Dietary analysis across breeding seasons of Eleonora's Falcon Falco eleonorae on the western coast of Algeria

The study of the contents of 318 Eleonora's Falcon Falco eleonorae pellets, collected from three islands off the western coast of Algeria, allowed us to identify 134 prey items. These are divided into 55 families, 21 orders and five classes. These represent 92 insect species, 39 birds, one mammal, one gastropod and one fish. In terms of abundance, insects constituted the main part of the diet (80.7%), followed by birds (18.5%), mammals (0.7%), and fish and gastropods (0.1% each). Among the insects, the Hymenoptera were the most numerous (45.2%), with ants being the most frequent family. In the class of birds, passeriforms were most frequently found (12.3%). The dominant family in the bird class was the Apodidae with a frequency of 5%. In terms of biomass, birds dominated with 98.1% of the total biomass, followed by insects with 1.2%. The diet of these Eleonora Falcons of Algeria was thus diverse, but varied with breeding status. The study of the dietary variation of the Eleonora Falcon during the breeding period shows that insects were most frequently encountered during the three breeding stages, whereas birds were highly consumed during the fledging stage, with frequencies of 43.9%.     

Cooperative breeding in birds: a comparative test of the life history hypothesis

In approximately 3.2% of bird species individuals regularly forgo the opportunity to breed independently and instead breed cooperatively with other conspecifics, either as non-reproductive ''helpers'' or as co-breeders. The traditional explanation for cooperative breeding is that the opportunities for breeding independently are limited owing to peculiar features of the species'' breeding ecology. However, it has proved remarkably difficult to find any common ecological correlates of cooperative breeding in birds. This difficulty has led to the ''life history hypothesis'', which suggests that the common feature of cooperatively breeding birds is their great longevity, rather than any particular feature of their breeding ecology. Here, we use a comparative method to test the life history hypothesis by looking for correlations between life history variation and variation in the frequency of cooperative breeding. First, we find that cooperative breeding in birds is not randomly distributed, but concentrated in certain families, thus supporting the idea that there may be a common basis to cooperative breeding in birds. Second, increases in the level of cooperative breeding are strongly associated with decreases in annual adult mortality and modal clutch size. Third, the proportion of cooperatively breeding species per family is correlated with a low family-typical value of annual mortality, suggesting that low mortality predisposes cooperative breeding rather than vice versa. Finally, the low rate of mortality typically found in cooperatively breeding species is associated with increasing sedentariness, lower latitudes, and decreased environmental fluctuation. We suggest that low annual mortality is the key factor that predisposes avian lineages to cooperative breeding, then ecological changes, such as becoming sedentary, further slow population turnover and reduce opportunities for independent breeding. As the traditional explanation suggests, the breeding habitat of cooperatively breeding species is saturated, but this saturation is not owing to any peculiar feature of the breeding ecology of cooperative breeders. Rather, the saturation arises because the local population turnover in these species is unusually slow, as predicted by the life history hypothesis.     

Is the range size of migratory birds constrained by their migratory program?

Aim Intuitively, species in which the individuals migrate long distances between summer and winter quarters should be more likely to disperse and colonize new breeding areas than resident species. However, it has repeatedly been noted that many bird species with large ranges are residents. This paradox was tested on land birds breeding in the boreal forest of the Palaearctic, the largest uninterrupted stretch of habitat on earth. Methods The longitudinal distribution of two land bird communities on each side of the Eurasian continent, in Scandinavia and eastern Siberia, were used to test whether migratory birds indeed have a lower colonization success than resident birds. Results The migratory species are significantly less likely than resident species to have a range including both regions. The pattern held true even after controlling for latitudinal effects and local abundance, and was also observed at the level of genus and family. Main conclusions The relatively low colonization success of migratory species into new breeding areas may be because these new areas require novel migratory programs (migratory distance, direction and timing) in order for the birds to reach suitable wintering grounds.     

