Extent Of Moult Research Articles

Timing and extent of primary moult in breeding Black-legged Kittiwakes Rissa tridactyla at different colonies in the north-east Atlantic

ABSTRACT Timing of moult of the inner primaries by breeding Black-legged Kittiwakes is very similar among colonies ranging from southern England to northern Norway, but can be much later at very high-latitude colonies, such as at Svalbard, where breeding is delayed by the late spring thaw. Breeding adult Black-legged Kittiwakes almost all replaced the first and second (innermost) primary feathers on their wings while breeding.

Plumage dimorphism and moult patterns of weaverbirds – a review

The colourful plumages of weaverbirds (family Ploceidae, with 118 species recognised) provide a well-known and in part iconic showcase of sexual selection, with widespread sexual dimorphism (93 species) as well as seasonal dimorphism (62 species). The tremendous diversity in both the type and degree of plumage dimorphism is poorly known, which calls for a better and extended understanding of the highly variable moult patterns in this group. Here, we lay a foundation for this by reviewing and discussing what is known of the timings and patterns of moult in the Ploceidae. The extent of post-juvenile moult is poorly known in weavers: it is known to be complete in 10 species, partial in two species, and either complete or partial in six species. However, it is likely that there is more variation than previously thought. Weavers typically have a complete moult after breeding, and before breeding a partial prenuptial moult, restoring the male (and, in some species, female) breeding plumage; this usually involves only body feathering, one exception being the Seychelles Fody Foudia sechellarum, which has a complete prenuptial moult. We compiled primary moult data based on the proportion of feather mass grown, for 11 weaver species, three of which are newly reported on. Timing of primary moult is discussed in relation to sex, location and annual timing. The duration of primary moult varies widely between and within species, from 46 days (1.5 months) in a widowbird to 215 days (7 months) in an arid species. Weavers in arid regions have longer moult durations than weavers in other regions. Examples of the overlap of primary moult and breeding are presented.

Evolutionary trade-off between male colouration and feather moult extent also indirectly determines female moult.

Males and females are often influenced by different selective forces, frequently resulting in diverging phenotypes, for example in colouration. Since an animal's colouration may strongly influence its fitness, causes and consequences of sexual dichromatism in birds could aid in understanding important factors affecting sexual and natural selection. Variation in plumage ornamentation may affect mate attraction or intraspecific antagonistic behaviour. In most passerines, body plumage colouration of juveniles is obtained through the process of feather moult. The number of moulted wing and tail feathers, which also influences the bird's appearance, may affect its fitness. Here, we show that body plumage colouration of male, but not female, passerines is correlated with the number of moulted wing and tail feathers in the early stage of the bird's life for both sexes. Thus, the extent of wing and tail moult in females is not modulated by the female's colouration and can prevent females from reaching their sex-specific optima. This result could be explained by high intersexual genetic correlations, which might make it impossible for the sexes to reach their own trait fitness optima. Our findings may indicate that species-specific, rather than sex-specific, internal correlations shaped bird moult strategy, an important avian life-history trait.

Clarification of molt strategies in three Empidonax flycatchers

We studied plumages and molt patterns of Yellow-bellied (Empidonax flaviventris), Least (E. minimus), and Alder (E. alnorum) flycatchers, primarily on the breeding grounds but with additional data from wintering grounds and a migration stopover site, in order to clarify our knowledge of molt strategies in these species. We determined that these 3 species have a similar overall molt strategy: (1) a partial-to-incomplete preformative molt begun on the breeding grounds, suspended over migration, and completed on the wintering grounds; (2) a limited-to-partial first prealternate molt on the wintering grounds that can overlap the final stages of the preformative molt; (3) a complete definitive prebasic molt begun on summer grounds and completed on wintering grounds; and (4) a limited-to-partial definitive prealternate molt that may overlap with the final stages of the prebasic molt. Our study clarifies previous terminologies and allows these molts to be interpreted in an evolutionary framework. We suggest that observed differences in molt extents among species may be linked to differences in wintering latitude and habitat. The broadleaf forest preferred by Yellow-bellied Flycatcher likely retains insect biomass later into the winter season than the scrub habitat preferred by Least Flycatcher, and this may promote more extensive preformative feather replacement in that species. The much more extensive preformative molt of Alder Flycatcher may be due to its wintering farther south, where there is greater annual solar exposure, perhaps resulting in higher rates of feather degradation. Our data also suggest that the extent of prealternate molt in these species may vary with proximate factors on the winter grounds affecting individuals, rather than body condition at the beginning of winter.

