evolution of naturally‐ and sexually‐selected traits can be intertwined if they share part of their genetic machinery or if sex traits impair foraging success or increase the risk of depredation. The present study investigated phenotypic correlations between naturally‐ and sexually‐selected plumage traits in the Tytonidae (barn owls, grass owls, and masked owls). Phenotypic correlations indicate the extent to which selection on one trait will indirectly influence the evolution of another trait. In this group of birds, the ventral body side varies from white to dark reddish, a naturally‐selected pheomelanin‐based colour trait with important roles in predator–prey interactions. Owls also exhibit eumelanin‐based black spots, for which number and size signal different aspects of individual quality and are used in mate choice. These three plumage traits are strongly heritable and sexually dimorphic, with females being on average darker reddish and more spotted than males. Phenotypic correlations were measured between these three plumage traits in 3958 free‐living barn owls in Switzerland and 10 670 skin specimens from 34 Tyto taxa preserved in museums. Across Tyto taxa, the sexually‐selected plumage spottiness was positively correlated with the naturally‐selected reddish coloration, with redder birds being more heavily spotted. This suggests that they are genetically constrained or that natural and sexual selection are not antagonistically exerted on plumage traits. In a large sample of Swiss nestlings and within 34 Tyto taxa, the three plumage traits were positively correlated. The production of melanin pigments for one plumage trait is therefore not traded off against the production of melanin pigments for another plumage trait. Only in the most heavily‐spotted Tyto taxa do larger‐spotted individuals display fewer spots. This indicates that, at some threshold value, the evolution of many spots constrains the evolution of large spots. These analyses raise the possibility that different combinations of melanin‐based plumage traits may not be selectively equivalent.     

Geographic variation in sexual dimorphism in the barn owl Tyto alba: a role for direct selection or genetic correlation?

Geographic variation in sexually selected traits is commonly attributed to geographic variation in the net benefit accrued from bearing such traits. Although natural and sexual selection are potentially important in shaping geographic variation, genetic constraints may also play a role. Although a genetic correlation between two traits may itself be the outcome of natural or sexual selection, it may indirectly reinforce the establishment and maintenance of cline variation with respect to one particular trait when across the cline different values of other traits are selected. Using the barn owl Tyto alba, a species in which the plumage of females is more reddish‐brown and more marked with black spots than that of males, I report results that are consistent with the hypothesis that both direct selection and genetic constraints may help establish and maintain cline variation in sexual dichromatism. In this species, inter‐individual variation in plumage coloration and spottiness has a genetic basis, and these traits are not sensitive to the environment. Data, based on the measurement of skin specimens, is consistent with the hypothesis that the stronger European cline variation in male spottiness than in female spottiness depends on the combined effects of (1) the similar cline variation in male and female plumage coloration and (2) the more intense phenotypic correlation between plumage coloration and spottiness in males (darker birds are more heavily spotted in the two sexes, but especially males) which is a general feature among the globally distributed barn owls. In northern Europe, male and female T. a. guttata are reddish‐brown and heavily spotted, and in southern Europe male and female T. a. alba are white, but only females display many spots. Here, I discuss the relative importance of direct selection, genetic correlation and the post‐ice age invasion of Europe by T. alba, in generating sex‐specific cline variation in plumage spottiness and non‐sex‐specific cline variation in plumage coloration.     

Evolution of a sexually dimorphic trait in a broadly distributed topminnow (Fundulus olivaceus)

Understanding the interaction between sexual and natural selection within variable environments is crucial to our understanding of evolutionary processes. The handicap principle predicts females will prefer males with exaggerated traits provided those traits are indicators of male quality to ensure direct or indirect female benefits. Spatial variability in ecological factors is expected to alter the balance between sexual and natural selection that defines the evolution of such traits. Male and female blackspotted topminnows (Fundulidae: Fundulus olivaceus) display prominent black dorsolateral spots that are variable in number across its broad range. We investigated variability in spot phenotypes at 117 sites across 13 river systems and asked if the trait was sexually dimorphic and positively correlated with measures of fitness (condition and gonadosomatic index [GSI]). Laboratory and mesocosm experiments assessed female mate choice and predation pressure on spot phenotypes. Environmental and community data collected at sampling locations were used to assess predictive models of spot density at the individual, site, and river system level. Greater number of spots was positively correlated with measures of fitness in males. Males with more spots were preferred by females and suffered greater mortality due to predation. Water clarity (turbidity) was the best predictor of spot density on the drainage scale, indicating that sexual and natural selection for the trait may be mediated by local light environments.     

