Differences In Plumage Coloration Research Articles

Integrative taxonomy of Cercomacroides serva (Sclater, 1858) demonstrates the validity of C. hypomelaena (Sclater, 1890) comb. nov. (Aves: Thamnophilidae)

Abstract Cercomacroides serva is widely distributed in northern South America. However, this species has never been thoroughly evaluated taxonomically. We conducted a taxonomic study of three taxa currently classified under Cercomacroides serva, based on a study of 307 skins and 145 recordings of male loudsongs. Females from the northwest Amazonian population differ qualitatively from populations from the southwest Amazon in the coloration of the upperparts, primary, and tail. Male loudsongs are superficially similar between these two populations, but the shape of the notes differs significantly. There is no evidence of intergradation or clinal variation in female plumage or male loudsongs. Based on differences in plumage coloration, loudsongs, and lack of evidence of intergradation, we suggest that two species are best recognized. The name Cercomacroides serva is here restricted to populations north of the Marañon River in Peru, to the north in Ecuador, and in southwestern Colombia. The name Cercomacroides hypomelaenacomb. nov. is revived. This species is found south of the Marañon River, and on both banks of the Ucayali River in Peru, to the eastern left bank of the Madeira River in Brazil, and in northern Bolivia.

Plumage coloration differs between offspring raised in natural cavities and nestboxes

Abstract Most of our knowledge of secondary hole-nesting birds comes from populations breeding in human-provided nestboxes, yet these might differ from natural cavities in a number of parameters, including internal dimensions or microclimate, leading to differences in reproductive ecology. Here, we demonstrate differences in plumage coloration, an important visual signal of individual quality, in Blue Tit (Cyanistes caeruleus) and Great Tit (Parus major) nestlings raised in natural cavities and nestboxes. For this study, we collected feather samples over two breeding seasons and applied reflectance spectrophotometry to calculate color metrics. Carotenoid chroma was higher in nestbox-reared Blue Tits, whereas brightness was higher in nestbox-reared Great Tits (with a similar tendency for Blue Tits). The latter result might be explained by the better nutritional condition of Great Tit nestlings raised in nestboxes. Furthermore, we found no evidence for preference of adults expressing more elaborate plumage towards a specific cavity type in either species. Consequently, we assume that differences in nestling plumage reported here are driven by rearing conditions (nestboxes vs. natural cavities) and not by differences in plumage-based parental quality. Our study adds to the growing body of evidence confirming that anthropogenic environmental modifiers, such as nestboxes, might influence avian physiology and the resulting phenotype.

Age-related changes in the temporal structure of song in the common rosefinch Erythrina erythrina

AbstractBird species that have visual differences in plumage coloration between young and older males may also differ in their song parameters. We have studied the difference in song rate between yearlings vs. older males in the common rosefinch Erythrina erythrina, a species with delayed plumage maturation. Yearlings sang 2.3 more strophes per minute compared to older males, and the breaks between strophes were 1.3 s shorter in young males. The higher singing rate of yearling males is probably a form of compensation for lower age (male quality), which may be important in finding a mate or avoiding aggression from older males.

Replicate contact zones suggest a limited role of plumage in reproductive isolation among subspecies of the Variable Seedeater (Sporophila corvina).

After establishing secondary contact, recently diverged populations may remain reproductively isolated or may hybridize to a varying extent depending on factors such as hybrid fitness and the strength of assortative mating. Here, we used genomic and phenotypic data from three independent contact zones between subspecies of the Variable Seedeater (Sporophila corvina) to examine how coloration and genetic divergence shape patterns of hybridization. We found that differences in plumage coloration are likely maintained by divergent selection across contact zones; however, the degree of plumage differentiation does not match overall patterns of hybridization. Across two parallel contact zones between populations with divergent phenotypes (entirely black vs. pied plumage), populations hybridized extensively across one contact zone but not the other, suggesting that plumage divergence is not sufficient to maintain reproductive isolation. Where subspecies hybridized, hybrid zones were wide and formed by later-generation hybrids, suggesting frequent reproduction and high survivorship for hybrid individuals. Moreover, contemporary gene flow has played an important role in shaping patterns of genetic structure between populations. Replicated contact zones between hybridizing taxa offer a unique opportunity to explore how different factors interact to shape patterns of hybridization. Overall, our results demonstrate that divergence in plumage coloration is important in reducing gene flow but insufficient in maintaining reproductive isolation in this clade, and that other factors such as divergence in song and time since secondary contact may also play an important role in driving patterns of reduced hybridization and gene flow.

