The effect of migration strategy and food availability on White Stork Ciconia ciconia breeding success

In the mid 1970s, the breeding populations of the migrant White Stork Ciconia ciconia were close to extinction in the northeastern region of France (Alsace). A re-introduction project was implemented, resulting in the year-round settlement of some individuals in the region, which rely on additional food supplied by humans during the winter. Today, both resident and migrant birds breed in the same areas and take food from rubbish dumps and humans (farmers). The effects of these anthropogenic influences, altering Stork behaviour, on Stork reproductive success are not known. The aim of this study was to test the influence of bird status (resident vs. migrant) and food availability (control nests vs. nests that benefit from high food supply) on reproductive success. In control nests, the mean laying date was earlier in resident than in migrant White Storks. There was also a clear seasonal decline in clutch size. For all nests, the numbers of eggs and hatchlings were higher in resident birds than in migrants, which can be attributed to the earlier breeding of resident Storks. The large broods of resident birds showed a high mortality rate, leading to the same fledgling success (fledglings/hatchlings) and number of fledglings as in migrants. Fledgling success and the number of fledglings were higher for nests close to a reliable food supply. In summary, although resident birds can breed earlier and produce more eggs than migrants, we found no advantage in terms of number of fledglings. The higher mortality rate of chicks found in pairs with a large brood could be caused by the deterioration of their habitat. Thus, the year-round settlement of Storks may not present a biological advantage if the quality of their habitat is not guaranteed by the conservation of their grasslands.     

Population fluctuations and survival of Great Tits Par us major dependent on food supplied by man in winter

The 16-year data of a Great Tit population, breeding and overwintering in a nest box area at Oulu, northern Finland, were studied to reveal the factors governing the annual fluctuations in density and local survival. The breeding density at Taskila was high after a cold spring (March-April) and a warm August the year before was also followed by a large breeding population. A similar relationship resulted for the local survival of fledglings, and there was a tendency for immigrant yearlings to settle to breed in large numbers when the spring was cold. In the north, Great Tits cannot survive the winter in the forests but gather around feeding tables near human settlements. A cold spring evidently suppresses the birds' dispersal before the breeding season. For a population which is time-limited, it is adaptive to remain in order to breed nearby instead of searching for territories out in the forests when conditions become favourable late in the spring. Thus, the negative correlation between spring temperature and the size of the following breeding population may be the result of a spatial distribution of juveniles achieved by behavioural responses to unfavourable conditions. The causality behind the high survival of resident juveniles after a warm August may be attributable to food availability during the time when the birds undergo their postjuvenile moult, which is an energy-demanding process. The survival rate of breeding adults was highly dependent on the intensity of nightly predation upon individuals roosting in nest boxes. Stoats Mustela erminea, the prime predators, preyed on tits when the populations of their main prey species, small rodents, were low. When the effect of predation was eliminated, the density-dependent survival of adult birds disappeared. During low predation years the adult survival rate was negatively related to the number of fledglings produced per pair; this suggests that investment in descendants is a substantial survival cost for reproducing individuals.     

Breeding success and chronology of Wood Storks Mycteria americana in northern and central Florida, U.S.A.

The breeding success and chronology of Wood Storks Mycteria americana were studied at eight colonies in northern and central Florida during 1981–1985. Mean ± s.d. clutch size for all colony-years was 3.07 ± 0.56 (n = 2694 nests), with three-egg clutches (72%) most frequent. Mean clutch size among all colonies and years ranged from 2.73 ± 0.55 to 3.41 ± 0.61. Many colonies exhibited significant negative trends in clutch size with, hatching date because of a proportional decrease in four-egg clutches later in the season. Mean colony clutch size was not correlated with nest numbers, nesting density or mean hatching date within most years. Mean ± s.d. number of fledglings for all colonies and years was 1.29 ± 1.16 fledglings per nest (n = 2812 nests). Mean annual fledging rates in colonies ranged from 0 (colony failed) to 2.66 fledglings per nest. Most breeding failure occurred prior to egg hatching, and the second highest mortality occurred between hatching and 2 weeks of age. Four-egg clutches fledged more storks than three-egg clutches, which in turn were more successful than two-egg clutches. However, all clutch sizes showed similar fledgling per egg rates. The seasonal decline in productivity was associated proportionally with smaller clutch sizes later in the breeding season. An increase in mean hatching date was correlated with an increase in latitude. There was greater within-year breeding synchrony among colonies than interyear breeding synchrony within each colony. Breeding synchrony was not correlated with mean hatching date, latitude, longitude, nest numbers or nesting density.     

