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.     

Timing of migration and residence areas during the non‐breeding period of barn swallows Hirundo rustica in relation to sex and population

We investigated sex‐ and year‐dependent variation in the temporal and spatial movement pattern of barn swallows Hirundo rustica during the non‐breeding period. Hundred and three individuals equipped with miniaturized light‐level geolocators at three different breeding areas in southern Switzerland and northern Italy provided data for the analysis. We identified a region 1000 km in radius centred in Cameroon as the main non‐breeding residence area of these three geographical populations. Five residence areas of males only were in southern Africa, south of 19°S. Most individuals occupied a single site during their stay south of the Sahara. The timing of migration broadly overlapped between sexes and all geographical breeding populations. Between the two study years there was a distinct difference of 5 to 10 d in departure dates from and arrival at the breeding sites. Remarkably, the period of residence in sub‐Saharan Africa was very similar (157 d) in the two study years, but their positions in the first year (2010–2011) were about 400 km more to the north than in the second (2011–2012). Independent of the year, individuals with sub‐Saharan residence areas further north and east had a shorter pre‐breeding migration and arrived earlier than those staying further south and west. In addition, birds breeding in southern Switzerland arrived at their breeding colony 7–10 d later than those breeding only 100 km south, in the Po river plain. Our study provides new information on the variance in migration phenology and the distribution of residence areas in sub‐Saharan Africa in relation to sex, population and year. It supports the usefulness of light‐level geolocators for the study of annual routines of large samples of small birds.     

An Ornithological Trip in the Gulf of Suez and Red Sea.

From what I personally observed on this trip and from information gathered en route and elsewhere, it would seem that-in spring at any rate-the migration along the Red Sea and Gulf of Suez is not very extensive, particularly with regard to the smaller birds. White Storks and Lesser Black-backed Gulls, however, follow this line in vast numbers on their journey north, though, as regards the first-named species, the vast majority had passed through earlier than the date of my visit to that district.
As will be noted from the list of species appended to this paper, very little collecting was done with the gun. The principal object of the trip was to obtain live specimens of the Osprey and other of the larger birds breeding in the locality for the Giza Zoological Gardens. In respect of the Osprey only was I successful, and returned with three young which were still flourishing in the Zoo collection when I left Egypt in July 1927. I was disappointed in not finding more species engaged in nesting operations, and it would appear that such birds as Sula leuco- gaster , Phaëton indicus , Casmerodius albus melanorhynchus , Platalea leucorodia , Larus leucophthalmus , and Sterna bergii welox , which undoubtedly breed in the latitude I visited, do so considerably later in the year than the month of April. Further south, on the Farsan Group of Islands Lat. N. 17°, the Brown Booby was breeding in October. Eggs were found at the end of that month and young birds early in November 1926.     

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.     

Timing and duration of moult in three populations of Purple Sandpipers Calidris maritima with different moult/migration patterns

Timing and duration of primary moult in three populations of Purple Sandpipers Calidris maritima were described and discussed in relation to the birds’ need to complete moult before the onset of winter, when resources are required for survival. We predicted that moult would be completed earlier by birds wintering at higher latitudes. The south Norwegian breeding population, which moults and winters along the coast of east Britain (54–57°N) had a mean starting date of 21 July for primary moult (16 July for females and 24 July for males), a mean duration of 61 days, and completed on 20 September. Resident Icelandic (64–65°N) birds had a mean starting date of 22 July for primary moult (17 July for females and 25 July for males), a mean duration of 51 days, and completed on 11 September. Birds moulting in north Norway (70°N) arrived in north Norway in suspended primary moult or without having started moult, and completed it there. They had a mean completion date of 2 November for primary moult (31 October for females and 3 November for males). Starting date and duration could not be estimated because some suspended moult for an undetermined period, but it was thought that they started in late August. It is likely that most originated from Russia. The onset of moult appears to be set by the end of breeding and there is little overlap in these two events. The earlier start of moult by females in all three populations may be because they abandon the males when the chicks hatch, leaving the males to attend the chicks. Although the duration of primary moult followed the expected trend, being fastest in north Norway and slowest in Britain, the onset of moult was so late in north Norway that they had an unexpectedly late completion date, despite their rapid moult. The late completion of primary moult in north Norway suggests that wintering in the far north may not pose the energetic constraints on Purple Sandpipers that had previously been supposed.     