Marginal-covert moult in the House Sparrow Passer domesticus

ABSTRACT Marginal coverts are often neglected in passerine moult studies due to their small size and large number. Here, we document eight moult components of this group of wing coverts in a House Sparrow population from Barcelona in 2018–21: timing, growth rate, intensity, speed, duration, sequence, extent and barb density. We also tested the influence of various intrinsic and extrinsic factors on marginal-covert moult. Our adult population started marginal-covert moult on 29 July and finished it on 29 August, with the moult of hatch-year birds delayed 13 days in relation to the moult of adults. Growth rate of the largest marginal covert increased significantly with its size but did not differ between sexes. Intensity of marginal-covert moult replacement was not constant during the moult progress, which took 32 days on average. Moult sequence of marginal coverts started with the proximal feathers, proceeded distally replacing the central rows and was completed toward the front and rear rows. Moult extent was complete except in one case. Size of the largest marginal covert increased with calamus width, but not significantly, and barb density decreased with feather size, but not significantly, and neither measure differed between sexes. Comparison with published results indicated that growth rate is lower in marginal coverts than in primaries and rectrices, whereas barb density is greater. Linear regression of marginal-covert size on both growth rate and barb density can be used to predict growth rate and barb density of flight feathers in the House Sparrow.

Extent and symmetry of tail moult in Amur Falcons

Amur Falcons Falco amurensis undergo one of the most extreme migrations of any raptor, crossing the Indian Ocean between their Asian breeding grounds and non-breeding areas in southern Africa. Adults are thought to replace all their flight feathers on the wintering grounds, but juveniles only replace some tail feathers before migrating. We compare the extent and symmetry of flight feather moult in a large sample of Amur Falcons killed at communal roosts during two hailstorms in KwaZulu-Natal, South Africa in March 2019, shortly before their northward migration. Most adults had completed replacing their remiges, with only a few still growing 1–3 feathers (mainly secondaries), but most were still growing their tail feathers. Juveniles only replaced tail feathers. Moult typically was distal from the central rectrices, but 25% of adults and 1% of juveniles replaced the outer tail first, and a few individuals exhibited other moult patterns (simultaneous moult across the tail, or among the inner and outer feathers). These different moult strategies were independent of sex. Adults that replaced the outer tail first typically had replaced a greater proportion of the rectrices (mean ± SD; 0.81 ± 0.19) than adults starting from the central tail (0.17 ± 0.08). Proportionally fewer distal moulting adults were killed on 9 March than 21 March, resulting in the average proportion of rectrices replaced by adults decreasing between the two storm events from 0.52 ± 0.26 to 0.43 ± 0.23. By comparison, juvenile tail moult increased from 9 March (0.34 ± 0.18) to 21 March (0.40 ± 0.15). Overall, the probability of replacement for T1 was similar for adults (0.82) and juveniles (0.83), but adults were more likely to have replaced T2–6 (0.40–0.45) than juveniles (0.18 for T2 and 0.04–0.07 for T3–6). Asymmetry in tail moult was greater at T1 for adults (15%) than juveniles (10%), but asymmetry for T2 to T6 was greater in juveniles (3–10%) than adults (1–4%), especially given the greater probability of feather replacement in adults. Despite these differences, the degree of asymmetry was less than expected by random replacement across all rectrices in both age classes. Interestingly, moult tended to be more advanced on the left than right side of the tail. The extent of tail moult was correlated with body condition in adults and juveniles, suggesting that moult pattern might be used as an indicator of fitness in falcons.

