SOME OBSERVATIONS ON THE DIDRIC CUCKOO

Earlé R. A. 1986. The breeding biology of the South African Cliff Swallow. Ostrich 57: 138–156.

The South African Cliff Swallow Hirundo spilodera breeds in dense colonies usually under man-made concrete bridges. The clutch size is 1–4 eggs but most 4-egg clutches are probably the result of conspecific brood parasitism. The incubation period averages 14,6 days and the fledling period 24,1 days. Although only the female Cliff Swallow has a featherless brood-patch, both males and females incubate effectively. Nestlings reach a maximum weight of up to 31 g between 19 and 22 days, about 10 g more than average adult weights. This weight increase of nestlings is mostly the result of an increase in water content of the body. Both parents feed the chicks, with the highest rate of feeding during the midday hours. In all, 56% of all eggs laid produced flying young, with a recruitment rate of 0,9 young: 1 adult per season.     

A RINGING STUDY OF MIGRATORY BARN SWALLOWS IN WEST MALAYSIA

The Barn Swallow is a non-breeding winter visitor to West Malaysia (Malaya), abundant in season, by day feeding aerially over a wide range of habitats and by night normally roosting gregariously in trees, reed-beds or on service wires in towns. Records of ringed birds have demonstrated that those reaching Malaya breed in the Palaearctic region from 108°E eastwards between 37° and 51°N. Recoveries south of the breeding range suggested that migrating birds may follow either a continental route or a more easterly track through the Philippines and Borneo. Counts at roost sites in a reed-bed and in towns demonstrated a seasonal increase in numbers from late July to a peak in November, followed by a decline of about 20% to a level maintained until mid-February when departure commenced. Most birds had left by early May, but a few lingered and possibly overlapped with the first returning migrants in June. There was no evidence that any individuals remained in Malaya through the nuptial period. Repeats during winter at three regularly sampled urban roosts indicated that many birds on passage were present until November and again in late March–early April; from December to February the winter population was relatively stable and comparatively sedentary. Although the distances between towns were small in relation to the demonstrated foraging range of Barn Swallows, only 17% of 1,955 repeats of ringed birds represented a shift in roost site. Most shifts were towards the centrally situated and most populous roost of the three; interchanges between the outer pair of towns were few. A complete moult occurred on the wintering grounds, during which young of the year acquired adult plumage. Replacement of the primaries extended virtually throughout the moulting period, at an average rate of 2.4 feathers per month in the proximal part of the tract and 1.3 feathers per month in the distal part. Adults on average moulted slightly earlier than juveniles, but there was a wide scatter in timing between individuals of both age groups. There was no evidence that the initiation of moult was related to the dates of post-nuptial migration. The date of departure on prenuptial migration, however, was normally delayed until primary moult was complete. Large weight gains in March and April occurred only in swallows which had completed the moult. At this period the mean weight of birds in fresh plumage was about 30% above the lowest winter mean, and was significantly higher than that of contemporary samples of birds in which moult was continuing. In final samples in late April and early May mean weights showed a decline, indicating that late birds departed with reduced deposits of metabolic reserves. The gonads of adults of both sexes among passage and arriving birds in July and August had largely completed post-nuptial regeneration, and subsequently remained quiescent. Preliminary stages of recrudescence were observed in females from February onwards, and in males from March. Recrudescence was most advance in specimens which had completed the moult, but did not approach breeding condition in any bird before departure. Returning birds tended to be conservative in their choice of winter roost. Among 1,276 records, 82% were recaptured in the town of original ringing. Again shifts towards the centrally situated roost were more numerous than between the peripheral pair. The frequency of returns varied significantly with the month of ringing, being higher for December-March, lower for July-November and April-May. Survival rates, calculated from returns after one and two breeding seasons, indicated an annual mortality of 60–72%, higher among juveniles than adults. Comparison of results of successive years suggested that unfavourable conditions in 1967 resulted in lower survival of juveniles in particular than in 1966. There was no evidence of mortality at the roost sites, and it is argued that heavy losses probably occur during the migratory journeys.     

