Effects of fragmentation on artificial nest predation in a tropical forest in Kenya

Nest predation has been established as a leading source of reproductive failure in songbirds. Numerous studies, conducted primarily in the Northern Hemisphere, have linked high rates of nest predation with fragmentation and habitat edges. To date, virtually no such studies have been conducted in Tropical Africa. Here we investigate the effects of disturbance level and edge on depredation of artificial avian nests in six fragments of Kakamega Forest, Kenya. We found that nest losses were higher at the edge than in the interior as often reported in previous studies. Surprisingly, nest predation was highest in the least disturbed fragments. One possible explanation for these findings is that top predators are missing from Kakamega Forest, allowing nest predator populations to increase in all fragments, while in the highly disturbed fragments, domestic dogs might be surrogates for top predators. Alternatively, human activity may itself lead to a decline in mesopredator populations.     

Water depth influences nest predation for a wetland-dependent bird in fragmented bottomland forests

The alteration and fragmentation of natural habitats has resulted in increased rates of nest predation and poor reproductive success for many bird species. The development of effective conservation strategies to reduce elevated rates of nest predation has been hindered by difficulties in fully understanding mechanisms underlying patterns and rates of nest predation in particular habitats. I recorded the outcome for 2726 nesting attempts of prothonotary warblers (Protonotaria citrea) breeding in fragmented bottomland forests and quantified the effect of nest predation on annual fecundity, determined the influence of different nest predators on rates of nest predation, and identified the factor driving rates of nest predation. There was a highly significant negative correlation between rates of nest predation and the actual annual reproductive output of prothonotary warblers. Of 1156 nest predation events, 73% were attributed to raccoons (Procyon lotor), 15% to snakes and 7% to southern flying squirrels (Glaucomys volans). Rates of nest predation decreased with increasing water depth as a result of nest predation by raccoons. Nests that were over water deeper than 60 cm were particularly successful. Habitat fragmentation, the draining of wetlands, and stream channelization may act synergistically to elevate rates of nest predation for those birds breeding in forested wetlands. Conservation actions designed to stop or reverse these processes will be especially beneficial to birds breeding in bottomland forest ecosystems.     

Wader nest distribution and predation in relation to man-made structures on coastal pastures

Coastal pastures and other wet grasslands are important but decreasing breeding habitats for many waders (Charadrii). Since loss of suitable habitat is a major reason for population declines, protection and restoration of these habitats is crucial. Reduction of the often high rate of nest predation is a potentially important tool in future conservation work. Here, we focus on predators’ use of raised structures in the landscape when searching for prey. Hooded crows (Corvus corone cornix) use man-made structures such as stone walls and barbed wire fences when foraging on coastal pastures in SW Sweden. However, few studies have examined wader breeding success in relation to man-made structures, and the extent to which such structures are used by searching nest predators. We measured the spatial distribution and rate of predation on wader nests in relation to such structures. Crows spent more time at or near man-made structures than expected by chance, but we found no significant difference in nest predation relative to distance from man-made structures. However, wader nests were placed farther away from man-made structures than expected by chance in two out of three years. Waders thus tend to avoid breeding close to man-made structures, which therefore reduce the suitable breeding area and probably also the local wader population size.     

Predation of artificial nests in a fragmented landscape in the tropical region of Los Tuxtlas, Mexico

