Effects of the risk of competition and predation on large secondary cavity breeders

The effects of competition and risk of predation on secondary cavity breeders were examined between the 2008 and 2009 breeding seasons using an experimental design manipulating two nest entrance sizes (large entrances allowed Barn Owls (Tyto alba) to enter, while the small entrances excluded them). During the 2009 breeding season, the entrance sizes of nest boxes were exchanged, so that if during one year a nest box in a particular location had a small entrance, the second year it had a large entrance and vice versa. Barn Owls and Eurasian Kestrels (Falco tinnunculus) occupied 67.3 and 17.3%, respectively, of large entrance nest boxes. Significantly more Jackdaws (Corvus monedula), House Sparrows (Passer domesticus) and Scops Owls (Otus scops) bred in nest boxes with small than with large entrances. After nest box entrance sizes were exchanged, Barn Owls and smaller species did not breed in the same nest boxes with the new entrance size. Jackdaws probably did not breed in large entrance nest boxes due both to exploitation competition (Barn Owls and Eurasian Kestrels occupied the majority of large entrance nest boxes), and may also have avoided empty nest boxes because of the risk of interference competition; whereas smaller species may have also avoided large entrance nest boxes due to risk of predation.     

Geographic and temporal variation in the consumption of bats by European Barn Owls

Capsule We report a review of the occurrence of bats in the Barn Owl diet Tyto alba in Europe. Based on 802 studies reporting 4.02 million prey items identified in pellets, 4949 were bats (0.12%). We found that bat predation decreased during the last 150 years, is more frequent on islands than mainland, and is higher in eastern than western Europe and in southern than northern Europe. Although Barn Owls usually capture bats opportunistically, they can sometimes specialize on them.     

FIRST ANNUAL REPORT ON THE RHODESIAN ORNITHOLOGICAL SOCIETY'S NEST RECORD SCHEME FOR THE YEAR ENDED 30 JUNE, 1956

MENDELSOHN, J. M. 1989. Habitat preferences, population size, food and breeding of six owl species in the Springbok Flats, South Africa. Ostrich 60:183-190.

Information on the habitat preferences, population size, food and breeding of Barn, Grass, Whitefaced, Marsh, Pearlspotted and Spotted Eagle Owls was obtained in a 6900-ha area in the Springbok Flats, South Africa. Seventy-two per cent of the area consisted of cultivated fields not usually used by owls. Hunting, roosting and nesting requirements were largely met in 1930 ha of verges, farmyards and patches of wood land ant grassland, here was an estimated total population of 303 owls in the area, giving an overall density of 22,7 ho/owl for the whole area or 6.4 ha/owl for those areas used by owls. These high densities were attributed to an abundance of Mastomys natalensis, the most important prey item for all except Pearlspotted Owls. Rates of predation on M. natalensis varied in relation to their population density, as indicated by rodent trapping results. Marsh Owls ate more insects in summer than at other times. Barn and Marsh Owls usuall laid in March-April and August-September, while other species started breeding in July-October. de timing of breeding of some owls may be related to changes in rates of recruitment of juvenile M. natalensis. Most Marsh Owl nests were placed on the southwestern sides of grass clumps or shrubs.     

Spatial,road geometric and biotic factors associated with Barn Owl mortality along an interstate highway

Highway programmes typically focus on reducing vehicle collisions with large mammals because of economic or safety reasons, while overlooking the millions of birds that die annually from traffic. We studied wildlife–vehicle collisions along an interstate highway in southern Idaho, USA, with among the highest reported rates of American Barn Owl Tyto furcata road mortality. Carcass data from systematic and ad hoc surveys conducted in 2004–2006 and 2013–2015 were used to explore the extent to which spatial, road geometric and biotic factors explained Barn Owl–vehicle collisions. Barn Owls outnumbered all other identified vertebrate species of roadkill and represented > 25% of individuals and 73.6% of road‐killed birds. At a 1‐km highway segment scale, the number of dead Barn Owls decreased with increasing numbers of human structures, cumulative length of secondary roads near the highway and width of the highway median. The number of dead Barn Owls increased with higher commercial average annual daily traffic (CAADT), small mammal abundance index and grass rather than shrubs in the roadside verge. The small mammal abundance index was also greater in roadsides with grass vs. mixed shrubs, suggesting that Barn Owls may be attracted to grassy portions of the highway with more abundant small mammals for hunting prey. When assessed at a 3‐km highway segment scale, the number of dead Barn Owls again increased, with higher CAADT as well as with greater numbers of dairy farms. At a 5‐km scale, the number of dead Barn Owls increased with a greater percentage of cropland near the highway. Although human conversion of the environment from natural shrub‐steppe to irrigated agriculture in this region of Idaho has probably enhanced habitat for Barns Owls, it simultaneously has increased risk for owl–vehicle collisions where an interstate highway traverses the altered landscape. We review some approaches for highway mitigation and suggest that reducing wildlife–vehicle collisions involving Barn Owls may contribute to the persistence of this species.     

