Landscape features associated to wind farms increase mammalian predator abundance and ground-nest predation

Wind farm implementation is a rapidly growing source of landscape transformation that may alter ecological processes such as predator–prey interactions. We tested the hypothesis that wind farms increase the activity of nest predators and, ultimately, increment ground-nest predation rates. We placed 18 plots in Iberian shrub-steppes (11 at control and seven at wind farm sites), each one comprised nine artificial ground-nests (three quail eggs/nest). Artificial nests were placed during two events: at the beginning (April) and at the end (June) of the breeding season in 2016 (n?=?324 artificial nests). We estimated the relative abundance of avian and large mammalian predators in the surroundings of each plot and recorded nest fate after 12 days exposure. We also measured variables at landscape and microhabitat scale that potentially affect predator abundance and nest predation. Wind farm sites contained higher cover of gravel roads and more large mammalian predators. Moreover, the abundance of large mammalian predators increased with surrounding cover of both trees and gravel-roads. Avian predator abundance and nest predation rates did not differ between control and wind farm sites, though nest predation did increase with the surrounding cover of crops and gravel roads. Lastly, nest predation was higher at the end of the breeding season and decreased with moss and lichen cover. Our results support previous evidence on the increase of mammalian predator abundance as the surface area of gravel-roads increases, pointing towards a potential mechanism for wind farms leading to rise ground-nest predation. Future wind energy projects should minimize the development of gravel-roads for wind turbine access or maintenance.

     

Does cowbird parasitism increase predation risk to American redstart nests?

Brood parasitism and nest predation are major causes of reproductive failure for many bird species nesting in fragmented landscapes. While brood parasites and predators may act independently, they could also interact if brood parasites increase the likelihood that predators detect nests. In this study, we examined the interaction between cowbird parasitism and nest predation in a 10 year study on 466 American redstart Setophaga ruticilla nests in central Alberta, Canada. We used advanced nest survival models to examine the support for three mechanisms that might lead to a positive correlation between brood parasitism and nest predation: 1) the presence of a cowbird nestling might increase the detection of the nest by predators, 2) nests with lower cover are more likely to be detected by both cowbirds and predators, and 3) cowbirds and predators may co-occur in landscapes of similar structure. Twelve percent of nests were parasitized and those nests had a 16–19% higher rate of failure due to predators compared to unparasitized nests. Daily nest predation rates increased during the nestling stage for both groups, but more strongly for parasitized nests. Loud begging by the cowbird nestling and/or higher parental feeding rates for the cowbird may have increased nest detectability to predators. Brood parasitism and nest predation were also positively related to forest cover, indicating landscape level effects were influential. Most nest predators were forest species and we suspect cowbirds responded positively to forest cover because of the increased abundance of songbird hosts. Nest-site features had less of an impact on nest predation or brood parasitism, although nests with higher overhead cover were less susceptible to predators. Our study shows how multiple mechanisms, particularly the behavioral effects of the brood parasite nestling and landscape structure, can lead to a positive relationship between nest predation and brood parasitism.     

Parental defence in Long-eared Owls Asio otus: effects of breeding stage, parent sex and human persecution

The responses of male and female Long-eared Owls to a human approaching the nest were examined. Each nest was only tested once. Nest defence increased significantly throughout the breeding season because older chicks were defended more strongly than younger chicks and eggs. No correlations were however found between defence intensity and laying date, clutch- or brood-size. These results generally do not support either the renesting-potential hypothesis or the positive reinforcement hypothesis but are in accordance with both the age-investment hypothesis and the vulnerability hypothesis. Females defended nestlings more often and more vigorously than did males. Given division of labour between sexes and the related reversed sexual dimorphism in size, female Long-eared Owls may be more willing to engage in nest defence simply because they are always nearer eggs and chicks during all breeding stages and are larger/heavier than males; consequently they may allocate more time and energy to this activity. Finally, owls experiencing higher levels of human persecution took smaller risks when defending nests than owls breeding in an undisturbed area.     