Sex allocation according to multiple sexually dimorphic traits of both parents in the barn swallow (Hirundo rustica)

Parents should differentially invest in sons or daughters depending on the sex‐specific fitness returns from male and female offspring. In species with sexually selected heritable male characters, highly ornamented fathers should overproduce sons, which will be more sexually attractive than sons of less ornamented fathers. Because of genetic correlations between the sexes, females that express traits which are under selection in males should also overproduce sons. However, sex allocation strategies may consist in reaction norms leading to spatiotemporal variation in the association between offspring sex ratio (SR) and parental phenotype. We analysed offspring SR in barn swallows (Hirundo rustica) over 8 years in relation to two sexually dimorphic traits: tail length and melanin‐based ventral plumage coloration. The proportion of sons increased with maternal plumage darkness and paternal tail length, consistently with sexual dimorphism in these traits. The size of the effect of these parental traits on SR was large compared to other studies of offspring SR in birds. Barn swallows thus manipulate offspring SR to overproduce ‘sexy sons’ and potentially to mitigate the costs of intralocus sexually antagonistic selection. Interannual variation in the relationships between offspring SR and parental traits was observed which may suggest phenotypic plasticity in sex allocation and provides a proximate explanation for inconsistent results of studies of sex allocation in relation to sexual ornamentation in birds.     

Female barn owls (Tyto alba) advertise good genes

The good genes hypothesis of sexual selection postulates that ornamentation signals superior genetic quality to potential mates. Support for this hypothesis comes from studies on male ornamentation only, while it remains to be shown that female ornamentation may signal genetic quality as well. Female barn owls (Tyto alba) display more black spots on their plumage than males. The expression of this plumage trait has a genetic basis and it has been suggested that males prefer to mate with females displaying more black spots. Given the role of parasites in the evolution of sexually selected traits and of the immune system in parasite resistance, we hypothesize that the extent of female plumage 'spottiness' reflects immunological defence. We assessed the genetic variation in specific antibody production against a non-pathogenic antigen among cross-fostered nestlings and studied its covariation with the plumage spottiness of genetic parents. The magnitude of the antibody response was positively correlated with the plumage spottiness of the genetic mother but not of the genetic father. Our study thereby provides the first experimental support, to our knowledge, for the hypothesis that female ornamentation signals genetic quality.     

Effect of the MC1R gene on sexual dimorphism in melanin‐based colorations

Variants of the melanocortin‐1 receptor (MC1R) gene result in abrupt, naturally selected colour morphs. These genetic variants may differentially affect sexual dimorphism if one morph is naturally selected in the two sexes but another morph is naturally or sexually selected only in one of the two sexes (e.g. to confer camouflage in reproductive females or confer mating advantage in males). Therefore, the balance between natural and sexual selections can differ between MC1R variants, as suggest studies showing interspecific correlations between sexual dimorphism and the rate of nonsynonymous vs. synonymous amino acid substitutions at the MC1R. Surprisingly, how MC1R is related to within‐species sexual dimorphism, and thereby to sex‐specific selection, has not yet been investigated. We tackled this issue in the barn owl (Tyto alba), a species showing pronounced variation in the degree of reddish pheomelanin‐based coloration and in the number and size of black feather spots. We found that a valine (V)‐to‐isoleucine (I) substitution at position 126 explains up to 30% of the variation in the three melanin‐based colour traits and in feather melanin content. Interestingly, MC1R genotypes also differed in the degree of sexual colour dimorphism, with individuals homozygous for the II MC1R variant being 2 times redder and 2.5 times less sexually dimorphic than homozygous individuals for the VV MC1R variant. These findings support that MC1R interacts with the expression of sexual dimorphism and suggest that a gene with major phenotypic effects and weakly influenced by variation in body condition can participate in sex‐specific selection processes.     

