STRUCTURALLY COLOURED PATTERN MARKS ON THE INNER WEBS OF FLIGHT FEATHERS.

Some Psittacidae and Coraciidae show the unusual feature of blue and green pattern marks restricted to reverse surfaces of flight feathers.
The optical causes of the colours of these marks are identical with, and the morphological configurations similar to, those which typically cause these colours on obverse surfaces of feathers in the same families. The atypical marks may, however, have been evolved independently from the typically located colour.
Colour patterns on flight feathers are discussed in relation to the mechanics of flight and to optical effect.     

Variations of Mesozoic feathers: Insights from the morphogenesis of extant feather rachises

The rachises of extant feathers, composed of dense cortex and spongy internal medulla, are flexible and light, yet stiff enough to withstand the load required for flight, among other functions. Incomplete knowledge of early feathers prevents a full understanding of how cylindrical rachises have evolved. Bizarre feathers with unusually wide and flattened rachises, known as “rachis-dominated feathers” (RDFs), have been observed in fossil nonavian and avian theropods. Newly discovered RDFs embedded in early Late Cretaceous Burmese ambers (about 99 million year ago) suggest the unusually wide and flattened rachises mainly consist of a dorsal cortex, lacking a medulla and a ventral cortex. Coupled with findings on extant feather morphogenesis, known fossil RDFs were categorized into three morphotypes based on their rachidial configurations. For each morphotype, potential developmental scenarios were depicted by referring to the rachidial development in chickens, and relative stiffness of each morphotype was estimated through functional simulations. The results suggest rachises of RDFs are developmentally equivalent to a variety of immature stages of cylindrical rachises. Similar rachidial morphotypes documented in extant penguins suggest that the RDFs are not unique to Mesozoic theropods, although they are likely to have evolved independently in extant penguins.     

The peacock's train (Pavo cristatus and Pavo cristatus mut. alba) II. The molecular parameters of feather keratin plasticity

Thermal activation analysis of plastic deformation of peacock tail feathers, by temperature changes and stress relaxation, gave for the keratin cortex an activation enthalpy of 1.78 ± 0.89?eV and an activation volume of 0.83 ± 0.13?nm3, for both the blue and the white subspecies. These values suggest that breaking of electrostatic bonds is responsible for plasticity in feather keratin. These might be bonds between keratin and nonkeratinous matrix or keratin-keratin cross-links. The mechanical properties of the rachis cortex are surprisingly uniform along the length of the feathers.     

Environmental conditions but not nest composition affect reproductive success in an urban bird

Adjusting the composition of their nests, breeding birds can influence the environmental conditions that eggs and offspring experience. Birds often use feathers to build nests, presumably due to their insulating properties. The amount of feathers in nests is often associated with increased nestling survival and body condition. However, it is unclear whether these putative beneficial effects of adding feathers to nests are relevant in a wide range of environmental conditions. Here, we combine data on weather conditions and feathers in nests (i.e., nest composition) to investigate their relative contribution to reproductive success in the Eurasian tree sparrow (Passer montanus). Specifically, we investigate whether the effect of weather conditions on breeding success is modulated by the amount of feathers added to the nest. We found a strong negative effect of rainfall on the number of nestlings that successfully fledged per breeding attempt, but this negative effect was not mitigated by the amount of feathers in nests. We also found that the amount of feathers in nests varied along the breeding season, with nests containing more feathers early in the breeding season, when temperatures were lower. Despite considerable variation in nest composition, our results do not suggest an important role of feathers in nests protecting eggs or nestling tree sparrows against fluctuations in environmental conditions.     

ON THE NATURE AND ORIGIN OF THE FEATHER COLOURATION IN THE GREAT WHITE PELICAN PELECANUS ONOCROTALUS ROSEUS IN ETHIOPIA

The yellow or orange-brown colour on the breast feathers and to a lesser extent on other feathers of the Great White Pelican in a breeding colony on an island in Lake Shala, Ethiopia, is due to the presence of ferric oxide.
The feathers most probably become stained when the birds are in the water, and the source of the ferric oxide may be iron–rich silt carried into the lake by the Gidu River.     

