Sorting out the Snakebirds: The species status,phylogeny, and biogeography of the Darters (Aves: Anhingidae)

Although the avian family Anhingidae is unequivocally monophyletic, the number and relationships of the component species within the single genus (Anhinga) have long remained unclear. Here, we use extensive mitochondrial and nuclear DNA sequence data (8,878 bp) to show that four species should be recognized. Our fully resolved and well‐supported tree shows that the American Anhinga (Anhinga anhinga) is sister to the three Old World species, with the Oriental (A. melanogaster) and African (A. rufa) Darters sister within the Old World clade, which also includes the Australian Darter (A. novaehollandiae). We estimate that the divergence between the New World and Old World branches occurred 19–22 mya, with the Australian Darter separating from its Old World congeners 14–16 mya and the Oriental and African species splitting ~10 mya. The genus is yet another example of osteological conservatism in the Suliformes, which is comparable to that shown by the cormorants and shags. Nevertheless, the relationships we infer are congruent with recent plumage studies and are biogeographically plausible. We suggest that further investigation of the variation within the African and Australian Darters would be of interest.     

Body mass and locomotor habits of the smallest darter,Anhinga minuta (Aves,Anhingidae)

During the Neogene of South America, Anhingidae was represented by several species, mainly with greater sizes than the extant members. In the present contribution, body mass and locomotor habits of Anhinga minuta, the smallest known darter, were inferred. Body mass was estimated using two methods, one with measures of a tibiotarsus (the holotype) and the other, with measurements of a humerus; locomotor habits were inferred through muscular reconstructions and wing parameters (wing span, wing area and wing loading). Estimates of wing span and wing area were based on the length of humerus, assuming a condition of isometry with respect to Anhinga anhinga; wing loading was obtained through a relation formula between wing area and body mass. The results obtained indicate a body mass of about 729 g, a wing span of 0.958 m, a wing area of 0.117 m² and a corresponding wing loading of 61 N/m². These values and also the proximal insertion of the musculus pectoralis are consistent with those of a soaring bird but with more frequent flapping than extant anhingids. Furthermore, the inferred musculature for tibiotarsus indicates abilities for swimming, climbing and moving through the vegetation as in extant representatives.     

Water repellency and feather structure of the Blue Swallow Hirundo atrocaerulea

Rijke, A.M., Jesser, W.A., Evans, S.W & Bouwman, H. 2000. Water repellency and feather structure of the Blue Swallow Hirundo atrocaerulea. Ostrich 71 (1 & 2): 143–145.

The Blue Swallow is an endangered species in southern Africa and is probably the most endangered passerine. It is restricted to escarpments with grasslands above 1 000 m where mists are frequent. It appears to forage on the wing even in thick mist raising the question of feather wettability in relation to its adaptation. Extensive physical and behaviourial adaptations are known to occur in a wide variety of birds to deal with the problem of shedding water continuously. To study the water repellency and resistance to water penetration of Blue Swallow feathers, we have examined the microscopic structure of head, back, throat, breast and abdominal feathers as well as remiges and tail feathers by transmission light microscopy. The width (2R) and separation (2D) of rami and barbules have been measured and were used to calculate the parameter (R + D)/R that serves as an indicator ofwater shedding potential. For the remiges and tail feathers the values of the (R+D)/R range from 5 to 10 which is comparable to values for other terrestrial birds. However, for body feathers the range is from 10 (head) and 35 (abdomen)-higher than previously observed for any other bird including Swifts, Apodidae. Blue Swallow feathers are thus the most effective feather yet discovered at repelling water drops. The water repellency is highest in those feathers that are relatively shielded From the direct impact of small water drops (throat, breast, abdomen, back). By contrast, the flight feathers must possess a relatively large resistance to water penetration to avoid becoming waterlogged and this is coupled to low (R+D)/R values. Values for the barbules lay between 2 and 6—the same as found for other bird families—supporting an earlier conclusion that they have little direct effect in repelling water.     

The discriminant power of biometrics for sex determination in European Bee-eaters Merops apiaster

ABSTRACT

Capsule A combination of several biometric measures enables the reliable sexing of the European Bee-eater Merops apiaster, a species with subtle sex differences in plumage and morphometry.

Aims To explore variation in biometrics and their suitability to discriminate sex in adult European Bee-eaters Merops apiaster.

