A sexual conflict in collared flycatchers,Ficedula albicollis: early male moult reduces female fitness

A sexual conflict over levels of parental care occurs in most animals with biparental care, and studies of sexual differences in levels of parental care have usually focused on its intra-annual fitness consequences. We investigated inter-annual fitness consequences of a sexual difference in timing of feather replacement (moult) in collared flycatchers (Ficedula albicollis). In this study, males overlapped reproduction and moult more often than females, they also initiated their moult at an earlier stage of breeding than females. Females mated to males with a moult-breeding overlap had significantly lowered survival chances than females mated with males initiating moult after breeding. Furthermore, females mated with moulting males risked a lowered future fecundity in terms of a delayed start to breeding in the following season. However, early moulting males achieved a similar reproductive success as males initiating moult after breeding. Likewise, male survival probability to the following breeding season did not differ between early and late moulting individuals, nor was there any evidence that males gained or lost in future mating advantages by moulting early. These results show not only that a sexual conflict over timing of moult may operate, but also that it can impose severe fitness consequences, in terms of reduced future fecundity and survival probability, upon the ''losing'' sex.     

Effects of latitude on the trade-off between reproduction and moult: a long-term study with pied flycatcher

Long-distance migratory passerine birds are generally time constrained by reproduction and moult, which need to be completed before migration. Breeding and post-nuptial moult may overlap especially under time-constrained conditions (northern latitudes). Here, we analysed the timing of adult moult in relation to latitude, timing of breeding and reproductive effort in pied flycatchers (Ficedula hypoleuca) breeding in four widely separated populations (40-68° N). In males but not females, the proportion of moulting birds while provisioning nestlings increased with increasing latitude. This may suggest that a moult-breeding overlap is a strategy employed by male pied flycatchers to adjust to the short breeding season at northern latitudes. However, the moult-breeding overlap was more pronounced among males in the southernmost study population (Spain). In this population, males may decide not to invest more in reproduction, and start moulting at earlier breeding stage than in northern populations,or, alternatively, birds in the Mediterranean region are time constrained by the hot and dry summer. The trade-off between breeding and post-nuptial moult may be more important in some populations than in others, depending on the latitude of the breeding site. Our results show that a moult-breeding overlap imposes a fitness cost on males in terms of fecundity and breeding success.     

Annual variation in the timing of breeding and moulting in male and female Pied Flycatchers Ficedula hypoleuca

During five breeding seasons, the timing of breeding and moulting was studied in the Pied Flycatcher Ficedula hypoleuca. In central Sweden, on average 67% of the males and 41% of the females started moulting before the young fledged. The proportion of individuals with an overlap between breeding and moulting varied considerably between years, with the highest proportion of moulting males being recorded in the year when the females started egg-laying on the latest date. Despite a large annual variation in the proportion of individuals showing a moult/breeding overlap, the duration of this overlap varied insignificantly between years. The onset of moult in males seemed to be related to both calendar date and timing of the current breeding attempt. Most females postponed their moult until just before or just after the fledging of their young, independent of calendar date. There was no significant relationship between male and female moult scores and nestling weight at fledging or fledging success of their brood. Thus, in long-distance migrants such as Pied Flycatchers, it may be adaptive to have some overlap between reproduction and moult, but there seems to be a limit to how early in the breeding cycle they are able to start moulting.     

The timing of gonadal development and moult in three raptors with different breeding seasons: effects of gender, age and body condition

Differences between species in breeding seasons are thought to be mediated through differences in their reproductive physiology. Little is known about how the timing and duration of gonadal maturation varies between raptor species, how the timing of moult relates to the gonadal cycle, whether the timing and degree of sexual maturation varies between juveniles and adults or whether body condition has a significant effect. To address these questions, data on gonadal size and moult for adults and juveniles of both sexes of three raptor species were extracted from the Predatory Bird Monitoring Scheme (based on birds found dead by members of the public). The three species, Sparrowhawk Accipiter nisus, Kestrel Falco tinnunculus and Barn Owl Tyto alba, have different ecologies – diurnal bird predator, diurnal mammal predator and nocturnal mammal predator, respectively. All are single‐brooded but have different breeding seasons. The duration of gonadal maturation was markedly different between the species. Barn Owls showed the earliest maturation and the latest gonad regression, and Sparrowhawks the latest maturation and earliest gonad regression. Kestrels were intermediate. In males of all species, the testes remained fully mature throughout their respective breeding seasons. In females, the ovaries remained partially mature throughout the breeding season. Moult started slightly earlier in Sparrowhawks than in Kestrels and coincided with gonadal regression in the two species. Although females of the two species started to moult earlier than males, moult duration was similar between the sexes. Barn Owls showed no distinct annual pattern of moult. In juveniles of all three species, the gonads were smaller than in adults throughout spring and started to mature later. Gonad size in birds that had starved tended to be smaller than in birds dying from other causes, but did not influence the difference in gonad mass between adults and juveniles and between seasons. Body condition had no effect on moult. Whilst ecology has led to the evolution of different breeding seasons, differences between species, and between adults and juveniles, are mediated through adaptive differences in their reproductive physiology.     

