Do artificial nests reveal relative nest predation risk for real nests?

Present knowledge of the effects of nest predation on spatial distribution, habitat selection and community structure of birds is to a large extent based on results from experiments with artificial nests. Although nest predation risk is likely to differ between artificial and real nests, most previous studies of nest predation using artificial nests have been lacking a proper control. We investigated whether predation rates on artificial nests predicted those on real nests by simultaneously comparing the fate of real and artificial nests (containing quail Coturnix coturnix and plasticine eggs) in 92 territories of the northern wheatear Oenanthe oenanthe in 1996. We also investigated whether risk for artificial nests was related to relative average risk for real nests in these territories (based on data collected two years before and two years after the experiment). Nest predation on artificial nests did predict relative predation risk for real nests only when quail egg depredation was used as the criterion for artificial nest predation. Despite plasticine egg depredation being the most common type of predation it was not associated with predation risk for real nests. Small mice and vole species dominated among cases with only plasticine egg depredation, while predatory mammals and snakes destroyed most quail eggs in artificial nests and most eggs in real wheatear nests. The results suggest that artificial nests may only predict the risk for real nests when the nest predator species are similar among the two types of nest. Furthermore, our data suggest that small mice and vole species rarely depredate nests of mid-sized passerine birds . Our results cast doubt on many previous conclusions based on experiments with artificial nests, since predation risk for such nests is likely to be uncorrelated with risk for real nests due to nest-type-specific differences in nest preying species.     

The effect of recreational homes on willow ptarmigan (Lagopus lagopus) in a mountain area of Norway

The increasing development of recreational resorts and second homes in mountain regions worldwide require substantial infrastructure, and have large impact on habitats and ecosystems. We hypothesized that developed areas would attract predators and lead to higher predation on willow ptarmigan and lower their abundance. In a 500-km² study area in south-central Norway, we sampled the density of territorial cocks in spring and the breeding success of willow ptarmigan along a 3-km gradient extending out from clusters of cabins. We also sampled red fox scats and corvid birds and measured nest predation on artificial nests across this gradient. Densities of cocks in the spring and of adults and brood sizes in August did not vary along the gradient. However, the density of chicks in August was higher beyond 1.5 km from cabin areas, presumably because more hens lost their clutches in the vicinity of cabins. This was supported by the results from the artificial nest experiment where significantly more nests were depredated near cabin areas than further away. The number of scats of red fox along trails increased with distance from cabins, whereas more corvid birds were observed near cabins. We conclude that corvid birds were the main cause of higher loss of ptarmigan nests near cabin areas, which led to lower production of chicks. Breeding density, however, did not seem to vary along the gradient, presumably because of suitable habitat for breeding and little human activity in these areas during the period of pair formation and nesting.     

Forest vegetation structure has more influence on predation risk of artificial ground nests than human activities

As a major process affecting the reproductive success of birds, nest predation influences population density and dynamics and forces species to adapt to ecological and evolutionary time scales. The disentangling of potential natural and anthropogenic drivers of nest predation is crucial for the conservation of species. Thus, we investigated the effects of elevation, egg characteristics, vegetation structure and human activities on daily nest predation rates of artificial ground nests by baiting 700 artificial nests with quail eggs along an elevational gradient of about 1100 m. After 25 days, we found an overall daily nest predation rate of 0.045. Our generalized linear mixed model revealed increasing daily predation rates with increasing forest management, no impact of recreational activities, and lower daily predation rates in the vicinity of buildings. Furthermore, daily predation rates declined with increasing density of near-ground vegetation and increased with increasing tree cover. Finally, we found no influence of elevation, matching of egg and ground colouration, and dead wood on daily nest predation rates. Our results revealed that the risk of nest predation depends more on vegetation structure than on current levels of recreational activities. Moreover, the negative relation of nest predation risk and near-ground vegetation indicates that the changing forest structure after natural disturbances (e.g. wind throw or bark beetle infestation), which is tolerated within the benign neglect strategy applied by the authorities of protected areas, decreases the predation risk, whereas salvage logging increases this risk.     

