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Plumage
Terms modified by Plumage Selected AbstractsPlumage-based phylogenetic analyses of the Merops bee-eatersIBIS, Issue 3 2004D. BRENT BURT I review previous systematic work on the family Meropidae and present phylogenetic hypotheses derived from my analyses of colour, pattern and shape variation in 30 plumage regions among species and subspecies in this family. Consistent patterns are seen across shallow portions of the trees. Uncertainty remains concerning the placement of several deep branches within this group's phylogeny. In particular, the phylogenetic placement of Meropogon forsteni and Merops breweri, M. ornatus, M. hirundineus and M. boehmi remains uncertain. The biogeographical patterns in the resultant trees are similar with either a Southeast Asian or African origin for the family, with most of the early diversification occurring in Africa, and with multiple independent subsequent invasions of non-African areas. [source] Influence of ambient light on the evolution of colour signals: comparative analysis of a Neotropical rainforest bird communityECOLOGY LETTERS, Issue 4 2004Doris Gomez Abstract Rainforests offer two contrasted light environments: a bright canopy rich in blue and UV and a dark understorey, rich in green and orange. Therefore, natural selection for crypsis should favour dark brown signals in understorey and bright green signals in canopy, whereas sexual selection for conspicuousness should favour bright yellow-red signals in understorey and dark blue and UV signals in canopy. Using spectrometry and comparative analyses, we examined the relationship between ambient light and colour signals in a bird community of French Guiana. It appears that brightness and hue are mostly naturally selected, while UV content of plumage is more likely sexually selected. At each height, both sexes present similar coloration but males display more conspicuous sexually selected patterns than females. These results show that ambient light drives the evolution of colour signals at community scale, and should be considered when studying signalling in other communities and light-contrasted ecosystems. [source] The effects of polychlorinated biphenyls (Aroclor 1242) on thyroxine, estradiol, molt, and plumage characteristics in the American kestrel (Falco sparverius)ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 7 2002Michael J. Quinn Jr. Abstract The purpose of this experiment was to determine the effects of Aroclor 1242, a mixture of polychlorinated biphenyls (PCBs), on plumage characteristics and molt in the American kestrel, Falco sparverius. Several characteristics of plumage, including color and molt schedule, are modulated by hormonal signals and hence may be modified by endocrine-active contaminants. If so, the functions of plumage (e.g., communication for mating or territorial defense) may be compromised by exposure to such compounds. Captive American kestrels were fed Aroclor 1242 at 0, 6.0, and 60.0 ppm (n = 6 males and 6 females per treatment) mixed in their normal diet. Concentrations of plasma estradiol and thyroxine were measured weekly from the beginning of treatment. Measured plumage characteristics included width of the black subterminal band on the tail, color (a composite index of hue and saturation), reflectance from 230 to 800 nm, pattern of feather loss and regrowth on the tail and wing, and timing of onset and duration of molt. Aroclor 1242 depressed plasma thyroxine. Plasma estradiol levels remained low due to the phase of the breeding cycle. Treatments did not disrupt the measured plumage characteristics. This may be due to timing or dose of exposure or to genetic factors. [source] Is Preening Behaviour Sexually Selected?ETHOLOGY, Issue 12 2006An Experimental Approach Elaborate or colourful feathers are important traits in female mate choice in birds but little attention has been given to potential costs of maintaining these traits in good condition with preening behaviour. Recent studies indicate that the time and energy required to maintain ornamental plumage in good condition reinforces the honesty of plumage trait. It has been proposed that some behaviours, whose primary function is not to transfer information, can also evolve as signalling components. Here we investigate whether the preening behaviour intensity has a signalling component: we hypothesized that if only high quality males can invest a lot of time in preening, this behaviour may be used by females as a quality signal (attractive preening hypothesis). We tested this hypothesis by using female budgerigars in mate-choice tests in captivity. We tried to experimentally manipulate the preening behaviour of two groups of budgerigar males (treatment and control group). The proportion of time in which treated males preened in front of females was statistically higher than for control males, however, females spent similar amounts of time with treated males and control males. Moreover, males did not show significant quantitative changes in preening (for both groups) when females were present, suggesting that male budgerigars did not use this behaviour to convey information. These results are inconsistent with the ,attractive preening' hypothesis which predicts that preening behaviour itself provides information on condition and is used in female choice. [source] Achromatic Plumage Reflectance, Social Dominance and Female Mate Preference in Black-Capped Chickadees (Poecile atricapillus)ETHOLOGY, Issue 10 2005Elisabeth A. Woodcock Individual variation in achromatic plumage reflectance of male Black-capped Chickadees (Poecile atricapillus) is correlated with social rank and reproductive success, suggesting it may play an important role in sexual signaling. We asked whether female chickadees could assess male quality based on plumage, in the absence of information about relative social dominance. Sexually mature but inexperienced females captured during the pair formation period in late fall and early winter were presented with a choice of two unfamiliar, sexually experienced males in separate compartments of an outdoor mate choice arena. Following each preference trial, we released the males into a single compartment and scored their pairwise dominance interactions. In 10 of 11 trials, females spent significantly more time with the male subsequently identified as dominant, despite not witnessing the males interact. Spectral analysis of male plumage reflectance revealed that UV-chroma of dark body regions (bib, cap and mantle) was significantly greater in dominant, preferred males and that dominant, preferred males had significantly brighter white cheek patches. There were no differences in vocalization rates of preferred and non-preferred males. These results show that female chickadees can rapidly assess unfamiliar males based on visual cues, and suggest that variation in achromatic plumage functions in sexual signaling. [source] Multiple Ornaments in Male Northern Cardinals, Cardinalis cardinalis, as Indicators of