The color of greater flamingo feathers fades when no cosmetics are applied

Greater flamingos use cosmetic coloration by spreading uropygial secretions pigmented with carotenoids over their feathers, which makes the plumage redder. Because flamingos inhabit open environments that receive direct solar radiation during daytime, and carotenoids bleach when exposed to solar radiation, we expected that the plumage color would fade if there is no maintenance for cosmetic purposes. Here, we show that the concentrations of pigments inside feathers and on the surface of feathers were correlated, as well as that there was a correlation between the concentrations of pigments in the uropygial secretions and on the surface of feathers. There was fading in color (becoming less red) in feathers that received direct solar radiation when there was no plumage maintenance, but not so in others maintained in darkness. When we controlled for the initial color of feathers, the feathers of those individuals with higher concentration of pigments on the feather surfaces were those that lost less coloration after experimental exposure of feathers to sunny conditions. These results indicate that exposure to sunlight is correlated with the fading of feather color, which suggests that individuals need to regularly apply makeup to be more colorful. These results also reinforce the view that these birds use cosmetic coloration as a signal amplifier of plumage color. This may be important in species using highly variable habitats, such as wetlands, since the conditions experienced when molting may differ from those when the signal should be functional, usually months after molting.     

解淀粉芽孢杆菌3-2发酵羽毛产氨基酸

【目的】建立废弃羽毛液体发酵工艺,优化发酵条件,提高羽毛降解率及氨基酸产量,研发新型、高效复合氨基酸肥料。【方法】利用解淀粉芽孢杆菌3-2发酵羽毛,探究温度、发酵时间、羽毛含量、单一碳源、复合碳氮源、金属离子等对废弃羽毛降解效果以及发酵液中氨基酸种类和含量的影响。【结果】废弃羽毛降解率与氨基酸总产量呈负相关。随着发酵时间延长,羽毛降解率增加,当发酵温度为37°C、羽毛添加量为1%、以乳糖为外加碳源、添加Mg2+时,羽毛降解率最高,达到81.92%。随着羽毛添加量增加,氨基酸总含量也增加(在20%范围以内),当发酵温度为37°C、降解时间为108 h、羽毛添加量为10%、乳糖添加量为0.5%、不添加复合碳氮源、不添加金属离子时,氨基酸的种类最全(富含17种氨基酸),总含量最高,达到20.861 g/kg。【结论】利用解淀粉芽孢杆菌3-2发酵废弃羽毛生产氨基酸复合肥料是一种可靠、环保、经济的方法,获得的氨基酸肥料营养齐全。研究结果为新型复合氨基酸肥料的研发提供技术支撑。     

THE MOULT OF THE BULLFINCH PYRRHULA PYRRHULA

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

THE LITTLE SWIFT AND OTHERS AT KASAMA

Rijke, A. M., Jesser, W. A. &; Mahoney, S. A. 1989. Plumage wettability of the African Darter Anhinga melanogaster compared with the Double-crested Cormorant Phalacrocarax auritus. Ostrich 60:128-132.

Darters emerge from water “dripping wet” but are able to become airborne without delay. Their plumage is, on the whole, three times more wettable than that of cormorants. We investigated the microscopic structure and resistance to water penetration of the body, wing and tail feathers of the African Darter, Anhinga melanogaster.

The results show values of the structural parameter (r + d)/r for body feathers in the range of 9 to 12, whereas for rectrices, primaries, secondaries and tertiaries, a range of 2 to 3 was observed, with barbules measuring 2 to 3. Penetration pressures measure zero to 1 cm water head for the body feathers and 6 to 15 cm for the wing and tail feathers. These findings suggest that on submersion, the body feathers wet out entirely but wing and tail feathers resist becoming waterlogged which may reduce buoyancy when stalking prey underwater and permit the darter to take to the air immediately after a dive. The results have been compared with those of similar measurements on cormorant feathers, which underscore the dual nature of the darter plumage in terms of water repellency and resistance to water penetration.     

What makes a feather shine? A nanostructural basis for glossy black colours in feathers

Colours in feathers are produced by pigments or by nanostructurally organized tissues that interact with light. One of the simplest nanostructures is a single layer of keratin overlying a linearly organized layer of melanosomes that create iridescent colours of feather barbules through thin-film interference. Recently, it has been hypothesized that glossy (i.e. high specular reflectance) black feathers may be evolutionarily intermediate between matte black and iridescent feathers, and thus have a smooth keratin layer that produces gloss, but not the layered organization of melanosomes needed for iridescence. However, the morphological bases of glossiness remain unknown. Here, we use a theoretical approach to generate predictions about morphological differences between matte and glossy feathers that we then empirically test. Thin-film models predicted that glossy spectra would result from a keratin layer 110-180 nm thick and a melanin layer greater than 115 nm thick. Transmission electron microscopy data show that nanostructure of glossy barbules falls well within that range, but that of matte barbules does not. Further, glossy barbules had a thinner and more regular keratin cortex, as well as a more continuous underlying melanin layer, than matte barbules. Thus, their quasi-ordered nanostructures are morphologically intermediate between matte black and iridescent feathers, and perceived gloss may be a form of weakly chromatic iridescence.     

