NOTICES

Schmitt, M. B., Baur, S. &; Von Malitz, F. 1980. Observations on the Steppe Buzzard in the Transvaal: Ostrich 51:151-159.

During a three year study 247 Steppe Buzzards Buteo buteo vulpinus were captured in the Transvaal, South Africa. Density, mensural data and moult are discussed and compared with findings from the Cape Province. Linear density is 7,3 times lower in the Transvaal as compared with the Cape. Identification criteria for second-year birds are given. Second-year birds moult primaries descendently and symmetrically, secondary moult is mainly ascendent and symmetrical, tail moult irregular but symmetrical. Adult birds moult irregularly. Recorded food items are listed.     

3. THE GENERA TURDUS,GEOKICHLA, PSOPHOCICHLA,MONTICOLA AND COSSYPHA IN NYASALAND

Summary

Hanmer, D. B. 1981. Mensural and moult data of nine species of sunbird from Moçambique and Mala?i. Ostrich 52: 156–178.

Wing length, culmen length, weight and moult data are given for the Coppery Sunbird Nectarinia cuprea, Purplebanded Sunbird N. bifnsclata, Yellowbellied Sunbird N. venusta, Whitebellied Sunbird N. talatala. Grey Sunbird N. veroxii, Black Sunbird N. amethystina. Scarletchested Sunbird N. senegalensis. Collared Sunbird Anthreptes collaris and Violet-backed Sunbird A. longuemarei from Mopeia (Moçambique) and Nchalo (Mala?i). Moulting seasons, immature age at moult, the duration of primary moult, its relation to the breeding season, weight changes with moult, the breeding season, altitude and latitude, and the sequence and timing of moult in remiges and rectrices are discussed for all species except N. veroxii, N. amethystina and A. longuemarei. Softpart and plumage colour changes with age are discussed and some data are given on habits and migration.     

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.     

Moult in the Loggerhead Shrike Lanius ludovicianus is influenced by sex,latitude and migration

We investigated moult strategies in Loggerhead Shrikes by examining first prebasic or preformative moult patterns and by assessing the general location where individual feathers were grown using stable hydrogen isotope (δ²H) analysis. We tested the relative importance of factors known to impact moult timing and pattern, including age, sex, body size, food availability and migration. Migratory Shrikes showed evidence of suspended moult, in which feathers are moulted on both the breeding and the non‐breeding grounds with a suspension of moult during migration. Extent of moult was best explained by sex, longitude, migratory behaviour and breeding‐ground latitude. Male Hatch Year (HY) Shrikes replaced more feathers on the breeding grounds prior to migration than did HY females and moulted more extensively on the breeding grounds than did females. Non‐migratory HY Shrikes underwent a more extensive preformative moult than migratory HY Shrikes. Individuals in more southerly migratory populations moulted more extensively on the breeding grounds than did those breeding further north. Our data also indicate that individuals in the northeastern populations moulted more extensively on the breeding grounds than did those in the north and southwest. Our study underlines the complex structure and variation in moult possible within species, revealing surprising levels of differentiation between sexes and age cohorts, linked to environmental factors on the breeding grounds. Our study highlights the utility of an intrinsic marker, specifically δ²H analysis, to test hypotheses regarding the evolutionary and ecological forces driving moult. Although the methodology has not commonly been applied to this area of research, our results indicate that it can provide unprecedented insight into inter‐ and intra‐specific adaptive response to constraints, whereby individuals maximize fitness.     

REVIEWS

Jones, P. J. 1978. Overlap of breeding and moult in the Whitebrowed Sparrowweaver in northwestern Botswana. Ostrich 48:21-24.

Female Whitebrowed Sparrowweavers Plocepasser mahali trapped on the nest while incubating showed advanced active moult of wing and tail feathers, indicating a complete overlap of moulting and breeding schedules. Additional moult data indicated an unusually protracted primary moult of 183 days. It is suggested that the low daily metabolic demands of a slow moult enable it to be compatible with breeding activities, which may be of advantage to some species living in semi-arid environments.     

