Intraflock variation in the speed of escape-flight response on attack by an avian predator

The benefits of flocking to prey species, whether through collective vigilance,dilution of risk, or predator confusion, depend on flock members respondingin a coordinated way to attack. We videotaped sparrowhawks attackingredshank flocks to determine if there were differences in thetiming of escape flights between flock members and the factorsthat might affect any differences. Sparrowhawks are surpriseshort-chase predators, so variation in the time taken to takeflight on attack is likely to be a good index of predation risk.Most birds in a flock flew within 0.25 s of the first bird flying,and all birds were flying within 0.7 s. Redshanks that werevigilant, that were closest to the approaching raptor, and thatwere close to their neighbors took flight earliest within aflock. Birds in larger flocks took longer, on average, to takeflight, measured from the time that the first bird in the flockflew. Most birds took flight immediately after near neighbors tookoff, but later flying birds were more likely to fly immediatelyafter more distant neighbors took flight. This result, alongwith the result that increased nearest neighbor distance increasedflight delay, suggests that most redshanks flew in responseto conspecifics flying. The results strongly suggest that thereis significant individual variation in predation risk withinflocks so that individuals within a flock will vary in benefitsthat they gain from flocking.     

Differential habitat selection by immature and adult Grey Eagle-buzzards Geranoaetus melanoleucus

During the 1992 breeding season, we studied the habitat selection, behaviour, aggressive interactions and diet of immature and adult Grey Eagle-buzzards Geranoaetus melanoleucus in an area of the Argentinean Patagonia. Immature eagles selected areas rich in prey, had no preference for flat or rugged areas and did not avoid areas close to active nests or those used by adult eagles. The density of the European Hare Lepus europaeus was the best predictor of the distribution of immature eagles. Adult eagles preferred rugged to flat areas but were not significantly affected by prey distribution. Immature eagles used flapping flight more frequently than did adult eagles. Wing-flapping frequency of immatures did not differ when flying over slopes or plains. In contrast, adults used a more economic flight with a lower wing-flapping frequency than that of immatures, especially when flying over slopes. Adults, in contrast to immatures, tended to select slopes when flying over predominantly flat country. Only in 22% of the occasions when adult and immatures were seen together were immatures attacked by adults, a rate of aggressive encounters similar to that observed between immatures (32%). This similarity indicates that adults do not actively exclude immatures from certain areas. The main prey of both immature and adult eagles was the introduced European Hare followed by native rodents and birds. Immatures ate significantly more carrion and fewer birds than did adults. These observations suggest that differences in flight behaviour and in the flight silhouette between adult and immature eagles may be responsible for their different habitat selection in relation to topography. While immatures apparently cue on prey density for habitat selection, adults select areas that allow more economic foraging flights     

Spatial segregation between immatures and adults in a pelagic seabird suggests age‐related competition

Individual competitiveness conditions access to resources when they are limited. Immature individuals that are less skilled than adults have to adapt their foraging strategies to survive. Among strategies to reduce competition, spatial segregation has been widely demonstrated. However, the use of spatial segregation by immatures to limit intra‐specific competition with adults has rarely been tested. In this study, we investigated and compared habitat preferences and distributions of free‐ranging immature and breeding adult northern gannets Morus bassanus in order to determine whether they compete for similar habitats during the year, and if this results in a spatial segregation between birds of different age groups. Based on > 66 000 km of aerial surveys conducted in the North‐East Atlantic Ocean during winter and summer 2012, habitats selected by immatures and adult birds were modelled independently, linking gannet density to a set of oceanographic and physiographic predictors. Their large‐scale seasonal distribution was then predicted. We found that gannets displayed a strong season‐dependent competition between immatures and adults, as a consequence of immatures and adults using similar habitats in both summer and winter. During summer, when adults are constrained by reproduction, both groups were spatially highly segregated despite similar habitat preferences (thermal fronts), with youngest individuals selecting habitats out of range of central‐place foragers, highlighting intra‐specific competition. Contrastingly during winter, when reproductive constraints disappear, immature and adult distributions largely overlapped. Our study provides new insights into the role played by age, foraging experience and reproductive constraints on the distribution of marine predators. More specifically, these results highlight in seabirds how the youngest fraction mitigates, through spatial segregation, the competition with experienced adults, and suggest a progressive strategy along the maturation process.     

