Exogenous and endogenous corticosterone alter feather quality

We investigated how exogenous and endogenous glucocorticoids affect feather replacement in European starlings (Sturnus vulgaris) after approximately 56% of flight feathers were removed. We hypothesized that corticosterone would retard feather regrowth and decrease feather quality. After feather regrowth began, birds were treated with exogenous corticosterone or sham implants, or endogenous corticosterone by applying psychological or physical (food restriction) stressors. Exogenous corticosterone had no impact on feather length and vane area, but rectrices were lighter than controls. Exogenous corticosterone also decreased inter-barb distance for all feathers and increased barbule number for secondaries and rectrices. Although exogenous corticosterone had no affect on rachis tensile strength and stiffness, barbicel hooking strength was reduced. Finally, exogenous corticosterone did not alter the ability of Bacillus licheniformis to degrade feathers or affect the number of feathers that failed to regrow. In contrast, endogenous corticosterone via food restriction resulted in greater inter-barb distances in primaries and secondaries, and acute and chronic stress resulted in greater inter-barb distances in rectrices. Food-restricted birds had significantly fewer barbules in primaries than chronic stress birds and weaker feathers compared to controls. We conclude that, although exogenous and endogenous corticosterone had slightly different effects, some flight feathers grown in the presence of high circulating corticosterone are lighter, potentially weaker, and with altered feather micro-structure.     

Increase of feather quality during moult: a possible implication of feather deformities in the evolution of partial moult in the great tit Parus major

Here we investigate the change in feather quality during partial post‐juvenile and complete post‐breeding moult in great tit Parus major by measuring the change in the number of fault bars and feather holes on wing and tail feathers. Feathers grown during ontogeny usually are of lower quality than feathers grown following subsequent moults at independence. This is reflected by higher number of fault bars and feather holes on juveniles compared to adults. Fault bars are significantly more common on tail and proximal wing feathers than on the distal remiges, indicating a mechanism of adaptive allocation of stress induced abnormalities during ontogeny into the aerodynamically less important flight feathers. On the contrary, feather holes produced probably by chewing lice have a more uniform distribution on wing and tail feathers, which may reflect the inability of birds to control their distribution, or the weak natural selection imposed by them. The adaptive value of the differential allocation of fault bar between groups of feathers seems to be supported by the significantly higher recapture probability of those juvenile great tits which have fewer fault bars at fledging on the aerodynamically most important primaries, but not on other groups of flight feathers. The selection imposed by feather holes seems to be smaller, since except for the positive association between hatching date, brood size and the number of feather holes at fledging, great tits' survival was not affected by the number of feather holes. During post‐juvenile moult, the intensity of fault bars drops significantly through the replacement of tail feathers and tertials, resulting in disproportional reduction of the total number of fault bars on flight feathers related to the number of feathers replaced. The reduction in the number of fault bars during post‐juvenile moult associated with their adaptive allocation to proximal wing feathers and rectrices may explain the evolution of partial post‐juvenile moult in the great tit, since the quality of flight feathers can be increased significantly at a relatively small cost. Our results may explain the widespread phenomenon of partial post‐juvenile moult of flight feathers among Palearctic passerines. During the next complete post‐breeding moult, the total number of fault bars on flight feathers has remained unchanged, indicating the effectiveness of partial post‐juvenile moult in reducing the number of adaptively allocated fault bars. The number of feather holes has also decreased on groups of feathers replaced during partial post‐juvenile moult, but the reduction is proportional with the number of feathers moulted. In line with this observation, the number of feather holes is further reduced during post‐breeding moult on primaries and secondaries, resulting in an increase in feather quality of adult great tits.     

Allometry of the Duration of Flight Feather Molt in Birds

We used allometric scaling to explain why the regular replacement of the primary flight feathers requires disproportionately more time for large birds. Primary growth rate scales to mass (M) as M^0.171, whereas the summed length of the primaries scales almost twice as fast (M^0.316). The ratio of length (mm) to rate (mm/day), which would be the time needed to replace all the primaries one by one, increases as the 0.14 power of mass (M^0.316/M^0.171=M^0.145), illustrating why the time required to replace the primaries is so important to life history evolution in large birds. Smaller birds generally replace all their flight feathers annually, but larger birds that fly while renewing their primaries often extend the primary molt over two or more years. Most flying birds exhibit one of three fundamentally different modes of primary replacement, and the size distributions of birds associated with these replacement modes suggest that birds that replace their primaries in a single wave of molt cannot approach the size of the largest flying birds without first transitioning to a more complex mode of primary replacement. Finally, we propose two models that could account for the 1/6 power allometry between feather growth rate and body mass, both based on a length-to-surface relationship that transforms the linear, cylindrical growing region responsible for producing feather tissue into an essentially two-dimensional structure. These allometric relationships offer a general explanation for flight feather replacement requiring disproportionately more time for large birds.     

