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1.
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.  相似文献   

2.
Endogenous circannual rhythms control the time course for moult, migratory fattening and autumn migration in juveniles of several bird species that breed in the temperate zone. Exogenous factors, such as daylength, can also exert a measure of control: photoperiodic cues detected by birds that hatch late in the season induce accelerated juvenile development, assuring that late-hatched young migrate at the same time as early-hatched young. Whether these same mechanisms of control also apply to birds that migrate between breeding and nonbreeding areas entirely within the tropics at latitudes characterized by little seasonal variation in photoperiod is unknown. We conducted a common-garden experiment in Panama (9°N) in which we hand-reared wild-caught nestling yellow-green vireos, Vireo flavoviridis, under a constant photoperiod and monitored them for the expression of juvenile moult, migratory fattening and migratory activity. Even in the absence of a seasonal photoperiodic cue, juveniles moulted, accumulated fat reserves and initiated migratory activity, suggesting endogenous control of these processes. Age at the onset of moult, migratory fattening and migratory activity were each significantly negatively correlated with hatch date, however, so that the expression of these three processes was synchronized among juveniles with respect to the time of the season. We suggest that the slight differences in daylength perceived either by the nestlings themselves in the short time before they were collected (at 6-8 days of age) or by the adult females during egg production influenced rate of nestling development, thus allowing later-hatched young to moult, accumulate fat and migrate at a younger age than early-hatched young. Remarkably, photoperiod differed between the earliest and latest hatch dates in this study by only 33 min.  相似文献   

3.
Birds moult to maintain plumage function through life, but the factors that determine moult duration are poorly understood. In temperate areas, variation in moult duration could be largely associated with between-species differences in migratory behaviour (migrants have less time for moulting after breeding), and body mass (because the aerodynamic cost of rapid moult increases allometrically with body size). Moreover, if the energetic cost of transport favours a smaller body size in migratory species, then the effects of migratory behaviour and body mass on moult duration could be confounded. We conducted a comparative study of the duration of adult complete moult in 48 European passerine species, in relation to body mass and migratory behaviour (sedentary, short-distance migrants and long-distance migrants). Lighter and more migratory species moulted faster than heavier and more sedentary species, but migration was not associated with body mass. If accelerated moult compromises the success of migration, changes in the physiology or phenology of moult in migratory birds are better interpreted as adaptive responses to compensate for such costs.  相似文献   

4.
The question “Which factors govern the timing of migration in birds?” has fascinated researchers for a long time. It was initially assumed that avian migration is triggered by environmental factors, such as ambient temperature and food availability. Later laboratory experiments in various avian species convincingly showed that timing of spring migration is mainly governed by daylength (photoperiod) and is controlled by circannual rhythms. As a result, the concept that environmental factors (air temperature, precipitation, food availability) have no significant impact on timing of spring migration generally took hold. However, in recent decades more and more data has become available showing that the timing of spring migration in many bird species has significantly changed. These data allow the formulation of a novel concept of regulation mechanisms of timing of spring migration which accounts not only for photoperiodic and endogenous control, but also for the already mentioned extrinsic factors. Studies of endocrine control of spring migratory disposition showed that features of endocrine mechanisms governing the onset of spring migration depend on speciesspecific migratory strategies and the stability of environmental conditions in winter quarters and on migratory routes. It is becoming clear precisely which endocrine mechanisms are involved in adjusting migratory behaviour to variation of the local environment. In recent years, progress has also been made in finding genetic mechanisms controlling the timing of spring migration.  相似文献   

5.
In recent decades, global temperature has increased at an unprecedented rate. This has been causing rapid environmental shifts that have altered the selective regimes determining the annual organization of birds. In order to assess the potential for adaptive evolution in the timing of autumn migration, we estimated heritabilities of the onset of migratory activity in a southern German blackcap (Sylvia atricapilla) population. Heritabilities (h2=0.34-0.45) and coefficients of additive genetic variation (CV(A)=4.7-5.7) were significant and consistent when estimated by different methods, irrespective of whether they were derived from birds hatched in the wild or bred in captivity. In an artificial selection experiment, we selected for later onset of migratory activity, simulating expected natural selection on this trait. We obtained a significant delay in the mean onset of migratory activity by more than one week after two generations of selection. Realized heritability (h2=0.55) was in agreement with expected heritability in the cohort that the selection line was derived from. Our results suggest that evolutionary changes in the timing of autumn migration may take place over a very short time period and will most probably be unconstrained by the lack of additive genetic variation.  相似文献   

