Effects of captivity and testosterone on the volumes of four brain regions in the dark‐eyed junco (Junco hyemalis)

This study investigates the effects of captivity and testosterone treatment on the volumes of brain regions involved in processing visual and spatial information in adult dark‐eyed juncos (Junco hyemalis). We treated captive and free‐living male juncos with either testosterone‐filled or empty implants. Captive juncos had a smaller hippocampal formation (HF) (both in absolute volume and relative to telencephalon) than free‐living birds, regardless of hormone treatment. Testosterone‐treated males (both captive and free‐living) had a smaller telencephalon and nucleus rotundus, but not a smaller HF or ectostriatum, than controls. We found that free‐living testosterone‐treated males had larger home ranges than free‐living controls in agreement with earlier experiments, but we found no corresponding difference in HF volume. We discuss the implications of the effect of captivity on HF volume for past and future laboratory experiments. © 2000 John Wiley & Sons, Inc. J Neurobiol 43: 244–253, 2000     

Female dark‐eyed juncos Junco hyemalis thurberi produce male‐like song in a territorial context during the early breeding season

Reports of female song, once considered a rarity, have recently increased across a variety of avian taxa. Females of many species can be induced to produce male‐like song with exogenous testosterone, but observations of female song in free‐living birds remain limited by incomplete sampling of females. Here, we report three independent observations of female dark‐eyed juncos Junco hyemalis producing male‐like song early in the breeding season (i.e. post‐territory establishment, pre‐nesting) in a recently established non‐migratory, urban population. To elicit song, we presented 17 free‐living junco pairs with a live, caged female conspecific. Three unique females responded to our trials by diving at the intruding female, chasing their (male) mate, fanning their tail feathers, and singing a trilled song similar in structure to male long‐range (broadcast) song. We compared male and female songs quantitatively and found that the two sexes were statistically similar in many spectral and temporal characteristics, but female songs had significantly lower minimum and peak frequencies than males. This result is particularly surprising, as males in this urban population are known to sing at a significantly higher minimum frequency than males in a nearby montane population. Both the seasonal and social context in which these songs were observed suggest a potential function for female song in mate guarding and polygyny prevention, but more data are needed to test this hypothesis. Whether female song is common in all dark‐eyed juncos during the early breeding season or if it is restricted to this particular urban and non‐migratory population remains an important question for future research.     

Intensity of mouth coloration in Blackcap Sylvia atricapilla nestlings affects food distribution among siblings but not provisioning of the whole brood

Among various begging stimuli, mouth coloration has received increasing attention in recent years, and previous research has demonstrated that mouths of nestling Canaries Serinus canaria get redder with the extent of food deprivation and that parents preferentially feed nestlings of redder gapes. This study assesses whether the intensity of red mouth colour in nestling Blackcaps Sylvia atricapilla is a signal in parent–offspring communication. This is one of the few species with a naturally red gape in which the function of mouth redness has been tested. Three predictions were experimentally tested: (1) reddening the gape of a single nestling within a brood increases its provisioning in relation to other siblings; (2) reddening the gapes of all nestlings within a brood increases parental feeding rate; and (3) food deprivation increases nestling mouth redness. The effect of nestling quality on mouth redness was also assessed. The intensity of gape coloration affected food distribution, but in a way opposite to that expected: an increase in mouth redness of the nestling caused reduced feeding by parents. However, reddening the gapes of all nestlings had no effect on provisioning of the whole brood, suggesting that Blackcap parents use different cues for provisioning particular nestlings and the whole brood. Intensity of mouth redness in Blackcap nestlings was not affected either by food deprivation or by nestling quality in terms of mass and rank in the nest.     

Decoding colouration of begging traits by the experimental addition of the appetite enhancer cyproheptadine hydrochloride in magpie Pica pica nestlings

