Differential behavioural and hormonal responses of voles and spiny mice to owl calls

Rodents usually respond to the presence of owls by reducing overall activity, in particular foraging. In this study, a playback of recorded tawny owl, Strix aluco, calls was sufficient to induce a marked effect in the social (Gunther's) vole, Microtus socialis. Some of the voles exposed to owl calls reduced their activity ('freeze' pattern) unlike control voles exposed to a human voice. Other voles, however, dashed around the cage ('flee' pattern). Owl calls also increased corticosterone levels in the voles, showing that the calls induced stress. We suggest that the behavioural dichotomy to freeze or flee in voles is a result of differences in individual normal behaviour and/or in stimulus interpretation. In the common spiny mouse, Acomys cahirinus, no behavioural changes were detected after exposure to owl calls, despite increased cortisol levels which are indicative of stress. Differences in the habitats of voles and spiny mice may explain the apparent lack of behavioural response in the latter. They are rock-dwelling rodents preferentially foraging between boulders and in rock crevices, where they are relatively protected from aerial predation, whereas voles forage in relatively open spaces. Copyright 1999 The Association for the Study of Animal Behaviour.     

Impacts of Agriculture on the Diet and Productivity of Mackinder's Eagle Owls (Bubo capensis mackinderi ) in Kenya

Land conversion for agriculture is an increasing threat to biodiversity conservation, but its ecological effects on African birds is practically unknown. We investigated the impacts of agriculture on the diet and productivity of a small, disjunct population of Mackinder's eagle owls ( Bubo capensis mackinderi  ) in central Kenya. Owl diet was determined by analysis of pellets and other remains and compared to small mammal populations estimated by live trapping in two habitats. Small mammal abundance was low and averaged 7.4 small mammals/ha in farms and 0.5 small mammals/ha in grassland. Owls consumed a wide diversity of prey. The majority were mammals (87%) followed by birds (7%) and insects (5%). The percentage of small mammals in owl diet correlated positively with the relative abundance of small mammals during monthly trapping sessions. Diet composition did not influence owl breeding success. Farming activities affected owl diet composition through crop production. The amount of maize, peas, and carrots growing in farms was correlated with the abundance of Mastomys sp. and Procavia sp. in the owl's diet. Agricultural activities had a large effect on Mackinder's eagle owl diet by increasing the abundance of certain small-mammal prey and attracting owl prey to farms, though farming practices harmful to owls were observed.     

The trigger for barn owl (Tyto alba) attack is the onset of stopping or progressing of the prey

Aiming at the question of whether barn owls favor to strike a moving or a stationary prey, we scrutinized the timing of launching 50 attacks of five barn owls (10 attacks/owl) in a captive environment. Attacks on stationary voles outnumbered attacks on moving voles, but this could merely reflect the higher portion of time during which voles were stationary. Notably, the majority of attacks (85-100%) were launched in less than 2 s (measured at accuracy of 0.04 s) after the voles ceased to progress or initiated progression. Therefore, the trigger for launching an attack is the transition of the prey from locomotion to still posture or vice versa.     

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.     

Predation on rodents in Białowieza primeval forest, Poland

Autumn and winter predation on bank vole Clethrtonomys glareolus and yellow-necked mouse Apodemus flavicollis was studied in 1985/86-88/89 in an 11 2 km² area of the Bialowieza National Park Rodents regularly increased in numbers from spring to autumn and decreased throughout winter Out of 23 species of predators, the most common were tawny owl Strix aluco (43-57 adult ind 10 km⁻²) weasel Mustela ntvahs (17-27 ind), buzzard Buteo buteo (12-16) and pine marten Martes martes (5-8) Voles and mice were the staple food for two specialists the stoat Mustela erminea and the weasel, and two generahsts the tawny owl and the pine marten The generalists exploited different alternative prey when rodents were scarce tawny owl -amphibians, marten - small mammals, and the red fox Vulpes vulpes - ungulate carcasses and hares The depth of snow and abundance of voles were two major factors shaping the contribution of voles to tawny owl and marten diets No such relationships were found for mice and generalist predators The predation by 8 species (tawny owl, buzzard, marten, weasel, stoat, polecat Mustela putortus fox, and raccoon dog Nyctereutes procyonoides) from 1 October to 15 April in 1986/87, 87/88, and 88/89 was estimated to be on average 28-35 voles and 14-17 mice ha Estimates suggested that three species were responsible for 86-95% of the total predation impact tawny owl (56-71%), weasel (11-21%) and marten (10-15%) The predation impact was similar to the annual decrease in rodent numbers from autumn till spring voles 35 (SD 111) lnds ha^-1in autumn and 8 (SD 2 6) lnds ha^-1in spring, and mice 24 (SD 16 3) mds ha⁻¹ in autumn and 3 (SD 2 5) in spring Predation, therefore, was regarded as the main agent of rodent mortality throughout autumn and winter     