Predation risk effects on fitness related measures in a resident bird

Predation risk is thought to be highly variable in space and time. However, breeding avian predators may create locally fixed and spatially fairly predictable predation risk determined by the distance to their nest. From the prey perspective, this creates predation risk gradients that potentially have an effect on fitness and behavioural decisions of prey. We studied how breeding avian predators affect habitat selection (nest location) and the resulting fitness consequences in a northern population of resident willow tit ( Parus montanus ). Data included 429 willow tit nests over a four year period in a landscape containing a total of 33 avian predator nests. Willow tit nests were located randomly in the landscape and no predator avoidance in habitat selection or emptying of territories in proximity to predators was observed. Nestling size, however, was positively associated with distance from predator nests (n=252). Nestling mass and wing length were about 4.5% smaller close to predator nests compared to nestlings raised far from predator nests. Tarsus length also exhibited a positive relationship with increasing distance from predator nest but this was limited to habitats of young forests and pine bogs or dense mixed forests (4% increase). It is likely that habitat structural complexity influenced the perception of predation risk in different habitats. Our results indicate that willow tits do not provide reliable cues of predator free habitats for settling migrants. Nonetheless, breeding avian predators may create predictable predation risk in the landscape which is an important factor affecting reproductive success and potentially the demography of prey populations.     

Environmental factors affecting patterns of distribution and co‐occurrence of two competing raptor species

Habitat selection is a complex process, that is affected by several factors, including habitat characteristics, environmental conditions, and both intra‐ and interspecific interactions. We analysed habitat preferences of two top avian predators, Peregrine Falcon Falco peregrinus, a medium‐sized diurnal raptor, and Eagle Owl Bubo bubo, a large nocturnal raptor. These two species are known to compete for preferred nest‐sites, and proximity to cliffs with Eagle Owls may reduce Peregrine breeding output through predation of young Falcons. We investigated the environmental factors affecting occurrence and coexistence of the two species and the potential role of habitat suitability in favouring co‐occurrence in 3519 km² of the central pre‐Alps of Italy, where the two species breed on cliffs and sometimes co‐occur on the same cliff. Peregrines settled on long, steep and favourably orientated cliffs in woodland landscapes close to urban areas. Eagle Owls settled on topographically similar cliffs, but in lower rainfall areas compared with cliffs occupied by Peregrines and cliffs unoccupied by either species. Sites where the two species co‐occurred were characterized by more horizontally extended cliffs compared with sites of exclusive occurrence of each species. An analysis of relative habitat suitability revealed that sites where the two species co‐occurred had the highest predicted probability of occupancy for both species, suggesting that those sites should be regarded as high‐quality sites. Breeding productivity of Eagle Owls was negatively affected by the co‐occurrence of Peregrines, whereas the effect of Eagle Owl proximity on Peregrine productivity varied according to cliff suitability for the Peregrines. Habitat selection had fitness consequences for Eagle Owls because breeding productivity increased with cliff length. Environmental conditions, particularly climatic factors, could allow the widespread coexistence of these competing raptors at the landscape scale, whereas at the local scale co‐occurrence could take place only on larger cliffs. These were preferred sites for both species, presumably because breeding at such sites offsets the costs of settling close to the competitor species.     

Breeding of waders (Charadrii) and Brent Geese Branta bernicla bernicla at Pronchishcheva Lake, northeastern Taimyr, Russia, in a peak and a decreasing lemming year

During summer 1991, lemmings occurred at high densities in Arctic tundra at Pronchishcheva Lake in the northeastern Taimyr Peninsula, whereas, in 1992, lemming densities were substantially lower and decreased further during the summer. In 1991, avian predators such as Snowy Owls Nyctea scandiaca, gulls and skuas bred well; Arctic foxes Alopex lagopus were rarely observed in the study area but bred in the immediate vicinity. In both years there was a late thaw, but this did not deter breeding by birds. The insect food supply for waders showed similar patterns of abundance in both years. In 1991, 73 nests of nine species of wader were found within a 14-km² study area, and Dark-bellied Brent Geese Branta bernicla bernicla nested in association with Snowy Owls. The overall density of wader nests was estimated to be 7 per km². Clutches disappeared at only two wader nests and no Brent Goose nests, and the Mayfield estimate of the daily probability of predation for waders was 0.0022. In contrast, the daily probability of predation was 0.20 in 1992, when there was a similar breeding density of waders. Arctic foxes were seen searching for food daily within the study area, and fox droppings were found associated with nests taken by predators. The predicted scenarios for peak and decreasing lemming years (the Roselaar-Summers hypothesis), i.e. low predation and high nest success in the peak year and high predation and low nest success in the decreasing year, therefore occurred.     

