Owls and rabbits: predation against substandard individuals of an easy prey

The interactions among the multiple factors regulating predator-prey relationships make predation a more complex process than previously thought. The degree to which substandard individuals are captured disproportionately seems to be better a function of the difficulty of prey capture than of the hunting techniques (coursing vs. ambushing predators). That is, when the capture and killing of a prey species is easy, substandard individuals will be predated in proportion to their occurrence in the prey population. In the present study, we made use of eagle owls Bubo bubo and their main prey, the rabbit Oryctolagus cuniculus : (a) the brightness of the white tails of rabbits seems to be correlated with the physical condition of individuals, (b) by using the tails of predated rabbits as an index of individual condition, we found that eagle owls seem to prefer substandard individuals (characterized by duller tails), and (c) by using information from continuous radiotracking of 14 individuals, we suggest that the difficulty of rabbit capture could be low. Although the relative benefits of preying on substandard individuals should considerably decrease when a predator is attacking an easy prey, we hypothesise that the eagle owl preference for substandard individuals could be due to the easy detection of poor individuals by a visual cue, the brightness of the rabbit tail. Several elements allow us to believe that this form of visual communication between a prey and one of its main predators could be more widespread than previously thought. In fact: (a) visual signalling plays a relevant role in intraspecific communication in eagle owls and, consequently, visual signals could also play a role in interspecific interactions, and (b) empirical studies showed that signals may inform the predator that it has been perceived, or that the prey is in a sufficiently healthy state to elude the predator.     

Colour also matters for nocturnal birds: owlet bill coloration advertises quality and influences parental feeding behaviour in little owls

Chromatic signals of offspring quality have been shown to play a role in parent–offspring communication in diurnal birds, but are assumed to be useless in dim light conditions because colour-based discrimination probably requires more light. A major ecological and evolutionary conundrum in this scenario is why the nestlings of some nocturnal owls display colourful beaks. Here, we test the hypothesis that yellow bill coloration of owlets of the nocturnal little owl Athene noctua may function as a chromatic signal revealing to parents aspects of quality of their offspring. In a first step, we examined physical variation in bill coloration and its covariation with owlet quality. Secondly, we studied parental provisioning in relation to an experimental manipulation of bill coloration of owlets. Bills of owlets showed higher within-nest variation in yellow–red chroma than in brightness. Plasma carotenoid concentration and nestling immunological status were not associated with chromatic or achromatic features of the bill. Interestingly, however, heavier owlets displayed more yellow bills than lighter ones. The effect of bill coloration on parental favouritism changed with brood size. Parents holding large broods preferentially fed owlets with enhanced over reduced yellow bill coloration, whereas those with small broods did not significantly bias feeding in relation to owlet bill coloration. Our results, based on integration of objective spectrophotometric assessment of colour and experimental procedures, confirm that parent little owls use bill coloration to reveal information on owlet body mass to adjust their feeding strategies, thus highlighting the importance of considering potential chromatic signals for a full comprehension of parent–offspring communication processes in nocturnal bird species.     

The importance of visual cues for nocturnal species: eagle owls signal by badge brightness

Nocturnal species may communicate by visual signals more frequentlythan previously thought. In fact, such species are habituallyactive around sunset and sunrise, when light conditions arestill suitable for visual communication. We investigated thecommunication function of a visual cue in the eagle owl Bubobubo, a nocturnal predator. In this species, territorial andcourtship displays peak during the sunset and sunrise periodsand involve the display of a white badge located on the throatwhose reflectance properties are sex and period dependent. Experimentalintrusions were conducted at 30 eagle owl territories in orderto understand the function of the white badge during contests.We analyzed the reactions of both male and female owners towarda taxidermic mount with a normal brightness and a brightness-reducedwhite badge, with both male and female territorial calls. Ourresults indicate that the white badge of eagle owls plays animportant role in visual communication during contests. Malesdisplayed more frequently toward male low-brightness mounts,which were also approached more closely or attacked. Femalebehavior did not differ between experimental groups. Furthermore,a positive relationship between male badge brightness and breedingoutput suggested a potential role of the white badge as an honestsignal of male quality. The need to convey information by visualcommunication in a nocturnal species may have promoted the evolutionof visual signals employed at crepuscule.     