Avian predation upon a mixed community of common voles (Microtus arvalis) and wood mice (Apodemus sylvaticus)

Summary Pellets of diurnal avian predators (mainly kestrels and buzzards) were analysed to prove the hypothesis of selective predation for a mixed population of small rodents. It was found that voles heavily predominated as prey over mice (up to a factor of 19 during winter). Within both prey species, predation focussed on distinct parts of the populations: during winter the heaviest specimens were preferentially captured, during summer the subadults were in an exposed position. In the voles, an additional predominance of males occurred (up to a factor of 5.2 during summer). These findings verify the assumption of Errington (1956) that speciments of a low social rank are susceptible to the highest risk 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.     

The effect of barn owls (Tyto alba) on the activity and microhabitat selection of Gerbillus allenbyi and G. pyramidum

Predation plays an important role in ecological communities by affecting prey behavior such as foraging and by physical removal of individual prey. In regard to foraging, animals such as desert rodents often balance conflicting demands for food and safety. This has been studied in the field by indirectly manipulating predatory risk through the alteration of cues associated with increased risk such as cover or illumination. It has also been studied by directly manipulating the presence of predators in aviaries. Here, we report on experiments in which we directly manipulated actual predatory risk to desert rodents in the field. We conducted a series of experiments in the field using a trained barn owl (Tyto alba) to investigate how two species of coexisting gerbils (Gerbillus allenbyi and G. pyramidum) respond to various cues of predatory risk in their natural environment. The gerbils responded to risk of predation, in the form of owl flights and owl hunger calls, by reducing their activity in the risky plot relative to the control plot. The strongest response was to owl flights and the weakest to recorded hunger calls of owls. Furthermore, when risk of predation was relatively high, as in the case with barn owl flights, both gerbil species mostly limited their activity to the safer bush microhabitat. The response of the gerbils to risk of predation disappeared very quickly following removal of the treatment, and the gerbils returned to normal levels of activity within the same night. The gerbils did not respond to experimental cues (alarm clock), the presence of the investigators, the presence of a quiet owl, and recorded white noise. Using trained barn owls, we were able to effectively manipulate actual risk of predation to gerbils in natural habitats and to quantify how gerbils alter their behavior in order to balance conflicting demands of food and safety. The method allows assessment of aspects of behavior, population interactions, and community characteristics involving predation in natural habitats.     

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.     

Refuge sites of voles under owl predation risk: priority of dominant individuals?

In an aviary experiment, we studied whether body size or habitatfamiliarity of field voles (Microtus agrestis) affected predationrisk by Tengmalm's owls (Aegolius funereus). In the field, wecompared the body size of field voles snap-trapped in good (covered)and poor (open) habitats in 1992 and 1994 to determine whetherthere were habitat-related differences in the body size of voles.In the aviary, large individuals occupied the good habitat significantlymore than small individuals both in the control (owl not present)and experimental treatments (owl present). Furthermore, habitat-familiarvoles inhabited the good habitat more than habitat-unfamiliarvoles did when an owl was present Our field data were consistentwith our aviary data: larger field voles were more frequentlyfound in good habitats than in poor habitats. In the aviary,Tengmalm's owl predation risk was higher for small and habitat-unfamiliarvoles. This suggests that large field voles may have priorityto sheltered habitats. Furthermore, habitat familiarity mayplay a central role in avoiding risky habitats.     

Using Detection Dogs to Conduct Simultaneous Surveys of Northern Spotted (Strix occidentalis caurina) and Barred Owls (Strix varia)