Predation on artificial bird nests along an urban gradient: predatory risk or relaxation in urban environments?

Urbanization - the anthropogenic conversion of natural ecosystems into human-dominated ecosystems - has occurred on global scales. The human-dominated landscape presents particular challenges to researchers because the effects of urbanization on ecological processes are not well understood. We investigated the influence of urbanization on predation by conducting an artificial nest experiment along an urban gradient of six sites ranging from natural to urbanized ecosystems. Previous hypotheses suggest that predation pressures in urban environments will either 1) increase because of the high abundance of exotic species which act as predators or 2) decrease due to the lack of natural predators. To determine relative predation pressures among sites along the urban gradient, we monitored the fates of 16 artificial avian nests at each of the six sites for a total of 96 nests in each year (1996, 1997). We analyzed the dependency of nest fate (depredated or undisturbed) on intensity of urbanization (sites along the urban gradient), nest height (ground, above-ground), and year using loglinear models. The frequency of nest predation was strongly dependent on site along the urban gradient, indicating that urbanization intensity was an important determinant of nest fate. Predation pressure exhibited an overall decline from natural to urban sites in both years, suggesting that urban environments have low predation pressures relative to natural areas. The predatory relaxation in urban environments may partially explain the greater abundance of some species in urban environments, particularly urban exploiters such as european starlings Sturnis vulgaris. house sparrows Passer domesticus. and rock doves Columba livia.     

千岛湖栖息地片段化效应对鸟类巢捕食风险的影响

为了解栖息地片段化对鸟类巢捕食风险的影响,我们于2010年4-8月,在千岛湖地区选取16个岛屿,分别在岛屿边缘和内部区域用放置鸡蛋(大型卵)和鹌鹑(Coturnix japonica)蛋(小型卵)的方法进行人工模拟地面巢试验,研究不同体积大小鸟卵的巢捕食率及其差异,分析巢捕食率与岛屿面积、隔离度、形状指数和植物物种丰富...     

Predation on artificial nests in relation to forest type: contrasting the use of quail and plasticine eggs

Previous studies of avian nest predation have focused on how human-induced changes in the landscape influence the frequency of predation However, natural variation in the abundance of predators due to their choice of habitat can also influence predation rate To determine if predation on artificial nests was influenced by forest stand type, we placed ground and shrub nests containing quail and plasticine eggs in contiguous coniferous, mixedwood and deciduous stands in the southern boreal mixedwood forest of central Canada Nest predators were identified using remotely triggered cameras and marks left in plasticine eggs, while the relative abundance of nest predators such as squirrels and corvids were estimated using acoustic-visual surveys Using the fate of quail eggs to calculate predation rate, we found that predation was significantly higher in coniferous (67%) than in deciduous (17%) or mixedwood (25%) forest, with similar predation on ground (37%) and shrub (29%) nests Using plasticine eggs to calculate predation rate, nests in coniferous forest still suffered higher rates of predation, although predation rates were 15–20% higher, and ground nests suffered significantly higher rates of predation than shrub nests Quail eggs seemed to suffer lower rates of predation because small mammals were unable to penetrate the shell, but could leave marks on plasticine eggs The higher predation rate in coniferous forest was likely caused by higher abundance of red squirrels Tamiasciurus hudsonicus , the presence of fishers Martes pennanti and a simplified understory which may have made it easier for predators to find nests relative to the deciduous and mixedwood forest Plasucine eggs provide new insights into nest predation by identifying predation events by smaller predators such as mice that are missed when using quail eggs     