Adaptive fault bar distribution in a long‐distance migratory,aerial forager passerine?

Fault bars are translucent bands produced by stressful events during feather formation. They weaken feathers and increase their probability of breakage, and thus could compromise bird fitness by lowering flight performance. It has been recently suggested ('fault bar allocation hypothesis') that birds could have evolved adaptive mechanisms for reducing fault bar load on the feathers with the highest function during flight. We tested this hypothesis by studying first-year individuals of the long-distance migratory, aerial forager barn swallow Hirundo rustica . We predicted that fault bars should be less abundant on the outermost wing and tail feathers, but more frequent on the tail than on the outermost wing feathers. Accordingly, we found that fault bars occurred more often in tertials than in primaries or secondaries. Tail feathers had fewer fault bars than tertials, but more than primaries. Within the tail, the distribution pattern of fault bars was W-shaped, with the highest fault bar load occurring on the streamers and on the two central feathers. Because streamers are the most important tail feathers for flight performance, this finding seems to contradict the 'fault bar allocation hypothesis'. However, flight performance is much less sensitive to changes in the shape of the tail than of the wings, which could explain why evolutionary forces have not counteracted the increase of fault bars associated with feather elongation during the recent evolution of streamers in the tail of hirundines.  © 2005 The Linnean Society of London, Biological Journal of the Linnean Society , 2005, 85 , 455–461.     

Temporal and spatial patterns of flight and body feather molt of Bank,Barn, and Cliff swallows in North and South America

Molt is energetically demanding and various molt strategies (i.e., molt series, duration, intensity, timing, and location) have evolved to reduce the negative fitness consequences of this process. As such, molt varies considerably among species. Identifying where and when specific feathers are molted is also crucial to inform species‐specific studies using stable isotope markers to assign individuals to geographical regions where they molt. Using museum specimens, we examined the molt of three species of migratory swallows in the Americas: Bank Swallows (Riparia riparia), Barn Swallows (Hirundo rustica), and Cliff Swallows (Petrochelidon pyrrhonota). All three species have one primary and two secondary molt series. Bank and Cliff swallows had one rectrix molt series, and Barn Swallows molted the outer rectrix (R6) separately from the inner five rectrices (R1‐5). All three species have a relatively long flight feather molt duration (i.e., 140–183 days) and low molt intensity. Barn Swallows initiated flight feather molt in the fall, about 2 months later than Bank and Cliff swallows. Barn Swallows likely delay molt because of constraints associated with double brooding. For all three species, molt started with the primaries and inner secondaries and was closely followed by the rectrices and, finally, the outer secondaries. For those that began and then interrupted molt either in breeding areas or during fall migration, the first feathers molted were predominantly S8 and P1. All three species underwent body molt throughout the year, but most individuals molted their body plumage in wintering areas. We recommend that the most appropriate feathers for stable isotope research examining migratory connectivity and habitat use are either R2‐R4 or S2‐S4.     

Does ultraviolet reflectance accentuate a sexually selected signal in terns?

Unlike the majority birds that replace their primaries once each year, most Sterna terns practice an unusual repeated wing molt, wherein a variable number of inner primaries are replaced twice or even three times in a single year. This seemingly redundant replacement of the primaries may serve as a sexually selected indicator of quality in that terns may evaluate potential mates based on the number of primaries they were able to replace twice or three times prior to the breeding season. To evaluate the potential of repeated molt as a social signal, we compared light-reflectance curves and photon catches for new (twice-molted) and old (once-molted) primaries in three species of terns. We observed that old feathers reflected considerably less light across all wavelengths and found that in two of the three species examined the ultraviolet reflectance was disproportionably reduced in old feathers relative to the reduction in visible reflectance. Thus, the UV component of coloration in tern wing feathers may accentuate the difference between the new feathers generated by repeated wing molt and older, more worn feathers, thereby reinforcing a sexually selected signal of quality.     

