BIOLOGY OF THE BANK CORMORANT,PART 2: MORPHOMETRICS,PLUMAGE, BARE PARTS AND MOULT

Cooper J. 1985. Biology of the Bank Cormorant, Part 2: Morphometrics, plumage, bare parts and moult. Ostrich 56: 79–85.

The Bank cormorant Phalacrocorax neglectus is a medium-sized, heavily built but relatively short-tailed cormorant. Males average 2 107 g, females 1794 g. There are significant differences, but overlaps, in mass, wing length, bill, tarsus and tail length between the sexes of breeding adults. The species is all black; adults have a white rump patch and white filoplumes on the head and neck in prenuptial plumage. The white rump patch is lost during breeding. Bare parts are black except for the iris (the only useful aging character) which is dark brown in juveniles, green in subadults and horizontally divided orange-brown above, green below, in adults. Partial albinism is common but leucism is not. Adults can moult while breeding but it seems likely that most moult occurs outside the breeding season. Adults and a single subadult examined exhibited Staffelmauser or stepwise moult of the primaries.     

Do melanin-based tail patterns predict individual quality and sex in Lesser Grey Shrikes Lanius minor ?

In many bird species, males display colourful, usually carotenoid or structurally based plumage ornaments. On the other hand, there are many bird species and entire avian genera that are achromatic, i.e. with predominantly white, grey and black plumage colours. Achromatic plumage is a typical feature in many shrikes for example. In this study, we examine the importance of an achromatic plumage pattern, namely, the black tail spots on the two outermost tail feathers (T6 and T5) of Lesser Grey Shrikes (LGS) for sex discrimination and as an indicator of individual quality. Our results suggest that the black tail patterns, especially spots on T5, are important for sex discrimination, but only in combination with other melanin-based or morphological features. The presence of black tail spots on T5 is also an indicator of male age. However, there is no indication that presence, size and asymmetry of these black spots are indicators of individual quality of both sexes in the terms of breeding performances.     

Reconstructing plumage evolution in orioles (Icterus): repeated convergence and reversal in patterns

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.     

Sexual Signals of the Male American Goldfinch

Male American goldfinches (Carduelis tristis) exhibit conspicuous yellow plumage, orange bills, and black caps during the breeding season. These secondary sexual characteristics may serve as criteria by which females evaluate males as potential mates because the traits vary among individuals and are likely to be costly. We quantified plumage and bill color and cap characteristics of wild, free‐ranging American goldfinches during the breeding season and tested for relationships between those features, body condition and individual genetic diversity in males. Overall, male and female goldfinches were highly sexually dichromatic, with plumage saturation and brightness and bill brightness contributing strongly to the dimorphism. Body condition decreased significantly with Julian date, even over the 2‐wk period immediately prior to the onset of nesting during which we collected our color and cap measurements. Principal components describing color of the back and the bill significantly predicted date‐corrected body condition based on quadratic regressions, suggesting that there is reliable information in back and bill color that females could use when choosing mates. In a subset of captive males, we found that bill hue faded from orange to yellow within 24 h of capture, suggesting that bill color may reflect short‐term changes in health status or carotenoid availability. Individual genetic diversity based on a panel of eight microsatellite loci was correlated with back brightness and perhaps with cap symmetry. Based on the results of this field study, ornamentation of male American goldfinches appears to signal both long‐ and short‐term aspects of phenotypic quality.     

Sexually selected male plumage color is testosterone dependent in a tropical passerine bird, the red-backed fairy-wren (Malurus melanocephalus)

Background

Sexual signals, such as bright plumage coloration in passerine birds, reflect individual quality, and testosterone (T) may play a critical role in maintaining signal honesty. Manipulations of T during molt have yielded mixed effects on passerine plumage color, in most cases delaying molt or leading to production of drab plumage. However, the majority of these studies have been conducted on species that undergo a post-nuptial molt when T is low; the role of T in species that acquire breeding plumage during a pre-nuptial molt remains largely unexplored.