The colouration of some traits in nestlings of altricial birds may influence parental food allocation as it may reflect physical condition or hunger. There is increasing evidence of the relationship between colouration of begging traits and nestling performance. However, evidence of the influence of hunger level on nestling colouration is scarce, mainly because of difficulty of distinguishing between the effects of physical condition and hunger levels. Here, we used the appetite stimulant cyproheptadine hydrochloride to increase the sensation of hunger of magpie Pica pica nestlings for eight days and assessed the effect on the colouration of rictal flanges, mouth and body skin. We found that nestlings administered with cyproheptadine had flanges more conspicuous (chromatic visual contrast), more UV coloured and less yellow coloured than their control nestmates. Conversely, mouths of experimental nestlings were more yellow coloured and less UV coloured than controls. Our pharmacological experiment affected the strength of the relationship between body mass and some colour components of body skin (chromatic and achromatic visual contrasts, UV–chroma and yellow–chroma) and of rictal flanges (chromatic visual contrasts, UV–chroma and yellow–chroma), but not for mouth colouration. These results taken together suggest that the effect of the cyproheptadine on nestling colourations is probably mediated by an increase in hunger levels of nestlings for rictal flanges and body skin colourations, and by an increase in physical condition in the case of mouth coloration.     

Non‐Redundant Social Information Use in Avian Flocks with Multisensory Stimuli

Animals generally live in multisensory worlds; however, our understanding of multisensory perception is rather limited, despite its relevance for explaining the mechanisms behind social interactions, such as collective detection while foraging in groups. We tested how multisensory stimuli affected the antipredator behavior of dark‐eyed juncos (Junco hyemalis) using alarm calls as an auditory signal and flushing behavior as a visual cue. We varied the degree of risk within the group by manipulating the number of group mates alarm calling and/or flushing using robotic birds. We assumed that alarm calling and flushing were redundant stimuli and predicted that they could generate one of three types of responses (enhancement, equivalence, or antagonism) depending on the mechanism of multisensory perception. We set up an artificial flock with three robotic juncos surrounding a live junco and controlled for multiple confounding factors (e.g., identity of the focal, body mass, food deprivation time). We found that the degree of alarm of live juncos increased when at least one robot flushed. However, the time it took the live individuals to react to the robots' behavior increased, rather than decreased, with at least one alarm call. This could be the result of an orienting response or sensory overload, as live juncos increased scanning behavior after being exposed solely to alarm calls. Contrary to some theoretical assumptions, alarm calling and flushing behavior elicited independent unimodal responses, suggesting that they are non‐redundant stimuli and that together they could reduce the occurrence of false alarms and facilitate flock cohesion.     

Testosterone Manipulation of Male Attractiveness has no Detectable Effect on Female Home-Range Size and Behavior During the Fertile Period

Female dark‐eyed juncos (Junco hyemalis) are socially monogamous, but they engage in extra‐pair copulations (EPCs). We examined spatial activity and behavior of female juncos during their fertile period to determine whether they engaged in tactics likely to facilitate EPCs and whether any such tactics varied with the attractiveness of their social mates. We manipulated the attractiveness of social mates by implanting experimental males with tubes containing testosterone (T‐males) and control males with empty tubes (C‐males). Previous findings in free‐living juncos showed that females mated to C‐males were more likely to produce extra‐pair young than females mated to T‐males. We radio‐tracked 13 females (eight C‐mated, five T‐mated) for an average of 15 h each over 3 d during their fertile periods. We predicted that C‐mated females, to compensate for the induced relative unattractiveness of their social mates, would foray from their territories to seek EPCs and as a result would have larger home ranges than T‐mated females. Females of both treatment groups made extra‐territorial forays, some of considerable distances, but we observed no EPCs during forays. Further, neighboring T‐ and C‐males frequently made incursions into the home ranges of T‐ and C‐mated females but we saw no EPCs during these incursions. Our ability to detect statistical differences was limited by sample size, but given that constraint, we found no detectable difference in female home‐range size in relation to the treatment of their mates, nor did other female behavior differ according to male treatment. Male behavior was significantly affected by testosterone treatment. C‐males guarded their mates more closely than did T‐males. We conclude that female juncos make extra‐territorial movements during their fertile period without regard to male attractiveness (testosterone treatment), but we found no evidence that these function as a special tactic to gain EPCs.     

