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.     

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     

Occupancy patterns of an apex avian predator across a forest landscape

Apex predators are integral parts of every ecosystem, having top‐down roles in food web maintenance. Understanding the environmental and habitat characteristics associated with predator occurrence is paramount to conservation efforts. However, detecting top order predators can be difficult due to small population sizes and cryptic behaviour. The endangered Tasmanian masked owl (Tyto novaehollandiae castanops) is a nocturnal predator with a distribution understood to be associated with high mature forest cover at broad scales. With the aim to gather monitoring data to inform future conservation effort, we trialled an occupancy survey design to model masked owl occurrence across ~800 km² in the Tasmanian Southern Forests. We conducted 662 visits to assess masked owl occupancy at 160 sites during July–September 2018. Masked owl site occupancy was 12%, and estimated detectability was 0.26 (±0.06 SE). Cumulative detection probability of masked owls over four visits was 0.7. Occupancy modelling suggested owls were more likely to be detected when mean prey count was higher. However, low detection rates hindered the development of confident occupancy predictions. To inform effective conservation of the endangered Tasmanian masked owl, there is a need to develop novel survey techniques that better account for the ecology of this rare, wide‐ranging and cryptic predator. We discuss the potential to combine novel census approaches that exploit different aspects of masked owl ecology to obtain more robust and detailed data.     

Factors affecting breeding habitat selection in a cliff-nesting peregrine Falco peregrinus population

We studied factors affecting breeding habitat selection in a population of cliff-nesting peregrines Falco peregrinus across multiple spatial levels (cliff site, cliff context and land-use of the surrounding landscape), over a 2,100 km² study area in the Alps (Italy and Switzerland). We detected 30 breeding pairs (density: 1.43 territorial pairs/100 km²), whose territories were uniformly distributed over the study area. We compared 15 habitat features characterising occupied cliffs and 30 randomly selected unoccupied cliffs by means of stepwise forward logistic regression and hierarchical partitioning. The logistic regression analysis showed that occupied cliffs were longer (horizontal length), steeper, and had a greater extension of urban areas in the surrounding landscape compared to non-occupied cliffs. The model had a discrimination ability of 0.95. Hierarchical partitioning indicated that the logistic regression model was appropriate. Neither the distance of cliffs to the nearest site occupied by a potential competitor and predator, the eagle owl Bubo bubo, which occurred at a low density (0.67 pairs/100 km²), nor the distance to the nearest site occupied by peregrines had any effect on the cliff suitability model. Therefore, habitat selection in cliff-nesting peregrines was mainly influenced by cliff site features and surrounding landscape characteristics, whereas the proximity to conspecifics and to an intraguild predator had no apparent effects on peregrine settlement in our study population.     

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.     

Home range and habitat selection of spotted owls in the central Sierra Nevada

We studied home range and habitat selection of radio-marked adult California spotted owls (Strix occidentalis occidentalis) randomly selected from among the breeding population of owls in the central Sierra Nevada, California from June to October 2006. The most parsimonious home-range estimate for our data was 555 ha (SE = 100 ha). Home-range size was positively correlated with the number of vegetation patches in the home range (habitat heterogeneity). We used resource selection ratios to examine selection of vegetation types by owls within our study area. Owl home ranges contained a high proportion of mature conifer forest, relative to its availability, although the confidence interval for this estimate overlapped one. We also used resource selection functions (RSF) to examine owl foraging habitat selection. Relative probability of selection of foraging habitat was correlated with vegetation classes, patch size, and their interaction. Owls showed highest selection rates for large patches (>10 ha) of pole-sized coniferous forest. Our results suggested that spotted owls in the central Sierra Nevada used habitat that contained a high proportion of mature conifer forest at the home-range scale, but at a finer scale (foraging site selection) owls used other vegetation classes interspersed among mature forest patches, consistent with our hypothesis that spotted owls may use other forest types besides old growth and mature forests when foraging. Our study provides an unbiased estimate of habitat use by spotted owls in the central Sierra Nevada. Our results suggest that forest managers continue to protect remaining mature and old-growth forests in the central Sierra Nevada because owl home ranges contain high proportions of these habitats. However, our results also showed that owls used younger stands as foraging habitat so that landscape heterogeneity, with respect to cover types, may be an important consideration for management but we did not attempt to relate our findings to fitness of owls. Thus management for some level of landscape heterogeneity for the benefit of owls should proceed with caution or under an adaptive management framework. © 2011 The Wildlife Society.     