The influence of flocking on the foraging behaviour of the chough (Pyrrhocorax pyrrhocorax) and the Alpine chough (P. graculus) coexisting in the Alps

We studied the flocking and foraging behaviour of the chough Pyrrhocorax pyrrhocorax and the Alpine chough P. gruculus coexisting in the south-western Italian Alps in order to evaluate the costs and benefits of foraging in single- and mixed-species flocks.
In the single-species context, flock size significantly affected the foraging behaviour of the Alpine chough; in larger flocks, the birds stayed for a shorter time in a patch and fed more quickly than in smaller flocks. Flock size did not significantly affect the foraging behaviour of the chough, probably because of the small number of individuals per flock.
The propensity for mixed-species flocking was rather low. The observed frequencies of single-species flocks of choughs and Alpine choughs were significantly higher than those expected on the basis of random flocking, whereas the observed frequencies of mixed-species flocks of the two species were lower than those expected. The stay times became significantly shorter for the chough in the presence of the Alpine chough. Moreover, feeding rates of the Alpine chough were significantly lower in the presence of the dominant chough.
The present study does not confirm the hypothetical foraging advantages of flocking. In single-species flocks, the benefits for the Alpine chough (higher feeding rates in larger flocks) were roughly compensated by the costs (shorter stay times in larger flocks), whereas the chough apparently neither gained benefits nor endured costs.
In mixed-species flocks, the Alpine chough sustained costs due to a reduction of feeding rates and the chough suffered costs due to a reduction of stay times. Hence, on average, single-species flocking gives no evident foraging advantages to either the chough or the Alpine chough, whereas mixed-species flocking provides some disadvantages for both species.     

The feeding success of cattle egrets in flocks

The feeding rates of grouped (<1.5 m from conspecifics) and solo (>5 m from conspecifics) cattle egrets (Bubulcus ibis) in loose flocks away from cows were compared, to test the hypothesis that grouped cattle egrets benefit from feeding on prey flushed inadvertently by nearby conspecifics. The flock feeding rates were also compared to those of grouped and solo egrets near cows, to determine the effects of flock membership on feeding rates. Birds in flocks captured prey faster than those with cows, and tended to capture larger prey, but field observations and captive experiments failed to show that the feeding success of flock members was enhanced by the hypothesized ‘beater’ effect. Increases in prey density, however, always resulted in higher feeding rates, so some cattle egret groups may form in response to local concentrations of prey. Prey size may also play a role in group formation, because birds in the field tended to feed at greater distances from their neighbours when larger prey were captured, regardless of prey density. When small groups did form among cattle egrets feeding on relatively large prey, group members occasionally captured prey items that had been discovered by nearby conspecifics. This behaviour was not observed among birds in dense aggregations, which fed on small, highly abundant prey. These data indicate that there is a potential cost associated with feeding too near others unless the prey are relatively small and abundant.     

Flocking and feeding in the white-fronted chat Ephthianura albifrons: The relationship between diet,food availability and patch selection

Censuses of white-fronted chats were conducted three times per day, four times per month for more than 2 years in a salt-marsh/grassland near Melbourne. Most birds Were in flocks of less than 10, although flocks of up to 50 were recorded. Diet was determined by stomach flushing 226 birds over a 12 month period and the abundance of their arthropod prey was sampled in pitfall and sticky traps located in areas where flocks aggregated and in areas where few birds were found. Diptera and Coleoptera were the major components of the diet, although the actual species varied throughout the year. On 8 of 9 occasions when differences in prey density were detected, birds aggregated in the more profitable patches. These observations suggest a relationship between food-finding and flock formation but cannot eliminate the possibility of flocking functioning as an anti-predator strategy.     