Feather development under environmental stress: lead exposure effects on growth patterns in Great Tits Parus major

Capsule Regrowth rate of tail feathers is more strongly affected compared to feather length and symmetry.

Aims To assess the value of avian feathers as bioindicators.

Methods The origin and persistence of fluctuating asymmetry (FA) in homologous pairs of regrowing feathers was studied in captive birds under different levels of environmental stress, respresented by exposure to lead (Pb). Homologous feathers of individually housed birds were plucked synchronously or with a delay of seven days. We measured growth rate, regeneration time, final size and FA of regrown feathers and related them to Pb stress.

Results Asymmetry decreased as feathers reached their final length. This was not due to compensatory growth but rather a consequence of the programmed growth trajectory of single feathers. Tail feathers grown under higher Pb pollution showed increased regeneration times, decreased growth rates and shorter lengths, but no changes in development times nor in FA. For differences between both (i) original and induced feathers and (ii) control and Pb treatment, effect sizes of parameters related to feather development (growth bar width, growth rate, regeneration and development time) were consistently larger than those related to the resulting phenotype (feather length and FA).

Conclusions Growth bar widths in particular provide an applicable, sensitive and reliable indicator of adverse conditions such as Pb pollution and experimental conditions. In general, phenotypic characteristics that retrospectively allow estimation of growth rates may be more suitable for monitoring environmental stress than sizes or asymmetries of full-grown traits.     

MOULT IN THE SHAG PHALACROCORAX ARISTOTELIS, AND THE ONTOGENY OF THE "STAFFELMAUSER"

There are three main types of plumage in the Shag, the juvenal which is brown, the post-juvenal which is dark brown and the nuptial which is black-green. The replacement of these plumages and the ontogeny of the Staffelmauser was studied in a sample of 566 Shags mainly from northeast England. The replacement of the juvenal primaries starts at the age of eight months with the loss of the innermost primary and continues outwards at a rate of about one primary per 17 days. Another cycle starts when the first reaches the 8th primary but both cycles soon pause for the winter. Successive cycles are established annually in August or September in this way, so that cycles which take longer than one year to complete result eventually in a Staffelmauser in which each feather is replaced once annually. Most individual Shags in a breeding population will retain feathers from two or three cycles, but a large sample of breeding adults of the same age will retain the feathers of four cycles. The winter pause is considered an adaptation to the increased probability of adverse conditions at this time. The system described for the ontogeny of the Staffelmauser is applicable to those other sea-birds which have been studied in detail, and is probably advantageous since it combines slow moult during the difficult early years with a highly efficient moult during the breeding years, especially where moult and breeding occur together.     

Is the structural and psittacofulvin‐based coloration of wild burrowing parrots Cyanoliseus patagonus condition dependent?

The bright colours of parrots are caused by psittacofulvin pigments, which appear unique to this Order, and by structural colours. We measured red (psittacofulvin), green (mixed) and blue (structural) colours of wild burrowing parrots Cyanoliseus patagonus of northeastern Patagonia, Argentina, and measured nestlings regularly to obtain data on breeding success and nestling growth. As adult feathers are moulted outside the breeding season, adult body condition could not be measured directly during feather growth, and climatic conditions were used as an indirect parameter. The colony of burrowing parrots is surrounded by Monte steppe habitat, the breeding success has been shown to depend strongly on the climatic patterns. The area experienced a drought with very poor breeding success as well as a year of above‐average precipitation during the study period, serving as a natural experiment. We thus analysed the variability of colouration within the population among and within breeding seasons. We observed strong inter‐annual differences in nestling and adult colouration. Nestlings grew blue feathers with lower achromatic brightness during better conditions, and when controlling for year effects, nestlings with higher mass and from more successful families also had blue feathers with lower achromatic brightness. Adult blue feathers showed the same trend, with lower achromatic brightness in the moult following breeding seasons of better conditions. In contrast, during better conditions, adults grew red feathers with higher achromatic brightness and the colour hue was also affected, and the hue of the red region of nestlings varied with the hatching order. The colour of all three regions of nestlings varied between nests, and the colour of the red region of adult males positively correlated with breeding success (clutch size, brood size). In summary, the present data suggest that environmental conditions contribute to variability in both structural and the psittacofulvin‐based colours of wild burrowing parrots.     