Predation rates of artificial nests were investigated in a fragmented landscape in the lowlands of Los Tuxtlas in southern Mexico. Hen and plasticine eggs were used to assess predation pressure in four habitats: the interior of forest fragments, the forest-pasture edge, corridors of residual forest vegetation and linear strips of live fences across pastures. Three sites per habitat were used in three experimental trials. Hen and plasticine ground nests with three eggs each were alternated every 50 m along transects at each site. Predation rates on each type of nest were monitored for 9 days. Survey of potential avian and mammalian potential nest predators were conducted at each site prior to the experimental trails. Readings of amount of light illuminating the ground were taken by each nest at each site to assess exposure of nests. In general, average predation rates were significantly higher for both hen and plasticine nests in the forest-pasture edge and in the corridors than in the interior of the forest fragments. While birds and mammals were the principal predators on hen eggs in the forests, mammals were responsible for the majority (?70%) of eggs damaged at the other habitats. Surveys of potential nest predators showed that avian and mammalian potential nest predators were significantly more common at the forest-pasture edges and at the other habitats than in the forests. Readings of light reaching the ground suggest that concealment of nests by the vegetation may play an important role in predation risk. Our results are consistent with reports from other Neotropical rainforests indicating an increase of artificial nest predation pressures from forest interior to open habitats. Restoration of forest fragments, allowing the vegetation to grow along the forest-pasture edge and the planting of arboreal crops at the forest-pasture edges may be measures that could increase cover and nest protection.     

Implications of intraguild predation for sea turtle nest protection

In the United States, raccoons Procyon lotor are often removed from sea turtle nesting beaches to decrease egg mortality. However, raccoons also consume ghost crabs Ocypode quadrata, another common egg predator. Reducing predator populations can benefit secondary predators, inflating total predation pressure and leading to a decline in prey species. We used track and burrow counts to compare raccoon and ghost crab abundance at four beaches in Florida, USA, that differ in management activity and determined predation rates on loggerhead Caretta caretta nests by each predator. Mean raccoon abundance (range 0.12-0.46 tracks plot⁻¹ night⁻¹) and ghost crab density (0.09-0.19 burrows m⁻²) were inversely correlated. Ghost crabs were largest at the site with the fewest raccoons. The stable nitrogen isotope ratios of ghost crabs (mean 9.8‰) were positively correlated with body mass, indicating larger ghost crabs feed at a higher trophic level and suggesting large ghost crabs may consume more loggerhead eggs. The highest rates of egg predation by both predators (31%) occurred where raccoon abundance was lowest and ghost crab abundance was highest, suggesting ghost crab burrows may facilitate predation by raccoons. Our data suggest that predation by raccoons limits ghost crabs and that removing raccoons can increase ghost crab abundance and sea turtle egg mortality. Although predator removal can be effective when nest predation rates are quite high, maintaining moderate raccoon densities may be important for controlling ghost crabs. These results highlight the importance of understanding food web connectivity in developing management strategies to achieve conservation goals, especially when the species of concern are threatened or facing extinction.     

Use of landscape metrics to predict avian nest survival in a fragmented midwestern forest landscape

Habitat fragmentation fundamentally affects trophic interactions and ecosystem function. Understanding how the landscape matrix modulates such interactions can improve our understanding of fragmentation ecology. Studies of breeding birds provide clear examples of the consequences of habitat fragmentation, but the landscape context of these effects are unclear. We sampled avian nesting success in 12 moderately-large forest patches (>250 ha) embedded in different types of landscapes in southern Illinois, USA. We then evaluated eight models that predicted the probability of nest success and brood parasitism by Brown-headed Cowbirds. These models incorporated landscape composition (% grassland, % agriculture, fragmentation), year and seasonal effects, conspecific density, predator density, and combinations of these variables. Temporal factors (stage of nesting cycle, seasonal effects, annual variation) had the most effect on nesting success; landscape factors had little influence on nesting success. The rate and intensity of brood parasitism were significantly influenced by the amount of grassland for the Wood Thrush, but not for the Acadian Flycatcher. Fine-scale management of the matrix surrounding the patches may dictate the local abundance and movements of nest predators and parasites. Other major nest predators may prefer the forest interior and at least partially compensate for the lower abundance of nest predators that depend upon the matrix. Overall, landscape metrics were weak predictors of avian nesting success in complex landscapes that have diverse predator communities.     