Interrelation between moulting and breeding in a tropical population of the House Sparrow Passer domesticus

Under the tropical regime in Rajkot, India, the House Sparrow Passer domesticus had a prolonged breeding season, so that breeding and moulting of the primaries overlapped. The moult was interrupted commonly in the nesting birds and was observed more frequently in females than in males. It is concluded that moult initiation was not controlled by reproductive hormones in any way. It is also suggested that the reproductive hormones may not be directly involved with moult interruption.     

Breeding plumage honestly signals likelihood of tapeworm infestation in females of a long-distance migrating shorebird, the bar-tailed godwit

The indicator mechanism for sexual selection proposed by Hamilton and Zuk (i.e. that sexually selected ornaments signal parasite resistance) has received rather little observational support, and none in the case of long-distance migrant birds. Here we present a test by examining the association between helminth infestations and breeding plumage quality in bar-tailed godwits Limosa lapponica taymyrensis during their spring staging period in the Wadden Sea, The Netherlands. After a non-stop flight from West Africa, these shorebirds refuel in the Wadden Sea in preparation for a second flight to the central Siberian Arctic breeding grounds. Earlier studies have shown that only relatively heavy and well ornamented birds carry out a "top-up" moult during stopover, in which part of the contour feathers recently grown in West Africa are replaced by even fresher ones. Active body moult was therefore taken as the primary indicator of ornament quality. Of 78 birds collected between 1992 and 1997, 42% carried helminths, including four species of digenean trematodes (flukes), three species of cestodes (tapeworms) and an acanthocephalan (spiny-headed worm). Faecal samples examined for helminth eggs in another 92 birds in 1998 and 2000 showed similar rates of infestation. Actively moulting bar-tailed godwits were confirmed to be heavier and to show more extensive breeding plumage than non-moulting birds. In females, but not in males, active moult was associated with fewer cestodes and acanthocephalans. Also, breeding plumage and presence of cestodes were negatively associated in females. We argue that the quality of the breeding plumage reliably indicates parasite resistance in female godwits. The repeatability of plumage scores of females between years is consistent with such resistance having a heritable component. In contrast, male ornaments may demonstrate other qualities, e.g. an ability to combine adequate fuelling and flight performances with moult during the time-stress of migration.     

POPULATION,DIET AND THE ANNUAL CYCLE OF THE LAUGHING DOVE AT BARBERSPAN,PART 3: THE ANNUAL CYCLE

Dean, W. R. J. 1979. Population, diet and the annual cycle of the Laughing Dove at Barbers-pan, Part 3: The annual cycle. Ostrich 50:234-239.

Laughing Doves Streptopelia senegalensis were collected each month from July 1976 to June 1977. In each sample some males and females were breeding. Breeding and primary moult overlapped, and some birds began to moult after starting to breed, and began to breed after starting moult. Adult Laughing Doves require about 120 days to complete primary moult, and juveniles require about 90 days. Weights of moulting birds were not significantly different from those of non-moulting birds, and there were no seasonal trends in the weights of either group. The mean weight of 79 males was 101,6 g and of 39 females was 100,2 g.     