Comparative morphology of dark-eyed juncos Junco hyemalis breeding at two elevations: a common aviary experiment

Morphologies of bird species often vary along elevation gradients, yet causes of the variation have not been examined experimentally. We investigated variation in morphological traits of the dark‐eyed junco Junco hyemalis, breeding at 1,000 m a.s.l. (low‐elevation; i.e. low) and 2,000 m asl (high‐elevation; i.e. high) in the Rocky Mountains, Canada. Eight morphological traits were measured in free‐living birds. We found two consistent differences in populations between elevations: at high‐elevation sites, females had longer wings and males had longer tails than birds from low‐ elevation sites. Other age‐ and gender‐ specific results were observed in free‐living birds between elevations: tarsi were shorter in high‐elevation second year (SY) females and after second year (ASY) males, beak lengths were slightly longer in low‐elevation SY females, and high‐elevation ASY females tended to have lower fat than low‐elevation ASY females. Morphological differences may result from genetic differences between elevations, or phenotypic flexibility resulting from exposure to the different environmental conditions. To identify which mechanism caused the difference in morphometrics, hand‐reared birds from low‐ and high‐elevation habitats were raised in identical conditions with unlimited access to high quality food until they had replaced all feathers. The traits measured in the lab (wing and rectrix length, weight and fat score) tended to increase in magnitude compared to field values. Juncos from high‐ and low‐elevations had similar responses to the aviary environment, with one exception: males from high‐elevation sites had greater weight gain relative to free‐living juncos than males from low‐elevation sites. Thus, morphological traits in dark‐eyed juncos were phenotypically flexible, capable of growing larger in the laboratory environment. However, there were also persistent genetic or perinatal/maternal differences underlying population responses that prevented traits from converging under aviary conditions. As a result, trait size differences between high‐ and low‐elevation populations were maintained or exacerbated in the common aviary environment.     

Nestling birds put their best flange forward

The offspring of caring parents may evolve specialized traits uniquely adaptive during their dependence on parental care. For example, the mouths of passerine nestlings are often bordered by enlarged and colorful rictal flanges expressed only during the nestling period. Although these traits are commonly hypothesized to act as visual signals during begging, non‐communication functions for the specialized mouth have been proposed as well. To test the hypothesis that nestling flange colors have evolved largely or exclusively as visual signals, I compared the reflectance of flange tissue that would be visible to parents during begging to that of flange tissue not exposed during begging in nestling house sparrows Passer domesticus and cliff swallows Petrochelidon pyrrhonota. Specifically, I tested the prediction that both condition‐dependent color parameters and those associated with visual conspicuousness would be expressed more intensely in tissue displayed during begging. Consistent with this prediction, flange tissue exposed during begging was brighter (reflected more total light), more UV‐rich, and had more intense carotenoid‐based coloration than hidden tissue. These differences do not exclude a non‐signaling function for flanges, but are consistent with the hypothesis that flange colors have evolved as visual signals.     

Behavioral responses of nesting female dark‐eyed juncos Junco hyemalis to hetero‐ and conspecific passerine preen oils

Several studies have suggested a greater role for olfactory cues in avian social interactions than previously recognized, but few have explicitly investigated the effect of odor on parental behavior. We present results from a preliminary study in which we applied hetero‐ and conspecific preen gland secretions, which are known to contain volatile compounds, to the nests and eggs of incubating female dark‐eyed juncos Junco hyemalis. The responses to these two conditions were compared to the responses of females whose nests were treated with their own preen oil as a control condition, and to females whose nests were treated with the vehicle only. We found that females significantly reduced incubation bout length, a form of parental care, in response to alien secretions, more so if they came from a heterospecific than a conspecific. Females did not reduce incubation bout length in response to their own preen oil or to a vehicle‐only control. These results suggest that odors in the nest may influence avian parental care. However, the behavioral change was only temporary and had no effect on later hatching success. In our study population, brood parasitism by brown‐headed cowbirds is common, but resulting nest abandonment is rare; juncos are frequently able to successfully breed even with cowbird nestlings in their nests. Thus, we suggest that more extreme behavioral responses to alien odor, such as nest abandonment or egg ejection, may not be adaptive and should not be expected.     

Ectoparasite density is associated with mouth colour and size in nestling House Sparrows Passer domesticus

Dependent offspring influence allocation of parental investment using specialized traits thought to contain information about offspring condition. To test this hypothesis, we examined the relationship between one component of avian begging, the phenotype of the nestling mouth, and the density of a haematophagous mite, Pellonyssus reedi, in nestling House Sparrows Passer domesticus. Ectoparasite density in broods was negatively associated with average nestling mass and flange colour intensity and positively associated with mouth width, but was not related to the intensity of blood‐based gape coloration or flange width. These results support the hypothesis that components of offspring solicitations signal high quality, and highlight the diverse selective pressures shaping offspring–parent communication.     