Causes and consequences of individual variation in the extent of post‐juvenile moult in the blue tit Cyanistes caeruleus (Passeriformes: Paridae)

Moult, comprising the growth or replacement of feathers in birds, is an energetically demanding process. As a result, in many species, the extent of the post‐juvenile moult can vary substantially. However, the reasons underlying this variation remain poorly understood, and the potential life‐history consequences of variation in moult extent are even less clear. In the present study, we aimed to use individual‐specific data to identify factors affecting the extent of the post‐juvenile moult in a population of over 2500 blue tits Cyanistes caeruleus Linnaeus 1758, and to assess the consequences of individual variation in moult extent on reproduction in the first year of life. There was a substantial sex difference in post‐juvenile moult extent, with males moulting more extensively than females. Putative immigrant birds had moulted on average less than those born locally. However, there was little evidence of carry‐over effects of the natal environment on moult extent because we found no relationship between moult extent and fledging date or nestling mass. Evidence that moult extent, and hence feather brightness, affected subsequent reproductive success was limited. Moult extent had no effect on recruitment in males, although female recruits had moulted significantly less than nonbreeders. Because it was not influenced by features of the natal environment, moult extent may not be an honest signal of individual quality in C. caeruleus. As a result, the potential consequences of variation in moult extent for fitness are likely to be small.     

Species and sexual isolating mechanisms in sibling species of giant petrels Macronectes

Summary The two sibling species of giant petrels Macronectes halli and M. giganteus are the dominant avian scavengers in the Southern Ocean ecosystem. They breed sympatrically at a number of sub-Antarctic sites. This paper synthesises data from a detailed study at South Georgia to examine the importance of various interspecific and intersexual differences between these closely related species. Morphological, breeding, dietary, feeding and moult characteristics were investigated. The most significant interspecific differences are a six week separation in the onset of breeding and the importance of seal carrion to male M. halli, the earlier breeding species. There is a strong sexual size dimorphism with females being only 75–80% of the weight of males in both species. Intersexual dietary differences are stronger than interspecific ones and females also have later primary moult schedules. Reproductive isolation and ecological adaptations are discussed in relation to the present distribution of giant petrels, comprising a more restricted sub-Antarctic species (M. halli) and a widespread Antarctic species (M. giganteus). It is suggested that the marked sexual dimorphism evolved before the two taxa became specifically distinct.     

A model for avian primary moult

The regression methods frequently used to estimate the parameters associated with primary moult in birds are unsatisfactory. Results obtained using least squares regression, and various ad hoc adaptations, are so obviously incorrect that many authors have fitted lines ‘by eye’ (Newton 1968, Thomas & Dartnall 1971, Elliott et al. 1976, Morrison 1976, Appleton & Minton 1978). In a comparison of seven regression methods, estimates of the average starting date varied between 29 June and 31 July, completion date between 2 and 24 October, and duration of moult between 72 and 109 days for the Redshank Tringa totanus, in spite of the very large sample of 1482 observations (Summers et al. 1983). In this paper we present a new approach to the analysis of primary moult and develop a mathematical model specifically designed for moult data.     

Frequency of complete moult in adult and juvenile Great Reed Warblers(Acrocephalus arundinaceus) in Spain

Summary We examined a large data set of adult and juvenile Great Reed Warblers (Acrocephalus arundinaceus), caught over five years, to study the occurrence of complete moult in a Spanish population. A total of 27 adults and 5 juveniles were in active moult. The proportion of birds moulting each year varied between 0.03 and 0.19. Nearly half the adults were finishing moult. At least one bird was certainly of local origin, rather than on passage, and four more were moulting when retrapped in subsequent years, suggesting that they too were resident breeders in the area. Some other birds were probably resident also, because they were in moult when caught at the beginning of August. Two of the five juveniles finished their moult in the area. In conclusion, our data seem to show that complete moult before departure to the wintering quarters is a regular process undertaken by some of the breeding population of Great Reed Warblers in north-east Spain.

