Tail Feathers (tail + feather)

Distribution by Scientific Domains


Selected Abstracts


Use of trace elements in feathers of sand martin Riparia riparia for identifying moulting areas

JOURNAL OF AVIAN BIOLOGY, Issue 3 2003
Tibor Szép
We investigated whether trace elements in tail feathers of an insectivorous and long-distance migratory bird species could be used to identify moulting areas and hence migratory pathways. We analysed tail feathers from birds of different age and sex collected from a range of different breeding sites across Europe. The site of moult had a large effect on elemental composition of feathers of birds, both at the European and African moulting sites. Analysis of feathers of nestlings with known origin suggested that the elemental composition of feathers depended largely upon the micro-geographical location of the colony. The distance between moulting areas could not explain the level of differences in trace elements. Analysis of feathers grown by the same individuals on the African wintering grounds and in the following breeding season in Europe showed a large difference in composition indicating that moulting site affects elemental composition. Tail feathers moulted in winter in Africa by adults breeding in different European regions differed markedly in elemental composition, indicating that they used different moulting areas. Analysis of tail feathers of the same adult individuals in two consecutive years showed that sand martins in their first and second wintering season grew feathers with largely similar elemental composition, although the amounts of several elements in tail feathers of the older birds was lower. There was no difference between the sexes in the elemental composition of their feathers grown in Africa. Investigation of the trace element composition of feathers could be a useful method for studying similarity among groups of individuals in their use of moulting areas. [source]


Experimental tail shortening in Barn Swallows (Hirundo rustica) affects haematocrit

FUNCTIONAL ECOLOGY, Issue 5 2005
J. J. CUERVO
Summary 1Recent studies in Scotland suggest that the outermost tail feathers of Barn Swallows (Hirundo rustica Linnaeus) may be around 10,12 mm longer than the aerodynamic optimum, with sexual selection for long tails accounting for this extra length. 2To test this hypothesis, we shortened the outermost tail feathers in male and female Barn Swallows in southern Spain by cutting 1, 11 or 21 mm from the tips of the feathers, and checked for change in haematocrit 1 month later. Haematocrit levels were high when birds arrived at the breeding grounds due to an intense effort for flight during migration, but these levels decreased during the breeding season. We predicted that this decrease would be more pronounced when tail length was closer to the aerodynamic optimum (tails shortened by 11 mm), and less pronounced as tail length was displaced from that optimum (tails shortened by 1 or 21 mm). 3Contrary to expectations, we found that the smaller the experimental reduction in tail length, the more pronounced the decrease in haematocrit. Barn Swallows with little parental effort and originally long tail feathers experienced a more pronounced decrease in haematocrit than individuals with strong parental effort and originally short tail feathers, respectively, although only in the group of birds with tails shortened by 21 mm. 4These results do not support the hypothesis that outermost tail feathers in Barn Swallows have been elongated because of sexual selection, at least in the population studied, but are consistent with tail length being at an aerodynamic optimum, or very close to it. Differences in tail length among populations might help to understand the disagreement with previous studies. [source]


How feather colour reflects its carotenoid content

FUNCTIONAL ECOLOGY, Issue 4 2003
Lauri Saks
Summary 1Many birds sequester carotenoid pigments in colourful patches of feathers to advertise or compete for mates. Because carotenoids can be scarce in nature and serve valuable physiological functions, only the highest-quality individuals are thought to acquire or allocate more pigments for use in sexual displays. 2A critical but rarely tested assumption of carotenoid-based signals is that the colour of pigmented feather patches directly reveals the total amount of carotenoids contained within them. 3We studied the relationship between carotenoid-based coloration (hue, chroma and brightness) and the pigment content of tail feathers in wild-caught and captive male greenfinches (Carduelis chloris[Linnaeus]). Greenfinches incorporate two main carotenoids , canary xanthophylls A and B , into feathers to develop yellow patches of colour in their tail. 4Variation in feather carotenoid content explained 32,51% of variation in chroma and hue of the yellow parts of tail feathers, while feather brightness was not significantly related to carotenoid concentration. Hence, chroma and hue appear good candidates to indicate feather carotenoid content. 5Birds with the most colourful feathers deposited significantly more of both canary xanthophylls into plumage. Thus, there does not appear to be a specific biochemical strategy for becoming colourful in greenfinches; males instead follow the general decision rule to deposit as many xanthophylls as possible into feathers to become yellow. [source]


Use of TLC-FID and GC-MS/FID to examine the effects of migratory state, diet and captivity on preen wax composition in White-throated Sparrows Zonotrichia albicollis