Post‐breeding movements of northeast Atlantic ivory gull Pagophila eburnea populations

The post‐breeding movements of three northeast Atlantic populations (north Greenland, Svalbard and Franz Josef Land) of the ivory gull Pagophila eburnea, a threatened high‐Arctic sea‐ice specialist, were studied between July and December 2007 using 31 satellite transmitters. After leaving their breeding grounds, all birds first dispersed eastward in August–September, to an area extending from the Fram Strait to the northwestern Laptev Sea (off Severnaya Zemlya). Most returned along the same flyway in October–November, hence describing a loop migration before moving south, off east Greenland. Wintering grounds were reached in December, in southeast Greenland and along the Labrador Sea ice‐edge, where Canadian birds also overwinter. One to two birds from each population however continued eastwards towards a third wintering area in the Bering Strait region, hence demonstrating a bi‐directional migration pattern for the populations and elucidating the origin of the birds found in the north Pacific during winter time. Overall, all birds breeding in the northeast Atlantic region used the same flyways, had similar rates of travel, and showed a peak in migratory activity in November. Though the total length of the main flyway, to the Labrador Sea, is only and at most 7500 km on a straight line, the mean total distance travelled by Greenland birds between July and December was 50 000 km when estimated from hourly rates of travel. Our study presents the first comprehensive and complete picture for the post‐breeding movements of the different ivory gull populations breeding in the northeast Atlantic.     

The flightless period of free-living male Teal Anas crecca in northern Sweden

A total of 126 flightless adult male Teal was caught in 1982 and 1983 in a moulting area in northern Sweden (63° 53'N). The birds were weighed and the stage of development of their primaries and secondaries measured. During the flightless period, the weight of the birds decreased by an average of 10% in 1982 and 19% in 1983. This weight decrease allows the birds to fly before their primaries and secondaries are full-grown. The weight loss is considered to be an adaptation making it possible, for example, for lighter birds to escape predators sooner after moulting. Birds varied greatly in the dates at which they initiated their flightless period, that is, from the end of June to the end of July. Thus, it is probable that both local birds and birds from distant breeding grounds were present in the moulting area.     

Effects of supplementary food on density-reduced breeding in an African eagle: adaptive restraint or ecological constraint?

Increased population density often reduces reproductive output in breeding birds, but the underlying mechanisms (adaptive restraint v reduced food resources) behind decreased productivity are poorly understood. Here I correlatively and experimentally investigated the roles of food, breeding density, latitude, altitude and rainfall in limiting productivity of Wahlberg's Eagles Aquila wahlbergi throughout Africa. Breeding success in equatorial and subtropical Africa (0°–30°S) was highly density-dependent but showed no latitudinal or rainfall-related trends. Pairs in dense populations produced half as many young annually as pairs in low-density populations. Density (but not rainfall or latitude) also explained much of the geographic variation in the mean proportion of pairs attempting to breed each year and the incidence of two-egg clutches.
Breeding within populations was consistent with these density-dependent trends: incidence of two-egg clutches increased in a declining population, and productivity was inversely related to breeding density and rainfall combined. To determine if reduced food resources accounted for reduced output in dense populations, eight pairs were food supplemented: supplementary food failed to induce nonbreeding pairs to breed: nor did it induce earlier laying or increase egg size or clutch-size. Population density itself was unrelated to two correlates of food resources, rainfall and latitude. I conclude that population density influences most aspects of breeding in Wahlberg's Eagles, and reduced food resources do not appear to explain these trends. Hence, adaptive restraint may account for decreased annual reproduction in this species.     