Compounding effects of habitat fragmentation and predation on bird nests

Habitat fragmentation and invasive species are two of the greatest threats to species diversity worldwide. This is particularly relevant for oceanic islands with vulnerable endemics. Here, we examine how habitat fragmentation influences nest predation by Rattus spp. on cup‐nesting birds in Samoan forests. We determined models for predicting predation rates by Rattus on artificial nests at two scales: (i) the position of the bird's nest within the landscape (e.g. proximity to mixed crop plantations, distance to forest edge); and (ii) the microhabitat in the immediate vicinity of the nest (e.g. nest height, ground cover, slope). Nest cameras showed only one mammal predator, the black rat (Rattus rattus), predating artificial nests. The optimal model predicting nest predation rates by black rats included a landscape variable, proximity to plantations and a local nest site variable, the percentage of low (<15 cm) ground cover surrounding the nest tree. Predation rates were 22 ± 13% higher for nests in forest edges near mixed crop plantations than in edges without plantations. In contrast, predation rates did not vary significantly between edge habitat where the matrix did not contain plantations, and interior forest sites (>1 km from the edge). As ground cover reduced, nest predation rates increased. Waxtags containing either coconut or peanut butter were used as a second method for assessing nest predation. The rates at which these were chewed followed patterns similar to the predation of the artificial nests. Rural development in Samoa will increase the proportion of forest edge near plantations. Our results suggest that this will increase the proportion of forest birds that experience nest predation from black rats. Further research is required to determine if rat control is needed to maintain even interior forest sites populations of predator‐sensitive bird species on South Pacific islands.     

Nest predation in forest birds: influence of predator type and predator's habitat quality

We used the introduction of a generalist nest predator, the red squirrel Tamiasciurus hudsonicus, and of a large herbivore, the Sitka black-tailed deer Odocoileus hemionus sitkensis, to the islands of Haida Gwaii (Queen Charlotte Islands, British Columbia, Canada) to study how predator assemblage and habitat quality and structure influenced nest predation in forest birds. We compared losses of natural nests to predators on islands with and without squirrels. We selected nine islands with or without squirrel or deer and used 506 artificial nests put on the ground or in shrubs to further analyse variation of nest predation with predator assemblage and habitat quality for the predators. For both natural and artificial nests predation risk was higher in presence of squirrels. But predation risk varied within island categories. In presence of squirrels it was highest in stands with mature conifers where it fluctuated from year to year, in response to fluctuations in squirrel abundance. Vegetation cover around the nest had little effect on nest predation by squirrels. Where squirrels were absent, nest predation concentrated near predictable food sources for corvids, the main native predators, and increased with decreasing vegetation cover, suggesting that removal of the vegetation by deer increased the risk of predation by native avian nest predators that use visual cues. Predation risk in these forests therefore varies in space and time with predator composition and with quality of the habitat from the predators' perspective. This temporal and spatial variation in predation risk should promote trade-offs in the response of birds to nest predation, rather than fine-tuned adaptations to a given predation pattern.     

Nest Predation Risk on Ground and Shrub Nests in Forest Margin Areas of Sulawesi, Indonesia

Forest loss and fragmentation in Indonesia may seriously affect the survivorship of forest birds and lead to local extinction of bird populations. We used 786 artificial nests baited with quail eggs to examine the effect of habitat alteration on nest predation in Lore Lindu National Park, Sulawesi. Natural forest and four habitats of forest margin areas: forest edge, forest gardens, coffee plantations, and secondary forest, were studied. Two types of artificial nests, ground and shrub nests were placed in these habitats at two different locations for a period of 8 days. In addition, we used automatic cameras and cage-traps to identify the predators. Nests in shrubs experienced significantly higher predation rates in forest margin areas than in natural forest. Predation on ground nests did not differ significantly between these habitat types, but was significantly higher than that on shrub nests in each habitat except forest edge. Rodents were the most common predators of both nests, but shrub nests were also susceptible to Dwarf cuscus (Strigocuscus celebensis), squirrels, and tree snakes. The nest predation rates we found were among the highest found in tropical rainforests, probably a consequence of the unique predator assemblages of Sulawesi. These results suggest that egg survival is negatively affected by human intervention and that human-induced habitats might have only limited importance for the conservation of Sulawesi's largely endemic understorey avifauna. These considerations might be important since forest margins comprise significant proportions of protected areas on Sulawesi and play an important role in future Park zoning concepts as well as in conservation-oriented land use management.     