Early‐breeding females experience greater telomere loss

Annual reproductive success is often highest in individuals that initiate breeding early, yet relatively few individuals start breeding during this apparently optimal time. This suggests that individuals, particularly females who ultimately dictate when offspring are born, incur costs by initiating reproduction early in the season. We hypothesized that increases in the ageing rate of somatic cells may be one such cost. Telomeres, the repetitive DNA sequences on the ends of chromosomes, may be good proxies of biological wear and tear as they shorten with age and in response to stress. Using historical data from a long‐term study population of dark‐eyed juncos (Junco hyemalis), we found that telomere loss between years was greater in earlier breeding females, regardless of chronological age. There was no relationship between telomere loss and the annual number of eggs laid or chicks that reached independence. However, telomere loss was greater when temperatures were cooler, and cooler temperatures generally occur early in the season. This suggests that environmental conditions could be the primary cause of accelerated telomere loss in early breeders.     

Parental Distribution of Resources in Relation to Larval Hunger and Size Rank in the Burying Beetle Nicrophorus vespilloides

In altricial birds, the parents' distribution of resources within the brood is influenced by variation in at least two components of nestling condition: hunger level and size rank. Here, we examine whether variation in larval hunger and size rank had similar influences on the parents' distribution of resources in the burying beetle Nicrophorus vespilloides . To this end, we analyzed hitherto unpublished data on parental resource distribution among individual larvae derived from three previous experiments. Our first experiment showed that resource distribution was biased towards hungry larvae at the expense of control larvae, but that actively begging hungry larvae were as likely to obtain resources from parents as actively begging control larvae. Thus, resource distribution was biased towards hungry larvae because hungry larvae spent more time begging than control larvae. Our second experiment showed that actively begging senior larvae (i.e. larvae that were older and larger) were more likely to obtain resources than actively begging junior larvae, suggesting that senior larvae had a competitive advantage or were treated preferentially by the parents. Our third experiment found no evidence that the interaction between larval hunger and size rank had an effect on parental resource distribution, suggesting that hunger level had a similar effect on resource distribution to seniors and juniors. We conclude that offspring hunger and size rank have remarkably similar effects in the burying beetle N. vespilloides as reported in studies on altricial birds.     

Age-Related Changes in Signalling of Need by Nestling Tree Swallows (Tachycineta bicolor)

Despite a large literature on the ontogeny of behaviour, few studies have examined how the function of juvenile behaviour changes during development. One of the most widespread and important juvenile behaviours is begging, the display used by young animals to solicit food from their parents. Begging signals generally vary reliably with offspring need for food and have served as models for understanding the evolution of honest signalling. Little is known, however, about whether the relationship between begging and need varies over the period of rapid juvenile development. Here, we examine whether tree swallow, Tachycineta bicolor, begging calls consistently reflect hunger levels across the 20 d nestling period. We recorded begging calls at 5, 10 and 15 d post‐hatch, during an hour of food deprivation, and related call features to time without food (i.e. hunger) at each age. The overall correlation between call structure and hunger, as measured by canonical correlation, was consistent across ages. The particular features that correlated with hunger varied, however. Call rate and length increased with hunger at all ages, but call amplitude and frequency range increased with hunger at days 10 and 15 only. The results of our study suggest that begging calls consistently convey information about offspring hunger throughout the nestling period, with the number of call features encoding hunger increasing with nestling age. This change may enhance the ability of parents to assess offspring hunger levels by adding redundancy to the signal.     

Nestling detectability affects parental feeding preferences in a cavity-nesting bird

In many avian species, nestlings have evolved striking plumage, behaviours and mouth colours to obtain a greater share of parental investment. Studies revealing parental feeding preferences for nestlings with red gapes have proposed that red mouth colour in songbirds can act as a signal of nestling need or condition. Alternative hypotheses suggest that bright nestling mouths in cavity-nesting birds evolved to increase nestling detectability by the parents. We tested whether nestling mouth colour affects parental feeding preferences in great tits, Parus major L. In broods of six young, we experimentally painted mouth gapes and flanges either red or yellow and tested the effect of mouth colour on nestlings' mass gain under two lighting conditions. In nests with high luminosity, there was no significant effect of mouth colour on mass gain. In nests with low luminosity, nestlings with red gapes and flanges gained less mass than nestlings with red gapes and yellow flanges or both yellow gapes and flanges. Our results suggest that, in nests with low luminosity, red mouths decreased nestling detectability to the feeding parents and support the hypothesis that poor luminosity in nesting cavities can select for pale mouths. Overall, our results do not support the hypothesis that red mouth colour signals nestling need or condition to parent great tits.     