Wing Colour Properties do not Reflect Male Condition in the American Rubyspot (Hetaerina americana)

Adult males of the American rubyspot ( Hetaerina americana ) dispute riverine territories where females arrive to mate. On the wing basis, these males bear a red pigmentation spot whose area correlates with territorial disputes and mating rate: males with larger spots are more successful. This is explained by the fact that spot size correlates with fat muscular reserves which fuel flight during territorial intrusions. To further our understanding of sexual selection acting on the spot, here we have examined possible differences in three spot colour properties (red chroma, hue and brightness) in three distinct adult male ages [young, middle-aged (when males are more likely to defend a territory) and old], social status (territorial and non-territorial in middle-aged males), and under two potentially, energetically and costly situations: when faced with an immune challenge [comparing a nylon-implanted male group vs. a non-implanted male group in two ages, teneral (previous to colour formation) and middle-aged] and low diet levels (comparing a male set of middle-aged animals that received food ad libitum vs. a male set that received no food). Our results indicate no change in colour properties across any of these comparisons. Taken together, these and previous results suggest that only spot size but not the spot characteristics we measured here, is sexually selected in males of this species at least in terms of pre-copulatory male–male competition. That some of these colour properties have been related to male condition in other calopterygid damselflies cannot be generalized to the American rubyspot.     

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.     

Relationship between algal-foraging ability and expression of sexually selected traits in male guppies

In the guppy Poecilia reticulata, males exhibit orange spots on their body and tail, and the orange spot patterns are often criteria for female mate choice. The orange spot coloration of males is determined by the intake of algae, a natural source of carotenoids. Therefore, males exhibiting conspicuous orange coloration are considered to possess high algal-foraging ability. In the present study, we examined the influence of algal-foraging ability, measured by algal-searching ability and algal-foraging frequency, on the expression of orange spot patterns and on other sexually selected traits in male guppies. Males exhibiting better performance in terms of both algal-searching ability and algal-foraging frequency grew larger. The size of the orange spots on males also increased with algal-foraging ability. However, neither algal-searching ability nor algal-foraging frequency influenced the coloration of the orange spots. In this experiment, a limited supply of carotenoids possibly prevented the males from completely developing their spots to the intrinsic size. The results of this study suggest that in male guppies under a carotenoid-limited situation, the allocation of carotenoids is directed toward enlargement of the size of the orange spots rather than enhancement of their coloration. Since both the body size and orange spot patterns of males contribute to their sexual attractiveness to females, high algal-foraging ability may enhance their mating success.     

Sexy Faces in a Male Paper Wasp

Sexually selected signals are common in many animals, though little reported in social insects. We investigated the occurrence of male visual signals mediating the dominance relationships among males and female choice of sexual partner in the paper wasp Polistes simillimus. Males have three conspicuous, variable and sexually dimorphic traits: black pigmentation on the head, a pair of yellow abdominal spots and body size differences. By conducting behavioral assays, we found that none of the three visual traits are associated with male-male dominance relationship. However, males with higher proportion of black facial pigmentation and bigger yellow abdominal spots are more likely chosen as sexual partners. Also, after experimentally manipulating the proportion of black pigment on males'' face, we found that females may evaluate male facial coloration during the choice of a sexual partner. Thus, the black pigmentation on P. simillimus male''s head appears to play a role as a sexually selected visual signal. We suggest that sexual selection is a common force in Polistes and we highlight the importance of this group as a model for the study of visual communication in insects.     

Uninformative exaggeration of male sexual ornaments in barn swallows

Models of sexual selection suggest that mate-choice preferences are favored because differences between males in their degree of ornamental exaggeration convey useful information about the direct or indirect benefits they have to offer [1-5]. Such arguments assume that variation in male ornament size can be attributed to variation in the degree of sexually selected exaggeration. We provide the first test of this assumption by conducting tail-length experiments in male barn swallows. Over the last twenty years, a large amount of work has shown that female barn swallows are influenced by male tail length when choosing a mate [6-12]. Recent experiments have shown that a combination of natural and sexual selection results in the elongated tail streamer--a tail that is on average across the population about 12 mm (approximately 10%) longer than the aerodynamic optimum [13, 14]. We show that the aerodynamically optimal tail length varies significantly between males, whereas the extent of streamer elongation beyond the optimum does not. Similarly, the aerodynamically optimal tail length significantly predicts observed tail length and conveys information about flight performance, whereas the extent of sexually selected exaggeration of streamer length does not. Therefore, contrary to handicap models of sexual selection, the sexually selected exaggeration of this trait provides females with little information about any aspect of mate quality     