Evolution of the preformative molt in Cardinalidae correlates with transitions from forest to open habitats

Abstract We explored adaptive factors affecting the preformative molt in the passerine family Cardinalidae, and concluded that the ancestor inhabited forest habitats and underwent a partial preformative molt that included wing coverts but not primaries. Later radiations within the family appeared to be characterized by transitions from forests toward more open habitats, and such transitions also correlated positively with increased preformative molt investment, plumage signaling, and flight. While previous studies had highlighted the role of time and energy constraints in the evolution of the preformative molt in passerines, we conclude that adaptation to the physical environment has had a greater influence than constraints on the evolution of this molt in Cardinalidae. Using molt data from 430 individuals from 41 of the 51 Cardinalidae species, we tested whether social and environmental factors (delayed plumage maturation and habitat openness), as well as that of physiological and time constraints (body mass, migration distance, and breeding latitude), have influenced the evolution of the preformative molt in this family. We predicted that these five factors could relate to the extent of the preformative molt in terms of energy investment, plumage signaling, and flight. We also examined whether or not the presence of an auxiliary preformative molt correlated to the extent of the preformative molt. We found a strong phylogenetic signal for the preformative molt in Cardinalidae due to shared ancestry, with habitat openness correlating significantly with increased molt extent. We also found a very strong relationship with the auxiliary preformative molt, indicating that both episodes form part of the early life molt strategy in this family. Evolutionary histories and the environments to which each taxonomic group has adapted can diverge across passerines, and we expect that future studies will further discover the nature and strength of the evolutionary drivers of preformative molt.

Sex, age, molt strategy, and migration distance explain the phenology of songbirds at a stopover along the East Asian flyway

Sex- and age-specific differences in the timing of migration are widespread among animals. In birds, common patterns are protandry, the earlier arrival of males in spring, and age-differential migration during autumn. However, knowledge of these differences stems mainly from the Palearctic-African and Nearctic-Neotropical flyways, while detailed information about the phenology of migrant birds from the East Asian flyway is far scarcer. To help fill parts of this gap, we analyzed how migration distance, sex, age, and molt strategy affect the spring and autumn phenologies of 36 migrant songbirds (altogether 18,427 individuals) at a stopover site in the Russian Far East. Sex-differential migration was more pronounced in spring than in autumn, with half of the studied species (6 out of 12) showing a protandrous migration pattern. Age-differences in migration were rare in spring but found in nearly half of the studied species (11 out of 25) in autumn. These age effects were associated with the birds’ molt strategy and the mean latitudinal distances from the assumed breeding area to the study site. Adults performing a complete molt before the onset of autumn migration passed the study site later than first-year birds undergoing only a partial molt. This pattern, however, reversed with increasing migration distance to the study site. These sex-, age-, and molt-specific migration patterns agree with those found along other flyways and seem to be common features of land bird migration strategies.Significance statementThe timing of animal migration is shaped by the availability of resources and the organization of annual cycles. In migrant birds, sex- and age-differential migration is a common phenomenon. For the rarely studied East Asian flyway, we show for the first time and based on a large set of migrant songbirds that earlier migration of males is a common pattern there in spring. Further, the timing and extent of molt explained age-differential migration during autumn. Adults molting their complete plumage at the breeding area before migration showed delayed phenology in comparison to first-year birds, which perform only a partial molt. This pattern, however, reversed with increasing migration distance to the study site. Since our results agree with the general patterns from the other migration flyways, similar drivers for differential migration may act across different flyway systems, provoking a similar evolutionary response.

Complex postbreeding molt strategies in a songbird migrating along the East Asian Flyway, the Pallas's Grasshopper Warbler Locustella certhiola.

