Exposure affects the risk of an owl being mobbed – experimental evidence

Mobbing is a widespread anti‐predator strategy in birds, and predators are generally expected to avoid mobbing. For example, observational studies suggest that the cryptic roosting behaviour of nocturnal predators, such as many owls, may be a strategy to limit mobbing. In this paper, we present the results of the first experimental study investigating to what degree roost exposure influences the risk of being mobbed, and the intensity of a mobbing incidence once initiated. To determine these factors, we used an experimental setup with taxidermic mounts of tawny owls Strix aluco in Grib Skov forest, Denmark. The risk of an owl being mobbed during a 50 min morning survey period increased with the exposure of its roosting position, from 24% when hidden to 85% when openly exposed. The corresponding increase in the afternoon was from 6% to 36%. This suggests that an owl may minimize the mobbing rate by reducing the encounter rate with potential mobbers through its choice of roost. Once initiated, the duration of the mobbing (a proxy for the presumed cost of being mobbed) was independent of the roosting position of the mounted owl, but was positively correlated with the number of birds in the mob.     

Exposure affects the risk of an owl being mobbed – experimental evidence

Mobbing is a widespread anti-predator strategy in birds, and predators are generally expected to avoid mobbing. For example, observational studies suggest that the cryptic roosting behaviour of nocturnal predators, such as many owls, may be a strategy to limit mobbing. In this paper, we present the results of the first experimental study investigating to what degree roost exposure influences the risk of being mobbed, and the intensity of a mobbing incidence once initiated. To determine these factors, we used an experimental setup with taxidermic mounts of tawny owls Strix aluco in Grib Skov forest, Denmark. The risk of an owl being mobbed during a 50 min morning survey period increased with the exposure of its roosting position, from 24% when hidden to 85% when openly exposed. The corresponding increase in the afternoon was from 6% to 36%. This suggests that an owl may minimize the mobbing rate by reducing the encounter rate with potential mobbers through its choice of roost. Once initiated, the duration of the mobbing (a proxy for the presumed cost of being mobbed) was independent of the roosting position of the mounted owl, but was positively correlated with the number of birds in the mob.     

Diurnal exposure as a risk sensitive behaviour in tawny owls Strix aluco?

Tawny owls Strix aluco generally roost in cryptic locations during the day. To test the hypothesis that this cryptic behaviour is an effort to avoid mobbers or avian predators, we measured diurnal behaviour and cause-specific mortality of radio-tagged birds. Non-breeding adults (assumed to be well fed individuals, optimising their own survival) roosted in less exposed locations than adults with young and newly independent juveniles. Parents roosted in the most exposed sites when their young were immature and vulnerable to depredation, probably to guard offspring. Newly independent juveniles apparently selected roosting sites in exposed places to get access to food, as this behaviour was associated with lower perching heights and higher prey abundance beneath their roosting sites. They also perched in more exposed sites, closer to the ground, in summers with low prey abundance compared to summers with high prey abundance. After previous encounters with goshawks Accipiter gentilis , dependent juveniles roosted in less exposed places compared to other young. The increased risk of being mobbed was highly significant with increasing roosting exposure. Once an owl was mobbed, the intensity of the mobbing correlated positively with the mass of the mobbers, but mobbing birds never killed any owls. In contrast, diurnal raptors caused 73% of natural owl deaths (n=15) and the depredation rate by raptors was 3.8 times higher in population classes that generally roosted in more exposed locations than did non-breeding adults. We therefore suggest that depredation by diurnal raptors is the main factor shaping the diurnal behaviour of tawny owls.     