K-Means Clustering으로 분류한 닭 깃털색 표현형의 분석

Chickens are a species of vertebrate with varying colors. Various colors of chickens must be classified to find color-related genes. In the past, color scoring was performed based on human visual observation. Therefore, chicken colors have not been measured with precise standards. In order to solve this problem, a computer vision approach was used in this study. Image quantization based on k-means clustering for all pixels of RGB values can objectively distinguish inherited colors that are expressed in various ways. This study was also conducted to determine whether plumage color differences exist in the reciprocal cross lines between two breeds: black Yeonsan Ogye (YO) and White Leghorn (WL). Line B is a crossbred line between YO males and WL females while Line L is a reciprocal crossbred line between WL males and YO females. One male and ten females were selected for each F₁ line, and full-sib mating was conducted to generate 883 F₂ birds. The results indicate that the distribution of light and dark colors of k-means clustering converged to 7:3. Additionally, the color of Line B was lighter than that of Line L (<i>P</i>&lt;0.01). This study suggests that the genes underlying plumage colors can be identified using quantification values from the computer vision approach described in this study.

Differences in plumage coloration predict female but not male territorial responses in three antbird sister species pairs

Social selection, via intra- and intersexual competition for sexual (e.g. mates) and/or nonsexual (e.g. territories) resources, is thought to drive the evolution of ornaments in both sexes. However, the relative importance of intra- and intersexual competition in promoting the evolution of female and male ornamentation and, hence, sexual dichromatism remains poorly understood. We addressed this issue in antbirds (Thamnophilidae), a radiation of sexually dichromatic passerines wherein eumelanic plumage patches have evolved multiple times in both sexes. In antbirds, the degree of sexual dichromatism differs between closely related species primarily due to eumelanic dark patches in either sex. If eumelanic patches evolved by social selection, individuals of species bearing more conspicuous eumelanic patches should display stronger territorial responses regardless of their sex. Using playback experiments, we simulated three conspecific territorial intrusion types – a social pair, a female and a male – and measured responses by social pairs of two sister species pairs exhibiting greater interspecific differences in female coloration and one sister species pair exhibiting greater interspecific differences in male coloration. We found that females of species bearing more conspicuous eumelanic patches responded more strongly than females of species bearing less conspicuous eumelanic patches, but only towards simulated female and/or male intruders. However, males responded similarly to all intrusions regardless of interspecific coloration differences. Our results suggest that eumelanic patches in antbirds may function as ornaments and that greater female ornamentation may function in intra- and intersexual contexts and reflect stronger social competition in ornamented females for territories and, possibly, mates. In contrast, in species pairs with greater interspecific differences in male ornamentation, territorial competition may occur predominantly among males and female mate choice may drive the evolution of male ornamentation. Our study highlights that social selection pressures acting on both sexes may drive the evolution of contrasting sexual dichromatism patterns. • Antbird sister species differed in female or male eumelanic coloration. • Female coloration was positively associated with female territorial responses. • Male coloration was not associated with male territorial responses. • Both sexes may show intra- and intersexual territorial responses. • Patterns of sexual dichromatism may evolve by social selection acting on both sexes.

Sexual Dimorphism in Morphology and Plumage of Endangered Yuma Ridgway's Rails: A Model for Documenting Sex

Abstract Many applications in wildlife management require knowledge of the sex of individual animals. The Yuma Ridgway's rail Rallus obsoletus yumanensis is an endangered marsh bird with monomorphic plumage and secretive behaviors, thereby complicating sex determination in field studies. We collected morphometric measurements from 270 adult Yuma Ridgway's rails and quantified the plumage and mandible color of 91 of those individuals throughout their geographic range to evaluate intersexual differences in morphology and coloration. We genetically sexed a subset of adult Yuma Ridgway's rails (n = 101) and used these individuals to determine the optimal combination of measurements (based on discriminant function analyses) to distinguish between sexes. Males averaged significantly larger than females in all measurements, and the optimal discriminant function contained whole leg, culmen, and tail measurements and classified correctly 97.8% (95% CI: 92.5–100.0%) of genetically sexed individuals. We used two additional functions that classified correctly ≥ 95.6% of genetically sexed Yuma Ridgway's rails to assign sex to individuals with missing measurements. These simple models provide managers and researchers with a practical tool to determine the sex of Yuma Ridgway's rails based on morphometric measurements. Although color measurements were not in the most accurate discriminant functions, we quantified subtle intersexual differences in the color of mandibles and greater coverts of Yuma Ridgway's rails. These results document sex-specific patterns in coloration that allow future researchers to test hypotheses to determine the mechanisms underlying sex-based differences in plumage coloration.