Modelling the energy budget of a colonial bird of prey, the Ruppell's griffon vulture, and consequences for its breeding ecology

Colonial nesting is rare in birds of prey. In this study we develop further Pennycuick's (1979 ) model of energy balance to consider the implications of colonial nesting for the breeding ecology of Ruppell's griffon vultures. To achieve a realistic foraging range, and remain in energy balance, the birds need to do more than fill their crop once on each foraging trip. They must remain in the feeding area and digest some of this food and refill the crop to obtain sufficient energy to pay for the flight costs and have sufficient energy to satisfy their own requirements and that of the chick. Given the known distances that the birds have to travel to forage, it would be impossible for them to rear more than one chick. The low growth rate of griffon vulture chicks may be an adaptation to the low rate at which energy can be delivered by the parents. The optimal time for a bird to be away from the nest changes with the distance they have to travel. Assuming that one parent remains on the nest at all times to guard the chick, it is optimal for both parents to take turns to forage on the same day if the distance to a feeding area is under 150 km, but to switch to each parent being away for a whole day when the distance is greater than this. Soaring flight is essential for such a scavenger, because of the low energy expenditure. If a vulture relied on the more energetically demanding flapping flight its maximum foraging range would be under 40 km. Griffon vultures are known to be able to depress their basal metabolic rate, and this has major implications for their foraging range, which then becomes constrained by the flight speed rather than by the amount of food they need to obtain. Griffon vultures minimize energy expenditure on all activities, because even small increases in their energy demands have a large impact on the foraging range that the bird can use.     

SEASONAL CHANGES IN BODY-WEIGHT OF OYSTERCATCHERS HAEMATOPUS OSTRALEGUS

The body-weights of Oystercatchers Haematopus ostralegus wintering in Morecambe Bay, north-west England, showed marked seasonal changes between late summer and late winter, with considerable differences apparent between adult and immature birds. An attempt is made to relate these changes to recorded seasonal variations in prey biomass and to the annual cycles of breeding, moult and migration of the Oystercatcher. The mean weight of females invariably exceeded the mean weight of males in samples collected on the same dates, regardless of age. Adults returned from northern breeding areas in very lean condition, with mean weights ranging from 526 g in males to 540 g in females. Mean weight then increased progressively, due mainly to fat deposition, to a peak in March (up to 662 g in males and 675 g in females) around the time of their main departures for breeding. Heaviest birds then exceeded 800 g. Birds migrating to Iceland in spring would need to be of above average weight in March to make the shortest crossing (850 km, 13 h), via Scotland, while Oystercatchers of 700 g and over could probably make a direct flight (1500 km, 25 h) from Morecambe Bay in favourable weather. Breeding weights of British Oystercatchers were similar to those of post-breeders returning to Morecambe Bay in late August. The mean weights of first-year Oystercatchers arriving in August were very low, 449 g in males and 478 g in females. Their weights, and those of second- and third-year immatures, then rose rapidly in autumn, with some fat deposition, and reached mean values ranging between 551 g (males) and 597 g (females) by November-December. Mean weight then fell by 10–17% from December to March returning close to or below the September levels, whereas adults gained a further 6% during these winter months. Summer and autumn weight gains, and the major moult of adults and older immatures, occurred when the biomass of their two staple mollusc preys, Mytilus edulis (mussel) and Cardium edule (cockle), was maximal. Winter loss in mean weight of immatures corresponded with declining prey biomass, suggesting either that they were less efficient than adults in coping with deteriorating winter food supplies, or that they had no need to accumulate further (premigratory) fat reserves. The autumnal increases in mean weight of immatures are interpreted as an adaptation for withstanding adverse feeding conditions in winter. The Oystercatcher appears to be the only wader species in Britain in which adults increase, rather than lose, weight during the winter. This may be a consequence of an early breeding season, but it may be regarded also as a measure of the success Oystercatchers have achieved by specializing on a difficult but plentiful prey source.     

