Moult Strategies Affect Age Differences in Autumn Migration Timing in East Mediterranean Migratory Passerines

Adult passerines renew their flight feathers at least once every year. This complete moult occurs either in the breeding areas, just after breeding (summer moult), or, in some long-distance migratory species, at the non-breeding areas, after arrival to the southern wintering area at the end of autumn migration (winter moult). The aim of this study was to relate moult strategies with the DMD, the difference in median migration date, through Israel, between juveniles and adults. Our data on autumn migration timing in juveniles and adults was based on ringing data of 49,125 individuals belonging to 23 passerine species that breed in Europe and Western Asia and migrate through Israel. We found that DMD was associated with moult timing. In all species that perform a winter moult, adults preceded juveniles during autumn. Among migrants who perform a summer moult, we found evidence of both migration timing patterns: juveniles preceding adults or adults preceding juveniles. In addition, in summer moulters, we found a significant, positive correlation between mean breeding latitude and DMD. Although previous studies described that moult duration and extent can be affected by migration, we suggest that moult strategies affect both migration timing and migration strategy. These two moult strategies (summer or winter moult) also represent two unique migration strategies. Our findings highlight the evolutionary interplay between moult and migration strategies.     

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.     

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.     

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.     

AUTUMN MOVEMENTS, MOULT AND MEASUREMENTS OF THE LESSER REDPOLL CARDUELIS FLAMMEA CABARET

The annual cycle of Lesser Redpolls breeding in Northumberland is described. Birds return in late April and could rear at least two broods, in the absence of predation, before they begin to moult in early August. The complete moult of both sexes usually begins just after the last brood of young reaches independence. Moult ends in late September and the adults then move southwards immediately. Juveniles also finish their partial moult before they migrate, but those which finish moult well before the adults, apparently wait for the latter before undertaking extensive southward movements, though some disperse over short distances in early September. Some adults and juveniles caught during moult at one site returned to moult there in later autumns, even though they did not breed there. Movement in autumn from Britain to the Continent takes place only at the short sea-crossings. More recoveries are obtained abroad in years of poor birch seed crop in southern England. Moult of the remiges and rectrices of the adults is described, and its progress recorded by a numerical scoring system whose merits are discussed. The moult score of the primary feathers follows an approximately linear relationship with date, and the moult scores of all individuals of each sex in each year have been used in regression analyses to yield averages of the duration, start and end of moult, an average daily increase of primary moult score, and the spread of the start of moult within each sample of birds. The results are discussed in relation to breeding and migration. The rates of moult of the primaries, secondaries and tail are not independent of each other, though, in contrast to the primaries, the secondary moult score does not increase linearly with date. The average daily increase of primary moult score is closely correlated with the number of primaries growing simultaneously. Each primary took about 16 days to complete growth in each year, but the duration of moult varied between 43 and 56 days in different years. Variation in the timing and duration of moult of Redpolls in Norway, Iceland and Britain is discussed in relation to the breeding season. Plumage sequences of the Lesser Redpoll are reviewed, with emphasis on their application to separation of sex and age classes. Wing lengths of the males and females of a given age overlap considerably, and abrasion alters these lengths only slightly. Older birds have longer wings. Weight changes of adults and juveniles in autumn are examined in detail. Weight variation of individual birds in August and September is more often due to hourly changes in response to feeding than day-to-day changes in response to temperature. Weights of adults, but not first-year birds, decrease at the start but then increase towards the end of the moult, but apparently there is no deposition of fat for migration. Weights of birds caught during their southward movement also show no increase, nor did a group of Lesser Redpolls caught near Oxford in December. It is suggested that day length may be an additional reason for southward migration, besides a reduction in food supply.     

