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.     

Annual survival of Gurney's Sugarbird,Promerops gurneyi

Seasonal variation in body mass and wing length, and the onset and duration of primary moult, were investigated for Chestnut Weavers from northern Namibia. Body mass of adult males was 31.2g (SD 2.6), and adult females weighed 27.4g (SD 1.9). Body mass declined from March to April, and started increasing after August (i.e. near the end of moult) in males and females. Wing length in adult males with new primaries (Oct–Feb) was 80.7mm (SD 2.7) and for adult females (Oct–Feb) 76.8mm (SD 2.6). For both sexes wing length declined during and after the breeding season, due to extensive feather wear. Adult males started primary moult significantly earlier than females (9 April vs 30 April) and moult lasted longer (206 days vs 189 days). The peak summer rainfall and the start of primary moult was earliest in 2000 and latest in 2004 for males and females. Individual primary feathers took 11–18 days to grow.     

BODY MEASUREMENTS,PLUMAGE AND MOULT OF THE SACRED IBIS IN SOUTH AFRICA

Lowe, K. W., Clark, A. & Clark, R. A. 1985. Body measurements, plumage and moult of the Sacred Ibis in South Africa. Ostrich 56: 111–116.

Body measurements, plumage and moult of Sacred Ibis Threskiomas aethiopicus were studied at Pretoria from July 1973 to June 1974. Adult and immature Sacred Ibises are sexually dimorphic in size. Bill length alone can be used to sex most birds. Body mass, wing, tarsus and tail lengths overlap greatly between the sexes but males are generally larger than females. The sexes show similar patterns of variation in body mass and gonad size throughout the year. Juveniles follow a different pattern of variation in these parameters. The plumages of adults, immatures and juveniles are described and compared. There is no sexual dimorphism in plumage pattersn. Moult in adults occurs mainly in the post-breeding period from January to August, and in juveniles and immatures throughout the year. Adult Sacred Ibises have an-extensive, irregular and asymmetrical moult. Factors affecting sexual size dimorphism in African and Australian populations are discussed.     

Marine moult migration of the freshwater Scaly‐sided Merganser Mergus squamatus revealed by stable isotopes and geolocators

Scaly‐sided Mergansers Mergus squamatus breed on freshwater rivers in far eastern Russia, Korea and China, wintering in similar habitats in China and Korea, but nothing was known of their moulting habitat. To investigate the moult strategies of this species, we combined wing feather stable isotope ratios (males and females) with geolocator data (nesting females) to establish major habitat types (freshwater, brackish or saltwater) used by both sexes during wing moult. Although most Scaly‐sided Mergansers of both sexes probably moult on freshwater, some males and non‐breeding and failed breeding females appeared to undertake moult migration to brackish and marine waters. Given the previous lack of any surveys of coastal or estuarine waters for this species during the moult period, these findings suggest important survey needs for the effective conservation of the species during the flightless moult period.     