Pursuit plunging by northern gannets (Sula bassana) feeding on capelin (Mallotus villosus)

Northern gannets (Sula bassana) are considered to obtain prey usually by rapid, vertical, shallow plunge dives. In order to test this contention and investigate underwater foraging behaviour, we attached two types of data-logging systems to 11 parental northern gannets at Funk Island in the North-Wiest Atlantic. We documented, for the first time to the authors' knowledge, gannets performing long, flat-bottomed, U-shaped dives that involved underwater wing propulsion as well as rapid, shallow, V-shaped dives. The median and maximum dive depths and durations were 4.6 and 22.0 m and 8 and 38 s, respectively. Short, shallow dives were usually V-shaped and dives deeper than 8 m and longer than 10 s were usually U-shaped, including a period at constant depth (varying between 4 and 28s with median 8s). Diving occurred throughout the daylight period and deepest dives were performed during late morning. On the basis of motion sensors in the loggers and food collections from telemetered birds, we concluded that extended, deep dives were directed at deep schools of capelin, a small pelagic fish, and we hypothesized that V-shaped dives were aimed at larger, pelagic fishes and squids. Furthermore, these V-shaped dives allowed the birds to surprise their pelagic prey and this may be critical because the maximum swimming speeds of the prey species may exceed the maximum dive speeds of the birds.     

Composition of mixed‐species flocks and shifts in foraging location of flocking species on Hainan Island,China

A total of 134 bird species were recorded at Jianfengling, Hainan Island, in China from May 2000 to September 2004, of which 44 participated in one or more of 134 mixed‐species flocks. These flocks averaged 3.8 ± 0.2 species and 20.3 ± 1.2 individuals. Flocking propensity in a given species ranged from 1.5 to 100%. For flocking species, frequency of flocking and number of individuals in flocks was positively correlated with frequency and number in point counts. Among all species pairs with flocking frequency above 5%, cluster and correlation analysis indicated there were two principal groups of flocking birds – canopy species and understorey species: associations were positive within a group, but negative between groups. Canopy birds had a higher flocking propensity than understorey birds. They also made significantly less use of inner branches and trunks and greater use of middle branches, and foraged at a significantly greater height when in mixed‐species flocks than when solitary. For understorey bird species, there were no significant differences in foraging locations between solitary and mixed‐species flocks. Higher flocking frequency occurred in the wet season for canopy birds, but in the dry season for understorey birds. Overall patterns were consistent with the explanation that flocking enables an expansion of foraging niche by reducing the risk of predation.     

Mixed species flocking of tits (Parus spp.): a field experiment

Summary We tested two general models of flocking behaviour, namely the antipredation model and foraging efficiency model on mixed-species tit flocks (Parus spp.). After food addition the size of mixed-species flocks was significantly less than in the control samples. In the presence of extra food significantly more birds were observed either in monospecific flocks or solitary, than during the control observations. In the presence of a living predator the birds foraged in larger mixed-specifies flocks than during the control observations. In addition, the social behaviour of Great Spotted Woodpecker, Middle Spotted Woodpecker and Nuthatch shifted to mixed-specific flocking. The size of monospecific flocks was independent of both treatments. The density of birds increased significantly after food addition, while in the predator presence the birds tended to leave the forest. These results support the view that both the antipredation model and foraging efficiency model seem to be valid for mixed-species flocking. However, in the case of monospecific flocks, the territory maintenance could be the most important factor.     