Survival during the Breeding Season: Nest Stage,Parental Sex,and Season Advancement Affect Reed Warbler Survival

Avian annual survival has received much attention, yet little is known about seasonal patterns in survival, especially of migratory passerines. In order to evaluate survival rates and timing of mortality within the breeding season of adult reed warblers (Acrocephalus scirpaceus), mark-recapture data were collected in southwest Poland, between 2006 and 2012. A total of 612 individuals (304 females and 308 males) were monitored throughout the entire breeding season, and their capture-recapture histories were used to model survival rates. Males showed higher survival during the breeding season (0.985, 95% CI: 0.941–0.996) than females (0.869, 95% CI: 0.727–0.937). Survival rates of females declined with the progression of the breeding season (from May to August), while males showed constant survival during this period. We also found a clear pattern within the female (but not male) nesting cycle: survival was significantly lower during the laying, incubation, and nestling periods (0.934, 95% CI: 0.898–0.958), when birds spent much time on the nest, compared to the nest building and fledgling periods (1.000, 95% CI: 1.00–1.000), when we did not record any female mortality. These data (coupled with some direct evidence, like bird corpses or blood remains found next to/on the nest) may suggest that the main cause of adult mortality was on-nest predation. The calculated survival rates for both sexes during the breeding season were high compared to annual rates reported for this species, suggesting that a majority of mortality occurs at other times of the year, during migration or wintering. These results have implications for understanding survival variation within the reproductive period as well as general trends of avian mortality.     

Breeding and survival of New Zealand Pigeons Hemiphaga novaeseelandiae

The breeding and survival of New Zealand Pigeons Hemiphaga novaeseelandiae were studied by radiotelemetry at three contrasting native forest sites in the North and South Islands of New Zealand. At each site, mean annual productivity was low (0-0.12 fledglings/adult) in relation to the mean annual rate of adult mortality (0.18-0.53). Losses of eggs and chicks to introduced mammals were the main identified causes of nest failure. Causes of adult mortality included episodic predation by introduced mammals and apparent starvation in spring at one site. At the most intensively-studied site (Pelorus Bridge), where 75 birds were radiotagged over 7 years, there was a marked annual variation in breeding success (0-0.3 fledglings/adult), including one season (1986–1987) when no breeding activity was detected at all. New Zealand Pigeons were legally hunted in the past, but our results indicate that harvesting is unlikely to be sustainable under current ecological conditions.     

Nest predation reduces benefits to early clutch initiation in northern cardinals Cardinalis cardinalis

Life history theory and empirical studies suggest that early breeding confers higher reproductive success, but the extent to which this advantage can be generalized to human‐dominated systems and across species is less well understood. We studied the fitness consequences of clutch initiation for 181 female northern cardinals Cardinalis cardinalis and 1228 nests in forests within urban and rural landscapes of Ohio, USA between 2004–2007. Cardinals that bred earlier made significantly more nesting attempts, but cumulative number of young fledged was similar to that of later‐breeding individuals. The expected number of fledglings produced per successful nest was unrelated to date and remained ~1.8 fledglings across the season, despite the fact that nest survival rates improved dramatically as the season progressed. Because the probability of resighting breeding individuals in subsequent years was unrelated to first clutch initiation date, we have no evidence that clutch initiation affected adult survival. The absence of a clear benefit to early breeding appears to be a consequence of high rates of nest predation early in the breeding season.     

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.     

High annual variability in reproductive success and survival of an Antarctic seabird,the snow petrel Pagodroma nivea