The timing, duration and pattern of moult and its relationship to breeding in a population of the European Greenfinch Carduelis chloris

Moult was studied in 1 year among Greenfinches trapped in a garden in east‐central England. Over the period June–December 2003, 333 captures of 179 individual adults provided information on breeding condition, moult, body weight, sex and age (yearling or older adult, equivalent to birds in their second or later calendar years, respectively). About 95% of all birds (sex and age groups combined) started primary feather moult from 2 July to 14 August, and finished from 10 October to 22 November. The mean date of moult onset in the population as a whole was 24 July. On average, males began 8 days before females, and yearlings began 6 days before older birds. The mean duration of moult was 100 days, whether the figure was calculated for the population as a whole or just for the 36 individual birds that were caught more than once during moult. However, moult rate was slightly slower, and moult duration slightly longer, in yearlings than in older adults of both sexes. No evidence was found for any systematic relationship between moult onset date and rate (duration). Breeding and moult overlapped by up to 5 weeks or more in individual birds, and some birds probably started to moult as early as the incubation stage of their last clutch of the season. The cloacal protuberance (taken as indicative of breeding condition) had regressed in all males by the time the fifth primary was shed, and the brood patch had regressed and re‐feathered in all females by the time the fourth primary was shed. The bulk of feather replacement in the secondary, tail and body tracts occurred in the second half of primary moult, and after cloacal protuberances and brood patches were completely regressed. In all birds examined near the end of primary moult the secondaries were still growing, and would have continued growth for up to another 19 days or more, extending the end of the moulting season into December. Body mass during moult was affected significantly by sex and age, as well as by time of day, amount of food in gullet, reproductive condition and date. No firm evidence emerged that body mass was affected by moult stage, after allowing for effects of date and other variables (although there was a non‐significant negative relationship between moult stage and body mass in males). In the population as a whole, the breeding season (from first egg‐laying to independence of last young) was spread over 21 weeks and moult over 24 weeks. With an overlap between the two events at the population level of up to 9 weeks, the two processes together took up to 36 weeks, some 69% of the year.     

Daily energy expenditure and cell-mediated immunity in pied flycatchers while feeding nestlings: interaction with moult

Ecological immunology posits a trade-off between parental effort and immunocompetence underlying the cost of reproduction. The moult-breeding overlap observed in several bird species represents a conflict in resource allocation between two energy-demanding processes. Moult processes have been associated with enlargements of immune system organs. In the present study. we measured simultaneously daily energy expenditure (DEE) and the T-cell-dependent immune response of pied flycatchers, Ficedula hypoleuca, caring for grown nestlings. We used the doubly labelled water technique and the phytohaemagglutinin (PHA) injection assay on both males and females, while recording provisioning rates and moult scores. DEE and the PHA response were negatively correlated for females, but not for males. A significantly higher proportion of males than females initiated moult. Provisioning rates were strongly correlated with DEE for females but only for non-moulting males. The DEE of moulting males was marginally correlated with moult score. For moulting males, there was a marginally significant positive correlation between moult score and immune response. The trade-off between DEE and immunity for females could underlie the cost of reproduction. However, the moult-breeding overlap found in males may offset this trade-off, thereby reducing the implications of immunosuppression for parental survival.     

Trade-off between reproduction and moult – a comparison of three Fennoscandian pied flycatcher populations

Organisms that reproduce at high latitudes are assumed to have evolved several adaptations to the short summer. For birds, and especially for long-distance migrants, there is a time constraint because both reproduction and moult must be completed before autumn migration. It has therefore been assumed that birds at northern latitudes must initiate their moult during reproduction more often than birds at low latitudes. To investigate how passerine birds breeding at different latitudes allocate their time between reproduction and moult, we compared timing of these activities during three consecutive breeding seasons in three widely separated populations of the pied flycatcher Ficedula hypoleuca. Our results show that the frequency of individuals with moult-breeding overlap, and moult initiation in relation to breeding stage, varied considerably among populations and years. In all three populations, female moult initiation was restricted to the late nestling period. The males had a more pronounced moult-breeding overlap than the females, but its duration was similar in all three study areas. Thus, there was no evidence for a more pronounced moult-breeding overlap at high compared with low latitudes. These results suggest that pied flycatchers sometimes accept a moult-breeding overlap, but that the time gained by having too extensive an overlap between reproduction and moult does not outweigh the associated costs. Long-distance migrants breeding at northern latitudes apparently experience a trade-off between reproduction and somatic investment during moult. We therefore suggest that a pronounced moult-breeding overlap is not a typical strategy used by long-distance migrants to adjust to the short breeding season at northern latitudes. Received: 7 May 1998 / Accepted: 24 August 1998     