6.
Studies of Zugunruhe – the ‘migratory restlessness’ behaviour of captive birds – have been integral to our understanding of animal migration, revealing an inherited propensity to migrate and an endogenous timing and navigation system. However, differences between Zugunruhe in captivity and migration in the wild call for more data, in particular on variation within and among taxa with diverse migration strategies. Here, we characterise Zugunruhe in a long‐term dataset of activity profiles from stonechats (genus Saxicola) with diverse migratory phenotypes (976 migration periods from 414 birds), using a flexible and consistent quantitative approach based on changepoint analysis. For east African, Austrian, Irish, and Siberian stonechats and hybrids, we report key inter‐population differences in the occurrence, timing, and intensity of Zugunruhe. In line with expectations, we found the highest Zugunruhe intensity in the longest‐distance migrants, more variable patterns in short‐distance migrants, and intermediate characteristics of hybrids relative to their parental groups. Inter‐population differences imply high evolutionary lability of Zugunruhe timing within a robustly structured annual cycle. However, counter to theory, Irish partial migrants showed no segregation between migrant and resident individuals, and previously reported nocturnal restlessness was confirmed for resident African stonechats. Further features of nocturnal restlessness that did not align with migratory behaviour of stonechats were juvenile nocturnal restlessness even prior to postjuvenile moult, and protandry in spring, although stonechats winter in heterosexual pairs. Importantly, Zugunruhe of all populations declined with age, and the intensity of an individual bird's Zugunruhe was correlated with activity levels during other parts of the annual cycle. Our results confirm endogenous, population‐specific migration programmes but also reveal apparent discrepancies between Zugunruhe and migration in the wild. We thus highlight both the continued potential of Zugunruhe study and the need for circumspect interpretation when using migratory restlessness to make inferences about migration in the wild.  相似文献   

7.
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.  相似文献   

8.
Christer Hemborg 《Ibis》1999,141(2):226-232
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.  相似文献   

9.
Summary In a constant 12 h, 50 min equatorial photoperiod postjuvenile moult started earlier and lasted shorter in European stonechats than in their African conspecifics. F1-hybrids showed an intermediary time course of moult indicating that the differences found between these two subspecies are genetically determined.  相似文献   

10.
Moult is an important process in the life cycle of birds. Passerines differ widely in the number, seasonality and extension of moult episodes, but the incidence of birds ecology on this variation remains largely uninvestigated. We analysed the patterns of moult in European passerines in relation to their distribution, migration and sexual dichromatism. Longer migrations and southern wintering quarters were characteristic of species with complete moults in summer and an additional moult in winter. The main moult in species with larger seasonal changes in sexual dimorphism tended to be scheduled just before the start of the breeding season, suggesting a link between sexual selection and the timing of moult. These patterns strongly support the importance of migration and dichromatism on the evolution of moult strategies.  相似文献   

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

12.
Shifts in reproductive phenology due to climate change have been well documented in many species but how, within the same species, other annual cycle stages (e.g. moult, migration) shift relative to the timing of breeding has rarely been studied. When stages shift at different rates, the interval between stages may change resulting in overlaps, and as each stage is energetically demanding, these overlaps may have negative fitness consequences. We used long‐term data of a population of European pied flycatchers (Ficedula hypoleuca) to investigate phenological shifts in three annual cycle stages: spring migration (arrival dates), breeding (egg‐laying and hatching dates) and the onset of postbreeding moult. We found different advancements in the timing of breeding compared with moult (moult advances faster) and no advancement in arrival dates. To understand these differential shifts, we explored which temperatures best explain the year‐to‐year variation in the timing of these stages, and show that they respond differently to temperature increases in the Netherlands, causing the intervals between arrival and breeding and between breeding and moult to decrease. Next, we tested the fitness consequences of these shortened intervals. We found no effect on clutch size, but the probability of a fledged chick to recruit increased with a shorter arrival‐breeding interval (earlier breeding). Finally, mark–recapture analyses did not detect an effect of shortened intervals on adult survival. Our results suggest that the advancement of breeding allows more time for fledgling development, increasing their probability to recruit. This may incur costs to other parts of the annual cycle, but, despite the shorter intervals, there was no effect on adult survival. Our results show that to fully understand the consequences of climate change, it is necessary to look carefully at different annual cycle stages, especially for organisms with complex cycles, such as migratory birds.  相似文献   

13.
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.  相似文献   

14.
Moult in birds is highly variable both within and among bird genera. The aim of the present study was to make an extended phylogenetic analysis of the diversity of moult strategies within Sylviidae in light of the recent phylogenies based on molecular data, and with the methodology of matched-pairs analysis. In the present study we analysed 141 sylviid taxa and, to improve character reconstruction, 22 outgroup taxa. The study could corroborate the earlier results that post-breeding moult is the ancestral state in Sylviidae. Migratory habits were found to be ancestral within Sylviidae but resident habits have evolved several times with a few reverse transitions back to migratory habits. Transitions in main moult strategy were significantly related to both migratory vs. resident habits and to migratory distance, giving support to the hypothesis that moult in the non-breeding season is related to migration as such and long-distance migration, respectively. Both resident and migratory taxa used minor alternative moult strategies besides the main moult strategy and such within-taxon flexibility might be a basal trait in Sylviidae. We investigated three variables that included minor strategies and found no relationship between these and migratory habits. However, two of these variables (the potential to interrupt moult and the occurrence of moult in both the post- and non-breeding seasons) were significantly related to migration distance. We conclude that migration patterns has some influence on the choice of moult strategy, and that flexibility in timing of moult is widespread within Sylviidae and might be a basal trait. We argue that such flexibility might be a prerequisite for changes in migratory strategies.  相似文献   