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

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

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

THE WINTERING AND MOULT OF RUFFS PHILOMACHUS PUGNAX IN THE KENYAN RIFT VALLEY

Some 5700 Ruffs were ringed in the southern Kenyan rift valley during 1967–79, mainly at Lakes Nakuru and Magadi. These have produced 15 recoveries outside East Africa, 14 in Siberia between 73° and 154°E and one in India. Adult males returned to Kenya mainly during August, and females during late August and early September. Females greatly outnumbered males at all times. Most wintering males departed late in March and early in April, but females not until about a month later. First-year birds appeared from the end of August, but remained in low numbers until late October or November. Most departed during April and May, but a few females oversummered. First-year birds typically accounted for about 25% of the wintering Nakuru females, but about 50% of those at Magadi. At both sites they accounted for a higher proportion of male birds than females. Most of the birds at Nakuru throughout late August to May appeared to be local winterers, and many individuals remained in the area for many months each year. Retrapping indicated that approximately 60% of each season's birds returned the following season. Adult males and most adult females commenced pre-winter wing moult before arrival, but completed most of it in Kenya. Males moulted 3–4 weeks ahead of females, and most had finished before December. Females typically finished during December and early January. Most second year birds timed their pre-winter moult similarly to older adults. Suspension was recorded in over 15% of all moulting birds examined. Adult pre-summer moult involved most or all of the tertials, some or all of the tail feathers, most of the inner wing coverts and the body and head plumage. It occurred mainly during January to March (males) or February to April (females), although tertial renewal commonly began a month earlier. Males showed no sign in Kenya of the supplementary prenuptial moult. First-year birds moulted from juvenile into first winter body plumage during late September to November. They underwent a pre-summer moult similar in extent and timing to that of adults, and again about a month earlier in males than females. Spring feathers acquired were often as brightly coloured as those of adults. About 15% of first-year birds renewed their outer 2–4 pairs of large primaries during January to April. Adult and first-year birds fattened before spring departure, commonly reaching weights 30–60% above winter mean. Weights of adult males peaked early in April, those of adult females early in May, and those of first-winter females later in May. Weights were relatively high also during August and September. This was due to the arrival of wintering birds carrying ‘spare’ reserves, and also apparently to the presence of a late moulting fattening passage contingent. The wing length of newly moulted adults was about 3 mm longer than that of newly arrived first-year birds, but there was no evidence of an increase in the wing kngth of adults with successive moults. Adult wing length decreased by 4–5 mm between the completion of one moult and the middle stages of the next. The migrations and annual timetable of Kenyan wintering Ruffs are discussed, and their moult strategy is compared with that of other Holarctic waders.     

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.     

Body weight, gonad development and moult in the Tawny owl (Strix alum)

Gonad development, moult and seasonal changes in body weight and composition in the Tawny owl Strix aluco were studied by examining the carcasses of 369 owls (mostly road casualties) supplemented by 112 weights of live birds. In breeding females laying was preceded by the accumulation of fat and to a lesser extent protein which meant that they weighed more at this time (February/March) than at any other. Females declined in weight after laying but were still heavy during incubation. In contrast, males and non-breeding females did not increase in weight before the start of the breeding season. Juveniles reached or even exceeded adult weight well before independence due to the deposition of fat. Even after the exclusion of diseased or contaminated individuals, 9·4% of the birds examined were identified as starving; most of these were in the autumn and were probably newly-independent young wandering in search of territories. In both sexes gonad maturation was of brief duration coinciding with the period (mid-March to mid-April) in which eggs are normally laid. Ovarian growth was biphasic. In the three months prior to the breeding season ovarian condition in different birds was positively correlated with body weight and it appeared that the largest ovarian follicles of females in poor condition failed to attain the size from which rapid growth to final ovulation occurs. in males testis size in the breeding season was correlated with pectoral muscle weight (an index to protein condition) but not body weight. The majority of adults commenced wing moult in June. The average duration of primary moult was estimated to be 77 days. Healthy birds replaced the primaries of both wings at the same rate but most diseased birds moulted asymmetrically and/or out of season. First-year birds renewed their body feathers between September and November. In the Tawny owl territory establishment, breeding and moult are temporally separated.     

Breeding barnacle geese in Kolokolkova Bay,Russia: number of breeding pairs,reproductive success and morphology

We report the results of an expedition to a barnacle-goose (Branta leucopsis) breeding area in Kolokolkova Bay, west of the lower Pechora delta in northern Russia, undertaken in July 2002. In total, 6 breeding colonies were found within the study area, harbouring 1,324 nests. Mean clutch size was 2.77±0.10 but may have been underestimated because of nest predation. Nest predation was high and correlated with the density of breeding gulls, Larus. The 2002 season was relatively cold and peak hatch occurred late, on 14 July. More than 11,000 barnacle geese were found to moult in the area which, together with the large number of nests found, emphasises the importance of Kolokolkova Bay for barnacle geese. Adult barnacle geese (341) were captured, marked and measured during their annual wing moult. Birds with broods started to moult approximately 2 weeks later than non- and failed breeders. Weight loss during moult was 3 times as rapid as reported for barnacle geese breeding in the Baltic, and a large cost of reproduction seemed to exist in the form of reduced body weight at the onset of moult for birds leading broods. Work in the area will continue over the coming years to document and explain the differences in major life-history parameters, dynamics and environmental effects between arctic and temperate breeding barnacle-goose populations.     