Out of Gondwanaland; the evolutionary history of cooperative breeding and social behaviour among crows, magpies, jays and allies

Cooperative breeding is comparatively rare among birds in the mainly temperate and boreal Northern Hemisphere. Here we test if the distribution of breeding systems reflects a response to latitude by means of a phylogenetic analysis using correlates with geographical range among the corvids (crows, jays, magpies and allied groups). The corvids trace their ancestry to the predominantly cooperative 'Corvida' branch of oscine passerines from the Australo-Papuan region on the ancient Gondwanaland supercontinent, but we could not confirm the ancestral state of the breeding system within the family, while family cohesion may be ancestral. Initial diversification among pair-breeding taxa that are basal in the corvid phylogeny, represented by genera such as Pyrrhocorax and Dendrocitta, indicates that the corvid family in its current form could have evolved from pair-breeding ancestors only after they had escaped the Australo-Papuan shield. Within the family, cooperative breeding (alloparental care/family cohesion) is strongly correlated to latitude and its predominance in species maintaining a southerly distribution indicates a secondary evolution of cooperative breeding in the lineage leading away from the basal corvids. Multiple transitions show plasticity in the breeding system, indicating a response to latitude rather than evolutionary inertia. The evolutionary background to the loss of cooperative breeding among species with a northerly distribution is complex and differs between species, indicating a response to a variety of selection forces. Family cohesion where the offspring provide alloparental care is a main route to cooperatively breeding groups among corvids. Some corvid species lost only alloparental care, while maintaining coherent family groups. Other species lost family cohesion and, as a corollary, they also lost the behaviour where retained offspring provide alloparental care.     

Family-based winter territoriality in western bluebirds, Sialia mexicana: the structure and dynamics of winter groups

Winter residency is characteristic of the majority of cooperatively breeding birds, but the composition and dynamics of winter groups have been examined in relatively few. In 1996-1998, we examined winter territoriality in the western bluebird, a year-round resident that shows a limited degree of helping behaviour in central coastal California, U.S.A. In spring, most western bluebirds breed as socially monogamous pairs, but a small proportion of pairs (3-16%) have additional breeding-age males helping at the nest, usually assisting parents or brothers. We found that year-round residents commonly wintered in family groups that defended territories similar to those used in spring. Winter groups had an even sex ratio and formed early in the autumn, when hatch-year birds dispersed. More females than males left their natal groups to be replaced by an influx of immigrant hatch-year birds. Winter groups typically consisted of breeders and one or two sons from the prior breeding season along with one or more immigrant females. A second period of dispersal occurred in spring when winter groups broke up and most birds other than the breeding pair left the winter territory. When they bred, yearling males and females often bred with unrelated individuals from their winter groups. Sons were more likely to remain on the study area as yearlings when they wintered with both parents than when they wintered with just one parent. We suggest that young males stay the winter due to benefits of remaining in family groups on mistletoe-based winter territories. Subsequent localized dispersal of sons then leads to opportunistic kin-based interactions later in life. Copyright 2001 The Association for the Study of Animal Behaviour.     

2. NOTES ON THE MASKED WEAVER

Radiotelemetry is an important tool used to aid the understanding and conservation of cryptic and rare birds. The two bird species of the family Picathartidae are little-known, secretive, forest-dwelling birds endemic to western and central Africa. In 2005, we conducted a radio-tracking trial of Grey-necked Picathartes Picathartes oreas in the Mbam Minkom Mountain Forest, southern Cameroon, using neck collar (two birds) and tail-mounted (four birds) transmitters to investigate the practicality of radio-tracking Picathartidae. Three birds with tail-mounted transmitters were successfully tracked with the fourth, though not relocated for radio tracking, resighted the following breeding season. Two of these were breeding birds that continued to provision young during radio tracking. One neck-collared bird was found dead three days after transmitter attachment and the other neither relocated nor resighted. As mortality in one bird was potentially caused by the neck collar transmitter we recommend tail-mounted transmitters in future radio-tracking studies of Picathartidae. Home ranges, shown using minimum convex polygon and kernel estimation methods, were generally small (<0.5 km²) and centred around breeding sites. A minimum of 60 fixes were found to be sufficient for home range estimation.     