Differential gene regulation underlies variation in melanic plumage coloration in the dark-eyed junco (Junco hyemalis).

Colour plays a prominent role in species recognition; therefore, understanding the proximate basis of pigmentation can provide insight into reproductive isolation and speciation. Colour differences between taxa may be the result of regulatory differences or be caused by mutations in coding regions of the expressed genes. To investigate these two alternatives, we studied the pigment composition and the genetic basis of coloration in two divergent dark-eyed junco (Junco hyemalis) subspecies, the slate-coloured and Oregon juncos, which have evolved marked differences in plumage coloration since the Last Glacial Maximum. We used HPLC and light microscopy to investigate pigment composition and deposition in feathers from four body areas. We then used RNA-seq to compare the relative roles of differential gene expression in developing feathers and sequence divergence in transcribed loci under common-garden conditions. Junco feathers differed in eumelanin and pheomelanin content and distribution. Within subspecies, in lighter feathers melanin synthesis genes were downregulated (including PMEL, TYR, TYRP1, OCA2 and MLANA), and ASIP was upregulated. Feathers from different body regions also showed differential expression of HOX and WNT genes. Feathers from the same body regions that differed in colour between the two subspecies showed differential expression of ASIP and three other genes (MFSD12, KCNJ13 and HAND2) associated with pigmentation in other taxa. Sequence variation in the expressed genes was not related to colour differences. Our findings support the hypothesis that differential regulation of a few genes can account for marked differences in coloration, a mechanism that may facilitate the rapid phenotypic diversification of juncos.

Age and sex differences in niche use at molt and its effect on plumage coloration characteristics in a bird.

Bird plumage is often very colorful and can communicate the quality of the bearer to conspecifics. These plumage-based signals of quality are composed of multiple pigments (e.g., melanin and carotenoids). Therefore, sex and age classes, which often show marked differences in plumage coloration, may have different dietary needs for the different plumage components and this might promote preferences for different dietary niches at different molting stages. However, no study has addressed the role that changes in niche use play in the expression of multiple component plumage signals in birds. We used stable isotope analysis to test the hypothesis that niche use is related to age and sex and to differently cultured plumage patches, yellow carotenoid-based and black melanin-based, in great tits Parus major. We recorded high niche overlap between plumage patches, although δ15N was higher in black than yellow plumage. Niche overlap was relatively low for age classes and relatively high for sex classes, and age classes showed a contrasting pattern of niche overlap between carotenoid- and melanin-based plumages. Moreover, δ13C, but not δ15N, had a significant negative relationship with carotenoid-based plumage, which was only apparent in juveniles. Taken together, our results demonstrate that niche use had a moderate influence on plumage coloration characteristics of great tit individuals, mostly associated with δ13C rather than with δ15N and with age rather than with sex. Therefore, our study is significant because it confirms the relevance of niche use during ornament production in free-living birds.

Plumage Colouration and the Provisioning Behaviour of Male and Female Eastern Phoebes

Many factors, including nestling age, brood size, and mate quality, can influence the provisioning behaviour of adult birds. Mate quality may affect provisioning behaviour because high-quality individuals may be ‘good parents’ and provision at higher rates. Alternatively, individuals paired to high-quality mates may provision at higher rates because the benefits provided by such mates ( e.g. good genes) increase the likelihood of reproductive success. We examined variation in the plumage colour of male and female Eastern Phoebes ( Sayornis phoebe) and the possible relationship between such variation and provisioning behaviour. During the 2006–2007 breeding seasons, we captured, banded, and measured adult Eastern Phoebes and collected belly feathers for spectral analyses. We also videotaped nests to quantify provisioning behaviour. Male Eastern Phoebes were larger than females, but the plumage (belly feathers) of males and females did not differ in brightness, hue, and carotenoid chroma (all P ≥ 0.37). Females provisioned nestlings at higher rates than males ( P = 0.009), but we found no significant relationship between provisioning rates of males and females and plumage colour. However, relationships between female provisioning rates and the brightness and carotenoid chroma of their mates’ belly feathers approached significance ( P ≤ 0.08). The larger size of male Eastern Phoebes suggests there is male–male competition for access to resources ( e.g. nest sites and mates), with larger size conferring a selective advantage. However, the absence of intersexual differences in plumage colour suggests limited sexual selection driven by female choice for extra-pair partners. Differences in provisioning rates of males and females may be due to male uncertainty of paternity status or to intersexual differences in foraging behaviour. The relationship between female provisioning rates and male plumage quality suggests that females may invest more in reproduction if male Eastern Phoebes with brighter, carotenoid-rich belly plumage are better able to provide quality nest sites and territories or, perhaps, high-quality genes that can potentially enhance female fitness (differential-allocation hypothesis).