It’s a dog-eat-croc world: dingo predation on the nests of freshwater crocodiles in tropical Australia

Predation on eggs is an important source of mortality for many long-lived organisms, but causes of egg mortality from specific predators remain poorly known in most cases. Understanding the identity of predators, and the rates and determinants of their effects on a cohort of recruits, can provide a valuable background for attempts to exploit, control or conserve populations. We used remotely triggered cameras to study predation on the nests of freshwater crocodiles (Crocodylus johnstoni) inhabiting Lake Argyle, in tropical Australia. We also supplemented our work on natural crocodile nests with artificial nests. Overall, 80 of 111 natural nests were opened by predators, and predation occurred throughout the study period (7 weeks). Unlike in other parts of the species’ range, most nest-robbers were dingoes (Canis lupus dingo, responsible for 98% of all predator visits in the northern sites, and 54% in the Ord River site), with minimal additional predation by reptiles and birds. Contrary to expectation, rates of nest predation were not influenced by spatial clumping of nests: the probability of predation per nest did not change with total numbers of nests laid in an area, and artificially aggregated versus dispersed nests experienced similar levels of predation. Nest vulnerability was linked to abiotic features including slope of surrounding banks, compactness of nesting substrate, and distance from the nearest forest. Abundant aquatic food resources support a large crocodile population, but a lack of suitable nest-sites forces the crocodiles to concentrate nesting in small areas readily accessible to wide-ranging nest predators. Collectively, our results suggest that distinctive attributes of the lakeside landscape alter predator guilds and fashion unique predator–prey interactions.     

吉林向海自然保护区占用喜鹊巢繁殖的鸟类巢记述

部分鸟类在繁殖过程中,为避免被捕食、减少繁殖投入等而选择占用其他鸟类的巢。2014~2016年每年的4~8月,在吉林向海国家级自然保护区记录到4种占用喜鹊巢进行繁殖的鸟类,其中绿头鸭(Anas platyrhynchos)8巢,纵纹腹小鸮(Athene noctua)4巢,长耳鸮(Aiso otus)5巢,麻雀(Passer montanus)6巢。大部分(82.6%)为利用喜鹊的废弃旧巢,而绿头鸭(1巢)、长耳鸮(2巢)和纵纹腹小鸮(1巢)少数侵占喜鹊当年新建的巢。     

Habitat preferences for Long-eared Owls Asio otus and Little Owls Athene noctua in semi-arid environments at three spatial scales

Capsule There is a relationship between owl numbers and the availability of the agri-forest patchwork.

Aims To model habitat preferences at three different scales of two predators largely neglected within the framework of Environmental Impact Assessment (EIA) studies.

Methods We studied habitat preferences of Long-eared Owls and Little Owls by comparing habitat composition around 28 and 78 occupied territories respectively with 55 non-occupied territories in Alicante (eastern Spain). Generalized linear models were used to examine patterns of habitat preference at three different spatial scales: nest-site, home range and landscape.

Results At the nest-site scale, Long-eared Owls preferred wooded areas with few paved roads while Little Owls preferred arid plantations. Furthermore, the probability of finding an occupied territory increased with the proximity of another occupied territory in the surroundings. The home range scale models mirror the feeding requirements of the owls. Thus, Long-eared Owls occupied areas with high percentages of forest, arid plantations, edges between these two land uses, short distances between nests, with presence of conspecifics and little human disturbance. Little Owls occupied arid plantations with high availability of linear structures and the proximity of villages. At the landscape scale, Long-eared Owls eluded extensive forests, and Little Owls preferred arid plantations.

Conclusions We suggest a hierarchical process of habitat selection for both owls regarding fitting trophic resources at the broadest scales and adequate sites for breeding and roosting at the smallest scale. EIA studies must consider that protecting small areas around single nests may not be an efficient conservation option compared with preserving clusters of territories for both species.     

Fear factor: prey habitat selection and its consequences in a predation risk landscape

Predation risk influences prey use of space. However, little is known about how predation risk influences breeding habitat selection and the fitness consequences of these decisions. The nest sites of central-place foraging predators may spatially anchor predation risk in the landscape. We explored how the spatial dispersion of avian predator nests influenced prey territory location and fitness related measures. We placed 249 nest boxes for migrant pied flycatchers Ficedula hypoleuca , at distances between 10 and 630 m, around seven different sparrowhawk nests Accipiter nisus . After closely monitoring flycatcher nests we found that flycatcher arrival dates, nest box occupation rates and clutch size showed a unimodal relationship with distance from sparrowhawk nests. This relationship suggested an optimal territory location at intermediate distances between 330 and 430 m from sparrowhawk nests. Furthermore, pied flycatcher nestling quantity and quality increased linearly with distance from sparrowhawk nests. These fitness related measures were between 4 and 26% larger in flycatcher nestlings raised far from, relative to those raised nearby, sparrowhawk nests. Our results suggest that breeding sparrowhawk affected both flycatcher habitat selection and reproductive success. We propose that nesting predators create predictable spatial variation in predation risk for both adult prey and possibly their nests, to which prey individuals are able to adaptively respond. Recognising predictable spatial variation in perceived predation risk may be fundamental for a proper understanding of predator-prey interactions and indeed prey species interactions.     