Lack of seasonal and moult-related stress modulation in an opportunistically breeding bird: The white-plumed honeyeater (Lichenostomus penicillatus)

This article is part of a Special Issue “SBN 2014”.In most vertebrate species, glucocorticoid levels and stress sensitivity vary in relation to season and life-history stage. In birds, baseline corticosterone (CORT) and stress sensitivity are typically highest while breeding and decrease substantially during moult. Because elevated CORT adversely affects protein synthesis, moult-related CORT suppression is thought to be necessary for forming high-quality feathers. Surprisingly, some passerine species lack moult-related CORT suppression, but these are distinguished by having slow rates of moult and being opportunistic breeders. We examined baseline and stress-induced CORT levels in an opportunistically breeding Australian passerine, the white-plumed honeyeater (Lichenostomus penicillatus). Although this species has a slower moult rate than high-latitude breeders, it differs little from north-temperate passerines. Neither baseline nor stress-induced CORT levels varied with season (winter, spring or summer), sex or moult status in adult birds. While breeding tended to be highest in early spring through late summer, laparotomies revealed only limited reduction in testicular size in males the year round. In all but one sampling period, at least some females displayed follicular hierarchy. Breeding usually coincides with outbreaks of phytophagous insects, which can happen at any time of the year. This results in moult/breeding overlap when infestations occur in late spring or summer. The ability of this species to moult and breed at the same time while having breeding-levels of CORT demonstrates that CORT suppression is not a prerequisite for synthesis of high-quality feathers. An experimental design incorporating moulting and non-moulting phenotypes is suggested to test the functional significance of CORT suppression in other species.     

Absence of seasonal variation in great tit offspring sex ratios

When the timing of breeding affects the reproductive value of sons and daughters differently, parents are expected to increase their fitness by changing the offspring sex ratio during the course of the breeding season. Previous studies have shown that in great tits Parus major hatching date has a stronger effect on the fitness of juvenile males than on that of juvenile females. We tested whether this difference was reflected in a seasonal decline in the proportion of sons per breeding attempt. Although offspring sex ratio was more variable than would be expected from a binomial distribution, there was no significant relationship between the proportion of sons and the laying date of the clutch. Moreover, individual females did not adjust the sex ratio of their offspring following an experimental delay of breeding. This study therefore fails to demonstrate adaptive seasonal variation in great tit offspring sex ratios.     

Balancing moult data by subsampling non-moulting birds prior to regression analysis

During the analysis of moult records from the SAFRING database it was found that for some datasets the records were not evenly distributed temporally and the proportion of moulting to non-moulting birds was not what would be expected from random sampling. In an attempt to balance these data, the records of non-moulting birds were subsampled with different sample sizes prior to moult regression analysis, and the resulting moult estimates were then compared. The results suggest that subsampling non-moulting birds such that they occur in the expected proportion to actively moulting birds, based on the duration of moult, provides the best estimates of moult.     

Sex‐specific patterns of fuelling and pre‐breeding body moult of Little Stints Calidris minuta in South Africa

The timing and duration of each stage of the life of a long‐distance migrant bird are constrained by time and resources. If the parental roles of males and females differ, the timing of other life stages, such as moult or pre‐migratory fuelling, may also differ between the sexes. Little is known about sexual differences for species with weak sexual dimorphism, but DNA‐sexing enables fresh insights. The Little Stint Calidris minuta is a monomorphic long‐distance migrant wader breeding in the Arctic tundra. Males compete for territories and perform elaborate aerial displays. Females produce two clutches a season. Each sex may be a bigamist and incubate one nest a season, each with a different partner. We expect that these differences in breeding behaviour entail different preparations for breeding by males and females, so we aimed to determine whether Little Stints showed any sex differences in their strategies for pre‐breeding moult and pre‐migratory fuelling at their non‐breeding grounds in South Africa. We used body moult records, wing length and body mass of 241 DNA‐sexed Little Stints that we caught and ringed between 27 January and 29 April in 2008–2018 at two neighbouring wetlands in North West Province, South Africa. For each individual we assessed the percentage of breeding plumage on its upperparts and took blood samples for DNA‐sexing. We calculated an adjusted Body Moult Index and an adjusted Wing Coverts Moult Index, then used the Underhill–Zucchini moult model to estimate the start dates and the rate of body moult in males and females. We estimated the changes in the sex ratio of the local population during their stay in South Africa, and also estimated the timing and rate of pre‐migratory fuelling and the potential flight ranges for males and females. The males started body moult on average on 7 February and the females on 12 February, but the sexes did not differ in their timing of wing covert moult, which started on average on 10 February. In January to mid‐February, males constituted c. 57% of the population, but their proportion declined afterwards, indicating an earlier departure than females. We estimated that both sexes began pre‐migratory fuelling on average on 15 March. The sexes did not differ in fuelling rate, but most females stayed at the non‐breeding site longer than the males, and thus accumulated more fuel and had longer potential flight ranges. These patterns of moult and fuelling suggest sex differences in preparations for breeding. We suggest that the males depart from South Africa earlier but with smaller fuel loads than the females to establish breeding territories before the females arrive. We conclude that for each sex the observed trade‐offs between fuelling and moult at the non‐breeding grounds are precursors to different migration strategies, which in turn are adaptations for their different roles in reproductive behaviour.     

