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.     

Variation in body condition of breeding Savi’s Warblers Locustella luscinioides: the reproductive stress and flight adaptation hypothesis revisited

Current theory suggests that mass change in adult birds while breeding may be adaptive (to reduce wing-loading during nestling feeding) or result from physiological stress. To test which might be more important in determining mass loss in breeding Savi’s Warblers (Locustella luscinioides), we used a new approach in which the variation in four indices of body condition was described: weight, fat score, muscle score and lean weight (i.e. excluding fat and muscle). We expected weight variations to be adaptive if they involved changes in fat and lean weight, whereas physiological stress should influence the muscle score to a greater extent. As in other species, females showed a greater variation in weight, and carried more fat, than males during the breeding cycle. During incubation, females had greater weight and fat score than males. The weight remained constant and lean weight declined in both sexes, whereas females increased in muscle, which probably reflects the regression of the reproductive organs. During the nestling stage, both sexes declined significantly in all four indices of condition, showing evidence of physiological stress. However, the greater decline in weight in females than in males is consistent with the flight-adaptation hypothesis, as are the cyclic changes in lean weight associated with the various nesting attempts. The fact that both sexes declined significantly in weight, muscle and lean weight with an increasing number of nesting attempts, but not in fat, which was recovered after each nestling period, also indicates that both reproductive stress and adaptive changes occur during breeding. When the whole breeding season was considered, females showed a greater decline in muscle than males, which we interpret to be evidence for a greater reproductive stress in females. We suggest that the small breast muscle size and depleted protein reserves at the end of the breeding period might influence future survival through impaired flight ability and a compromised post-breeding moult.     

The rôle of fat and protein during breeding in the White-bellied swiftlet (Collocalia esculents)

The breeding biology of the White-bellied swiftlet was studied in Malaysia. Birds were captured every month, and more intensively during the breeding season. To investigate the role of fat and protein reserves in the annual cycle, carcasses were fat extracted after separating the pectoral muscles. The stage of the laying cycle was investigated by histological examination of the ovaries.
Fat and protein reserves were correlated with the body size of the birds. In non-laying females and males, both reserves were correlated with date and feeding conditions determined by the weather. In egg-laying birds, protein reserves were again correlated with feeding conditions, but fat reserves were negatively correlated with the day of the laying cycle. Assessment of the daily foraging abilities of the birds showed that, for egg-layers, proteins were likely to be in greatest supply and fats in least supply. It is suggested that a fat reserve serves as an insurance against poor feeding conditions for laying birds.     

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.     

Annual cycles of migratory fattening, reproduction and moult in European quail (Coturnix coturnix)

Experimental studies of the physiological mechanisms underlying avian migration have concentrated on small passerines. The present study is concerned with the regulation of migratory fat deposition in a galliform. the European quail (Coturnix coturnix). The increased mass associated with migration was due exclusively to the deposition of fat whereas the increased body mass of laying females was due to increases in lean tissue and water as well as fat. Annual cycles of body mass, moult, gonadal size and plasma luteinizing hormone were measured every other week in captive males and females held outdoors under natural daylengths and temperatures in Bristol, UK (51° 27' N). Males and females showed two peaks of fat deposition each year which occurred at the migratory passage times reported in wild birds. Luteinizing hormone levels and gonadal size increased in parallel with vernal fat deposition, and remained high until late summer. The pattern of primary feather moult in the intact birds was similar to that of wild quail, with moult following gonadal regression and being suspended during autumnal fattening. Castration of European quail did not inhibit the expression of migratory fattening, as it does In certain passerines. In fact, castrates displayed fattening cycles that were more clearly defined and of greater amplitude than those in the intact males. The annual cycle of European quail differs from that of other well-studied passerine migrants such as Zonotrichia sparrows, and this is most likely associated with differences in breeding ecology. In addition, the ability of quail to express vernal fattening independently of the presence of the gonads suggests that taxonomic differences between migratory species are also apparent in the physiological mechanisms of migratory fattening.     

