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。     

Breeding success and predation at nests of banded dotterel (

Egg and chick loss at banded dotterel (Charadrius bicinctus) nests was studied over the 1992/93 season on the Tekapo, Ohau and Ahuriri Rivers in the Central South Island. Egg loss at nests was higher on the Ohau and Tekapo Rivers than on the Ahuriri River, especially early in the season. Only 11% and 12% of nests fledged one or more chicks on the Tekapo and Ohau Rivers respectively, compared to 42% of nests on the Ahuriri River. Nests on islands within the braided riverbeds were more successful than nests on the mainland. Proximity of nests to potential predator cover did not influence hatching success although close proximity of nests to rabbit burrows increased the risk of predation. A lack of knowledge of the predator species involved in this study hampers assessment of the impact of various factors on the breeding success of banded dotterels. Further research to identify predators is necessary to target conservation management and better protect banded dotterel and endangered riverbed birds.     

INTRASPECIFIC PREDATION AND COLONIAL BREEDING IN LESSER BLACK-BACKED GULLS LARUS FUSCUS

The breeding biology of Lesser Black-backed Gulls was studied on Skokholm Island, Pembrokeshire, where the number of breeding pairs has been increasing at about 20% per annum since 1963. Laying was found to be synchronous within small groups. Clutch size and breeding success showed seasonal declines over the spread of breeding. The loss mainly of eggs, but to a lesser extent of chicks also, caused this overall decline in success. Hide observations indicated that the bulk of these losses arose through predation by nesting adult Lesser Black-backed Gulls on their nearest neighbours. Not infrequently the protagonist had lost its own clutch shortly before turning predator, and such a chain-sequence should lead to a steady build-up of aggressive failed breeders and so account for the observed seasonal increase in egg loss. Attentiveness to the clutch decreased with season but this was unlikely to have been important in precipitating the predation. Intermediate plant cover was associated with highest nest density and also with highest chick survival. In addition, nest density was directly correlated with chick survival. Whether plant cover and nest density separately affect chick production remains unresolved. Nevertheless, the increasing nest densities in this colony caused by the growth of the gull population are thought to be responsible for the widespread intraspecific predation, the intensity of which is probably a new feature of the gulls' breeding behaviour. The implications of this 'internal' predation for laying synchrony and aggregated nesting are discussed; these two factors of the breeding pattern probably evolved largely to combat 'external' predators. Not only are they no protection against inter-neighbour predation but appear to facilitate it. It remains to be seen whether this kind of predation will significantly affect breeding patterns with further increases in nest density.     

Predator‐mediated interactions between preferred,alternative and incidental prey in the arctic tundra

Apparent competition between prey is hypothesized to occur more frequently in environments with low densities of preferred prey, where predators are forced to forage for multiple prey items. In the arctic tundra, numerical and functional responses of predators to preferred prey (lemmings) affect the predation pressure on alternative prey (goose eggs) and predators aggregate in areas of high alternative prey density. Therefore, we hypothesized that predation risk on incidental prey (shorebird eggs) would increase in patches of high goose nest density when lemmings were scarce. To test this hypothesis, we measured predation risk on artificial shorebird nests in quadrats varying in goose nest density on Bylot Island (Nunavut, Canada) across three summers with variable lemming abundance. Predation risk on artificial shorebird nests was positively related to goose nest density, and this relationship was strongest at low lemming abundance when predation risk increased by 600% as goose nest density increased from 0 to 12 nests ha^?1. Camera monitoring showed that activity of arctic foxes, the most important predator, increased with goose nest density. Our data support our incidental prey hypothesis; when preferred prey decrease in abundance, predator mediated apparent competition via aggregative response occurs between the alternative and incidental prey items.     

Large-scale spatio-temporal shifts in the diet of a predator mediated by an emerging infectious disease of its main prey

