Beak colouration as a possible sexual ornament in gentoo penguins: sexual dichromatism and relationship to body condition

Gentoo penguins (Pygoscelis papua) have conspicuous red beak spots, the function of which is currently unknown. We hypothesized that beak spots might be sexual ornaments and investigated sexual dichromatism, assortative mating and the possible relationship between beak spot colouration and body condition. Beak colouration was measured with a portable spectroradiometer in 19 breeding pairs of gentoo penguin. Body mass and body mass relative to structural body size were used as estimates of body condition. We found that beak spots were sexually dichromatic, as they were more UV in males and more violet in females, but males and females did not mate assortatively in relation to beak spot colouration. Body condition was strongly related to red colouration in males, with individuals in good condition having redder beaks and individuals in poor condition more orange beaks. The beaks of males in good condition were also brighter. Body condition was not significantly related to beak spot colouration in females, so females might show red beak spots because of genetic correlation with the male trait. These results suggest that the red colour of the beak spot has the potential to be a secondary sexual character in males. Interpretation of the sexual dichromatism in the UV colour will require further knowledge of the capability of gentoo penguins to discriminate small differences in UV wavelengths. In any case, experimental manipulation of beak colouration will be needed to ascertain the role of this trait.     

Ornamental colors reveal age in the king penguin

We investigated whether delayed plumage maturation occurred in king penguins (Aptenodytes patagonicus). Therefore we examined the relationships between age and sex on spectral properties and size of two colored plumage patches and a UV-reflective beak spot, using known-age cohorts. Unlike the colored patch on the breast, we found age differences in ear and beak coloration. These results suggest that head ornaments in king penguins could signal sexual maturity or social status. No sex differences were found in the intensity of colored ornaments, which can result from mutual mate choice or genetic correlation between sexes. Size of colored patches did not relate to age or sex.     

Winter male plumage coloration correlates with breeding status in a cooperative breeding species

The function of colored ornaments is usually related to thesignaling of individual quality in intra- and intersexual interactions.In cooperative breeding species, where only a fraction of themale population access the breeding status and the other fractionhas the option to help breeding pairs, colored traits mightprovide the females with a reliable information on the qualityof potential mate. Males of the cooperative breeding azure-wingedmagpies (Cyanopica cyanus) display conspicuous blue plumagecoloration. Here we explored the role played by structural bluecoloration of males and the probability of becoming a breederor a helper. Birds were trapped during 4 consecutive years,and feather coloration was measured with a spectrometer. Malesthat became breeders had a more brilliant and saturated bluecoloration and showed a more violet hue in the nonbreeding periodcompared with birds that became helpers. Breeding males alsoshowed a seasonal decline in blueness, whereas the color propertiesof helpers were constant throughout the year. Blueness of individualstrapped in the nonbreeding period was positively correlatedwith body size and condition. These findings are consistentwith a scenario in which nonbreeding blue plumage colorationmay function as a signal of individual quality in the azure-wingedmagpie at the pair formation time and add to growing evidencesuggesting that the nonbreeding season appears particularlyimportant in impacting breeding roles in cooperative breedingbirds.     

Mutually honest? Physiological ‘qualities’ signalled by colour ornaments in monomorphic king penguins

Mate choice is expected to be important for the fitness of both sexes for species in which successful reproduction relies strongly on shared and substantial parental investment by males and females. Reciprocal selection may then favour the evolution of morphological signals providing mutual information on the condition/quality of tentative partners. However, because males and females often have differing physiological constraints, it is unclear which proximate physiological pathways guarantee the honesty of male and female signals in similarly ornamented species. We used the monomorphic king penguin (Aptenodytes patagonicus) as a model to investigate the physiological qualities signalled by colour and morphological ornaments known to be under sexual selection (coloration of the beak spots and size of auricular feather patches). In both sexes of this slow‐breeding seabird, we investigated the links between ornaments and multiple indices of individual quality; including body condition, immunity, stress and energy status. In both sexes, individual innate immunity, resting metabolic rate, and the ability to mount a stress response in answer to an acute disturbance (capture) were similarly signalled by various aspects of beak coloration or auricular patch size. However, we also reveal interesting and contrasting relationships between males and females in how ornaments may signal individual quality. Body condition and oxidative stress status were signalled by beak coloration, although in opposite directions for the sexes. Over an exhaustive set of physiological variables, several suggestive patterns indicated the conveyance of honest information about mate quality in this monomorphic species. However, sex‐specific patterns suggested that monomorphic ornaments may signal different information concerning body mass and oxidative balance of males and females, at least in king penguins.     