Methodology/Principal Findings

We experimentally tested the effects of increased T on plumage color in second-year male red-backed fairy-wrens (Malurus melanocephalus), a species in which after-second-year males undergo a pre-nuptial molt into red/black (carotenoid and melanin-based) plumage and second-year males either assume red/black or brown breeding plumage. T treatment stimulated a rapid and early onset pre-nuptial molt and resulted in red/black plumage acquisition, bill darkening, and growth of the sperm storage organ, but had no effect on body condition or corticosterone concentrations. Control males molted later and assumed brown plumage. T treated males produced feathers with similar but not identical reflectance parameters to those of unmanipulated after-second-year red/black males; while reflectance spectra of red back and black crown feathers were similar, black breast feathers differed in UV chroma, hue and brightness, indicating a potentially age and plumage patch-dependent response to T for melanin- vs. carotenoid-pigmentation.

Conclusions/Significance

We show that testosterone is the primary mechanism functioning during the pre-nuptial molt to regulate intrasexually variable plumage color and breeding phenotype in male red-backed fairy-wrens. Our results suggest that the effects of T on plumage coloration may vary with timing of molt (pre- vs. post-nuptial), and that the role of T in mediating plumage signal production may differ across age classes, plumage patches, and between pigment-types.     

Sexing sooty terns on Ascension Island from morphometric measurements

Sooty terns Onychoprion fuscata are one of the most abundant seabirds but breeding populations in many colonies have diminished. Rapid sexing of sooty terns in the field could be crucial in advancing our understanding of their reproductive biology, and in promoting conservation. However, sooty tern males and females are identical in their plumage and, thus, difficult to sex in the field. Morphometric measurements were taken from 63 adult sooty terns breeding on Ascension Island in 2005. A small blood sample was taken from the brachial vein to determine the bird's sex using standard PCR-based molecular techniques. Males were consistently larger in all morphometric measurements than females but considerable overlap between the sexes resulted in no single measurement being a useful discriminator of sex. A principal components analysis on a correlation matrix of seven morphometric measurements indicated that the first principal component (PC1) was a good 'body size' axis explaining 40.5% of the variance in the original matrix. The suite of head measurements all had high character loadings on PC1 and were, therefore, good indicators of the body size of sooty terns. Tarsus length and wing length were less reliable predictors of sex. Discriminant analyses revealed that a disciminant function incorporating head measurements and wing length allowed 77.8% of sooty terns to be sexed correctly based upon morphometric measurements alone. Further morphometric approaches to sexing should be explored with sooty terns captured in subsequent years.     

Is black plumage an adaptation to high elevations in a cosmopolitan bird genus?

Black plumage is expected to absorb and retain more heat and provide better protection against UV radiation compared with lighter plumages. Black plumage is common in species of the genera Turdus and Platycichla that inhabit highlands across different regions of the world. Considering this geographical recurrent pattern we tested the hypothesis that black plumage in these two genera has evolved as a co‐adaptive response to inhabiting highlands, reconstructing ancestral character states for plumage and altitudinal distribution using maximum‐likelihood methods, and a Pagel's multistate discrete method. For these analyses, we used a phylogeny based on mitochondrial and nuclear DNA regions that included 60 of the 66 recognized species in the genera Turdus and Platycichla. We found that black‐plumage coloration evolved independently on eight occasions within these two genera, and species with black plumage occur more often at highlands. Our results support the hypothesis that black‐plumage is adaptative in highlands; but, studies in other bird groups with black‐plumage inhabiting at the same elevations will provide evidence for this adaptive hypothesis or if the evolution of black‐plumage in other groups is explained by other evolutionary forces.     

Astaxanthin is responsible for the pink plumage flush in Franklin's and Ring-billed gulls

ABSTRACT.   Carotenoid pigments produce the red, orange, and yellow plumage of many birds. Carotenoid-containing feathers are typically rich in color and displayed by all adult members of the species. In many gulls and terns, however, an unusual light pink coloring (or flush) to the normally white plumage can be found in highly variable proportions within and across populations. The carotenoid basis of plumage flush was determined in an Elegant Tern ( Sterna elegans ; Hudon and Brush 1990 ), but it is not clear if all larids use this same mechanism for pink plumage coloration. We examined the carotenoid content of pink feathers in Franklin's ( Larus pipixcan ) and Ring-billed ( Larus delawarensis ) gulls and found that a single carotenoid—astaxanthin—was present. Astaxanthin was primarily responsible for the flush in Elegant Terns as well, but was accompanied by other carotenoids (e.g., canthaxanthin and zeaxanthin), as is typical of most astaxanthin-containing bird feathers. In both gull and tern species, carotenoids were contained within feathers and did not occur on the plumage surface in preen oil, as some have previously speculated. We hypothesize that some gulls turn pink because they acquire unusually high amounts of astaxanthin in their diets at the time of feather growth. It is tempting to link the increase in sightings of pink Ring-billed Gulls since the late 1990s with the introduction of pure, synthetic astaxanthin to the diets of hatchery-raised salmon.     

