Viability selection on prey morphology by a generalist predator

Prey use their locomotory capacity to escape predators, and there should thus be strong viability selection on locomotory morphology of prey. We compared feather morphology of wood pigeons Columba palumbus killed by goshawks Accipiter gentilis with that of survivors to quantify directional and quadratic selection on primary and rectrix feathers. The goshawk is mainly a predator attacking by surprise, leaving wood pigeons with an ability to accelerate fast at a selective advantage. There was directional selection for light primary feathers with a narrow calamus. In addition, there was directional selection for increased area of rectrices. These patterns of natural selection were confirmed in multivariate analyses of selection that showed selection for light primary feathers with a large area and narrow calamus and for a large area of rectrix feathers. These results provide evidence of selection on different aspects of feather morphology directly related to flight performance and thus escape ability from predators.     

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.     

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.     

Moult patterns in the Long-tailed Hawk Urotriorchis macrourus

Information is presented on moult of the Long-tailed Hawk Urotriorchis macrourus, based on 51 specimens. The postjuvenile primary moult is descendant, but the annual primary moult is descendant in about half of the cases only and regular serial descendant moult was found in a few, but different asymmetrical patterns occur in other specimens, probably in relation to accidental replacements, physiological stress or consecutive breeding attempts. As in some other raptors, the brown juvenile central pair of rectrices is replaced by the piebald new generation of feathers before the body and primary moults. These feathers probably signal the individual's status as a potential breeder. As in several other very long-tailed birds, annual rectrix replacement is a permanent ongoing process, which is largely asymmetrical, particularly in the central two pairs, resulting in one feather having always a new contrasting aspect, which may help in signalling status.     

Using stable isotopes to investigate the dietary trophic level of fledgling songbirds

ABSTRACT Use of early successional habitat by mature forest birds during the postfledging period is well documented, but reasons for this habitat shift remain elusive. Although forest‐breeding songbirds are primarily insectivorous during the nestling and early fledgling periods due to high protein requirements, older fledglings may adopt a heavily frugivorous diet. Our objectives were to use stable isotopes to examine the dietary trophic level of juveniles of three species of mature forest songbirds to determine if juvenile songbirds heavily consume fruit resources during the postfledging period and to evaluate a possible link between diet and energetic condition. We collected the outer right rectrix and several body feathers from 34 Wood Thrushes (Hylocichla mustelina), 34 Ovenbirds (Seiurus aurocapilla), and 35 Scarlet Tanagers (Piranga olivacea) captured in regenerating clearcuts in southeastern Ohio in 2005 and 2006. We also collected fruit and arthropod samples from each clearcut. Isotopic values of body feathers were significantly higher (more enriched) than those of rectrices in all cases except values of δ¹³C for Ovenbirds where we found no difference between body and rectrix feathers. These results suggest that juvenile songbirds did not undergo a strong shift to frugivory during the postfledging period, and arthropods were the primary source of protein during the period when rectrix and body feathers were growing. In addition, the energetic condition of birds was not related to the isotopic signature of feathers. Although our results are inconsistent with the hypothesis that juveniles move into regenerating clearcuts enabling them to shift to a primarily frugivorous diet during the postfledging period, they may consume fruit for nonprotein requirements, such as lipids and carbohydrates.     

Moulting strategies of a long-distance migratory seabird, the Mediterranean Cory's Shearwater Calonectris diomedea diomedea

Seabird moult is poorly understood because most species undergo moult at sea during the non-breeding season. We scored moult of wings, tail and body feathers on 102 Mediterranean Cory's Shearwaters Calonectris diomedea diomedea accidentally caught by longliners throughout the year. Primary renewal was found to be simple and descendant from the most proximal (P1) to the most distal (P10) feather. Secondaries showed a more complex moulting pattern, with three different asynchronous foci: the first starting on the innermost secondaries (S21), the second on the middle secondaries (S5) and the latest on the outermost secondaries (S1). Rectrix moult started at a later stage and was simple and descendant from the most proximal feather (R1) expanding distally. Although a few body feathers can be moulted from prelaying to hatching, moult of ventral and dorsal feathers clearly intensified during chick rearing. Different moulting sequences and uncoupled phenology between primary and secondary renewal suggest that flight efficiency is a strong constraint factor in the evolution of moulting strategies. Moreover, moult of Cory's Shearwaters was synchronous between wings and largely asynchronous between tail halves, with no more than one rectrix moulted at once. This result is probably related to the differential sensitivity of wings and the tail on flight performance, ultimately derived from different aerodynamic functions. Finally, Cory's Shearwater females renewed feathers earlier and faster than males, which may be related to the lower chick attendance of females.     