Vererbung einer populationsspezifischen Mauser bei Kreuzung von M?nchsgrasmücken (Sylvia atricapilla) verschiedener Populationen

A comparative study of migratory blackcaps from Central Europe (S. Germany) and resident conspecifics from the Cape Verde Islands revealed marked differences in annual periodicity. European blackcaps, with one breeding season per year, have a single-peaked annual gonadal cycle whereas the African birds with two breeding seasons per annum have a two-peaked gonadal cycle. The European birds go through a post-juvenile moult (partial moult in first-year birds) or postnuptial moult (complete moult in adults) and, in addition, through a partial winter moult (all age classes) before the next gonadal cycle and breeding season. Their African conspecifics, on the other hand, have only one moult between two gonadal cycles, the summer moult also being the complete one. Here, we demonstrate that the additional winter moult of European blackcaps is heritable and can be transmitted into interpopulational hybrids. When blackcaps from S. Germany and the Cape Verdes were cross-bred, 16 out of 21 hybrids displayed the partial winter moult of their German parents. The fact that not all but only 76% of the F1 hybrids passed through this moult favours the idea that its incidence is controlled by a polygenic rather than a single locus system. Most likely winter moult in European blackcaps represents a threshold character as several migratory features do.     

The moult of Barred Warblers Sylvia nisoria in Kenya—evidence for a split wing-moult pattern initiated during the birds' first winter*

The moult of Barred Warblers Sylvia nisoria was studied during three winter seasons in southeastern Kenya at a southward passage site (Ngulia) and a wintering site (Mtito Andei). Most Barred Warblers migrating through Ngulia in November had yet to commence winter moult. These birds probably moulted subsequently in winter in northern Tanzania. In December, birds were found in heavy moult at Mtito Andei, and some of these birds were known to stay throughout the winter. By contrast, most birds reaching southeastern Kenya from late December onwards had already completed part or all of their winter moult, presumably at stopover sites in northern and eastern Kenya or in Ethiopia. Thus, winter moult in Barred Warblers takes place mainly in late November and December, either just before or soon after the final leg of autumn migration. In general, first-year birds renewed all tertials and tail feathers, about three to five secondaries per wing and commonly also the outer one to four large primaries per wing. Adults renewed all tertials and tail feathers, almost all secondaries and only occasionally an outer primary. The replacement of relatively fresh juvenile secondaries during the birds' first winter implies that the split moult pattern of this species (secondaries, tertials and tail moulted in winter; primaries and tertials in summer) is endogenously controlled.     

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.     

Of squeezers and skippers: factors determining the age at moult of immature African Penguins Spheniscus demersus in Namibia

We used banding and resighting records of 391 African Penguins Spheniscus demersus banded as chicks and later resighted during immature moult to explain the roles of date of fledging and age at moult in determining the season of moult and its timing within the season. Breeding was continuous, but immature moult occurred mainly during spring and summer. Age at immature moult extended over 11 months, from 12 to 23 months after hatching. Birds that fledged during summer and early autumn generally moulted during the next moult season (squeezers), whereas birds that fledged in late autumn, winter and spring skipped the next moult season to moult only the following season (skippers). There was a significant relationship between age at moult and moult date, with young birds moulting later in the season than older birds. The age at moult of immature birds appears to be constrained by minimum age, moult seasonality and plumage wear. Birds that fledged over nearly 2 years moult during one season. Counts of moulting immature African Penguins have not been used to estimate year-class strength and post-fledging survival owing to the wide range of ages at immature moult. Our results provide the means of assigning recruits to specific age groups.     

The timing of breeding and moult of the Lesser Striped Swallow Hirundo abyssinica

The Lesser Striped Swallow seems to have two different breeding populations. The birds south of 10°S breed largely during the spring and summer (July to April) and moult from about April to August. Birds further north breed throughout the year, but mainly during the first seven months of the year. Moult in the birds north of 10°S is from July to February when few birds are breeding. There seem to be two clearly defined moulting populations, with the southern breeding population moulting largely south of 10°S and the east African breeding population moulting largely north of the equator. In both populations moult and breeding seem to be separated in time, at least at the individual level.     

Moult of three Palaearctic migrants in their West African winter quarters

Some theories about moult strategies of Palaearctic passerine migrants assume that birds adapt timing of moult to environmental conditions such as rainfall on their African wintering grounds. Species wintering in the northern tropics should limit moult to the period shortly after their arrival at the end of the rainy season. Passerine migrants wintering in West Africa should also moult more rapidly compared to related species or conspecific populations that moult elsewhere. We investigated the moult of melodious warblers Hippolais polyglotta, willow warblers Phylloscopus trochilus and pied flycatchers Ficedula hypoleuca wintering in Comoé National Park, Ivory Coast, between October 1994 and April 1998. In contrast to previous studies we did not restrict our analyses to moult of flight feathers but also included moult of body feathers. The results differed partially from the general assumptions of previous authors. Melodious warblers moulted twice: a complete moult shortly after their arrival, and a moult of body feathers and in some cases some tertials and secondaries in spring. Willow warblers moulting flight feathers were found between December and March with the majority moulting in January and February. Primary moult was not faster compared to populations moulting in central Africa and South Africa. Body feather moult varied strongly among individuals with birds in heavy moult between December and April. Pied flycatchers moulted body feathers and tertials between January and April. Birds with growing feathers were found throughout the whole period including the entire dry season. Moult strategies are thus not readily related to a few environmental factors in general and our results show that factors other than mere resource availability during certain times on the wintering grounds are likely to govern the timing of moult.Communicated by F.Bairlein     