Activity patterns at the Arctic Circle: nocturnal eagle owls and interspecific interactions during continuous midsummer daylight

Circadian rhythms result from adaptations to biotic and abiotic environmental conditions that cycle through the day, such as light, temperature, or temporal overlap between interacting species. At high latitudes, close to or beyond the polar circles, uninterrupted midsummer daylight may pose a challenge to the circadian rhythms of otherwise nocturnal species, such as eagle owls Bubo bubo. By non‐invasive field methods, we studied eagle owl activity in light of their interactions with their main prey the water vole Arvicola amphibius, and their competitor the white‐tailed eagle Haliaeetus albicilla during continuous midsummer daylight on open, treeless islands in coastal northern Norway. We evaluated circadian rhythms, temporal overlap, exposure, and spatial distribution. The owls maintained a nocturnal activity pattern, possibly because slightly dimmer light around midnight offered favourable hunting conditions. The eagles were active throughout the 24‐h period as opposed to the strictly diurnal rhythm reported elsewhere, thus increasing temporal overlap and the potential for interference competition between the two avian predators. This may indicate an asymmetry, with the owls facing the highest cost of interference competition. The presence of eagles combined with constant daylight in this open landscape may make the owls vulnerable to interspecific aggression, and contrary to the available literature, eagle owls rarely exposed themselves visually during territorial calls, possibly to avoid detection by eagles. We found indications of spatial segregation between owls and eagles reflecting differences in main prey, possibly in combination with habitat‐mediated avoidance. Eagle owl vocal activity peaked in the evening before a nocturnal peak in visual observations, when owls were active hunting, consistent with the hypothesis of a dusk chorus in nocturnal bird species. The owls may have had to trade‐off between calling and foraging during the few hours around midnight when slightly dimmer light reduced the detection risk while also providing better hunting conditions     

No need to shout: Effect of signal loudness on sibling communication in barn owls Tyto alba

In animal communication, signal loudness is often ignored and seldom measured. We used a playback experiment to examine the role of vocal loudness (i.e., sound pressure level) in sibling to sibling communication of nestling barn owls Tyto alba. In this species, siblings vocally negotiate among each other for priority access to parental food resources. Call rate and call duration play key roles in this vocal communication system, with the most vocal nestlings deterring their siblings from competing for access to the food item next delivered by parents. Here, we broadcast calls at different loudness levels and call rate to live nestlings. The loudness of playback calls did not affect owlets' investment in call rate, call duration or call loudness. The rate at which playback calls were broadcast affected owlets' call rate but did not influence their response in terms of loudness. This suggests that selection for producing loud signals may be weak in this species, as loud calls may attract predators. Moreover, given that owlets do not overlap their calls and that they communicate to nearby siblings in the silence of the night, loud signals may not be necessary to convey reliable information about food need.     

Is the denser contour feather structure in pale grey than in pheomelanic brown tawny owls Strix aluco an adaptation to cold environments?

In colour polymorphic species morphs are considered to be adaptations to different environments, where they have evolved and are maintained because of their differential sensitivity to the environment. In cold environments the plumage insulation capacity is essential for survival and it has been proposed that plumage colour is associated with feather structure and thereby the insulation capacity of the plumage. We studied the structure of contour feathers in the colour polymorphic tawny owl Strix aluco. A previous study of tawny owls in the same population has found strong selection against the brown morph in cold and snowy winters whereas this selection pressure is absent in mild winters. We predicted that grey morphs have a denser and more insulative plumage, enabling them to survive better in cold climate compared to brown ones. The insulative plumulaceous part of the dorsal contour feathers was larger and the fine structure of the plumulaceous part of the feather was denser in grey tawny owls than in brown ones. In the ventral contour feathers the plumulaceous part of the feather was denser in females than in males and in older birds without any differences between morphs. Our study suggests that insulative microscopical feather structures differ between colour morphs and we propose that feather structure may be a trait associated with morph‐specific survival in cold environments.     