Interspecific offspring killing in owls

In Baranya County (Southern Hungary), tawny owls (Strix aluco) and barn owls (Tyto alba) sequentially use the same nest boxes in a significant number of cases. A total of 460 broods were observed between 1996 and 2003 and, in 12 cases, whole broods of dead tawny owl chicks were registered that had apparently been killed. On investigating the reproductive life characteristics, population sizes, and frequency of killing in these two species, it was concluded that: (1) with growing barn owl population, the number of sequential broods increases but changes in tawny owl population size have no effect on the frequency of sequential broods; (2) the number of killings depends on the number of sequential broods; and (3) with growing barn owl population, the number of killings also grows and this change is unaffected by the size of the tawny owl population. However, no killing occurs as long as 50–60% of the nest boxes are unoccupied. There is no killing either until the percentage of nest boxes occupied by barn owls reaches 40%, although a threshold value like this cannot be shown for the tawny owl. In the cases when a barn owl breeding follows the tawny owl's, the percentage of killing is significantly higher compared to that when barn owls do not breed in the same box. These results indicate that barn owls kill the offspring of tawny owls. By these means, they obtain a breeding place earlier than without killing the chicks of the other species, and this results in higher reproductive success. © 2008 The Linnean Society of London, Biological Journal of the Linnean Society, 2008, 95 , 488–494.     

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.     

Response of Captive Raptors to Avian Mobbing Calls: the Roles of Mobber Size and Raptor Experience

The ‘move on’ hypothesis for avian mobbing proposes that mobbing induces stress in potential predators, thereby provoking them into moving elsewhere. We tested whether mobbing is stress inducing by subjecting captive owls, hawks, and falcons to the mobbing calls of four species of co‐occurring passerine birds that vary considerably in body size. Test subjects comprised 15 individuals of seven species of birds of prey that were housed at a wildlife rehabilitation center in northwestern Pennsylvania, USA. Playback treatments included mobbing calls of the black‐capped chickadee (Poecile atricapillus), blue‐headed vireo (Vireo solitarius), blue jay (Cyanocitta cristata), and American crow (Corvus brachyrhynchos), which vary in size from 12 g (chickadee) to 500 g (crow). A non‐mobbing vocalization (song of the black‐capped chickadee) was included in the playback treatments as a control. Playback treatment produced pronounced effects on three behavioral indicators of probable stress: head orientation toward the playback speaker, raising of feathers or spreading of wings, and changing of perch positions. Test subjects responded more vigorously to mobbing calls of the large passerines (jays and crows) than to those of the smaller passerines (chickadees and vireos). In addition, raptors that had entered the rehabilitation facility as adults generally responded more vigorously to the mobbing calls of jays and crows than did naive individuals that had entered the facility as fledglings or young juveniles. Our results are therefore consistent with the ‘move on’ hypothesis and suggest (1) that the mobbing calls of large passerines are more effective in provoking stress and altering the behavior of potential predators than are the mobbing calls of small passerines and (2) that a raptor's previous experience with mobbing in the wild can exaggerate the strength of its response, particularly to the mobbing calls of large passerines.     

Effects of avian mobbing on roost use and diet of powerful owls,Ninox strenua

We observed the species and numbers of mobbing birds and their effects on a large, nocturnal, bird-eating predator, the powerful owl, together with the pattern of owl predation on mobbing and non-mobbing species. Owls were mobbed on 35 occasions by seven of 44 species of forest birds at a site composed of open forest (88% by area) and rainforest (12%). The majority of bouts involved individuals of a single species, although mixed groups were observed on nine occasions. Regular mobbers were between 4 and 26% of the owls’ body weight. Owls abandoned their daytime roosts during 20% of bouts and responded by calling or actively monitoring mobbers during 54% of bouts. Mobbing appeared to explain why owls roosted in rainforest significantly more often than expected by its availability, mobbing being significantly less frequent in rainforest than in open forest. Only one mobbing species regularly occupied rainforest and the canopy of roosts in rainforest was denser than that in open forest, thus reducing the chances of an owl being detected by potential mobbers. Twelve species of forest birds were within the range of prey size of the powerful owl (75–800 g): six were mobbers and six non-mobbers. The frequency of owl predation on non-mobbers was 8.75 times that on mobbers. The species in this study took a high risk by mobbing a very large predator, but benefited by greatly reducing their chances of predation.     