Haste makes waste but condition matters: molt rate-feather quality trade-off in a sedentary songbird

Background

The trade-off between current and residual reproductive values is central to life history theory, although the possible mechanisms underlying this trade-off are largely unknown. The ‘molt constraint’ hypothesis suggests that molt and plumage functionality are compromised by the preceding breeding event, yet this candidate mechanism remains insufficiently explored.

Methodology/Principal Findings

The seasonal change in photoperiod was manipulated to accelerate the molt rate. This treatment simulates the case of naturally late-breeding birds. House sparrows Passer domesticus experiencing accelerated molt developed shorter flight feathers with more fault bars and body feathers with supposedly lower insulation capacity (i.e. shorter, smaller, with a higher barbule density and fewer plumulaceous barbs). However, the wing, tail and primary feather lengths were shorter in fast-molting birds if they had an inferior body condition, which has been largely overlooked in previous studies. The rachis width of flight feathers was not affected by the treatment, but it was still condition-dependent.

Conclusions/Significance

This study shows that sedentary birds might face evolutionary costs because of the molt rate–feather quality conflict. This is the first study to experimentally demonstrate that (1) molt rate affects several aspects of body feathers as well as flight feathers and (2) the costly effects of rapid molt are condition-specific. We conclude that molt rate and its association with feather quality might be a major mediator of life history trade-offs. Our findings also suggest a novel advantage of early breeding, i.e. the facilitation of slower molt and the condition-dependent regulation of feather growth.     

THE MOULT OF REMIGES AND RECTRICES IN GREAT BLACK-BACKED GULLS LARUS MARZNUS AND GLAUCOUS GULLS L. HYPERBOREUS IN ICELAND

The moult of primaries, secondaries, and rectrices in two closely-related gulls, the Great Black-backed Gull Larus mavinus and the Glaucous Gull L. hyperboreus, was studied in Iceland. Both gulls moult their primaries in an extremely regular sequence, starting with the 1st (innermost) and ending with the 10th (oiltermost) feather. Usually two, less often one or three, primaries are growing per wing during the primary moult, which lasts for about six or seven months. Growlng primaries were estimated to lengthen on the average by 8.7 mm per day in marinus and 7.8 mm per day in hyperboreus. The secondaries, usually 24 in number, are shed in two moult waves, one starting with the innermost feather soon after the start of the primary moult and then progressing slowly outwards, the other beginning with the outermost secondary after the primary moult is about half completed and then progressing rapidly inwards. The moult is completed just before the end of the primary moult as the two moult waves meet at about the 16th secondary. There are no marked differences between the two gulls in the moult of secondaries. The moult of rectrices shows large variations in both species, some feathers being much more irregular than others in their time of shedding. In both species, indications of an obscured centrifugal pattern of replacement are seen, although the 5th (next to the outermost) rectrix is usually the last one to be shed. Significant differences were observed between the two species in the degree of regularity of shedding of some feathers and in the average position in the moulting sequence of others. The moult of rectrices starts soon after the moult of primaries is half completed. The feathers are then shed in rapid succession, and the moult is completed some time before the end of the primary moult. The need for good powers of flight at all times is undoubtedly the reason for the protracted primary moult. This in turn causes the moult to start early, in adults sotnetimes before the eggs are laid; immatures moult even earlier than this. The rectrix moult and the main part of the secondary moult do not begin in adults until the young have fledged, but then progress very rapidly. Presumably, the loss of some of these feathers would impair the flying ability to an extent sufficient to make it difficult for the gulls to care for their young, while the rapid moult is necessary in order for the replacement of these feathers to be completed by the time the primary moult is over.     