Differential moult patterns in relation to antipredator behaviour during incubation in four tundra plovers

Golden plovers and Grey Plovers Pluvialis spp. all have very distinct breeding plumage rich in contrast, with a conspicuous black belly and breast bordered by a bright white fringe. Eurasian Golden Plovers are known partly to replace their breeding plumage with striped yellow feathers during incubation, different from both breeding and non-breeding plumages. In this study a similar partial breeding moult was observed in Pacific Golden Plovers and American Golden Plovers caught on the nest or collected during incubation, although the feathers did not differ clearly from those of non-breeders. This moult starts during incubation and precedes the post-breeding moult into non-breeding plumage. Because the lighter feathers reduce the contrast between the black belly and the white flanks, we suggest that during incubation the plumage characteristic that plays an important role in mate choice is no longer important; at this stage it is better for the bird to be inconspicuous. Additional information on museum skins of golden plovers and of Grey Plovers indicated that only the three golden plovers undergo this partial moult, but that Grey Plovers in general retain full breeding plumage throughout incubation. The three golden plovers also resemble each other in their generally very passive nest defence strategies. In contrast, the larger Grey Plovers actively chase and attack aerial and ground predators. Thus, a reduced conspicuousness of the body plumage during incubation is likely to benefit the golden plovers more than the Grey Plover. We suggest that nest defence behaviour, plumage characteristics and perhaps size have co-evolved as a response to different selection pressures in golden plovers and Grey Plover, but alternative hypotheses are also discussed.     

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.     

Timing of breeding and offspring number covary with plumage colour among Gyrfalcons Falco rusticolus

Plumage colour variation exists among Gyrfalcons throughout their Arctic and sub‐Arctic circumpolar distribution, ranging from white through silver and grey to almost black. Although different colour variants coexist within many populations, a few geographical regions, such as northern Greenland, possess a single variant, suggesting that local environments may influence plumage colour variation. In central‐west Greenland (66.5–67.5°N), where multiple colour variants exist, white male Gyrfalcons fathered significantly earlier clutches than grey males. No significant association was observed between female colour and lay date. However, significantly more offspring were produced by both male and female white Gyrfalcons than by grey variants when controlling for lay date, and silver Gyrfalcons produced an intermediate number of offspring for both sexes. This pattern was further supported by breeding plumage colour pairings. Grey females paired with grey males nested significantly later in the season and produced fewer offspring than those paired with white males, whereas no difference in lay date or offspring number was found between white males paired with white or with grey females. The difference in the number of offspring produced at each nest‐site was also inversely correlated with the distance to the nearest neighbouring nest, and grey males nested in closer proximity to other nests compared with white and silver colour variants. These results suggest that factors associated with territory occupancy and timing of breeding may regulate reproductive success differently between colour variants, with directional selection favouring light‐coloured Gyrfalcons and resulting in earlier lay date and a high frequency of white plumage colour variants in this population. Although gene flow exists between our study population and those further north (>75°N), white Gyrfalcons prevail where the breeding season duration is even shorter, suggesting that nesting chronology in combination with genetic drift may play an important role in influencing plumage colour polymorphism among Gyrfalcon populations.     

Alula size signals male condition and predicts reproductive performance in an Arctic‐breeding passerine

While studies of achromatic plumage signaling are scarce relative to chromatic ornaments, achromatic ornaments have the potential to act as an efficient form of visual communication due to the highly conspicuous contrast between black and white body regions. Recently, achromatic plumage reflectance has been shown to indicate condition, yet the condition‐dependence of achromatic patch size remains unstudied. Here we show the first evidence that alula size, an achromatic plumage patch, has the potential to signal a male’s condition and predict reproductive performance. In Arctic‐breeding snow buntings Plectrophenax nivalis, the size of the alula simultaneously predicted pre‐breeding physiological health and the number of offspring produced, through an intermediate variable (lay date). Snow buntings appear to pair assortatively; males and females arriving earlier pair together, and changes in body condition over the breeding season are positively related within pairs. We suggest that simple achromatic plumage patches, like alula size, have the potential to act as condition‐dependent signals. Consequently, females may benefit from assessing these signals to reliably evaluate a male’s condition and reproductive potential as a means of maximizing their reproductive success.     