An ecological paradox: More woodland predators and less artificial nest predation in landscapes colonized by noisy miners

Many passerine bird populations, particularly those that have open‐cup nests, are in decline in agricultural landscapes. Current theory suggests that an increase in habitat generalist predators in response to landscape change is partially responsible for these declines. However, empirical tests have failed to reach a consensus on how and through what mechanisms landscape change affects nest predation. We tested one hypothesis, the Additive Predation Model, with an artificial nest experiment in fragmented landscapes in southern Queensland, Australia. We employed structural equation modelling of the influence of the relative density of woodland and habitat generalist predators and landscape features at the nest, site, patch and landscape scales on the probability of nest predation. We found little support for the Additive Predation Model, with no significant influence of the density of woodland predators on the probability of nest predation, although landscape features at different spatial scales were important. Within woodlands fragmented by agriculture in eastern Australia, the presence of noisy miner colonies appears to influence ecological processes important for nest predation such that the Additive Predation Model does not hold. In the absence of colonies of the aggressive native bird, the noisy miner, the influence of woodland predators on the risk of artificial nest predation was low compared with that of habitat generalist predators. Outside noisy miner colonies, we found significant edge effects with greater predation rates for artificial nests within woodland patches located closer to the agricultural matrix. Furthermore, the density of habitat generalist predators increased with the extent of irrigated land‐use, suggesting that in the absence of noisy miner colonies, nest predation increases with land‐use intensity at the landscape scale.     

Birds nesting survival in disturbed and protected Neotropical savannas

Fragmentation and other habitat disturbances are long known to negatively affect birds, in large part by decreasing nest success due to high nest predation rates. The factors, however, that cause this decrease in nest success are still poorly understood and may vary among regions or species. Here, we show that nest survival is also lower in a disturbed landscape versus a protected cerrado (savanna-like) Neotropical landscape. Also, we tested the importance of garbage in the nest, brood parasitism, microhabitat and bird family in nest survival, controlling for temporal effects. We monitored 144 birds’ nests in a disturbed landscape and 150 nests in a natural reserve of cerrado vegetation in central Brazil, between September and December 2006. We used Program MARK to estimate nest survival probabilities and evaluate the effect of covariates in nest success in the disturbed area. Nest daily survival rate (DSR) was higher in the reserve (survival probability = 29.4%) than in the disturbed landscape (survival probability = 16.6%). Nest daily survival rate (DSR) was smaller in nests with garbage (survival probability = 9.3%) than in nests without garbage (survival probability = 19.5%) in the disturbed landscape. Effects of habitat disturbance on nest survival differed among bird families, with finches and tanagers being more affected mostly due to high nest predation rates. Conservation and management of birds in disturbed landscapes should include actions to decrease nest predation. In poor rural or suburban areas in developing countries, such as Brazil, actions like better garbage treatment may help conserve birds in disturbed landscapes.     

Testing sources of variation in nestling‐stage nest success of Florida Scrub‐Jays in suburban and wildland habitats

