Anti-predator function of not covering eggs in the initial phase of nesting in Grey Partridge Perdix perdix: a field experiment

ABSTRACT

Capsule: An experiment in the field supports the hypothesis that Grey Partridges Perdix perdix purposely expose their first laid eggs in order to test the predation risk at their nest site.

Aims: To test the hypothesis that female Grey Partridges leave first laid eggs uncovered to assess the predation risk at their chosen nesting site.

Methods: Four area-independent experiments with artificial nests were used. Predation risk was estimated by daily nest failure rate. Generalized linear mixed-effects models were used in statistical analysis.

Results: We found that Grey Partridge females could predict nest site safety. At nest sites where the first uncovered egg was depredated, there was a higher predation risk for the whole clutch.

Conclusion: Our data statistically support the hypothesis that leaving the first egg uncovered serves to provide a more conspicuous bait for potential predators and could be a female tactic for better recognizing predation risk at a nesting site. Thus, if the first uncovered egg is depredated, the female may start a new clutch elsewhere without wasting investment in the clutch at a site under high predation risk.     

Different nest predator guild associated with egg size in the Patagonian temperate forest

Capsule: Studies of nest predation using artificial nests need to consider the effect of egg size on the types of predator that are detected.

Aims: To estimate the nest predation rate in the Patagonian temperate forest and evaluate the influence of egg size on predator guild.

Methods: On different plant species, we placed 108 nests each containing eggs of either Atlantic Canary Serinus canaria or Common Quail Coturnix coturnix, and a model clay egg of equal size to the real egg. Nest predators were identified from the marks left on the clay eggs or by videos recorded using camera traps.

Results: 86% of the nests were predated. Birds, mainly Chimango Caracara Milvago chimango, were the main nest predators. A marsupial, the Monito del Monte Dromiciops gliroides, and rodents also contributed to nest predation. Nest predation rates were similar for both egg sizes but the nest predator guild was different. Birds and rodents preyed on both eggs but the Monito del Monte consumed mainly small eggs.

Conclusion: Egg size did not influence the rate of nest predation but, instead, affected the nest predator guild. Consequently, in order to avoid underestimating the impacts of small predators, egg size should be considered in studies of nest predation.     

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     

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.

     

Predation on artificial and natural nests in the lowland rainforest of Papua New Guinea

Capsule: Although survival of nests was similar between forest fragments and continuous forest, the range of predators differed. Artificial nests provide an under-estimate of nest predation by snakes.

Aims: To estimate the natural nest predation rate in continuous primary forest, compare it with predation rates in forest fragments. To assess the reliability of nest survival rates determined by the use of artificial nests with clay eggs and identify the main nest predators.

Methods: We observed survival of natural nests during the incubation period in continuous primary forest in Papua New Guinea. Some nests were monitored with infrared cameras. We also used artificial nests deployed with clay eggs to identify predators.

Results: There was a predation rate of 50% for natural nests and snakes were major predators of nest contents. Clutch daily survival rates (DSRs) differed among nest types. The DSR of artificial nests (0.977) was not significantly different to that of natural cup nests (0.969). Survival rates of artificial nests were similar in forest fragments and continuous forest. Forest fragments had, however, a higher proportion of avian predators than continuous forest.

Conclusion: Although, we observed similar survival rates in artificial and natural nests, the composition of nest predators was different between natural and artificial nests. Artificial nests were not suitable for estimating the real predation caused by reptiles. Nevertheless, we find that participation of avian nest predators can be estimated correctly with the use of artificial nests.     

Do alien predators pose a particular risk to duck nests in Northern Europe? Results from an artificial nest experiment