SOARING BEHAVIOUR AND PERFORMANCE OF SOME EAST AFRICAN BIRDS, OBSERVED FROM A MOTOR-GLIDER

Various species of soaring birds were studied by following them in a motor-glider, mainly over the Serengeti National Park, Tanzania. The characteristics of thermal convection in the study area are described in general terms. The two vulture species of the genus Gyps live by scavenging among the herds of migratory ungulates, especially Wildebeest. They are not territorial, and gather in large numbers on kills. When raising young they may be obliged by game movements to forage at long distances from their nests. Their cross-country performance is adequate for a foraging radius of over 100 km in dry-season conditions. Their ability to compete with Spotted Hyaenas is thought to depend partly on this factor and partly on an advantage in arriving early at kills. These two species appear to find food more by watching other vultures than by searching for it directly. The Lappet-faced and White-headed Vultures are thought to be sedentary, and to depend on thorough searching of a fixed foraging territory, rather than on following migratory game. They have lower wing loadings than the Gyps vultures, and were not seen cross-country flying. They never gather in large numbers. The Hooded Vulture is a solitary nester, but it does fly across country, and does gather at kills. Vultures soar individually, and seem to be good at exploiting such phenomena as thermal streets. They do not travel in flocks. Tawny and Martial Eagles react positively to the glider, and are suspected of regarding it as potential prey. White Storks migrate between Europe and Africa, and also travel about within East Africa, by thermal soaring. They soar in flocks, and unlike vultures rely on co-ordinated social behaviour to locate thermals. In choosing their route, they often fail to react to obvious weather signs. They enter cumulus clouds from the bottom when thermalling, but probably do not climb far above cloudbase. Marabou Storks soar individually, but also sometimes travel in flocks. When doing so, they show less lateral spreading than White Storks, which reduces the effectiveness of the flock as a thermal-finding unit; on the other hand, they do seem to react to visible weather signs, like vultures or glider pilots. White Pelicans, which travel by thermal soaring between different lakes in the Rift Valley, show the most highly co-ordinated social soaring behaviour. Unlike White Storks, they fly in formation even when circling. Storks and pelicans showed more signs of alarm when approached by the glider than did the vultures or birds of prey. This could be due to their being preyed upon in flight, for instance by Martial Eagles. The basis of conventional thermal cross-country flying is outlined, and it is explained why the high wing loadings of the Gyps vultures are appropriate to their peripatetic habits. A method of thermal soaring without circling is discussed, and shown to be more readily feasible for small than for large birds. Some differences in soaring techniques between birds and glider pilots are interpreted in the light of this calculation. A case in which Black Kites apparently used this technique to soar in random turbulence is described. The cross-country speed attainable by thermal soaring should be similar to the cruising speed under power in both large and small birds. Rough calculations of the energy costs suggest that a large bird (White Stork) should reduce its fuel consumption by a factor of 23 by soaring rather than flying under power, whereas this factor would be only 2–4 for a small bird (Bonelli's Warbler). Other reasons why thermal soaring is an advantageous means of travel for large but not for small birds are also indicated.     

Body mass change and diet switch tracked by stable isotopes indicate time spent at a stopover site during autumn migration in dunlins Calidris alpina alpina

Birds may change their diet and foraging habitat during or after migration. Dunlins Calidris alpina alpina breed in the tundra of northern Europe and Russia where they feed exclusively on terrestrial prey. However, up to 80% of the flyway population uses the Wadden Sea as their first important staging site on the way to wintering grounds, feeding exclusively on marine prey. Adult birds migrate earlier than immatures and tend to fly non‐stop, whereas immatures may stage for at least a few days en route, mainly in the Baltic region. There they mostly feed on brackish water prey showing similar isotopic values compared to terrestrial prey. When they arrive in the Wadden Sea, dunlin body reserves are depleted and lower than those of individuals that have already staged for several days. We hypothesized that lighter individuals should retain a strong terrestrial isotopic blood signature, while heavier ones should show a stronger marine signature. We found a significant positive correlation between scaled mass index and carbon (δ¹³C) and nitrogen (δ¹⁵N) stable isotopes, reflecting the switch from terrestrial to marine prey during migration. A mixing model revealed differences in isotopic values between heavy and light adults and immatures, respectively, in relation to the isotopic prey signatures. Adults showed stronger marine signals compared with immatures, emphasizing the different modes of migration (i.e. a later departure in immatures) as well as the known spatial segregation of age classes in the Wadden Sea, i.e. adults use tidal flats distant from the shore while immatures use coastal areas influenced by terrestrial carbon sources. The results of this study demonstrate the value of scaled mass index in migratory birds as an indicator of time elapsed after diet switching following migration. Furthermore, this study extents the existing knowledge on the timing of dunlin migration by using an isotopic approach.     