<Emphasis Type="Italic">Apodemus</Emphasis> mice as the main prey that determines reproductive output of tawny owl (<Emphasis Type="Italic">Strix aluco</Emphasis>) in Central Europe

During the years 2008–2014, we studied diet composition, the number of breeding pairs, and reproductive output of tawny owls in Central Europe (Czech Republic) in relation to availability of main prey in the field. We also performed a meta-analysis on diet composition of tawny owl in Europe that confirmed the important role of Apodemus mice in tawny owl diet in Central Europe. In concordance, Apodemus mice were the main prey of tawny owl in our study area (38.7%), and Microtus/Myodes voles (15.4%), birds (12.1%) and others (33.8%) were alternative prey. We found a positive relationship between the proportion of Apodemus mice in the diet and their abundance in the field (beta = 0.23, P = 0.001). Availability of main prey (Apodemus mice, Microtus/Myodes voles or Sorex shrews) in the field was not correlated with the number of breeding pairs. Proportion of birds in diet (expressed by scores from multivariate analysis), which was inversely related to proportion of Apodemus mice, was positively correlated with laying date (beta = 0.66, P = 0.012) and negatively correlated with clutch size (beta = − 0.45, P = 0.004) and brood size (beta = − 0.16, P = 0.076). We also found negative relationships between laying date and clutch size (beta = − 0.13, P = 0.014) and brood size (beta = − 0.07, P = 0.057). Our results support the idea that diet and breeding ecology of owls in Central Europe is mainly driven by the availability of Apodemus mice that are suitable prey due to their similar habitat requirements and nocturnal activity.     

Fluctuating Asymmetry in Body Traits Increases Predation Risks: Tawny Owl Selection Against Asymmetric Woodmice

During the last decade, the study of fluctuating asymmetry (FA) in relation to different fitness aspects has become a popular issue in evolutionary biology. There has been much recent debate in subtle departures from perfect symmetry in bilaterally paired morphological characters, and the extent to which such departure actually reflects aspects of individual quality and fitness. We used data from pellet collection and trapping sessions involving the trophic system Apodemus – Strix aluco, to test the hypothesis that asymmetric woodmice disproportionately fell prey to the tawny owl compared with “normal” woodmice. We found that woodmice preyed on by owls had significantly more asymmetric leg bones than survivors, particularly hind legs, those devoted to jumping. Thus asymmetry in locomotory traits apparently increased predation risks due probably to minor efficiency of asymmetric woodmice in evading predators or to their general low quality. These results suggest that FA affects fitness and consequently may be a good predictor of survival chances for woodmice, i.e. their quality; on the other hand, by removing asymmetric individuals, tawny owls can exert a stabilising selection on prey populations.Co-ordinating editor: M. Klaassen     

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.     

Effect of spatial context on the mobbing reaction of pied flycatchers to a predator model

Seven pairs of breeding pied flycatchers (Ficedula hypoleuca) were repeatedly presented a stuffed owl from a specific location until their mobbing response had waned. Subsequent change in the location of the ‘predator’ evoked renewed responsiveness from the birds, as measured by their increased calling rate. The results suggest that predator recognition incorporates an evaluation of the spatial context and, furthermore, support the view that the relative lack of habituation to recurring predators in nature is due, in part, to ever-changing spatial relationships of the predator relative to the inanimate environment.     