Several alien predator species have spread widely in Europe during the last five decades and pose a potential enhanced risk to native nesting ducks and their eggs. Because predation is an important factor limiting Northern Hemisphere duck nest survival, we ask the question, do alien species increase the nest loss risk to ground nesting ducks? We created 418 artificial duck nests in low densities around inland waters in Finland and Denmark during 2017–2019 and monitored them for seven days after construction using wildlife cameras to record whether alien species visit and prey on the nests more often than native species. We sampled various duck breeding habitats from eutrophic agricultural lakes and wetlands to oligotrophic lakes and urban environments. The results differed between habitats and the two countries, which likely reflect the local population densities of the predator species. The raccoon dog (Nyctereutes procyonoides), an alien species, was the most common mammalian nest visitor in all habitats and its occurrence reduced nest survival. Only in wetland habitats was the native red fox (Vulpes vulpes) an equally common nest visitor, where another alien species, the American mink (Neovison vison), also occurred among nest visitors. Although cautious about concluding too much from visitations to artificial nests, these results imply that duck breeding habitats in Northern Europe already support abundant and effective alien nest predators, whose relative frequency of visitation to artificial nests suggest that they potentially add to the nest predation risk to ducks over native predators.

     

Foraging behaviour of nest predators at open-cup nests of woodland passerines

Nest predation patterns and processes cannot be understood without studying the behaviour of predators. I videotaped the behaviour of 22 species of predators at 171 depredated nests of 13 passerine species, in woodland in the Czech Republic. About 32% (60/187) of all events occurred during the night; mammals accounted for 95% (57/60) and 22% (28/127) of nocturnal and diurnal predation, respectively. About 67% (57/85) of mammalian predation, but only 3% (3/102) of avian predation, occurred during night. Multiple predations by the same species were detected in at least 7% (6/82) and 42% (37/88) of nests depredated by mammals and birds, respectively. Martens Martes martes/foina took nest content mostly all at once; birds (mainly Jay Garrulus glandarius) revisited partially depredated nest during 1–4 consecutive days. Martens stayed at the depredated nest about five times longer than Jays. Martens spent similar time at nests with eggs and nestling, while Jays stayed about twice longer at nests with eggs. Mammals consumed eggs always at the nest (23/23), but took nestlings away in at least 48% (31/64) cases. Birds took the eggs and nestling away in at least 31% (18/58) and 76% (71/94) cases, respectively. Predator visits to active nests without taking the content, repeated partial predation and revisitation of previously depredated nests suggest an effect of memory on predator’s foraging behaviour.     

Predators of Spotted Flycatcher Muscicapa striata nests in southern England as determined by digital nest-cameras

Capsule Avian predators are principally responsible.

Aims To document the fate of Spotted Flycatcher nests and to identify the species responsible for nest predation.

Methods During 2005–06, purpose-built, remote, digital nest-cameras were deployed at 65 out of 141 Spotted Flycatcher nests monitored in two study areas, one in south Devon and the second on the border of Bedfordshire and Cambridgeshire.

Results Of the 141 nests monitored, 90 were successful (non-camera nests, 49 out of 76 successful, camera nests, 41 out of 65). Fate was determined for 63 of the 65 nests monitored by camera, with 20 predation events documented, all of which occurred during daylight hours. Avian predators carried out 17 of the 20 predations, with the principal nest predator identified as Eurasian Jay Garrulus glandarius. The only mammal recorded predating nests was the Domestic Cat Felis catus, the study therefore providing no evidence that Grey Squirrels Sciurus carolinensis are an important predator of Spotted Flycatcher nests. There was no evidence of differences in nest survival rates at nests with and without cameras. Nest remains following predation events gave little clue as to the identity of the predator species responsible.

Conclusions Nest-cameras can be useful tools in the identification of nest predators, and may be deployed with no subsequent effect on nest survival. The majority of predation of Spotted Flycatcher nests in this study was by avian predators, principally the Jay. There was little evidence of predation by mammalian predators. Identification of specific nest predators enhances studies of breeding productivity and predation risk.     

Nesting success in Redshank Tringa totanus breeding on coastal meadows and the importance of habitat features used as perches by avian predators

Capsule Nest survival rates could not be explained by distance to habitat edges or other features used by predators.

Aims To investigate if predation on Redshank nests was affected by habitat characteristics at a local scale.

Methods We examined survival rates of Redshank nests on coastal meadows on the Baltic island of Gotland, Sweden, over two breeding seasons. We analysed nest survival rates in relation to several habitat characteristics that may benefit predators searching for nests. We examined existing studies concerning predation rates on wader nests in relation to edges and habitat features potentially used by avian predators.