Human modification of habitats can reduce reproductive success by providing novel cues to which birds may respond with behaviors that are actually maladaptive in those environments. Ad libitum human‐provided foods may provide the perception that urban habitats are food‐rich even as natural food availability decreases. Similarly, human activity may increase the perception that predation risk is high even as natural predators may decrease in abundance. In response, birds may reduce parental care with a subsequent cost to successful reproduction. Florida Scrub‐Jays (Aphelocoma coerulescens) in suburban areas have lower nest success during the nestling period than do wildland jays, possibly the result of such maladaptive responses, but maybe because of ecological differences with wildlands. We manipulated adult perception of predation risk and the availability of nestling foods in suburban and wildland areas to determine if these factors influenced parental care and nestling begging, and if the behavioral responses of adults influence nest survival during the nestling stage. Experimentally increasing perception of predation risk reduced parental care by both suburban and wildland females, but did not influence care by males. Increasing food availability, but not predation risk, had little influence on parental care, but resulted in decreased nestling begging rates and an increase in the frequency (pitch) of begging calls in both habitats. However, neither parental care nor food availability influenced nest survival during the nestling stage. Instead, the presence of helpers was the most important variable in nest survival analyses, suggesting that habitat‐specific differences in nest survival during the nestling stage were not simply the result of maladaptive parental behavior or shortage of nestling food resources in the suburban habitat. The lack of helpers combined with ecological differences, such as the abundance of nest predators, may be why fewer nests of Florida Scrub‐Jays survive during this stage in suburban areas.     

Urban-associated habitat alteration promotes brood parasitism of Acadian Flycatchers

ABSTRACT.   High rates of brood parasitism are generally associated with agricultural landscapes, but recent evidence suggests that urbanization may also increase the likelihood of brood parasitism. I evaluated the extent to which brood parasitism by Brown-headed Cowbirds ( Molothrus ater ) was explained by differences in (1) body size of adult hosts, presumably relating to the ability to defend nest from cowbirds, (2) nest placement in substrate and relative to habitat edges, (3) habitat structure surrounding nests, (4) host density, (5) cowbird abundance, both absolute and relative to host numbers, (6) landscape composition, and (7) Julian date. From 2001 to 2006, I monitored nest fate and measured vegetation characteristics surrounding nests of Acadian Flycatcher ( Empidonax virescens ) breeding in mature riparian forests in central Ohio, USA. The likelihood that a nest would be parasitized was best explained by the number of understory stems surrounding the nest and, to a lesser extent, by the amount of urbanization in the surrounding 1-km-radius landscape. Parasitized nests were surrounded by 1.6 times more stems and nearly twice the amount of urbanization than nonparasitized nests. Numbers of understory stems were positively associated with increasing urbanization, primarily due to invasion of urban forests by Amur honeysuckle ( Lonicera maackii ). Thus, urban-associated changes in habitat characteristics around nests may be important contributors to the greater vulnerability of urban nests to brood parasitism than nests in more rural landscapes. This pattern suggests that ecological restoration, such as removing exotic shrubs, may be an effective strategy to ameliorate certain negative consequences of urbanization near wooded reserves.     

Predators at bird nests in a northern hardwood forest in New Hampshire

ABSTRACT.   Nest predation is the primary cause of nest failure in most passerine birds, and increases in nest predation associated with anthropogenic habitat disturbance are invoked as explanations for population declines of some bird species. In most cases, however, the identity of the nest predators is not known with certainty. We monitored active bird nests with infrared time-lapse video cameras to determine which nest predators were responsible for depredating bird nests in northern New Hampshire. We monitored 64 nests of 11 bird species during three breeding seasons, and identified seven species of predators during 14 predation events. In addition, we recorded two instances of birds defending nests from predators and, in both cases, these nests were ultimately lost to predation. These results contrast with other studies in terms of the relatively high proportion of nests depredated by raptors and mice, as well as the absence of any predation by snakes. The diverse suite of predators in this and other studies is likely to confound our understanding of patterns of nest predation relative to fragmentation and habitat structure.     