Molt strategies have received relatively little attention in current ornithology, and knowledge concerning the evolution, variability and extent of molt is sparse in many bird species. This is especially true for East Asian Locustella species where assumptions on molt patterns are based on incomplete information. We provide evidence indicating a complex postbreeding molt strategy and variable molt extent among the Pallas's Grasshopper Warbler Locustella certhiola, based on data from six ringing sites situated along its flyway from the breeding grounds to the wintering areas. Detailed study revealed for the first time that in most individuals wing feather molt proceeds from the center both toward the body and the wing‐tip, a molt pattern known as divergent molt (which is rare among Palearctic passerines). In the Russian Far East, where both breeding birds and passage migrants occur, a third of the adult birds were molting in late summer. In Central Siberia, at the northwestern limit of its distribution, adult individuals commenced their primary molt partly divergently and partly with unknown sequence. During migration in Mongolia, only descendantly (i.e., from the body toward the wing‐tip) molting birds were observed, while further south in Korea, Hong Kong, and Thailand the proportion of potential eccentric and divergent feather renewal was not identifiable since the renewed feathers were already fully grown as expected. We found an increase in the mean number of molted primaries during the progress of the autumn migration. Moderate body mass levels and low‐fat and muscle scores were observed in molting adult birds, without any remarkable increase in the later season. According to optimality models, we suggest that an extremely short season of high food abundance in tall grass habitats and a largely overland route allow autumn migration with low fuel loads combined with molt migration in at least a part of the population. This study highlights the importance of further studying molt strategy as well as stopover behavior decisions and the trade‐offs among migratory birds that are now facing a panoply of anthropogenic threats along their flyways.

Preformative molt in Neotropical Cardinalidae

Neotropical Cardinalidae consists of 40 species in 10 genera that have diversified across the Americas. We provide quantitative information on the preformative molt of 21 Cardinalidae species of seven genera, plus one Thraupidae species placed within Cardinalidae until recently. From 155 preformative molt cards, we calculated molt extent estimates, computed frequencies of molt patterns, and summarized observed frequencies of wing-feather replacement in wing diagrams. We found 17 species with partial preformative molts, four species with eccentric preformative molts (outer but not inner primaries replaced), and one species with a complete preformative molt. Preformative molt extent and patterns were similar within Cardinalidae genera, including genera with Nearctic representatives, such as the complete preformative molt of Northern Cardinal Cardinalis cardinalis or the eccentric molt of Passerina buntings. Our results cover an important gap in the knowledge of the natural history of Cardinalidae, generate important criteria to determine the age of Neotropical Cardinalidae, and provide essential information to test hypotheses on the ecology and evolution of molt in this passerine family.

Time available for moulting shapes inter- and intra-specific variability in post-juvenile moult extent in wheatears (genus Oenanthe)

Moult is a vital and endogenously controlled process in the avian life. However, birds may modulate their feather renovation properties, such as the extent of moult, based on exogenous factors. Despite the large body of knowledge about moult patterns, numerous questions remain unclear. In this study, we aimed to improve our knowledge about the factors that affect variation in the extent of the post-juvenile moult in passerines by performing inter- and intra-specific comparative analyses. We assessed the effect of internal and external factors on passerines’ moult by comparing post-juvenile moult extent among 16 wheatear species (genus Oenanthe) from the Palearctic Ecozone. The tested factors included migration distance used as a proxy of time available for moulting and habitat type. We also explored the relationship between the extent of the moult, migration distance, and sex in the Northern Wheatear Oenanthe oenanthe across a latitudinal gradient in Western Europe. The results indicate that post-juvenile moult extent in wheatears was negatively related to migration distance, such that species with shorter migration distances moult extensively compared to long-distance migratory species. In contrast, the extent of post-juvenile moult in the Oenanthe genus was not related to preferred habitat type (arid or non-arid) of the species. Migration distance was also related to post-juvenile moult extent in the Northern Wheatear, with fewer renewed feathers in northern populations. However, the extent of the post-juvenile moult did not differ between sexes. Thus, our results support that time constraints affect moult extent in long-distance migratory species and populations.

