Forest fragmentation and avian nest predation in forested landscapes

Summary The size of forest fragments, the use of land bordering fragments, and the distance of nests from an edge all affect the frequency of predation upon bird nests in Maine (USA), an area where the forest has been fragmented by roads, but not significantly reduced in area. We placed artificial nests containing quail eggs in forests of different sizes and at various distances from the edge to test which of these factors was most important in describing predation. Predation was greatest in small tracts surrounded completely by land. Large areas and those bordered on at least one side by a large water body had lower predation rates. This suggests that influx of predators from nearby habitats may be responsible for much of the nest predation in forest fragments.     

Artificial nest predation and habitat fragmentation: different trends in bird and mammal predators

Predation on artificial nests was studied in Belgian deciduous forest fragments between 1 and 200 ha Predation rates were compared to fragment size, distance from the forest edge, time period (three replicates), and nest type (ground and tree) Logistic regression analysis showed that overall nest predation did not vary with distance from the edge, forest size, and time period Birds represented over 70% of all predator attacks but their importance decreased in larger areas and away from the forest edge where mammals were responsible for much of the nest predation It is concluded that the effect of habitat fragmentation depends on the composition of the local predator community     

Edge effect on bird nest predation in the fragmented caldén (<Emphasis Type="Italic">Prosopis caldenia</Emphasis>) forest of central Argentina: an experimental analysis

Clearing of caldén (Prosopis caldenia) forests for agriculture and cattle raising in east-central La Pampa Province, central Argentina, has created a highly fragmented landscape, a condition that has resulted in adverse effects on birds in other forests, mainly through increased predation rates near forest edges. We evaluated bird nest predation rates using artificial nests, assessing the effects of forest fragment size, distance to the edge and nest height. We measured survival rate of 570 artificial nests located in trees, in bushes and on the ground, at different distances from the edge, in six forest fragments ranging in size from 2.1 to 117.6 ha, during two consecutive breeding seasons. Nest predation rates were significantly related with the number of days of exposition of the nest, nest height and distance to the edge, whereas fragment size and year of the experiment were not associated with predation rates. Ground nests were less likely to be predated than those located in bushes and trees. Predation rates decreased with the distance to the edge, showing a pattern consistent with the existence of an edge effect.     

Different nest predator faunas and nest predation risk on ground and shrub nests at forest ecotones: an experiment and a review

This study examined predator faunas of artificial ground and shrub nests and whether nest predation risk was influenced by nest site, proximity to forest edge, and habitat structure in 38 grassland plots in south-central Sweden. There was a clear separation of predator faunas between shrub and ground nests as identified from marks in plasticine eggs. Corvids accounted for almost all predation on shrub nests whereas mammals mainly depredated ground nests. Nest predation risk was significantly greater for shrub than for ground nests at all distances (i.e. 0, 15 and 30 m) from the forest edge. However, nest predation risk was not significantly related to distance to forest edge, but significantly increased with decreasing distance to the nearest tree. Different corvid species robbed nests at different distances from the forest edge, with jays robbing nests closest to edges. We conclude that the relationship between the predation risk of grassland bird nests and distance to the forest edge mainly depends on the relative importance of different nest predator species and on the structure of the forest edge zone. A review of published articles on artificial shrub and ground nest predation in the temperate zone corroborated the results of our own study, namely that shrub nests experienced higher rates of depredation in open habitats close to the forest edge and that avian predators predominantly robbed shrub nests. Furthermore, the review results showed that predation rates on nests in general are highest <50 m inside the forest and lower in open as well as forest interior habitats (≥50 m from the edge). Received: 16 March 1998 / Accepted: 30 July 1998     

Artificial nest and seed predation experiments on tropical southeast Asian islands

Southeast Asia is rapidly losing native habitats and the consequences of this are poorly understood. Because habitat loss and disturbance can affect avian and seed survivorship, we conducted artificial nest and seed predation experiments on tropical southeast Asian islands. Data among islands and fragments or different forest types (e.g. primary versus exotic forest) within the islands are compared. On Singapore Island, predation among different forest types (primary, secondary and woodland) did not differ. Only at one of the sites, nest predation was higher at 75 m from the forest edge than at 25 m. In other sites, predation did not differ in relation to the distance from the forest edge. Predation among 10 small (0.8–1026 ha) Singaporean islands differed. However, none of the environmental variables (e.g. island area) could explain the predation differences. The lowest predation of both nests and seeds was recorded in the primary forest areas of a contiguous forest (25 500 ha) in central Java (Linggoasri). Small mammals were the main predators on Singapore and other surrounding islands. However, the index of potential predator abundance, overall, did not correlate with predation. While larger and more pristine forests may be better for avian and seed survivorship, pinpointing variables affecting both artificial nest and seed predation may be difficult.     