No phylogeographic structure in the circumpolar snowy owl (Bubo scandiacus)

The snowy owl (Bubo scandiacus) is a nomadic species with a circumpolar distribution. It has recently declined in the western Palearctic and may thus be worthy of special consideration for conservation. We investigated genetic structure in three well separated geographic regions within the snowy owls’ breeding range. We sequenced two mitochondrial genes; the control region and cytochrome b, and two Z-chromosome introns; VLDLR-9 and BRM-15. We found no phylogeographic structure among the sampled regions, indicating high levels of gene flow in the recent past and possibly still today. Intra-population diversity did not vary between regions for the control region, but for Cyt b, North American birds had higher haplotype diversity than Scandinavian and eastern Siberian birds. Western Palearctic birds do not seem to be genetically deprived or inbred. Genetic diversity in the snowy owl was not lower than Scandinavian populations of three other owl species: tawny owls (Strix aluco), Tengmalm’s owls (Aegolius funereus) and eagle owls (Bubo bubo).     

Comparing food limitation among three stages of nesting: supplementation experiments with the burrowing owl

Food availability is an important limiting factor for avian reproduction. In altricial birds, food limitation is assumed to be more severe during the nestling stage than during laying or incubation, but this has yet to be adequately tested. Using food‐supplementation experiments over a 5‐year period, we determined the degree and timing of food limitation for burrowing owls (Athene cunicularia) breeding in Canada. Burrowing owls are an endangered species and food limitation during the nestling stage could influence reproductive performance of this species at the northern extent of their range. Supplemented pairs fledged on average 47% more owlets than unfed pairs, except during a year when natural food was not limiting (i.e., a prey irruption year). The difference in fledgling production resulted from high nestling mortality in unfed broods, with 96% of all nestling deaths being attributed to food shortage. Supplemental feeding during the nestling period also increased fledgling structural size. Pairs fed from the start of laying produced the same number of hatchlings as pairs that received no supplemental food before hatch. Furthermore, pairs supplemented from egg laying to fledging and pairs supplemented during the nestling period alone had the same patterns of nestling survival, equal numbers of fledglings, and similar fledgling mass and structural size. Our results provide empirical support for the hypothesis that the nestling period is the most food‐limited phase of the breeding cycle. The experimental design we introduce here could be used with other altricial species to examine how the timing of food limitation differs among birds with a variety of life‐history strategies. For burrowing owls, and other species with similar life histories, long‐term, large‐scale, and appropriately timed habitat management increasing prey abundance or availability is critical for conservation.     

Disentangling the effects of genetic and environmental factors on movement behaviour

Individual variability in animal movement behaviour is well documented for many species. However, it remains unclear whether this variability reflects genetic variation, environmental variation or a combination of the two. Here, we conduct a cross‐fostering experiment with the aim of investigating the role of these two components in movement patterns during the post‐fledging dependence period and early natal dispersal of 21 eagle owls Bubo bubo. Our experiment showed that cross‐fostering did not influence any of the movement parameters considered. Movement parameters were, however, affected by the age and sex of the owlets. We therefore suggest that individual variability and family resemblance in movement behaviour during the post‐fledging dependence period and early natal dispersal might not be due to the common genetic origin of siblings, but rather that it originates from factors related to the rearing environment.     