ConditionETHOLOGY, Issue 2 2004Jodie M. Jawor Investigations of male ornaments in the context of sexual selection have tended to focus on single ornaments, although many species of birds possess multiple ornaments. Understanding the evolution of multiple ornaments requires knowledge of correlations among ornaments in the same individual and the extent to which ornament expression reflects individual condition and behavior. Variation in four male ornaments in socially monogamous, biparental northern cardinals (Cardinalis cardinalis) was related to body size, indices of condition, level of paternal care, and reproductive success. Redness of breast plumage positively predicted body size and negatively predicted nestling feeding rate. Bill color predicted current body condition, with birds with redder bills in better condition. Birds with smaller black face masks had greater reproductive success. These results are consistent with the hypothesis that different ornaments in male cardinals provide information on different aspects of condition and behavior. [source] CORRELATED EVOLUTION OF MIGRATION AND SEXUAL DICHROMATISM IN THE NEW WORLD ORIOLES (ICTERUS)EVOLUTION, Issue 12 2009Nicholas R. Friedman The evolution of sexual dimorphism has long been attributed to sexual selection, specifically as it would drive repeated gains of elaborate male traits. In contrast to this pattern, New World oriole species all exhibit elaborate male plumage, and the repeated gains of sexual dichromatism observed in the genus are due to losses of female elaboration. Interestingly, most sexually dichromatic orioles belong to migratory or temperate-breeding clades. Using character scoring and ancestral state reconstructions from two recent studies in Icterus, we tested a hypothesis of correlated evolution between migration and sexual dichromatism. We employed two discrete phylogenetic comparative approaches: the concentrated changes test and Pagel's discrete likelihood test. Our results show that the evolution of these traits is significantly correlated (CCT: uncorrected P < 0.05; ML: LRT = 12.470, P < 0.005). Indeed, our best model of character evolution suggests that gains of sexual dichromatism are 23 times more likely to occur in migratory taxa. This study demonstrates that a life-history trait with no direct relationship with sexual selection has a strong influence on the evolution of sexual dichromatism. We recommend that researchers further investigate the role of selection on elaborate female traits in the evolution of sexual dimorphism. [source] RECONSTRUCTING PLUMAGE EVOLUTION IN ORIOLES (ICTERUS): REPEATED CONVERGENCE AND REVERSAL IN PATTERNSEVOLUTION, Issue 6 2000Kevin E. Omland Abstract. Several empirical studies suggest that sexually selected characters, including bird plumage, may evolve rapidly and show high levels of convergence and other forms of homoplasy. However, the processes that might generate such convergence have not been explored theoretically. Furthermore, no studies have rigorously addressed this issue using a robust phylogeny and a large number of signal characters. We scored the appearance of 44 adult male plumage characters that varied across New World orioles (Icterus). We mapped the plumage characters onto a molecular phylogeny based on two mitochondrial genes. Reconstructing the evolution of these characters revealed evidence of convergence or reversal in 42 of the 44 plumage characters. No plumage character states are restricted to any groups of species higher than superspecies in the oriole phylogeny. The high frequency of convergence and reversal is reflected in the low overall retention index (RI = 0.66) and the low overall consistency index (CI = 0.28). We found similar results when we mapped plumage changes onto a total evidence tree. Our findings reveal that plumage patterns and colors are highly labile between species of orioles, but highly conserved within the oriole genus. Furthermore, there are at least two overall plumage types that have convergently evolved repeatedly in the three oriole clades. This overall convergence leads to significant conflict between the molecular and plumage data. It is not clear what evolutionary processes lead to this homoplasy in individual characters or convergence in overall pattern. However, evolutionary constraints such as developmental limitations and genetic correlations between characters are likely to play a role. Our results are consistent with the belief that avian plumage and other sexually selected characters may evolve rapidly and may exhibit high homoplasy. The overall convergence in oriole plumage patterns is an interesting evolutionary phenomenon, but it cautions against heavy reliance on plumage characters for constructing phylogenies. [source] Different roles of natural and sexual selection on senescence of plumage colour in the barn swallowFUNCTIONAL ECOLOGY, Issue 2 2009Ismael Galván Summary 1Colour may show effects of senescence because the pigment or structures involved in production of colouration deteriorate with age. 2We tested this hypothesis by investigating age-related changes in plumage colour for two feather tracts coloured by eumelanin or pheomelanin in a longitudinal study of a cohort of barn swallows Hirundo rustica that reached very old age (at least 5 years). 3The level of melanization of the throat increased with age in both sexes, but particularly in females. In contrast, the black colour of the plumage of the back was unrelated to age in both sexes. 4These age-dependent patterns of colouration of different feather tracts of male and female barn swallows suggest that effects of senescence are trait-specific depending on their importance in sexual signalling. The red throat colour based on pheomelanin is involved in sexual selection, with a strong effect in males, but not in females. In contrast, the black colour of the back based on eumelanin is unrelated to sexual selection, but is under natural selection due to intense abrasion of this feather tract. 5These findings suggest that the relative importance of natural and sexual selection are important determinants of the pattern and rate of senescence of colour. [source] Carotenoid accumulation strategies for becoming a colourful House Finch: analyses of plasma and liver pigments in wild moulting birdsFUNCTIONAL ECOLOGY, Issue 4 2006K. J. MCGRAW Summary 1Male House Finches (Carpodacus mexicanus) colour their sexually selected plumage with carotenoid pigments, and there has been much interest in the factors that affect their ability to become bright red rather than drab yellow. 2There is good support for the notions that health, nutritional condition and total carotenoid intake influence colour expression, but there are also suggestions that acquiring particular types of carotenoids from the diet may be important for developing red plumage. 3We used high-performance liquid chromatography (HPLC) to analyse the types and amounts of endogenous (in plasma and liver) and integumentary (in newly grown feathers) carotenoids in a wild, native population of moulting male and female House Finches from the south-western United States to determine the carotenoid-accumulation strategies for becoming optimally colourful. 