Nest predation in a fragmented Afrotropical forest: evidence from natural and artificial nests

Nest predation accounts for a substantial share of nest failure and low reproductive success in most tropical songbirds. Normally, forest fragmentation leads to an increase in nest predation pressure due to reduced cover, fewer (and poorer) nest sites and predator influxes from the surrounding habitats. To test this hypothesis, we studied natural nesting behaviour and nest success of the white-starred robin (Pogonocichla stellata) in seven Afrotropical forest fragments differing in size and level of habitat disturbance. Based on data from 12 nests, we estimate that 29% of all natural nests initiated by the robins survive to produce fledglings across all fragments. We also conducted an experiment using artificial (plasticine) model-eggs to reveal potential predators and compare relative predation rates amongst fragments. This experiment revealed that small mammals might be the major predators on robin nests at the egg-stage. In addition, it showed that the highest incidences of nest disturbance during this stage were in the most heavily disturbed fragment. This was presumably attributable to an influx of mammalian predators from the surrounding habitats as forest degradation created suitable habitats for them. Such an infiltration was recently reported in this study site. Both nest placement and microhabitat did not significantly affect depredation levels in our experiment. This suggests that depredation was predominantly incidental (i.e., predators mainly encountered nests fortuitously while foraging for other food items), where the likelihood of encountering a nest largely depended upon the prevalence of the principal potential predators - the small mammals.     

Managing predation on ground-nesting birds: The effectiveness of nest exclosures

Ground-nesting birds have declined world-wide, probably partly due to high nest predation. A non-lethal method for decreasing predation uses protective cages at nests. Tests have mainly looked at the effect of such nest exclosures on hatching success and adult predation, but several additional aspects need to be explored for a comprehensive evaluation of this conservation technique. Here, we test the effect of nest exclosures in two common European shorebirds: northern lapwing (Vanellus vanellus) and redshank (Tringa totanus), measuring hatching success, incubation length, hatching synchrony, hatchability, partial clutch loss, chick condition, and adult predation. In both species, protected nests had higher hatching success than unprotected nests. Taking into account incubation time, nest abandonment, hatchability and partial clutch loss, protected nests still hatched more young than unprotected controls. In lapwings, but not in redshanks, protected nests were incubated longer, but this did not impair the condition of lapwing chicks. Protected redshanks suffered increased predation on incubating adults, which often sit on the nest until a predator is close by. Our results emphasize the need for caution in the use of nest exclosures, particularly in redshanks and other species with similar incubation behaviour. Exclosures can, however, be a useful management tool in shorebirds that leave their nest early, when an approaching predator is still far away.     

Effects of landscape composition, habitat features, and nest distribution on predation rates of simulated turtle nests

We investigated predation of simulated turtle nests in an effort to understand how land-use patterns and the availability of nesting habitat may affect turtle recruitment in a region where human populations and associated development are increasing. Simulated nests were patterned after those created by painted turtles (Chrysemys picta), a common aquatic turtle in our study area, and distributed in four patterns (clustered and near pond, scattered and near pond, clustered and far from pond, and scattered and far from pond) around 36 ponds. Landscape composition (500-2000 m from pond perimeters) and habitats surrounding pond edges (an area extending 250 m from the shore of each pond) were then compared with rates of predation at each pond. Nest-site characteristics also were compared to the fate of individual nests. Landscape composition and habitats surrounding ponds apparently had little influence on predation rates. Nest distribution and the immediate habitat features associated with each nest did affect vulnerability to predation. Clumped nests were preyed upon at a higher rate than scattered nests, and nests close to ponds (within 50 m) were more vulnerable to predators than those created far (100-150 m) from a pond. Counter to our expectations, proximity to edge habitats (other than the shore of a pond) reduced the probability that a nest would be detected by predators. Also, nests placed near roads and suburban lawns had a reduced likelihood of predation whereas those placed in agricultural areas or disturbed sites had a greater probability of being preyed upon. Our results suggest that predation of simulated turtle nests may be a consequence of their distribution and location relative to the foraging activities of common nest predators, especially raccoons (Procyon lotor). Efforts to enhance recruitment among declining populations of turtles should consider the abundance and distribution of nesting habitat. Providing additional nesting sites away from predator foraging habitats may reduce nest predation and increase the recruitment of hatchlings into a population.     