Bird predation by tawny owls (Strix aluco L.) and its effect on the reproductive performance of tits

The density of great tit Parus major L. and blue tit Parus caeruleus L. was artificially increased by placing nest-box colonies for these species in the vicinity of the nests of breeding tawny owls during 1993–1997. Bird prey composition in the owl nests, the proportion of parents disappearing from the breeding tit populations and the reproductive performance of the widowed parents were analysed. The frequency of predation on tits by tawny owls was greater in areas where tit density had been artificially increased. Owls preyed more on tits during the feeding period of owlets than during the incubation period and more in years when snow covered the ground during the incubation period than when it did not. Mortality due to predation was male biased and more females lost their mates in populations breeding near tawny owl nests. Reproductive performance of the widowed parents was lower and their body weights were lighter at the end of the nestling period than those found in birds rearing youngs with their mates. Predation by owls increased the between-year turnover in the breeding tit population: widowed parents did not return to the nesting site for the next breeding season.     

The Sound Suppression Characteristics of Wing Feather of Owl (Bubo bubo)

Many species of owls are able to fly noiselessly,and their wing feathers play an important role for the silent flight.In this paper,we studied the sound suppression mechanism of the eagle owl (Bubo bubo) by Stereo Microscope (SM),Scanning Electron Microscopy (SEM) and Laser Scanning Confocal Microscope (LSCM).To investigate the effects of special characteristics of wing feather on owl silent flight,the acoustic properties,including the sound absorption coefficient and flight noise,were compared between the eagle owl and common buzzard (Buteo buteo).The results show that the eagle owl generates lower noise than common buzzard during flight,and its wing feather has better sound absorption properties.The leading edge serration and trailing edge fringe can improve the pressure fluctuation of turbulence boundary,and suppress the generation of vortex sound.The elongated distal barbules form a multi-layer grid porous structure which also has an effect on sound absorption.This research not only can give the inspiration for solving the aerodynamic noise of aircraft and engineering machine,but also can provide a new idea for the design of low-noise devices.     

Role of prey and intraspecific density dependence on the population growth of an avian top predator

Exploring predator–prey systems in diverse ecosystems increases our knowledge about ecological processes. Predator population growth may be positive when conspecific density is low but predators also need areas with prey availability, associated with competition, which increases the risk of suffering losses but stabilises populations. We studied relationships between European rabbits Oryctolagus cuniculus (prey) and adult eagle owls Bubo bubo (predators) in south-western Europe. We assessed models explaining the predator population growth and stability. We estimated the abundance of rabbits and adult eagle owls during three years in eight localities of central-southern Spain. We explored models including rabbit and adult eagle owl abundance, accounting for yearly variations and including the locality as a random variable. We found that population growth of adult eagle owls was positive in situations with low conspecific abundance and tended to be negative but approaching equilibrium in situations of higher conspecific abundance. Population growth was also positively related to previous summer rabbit density when taking into account eagle owl conspecific abundance, possibly indicating that rabbits may support recruitment. Furthermore, abundance stability of adult eagle owls was positively related to previous winter–spring rabbit density, which could suggest predator population stabilisation through quick territory occupation in high-quality areas. These results exemplify the trade-off between prey availability and abundance of adult predators related to population growth and abundance stability in the eagle owl–rabbit system in south-western Europe. Despite rabbits have greatly declined during the last decades and eagle owls locally specialise on them, eagle owls currently have a favourable conservation status. As eagle owls are the only nocturnal raptor with such dependence on rabbits, this could point out that predators may overcome prey decreases in areas with favourable climate and prey in the absence of superior competitors with similar foraging mode.     

Tawny owl vocal activity is constrained by predation risk

The vocal behaviour of birds may be influenced by many factors, including the risk of being detected by a predator. In Doñana Protected Area, the tawny owl co‐exists alongside its intraguild predator, the eagle owl Bubo bubo. We considered four scenarios to study the vocal behaviour of tawny owls at dusk by analysing: A) the calling rate of all males in 29 sites; B) the calling rate at dusk of males living within the home range of the intraguild predator; C) the calling rate of males living within the home range of the intraguild predator between 60 and 90 min after sunset; and D) the duration of male vocal bouts in visits where eagle owls have called. In scenario A we found that only the number of conspecific males affected the calling rate of tawny owls. In scenario B we observed that the presence of an eagle owl calling constrained the calling rate of the intraguild prey. In scenario C we found that this effect seemed mostly associated to a contemporaneous detection of the intraguild predator’s calls. Finally, in scenario D we found no significant effects on bout duration. These results seem to indicate that tawny owls use their intraguild predator’s calls as a cue to assess predation risk, and then adjust their vocal behaviour in order to minimize predation risk by a predator that may locate its prey by its vocalizations.     