State and federal actions to conserve northern spotted owl (Strix occidentalis caurina) habitat are largely initiated by establishing habitat occupancy. Northern spotted owl occupancy is typically assessed by eliciting their response to simulated conspecific vocalizations. However, proximity of barred owls (Strix varia)-a significant threat to northern spotted owls-can suppress northern spotted owl responsiveness to vocalization surveys and hence their probability of detection. We developed a survey method to simultaneously detect both species that does not require vocalization. Detection dogs (Canis familiaris) located owl pellets accumulated under roost sites, within search areas selected using habitat association maps. We compared success of detection dog surveys to vocalization surveys slightly modified from the U.S. Fish and Wildlife Service's Draft 2010 Survey Protocol. Seventeen 2 km ×2 km polygons were each surveyed multiple times in an area where northern spotted owls were known to nest prior to 1997 and barred owl density was thought to be low. Mitochondrial DNA was used to confirm species from pellets detected by dogs. Spotted owl and barred owl detection probabilities were significantly higher for dog than vocalization surveys. For spotted owls, this difference increased with number of site visits. Cumulative detection probabilities of northern spotted owls were 29% after session 1, 62% after session 2, and 87% after session 3 for dog surveys, compared to 25% after session 1, increasing to 59% by session 6 for vocalization surveys. Mean detection probability for barred owls was 20.1% for dog surveys and 7.3% for vocal surveys. Results suggest that detection dog surveys can complement vocalization surveys by providing a reliable method for establishing occupancy of both northern spotted and barred owl without requiring owl vocalization. This helps meet objectives of Recovery Actions 24 and 25 of the Revised Recovery Plan for the Northern Spotted Owl.     

Owl predation on snowshoe hares: consequences of antipredator behaviour

We show evidence of differential predation on snowshoe hares (Lepus americanus) by great horned owls (Bubo virginianus) and ask whether predation mortality is related to antipredator behaviour in prey. We predicted higher predation on (1) young and inexperienced hares, (2) hares in open habitats lacking cover to protect from owl predation, and (3) hares in above average condition assuming that rich food patches are under highest risk of predation. Information on killed hares was obtained at nest sites of owls and by monitoring hares using radio-telemetry. The availability of age classes within the hare population was established from live-trapping and field data on reproduction and survival. Great horned owls preferred juvenile over adult hares. Juveniles were more vulnerable to owl predation before rather than after dispersal, suggesting that displacement or increased mobility were not causes for this increased mortality. Owls killed ratio-collared hares more often in open than in closed forest types, and they avoided or had less hunting success in habitats with dense shrub cover. Also, owls took hares in above average condition, although it is unclear whether samples from early spring are representative for other seasons. In conclusion, these results are consistent with the hypothesis that variation in antipredator behaviours of snowshoe hares leads to differential predation by great horned owls.     

The role of Apodemus mice and Microtus voles in the diet of the Tengmalm’s owl in Central Europe

Based on a long-term dataset (1999–2010), we investigated how the availability of main prey affects the breeding density and food ecology of the Tengmalm’s owl (Aegolius funereus) in the Czech Republic. In particular, we assessed the role of Microtus voles and Apodemus mice in the diet, based on the main predictions of the optimal diet theory that the diet composition depends on the availability of the main prey. We found that (i) the Tengmalm’s owl exhibited no numerical response to the availability of Microtus voles and Apodemus mice in the field; (ii) the availability of Apodemus mice in the field positively affected their proportion in the diet (26 %), and despite a high proportion of Microtus voles in the owls’ diet (47 %), no relationship was found between their availability in the field and proportion in the diet; (iii) the proportion of Apodemus mice was negatively correlated to the proportion of Microtus voles, Sorex shrews and birds in the diet, but no similar relationship was detected for Microtus voles; (iv) the reproductive output of Tengmalm’s owls was positively correlated to the proportion of Apodemus mice in the diet, as well as to Apodemus mice and Microtus vole availability in the field; and (v) diet diversity and diet overlap were not significantly affected by the abundance of Apodemus mice and Microtus voles. Therefore, the validity of these main optimal diet theory predictions was not confirmed, especially for Microtus vole prey, due to an opportunistic choice between Apodemus mice and Microtus voles. We suggest that the reproductive output of nocturnal raptors in Central Europe may be less dependent on Microtus vole supply than that of their northern counterparts.     

Live blind snakes (Leptotyphlops dulcis) in eastern screech owl (Otus asio) nests: a novel commensalism

Summary Eastern screech owls bring live blind snakes to their nestlings, whereas all other prey are delivered dead. Some of the snakes are eaten but most live in nest debris, where they eat soft-bodied insect larvae from the decomposer community in fecal matter, pellets, and uneaten prey. Consumption of larvae may reduce larval parasitism on owl nestlings or larval competition with nestlings for food stored in the nest, because nestlings with live-in blind snakes grow faster and experience lower mortality than same-season broods lacking snakes. We propose a commensalistic association in which the screech owl benefits reproductively and the live-in blind snake is not affected.     

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.     