IBIS, Issue 4 2010
RAYMOND H. THOMAS
Preen wax is important for plumage maintenance and other functions. Its chemical composition is complex, and separating and quantifying its components, commonly by gas chromatography (GC), can be challenging. We present a simple analytical system consisting of thin-layer chromatography/flame ionization detection (TLC-FID) using a solvent system of 100% toluene to analyse the complex compound classes present in preen wax. We used GC and TLC-FID to investigate the effects of migratory status, diet and captivity on the preen wax composition of White-throated Sparrows Zonotrichia albicollis, and to measure the quantity of preen wax on the head, primary and tail feathers. White-throated Sparrows produced preen wax containing only monoesters regardless of migratory state. The monoesters contained several isomers consisting of homologous series of fatty alcohols (C10,C20) and fatty acids (C13,C19) esterified together in different combinations to form monoesters with total carbon numbers ranging from C23 to C38. Weighted average monoester carbon number was greater in captive birds than in wild birds and was greater in captives fed a formulated diet enriched with sesame oil than in birds fed the same diet enriched with fish oil. Captivity and migratory state also affected the complexity of the mixture of monoesters. There was significantly more preen wax on head feathers compared with primary and tail feathers. We suggest that among its many functions, preen wax may play a role in drag reduction by affecting the physical properties of feathers, and/or the fluid flow at their surfaces. [source]


Poor nutritional condition as a consequence of high dominance status in the Coal Tit Parus ater

IBIS, Issue 1 2004
Jacqueline M. Hay
The costs and benefits of dominance status have been investigated in the past and it has generally been reported that subdominant birds are at a nutritional disadvantage owing to their low dominance status. The nutritional condition of birds during winter can be important in determining their likelihood of survival. This is particularly so in small passerines that are sensitive to severe weather conditions. Ptilochronology is an accurate method used to produce a long-term estimate of body condition spanning the number of days that it takes to grow a new feather. Ptilochronology was used during this study to estimate the nutritional condition of Coal Tits Parus ater during one winter and how condition was affected by dominance status. Dominant Coal Tits produced poorer quality feathers, which they grew at a slower rate, than did subdominant conspecifics. This study highlights a nutritional cost to high dominance status that could have long-term consequences because the induced tail feathers will not be replaced for at least 5 months. [source]


A new Eocene swift-like bird with a peculiar feathering

IBIS, Issue 3 2003
Gerald Mayr
A new taxon of swift-like birds is described from the Middle Eocene of Messel (Germany). It is tentatively assigned to the extinct family Jungornithidae and exhibits a completely unexpected feathering, which contrasts sharply with that of recent swifts. The short and rounded wings clearly show that it was not adapted to gliding, but might have caught its prey by sallying flights from a perch. The tail of the new taxon is very long and the tail feathers are broad and nearly symmetrical. The phylogenetic relationships between the Jungornithidae and other apodiform birds are still not convincingly resolved. The early Oligocene genus Jungornis itself shares unique derived characters with hummingbirds which are, however, absent in the Eocene genus Argornis and in the new taxon from Messel. [source]


Lack of melanized keratin and barbs that fall off: how the racketed tail of the turquoise-browed motmot Eumomota superciliosa is formed

JOURNAL OF AVIAN BIOLOGY, Issue 2 2007
Troy G. Murphy
The racket-tipped tail of the motmots is uniquely shaped and its formation has attracted much attention. Barbs that grow along the wire of the motmot's two central tail feathers are weakly attached and shed soon after development. The cause of the weak attachment of these barbs is unclear. I induced feather growth by plucking the central tail feathers from seven turquoise-browed motmots Eumomota superciliosa and then collected the regrown feathers before the barbs along the wire had fully shed. I compared the barb-rachis junction (petiole of the ramus) along the distal flag (the racket-tip of the tail) where barbs are not shed, to the barb-rachis junction along the wire where barbs would later be shed. In these two regions, I examined the size and structure of the attachment of the barb to the rachis with a scanning electron microscope (SEM). I also used a light microscope to score the grayness of the proximal rami of these two regions to estimate the amount of melanized keratin. SEM imaging showed that the barbs are attached to the rachis with a larger supporting flange along the distal flag compared to along the wire. Images from a light microscope showed that the rami along the distal flag were black, whereas rami along the wire were translucent or gray. The lower gray-scale color score of the rami along the wire is likely due to reduced melanized keratin. These data suggest that that the barbs along the wire are weakly attached due to a combination of a reduced structural attachment and a lack of structurally enhancing melanin. [source]


