A small badge of longevity: opposing survival selection on the size of white and black wing markings

According to handicap principle, exaggerated ornamental traits are supposed to exert costs on their bearers. However, there is much less theoretical and practical consensus about whether and under which conditions ornament expression should positively correlate with survival. We measured age‐related variation and survival selection on the size of white wing patches and black wing tips in a long‐lived monogamous seabird, the common gull Larus canus. Males had larger white patches than females but patch size showed concave relationship with age irrespective of sex, suggesting that white patch size was prone to senescence in both sexes. Extent of wing tip abrasion correlated negatively with the size of white patch, suggesting, in agreement with the Zahavian handicap hypothesis that only individuals with largest ornaments are able of maintaining them and not paying cost of displaying them. Areas of white wing patches and black wing tips correlated negatively. Irrespective of sex, survival selection favored birds with larger white wing patches and smaller black wing tips, which suggests that white and black wing markings may have coevolved as reverse components of a single ornament. Altogether, our results provide an evidence for the case where survival selection on ornamental traits in females is not weaker than in males. Absence of sex differences with respect to most of observed patterns is consistent with a prediction that among monogamous long‐lived species with biparental care, mutual mate choice leads to evolution of elaborate ornamental traits in both sexes.     

Moult strategies in the Common Whitethroat Sylvia c. communis in northern Nigeria

Moult strategies in the Common Whitethroat Sylvia c. communis trapped in northern Nigeria in April 1999 are analysed. Differences in the extent of moult between age and sex classes are presented. The secondary moult of adult birds is considered to belong to a new pre-breeding moult or an arrested moult, beginning at the normal starting positions on the wing, and not as a continuation of a suspended post-breeding moult. Eccentric moult of primaries was found in nearly 19% of the yearling birds, a pattern that is unusual for Western Palearctic passerines. Some individuals showed resemblance to the split moult pattern described for the Barred Warbler S. nisoria .     

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.     

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.     

Multitrait aposematic signal in Batesian mimicry

Batesian mimics can parasitize Müllerian mimicry rings mimicking the warning color signal. The evolutionary success of Batesian mimics can increase adding complexity to the signal by behavioral and locomotor mimicry. We investigated three fundamental morphological and locomotor traits in a Neotropical mimicry ring based on Ithomiini butterflies and parasitized by Polythoridae damselflies: wing color, wing shape, and flight style. The study species have wings with a subapical white patch, considered the aposematic signal, and a more apical black patch. The main predators are VS‐birds, visually more sensitive to violet than to ultraviolet wavelengths (UVS‐birds). The white patches, compared to the black patches, were closer in the bird color space, with higher overlap for VS‐birds than for UVS‐birds. Using a discriminability index for bird vision, the white patches were more similar between the mimics and the model than the black patches. The wing shape of the mimics was closer to the model in the morphospace, compared to other outgroup damselflies. The wing‐beat frequency was similar among mimics and the model, and different from another outgroup damselfly. Multitrait aposematic signals involving morphology and locomotion may favor the evolution of mimicry rings and the success of Batesian mimics by improving signal effectiveness toward predators.     

Thermal impact of migrating birds’ wing color on their flight performance: Possibility of new generation of biologically inspired drones

The thermal impact of the birds’ color on their flight performance are investigated. In most of the large migrating birds, the top of their wings is black. Considering this natural phenomenon in the migrating birds, such as albatross, a thermal analysis of the boundary layer of their wings is performed during the year depending on the solar insulation. It is shown that the temperature difference between the bright and dark colored top wing surface is around 10 °C. The dark color on the top of the wing increases the temperature of the boundary layer over the wing which consequently reduces the skin drag force over the wing. This reduction in the drag force can be considered as one of the effective factors for long endurance of these migrating birds. This research should lead to improved designs of the drones by applying the inspired colors which can help drones increase their endurance.     