Tallgrass prairie management and bird nest success along roadsides

The attributes of roadside vegetation, an important bird habitat in grassland ecosystems, have been shown to affect bird abundance, distribution composition, and diversity, yet there are relatively few works on reproductive success of birds nesting along roadsides. Because roadsides are linear habitats, management at the landscape scale can affect nest success in roadsides through bottom-up and top-down effects. In northeastern Oklahoma tallgrass prairie is subjected annually to prescribed spring fires. In the short term fires can alter both arthropod abundance and predator access to nests. We explored effects of burning on bird nest success with a five-year study along roads that traversed tallgrass prairie habitat. Using data from ∼1400 nests of 23 species, we generated nest survival curves for groups of altricial species defined by nest substrate (ground, shrub, tree, or culvert). We then determined if these curves were affected by management practice (spring burning), food abundance (arthropod biomass), and habitat attributes (tree density and height). Nest substrate had a large effect on nest success: despite their shorter nest exposure period, ground nests were least successful and culvert nests were most successful. An increase in arthropod biomass following burning was possibly the cause for the increased nest success in burned plots, regardless of substrate, suggesting bottom-up control. Tree height and nest height were correlated positively with nest success, whereas tree density had no effect. Conversely, nest predation rates were correlated negatively with nest success, with ground nests experiencing the highest predation, culvert nests the lowest. Our results suggest that burning may increase nest success through bottom-up processes, but some species may not benefit from the increase in food abundance as a result of a concomitant increase in predation.     

Influence of food availability, predator density and forest fragmentation on nest survival of New Zealand robins

The decline of avian populations in fragmented landscapes is often attributed to a decrease in nest survival rates for species breeding within these habitats. We tested whether fragment size and connectivity, livestock grazing, predator density or invertebrate biomass were correlated with nest survival rates for an endemic New Zealand species, the North Island robin (Petroica longipes). Across three breeding seasons (2002-2005) daily nest survival rate for the 203 robin nests monitored in 15 forest fragments was 0.315 (SE 0.003), with nest survival rates increasing with invertebrate biomass (indexed with pitfall traps) and marginally decreasing with fragment size. Footprint tracking rates for exotic ship rats (Rattus rattus), which are likely to be the key nest predator, varied greatly among fragments, but were not a useful predictor of nest survival. We found no relationship between the number of fledglings per successful nesting attempt and invertebrate biomass. We conclude that fragment size and connectivity does not appear to be negatively influencing robin nest survival, potentially because of the already high impact that mammalian nest predators have in this unique system.     

Habitat management and patterns of predation of Northern Lapwings on wet grasslands: The influence of linear habitat structures at different spatial scales

In managed landscapes, habitat structure is frequently manipulated through the creation of features such as tracks, hedges, and waterways. If predator and prey activity are concentrated around these features, levels of predation may be elevated in these landscapes. This issue is of particular importance when habitat structures are used to attract species of conservation concern. For example, the installation of linear waterways in wet grasslands is a common form of habitat management to benefit breeding waders and wader nests and foraging chicks tend to be aggregated around wet features. If predator activity is also focused around these features, and if their linearity increases the probability of prey being located, then the conservation benefits of this management technique may be eliminated. We explore predator movement in relation to the structure and complexity of linear wet features within a lowland wet grassland landscape. We examine patterns of nest and chick predation in lapwing (Vanellus vanellus) at the whole-site, between-field and within-field scales. Mammalian predators were responsible for the majority of nest predation. However, we found no evidence that mammalian predators used linear wet features disproportionately within the landscape, or that wet feature distribution influenced the probability of nest or chick predation. At the whole-site scale, nest predation rates were significantly higher in areas with greater predator presence and lowest where the number of breeding neighbours was high. Thus, predation levels were influenced by large-scale patterns of predator presence and lapwing density but not by the use of linear wet features as a habitat management tool. Managing predator impacts is therefore likely to require empirical assessments of local predator distribution and abundance in order to target measures effectively.     