The life cycle of the Upland Goose Chloëphaga picta in the Falkland Islands

Upland Geese Chloëphaga picta were studied between 1977 and 1980, primarily around Darwin, East Falkland, in order to describe their breeding biology, moulting and adult survival. The population of breeding birds in a valley reached a peak from mid-September to late November when nesting took place. The average territory length was 240 m in five valleys. Breeding adults generally returned to breed in the same territory each year and with the same mate. Nests were on the ground, usually amongst whitegrass Cortaderiapilosa. The mean clutch size was 6-1, brood size was 5-1 and fledged family 3–9. Incubation took 30 days and the fledgling period was about 70 days. Most broods were raised in the nesting territory. Growth of goslings is described. The breeding success between laying and fledging was 0–34 (in 1977) and 0–29(in 1978), giving an annual production of 21 and 1–8 young per breeding pair. Fledglings remained in family parties through the autumn and winter and were evicted by their parents in early spring. Some siblings stayed together for short periods and then joined other non-breeders. Females started pairing at ten months of age and most were paired at 17–18 months. Some bred for the first time at 23 months. Males started pairing at about 20 months of age. Flightless moult (shedding) took place at ponds or in sheltered inlets of the sea, in flocks of up to several hundred birds. Flightless birds were found between 14 November and 11 February, though 50% were flightless between 26 November and 2 January. Individuals were flightless for 36 days. First-year birds were more synchronized in shedding than adults. The percentage of first-year males (in the male component) varied from 16-5 to 45-9% in shedding flocks, and significantly more males were present in some flocks. The flocks were composed of first-year and second-year birds too young to breed and failed breeders. The percentage of a shedding population which returned to the same site in successive years was 25-3 and 15-1% at two localities. The moult of other feather tracts is described. The annual survival rate of breeding adults was 82%. A model of the population dynamics is presented. The current level of culling to control the goose population is less than the number which must die each year to maintain a stable population.     

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.     

Cooperative breeding in corvids (Passeriformes,Corvidae)

The family of corvids differs from most other passerines by the significant number of species (at least 33) in which the feeding of nestlings and fledglings involves not only parents, but also individuals from their already grown broods (one-year-old and older). A review of the currently known data on cooperative breeding (or helping behavior) in corvids is given. This paper discusses factors that can contribute to the manifestation of delayed dispersion of young birds and the appearance of their helping behavior. It emphasizes the importance of long-term social bonds between parent birds and their offspring in delayed dispersion. At the heart of such social relationships is the tolerance of adult birds to their offspring and prolonged care for the young birds. The appearance of irregular helpers near the nests may be a prerequisite for the emergence of the helping behavior in certain family groups and populations.     

Individual breeding decisions and long-term reproductive strategy in the King Penguin Aptenodytes patagonicus

Although studied for 35 years, knowledge of the reproductive biology of the King Penguin Aptenodytes patagonicus remains incomplete. The chick requires more than 12 months of care, which extends the breeding cycle, including moult, to more than one year, i.e. the King Penguin is neither annual nor biennial. In an attempt to resolve ambiguities in the literature and to elucidate the long-term breeding strategy of the species, we studied breeciing frequency at the individual level, considering the decision to breed in relation to breeding history over the previous few years. Although adult birds attempted to breed annually (0.83 breeding attempts per year), successful rearing occurred, at best, every two years only (maximum of 0.41 fledged chick per pair). Comparing successive years, the number of breeding birds in the colony was stable but the number of fledged chicks varied from 29 to 278 over eight years. These results suggest that King Penguins adopt (as individuals) an opportunistic reproductive strategy, in that they usually lay an egg every year, even when failure is certain. Nevertheless, the decision to breed was not entirely blind, and we identified groups of birds that invested differentially in breeding attempts. The decision to breed was related to the previous breeding frequency, i.e. 81% of the birds that had bred continuously in the past started a new breeding attempt, but only 67% of birds that had missed a year did so. In intermittent breeders, birds that had bred frequently, more often started a new breeding attempt than birds that had largely missed years (71% versus 57%, respectively). Classes of breeders could correspond to age classes, to birds of different breeding quality or to alternative breeding strategies coexisting in the species. Testing the hypothesis that reproductive effort increases with age should be possible in future.     

Factors influencing plasticity in the arrival‐breeding interval in a migratory species reacting to climate change

Climate change is profoundly affecting the phenology of many species. In migratory birds, there is evidence for advances in their arrival time at the breeding ground and their timing of breeding, yet empirical studies examining the interdependence between arrival and breeding time are lacking. Hence, evidence is scarce regarding how breeding time may be adjusted via the arrival‐breeding interval to help local populations adapt to local conditions or climate change. We used long‐term data from an intensively monitored population of the northern wheatear (Oenanthe oenanthe) to examine the factors related to the length of 734 separate arrival‐to‐breeding events from 549 individual females. From 1993 to 2017, the mean arrival and egg‐laying dates advanced by approximately the same amount (~5–6 days), with considerable between‐individual variation in the arrival‐breeding interval. The arrival‐breeding interval was shorter for: (a) individuals that arrived later in the season compared to early‐arriving birds, (b) for experienced females compared to first‐year breeders, (c) as spring progressed, and (d) in later years compared to earlier ones. The influence of these factors was much larger for birds arriving earlier in the season compared to later arriving birds, with most effects on variation in the arrival‐breeding interval being absent in late‐arriving birds. Thus, in this population it appears that the timing of breeding is not constrained by arrival for early‐ to midarriving birds, but instead is dependent on local conditions after arrival. For late‐arriving birds, however, the timing of breeding appears to be influenced by arrival constraints. Hence, impacts of climate change on arrival dates and local conditions are expected to vary for different parts of the population, with potential negative impacts associated with these factors likely to differ for early‐ versus late‐arriving birds.     