PRIMARY MOULT,WEIGHT AND BREEDING CYCLES OF THE ROCK PIGEON ON DASSEN ISLAND

Cooper, J. 1975. Primary moult, weight and breeding cycles of the Rock Pigeon on Dassen Island. Ostrich 46:154-156.

The primary moult season of the adult Rock Pigeon Columba guinea on Dassen Island is spread over at least nine months. Individual duration is estimated at eight months. Adult birds were heaviest in the winter months outside the breeding season. Overlap between the breeding and moulting seasons occurred and evidence was obtained of incubating birds with active primary moult. Juveniles were lighter than adults. Adults fed on the mainland and probably made daily flights there.     

Food niche segregation between the Malachite Kingfisher,Alcedo cristata,and the Pied Kingfisher,Ceryle rudis,at Lake Nokoué, Bénin

Several species of kingfisher occur on Lake Nokoué, southern Bénin, including Malachite (Alcedo cristata) and Pied Kingfishers (Ceryle rudis). Here, we compare their diet and estimate the degree of overlap in food niche by analysing contents of regurgitated pellets collected near nesting sites of Pied Kingfishers or inside the nest chambers of Malachite Kingfishers. Characteristic fish skull bones were identified using a reference collection of local fish skeletons. Malachite Kingfishers feed most frequently on fish that occur around floating vegetation, mainly Kribia sp. (56%), Hemichromis fasciatus (28%) and Sarotherodon melanotheron (8%). Important differences were found between different pairs, and between adults and nestlings, the latter being fed almost exclusively on Kribia sp. Larger fish are fed to nestlings than are eaten by the adults. Pied Kingfishers prey upon 14 different fish species, some of them being caught in the pelagic region of the lake, particularly clupeids taken by hovering. By comparison with Malachite Kingfishers, Pied Kingfishers feed on a wider diversity of prey, and take larger fish, so that the dietary overlap between the species is relatively low (O = 0.181).     

SOME NOTES ON THE BIRDS OF THE ISOKA DISTRICT OF THE NORTHERN PROVINCE OF NORTHERN RHODESIA

Dean, W. R. J. 1978. Moult seasons of some Anatidae in the western Transvaal. Ostrich 49:76-84.

Spurwinged Geese Plectropterus gambensis, Egyptian Geese Alopochen aegyptiacus, Yellow-billed Ducks Anas undulata, Redbilled Teal A. erythrorhyncha and Southern Pochard Netta erythrophthalma have a flightless moult mainly during the dry season, from April to August, in the western Transvaal. South African Shelduck Tadorna cana moult during October to February after breeding during July and August. The Cape Shoveller Anas smithii has two main flightless periods, April-May and October-January. Cape Teal A. capensis have been recorded in flightless moult in October, December and January.

The duration of the flightless period correlates with wing length; larger and longer winged Anatidae require proportionally more time for wing moult than do smaller and shorter winged Anatidae.

Geese and shelducks moult on large open lakes with an open shore. Ducks have been recorded flightless on lakes and dams, with or without emergent vegetation.     

REVIEWS

Jones, P. J. 1978. Overlap of breeding and moult in the Whitebrowed Sparrowweaver in northwestern Botswana. Ostrich 48:21-24.

Female Whitebrowed Sparrowweavers Plocepasser mahali trapped on the nest while incubating showed advanced active moult of wing and tail feathers, indicating a complete overlap of moulting and breeding schedules. Additional moult data indicated an unusually protracted primary moult of 183 days. It is suggested that the low daily metabolic demands of a slow moult enable it to be compatible with breeding activities, which may be of advantage to some species living in semi-arid environments.     