Large‐scale longitudinal climate gradient across the Palearctic region affects passerine feather moult extent

Large‐scale spatial gradients of environmental conditions shape organisms, populations and ecosystems. Even though environmental gradients are a key research theme in macro‐ecology and biogeography, the effects of large‐scale, east–west, environmental gradients are largely overlooked compared with north–south gradients. Our study focused on feather moult, an important and energy demanding process in birds. By comparing Western and Eastern Palearctic populations of 21 species, we found that juvenile passerines in the Western and Eastern Palearctic differ in the number of feathers moulted as part of their post‐juvenile moult. This difference is most likely the result of a large‐scale climatic gradient in cold season duration and consequent differences in the time available for moulting. Eastern populations were characterized by a limited extent of feather moult that was additionally affected by migration distance and body mass. The longer migration distance in the Eastern Palearctic caused a generally less extensive moult while high body mass was correlated with a low difference in moult extent between the Western and Eastern Palearctic regions. These results highlight the importance of linking annual cycle processes at the organismal level to the specific environmental conditions within the distribution range of each species.

Feather moult and bird appearance are correlated with global warming over the last 200 years

Global warming alters various avian phenological processes, including advanced reproduction and migration schedules. In birds, individual appearance is largely determined by plumage, influencing, for example, bird attractiveness, social status and camouflage. Juveniles of most passerine species replace their nest-grown plumage during the first months of life, a process that is called post-juvenile feather moult. Using data from ten natural history collections, we show that the extent of the post-juvenile moult has increased significantly over the last 212 years (1805–2016), a trend that is positively correlated with the temperature of the environment. Therefore, it seems that birds replaced more feathers under warmer conditions, causing juveniles to appear more similar to adult birds. Moreover, in several species, we describe a male–female switch in the extent of moult, with females currently replacing more feathers than males compared to the past. These results demonstrate different biological responses to climate warming by different phenotypes.

Molt strategy and aging of Rufous-collared Sparrow (Zonotrichia capensis) in Bogotá, Colombia

La muda es un proceso importante de la historia natural de las aves y aprender sobre este proceso permite entender varios aspectos de su vida. En zonas templadas, el conocimiento sobre las estrategias de muda, las características de cada tipo de plumaje y su relación con la edad del ave, son bien conocidas. Por el contrario, en el neotrópico, este conocimiento no está bien desarrollado. Una especie con bastantes estudios sobre muda en varias localidades es el ampliamente distribuido Copetón (Zonotrichia capensis). Esos estudios cubren localidades de su ámbito geográfico facilitando comparaciones entre poblaciones y proveyendo un excelente modelo para estudiar la variación del plumaje y la muda. En este estudio, determiné el alcance y la estrategia de muda de Z. capensis costaricensis mediante muestreos durante un año en dos localidades de Bogotá. Capturé y anillé individuos de Z. capensis y tomé información de características como los límites de muda, osificación del cráneo y color del iris que me permitieron identificar el tipo de plumaje/muda y relacionarlo con una categoría de edad del sistema de clasificación de edad basado en los ciclos de muda. Encontré que Z. capensis tiene una estrategia de muda básica compleja, donde todas las mudas prebásicas, incluida la prejuvenil, son completas y la muda preformativa es parcial. Estos resultados son congruentes con los de otras regiones. Sin embargo, la muda de Z. capensis varía mucho, e individuos lejos de los trópicos tienen una muda alterna parcial-incompleta adicional y aún desconocemos por qué.