15.
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.  相似文献   

16.
J. C. SENAR  J. L. COPETE  A. J. MARTIN 《Ibis》1998,140(4):661-669
Siskins Carduelis spinus show great variation in the acquisition of adult plumage, so that yearling birds can be classified as either "delayed" (i.e. still showing yearling plumage) or "advanced" (i.e. with an adult plumaged appearance). The extent of moult in males is related to the size of their black bib, which in turn is highly correlated with their social dominance rank. Autumn male body mass is higher in advanced than in delayed moult birds, but by winter the relationship is reversed, suggesting a trade-off between investment in moult and subsequent body condition. Results were similar in Spain and Britain. A possible cost of advancing moult is suggested by an analysis of aggressive interactions at bird feeding tables which showed that adult males discriminate between delayed and advanced birds, directing most aggression towards adult-looking yearling males. The results suggest that the variation in the extent of postjuvenile moult is not only related to energetic constraints but has other important behavioural and ecological implications.  相似文献   

17.
The evolution of migratory strategies in birds is likely to have been influenced by ecological as well as socio-sexual factors in both wintering and breeding areas. In this comparative study, we analysed timing of spring passage of 38 long-distance migratory bird species that winter south of the Sahara desert and breed in Europe, in relation to wintering and breeding latitudes, moult strategy, nesting site (open vs. cavity), and sexual dimorphism in size and coloration, which may reflect intensity of sexual selection. We employed a large data set consisting of more than 190 000 individuals ringed during spring migration in the Mediterranean Sea. We found that the species that migrated earlier were those wintering farther north, nesting in cavities and showing the largest degree of sexual size dimorphism (SSD). However, sexual dichromatism was not related to migration date. Among passerine species, moulting wing-feathers in Africa delayed migration. We found no support for the energetic constraint hypothesis, which proposes that early arrival selects for large male size, since early arriving species were not larger than late arriving ones. Thus, the observed associations suggest that variation in migration schedules at the interspecific level may have evolved in relation to ecological factors and SSD, possibly reflecting the intensity of mating competition.  © 2005 The Linnean Society of London, Biological Journal of the Linnean Society , 2005, 85 , 199–210.  相似文献   

18.
The Willow Warbler Phylloscopus trochilus is one of the few bird species that undergoes two primary moults a year, a post-nuptial moult in the breeding area and a moult in the wintering area. Primary-moult data for Willow Warblers from Finland, Sweden, Britain, the Netherlands, Belgium. Guinea-Bissau, Uganda, Kenya, Malawi, Zambia, Zimbabwe, Botswana and South Africa are analysed. The parameters of primary moult (mean starting date, standard deviation of starting date, and duration) are estimated using the techniques of Underhill & Zucchini (T.988 Ibis 1 30: 358–372) and Underhill, Zucchini & Summers (1990 Ibis 132: 118-12 3). The scheduling of moult in relation to theother main components of the annual cycle, breeding and migration, is considered. The mean durations of post-nuptial moult for P. t. trochilus and P. t. acredula are 36.5 and 38.3 days, respectively; the start and termination of moult for P. t. trochilus are about 3.5 days later for each degree of latitude northwards, and the start and termination of moult for P. t. acredula, are about 10 days later than that of the most northerly populations of P. t. trochilus studied. Females start their postnuptial moult about 10 days later than males. Southward migration commences as soon as post-nuptial moult is complete. There is an increasing constraint on the timing of breeding and post-nuptial moult events at higher latitudes, leading to overlap between them. The duration of pre-nuptial moult is longer than that of post-nuptial moult, and is completed shortly prior to northward migration.  相似文献   

19.
Many migratory birds start prebreeding moult and premigratory fuelling some months before the breeding season and face severe time constraints, while travelling up to 15,000 km between non-breeding and breeding grounds. Shorebirds typically leave Southern Hemisphere non-breeding areas over a 3-4 week period, but whether they benefit from interannually consistent timing of departure is unknown. Here, I show that individual bar-tailed godwits (Limosa limosa baueri) from New Zealand are highly consistent in their migratory scheduling. Most birds left within the same week each year (between-year repeatability, r, of 0.83) and adult males, which moult into a bright breeding plumage, were also highly repeatable in the extent of their prebreeding moult (r=0.86). This is consistent with the hypothesis that birds have individually optimized migration schedules. Within adult males, but not females, smaller birds tended to migrate earlier than large birds. Whether this reflects differences in size-related migration speed, optimal breeding time at different sites or size-related natural or sexual selection pressures, remains unknown.  相似文献   

20.
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.  相似文献   

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