4Four plant carotenoids , lutein, zeaxanthin, ,-cryptoxanthin and ,-carotene , were detected in plasma and liver. However, as was found previously, 11 carotenoids were observed in colourful plumage, with xanthophylls (e.g. lutein, dehydrolutein) predominant in yellow feathers and ketocarotenoids (e.g. adonirubin, 3-hydroxy-echinenone) in red feathers. This indicates endogenous modification of ingested carotenoids. 5Birds that accumulated more of one type of carotenoid in plasma and liver did not necessarily accumulate more of all other types, suggesting that individuals are not employing a simple ,more is better' strategy for coloration. Instead, when forward stepwise regression was used to examine the ability of individual types of carotenoids in plasma and liver to explain variation in red plumage pigments and plumage redness, we found that the lone variable remaining in all models was ,-cryptoxanthin concentration. 6This supports the idea that, unlike some other songbirds (e.g. yellow Carduelis finches), there is a specialized biochemical strategy that male House Finches follow to become red and most sexually attractive , to accumulate as much ,-cryptoxanthin in the body as possible. ,-Cryptoxanthin is a less common dietary carotenoid than the typical xanthophylls and carotenes in grains and fruits and may be limited enough in the diet that, to become colourful, House Finches might adopt selective foraging strategies for the most ,-cryptoxanthin-rich foods. [source] How feather colour reflects its carotenoid contentFUNCTIONAL ECOLOGY, Issue 4 2003Lauri Saks Summary 1Many birds sequester carotenoid pigments in colourful patches of feathers to advertise or compete for mates. Because carotenoids can be scarce in nature and serve valuable physiological functions, only the highest-quality individuals are thought to acquire or allocate more pigments for use in sexual displays. 2A critical but rarely tested assumption of carotenoid-based signals is that the colour of pigmented feather patches directly reveals the total amount of carotenoids contained within them. 3We studied the relationship between carotenoid-based coloration (hue, chroma and brightness) and the pigment content of tail feathers in wild-caught and captive male greenfinches (Carduelis chloris[Linnaeus]). Greenfinches incorporate two main carotenoids , canary xanthophylls A and B , into feathers to develop yellow patches of colour in their tail. 4Variation in feather carotenoid content explained 32,51% of variation in chroma and hue of the yellow parts of tail feathers, while feather brightness was not significantly related to carotenoid concentration. Hence, chroma and hue appear good candidates to indicate feather carotenoid content. 5Birds with the most colourful feathers deposited significantly more of both canary xanthophylls into plumage. Thus, there does not appear to be a specific biochemical strategy for becoming colourful in greenfinches; males instead follow the general decision rule to deposit as many xanthophylls as possible into feathers to become yellow. [source] Unexplained recurrent features of the plumage of birdsIBIS, Issue 4 2010M. de L. BROOKE No abstract is available for this article. [source] Preen waxes do not protect carotenoid plumage from bleaching by sunlightIBIS, Issue 2 2008ADRIAN SURMACKI The plumage coloration of wild birds often changes during the breeding season. One of the possible reasons for this is that sunlight, and particularly ultraviolet (UV) wavelengths, degrades the pigments responsible for plumage coloration. It has been suggested that birds may apply preen wax to feathers to protect feathers from bleaching. This hypothesis is tested by exposing carotenoid-based breast feathers of Great Tits to ambient light, light filtered to exclude UV and darkness. Preen waxes were experimentally removed from feather samples and the effect of light on coloration of treatment and control feathers compared. Ambient light had an effect on feather colour but preen wax did not. Feathers exposed to sun gradually became less saturated and hues shifted towards shorter wavelengths. This was not apparent in control feathers kept in darkness. Feathers exposed to full-spectra sunlight faded more than those that were kept in light with UV wavelengths removed. There was a decrease in brightness of feathers in both experimental and control groups, which was assumed to be an effect of dirt accumulation. This experiment confirmed earlier suspicions regarding the detrimental effects of UV irradiation on carotenoid-based coloration of avian feathers but failed to show any protective function of preen waxes. The possible consequences of these mechanisms of colour change for birds with regard to mating strategies are discussed. [source] Fast fuelling but light flight in Broad-billed Sandpipers Limicola falcinellus: stopover ecology at a final take-off site in spring (Sivash, Ukraine)IBIS, Issue 2 2006YVONNE VERKUIL We studied phenology, staging time and refuelling in Broad-billed Sandpipers Limicola falcinellus stopping over during spring migration in the Sivash (Black Sea, Ukraine) in May 1991,94. In the study area, peak staging numbers of 2000,2500 individuals occurred in the third week of May. In May 1993, 460 birds were marked with a yellow dye and 126 of these were colour-ringed. Before 28 May no departure of birds dyed yellow could be detected; by 3 June all birds had departed. Colour-ringed adults in mid May 1993 staged for a minimum of 8.2 days. After the observed departure of large flocks (24 May and later) the staging time of colour-ringed birds decreased significantly with body mass at the time of capture. Of birds mist-netted in 1991,94, 99.3% were in full summer plumage and 89% were adults. In second-year birds, fuel deposition rate (measured between individuals) was 0.44 g/day. In adults caught from early May to 24 May, overall fuel deposition rate was 1.04 g/day (3.4% of lean body mass). Mean adult body mass in early May was 34.8 g, increasing to 45.5 g after 24 May. Estimated body mass at departure was 51 g. Departure body mass and flight range estimates suggest that although birds refuelled quickly, fuel loads are only just sufficient for an unbroken flight to Scandinavia and the Kola Peninsula. We suggest that Broad-billed Sandpipers use the Sivash as a crucial final take-off stopover site, and that they follow a ,jumping' migration strategy, performed under narrow time constraints. [source] The effects of delaying the start of moult on the duration of moult, primary feather growth rates and feather mass in Common Starlings Sturnus vulgarisIBIS, Issue 3 2004Alistair Dawson In many species of birds there is a close relationship between the end of breeding and the start of moult. Late-breeding birds therefore often start to moult late, but then moult more rapidly. This is an adaptive mechanism