Dyed birds achieve higher social status than controls in Harris' sparrows

The status-signalling hypothesis has been proposed to explain colour variation among individuals in flocking birds. Its fundamental assumption is that colour may affect the determination of an individual's social rank in a flock. Here I show for winter Harris' sparrows (Zonotrichia querula) that birds dyed to resemble adults dominate control birds within experimental flocks of young males and young females. The domination of controls by the dyed birds was achieved by a two-step process in both experiments: immediately after the two groups were combined, the controls avoided the dyed birds; then, shortly thereafter, the dyed birds began actively to displace the control birds.     

Bird mixed‐species flock formation is driven by low temperatures between and within seasons in a Subtropical Andean‐foothill forest

According to both the predation avoidance and foraging efficiency hypotheses, birds within mixed flocks increase their foraging efficiency and/or can spend more time feeding and less time looking out for predators. These hypotheses predict that birds in mixed flocks obtain benefits. Thus, mixed flock formation could serve as a strategy to cope with difficult conditions imposed on birds such as climatic conditions that ultimately result in a change in predation pressure or food resources. We evaluate the hypotheses that forming part of a flock confers benefits to its members and the associated prediction that birds will take advantage of these benefits and flock more often under cold and dry weather conditions between and within seasons to cope with such conditions. We surveyed the presence of mixed flocks, flocking propensity, number of species and individuals in mixed flocks in the Subtropical Yungas foothill of Argentina, to examine seasonality, flocking behavior of birds and their responses to two climatic variables: temperature and humidity. Bird species presented a higher flocking propensity and mixed flocks occurred more frequently during the dry and cold seasons than during the more benign seasons, and lower values of temperature within seasons triggered the flocking behavior. Although effects between seasons were expected, birds also showed a short‐term response to small changes in temperature within seasons. These results strengthen the ideas proposed by the foraging hypothesis. Although benefits derived from flocking have yet to be determined, whatever they are should be understood in the context of seasonal variation in life‐history traits.     

Does prey capture induce area-restricted search? A fine-scale study using GPS in a marine predator, the wandering albatross

In a patchy environment, predators are expected to increase turning rate and start an area-restricted search (ARS) when prey have been encountered, but few empirical data exist for large predators. By using GPS loggers with devices measuring prey capture, we studied how a marine predator adjusts foraging movements at various scales in relation to prey capture. Wandering albatrosses use two tactics, sit and wait and foraging in flight, the former tactic being three times less efficient than the latter. During flight foraging, birds caught large isolated prey and used ARS at scales varying from 5 to 90 km, with large-scale ARS being used only by young animals. Birds did not show strong responses to prey capture at a large scale, few ARS events occurred after prey capture, and birds did not have high rates of prey capture in ARS. Only at small scales did birds increase sinuosity after prey captures for a limited time period, and this occurred only after they had caught a large prey item within an ARS zone. When this species searches over a large scale, the most effective search rule was to follow a nearly straight path. ARS may be used to restrict search to a particular environment where prey capture is more predictable and profitable.     

Age bias in the bag of pink-footed geese <Emphasis Type="Italic">Anser brachyrhynchus</Emphasis>: influence of flocking behaviour on vulnerability