Wing and tail myology of Tyto furcata (Aves,Tytonidae)

Barn Owls (Tytonidae) are nocturnal raptors with the largest geographical distribution among Strigiformes. Several osteological, morphometrical, and biomechanical studies of this species were performed by previous authors. Nevertheless, the myology of forelimb and tail of the Barn Owls is virtually unknown. This study is the first detailed myological study performed on the wing and tail of the American Barn Owl (Tyto furcata). A total of 11 specimens were dissected and their morphology and muscle masses were described. Although T. furcata has the wing and tail myological pattern present in other species of Strigiformes, some peculiarities were observed including a difference in the attachment of m. pectoralis propatagialis due to the lack of the os prominence, and the presence of an osseous arch in the radius that seems to widen the anchorage area of the mm. pronator profundus, extensor longus alulae, and extensor longus digiti majoris. Furthermore, the m. biceps brachii has an unusual extra belly that flexes the forearm. The interosseous muscles have a small size and lacks ossified tendons. This feature may be indicative of a lower specialization in the elevation and flexion of the digiti majoris. Forelimb and tail muscle mass account for 10.66 and 0.24% of the total body mass, respectively. Forelimb muscle mass value is similar to the nocturnal (Strigiformes) and diurnal (Falconidae and Accipitridae) raptors, while the tail value is lower than in the diurnal raptors (Falconidae and Accipitridae). The myological differences with other birds of prey are here interpreted in association with their “parachuting” hunting style. This work complements our knowledge of the axial musculature of the American Barn owls, and provides important information for future studies related to functional morphology and ecomorphology.     

Behavioural and body mass changes before egg laying in the Barn Owl: cues for clutch size determination?

To investigate laying decision and clutch size determination in indeterminate layers, we analysed in-nest activity (nest presence, and copulation, prey deliveries, and entrance frequencies) and female body mass change, as well as their relation to clutch size variation in five Barn Owl pairs (Tyto alba) nesting in eastern France. Body mass of the female and behaviour [copulation frequency, entrance frequency, and prey delivery to the nest by the male (in number and mass)] were monitored using an automated weighing system and a video camera. There was a consistent change of behaviour and foraging activity among pairs ca. 18 days before laying indicating that the females may be tied to the nest at this time. Barn Owls being indeterminate layers have their clutch size determined at the oviposition of the first egg of the clutch. Window correlation analyses between the clutch size and the female body mass gain indicate that the clutch size might be determined no later than a few days before the laying of the first egg. Our results suggest that female Barn Owls may use the pre-laying period to determine the clutch size using cues such as the male food deliveries (a proxy for male quality).     

Food partitioning between breeding White-tailed Kites (Elanus leucurus; Aves; Accipitridae) and Barn Owls (Tyto alba; Aves; Tytonidae) in southern Brazil.

I examined the diet of breeding White-tailed Kites (Elanus leucurus; Aves; Accipitridae) and Barn Owls (Tyto alba; Aves; Tytonidae) in an agrarian area of southern Brazil by analyzing regurgitated prey remains. The objective was to evaluate how these raptors, which differ markedly in their hunting activity periods (owls are nocturnal and kites diurnal), share their mammalian food component. 2,087 prey consumed by Barn Owls and 1,276 by White-tailed Kites were identified. They presented a high overlap of food-niches (Piankas index was 0.98). Based on the daily activity period of their main small mammal prey, a lower overlap would be expected. The crepuscular/nocturnal Mus musculus was the main prey for the diet of breeding Barn Owls (81%) and White-tailed Kites (63%). This small exotic rodent provided 63% of the small mammal biomass ingested by owls and 44% by kites. Larger native small mammals were also considered important for the diet of kites, mainly because of their biomass contribution. Although these raptors differ markedly in their hunting activity periods, Barn Owls and White-tailed Kites are very similar predators in southern Brazil, overlapping their diets.     