Moult of the giant petrels Macronectes halli and M. giganteus at South Georgia

Moult scores were collected from colour-ringed individuals of known reproductive status of the two species of giant petrel, Macronectes halli and M. giganteus , at Bird Island, South Georgia between 1978–81.
Both species showed a substantial overlap between breeding and wing-moult, unlike most other Southern Ocean seabirds. Males started moult before females and both sexes of M. giganteus moulted at an earlier stage of the breeding cycle than M. halli , which breeds six weeks earlier than its congener.
Changes in moult rate during the breeding season are documented for both species, with Id. halli showing a rapid increase as the chick nears fledging. Male M. giganteus show a notably different pattern to the other three species-sex groups, starting moult much earlier (at egg-laying), with greater individual synchrony and usually suspending primary moult throughout the main chick growth period, whereas only two male M. halli and no females of either species suspended moult. Differences in pattern, timing and rate of moult are interpreted in terms of availability of food resources and the competing energy demands of other activities, especially chick-rearing.
Completion of primary moult could not be observed in the field but was estimated using data frcsm non-breeding birds and failed breeders; the latter started a rapid moult almost immediately they failed. In both sexes of both species moult is probably concluded at least by early winter.
The general pattern of moult in giant petrels at Bird Island is contrasted with that of other populations and species of Southern Ocean seabirds. It is suggested that the unusually extensive overlap between breeding and moult in giant petrels is a consequence of the very abundant and easily available summer food supplies (especially carrion) and the much diminished winter resources, favouring a completion of moult by the beginning of the winter.     

Moult in Black-browed and Grey-headed Albatrosses Diomedea melanophris and D. chrysostoma

We recorded the age of individual wing and tail feathers of Black-browed and Grey-headed Albatrosses Diomedea melanophris and D. chrysostoma of known age and breeding status at Bird Island, South Georgia. Breeders and non-breeders of both species moult their rectrices annually. Non-breeders moult primaries biennially. In the first year of a cycle, the outer three and some inner primaries are moulted descendantly; in the next year the inner primaries are moulted ascendantly, starting from primary seven. There is a general progression to moulting equal numbers of primaries in each half of the cycle by the time breeding starts at about 10 years of age. Grey-headed Albatrosses usually moult fewer primaries than Black-browed Albatrosses, particularly as 3-year-olds, when they undertake substantial plumage change in body moult. Most secondaries in Black-browed Albatrosses have been replaced once by age 4 years. Breeding Black-browed Albatrosses continue the moult pattern established as immatures whether they fail or not, as do failed Grey-headed Albatrosses. Successful Grey-headed Albatrosses, which breed again 16 months later, moult their three innermost primaries after breeding in the remainder of the current year and, after a period when moult is interrupted, renew the remaining primaries the following year. Comparisons between species and between failed and successful birds within species indicate that moult rate is not closely linked to the length of the interval between breeding attempts. Interspecies differences are better explained by breeding latitude, with tropical albatrosses moulting twice as fast as sub-Antarctic species, possibly reflecting food availability outside the breeding season.     

Resting metabolic rate in migratory and non‐migratory geese following range expansion: go south,go low

While many species suffer from human activities, some like geese benefit and may show range expansions. In some cases geese (partially) gave up migration and started breeding at wintering and stopover grounds. Range expansion may be facilitated and accompanied by physiological changes, especially when associated with changes in migratory behaviour. Interspecific comparisons found that migratory tendency is associated with a higher basal or resting metabolic rate (RMR). We compared RMR of individuals belonging to a migratory and a sedentary colony of barnacle geese Branta leucopsis. The migratory colony is situated in the traditional arctic breeding grounds (Russia), whereas the sedentary colony has recently been established in the now shared wintering area (the Netherlands). We measured RMR by oxygen consumption () during two ontogenetic phases (juvenile growth and adult wing moult). We also investigated juvenile growth rates and adult body mass dynamics. Mass‐independent was 13.6% lower in goslings from the sedentary colony than in goslings from the migratory colony. Similarly, in adult geese, mass‐independent was 15.5% lower in sedentary than in migratory conspecifics. Goslings in the Netherlands grew 36.2% slower than goslings in Russia, while we found no differences in body dimensions in adults. Adult geese from both colonies commenced wing moult with similar body stores, but whereas Russian barnacle geese maintained this level throughout moult, body stores in geese from the Netherlands fell, being 8.5% lower half‐way through the moult. We propose that the colony differences in resting metabolic rate, growth rate and body mass dynamics during moult can be explained by environmental and behavioural differences. The less stringent time constraints combined with poorer foraging opportunities allow for a smaller ‘metabolic machinery’ in non‐migratory geese. Our analysis suggests that range expansion may be associated with changes in physiology, especially when paired with changes in migratory tendency.     