Predation on artificial nests in a forest dominated landscape – the effects of nest type, patch size and edge structure

We studied the effects of forest patch size and forest edge structure on nest predation in a boreal coniferous forest landscape. The following predictions were tested. Nest predation should be higher in small than in large stands, in edges than in interior areas of forest stands, and in barren forest/clear–cut edges created by forestry than in natural forest/open marsh edges. Four types of artificial above ground nests (total of 261) were used; open cup nests with reindeer Rangifer t. tarandus hair, open cup nests with domestic hen Gallus domesticus feathers, and unlined open cup and nest–box nests. Nests were baited with one Japanese quail Coturnix coturnix japonica egg. Nest–boxes were depredated significantly less than open cup nests of all types. No edge- or stand size–related nest predation was found. The predation rate, regardless of the nest type, did not differ relative to the edge type and vegetation characteristics. However, better horizontal visibility of open cup nests due to more open vegetation structure increased predation risk in man–made edges compared to inherent edges. The results suggest that edge–related nest predation is absent or weak in forest dominated landscapes. This may be due to predator types present in the landscape and/or predators habitat use in forest dominated areas. Therefore, it might be that findings documented in other areas, such as in agricultural dominated landscapes, cannot be directly applied to managed forest landscapes.     

人工巢箱条件下的大山雀巢捕食

于2004—2008年在次生阔叶林中,采用悬挂巢箱的方法对大山雀的巢捕食作了研究。结果表明:不同年龄巢箱的被捕食率显著不同,新巢箱被捕食率最低,第2年被捕食率最高,第3年下降很大,第4年又略有上升。被捕食巢的窝卵数极显著的低于未被捕食巢的窝卵数。影响巢捕食的主要生境因子为巢箱高度和巢上盖度,其次为灌木的密度和高度。     

Cropland edge,forest succession,and landscape affect shrubland bird nest predation

The effects of habitat edges on nest survival of shrubland birds, many of which have experienced significant declines in the eastern United States, have not been thoroughly studied. In 2007 and 2008, we collected data on nests of 5 shrubland passerine species in 12 early successional forest patches in North Carolina, USA. We used model selection methods to assess the effect of distance to cropland and mature forest edge on nest predation rates and additionally accounted for temporal trends, nest stage, vegetation structure, and landscape context. For nests of all species combined, nest predation decreased with increasing distance to cropland edge, by nearly 50% at 250 m from the cropland edge. Nest predation of all species combined also was higher in patches with taller saplings and less understory vegetation, especially in the second year of our study when trees were 4–6 m tall. Predation of field sparrow (Spizella pusilla) nests was lower in landscapes with higher agricultural landcover. Nest predation risk for shrubland birds appears to be greater near agricultural edges than mature forest edges, and natural forest succession may drive patterns of local extirpation of shrubland birds in early successional forest patches. Thus, we suggest that habitat patches managed for shrubland bird populations should be considerably large or wide (>250 m) when adjacent to crop fields and maintained in structurally diverse early seral stages. © 2011 The Wildlife Society.     

Relative effects of nest size and site on the risk of predation in open nesting passerines

Large nests may incur fitness cost in terms of conspicuousness to predators, but the effect of nest size on predation risk can be confounded by effects of nest site and parental characteristics. I examined relative effects of nest size and placement by experimentally exchanging subsets of inactive nests baited with artificial clutches, among three open-cup nesting passerine species characterized by different nest size, placement and predation rate. The prediction that increasing nest size (original nest replaced by nest of the larger species) would increase predation, while decreasing nest size (replacement by nest of the smaller species) would decrease predation, relative to control (replacement by conspecific nest) was not supported in any species. The prediction that predation should be higher for large nests compared to small ones, even after exchanging nests among species-specific sites, was not supported. Predation rate differed among species (combined site/nest effect) before manipulation, whereas only the effect of nest site was significant after manipulation. This means that predation differed between species-specific nest sites, irrespective of the nest placed at these sites, but not between large (thrush) and small (warbler) nests, irrespective of their placement. Results do not suggest that nest predation selects directionally for smaller nest size. This conclusion could be specific to the study system characterized by high nest densities and high predation rate.     

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.     