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Das Vorkommen von Vollmauser bei Alt- und Jungvögeln des Drosselrohrsängers(Acrocephalus arundinaceus) in Spanien

Zusammenfassung Von 837 zwischen 1992 und 1996 im Ebro Delta gefangenen Drosselrohrsängern mauserten 27 Alt-und 5 Jungvögel. Der jährlichen Anteil mausernder Vögeln betrug zwischen 0,03 und 0,19%. Etwa die Hälfte der mausernden Altvögel und zwei der Jungvögel beendeten ihre Mauser im Untersuchungsgebiet. Diese Daten zeigen, daß Drosselrohrsänger in Spanien wenigstens teilweise auch schon vor Beginn des Wegzuges eine Vollmauser durchführen.

     

MEASUREMENTS AND MOULT OF FIVE SPECIES OF BULBUL FROM MOÇAMBIQUE AND MALAŴI

Summary

Hanmer, D. B., 1978. Measurements and moult of five species of bulbul from Moçambique and Mala?i. Ostrich 49:116-131.

The wing length, weight and moult of five species of bulbul, Blackeyed Pycnonotus barbatus, Sombre Andropadus importunus, Yellowbellied A. flaviventris, Terrestrial Phyllas-trephus terrestris and Yellowspotted Nicator Nicator gularis, are given for two localities in tropical lowland (Mopcia, Moçambique and Nchalo, Mala?i). The characters identifying immatures and the length of time these are retained, are given with reference to skull pneumatization, retrapped birds and the breeding season, for Pycnonotus barbatus, Andropadus intportunus and Phyllastrephus terrestris. Weights are compared with some published for other parts of Africa. The months during which moult occurred are given. Duration and timing of primary moult and its relation to the breeding season, are given for Pycnonotus barbatus, Andropadus importunus and Phyllastrephus terrestris. The age at which immatures moult is given for these three species. Instances of interrupted moult are mentioned.     

Using field photography to study avian moult

Methods to obtain moult data from wild birds have not changed much over the last century and most studies still depend on checking museum specimens or capturing birds. Here we assess the applicability of systematic field photography for detecting and scoring moult in adult Black Skimmers Rynchops niger from southern Brazil. Moult data extracted from photographs have a high within‐ (R_GLMM = 0.98) and between‐observer repeatability (R_GLMM = 0.97) and show very good fit to current Underhill–Zucchini moult models (R² = 0.75). Photography offers the advantages of being less invasive, requiring less equipment and human effort, being feasible in areas where captures may not be possible, and causing less disturbance, so enhancing the number of sampled individuals.     

Experiments on the physiology of southern and northern krill,Euphausia superba and Meganyctiphanes norvegica,with emphasis on moult and growth – a review

Physiological data are needed for life history studies on krill, and as parameters for input into energy budgets and models. In conjunction with moult and growth data, these may also prove useful for assessing the fishable biomass of krill. Here, the development of physiological concepts in experimental krill research is briefly evaluated, with emphasis on the gaps to be filled. Krill growth is very flexible, as well as strongly temperature and nutrition dependent. The polar Antarctic krill Euphausia superba grows as fast as the boreal species Meganyctiphanes norvegica, at least during the first 2.5 years, and the species are comparable in terms of physiological plasticity. Accordingly, as krill appear to adjust quickly to specific laboratory conditions, short-term experiments are essential if field conditions are to be reflected as closely as possible. Furthermore, direct comparisons between laboratory experiments and swarming studies in the field are advantageous. For these, M. norvegica is particularly well-suited, as swarms can be followed over longer times and more easily than in E. superba. For example, processes of moult and reproduction were found to be highly coordinated in swarms and populations of Northern krill. For this species a conceptual model of reproduction was developed based on a combination of short-term laboratory observations coupled with field data on moult and ovary stages. In further physiological experiments krill should be studied as groups when swarming. Using proxies, that is applying physiological and/or biochemical methods side by side, is a promising way to enhance the reliability of life history data.     