A provisional checklist of the avifauna of Turaif province,the Kingdom of Saudi Arabia

The richness and diversity of avian species inhabiting Turaif province of Saudi Arabia were surveyed for a period of one-year (2014–2015) using walked belt transects in different habitats of the studied area. Bird species were observed and recorded by sightings or vocal calls. A total of thirty-three bird species belonging to fifteen families were observed across all the surveys in the Turaif area. During a breeding season, species abundance was higher as compared to non-breeding season. Out of 33, eighteen species were passage migrants and fifteen species were noted as breeding residents. Family Muscicapidae which showed the highest proportion (24.24%) was represented by 8 bird species followed by family Alaudidae and family Falconidae represented by 4 species each. According to this survey relatively a fair quantity of bird species still exists in the Turaif region. This area is of significant interest in terms of conservation of birds due to higher densities of endemic, breeding or resident avian species.     

Alternate Routes to Sociality in Jays--With a Theory for the Evolution of Altruism and Communal Breeding

The social systems of New World species of jays are comparedbehaviorally and ecologically. Two lines leading to socialityare identified, one connecting the pair-in-territory systemwith the colonial system and a second connecting the pair-in-territorysystem with the communal system. Ecological factors in the evolution of communal breeding andits associated altruistic behavior are considered mainly inthe genus Aphelocoma, but other birds are treated briefly. Threeprincipal origins of communality and altruism in birds are identified:from colonies, from a surplus of males, and by retention ofyoung in the family, the latter being of greatest importance.The theory proposed for the evolution of communal breeding andaltruism emphasizes three main processes: 1) K-selection, (2)kin selection, and (3) kin-group selection in the same chronologicalorder.     

Density-dependent age at first reproduction in the eastern kingbird

Theory predicts that maximal fitness is obtained by individuals who begin to breed immediately upon reaching sexual maturity. However, delayed breeding occurs regularly in some taxa, and in birds and mammals is most often associated with long lifespan and/or limited access to suitable habitats. Delayed breeding is not expected among relatively short-lived species such as migratory passerine birds, but this assumption remains untested in many species. Here we quantify age at first reproduction in an eastern kingbird Tyrannus tyrannus population breeding in an ecological island, and through both observational and experimental approaches, investigate the potential causes for the high frequency of delayed breeding that occurs in this population. Nearly half of the fledged nestlings that returned to the breeding grounds did not breed in their first potential breeding season. Some non-breeders occupied territories, for at least some period, but most remained as non-territorial 'floaters'. Parentage analysis failed to show any reproductive success for female floaters, and only limited success for male floaters, indicating that floating was not a successful reproductive tactic. On the other hand, a strong negative relationship existed between population size and the proportion of young birds that bred in their first year, and non-territorial birds of both sexes quickly filled territory vacancies created by experimental adult removals. Limited breeding habitat and territorial behavior of older birds thus appear to be the main causes of delayed breeding in kingbirds. The frequency of delayed breeding in most species is unknown but of potential significance because failure to incorporate accurate estimates of age at first reproduction in population models may lead to flawed population projections.     

Factors determining the laying date of the Waved Albatross Diomedea irrorata

The Waved Albatross laying period is between mid-April and the end of June. This paper investigates the factors determining when, during this period, a female lays. It is shown that birds breeding for the first time lay relatively late. For older birds, the laying date depends on date and outcome of the previous year's attempt: females that bred successfully in the previous year lay slightly later than in that year, while birds that failed lay earlier. A corresponding difference exists in the dates of arrival at the breeding grounds of successful and failed males. It is argued that one calendar year is not quite sufficient for pairs that have reared a chick successfully to regain breeding condition, while failed breeders can choose the laying date more freely.
Under catastrophic El Niño weather conditions in 1983, all albatrosses arrived late at the breeding grounds, but still the birds that had failed in 1982 were clearly earlier than those that had reared a chick.     

Reduced reproductive performance prior to death in the Black‐legged Kittiwake: senescence or terminal illness?

