How do birds search for breeding areas at the landscape level? Interpatch movements of male ortolan buntings

Animal movements at large spatial scales are of great importance in population ecology, yet little is known due to practical problems following individuals across landscapes. We studied the whole Norwegian population of a small songbird (ortolan bunting, Emberiza hortulana ) occupying habitat patches dispersed over nearly 500 km². Movements of colour-ringed males were monitored during ten years, and extensive long-distance dispersal was recorded. More than half of all cases of breeding dispersal took place within one breeding season, and males moved up to 43 km between singing territories, using 1–22 d. Natal dispersal was usually to a habitat patch close to the natal patch, or within the natal patch if it was large. Breeding dispersal movements were often long-distance, beyond neighbouring patches, and up to 11–19 patches were overflown. Movements of at least 6–9 km across areas of unsuitable habitat occurred regularly. The number of patches visited was low (1–4) even though search costs in terms of time spent moving from one site to another were relatively low (often only a few days even for distances >10 km). Most males seemed to use a threshold tactic when choosing a patch, but returns to previously visited patches were recorded, including some cases of commuting. In conclusion, male ortolan buntings have a surprising ability to move quickly at the landscape level, and this resulted in a high connectivity of patches. We discuss our results in relation to optimal searching strategies, in particular the use of within-breeding season versus post-breeding season search, conspecific attraction and adaptive late arrival of young birds.     

FACTORS AFFECTING BREEDING OF RAZORBILLS ALCA TORDA ON SKOKHOLM

A study of the breeding biology of the Razorbill was carried out on Skokholm (South Wales) during 1971-73. Birds ringed or colour ringed before the study began provided additional information upon the effects of age on breeding. Mean laying date was delayed in 1972, compared with 1971; the effect is attributed chiefly to stormy weather which upset colony attendance. Eggs were also smaller in 1972. A seasonal decline in egg size (volume) was noted in all three years, attributed mainly to the later laying of young birds. Egg size increased with age, at least up to the fifteenth year. Eggs lost totalled 30% of those laid; 73% of this total was due to predation by Herring Gulls and of Jackdaws. Most losses (45%) occurred during the first 10 days after laying. Of lost eggs, 25% were replaced, usually 14 days after the loss of the original; only eggs laid and lost early in the season could be replaced. Only 7% of the chicks which hatched failed to fledge. Most (62.5%) chick losses occurred in the first week of nestling life, when chick weight was related to egg size. Afterwards, both growth rate and fledging weight were independent of egg size. The chicks fledging early in the season were heavier than later chicks. Failure to fledge was mainly due to a breakdown in behaviour between parent and young, rather than to predation. Breeding success was highest for birds breeding early in the season, most of which were older, more experienced breeders. These laid early enough to replace an egg if it was lost; they produced large eggs, and their chicks were therefore both heavier than average during the critical first 7–10 days of life, and fledged at a high weight. Thus experience accumulated with age, and the ability to lay early in the season are important for successful breeding in the Razorbill.     

Age at first breeding, philopatry and breeding site-fidelity in the Lapwing Vanellus vanellus

Breeding Lapwings Vanellus vanellus were studied in the Eden Valley (Cumbria) and in Teesdale (County Durham) between 1990 and 1992. A total of 300 adult Lapwings and 801 near-fledged young were uniquely colour-ringed. Breeding adults were highly site-faithful, almost always nesting in the same or an adjacent field in successive years. Second-year birds were less site-faithful, with more birds nesting in adjacent and other fields and fewer in the same field in successive years. In Teesdale, 74% of colour-ringed young Lapwings returned in their first or second year of life to within 5 km from where they hatched. In contrast, in the Eden Valley only 37% of young birds in their first or second year of life returned to within 5 km from where they hatched. From an analysis of British ringing recoveries in April and May, 61% of Lapwings were recovered within 10 km from where they were ringed as chicks. A further 11% were recovered more than 100 km from where they were ringed. Young Lapwings were highly philopatric, with 45% of males and 52% of females breeding in the same field or a field adjacent to where they hatched. The majority of Lapwings (67%) began breeding at 1 year old. Of the remaining birds, 27% bred for the first time when 2 years old and 6% for the first time in their third year of life. There was no difference between the sexes. Chicks hatching and subsequently fledging late in the season returned less frequently to the study areas in subsequent years than did chicks hatching earlier in the season.     