Aim To explore the influence of an emerging infectious disease (EID) affecting a prey species on the spatial patterns and temporal shifts in the diet of a predator over a large geographical scale. We reviewed studies on the diet of Bonelli’s eagles (Hieraaetus fasciatus) in order to determine the repercussions of the reduction in the density of its main prey, the rabbit (Oryctolagus cuniculus), caused by outbreaks of rabbit haemorrhagic disease (RHD) since 1988. Location Western continental Europe. Methods We compiled published and unpublished information on the diet of breeding Bonelli’s eagles from Portugal, Spain and France for a 39‐year study period (1968–2006). Nonparametric tests were used in order to analyse temporal shifts in diet composition and trophic diversity (H′) between the periods of ‘high’ (before outbreak of RHD) and ‘low’ rabbit density (after outbreak of RHD). A combination of hierarchical agglomerative clustering and non‐metric multidimensional scaling (NMDS) analyses were used to test for the existence of geographical patterns in the diet of Bonelli’s eagles in each period. Results The diet of the Bonelli’s eagle consisted of rabbit (28.5%), pigeons (24.0%), partridges (15.3%), ‘other birds’ (11.6%), ‘other mammals’ (7.1%), corvids (7.0%), and herptiles (6.4%). However, RHD had large consequences for its feeding ecology: the consumption of rabbits decreased by one‐third after the outbreak of RHD. Conversely, trophic diversity (H′) increased after outbreak of RHD. At the same time, the analyses showed clear geographical patterns in the diet of the Bonelli’s eagle before, but not after, RHD outbreak. Main conclusions Geographical patterns in the diet of the Bonelli’s eagle in western Europe seem to be driven mainly by spatio‐temporal variation in the abundance of rabbits and, to a lesser extent, by the local (territorial) environmental features conditioning the presence and density of alternative prey species. We show that an EID can disrupt predator–prey relationships at large spatial and temporal scales through a severe decline in the population of the main prey species. Hence we argue that strict guidelines should be drawn up to prevent human‐aided dissemination of ‘pathogen pollution’, which can threaten wildlife not only at the population and species level but also at the community and ecosystem scale.     

Food use is affected by the experience of nest predation: implications for indirect predator effects on clutch size

Indirect predator effects on prey demography include any effect not attributable to direct killing and can be mediated by perceived predation risk. Though perceived predation risk clearly affects foraging, few studies have yet demonstrated that it can chronically alter food intake to an extent that affects demography. Recent studies have used stable isotopes to gauge such chronic effects. We previously reported an indirect predator effect on the size of subsequent clutches laid by song sparrows (Melospiza melodia). Females that experienced frequent experimental nest predation laid smaller clutches and were in poorer physiological condition compared to females not subject to nest predation. Every female was provided with unlimited supplemental food that had a distinctive ¹³C signature. Here, we report that frequent nest predation females had lower blood δ¹³C values, suggesting that the experience of nest predation caused them to eat less supplemental food. Females that ate less food gained less fat and were in poorer physiological condition, consistent with the effect on food use contributing to the indirect predator effect on clutch size. Tissue δ¹⁵N values corroborated that clutch size was not likely constrained by endogenous resources. Finally, we report that the process of egg production evidently affects egg δ¹³C values, and this may mask the source of nutrients to eggs. Our results indicate that perceived predation risk may impose food limitation on prey even where food is unlimited and such predator-induced food limitation ought to be added to direct killing when considering the total effect of predators on prey numbers.     

Breeding Phenology of Birds: Mechanisms Underlying Seasonal Declines in the Risk of Nest Predation

Seasonal declines in avian clutch size are well documented, but seasonal variation in other reproductive parameters has received less attention. For example, the probability of complete brood mortality typically explains much of the variation in reproductive success and often varies seasonally, but we know little about the underlying cause of that variation. This oversight is surprising given that nest predation influences many other life-history traits and varies throughout the breeding season in many songbirds. To determine the underlying causes of observed seasonal decreases in risk of nest predation, we modeled nest predation of Dusky Flycatchers (Empidonax oberholseri) in northern California as a function of foliage phenology, energetic demand, developmental stage, conspecific nest density, food availability for nest predators, and nest predator abundance. Seasonal variation in the risk of nest predation was not associated with seasonal changes in energetic demand, conspecific nest density, or predator abundance. Instead, seasonal variation in the risk of nest predation was associated with foliage density (early, but not late, in the breeding season) and seasonal changes in food available to nest predators. Supplemental food provided to nest predators resulted in a numerical response by nest predators, increasing the risk of nest predation at nests that were near supplemental feeders. Our results suggest that seasonal changes in foliage density and factors associated with changes in food availability for nest predators are important drivers of temporal patterns in risk of avian nest predation.     

Continuing influences of introduced hedgehogs <Emphasis Type="Italic">Erinaceus europaeus</Emphasis> as a predator of wader (Charadrii) eggs four decades after their release on the Outer Hebrides,Scotland

Non-native predators can cause major declines or even localised extinctions in prey populations across the globe, especially on islands. The removal of non-native predators can, therefore, be a crucial conservation management tool but there can be challenges when they are viewed as charismatic in their own right. Four decades after their introduction to islands in the Outer Hebrides, Scotland, European hedgehogs Erinaceus europaeus continue to be an important nest predator for a declining population of breeding waders. Where hedgehogs were rare, clutch survival rates (assessed using nest temperature loggers) of five species of waders (dunlin Calidris alpina, lapwing Vanellus vanellus, redshank Tringa totanus, snipe Gallinago gallinago and ringed plover Charadrius hiaticula) were higher than where hedgehogs were relatively more abundant. Hedgehogs were the most frequent nest predator identified using cameras. However, factors influencing population sizes of breeding waders are complex and unlikely to be attributable to a single species of predator. The interactions between predation, land use, habitat and the changes in each deserve further attention.     