Seasonal changes in male and female bill knob size in the mute swan Cygnus olor

Sexual selection theory predicts that sexually selected ornaments are costly to maintain and, as condition-dependent signals, are likely to vary in attractiveness with season and age. Mute swans Cygnus olor possess a black, fleshy knob at the base of the bill, which is present in both sexes. Using measures calculated from digital photographs taken over two years we monitored changes in the size of the bill knob in individual swans throughout the breeding season. Our longitudinal data show that bill knob size is highly dynamic. Relative bill knob size was larger in males than females and was consistently greater for breeding males than for non-breeders. For males, relative bill knob size peaked during cygnet hatching, when male protection of the brood is most important, and was smallest during moult. In females, breeders had larger bill knobs than non-breeders at all times apart from immediately after egg-laying and incubation, when the reverse was true, presumably reflecting the costs of reproduction. Body mass was a highly significant predictor of relative bill knob size in both sexes, as was age, with an initial increase and then later a decline in relative ornament size across the lifetime of male birds. The bill knob ornament in mute swans thus appears to be a condition-dependent, highly malleable trait. It accurately reflects the differing pressures experienced by individual birds as they progress through the breeding season, suggesting selection by both intra- and inter-sexual forces.     

Egg Mimics in Haplochromine Cichlids (Pisces,Perciformes) from Lake Victoria

An ecomorphological explanation is given of the anal spots of haplochromine cichlids from Lake Victoria. Anal spots are ovoid orange-yellow spots on the anal fins of these fishes. The possible roles of sexual selection and predation as determinants of the form of these spots are discussed. Evidence is given that the anal spots are egg mimics and thus examples of intra-specific mimicry. Mimicking an egg to stimulate sexually active females presumably is an important demand on the form of the anal spots. However, no positive correlation was found between anal spot size and egg size. Light intensities of the habitat of the species investigated showed a negative correlation with anal spot size. In contrast to this, egg size did not show a negative correlation with light intensities. It is suggested that, besides mimicry, at least one more demand is involved in determining spot size: that of being conspicuous. Conspicuousness is likely to have a positive impact (benefits) on courting conspecific females, but a negative one (costs) with regard to predators who hunt visually for either adults or eggs. The actual appearance of anal spots may be a compromise. This may explain the mismatch between egg size and spot size in many species. Qualitative evidence is presented that predation pressures on adult haplochromines exerted by visually hunting predators are relatively high in lighter habitats, viz. near the rocks and near the surface. An alternative hypothesis that spots in dark surroundings cannot be seen unless they are supra-normal is discussed.     

Sex‐ and age‐dependent morphology and selection on wing shape in the barn swallow Hirundo rustica

Wings have evolved in phylogenetically distant organisms with morphologies that depend on the combined effects of diverse, potentially contrasting selective forces. In birds, long pointed wings boost speed and energetic efficiency during cruising flight but reduce manoeuvrability. Migratory behavior is believed to lead to the evolution of more pointed wings, but selection on pointedness has never been estimated. Because annual routines of migrants are tightly scheduled, wing pointedness may be selected for because it allows for earlier arrival to the breeding grounds. In long‐distance migratory barn swallows Hirundo rustica we showed that selection via breeding date and thus annual fecundity operates on wing pointedness, but not on other wing traits, among yearling females but not among older females or males. Selection on wing pointedness specifically in yearling females may result from climatic effects, which favour earlier arrival from migration, and from yearling females being the sex‐by‐age class with the latest migration and the smallest wing pointedness. Wing morphology differed between sexes and age classes because of change in size of the outermost but not the innermost wing feathers. Hence, sex‐ and age‐specific selection on wing pointedness operates in a species with sex‐ and age‐dependent variation in phenology and wing morphology.     