Interrelationships between breeding frequency,timing and outcome in King Penguins Aptenodytes patagonicus: are King Penguins biennial breeders?

King Penguin Aptenodytes patagonicus chick growth is interrupted by a winter fast which extends the length of the breeding cycle (laying to chick independence) to 14–16 months, so that continuous annual successful breeding appears to be impossible. The 3–month laying period imposes further constraints with respect to timing of breeding attempts in relation to the onset of fasting. By the frequent resighting of individually marked birds at Marion Island, we examined the frequency of breeding and the relationships between timing, outcome and frequency in the same and in consecutive years. A total of 3101 adult King Penguins were banded between 1984 and 1991, yielding continuous breeding histories spanning a maximum of 5 years. Most penguins attempted to breed in consecutive years, although the likelihood of taking a year off increased with the number of consecutive attempts. In any one season, about 19% of potentially breeding adults did not breed. Early breeders were more likely to succeed than late breeders and comprised 84% of breeding attempts of known timing. Successful birds in one season usually bred late in the following season, whereas failed attempts were usually followed by an early attempt. Non-breeding was more likely to occur after a successful outcome than a failed one, and after a year off 93% of birds bred early. It is incorrect to refer to the King Penguin as a biennial breeder.     

Mutual Mate Choice for Colorful Traits in King Penguins

While studies of mate choice based on male color pattern are ubiquitous, studies of mate choice based on ornamental color traits in sexually monomorphic species are less common. We conducted manipulative field experiments on two color ornaments of king penguins (Aptenodytes patagonicus), the size of auricular patches of orange feathers and degree of UV reflectance from beak spots, to determine how the degree of ornamentation influenced pairing rate. In a reduction of auricular patch size, females paired significantly more quickly than males in both control and experimental samples. When this bias was taken into account statistically, pairing of individuals with reduced auricular patches was significantly delayed. We also reduced, but did not eliminate, UV reflectance from beak spots by applying a UV filter; no sex difference in pairing rate was evident in this experiment. Treated birds paired significantly more slowly than untreated control individuals, taking more than a week longer to pair on average than their unmanipulated counterparts, a result that was significant for males and approached significance for females. Our results may indicate mutual mate choice via UV reflectance of the beak spot. Given that this is a species where breeding is extremely slow and considerable investment by both males and females is required for successful reproduction, our results support the hypothesis that in such species, sexual selection might act on the same ornament in both sexes.     

Experimental stress during molt suggests the evolution of condition‐dependent and condition‐independent ornaments in the king penguin

Sexual selection and social selection are two important theories proposed for explaining the evolution of colorful ornamental traits in animals. Understanding signal honesty requires studying how environmental and physiological factors during development influence the showy nature of sexual and social ornaments. We experimentally manipulated physiological stress and immunity status during the molt in adult king penguins (Aptenodytes patagonicus), and studied the consequences of our treatments on colourful ornaments (yellow‐orange and UV beak spots and yellow‐orange auricular feather patches) known to be used in sexual and social contexts in this species. Whereas some ornamental features showed strong condition‐dependence (yellow auricular feather chroma, yellow and UV chroma of the beak), others were condition‐independent and remained highly correlated before and after the molt (auricular patch size and beak UV hue). Our study provides a rare examination of the links between ornament determinism and selection processes in the wild. We highlight the coexistence of ornaments costly to produce that may be honest signals used in mate choice, and ornaments for which honesty may be enforced by social mediation or rely on genetic constraints.     