Methods We sampled populations of a long-distance migratory species with low sexual size dimorphism, the European Bee-eater Merops apiaster, from colonies in western Iberia (Portugal) and Central Europe (Germany) to investigate body size variation and derive population-specific and general sex discriminant functions.

Results Overall, male Bee-eaters were larger than females while Bee-eaters from Germany and Portugal did not differ in size, except for primary length and tail length. The best single measurement to discriminate sex was wing length for Portuguese birds and tail tip length for German birds, as in the combined dataset. Multivariate discriminant functions of head-bill, wing and tail tip lengths provided the highest discriminant accuracy, discriminating sex for 91% of the birds from Portugal, 96% from Germany and 94% when using the combined dataset. Nonetheless, the discriminant accuracy remained high in the functions using only two variables for Portugal (head-bill and tail tip 91%, head-bill and wing 88%, wing and tail tip 88%), Germany (head-bill and tail tip 95%, wing and tail tip 97%) and in the combined dataset (head-bill and tail tip 92%, wing and tail tip 93%).

Conclusions Population specific discriminant functions allow sexing of European Bee-eaters by morphometry with high degree of accuracy at least for Iberia and Central European populations. Such discriminant functions can be used to assign the sex of adult Bee-eaters reliably and swiftly while the bird is still in the hand, highlighting the potential of these functions for rapidly sexing species with low degrees of sexual size and plumage dimorphism.     

CORMORANT AND DARTER PREY SIZE SELECTION UNDER EXPERIMENTAL CONDITIONS

Hustler, 1995. Cormorant and Darter prey size selection under experimental conditions. Ostrich 66:109-113.

The most profitable sized cichlid fish for Reed Phalacrocorax africanus and Whitebreasted Cormorants P. carbo lucidus and Darter Anhinga melanogaster were determined experimentally. A range of sizes was fed to all three species in captivity to determine whether, given a choice, they would choose the most profitable fish. All species chose certain sizes of fish preferentially, but not in accordance with their profitability. The hunger status of the birds at the time of the experiment and the way in which the experiments were designed and carried out probably influenced the size of fish chosen by the birds.     

Winter body condition in relation to age,sex and plumage ornamentation in a migratory songbird

Winter body condition may play important roles in the life history of migratory birds, but it is difficult to estimate. We used the growth rate of winter‐grown tail feathers of Collared Flycatchers Ficedula albicollis as an indicator of winter body condition, comparing this trait between age classes and sexes and relating it to plumage ornamentation (forehead and wing patch sizes). Adults and males were in better nutritional condition during winter, as indicated by their faster tail feather growth rates, than were yearlings and females, respectively, which could indicate differences in individual quality and foraging ability with age, or age‐ and sex‐related winter habitat segregation. However, feather growth rate was related neither to the size of the winter‐grown forehead patch nor to the size of the summer‐grown wing patch, suggesting weak condition‐dependence for the winter‐grown ornament and complex life‐history consequences for the summer‐grown ornament.     

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.     

BODY MEASUREMENTS,PLUMAGE AND MOULT OF THE SACRED IBIS IN SOUTH AFRICA

Lowe, K. W., Clark, A. & Clark, R. A. 1985. Body measurements, plumage and moult of the Sacred Ibis in South Africa. Ostrich 56: 111–116.

Body measurements, plumage and moult of Sacred Ibis Threskiomas aethiopicus were studied at Pretoria from July 1973 to June 1974. Adult and immature Sacred Ibises are sexually dimorphic in size. Bill length alone can be used to sex most birds. Body mass, wing, tarsus and tail lengths overlap greatly between the sexes but males are generally larger than females. The sexes show similar patterns of variation in body mass and gonad size throughout the year. Juveniles follow a different pattern of variation in these parameters. The plumages of adults, immatures and juveniles are described and compared. There is no sexual dimorphism in plumage pattersn. Moult in adults occurs mainly in the post-breeding period from January to August, and in juveniles and immatures throughout the year. Adult Sacred Ibises have an-extensive, irregular and asymmetrical moult. Factors affecting sexual size dimorphism in African and Australian populations are discussed.     