Demographic parameters were estimated for snow petrels Pagodroma nivea nesting at Pointe Géologie Archipelago, Adélie Land, Antarctica between 1963 and 1990; 21 years of data on adult survival and 27 years of data on breeding success are available. The average age of first return and first breeding were 8.1 and 9.9 years respectively and there was no signifcant difference between the sexes. The overall breeding success averaged 51.3% and was very variable between years (21–80%). Breeding failure was mostly due to incubation failure and annual breeding success was negatively correlated with average snow falls in October–November and October–March. Breeding frequency was very low, averaging 52% of seasons during a reproductive lifetime. Good quality sites, with high occupancy rate and high breeding success were few in the study plots. Poor years in 1966–1967, 1976–1977 and 1983–1984, with low breeding success, very low proportions of nets with breeding attempts and high numbers of non-breeders, occurred 1 year after large-scale El Niño Southern Oscillation (ENSO) events. Snow petrels exhibited very low philopatry. Only 45 birds have been recovered in the study plots from a total of 1115 banded fledglings giving an estimated rate of return of 12.9% between fledging and 3 years old. Annual survival between 3 and 10 years was 91.4%. Annual adult survival (93.4%), though variable, was low during poor years of 1977–1978 and 1983–1984. Adult survival of males (94.7%) was not significantly different from that of females (93.9%). Over the study period, the population of Pointe Géologie was stable. Using the estimated parameters, a Leslie model gave a growth rate of 0.948%, which was probably compensated by immigration (5.7% per year). Restricted numbers of good-quality sites at the place of birth could have led young birds to prospect other colonies and could have selected low philopatry. High adult survival, strong site tenacity and capacity to spread breeding over a long lifetime are probably part of the adaptive strategy of this small fulmarine petrel facing highly variable environmental conditions.     

The effect of age and year on the survival of breeding adult Great Skuas Catharacta skua in Shetland

The survival rates of breeding adult Great Skuas Catharacta skua were examined at Foula, the largest colony in the world, where numbers have been declining since the late 1970s. Resightings of colour-ringed breeding adults over a 12-year period were analysed using Cormack-Jolly Seber models to estimate survival rates. Annual survival rates averaged 0.89 but varied among years between 0.82 and 0.93, with annual variations being temporally associated with variations in sandeel abundance during the breeding season. Most birds appeared to die outside the breeding season and so it is possible that nutritional stress and reproductive costs of breeding in years of poor food supply affect survivorship on migration or in the wintering range. Survival rates of adult Great Skuas were affected by their age according to a quadratic equation, with survival increasing significantly with age from 0.73 in 5-year-old-birds to between 0.85 and 0.96 in birds from 7 to 22 years old, with a sharp decline to between 0.75 and 0.87 in birds over 22 years old. Year effects were evident when controlling for age, indicating that annual variations in survival rates are not explained by changes in age-composition of the marked population among years.     

Survival rates of Redshank Tringa totanus wintering on the Moray Firth

Long-term mark–recapture data were used to estimate the annual survival rates of Redshank wintering on the Moray Firth in Scotland. Survival modelling required the exclusion of all birds caught during the main passage months (August, March and April), and a highly variable annual catching effort limited the precision of annual survival estimates. Survival rates of juvenile Redshank (between the first and second winters of life) varied markedly from year to year and averaged 43% (se 3.6%). Adult survival rates were less variable between years and were age-dependent, with 67% (se 5.0%) surviving and returning between the second and third winters of life, compared to 74% (se 1.4%) for older birds. Year-to-year variation in adult survival was weakly (and negatively) related to the number of snow days in winter. Year-to-year variation in first-year survival was non-linearly related to winter rainfall, with low survival during dry (and cold) winters, higher survival during winters with average rainfall and lower survival during wet winters. Having accounted for these weather relationships there was no evidence that survival was related to the size of the local wintering Redshank population. Organized annual ringing programmes of wintering waders on British estuaries have the potential to monitor long-term changes in survival rates and productivity. Although constant effort sampling may be difficult to achieve for wintering waders, the utility of mark–recapture data collected on estuaries is likely to depend heavily on careful study design.     

BREEDING OF THE WHITE-BACKED AND RÜPPELL'S GRIFFON VULTURES, GYPS AFRICANUS AND G. RUEPPELLII

The breeding season of two species of griffon vultures are described. Rüppell's Griffon Vulture lays 2–3 months earlier than the White-backed Griffon. Young birds were hand-reared to determine their food requirements during growth; these estimates were combined with the food requirements of adult birds to make an estimate of the amount of food a parent bird needs to obtain when it is rearing young. The amount of food actually obtained by a group of birds was recorded from the size of the crops of birds returning to the breeding colony in the afternoon. The comparison of the estimates of the food obtained and the food required through the breeding season suggested that there may be a period during rearing when there was insufficient food available to satisfy the food requirements of both chick and adult. Chicks were found to have a very high survival rate and were probably receiving sufficient food. Presumably adult birds were not therefore receiving sufficient food, and the examination of a sample of adult birds for body condition through the breeding season showed a clear decline in their fat deposits. It was considered that in both species, breeding was timed so that the young left the nest at a period in the year when food conditions were good and the young birds could feed with little competition from adults. The parent birds therefore had to rear young during a season in the year when food conditions were not always adequate and they had to rely on utilising fat reserves. The food conditions for vultures during this study were probably favourable and during years of food shortage breeding may become impossible, or restricted to the most aggressive and dominant individuals.     