Avian brachial index and wing kinematics: putting movement back into bones

The relationship between wing kinematics, wing morphology and the brachial index of birds (BI=humerus length/ulna length) was examined. BI was found to differ between three groups of birds, which were classified on the basis of similar wing kinematics. In addition, a comparative analysis of a large dataset, using phylogenetically independent contrasts, suggested a significant, albeit weak, correlation between BI and four measures of wing morphology (wing loading, wing area, wing length and aspect ratio). Although wing kinematics and wing morphology are both correlated with BI in birds, the dominant selective pressure upon this ratio is probably wing kinematics. The previously identified clade specificity of BI within Neornithes is most likely because birds with similar BIs fly with kinematic similarity and closely related birds have similar flight styles. A correlation between BI and wing kinematics means that it may be possible to characterize the wing beat of fossil birds. A more robust relationship between wing morphology and BI may emerge, but only after the relationship between wing kinematics and BI is quantified. A comparative and quantitative study of wing-bone anatomy and wing kinematics is a priority for future studies of avian wing-skeleton evolution and functional morphology.     

HOW TO COMPENSATE FOR COSTLY SEXUALLY SELECTED TAILS: THE ORIGIN OF SEXUALLY DIMORPHIC WINGS IN LONG-TAILED BIRDS

Recent work on birds suggests that certain morphological differences between the sexes may have evolved as an indirect consequence of sexual selection because they offset the cost of bearing extravagant ornaments used for fighting or mate attraction. For example, long-tailed male sunbirds and widowbirds also have longer wings than females, perhaps to compensate for the aerodynamic costs of tail elaboration. We used comparative data from 57 species to investigate whether this link between sexual dimorphism in wing and tail length is widespread among long-tailed birds. We found that within long-tailed families, variation in the extent of tail dimorphism was associated with corresponding variation in wing dimorphism. One nonfunctional explanation of this result is simply that the growth of wings and tails is controlled by a common developmental mechanism, such that long-tailed individuals inevitably grow long wings as well. However, this hypothesis cannot account for a second pattern in our data set: as predicted by aerodynamic theory, we found that, comparing across long-tailed families, sexual dimorphism in wing length varied with tail shape as well as with sex differences in tail length. Thus, wing dimorphism was generally greater in species with aerodynamically costly graduated tails than in birds with cheaper, streamer-shaped tails. This result was not caused by confounding phylogenetic effects, because it persisted when phylogeny was controlled for, using an independent comparisons method. Our findings therefore confirm that certain aspects of sexual dimorphism may sometimes have evolved through selection for traits that reduce the costs of elaborate sexually selected characters. We suggest that future work aimed at understanding sexual selection by investigating patterns of sexual dimorphism should attempt to differentiate between the direct and indirect consequences of sexual selection.     

Adaptive benefits of differential post-fledging development patterns in the Lesser Flamingo (Phoenicopterus minor)

Measurements of five morphological components (mass, skull length, culmen, flattened wing and tarsus) and blood samples were taken from 154 fledged wild Lesser Flamingos Phoenicopterus minor captured during 2001 and 2002 at Lake Bogoria, Kenya (0°11'–20'N, 036°06'E). The sample included adults (>3 years old), immature birds (2–3 years old) and first-year juvenile birds of both sexes. The sex of each bird was determined by PCR amplification of the CHD-Z and CHD-W genes, using DNA extracted from blood samples. Within each gender, there were significant differences in mass and tarsus length amongst the three age groups, indicating that the skeletal size and mass of Lesser Flamingos continue to increase between fledging and attainment of adult plumage at three to four years of age. The different morphological components increased in size at different rates, although the same components appeared to increase at similar rates in both males and females. Skull and culmen lengths had reached adult size in juvenile birds, while juvenile wing length, tarsus length and mass were approximately 95%, 85% and 75% of adult size, respectively. The adaptive significance of these findings is discussed.     

Sexual size dimorphism and morphometric sexing in a North African population of Laughing Doves Spilopelia senegalensis

Like the majority of Columbiformes, the Laughing Dove Spilopelia senegalensis is sexually monomorphic in plumage, but seems to be slightly dimorphic in size. However, due to the lack of studies little is known about the sexual size dimorphism in this species. In this work, we used morphometric data on a sample of 61 Laughing Doves from southern Tunisia, and sexed using a DNA-based method, to assess size differences between males and females and to determine a discriminant function useful for sex identification. The results showed that wing length was the most dimorphic trait, which could be due to the effects of sexual selection. The best function for the discrimination between sexes included wing length and head length, which is comparable with findings on other dove species. This discriminant function accurately classified 89% of birds, providing a rapid and accurate tool for sex identification in the studied population. Further data from different populations are needed for firmer conclusions about the extent of sexual size dimorphism and the reliability of the morphometric sexing approach in this dove species.     