mediated by decreasing day lengths that allows late-breeding birds to complete moult in time. This study asked how these birds complete moult of the primary feathers more rapidly, and the consequences of this on the mass of primary feathers. Common Starlings Sturnus vulgaris were induced to moult rapidly in one of two ways. In the first experiment, one group was exposed to artificially decreasing photoperiods from the start of moult, whereas the control group remained on a constant long photoperiod. The second experiment was a more realistic simulation. Two groups were allowed to moult in an outdoor aviary. One group started to moult at the normal time. In the other, the start of moult was delayed by 3 weeks with an implant of testosterone. The duration of moult was significantly reduced in both the group experiencing artificially decreasing photoperiods and the group in which the start of moult was delayed. The faster moult rate was achieved by moulting more feathers concurrently. The rate of increase in length of each of the primary feathers, and their final length, did not differ between groups. The rate at which total new primary feather mass was accumulated was greater in more rapidly moulting birds, but this was insufficient to compensate for the greater numbers of feathers being grown concurrently. Consequently, the rate of increase in mass of individual feathers, and the final feather mass, were less in the rapidly moulting birds. A 3-week delay in the start of moult is not an unrealistic scenario. That this caused a measurable decrease in feather mass suggests that late-breeding birds are indeed likely to suffer a real decrease in the quality of plumage grown during the subsequent moult. [source] Mate choice in Pied Flycatchers Ficedula hypoleuca: can females use song to find high-quality males and territories?IBIS, Issue 1 2003Helene M. Lampe High-quality male Pied Flycatchers Ficedula hypoleuca (defined by brighter plumage, better condition and more experience) have previously been shown to have larger syllable repertoires and greater song versatility than males of inferior quality. Thus, by preferring more complex songs, females could choose a high-quality male. Females may also use song as a cue to find a high-quality territory since early arriving males may obtain the best territories and these males have more complex songs than late-arriving males. We found that males with more complex songs had a greater chance of becoming paired and stayed unpaired for a shorter period than males with less elaborate songs. When controlling for arrival order, however, only strophe versatility was still correlated with pairing order. Males defending popular territories had more complex and longer songs and were also in better body condition than males in less popular territories. A multiple logistic regression showed that song length was important in explaining whether a male defended a popular nestbox or not. Thus, male arrival time seems to be important in deciding the quality of a male's territory, which in turn explains female choice. However, song quality seems to add important information. Thus, females could find both high-quality males and high-quality territories by using song cues during mate choice. [source] The evolution of black plumage from blue in Australian fairy-wrens (Maluridae): genetic and structural evidenceJOURNAL OF AVIAN BIOLOGY, Issue 5 2010Amy C. Driskell Genetic variation in the melanocortin-1 receptor (MC1R) locus is responsible for color variation, particularly melanism, in many groups of vertebrates. Fairy-wrens, Maluridae, are a family of Australian and New Guinean passerines with several instances of dramatic shifts in plumage coloration, both intra- and inter-specifically. A number of these color changes are from bright blue to black plumage. In this study, we examined sequence variation at the MC1R locus in most genera and species of fairy-wrens. Our primary focus was subspecies of the white-winged fairy-wren Malurus leucopterus in which two subspecies, each endemic to islands off the western Australian coast, are black while the mainland subspecies is blue. We found fourteen variable amino acid residues within M. leucopterus, but at only one position were alleles perfectly correlated with plumage color. Comparison with other fairy-wren species showed that the blue mainland subspecies, not the black island subspecies, had a unique genotype. Examination of MC1R protein sequence variation across our sample of fairy-wrens revealed no correlation between plumage color and sequence in this group. We thus conclude that amino acid changes in the MC1R locus are not directly responsible for the black plumage of the island subspecies of M. leucopterus. Our examination of the nanostructure of feathers from both black and blue subspecies of M. leucopterus and other black and blue fairy-wren species clarifies the evolution of black plumage in this family. Our data indicate that the black white-winged fairy-wrens evolved from blue ancestors because vestiges of the nanostructure required for the production of blue coloration exist within their black feathers. Based on our phylogeographic analysis of M. leucopterus, in which the two black subspecies do not appear to be each other's closest relatives, we infer that there have been two independent evolutionary transitions from blue to black plumage. A third potential transition from blue to black appears to have occurred in a sister clade. [source] Evidence that plumage bacteria influence feather coloration and body condition of eastern bluebirds Sialia sialisJOURNAL OF AVIAN BIOLOGY, Issue 4 2009Alex R. Gunderson Parasites influence the expression of secondary sexual traits and the health of infected individuals. We set out to test the influence of reputed exogenous parasites, plumage bacteria, including feather-degrading bacteria (FDB), on secondary sexual characteristics and body condition of wild adult eastern bluebirds Sialia sialis. Previous work has shown that FDB alter the coloration of structurally-colored bluebird feathers in vitro (Shawkey et al. 2007). In a correlational study of how bacteria affect birds in the wild, we found that female plumage got duller with increasing FDB intensity. Males tended to get brighter with increasing FDB intensity, but the relationship was not significant. We also found significant associations between plumage bacteria intensity and body condition, but, again, with gender-based differences. Female body condition was negatively associated with plumage bacteria intensity, while male body condition was positively associated with plumage bacteria intensity. Interestingly, plumage bacteria intensity of males and females in nesting pairs was significantly positively correlated. We also report the highest prevalence of FDB measured in a wild bird population, with FDB detected on 67/68 (99%) of individuals. Further work is needed to fully understand the relationships between plumage bacteria and birds, but our data indicate that plumage bacteria may have