Does feeding effort of Tengmalm's owls reflect offspring survival prospects in cyclic food conditions?

In an environment fluctuating in a predicatable manner with wide among-year variation in offspring mortality, fitness is largely influenced by the timing of reproductive investment. In vole-eating nocturnal Tengmalm's owls (Aegolius funereus), within-cycle variation in 1st-year survival of owlets is 3-fold as estimated by the recruitment probability of an offspring. It increases from the peak through the low to the increase phase of the vole cycle. We recorded prey delivery rates of males during a 3-year vole cycle using 4 h continuous recording at night. Males brought significantly more prey items per offspring in a low-vole year than in the increase and peak vole years. In the early night (10 p.m.–12 p.m.), males fed their families equally in the increase and peak vole years, whereas in the late night (0.01–2.00 a.m.) males reduced their feeding rate in the peak year but not in other years. Both prey number and prey mass per offspring were larger in the low and increase vole years than in the peak year, though in the peak phase food is most abundant. We suggest that feeding effort of site-tenacious, long-lived (mean lifespan 3.5 years) male owls culminates in the increase rather than in the peak phase of the vole cycle, because offspring survive better in the former phase.     

Helminth Communities of Owls (Strigiformes) Indicate Strong Biological and Ecological Differences from Birds of Prey (Accipitriformes and Falconiformes) in Southern Italy

We compared the helminth communities of 5 owl species from Calabria (Italy) and evaluated the effect of phylogenetic and ecological factors on community structure. Two host taxonomic scales were considered, i.e., owl species, and owls vs. birds of prey. The latter scale was dealt with by comparing the data here obtained with that of birds of prey from the same locality and with those published previously on owls and birds of prey from Galicia (Spain). A total of 19 helminth taxa were found in owls from Calabria. Statistical comparison showed only marginal differences between scops owls (Otus scops) and little owls (Athene noctua) and tawny owls (Strix aluco). It would indicate that all owl species are exposed to a common pool of ‘owl generalist’ helminth taxa, with quantitative differences being determined by differences in diet within a range of prey relatively narrow. In contrast, birds of prey from the same region exhibited strong differences because they feed on different and wider spectra of prey. In Calabria, owls can be separated as a whole from birds of prey with regard to the structure of their helminth communities while in Galicia helminths of owls represent a subset of those of birds of prey. This difference is related to the occurrence in Calabria, but not Galicia, of a pool of ‘owl specialist’ species. The wide geographical occurrence of these taxa suggest that local conditions may determine fundamental differences in the composition of local communities. Finally, in both Calabria and Galicia, helminth communities from owls were species-poor compared to those from sympatric birds of prey. However, birds of prey appear to share a greater pool of specific helmith taxa derived from cospeciation processes, and a greater potential exchange of parasites between them than with owls because of phylogenetic closeness.     

Feather eating in individually caged hens which differ in their propensity to feather peck

Two experiments examined the responses of 16 individually caged laying hens to the presentation of feathers plucked from dead birds of the same genetic line. In the first experiment, hens known from a previous experiment to be either feather 'peckers' or 'non-peckers' (8 of each) were tested for their propensity to eat feathers in four 10min trials, in which they were offered fresh semiplumes measuring 4-6cm (length), one at a time, in front of their cage. Wide variation between birds was observed in numbers of feathers eaten, pecked, picked-up and manipulated. Fourteen out of 16 birds readily ate presented feathers on one or more occasion and both birds that ate no feathers were non-peckers. Peckers ate, picked-up and manipulated feathers significantly more often than did non-peckers (P<0.05, P<0.01 and P<0.01, respectively). A second experiment investigated the possibility that presence of preen (uropygial) oil might contribute to the attractiveness of feathers to eat. The same group of 16 pecker and non-pecker hens were offered a choice between 20 washed and 20 unwashed semiplumes, presented simultaneously in separate containers, in two 10min trials. Unwashed feathers were eaten, pecked and picked-up in preference to washed feathers by both peckers and non-peckers (P<0.05, P<0.01, and P<0.01, respectively), indicating an attraction towards unwashed feathers, or an avoidance of washed feathers for some reason. Peckers and non-peckers did not differ significantly in their preferences. These results provide evidence of a relationship between feather eating and feather pecking at an individual level. The finding that hens could distinguish between normal feathers and those treated in such a way as to alter their olfactory (but not visual) properties suggests olfactory cues may be of importance in determining the attractiveness of conspecific feathers.     