Of 11 candidate steroids,corticosterone concentration standardized for mass is the most reliable steroid biomarker of nutritional stress across different feather types

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Moult topography and its application to the study of partial wing‐moult in two neotropical wrens

During partial moults birds replace a variable number or percentage of old feathers. This quantity, known as moult extent, has been a primary variable used in comparative studies. However, different spatial configurations of feather replacement may result from an equal number of renewed feathers. Few studies have addressed spatial aspects of moult, which may vary among species, among individuals of the same species and between episodes at the individual level. We present a novel approach to quantify the spatial configuration of a wing‐moult episode, hereafter referred to as moult topography, which comprises two elements, namely extent and vector, the latter condensing the spatial configuration of the replaced feathers on the wing plane. We apply this method to investigate preformative (post‐juvenile) wing‐feather moult pattern in the Spot‐breasted Wren Pheugopedius maculipectus and the White‐breasted Wood‐Wren Henicorhina leucosticta. We specified a null model of wing‐moult topography by which feather replacement follows a discrete anterior–posterior (vertical) axis between tracts and a discrete proximal–distal (horizontal) axis within tracts, and whereby wing feathers from a new tract are replaced only if all the feathers from the previous (anterior) tract have been replaced. Our sample of Spot‐breasted Wrens showed a strict single pattern of replacement that did not differ significantly from the null model. Our sample of White‐breasted Wood‐Wrens, however, differed significantly from the null model, showing prioritization of proximal wing feathers closer to the body. These differences might have biological relevance, for example in mate selection or in response to different environmental stressors, and might reveal the influence of these factors on the evolution of moult strategies. Overall, moult topography provides a new approach to future ecological and evolutionary studies of moult.     

MOULT IN FIVE SPECIES OF CORVIDAE IN BRITAIN

This paper presents objective methods for measuring moult and uses them to describe the pattern and rate of the complete moult as a component of the annual cycle in Corvus corone, C. frugilegus, C. monedula, Pica pica and Garrulus glandarius in Britain. The basis of the methods used to measure the rate of moult was the dry weight of the whole plumage and its component tracts and feathers. Within whole tracts of flight feathers showing diversity of size, the longer feathers grew in length a little faster than the others by accumulating feather material very much faster. Thus, for the flight feathers at least length by itself was a poor indicator of size, but, if first related to weight, could be used to predict weight. Hence, to enable realistic comparisons to be made between different flight feathers and tracts of flight feathers on a given individual bird or on individuals of different species, a ‘units’ system was created which would take account of such variations in size. This information provided a standard against which the growth of new flight feathers in a specimen collected in the field could be measured. The progress of moult in each tract was indicated by the sum of the units. In addition, for both the flight feathers and all other tracts, the duration of moult was measured from the start and finish in each tract as indicated by the proportion of birds having either growing or entirely fully-grown feathers in each tract. In the annual cycle body weight and abdominal fat weight were at a maximum in mid-winter and at a minimum in mid-summer in Corvus; variations in these items were apparently absent in G. glandarius. In Corvus probably only post-second-year birds breed, but in P. pica some second-year individuals do so as well; also, increase in testes size in second-year males was greatest in P. pica. The patterns of the relative seasonal timing of the start and finish of moult in each tract were most similar in the three Corvus species, in which moult in the whole plumage began in the primary tract and finished in tracts on the body; P. pica differed principally in the extended growth of the secondary tract; G. glandarius differed in that moult began in the dorsal tract. By summing the data from individual tracts, a measure of the rate of growth in the whole plumage was obtained: all five species moulted at essentially the same time of year. In the primary, secondary, tertiary and rectricial tracts the seasonal accumulation of dry weight of feather material in each tract followed a sigmoid pattern; in the alula tract dry weight increased most rapidly at the beginning. These patterns were correlated with the numbers of feathers growing at different stages in each tract. The primary tract accumulated dry matter at the highest relative rate, while the rectricial, secondary, tertiary and alula tracts did so at successively lower rates. The maximum relative rate of increase in dry weight in any given tract of flight feathers was fairly similar in all five species, but was possibly related inversely to body weight. Maximum absolute rates of increase in dry tract weight were also calculated. During the springtime period when non-moulting and moulting birds were present simultaneously in the population, no difference could be detected between these groups in any species in body and fat weights; in individuals obtained together with evidence of reproductive activity, few had begun primary moult, but in post-second-year C. frugilegus with branchers, males began before females; in C. corone and C. frugilegus testes weight was lower in moulting than in non-moulting birds. In conclusion, some aspects of moult for further research are suggested.     