Herbaceous ground cover reduces nest predation in olive groves

Capsule Bare ground increases artificial nest predation in olive groves.

Aims To assess the effect of different soil management regimes on nest predation rates in olive groves.

Methods We performed nest predation experiments with artificial nests during the breeding season in 2013, in two areas of southern Spain. Each artificial nest (n?=?300) contained three quail Coturnix eggs, two of which were unmanipulated and the third one was emptied and injected with plaster. Predators were identified by marks on eggs filled with plaster.

Results Ground nests were significantly more depredated, irrespective of the presence of ground cover; tree nests were less depredated in fields with ground cover. There was a clear difference in nest predators of ground and tree nests. Rodents were the most frequent predators of tree nests.

Conclusion Lower predation rates of tree nests in orchards with ground cover are probably linked to a change in the foraging behaviour of rodents, which in these more complex habitats might be restricted by rodents' own risk of predation. This study underscores the important role of agricultural practices in preserving farmland bird communities, particularly tree-nesting species, suggesting that for this group, implementation of ground cover in olive groves might enhance breeding success by reducing nest predation rates.     

Nest predation and habitat change interact to influence Siberian jay numbers

We studied Siberian jays, breeding in northern Sweden, to examine the potential for interactions between nest predation and reduced vegetation heterogeneity around nest sites to cause a decrease in jay numbers. Parent behaviour and nests are highly cryptic in the species. Our 12-year data showed, however, that nests had a probability of only 0.46 to be successful and produce at least one nestling. Nest predation was intense and a main cause of nest failure. All predators that could be identified were visually oriented hunters, mostly other corvids able to colonize taiga forest only close to human settlements. Consistent with the idea that predators used visual cues, nest predation increased with parental activity, which suggests that predators used parental provisioning trips to locate nests. Furthermore, a reduction in daily nest survival rates with decreasing amount of nesting cover was more pronounced in areas with high corvid activity as predicted when cover mediates the hunting efficiency of visual oriented predators. Declining temperatures interacted with the effects of habitat characteristics to further reduce daily nest survival rates suggesting that parents were not able to increase nest visitation rates to satisfy the higher energy demands of their nestlings without endangering the nest. Our results identify a mechanism through which predation and human-induced reduction in nesting cover on a larger scale may interact to cause a reduction in Siberian jay numbers larger than expected from habitat loss alone.     

Nest-site selection of the Long-eared Owl Asio otus in northwestern Switzerland

Capsules Sites are selected as part of an antipredator strategy.

Aims To assess if site choice depends on habitat variables at nest sites and if habitat quality influences reproduction.

Methods Breeding density was explored in northwestern Switzerland from 1992 to 1996. Habitat variables were examined at 38 breeding sites and were compared with data collected from random sites. Habitat quality was estimated using the discriminant function scores of the nesting sites.

Results Breeding density was found to vary between years; more pairs bred and raised more young in 1993, a year of high vole abundance. Long-eared Owls tended to avoid the vicinity of buildings; they occupied sites with denser forest edges, greater canopy cover, and with more conifers than random sites. I found no statistical evidence that they used less optimal sites when the population was high. The number of fledglings increased with habitat quality, but did not vary with any of the habitat variables taken separately.

Conclusion Long-eared Owl selects nesting habitat as part of an anti-predator strategy, but the measures of territory quality did not seem to be a limiting factor for the population.     