Spatio-temporal shifts in gradients of habitat quality for an opportunistic avian predator

We used the conceptual framework of the theory of natural selection to study breeding habitat preferences by an opportunistic avian predator, the black kite Milvus migrans. In Europe, black kite populations are mostly found near large networks of aquatic habitats, usually considered optimal for foraging and breeding. We hypothesized that proximity to wetlands could vary among individuals and affect their fitness, and thus be subject to natural selection. We tested the hypothesis first on a population on Lake Lugano (Italian pre‐Alps) which has been monitored for nine years, and then on seven other populations, each studied for four–five years, located along a continuum of habitat from large water bodies to scarce aquatic habitat of any kind. In the Lake Lugano population, black kite abundance was negatively related to distance to the lake in all the nine years of study, consistent with long‐term natural selection. There was evidence of ongoing directional selection on strategic nest location in three of the years, and evidence of stabilizing selection in two years. In eight of the nine years the trend was for a linear increase in fitness with increasing proximity to the lake. At the population level, results were consistent with adaptive habitat choice in relation to the previous year's spatial variation in fitness: higher associations between fitness and distance to the lake (i.e. higher selection gradients) resulted in higher density variations in the following year, in turn related to the availability of fish, the main local prey. The progressive decline of inland pairs and increase in the density of lakeshore pairs caused a directional long‐term trend of declining mean distance to the lake. Breeding near aquatic habitats was associated with higher foraging success, and higher frequency and biomass of prey deliveries to offspring. There was weak evidence of selection in other populations. The inland‐wetland gradient of habitat quality may have been affected by predation risk, as estimated by density of a major predator of adults and nestlings, the eagle owl Bubo bubo. Behavioral decisions at the level of the individual probably translated into population effects on density and distribution at various spatial scales. Populations in optimal habitats showed higher density and produced six times as many young per unit space as those in sub‐optimal habitats.     

Winter distribution and conservation status of the Sierra Nevada great gray owl

Little information is available on the winter ecology of the small, geographically isolated, genetically-unique population of great gray owls (Strix nebulosa) in the central Sierra Nevada, California. This population is comprised of facultative, elevational winter migrants and access to winter habitat is an important component of their ecology. Winter observations and remotely sensed habitat variables were used to inform a predictive model of the environmental requirements and geographic distribution of this owl population. Using the modeled distribution map we assessed the distribution of 20% probability of occurrence classes relative to owl habitat associations, ownership, current development, and projected future development patterns. Our findings indicate that high probability class (81–100%) areas and the broader joint medium/medium-high/high probability class (41–100%) areas are uncommon on the landscape (0.2% and 5.0% of study area, respectively). High probability areas were characterized by Sierran Yellow Pine forest surrounding relatively small, flat areas of grassland, wet meadow, and riparian habitats, within the mid-elevation range. Approximately 32% of the high probability areas and 48% of the medium/medium-high/high probability areas occur on private lands. Of the areas on private lands, 32% of the high probability and 42% of the medium/medium-high/high probability areas occur on currently developed lands. Projected future development on private lands indicated that an additional 12% of the high and 18% of medium/medium-high/high suitability areas are slated for development by the year 2040. Future conservation planning efforts for the great gray owl in the Sierra Nevada will need to address management issues on both public and private lands. For future planning of development projects around great gray owl wintering habitat, the results from our study supplement current knowledge of breeding distributions to provide land and wildlife managers guidance on conservation priorities. © 2011 The Wildlife Society.     

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.     