The Effects of Experimentally Elevated Testosterone and Food Deprivation on Food Consumption and Prey Size Preferences in Male Dark-Eyed Juncos (Junco hyemalis, Emberizidae: Passeriformes)

Numerous studies have shown that the experimental elevation of circulating levels of testosterone reduces parental behaviour in male birds, particularly the provisioning of young. The mechanisms responsible for this change in behaviour are not fully understood. In this study, we examine the effects of elevated testosterone on food consumption and prey selection, both of which have potential consequences for nestling provisioning behaviour. We manipulated testosterone and performed two experiments on a captive, non-breeding population of male dark-eyed juncos ( Junco hyemalis ) on long day-lengths. In the first experiment, we subjected juncos to 3 h of food deprivation and compared food consumption and prey size selection by males with elevated testosterone (testosterone males) to that of control males. Testosterone males consumed more food than control males and showed a preference for larger prey. In a second experiment in which small prey were more abundant than large prey, food consumption and prey size preferences did not differ between testosterone and control males. We also manipulated the duration of food deprivation in the second experiment. Males of both treatments consumed more small prey under conditions of mild (1 h) or moderate (5 h) food deprivation and consumed more large prey under conditions of intermediate (3 h) food deprivation. We discuss our results and the effects that testosterone has on self-maintenance behaviour and male parental effort.     

A pre‐breeding immune challenge delays reproduction in the female dark‐eyed junco Junco hyemalis

Precise timing of life‐history transitions in predictably changing environments is hypothesized to aid in individual survival and reproductive success, by appropriately matching an animal's physiology and behavior with prevailing environmental conditions. Therefore, it is imperative for individuals to time energetically costly life‐history stages (i.e. reproduction) so they overlap with seasonal peaks in food abundance and quality. Female lifetime reproductive fitness is affected by several factors that influence energy balance, including arrival date, timing of egg production, and energetic condition. Therefore, any extra energetic costs during reproduction may negatively affect timing of egg production, and ultimately a female's fitness. For example, mounting an immunological response elicits a high energetic cost, and this transfer of resources towards cell and immune system maintenance could have direct negative effects on reproductive timing. In order to determine whether an immune challenge delays onset of breeding (i.e. egg production), we administered either a humoral immune challenge (keyhole limpet hemocyanin (KLH)) (treatment) or physiological saline (control) to free‐living female dark‐eyed juncos Junco hyemalis in the period immediately prior to egg‐laying (～4 weeks). We found that KLH‐injected females artificially delayed clutch initiation when compared to control females. These data help to refine our understanding of how free‐living birds allocate resources between reproduction and self‐maintenance processes during the critical pre‐laying period of the annual cycle.     

Reliable Information Content and Ontogenetic Shift in Begging Calls of Grey Warbler Nestlings

The most critical assumption of communication models regarding parent–offspring conflict is that food solicitation displays of genetic offspring are honest signals to elicit beneficial parental care. A critical requirement of honesty is the reliable change of perceivable aspects of begging calls with physiological needs. We experimentally tested whether and how the acoustic structure and begging call rate of individual Grey Warbler Gerygone igata nestlings change with hunger level and age. We also examined a rarely documented component of chick begging calls, namely the temporal dynamics of acoustic modulation after nestlings heard parental feeding calls. Begging call structure narrowed in frequency range and, surprisingly, decreased in amplitude as chick hunger levels increased. We also found that begging calls changed with chick age, with the frequency increasing and the duration decreasing for older chicks. These results indicate that the acoustic properties of nestling Grey Warbler begging calls are complex and may be used to signal several aspects of nestling traits, including hunger level and age (or size, a correlate of age). Overall, begging calls of Grey Warbler chicks appear to be honest, implying that parents are likely to benefit from relying on the acoustic features of their progeny’s calls which predict chick need. Our results have important implications regarding the reliability and information content of nestling solicitation signals for the brood parasite shining cuckoo Chrysococcyx lucidus exploiting Grey Warbler parental care, in that these begging‐call mimetic specialist cuckoos might also need to match closely the dynamics of acoustic features of their host chicks’ calls.     