Impact of brood parasitism and predation on nest survival of the fan-tailed gerygone in New Caledonia

Predation and brood parasitism are common reasons for nesting failure in passerine species and the additive impact by invasive species is a major conservation concern, particularly on tropical islands. Recognising the relative contribution of the different components of nesting failure rates is important to understand co-evolutionary interactions within brood parasite–host systems. In the remote archipelago of New Caledonia, the fan-tailed gerygone Gerygone flavolateralis is the exclusive host of the brood-parasitic shining bronze-cuckoo Chalcites lucidus. Additionally, invasive rodents also possibly have an impact on breeding success. To estimate the impact of potential nest predators, we 1) video monitored nests to identify predators, 2) estimated the probability of predation based on nest visibility and predator abundance and 3) tested the possibility that the location of experimental nests and lack of odour cues decrease the predation by rodents. In addition, we estimated nest survival rates using data collected in different habitats over the course of eight breeding seasons. Nesting success of fan-tailed gerygones was relatively low and predation was the main cause of nesting failure. We recorded mainly predation by native birds, including the shining bronze-cuckoo, whereas predation by rats was rare. In open habitats predation by cuckoos was much lower than predation by other avian predators. Neither predator activity around nests nor nest visibility influenced the probability of predation. Experimental nests in more accessible locations and containing an odorous bait were more exposed to rodent predation. Apparently, the fan-tailed gerygone has either never been specifically vulnerable to predation by rats or has developed anti-predator adaptations.     

Nest site selection and predation driven despotic distribution of breeding long-eared owls Asio otus

Long-eared owls Asio otus do not build their own nests. They occupy old corvid nests in either coniferous or deciduous trees. In my study area owls favoured coniferous over deciduous trees for nesting and occupied nest sites in that order. Comparing overall breeding output, I found no difference between the two kinds of nest sites, but among early nests there was a higher proportion of unsuccessful nests in deciduous trees. This difference was due to differences in predation rate, indicating that the owls' pattern of nest site occupation followed predictions from the ideal despotic distribution model. I also show that, due to a seasonal change in habitat quality, predator driven despotism, although present, can be well masked and hence difficult to detect.     

Nestbox provisioning in a rural population of Eurasian Kestrels: breeding performance,nest predation and parasitism

The breeding biology of the Eurasian Kestrel Falco tinnunculusin nestboxes in farmland was studied to test for differences between artificial and natural sites. We report on the direct effect of nestbox provisioning on some life-history traits and how nestbox use affects nest predation and parasitism. Five types of nest-sites were available: nestboxes on poles and trees (artificial sites), stick nests on trees, stick nests on pylons and holes in buildings (‘natural’ sites). The Kestrel population increased from 23 pairs in 1993 (prior to nestbox installation) to 55 in 1998 as nestboxes were provided. In general, pairs breeding in trees started to lay later than those nesting in nestboxes on poles or in building holes, but this difference was probably associated with habitat quality rather than nest type. Differences in clutch size were found between nest-sites in some years, and were associated with laying date and, probably, with variation in territory quality. Using only data from successful nests, pairs breeding in nestboxes produce more fledglings than those in building holes or pylons. The frequency of nest predation was higher in natural sites than in nestboxes. The number of fledglings from pairs breeding in nestboxes was higher than from those breeding in old stick nests in trees when all nests were considered. Nestbox provisioning had no effect on the occurrence of the ectoparasite Carnus hemapterus, but chicks from nestboxes showed higher intensity of infection. Our results suggest that nestbox provisioning increases reproductive success and the frequency of nest predation or intensity of parasite infestation in Kestrels.     

The exclusion of avian predators from aggregations of nesting lapwings (Vanellus vanellus)

Territorial lapwings in Aberdeenshire, Scotland, largely prevented carrion crows, (Corvus corone), their main egg predators, from approaching close to nest-sites and from entering the area within an aggregation of 11 nests. Predation rates of artifical nests were significantly lower when placed within 10 m of active lapwing nests than when>200 m from nest-sites, indicating that the presence of lapwings afforded protection from crow predation. Further artificial nest experiments showed that the amount of protection declined linearly with increasing distance from the nest-site, and some degree of protection occurred to at least 30–50 m from it. The size of this protected zone was apparently related to the number of lapwing nests present, and the survival time of eggs in artificial nests reflected the lapwings' nesting density. The defended zones around each lapwing nest overlapped appreciably in dense or large nesting aggregations, leading to the observed protection by generally excluding crows, from the nesting area.     