Interrelationships between breeding frequency,timing and outcome in King Penguins Aptenodytes patagonicus: are King Penguins biennial breeders?

King Penguin Aptenodytes patagonicus chick growth is interrupted by a winter fast which extends the length of the breeding cycle (laying to chick independence) to 14–16 months, so that continuous annual successful breeding appears to be impossible. The 3–month laying period imposes further constraints with respect to timing of breeding attempts in relation to the onset of fasting. By the frequent resighting of individually marked birds at Marion Island, we examined the frequency of breeding and the relationships between timing, outcome and frequency in the same and in consecutive years. A total of 3101 adult King Penguins were banded between 1984 and 1991, yielding continuous breeding histories spanning a maximum of 5 years. Most penguins attempted to breed in consecutive years, although the likelihood of taking a year off increased with the number of consecutive attempts. In any one season, about 19% of potentially breeding adults did not breed. Early breeders were more likely to succeed than late breeders and comprised 84% of breeding attempts of known timing. Successful birds in one season usually bred late in the following season, whereas failed attempts were usually followed by an early attempt. Non-breeding was more likely to occur after a successful outcome than a failed one, and after a year off 93% of birds bred early. It is incorrect to refer to the King Penguin as a biennial breeder.     

THE BIOLOGY OF THE WAVED ALBATROSS DIOMEDEA IRRORATA OF HOOD ISLAND, GALAPAGOS

As a nesting species, the Waved Albatross Diomedea irrorata is restricted to Hood Island in the Galapagos archipelago where 12,000 pairs bred in 1971. Outside the islands the species occurs over the northern parts of the Humboldt Current. Two colonies were studied in detail (1970–1971). At the start of a season, males returned first to the colonies and defended a small territory. Copulation occurred without any elaborate ceremony and the female spent little time on land before laying. There was no fixed nest-site, even within a season, and birds moved their eggs considerable distances. This resulted in heavy egg losses. Younger birds bred later than older birds and laid longer but narrower eggs. The average incubation spell varied from four to five days at the extremes of the incubation period to 19 days in the middle. The average incubation and fledging periods were 60 and 167 days respectively. Pairs which lost an egg sometimes adopted the abandoned egg of another bird and successfully reared the chick. Most pairs nested in both seasons. Nesting success was extremely variable, both between years and between colonies. Between 1961 and 1971 at Punta Suarez, virtually no young were reared in four seasons. Even in 1970–71, where nesting success was good, some groups of birds deserted their eggs en masse whereas in neighbouring areas up to 80% of the pairs reared young. The main foods of the young were squid and fish. Birds did not moult wing and tail feathers at the breeding colonies, and about 50% retained some primaries for more than one season, suggesting that successful pairs had difficulty in fitting in a complete moult between breeding attempts. Old feathers were normally found among the inner primaries and at the next moult were preferentially replaced, though adjacent newer feathers were sometimes retained for another season. Some birds bred in their fourth years, but most not until a year or two older. Immatures were present at the colonies late in the breeding cycle, the youngest returning latest and remaining until the last young fledged. Survival of adults and young averaged at least 95% and 93% per annum over many years. Adults and young ringed in 1961 survived equally well. The significance of the timing of the return of immatures and of the large-scale desertion of eggs, apparently not due to food shortage or disturbance, is discussed.     

Estimating dispersal distributions at multiple scales: within‐colony and among‐colony dispersal rates,distances and directions in European Shags Phalacrocorax aristotelis