sex-dependent effects on multiple phenotypic traits. [source] Inferring the phylogeography and evolutionary history of the splendid fairy-wren Malurus splendens from mitochondrial DNA and spectrophotometryJOURNAL OF AVIAN BIOLOGY, Issue 1 2009Anna M. Kearns The phylogeographic structure of the widely distributed arid and semi-arid Australian splendid fairy-wren Malurus splendens was investigated by using variation in plumage characters and mitochondrial DNA (mtDNA). We examined sequences of the mtDNA ND2 gene and used spectrophotometry to quantify chromatic variation in plumage in order to test the current morphology-based intraspecific taxonomy of M. splendens and to discriminate between hypotheses invoking allopatric and parapatric processes in the origin of diversity in the complex. Genetic diversity of M. splendens fell into three divergent geographically structured clades. One represents populations ascribed to the western subspecies M. s. splendens, the other populations of central M. s. musgravi and the third all eastern populations currently ascribed to M. s. emmottorum and M. s. melanotus. Plumage patterns clearly differentiate M. s. splendens and M. s. musgravi, and spectrophotometry identified a step-wise transition in spectra between M. s. melanotus and M. s. emmottorum. Congruence of patterns of phenotypic and genetic variation among western, central and eastern populations of M. splendens strongly suggests that these populations have diverged in allopatry on either side of historical biogeographic barriers in this region. Decoupled patterns of phenotypic and genetic diversity suggest that the divergence of M. s. melanotus and M. s. emmottorum may have occurred without periods of isolation perhaps in response to differences in local environmental conditions, or alternatively, mtDNA and plumage may have different rates of evolution. Critically, we encountered issues with the placement of the root of the M. splendens complex. The root was placed within the subspecies M. s. splendens separating its northern and southern populations and rendering the subspecies paraphyletic. [source] Ultraviolet-blue reflectance of some nestling plumage patches mediates parental favouritism in great tits Parus majorJOURNAL OF AVIAN BIOLOGY, Issue 3 2008Ismael Galván The colouration exhibited by nestling birds is generally cryptic, but in some species it has a conspicuous appearance. The adaptive function of these nestling displays is poorly known, especially in altricial species. We performed an experimental study in which the ultraviolet-blue reflectance of the carotenoid-based plumage of great tit Parus major nestlings was reduced in order to find possible evidence of parental favouritism. Tarsus length increment in a three-day period was significantly lower in manipulated nestlings than in their control siblings. As tarsus length may be a good predictor of survival, the parents may increase their fitness return by investing more in those nestlings reflecting more in the UV-blue spectral region. Interestingly, this effect was only found in a yellow patch located at the nape of nestlings that has been previously overlooked, as all the studies on plumage colouration in this species have focused on the breast plumage. Some quality indicators are proposed for the colour of nestling plumage, though the possibility exists that selection may operate through aspects of signal efficacy instead of aspects of signal content. [source] Diving in shallow water: the foraging ecology of darters (Aves: Anhingidae)JOURNAL OF AVIAN BIOLOGY, Issue 4 2007Peter G. Ryan Diving birds have to overcome buoyancy, especially when diving in shallow water. Darters and anhingas (Anhingidae) are specialist shallow-water divers, with adaptations for reducing their buoyancy. Compared to closely-related cormorants (Phalacrocoracidae), darters have fully wettable plumage, smaller air sacs and denser bones. A previous study of darter diving behaviour reported no relationship between dive duration and water depth, contrary to optimal dive models. In this study I provide more extensive observations of African darters Anhinga melanogaster rufa diving in water<5 m deep at two sites. Dive duration increases with water depth at both sites, but the relationship is weak. Dives were longer than dives by cormorants in water of similar depth (max 108 s in water 2.5 m deep), with dives of up to 68 s observed in water<0.5 m deep. Initial dives in a bout were shorter than expected, possibly because their plumage was not fully saturated. Dive efficiency (dive:rest ratio) was 5,6, greater than cormorants (2.7±0.4 for 18 species) and other families of diving birds (average 0.2,4.3). Post-dive recovery periods increased with dive duration, but only slowly, resulting in a strong increase in efficiency with dive duration. All dives are likely to fall within the theoretical anaerobic dive limit. Foraging bouts were short (17.8±4.3 min) compared to cormorants, with birds spending 80±5% of time underwater. Darters take advantage of their low buoyancy to forage efficiently in shallow water, and their slow, stealthy dives are qualitatively different from those of other diving birds. However, they are forced to limit the duration of foraging bouts by increased thermoregulatory costs associated with wettable plumage. [source] Red-winged blackbirds Agelaius phoeniceus use carotenoid and melanin pigments to color their epauletsJOURNAL OF AVIAN BIOLOGY, Issue 6 2004Kevin J. McGraw Over the past three decades, the red-winged blackbird Agelaius phoeniceus has served as a model species for studies of sexual selection and the evolution of ornamental traits. Particular attention has been paid to the role of the colorful red-and-yellow epaulets that are striking in males but reduced in females and juveniles. It has been assumed that carotenoid pigments bestow the brilliant red and yellow colors on epaulet feathers, but this has never been tested biochemically. Here, we use high-performance liquid chromatography (HPLC) to describe the pigments present in these colorful feathers. Two red ketocarotenoids (astaxanthin and canthaxanthin) are responsible for the bright red hue of epaulets. Two yellow dietary precursors pigments (lutein and zeaxanthin) are also present in moderately high concentrations in red feathers. After extracting carotenoids, however, red feathers remained deep brown in color. HPLC tests show that melanin pigments (primarily eumelanin) are also found in the red-pigmented barbules of epaulet feathers, at an approximately equal concentration to carotenoids. This appears to be an uncommon feature of carotenoid-based ornamental plumage in birds, as was shown by comparable analyses of melanin in the yellow feathers of male American goldfinches Carduelis tristis and the red feathers of northern cardinals Cardinalis cardinalis, in which we detected virtually no melanins. Furthermore, the yellow bordering feathers of male epaulets are devoid of carotenoids (except when tinged with a carotenoid-derived pink coloration on