Different scales of spatial segregation of two species of feather mites on the wings of a passerine bird

The "condition-specific competition hypothesis" proposes that coexistence of 2 species is possible when spatial or temporal variations in environmental conditions exist and each species responds differently to those conditions. The distribution of different species of feather mites on their hosts is known to be affected by intrinsic host factors such as structure of feathers and friction among feathers during flight, but there is also evidence that external factors such as humidity and temperature can affect mite distribution. Some feather mites have the capacity to move through the plumage rather rapidly, and within-host variation in intensity of sunlight could be one of the cues involved in these active displacements. We analyzed both the within- and between-feather spatial distribution of 2 mite species, Trouessartia bifurcata and Dolichodectes edwardsi , that coexist in flight feathers of the moustached warbler Acrocephalus melanopogon. A complex spatial segregation between the 2 species was observed at 3 spatial levels, i.e., "feather surfaces," "between feathers," and "within feathers." Despite certain overlapping distribution among feathers, T. bifurcata dominated proximal and medial regions on dorsal faces, while D. edwardsi preferred disto-ventral feather areas. An experiment to check the behavioral response of T. bifurcata to sunlight showed that mites responded to light exposure by approaching the feather bases and even leaving its dorsal face. Spatial heterogeneity across the 3 analyzed levels, together with response to light and other particular species adaptations, may have played a role in the coexistence and segregation of feather mites competing for space and food in passerine birds.     

HISTORICAL EXAMINATION OF DELAYED PLUMAGE MATURATION IN THE SHOREBIRDS (AVES: CHARADRIIFORMES)

Delayed plumage maturation refers to the presence of nonadultlike immature plumages (juvenal plumage excluded). It is usually considered the result of selection for distinctive first-winter or first-summer appearance. In the present study, evolution of delayed plumage maturation is examined in the shorebirds: the sandpipers, plovers, gulls, and their allies. Nine plumage-maturation characters were identified, and their states were superimposed onto topologies generated during two recent investigations of shorebird relationships (Sibley and Ahlquist; revised Strauch). The characters were then optimized so as to assign character states to interior nodes of the trees in the most parsimonious way. Reconstructions of character evolution on six of the shortest revised Strauch trees were ambiguous with respect to delayed plumage maturation in the hypothetical ancestral shorebird. If plumage maturation was not delayed in the shorebird ancestor, optimization indicated that delay appeared when nonadultlike juvenal feathers were acquired. In contrast, on the single Sibley and Ahlquist tree, absence of delayed plumage maturation in the shorebird ancestor was indicated unambiguously, with three evolutionary novelties (nonadultlike juvenal feathers, seasonal plumage change, and a reduced first-spring molt) implicated in its acquisition. Optimization indicated that delayed plumage maturation in shorebirds can be explained plausibly without invoking selection for distinctive first-winter or first-summer appearance. Two of the novel conditions generating delayed plumage maturation (modified juvenal feathers and seasonal plumage change) did so only because they were acquired in a taxon possessing restricted first-year molts, which are primitive. Given these observations, it seems simplest to explain the delay in plumage maturation as an incidental consequence of the phylogenetic inertia of shorebird molts. The third novelty that generates delayed plumage maturation, a reduced first-spring molt, may have been acquired to reduce molt-associated energetic demands in young birds.     

Circannual pupation rhythm in the varied carpet beetle Anthrenus verbasci under different nutrient conditions

Anthrenus verbasci pupates in spring and the timing of pupation is controlled by a circannual rhythm. Although A. verbasci is considered to be a univoltine species in Japan, it is assumed that larval development in its natural habitats, including bird nests, varies with nutrient availability, and that the life cycle often takes two or more years to complete. In the present study, larval development and pupation times were compared under constant and outdoor conditions in larvae provided a diet of either high‐nutrient bonito powder or low‐nutrient pigeon feathers. Although a circannual pupation rhythm was observed irrespective of the diet used, larval development was slower on feathers than on bonito powder. The pupation times on feathers varied over three years or more under both constant and outdoor conditions. Under outdoor conditions, larvae grown on feathers needed three years to approach the weight gained within a year by larvae grown on bonito powder. It is considered that life cycle length in A. verbasci is often two years or more in nutritionally unstable natural habitats, and that this species has probably evolved a circannual rhythm as a seasonal adaptation to nutrient‐poor environments.     