THE MOULT OF THE BULLFINCH PYRRHULA PYRRHULA

The distribution of feather tracts and their sequence of moult in the Bullfinch is described. The adult post-nuptial moult, which is complete, lasted 10–12 weeks, and the post-juvenile moult, which is partial, 7–9 weeks. Adult moult began with the shedding of the first (innermost) primary and ended with the replacement of the last. Variations in the rate of moult in the flight feathers were mainly achieved, not by changes in the growth rates of individual feathers, but in the number of feathers growing concurrently. The primaries were shed more slowly, and the onset of body moult delayed, in birds which were still feeding late young. In 1962, the onset of moult in the adults was spread over 11 weeks from thc end of July to the beginning of October, and in the two following years over the six weeks, from the end of July to the beginning of September. The onset of moult was delayed by late breeding, which itself occurred in response to a comparative abundance of food in late summer, markedly in 1962. In all years, the first juveniles to moult started at the end of July, and the last, three weeks after the latest adults. Juveniles moulting late in the season retained more juvenile feathers than those moulting earlier. During moult, adult and juvenile Bullfinches produce feathers equivalent to 40% and 33% respectively of their dry weights. In both, for much of the moult, an average of nearly 40 mgm. of feather material—some 0.6% of their dry-weight–is laid down each day. The remiges of the adult comprise only a seventh of the weight of the entire plumage, and it is suggested that their protracted moult results not so much from their energy requirements, as from the need to maintain efficient flight. Variation in the rate of moult in the remiges was much less pronounced than in the body feathers. Bullfinches were less active during moult than at other times of the year. The weights of both adults and juveniles increased during moult. The food during the moult period is described. In all years, most Bullfinches finished moulting just before food became scarce, even though this occurred at different times in different years. In one year, adults moulting latest in the season probably survived less well than those moulting earlier; the same was apparently true of the juveniles in all years. The timing of moult in the Bullfinch, and the factors initiating it, are discussed in relation to the breeding season and foodsupply near Oxford.     

Keeping up with early springs: rapid range expansion in an avian herbivore incurs a mismatch between reproductive timing and food supply

Within three decades, the barnacle goose population wintering on the European mainland has dramatically increased in numbers and extended its breeding range. The expansion has occurred both within the Arctic as well as by the colonization of temperate areas. Studies of performance of individuals in expanding populations provide information on how well species can adapt to novel environments and global warming. We, therefore, studied the availability of high quality food as well as timing of reproduction, wing moult, fledgling production and postfledging survival of individually marked geese in three recently established populations: one Arctic (Barents Sea) and two temperate (Baltic, North Sea). In the Barents Sea population, timing of hatching was synchronized with the peak in food availability and there was strong stabilizing selection. Although birds in the Baltic and North Sea populations bred 6–7 weeks earlier than Arctic birds, timing of hatching was late in relation to the peak in food availability, and there was moderate to strong directional selection for early breeding. In the Baltic, absolute timing of egg laying advanced considerably over the 20‐year study period, but advanced little relative to spring phenology, and directional selection on lay date increased over time. Wing moult of adults started only 2–4 weeks earlier in the temperate populations than in the Arctic. Synchronization between fledging of young and end of wing moult decreased in the temperate populations. Arctic‐breeding geese may gradually accumulate body stores from the food they encounter during spring migration, which allows them to breed relatively early and their young to use the peak of the Arctic food resources. By contrast, temperate‐breeding birds are not able to acquire adequate body stores from local resources early enough, that is before the quality of food for their young starts to decrease. When global temperatures continue to rise, Arctic‐breeding barnacle geese might encounter similar problems.     

Breeding status influences timing but not duration of moult in the Northern Fulmar Fulmarus glacialis

Seabirds are key marine top predator species that are often used as indicators of the environmental quality of the oceans. Their breeding phenology has been studied extensively, but their pelagic habits mean less is known about the phenology of other events during the non-breeding period. Here, we used miniaturized saltwater immersion light-based geolocators (GLS) to investigate moult phenology in individuals with known breeding histories in a population of Northern Fulmar Fulmarus glacialis in Orkney, Scotland. As seabirds spend more time on the water during moult, moulting periods can be identified from patterns of variation in the amount of time that birds are in contact with saltwater. Estimates of daily variation in this behaviour during the non-breeding period were based upon wet/dry sensors and then modelled to characterize the timing of the moult. Light-based geolocation provided information on the areas used by each individual during its moult period. Inter-individual variability in moult timing was investigated in relation to sex and breeding success in the previous summer. We found a sex difference in the location of the moult, but not in its timing. However, the timing of moult did differ between individuals that had succeeded or failed in their previous breeding attempt, with successful breeders moulting the latest. In contrast, the duration of moult did not depend on prior reproductive success, but there was evidence of inter-annual variation in moult duration. GLS studies have provided a step change in our understanding of the at-sea distribution of pelagic seabirds. Our work highlights how activity data from these devices can add value to such studies by identifying key phases of the annual cycle, and locations at these times, when seabirds may be at particular risk. Furthermore, our findings indicate that individual and inter-annual variation in breeding success may influence phenological patterns in other phases of the Northern Fulmar annual cycle.     

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.     

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.     