Moult in the Loggerhead Shrike Lanius ludovicianus is influenced by sex, latitude and migration

We investigated moult strategies in Loggerhead Shrikes by examining first prebasic or preformative moult patterns and by assessing the general location where individual feathers were grown using stable hydrogen isotope (δ2H) analysis. We tested the relative importance of factors known to impact moult timing and pattern, including age, sex, body size, food availability and migration. Migratory Shrikes showed evidence of suspended moult, in which feathers are moulted on both the breeding and the non‐breeding grounds with a suspension of moult during migration. Extent of moult was best explained by sex, longitude, migratory behaviour and breeding‐ground latitude. Male Hatch Year (HY) Shrikes replaced more feathers on the breeding grounds prior to migration than did HY females and moulted more extensively on the breeding grounds than did females. Non‐migratory HY Shrikes underwent a more extensive preformative moult than migratory HY Shrikes. Individuals in more southerly migratory populations moulted more extensively on the breeding grounds than did those breeding further north. Our data also indicate that individuals in the northeastern populations moulted more extensively on the breeding grounds than did those in the north and southwest. Our study underlines the complex structure and variation in moult possible within species, revealing surprising levels of differentiation between sexes and age cohorts, linked to environmental factors on the breeding grounds. Our study highlights the utility of an intrinsic marker, specifically δ2H analysis, to test hypotheses regarding the evolutionary and ecological forces driving moult. Although the methodology has not commonly been applied to this area of research, our results indicate that it can provide unprecedented insight into inter‐ and intra‐specific adaptive response to constraints, whereby individuals maximize fitness.

Age‐specific variation in relationship between moult and pre‐migratory fuelling in Wood SandpipersTringa glareolain southern Africa

Trans‐equatorial avian migrants tend to breed, moult and migrate – the main energy‐requiring events in their lifecycle – at different times. Little is known about the relationship between wing moult and pre‐migratory fuelling in waders on their non‐breeding grounds, where time is less constrained than during their brief high‐latitude breeding season. We determined age‐related strategies of Wood SandpipersTringa glareolato balance the energetic demands of primary moult against pre‐migratory fuelling in southern Africa by analysing body mass and primary moult at first capture of 1721 birds mist‐netted in 1972–96 at waterbodies in Zimbabwe. Adults moulted all their primaries in August–December, but immatures underwent a supplemental moult of varying numbers of outer primaries in December–April, close to departure. We used locally weighted linear regression to estimate trends in Wood Sandpiper body mass from 1 July to 1 May. They maintained low mass from arrival in July–September to February–early March. Adults fuelled from 10 February to 1 May at a mean rate of 0.25 g/day (sd = 0.16). Most adults (98%) began fuelling 10–75 days after completing primary moult. Immatures fuelled from 4 March to 13 April at 0.24 g/day (sd = 0.14). They used varying strategies depending on their condition: a brief gap between moult and fuelling; an overlap of these processes near departure, leading to slower fuelling; or skipping fuelling altogether and staying in southern Africa for a ‘gap year’. Immatures moulting three or five outer primaries fuelled more slowly than post‐moult birds. Immatures moulting four outer primaries started fuelling 3 weeks later but at a higher rate than did post‐moult birds of this group. In post‐moult immatures, the later they ended moult, the later and faster they fuelled. The heaviest adults and immatures using all moult patterns accumulated fuel loads ofc. 50% of lean body mass, and could potentially cross 2397–4490 km to reach the Great Rift Valley in one non‐stop flight. Immatures were more flexible in the timing and extent of moult and in the timing and rate of fuelling than adults. This flexibility enables inexperienced Wood Sandpipers to cope with inter‐annual differences in feeding conditions at Africa's ephemeral inland waterbodies.

Factors influencing the evolution of moult in the non-breeding season: insights from the family Motacillidae

The number of moults per annual cycle and their final spatial pattern (i.e. topography) show high interspecific variation in the order Passeriformes. Factors behind this variability remain obscure, especially for variability in spatial pattern among species. Here, we explored the relative influence of ten ecological, ontogenetic, social and sexual factors on the evolution of autumn moult (feather replacement largely undertaken by migratory species, which is not necessarily an independent episode within their moult cycle) and prealternate moult among Northern Hemisphere species of the family Motacillidae using phylogenetically controlled analyses, ancestral state reconstruction and analyses of correlated evolution. The results strongly support the presence of prealternate moult and absence of autumn moult as ancestral states in this family. A high rate of change between related species indicates phylogenetic independence among prealternate moult patterns and examined factors. Migration distance and gregariousness are the most important factors influencing prealternate moult evolution, and point toward natural selection and sociality as the most important evolutionary drivers of prealternate moult in Motacillidae. Breeding latitude, seasonal plumage change, winter plumage conspicuousness, sexual dichromatism, plumage maturation and extent of preformative moult show a minor influence, and suggest that ontogeny and sexual selection may have played a limited role in shaping prealternate moult in Motacillidae.