Brood size manipulations reveal relationships among physiological performance,body condition and plumage colour in Northern Flicker Colaptes auratus nestlings

Visual signals of quality in offspring, such as plumage colour, should honestly advertise need and/or body condition, but links between nutritional status, physiological performance and the expression of colours are complex and poorly understood. We assess how food stress during rearing affected two physiological measures (T‐cell‐mediated immune function and corticosterone level in feathers: CORT_f) and how these two variables were related to carotenoid and melanin coloration in Northern Flicker Colaptes auratus nestlings. We were also interested in how these two physiological measures were influenced by the sex of the nestling. We experimentally manipulated brood size to alter levels of food availability to nestlings during development. We measured carotenoid‐based colour (chroma and brightness) in wing feathers and the size of melanin spots on breast feathers. In agreement with our prediction, nestlings in the reduced brood treatment had better body condition and stronger immune responses than those in the control and brood enlargement treatments. This supports the hypothesis that immune responses are energetically costly. In contrast, CORT_f was not related to nestling body condition or sex and was unaffected by brood size manipulation. Nestlings of both sexes with stronger T‐cell‐mediated immune responses had larger melanin spots but only males with higher immune responses also had brighter flight feathers. Feather brightness decreased with increasing CORT_f levels. Our study is one of the few to examine the relationship between multiple physiological and plumage measures in nestlings and shows that plumage colour and immune function signalled body condition of nestlings, but that feather corticosterone levels did not.     

Do the contour feathers of Cisticolae exhibit adaptations to annual rainfall in their habitats?

Birds of the genus Cisticola occur over most of Southern Africa in varying habitats ranging from low to high altitudes and wet to dry areas causing species to have unique distributions. In order to determine if Cisticolas have evolved species‐specific water repellency and resistance to water penetration compatible with their habitats, we have measured the barb diameter and spacing of abdominal, breast and throat feathers of six cisticola species and related the results to mean annual rainfall and altitudes in five different locations. Water repellency was not significantly associated with altitude or maximum mean summer temperatures. However, water repellency increased markedly with annual rainfall in the 550 to 600 mm/year range for abdominal and breast feathers, but not for throat feathers. This increase was evident both among species occurring at multiple sites and among different species occurring at single sites. However, the two species occurring at the wettest sites showed low water repellency, but increased resistance to water penetration. These findings suggest that water repellency and resistance to water penetration are part of the evolutionary forces that shape the microstructure of Cisticola contour feathers.     

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.     

Variation in the wing-clapping display of Clapper Larks

The pied plumage of the adult Black Sparrowhawk is rather exceptional in the genus Accipiter and it could be explained by functionality or by phylogenetic relationships. The moult pattern of museum specimens is presented, supplementing information from captive birds. The post-juvenile moulting sequence is similar to that of the Northern Goshawk. The moult of primaries starts at, or just after, the beginning of body moult; moult of the secondaries also starts early and progresses from three consecutive foci, and tail moult starts early but is less predictable. A few body feathers and tail feathers may remain in place until the second moult. The pied flank feathers appear at an early stage. Some adult specimens are in arrested annual moult. Two with definite serially-descendant moult were discovered; this is related to the fact that the species is known to be double-brooded. Serially descendant moult was not known in this species and is rarely mentioned in the genus. Possible functions of the pied plumage are discussed: crypsis, mimicry, hunting strategy, and sexual attraction. Its taxanomic status is obscure. Although the streaked juvenile plumage of the Black Sparrowhawk is similar to those of the Northern Goshawk A. gentilis, Meyer's Goshawk A. meyerianus and Henst's Goshawk A. hentsi, adult and juvenile plumages are variable within the genus, and thus are not a reliable indicator of taxanomic relationships.     

Size,plumage, moult and supposed hybrids of African Goshawks (Accipiter tachiro/toussenelii group) in DR Congo