A new swallow from the Red Sea

A single specimen (Fig. 1), found dead on an islet off Port Sudan in spring 1984 is described as a distinctive new allospecies of African Cliff Swallow Hirundo spilodera.     

Primary moult, body mass and migration of Grey Plovers Pluvialis squatarola in Britain

Long-distance migrants have evolved complex strategies for the timing of their annual moult, fattening and migration cycles. These strategies are likely to vary at different stages of a bird's life. Ringing data on 6079 Grey Plovers Pluvialis squatarola , caught on the Wash, England, between 1959 and 1996, were analysed to relate migratory strategies to patterns of primary moult and body mass changes. Adults returning from breeding grounds had a shorter and delayed primary moult (duration 90 days, starting date 19 August) in comparison with over-summering birds (duration 109 days, starting date 5 June). Three categories of migrant adults were identified on the basis of primary moult and body mass: (1) birds which did not moult, but increased body mass and migrated further south; (2) birds which moulted 1–3 inner primaries, suspended moult, increased body mass and migrated; and (3) birds which completed or suspended moult and wintered locally. In birds of the second category, timing of primary moult and body mass increase overlapped. Among wintering birds, 38% were in suspended moult. Ninety-six per cent of birds that suspended moult at the beginning of winter were males and almost all completed moult in spring. Grey Plovers which left Britain in autumn had an average body mass of 280 g, enough to reach southern Morocco without refuelling. Both wintering adults and first-year birds showed a prewinter body mass increase, peaking in December. Adults had a synchronized premigratory body mass increase in May, which suggested a negligible presence of African migrants. The average departure mass for spring migration, estimated at 316 g, would allow birds to fly non-stop to the Siberian breeding grounds in western Taymyr.     

The timing of breeding and moult of the Lesser Striped Swallow Hirundo abyssinica

The Lesser Striped Swallow seems to have two different breeding populations. The birds south of 10°s breed largely during the spring and summer (July to April) and moult from about April to August. Birds further north breed throughout the year, but mainly during the first seven months of the year. Moult in the birds north of 10°s is from July to February when few birds are breeding. There seem to be two clearly defined moulting populations, with the southern breeding population moulting largely south of 10°s and the east African breeding population moulting largely north of the equator. In both populationsmoult and breeding seem to be separated in time, at least at the individual level.     

The timing of breeding and wing-moult of four African Sturnidae

Wing-moult of the Cape Glossy Starling, Red-winged Starling, Pale-winged Starling and Pied Starling was examined primarily from specimens in southern African museums. Breeding data were obtained from nest record cards.
The Cape Glossy Starling breeds from October to March, with the moult period from December to May. There is no evidence of moult-breeding overlap in individual birds. The Red-winged Starling breeds from September to March, while the moult takes place between November and April, overlapping with the second broods. The Pale-winged Starling breeds from October to April and moults between November and May. The Pied Starling moults between November and April, while breeding varies regionally, occurring concurrently with moulting in some areas.     

Post-breeding dispersal of Ad��lie penguins (Pygoscelis adeliae) nesting at Signy Island, South Orkney Islands

ARGOS satellite telemetry and Global Location Sensors (geolocators) were used to identify the moult locations and the winter foraging dispersal of Adélie penguins after they left their breeding colonies on Signy Island in the South Orkney Islands. Animals were tracked during the period December 2004 to October 2005. All birds displayed a similar pattern of migratory behaviour, remaining away from colonies for approximately 9 months, at distances of up to 2,235 km. Moult locations were within the pack ice. Mean daily travel speeds to the moult locations were significantly faster when moving through open water than through pack ice. Moult occurred during February/March within a narrow latitudinal range (65–71°S), at a mean distance of 126 km from the ice edge; the mean duration of individual moult was c. 18.6 days. After moult, penguins spent the subsequent winter months moving north or north-eastward within the expanding winter pack ice, at a mean distance of 216 km from the ice edge, and in areas with ice cover >80%. The penguins returned to the vicinity of their colony between September 26 and October 22, 2005. This dependence of Adélie penguins on sea ice habitat suggests that any further reductions in sea ice extent in the Weddell Sea region would potentially have important impacts on the population processes of this pagophilic species.     