Taphonomic experiments resolve controls on the preservation of melanosomes and keratinous tissues in feathers

Fossils are a key source of data on the evolution of feather structure and function through deep time, but their ability to resolve macroevolutionary questions is compromised by an incomplete understanding of their taphonomy. Critically, the relative preservation potential of two key feather components, melanosomes and keratinous tissue, is not fully resolved. Recent studies suggesting that melanosomes are preferentially preserved conflict with observations that melanosomes preserve in fossil feathers as external moulds in an organic matrix. To date, there is no model to explain the latter mode of melanosome preservation. We addressed these issues by degrading feathers in systematic taphonomic experiments incorporating decay, maturation and oxidation in isolation and combination. Our results reveal that the production of mouldic melanosomes requires interactions with an oxidant and is most likely to occur prior to substantial maturation. This constrains the taphonomic conditions under which melanosomes are likely to be fossilized. Critically, our experiments also confirm that keratinous feather structures have a higher preservation potential than melanosomes under a range of diagenetic conditions, supporting hitherto controversial hypotheses that fossil feathers can retain degraded keratinous structures.     

The possible evolutionary significance of differences in feather structure between closely related Pittidae (Passeres: Mesomyodes)

The Pittidae of the subgenus Cervinipitta are practically uniform in the colour pattern of their plumage, but the African forms differ from the remaining (namely, Asian and Australasian) forms of the subgenus in the structure and pigmentation of their green (Tyndall-coloured) feathers.
In these feathers, the Africans appear to show certain ancestral characters: small numbers of medullary cells, some of which may contain small, fluctuating amounts of dark-pigmented granules.
These characters coexist there with specialized features, which may intensify the colour effect: absence of the granules from most medullary cells and aggregation of such granules in lateral portions of the cortex.
In the Eastern forms of the subgenus, the number of medullary cells appears to be secondarily increased, and the amount of granules enlarged and concentrated in axial cells of the medulla–again serving the intensification of the colour.
In this way the African and the Eastern branches of the subgenus have undergone divergent specialization in histological details, but show practically identical colour effects. However, the African branch appears to have retained some primitive characters and shows incompletely stabilized conditions.     

Colourful parrot feathers resist bacterial degradation

The brilliant red, orange and yellow colours of parrot feathers are the product of psittacofulvins, which are synthetic pigments known only from parrots. Recent evidence suggests that some pigments in bird feathers function not just as colour generators, but also preserve plumage integrity by increasing the resistance of feather keratin to bacterial degradation. We exposed a variety of colourful parrot feathers to feather-degrading Bacillus licheniformis and found that feathers with red psittacofulvins degraded at about the same rate as those with melanin and more slowly than white feathers, which lack pigments. Blue feathers, in which colour is based on the microstructural arrangement of keratin, air and melanin granules, and green feathers, which combine structural blue with yellow psittacofulvins, degraded at a rate similar to that of red and black feathers. These differences in resistance to bacterial degradation of differently coloured feathers suggest that colour patterns within the Psittaciformes may have evolved to resist bacterial degradation, in addition to their role in communication and camouflage.     

Brown tawny owls moult more flight feathers than grey ones

The mechanisms by which melanin‐based colour polymorphism can evolve and be maintained in wild populations are poorly known. Theory predicts that colour morphs have differential sensitivity to environmental conditions. Recently it has been proposed that colour polymorphism covaries genetically with intrinsic and behavioural properties. Plumage moult is a costly and crucial somatic maintenance function in birds. We used a long‐term data set consisting of 761 observations on 307 individuals captured between 1985 and 2010 to examine differences in partial flight feather moult between grey (pale) and brown (pheomelanic dark) colour morphs of the tawny owl. We find that the brown morph consistently moult more primary flight feathers than the grey morph whereas there is no clear difference between colour morphs in the moulting of secondary feathers. Contrary to expectations, the difference in the number of moulted flight feathers between the morphs was independent of environmental conditions, as quantified by the abundance of prey. We discuss the potential physiological and behavioural causes for and costs of the observed difference in maintenance functions between colour morphs.