Genomic evidence for convergent evolution of a key trait underlying divergence in island birds.

Reproductive isolation can be initiated by changes in one or a few key traits that prevent random mating among individuals in a population. During the early stages of speciation, when isolation is often incomplete, there will be a heterogeneous pattern of differentiation across regions of the genome between diverging populations, with loci controlling these key traits appearing the most distinct as a result of strong diversifying selection. In this study, we used Illumina-sequenced ddRAD tags to identify genomewide patterns of differentiation in three recently diverged island populations of the Monarcha castaneiventris flycatcher of the Solomon Islands. Populations of this species have diverged in plumage colour, and these differences in plumage colour, in turn, are used in conspecific recognition and likely important in reproductive isolation. Previous candidate gene sequencing identified point mutations in MC1R and ASIP, both known pigmentation genes, to be associated with the difference in plumage colour between islands. Here, we show that background levels of genomic differentiation based on over 70,000 SNPs are extremely low between populations of distinct plumage colour, with no loci reaching the level of differentiation found in either candidate gene. Further, we found that a phylogenetic analysis based on these SNPs produced a taxonomy wherein the two melanic populations appear to have evolved convergently, rather than from a single common ancestor, in contrast to their original classification as a single subspecies. Finally, we found evidence that the pattern of low genomic differentiation is the result of both incomplete lineage sorting and gene flow between populations.

Intraspecific geographic variation in rod and cone visual pigment sensitivity of a parrot, Platycercus elegans

Variation in wavelength sensitivity among subspecies is unknown among vertebrates. The parrot Platycercus elegans has extreme plumage variation between subspecies ranging from pale yellow to crimson which, with differences in background colour and light environment between subspecies, makes it a good candidate for the evolution of within-species differences in vision. We report differences in visual pigments between populations of P. elegans from two subspecies, providing the first known support for population and subspecies variation in visual pigments within a vertebrate species; it is also the first instance of intraspecific variation in rod sensitivity within any vertebrate species. Differences in wavelength sensitivity of rods and cones corresponded to geographic differences in plumage colour. Between study populations, visual pigments varied but not oil droplets. Adaptive functions for the visual pigment differences are untested but they could cause divergence in behaviours associated with colour as well as in dim light, and provide insights into the role of senses in divergence and speciation.

Sex Differences in Long-eared Owl Plumage Coloration

Abstract Most species of owls lack distinctive sexual color dimorphism, and plumage is not considered reliable for distinguishing sex. In North America, Long-eared Owls (Asio otus) are generally considered monomorphic in color, although there are subtle color differences between the sexes. From 1987 to 2015, we investigated differences in plumage coloration of male and female Long-eared Owls in western Montana. We initially used an observational method (1987–1993), followed by a quantitative method (1994–1999), and then a simplified method (2000–2015). When we used the observational method, we correctly sexed all 22 Long-eared Owls. For the quantitative method, we used a Munsell Soil Color Chart to score underwing coverts, tarsometatarsus, and facial disc of breeding males and females and museum specimens purportedly sexed correctly. We found significant sex-specific color differences: underwing coverts (G = 136.77, df = 5, P < 0.01), tarsometatarsus (G = 44.50, df = 4, P < 0.01), and facial disc (G = 50....