Results We found no significant effects of distance to habitat edge or to nearest potential lookout for avian predators or to shoreline. Abundance of Lapwings Vanellus vanellus, an aggressive species with active nest-defence, did not have any significant effect on nest survival rate, nor did vegetation concealment of nests. Nest survival rates were significantly different between years and lower later in the season.

Conclusions There is only weak support for general effects on wader nest predation rates of proximity to edges and features used by avian predators. Simple mechanical management actions such as removal of trees and bushes on coastal meadows may not directly, and by itself, result in higher reproductive success of waders. Further understanding is needed of the behaviour of predators and the composition of the predator community in different landscapes in order to increase the efficiency of management actions to remove threats to vulnerable species on coastal meadows.     

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.     

Mortality of Wood Warbler Phylloscopus sibilatrix nests in Welsh Oakwoods: predation rates and the identification of nest predators using miniature nest cameras

Capsule Predation was the main cause of nest failure, but predation rates have remained unchanged since the 1980s. Eurasian Jays Garrullus glandarius were the most common predator.

Aims To quantify, and compare, nest predation rates for 1982–84 and 2009–11, and to identify predators of Wood Warbler Phylloscopus sibilatrix nests in Welsh oakwoods.

Methods During 2009–11, 167 Wood Warbler nests were monitored and purpose-built miniature nest cameras deployed at 73 of them. Nest predation rates were compared with 67 nests monitored during 1982–84.

Results Of 167 nests monitored from 2009 to 2011, 62 failed due to predation (32/73 camera nests, 30/94 non-camera nests), giving an overall Daily Survival Rate (DSR?±?se) of 0.979?±?0.003. This was not significantly different from the rate during 1982–84 (0.967?±?0.006). In 2009–11, the DSR of nests declined temporally during the season at both the egg and chick stages. For chick stage nests, DSR varied annually and nonlinearly with age of nestlings. There was no evidence for an effect of cameras at either stage. Of 32 camera nests lost to predation, the predator was identified from 28, resulting in 30 predators being identified. There was one case of multiple predators at a single nest. The majority of nest predation was carried out by birds (28/30), predominantly Eurasian Jays (18/28), but also Common Buzzards Buteo buteo (5/28), Great Spotted Woodpeckers Dendrocopos major (3/28) and Eurasian Sparrowhawks Accipiter nisus (2/28). There was one predation by both a Eurasian Badger Meles meles and a Red Fox Vulpes vulpes. There were no records of Grey Squirrels Sciurus carolinensis depredating nests.

Conclusions Nest predation rates were similar in both periods, suggesting that increased rates of nest predation have not been driving the decline of the Wood Warbler population in Wales. Deployment of nest cameras did not affect nest survival rates and were successful in identifying nest predators, the majority of which were avian, especially Eurasian Jays. Knowledge of the identity of nest predators can aid the development of conservation measures.     

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     

Nest predation and semicolonial breeding in Linnets Carduelis cannabina

Capsule Nest predation in Linnets in Denmark was caused mainly by Hooded Crows Corvus corone cornix and Magpies Pica pica with no experimental evidence of antipredator aggression.

Aims To investigate the influence of nest clumping on the risk of nest predation in Linnets, a species that often breeds semi-colonially.

Methods The predation rates on clumped and randomly distributed nests were compared by the use of artificial nest experiments. Additionally, the behaviour of Linnets towards a potential nest predator was studied by presenting a mounted Magpie near the nest of breeding Linnets.

Results The artificial nest experiments showed that semi-colonial breeding was not likely to increase the risk of nest predation, and an experiment with the mounted Magpie showed that Linnets did not exhibit anti-predator aggression.

Conclusion Semi-colonial breeding, resulting in increased local nest density, did not appear to influence the risk of nest predation in Linnets. We suggest that semi-colonial breeding in Linnets is a means of pooling information on food sources.     