Parapatric A. tachiro sparsimfasciatus and A. toussenelii canescens are in a size cline from large east African to small west African birds. While their plumage colour is different, the pattern of spotting (juvenile) and barring (adult) of the breast feathers is similar. No general hybridisation is found in the contact region in Kivu: the plumage of some aberrant individuals can be due to great age or to individual variation. One supposed hybrid was obtained far from the contact region. I consider them as paraspecies. Based on direct evidence and on annual moult I conclude that the breeding period is prolonged in both taxa in equatorial DR Congo, and that it is seasonal in tachiro sparsimfasciatus in southern DR Congo. In the latter population, the postjuvenile moult starts probably just before the age of one year but it lasts many months, leaving the juvenile upper tail coverts in place for one more year. Plumage characteristics are related to habitat. The female of the woodland sparsimfasciatus is cryptically coloured, with individual variation, possibly helpful for 'image avoidance'. The male is even more variable in colour, in part age related: a 'sepia' morph is described for the first adult plumage. Older birds are grey with reddish flanks, becoming darker with age. The adult evergreen forest canescens shows enforcement of colourful advertising plumage and loss of sexual plumage dimorphism. The first adult is advertised by the late moult of the barred juvenile flank feathers in both sexes. Its juvenile is peculiar; it lacks breast spots, suggesting image avoidance, but possibly also character displacement or mimicry.     

Ornamental plumage coloration and condition are dependent on age in eastern bluebirds Sialia sialis

Male eastern bluebirds Sialia sialis have striking ultraviolet (UV)-blue coloration on their heads, backs, rumps, wings, and tails and bold chestnut coloration on their breasts. These colored areas are ornaments that correlate with pairing date and reproductive effort, and thus probably influence the choice of mates by females. Such ornaments are expected to increase in color with age and body condition. We investigated the effects of age on body condition and the UV-blue and chestnut coloration of males over four years using both cross-sectional (comparing age classes) and longitudinal analyses (following individuals as they age). We found that both the body condition index and brightness of UV-blue rump coloration increased with age, while UV-blue tail plumage coloration increased between yearling and older males, and the chestnut breast coloration decreased in the oldest age class. The proximate mechanisms whereby individuals reliably signal age via rump brightness and tail coloration are probably different. Contour feathers, including rump feathers, are molted at approximately the same time in all age classes and are likely subject to the same production costs in all age classes. In contrast, the molt schedule of the tail and wing feathers differs between individuals of yearling and older age classes, with yearlings retaining wing and tail feathers for several months longer than adults. The relationship between tail color and age was probably, in part, a consequence of yearlings expressing tails that have increased feather wear and accumulation of dirt. In general, UV-blue coloration increased with age while chestnut plumage decreased with age, indicating that older individuals may tradeoff investing energy in structural and melanin ornaments. By assessing overall plumage coloration, female eastern bluebirds could estimate age class when choosing mates.     

Male achromatic wing colouration is related to body condition and female reproductive investment in a dichromatic species,the upland goose

In many bird species, achromatic plumage patch size can serve as a male status signal, but the use of variations in the achromatic colours themselves as a quality signal has only recently come into focus. In our study, we sought to determine whether achromatic plumage reflects individual quality in the upland goose (Chloephaga picta leucoptera). We examined the relationship between male head and wing reflectance, male condition and female reproductive investment. We found that males with darker specula and greater contrast between the white wing coverts and the speculum were in a better body condition. Variations in the brightness of the white plumage were not a quality signal in the upland goose. The information gleaned from the wing colouration of male upland geese could be used during mate selection, when females choose their mate on the basis of the outcomes of aggressive encounters. During these fights, the males expose their white coverts and their specula, which are normally tucked beneath body feathers.     

Takeoff flight performance and plumage wettability in Cassin’s Auklet Ptychoramphus aleuticus, Xantus’s Murrelet Synthliboramphus hypoleucus and Leach’s Storm-petrel Oceanodroma leucorhoa

Due to their marine habitats and distinctive foraging modes, seabirds face unique challenges with respect to flying that are negotiated differently by various species. One such challenge is taking off from the water with wet plumage. This study evaluated plumage wettability and takeoff performance in three seabird species: two wing-propelled divers with high wing loading, Cassin’s Auklet Ptychoramphus aleuticus and Xantus’s Murrelet Synthliboramphus hypoleucus; and Leach’s Storm-petrel Oceanodroma leucorhoa, a surface feeder with low wing loading. The plumages of the diving birds held less water than that of O. leucorhoa (~6.7% of body mass vs 9.5%). This difference is explained by O. leucorhoa’s surface to volume ratio being larger than that of the alcids. Furthermore, the alcids have afterfeathers larger than those of O. leucorhoa, which promotes a better insulation during diving. Examination of takeoff performance both before and after experimentally submerging the birds indicated that wingbeat frequency, speed and mass-specific power (peak and mean), and energy per wingbeat decreased in all species when plumage was experimentally wetted, whereas mean acceleration increased. O. leucorhoa was more strongly affected by wet plumage than the alcids, with a 32% of reduction in mass-specific energy per wingbeat compared to ≤25% in the alcids. Takeoff angle was reduced in alcids, but not significantly so in O. leucorhoa. Our results offer insights into the takeoff mechanics problems of wet seabirds given their differences in life history and morphology.     