Mate desertion by male Great Reed Warblers Acrocephalus arundinaceus at the end of the breeding season

Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains.     

Timing and duration of moult in three populations of Purple Sandpipers Calidris maritima with different moult/migration patterns

Timing and duration of primary moult in three populations of Purple Sandpipers Calidris maritima were described and discussed in relation to the birds’ need to complete moult before the onset of winter, when resources are required for survival. We predicted that moult would be completed earlier by birds wintering at higher latitudes. The south Norwegian breeding population, which moults and winters along the coast of east Britain (54–57°N) had a mean starting date of 21 July for primary moult (16 July for females and 24 July for males), a mean duration of 61 days, and completed on 20 September. Resident Icelandic (64–65°N) birds had a mean starting date of 22 July for primary moult (17 July for females and 25 July for males), a mean duration of 51 days, and completed on 11 September. Birds moulting in north Norway (70°N) arrived in north Norway in suspended primary moult or without having started moult, and completed it there. They had a mean completion date of 2 November for primary moult (31 October for females and 3 November for males). Starting date and duration could not be estimated because some suspended moult for an undetermined period, but it was thought that they started in late August. It is likely that most originated from Russia. The onset of moult appears to be set by the end of breeding and there is little overlap in these two events. The earlier start of moult by females in all three populations may be because they abandon the males when the chicks hatch, leaving the males to attend the chicks. Although the duration of primary moult followed the expected trend, being fastest in north Norway and slowest in Britain, the onset of moult was so late in north Norway that they had an unexpectedly late completion date, despite their rapid moult. The late completion of primary moult in north Norway suggests that wintering in the far north may not pose the energetic constraints on Purple Sandpipers that had previously been supposed.     

Annual cycle of the Helmeted Honeyeater Lichenostomus melanops cassidix, a sedentary inhabitant of a predictable environment

The annual cycle of breeding, moult and weight variation in the Helmeted Honeyeater Lichenostomus melanops cassidix , a sedentary bird of temperate southeast Australia, is documented. Breeding and moult were sequential unimodal annual events, whose timing was highly consistent between years. However, overlap of breeding and moult was frequent, and some individuals even commenced primary moult before laying their final clutch. The timing of the post-juvenile moult was coincident with that of adults. Early-hatched young moulted within a few months of hatching, but late-hatched young deferred moult for a year. Helmeted Honeyeaters were heaviest in autumn and early winter, and lightest in spring and early summer, a cycle most consistent with the redirection of all available resources to reproduction. The long breeding season (seven-and-a-half months) of the Helmeted Honeyeater, extensive overlap of breeding and moult, and other life-history attributes including small clutch size, are more consistent with the described bio-rhythmic patterns for birds in the humid tropics than the temperate zone. However, the Helmeted Honeyeater has a fairly rapid primary moult rate, unusual amongst species that overlap moult and breeding. This combination of attributes reflects the stable, somewhat seasonal environment occupied and the resource monopoly established by this tightly territorial subspecies. We speculate that extension of the breeding season, by overlapping breeding and moult, is one of the few options available to vary life-history strategies amongst 'old-endemic' Australian birds of the temperate zone.     