Knowledge of the rate, distance and direction of dispersal within and among breeding areas is required to understand and predict demographic and genetic connectivity and resulting population and evolutionary dynamics. However dispersal rates, and the full distributions of dispersal distances and directions, are rarely comprehensively estimated across all spatial scales relevant to wild populations. We used re‐sightings of European Shags Phalacrocorax aristotelis colour‐ringed as chicks on the Isle of May (IoM), UK, to quantify rates, distances and directions of dispersal from natal to subsequent breeding sites both within IoM (within‐colony dispersal) and across 27 other breeding colonies covering 1045 km of coastline (among‐colony dispersal). Additionally, we used non‐breeding season surveys covering 895 km of coastline to estimate breeding season detection probability and hence potential bias in estimated dispersal parameters. Within IoM, 99.6% of individuals dispersed between their natal and observed breeding nest‐site. The distribution of within‐colony dispersal distances was right‐skewed; mean distance was shorter than expected given random settlement within IoM, yet some individuals dispersed long distances within the colony. The distribution of within‐colony dispersal directions was non‐uniform but did not differ from expectation given the spatial arrangement of nest‐sites. However, 10% of all 460 colour‐ringed adults that were located breeding had dispersed to a different colony. The maximum observed dispersal distance (170 km) was much smaller than the maximum distance surveyed (690 km). The distribution of among‐colony dispersal distances was again right‐skewed. Among‐colony dispersal was directional, and differed from random expectation and from the distribution of within‐colony dispersal directions. Non‐breeding season surveys suggested that the probability of detecting a colour‐ringed adult at its breeding location was high in the northeastern UK (98%). Estimated dispersal rates and distributions were therefore robust to incomplete detection. Overall, these data demonstrate skewed and directionally divergent dispersal distributions across small (within‐colony) and large (among‐colony) scales, indicating that dispersal could create genetic and demographic connectivity within the study area.     

The social organization and behaviour of the Hoatzin Opisthocomus hoazin in central Venezuela

The social organization and behaviour of the Hoatzin Opisthocomus hoazin , a cooperatively-breeding folivorous bird, was studied in the central plains (llanos) of Venezuela. In this area Hoatzins nested in communal social units of two to eight individuals. Units were usually composed of a breeding pair and up to six helpers at the nest. Helpers, usually offspring retained from the previous years' nesting, aided in all breeding activities of their social unit except egg production. On the study site, Hoatzin units defended extremely small, all-purpose territories along watercourses during the rainy (breeding) season, but migrated up to 2 km to areas with permanent water during the dry season. Nesting extended from early May to October. Nest and egg measurements and growth rates of young are provided. Nesting success was low (27%), primarily due to predation by Cebus olivaceus and several other species. Annual survival of adults and young was high. Young did not breed during their first year; 90% of yearlings remained on their natal territories as helpers. Females appear to be the dispersing sex. The results are discussed in relation to previous work on the Hoatzin. The demography of the study population fits the criteria for several recent theories regarding the evolution of cooperative breeding in birds.     

SEASONALITY OF MARABOU STORKS LEPTOPTILOS CRUMENIFERUS IN EASTERN AFRICA

Nesting by Marabou Storks in eastern Africa is seasonal, and so are assemblages of non-breeding birds at places with a regular supply of food. In Uganda, where temperatures and day-length are almost constant, Marabous have nested at about the same time each year, despite considerable variations in rainfall from year to year. However, rainfall can have a modifying effect, delaying egg-laying by up to a few weeks. The timing of egg-laying varied regionally throughout eastern Africa, but in general nesting began during a dry season and continued into the next wet season. In drier areas the timing of nesting was more complex. Regional variations in the nesting season, and in the sizes of feeding assemblages, are consistent with north-south movements of individual Marabous to or across the equator, enabling them to avoid the late wet season and early dry season. These are times when the supply of natural foods is likely to be least. Figure 6 summarizes the data and indicates probable movements. In the wetter areas the main northwards movement is in October-November, returning four to six months later. In driet areas the timing is almost reversed.     

Site use and fidelity in the Common Guillemot Uria aalge

The site fidelity of 470 colour-ringed Common Guillemots Uria aalge with at least 1 year of breeding experience was followed on the Isle of May from 1982 to 1993. On average, 85.7% of birds recorded breeding at a site in any year were present at the same site in the following season. Of those which did not retain their site, 35% had moved to another site, 25% were nonbreeders and 40% were not seen. Site- fidelity of birds which returned to the colony the next year was 91%. There were no significant age or sex effects, but there were significant (and unexplained) year and area effects. Most birds which changed sites moved less than 2 m. Some birds which obtained a new site improved their nesting success, but many others became nonbreeders; it is speculated that the former chose to move site, whilst the latter had been evicted.     

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.     