Monitoring predators to optimize their management for marine turtle nest protection

The fundamental conservation focus for Hobe Sound National Wildlife Refuge (HSNWR), Florida is to provide protected nesting habitat for three threatened or endangered marine turtle species. Turtle nesting and hatching spans from early spring to fall each year. Left unchecked, nest predation by raccoons and armadillos would destroy most turtle nests. Predators are removed to protect nests, primarily with a one person-month contract using control specialists. We maximized the efficiency of predator removal by using a passive tracking index to: (1) optimize the timing and strategy for predator removal, (2) minimize labor by identifying areas where predator removal would have maximal effect, (3) examine beach invasion patterns of predators, (4) assess efficacy of removal efforts, (5) provide anticipatory information for future turtle nesting seasons, and (6) serve as a detection method for invasion by additional species known to depredate turtle nests. An overall nest predation rate of 28% resulted, whereas the rate for the previous year was 42% when the same level of contracted predator removal was applied, but without monitoring predators. One year before that, predator removal was done without contracts with specialists and predation was 48%. Up to 95% of the nests were destroyed in the years prior to predator removal. Using 2000 data on numbers of nests, clutch sizes, and emergence rates, we estimated the number of hatchlings that would have been lost assuming that the predation rates observed from four predator removal scenarios at HSNWR would have occurred in 2000. Historical predation of 95% would have resulted in 120,597 hatchlings lost in 2000. Predator removal as part of regular refuge operations would have reduced this number to 62,481. Addition of a contract with control specialists would have further reduced the number lost to 53,778. Addition of temporal and spatial monitoring for predator removal reduced losses to 36,637.     

Do domestic cats impose an unsustainable harvest on urban bird populations?

We assessed the impact of domestic cats on population persistence of native and exotic urban bird populations using a model adjusted for habitat-specific catch rates, cat ownership and hunting activity data. GPS-derived home ranges of 32 cats and resource selection indices demonstrated the degree of penetration and preference for native vegetation fragments. Owners reported on prey brought back by 144 domestic cats in Dunedin, New Zealand, during 12 months. One third of cats never brought back prey, and 21% returned more than one item/month. Cats brought back a mean of 13.4 prey items/year (median = 4), with cats aged <1 year returning more prey than older cats. Birds were the most common prey, followed by rodents. Although cats penetrated adjacent vegetation fragments they did not catch more birds and preferred garden habitat, suggesting that predation pressure may be reduced in fragments. Cat home range size appears to be constrained by cat density while the number of birds caught depends on the density of available prey. Estimates of city-wide catch for six bird species were either more than total urban population size estimates or close to lower confidence intervals. Modelling of three species indicated low likelihood of population persistence with cat predation. The observed persistence of these prey species suggests a meta-population structure with urban populations acting as sinks with source populations located on the city fringe.     

Vulnerability of ground-nesting waterbirds to predation by invasive American mink in the Cape Horn Biosphere Reserve, Chile

Biological invasions constitute one of the most important threats to biodiversity. This is especially true for “naïve” birds that have evolved in the absence of terrestrial predators in island ecosystems. The American mink (Mustela vison) has recently established a feral population on Navarino Island (55°S), southern Chile, where it represents a new guild of terrestrial mammal predators. We investigated the impact of mink on ground-nesting coastal waterbirds with the aim of deriving a vulnerability profile for birds as a function of different breeding strategies, habitat, and nest characteristics. We compared rates of nest survival and mink predation on 102 nests of solitary nesting species (Chloephaga picta, Tachyeres pteneres), on 361 nests of colonial birds (Larus dominicanus, Larus scoresbii, Sterna hirundinacea), and on 558 artificial nests. We calculated relative mink and bird densities at all nest sites. Nests of colonial species showed the highest nest survival probabilities (67-84%) and no predation by mink. Nest survival rates for solitary nesting species were lower (5-20%) and mink predation rates higher (10-44%). Discriminant analyses revealed that mink preyed upon artificial nests mainly at shores with rocky outcroppings where mink were abundant. High nest concealment increased the probability for predation by mink. Conservation planning should consider that invasive mink might severely affect the reproduction success of bird species with the following characteristics: solitary nesting, nesting habitat at rocky outcrop shores, and concealed nests. We recommend that work starts immediately to control the mink population with a priority in the nesting habitats of vulnerable endemic waterbirds.     