Factors associated with the geographic distribution of leucocytozoa parasitizing nestling eagle owls (<Emphasis Type="Italic">Bubo bubo</Emphasis>): a local spatial-scale analysis

Knowledge of the factors influencing the patterns and distribution of parasite infections and disease outbreaks is a major question in disease ecology and conservation research. In this study, we use a highly efficient PCR approach to detect blood parasites and investigate the factors influencing geographical variation in the distribution of leucocytozoids parasitizing nestling eagle owls (Bubo bubo) over a 3-year study period. We found that both prevalence and intensity of infections by the single lineage of Leucocytozoon ziemanni infecting nestling eagle owls in the study area increased with local owl population density and decreased with nest height above sea level. Overall, these results suggest that higher horizontal transmission rates under higher host density conditions together with the presence of adequate habitats for larval development of vectors are relevant factors influencing blood parasite distribution in the study system.     

Modelling habitat use and distribution of golden eagles <Emphasis Type="Italic">Aquila chrysaetos</Emphasis> in a low-density area of the Iberian Peninsula

We analyse the current situation of the Golden eagle (Aquila chrysaetos) in the region of Galicia in NW Spain. At present, the entire Galician population (five pairs) is located within an area of about 2000 km² in the province of Ourense. To identify high-priority areas for golden eagle conservation, we derived predictive models of habitat suitability using logistic regression and a Geographic Information System (GIS). Specifically, to model the distribution of the breeding population we considered topographic features, land use and degree of humanization, using a 10 × 10 km grid. Presence/absence of golden eagle nests was used as the dependent variable; analyses were performed both considering current nesting areas and considering old nesting areas (1960s and 70s). At the spatial scale considered, the best predictors of habitat suitability for breeding were topographical variables indicative of rugged relief. For current nesting areas the most parsimonious model included maximum altitude. We consider that the predictive models obtained may be of use for the monitoring and conservation management of the golden eagle population in this region. Conservation problems associated with habitat constraints such as food supply, availability of nesting sites, changes in land use and human disturbance are discussed.     

Predictive models of habitat preferences for the Eurasian eagle owl Bubo bubo: a multiscale approach

Habitat preference of eagle owls Bubo bubo were examined through comparing habitat composition around 51 occupied cliffs and 36 non-occupied cliffs in Alicante (E Spain). We employed Generalized Linear Models to examine patterns of habitat preference at three different spatial scales: nest site (7 km²), home range (25 km²), and landscape (100 km²). At the nest site scale, occupied cliffs were more rugged, had a greater proportion of forest surface in the surroundings, and were further from the nearest paved road than unoccupied cliffs. Additionally, probability of having an occupied cliff increased when there was another occupied territory in the surroundings. At both the home range scale and the landscape scale, high probabilities of presence of eagle owls were related to high percentages of Mediterranean scrubland around the cliffs, which are the preferred habitat of European rabbits Oryctolagus cuniculus , the main prey of the owls. We suggest a hierarchical process of habitat selection in the eagle owl concerning suitable trophic resources at the broadest scales and adequate sites for breeding and roosting at the smallest scale. However, it should be noted that some structural features such as the proximity of roads were not necessarily avoided by the owls, but their presence were possibly constrained by systematic killing of individuals. Our paper provides new evidence for the requirement of multi-scale approaches to gain insight into both the different limiting factors for the persistence of populations and the role of individual perception of the environment in the evolution of habitat selection.     

Mechanisms determining the spatial distribution of microtine predators on the Arctic tundra

1. We studied the spatial distribution of avian microtine predators using data from 19 study areas on the tundra of northern Siberia.
2. Numbers of snowy owls, and long-tailed skuas and pomarine skuas depended strongly on lemming density. However, a significant relationship between lemming density and number of rough-legged buzzards appeared first after removal of the effect of snowy owl abundance on the distribution of rough-legged buzzards.
3. We applied a recently developed method (Manly 1995) to examine co-occurrences of species and found that rough-legged buzzards and snowy owls did not co-occur while snowy owls, long-tailed skuas and pomarine skuas did.
4. There are large differences in nest construction and chick behaviour between rough-legged buzzards and the three other species. Moreover, the snow owl is a polyphagous predator preying also on large birds including raptor chicks. Therefore, we propose that reduced risk of nest predation favours rough-legged buzzards nesting away from snowy owls.
5. Variations in abundance of the two lemming species did not seem to influence the distributions of snowy owls and rough-legged buzzards. Neither was it likely that latitudinally related factors such as breeding season length affected the distribution of rough-legged buzzards.     