Tawny Owl Strix aluco as an indicator of Barn Owl Tyto alba breeding biology and the effect of winter severity on Barn Owl reproduction

In the temperate zone, food availability and winter weather place serious constraints on European Barn Owl Tyto alba populations. Using data collected over 22 years in a Swiss population, we analysed the influence of early pre‐breeding food conditions and winter severity on between‐year variations in population size and reproductive performance. To estimate pre‐breeding food conditions, we attempted a novel approach based on an index that combines Tawny Owl Strix aluco reproductive parameters and the occurrence of wood mice Apodemus sp. in their diet. Tawny Owls breed earlier in the season than Barn Owls and are strongly dependent on the abundance of wood mice for breeding. This index was strongly positively associated with the number of breeding pairs and early breeding in the Barn Owl. Winter severity, measured by snow cover and low temperatures, had a pronounced negative influence on the size of the breeding population and clutch size. Food conditions early in the breeding season and winter severity differentially affect the Barn Owl life cycle. We were able to use aspects of the ecology and demography of the Tawny Owl as an indicator of the quality of the environment for a related species of similar ecology, in this case the Barn Owl.     

Stable isotopes reveal unexpected relationships between fire history and the diet of Spotted Owls

Although the effects of shifting fire regimes on bird populations have been recognized as important to ecology and conservation, the consequences of fire for trophic interactions of avian species – and raptors in particular – remain relatively unknown. Here, we found that within national parks with long‐standing (40+ years) fire management programmes, California Spotted Owls Strix occidentalis occidentalis consumed predominantly Woodrats Neotoma spp. and Pocket Gophers Thomomys spp.; however, in contrast to our predictions, when their territories experienced more extensive and frequent fire, Spotted Owls consumed proportionally more Flying Squirrels Glaucomys oregonensis. We hypothesize this finding could have been driven by either changes to prey abundance following fires (e.g. increases in flying squirrels) or changes to prey availability (e.g. shifts in forest structure or flying squirrel spatial distribution that increased predation upon them by owls). Our work thus demonstrates that fire may have unexpected consequences for the trophic interactions of raptor species and provides valuable information for the conservation of Spotted Owls in fire‐prone forest landscapes.     

Wildflower areas within revitalized agricultural matrices boost small mammal populations but not breeding Barn Owls

Agro-ecosystems have recently experienced dramatic losses of biodiversity due to more intensive production methods. In order to increase species diversity, agri-environment schemes provide subsidies to farmers who devote a fraction of their land to ecological compensation areas (ECAs). Several studies have shown that invertebrate biodiversity is actually higher in ECAs than in nearby intensively cultivated farmland. It remains poorly understood, however, to what extent ECAs also favour vertebrates, such as small mammals and their predators, which would contribute to restoring functional food chains within revitalised agricultural matrices. We studied small mammal populations among eight habitat types—including wildflower areas, a specific ECA in Switzerland—and habitat selection (radiotracking) by the Barn Owl Tyto alba, one of their principal predators. Our prediction was that habitats with higher abundances of small mammals would be more visited by foraging Barn Owls during the period of chicks’ provisioning. Small mammal abundance tended to be higher in wildflower areas than in any other habitat type. Barn Owls, however, preferred to forage in cereal fields and grassland. They avoided all types of crops other than cereals, as well as wildflower areas, which suggests that they do not select their hunting habitat primarily with respect to prey density. Instead of prey abundance, prey accessibility may play a more crucial role: wildflower areas have a dense vegetation cover, which may impede access to prey for foraging owls. The exploitation of wildflower areas by the owls might be enhanced by creating open foraging corridors within or around wildflower areas. Wildflower areas managed in that way might contribute to restore functional links in food webs within agro-ecosystems.     

Larval sensory abilities and mechanisms of habitat selection of a coral reef fish during settlement