Do Embedded Shotgun Pellets Have a Chronic Effect on Body Condition of Pink-Footed Geese?

Abstract: Hunting with shotguns inevitably causes wounding of game that are hit by pellets but not retrieved by the hunter. We examined the effects of pellets on body condition in a total of 2,164 pink-footed geese (Anser brachyrhynchus) that were captured by cannon-nets, x-rayed, and banded with neck collars after the closure of the hunting season in Denmark. All geese were sexed, aged, weighed, and wing lengths measured. In the overall material, 23.8% and 11.6% of adults and first-winter birds, respectively, carried pellets outside the gizzard. We derived an index of the body condition of individual birds as the residuals of linear regression of log-transformed wing length and weight. Statistical analyses showed a highly significant relationship between body condition, sex, and year, whereas number of pellets was not significantly related to body condition. The results suggest that geese that have been hit by shotgun pellets but have survived the hunting season, so-called lightly crippled individuals, are not injured to an extent to have detectable chronic effects.     

The Role of Wing Coloration in Sex Recognition and Competitor Recognition in Rubyspot Damselflies (Hetaerina spp.)

The decision rules that animals use for distinguishing between conspecifics of different age and sex classes are relevant for understanding how closely related species interact in sympatry. In rubyspot damselflies (Hetaerina spp.), the red wing coloration of mature males is hypothesized to be a key trait for sex recognition and competitor recognition within species and the proximate trigger for interspecific male–male aggression. We tested this hypothesis by manipulating the wing coloration of tethered conspecific intruders and measuring the responses of territory holders of three species in the field. As predicted, covering the red spots of mature males with black ink nearly eliminated territorial responses, and in some cases, territorial holders clasped the blackened males as if they were females. Adding red spots to female wings triggered territorial responses and nearly eliminated sexual responses. Immature males with artificial red spots were attacked at the same rate as mature male intruders, and much more frequently than were immature male controls. The results varied somewhat by species. In H. titia, the only species of Hetaerina with substantial black wing pigmentation, the effects of blackening the red spots of intruders varied both geographically and seasonally. But even when blackening the red spots of male intruders did not reduce the aggressive response of H. titia territory holders, adding artificial red spots to female wings elicited aggressive responses and nearly eliminated sexual responses. The results of this study further strengthen the evidence that interspecific aggression in Hetaerina results from overlap in territorial signals and that the derived black wing pigmentation of H. titia reduces interspecific aggression.     

Changes in age and sex ratios amongst samples of hunter-shot wings from common duck species in Denmark 1982–2010

There are almost no long-term demographic monitoring programmes of commoner waterbird species, yet such data are fundamental to our understanding of drivers of population change. In the present study, we present annual age and sex ratios in samples of shot duck wings forwarded on a voluntary basis by hunters throughout Denmark from 1982 to 2010 for eight common quarry species. Wigeon, Shoveler, Pintail and Goldeneye showed statistically significant declines in the proportions of young birds in the samples, but only Wigeon showed a statistically significant decline in the proportion of females in the adult sample over this period. Amongst Wigeon, the proportions of first winter birds and females were lower amongst the sample shot over decoys compared with those shot without decoys, suggesting these two shooting methods differentially select for young birds and females. However, the slopes of declines in these proportions shot with and without decoys over time did not differ. We found no correlations between North Atlantic Oscillation index values and the proportions of young for any of the species or between May and June temperatures on the breeding areas of Wigeon and the proportions of young in samples derived the following winter. With the exception of Wigeon, little is known about how well the shot duck wing samples reflect the true ratios in the populations, and unravelling the error and bias associated with these samples remains a high future research priority. If long-term declines in age and sex ratio in the wing surveys reflect true trends in the Wigeon population as a whole, we have strong grounds for concern for this population, and effort should be invested in increased demographic surveillance to better understand the causes of these changes. We need improved methods to derive unbiased measures of annual breeding of our common duck species if we are to be better able to understand the population dynamics of these stocks and be effective in their management. In the meantime, the Danish wing survey represents a unique time series of reproductive success for many common migratory duck species and must be maintained and further exploited.     