The scaling of primary flight feather length and mass in relation to wing shape, function and habitat

The mass and length of each primary flight feather was measured in 120 species of birds (347 individuals) representing 37 families and 15 orders. The scaling relationship between mass and length was determined using the mass of each primary as a proportion of total primary feather mass for that individual and, similarly, length as a proportion of total length. This eliminated errors due to intra- and interspecific differences in absolute size. In every species there was a highly significant constant scaling relationship (log mass/log length) for all of the primary feathers proximal to the feather that formed the wing tip. This relationship was allometric and varied between 1.80 in Rooks Corvus frugilegus and 4.87 in Winter Wrens Troglodytes troglodytes . The mean scaling relationship for 120 species was 2.41 ± 0.42 sd, which was significantly less ( P  < 0.0001) than isometry (i.e. 3.00). In most species (117 of 120) the primary feather forming the wing tip and all feathers distal to it had a different scaling relationship, and had a greater mass than expected from their length. The greater relative mass of the outer primaries may reflect a protective role against physical abrasion, or an aerodynamic role in that each of these feathers provides a leading edge to the wing. Thus, there were two scaling relationships that pivoted about the feather forming the wing tip, resulting in a characteristic 'signature' for each species. Scaling relationships can be related to flight characteristics and habitat, rather than to phylogeny. Closely related species often had widely varying scaling relationships. In general, species exploiting dense vegetation had greater scaling relationships than more aerial species. However, species with a high scaling relationship did not have a greater mean feather mass, so the increased relative mass of the distal primaries was at the expense of proximal primary feather mass.     

The moult of the Little Stint Calidris minuta in the Kenyan rift valley

Moult data were collected during 1967–80 from some 6900 Little Stints in the southern Kenyan rift valley.
Adults typically moulted from summer to winter body and head plumage during September and early October, soon after arrival. The complete pre-winter wing and tail moult began in most adults between mid-September and early October. Some birds finished by December, but others continued until February and March. Individual duration was usually between 100 and 150 days. Adults which completed this moult early often remoulted outer primaries between January and early April.
Young birds acquired first-winter body plumage during October and early November. Some 90% had a complete pre-winter wing and tail moult. This usually began between December and early February, and finished during March or early April, taking about 70–100 days. In about 10% of young birds, flight feather moult was restricted to the outer primaries and inner secondaries. Birds adopting this strategy typically began moult late, during January or February. Short periods of suspension were common during pre-winter wing moult, particularly in adults. The difference in moult speed between adult arid first-winter birds was attributable in the primary, secondary and tail tracts to differences in numbers of growing feathers.
Practically all birds completed a pre-summer moult involving the entire body and head plumage, most of the tertials, some or all of the tail feathers and many wing coverts. Most birds began this moult between early February and late March, and finished between mid-April and early May. It was typically later and more rapid in first-year birds than adults. In late birds, the onset of pre-summer moult was linked to the final stages of pre-winter moult.
The wing moult of the Little Stint in different wintering areas is discussed. First-winter moult strategy is compared with that in other small Calidris species.     

The moult of Barred Warblers Sylvia nisoria in Kenya—evidence for a split wing-moult pattern initiated during the birds' first winter*

The moult of Barred Warblers Sylvia nisoria was studied during three winter seasons in southeastern Kenya at a southward passage site (Ngulia) and a wintering site (Mtito Andei). Most Barred Warblers migrating through Ngulia in November had yet to commence winter moult. These birds probably moulted subsequently in winter in northern Tanzania. In December, birds were found in heavy moult at Mtito Andei, and some of these birds were known to stay throughout the winter. By contrast, most birds reaching southeastern Kenya from late December onwards had already completed part or all of their winter moult, presumably at stopover sites in northern and eastern Kenya or in Ethiopia. Thus, winter moult in Barred Warblers takes place mainly in late November and December, either just before or soon after the final leg of autumn migration. In general, first-year birds renewed all tertials and tail feathers, about three to five secondaries per wing and commonly also the outer one to four large primaries per wing. Adults renewed all tertials and tail feathers, almost all secondaries and only occasionally an outer primary. The replacement of relatively fresh juvenile secondaries during the birds' first winter implies that the split moult pattern of this species (secondaries, tertials and tail moulted in winter; primaries and tertials in summer) is endogenously controlled.     