Theory of the development of curved barbs and their effects on feather morphology

Feathers exhibit an extraordinary diversity of shapes, which are used by birds to accomplish a diverse set of functions. Pennaceous feathers have a double branched morphology that develops from a tube of epidermis, and variation in branch geometry determines feather shape. Feather development is both complex (i.e., a simple developmental modification can have multiple effects on mature feather shape), and redundant (i.e., different developmental modifications can create the same shape). Due to this, it is not readily apparent how different feather shapes develop. In many feathers, barbs are not straight, but instead curve in toward, or away, from the feather tip. Barb curvature can affect the shape of mature feathers but the development of curved barbs is unknown. Previous research has hypothesized that barb curvature could develop either during the helical growth of barb ridges in the tubular feather germ, or during barb angle expansion as the feather unfurls from the sheath. To better understand the development of curved barbs and their effects on mature feathers we present a theoretical model of curved barb development and test the model with empirical investigations of feathers. We find that curved barbs affect many aspects of feather morphology including vane width, barb length, and barb spacing. In real feathers, curved barbs can develop both during helical barb ridge growth and during barb angle expansion, with most of the observed curvature due to barb angle expansion. Our results demonstrate that barb angle expansion as a feather unfurls from the sheath is a complex and dynamic process that plays an important role in determining the shape and structure of mature feathers. Curved barbs create heterogeneity in barb geometry within the feather vane, which could have important implications for aerodynamic function and the development of within feather pigmentation patterns. J. Morphol. 277:995–1013, 2016. © 2016 Wiley Periodicals, Inc.     

Bacterial community profiles on feathers during composting as determined by terminal restriction fragment length polymorphism analysis of 16S rDNA genes

Composting is one of the more economical and environmentally safe methods of recycling feather waste generated by the poultry industry, since 90% of the feather weight consists of crude keratin protein, and feathers contain 15% N. However, the keratin in waste feathers is resistant to biodegradation and may require the addition of bacterial inocula to enhance the degradation process during composting. Two keratin-degrading bacteria isolated from plumage of wild songbirds and identified as Bacillus licheneformis (OWU 1411T) and Streptomyces sp. (OWU 1441) were inoculated into poultry feather composts (1.13×10⁸ cfu g^–1 feathers) and co-composted with poultry litter and straw in 200-l compost vessels. Composting temperatures, as well as CO₂ and NH₃ evolution, were measured in these vessels to determine the effects of inoculation on the rate and extent of poultry feather decomposition during composting. Terminal restriction fragment length polymorphisms of 16S rRNA genes were used to follow changes in microbial community structure during composting. The results indicated that extensive carbon conversion occurred in both treatments (55.5 and 56.1%). The addition of the bacterial inocula did not enhance the rate of waste feather composting. The microbial community structure over time was very similar in inoculated and uninoculated waste feather composts.     

Air-permeable hole-pattern and nose-droop control improve aerodynamic performance of primary feathers

Primary feathers of soaring land birds have evolved into highly specialized flight feathers characterized by morphological improvements affecting aerodynamic performance. The foremost feathers in the cascade have to bear high lift-loading with a strong bending during soaring flight. A challenge to the study of feather aerodynamics is to understand how the observed low drag and high lift values in the Reynolds (Re) regime from 1.0 to 2.0E4 can be achieved. Computed micro-tomography images show that the feather responds to high lift-loading with an increasing nose-droop and profile-camber. Wind-tunnel tests conducted with the foremost primary feather of a White Stork (Ciconia ciconia) at Re = 1.8E4 indicated a surprisingly high maximum lift coefficient of 1.5 and a glide ratio of nearly 10. We present evidence that this is due to morphologic characteristics formed by the cristae dorsales as well as air-permeable arrays along the rhachis. Measurements of lift and drag forces with open and closed pores confirmed the efficiency of this mechanism. Porous structures facilitate a blow out, comparable to technical blow-hole turbulators for sailplanes and low speed turbine-blades. From our findings, we conclude that the mechanism has evolved in order to affect the boundary layer and to reduce aerodynamic drag of the feather.     