Identification and sex determination of Bicknell's Thrushes using morphometric data

ABSTRACT The similar plumage of Bicknell's (Catharus bicknelli) and Gray‐cheeked (C. minimus) Thrushes have hindered attempts to better understand the nonbreeding biology of these species. We used morphometric data, specifically primary formulae, from Bicknell's Thrushes of known sex and age throughout their breeding range in the United States and Canada to examine possible differences between sex and age classes. We compared these data with similar data from Gray‐cheeked Thrushes in Alaska, United States and Newfoundland, Canada to examine mensural characters for distinguishing the two species. We performed a discriminant function analysis (DFA) for each age class to examine morphometric differences between male and female Bicknell's Thrushes. For second‐year (SY) and after‐second‐year (ASY) birds, wing chord was the strongest differentiator, in conjunction with tarsus length. Wing chord and tail length were used to create a discriminant function to differentiate between the two Catharus species. The discriminant functions for both age classes did not permit unambiguous separation of male and female Bicknell's Thrushes nor did the DFA enable unequivocal species identity, but most individuals were correctly classified. Significant differences in the p8–p1 measurement of Bicknell's and Gray‐cheeked Thrushes and of male and female Bicknell's Thrushes suggest that this character may be useful to augment published wing chord criteria for species identification and sex determination. Our results indicate that wing chord, in combination with tail length, is the most useful measurement for distinguishing Bicknell's from Gray‐cheeked Thrushes and, when augmented with tarsus length, to differentiate between male and female Bicknell's Thrushes outside the breeding season.     

Winter body condition in relation to age,sex and plumage ornamentation in a migratory songbird

Winter body condition may play important roles in the life history of migratory birds, but it is difficult to estimate. We used the growth rate of winter‐grown tail feathers of Collared Flycatchers Ficedula albicollis as an indicator of winter body condition, comparing this trait between age classes and sexes and relating it to plumage ornamentation (forehead and wing patch sizes). Adults and males were in better nutritional condition during winter, as indicated by their faster tail feather growth rates, than were yearlings and females, respectively, which could indicate differences in individual quality and foraging ability with age, or age‐ and sex‐related winter habitat segregation. However, feather growth rate was related neither to the size of the winter‐grown forehead patch nor to the size of the summer‐grown wing patch, suggesting weak condition‐dependence for the winter‐grown ornament and complex life‐history consequences for the summer‐grown ornament.     

The redder the better: wing color predicts flight performance in monarch butterflies

The distinctive orange and black wings of monarchs (Danaus plexippus) have long been known to advertise their bitter taste and toxicity to potential predators. Recent work also showed that both the orange and black coloration of this species can vary in response to individual-level and environmental factors. Here we examine the relationship between wing color and flight performance in captive-reared monarchs using a tethered flight mill apparatus to quantify butterfly flight speed, duration and distance. In three different experiments (totaling 121 individuals) we used image analysis to measure body size and four wing traits among newly-emerged butterflies prior to flight trials: wing area, aspect ratio (length/width), melanism, and orange hue. Results showed that monarchs with darker orange (approaching red) wings flew longer distances than those with lighter orange wings in analyses that controlled for sex and other morphometric traits. This finding is consistent with past work showing that among wild monarchs, those sampled during the fall migration are darker in hue (redder) than non-migratory monarchs. Together, these results suggest that pigment deposition onto wing scales during metamorphosis could be linked with traits that influence flight, such as thorax muscle size, energy storage or metabolism. Our results reinforce an association between wing color and flight performance in insects that is suggested by past studies of wing melansim and seasonal polyphenism, and provide an important starting point for work focused on mechanistic links between insect movement and color.     