CHAIRMAN'S REPOST, 1954–55

Brown, C. R. 1986. Feather growth, mass loss and duration of moult in Macaroni and Rockhopper Penguins. Ostrich 57:180-184.

The development of new feathers, loss of body mass and the duration of moult were investigated in Macaroni Penguins Eudyptes chrysolophus and Rockhopper Penguins E. chrysocome at Marion Island, southern Indian Ocean. New feathers began developing under the skin before the birds returned ashore to moult, and only began protruding through the skin about five days later when they were already over half their final length. Feather synthesis was complete by 21 days after the birds returned ashore. Loss of body mass was similar to previous observations for the species, but previous reports on the duration of moult do not take into account that moult begins while the birds are still at sea.     

Plasticity of moult and breeding schedules in migratory European Stonechats Saxicola rubicola

Timing is crucial in seasonal environments. Passerine birds typically use a combination of physiological mechanisms and environmental cues to ensure that breeding, moult and migration occur without major temporal overlap and under the most favourable conditions. However, late in the breeding season some individuals initiate additional clutches , whereas others initiate moult. Such alternative strategies are thought to reflect trade‐offs between reproductive benefits and timely investment in maintenance and survival. The degree of seasonal plasticity differs between species, depending on the mechanisms that govern their annual routine. Migrants are generally under pressure to complete breeding and moult before the autumn departure and often show little plasticity. We studied seasonal plasticity of breeding and moult schedules in the European Stonechat Saxicola rubicola. This species, an obligate short‐distance migrant in Central Europe, sometimes initiates late clutches after typically at least two earlier breeding attempts. Based on life‐history theory and on observations in captivity, which revealed photoperiodic regulation of breeding and moult, we predicted relatively little seasonal plasticity in Stonechats. We further predicted that reproductive gains of late breeders should be offset by reduced survival. These predictions were tested on long‐term field data, using Underhill–Zucchini models to estimate moult. Late breeding occurred in c. 40% of pairs and increased their reproductive success by a third. Both sexes modified moult timing but in different ways. Late breeding females postponed moult approximately until chick independence without compensating for delay by faster moult. Males started moult on time and overlapped it with breeding, associated with markedly slowed plumage change. Sex differences in moult score increased with lay date, but due to their respective modifications, both sexes delayed moult completion. Nonetheless, we could not detect any evidence for survival costs of late breeding. Breeding and moult of European Stonechats appear relatively flexible, despite migratory schedules and photoperiodic programs for seasonal timing. Individuals can modify seasonal behaviour in late summer, presumably depending on their condition, and may profit considerably from extended breeding.     

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.     

Late‐moulting Black‐necked Grebes Podiceps nigricollis show greater body mass in the face of failing food supply

From August to December, thousands of Black‐necked Grebes Podiceps nigricollis concentrate during the flightless moult period in salt ponds in the Odiel Marshes, southern Spain, where they feed on the brine shrimp Artemia parthenogenetica. We predicted that because Black‐necked Grebes moulted in a food‐rich, predator‐free environment, there would be no net loss of body mass caused by the use of fat stored to meet energy needs during remigial feather replacement (as is the case for some other diving waterbirds). However, because the food resource disappears in winter, we predicted that grebes moulting later in the season would put on more body mass prior to moult because of the increasing risk of an Artemia population crash before the moult period is completed. Body mass determinations of thousands of birds captured during 2000–2010 showed that grebes in active wing‐moult showed greater mass with date of capture. Early‐moulting grebes were significantly lighter at all stages than late‐moulting birds. Grebes captured with new feathers post‐moult were significantly lighter than those in moult. This is the first study to support the hypothesis that individual waterbirds adopt different strategies in body mass accumulation according to timing of moult: early‐season grebes were able to acquire an excess of energy over expenditure and accumulate fat stores while moulting. Delayed moulters acquired greater fat stores in advance of moult to contribute to energy expenditure for feather replacement and retained extra stores later, most likely as a bet hedge against the increasing probability of failing food supply and higher thermoregulatory demands late in the season. An alternative hypothesis, that mass change is affected by a trophically transmitted cestode using brine shrimps as an intermediate host and Black‐necked Grebes as final host, was not supported by the data.     