Chemical Analysis of Melanin Pigments in Feather Germs of Japanese Quail Bh (Black at Hatch) Mutants

Bh (black at hatch) is a mutation of Japanese quails which causes darkening or lightening of the plumage in heterozygotes or homozygotes, respectively. We chemically analyzed melanin pigments in feather germs of Bh mutant embryos and in feathers of adult animals. Dark brown dorsal feathers of wild-type adult animals had white barrings, but heterozygous ones lacked clear barrings. The feathers of wild-type and heterozygote animals contained both eumelanins and pheomelanins, the latter being more pheomelanic. On the dorsal skin of 10-day old wild-type embryos, longitudinal stripes from black and yellow rows of feather germs developed; two or three longitudinal rows of black feather germs and then two or three rows of yellow feather germs next to the short central feather germs. Heterozygous embryos appeared black in plumage pigmentation, due to the presence of‘gray’feather germs in rows of dorsal feather germs that corresponded to yellow rows in wild-type embryos. Homozygous dorsal feather germs did not develop the black and yellow longitudinal stripes, but were brown. Chemical analysis showed that embryos of each genotype contained both eumelanins and pheomelanins in the feather germs; however, the eumelanin content in ho-mozygous feather germs was very low. These results suggest that the Bh mutation causes pheomelanic changes in feathers of quails.     

Resistance of melanized feathers to bacterial degradation: is it really so black and white?

Melanins are common feather pigments that contribute to signaling and crypsis. Melanins may also help feathers resist feather‐degrading bacteria (FDB). Two recent studies (Goldstein et al. 2004, Grande et al. 2004) tested the resistance of melanized versus unmelanized feathers to FDB using in vitro experiments, but draw opposite conclusions. Goldstein et al. (2004) concluded that melanized feathers resist FDB more than unmelanized feathers, while Grande et al. (2004) concluded that unmelanized feathers resist FDB more than melanized feathers. To resolve this conflict in the literature, we replicated previous studies but included additional tests not previously used. We inoculated melanized and unmelanized feathers of domestic geese Anser anser domesticus, with the FDB Bacillus licheniformis and measured bacterial activity every two days over two weeks. Three metrics of bacterial activity on feathers were measured: soluble protein content around feathers in solution, bacterial growth on feathers, and loss of feather mass. The latter two metrics were not considered in the aforementioned studies, which indirectly measured bacterial activity. We conducted two trials, one in which feathers were sterilized by autoclaving before inoculation (Goldstein et al. 2004, Grande et al. 2004), and a second in which feathers were sterilized by ethylene oxide gas. This allowed us to test whether autoclaving, done in previous studies, influences bacterial activity on feathers and could confound results. In both trials, unmelanized feathers degraded earlier, supported greater bacterial growth, and lost more mass than melanized feathers. These results support the findings of Goldstein et al. (2004); melanized feathers are more resistant to FDB than unmelanized feathers. Thus, using direct metrics of bacterial activity, we resolve a current conflict in the literature. We also found that autoclaving feathers influences FDB activity on them, and thus autoclaving should be avoided in future studies.     

Divergent rectrix moult: the implications and conditions of moult sequence

Wing and tail morphology strongly affect flight performance which may consequently decline during feather moult due to the creation of feather gaps in the flight‐surface. Hence, the size and shape of moult‐related gaps may directly affect flight capacity. Here, I examined the divergent rectrix moult sequence compared to the more common distal moult sequence. In the divergent moult, the focus of rectrix moult is shifted from the tail centre (R₁; rectrices numbered distally from mid‐tail outward) to another rectrix (R₂ or R₃), and then rectrices are moulted bidirectionally, towards the tail centre and outwards. The result of this moult sequence is the splitting of the tail gap into multiple smaller gaps. Using a large moult database including 5669 individuals of 47 Western Palaearctic passerine species, I found evidence of divergent moult sequence for only seven species. Using comparative and experimental approaches, I found that the divergent rectrix sequence is correlated with higher moult speed and lower aerodynamic cost. Furthermore, the divergent rectrix sequence is more common among adults than juveniles. This work focused on the feather moult sequence – a seldom studied aspect of the avian life‐history. I propose that moult‐related aerodynamic costs may be an important evolutionary factor not only in moult speed, but also in moult sequence.     