Corticosterone inhibits feather growth: potential mechanism explaining seasonal down regulation of corticosterone during molt

Corticosterone (CORT) is seasonally modulated in many passerines, with plasma CORT concentrations lowest during the prebasic molt when all feathers are replaced. To explain why, we proposed that the birds downregulate natural CORT release during molt in order to avoid CORT's degradative effects on proteins and its inhibition of protein synthesis. If CORT exerted these effects during molt, it could slow protein deposition during feather production and potentially result in a longer period of degraded flight performance. To test this hypothesis, either empty or CORT-filled silastic implants were inserted into captive European starlings (Sturnus vulgaris) and white-crowned sparrows (Zonotrichia leucophrys) undergoing induced (feather replacement after plucking) and natural molts. We then measured the rate of feather re-growth by regularly measuring the length of primary, secondary, and tail feathers. CORT implanted birds showed a significantly decreased rate of feather growth compared to control animals. Basal CORT concentrations of induced molt and non-molting birds were also compared but no difference was noted. The results suggest a tradeoff; a complete set of new feathers may be more important to the survival of a bird than the ability of CORT to respond maximally to a stressor.     

The phenology of molting,breeding and their overlap in central Amazonian birds

The energetically challenging periods of molting and breeding are usually temporally separated in temperate birds, but can occur simultaneously in tropical birds, a condition known as molt–breeding overlap. Here, we document great variation in the timing and duration of molting and breeding, and in the extent of molt–breeding overlap, among 87 species of understory passerines in central Amazonia. We analyzed molt and breeding from 26 871 birds captured over a 30‐yr period near Manaus, Brazil. Although most species typically bred during the late dry season (about October through January), many thamnophilids apparently bred year‐round, whereas a few other species from a variety of families bred mainly during the wet season (about January through May). Of all breeding birds with an active brood patch, 12.7% were simultaneously molting. Molt–breeding overlap was more frequently observed among suboscines (13.3%), especially thamnophilids (23.0%), than oscines (6.4%). Some families had <5% molt–breeding overlap frequency, including Tyrannidae (4.4%), Tityridae (0.0%), Pipridae (1.5%), Turdidae (0.0%), and Thraupidae (0.0%), indicating that not all tropical species exhibit molt–breeding overlap. Among 31 well‐sampled species (n ≥15 brood patches), variation in molt–breeding overlap frequency was positively correlated with each species’ average duration of flight feather replacement (range 98–301 d). We also measured feather growth rates of individual birds in nine species; in five of these, slower‐growing feathers increased with an individual's probability of having molt–breeding overlap. Among furnariids, molt–breeding overlap occurred either at the beginning or end of the molt cycle, suggesting that physiological mechanisms typically separate molting from breeding. Thamnophilids showed a much different pattern; molt–breeding overlap occurred at any stage of feather replacement, apparently not regulated to be independent of breeding. These results reveal substantial life‐history variation among Amazonian birds. Future work to resolve the physiological regulation of molting and breeding in tropical birds will greatly contribute to understanding these patterns and their relevance to avian diversity.     

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.     

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.     

Feather isotope analysis discriminates age-classes of Western, Least, and Semipalmated sandpipers when plumage methods are unreliable

ABSTRACT Avian age‐class discrimination is typically based on the completeness of the first prebasic molt. In several calidrid sandpiper species, juvenal flight feathers grown on Arctic breeding grounds are retained through the first three migrations. Thereafter, flight feathers are grown annually at temperate migratory stopover sites during the fall or on the subtropical wintering grounds. Standard methods for distinguishing age classes of sandpipers rely on a combination of traits, including body plumage, coloration of protected inner median covert edges, and extent of flight feather wear. We tested the ability of stable hydrogen isotope ratios in flight feathers (δD_f) to distinguish young birds in their first winter through second fall from older adults in three calidrid sandpiper species, Western (Calidris mauri), Least (C. minutilla), and Semipalmated (C. pusilla) sandpipers. We compared the apparent reliability of the isotope approach to that of plumage‐based aging. The large expected differences in δD_f values of flight feathers grown at Arctic versus non‐Arctic latitudes enabled use of this technique to discriminate between age‐classes. We determined δD_f values of known Arctic‐grown feathers from juveniles that grew their flight feathers on the breeding grounds. Flight feather δD_f values of southward‐migrating adults showed bimodal distributions for all three species. Negative values overlapped with species‐specific juvenile values, identifying putative second fall birds with high‐latitude grown juvenal feathers retained from the previous year. The more positive values identified older adults who grew their feathers at mid‐ and low latitudes. Importantly, δD_f analysis successfully identified first‐winter and second‐fall birds not detected by plumage‐based aging. Flight feather wear alone was a poor basis for age classification because scores overlapped extensively between putative second fall birds and older adults. Flight feather hydrogen isotope analysis enables more definitive assignment of age classes when standard plumage methods are unreliable.     