High survival rate and site fidelity in the Siberian Tit Parus cinctus, a focal species of the taiga

The Siberian Tit Parus cinctus population of Finland, and probably of the whole of Fennoscandia, has declined dramatically during this century. Understanding its population dynamics is essential for its conservation. We studied annual survival rate and dispersal distance of both breeding and fledgling Siberian Tits during 1989-97 in a moderately managed forest habitat near the southern border of its range in Kuusamo, northeastern Finland. Breeding density was low, averaging 0.51 pairs/km in a nestbox area of about 42 km². This was probably an underestimate, because we did not search for nests in natural holes. However, following its population decline, overall densities at the southern border of the range are low. The study area was, however, suitable breeding habitat as reflected by their high nesting success. Brood size at fledging averaged 7.45 young, and reproductive output was 6.16 young per breeding pair, including failed nests. Clutch size adjustment was successful among pairs producing fledglings because, on average, 92.6% of the eggs laid produced young in successful broods. Median distance between consecutive breeding attempts was 100 m for both males and females (range 0–2500 m and 0–6000 m, respectively). Natal dispersal distance was significantly longer in females than in males. We applied Cormack-Jolly-Seber modelling to estimate survival and recapture probabilities separately. Survival of breeding birds was not sex-related, averaging 0.69 annually. Some of the ringed fledglings (3.0%) were later captured as breeders in the area. This is an underestimate of local survival rate due to incomplete recapturing of breeding birds. The implications of these results with respect to the conservation status of the species are discussed.     

Postfledging dispersal in the endangered Lesser Kestrel Falco naumanni

Much is known about the breeding period of the threatened Lesser Kestrel, but little of the postfledging period. Here, I examine the postfledging dispersal of juvenile Lesser Kestrels, based on all ringing recoveries of Lesser Kestrels ringed as nestlings in Spain and recovered before September (migration) of the same year. Of 28 juveniles recovered, 19 (67.9%) dispersed and their median recovery distance was 210 km (range 41–578 km), with significantly northern directions. No difference was found in the dispersal distance between individuals ringed as nestlings in mid-north and mid-south Spain, nor was any correlation found between the recovery distance and ringing latitude. These findings for postfledging dispersal in juvenile Lesser Kestrels seem in accordance with predictions of a mental map hypothesis for homing, but they do not exclude food as a potential factor influencing such movements. However, these postfledging movements cannot be explained by the hypothesis of gathering information for identifying a future breeding site.     

Breeding dispersal and site-fidelity in three monogamous wader species in the Western Isles, U.K.

Adult and post-natal breeding-dispersal movements of Redshank Tringa totanus , Dunlin Calidris alpina and Ringed Plover Charadrius hiaticula were quantified in west Scotland. Data from 373 returning birds marked as breeding adults and 142 returning birds marked as chicks are presented. Unlike most previous studies, this study measured dispersal movements up to 40 km and attempted to overcome distance-related biases. For each species, adult males were significantly more nest site-faithful between years than were adult females. Likewise, first-time breeding males bred significantly closer to their natal site than did females. The settlement intensity per unit area of habitat showed marked differences between species, age classes and sex in the relative attractiveness of potential areas at different distances to settling birds. Adult dispersal was negatively and significantly related to breeding success in the previous year and positively related to capture on the nest in the previous year. Dispersal movements of adult Ringed Plover breeding on unstable cultivated habitats were significantly related to habitat quality (measured in terms of nest survival) and were always to habitat of better or equal quality.     

Limited dispersal by Nazca boobies Sula granti

We documented natal and breeding dispersal at several spatial scales by Galápagos Nazca boobies Sula granti, a wide‐ranging pelagic seabird. We found exceptionally low degrees of both types of dispersal despite these birds’ vagility. Median natal dispersal distances were 26 m and 105 m for males and females, respectively. Median breeding dispersal distances for both sexes were 0 m. No natal or breeding dispersals occurred from our study site at Punta Cevallos, Isla Española to six other colonies in the Galápagos, but we did document four long‐distance natal dispersals from Punta Cevallos to islands near the South American coast. Recaptures and dead recoveries of ringed birds showed long distance non‐breeding movements to the Central American coast and elsewhere in the eastern Pacific, contrasting with the very limited dispersal to breeding sites.     