Identification of genes related to white and black plumage formation by RNA-Seq from white and black feather bulbs in ducks

To elucidate the genes involved in the formation of white and black plumage in ducks, RNA from white and black feather bulbs of an F(2) population were analyzed using RNA-Seq. A total of 2,642 expressed sequence tags showed significant differential expression between white and black feather bulbs. Among these tags, 186 matched 133 annotated genes that grouped into 94 pathways. A number of genes controlling melanogenesis showed differential expression between the two types of feather bulbs. This differential expression was confirmed by qPCR analysis and demonstrated that Tyr (Tyrosinase) and Tyrp1 (Tyrosinase-related protein-1) were expressed not in W-W (white feather bulb from white dorsal plumage) and W-WB (white feather bulb from white-black dorsal plumage) but in B-B (black feather bulb from black dorsal plumage) and B-WB (black feather bulb from white-black dorsal plumage) feather bulbs. Tyrp2 (Tyrosinase-related protein-2) gene did not show expression in the four types of feather bulbs but expressed in retina. C-kit (The tyrosine kinase receptor) expressed in all of the samples but the relative mRNA expression in B-B or B-WB was approximately 10 fold higher than that in W-W or W-WB. Additionally, only one of the two Mitf isoforms was associated with plumage color determination. Downregulation of c-Kit and Mitf in feather bulbs may be the cause of white plumage in the duck.     

On the ecological basis of interspecific homoplasy in carotenoid-bearing signals

Evidence that similar color patterns occur in unrelated animals with different habits undermines the traditional view that homoplasy evolves through shared ecological selection pressures. Carotenoid pigments responsible for many yellow to red signals exhibit two related properties that could link ecology with appearance by nontraditional means. Ecologic homoplasy could arise through ecophenotypy because all animals must obtain carotenoids through their diet. Such homoplasy also could be hidden from view because increased carotenoid levels are more strongly encoded by decreased reflectance over ultraviolet (UV) wavelengths invisible to humans. To explore these possibilities, I examined apparent matches or mismatches between color and ecology among insectivorous (low carotenoid diet) and frugivorous (high carotenoid diet) bird species in relation to the typical yellow and black plumage pattern of insectivorous, UV-sensitive titmice (Paridae). Diagnostic features of reflectance spectra indicated that all yellow plumages resulted from carotenoids, black plumages from melanins, and olive green plumages from codeposition of both pigments. However, reflectance by carotenoid-bearing plumages correlated with diet independent of plumage pattern; compared to the insectivores, frugivores had reduced amounts of UV reflectance, and to a lesser extent, "red shifts" in longer-wavelength reflectance. Furthermore, an asymptotic decrease in amount of UV with increased redness implied that plumage reflectance of insectivorous species differed more over UV wavelengths, whereas that of frugivorous species differed more over longer wavelengths. I verified that dietary links to plumage reflectance resulted from greater amounts of plumage carotenoids in frugivores, presumably due to their carotenoid-rich diets. All of these ecological associations transcended post-mortem or post-breeding color change, and phylogeny. Thus, predictable associations between avian-visible plumage reflectance, pigmentation, and diet across evolutionary scales may arise directly (diet per se) or indirectly (honest signaling of diet) by ecophenotypy, although various genetic factors also may play a role.     

A molecular phylogeny of minivets (Passeriformes: Campephagidae: Pericrocotus): implications for biogeography and convergent plumage evolution

Jønsson, K. A., Irestedt, M., Ericson, P. G. P. & Fjeldså, J. (2009). A molecular phylogeny of minivets (Passeriformes: Campephagidae: Pericrocotus ): implications for biogeography and convergent plumage evolution.— Zoologica Scripta, 39 , 1–8.
Minivets are conspicuous and mostly intensely colourful birds inhabiting wooded environments in tropical and subtropical South and Southeast Asia and temperate East Asia. We present a robust phylogeny of the group based on nuclear and mitochondrial DNA data including all 12 recognized species and also many subspecies representing disjunct populations in the Oriental mainland and in Indonesia. The study indicates that minivets radiated within mainland Asia and dispersed to the Indonesian archipelago. We also demonstrate that in accordance with studies on other bird groups, plumage characters are highly plastic and that the diversity of plumage patterns and colouration represents an example of convergent evolution.     