Non-additivity among multiple cues of predation risk: a behaviorally-driven trophic cascade between owls and songbirds

Non-lethal effects of predators on prey are initiated in the form of responses to direct and indirect cues of predation risk. Like their lethal equivalents, non-lethal effects may affect species further down the food web initiating a behaviorally-driven trophic cascade. I presented a direct cue of predation risk, owl vocalizations, to white-footed mice ( Peromyscus leucopus ) during either a new or full moon (indirect cue). Mice reduced their activity in space by nearly two-thirds in response to playbacks of owl vocalizations during a full moon. However, neither moonlight (full vs new) nor the presence/absence of owl calls had an effect on space use when each cue varied singly. Previous studies have demonstrated a tight correlation between spatial activity in mice as used in the current experiment and nest predation rates on ground-nesting birds. Because moonlight is a ubiquitous deterrent of activity in nocturnal rodents I used of long-term nesting records the veery ( Catharus fuscescens ) to test whether nest predation rates were correlated negatively with moonlight. For half the lunar cycle (∼full moon to new moon) predation rates decreased with moonlight as predicted. During the second half of the lunar cycle predation and moonlight did not correlate as expected, but this was likely due to the depletion of vulnerable nests after a period of in which predation rates were at their maximum near the full moon. These studies suggest that the non-lethal effects of predatory risk on mice (i.e. changes in space use) cascade to affect their prey. Through the mechanism of reduced space use by rodents, perceived predation risk has the potential to significantly and indirectly affect songbird nest predation rates.     

Food habits of genetically identified pine marten (<Emphasis Type="Italic">Martes martes</Emphasis>) expanding in agricultural lowlands (NW Italy)

We assessed the diet of pine marten (Martes martes) expanding in the heavily human-altered agricultural plain of the River Po, northern Italy. Between February 2008 and November 2009, surveys were carried out twice a week during seasonal sampling sessions of three to four consecutive weeks. To distinguish the faecal samples from those of sympatric carnivores, a polymerase chain reaction-restriction fragment length polymorphism method was applied. The availability of small mammals was assessed by the analysis of 59 barn owl (Tyto alba) pellets. A total of 109 pine marten faeces were analysed. Its diet consisted of fruit, rodents, lagomorphs and birds. Seasonal variation occurred for fruit, which prevailed in summer, and rodents, which were more preyed upon in autumn. In winter, the diet of the pine marten was almost totally based on vertebrates, and lagomorphs were the main source of protein in summer. Use of small mammals differed significantly from their availability, voles, particularly bank vole Myodes glareolus, being preferred to mice (Apodemus sp.) and rats (Rattus sp.). Medium-size mammals formed about 18% of pine marten diet, a value generally reported for high-latitude habitats. In agricultural areas, the pine marten proved to be an opportunistic predator, able to face the reduced availability of small mammals by preying upon medium-size prey and fruit.     

Seasonal selectivity of Magellanic horned owl (Bubo magellanicus) on rodents

This study examines prey selection by Magellanic horned owls (Bubo magellanicus) in an ecotonal steppe area of northwestern Argentine Patagonia, and analyzes morphological and behavioral traits of the owls main rodent prey. The owls diet was studied for two years, along with field estimates of rodent abundance. The frequency distribution of rodents was significantly different from that estimated from trapping, indicating that Magellanic horned owl behaved as a selective predator. Eligmodontia morgani and Abrothrix xanthorhinus, the smallest species inhabiting open areas, were consumed in lower proportion than their occurrence estimated from the trapped sample, whereas the larger Abrothrix longipilis and Oligoryzomys longicaudatus, which inhabited bushy habitats, were eaten in a greater proportion than their estimated abundance. It is suggested that distinctive morphological and behavioral characteristics among prey interacting with the owl hunting strategy, accounted for their differential vulnerability to predation.     

The prey of the Barn owl (Tyto alba alba) in East Norfolk

Some 5000 Barn owl pellets, collected from sites in East Norfolk during the past decade, have been examined. The most important prey species, by weight, were the Field vole (Microtus agrestis) 52%, the Brown rat (Rattus norvegicus) 17%, and the Common shrew (Sorex araneus) 12%. The prey varies over different habitats; Wood mice (Apodemus sylvaticus) and Bank vole (Clethrionomys glareolus) forming a higher proportion in localities with hedges, scrub and woodland than in open grasslands. These results are comparable with those of other recent work. However, when compared with studies conducted over 30 years ago, it would appear that the Field vole now constitutes a higher proportion, and the Brown rat a lower proportion, of the prey taken.     

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.