Corticosterone responses of grey-faced petrels (Pterodroma macroptera gouldi) are higher during incubation than during other breeding stages

We report the results of the first field study examining seasonal changes in corticosterone responses of typically long-lived birds of the order Procellariiformes. In particular, we examined whether grey-faced petrels Pterodroma macroptera gouldi showed changes in circulating baseline corticosterone concentrations and corticosterone responses to a standardized handling protocol across the breeding season. Such changes have been associated with changes in body condition and variations in energy demands on adult birds through the breeding season. During early incubation, males were in significantly better condition than females that had just completed laying, whereas during late incubation, males were in significantly poorer condition than females. In spite of these differences, there was no significant difference in baseline corticosterone concentrations between sexes or among birds at different reproductive stages. However, we detected significant differences in corticosterone responses associated with a standardized handling protocol at different stages through the breeding season. Responses were significantly greater during incubation compared with the prelay period and late chick rearing. Body condition was weakly and negatively correlated with maximum and total integrated corticosterone level, indicating that some of the individual variability in stress corticosterone responses could be explained by variation in body condition. However, the largest stress response occurred during late incubation and was independent of sex, although males were in relatively poor condition and females in relatively good condition. This period coincided with the breeding stage in which energy constraints on individual adults were higher than at other periods of the reproductive cycle and birds may be physiologically primed for extended fasts.     

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.     

The importance of body reserves for successful reproduction in the Tawny owl (Strix aluco)

One-quarter of Tawny owl nests fail to hatch young, mainly because the eggs are chilled and/or deserted. In 1973–74 automatic photography was employed at four nests near Oxford to relate the incubation behaviour of females to the ration of prey supplied to them by their mates. The eggs did not hatch in two nests and young fledged from only one of the others. Females were less attentive at the nests which failed during incubation and on average received less prey, but even at successful nests there were some nights when the female was supplied with less than her estimated daily food requirement. Female Tawny owls accumulate large reserves of fat and protein before laying. These buffer against any temporary inability of the male to provide sufficient food during incubation, and enable the female to stay on the nest rather than hunt for herself and risk the eggs becoming chilled. When prey are scarce, many females do not lay at all, and the ultimate factor determining whether breeding takes place may be the female's ability to acquire body reserves sufficient to provide a chance of breeding successfully.     

Post-juvenile and post-breeding moult of Savi's Warblers Locustella luscinioides in Portugal

We describe the sequence and extent of the complex and little understood post-juvenile and post-breeding moults of Savi's Warblers Locustella luscinioides . In contrast to previous studies, the post-juvenile moult occurred in at least 44% of the birds, 5% of which moulted some or all tertials and greater coverts. The timing of overlap between the filling and the post-juvenile moults, and the fact that later-moulting birds had no post-juvenile moult, strongly suggests that the moult extent is dependent on fledging date. From July onwards, all adult males overlapped breeding and moult, whereas only 11% of the females did so. The start of moult varied from 6 June to 25 August, and was significantly earlier in males. Only 18% of the birds completed the moult, whereas the remaining individuals retained a variable number of inner primaries and/or secondaries. Interestingly, not only was the number of retained primaries positively associated with the date of moult, but so too was the primary number of birds in which the moult started. We view this as an adaptation allowing the replacement of the most important feathers for flight when the time available for moult is short. Body condition did not vary with the progress of moult when date was taken into account, but fat reserves still tended to decrease and then increase. The body condition was correlated positively with the wing raggedness, so Savi's Warblers do not compensate for an increasing wing load during moult.     