A non-invasive genetic evaluation of population size,natal philopatry,and roosting behavior of non-breeding eastern imperial eagles (<Emphasis Type="Italic">Aquila heliaca</Emphasis>) in central Asia

Roughly one-third of all eagle species are considered to be threatened or endangered, but the ecology of most eagles remains poorly understood. While the pronounced territoriality of breeding adults facilitates behavioral studies, the demography of non-breeding individuals (pre-adults and non-territorial floaters) is almost completely unknown. Traditionally, limited data on pre-adult and floater movement come from wing-tagging and/or telemetry studies. As an alternative to these methods we used genetic analyses of non-invasively collected feathers to investigate the population biology of non-breeding eastern imperial eagles (Aquila heliaca) in Kazakhstan. Microsatellite profiles of shed feathers indicate that eastern imperial eagles roost communally with other raptors. Furthermore, roosts are large and dynamic: 287 non-breeding eastern imperial eagles were detected in our sample, and a mark-recapture analysis estimated the total number to be 308 ± 8. The natal origins of these individuals were investigated by comparing their microsatellite profiles to those available for >90% of the eastern imperial eagle chicks hatched at the study site over the six previous breeding seasons. Only 4% of the individuals genetically matched a chick, suggesting that the reserve may serve as a critical refugium for pre-adults and itinerant floaters. Feathers have long been recognized as a suitable source of DNA, but few studies have used wide-scale, non-invasive collections of feathers (>1,000 samples) to investigate fundamental aspects of avian biology. Our research demonstrates that non-invasive genetic analyses of feathers can be used to evaluate population size, natal philopatry, and local movements of birds that are difficult to study using traditional means.     

Covariation between bill colouration and fitness components in a nocturnal bird

Vividly coloured chromatic signals play a key role in social and sexual signalling in diurnal birds, but their role is considered negligible in favour of achromatic (i.e. white, pure grey and black colourations) signals in nocturnal species. Here we studied colour variation and potential signalling of the yellow bill – a trait functioning as sexual signal in diurnal raptors during the breeding season in females of a truly nocturnal raptor, the little owl Athene noctua. We found that yellow‐red chroma of the bill was highly variable between individuals and positively correlated with female fitness prospects (i.e. brood size at fledging). In addition, we found that females with brighter bills were larger in size and produced owlets with a higher mass at fledging. This study suggests that yellow bill colouration in female little owls may potentially play a role in sexual signalling and may constitute the first evidence of chromatic colour signalling in a nocturnal bird.     

Head ornaments in owls: what are their functions?

We studied head ornamentation in owls by focussing on the hypothesis that it may serve both intra- and interspecific communication. We carried out pairwise comparisons of morphological, ecological and behavioural traits on a subset of closely related species with contrasting head ornamentation patterns. We found that the degree of head ornamentation was associated with habitat and activity rhythm, highly ornamented species (e.g., most of the genus Bubo ) living preferentially in open habitats and being active by day, but not with body size. Although our results do not exclude the possibility that head ornaments may represent a warning mechanism to startle predators and mobbers, they nevertheless suggest that such signals have evolved for visual communication with conspecifics, being more expressed in species that may use them more effectively without incurring the risk of predation or disturbance.