Feather melanin and microstructure variation in dark‐eyed junco Junco hyemalis across an elevational gradient in the Selkirk Mountains

Variation in feather melanism and microstructure can arise through sexual selection and ecological functional drivers. Melanin‐based plumage traits are associated with sexual dichromatism and the intensity of sexual selection in many avian species, but also have several ecological benefits such as protection against ultra‐violet (UV) radiation, camouflage, and feather strength. Additionally, feather microstructure influences thermoregulation. Plumage variation across species is well documented; however, the relative role of sexual selection and ecological drivers in intra‐specific and within‐population variation is less established. We investigated UV reflectance, melanism, and feather microstructure in a population of Oregon dark‐eyed juncos Junco hyemalis oreganus between high (1900–2200 m a.s.l.) and low (450–800 m a.s.l.) elevations in the Selkirk Mountains to evaluate potential sexual selection and ecological drivers of variation. We found no difference in UV reflectance or lightness (melanism) of head feathers between elevations, but individuals at high elevation had lighter (less melanism) and less brown (less pheomelanin) body contour feathers than at low elevations. High elevation individuals also had longer contour feathers with more pronounced plumulaceous regions. Sexual dichromatism did not vary between elevations, leading us to reject sexual selection in favour of ecological functional drivers of plumage variation in this system. To our knowledge, this is the first study to identify within‐population differences in feather melanism and microstructure between different elevations.     

Change in sexual signalling traits outruns morphological divergence across an ecological gradient in the post‐glacial radiation of the songbird genus Junco

The relative roles of natural and sexual selection in promoting evolutionary lineage divergence remains controversial and difficult to assess in natural systems. Local adaptation through natural selection is known to play a central role in promoting evolutionary divergence, yet secondary sexual traits can vary widely among species in recent radiations, suggesting that sexual selection may also be important in the early stages of speciation. Here, we compare rates of divergence in ecologically relevant traits (morphology) and sexually selected signalling traits (coloration) relative to neutral structure in genome‐wide molecular markers and examine patterns of variation in sexual dichromatism to explore the roles of natural and sexual selection in the diversification of the songbird genus Junco (Aves: Passerellidae). Juncos include divergent lineages in Central America and several dark‐eyed junco (J. hyemalis) lineages that diversified recently as the group recolonized North America following the last glacial maximum (ca. 18,000 years ago). We found an accelerated rate of divergence in sexually selected characters relative to ecologically relevant traits. Moreover, sexual dichromatism measurements suggested a positive relationship between the degree of colour divergence and the strength of sexual selection when controlling for neutral genetic distance. We also found a positive correlation between dichromatism and latitude, which coincides with the geographic axis of decreasing lineage age in juncos but also with a steep ecological gradient. Finally, we found significant associations between genome‐wide variants linked to functional genes and proxies of both sexual and natural selection. These results suggest that the joint effects of sexual and ecological selection have played a prominent role in the junco radiation.     

Brief communication: Blue eyes in lemurs and humans: Same phenotype,different genetic mechanism

Almost all mammals have brown or darkly‐pigmented eyes (irises), but among primates, there are some prominent blue‐eyed exceptions. The blue eyes of some humans and lemurs are a striking example of convergent evolution of a rare phenotype on distant branches of the primate tree. Recent work on humans indicates that blue eye color is associated with, and likely caused by, a single nucleotide polymorphism (rs12913832) in an intron of the gene HERC2, which likely regulates expression of the neighboring pigmentation gene OCA2. This raises the immediate question of whether blue eyes in lemurs might have a similar genetic basis. We addressed this by sequencing the homologous genetic region in the blue‐eyed black lemur (Eulemur macaco flavifrons; N = 4) and the closely‐related black lemur (Eulemur macaco macaco; N = 4), which has brown eyes. We then compared a 166‐bp segment corresponding to and flanking the human eye‐color‐associated region in these lemurs, as well as other primates (human, chimpanzee, orangutan, macaque, ring‐tailed lemur, mouse lemur). Aligned sequences indicated that this region is strongly conserved in both Eulemur macaco subspecies as well as the other primates (except blue‐eyed humans). Therefore, it is unlikely that this regulatory segment plays a major role in eye color differences among lemurs as it does in humans. Although convergent phenotypes can sometimes come about via the same or similar genetic changes occurring independently, this does not seem to be the case here, as we have shown that the genetic basis of blue eyes in lemurs differs from that of humans. Am J Phys Anthropol, 2009. © 2009 Wiley‐Liss, Inc.