Gray plumage color is more cryptic than brown in snowy landscapes in a resident color polymorphic bird

Camouflage may promote fitness of given phenotypes in different environments. The tawny owl (Strix aluco) is a color polymorphic species with a gray and brown morph resident in the Western Palearctic. A strong selection pressure against the brown morph during snowy and cold winters has been documented earlier, but the selection mechanisms remain unresolved. Here, we hypothesize that selection favors the gray morph because it is better camouflaged against predators and mobbers in snowy conditions compared to the brown one. We conducted an online citizen science experiment where volunteers were asked to locate a gray or a brown tawny owl specimen from pictures taken in snowy and snowless landscapes. Our results show that the gray morph in snowy landscapes is the hardest to detect whereas the brown morph in snowy landscapes is the easiest to detect. With an avian vision model, we show that, similar to human perceivers, the brown morph is more conspicuous than the gray against coniferous tree trunks for a mobbing passerine. We suggest that with better camouflage, the gray morph may avoid mobbers and predators more efficiently than the brown morph and thus survive better in snowy environments. As winters are getting milder and shorter in the species range, the selection periods against brown coloration may eventually disappear or shift poleward.     

Auditory Perception of Hawks and Owls for Passerine Alarm Calls

The auditory perception of eight species of raptors was examined to test the hypothesis of Marler (1955) that these avian predators are unable to locate certain songbird alarm calls. In particular, Marler proposed that mobbing calls have characteristics that enhance their locatability and that these characteristics are absent in the high-frequency 'seet' calls given by individual songbirds. To test this hypothesis, the behavioral responses of four species of owls and four species of hawks, housed at two different raptor rehabilitation sites, to tape recorded alarm calls were examined. Each raptor was exposed to a random order of 10 trials of mobbing calls and 10 trials of a seet call. Responses were scored based upon head angle orientations. Hawks and owls responded more often and more accurately to mobbing calls than to seet calls. In general, owls responded to significantly more calls than hawks. The results are consistent with Marler's hypothesis that raptors have difficulty locating passerine seet calls. Nevertheless, future studies should test mobbing calls that vary in their frequency and duration ( Ficken & Popp 1996 ) to determine whether some mobbing calls are more difficult to locate than others.     

The relationship between intra–guild diet overlap and breeding in owls in Israel

Even though intra-guild predators frequently prey on the same species, it is unclear whether diet overlap between two predators is a source of interspecific competition or whether predators simply use the same abundant prey resource. We measured the extent to which the diets of barn owls (Tyto alba) and long-eared owls (Asio otus) in Israel overlap and examined whether yearly differences in diet overlap correlate with barn owl breeding success. Pianka’s index of niche overlap was positively related to barn owl population size but not to its breeding success. The number of breeding barn owls was higher when long-eared owls consumed more rodents, suggesting that diet overlap most likely increased when rodents became more abundant. Therefore, in Israel, when these two owl species prey more often on rodents, their diets are more similar and interspecific competition is reduced. Unlike sympatric populations in Europe, in years when rodents are less abundant in Israel long-eared owls switch to hunting alternative prey (e.g., birds), perhaps to avoid competition with barn owls.     

Young and female‐biased irruptions in pygmy owls Glaucidium passerinum in southern Finland

Irruptive migrants often show biased sex and age ratio, and typically young females are the most abundant class participating in irruptions. Several hypotheses have been proposed to explain differential migration in birds. We examined these hypotheses in a sexually size‐dimorphic species (females being larger than males), the pygmy owl Glaucidium passerinum, whose migration behaviour has also been poorly documented. Migration data were collected at the Hanko Bird Observatory, SW Finland during 1979–2010. Pygmy owls showed large fluctuations in migration numbers between years. Most of the migrants were young birds and females migrated in larger numbers than males. Results support the ‘territory defence hypothesis’ since males showed weaker tendency to migrate despite the smaller body size, but the ‘dominance hypothesis’ was also supported (subordinate young outnumber dominant adults in migration numbers). Findings support the idea that in owl species, which are dependent on nesting cavities, males show lower migration behaviour than females, whereas the pattern is opposite in species which normally breed outside cavities. In addition, adults migrated later than young, likely because they need to moult remiges before departure. Early hatched young also migrated earlier than late hatched young, suggesting that more dominant young migrate first.     

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.     

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).     

Home range and movement patterns of Sokoke Scops Owl Otus ireneae

Virani, M. 2000. Home range and movement patterns of Sokoke Scops Owl Otus ireneae. Ostrich 71 (1 & 2): 139–142.