In most animals, siblings from a given reproductive event emerge over a very short period of time. In contrast, many species of birds hatch their young asynchronously over a period of days or weeks, handicapping last-hatched chicks with an age and size disadvantage. Numerous studies have examined the adaptive significance of this atypical hatching pattern, but few have attempted to explain the considerable intrapopulation variation that exists in hatching asynchrony. I explored proximate determinants of hatching asynchrony by monitoring 112 Burrowing Owl (Athene cunicularia) nests in the grasslands of southern Saskatchewan, Canada, over 4 years. Age disparities between first- and last-hatched siblings (i.e., hatching spans) varied considerably, ranging between 1 and 7 days (mode = 4 days). These hatching spans increased with increased hatching success. Hatching spans also increased with larger clutches, but the increase was less than predicted given the increased time required to lay more eggs. Hatching span was unrelated to number of prey cached in the nest during egg laying (an index of food availability), and was unaltered by a year of super-abundant prey. Furthermore, pairs given extra food during laying had hatching spans equal to those of unsupplemented control pairs. These results were inconsistent with both the energy constraint and facultative manipulation hypotheses, which predict that hatching asynchrony should vary with the level of food during laying, when incubation onset is determined. Burrowing Owls were apparently free of food limitation early in breeding, yet may not have been able to optimize hatching spans because food conditions during laying were largely unrelated to food conditions during brooding. Thus, one of the premises for facultative manipulation of hatching asynchrony—that laying females are able to forecast post-hatch food conditions—may not have been met for this population of Burrowing Owls.     

Changes in the food of British Barn Owls (Tyto alba) between 1974 and 1997

Comparison of the results of a 1993–97 Barn Owl Tyto alba pellet survey with those of a similar survey from 1956–74 showed that Barn Owl diet had changed significantly. The primary differences were a widespread decrease in the percentage of Common Shrew Sorex araneus, combined with an increase in Pygmy Shrew Sorex minutus. The percentage of Wood and Yellow‐necked mice Apodemus sylvaticus and A. flavicollis and Bank Vole Clethrionomys glareolus in the diet also increased. Changes in Barn Owl diet since 1974 were independent of land‐class group, but were dependent upon region. This was due primarily to a large increase in the percentage of Apodemus spp. in Eastern England. Whilst the percentage of Pygmy Shrew in Barn Owl diet showed significant regional variation, there was no significant variation between land‐class groups. The diversity of Barn Owl diet increased between 1974 and 1997, although it was still lower in 1997 than earlier in the century. This increase was dependent upon region, but independent of land‐class group. The combined results of both surveys showed significant interland‐class group variation in dietary diversity. Changes in diet are discussed in relation to the intensification of agriculture and other changes in land management since the 1970s. The effects on Barn Owls of these changes in prey abundance are discussed, particularly in relation to the decline in Barn Owl numbers during the twentieth century.     

On the diet of the Pharaoh Eagle Owl,Bubo ascalaphus (Savigny, 1809), in Qatar,with an overview of its feeding habits

The diet of Bubo ascalaphus in Qatar was assessed based on pellets collected from the first known nesting site of the species in the country. The pellets contained a total of 68 prey items, representing 9 different species: 4 mammals, 1 bird, 1 reptile, and at least 3 scorpions. Mammals clearly comprised the major food source (89.7% and 97.7% in frequency and biomass respectively). Our data suggest that Pharaoh Eagle Owls are opportunistic predators that feed on a variety of prey depending on their temporal/spatial availability, which is consistent with previous studies. A literature review clearly suggests that Eagle Owls in arid to semi-arid environments are opportunistic predators with small mammals being their main prey. Predation on migrating Blue-cheeked Bee-eaters Merops persicus supports this hypothesis.     

Habitat associations of small mammals in southern Brazil and use of regurgitated pellets of birds of prey for inventorying a local fauna.

We inventoried terrestrial small mammals in an agricultural area in southern Brazil by using trapping and prey consumed by Barn Owls (Tyto alba) and White-tailed Kites (Elanus leucurus). Small mammals were trapped in three habitat types: corn fields, uncultivated fields ("capoeiras"), and native forest fragments. A total of 1,975 small mammal specimens were trapped, another 2,062 identified from the diet of Barn Owls, and 2,066 from the diet of White-tailed Kites. Both trapping and prey in the predators' diet yielded 18 small mammal species: three marsupials (Didelphis albiventris, Gracilinanus agilis, and Monodelphis dimidiata) and 15 rodents (Akodon paranaensis, Bruceppatersonius iheringi, Calomys sp., Cavia aperea, Euryzygomatomys spinosus, Holochilus brasiliensis, Mus musculus, Necromys lasiurus, Nectomys squamipes, Oligoryzomys nigripes, Oryzomys angouya, Oxymycterus sp.1, Oxymycterus sp.2, Rattus norvegicus, and Rattus rattus (Linnaeus, 1758)). The greatest richness was found in the uncultivated habitat. We concluded that the three methods studied for inventorying small mammals (prey in the diet of Barn Owls, White-tailed Kites, and trapping) were complementary, since together, rather than separately, they produced a better picture of local richness.     