The flight feather moult pattern of the bearded vulture (Gypaetus barbatus)

Moult is an extremely time-consuming and energy-demanding task for large birds. In addition, there is a trade-off between the time devoted to moulting and that invested in other activities such as breeding and/or territory exploration. Moreover, it takes a long time to grow a long feather in large birds, and large birds that need to fly while moulting cannot tolerate large gaps in the wing, but only one or two simultaneously growing feathers. As a consequence, large birds take several years to complete a full moult cycle, and they resume the moult process during suboptimal conditions. A clear example of this pattern is the Bearded Vulture (Gypaetus barbatus), which needs 2–3 years for changing all flight feathers. Here we describe the sequence, extent, and timing of moult of 124 Bearded Vultures in detail for the first time. We found that extent and timing of flight feather moult was different between age classes. Subadults (from 3rd to 5th calendar year) started moult, on average, in early March, whereas adults only started moult, on average, in late April, possibly due to breeding requirements. Second calendar year individuals delayed onset of moult until the middle of May. In general, the moult lasted until November, and although adults started to moult later than subadults, they moulted more feathers. Subadults needed 3 years for moulting all flight feathers, whereas adults normally completed it in 2 years.

Causes and consequences of individual variation in the extent of post-juvenile moult in the blue titCyanistes caeruleus(Passeriformes: Paridae)

Moult, comprising the growth or replacement of feathers in birds, is an energetically demanding process. As a result, in many species, the extent of the post-juvenile moult can vary substantially. However, the reasons underlying this variation remain poorly understood, and the potential life-history consequences of variation in moult extent are even less clear. In the present study, we aimed to use individual-specific data to identify factors affecting the extent of the post-juvenile moult in a population of over 2500 blue tits Cyanistes caeruleus Linnaeus 1758, and to assess the consequences of individual variation in moult extent on reproduction in the first year of life. There was a substantial sex difference in post-juvenile moult extent, with males moulting more extensively than females. Putative immigrant birds had moulted on average less than those born locally. However, there was little evidence of carry-over effects of the natal environment on moult extent because we found no relationship between moult extent and fledging date or nestling mass. Evidence that moult extent, and hence feather brightness, affected subsequent reproductive success was limited. Moult extent had no effect on recruitment in males, although female recruits had moulted significantly less than nonbreeders. Because it was not influenced by features of the natal environment, moult extent may not be an honest signal of individual quality in C. caeruleus. As a result, the potential consequences of variation in moult extent for fitness are likely to be small.

Silver spoon effects on plumage quality in a passerine bird.

A silver spoon effect means that individuals who develop under favourable circumstances enjoy a fitness or performance advantage later in life. While there is large empirical support for silver spoon effects acting on different life-history traits in birds, such as survival and reproduction, the evidence for the carry-over effects of rearing conditions on the quality of future plumage generations is lacking. Here, we examined whether abilities of individuals to undergo extensive post-juvenile moult may depend on the quality of juvenile plumage developed during the nestling phase in a small passerine showing large individual variation in the extent of post-juvenile moult, the greenfinch (Carduelis chloris). We found that high structural quality and carotenoid chroma of juvenile feathers were positively linked to the extent of post-juvenile moult in this species, thus allowing young birds to attain more adult-like plumage. Silver spoon effects mediated by the juvenile plumage quality were also found to have other fitness-related consequences, as individuals with high-quality juvenile feathers were in better condition during their first winter. As far as we are aware, the results provide the first correlative evidence for a silver spoon effect acting on general plumage quality in birds.