The demography of a newly established Osprey Pandion haliaetus population in France

Using long‐term mark–resighting data acquired over 27 years in continental France, we estimated demographic parameters and modelled the dynamics of a newly established population of Ospreys Pandion haliaetus using a life‐history model. We then performed prospective and retrospective analyses to estimate the sensitivity of the population growth rate to demographic parameters, and to quantify their contribution to the observed variation in abundance. The observed population growth rate was estimated at 1.150 (from one to 38 pairs in the period 1985–2011), and the stochastic population growth rate was estimated at 1.156. The number of fledglings per nest made the largest contribution to the variance of the observed population growth rate. Breeding productivity was stable across years. In contrast, the prospective analysis indicated that the sensitivity of the population growth rate was greatest for immigration and adult survival. Our results suggest that the increase of a new and recently established breeding population of Ospreys was mainly driven by local dynamics (high productivity and high proportion of breeding individuals), with no sign of density‐dependence except for juvenile survival. This probably reflects highly favourable conditions for breeding. Our results show that productivity can be a major driver in recovering raptor populations, and conservation work should aim to protect occupied nest‐sites and their surrounding habitat and to maintain highly favourable foraging areas in the vicinity of breeding sites.     

Postfledging Survival and Development of Juvenile Lilac-Crowned Parrots

Abstract: We fitted radiotransmitters to 68 lilac-crowned parrot (Amazona finschi) fledglings from 1996 to 2003 to determine the survival and development of juveniles during their first year after leaving the nest. Overall, first-year survival was 73% (CI = 53–94%) and all mortalities occurred within 5 weeks of fledging, with highest mortality in the first week postfledging. Survival varied between years, influencing recruitment of independent young in the population. Nesting lilac-crowned parrots produced 0.70 independent young per egg-laying pair during 1996–2003. Lowest productivity of 0.25 independent young per pair occurred in 2003, with 40% postfledging survival. Juvenile development after fledging was characterized by variations in mobility, distance from the nest, and separation distance between siblings. Mobility and distance of young birds from the nest increased linearly with months postfledging. The first 2–3 weeks after fledging were characterized by low mobility and survival of young parrots, making this the most critical phase postfledging. The dependency period for young parrots extended to 4–5 months postfledging and was characterized by increased mobility and low separation between siblings, as juveniles traveled in family groups. Independence occurred in month 5 and was marked by a significant increase in mobility and separation between siblings, indicating the break-up of family groups. The first weeks after leaving the nest were crucial for survival and highlight the need for secure habitats where fledglings can improve flight and locomotory skills. The 4–5-month dependency of young parrots may be a key period for development, enhancing survival, and establishment in the breeding population. Release programs need to replicate learning and development acquired during the postfledging dependency phase to enhance survival of captive-reared psittacines. Researchers should conduct surveys of parrot group sizes during the dependency period 1–4 months after the end of nesting to provide reliable demographic data on annual recruitment of wild populations.     

The magnitude and timing of migration by soaring raptors, pelicans and storks over Israel

The magnitude and timing of the autumn and spring migrations of 35 species of medium-and large-sized raptors, White Pelicans Pelicanus onocrotalus and White Storks Ciconia ciconia were studied in Israel. Observations were carried out from the ground by a line of observers covering most of the width of Israel across the line of migration and by radar. There was a high correlation between the counts obtained by ground observers and by radar. On average, about half a million raptors (mainly Lesser Spotted Eagles Aquila po-marina, Honey Buzzards Pernis apivorus and Levant Sparrowhawks Accipiter brevipes), 250,000 White Storks and 70,000 White Pelicans passed during autumn, and about a million raptors (mainly Honey Buzzards, Steppe Buzzards Buteo vulpinus, Steppe Eagles Aquila nipalensis and Black Kites Milvus migrans) and 450,000 White Storks passed during spring. Peak numbers were higher–over a million raptors and half a million White Storks. There was high interyear variation in the number of migrants recorded during the study, probably caused by weather and counting efforts. For some species, the whole world (Lesser Spotted Eagle and Levant Sparrowhawk) or Palaearctic (White Pelican) population passes over Israel during migration, allowing an estimate of the world populations of these species. Mean dates of arrival of most raptors are highly predictable, with confidence limits ranging between 1.5 and 5.5 days. The migration periods of White Storks and White Pelicans are longer and their mean day of appearance is less predictable (confidence limits range from 4.2 to 13.8 days). During autumn, 90% of the migrating populations of nocking species, such as Levant Sparrowhawk, Lesser Spotted Eagle, Honey Buzzard and Red-footed Falcon Falco vespertinus, pass within 13, 15, 16 and 18 days, respectively, while nonflocking species, such as Egyptian Vulture Neophron percnopterus, Marsh Harrier Circus aeruginosus and Short-toed Eagle Circaetus gallicus, generally take twice as long to pass. Similar passage periods were recorded in spring. For most species, the autumn migration period was longer than the spring migration period, probably because in autumn adults move before the young birds. Three factors affected the timing and spread of the migration wave: age at first breeding, diet and size of the breeding area.     