Isotopic (δ2Hf) evidence of “loop migration” and use of the Gulf of Maine Flyway by both western and eastern breeding populations of Blackpoll Warblers

Declining numbers of Blackpoll Warblers (Setophaga striata) have been documented at long‐term migration monitoring sites as well as in breeding areas. However, the “loop migration” of Blackpoll Warblers makes it difficult to ascribe population change at migration monitoring sites to specific breeding populations. Individuals from all populations across the breeding range of Blackpoll Warblers concentrate in fall along the Atlantic coastline of eastern North America prior to initiating a transoceanic flight to wintering areas. In spring, Blackpoll Warblers return along a different route, moving north into the southeastern United States where birds from eastern and western breeding populations then diverge during migration to reach their respective breeding areas. To monitor breeding populations outside of breeding areas and identify factors potentially affecting those populations, we must be able to identify where birds captured during migration breed and map seasonal variation in population‐specific flyways. To “map” population‐specific migration movements of Blackpoll Warblers, we used feather deuterium (δ²H_f) values and a spatially explicit model to assign molt origins of 289 Blackpoll Warblers moving through sites in the Gulf of Maine (GOM) region and at three locations further west and south (northern Great Lakes area, Pennsylvania, and Florida). The assignment method was validated with feather samples from 35 birds captured during the breeding season at Churchill, Manitoba, Canada. As predicted, the spatial pattern of movement within and between seasons reflected “loop migration.” Blackpoll Warblers captured during fall migration in the GOM region included birds from across their breeding range, whereas birds captured during the spring were exclusively from northeastern populations. During fall migration, Blackpoll Warblers captured at two sites west of the GOM were from breeding areas further northwest than those from western Canada that were captured in the GOM. Blackpoll Warblers captured in eastern Florida during spring migration were assigned exclusively to breeding areas in the northeast, suggesting that eastern and western populations diverge soon after entering the United States. Finally, most Blackpoll Warblers sampled at Manomet Bird Observatory originated from breeding populations in Alaska and western Canada that have shown a similar (70–90%) decline over the same period. Our results, therefore, not only document the “loop migration” pattern of Blackpoll Warblers, but, by mapping patterns of connectivity between breeding and non‐breeding areas, may help target conservation efforts for breeding populations of Blackpoll Warblers where most needed.     

Variation in the abundance of Red-breasted Mergansers Mergus serrator on a Scottish river in relation to season, year, river hydrography, salmon density and spring culling

Red-breasted Mergansers Mergus serrator were counted in the river North Esk, Scotland, and on the sea nearby, 1987–1990. Pairs arrived at the river estuary from early winter, but the main influx to freshwater took place in late April and in May, when breeding pairs dispersed far upriver. Females began incubation from late May. Most young hatched in July and fledged by late September. Males left the river in June and congregated at an offshore moulting site, their numbers peaking in August, and dispersed rapidly in September.
Breeding density and total duckling production decreased with increasing distance upstream, decreasing river width and increasing gradient and elevation. The total number of breeding pairs and their distribution on the river were similar from year to year, despite variable numbers killed, suggesting a stable breeding population near the upper limit the habitat would support in those years. It also suggested that killing mergansers in April was an ineffective way to reduce the population. The spatial variation in merganser breeding density was not correlated with the density of their main spring food, parr of salmon Salmo salar , but could have been related to its availability.
The production of well-grown ducklings varied annually and was inversely correlated with river flow during the main period of hatch. It is argued that Red-breasted Mergansers breed late in the year because the hatching of ducklings in July coincides with an abundance of their food, large aquatic invertebrates and tiny juvenile fish.     