Role of predation in short-term population fluctuations of some birds and mammals in Fennoscandia

Summary We tested the hypothesis that synchronous fluctuations in small game species in boreal Fennoscandia are caused by varying predation pressure. The main prey of predators are the cyclically superabundant voles. Small game species (alternative prey) are rare compared to voles. The following 4 predictions were checked: (1) Predators should shift their diet from main prey to alternative prey as main prey decline. — This was confirmed using data on red fox (Vulpes vulpes L.) diet.; (2) The mortality rate of alternative prey should be inversely correlated to the abundance of main prey. — This was true for mountain hare (Lepus timidus L.) mortality rates and the rate of nest predation on black grouse (Tetrao tetrix L.).; (3) The total consumption of prey by all the predators should at least equal the critical losses in alternative prey during a decline year. — A tentative estimate of predator consumption amounted to 10 times the losses in grouse and hare.; and (4) The absence of synchrony between the species in the boreonemoral region should be associated with a more diverse diet of predators. — This was the case for red fox diets throughout Sweden. Although all 4 predictions were confirmed, we could not necessarily exclude other hypotheses involving changes in quality or quantity of plant food.     

Predation pressure on an imperfect Batesian micicry complex in the presence of alternative prey

Summary Differential predation pressure and the probability of predation on a Batesian mimicry complex and on alternative prey were estimatedin a field experiment. The mimicry complex was composed of a noxious model (Eleodes obscura (Say)) and a palatable mimic (Stenomorpha marginata (LeConte)). House crickets (Acheta domesticus) (Linn.) were used as alternative prey. The experiment was conducted for 23 nights in August and September to approximate the peak seasonal activity time period during which both models and mimics normally are exposed to predation while foraging and depositing eggs. Each night thirty prey in ratios of 16 models: 7 mimics: 7 crickets were exposed for 2.5 h to a suite of predators consisting of pallid bats (Antrozous pallidus), striped skunks (Mephitis mephitis) and ringtails (Bassariscus astutus) that had free access to the prey. The model-mimic ratio was similar to that found in nature. Predators obtained prey on 11 of the 23 nights and preferred the alternative prey (crickets) in proportions higher than was expected from a predation rate that was equal on all species of prey. Mimics were taken by predators at a rate proportional to their abundance, while models were taken at a rate considerably lower than their relative abundance. This suggests that at least some of the predators could distinguish between models and mimics and were willing to eat the mimics at higher frequencies than they were willing to eat the models. However, although the mimicry is not perfect with respect to the entire predator suite, the mimics still gain an advantage by resembling the models, compared to the predation levels on the alternate prey.     

What determines prey selection in owls? Roles of prey traits,prey class,environmental variables,and taxonomic specialization

Ecological theory suggests that prey size should increase with predator size, but this trend may be masked by other factors affecting prey selection, such as environmental constraints or specific prey preferences of predator species. Owls are an ideal case study for exploring how predator body size affects prey selection in the presence of other factors due to the ease of analyzing their diets from owl pellets and their widespread distributions, allowing interspecific comparisons between variable habitats. Here, we analyze various dimensions of prey resource selection among owls, including prey size, taxonomy (i.e., whether or not particular taxa are favored regardless of their size), and prey traits (movement type, social structure, activity pattern, and diet). We collected pellets of five sympatric owl species (Athene noctua, Tyto alba, Asio otus, Strix aluco, and Bubo bubo) from 78 sites across the Mediterranean Levant. Prey intake was compared between sites, with various environmental variables and owl species as predictors of abundance. Despite significant environmental impacts on prey intake, some key patterns emerge among owl species studied. Owls select prey by predator body size: Larger owls tend to feed on wider ranges of prey sizes, leading to higher means. In addition, guild members show both specialization and generalism in terms of prey taxa, sometimes in contrast with the expectations of the predator–prey body size hypothesis. Our results suggest that while predator body size is an important factor in prey selection, taxon specialization by predator species also has considerable impact.     