Satellite tracking of a White Stork from Italy to Morocco

Two young White Storks were tracked by satellite during a part of their first migratory journey from the nest colony (settled in Piedmont, NW Italy) to the wintering ground in Western Africa. Both birds left westward, but only one of the two birds provided reliable data which allowed the reconstruction of its migratory route along the coasts of France and Spain up to Morocco. A new aspect of the journey is that the bird did not pass from Europe to Africa at Gibraltar, the storks' known western route. Despite the storks' tendency to avoid flying over large stretches of sea, the tracked bird crossed the Alboran sea from De Gata Cape (Spain) to Tres Forcas Cape (Morocco), thus flying about 120 km over the open sea.     

The presence of kleptoparasitic fledglings is associated with a reduced breeding success in the host family in the barn owl

Fledgling birds sometimes abandon their own nest and move to neighboring nests where they are fed by host parents. This behaviour, referred to as ‘nest‐switching’, is well known in precocial birds that are mobile soon after hatching and can easily reach foster nests. In contrast, due to the difficulty of observing nest‐switching in territorial altricial birds, the causes and consequences of moving to others’ nests are poorly known in this group of birds. Nest‐switchers can be adopted by the foster parents or they can steal food from the host parents meant for their offspring, a form of kleptoparasitism, which may result in reduced breeding success of the host nest. In Israel, 12 barn owl fledglings left their natal nests and were found in 9 host nests out of 111 monitored nests (8.1%). Nest‐switchers that fledged earlier in the breeding season flew shorter distances to reach host nests probably because the density of nests with younger nestlings is higher early in the season. The number of host nestlings fledged and the percentage of nestlings fledged was lower in host nests than in nests without switchers. The occasional nest‐switchers were always older than host nestlings (respectively 80 and 50 days of age, on average) and host parents fledged fewer young when nest‐switchers occupied host nests with younger nestlings. This suggests that nest‐switchers are kleptoparasites because the presence of the older alien fledglings is associated with a lower breeding success of the host parents.     

Sex and migratory strategy influence corticosterone levels in winter-grown feathers,with positive breeding effects in a migratory pelagic seabird

To overcome unpredictable stressful transitory events, animals trigger an allostatic response involving the hypothalamic–pituitary–adrenal cortex. This hormonal response, which involves the release of glucocorticoids which in turn mediate between the main physiological mechanisms that regulate the energetic demands and resource allocation trade-off with behavioural responses to environmental perturbations and may ultimately lead to variation in fitness. We have used the Cory’s shearwater Calonectris borealis, a sexually dimorphic pelagic seabird with a partial migratory strategy, as a model bird species to analyse a number of traits related to the stress response. We investigated whether the activation of a stressful response, mediated by corticosterone, during the wintering period (1) correlated with the previous breeding success, (2) was affected by the migratory behaviour of male birds and (3) had consequences in the fitness of the birds. Corticosterone levels in feathers grown overwinter were analysed in 61 adult birds during three consecutive migratory periods (2009–2012) and in 14 immature birds in the wintering period 2010–2011. Moreover, the levels of corticosterone were analysed in experimental birds which were freed from their reproductive duties and compared with control birds which raised fledglings to the end of the breeding period. The results show that the levels of corticosterone were sex dependent, differed between years and were affected by the migratory strategy performed by the birds. The activation of the stressful response over the wintering period generated residual carry-over effects that positively affected the reproductive output in the subsequent breeding stage, a phenomenon previously undescribed in a long-lived pelagic seabird. Our study provides evidence that the analysis of corticosterone from feathers is a useful tool to evaluate carry-over effects in birds far away from breeding sites, opening new possibilities for future studies in this field.     