THE PRIMARY MOULT OF WADERS ON THE ATLANTIC COAST OF MOROCCO

Data from 3659 waders of 23 species live-trapped in the years 1971-73 on the Atlantic coast of Morocco during the period of autumn moult and migration are analysed to estimate duration and timing of primary moult. Common Sandpiper was the only species to moult primaries in its first autumn (unless published ageing criteria are incorrect). Several species showed a low incidence of arrested primary moult and a higher incidence was observed in Ringed, Kentish and Grey Plovers. This is discussed in relation to breeding and migration. Similar rates of primary feather replacement relative to specific moult duration were observed in all species for which information was available. Comparisons between species and with published studies showed that variations in rate of moulting between species and between different geographical populations of the same species were largely due to differences in feather growth rate rather than in the numbers of primaries concurrently in growth. Variations in rate between individuals of the same population were achieved, at least in the first part of moult, by differences in feather dropping rate resulting in differences in the numbers of primaries growing concurrently. The timing and duration of moult in different populations and differences between breeding and non-breeding components were closely related to the requirements of other annual cycle activities, notably breeding and migration. Non-breeding birds summering in Morocco had started moult early. Locally breeding birds had an early start to a fairly slow moult which overlapped with breeding and which in some cases passed through an arrested stage. Birds breeding in cold temperate and arctic regions and wintering in Morocco moulted in a short time soon after arrival. In some cases, notably in Ringed Plovers, birds had commenced moulting on the breeding grounds and arrested moult during migration. Most Redshank and possibly Dunlin migrated in active wing moult. The fastest primary moult was achieved by high arctic breeding birds, Curlew Sandpiper and possibly Little Stint, which stopped to moult in Morocco before moving on to wintering areas further south. This situation is contrasted with that of populations of these two and other species wintering in the southern hemisphere where moult occurs over an extended period during the northern winter.     

THE BREEDING SEASONS OF AFRICAN BIRDS—2. SEA BIRDS.

1. All the available data, largely unpublished, are assembled for sea-birds breeding in African waters, about 36° N.-36° S.
2. An ill-defined breeding season by any species at any station is exceptional.
3. North of the Equator practically all sea-birds breed in spring or summer.
4. South of the Equator there is much more variation. Round the Cape there is a good deal of mid-winter breeding, mainly in stations affected by the warm Agulhas current.
5. On the east coast most of the breeding takes place in the period June–August from the Gulf of Suez (27° N.) to the mouth of the Zambesi (19° S.) and beyond, i.e. in the hottest months north of the Equator and the coolest months south of it.     

Skipping‐type migration in a small Arctic wader,the Temminck's stint Calidris temminckii

By using morphometric data and geolocator tracking we investigated fuel loads and spatio‐temporal patterns of migration and non‐breeding in Temminck's stints Calidris temminckii. Body masses in stints captured at autumn stopover sites from Scandinavia to northern Africa were generally not much higher than during breeding and did not vary geographically. Thus, we expected migrating stints to make several stopovers and either circumventing the Sahara desert with low fuel loads or fuelling at north African stopover sites before desert crossing. Geolocation revealed that birds (n = 6) departed their Norwegian breeding site in the last part of July and all but one migrated south‐west over continental western Europe. A single bird headed south‐east to the Balkan Peninsula where the geolocator died. As predicted, southbound migration proceeded in a typical skipping manner with 1–4 relatively short stopovers (median 4 d) during 10–27 d of migration before reaching north‐west Africa. Here birds spent 11–20 d before crossing the Sahara. The non‐breeding sites were located at or near the Niger River in Mali and were occupied continuously for more than 215 d with no indications of itinerancy. Spring migration commenced in late April/early May when birds crossed the desert and used stopover sites in the western Mediterranean basin in a similar manner as during autumn. The lowest body masses were recorded in spring at islands in the central Mediterranean basin, indicating that crossing the Sahara and Mediterranean barriers is exhausting to these birds. Hence, the skipping‐type pattern of migration revealed by geolocators is likely to be natural in this species and not an effect of instrumentation.     