Predation on wader nests in Europe

The population declines of waders in Europe are widely considered to have resulted from habitat loss and degradation due to agricultural changes. However, recent empirical evidence suggests that levels of predation on wader nests are unsustainably high in many cases, even in some situations where breeding habitat is otherwise favourable. We review the published and 'grey' literature on nest predation on waders in Europe and quantify the relative importance of the major predators. Nest cameras offer the least biased method of identifying and quantifying nest predators. A small number of camera studies, in combination with others utilizing nest temperature loggers, indicate that nocturnal/mammalian predators make the largest contribution to wader nest predation. More than half of site-years or studies reviewed reported clutch failure rates of over 50% attributable to predation alone, a rate that is likely to be associated with declining populations, although parameters such as chick and adult survival will also affect population trends. Correlates of wader nest predation are documented, with time of season, field type and management, distance to habitat/field edge, wader nest density, and abundance of mammalian predators being most consistently identified. Future directions of research into wader productivity are discussed, and we suggest that studies quantify additional life-history parameters such as chick survival, as well as examining the predator community, wherever possible.     

Incidental nest predation in freshwater turtles: inter- and intraspecific differences in vulnerability are explained by relative crypsis

There has long been interest in the influence of predators on prey populations, although most predator–prey studies have focused on prey species that are targets of directed predator searching. Conversely, few have addressed depredation that occurs after incidental encounters with predators. We tested two predictions stemming from the hypothesis that nest predation on two sympatric freshwater turtle species whose nests are differentially prone to opportunistic detection—painted turtles (Chrysemys picta) and snapping turtles (Chelydra serpentina)—is incidental: (1) predation rates should be density independent, and (2) individual predators should not alter their foraging behavior after encountering nests. After monitoring nest survival and predator behavior following nest depredation over 2 years, we confirmed that predation by raccoons (Procyon lotor), the primary nest predators in our study area, matched both predictions. Furthermore, cryptic C. picta nests were victimized with lower frequency than more detectable C. serpentina nests, and nests of both species were more vulnerable in human-modified areas where opportunistic nest discovery is facilitated. Despite apparently being incidental, predation on nests of both species was intensive (57% for painted turtles, 84% for snapping turtles), and most depredations occurred within 1 day of nest establishment. By implication, predation need not be directed to affect prey demography, and factors influencing prey crypsis are drivers of the impact of incidental predation on prey. Our results also imply that efforts to conserve imperiled turtle populations in human-modified landscapes should include restoration of undisturbed conditions that are less likely to expose nests to incidental predators.     

Parent birds assess nest predation risk: influence of cavity condition and avian nest predator activity

Skutch hypothesized that nest predators visually assess parental activities to locate a prey nest, whereas parents modify fitness‐related traits to reduce the probability of nest predation. We examined how cavity condition and parental activity interact with avian nest predators to shape the nest success of two coexisting parid species, marsh tits Poecile palustris and oriental tits Parus minor, breeding in nest‐boxes during the incubation period. Nest‐boxes were manipulated to create a prolonged risk of nest predation (entrance diameter 2.6 cm control vs 5.5 cm treatment) soon after clutch completion. To measure changes in parental behavior, we also simultaneously simulated a pulsed risk of nest predation, using sound playbacks of a coexisting control bird and an avian nest predator. We found that the parent tits merely responded the pulsed risk, presumably due to an environment with high avian nest predator encounters, compared to the prolonged risk. Instead, both species spent more time on vigilance at the nest, only under prolonged risk conditions. The activity of corvids near the nest‐box was higher in the marsh tit than that in oriental tits. This activity was also higher in the treatment nest box than that in the control nest‐box. Nest predation during the incubation period was higher in marsh tits than in oriental tits, presumably due to higher and more plastic vigilance in oriental tits, compared to marsh tits. Our results highlight that the differences in cavity condition and parental activities at the nests of two coexisting non‐excavators may contribute to differential nest predation by attracting avian nest predators.     