Annual cycles in Jamaican forest birds

The annual cycles of forest birds in Jamaica were found to be very similar to those at higher latitudes. Most species bred between March and September, though a few possibly breed throughout the year, especially in cultivated areas. Primary moult followed immediately after breeding, and in some species was apparently arrested to allow a further breeding attempt. Several species were fatter outside the breeding season than during it, and this is interpreted as "winter fattening" comparable to that found in many birds at higher latitudes. Weights varied little but individuals retrapped were usually heavier outside the breeding season. In some species the first complete moult took place at the end of the first year, implying that the birds do not breed until at least two years old.     

Contrasting strategies for wing‐moult and pre‐migratory fuelling in western and eastern populations of Common Whitethroat Sylvia communis

Trade‐offs between moult and fuelling in migrant birds vary with migration distance and the environmental conditions they encounter. We compared wing moult and fuelling at the northern and southern ends of migration in two populations of adult Common Whitethroats Sylvia communis. The western population moults most remiges at the breeding grounds in Europe (e.g. Poland) and migrates 4000–5000 km to western Africa (e.g. Nigeria). The eastern population moults all remiges at the non‐breeding grounds and migrates 7000–10 000 km from western Asia (e.g. southwestern Siberia) to eastern and southern Africa. We tested the hypotheses that: (1) Whitethroats moult their wing feathers slowly in South Africa, where they face fewer time constraints than in Poland, and (2) fuelling is slower when it coincides with moulting (Poland, South Africa) than when it occurs alone (Siberia, Nigeria). We estimated moult timing of primaries, secondaries and tertials from moult records of Polish and South African Whitethroats ringed in 1987–2017 and determined fuelling patterns from the body mass of Whitethroats ringed in all four regions. The western population moulted wing feathers in Poland over 55 days (2 July–26 August) at a varying rate, up to 13 feathers simultaneously, but fuelled slowly until departure in August–mid‐September. In Nigeria, during the drier period of mid‐February–March they fuelled slowly, but the fuelling rate increased three‐fold in April–May after the rains before mid‐April–May departure. The eastern population did not moult in Siberia but fuelled three times faster before mid‐July–early August departure than did the western birds moulting in Poland. In South Africa, the Whitethroats moulted over 57 days (2 January–28 February) at a constant rate of up to nine feathers simultaneously and fuelled slowly from mid‐December until mid‐April–May departure. These results suggest the two populations use contrasting strategies to capitalize on food supplies before departure from breeding and non‐breeding grounds.     

The moults of captive Scottish ptarmigan (Lagopus mutus)

The moults of captive Scottish ptarmigan were studied at Banchory, north-east Scotland from December 1968 to February 1971. In the autumn moult (June to September) which included the primaries, cock ptarmigan moulted earlier and more completely than hens. In the winter moult (September to February) hens moulted earlier and both sexes moulted more completely than in spring. In the spring moult (February to June) cocks moulted more rapidly to begin with but by mid-April hens had caught up and thereafter moulted at least as rapidly as cocks. When kept indoors at slightly higher temperatures ptarmigan grew more pigmented feathers during the winter moult. In a colder winter the birds became whiter than in a milder one. First-winter ptarmigan completed the winter moult later than older birds. Birds from the Cairnwell hills had more dark feathers in winter than those from the eastern Cairngorms. There was no correlation between the start or finish of egg-laying and moulting.     

Wing moult in relation to autumn migration in adult Common Whitethroats Sylvia communis communis

Most long-distance passerine migrants in Sweden moult on breeding grounds before leaving on autumn migration to winter quarters. However, birds laying second or replacement clutches, or just breeding late, have too little time for a normal moult on the breeding grounds. When time is limited the birds may respond by making various adjustments to the moult, for example by moulting more quickly or by suspending the moult. In this study, the relationship between the performance of post-nuptial remex moult in Common Whitethroats breeding on Gotland, southeast Sweden, and autumn migration departure was investigated. The majority (77%) of the birds had interrupted moult in either the primaries or secondaries. Interruption of moult was more common among birds with a later onset date, as was asymmetry in moult between wings. The interruption of moult led to a significant time gain and moult completion was, consequently, more synchronized than moult onset. The results from this study indicate, in accordance with other data, that an early start of autumn migration is important. An early start may be crucial to facilitate the crossing of the Sahara Desert once the dry season has begun.     