Avian wing proportions and flight styles: first step towards predicting the flight modes of mesozoic birds

We investigated the relationship between wing element proportions and flight mode in a dataset of living avian species to provide a framework for making basic estimates of the range of flight styles evolved by Mesozoic birds. Our results show that feather length (f(prim)) and total arm length (ta) (sum of the humerus, ulna and manus length) ratios differ significantly between four flight style groups defined and widely used for living birds and as a result are predictive for fossils. This was confirmed using multivariate ordination analyses, with four wing elements (humerus, ulna/radius, manus, primary feathers), that discriminate the four broad flight styles within living birds. Among the variables tested, manus length is closely correlated with wing size, yet is the poorest predictor for flight style, suggesting that the shape of the bones in the hand wing is most important in determining flight style. Wing bone thickness (shape) must vary with wing beat strength, with weaker forces requiring less bone. Finally, we show that by incorporating data from Mesozoic birds, multivariate ordination analyses can be used to predict the flight styles of fossils.     

Does Feather Corticosterone Reflect Individual Quality or External Stress in Arctic-Nesting Migratory Birds?

The effects of environmental perturbations or stressors on individual states can be carried over to subsequent life stages and ultimately affect survival and reproduction. The concentration of corticosterone (CORT) in feathers is an integrated measure of hypothalamic–pituitary–adrenal activity during the molting period, providing information on the total baseline and stress-induced CORT secreted during the period of feather growth. Common eiders and greater snow geese replace all flight feathers once a year during the pre-basic molt, which occurs following breeding. Thus, CORT contained in feathers of pre-breeding individuals sampled in spring reflects the total CORT secreted during the previous molting event, which may provide insight into the magnitude or extent of stress experienced during this time period. We used data from multiple recaptures to disentangle the contribution of individual quality vs. external factors (i.e., breeding investment or environmental conditions) on feather CORT in arctic-nesting waterfowl. Our results revealed no repeatability of feather CORT within individuals of either species. In common eiders, feather CORT was not affected by prior reproductive investment, nor by pre-breeding (spring) body condition prior to the molting period. Individual feather CORT greatly varied according to the year, and August-September temperatures explained most of the annual variation in feather CORT. Understanding mechanisms that affect energetic costs and stress responses during molting will require further studies either using long-term data or experiments. Although our study period encompassed only five years, it nonetheless provides evidence that CORT measured in feathers likely reflects responses to environmental conditions experienced by birds during molt, and could be used as a metric to study carry-over effects.     

Prebasic molt initiation and progress in northern fulmars of the High Arctic: do molt and breeding overlap?

We examined feather molt progress of northern fulmars (Fulmarus glacialis) at Cape Vera in the Canadian High Arctic through opportunistic observation of individuals in flight from 2003 to 2006, and examination of bodies and wings of 127 individuals collected at the site, from 2003 to 2005. We found no evidence suggesting that fulmars shed primary feathers during breeding. Prebasic molt was initiated in the head, neck, sides, belly and back approximately 1 week before hatch. We failed to detect a sex effect on molt progress, but molt among breeders was delayed compared to molt in non- or failed breeders. This study constitutes a baseline we feel may be useful to: (1) researchers interested in feather replacement chronology, wherein feathers are used as sources of biological information; and (2) researchers interested in eventual assessment of relationships among large-scale environmental processes and molt progress in this species, especially in light of predicted changes to Arctic regions.     

Experimental evidence that a large raptor can detect and replace heavily damaged flight feathers long before their scheduled moult dates

Because many species of large birds must remain capable of flight during moult and breeding, complete replacement of all flight feathers often takes two or more years, with the result that their plumage normally includes many faded, worn and sometimes even broken feathers. It seems adaptive for such birds to have the ability to quickly replace severely damaged feathers. In search of such a feather replacement mechanism, we cut rectrices on a captive Golden Eagle Aquila chrysaetos and found that feathers cut in their first year of use were replaced, on average, after 11.4 months, whereas uncut feathers before and during the experiment were moulted, on average, after 24 months of use. Feather cutting advanced moult, on average, in excess of a year and thereby demonstrates the existence of a previously undescribed neurophysiological mechanism for preferentially replacing damaged feathers.