布氏田鼠标志种群的繁殖参数

采用标志重捕和染色观测法跟踪了内蒙古典型草原区布氏田鼠野外种群,按绝对时间年龄研究其种群繁殖参数。结果3表明：4－5月份出生的雄鼠能在当年达到性成熟,性成熟发育历期约为1．5个月,6月后出生的雄鼠当年达不到性成熟。在达到性成熟的当年雄鼠中,多数个体再度转入性休止期,其平均繁殖结束时间要林越冬雄鼠早1个月,而越冬雄鼠则在整个繁殖期保持性活动状态。雌鼠性成熟发育历期约为1个月,首次产仔时间约为2月龄。雌鼠在一年中的产仔窝数与其年龄有关;越冬鼠能产3－4窝,4月份出生的雌鼠能产2－3窝,5月份出生的雌鼠当年能产1－2窝,6月份出生的雌鼠能产0－1窝,7月份之后出生雌鼠当年不参加繁殖,在自然条件下,布氏田鼠一年中最多能产4窝。     

THE MIGRATION PATTERNS OF THE PURPLE SANDPIPER CALIDRIS MARITIMA

Summers, R. W. 1994. The migration patterns of the Purple Sandpiper Calidris maritima. Ostrich 65: 167–173.

The Purple Sandpiper breeds largely in the Arctic, and winters (boreal season) on the rocky shores of the north Atlantic, further north than any other sandpiper. As the populations from Canada, Greenland, Iceland, Svalbard, Norway and Russia differ in wing and bill lengths it is possible to match measurements taken from breeding birds with samples of birds caught in winter. Ringing recoveries, especially from colour marked birds, have also helped to determine migration routes and wintering areas. Four populations move to the nearest ice-free coast. Two populations move south of the nearest ice-free coast, being replaced by larger birds from a more northerly population (“chain migration”). Only the north Canadian population is believed to migrate a long distance, “leap-frogging” other winter populations. These patterns are discussed in relation to theories for the migration patterns of waders.     

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.     

Can Experience Alter the Avian Annual Cycle? Results of Migration Experiments with Indigo Buntings

Field experiments were conducted during 2 years testing whether premature release on their familiar, perennial breeding territories would cause indigo buntings (Passerina cyanea) to delete spring migration from their annual cycle. In the first year, male buntings were captured on their breeding territories in summer and held indoors for the winter on the photoregime that they would have encountered in nature as fall migrants and winter residents. The following spring they were released at the time buntings begin spring migration from the subtropics. Half were released on their breeding territories, to which they would normally have returned; half were released far to the south. Some of the males released on their territories remained and passed into breeding condition without having migrated, while some of those released to the south returned north to their territories. The results suggest that endogenous or photoperiodic mechanisms controlling the timing and occurrence of migration in this species can be overridden by experience. In the second year we tested alternative explanations for these results. Our second year's results seem to indicate (1) that birds that deleted migration in year one did not do so because of unfavourable weather and (2) that the birds that returned to their breeding sites in year one were actually migrating and not simply retracing their outward journey.     

Age‐specific variation in relationship between moult and pre‐migratory fuelling in Wood Sandpipers Tringa glareola in southern Africa