Meta‐analyses of nest predation in temperate Australian forests and woodlands

Nest predation is the leading cause of nesting failure. Thus it is a crucial area of research needed to inform conservation management and to understand the life history of birds. I surveyed the literature to review the identity of nest predators and the factors affecting nest predation, in Australia using 177 studies. Overall, 94 nest predators were identified when incorporating artificial nests, 69 without. Using only natural nests, the Pied Currawong Strepera graculina was the most frequently reported nest predator. Five nest predators, including Pied Currawong, depredated 40% of the prey measured by the number of prey species taken. Yet, 60% of predation was carried out by the other 64 species, which included by the order of importance birds, mammals, reptiles, frogs and ants. Predation at cup and dome nests was more frequently reported than at burrow, ground and hollow nests. Only 28% of predators were observed at both artificial and natural nests suggesting artificial nests have limited, but not negligible, ability as tools for identifying predators. There was a highly significant and positive correlation between predator and prey masses. The predator prey mass ratio was calculated with a mean 0.25 and a median 0.22, a result closely matching with the proportional size of prey taken by raptors. The finding that predator size is proportional to prey opens a pathway for more life history and conservation research.     

Effects of Edge Habitat and Nest Characteristics on Depredation of Artificial Nests in Fragmented Australian Tropical Rainforest

Variation in nest predation levels associated with rainforest fragmentation (edge effects) was assessed in Australia's Wet Tropics bioregion. Artificial nests were placed in the forest understorey at seven edge sites where continuous forest adjoined pasture, seven interiors (about 1 km from the edge), and six linear riparian forest remnants (50–100 m wide) that were connected to continuous forest. Four nest types were also compared, representing different combinations of two factors; height (ground, shrub) and shape (open, domed). At each site, four nests of each type, containing one quail egg and two model plasticine eggs, were interspersed about 15 m apart within a 160 m transect during September–October 2001. Predators were identified from marks on the plasticine eggs. The overall depredation rate was 66.5% of 320 nests' contents damaged over a three-day period. Large rodents, especially the rat Uromys caudimaculatus, and birds, especially the spotted catbird Ailuroedus melanotis, were the main predators. Mammals comprised 56.5% and birds 31.0% of predators, with 12.5% of unknown identity. The depredation rate did not vary among site-types, or between open and domed nests, and there were no statistically significant interactions. Nest height strongly affected depredation rates by particular types of predator; depredation rates by mammals were highest at ground nests, whereas attacks by birds were most frequent at shrub nests. These effects counterbalanced so that overall there was little net effect of nest height. Mammals accounted for 78.4% of depredated ground nests and birds for at least 47.4% of shrub nests (and possibly up to 70.1%). The main predators were species characteristic of rainforest, rather than habitat generalists, open-country or edge specialists. For birds that nest in the tropical rainforest understorey of the study region, it is unlikely that edges and linear remnants presently function as ecological population sinks due to mortality associated with increased nest predation.     

Predation of artificial nests by introduced rhesus macaques (<Emphasis Type="Italic">Macaca mulatta</Emphasis>) in Florida,USA

Native throughout Asia, rhesus macaques are believed to have the widest native range of any non-human primate and are capable of adapting to an extensive diversity of habitats. Rhesus macaques have caused environmental degradation in introduced habitats, including decreasing bird populations through nest predation. In the 1930s, rhesus macaques were intentionally introduced into what is today Silver Springs State Park (SSSP), central Florida, in an effort to increase tourism. Our objective was to determine whether introduced rhesus macaques in SSSP would consume eggs presented in artificial nests. We used camera traps adjacent to 100 open-cupped artificial bird nests baited with quail eggs near the Silver River. Nests were placed in shrubs and left in the field site for 12 days, representative of the incubation period of native passerine species. Twenty-one nests were depredated by rhesus macaques, nine by nest predators other than macaques, and five nests by an unidentified predator. Nests were more likely to be depredated by macaques when located in areas of high macaque relative abundance. This study suggests introduced rhesus macaques may influence nest predation rates of native bird species in natural areas.     