The ‘chaotic’ flight feather moult of the Steppe Buzzard Buteo buteo vulpinus

Steppe Buzzards breed in Eurasia and spend the non-breeding season in Africa. Adults moult some flight feathers during the breeding season and some during the non-breeding season. Moult is arrested during migration. The extent of moult of flight feathers in adults is highly variable between individuals in southern Africa, with the renewal of two primaries, three secondaries and five rectrices as the most frequently encountered pattern. Time spent on the non-breeding grounds in South Africa is too short to allow for a sequential moult. Moult of flight feathers is restricted to the almost synchronous dropping of a number of feathers upon arrival, with few being replaced subsequently. Any of the flight feathers can be replaced in southern Africa, and the pattern of renewal in primaries and secondaries cannot be distinguished from random. Tail feathers are replaced in an alternating (transilient) pattern. Moult in the non-breeding areas may primarily be complementary to moult on the breeding grounds, but these two partial moults per year are insufficient to renew all flight feathers annually. Middle secondaries and central tail feathers are regularly carried over to a third moult, but this is rare for primaries.     

Why renew fresh feathers? Advantages and conditions for the evolution of complete post‐juvenile moult

Juveniles of several passerine species renew all of their fresh juvenile feathers immediately after fledging (complete post‐juvenile moult), in contrast to the majority, which perform a partial post‐juvenile moult. To understand the adaptive roles of this phenomenon we compared the quality of juvenile plumage in species that perform a complete post‐juvenile moult with that of species which perform a partial post‐juvenile moult; we similarly compared juveniles and adults in each of these groups. The quality of feathers was measured by mass of primaries, colour, and length. In species which perform a complete post‐juvenile moult the plumage quality of second‐year individuals, in their first breeding season, is similar to the plumage quality of adults, unlike those species that perform a partial post‐juvenile moult. In species which perform complete post‐juvenile moult, the quality of the feathers grown in the nest is lower than the quality of adult post‐breeding feathers. In contrast, in species which perform partial post‐juvenile moult the quality of the feathers grown in the nest is similar to that of adult post‐breeding feathers. We found that a complete post‐juvenile moult strategy is much more common 1) in residents and short‐distance migrants than in long‐distance migrants, 2) in southern latitudes, 3) in species with medium body mass and 4) in omnivores and granivores. Our results indicate two adaptive roles of the complete post‐juvenile moult strategy: 1) achieving high quality plumage in the first year which may increase individual survival probability and fitness and 2) allocating fewer resources to nestling plumage and more to nestling development, which enables the nestlings to leave the nest earlier, thus reducing the probability of encountering nest predators. We suggest that the complete post‐juvenile moult, immediately after fledging, is an optimal strategy in favourable habitats and under low time constraints, as in some tropical ecosystems.     

The effects of long‐distance migration on the evolution of moult strategies in Western‐Palearctic passerines

Although feathers are the unifying characteristic of all birds, our understanding of the causes, mechanisms, patterns and consequences of the feather moult process lags behind that of other major avian life‐history phenomena such as reproduction and long‐distance migration. Migration, which evolved in many species of the temperate and arctic zones, requires high energy expenditure to endure long‐distance journeys. About a third of Western‐Palearctic passerines perform long‐distance migrations of thousands of kilometres each year using various morphological, physiological, biomechanical, behavioural and life‐history adaptations. The need to include the largely non‐overlapping breeding, long‐distance migration and feather moult processes within the annual cycle imposes a substantial constraint on the time over which the moult process can take place. Here, we review four feather‐moult‐related adaptations which, likely due to time constraints, evolved among long‐distance Western‐Palearctic migrants: (i) increased moult speed; (ii) increased overlap between moult and breeding or migration; (iii) decreased extent of plumage moult; and (iv) moult of part or all of the plumage during the over‐wintering period in the tropics rather than in the breeding areas. We suggest that long‐distance migration shaped the evolution of moult strategies and increased the diversity of these strategies among migratory passerines. In contrast to this variation, all resident passerines in the Western Palearctic moult immediately after breeding by renewing the entire plumage of adults and in some species also juveniles, while in other species juvenile moult is partial. We identify important gaps in our current understanding of the moult process that should be addressed in the future. Notably, previous studies suggested that the ancestral moult strategy is a post‐breeding summer moult in the Western Palearctic breeding areas and that moult during the winter evolved due to the scheduling of long‐distance migration immediately after breeding. We offer an alternative hypothesis based on the notion of southern ancestry, proposing that the ancestral moult strategy was a complete moult during the ‘northern winter’ in the Afro‐tropical region in these species, for both adults and juveniles. An important aspect of the observed variation in moult strategies relates to their control mechanisms and we suggest that there is insufficient knowledge regarding the physiological mechanisms that are involved, and whether they are genetically fixed or shaped by environmental factors. Finally, research effort is needed on how global climate changes may influence avian annual routines by altering the scheduling of major processes such as long‐distance migration and feather moult.     

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     

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.     