Trans‐equatorial range of a land bird lineage (Aves: Rallidae) from tropical forests to subantarctic grasslands

Despite the capacity for dispersal, range size varies considerably among birds species. Many species have restricted geographic spread, whilst others routinely travel long distances to reach preferred habitat. These alternatives are well expressed amongst the rails (Rallidae) and a varying tendency for movement results in overlapping distribution patterns. Here, we examine the situation of a particular lineage, the Lewinia rails (L. mirifica, L. pectoralis and L. muelleri) that inhabit a very wide spatial and ecological range. Lewinia occurs from the Philippines, north of the equator in Oceania, to Australia and the subantarctic Auckland Islands far to the south. Allopatric distribution and differences in plumage colour result in their treatment as distinct species but our mitochondrial molecular analysis (cyt b and CR) reveals genetic distances of less than &lt; 1%. The genetic and phylogeographical structure in the Lewinia lineage includes shared nuclear sequence alleles and this is consistent with a callibrated multigene phylogeny suggesting trans‐hemispheric dispersal since the middle Pleistocene. Despite this recent history, available morphometric data indicates that the subantarctic population has relatively small wings for its mass, and this implies adaptation away from flight. Lewinia provides a nice example of the way dispersal and adaptation intersect over short time frames to generate diversity.

SWS2 visual pigment evolution as a test of historically contingent patterns of plumage color evolution in warblers.

Distantly related clades that occupy similar environments may differ due to the lasting imprint of their ancestors-historical contingency. The New World warblers (Parulidae) and Old World warblers (Phylloscopidae) are ecologically similar clades that differ strikingly in plumage coloration. We studied genetic and functional evolution of the short-wavelength-sensitive visual pigments (SWS2 and SWS1) to ask if altered color perception could contribute to the plumage color differences between clades. We show SWS2 is short-wavelength shifted in birds that occupy open environments, such as finches, compared to those in closed environments, including warblers. Phylogenetic reconstructions indicate New World warblers were derived from a finch-like form that colonized from the Old World 15-20 Ma. During this process, the SWS2 gene accumulated six substitutions in branches leading to New World warblers, inviting the hypothesis that passage through a finch-like ancestor resulted in SWS2 evolution. In fact, we show spectral tuning remained similar across warblers as well as the finch ancestor. Results reject the hypothesis of historical contingency based on opsin spectral tuning, but point to evolution of other aspects of visual pigment function. Using the approach outlined here, historical contingency becomes a generally testable theory in systems where genotype and phenotype can be connected.

Major breeding plumage color differences of male ruffs (Philomachus pugnax) are not associated with coding sequence variation in the MC1R gene.

Sequence variation in the melanocortin-1 receptor (MC1R) gene explains color morph variation in several species of birds and mammals. Ruffs (Philomachus pugnax) exhibit major dark/light color differences in melanin-based male breeding plumage which is closely associated with alternative reproductive behavior. A previous study identified a microsatellite marker (Ppu020) near the MC1R locus associated with the presence/absence of ornamental plumage. We investigated whether coding sequence variation in the MC1R gene explains major dark/light plumage color variation and/or the presence/absence of ornamental plumage in ruffs. Among 821bp of the MC1R coding region from 44 male ruffs we found 3 single nucleotide polymorphisms, representing 1 nonsynonymous and 2 synonymous amino acid substitutions. None were associated with major dark/light color differences or the presence/absence of ornamental plumage. At all amino acid sites known to be functionally important in other avian species with dark/light plumage color variation, ruffs were either monomorphic or the shared polymorphism did not coincide with color morph. Neither ornamental plumage color differences nor the presence/absence of ornamental plumage in ruffs are likely to be caused entirely by amino acid variation within the coding regions of the MC1R locus. Regulatory elements and structural variation at other loci may be involved in melanin expression and contribute to the extreme plumage polymorphism observed in this species.

Agonistic behaviors between Chestnut-sided (Setophaga pensylvanica) and Golden-winged (Vermivora chrysoptera) warblers are unlikely a result of plumage misidentification

Plumage coloration within species is often a signal of competitive ability and can influence territorial aggression between males. Agonistic interactions among males of different co-occurring species could result from misidentification (misdirected conspecific aggression). Reflectance spectrometry of plumage coupled with models of avian vision can be used to infer whether plumage color differences can be distinguished by birds. Here we investigate crown coloration similarity as a potential explanation for aggression between the imperiled Golden-winged Warbler (Vermivora chrysoptera) and the comparatively abundant Chestnut-sided Warbler (Setophaga pensylvanica). Because the yellow crown coloration of the two species appears identical to humans, we hypothesized that misidentification of heterospecifics as conspecifics could escalate agonistic interactions. Using museum study skins, we tested whether the yellow crown coloration of the two species should be distinguishable to the birds. Spectral reflectance data demonstrate that plumage color differs between the two species and avian vision models suggest these color differences should be easily discriminated. Thus, we conclude that plumage coloration similarity between these wood warblers is unlikely to cause misidentification of heterospecifics as conspecifics and may just be a result of phylogenic constraint. As populations of Golden-winged Warblers are experiencing accelerating declines, research focusing on the role interspecific competition plays on reduced productivity and survival is warranted.