Woodpigeons nesting in association with hobby falcons: advantages and choice rules

Many bird species nest in close association with other bolder and more aggressive birds which provide protection against nest predators. The woodpigeons, Columba palumbus, that nest in poplar plantations in Northern Italy are found almost exclusively clumped around hobby, Falco subbuteo, nests. Woodpigeons settle in the area and build their nests after the hobby has started nesting. We carried out experiments with dummy nests and observations on woodpigeon nests. Dummy woodpigeon nests placed near a hobby's nest suffered less depredation by hooded crows, Corvus corone cornix, than those placed far from it. A logistic regression analysis showed that three variables, hobby nesting stage, distance from the hobby's nest and the hobby's aggressiveness, influenced the probability of nest predation. The degree of protection varied during the hobby's nesting period and was highest when chicks were in the nest. The hobby's aggressiveness against intruders varied both between and within individuals during different nesting phases. The predation rate of dummy nests associated with the falcon was negatively correlated with the aggressiveness score of the hobby during the 6 days of dummy nest exposure. Observations on real nests showed that woodpigeons selected hobbies that had a high fledging success, and a more vigorous defensive behaviour. Clues that would allow woodpigeons to choose the best protector may be early nesting by the hobby and its aggressiveness. Hobbies preyed on adult woodpigeons, but the risk incurred by the woodpigeons was low compared with the very high risk of nest predation in this area. Copyright 1999 The Association for the Study of Animal Behaviour.     

Forest fragmentation relaxes natural nest predation in an Afromontane forest

Nest predation is widely regarded as a major driver underlying the population dynamics of small forest birds. Following forest fragmentation and the subsequent invasion by species from non-forested landscape matrices, shifts in predator communities may increase nest predation near forest edges. However, effects of human-driven habitat change on nest predation have mainly been inferred from studies with artificial nests, despite being regarded as poor surrogates for natural ones. We studied variation in predation rates, and relationships with timing of breeding and characteristics of microhabitats and fragments, on natural white-starred robin Pogonocichla stellata nests during three consecutive breeding seasons (2004–2007) in a Kenyan fragmented cloud forest. More than 70% of all initiated nests were predated during each breeding season. Predation rates nearly quadrupled between the earliest and the latest nests within a single breeding season, increased with distance to the forest edge, and decreased with the edge-to-area ratio of forest fragments. These spatial relationships oppose the traditional perception of edge and fragmentation effects on nest predation, but are in line with results from artificial nest experiments in other East African forests. In case of inverse edge and fragmentation effects on nest predation, such as shown in this study, species that tolerate edges for breeding may be affected positively, rather than negatively, by forest fragmentation, while the opposite can be expected for species restricted to the forest interior. The possibility of inverse edge effects, and its conservation implications, should therefore be taken into account when drafting habitat restoration plans.     

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.     

Do trade‐offs between predation pressures on females versus nests drive nest‐site choice in painted turtles?

Predation strongly influences reproductive behaviours because reproducing individuals must balance mortality risks to themselves and to their offspring. In many freshwater turtles, the nest predation risk decreases with nest distance from water, whereas the predation risk to females increases farther from water. To determine whether predation pressure influences the distance from water at which female turtles nest, we measured predation pressure on nesting females and on nests, as well as the distances of nests to water, in two populations of painted turtles. Using models, we found that female survival in both populations was high and did not vary with distance from water. Nest survival was also uncorrelated with nest distance to water, although it was significantly lower than adult survival in both populations and was only 1.2% in one population. Our results suggest that nest sites are not predictably safe from predators. Instead, turtles may hedge their bets by nesting over a wide range of distances from water because any distance is risky for nests and no distance is particularly risky for the nesting female. We suggest that other factors, such as suitable incubation conditions and/or post‐emergence hatchling survival, probably play a larger role than predation in driving nest‐site choice in painted turtles.     

Nest position and type affect predation rates of artificial avian nests in the tropical lowland forest on Mount Cameroon

Nest predation is the leading cause of reproductive failure in birds and thus it shapes their life history strategies. Intensities of nest predation appear to differ among nest locations and types in both temperate and tropical regions. However, there is limited knowledge of factors influencing susceptibility of avian nests to predation in Africa. The aim of our study was to investigate artificial nest predation rates of different ground and shrub nests located at different heights in the rainforest undergrowth. We placed artificial avian nests within a homogeneous lowland forest interior with sparse forest undergrowth in the Mount Cameroon National Park, Cameroon. We exposed three sets of nests: 50 bare-ground, 50 cup-ground and 50 cup-shrub nests, for 10 d. Predation was higher for cup-ground nests compared to cup-shrub nests, and bare-ground nests were more depredated than cup-ground nests. We concluded that the presence of a cup as well as higher nest position significantly increased probability of artificial nest survival. The results of this study suggest a potential selection pressure on nest type and placement in lowland forest birds for a poorly known tropical region.     