In pink-footed goose (Anser brachyrhynchus) wintering in Denmark, The Netherlands and Belgium, the proportion of juveniles in the hunting bag is consistently higher than that observed in the autumn population. Such juvenile bias in the bag is usually ascribed to young geese lacking experience with hunting or disruption of juveniles from families. An alternative explanation may be that flocking behaviour of families make juveniles more vulnerable. Observations of morning flights of pink-footed geese to the feeding grounds from two of the major autumn-staging areas showed that geese were distributed in many small flocks (median flock size = 9). This was not significantly different from the flock size distribution shot at by hunters (median = 8), suggesting that hunters targeted goose flock size in proportion to the general probability of encounter. The rate at which hunters downed geese was independent of flock size. The ratio between juveniles and adults in flocks decreased with flock size and flocks of <60 individuals primarily comprised family groups. The likelihood of being shot at was 2.4 times higher for juveniles and 3.4 times higher for older birds in small flocks (<10 individuals) compared to larger flocks. The observations suggest that both juveniles as well as successful adult breeding birds were more vulnerable than non-breeding/failed breeding birds as a result of flocking behaviour.     

Aggression in shorebirds in relation to flock density and composition

The aggressive interactions of Turnstones and Purple Sandpipers feeding in wintering mixed-species wader flocks could be classified into those involving food and those involving space. All observed interspecific encounters were of short duration and were initiated and won by the larger species; the majority did not involve food and were resolved by low-intensity displays. Intraspecific interactions (a greater proportion of which involved food) were also resolved quickly and were usually won by the initiator. Space-related encounters between conspecifics were more likely to be resolved than food-related encounters just by threat displays. Aggression rates increased with flock densities. However, the increase in aggression with density was dependent on the species composition of the flock: both Turnstones and Purple Sandpipers were more likely to be involved in fights (both over food and over space) with conspecifics than with other species, indicating that the aggression costs of flocking were less in mixed-species flocks.     

Intraspecific differences in benefits from feeding in mixed-species flocks

The Madagascar Paradise Flycatcher Terpsiphone mutata and Common Newtonia Newtonia brunneicauda frequently form two-species flocks in the deciduous dry forest of western Madagascar. In T. mutata , some males have long tails, while other males and females have short tails. When foraging in mixed flocks, each type of bird captured prey more rapidly than otherwise, but the degree of increase in feeding rate was smaller in long-tailed males. When in mixed flocks, all T. mutata caught prey on leaves in the canopy where N. brunneicauda foraged. Long-tailed males changed feeding habits from sallying when not in mixed flocks, whereas short-tailed birds showed no change of feeding habit. The elongated tails of long-tailed males may have made their foraging less efficient owing to decreased agility in the canopy. N. brunneicauda is monomorphic and often formed groups of three to five individuals. In monospecific flocks, subordinates fed at low rates on branches owing to frequent hostile encounters. When foraging in mixed flocks, however, subordinates foraged among leaves, and their feeding rates increased because the frequency of intraspecific interference decreased greatly. Dominants did not show any difference in feeding pattern with social situation. Thus, heterospecific flocking was more advantageous for subordinates.     

Foraging by little auks in the distant marginal sea ice zone during the chick-rearing period

During the chick-rearing period, little auks Alle alle adopt a bimodal foraging strategy, alternating long trips with several short ones. It has been postulated that they reach more remote areas during long feeding trips than during short ones. However, the range of their foraging flights has never actually been measured. The aims of this study were to find the exact location of the little auk feeding grounds and to investigate whether they reach remote areas during long foraging trips using miniature GPS and temperature loggers. The study was conducted in 2009 in Magdalenefjorden (79°34′N, 11°04′E), one of the main breeding grounds of little auks on Spitsbergen. The temperature logger records indicated that during short trips, little auks visit warmer waters (situated close to the colony) than during long ones. The tracks of two GPS-equipped birds indicated that during long trips little auks foraged in the distant, food-abundant marginal sea ice zone, at least 100 km away from the colony. During long trips, birds make several stops at sea, perhaps sampling the foraging area with respect to prey distribution. Since food conditions near the studied colony are usually suboptimal, little auks may be exploiting distant feeding areas to compensate for the poorer-quality food available at nearby foraging grounds. The extended duration of long foraging trips may enable birds to collect food for chicks on food-abundant, remote foraging grounds as well as acquire, process and excrete food needed for self-maintenance, reducing the costs of flight to the colony.