黄腹山鹪莺稳定的配偶关系限制雄性欺骗者

多数鸟类通过性特征限制在同性竞争和配偶选择中的“欺骗者”存在,与此相反,雀形目扇尾莺科部分物种表现出繁殖季节性特征消退的身体特征变化模式.在广州市南沙区通过“目字笼”对黄腹山鹪莺配偶关系稳定性的限制机制进行研究,发现虽然雌性个体到访原配个体和对照个体的次数几乎相同,但是雌性个体对原配雄性的单次选择时间明显长于对照雄性个体,总计选择时间也明显长于对照雄性个体.选择实验过程中,原配雄性的跳动次数明显高于对照个体雄性,以竖尾扑哧和鸣声恐吓等为代表的威慑行为次数也明显高于对照雄性个体.结果说明,雌性更青睐于原配个体,配对时间越长,忠诚度越高,而且原配雄性比入侵雄性个体表现出更高的活跃度和威慑行为.繁殖季节性特征消退的物种可以通过保持稳定的配偶关系以限制“欺骗者”存在.可以推测繁殖的巨大投入和雌性之间的同性竞争可能是产生这种配偶稳定性的主要原因.     

The effect of food on laying date and clutch-size in Tengmalm's Owl Aegolius funereus

The breeding of Tengmalm's Owl Aegolius funereus was studied at Umeå, Sweden, during the 1984–85. Mean clutch-size was one egg larger in 1984 than in 1985 despite the later laying in 1984. The difference in clutch-size was related to a better food supply in 1984. Daily weight increase of females during the prelaying period showed a high negative correlation with laying date in 1985, and a high positive correlation with clutch-size independently of laying date in 1984–85. This suggested that food eaten before and during laying had a great and direct influence on both laying date and clutch-size. Many females increased in weight during laying and most others decreased only moderately (relative to egg weight), suggesting that body reserves were not a main source for egg production.
Late breeding females were provided with extra food during the prelaying and laying periods in 1985. Fed females weighed more, bred eight days earlier and laid one more egg than controls. At the same laying dates in mid season, and after heavy snow-fall, clutch-size and female weight were larger in the fed birds than in controls, but this was not so near the end of the laying season. Although the earliest of the fed late breeders weighed more, and probably were less restricted by food availability just before or during laying, they did not lay more eggs than did early breeders. This result suggested some limitation on clutch-size that could not be overcome by the supplementary feeding. Weights of females during laying did not show any consistent relationship with clutch-size during successive laying date intervals, suggesting that clutch-size was not directly related to body condition.     

SEASONAL CHANGES IN BODY-WEIGHT OF OYSTERCATCHERS HAEMATOPUS OSTRALEGUS

The body-weights of Oystercatchers Haematopus ostralegus wintering in Morecambe Bay, north-west England, showed marked seasonal changes between late summer and late winter, with considerable differences apparent between adult and immature birds. An attempt is made to relate these changes to recorded seasonal variations in prey biomass and to the annual cycles of breeding, moult and migration of the Oystercatcher. The mean weight of females invariably exceeded the mean weight of males in samples collected on the same dates, regardless of age. Adults returned from northern breeding areas in very lean condition, with mean weights ranging from 526 g in males to 540 g in females. Mean weight then increased progressively, due mainly to fat deposition, to a peak in March (up to 662 g in males and 675 g in females) around the time of their main departures for breeding. Heaviest birds then exceeded 800 g. Birds migrating to Iceland in spring would need to be of above average weight in March to make the shortest crossing (850 km, 13 h), via Scotland, while Oystercatchers of 700 g and over could probably make a direct flight (1500 km, 25 h) from Morecambe Bay in favourable weather. Breeding weights of British Oystercatchers were similar to those of post-breeders returning to Morecambe Bay in late August. The mean weights of first-year Oystercatchers arriving in August were very low, 449 g in males and 478 g in females. Their weights, and those of second- and third-year immatures, then rose rapidly in autumn, with some fat deposition, and reached mean values ranging between 551 g (males) and 597 g (females) by November-December. Mean weight then fell by 10–17% from December to March returning close to or below the September levels, whereas adults gained a further 6% during these winter months. Summer and autumn weight gains, and the major moult of adults and older immatures, occurred when the biomass of their two staple mollusc preys, Mytilus edulis (mussel) and Cardium edule (cockle), was maximal. Winter loss in mean weight of immatures corresponded with declining prey biomass, suggesting either that they were less efficient than adults in coping with deteriorating winter food supplies, or that they had no need to accumulate further (premigratory) fat reserves. The autumnal increases in mean weight of immatures are interpreted as an adaptation for withstanding adverse feeding conditions in winter. The Oystercatcher appears to be the only wader species in Britain in which adults increase, rather than lose, weight during the winter. This may be a consequence of an early breeding season, but it may be regarded also as a measure of the success Oystercatchers have achieved by specializing on a difficult but plentiful prey source.     