A radio-telemetric study of the endangered Sokoke Scops Owl Otus ireneae was conducted between July and December 1993. The aims were to determine the species' home range and movement patterns with respect to time and moon phases. Information gathered would then be used to formulate a rational conservation plan to ensure their survival. Six adult owls (from three adjacent pairs) were monitored during the study period. Pairs held exclusive home ranges with little (2.6%) or no overlap with their neighbours. Mean home range size (MCP) of individual owls was 8.8 ha while mean home range size of each pair was 11.0 ha. Peak owl activity took place immediately after dusk and prior to dawn. Periods of lulls occurred between 23h00 and 03h00. Movement per unit time was negatively correlated with distance from roost. The owls tended to forage further from their roosts on nights with decreased illumination from the moon. Maximum owl distances from roosts were attained between 00h00 and 02h00.     

Effects of episodic bamboo mast seeding on top predators in the southern Andes

Woody bamboos that undergo masting on a cyclic basis constitute large‐scale endogenous disturbances in forests of America, Africa and Asia, driving long‐ and short‐term effects on community structure and dynamics. Among the transient effects of these nonequilibrial phenomena are rodent outbreaks whose potential bottom‐up consequences on top predators have never been explored. We investigated the effects of unpredictable rodent outbreaks on the assemblage of nocturnal raptors of the southern Andes after a large‐scale (>140 000 ha), spatially heterogeneous, Chusquea culeou masting event in north Argentine Patagonia. We compared owl numbers and behaviours between pre‐masting (2009) and post‐masting (2011) at subsidized (outbreaking rodents) and unsubsidized (normal rodents) contiguous sites. Both generalist (opportunistic forest resident) and rodent‐specialist (forest‐facultative) owls were monitored, with emphasis on the resident territorial rufous‐legged owl (Strix rufipes). The resident owls behaved as predicted, perceiving the rodent increases soon and gathering at subsidized sites, while apparently relaxing territoriality. Contrary to our predictions, later at the rodent outbreak phase, resident territorial owls turned inconspicuous, coinciding – causally or not – with an irruption of forest‐facultative barn owls (Tyto alba tuidara), and influx of some open country short‐eared owls (Asio flammeus suinda, some of which took a chance to breed in the woods). Considering the whole rodent outbreak period, besides significant changes in owls’ numbers, we recorded a notable adjustment in owls’ foraging modes in response to food surplus (consuming prey heads only), and null interference behaviours among all observed species. This study provides a first quantitative assessment of the effects of bamboo episodic masting on top carnivores globally, and contributes novel data on the indirect effects of these events in forests of South America.     

Higher nest predation risk in association with a top predator: mesopredator attraction?

Breeding close to top predators is a widespread reproductive strategy. Breeding animals may gain indirect benefits if proximity to top predators results in a reduction of predation due to suppression of mesopredators. We tested if passerine birds gain protection from mesopredators by nesting within territories of a top predator, the Ural owl (Strix uralensis). We placed nest boxes for pied flycatchers (Ficedula hypoleuca) in Ural owl nest sites and in control sites (currently unoccupied by owls). The nest boxes were designed so that nest predation risk could be altered (experimentally increased) after flycatcher settlement; we considered predation rate as a proxy of mesopredator abundance. Overall, we found higher nest predation rates in treatment than in control sites. Flycatcher laying date did not differ between sites, but smaller clutches were laid in treatment sites compared to controls, suggesting a response to perceived predation risk. Relative nest predation rate varied between years, being higher in owl nest sites in 2 years but similar in another; this variation might be indirectly influenced by vole abundance. Proximity to Ural owl nests might represent a risky habitat for passerines. High predation rates within owl territories could be because small mesopredators that do not directly threaten owl nests are attracted to owl nest sites. This could be explained if some mesopredators use owl territories to gain protection from their own predators, or if top predators and mesopredators independently seek similar habitats.