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.     

Predation on artificial ground nests in relation to forest fragmentation, agricultural land and habitat structure

The impacts of forest fragmentation agricultural land and habitat structure on depredation of artificial ground nests were studied in the cultivated area in central Finland and in the forest dominated area in Finnish Lapland The overall predation rate did not differ between the regions The overall predation rate was also independent of landscape characteristics forest patch size and the distance to patch edge However, nest predation was clearly affected by the agricultural land since the robbing rate in forest edges was higher near farmlands than further away This effect was caused by avian predators which proportional importance in predation was higher in the agricultural landscape than in the forest landscape In both regions, depredation correlated positively with high numbers of pine and spruce This can be mainly explained by the preference of predators over coniferous forest habitat as a living or hunting area     

Predator–prey interactions between the South Polar skua Catharacta maccormicki and Antarctic tern Sterna vittata

Antarctic terns have to co‐exist in a limited space with their major nest predator, the skuas. We conducted artificial nest experiments to evaluate the roles of parental activity, nest location and nest and egg crypsis in this simple predator–prey system. Predation on artificial (inactive) nests was higher in traditional nesting sites than in sites previously not occupied by terns, which suggests that skuas memorized past tern breeding sites. Predation on artificial nests in inactive colonies was higher than in active (defended) colonies. Parental defense reduced predation in colonies to the level observed in artificial nests placed away from colonies. This suggests that communal defense can balance the costs of attracting predators to active colonies. Within colonies, predation was marginally higher on experimental eggs put in real nests than on bare ground. Although it seems that the presence of a nest is costly in terms of increased predation, reductions in nest size might be constrained by the need for protective nest structures and/or balanced by opposing selection on nest size. Predation did not differ markedly between artificial (quail) and real tern eggs. A simultaneous prey choice experiment showed that the observed predation rates reflected egg/nest detectability, rather than discrimination of egg types. In summary, nesting terns probably cannot avoid being detected, and they cannot defend their nest by attending them. Yet, by temporarily leaving the nest, they can defend it through communal predator mobbing, and at the same time, they can benefit from crypsis of unattended nest and eggs.     

Predator presence may benefit: kestrels protect curlew nests against nest predators

We studied whether the presence of breeding kestrels (Falco tinnunculus) affected nest predation and breeding habitat selection of curlews (Numenius arquata) on an open flat farmland area in western Finland. We searched for nests of curlews from an area of 6 km² during 1985–1993. For each nest found, we recorded the fate of the nest, and the distance to the nearest kestrel nest and to the nearest perch. We measured the impact of breeding kestrels on nest predation by constructing artificial curlew nests in the vicinity of ten kestrel nests in 1993. Curlew nests were closer to kestrel nests than expected from random distribution, eventhough kestrels fed on average 5.5% of curlew chick production. Predation risk by kestrels was lower than predation risk by corvids and other generalist predators, which predated 9% of curlew nests surviving farming practices and an unknown proportion of chicks. Artificial nest experiment showed that nest predation was lower close to kestrel nests than further away suggesting that the breeding association of curlews and kestrels was a behavioural adaptation against nest predation. Thus, the presence of a predator may sometimes be beneficial to prey, and prey animals have behavioural adaptations to these situations.     

Predation on artificial,solitary and aggregated wader nests on farmland

Predation rates on artificial wader nests, solitary curlew (Numenius arquata) and lapwing (Vanellus vanellus) nests and lapwing nests in colonies were studied on a farmland site in central Sweden. Predation rates were highest on artificial wader nests, intermediate on solitary curlew and lapwing nests and lowest on lapwing nests in colonies, probably because of active defence of adults at real nests and/or because of selection of nest sites with lower predation risk by breeding birds. A comparison of nests close to (50 m) and far away from (200 m) forest edges revealed no increased predation risk close to edges for any of the studied nest types. Predation risk changed during the season for artificial nests (highest in the middle of May), while predation rates on lapwing and curlew nests were more stable. Artificial nests seem to be inappropriate for measuring actual predation rates and temporal differences in predation rates on real nests, but they might be suitable for use as an index of spatial differences.