Non‐breeding Cackling,Ross's and Snow Geese on Baffin Island show no loss of body mass during wing moult

Non‐breeding Cackling Branta hutchinsii, Ross's Anser rossii and Lesser Snow Geese Anser caerulescens caerulescens captured during remigial moult on Baffin Island in 2015 showed no loss of body mass with moult stage, and individual variation in mass was largely explained by sex and measures of body size (tarsus length). Exceptional conditions in 2015 resulted in almost no reproductive effort or success in that year, so captured geese of all three species were likely to have been non‐breeding individuals that initiated moult early, whereas there were almost no failed or successful breeders, which would normally moult later. This suggests that in a non‐breeding year (i.e. in the absence of competition from large numbers of goslings), locally moulting geese can obtain sufficient exogenous energy to meet their needs during the flightless wing moult period without losing body mass. This also is consistent with the hypothesis that in other species of geese, accumulation of fat stores prior to, and depletion of such stores during, wing moult is adaptive and likely to be a feature of individual plasticity to meet particular needs, such as undertaking moult migration to remote sites where precise foraging and predation conditions cannot be anticipated, or where competition from more dominant individuals may restrict their access to a reliable food supply.     

OBSERVATIONS ON THE NESTING SITES AND NESTING BEHAVIOUR OF THE KITTLITZ'S SANDPLOVER CHARADRIUS PECUARIUS

Jackson, S. 1984. Predation by Pied Kingfishers and Whitebreasted Cormorants on fish in the Kosi estuary system. Ostrich 55:113-132.

Identification of otoliths from the regurgitated pellets of Pied Kingfishers Ceryle rudis and Whitebreasted Cormorants Phalacrocorax carbo from the Kosi estuary system provides information on the relative proportions of fish species in the diets of the birds. This information can be related to the feeding habits, distribution and abundance of their prey. It is also an indication of the feeding range of the birds. There is little overlap between both the size classes and the species of fish taken by the two predators. This is because of the difference in size and fishing techniques of C. rudis and P. carbo, and of differences in their feeding ranges. Competition for food between the two populations of birds studied is minimized by these differences.     

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.     

Carry‐over effects and compensation: late arrival on non‐breeding grounds affects wing moult but not plumage or schedules of departing bar‐tailed godwits Limosa lapponica baueri

In the annual cycle of migratory birds, temporal and energetic constraints can lead to carry‐over effects, in which performance in one life history stage affects later stages. Bar‐tailed godwits Limosa lapponica baueri, which achieve remarkably high pre‐migratory fuel loads, undertake the longest non‐stop migratory flights yet recorded, and breed during brief high‐latitude summers, may be particularly vulnerable to persistent effects of disruptions to their rigidly‐timed annual routines. Using three years of non‐breeding data in New Zealand, we asked how arrival timing after a non‐stop flight from Alaska (>11 000 km) affected an individual godwit's performance in subsequent flight feather moult, contour feather moults, and migratory departure. Late arrival led to later wing moult, but godwits partially compensated for delayed moult initiation by increasing moult rate and decreasing the total duration of moult. Delays in arrival and wing moult up to 34–37 d had no apparent effect on an individual's migratory departure or extent of breeding plumage at departure, both of which were extraordinarily consistent between years. Thus, ‘errors’ in timing early in the non‐breeding season were essentially corrected in New Zealand prior to spring migration. Variation in migration timing also had no apparent effect on an individual's likelihood of returning the following season. The bar‐tailed godwits’ rigid maintenance of plumage and spring migration schedules, coupled with high annual survival, imply a surprising degree of flexibility to address unforeseen circumstances in the annual cycle.