Factors affecting piping plover hatching success on Long Island,New York

Low hatching success may limit progress towards reaching productivity goals for Atlantic Coast piping plover (Charadrius melodus) recovery, despite management strategies to protect eggs from predators and decrease human disturbance of birds on nests. We measured piping plover hatching success on Eastern Long Island beaches and identified the major causes of egg failure to better understand why eggs that were otherwise intact (not depredated or destroyed by tidal flooding) failed to hatch. We documented egg and nest fates, dissected contents of unhatched eggs to determine viability, and recorded human and predator activity near a subset of plover nests on Suffolk County Parks properties. The low hatching success we recorded (0.60) in 2006 and 2007 would require higher chick survival rates than are typically observed for piping plovers to meet recovery targets for productivity. Few eggs showed signs of poor viability and overall egg hatchability was comparable to other ground nesting birds. Most egg failure was due to either depredation at unexclosed nests or nest abandonment by adults. The best predictor of nest abandonment was the maximum number of red fox tracks (Vulpes vulpes) counted on nearby transects (β = −1.16, 95% CI: −2.0 to −0.3) and we found evidence that plovers abandoned eggs in response to predation risk (e.g., a fox circling a nest exclosure). Adults from abandoned nests may have deserted eggs or been depredated. In either case, intact and viable eggs were abandoned. Nest abandonment was not related to human activity near nests, which were buffered from human disturbance by symbolic string fencing. Our results suggest that depredation and nest abandonment (e.g., desertion or death of adults) due to predator disturbance, not human disturbance or poor egg viability, contributed to the low hatching success we recorded. Active predator removal in addition to modification of predator exclosure use and design may be necessary to prevent direct (egg depredation) and indirect (nest abandonment) negative effects of predators on hatching success. © 2010 The Wildlife Society.     

Nest Predation of Greater Sage-Grouse in Relation to Microhabitat Factors and Predators

ABSTRACT Nest predation is a natural component of greater sage-grouse (Centrocercus urophasianus) reproduction, but changes in nesting habitat and predator communities may adversely affect grouse populations. We used a 2-part approach to investigate sage-grouse nest predation. First, we used information criteria to compare nest survival models that included indices of common raven (Corvus corax) abundance with other survival models that consisted of day of incubation, grouse age, and nest microhabitat covariates using measurements from 77 of 87 sage-grouse nests. Second, we used video monitoring at a subsample of 55 of 87 nests to identify predators of depredated nests (n = 16) and evaluated the influence of microhabitat factors on the probability of predation by each predator species. The most parsimonious model for nest survival consisted of an interaction between day of incubation and abundance of common ravens (w_{ravenXincubation day} = 0.67). An estimated increase in one raven per 10-km transect survey was associated with a 7.4% increase in the odds of nest failure. Nest survival was relatively lower in early stages of incubation, and this effect was strengthened with increased raven numbers. Using video monitoring, we found the probability of raven predation increased with reduced shrub canopy cover. Also, we found differences in shrub canopy cover and understory visual obstruction between nests depredated by ravens and nests depredated by American badgers (Taxidea taxus). Increased raven numbers have negative effects on sage-grouse nest survival, especially in areas with relatively low shrub canopy cover. We encourage wildlife managers to reduce interactions between ravens and nesting sage-grouse by managing raven populations and restoring and maintaining shrub canopy cover in sage-grouse nesting areas.     

Factors affecting egg predation in Black-tailed Gulls

In colonial seabirds, nesting density, egg-laying date and nest microhabitat affect the probability of eggs being taken by avian predators. Jungle Crows (Corvus macrorhynchos) are dominant predators of eggs of Black-tailed Gulls (Larus crassirostris). Factors affecting the probability of gulls allowing the crows to attack their nests or depredate their eggs and the probability of eggs being taken were studied by direct observation and egg census, respectively. The effect of vegetation heights, position in the colony, egg-laying date and neighbour nests on the probability of eggs being taken were examined at multiple spatial scales. Gull nests were depredated more easily by larger groups of crows. Nests in peripheral areas (<4 m from the edge of the colony) were also depredated more easily by the crows walking on the ground. Although the nests where eggs were laid early in the season were depredated more frequently, such nests highly synchronised in egg laying within a <2-m radius were less likely to be depredated than less-synchronised nests. The nests in tall vegetation were less likely to be depredated though those having neighbour nests in tall vegetation were not. The number of neighbour nests did not affect the probability of eggs being taken. Antipredation effects of nesting microhabitats vary with spatial scales at which the crows search and attack the nests of gulls.     

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.