Trans‐equatorial avian migrants tend to breed, moult and migrate – the main energy‐requiring events in their lifecycle – at different times. Little is known about the relationship between wing moult and pre‐migratory fuelling in waders on their non‐breeding grounds, where time is less constrained than during their brief high‐latitude breeding season. We determined age‐related strategies of Wood Sandpipers Tringa glareola to balance the energetic demands of primary moult against pre‐migratory fuelling in southern Africa by analysing body mass and primary moult at first capture of 1721 birds mist‐netted in 1972–96 at waterbodies in Zimbabwe. Adults moulted all their primaries in August–December, but immatures underwent a supplemental moult of varying numbers of outer primaries in December–April, close to departure. We used locally weighted linear regression to estimate trends in Wood Sandpiper body mass from 1 July to 1 May. They maintained low mass from arrival in July–September to February–early March. Adults fuelled from 10 February to 1 May at a mean rate of 0.25 g/day (sd = 0.16). Most adults (98%) began fuelling 10–75 days after completing primary moult. Immatures fuelled from 4 March to 13 April at 0.24 g/day (sd = 0.14). They used varying strategies depending on their condition: a brief gap between moult and fuelling; an overlap of these processes near departure, leading to slower fuelling; or skipping fuelling altogether and staying in southern Africa for a ‘gap year’. Immatures moulting three or five outer primaries fuelled more slowly than post‐moult birds. Immatures moulting four outer primaries started fuelling 3 weeks later but at a higher rate than did post‐moult birds of this group. In post‐moult immatures, the later they ended moult, the later and faster they fuelled. The heaviest adults and immatures using all moult patterns accumulated fuel loads of c. 50% of lean body mass, and could potentially cross 2397–4490 km to reach the Great Rift Valley in one non‐stop flight. Immatures were more flexible in the timing and extent of moult and in the timing and rate of fuelling than adults. This flexibility enables inexperienced Wood Sandpipers to cope with inter‐annual differences in feeding conditions at Africa's ephemeral inland waterbodies.     

Status and abundance of the African Black Oystercatcher Haematopus moquini at the eastern limit of its breeding range

From 1983 to 2004 the breeding population of African Black Oystercatchers along the East London coast has more than trebled. The population increase is probably due to immigration as local breeding success is low. There are three classes of birds: breeding pairs, tenants and visitors, and birds may change status during the breeding season. In the winter, birds aggregate into groups and some birds may disperse from the East London coast. The presence of African Black Oystercatchers in all months of the year shows that they are resident, but may only be resident in the general sense, and at a local level appear to be nomadic, wandering along the coast in search of resources and, in the summer, opportunities to breed. The birds remain at any locality only for as long as conditions are suitable, suggesting that the birds along the East London coast are mostly visitors that have dispersed from their natal areas in the south.     

State uncertainty models and mark‐resight models for understanding non‐breeding site use by Piping Plovers

Conservation of beach‐nesting medium‐distance migrants has focused on breeding areas because protection of nests is more tractable than protection of non‐breeding habitat. As breeding ground management has encountered diminishing returns, interest in understanding threats in non‐breeding areas has increased. However, robust estimates of non‐breeding demographic rates and abundance are generally lacking, hindering the study of limiting factors. Estimating such rates is made more difficult by complex population dynamics at non‐breeding sites. In South Carolina, endangered Piping Plovers Charadrius melodus start arriving in July and some depart prior to December (the autumn‐only population) while others remain through at least March (the wintering population). State uncertainty capture‐mark‐recapture models provide a means for estimating vital rates for such co‐occurring populations. We estimated the proportion of the population entering the study area per survey (entry probability) and proportion remaining per survey (persistence rate) for both populations during autumn, and abundance of the wintering population, at four sites in South Carolina in 2006/7 and 2007/8, taking advantage of birds previously colour‐ringed on the breeding grounds. We made fairly precise estimates of entry and persistence rates with small sample sizes. Cumulative entry probability was ~50% by the end of July and reached 95% for both populations by October. Estimated stopover duration for birds in the autumn‐only population was 35 days in year 1 and 42 days in year 2. We estimated a wintering super‐population size of 71 ± 16 se birds in the first year and 75 ± 16 in the second. If ringing programmes on the breeding grounds continue, standardized resighting surveys in the non‐breeding period and mark‐recapture models can provide robust estimates of entry and persistence rates and abundance. Habitat protection intended to benefit non‐breeding Piping Plovers at our coastal sites should be in effect by late summer, as many birds are resident from July to the end of winter.