Why some rails have white tails: the evolution of white undertail plumage and anti-predator signaling

Conspicuous plumage patches have evolved in birds as conspecific signals for mate attraction and assessment, intersexual competition or to signal alarm. Signals may alternatively be directed at potential predators to discourage pursuit. Rails (Family Rallidae) are ground-dwelling birds, many of which inhabit wetlands, while others occur in forests and grasslands. They are renown for their secretive nature and the tendency to flick their tails when observed. This behavior is more conspicuous in species with white undertail coverts that contrast sharply with darker body plumage. Using species comparisons and controlling for phylogeny, we investigated four hypotheses for the evolution of white undertail coverts in rails. We found little support for the hypothesis that white tails are sexually selected: white tails were not more common in species with polygamous as opposed to monogamous mating systems, species with sexual dimorphism, nor species that display their tails in courtship. Nor did our results support the hypothesis that white tail plumage evolved for intersexual competition during territorial interactions. Instead, we found that species that flock for at least part of the year and species found in open as opposed to concealing habitats were significantly more likely to have white undertail coverts. Rail species inhabiting concealing habitats are less commonly gregarious and more likely selected for crypsis. Using phylogenetically-controlled statistical inference we found that adaptation to open wetland habitats significantly precedes the evolution of white undertails, whereas gregariousness likely evolved later in some lineages. The inferred order of trait evolution suggests that this plumage characteristic could have been selected primarily for enhancement of an anti-predator signal rather than a social signal for conspecifics.     

The evolution of black plumage from blue in Australian fairy‐wrens (Maluridae): genetic and structural evidence

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.     

Polyphyly of the hawk genera Leucopternis and Buteogallus (Aves, Accipitridae): multiple habitat shifts during the Neotropical buteonine diversification

Background  

The family Accipitridae (hawks, eagles and Old World vultures) represents a large radiation of predatory birds with an almost global distribution, although most species of this family occur in the Neotropics. Despite great morphological and ecological diversity, the evolutionary relationships in the family have been poorly explored at all taxonomic levels. Using sequences from four mitochondrial genes (12S, ATP8, ATP6, and ND6), we reconstructed the phylogeny of the Neotropical forest hawk genus Leucopternis and most of the allied genera of Neotropical buteonines. Our goals were to infer the evolutionary relationships among species of Leucopternis, estimate their relationships to other buteonine genera, evaluate the phylogenetic significance of the white and black plumage patterns common to most Leucopternis species, and assess general patterns of diversification of the group with respect to species' affiliations with Neotropical regions and habitats.     

Testing whether macroevolution follows microevolution: Are colour differences among swans (<Emphasis Type="Italic">Cygnus</Emphasis>) attributable to variation at the <Emphasis Type="Italic">MC1R</Emphasis> locus?

Background  

The MC1R (melanocortin-1 receptor) locus underlies intraspecific variation in melanin-based dark plumage coloration in several unrelated birds with plumage polymorphisms. There is far less evidence for functional variants of MC1R being involved in interspecific variation, in which spurious genotype-phenotype associations arising through population history are a far greater problem than in intraspecific studies. We investigated the relationship between MC1R variation and plumage coloration in swans (Cygnus), which show extreme variation in melanic plumage phenotypes among species (white to black).     

Sexually selected dichromatism in the hihi Notiomystis cincta: multiple colours for multiple receivers

Why do some bird species show dramatic sexual dichromatism in their plumage? Sexual selection is the most common answer to this question. However, other competing explanations mean it is unwise to assume that all sexual dichromatism has evolved by this mechanism. Even if sexual selection is involved, further work is necessary to determine whether dichromatism results from competition amongst rival males, or by female choice for attractive traits, or both. Here, we test whether sexually dichromatic hihi (Notiomystis cincta) plumage is currently under sexual selection, with detailed behavioural and genetic analyses of a free‐living island population. Bateman gradients measured for males and females reveal the potential for sexual selection, whilst selection gradients, relating reproductive success to specific colourful traits, show that there is stabilizing selection on white ear tuft length in males. By correlating colourful male plumage with different components of reproductive success, we show that properties of yellow plumage are most likely a product of male–male competition, whilst properties of the black and white plumage are an outcome of both male–male competition and female choice. Male plumage therefore potentially signals to multiple receivers (rival males and potential mates), and this may explain the multicoloured appearance of one of the most strikingly dichromatic species in New Zealand.