Males with a Faster Courtship Display have More White Spots and Higher Pairing Success in the Diamond Firetail,Stagonopleura guttata

There is growing evidence that female mate choice could be based on a combination of multiple signals that often involve both ornamental colourful traits and behavioural displays. The Diamond Firetail is an Australian finch with a variable number of white spots on their black flank feathers. The number of white spots is a dimorphic characteristic: females have more spots than males, and males prefer females with many spots. Previously, we found assortative pairing for spot number despite the absence of experimental evidence for female preference for male spot number. Here, we test whether the male behavioural courtship display (bobbing while waving a grass stem) correlates with male spot number and pairing success. We also test whether male spot number predicts the outcome (winner or loser) of intrasexual competition over courtship materials (grass stem, perch, nest site). Males with many spots had higher pairing success, and male spot number correlated with the intensity of courtship display. In a multivariate statistical analysis, male courtship display was the stronger predictor of male pairing success. Finally, male spot number predicted the outcome of intrasexual interactions: males with many spots consistently won contests over grass stems, perches and nest sites. We suggest that intrasexual selection could favour male spot number, whereas courtship intensity appears to be under stronger intersexual selection.     

Ornaments or offspring: costs to reproductive success restrict sexual selection processes

If, in their partner choice, males seek direct benefits (fecund females), the result will be selection for traits indicating female quality rather than for arbitrary (Fisherian) traits. However, the costs of developing and maintaining the sexually selected traits (ornaments) may reduce the resources available to the female for allocation to reproduction and hence result in lower reproductive success per brood. This hitherto unrecognized fecundity cost of sexually selected traits will constrain both the potency of sexual selection mechanisms and the degree of elaboration of sexually selected traits in females, and can also apply to males which invest in their offspring: sexual selection becomes self-limiting. The fitness implications of these costs are examined for both sexes in a variety of mating and parental care patterns. Sexual selection acting on both sexes may lead to either dimorphism or monomorphism, the latter being the case when the quality indicators chosen by both sexes coincide. Ways of evasion or reduction of these reproductive costs of allocations to sexually selected traits include using different resource components for the ornament and for reproduction, or partitioning the two allocations in time.     

Sperm competition and sexually size dimorphic brains in birds

Natural selection may favour sexually similar brain size owing to similar selection pressures in males and females, while sexual selection may lead to sexually dimorphic brains. For example, sperm competition involves clear-cut sex differences in behaviour, as males display, mate guard and copulate with females, while females choose among males, and solicit or reject copulations. These behaviours may require fundamentally different neural government in the two sexes leading to sex-dependent brain evolution. Using two phylogenetic approaches in a comparative study, we tested for roles of both natural and sexual-selection pressures on brain size evolution of birds. In accordance with the natural-selection theory, relative brain size of males coevolved with that of females, which may be the result of adaptation to similar environmental constraints such as feeding innovation. However, the mode of brain size evolution differed between the sexes, and factors associated with sperm competition as reflected by extra-pair paternity may give rise to sexually size dimorphic brains. Specifically, species in which females have larger brains than males were found to have a higher degree of extra-pair paternity independently of potentially confounding factors, whereas species in which males have relatively larger brains than females appeared to have lower rates of extra-pair paternity. Hence, the evolution of sperm competition may select for complex behaviours together with the associated neural substrates in the sex that has a higher potential to control extra-pair copulations at the observed levels. Brain function may thus be affected differently in males and females by sexual selection.     

Age‐related change in melanin‐based coloration of Barn owls (Tyto alba): females that become more female‐like and males that become more male‐like perform better

Ornament expression fluctuates with age in many organisms. Whether these changes are adaptively plastic is poorly known. In order to understand the ultimate function of melanin‐based ornaments, we studied their within‐individual fluctuations and their covariation with fitness‐related traits. In barn owls (Tyto alba), individuals vary from reddish‐brown pheomelanic to white, and from immaculate to marked with black eumelanic spots, with males being less reddish and less spotted than females. During the first molt, both sexes became less pheomelanic, females displayed larger spots and males fewer spots, but the extent of these changes was not associated with reproduction. At subsequent molts, intra‐individual changes in melanin‐based traits covaried with simultaneous reproduction changes. Adult females bred earlier in the season and laid larger eggs when they became scattered with larger spots, whereas adults of both sexes produced larger broods when they became whiter. These results suggest that the production of melanin pigments and fitness‐related life‐history traits are concomitantly regulated in a sex‐specific way. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 101 , 689–704.