Aggressiveness in king penguins in relation to reproductive status and territory location

King penguins, Aptenodytes patagonicus, vigorously defend small territories in very dense colonies. The egg-laying season lasts approximately 4 months, but only pairs that reproduce during the first half of the period succeed in fledging a chick. I examined various factors affecting aggressiveness of king penguins during the breeding season and focused on the differences between central and peripheral territories. Pairs on peripheral territories experienced twice as many encounters with avian predators as did central birds. The vast majority of peripheral birds were late breeders, indicating that reproductive success was very low among penguins defending a territory on the edge of the colony. Time invested in territory defence and rate of agonistic encounters between breeding neighbours increased from the incubation to the brooding period. Parents gave most threat displays to territorial neighbours when the chick was very young and just before crèche formation. Distance to colony edge was not related to aggressiveness in incubating birds, however, the rate of pecking and flipper blows increased from the edge to the centre during brooding. In addition, aggressiveness of breeding penguins towards travelling birds trespassing into their territory increased with distance to edge. Early breeders were not more aggressive than late breeders but the proportion of time spent in territory defence increased with the number of days a bird had spent incubating. As expected, I did not detect any sex difference in aggressive behaviour. Birds occupying territories on the beach were generally more aggressive during the incubation period than those located on the valley sides. Reproductive status (incubating versus brooding) and territory location were the main factors explaining the various levels of aggressiveness observed in breeding king penguins. Copyright 2000 The Association for the Study of Animal Behaviour.     

Aspects of the breeding biology of the southern rockhopper penguin <Emphasis Type="Italic">Eudyptes c. chrysocome</Emphasis> and new consideration on the intrinsic capacity of the A-egg

The rockhopper penguins Eudyptes chrysocome have recently been split into the northern E. moseleyi and the southern E. chrysocome rockhopper penguin. It is therefore crucial to have a comprehensive understanding of the biology of each species in order to develop appropriate conservation measures. We investigated the breeding biology of the southern rockhopper on New Island, in the western part of the Falklands Islands, by following the breeding attempt of 160 pairs during the 2006/2007 season and examining the effect of lay time and colony habitat on breeding success. Specifically, we compared survival and growth parameters between A- and B-eggs and chicks from non-manipulated and artificially manipulated nests to investigate why southern rockhopper penguins in the Falkland Islands are more able to fledge an A-egg (first laid) than conspecifics elsewhere. Breeding was highly synchronous, with no significant difference in the breeding success between early and late breeders or between pairs breeding in different habitats. We demonstrate for the first time that the A-egg produced by the southern rockhopper penguin has, when alone, the same theoretical intrinsic potential to lead to a fledged chick as the B-egg. In contrast, the hatching success and survival of the B-chick was similar when alone or in a two-egg clutch.     

A test of the Darwin–Fisher theory for the evolution of male secondary sexual traits in monogamous birds

The Darwin–Fisher theory proposes that the presence of male secondary sexual traits in monogamous birds is selected for by early season breeding of females that are in good condition. These early breeding females have high fecundity because of their good condition, and they select mates based on secondary sex traits. We tested whether this hypothesis may be responsible for the presence of male sexual ornaments in the great frigatebird, a socially and genetically monogamous seabird. Consistent with the Darwin–Fisher theory, we found that reproductive success declined over the season. However, males with more exaggerated ornaments were not chosen as mates earlier in the season than males with less exaggerated ornaments, and selection gradients on these ornaments were not significantly different from zero.     

Restoration of body mass in King Penguins after egg abandonment at a critical energy depletion stage: early vs late breeders

In fasting‐incubating seabirds, it has been proposed that egg abandonment and refeeding should be induced when a low body mass (BM) threshold is attained, thus ensuring adult survival at the expense of immediate breeding. In the context of life‐history trade‐offs in long‐lived birds, we have tested this hypothesis by comparing short‐term survival and restoration of BM in King Penguins Aptenodytes patagonicus that abandoned their egg to those that were relieved normally by their mate at the end of the first incubation shift. Since King Penguins have an extended laying period, the possible influence of seasonal factors was also examined by comparing early and late breeders. Forty incubating males were experimentally forced to fast until egg abandonment by preventing relief by the female. At egg abandonment of both early and late breeding males, BM was below the BM threshold, fasting duration was eight days (about 30%) longer than for relieved birds, and plasma uric acid level was elevated (signature of increased body protein catabolism, phase III of fasting). All abandoning birds survived and came back from sea at a BM similar to that of relieved penguins. The duration of the foraging trip of abandoning early breeders was the same as that of relieved birds, and some abandoning birds engaged in a new breeding attempt. Abandoning late breeders, however, made foraging trips twice as long as those of relieved males. This difference can be explained by time constraints rather than nutritional constraints, abandoning early breeders having enough time left in the breeding season to engage in a new breeding attempt in contrast to abandoning late breeders. These observations lend support to the suggestion that not only BM but also an internal clock intervene in the decision to engage in breeding or not. By preventing a lethal energy depletion ashore and by acting at a fasting stage where the capacity to restore BM at sea is unaffected, abandonment at a low body condition threshold plays a major role in the trade‐off between adult penguin survival and reproduction.     