Evaluating cropland in the Canadian prairies as an ecological trap for the endangered Burrowing Owl Athene cunicularia

Anthropogenic development may influence the choices animals make and their resulting reproductive success and survival. If such choices are maladaptive, the impact of anthropogenic change can be catastrophic to small or declining populations. Over the past century, Canada's prairie landscapes have been altered dramatically, with over two-thirds of its native grasslands now having been converted to cropland. The decline of the endangered Burrowing Owl Athene cunicularia population is assumed to have resulted from this landscape change, yet no causal link has been demonstrated. One hypothesis to explain this population decline is that owls get caught in an ecological trap, whereby they prefer to establish nests at the start of each breeding season in landscapes that later confer lower reproductive success. Agricultural landscapes represent a plausible potential ecological trap because the short and sparse vegetation in annual crops (seeded each spring) is predicted to be attractive nesting/foraging habitat for Burrowing Owls when they arrive from northward migration, yet crops become substantially taller and denser over the growing season so prey are predicted to become less accessible by the time broods have hatched. We tested this ecological trap hypothesis in a 3-year study, involving 379 Burrowing Owl pairs, across the agricultural landscapes of southern Alberta and Saskatchewan. In support of the hypothesis, Burrowing Owls did prefer to settle in breeding home-ranges that contained a higher proportion of cropland, and their prey-delivery rates during brood-rearing were lower at nests with a higher proportion of cropland growing in the surrounding landscape. However, in contradiction to a key prediction, the number of fledglings produced (range = 0–9) was higher, not lower, for pairs with more actively growing cropland in their landscapes. Therefore, the decline of the Burrowing Owl in Canada does not appear to result from cropland forming an ecological trap during the breeding season. We also found a significant positive relationship between the amount of summer fallow within Burrowing Owl home-ranges and the quantity of vertebrate prey delivered to the nest and the number of juveniles fledged, highlighting the importance of this declining land use in raptor conservation.     

Increased behavioural responses to human disturbance in breeding Burrowing Owls Athene cunicularia

Human disturbance may have several negative impacts on bird biology. Although some species may habituate to human presence, other species do not show any signs of habituation, and may even be sensitized or affected by human disturbance. Furthermore, anthropogenic effects on bird behaviour rarely have been explored to address the alteration of frequencies of aggressive and fear‐associated behaviours. Such behavioural approaches may provide substantial data for bird conservation and management. Therefore, we assessed whether human disturbance disrupts the normal behaviour of Burrowing Owls Athene cunicularia. Specifically, we assessed whether guarding parents exhibited aggressive and fearful behaviours differentially in areas where human contact was more common. Burrowing Owls showed increased frequencies of threat displays in sites with more people walking by the nests, but not fear behaviours. These results suggest that different domains of behaviour (aggression vs. fear) may respond differently to human disturbance. We highlight the importance of quantifying a wide range of behavioural acts as indicators of bird stress in studies of anthropogenic impact.     

The decline of Common Kestrels Falco tinnunculus in a forested area of northern England: the role of predation by Northern Goshawks Accipiter gentilis

We have previously documented the decline of the Common Kestrel Falco tinnunculus over a 23‐year period in a large coniferous forest in northern England. Kestrels fed predominantly on Field Voles Microtus agrestis, which were most abundant in young plantations (1–11 years old). Over the 23 years, voles remained abundant in the study area, but their numbers fluctuated cyclically. Here we consider whether the decline of Kestrels was linked to predation by Northern Goshawk Accipiter gentilis. Goshawks first bred in the study area in 1973 and increased until 1989, after which numbers stabilized. We use a number of approaches to explore the role of Goshawk predation, all of which are correlative, but independent. First, there was a significant negative relationship between Kestrel and Goshawk numbers after controlling for a decline in vole habitat. Short‐eared Owls Asio flammeus, which also hunt by day, declined over the same period as Kestrels. Second, numbers of Tawny Owl Strix aluco and Long‐eared Owl Asio otus did not decline as Goshawk numbers increased. These two species are also vole‐dependent, but active by night, and less vulnerable to Goshawk attack. Third, six species of raptor comprised 4.5% of 5445 Goshawk prey items during the breeding season, but more Kestrels were killed than the combined total of all other raptors. Goshawks not only killed many adult Kestrels in early spring, prior to breeding, when it would have most impact on population levels, but there was also a temporal trend for predation on Kestrels to be inversely density‐dependent. Finally, we estimated that Goshawks removed more Kestrels than were recorded each spring in the study area. We interpreted this as indicating that immigrant Kestrels were being removed continually, mostly before they could breed. We conclude that the decline of Kestrels (and possibly Short‐eared Owls) was mainly due to predation by Goshawks. This study provides some of the strongest evidence yet of the role of predation in the hierarchical structuring of raptor communities.