The influence of fragment size and edge on nest predation in urban bushland

To test the effects of habitat fragmentation and edge on the rate of nest predation in an urban ecosystem, 20 artificial nests each containing 2 plasticine eggs were distributed in each of 24 bushland sites in Sydney, Australia. the eastern yellow robin Eopsaltria australis was adopted as a target species, and variables of nests, eggs and nesting behaviour were manipulated in experiments. Sites ranged in size from 3.8 ha to 14717 ha and were divided into three size classes: 1) 0–10 ha. 2) 11–100 ha and 3) ≥101 ha. Nests were positioned either around the edge of the fragment (within 50 m from the fragment boundary) or within the centre of the fragment (< 50 m from the fragment boundary). The predation rate was calculated as the percentage of nests that had one or both eggs damaged or removed after 15 d of exposure. Nest predation rates were high (average 70.6%) but were not affected by patch size or distance from fragment edges. Predators were identified by marks of the beak or teeth left in the plasticine eggs. Nest predators identified were birds, black rats, brown antechinus and ringtail possum, with the majority of predation being by birds (61.7%), Our findings differ from those of most previous studies of nest predation, and perhaps reflect the ubiquity of generalist predators and the degree of habitat modification throughout remnants of bushland in the urban environment.     

Provision of supplementary food for wild birds may increase the risk of local nest predation

In countries such as the UK, USA and Australia, approximately half of all households provide supplementary food for wild birds, making this the public's most common form of active engagement with nature. Year‐round supplementary feeding is currently encouraged by major conservation charities in the UK as it is thought to be of benefit to bird conservation. However, little is understood about how the provision of supplementary food affects the behaviour and ecology of target and non‐target species. Given the scale of supplementary feeding, any negative effects may have important implications for conservation. Potential nest predators are abundant in urban areas and some species frequently visit supplementary feeding stations. We assess whether providing supplementary food affects the likelihood of nest predation in the vicinity of the feeder, by acting as a point attractant for potential nest predators. We provided feeding stations (empty, peanut feeder, peanut feeder with guard to exclude potential nest predators) in an area of suburban parkland in the UK and monitored the predation rate of eggs placed in artificial nests located at distances that replicated the size of typical suburban gardens. Nest predators (Magpies Pica pica, Grey Squirrels Sciurus carolinensis) were frequent visitors to filled feeders, and predation caused by Magpies, European Jays Garrulus glandarius and Grey Squirrels was significantly higher when nests were adjacent to filled feeders. The presence of a feeder guard did not significantly reduce nest predation. As supplementary feeding is becoming increasingly common during the breeding season in suburban habitats, we suggest that providing point attractants to nest predators at this time may have previously unconsidered consequences for the breeding success of urban birds.     

Predation risk of artificial ground nests in managed floodplain meadows

Nest predation highly determines the reproductive success in birds. In agricultural grasslands, vegetation characteristics and management practices influences the predation risk of ground breeders. Little is known so far on the predation pressure on non-passerine nests in tall swards. Investigations on the interaction of land use with nesting site conditions and the habitat selection of nest predators are crucial to develop effective conservation measures for grassland birds.In this study, we used artificial nests baited with quail and plasticine eggs to identify potential predators of ground nests in floodplain meadows and related predation risk to vegetation structure and grassland management.Mean daily predation rate was 0.01 (±0.012) after an exposure duration of 21 days. 70% of all observed nest predations were caused by mammals (Red Fox and mustelids) and 17.5% by avian predators (corvids). Nest sites close to the meadow edge and those providing low forb cover were faced with a higher daily predation risk. Predation risk also increased later in the season. Land use in the preceding year had a significant effect on predation risk, showing higher predation rates on unmanaged sites than on mown sites. Unused meadows probably attract mammalian predators, because they provide a high abundance of small rodents and a more favourable vegetation structure for foraging, increasing also the risk of incidental nest predations. Although mowing operation is a major threat to ground-nesting birds, our results suggest that an annual removal of vegetation may reduce predation risk in the subsequent year.     