Conditions at the breeding grounds and migration strategy shape different moult patterns of two populations of Eurasian golden plover Pluvialis apricaria

Events in the life cycle of migrant birds are generally time‐constrained. Moult, together with breeding and migration, is the most energetically demanding annual cycle stages, but it is the only stage that can be scheduled at different times of the year. However, it is still not fully understood what factors determine this scheduling. We compare the timing of primary feather moult in relation to breeding and migration between two populations of Eurasian golden plover Pluvialis apricaria, the continental population breeding in Scandinavia and in N Russia that migrates to the Netherlands and southern Europe, and the Icelandic population that migrates mainly to Ireland and western UK. Moult was studied at the breeding grounds (N Sweden, N Russia, Iceland) and at stopover and wintering sites (S Sweden, the Netherlands). In both populations, primary moult overlapped with incubation and chick rearing, and females started on average 9 d later than males. Icelandic plovers overlapped moult with incubation to a larger extent and stayed in the breeding grounds until primary moult was completed. In contrast, continental birds only moulted the first 5–7 primaries at the breeding grounds and completed moult in stopover and wintering areas, such as S Sweden and the Netherlands. This overlap, although rare in birds, can be understood from an annual cycle perspective. Icelandic plovers presumably need to initiate moult early in the season to be able to complete it at the breeding grounds. The latter is not possible for continental plovers as their breeding season is much shorter due to a harsher climate. Additionally, for this population, moulting all the primaries at the stopover/wintering site is also not possible as too little time would remain to prepare for cold‐spell movements. We conclude that environmental conditions and migration strategy affect the annual scheduling of primary feather moult in the Eurasian golden plover.     

Sex‐dependent response of primary moult to simulated time constraints in the rock sparrow Petronia petronia

There is growing evidence that moult speed affects plumage quality. In many bird species, males and females differ in terms of breeding effort, survival expectation and the relationship between fitness and plumage quality. Consequently, differences in moult strategies between the sexes can be expected. The aim of this study was to assess whether, under simulated time constraints and with no parental investment in the previous breeding season, males and females differed in: a) timing and duration of primary moult, b) growth rates of individual primary feathers, and c) number of concurrently growing feathers. We investigated the effect of time constraints generated by a treatment consisting of two decreasing photoperiods (slow changing photoperiod, SCP=2 min day^?1 and fast changing photoperiod, FCP=8 min day^?1) on the primary post‐nuptial moult of captive rock sparrows Petronia petronia. Females started to moult on average 14 and 15 days later than males in both experimental groups. Primary moult duration was 10 (FCP) and 24 (SCP) days longer in males than in females, and, within sex, 34 (females) and 48 (males) days longer in SCP birds than in FCP ones. Females renewed a larger number of primaries simultaneously (5.7% in FCP and 12.8% in SCP) and had a higher total daily feather mass grown (9.9% in FCP and 22.4% in SCP), even though daily growth rates of individual primaries did not differ between sexes. As a result, males and females completed their primary moult at the same time within treatment. The observed differences in timing, duration and energy allocation for primary moult between the sexes probably have a genetic basis, as birds did not engage in reproduction during the preceding breeding season.     

Moult strategies of Cory’s Shearwaters Calonectris diomedea borealis: the influence of colony location, sex and individual breeding status

The replacement of old feathers is essential for birds, but it is also an energy-demanding task. As moult usually does not coincide with other stressful events in its annual cycle, such as reproduction and migration, the bird can optimise its use of time and energy allocated to different activities. There are very few studies comparing the moult strategies of populations with similar breeding calendars but occurring in areas of different habitat quality. Cory’s Shearwaters Calonectris diomedea have a partial moult–breeding overlap, an unusual phenomenon among pelagic seabirds. We have compared the moult schedules in Cory’s Shearwater colonies located in distinct environments (pelagic vs. coastal) and show that moult–breeding overlap is less extensive on Selvagem Grande, situated in deep oceanic waters, than on Berlenga, situated on the continental shelf. Colony attendance of failed breeders, most of which were moulting, was lower at Selvagem Grande than at Berlenga, which suggests that the feeding areas of birds from the former site are more distant from the colony. Failed breeders started to moult earlier than individuals still raising a chick, and breeding status had a stronger influence on determining the onset of wing-feather moult than colony location. Despite published evidence that internal circannual rhythms and external cues, such as variation in daylength, are important factors regulating moult schedules, it is clear that birds retain a considerable flexibility that allows them to respond to external factors in order to strategically manage time and energy in a way that is thought to maximise their fitness.