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.     

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.     

Sexual differences in moult–breeding overlap and female reproductive costs in pied flycatchers, Ficedula hypoleuca

1. In this study I show that a sexual difference in timing of the post-nuptial moult frequently occurs in a sub-arctic population of the pied flycatcher.
2. Most pairs started to moult after fledging of their young, but an overlap between moult and nestling feeding was more common among males than females. This sexual difference in moult–breeding overlap increased as the season progressed.
3. Females with moult–breeding overlap laid smaller clutches than non-moulting females. In addition to many other factors explaining the seasonal decline in clutch size that has been found for many bird species, it is possible that females adjust their clutch size according to their own risk of having to start moulting while still feeding the nestlings.
4. Nearly 24% of the females were deserted by their mate before the young fledged. Desertion imposed no fitness costs to males in terms of fledgling number or quality, suggesting that their females managed to adjust their care for the loss of male care.
5. Deserted females started moulting later than aided females, which may be a result of their increased reproductive investment.
6. Deserted females and females aided by moulting males had lower survival rate than females aided by non-moulting males.
7. These findings suggests that delayed moult may be one mechanism causing inter-annual reproductive costs in birds, and the relationship between a sexual difference in timing of moult and its fitness consequences may be widespread among passerine birds.     

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.     

5. LIVINGSTONE IN NORTH-EASTERN RHODESIA

Sugg, M. St. J. 1974. Mensural and moult data from a breeding colony of Pied Kingfishers. Ostrich 45: 227–234.

Pied Kingfishers were ringed over two breeding seasons at a breeding colony on the Kenyan shore of Lake Victoria. Data were collected on weight, wing and bill length, injury and moult. Bill abrasion and breakage from nest excavation was found in both sexes and regeneration of worn and broken bills was recorded.

Adult birds of both sexes returned to the colony to breed but no juvenile was recaptured the year after hatching. Females are slightly larger than males (wing length) and both sexes showed a weight increase in the evening prior to roosting. Juveniles had shorter wings and bills than adults but their weights were similar. Their bills were short, soft, weak and the gape was salmon pink. No juveniles showed any moult. Adult moult records support the sequence and duration of moult suggested by Douthwaite (1971) though no overall decrease of moult activity was recorded during the breeding season.     

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.     

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.     

Fat reserves of migrating passerines at arrival on the breeding grounds in Swedish Lapland

Mist-net capture data taken during 6 years (1988–1990 and 1992–1994) of field work were used to describe the arrival sequences and fat loads of nine species of migratory passerines which breed in a near-Arctic environment in Swedish Lapland. Long-distance migrants arrived with significantly larger mean fat reserves than did medium- and short-distance migrants. Long-distance migrants carried fat loads at arrival which corresponded to potential remaining flight distances between 242 and 500 km. When females and males arrived on the breeding grounds simultaneously, females carried significantly larger energy reserves than did males in seven out of nine species. In contrast, when the sexes showed a significant difference in median arrival date (two out of nine species), there was no difference in mean fat load carried into the breeding area. A relationship was found between the migratory habits and foraging ecology of each species and the amount of fat reserves at arrival, suggesting that species-specific migratory distances and feeding habits determine the amount of fat that is needed during the transition period between migration and onset of breeding. The short growing season in the study area restricts the time available for breeding and moult, and large energy reserves at arrival may speed up the breeding schedule to counteract possible time constraints. Overloading at the last stopover site during spring migration may be an adaptation allowing birds to cope with a restricted time frame for breeding and moult at high latitudes.