occasion) and instead are comprised of a high concentration of primarily phaeomelanin pigments. The dual pigment composition of red epaulet feathers and the melanin-only basis for yellow coloration may have important implications for the honesty-reinforcing mechanisms underlying ornamental epaulets in red-winged blackbirds, and shed light on the difficulties researchers have had to date in characterizing the signaling function of this trait. As in several other birds, the melanic nature of feathers may explain why epaulets are used largely to settle aggressive contests rather than to attract mates. [source] Temporal variation in glucocorticoid levels during the resting phase is associated in opposite way with maternal and paternal melanic colorationJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 10 2010A. ROULIN Abstract 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. [source] Interspecific variation in plumage colour among birds: species recognition or light environment?JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2002Melinda K. McNaught Abstract The traditional explanation for interspecific plumage colour variation in birds is that colour differences between species are adaptations to minimize the risk of hybridization. Under this explanation, colour differences between closely related species of birds represent reproductive character displacement. An alternative explanation is that interspecific variation in plumage colour is an adaptive response to variation in light environments across habitats. Under this explanation, differences in colour between closely related species are a product of selection on signal efficiency. We use a comparative approach to examine these two hypotheses, testing the effects of sympatry and habitat use, respectively, on divergence in male plumage colour. Contrary to the prediction of the Species Isolation Hypothesis, we find no evidence that sympatric pairs of species are consistently more divergent in coloration than are allopatric pairs of species. However, in agreement with the Light Environment Hypothesis, we find significant associations between plumage coloration and habitat use. All of these results remain qualitatively unchanged irrespective of the statistical methodology used to compare reflectance spectra, the body regions used in the analyses, or the exclusion of areas of plumage not used in sexual displays. Our results suggest that, in general, interspecific variation in plumage colour among birds is more strongly influenced by the signalling environment than by the risk of hybridization. [source] Using interpubic distance for sexing manakins in the fieldJOURNAL OF FIELD ORNITHOLOGY, Issue 1 2010Chase D. Mendenhall ABSTRACT Field methods for determining the sex of birds are often limited due to morphometric overlap between sexes, intermediate plumages, seasonality, and reliance on subjective age classification. Interpubic distance, characterized in birds as the distance between the distal ends of the pubic bones, has not been formally tested as a method for determining the sex of birds, despite references among parrot breeders and the frequent use of analogous measurements in mammals. We developed a harmless and easily performed field method for measuring interpubic distance in studies involving bird capture, and compared the interpubic distances of known sex White-ruffed Manakins (Corapipo altera), Orange-collared Manakins (Manacus aurantiacus), and Blue-crowned Manakins (Lepidothrix coronata) to evaluate the possible use of this measurement to determine sex. Using interpubic distance ranges based on 85% confidence intervals where overlap existed between sexes, the sex of 92.8,100% of all manakins in our study was accurately determined with no misclassification. Interpubic distance performed better than plumage-based methods that sexed 74.0% of all individuals and misclassified 1.5%. Using linear discriminant analysis, we developed classification equations that allowed us to accurately determine the sex of all individuals with 100% accuracy using mass and interpubic distance. Additionally, we compared the interpubic distances of female White-ruffed Manakins to evaluate the potential to determine age and reproductive status. Despite an apparent relationship between interpubic distance, age and reproductive status, we concluded that interpubic distance has limited use for determining age and reproductive status due to extensive overlap (31.6,100%), but shows potential in other applications. Based on these results, we endorse the use of interpubic distance to determine the sex of manakins. We encourage further study to develop additional classification equations using different morphometric measurements and to test the efficacy of interpubic distance to determine sex in other bird species. RESUMEN Los métodos del campo para distinguir el sexo de aves son limitados a causa de traslapes de medidas mórfometricas extremas entre sexos, plumajes intermedios, diferencias temporales y/o dependencia en clasificación sujeto de la edad. Distancia interpúbica, caracterizada en aves como la distancia entre los puntos distales de los huesos púbicos, no ha sido formalmente probada como un método para distinguir el sexo de las aves, a pesar de referencias por criadores de loros y uso de métodos similares en mamíferos. Diseñamos un método del campo rápido y sencillo que no tiene riesgo del daño para sacar la distancia interpúbica en estudios que capturan aves. Comparamos la distancia interpúbica de individuos de sexo conocido de Corapipo altera, Manacus aurantiacus, y Lepidothrix coronata para probar el método. Clasificamos correctamente el sexo de 92.8,100% de todos los individuos en este estudio por rangos determinados a través de intérvalos de confianza de 85%. La distancia interpúbica funcionó mejor que un método basado en plumaje, el cual que distinguió el sexo correcto de 74.0% pero falló en clasificar el sexo de 1.5% de los individuos estudiados. Usamos el análisis de discriminación linear para determinar el poder predictivo de la distancia interpúbica, longitud del ala y masa e hicimos ecuaciones de clasificación que distinguieron sexo con un 100% de éxito usando solo masa y distancia interpúbica. Además, comparamos distancia interpúbica de las hembras de C. altera para evaluar el potencial de distinguir edad y estadio reproductivo. A pesar de existir una conexión entre distancia interpúbica, edad y estadio reproductivo, concluimos que la distancia interpúbica es limitada en el contexto de distinguir edad y estadio reproductivo por traslape extensivo (31.6,100%), pero muestra potencial en otras aplicaciones. Basados en estos resultados recomendamos el uso de distancia interpúbica como un método para distinguir sexo de pipridos. Recomendamos más investigación para crear otras ecuaciones de clasificación usando medidas mórfometricas diferentes y probar la eficacia de la distancia interpúbica para distinguir el sexo de otras especies de aves. [source] Secrets in the eyes of Black Oystercatchers: a new sexing