Gene expression divergence and nucleotide differentiation between males of different color morphs and mating strategies in the ruff

By next generation transcriptome sequencing, it is possible to obtain data on both nucleotide sequence variation and gene expression. We have used this approach (RNA-Seq) to investigate the genetic basis for differences in plumage coloration and mating strategies in a non-model bird species, the ruff (Philomachus pugnax). Ruff males show enormous variation in the coloration of ornamental feathers, used for individual recognition. This polymorphism is linked to reproductive strategies, with dark males (Independents) defending territories on leks against other Independents, whereas white morphs (Satellites) co-occupy Independent's courts without agonistic interactions. Previous work found a strong genetic component for mating strategy, but the genes involved were not identified. We present feather transcriptome data of more than 6,000 de-novo sequenced ruff genes (although with limited coverage for many of them). None of the identified genes showed significant expression divergence between males, but many genetic markers showed nucleotide differentiation between different color morphs and mating strategies. These include several feather keratin genes, splicing factors, and the Xg blood-group gene. Many of the genes with significant genetic structure between mating strategies have not yet been annotated and their functions remain to be elucidated. We also conducted in-depth investigations of 28 pre-identified coloration candidate genes. Two of these (EDNRB and TYR) were specifically expressed in black- and rust-colored males, respectively. We have demonstrated the utility of next generation transcriptome sequencing for identifying and genotyping large number of genetic markers in a non-model species without previous genomic resources, and highlight the potential of this approach for addressing the genetic basis of ecologically important variation.

Plumage and Body Size Differentiation in Blue-Winged Teal and Cinnamon teal

Blue-winged Teal (Anas discors) and Cinnamon Teal (A. cyanoptera septentrionalium) are two closely related North American dabbling duck species that are ecological equivalents. Cinnamon Teal are primarily restricted to regions west of the Great Plains, whereas Blue-winged Teal occur primarily in the central and eastern part of the continent, only recently expanding westward. Males of the two species exhibit striking plumage color differences, while females are difficult to differentiate by plumage, and it is unclear if interspecific size differences exist between either sex due to inconsistencies in previous reports. Here we reassess body size differences, and quantify plumage color differences using avian color discrimination modeling. Like previous studies, significant differences were found for bill morphology; mean bill length was 7-10% longer in Cinnamon Teal. Based on avian visual modeling of plumage reflectance data, color differences not visible to human vision were found between species for several female feather patches (e.g. breast coloration) and male wing speculum coloration, potentially representing previously unrecognized interspecific signals to the avian visual system. Although color reflectance data yielded higher accuracy than morphometrics for identifying females, body size measurements (in addition to plumage to a lesser degree) also proved to be reliable in correctly classifying males of each species. In combination, morphometrics and plumage reflectance data represent useful identification tools for avian species that are otherwise difficult to distinguish.

Fluorescent and ultraviolet sexual dichromatism in the blue‐winged parrotlet

AbstractThe presence of sexual differences in plumage coloration (sexual dichromatism) is frequent in birds. However, in many cases, humans cannot detect colour differences that are discernible to birds and it is therefore necessary to employ objective methods that contemplate the characteristics of the avian visual system for the study of plumage coloration. An understudied property of feather coloration is the occurrence of fluorescence, which has been described almost exclusively in parrots from the Eastern Hemisphere using non‐objective methods and has been attributed to yellow pigments that are only present in psittacids. In this study, we explore fluorescence and sexual dichromatism through objective and quantitative methods in the plumage of a Neotropical species, the blue‐winged parrotlet Forpus xanthopterygius. We measured plumage reflectance and fluorescence emission on museum skins using spectrophotometry and spectrofluorometry, respectively. The reflectance analysis revealed the presence of ultraviolet sexual dichromatism that adds to the differences in the visible range of wavelengths that are detectable by humans. The spectrofluorometric analysis showed that fluorescence is indeed present in this species, both in green plumage patches, where fluorescent pigments are presumably located, and in the blue rump of males, where colour is considered to be purely structurally based. The sexes differed in the intensity and wavelength of their fluorescence emission, representing the first finding of fluorescence sexual dichromatism in birds.