Corvid response to human settlements and campgrounds: Causes, consequences, and challenges for conservation

Human development often favors species adapted to human conditions with subsequent negative effects on sensitive species. This is occurring throughout the urbanizing world as increases by generalist omnivores, like some crows and ravens (corvids) threaten other birds with increased rates of nest predation. The process of corvid responses and their actual effects on other species is only vaguely understood, so we quantified the population response of radio-tagged American crows (Corvus brachyrhynchos), common ravens (Corvus corax), and Steller’s jays (Cyanocitta stelleri) to human settlements and campgrounds and examined their influence as nest predators on simulated marbled murrelet (Brachyramphus marmoratus) nests on Washington’s Olympic Peninsula from 1995 to 2000. The behavior and demography of crows, ravens, and jays was correlated to varying degrees with proximity to human development. Crows and ravens had smaller home ranges and higher reproduction near human settlements and recreation. Annual survival of crows was positively associated with proximity to human development. Home range and reproduction of Steller’s jays was independent of proximity to human settlements and campgrounds. Local density of crows increased because home ranges of neighboring breeding pairs overlapped extensively (6× more than ravens and 3× more than Steller’s jays) and breeders far from anthropogenic foods traveled 10s of kilometers to access them. Corvids accounted for 32.5% of the predation events (n = 837) we documented on artificial murrelet nests. Small corvids (jays) were common nest predators across our study area but their contribution as predators did not vary with proximity to settlements and campgrounds. In contrast, large corvids (crows and ravens) were rare nest predators across our study area but their contribution varied greatly with proximity to settlements and campgrounds. Managers seeking to reduce the risk of nest predation need to consider the varied impacts and variable behavioral and population responses of potential nest predators. In our situation, removing large corvids may do little to reduce overall rates of nest predation because of the diverse predator assemblage, but reducing anthropogenic food in the landscape may be effective.     

What do artificial nests tells us about nest predation?

Artificial nests are commonly used to evaluate predation, but the assumption that this method mimics predation on natural nests has seldom been tested. Natural and artificial nests of eastern yellow robins (Eopsaltria australis) were monitored in four, 55-ha plots over two breeding seasons. Overall, daily survival rates were higher (P<0.001) for natural (95%/day) than for artificial nests (88%/day). Among plots, daily survival rates for the two types of nests were not correlated with one another (P=0.72) indicating that the spatial pattern of predation on artificial nests did not mimic that for natural nests. Seasonal variation was evident for natural nests in one year, when they were more successful at the beginning and end of the breeding season. No seasonal patterns were observed for artificial nests in either year. Neither natural nor artificial nests showed annual variation in predation. Previous researchers concluded that large birds were important predators on robin nests. In this study, predation by large birds on artificial nests was positively correlated with the numbers of large birds counted on the plots (P=0.04). However, large birds depredated only 16% of artificial nests. Daily survival rates for artificial nests were recalculated using predation by large birds only. These rates were compared with natural nests, but there was still no correspondence in the spatial and temporal patterns of predation for the two types of nests. These results suggest that inferences about predation on natural nests based on artificial nest studies should be avoided.     