Notes on the moult of red-backed shrikes ( Lanius collurio ) in their non-breeding range

Moult data from 302 museum skins and 11 trapped birds from sub-Saharan Africa show the course of flight feather moult. Most birds seem to start flight-feather moult soon after arrival in their southern African non-breeding ranges. About 75% of the birds had started before mid-December, i.e., during the main arrival time of the species. The mode of moult scores 1 and 2 was reached on 7 December; the last birds with a score of zero occurred in the first days of January. The mode of moult scores 5 and 6 was reached on 27 February. Thus, the time elapsed between the days when 50% of the population had reached the first and last stages of recorded moult was about 82 days; nine days later 75% had reached this last stage before moult was completed. Thus, individual moult may be estimated to cover about 80–90 days. The main moulting period is between mid-November and mid-March, thus covering about four months. No temporal difference was detected between males and females. A tendency for an advancement of adults compared to young birds was not statistically significant. According to the progress of the moult, sexing of young birds in the field is possible for 50% of the birds towards the end of January and for most birds before mid-February.     

Do body condition and plumage during fuelling predict northwards departure dates of Great Knots Calidris tenuirostris from north‐west Australia?

It is often assumed that strong selection pressures give rise to trade-offs between body condition and time in long-distance migrating birds. Birds that are 'behind schedule' in fuel deposition or moult should delay departure, and this should result in a negative correlation between initial condition and departure date. We tested this hypothesis in the Great Knot Calidris tenuirostris migrating from north-west Australia to eastern Asia en route to Siberia. Great Knot gain mass and moult into breeding plumage before leaving northern Australia in late March and early April, and fly 5400–6000 km to eastern China and Korea. We radiotracked 27 individuals (17 males and ten females) to determine departure dates; 23 migrated and four remained in Australia. We characterized body condition at capture using body mass, predicted pectoral muscle mass (based on ultrasound estimates of the size of the pectoral muscles) and breeding plumage scores. Residual condition indices were uncorrelated, indicating that at the individual level, variation in one fuelling component was not strongly associated with variation in the other components. Birds that did not depart had lower residual body mass and breeding plumage indices than those that did migrate; these four birds may have been subadults. Neither sex, size nor the condition indices explained variation in departure date of migrants. Reasons for this are explored. Departure dates for northward migrating waders indicate that the migration window (span over which birds depart) decreases with proximity to the northern breeding grounds. We suggest that migration schedules become tighter as birds get nearer to the breeding grounds. Thus the lack of a relationship between condition and departure date in Great Knots may reflect the fact that the departure episode under study is the first one in sequence and is still 4–8 weeks before breeding.     

Sociable Weaver biometrics and primary moult

The biometric and primary moult data housed at the South African Bird Ringing Unit (SAFRING) were analysed for the Sociable Weaver Philetairus socius. The average body mass and wing length was 27.9g (SD = 2.2) and 74.1mm (SD = 2.5), respectively. Variation in these parameters is not clearly correlated with region, season or climate, other than a negative correlation of body mass with average annual water deficiency. Body mass of Sociable Weavers near Kimberley showed a longterm decrease of 2.9g, probably due to stabilising selection on mass. Primary moult duration varied from 152 days to 169 days and started between 26 January and 31 December in two populations (socius and South African eremnus respectively). Individual primaries moulted mainly one at a time, each taking 20–28 days to grow fully. Prolonged moult duration in this species is probably an adaptation to reduce energy expenditure, and to grow more durable feathers due to abrasion in entering the nest. The lack of clear patterns of geographical variation in biometrics indicates that the contiguous populations of Sociable Weaver should belong to the nominate species. The biometric and primary moult data housed at the South African Bird Ringing Unit (SAFRING) were analysed for the Sociable Weaver Philetairus socius. The average body mass and wing length was 27.9g (SD = 2.2) and 74.1mm (SD = 2.5), respectively. Variation in these parameters is not clearly correlated with region, season or climate, other than a negative correlation of body mass with average annual water deficiency. Body mass of Sociable Weavers near Kimberley showed a longterm decrease of 2.9g, probably due to stabilising selection on mass. Primary moult duration varied from 152 days to 169 days and started between 26 January and 31 December in two populations (socius and South African eremnus respectively). Individual primaries moulted mainly one at a time, each taking 20–28 days to grow fully. Prolonged moult duration in this species is probably an adaptation to reduce energy expenditure, and to grow more durable feathers due to abrasion in entering the nest. The lack of clear patterns of geographical variation in biometrics indicates that the contiguous populations of Sociable Weaver should belong to the nominate species.