techniqueJOURNAL OF FIELD ORNITHOLOGY, Issue 2 2008Brian M. Guzzetti ABSTRACT Sexing oystercatchers in the field is difficult because males and females have identical plumage and are similar in size. Although Black Oystercatchers (Haematopus bachmani) are sexually dimorphic, using morphology to determine sex requires either capturing both pair members for comparison or using discriminant analyses to assign sex probabilistically based on morphometric traits. All adult Black Oystercatchers have bright yellow eyes, but some of them have dark specks, or eye flecks, in their irides. We hypothesized that this easily observable trait was sex-linked and could be used as a novel diagnostic tool for identifying sex. To test this, we compared data for oystercatchers from genetic molecular markers (CHD-W/CHD-Z and HINT-W/HINT-Z), morphometric analyses, and eye-fleck category (full eye flecks, slight eye flecks, and no eye flecks). Compared to molecular markers, we found that discriminant analyses based on morphological characteristics yielded variable results that were confounded by geographical differences in morphology. However, we found that eye flecks were sex-linked. Using an eye-fleck model where all females have full eye flecks and males have either slight eye flecks or no eye flecks, we correctly assigned the sex of 117 of 125 (94%) oystercatchers. Using discriminant analysis based on morphological characteristics, we correctly assigned the sex of 105 of 119 (88%) birds. Using the eye-fleck technique for sexing Black Oystercatchers may be preferable for some investigators because it is as accurate as discriminant analysis based on morphology and does not require capturing the birds. SINOPSIS El sexado de ostreros en el campo es sumamente difícil dado el caso de que tanto hembras como machos tienen plumaje idéntico y son similares en tamaño. Aunque los ostreros negros (Haematopus bachmani) son sexualmente dimórficos, el utilizar morfometría para determinar su sexo requiere capturar a ambos miembros de la pareja para compararlos, utilizando una análisis discriminativo a modo de asignar un sexo por probabilidad, basado en características morfométricas. Todos los adultos del ostrero negro tienen ojos amarillos y brillantes, pero algunos tienen manchas oscuras en el iris. Tomamos como hipótesis que estas peculiaridades observables estaban ligada al sexo, y que podían ser utilizadas como una herramienta novel de diagnóstico para identificar el sexo en dichas aves. Para poner a pruebas lo mencionado, comparamos datos de ostreros donde se utilizaron marcadores genéticos moleculares (CHD-W/CHD-Z y HINT-W/HINT-Z), análisis morfométrico, y categorías en las manchas en los ojos (manchas marcadas en los ojos, algunas manchitas en los ojos, sin manchas en los ojos). Comparado a marcadores moleculares, encontramos que el análisis discriminativo basado en características morfológicas ofrecía resultados variables asociados a diferencias morfológicas geográficas. Sin embargo, encontramos que las manchas en los ojos estaban ligadas al sexo. Utilizando un modelo de manchas en los ojos, en donde clasificamos como hembras aquellos individuos con manchas pronunciadas en los ojos y a machos con muy pocas manchitas o sin manchitas, le pudimos asignar correctamente el sexo a 117 de 125 (94%) individuos. Utilizando una análisis discriminativo basado en características morfológicas, le asignamos el sexo correctamente a 105 de 119 (88%) individuos. El utilizar la técnica de manchas en los ojos para el sexado de ostreros negros pudiera ser preferible para algunos investigadores porque es más exacto que el análisis discriminativo basado en morfología y porque no requiere que se tenga que capturar a las aves. [source] Continuous, age-related plumage variation in male Kirtland's WarblersJOURNAL OF FIELD ORNITHOLOGY, Issue 1 2007John R. Probst ABSTRACT The ability to age individual birds visually in the field based on plumage variation could provide important demographic and biogeographical information. We describe an approach to infer ages from a distribution of plumage scores of free-ranging male Kirtland's Warblers (Dendroica kirtlandii). We assigned ages to males using a scoring scheme (0,12 points) based on variation in plumage coloration, brightness, and contrast on three dorsal and three ventral body regions presumed to be age-related. The distribution of total additive plumage scores for 875 breeding males was normally distributed, indicating no distinct age classes. Thus, we developed provisional plumage-age classes of second year (SY) and after second-year (ASY), and compared them to the total plumage scores of a smaller subsample of known age (N= 92) and minimum age (N= 143) males. Plumage scores of known-age male Kirtland's Warblers increased nonlinearly with age (rs= 0.67), but with some overlap. The median plumage score for SY males (median = 5.0) was significantly lower than for third-year (TY) males (median = 7.0) and after third-year (3 year and older) males (median = 8.0), indicating that the plumage of male Kirtland's Warblers becomes more distinctive and brighter with age. Linear discriminant function analysis differentiated ASY male Kirtland's Warbler from SY males with 78.3% accuracy. Investigators could use the distribution of plumage scores and approximate age structures to document changes in male age structure during colonization, use, and abandonment of habitats by Kirtland's Warblers or other species that occupy early successional habitats. Aging free-ranging birds based on a plumage scoring scheme may be especially critical for demographic studies of less-studied species where it is unlikely that a banding program will be initiated, but where plumage-age inferences or management decisions must be made. SINOPSIS Describimos una forma para inferir la edad a través de una distribución de marcadores en machos silvestres de la reinita Dendroica kirtlandii. Utilizando dicho acercamiento, asignamos edad relativa a machos basándonos en un esquema de puntuación (0,12) para la coloración del plumaje, su brillantez, y contraste en tres localidades del dorso y la parte ventral, que han sido relacionadas con la edad de estos. La distribución de las puntuaciones de 875 machos fue normal, lo que indica que no hubo forma de distinguir las diferentes edades. Por ende, desarrollamos un divisiones de clases, basándonos en diferencias en el plumaje para individuos de segundo año (SA) y posterior al segundo año (PSA) y los comparamos a las puntuaciones de una pequeña muestra de aves (N= 92) cuya edad era conocida y a otra en que sabíamos la edad mínima (N= 143). La puntuación total para individuos de edad conocida aumento de forma no-lineal con la edad (Rs = 0.67), con un pequeño solapamiento en el plumaje total. La puntuación para machos de segundo año (SA) (mediana = 5.0) fue significativamente menor que para aves de tercer año (mediana = 7.0) y esta a su vez que para aves mayores a tres años (mediana = 8.0), lo que indica que el plumaje de los machos, en las aves estudiadas, se