The breeding of Black-legged Kittiwakes Rissa tridactyla in their last breeding season has been compared with that of pairs which survived to the next breeding season. The time of laying was not affected but the clutch size, breeding success and productivity were significantly lower and a higher proportion of pairs totally failed to rear any young in pairs where one of the partners died before the next breeding season. When both partners died before the next breeding season, the breeding performance was reduced to a greater extent, suggesting an additive influence. The depressive effect on the last breeding attempt was confirmed by comparing the breeding success of individual females in their ultimate and penultimate breeding attempts. The effect was present in breeding birds of all ages, from first time breeders to the oldest individuals, and so could not be interpreted as an effect of senescence. Most of the adults which died apparently did so several months after breeding, during the winter half of the year when the kittiwake is oceanic. It is suggested that this depressive effect on breeding is the result of terminal illness which caused the birds to lose condition progressively over several weeks or months. It is possible that stress in the form of disease or parasite infections is primarily responsible for the death of many of the individuals. Attention is drawn to the possible confusion between the effect reported here and claims that senescence leads to lower reproductive output in old birds. It is suggested that more critical examinations are needed of claims that senescence directly affects the breeding success of birds.     

Age-specific variation in reproduction is largely explained by the timing of territory establishment in the New Zealand stitchbird Notiomystis cincta

1. Using data from 327 nests over a consecutive 8-year period we examined age-specific variation in reproduction in a population of stitchbirds (or hihi) Notiomystis cincta and related how differences in reproductive performance were linked to the timing of territory establishment and breeding. 2. Across the population all reproductive parameters showed a quadratic relationship with an increase mainly between the first and second breeding season and a decline after the fourth year. A longitudinal analysis showed evidence of senescence by the sixth year in the numbers of chicks fledged and recruited. 3. Reproductive increases between years 1 and 2 were the result of poor-quality females dying after their first breeding season (differential selection hypothesis) in combination with surviving females showing improvements in reproduction in their second year (individual improvement/constraint hypothesis). 4. There was no effect of mate experience or territory quality on improvements in breeding between years. 5. The key variable influencing reproductive output was the timing of breeding. Birds that started laying earlier were more likely to lay multiple clutches in any given season. This was the main difference between first-year and older birds; generally first-year birds initiated egg laying later and consequently laid fewer clutches. 6. Approximately half of all first-year birds did not establish their territory until after the breeding season had begun. This delay in territory establishment resulted in these birds delaying breeding, which resulted in them having a lower reproductive output relative to all other birds. First-year birds that managed to establish their territory before breeding commenced, had similar rates of reproduction as older birds. 7. There was a positive relationship between the timing of territory establishment during a female's first year and her hatching date in the previous breeding season. We hypothesize that this was because late-hatched females were less able to effectively compete for territories against earlier-hatched members of their cohort, and this delayed their establishment and breeding in their first year. Thus, this social constraint is likely to be a major factor driving age-specific reproductive variation in this population.     

Partitioning phylogenetic and adaptive components of the geographical body-size pattern of New World birds

Aim To evaluate seasonal body‐size patterns for New World birds in geographical space, to develop environmental models to explain the gradients, and to estimate phylogenetic and adaptive contributions. Location The Western Hemisphere. Methods We used range maps to generate gridded geometric mean body masses. Summer and winter patterns were distinguished based on breeding and non‐breeding ranges. We first generated the geographical gradients, followed by phylogenetic eigenvector regression to generate body sizes predicted by the birds’ positions in a phylogenetic tree, which were used to generate the expected phylogenetic gradient. Subtracting the expected pattern from the observed pattern isolated the adaptive component. Ordinary least squares multiple‐regression models examined factors influencing the phylogenetic, adaptive and combined components of the seasonal body‐size patterns, and non‐spatial and spatial models were compared. Results Birds are larger in the temperate zones than in the tropics. The gradient is quantitatively stronger in winter than in summer. Regression models explained 66.6% of the variance in summer mass and 45.9% of the variance in winter mass. In summer, phylogenetic and adaptive responses of birds contribute equally to the gradient. In winter, the gradient in North America is much stronger than that expected by taxonomic turnover, and responses of species independent of their family membership drive the overall pattern. Main conclusions We confirm Bergmann's rule in New World birds and conclude that winter temperatures ultimately drive the pattern, exerting selection pressures on birds that overwhelm patterns expected by phylogenetic inertia at the family level. However, in summer, the movement of migratory species into the temperate zone weakens the gradient and generates a pattern more congruent with that expected from the taxonomic composition of the fauna. The analytical method we develop here represents a useful tool for partitioning the phylogenetic and non‐phylogenetic components of spatially explicit macroecological data.     

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.     

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

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