Annual cycles in Jamaican forest birds

The annual cycles of forest birds in Jamaica were found to be very similar to those at higher latitudes. Most species bred between March and September, though a few possibly breed throughout the year, especially in cultivated areas. Primary moult followed immediately after breeding, and in some species was apparently arrested to allow a further breeding attempt. Several species were fatter outside the breeding season than during it, and this is interpreted as "winter fattening" comparable to that found in many birds at higher latitudes. Weights varied little but individuals retrapped were usually heavier outside the breeding season. In some species the first complete moult took place at the end of the first year, implying that the birds do not breed until at least two years old.     

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.     

Short‐ and long‐term costs of reproduction in a migratory songbird

Costs of reproduction represent a common life‐history trade‐off. Critical to understanding these costs in migratory species is the ability to track individuals across successive stages of the annual cycle. We assessed the effects of total number of offspring fledged and date of breeding completion on pre‐migratory body condition, the schedule of moult and annual survival in a migratory songbird, the Savannah Sparrow Passerculus sandwichensis. Between 2008 and 2010, moult was delayed for individuals that finished breeding later in the breeding period and resulted in reduced lean tissue mass during the pre‐migratory period, suggesting an indirect trade‐off between the timing of breeding completion and condition just prior to migration. Lean tissue mass decreased as the number of offspring fledged increased in 2009, a particularly cool and wet year, illustrating a direct trade‐off between reproductive effort and condition just prior to migration in years when weather is poor. However, using a 17‐year dataset from the same population, we found that parents that fledged young late in the breeding period had the highest survival and that number of offspring fledged did not affect survival, suggesting that individuals do not experience long‐term trade‐offs between reproduction and survival. Taken together, our results suggest that adult Savannah Sparrows pay short‐term costs of reproduction, but that longer‐term costs are mitigated by individual quality, perhaps through individual variation in resource acquisition.     

Weak breeding seasonality of a songbird in a seasonally arid tropical environment arises from individual flexibility and strongly seasonal moult

In some tropical birds, breeding seasonality is weak at the population level, even where there are predictable seasonal peaks in environmental conditions. It therefore remains unclear whether individuals are adapted to breeding at specific times of the year or flexible to variable environmental conditions. We tested whether the relative year‐round breeding activity of the Common Bulbul Pycnonotus barbatus arises due to within‐individual variability in breeding dates. We collected data from 827 birds via mist‐netting over 2 years with corresponding local weather data. We used a combination of climate envelope and generalized linear mixed models to explore how the timing of breeding is influenced by time of year, individual variation, rainfall and temperature in a West African savannah where seasonal precipitation determines annual variation in environmental conditions. We also pooled 65 breeding records from 19 individuals recorded between 2006 and 2017 based on brood patch occurrence and behavioural observation to compare within‐individual and population variability in breeding dates. We show that the breeding dates of individuals may be as variable as for the population as a whole. However, we observed a seasonal peak in juvenile occurrence that varies significantly between years. Models suggest no relationship between nesting and moult, and within‐year variation in rainfall and temperature, and birds were unlikely to breed during moult but may do so afterwards. Moult was very seasonal, correlating strongly with day length. We suggest that because environmental conditions permit year‐round breeding, and because reproductive output is subject to high predation risk, there is probably a weak selection for individuals to match breeding with variable peak conditions in the environment. Instead, moult, which always occurs annually and successfully, is probably under strong selection to match variable peak conditions in the environment so that long‐term survival ensures future reproduction.     

Young But Not Old Adult African Striped Mice Reduce Their Activity in the Dry Season When Food Availability is Low

An individual′s survival and fitness depend on its ability to effectively allocate its time between competing behaviors. Sex, social tactic, season and food availability are important factors influencing activity budgets. However, few field studies have tested their influences. The African striped mouse (Rhabdomys pumilio) lives in highly seasonal habitats in southern Africa, and individuals can adopt different social tactics. We investigated seasonal changes in activity budgets of different tactics and predicted that individuals will reduce their activity in the non‐breeding season to save energy when food availability is low and that young non‐breeding adults (‘philopatrics’) invest mainly in activities related to gaining body mass to increase survival probability. We predicted old adults (‘breeders’), which bred during the previous breeding season, to invest mainly in maintenance of their social status. We conducted 90 focal observations during the non‐breeding season and 73 during the breeding season. Activity budgets of striped mice were season and tactic specific, with philopatrics, but not breeders, reducing activity when food availability was low, possibly to decrease energy expenditure. Philopatrics of both sexes foraged and basked more in the breeding season than during the non‐breeding season. Male philopatrics gained body mass and female philopatrics maintained their body mass in both seasons. Sex‐specific differences occurred during the breeding season, when female breeders foraged more than male breeders, while male breeders chased other individuals more than female breeders. These findings indicate that individuals adopting different social tactics display distinct behaviors to fulfill tactic‐specific energetic needs .