BREEDING BIOLOGY OF SOUTHERN ELEPHANT SEALS IN PATAGONIA

Abstract: Elephant seals breed in Patagonia (Península Valdés, Argentina) from late August to early November, reaching peak numbers during the first week in October. Observations of this population over the past ten years yielded similar results. Eighty percent of the pups were born by 2 October. Most (96%) of 663 females marked during three breeding seasons gave birth to a pup. Females stayed on land a mean of 28 d, gave birth 6 d after arrival, nursed their pups for 22 d, and copulated a mean of 2.5 times 20 d after parturition and 2 d before departure. Copulations peaked during the third week in October. Males spent 57–80 d on land fasting and defending harems of up to 134 females (median 11–13 females, depending on year). Most (96%) marked females that gave birth ( n = 636) also weaned their pups successfully. Pup sex ratio was unity. Harems were smaller and breeding occurred about three weeks earlier in Patagonia than in other colonies. Thermal conditions, day length and food availability may explain clines in the timing of breeding events between populations, Other parameters of the breeding season for the expanding Patagonia colony are similar to those for declining southern elephant seal populations elsewhere.     

THE SEASONAL MOVEMENTS OF GURNEY'S SUGARBIRD PROMEROPS GURNEYI IN THE LYDENBURG AREA,TRANSVAAL

De Swardt, D. H. 1991. The seasonal movements of Gurney's Sugarbird Promerops gurneyi in the Ly-denburg area, Transvaal. Ostrich 62: 40–44.

The seasonal movements of Gurney's Sugarbird Promerops gurneyi were studied in the Lydenburg area, eastern Transvaal, South Africa. Influx into the suburban habitat occurred durin the winter when the birds left the mountains at the end of the flowering period of Protea roupelliae. Birifs were mistnetted and each adult colour-ringed with a unique combination for individual recognition. In all, 256 Sugarbirds were ed in the mountain habitat and 50 in the suburban habitat. Of the unringed individuals 22,2 % were ted on cliffs with aloes and 79,3 % around P. roupelliae clumps late in the season. Of the ringed birds 25 (9,7%) were retrapped at sites in the mountain and 10 (3.9%) showed seasonal movements; 6 (8,3%) were recaptured in the same town localities where originally ringed. Mean distance moved was 7 km. An overall recapture rate of 7,5% was recorded during this study. When nectar became scarce the birds started moving away and utilized other food sources. Protea roupelliae showed a flowering peak from October to February which coincided with the sugarbirds' breeding season.     

THE WINTERING AND MOULT OF RUFFS PHILOMACHUS PUGNAX IN THE KENYAN RIFT VALLEY

Some 5700 Ruffs were ringed in the southern Kenyan rift valley during 1967–79, mainly at Lakes Nakuru and Magadi. These have produced 15 recoveries outside East Africa, 14 in Siberia between 73° and 154°E and one in India. Adult males returned to Kenya mainly during August, and females during late August and early September. Females greatly outnumbered males at all times. Most wintering males departed late in March and early in April, but females not until about a month later. First-year birds appeared from the end of August, but remained in low numbers until late October or November. Most departed during April and May, but a few females oversummered. First-year birds typically accounted for about 25% of the wintering Nakuru females, but about 50% of those at Magadi. At both sites they accounted for a higher proportion of male birds than females. Most of the birds at Nakuru throughout late August to May appeared to be local winterers, and many individuals remained in the area for many months each year. Retrapping indicated that approximately 60% of each season's birds returned the following season. Adult males and most adult females commenced pre-winter wing moult before arrival, but completed most of it in Kenya. Males moulted 3–4 weeks ahead of females, and most had finished before December. Females typically finished during December and early January. Most second year birds timed their pre-winter moult similarly to older adults. Suspension was recorded in over 15% of all moulting birds examined. Adult pre-summer moult involved most or all of the tertials, some or all of the tail feathers, most of the inner wing coverts and the body and head plumage. It occurred mainly during January to March (males) or February to April (females), although tertial renewal commonly began a month earlier. Males showed no sign in Kenya of the supplementary prenuptial moult. First-year birds moulted from juvenile into first winter body plumage during late September to November. They underwent a pre-summer moult similar in extent and timing to that of adults, and again about a month earlier in males than females. Spring feathers acquired were often as brightly coloured as those of adults. About 15% of first-year birds renewed their outer 2–4 pairs of large primaries during January to April. Adult and first-year birds fattened before spring departure, commonly reaching weights 30–60% above winter mean. Weights of adult males peaked early in April, those of adult females early in May, and those of first-winter females later in May. Weights were relatively high also during August and September. This was due to the arrival of wintering birds carrying ‘spare’ reserves, and also apparently to the presence of a late moulting fattening passage contingent. The wing length of newly moulted adults was about 3 mm longer than that of newly arrived first-year birds, but there was no evidence of an increase in the wing kngth of adults with successive moults. Adult wing length decreased by 4–5 mm between the completion of one moult and the middle stages of the next. The migrations and annual timetable of Kenyan wintering Ruffs are discussed, and their moult strategy is compared with that of other Holarctic waders.     