Sex and environmental sensitivity in blue tit nestlings

In birds and mammals with sexual size dimorphism (SSD), the larger sex is typically more sensitive to adverse environmental conditions, such as food shortage, during ontogeny. However, some recent studies of altricial birds have found that the larger sex is less sensitive, apparently because large size renders an advantage in sibling competition. Still, this effect is not an inevitable outcome of sibling competition, because several studies of other species of altricial birds have found the traditional pattern. We investigated if the sexes differ in environmental sensitivity during ontogeny in the blue tit, a small altricial bird with c. 6% SSD in body mass (males larger than females). We performed a cross-fostering and brood size manipulation experiment during 2 years to investigate if the sexes were differently affected as regards body size (body mass, tarsus and wing length on day 14 after hatching) and pre-fledging survival. We also investigated if the relationship between body size and post-fledging survival differed between the sexes. Pre-fledging mortality was higher in enlarged than in reduced broods, representing poor and good environments, respectively, but the brood size manipulation did not affect the mortality rate of males and females differently. In both years, both males and females were smaller on day 14 after hatching in enlarged as compared to reduced broods. In one of the years, we also found significant Sex × Experiment interactions for body size, such that females were more affected by poor environmental conditions than that of males. Body size was positively correlated with post-fledging survival, but we found no interactive effects of sex and morphological traits on survival. We conclude that in the blue tit, females (the smaller sex) are more sensitive to adverse environmental conditions which, in our study, was manifest in terms of fledgling size. A review of published studies of sex differences in environmental sensitivity in sexually size-dimorphic altricial birds suggests that the smaller sex is more sensitive than the larger sex in species with large brood size and vice versa.     

Female wing plumage reflects reproductive success in Common Goldeneye Bucephala clangula

Recent studies on the function of female plumage characteristics have yielded ambiguous results. Some studies have found an association between different physiological, ecological or behavioural traits and female plumage, while others have found no association and interpret female plumage as neutral in function. We observed a high variance among females in both wing plumage and breeding success in female Common Goldeneyes Bucephala clangula , a sexually plumage-dimorphic diving duck. We studied the association between female wing plumage and hatching date. Principal component analysis of four wing patch area measurements derived a single factor describing wing plumage. Wing plumage was strongly associated with hatching date, which is the most important determinant of goldeneye recruit production; irrespective of age, females with more white in the wing bred earlier than individuals with more black in the wing. We propose that the wing pattern in Common Goldeneye females reflects individual quality.     

Ecological implications of the correlation of avian footprints with wing characteristics: a mathematical approach

The characteristics of avian wings that evolved for flying appear to show a distinct relationship to the shape of the pes and walking abilities as reflected in footprints. Wing area, wing span and body weight data of modern birds were collected and analysed in order to quantify the possible correlation, which was previously only inferred from empirical data. Discriminant analysis demonstrated that avian wings can be divided into three habitat groups, in a similar way to footprints. Multiple regression analyses revealed that the avian wing loading and aspect ratio were correlated with the parameters of footprint shape and can be expressed by a simple equation. The results may reflect the adaptation of avian locomotion to habitat. The relationships between wing area and wing span, and between wing area and footprint area, which are apparent in modern avians, were derived and used to estimate wing area and wing span from the footprints of extinct Cretaceous avian taxa. The estimated values of body weight, wing span and wing area suggest that the trackmakers of Archaeornithipus meijidei, Hwangsanipes choughi and Yacoraitichnus avis had bodies similar to herons (or cranes), large sandpipers (or small sea birds) and medium‐sized gull‐like birds, respectively.     

Do migrant birds have more pointed wings?: A comparative study

Summary Do birds that migrate over longer distances have more pointed wings than more sedentary birds? Within several bird genera, species differ considerably in their migration distances. This makes it possible to study the extent to which different taxa show similar morphological solutions to common selection pressures. I selected 14 species, two from each of seven passerine genera, to maximize within-genus differences in migration distance. Wing lengths and the lengths of eight primary feathers around the wing tip were measured to assess wing length and shape. Primary lengths were transformed to take into account the allometric relationship between the length of each feather and wing length and then collapsed into summary measures of shape by principal component analysis. I used the method of independent contrasts to address the effects of phylogeny. Wing length showed no relationship with migration distance. There was a correlation between migration distance and wing shape. It is concluded that long-distance migration has resulted in convergent morphological evolution of long distal and short proximal primaries, resulting in wing tips close to the leading edge of the wing.