torna más brillante con la edad. Un análisis lineal de función discriminativa pudo diferenciar entre aves PSA y SA con un 78.3% de exactitud. Los investigadores han utilizado estas diferencias en el plumaje para clasificar entre los grupos machos territoriales que no han sido anillados. También pudieran utilizar estas particularidades y diferencias en el plumaje para aproximar la estructura de edades entre machos silvestres y hacer inferencias sobre la demografía y reclutamiento de aves en habitats de diferente calidad. [source] Sexual dimorphism and dichromatism in Steere's Liocichla (Liocichla steerii)JOURNAL OF FIELD ORNITHOLOGY, Issue 4 2006Herman L. Mays Jr ABSTRACT Although sexual differences in birds can be extreme, differences between males and females in body size and plumage color are more subtle in many species. We used a genetic-based approach to determine the sex of male and female Steere's Liocichla (Liocichla steerii) and examine the degree of size dimorphism and plumage dichromatism in this apparently monomorphic species. We found that males were significantly larger than females. In addition, Steere's Liocichla have a prominent yellow plumage patch on the lores that was significantly larger in males than females for both live birds and museum specimens. We also used reflectance spectrometry to quantify the color of the yellow-green breast feathers of Steere's Liocichla and found no significant differences between males and females in brightness, intensity, saturation, or hue. However, females tended to have brighter breast plumage, particularly at long wavelengths. Collectively, these color variables were useful in discriminating birds according to sex when used in a discriminant function analysis. Our study suggests that sexual selection may be more widespread than once assumed, even among birds considered monomorphic, and emphasizes the need for additional data from tropical and subtropical species. SINOPSIS Aunque las diferencias sexuales entre algunas especies puede ser estrechas, un muchas de estas las diferencias corporales entre los sexos pudiera ser sutiles. Abordamos el asunto basados en genética para determinar el sexo en Liocichla steerii y examinamos el grado de dimorfismo sexual y dicromatismo en el plumaje en esta especie la cual aparentemente es monomórfica. Encontramos que los machos eran significativamente de mayor tamaño que las hembras. Además encontramos en los machos un parcho amarillo en los lores significativamente más grande que en las hembras, tanto en aves del estado silvestre como en pieles de museos. Usamos espectrometría para cuantificar el color de las plumas verde-amarillentas del pecho de las aves y no encontramos diferencias significativas entre los sexos, con respecto a la brillantez, insensidad, saturación o matiz color. Sin embargo, las hembras tuvieron la tendencia a tener el plumaje más brillante en el pecho particularmente en el espectro de onda larga. Colectivamente, estas variables de color fueron útiles para discriminar entre el sexo de las aves, particularmente cuando fueron examinadas utilizando un análisis discriminante de funciones. Nuestro estudio sugiere que la selección sexual pudiera estar más ampliamente distribuida que lo previamente asumido, aún en aves consideradas monomórficas. Además el trabajo enfatiza la necesidad de llevar a cabo estudios adicionales, de este tipo, tanto en especies del trópico como de la zona templada. [source] A female Lucifer Hummingbird (Calothorax lucifer) with iridescent chin feathersJOURNAL OF FIELD ORNITHOLOGY, Issue 1 2006Raúl Ortiz-Pulido ABSTRACT We report an observation of a female Lucifer Hummingbird (Calothorax lucifer) with iridescent feathers on the chin, resembling the plumage of the juvenile male. The female and nest were found in a xeric shrubland in Barranca de Metztitlán Biosphere Reserve, Hidalgo State, Mexico. This is the first definitive report of a breeding female with such plumage, supporting a previous observation in which sex was not confirmed by behavior. Although this condition appears be rare in female Lucifer Hummingbirds, females in other species of hummingbirds exhibit much variation in the amount of iridescent plumage on the chin and in some, such as Costa's Hummingbirds (Calypte costae), females commonly exhibit colored feathers on the chin. SINOPSIS Reportamos una observacion de una hembra de colibrí Lucifer (Calothorax lucifer) con plumas iridiscentes en el babero, parecidas al plumaje de un macho juvenil. La hembra, la cual estaba incubando, fue encontrada en un área arbustiva xerofítica en la Reserva Biosférica Barranca de Metztitlan, en Hidalgo, México. Este es el primer informe definitivo de una hembra reproductora con este tipo de plumaje, en apoyo a una observación previa en donde el sexo no fue confirmado. Esta condición parece ser rara en estas aves en contraste con otras especies de zumbadores como Calypte costae, pero común en otras especies dimórficas de México y de los Estados Unidos. [source] Sex determination of Red-tailed Hawks (Buteo jamaicensis calurus) using DNA analysis and morphometricsJOURNAL OF FIELD ORNITHOLOGY, Issue 1 2006Kara C. Donohue ABSTRACT Currently, the sex of Red-tailed hawks (Buteo jamaicensis) cannot be determined by in-hand methods. Males and females do not differ in plumage and overlap in size. We collected feather samples and morphological measurements from migrating birds at four sites in the western United States. Sex was determined for individual birds using sex-specific DNA markers and polymerase chain reaction was used to identify these DNA markers. Using discriminant function analysis, we created equations for determining the sex of Red-tailed Hawks using in-hand measurements based on the DNA-determined sexes. We formed two equations, one for adults that was 98% accurate, and one for hatch-year birds that was 97% accurate. The ability to determine the sex of western Red-tailed Hawks using morphological measurements will be useful to investigators examining possible intra- or intersexual differences. SINOPSIS Actualmente no se puede determinar el sexo de Buteo jamaicensis, aun teniendo al ave en la mano. Durante el periodo migratorio tomamos medidas morfométricas y coleccionamos plumas de estas aves en cuatro localidades de la parte oeste de los Estados Unidos. Determinamos el sexo de los individuos utilizando marcadores específicos de ADN para el sexo y reacciones en cadena de polimerasa para identificar los marcadores de ADN. Una vez determinado el sexo por medio de ADN, se hizo un análisis de función discriminativa de los datos para producir una ecuación que permitiera identificar el sexo de las medidas morfométricas de individuos capturados. Se produjeron dos ecuaciones, una para los adultos y otra para jóvenes de un año con 98 y 97% de exactitud, respectivamente. La capacidad para determinar el sexo en la especie, utilizando morfometría será de gran utilidad para investigadores interesados en determinar posibles diferencias intra e intersexuales. [source] | |||||||||||||||||||||||||