Does wintering north or south of the Sahara correlate with timing and breeding performance in black‐tailed godwits?

Migrating long distances requires time and energy, and may interact with an individual's performance during breeding. These seasonal interactions in migratory animals are best described in populations with disjunct nonbreeding distributions. The black‐tailed godwit (Limosa limosa limosa), which breeds in agricultural grasslands in Western Europe, has such a disjunct nonbreeding distribution: The majority spend the nonbreeding season in West Africa, while a growing number winters north of the Sahara on the Iberian Peninsula. To test whether crossing the Sahara has an effect on breeding season phenology and reproductive parameters, we examined differences in the timing of arrival, breeding habitat quality, lay date, egg volume, and daily nest survival among godwits (154 females and 157 males), individually marked in a breeding area in the Netherlands for which wintering destination was known on the basis of resightings. We also examined whether individual repeatability in arrival date differed between birds wintering north or south of the Sahara. Contrary to expectation, godwits wintering south of the Sahara arrived two days earlier and initiated their clutch six days earlier than godwits wintering north of the Sahara. Arrival date was equally repeatable for both groups, and egg volume larger in birds wintering north of the Sahara. Despite these differences, we found no association between wintering location and the quality of breeding habitat or nest survival. This suggests that the crossing of an important ecological barrier and doubling of the migration distance, twice a year, do not have clear negative reproductive consequences for some long‐distance migrants.     

Searching for potential wintering and migration areas of a Danish Barn Swallow population in South Africa by correlating NDVI with survival estimates

On the basis of correlation analyses between annual Normalised Difference Vegetation Index (NDVI) values in Africa and the annual survival rate estimated for a breeding population of barn swallows Hirundo rustica from Denmark, we identified potential wintering and migration areas in South Africa during December–February and March–May, when barn swallows commonly occur in South Africa. During December–February we identified potential wintering areas only in the western part of South Africa, in the Karoo. Potential areas in the central and eastern parts of the country were only identified during March–May. NDVI values in the Karoo during March–May explained most of the variance in annual adult survival rate of the population. The high ratio of European ringed barn swallows among controlled individuals in the Karoo was similar to the ratio that would be expected based on the number of ringed barn swallows and the population sizes of barn swallows in north-western European breeding populations. The level of this ratio in the Karoo was higher than in any other locality in the central and eastern parts of South Africa and Botswana, indicating that ringed birds from the eastern flyway are absent to a much smaller extent than ringed birds from the western flyway. This approach shows that the NDVI and survival method can focus ringing efforts to regions and areas that are likely to harbour specific breeding populations, thereby helping to identify potential wintering and migration areas for breeding populations of migratory birds.     

Growth and demography of a re‐introduced population of White‐tailed Eagles Haliaeetus albicilla

White‐tailed Eagles Haliaeetus albicilla became extinct in Britain in 1918 following prolonged persecution. Intensive conservation efforts since the 1970s have included the re‐introduction of the species to Britain through two phases of release of Norwegian fledglings in western Scotland in 1975–85 and 1993–98. Population growth and breeding success have been monitored closely to the present day, aided by the use of patagial tags to individually mark most released birds as well as a high proportion of wild‐bred nestlings. This study reviews the growth and demography of this re‐introduced population, and makes comparisons with other European populations. For the first time, we compare the demographic rates of released and wild‐bred birds in the Scottish population. Breeding success in the Scottish population has increased over time as the average age and experience of individuals in the population have increased, and success tends to be higher where one or both adults are wild‐bred. Current levels of breeding success remain low compared with some other populations in Europe, but similar to those in Norway where weather conditions and food availability are likely to be most similar. Survival rates in Scotland are similar to those recorded elsewhere, but survival rates of released birds are lower than those of wild‐bred birds, especially during the first 3 years of life. Despite the effect of lower survival rates of released birds in limiting overall population growth rate, the recent rate of growth of the Scottish population remains high relative to other recovering populations across Europe. Differences in demographic rates of wild‐bred and released birds suggest that in future re‐introduction programmes, steps to maximize the success and output of the earliest breeding attempts would help ensure the most rapid shift to a population composed largely of wild‐bred birds, which should then have a higher rate of increase.