Nest Crypsis, Reproductive Value of a Clutch and Escape Decisions in Incubating Female Mallards Anas platyrhynchos

In cryptically coloured birds, remaining on the nest despite predator approach (risk‐taking) may decrease the likelihood that the nest will be detected and current reproductive attempt lost. By contrast, flushing may immediately reveal the nest location to the predator. Escape decisions of incubating parents should therefore be optimized based on the risk‐to‐parent/cost of escape equilibrium. Animal prey may assess predation risk depending on a variety of cues, including the camouflage that vegetation provides against the predator. We examined interactive effects of nest crypsis and the current reproductive value of a clutch on flushing distances in incubating mallards (Anas platyrhynchos) approached by a human. Our results were consistent with predictions of parental investment theory: flushing distances were inversely correlated with measures of the reproductive value of the current clutch, namely with clutch size, stage of incubation and mean egg volume. Independently of a reproductive value of a clutch, nest concealment explained a significant portion of the variation in flushing distance among females; individual females tended to increase/decrease flushing distances according to change in nest cover. The results further suggest that vegetation concealment greatly influenced the risk of nest detection by local predators, suggesting that vegetation may act as a protective cover for incubating female. A female's ability to delay flushes according to the actual vegetation cover might thus be viewed as an antipredator strategy that reduces premature nest advertising to visually oriented predators. We argue, however, that shorter flying distances from densely covered sites might be maladaptive in areas where a predator's ability to detect incubating female does not rely on visual cues of nests.     

Testing models for equilibrium distribution and abundance of insects

We evaluated willow removal as a technique for enhancing habitat for birds of braided rivers by monitoring five bird species at three sites in the Mackenzie Basin, New Zealand, from 1991 to 1994 Four species—banded dotterel (Charadrius bicinctus), pied stilt (Himantopus novaezelandiae), black- fronted tern (Sterna albostriata) and South Island pied oystercatcher (Haematopus ostralegus) used the areas of riverbed cleared of willows for nesting and foraging, at the same or greater density than other areas of riverbed already free from willows. Wrybills (Anarhynchus frontalis) were occasionally seen in cleared areas of riverbed but were not nesting there during the study. Densities of banded dotterel and wrybill were lowest at sites with the greatest densities of willows, and only three out of 327 monitored nests were located in willow habitat. Nest predation rates did not differ significantly among sites with differing levels of willow infestation, nor did they differ between areas of cleared riverbed and riverbed already free from willow. In addition to weed control, predator control may be necessary to increase bird populations. This study indicates that willow removal increases foraging and nesting habitat for some river bird populations, but further surveys are necessary to assess whether willow removal has any long-term benefits.     

Of mice and mallards: positive indirect effects of coexisting prey on waterfowl nest success

Coexisting prey species interact indirectly via their shared predators when one prey type influences predation rates of the second prey type. In a temperate system where the predominant shared predator is a generalist, I studied the indirect effects of rodent populations on waterfowl nest success, both within the nesting season among sites and among years. Among six to ten upland fields (14 to 27 ha), mallard ( Anas platyrhynchos ) nest success was positively correlated with rodent abundance in all three years of the study. After removing year effects, mallard nest success remained positively correlated with the relative abundance of rodents. Of the rodent species present, California voles ( Microtus californicus ) were the most important coexisting prey type influencing nest success. Among years, mallard nest success was positively correlated with vole abundance; the asymptotic relationship suggests a threshold response to vole abundance, beyond which predators become satiated and additional voles do little to affect nest success. I tested and rejected three alternative explanations for the observed positive correlation between mallard nest success and rodent abundance that do not involve an indirect effect of coexisting prey populations. The influences of dense nesting cover, nesting density, and predator activity did not explain the observed patterns of nest success. These results suggest that rodent populations buffer predation on waterfowl nests, both within and among years, via the behavioral responses of shared predators to coexisting prey.     

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.

     

Can widespread generalist predators affect keystone prey? A case study with red foxes and European rabbits in their native range

Widespread generalist predators may affect declining keystone prey populations. However, this phenomenon is not well understood. In this paper, we assessed whether the abundance and population growth of European rabbits Oryctolagus cuniculus, a keystone prey species in Mediterranean Iberia, was related to the abundance and diet of red foxes, Vulpes vulpes, a widespread generalist predator. In a locality in central Spain, where rabbit population abundance declined, we estimated rabbit abundance during almost 3 years and determined fox abundance and diet during two concurrent years. We calculated a fox predation index (percentage of consumed rabbit biomass × fox abundance) to assess the importance of rabbits to foxes. We employed a multi–model approach to explain rabbit abundance and population growth. Foxes consumed between 60 and 99 % rabbit biomass in their diets, and this was independent of rabbit abundance. Periods of higher fox predation index coincided with lower rabbit density and vice versa. Two models best explained rabbit abundance and four rabbit population growth. They included the fox predation index and its interaction with rabbit abundance during the previous month. Altogether, fox predation, intraspecific density dependence, and their interaction partly explained rabbit population dynamics. We conclude that in order to propel the recovery of the rabbit in Iberia, it is essential to better understand the role of these factors in driving the abundance of the species.     