Non‐moulted primary coverts correlate with rapid primary moulting

Time constraint is a main factor which affects the moult strategies in passerines, mainly during the first year of life. The variability of moult strategies between species is associated with the extent of the moult. In the first year of life, the extent of the moult is highly variable between species and individuals. In most passerine species, juveniles only renew some of their feathers, but the factors that govern which feathers are renewed and which are retained have been largely overlooked. Here we examine the common pattern of non‐moulted primary coverts (PC) in passerines during the first‐year moult cycle (post‐juvenile and first‐year pre‐breeding moults). On the interspecific level we found that among 63 species of passerines, PCs are the least commonly moulted feather tract. For five species (Hirundo rustica, Pycnonotus xanthopygos, Prinia gracilis, Acrocephalus stentoreus and Passer moabiticus) which perform a complete post‐juvenile moult, we found that the PC moult occurs over a longer period than greater coverts (GCs) and is sequential (non‐simultaneous). At the intraspecific level, we found that the main difference between a partial and complete moult in Prinia gracilis is the moulting or non‐moulting of the PCs. We also demonstrate that for Prinia gracilis 1) juveniles which do not moult their PCs, moult their primaries at a higher speed than those which moult their PCs and 2) area/mass ratio of PCs is lower than of GCs. These two findings may explain why many passerines skip PC renewal during the first year of life. Because the PC moult lasts a long time, forgoing this moult enables long term resource savings that allow for dealing with time constraints. Our results highlight the adaptive advantages of non‐moulted PCs in cases of time constraints.     

Ascendente Handschwingen-Mauser beiMuscicapa striata

Zusammenfassung Ascendente Mauser der Handschwingen beiMuscicapa striata wird beschrieben. Der Ersatz der Handschwingen von der äußeren zur inneren fortschreitend ist einzigartig bei den Passeres. Bisher war von allen untersuchten Passeres nur die descendente, von innen nach außen fortschreitende Mauser der Handschwingen bekannt. Auch die nächstverwandten ArtenMuscicapa gambagae, M. sibirica undM. latirostris mausern descendent. Vermutlich verlaufen auch die Mauser der Armschwingen und der Schwanzfedern beiM. striata nach einem anderen Schema als bei den übrigen Passeres. Die mögliche Bedeutung der Erscheinung wird diskutiert.

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Summary The examination of eight specimens of the palearctic FlycatcherMuscicapa striata collected in the wintering grounds in Tanganyika Territory and Kenya Colony, all in different stages of complete prenuptial moult, yielded the unexpected result of ascending primary moult (beginning with the outermost primary), in contrast to the descending mode so far known to be followed by all Passeriformes.With regard to the moult of secondaries and tail-feathers the material, somewhat scanty in this respect, seems to show that in both these feather-tracts too the ordinary Passerine sequence is reversed, the rectrices being moulted centripetally and the secondaries diverging from a single moult centre represented by the sixth, but this needs corroboration.A superficial search among other members of the genusMuscicapa, includingM. gambagae, and among other genera of Flycatchers disclosed the usual descending primary moult in all these forms (listed in the text).A possible functional meaning of the ascending primary moult inMuscicapa striata is discussed.