Foraging movements of emperor penguins at Pointe Géologie, Antarctica

The foraging distributions of 20 breeding emperor penguins were investigated at Pointe Géologie, Terre Adélie, Antarctica by using satellite telemetry in 2005 and 2006 during early and late winter, as well as during late spring and summer, corresponding to incubation, early chick-brooding, late chick-rearing and the adult pre-moult period, respectively. Dive depth records of three post-egg-laying females, two post-incubating males and four late chick-rearing adults were examined, as well as the horizontal space use by these birds. Foraging ranges of chick-provisioning penguins extended over the Antarctic shelf and were constricted by winter pack-ice. During spring ice break-up, the foraging ranges rarely exceeded the shelf slope, although seawater access was apparently almost unlimited. Winter females appeared constrained in their access to open water but used fissures in the sea ice and expanded their prey search effort by expanding the horizontal search component underwater. Birds in spring however, showed higher area-restricted-search than did birds in winter. Despite different seasonal foraging strategies, chick-rearing penguins exploited similar areas as indicated by both a high ‘Area-Restricted-Search Index’ and high ‘Catch Per Unit Effort’. During pre-moult trips, emperor penguins ranged much farther offshore than breeding birds, which argues for particularly profitable oceanic feeding areas which can be exploited when the time constraints imposed by having to return to a central place to provision the chick no longer apply.     

Spontaneous egg or chick abandonment in energy-depleted king penguins: a role for corticosterone and prolactin?

Various exogenous or endogenous factors may induce an emergency response in birds, redirecting current activity towards survival. In fasting, breeding penguins, the achievement of a critical energy depletion was suggested to induce egg abandonment and departure to sea for re-feeding. How such a behavioral shift is hormonally controlled remains unknown. The possible involvement of corticosterone and prolactin was examined by characterizing the nutritional and hormonal states of king penguins at egg abandonment. Further, we tested if these states differ according to whether an egg or a chick is abandoned, and according to the timing of breeding. In every case of abandonment, birds were in phase III fasting characterized by accelerated protein catabolism. However, body condition at egg abandonment was lower in early than in late breeders, suggesting that king penguins are willing to tolerate a larger energy depletion when their potential breeding success is high. At egg and chick abandonment, plasma corticosterone levels were, respectively, increased by 2- and 4-fold, whereas plasma prolactin levels were, respectively, depressed by 3- and 1.4-fold. The increase in plasma corticosterone and the decrease in plasma prolactin could be involved in the control of abandonment by, respectively, stimulating the drive to re-feed and diminishing the drive to incubate or brood. The smaller decrease in prolactin levels and the greater increase in corticosterone levels observed at chick vs egg abandonment suggest that, in addition to nutritionally-related stimuli, tactile or audible stimuli from the egg or chick could intervene in the endocrine control of abandonment.     

FACTORS AFFECTING BREEDING OF RAZORBILLS ALCA TORDA ON SKOKHOLM

A study of the breeding biology of the Razorbill was carried out on Skokholm (South Wales) during 1971-73. Birds ringed or colour ringed before the study began provided additional information upon the effects of age on breeding. Mean laying date was delayed in 1972, compared with 1971; the effect is attributed chiefly to stormy weather which upset colony attendance. Eggs were also smaller in 1972. A seasonal decline in egg size (volume) was noted in all three years, attributed mainly to the later laying of young birds. Egg size increased with age, at least up to the fifteenth year. Eggs lost totalled 30% of those laid; 73% of this total was due to predation by Herring Gulls and of Jackdaws. Most losses (45%) occurred during the first 10 days after laying. Of lost eggs, 25% were replaced, usually 14 days after the loss of the original; only eggs laid and lost early in the season could be replaced. Only 7% of the chicks which hatched failed to fledge. Most (62.5%) chick losses occurred in the first week of nestling life, when chick weight was related to egg size. Afterwards, both growth rate and fledging weight were independent of egg size. The chicks fledging early in the season were heavier than later chicks. Failure to fledge was mainly due to a breakdown in behaviour between parent and young, rather than to predation. Breeding success was highest for birds breeding early in the season, most of which were older, more experienced breeders. These laid early enough to replace an egg if it was lost; they produced large eggs, and their chicks were therefore both heavier than average during the critical first 7–10 days of life, and fledged at a high weight. Thus experience accumulated with age, and the ability to lay early in the season are important for successful breeding in the Razorbill.     