Repeatability of nest predation in passerines depends on predator species and time scale

It has been proposed that some specific locations of bird's nests have higher intrinsic chances of being depredated than other locations. This predicts that fates of consecutive nesting attempts at the same site should be repeatable. We used 20 pairs of old thrush nests to simulate repeated nesting attempts at the same sites, both within and between breeding seasons (n=40  sites×2  trials×2  years=160). Each nest was monitored by a camera to record multiple predation events and to identify predators. Predation by all predator species was repeatable during a 15-day trial. Predation by principal predators (jay Garrulus glandarius , marten Martes martes / foina ) and total predation (all species combined) was not correlated within pairs of simultaneously exposed nests or within samples of nests from particular study plot, and not repeatable for individual nests between-trials or between-years. These findings suggest short-term effect of predator memory causing revisitation of previously depredated nests during a current nesting trial (all predators); do not support an effect of nest site features on multiple nest discoveries and/or an effect of nest location on repeated random encounters with the same nest (principal predators). Long-term repeatability and correlation within pairs of simultaneously exposed nests was detectable only in occasional predators (great spotted woodpecker Dendrocopos major , possibly also squirrel Sciurus vulgaris ), which suggests effect of nest location combined with site fidelity and individual foraging specialization of these predators. We conclude that repeatability of nest predation depends on the time scale considered and the local predator community. We caution against spurious findings of repeatable nest predation resulting simply from statistical properties of correlation in binary data (nest fates).     

Predators and the breeding bird: behavioral and reproductive flexibility under the risk of predation

A growing body of work suggests that breeding birds have a significant capacity to assess and respond, over ecological time, to changes in the risk of predation to both themselves and their eggs or nestlings. This review investigates the nature of this flexibility in the face of predation from both behavioural and reproductive perspectives, and also explores several directions for future research. Most available work addresses different aspects of nest predation. A substantial change in breeding location is perhaps the best documented response to nest predation, but such changes are not always observed and not necessarily the best strategy. Changes in nesting microhabitat (to more concealed locations) following predation are known to occur. Surprisingly little work addresses the proactive avoidance of areas with many nest predators, but such avoidance is probably widespread. Individual birds could conceivably adopt anti‐predator strategies based on the nest predators actually present in an area, but such effects have yet to be demonstrated. In fact, the ways in which birds assess the risk of nest predation is unclear. Nest defence in birds has historically received much attention, but little is known about how it interacts with other aspects of decision‐making by parents. Other studies concentrate on predation risk to adults. Some findings suggest that risk to adults themselves influences territory location, especially relative to raptor nests. An almost completely unexplored area concerns the sorts of social protection from predators that might exist during the breeding season. Flocking typical of the non‐breeding season appears unusual while breeding, but a mated pair may sometimes act as a “flock of two”. Opportunistic heterospecific sociality may exist, with heterospecific protector species associations more prevalent than currently appreciated. The dynamics of singing during the breeding season may also respond to variation in predation risk, but empirical research on this subject is limited. Furthermore, a few theoretical and empirical studies suggest that changes in predation risk also influence the behaviour of lekking males. The major influence of predators on avian life histories is undoubtedly expressed at a broad phylogenetic scale, but several studies hint at much flexibility on an ecological time scale. Some species may forgo breeding completely if the risk of nest predation is too high, and a few studies document smaller clutch sizes in response to an increase in nest predation. Recent evidence suggests that a female may produce smaller eggs rather than smaller clutches following an increase in nest predation risk. Such an increase may also influence decisions about intraspecific brood parasitism. There are no clear examples of changes in clutch/egg size with changes in risk experienced by adults, but parental responses to predators have clear consequences for offspring fitness. Changes in risk to adults may also influence body mass changes across the breeding season, although research here is sparse. The topics highlighted herein are all in need more empirical attention, and more experimental field work whenever feasible.     

Noise pollution and decreased size of wooded areas reduces the probability of occurrence of Tawny Owl Strix aluco

At present, urban areas cover almost 3% of the Earth's land surface, and this proportion is constantly increasing along with human population growth. Although urbanization leads to biodiversity decline, at the same time it creates a novel and extensive environment that is exploited by whole assemblages of organisms. These include predators, which use the matrix of different habitat types within the urban environment for breeding and/or foraging. This study investigated how attributes of the urban landscape influence the distribution pattern of a nocturnal acoustic predator, the Tawny Owl Strix aluco. The probability of occurrence of this species was correlated with the presence of natural forests, and the increasing size of wooded habitat patches within the urban landscape; however, Tawny Owls were less likely to occur at sites with high noise levels at night. Our study suggests that the distribution pattern of acoustic predators is shaped by the availability of primary habitat but reduced by noise intensity (which may decrease hunting efficiency). The Tawny Owl is a top predator in the urban environment and its presence/absence may therefore affect populations of other species; this provides clear evidence of the indirect effect of noise pollution on animal populations inhabiting urban environments.