SEX RATIOS,MORPHOLOGY AND GROWTH OF THE AFRICAN BUCK DUCK

Frost, P. G. H., Ball, I. J., Siegfried, W. R. & McKinney, F. 1979. Sex ratios, morphology and growth of the African Black Duck. Ostrich 50:220-233.

Black Ducks Anus sparsa were trapped regularly in the Eerste River Valley near Stellenbosch, South Africa. The sex ratio of adult Black Ducks did not differ significantly from parity. Males were larger and heavier than females and also had proportionately larger wing spurs which are used when fighting over mates and territories. Body mass fluctuated seasonally, being lowest during summer and highest in autumn-winter. In the southwestern Cape breeding took place from July to December after the peak of the early winter rains. Ducklings hatched when waters were dropping and there was an increase in the emergence of aquatic insects. The growth rate of ducklings in the Eerste River Valley was severely retarded compared with that of ducklings reared in captivitly. Black Ducks moulted their body feathers twice a year, the moults corresponding to the pre- and post-nuptial moults of northern hemisphere waterfowl. Moults were not accompanied by any change in plumage coloration. Body and rectrix moult took more than five weeks to complete while remex replacement required about 30 days. Males began wing moult about a month earlier than females which delayed moulting until after their young had been reared. Forty-six percent of Black Ducks trapped had noticeable plumage aberrations; individual recognition among Black Ducks appears to be an important element in their social behaviour.     

Juvenile coloration of Florida Scrub-Jays ( Aphelocoma coerulescens ) is sexually dichromatic and correlated with condition

The Florida Scrub-Jay is a monogamous cooperative breeder in which both males and females display extensive structurally based blue plumage. Juveniles of this species exhibit blue tail and wing feathers that they begin growing as nestlings, and some of these feathers are retained throughout their first year. Although the birds appear to be sexually monochromatic, we assessed whether cryptic dichromatism exists in both the magnitude and pattern of coloration in tail feathers of juvenile Florida Scrub-Jays. We then determined whether variation in plumage coloration is associated with nutritional condition during molt. Tails of juvenile male Florida Scrub-Jays exhibit a greater proportion of UV reflectance than those of females. Mass at age 11 days and ptilochronology of the juvenile tail feathers were used as measures of individual nutritional condition during feather growth, and the latter was found to be positively associated with UV chroma. These data demonstrate that Florida Scrub-Jays are sexually dichromatic and suggest that variation in plumage color may be condition dependent, although we cannot rule out alternative explanations. Juvenile plumage coloration, therefore, has the potential to function as a signal of individual quality in both males and females.     

Color expression in experimentally regrown feathers of an overwintering migratory bird: implications for signaling and seasonal interactions

Plumage coloration in birds plays a critical role in communication and can be under selection throughout the annual cycle as a sexual and social signal. However, for migratory birds, little is known about the acquisition and maintenance of colorful plumage during the nonbreeding period. Winter habitat could influence the quality of colorful plumage, ultimately carrying over to influence sexual selection and social interactions during the breeding period. In addition to the annual growth of colorful feathers, feather loss from agonistic interactions or predator avoidance could require birds to replace colorful feathers in winter or experience plumage degradation. We hypothesized that conditions on the wintering grounds of migratory birds influence the quality of colorful plumage. We predicted that the quality of American redstart (Setophaga ruticilla) tail feathers regrown after experimental removal in Jamaica, West Indies, would be positively associated with habitat quality, body condition, and testosterone. Both yearling (SY) and adult (ASY) males regrew feathers with lower red chroma, suggesting reduced carotenoid content. While we did not observe a change in hue in ASY males, SY males shifted from yellow to orange plumage resembling experimentally regrown ASY feathers. We did not observe any effects of habitat, testosterone, or mass change. Our results demonstrate that redstarts are limited in their ability to adequately replace colorful plumage, regardless of habitat, in winter. Thus, feather loss on the nonbreeding grounds can affect social signals, potentially negatively carrying over to the breeding period.