Breeding time, health and immune response in the chinstrap penguin Pygoscelis antarctica

Health status and immunocompetence have been proposed as important factors affecting individual variation in the attainment of breeding condition in birds. We studied individual variation in serological variables indicating health status (blood sedimentation rate, haematocrit, `buffy coat' layer, proportions of different types of leucocytes) in two groups of breeding chinstrap penguins Pygoscelis antarctica with breeding dates 9 days apart. We sampled these individuals shortly after hatching of their young and at the end of the chick-raising period. A group of failed breeders was also sampled. Birds of both sexes were included. We also measured the T-cell-mediated immune response as indicated by an in vivo hypersensitivity response to an intradermal injection of a mitogen (phytohaemagglutinin) in early and late breeders. Sex had no significant effect on most variables. Late breeders had poorer health (more leucocytes, especially heterophils and lymphocytes) and a lower T-cell-mediated immune response than early breeders. Failed breeders were more similar to late than to early breeders. Early breeders suffered a decline in health status throughout the chick-raising period. The impact of pathogens on variation in life history traits in avian populations may be important even in extreme Antarctic environments. Received: 18 December 1997 / Accepted: 1 March 1998     

Endocrine correlates of parental care in an Antarctic winter breeding seabird, the emperor penguin, Aptenodytes forsteri

Plasma levels of luteinizing hormone (LH) and prolactin associated with parental behavior were measured in the Antarctic winter breeding emperor penguin, Aptenodytes forsteri. Males exclusively incubate the egg while females exclusively brood the nonhomeothermic young; both sexes alternate in rearing the homeothermic young. Birds were sampled on arrival from the sea through egg laying, incubation, and brooding. All parent birds lost their chicks at the end of the brooding period due to harsh weather but sampling continued. In females, LH titers dropped after egg laying but levels were restored when the birds returned from the sea to brood the chicks and were not depressed by high prolactin levels. Plasma prolactin remained low in males captured on arrival and kept until the free-living males finished incubation. In breeders, prolactin secretion increased during the prelaying period when day length decreased. Prolactin levels stayed elevated in males during incubation and in brooding females returning after a 2-month absence at sea. Prolactin values were higher in brooding females than in males ending incubation or returning in late brooding. These levels did not drop after chick loss, and the sexual difference in prolactin values was maintained after breeding failure. In emperor penguins, increased prolactin secretion appears to be triggered around the time of egg laying and continues, driven by an endogenous mechanism, through incubation and brooding until rearing is completed. Prolactin secretion independent of external stimuli may have evolved in pelagic seabirds to maintain parental care despite long absences at sea from the breeding colony.     

BREEDING OF THE ADÉLIE PENGUIN PYGOSCELIS ADELIAE AT CAPE BIRD

Observations were made during four seasons (1967–68, 1968–69, 1969–70, 1970–71) on the breeding of Adelie Penguins at Cape Bird, Ross Island, Antarctica. Breeding data from individuals were related to date of return, laying date, clutch-size, nest location, and change of mate. Some females consistently laid near the mean date of laying, while others were consistently early or late layers. Laying date may be under direct genetic control, or may reflect feeding ability. The mean clutch-size was smaller in peripheral compared to central nests, and smallest of all in isolated nests. Clutches laid late in the season were smaller than those laid near the peak date, and small, late clutches were laid in peripheral rather than central nests. These differences may reflect age and/or feeding ability. Penguins that are better able to find food will return earlier, obtain central sites, and have larger clutches than those with a lesser ability. The two main causes of egg and chick losses were predation and parental failure. Losses were highest in single-egg clutches, at isolated and peripheral nests, and among eggs laid late in the season. These results may be partly related to the age and experience of the penguins. However, regardless of age, peripheral nesting and late laying were always disadvantageous. The sex ratio of adults in the colonies was 117♂:100♀. This may be explained by the higher mortality of females. Some males could not find partners, but females that did not breed had probably been unable to obtain sufficient food for gonad development. The return of penguins, incidence of non-breeding, adult mortality, clutch-size, and breeding success at Cape Bird were all markedly different in 1968–69 compared to the other three seasons studied. This season was marked by the persistence of sea-ice along the northwestern shores of Ross Island. The low reproductive output in 1968–69 was thought to result from a shortage of food for egg-laying and incubation.     