Predation determines the outcome of 10 reintroduction attempts in arid South Australia

Ten reintroduction attempts were conducted in and around the Arid Recovery Reserve in northern South Australia between 1998 and 2008. Five locally-extinct mammal species and one reptile species were reintroduced into a fenced Reserve where cats, foxes and rabbits were excluded. Reintroductions of the nationally threatened greater stick-nest rat, burrowing bettong, greater bilby and western barred bandicoot were all considered successful based on short and medium-term success criteria. These criteria included continued survival after 8 years, increased distribution across the large Reserve and, most importantly, recovery after a drought event. The trial reintroductions of the numbat and woma python into the Reserve were unsuccessful due to predation by native avian and reptilian predators respectively. Outside the Reserve, where cats and foxes were present but controlled through poison baiting, reintroduction attempts of the greater bilby and burrowing bettong were unsuccessful. High mortality was attributed to cat and fox predation with dingoes also contributing to post-release mortality in bettongs. However, a reintroduction of burrowing bettongs into a fenced area with low rabbit and cat abundance has, to-date, met short-term and medium-term success criteria. Results suggest that the absence or severe restriction of exotic mammalian predators was the critical factor responsible for the success of the mammal reintroductions. Determining thresholds of predator activity below which successful reintroduction of threatened species can occur, are needed to improve the science of reintroduction biology in Australia.     

Causes of mortality at nests of ground-nesting birds in the Upper Waitaki Basin, South Island, New Zealand: a 5-year video study

We used video cameras over 5 years to quantify causes of mortality at 172 nests of three species of ground-nesting birds that nest on braided riverbeds of the Upper Waitaki Basin, South Island, New Zealand. The species were banded dotterels Charadrius bicinctus (n=114), black stilts Himantopus novaezelandiae (n=23), and black-fronted terns Sterna albostriata (n=35). Of 77 recorded lethal events (excluding four desertions caused by us), 66 involved deaths of only eggs, and 11 involved deaths of adults and/or chicks, and/or eggs. The main predators were cats Felis catus, hedgehogs Erinaceus europaeus, and ferrets Mustela furo, which were responsible for 43, 20, and 18% of lethal events, respectively. Cats were the only predator species to take adult birds. We recorded only two avian predations: a harrier Circus approximans took a chick and a hatching egg from one nest, and an Australian magpie Gymnorhina tibicen ate chicks at one nest. Other causes of mortality were incubating adult birds, floods, and sheep Ovis aries. Each accounted for <4% of lethal events. Ninety percent of visits (151 of 168) by predators or potential predators happened between sunset and sunrise. We found no evidence that video cameras or infra-red lighting influenced predation rates during 2 years of testing for such effects.     

Introduced cane toads Bufo marinus are active nest predators and competitors of rainbow bee-eaters Merops ornatus: observational and experimental evidence

During a three-year study, introduced cane toads (Bufo marinus) ruined one-third of nest attempts of ground-nesting rainbow bee-eaters (Merops ornatus) by usurping their nest burrows and preying upon their eggs and young nestlings. Birds that had lost their nest to cane toads were less likely to be recaptured in subsequent years. Cane toads are having a significant negative effect at the population level: at present, rainbow bee-eaters produce 0.8 fledglings per nest. However, in the absence of cane toads each nest would produce 1.2 fledglings. Rainbow bee-eaters had little defence against the cane toads. The diurnal birds were not able to mob the nocturnal toads, nor were they able to eject cane toads from the nest. Deep nests and nests built on steep slopes were still preyed upon by the toads. Cane toads that were removed from the nest had the ability and motivation to return to the nest when displaced up to 1200 m away, suggesting that the nest is a valuable resource to toads. Cane toads were significantly more likely to: (a) prey upon nests containing hatchlings rather than eggs; (b) enter and occupy artificial nest tunnels (1.2 m deep) containing a small food item (20 g of raw chicken) rather than artificial nests that were empty. These results indicate that cane toads actively prey upon nests using olfactory cues. The predatory and homing abilities of cane toads are reviewed, as well as their need for diurnal shelter sites. The possibility that cane toads are having a negative impact upon other native, ground-dwelling vertebrate fauna via their role as opportunistic predators requires urgent investigation.