     

Modelling developmental changes in the carbon and nitrogen budgets of larval brachyuran crabs

The uptake and partitioning of nutritional carbon (C) and nitrogen (N) were studied during the complete larval development of a brachyuran crab,Hyas araneus, reared under constant conditions in the laboratory. Biochemical and physiological data were published in a foregoing paper, and complete budgets of C and N were now constructed from these data. Regression equations describing rates of feeding (F), growth (G), respiration (R), and ammonia excretion (U) as functions of time during individual larval moult cycles were inserted in a simulation model, in order to analyse time-dependent (i.e. developmental) patterns of variation in these parameters as well as in bioenergetic efficiencies. Absolute daily feeding rates (F; per individual) as well as carbon and nitrogen-specific rates (F/C, F/N) are in general maximum in early, and minimum in late stages of individual larval moult cycles (postmoult and premoult, respectively). Early crab zoeae may ingest equivalents of up to ca 40% body C and 30% body N per day, respectively, whereas megalopa larvae usually eat less than 10%. Also growth rates (G; G/C, G/N) reveal decreasing tendencies both during individual moult cycles and, on the average, in subsequent instars. Conversion of C and N data to lipid and protein, respectively, suggests that in all larval instars there is initially an increase in the lipid: protein ratio. Protein, however, remains clearly the predominant biochemical constituent in larval biomass. The absolute and specific values of respiration (R; R/C) and excretion (U; U/N) vary only little during the course of individual moult cycles. Thus, their significance in relation toG increases within the C and N budgets, and net growth efficiency (K ₂) decreases concurrently. Also gross growth and assimilation efficiency (K ₂; A/F) are, in general, maximum in early stages of the moult cycle (postmoult). Biochemical data suggest that lipid utilization efficiency is particularly high in early moult cycle stages, whereas protein utilization efficiency is higher in later stages. Only the zoea II appears to accumulate lipid from food constantly with a higher conversion efficiency than protein. The cumulative C and N budgets show in subsequent larval instars conspicuously increasing figures in all of their parameters.F andG increase to a particularly high extent from the first to the second zoeal instar, whereasR, U, exuvia production (G _E), and total assimilation (A) reveal a greater increase from the zoea II to the megalopa. Respiratory, excretory, and exuvial losses increase in subsequent larval instars at higher rates than tissue growth and, hence,K ₂ decreases in the same order. In the C budget,K ₂ values of 0.63 (zoea I). 0.56 (zoea II), and 0.29 (megalopa) were calculated (or: 0.56, 0.46, and 0.16 after subtraction of exuviae). In the N budget, corresponding values of 0.76, 0.66, and 0.45 (or: 0.72, 0.62, 0.38 without exuviae) were obtained. AlsoK ₁ decreases slightly in subsequent instars, whereasA/F reveals rather an increasing tendency, at least from the zoeal instars to the megalopa. Changes in the uptake and partitioning of matter in crab larvae are discussed in relation to developmental events and changes in life style before metamorphosis.     

SOME NOTES ON THE BIRDS OF THE ISOKA DISTRICT OF THE NORTHERN PROVINCE OF NORTHERN RHODESIA

Dean, W. R. J. 1978. Moult seasons of some Anatidae in the western Transvaal. Ostrich 49:76-84.

Spurwinged Geese Plectropterus gambensis, Egyptian Geese Alopochen aegyptiacus, Yellow-billed Ducks Anas undulata, Redbilled Teal A. erythrorhyncha and Southern Pochard Netta erythrophthalma have a flightless moult mainly during the dry season, from April to August, in the western Transvaal. South African Shelduck Tadorna cana moult during October to February after breeding during July and August. The Cape Shoveller Anas smithii has two main flightless periods, April-May and October-January. Cape Teal A. capensis have been recorded in flightless moult in October, December and January.

The duration of the flightless period correlates with wing length; larger and longer winged Anatidae require proportionally more time for wing moult than do smaller and shorter winged Anatidae.

Geese and shelducks moult on large open lakes with an open shore. Ducks have been recorded flightless on lakes and dams, with or without emergent vegetation.