Predation as a landscape effect: the trading off by prey species between predation risks and protection benefits

1. Predators impose costs on their prey but may also provide benefits such as protection against other (e.g. nest) predators. The optimal breeding location in relation to the distance from a nesting raptor varies so as to minimize the sum of costs of adult and nest predation. We provide a conceptual model to account for variation in the relative predation risks and derive qualitative predictions for how different prey species should respond to the distance from goshawk Accipiter gentilis nests. 2. We test the model predictions using a comprehensive collection of data from northern Finland and central Norway. First, we carried out a series of experiments with artificial bird nests to test if goshawks may provide protection against nest predation. Second, we conducted standard bird censuses and nest-box experiments to detect how the density or territory occupancy of several prey species varies with distance from the nearest goshawk nest. 3. Nest predation rate increased with distance from goshawk nest indicating that goshawks may provide protection for birds' nests against nest predation. Abundance (or probability of presence) of the main prey species of goshawks peaked at intermediate distances from goshawk nests, reflecting the trade-off. The abundance of small songbird species decreased with distance from goshawk nests. The goshawk poses little risk to small songbirds and they may benefit from goshawk proximity in protection against nest predation. Finally, no pattern with distance in pied flycatcher territory (nest box) occupation rate or the onset of egg-laying was detected. This is expected, as flycatchers neither suffer from marked nest predation risk nor are favoured goshawk prey. 4. Our results suggest that territory location in relation to the nest of a predator is a trade-off situation where adult birds weigh the risk of themselves being predated against the benefits accrued from increased nest survival. Prey species appear able to detect and measure alternative predation risks, and respond adaptively. From the prey perspective, the landscape is a mosaic of habitat patches the quality of which varies according to structural and floristic features, but also to the spatial distribution of predators.     

Predictable changes in predation mortality as a consequence of changes in food availability and predation risk

Theory predicts that animals will have lower activity levels when either the risk of predation is high or the availability of resources in the environment is high. If encounter rates with predators are proportional to activity level, then we might expect predation mortality to be affected by resource availability and predator density independent of the number of effective predators. In a factorial experiment, we tested whether predation mortality of larval wood frogs, Rana sylvatica, caused by a single larval dragonfly, Anax junius, was affected by the presence of additional caged predators and elevated resource levels. Observations were consistent with predictions. The survival rate of the tadpoles increased when additional caged predators were present and when additional resources were provided. There was no significant interaction term between predator density and food concentration. Lower predation rates at higher predator density is a form of interference competition. Reduced activity of prey at higher predator density is a potential general mechanism for this widespread phenomenon. Higher predation rates at low food levels provides an indirect mechanism for density-dependent predation. When resources are depressed by elevated consumer densities, then the higher activity levels associated with low resource levels can lead to a positive association between consumer density and consumer mortality due to predation. These linkages between variation in behaviour and density-dependent processes argue that variation in behaviour may contribute to the dynamics of the populations. Because the capture rate of predators depends on the resources available to prey, the results also argue that models of food-web dynamics will have to incorporate adaptive variation in behaviour to make accurate predictions.     

Studies on the basic components of the predation ofPhytoseiulus persimilis Athias-Henriot (Acarina: Phytoseiidae)

The basic components of the predation of Phytoseiulus persimilisAthias-Henriot feeding upon eggs of Tetranychus urticaeKoch were studied in an open system where the predator could disperse freely. The type of the functional response of the predator to the density of its prey was the same as that studied so far in a closed system, i.e.,Holling's Type 2. The search rate of the predator, however, was much lower in comparison with the result from a closed system. The oviposition of the predator per day was only weakly related to prey densities higher than 10 per leaf disc. But the emigration rate was inversely dependent upon the initial prey density up to 60 per leaf disc. The searching behaviour of the predator was influenced by both the web density spun by T. urticae and the density of the prey: the predator searched for its prey intensively only after it had contact with web. Mutual interference was observed in prey consumption, but not in the emigration rate. The emigration rate was largely dependent upon the prey density available per predator.