Mate Choice and Colored Beak Spots of King Penguins

The theory of sexual selection explains sexual dimorphisms in ornaments used in mate choice. Mutual mate choice is a form of sexual selection that might explain sexually monomorphic ornamental traits. Under mutual mate choice, both sexes select partners based on the same ornament. We tested the mutual mate choice hypothesis in a mutually ornamented seabird, the king penguin (Aptenodytes patagonicus), through observations of the pair formation process in the field. Penguins that were ready to mate formed displaying pairs at the edge of the colony. Some of these pairs moved into the breeding colony and produced an egg (definitive pairs), while other pairs separated and often switched to another potential partner (temporary pairs). Colored ornaments were quantified using color vision modeling. We predicted that birds would mate assortatively by their elaborate ornamental traits (specifically, colors of beak spots, auricular patches of feathers, and breast patch of feathers). We also predicted that definitive pairs would exhibit more elaborate ornaments than temporary pairs. The mutual mate choice hypothesis was supported by assortative pairing for color of the beak spots, but not for color or size of the auricular patches or for the color of the breast patch. An alternative hypothesis was also consistent with our results, that female choice for a male ornamental trait and superior female condition associated with the same trait produced assortative pairing patterns. More UV‐ and yellow‐colored beak spots for females in definitive than temporary pairs supported the female choice hypothesis over the mutual mate choice hypothesis, but previous experimental results from altered beak spot colors supported the latter. Evidence to date thus supports both the mutual mate choice and female choice hypotheses.     

Male ornamentation, timing of breeding, and cost of polygyny in the collared flycatcher

Highly ornamented males are often thought to be better ableto provide females with resources, parental assistance, or goodgenes. Individual variation in such male abilities may overridethe costs of polygyny and therefore largely explain within-populationvariation in mating patterns. We investigated the influenceof variation in male ornamentation and the environment on thecosts of polygyny for female collared flycatchers (Ficedulaalbicollis), using data from a long-term study involving 2733breeding attempts over 19 years. We show that females sufferreduced reproductive success when mated polygynously but thatthe costs of polygyny depend on an interaction between maleornamentation and timing of breeding. Among early breeders,polygynously mated females experience higher reproductive successwhen mated to less ornamented males, but among late breeders,females mated polygynously to highly ornamented males were moresuccessful. We suggest that a high effort spent on obtainingextrapair matings early in the season renders highly ornamentedmales less able to assist two females in caring for the young.Thus, a male's ability to simultaneously gain from extrapairmatings and polygyny may be limited through direct effects onfemale reproductive success. Given such limitation, extrapairmatings may be expected to be less frequent in species withbiparental care and a high level of social polygyny.     

Plumage redness predicts breeding onset and reproductive success in the House Finch: a validation of Darwin's theory

Darwin (1871) and later Fisher (1958) suggested that sexual selection can drive the evolution of ornamental traits in monogamous species when female preferences for these traits allow well-ornamented males to begin breeding earlier in a season and, as a result, gain reproductive advantages over poorly ornamented males. However, few studies have been conducted to test this fundamental concept upon which much of the sexual selection theory for monogamous species has been based. In this study, we examined the relationship between breeding onset, reproductive success, and male ornamentation in the House Finch Carpodacus mexicanus , a species in which males display bright carotenoid-based plumage pigmentation. In previous work, it has been shown that bright male House Finches are preferred as social mates by females and, as a result, begin nesting earlier in the season than do drab orange and yellow males. Here we show that, by initiating breeding earlier in the season, brightly colored males fledge more offspring in a season than do drab males. Thus, differential timing of breeding generates considerable variance in reproductive success among male House Finches and contributes to sexual selection for male plumage ornamentation in this species.