Urban flight: understanding individual and population-level responses of Nearctic-Neotropical migratory birds to urbanization

1. Despite the fact that studies of urban ecology have become commonplace in the literature, ecologists still lack empirical evidence of the underlying mechanisms responsible for relationships between urbanization and animal community structure. In an effort to understand the processes that govern an apparent avoidance of urban landscapes by many Nearctic-Neotropical migratory birds, we examined population- and individual-level responses of the Acadian flycatcher (Empidonax virescens) to urbanization within the landscapes surrounding 35 riparian forest stands in Ohio, USA. 2. From May to August 2001-06 we surveyed birds, banded 175 territorial flycatchers to estimate both condition and survival, tracked nest initiation dates, monitored success of 387 nests and estimated annual reproductive productivity of 163 breeding pairs. 3. Neither apparent annual survival of males (phi = 0.53 +/- 0.056 SE) nor females (phi = 0.23 +/- 0.064 SE) was related to the amount of urban development within the landscape. Similarly, daily survival rates of nests, which ranged from 0.92 to 0.98 across sites, was not associated significantly with urbanization. In contrast, reproductive productivity was related negatively to the amount of urbanization surrounding riparian forests, perhaps due in part to the greater incidence of brood parasitism and fewer numbers of nesting attempts made by pairs in urban compared to rural forests. 4. Forests within urban landscapes experienced higher levels of turnover in site occupancy, and birds settling in urban areas initiated nests later, had marginally smaller body sizes and exhibited lower return rates following nest predation than birds in more rural landscapes. In this way, behavioural processes governing habitat selection, settlement patterns and site fidelity probably contributed to the lower levels of reproductive productivity achieved by pairs nesting in urban landscapes. 5. This study provides evidence that the negative association between Acadian flycatchers and urbanization results from both population- and individual-level responses to urbanizing landscapes surrounding their riparian forest habitats.     

Prevalence of nest predators in a sub-Arctic ecosystem

High nest loss is an important driver of gallinaceous bird population dynamics. Identifying factors determining the spatial distribution of potential nest predators and thereby indirectly risk of nest losses is therefore essential. The aim of this 1-year study was to estimate relative predation rates on artificial ground nests in willow ptarmigan (Lagopus lagopus) habitats, along replicate altitudinal gradients (transects, n?=?60) spanning from sub-Arctic birch forest to the low-alpine tundra in three locations in northern Norway. In each transect, one artificial nest (track board) was placed in three different habitats: (1) birch forest, (2) edge between birch forest and low-alpine tundra and (3) low-alpine tundra. Total predation rates over all habitats within locations ranged from 47.4% to 77.5% and did not vary systematically in space and time. The average predation rate by avian predators was consistently high (58%), and mammalian predation rate was consistently low (5.6%). The consistently high level of predation inflicted by birds was mainly due to omnipresent corvids, especially the hooded crow (Corvus cornix). Analysis of species-specific predation rates showed that habitat and location effects were insignificant for all species, except for raven (Corvus corax) that showed clearly higher predation in one of the locations. The results indicate that from the perspective of the spatial distribution of potential nest predators in sub-Arctic birch forest, ground nesting birds like willow ptarmigan should not be expected to be selective with respect to nesting habitat in the ecotone between birch forest and the low-alpine tundra.     

Nest-predation at the edge: an experimental study contrasting two types of edges in the dry Chaco, Paraguay

Forest fragmentation leads to the creation of isolated forest patches with subsequent impact on forest-interior flora and fauna. Forested corridors have been suggested to alleviate some of the impact by increasing the connectivity between remnant forest patches. However, both fragmentation and corridors increase the ratio of edge to core habitat. We studied nest predation of artificial nests at edges between I) contiguous forests and pastures and 2) forested corridors and pastures, in a forest-dominated landscape in the dry Chaco, Paraguay, The aim was lo determine if nest predation was higher near habitat edges compared to within forests and pastures, with special emphasis on edges at forested corridors. We found that predation rates were similar at edges and in interior habitats. Nest predation was higher for both ground and shrub nests in forested areas than in pastures, Predation rates were also higher for both ground and shrub nests at edges along forested corridors compared to edges neighbouring contiguous forests. Forested corridors connecting contiguous forests may thus act as an ecological sink for some species breeding here. Analysis of predator categories revealed that ground nests in pastures were relatively more depredated by mammals and less by birds, compared to both shrub nests in pastures and ground nests in forests.