An avian terrestrial predator of the Arctic relies on the marine ecosystem during winter

Top predators of the arctic tundra are facing a long period of very low prey availability during winter and subsidies from other ecosystems such as the marine environment may help to support their populations. Satellite tracking of snowy owls, a top predator of the tundra, revealed that most adult females breeding in the Canadian Arctic overwinter at high latitudes in the eastern Arctic and spend several weeks (up to 101 d) on the sea‐ice between December and April. Analysis of high‐resolution satellite images of sea‐ice indicated that owls were primarily gathering around open water patches in the ice, which are commonly used by wintering seabirds, a potential prey. Such extensive use of sea‐ice by a tundra predator considered a small mammal specialist was unexpected, and suggests that marine resources subsidize snowy owl populations in winter. As sea‐ice regimes in winter are expected to change over the next decades due to climate warming, this may affect the wintering strategy of this top predator and ultimately the functioning of the tundra ecosystem.     

Fostering orphan Eagle Owls (Bubo bubo) as a successful conservation technique: A first for the species

For many species, the artificial raising of orphaned nestlings is a time and cost-prohibitive task, usually accompanied by low survivability. The introduction of orphaned nestlings to other natural nests was found to be a successful technique wherein fostered nestling(s) developed better in the wild and imprinting on humans is avoided. To date, the number of diurnal species in which induced alloparenting has been conducted is limited to several eagle species, falcons, buzzards, and vultures. In the owls, it has only been demonstrated to work in two species, but the eagle owl has not been studied in this aspect. Eagle Owls, amongst the largest of the owls with a geographic distribution stretching across Europe and Asia, are a favored species in the wildlife trade, and many a nestling is removed from the nest. In Israel, when reported or rescued, the nestlings are removed to the wildlife hospital where they are rehabilitated and then introduced into a wild nest with similarly aged nestlings. From 2009 to 2021 we conducted 44 successful adoptions of Eagle Owl orphans into active, wild nests. This success stresses the importance of our work as a conservation tool for the preservation of an apex predator across its breeding range.     

Barred Owl Space Use and Habitat Selection in the Eastern Cascades,Washington

ABSTRACT Competition with barred owls (Strix varia varia) is an important factor contributing to the continued decline of threatened northern spotted owl (Strix occidentalis caurina) populations in the Pacific Northwest, USA, but basic information on habitat selection and space use patterns of barred owls is lacking for much of the region. We investigated space use and habitat selection by tracking radiotagged barred owls in the Eastern Cascade Range of Washington, USA, from 2004 to 2006. We surveyed for barred owls across the 309-km² study area and confirmed presence of barred owl pairs at 21 sites. We collected movement data on 14 barred owls from 12 sites. Mean annual 95% fixed-kernel home-range size was 194 ha for females (n = 4, SD = 70) and 288 ha for males (n = 5, SD = 114). Home ranges were located more frequently than expected in areas with low topographic position, gentle slopes, large overstory tree-crown diameter, high normalized difference vegetation index (NDVI), overstory tree canopy closure >72%, and a moderate amount of solar insolation. Within home ranges, areas that had large tree-crown diameters, low topographic positions, and gentle slopes were used more frequently than expected. The resource selection function we developed for barred owls in our study area indicated that barred owls used areas with the combination of low values for topographic position and slope and higher values for NDVI, solar insolation, and an interaction term for canopy closure and tree-crown diameter. In comparison to published information on northern spotted owls, barred owls used areas with similar canopy closure and tree size classes, but barred owl home ranges were much smaller and more concentrated on gentler slopes in valley bottoms. This information may contribute to the development of management practices that maintain forest characteristics appropriate for spotted owl habitat and prey in areas where spotted owls are least likely to be excluded by territorial barred owls in the Eastern Cascades of Washington.     