THE WINTERING AND MIGRATION OF PALAEARCTIC PASSERINES AT KAMPALA, SOUTHERN UGANDA

Palaearctic passerines were observed and trapped over three seasons near Kampala, in southern Uganda. Passage migration and wintering are described.
Only 11 species were encountered at all frequently. Three of these were common as passage migrants only, the rest remained in numbers throughout the northern winter. Most migrants reached Kampala during October and November, but the majority of Acrocephalus warblers appeared later. Spring departure commenced at the end of March, and continued throughout April. Autumn passage was in progress from late September to December, but appreciable spring movement was confined to a period of a few weeks only.
Ringing revealed that most wintering warblers were highly sedentary, and that a high proportion of surviving birds returned to the same site in successive winters. No fewer than 12–5% of the 220 Acrocephalus warblers ringed during 1966/67 were retrapped during the following season.
Wing measurements were recorded for most migrants trapped. Plumage details were noted, and representative specimens of several species were subsequently compared with museum series. It was concluded that most migrant passerines which occurred at Kampala were of eastern origin.
Migration times were compared with those recorded for some other areas. The spring movement from southern Uganda to the Middle East tends to be more rapid than the return journey. Some species apparently spend weeks or even months of the autumn in northeast Africa before reaching the equator,     

Behavioral and Social Structure Effects on Seed Dispersal Curves of a Forest‐Interior Bulbul (Pycnonotidae) in a Tropical Evergreen Forest

Movement patterns of animals can vary dramatically as a function of their reproductive cycle or social structure; however, little is known about how changes in the social structure of dispersers affect patterns of seed dispersal. We examined the movement patterns of the forest‐dwelling and cooperatively breeding Puff‐throated Bulbul (Alophoixus pallidus) in relation to different stages of their reproductive cycle, time of day, and group size, to determine potential impacts on the shape and scale of dispersal curves generated using a combination of gut passage time and displacement distance data. There were significant differences in dispersal distances depending on group size, season (breeding, non‐breeding), incubation (vs. other times of the year), and time of the day. The estimated median seed dispersal distance was 28 m. The median dispersal distances produced by birds in larger groups were longer than those of smaller groups (29 m vs. 25 m). During the breeding season, median dispersal distances were longer than during the non ‐ breeding season (31 m vs. 25 m), but the median dispersal distances were significantly shorter during incubation than during outside incubation (24 m vs. 28 m). The median dispersal distance produced in the early morning (30 m) was also longer than that of other times of the day (23 m late morning, 28 m early afternoon, and 26 m late afternoon). This study suggests that various aspects of an animal's behavior are likely to have significant effects on seed shadows and that this may vary significantly even among individuals of the same species.     

Early age at first breeding and high natal philopatry in the Red‐necked Nightjar Caprimulgus ruficollis

Recruitment rates, natal philopatry and the onset of breeding activity are documented for the first time for the order Caprimulgiformes. Of 171 Red‐necked Nightjars Caprimulgus ruficollis ringed as fledglings in southwestern Spain between 2008 and 2011, 31 (18%) were later recovered. Females tended to disperse slightly further (680 m) than males (570 m), and no individual from the study site or nearby locations was ever recovered outside the area where it hatched, suggesting high natal philopatry. Most males (94%) and females (73%) recruited into the breeding population in their first year of life, and only a few individuals were not recovered until their second (10%) or third (7%) year of life. In contrast to most long‐lived birds, nearly all (95.5%) Red‐necked Nightjars started to reproduce in their first potential breeding season.