Demographic variation in timing and intensity of feather molt in migratory Fork‐tailed Flycatchers (Tyrannus s. savana)

Understanding the annual cycle of migratory birds is imperative for evaluating the evolution of life‐history strategies and developing effective conservation strategies. Yet, we still know little about the annual cycle of migratory birds that breed at south‐temperate latitudes of South America. We aged, sexed, and determined the progression and intensity of body, remige, and rectrix molt of migratory Fork‐tailed Flycatchers (Tyrannus s. savana) at breeding sites in southern South America and at wintering sites in northern South America. Molt of both body and flight feathers occurred primarily during the winter. In early winter, a similar proportion of young and adult flycatchers molted remiges and rectrices, but remige molt intensity (number of remiges molting) was greater and primary molt progression (mean primary feather molting) more advanced in adults. In late winter, remige molt intensity and primary molt progression did not differ between age groups. We found no difference between males and females either in the proportion of individuals molting in winter or in the intensity or progress of remige molt. Our results suggest that the nominate subspecies of Fork‐tailed Flycatcher undergoes one complete, annual molt on the wintering grounds, and represents the first comprehensive evaluation of molt timing of a migratory New World flycatcher that overwinters in the tropics. Given that breeding, molt, and migration represent three key events in the annual cycle of migratory birds, knowledge of the timing of these events is the first step toward understanding the possible tradeoffs migratory birds face throughout the year.     

Variation in the mechanical properties of flight feathers of the blackcap Sylvia atricapilla in relation to migration

Migration causes temporal and energetic constraints during plumage development, which can compromise feather structure and function. In turn, given the importance of a good quality of flight feathers in migratory movements, selection may have favoured the synthesis of feathers with better mechanical properties than expected from a feather production constrained by migration necessities. However, no study has assessed whether migratory behaviour affects the relationship between the mechanical properties of feathers and their structural characteristics. We analysed bending stiffness (a feather mechanical property which is relevant to birds’ flight), rachis width and mass (two main determinants of variation in bending stiffness) of wing and tail feathers in migratory and sedentary blackcaps Sylvia atricapilla. Migratory blackcaps produced feathers with a narrower rachis in both wing and tail, but their feathers were not significantly lighter; in addition, bending stiffness was higher in migratory blackcaps than in sedentary blackcaps. Such unexpected result for bending stiffness remained when we statistically controlled for individual variation in rachis width and feather mass, which suggests the existence of specific mechanisms that help migratory blackcaps to improve the mechanical behaviour of their feathers under migration constraints.     

Population differences in the structure and coloration of great tit contour feathers

Contour feathers cover most of the avian body and play critical roles in insulation, social communication, aerodynamics, and water repellency. Feather production is costly and the development of the optimum characteristics for each function may be constrained by limited resources or time, and possibly also lead to trade‐offs among the different characteristics. Populations exposed to different environmental conditions may face different selective pressures, resulting in differences in feather structure and coloration, particularly in species with large geographical distributions. Three resident populations of great tit Parus major L. from different latitudes differed in feather structure and coloration. Individuals from the central population exhibited less dense and longer contour feathers, with a higher proportion of plumulaceous barbs than either northern or southern birds, which did not differ in their feather structure. Ultraviolet reflectance and brightness of the yellow of the contour feathers of the breast was higher for the southern than for the northern population. Birds with greener plumage (higher hue) had less dense but longer feathers, independently of the population of origin. Differences in feather structure across populations appear to be unrelated to the contour feather colour characteristics except for hue. Nutritional and time constraints during molt might explain the pattern of feather structure, whereas varying sexual selection pressure might underlie the coloration patterns observed. Our results suggest that different selective pressures or constraints shape contour feather traits in populations exposed to varying environmental conditions. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 114 , 82–91.     

Colour composition of nest lining feathers affects hatching success of barn swallows,Hirundo rustica (Passeriformes: Hirundinidae)

Many bird species use feathers as lining material, and its functionality has traditionally been linked to nest insulation. However, nest lining feathers may also influence nest detection by predators, differentially affect reproductive investment of mates in a post‐mating sexual selection process, and affect the bacterial community of the nest environment. Most of these functions of nest lining feathers could affect hatching success, but the effect might vary depending on feather coloration (i.e. pigmented versus white feathers). This would be the case if coloration is related to: (1) thermoregulatory properties; (2) attractiveness of feathers in the nest for mates; (3) eggshell bacterial density. All of these hypothetical scenarios predict that feathers of different colours would differentially affect the hatching success of birds, and that birds should preferentially choose the most beneficial feather colour for lining their nests. Results from two different experiments performed with a population of Danish barn swallow, Hirundo rustica, were in accordance with these predictions. First, H. rustica preferentially selected white experimentally offered feathers for lining their nests. Second, the experimental manipulation of the feather colour composition of nests of H. rustica had a significant effect on hatching success. Experimental nests with more white feathers added at the beginning of incubation had a lower probability of hatching failures, suggesting differential beneficial effects of lining nests with feathers of this colour. We discuss the relative importance of hypothetical functional scenarios that predicted the detected associations, including those related to sexual selection or to the community of microorganisms associated with feathers of different colours. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 67–74.