Biodiversity gradients in the Alps: the overriding importance of elevation

Land abandonment is causing woodland expansion and loss of open habitats in the Alps, coupled with a shift in forestry practices from coppice management to high forest. Despite such rapid large-scale changes, there has been very little investigation of the environmental predictors of biodiversity in the Alpine landscape. We assessed the richness of amphibians, reptiles and breeding birds (n = 189 species), used as a surrogate of biodiversity, in 58 quadrats of 100 km², located within a well surveyed area of the province of Trento (central-eastern Italian Alps). The surrogates were then related to a series of environmental variables by means of stepwise multiple regression. Depending on the surrogate analysed, species richness declined linearly or quadratically with elevation, and increased with habitat heterogeneity and the availability of grassland and arid-rocky habitats. The same results were obtained when incorporating a measure of species threat into the biodiversity estimates. Different surrogates were positively inter-correlated, probably because of a common response to the same factor, namely elevation, which was the only variable to enter all models. Such elevational gradient produced a clear biodiversity peak in low-elevation areas, generating potential conflict between efficient biodiversity conservation and economic interests linked to human development, a scenario which probably applies to many mountain regions worldwide. The current network of protected areas was quite satisfactory in terms of area covered but biased towards high-elevation areas, of high scenic beauty but relatively low in animal biodiversity value. Low-elevation reserves were small and isolated. Proposed conservation targets include the establishment of corridors increasing the connectivity of low-elevation reserves and the promotion of incentives for the extensive management of grassland, an agro-ecosystem of high historical and biological value.     

Fauna habitat modelling and mapping: A review and case study in the Lower Hunter Central Coast region of NSW

Abstract Habitat models are now broadly used in conservation planning on public lands. If implemented correctly, habitat modelling is a transparent and repeatable technique for describing and mapping biodiversity values, and its application in peri‐urban and agricultural landscape planning is likely to expand rapidly. Conservation planning in such landscapes must be robust to the scrutiny that arises when biodiversity constraints are placed on developers and private landholders. A standardized modelling and model evaluation method based on widely accepted techniques will improve the robustness of conservation plans. We review current habitat modelling and model evaluation methods and provide a habitat modelling case study in the New South Wales central coast region that we hope will serve as a methodological template for conservation planners. We make recommendations on modelling methods that are appropriate when presence‐absence and presence‐only survey data are available and provide methodological details and a website with data and training material for modellers. Our aim is to provide practical guidelines that preserve methodological rigour and result in defendable habitat models and maps. The case study was undertaken in a rapidly developing area with substantial biodiversity values under urbanization pressure. Habitat maps for seven priority fauna species were developed using logistic regression models of species‐habitat relationships and a bootstrapping methodology was used to evaluate model predictions. The modelled species were the koala, tiger quoll, squirrel glider, yellow‐bellied glider, masked owl, powerful owl and sooty owl. Models ranked sites adequately in terms of habitat suitability and provided predictions of sufficient reliability for the purpose of identifying preliminary conservation priority areas. However, they are subject to multiple uncertainties and should not be viewed as a completely accurate representation of the distribution of species habitat. We recommend the use of model prediction in an adaptive framework whereby models are iteratively updated and refined as new data become available.     

Review of the effects of barred owls on spotted owls

Barred owls (Strix varia) are forest-dwelling owls, native to eastern North America, with populations that expanded westward into the range of the spotted owl (Strix occidentalis). Barred owls exert an overwhelmingly negative influence on spotted owls, thereby threatening spotted owl population viability where the species co-occur. In this review, we provide an overview of the barred owl's range expansion and detail and synthesize previously published literature on spotted and barred owls within the range of the spotted owl as related to potential future outcomes for the northern spotted owl (S. o. caurina). We include research on diet, habitat use and selection, effects of barred owls on spotted owl demography and behavior, hybridization with spotted owls, parasites, contemporary management, and future research needs for spotted owl populations given continued barred owl expansion throughout western North America. Our literature review and synthesis should provide managers with the information necessary to develop strategies that mitigate deleterious effects of barred owls at local and landscape scales. © 2019 The Wildlife Society.