Use of trace elements in feathers of sand martin Riparia riparia for identifying moulting areas

JOURNAL OF AVIAN BIOLOGY, Issue 3 2003
Tibor Szép
We investigated whether trace elements in tail feathers of an insectivorous and long-distance migratory bird species could be used to identify moulting areas and hence migratory pathways. We analysed tail feathers from birds of different age and sex collected from a range of different breeding sites across Europe. The site of moult had a large effect on elemental composition of feathers of birds, both at the European and African moulting sites. Analysis of feathers of nestlings with known origin suggested that the elemental composition of feathers depended largely upon the micro-geographical location of the colony. The distance between moulting areas could not explain the level of differences in trace elements. Analysis of feathers grown by the same individuals on the African wintering grounds and in the following breeding season in Europe showed a large difference in composition indicating that moulting site affects elemental composition. Tail feathers moulted in winter in Africa by adults breeding in different European regions differed markedly in elemental composition, indicating that they used different moulting areas. Analysis of tail feathers of the same adult individuals in two consecutive years showed that sand martins in their first and second wintering season grew feathers with largely similar elemental composition, although the amounts of several elements in tail feathers of the older birds was lower. There was no difference between the sexes in the elemental composition of their feathers grown in Africa. Investigation of the trace element composition of feathers could be a useful method for studying similarity among groups of individuals in their use of moulting areas. [source]


Phylogenetics, biogeography and classification of, and character evolution in, gamebirds (Aves: Galliformes): effects of character exclusion, data partitioning and missing data

CLADISTICS, Issue 6 2006
Timothy M. Crowe
The phylogenetic relationships, biogeography and classification of, and morpho-behavioral (M/B) evolution in, gamebirds (Aves: Galliformes) are investigated. In-group taxa (rooted on representatives of the Anseriformes) include 158 species representing all suprageneric galliform taxa and 65 genera. The characters include 102 M/B attributes and 4452 nucleic acid base pairs from mitochondrial cytochrome b (CYT B), NADH dehydrogenase subunit 2 (ND2), 12S ribosomal DNA (12S) and control region (CR), and nuclear ovomucoid intron G (OVO-G). Analysis of the combined character data set yielded a single, completely resolved cladogram that had the highest levels of jackknife support, which suggests a need for a revised classification for the phasianine galliforms. Adding 102 M/B characters to the combined CYT B and ND2 partitions (2184 characters) decisively overturns the topology suggested by analysis of the two mtDNA partitions alone, refuting the view that M/B characters should be excluded from phylogenetic analyses because of their relatively small number and putative character state ambiguity. Exclusion of the OVO-G partition (with >,70% missing data) from the combined data set had no effect on cladistic structure, but slightly lowered jackknife support at several nodes. Exclusion of third positions of codons in an analysis of a CYT B + ND2 partition resulted in a massive loss of resolution and support, and even failed to recover the monophyly of the Galliformes with jackknife support. A combined analysis of putatively less informative, "non-coding" characters (CYT B/ND2 third position sites + CR +12S + OVO-G sequences) yielded a highly resolved consensus cladogram congruent with the combined-evidence cladogram. Traditionally recognized suprageneric galliform taxa emerging in the combined cladogram are: the families Megapodiidae (megapodes), Cracidae (cracids), Numididae (guineafowls), Odontophoridae (New World quails) and Phasianidae (pheasants, pavonines, partridges, quails, francolins, spurfowls and grouse) and the subfamilies Cracinae (curassows, chachalacas and the horned guan), Penelopinae (remaining guans), Pavoninae sensu lato (peafowls, peacock pheasants and argus pheasants), Tetraoninae (grouse) and Phasianinae (pheasants minus Gallus). The monophyly of some traditional groupings (e.g., the perdicinae: partridges/quails/francolins) is rejected decisively, contrasted by the emergence of other unexpected groupings. The most remarkable phylogenetic results are the placement of endemic African galliforms as sisters to geographically far-distant taxa in Asia and the Americas. Biogeographically, the combined-data cladogram supports the hypothesis that basal lineages of galliforms diverged prior to the Cretaceous/Tertiary (K-T) Event and that the subsequent cladogenesis was influenced by the break-up of Gondwana. The evolution of gamebirds in Africa, Asia and the Americas has a far more complicated historical biogeography than suggested to date. With regard to character evolution: spurs appear to have evolved at least twice within the Galliformes; a relatively large number of tail feathers (, 14) at least three times; polygyny at least twice; and sexual dimorphism many times. © The Willi Hennig Society 2006. [source]