Ruff Philomachus pugnax staging in the Netherlands forage in agricultural grasslands, where they mainly eat earthworms (Lumbricidae). Food intake and the surface availability of earthworms were studied in dairy farmland of southwest Friesland in March–April 2011. Daily changes in earthworm availability were quantified by counting visible earthworms. No earthworms were seen on the surface during daytime, but their numbers sharply increased after sunset and remained high during the night. Nevertheless, intake rates of individual Ruff in different grasslands measured during daytime showed the typical Holling type II functional response relationship with the surfacing earthworm densities measured at night. Radiotagging of Ruff in spring 2007 revealed that most, if not all, feeding occurs during the day, with the Ruff assembling at shoreline roosts at night. This raises the question of why Ruff do not feed at night, if prey can be caught more easily than during daytime. In March–May 2013 we experimentally examined the visual and auditory sensory modalities used by Ruff to find and capture earthworms. Five males were kept in an indoor aviary and we recorded them individually foraging on trays with 10 earthworms mixed with soil under various standardized light and white noise conditions. The number of earthworms discovered and eaten by Ruff increased with light level, but only when white noise was played, suggesting that although they can detect earthworms by sight, Ruff also use auditory cues. We suggest that although surfacing numbers of earthworms are highest during the night, diurnal intake rates are probably sufficient to avoid nocturnal foraging on a resource that is more available but perhaps less detectable at that time. 相似文献
Prey often reduce predation risk at the cost of lower resource intake. The cumulative effects of such tradeoffs can alter resource allocation, demography and evolutionary processes. We show how the accumulation of risk effects reduces the growth rate of wild North American porcupines Erethizon dorsatum, and simulate three evolutionary responses related to lifetime reproductive success. Individual porcupines experiencing predation risk from fishers Pekania pennanti grew slower and gave birth to fewer offspring. Simulations show that predation risk alone can lead to population declines, and that a female can replace herself by investing more energy into reproduction or adult survival; females that only invest energy in juvenile survival cannot. We show that the accumulation of predation risk can reduce lifetime reproductive success in natural ecosystems. Estimating the contribution of predation risk, and how evolutionary responses can mediate consequences associated with predation risk, is necessary to understand the evolution of predator–prey systems. 相似文献
Many wetlands undergo seasonal cycles in precipitation and water depth.This environmental seasonality is echoed in patterns of production of fishbiomass, which, in turn, influence the phenology of other components of thefood web, including wading birds. Human activities, such as drainage orother alterations of the hydrology, can exacerbate these natural cycles andresult in detrimental stresses on fish production and the higher trophic levels dependent on this production. In this paper we model theseasonal pattern of fish production in a freshwater marsh, with specialreference to the Everglades/Big Cypress region of southern Florida.The model illustrates the temporal pattern of production through theyear, which can result in very high densities of fish at the end of ahydroperiod (period of flooding), aswell as the importance of ponds and other deep depressions, both as refugia and sinks during dry periods. The model predicts that: (1) there is an effective threshold in the length of the hydroperiod that must beexceeded for high fish-population densities to be produced, (2) large,piscivorous fishes do not appear tohave a major impact on smaller fishes in the marsh habitat, and (3) therecovery of small-fish populations in the marsh following a major droughtmay require up to a year. The last of these results is relevant toassessing anthropogenic impacts on marsh production, as these effectsmay increase the severity and frequency of droughts. 相似文献
The structure of the food web including the endangered lycaenid butterfly Shijimiaeoides divinus asonis (Matsumura) was analyzed to identify species contributing most to maintaining the equilibrium of the food web. Twenty‐seven species belonging to 17 families fed on Sophora flavescens Aiton, the host‐plant of S. divinus asonis: 15 species were leaf and stem feeders, seven (including S. divinus asonis) fed on flower buds, four were flower feeders and one fed on the seeds of So. flavescens. Of these 27 species, four were omnivores. The natural enemies of S. divinus asonis comprised six insect species, 11 spider species and one entomopathogenic fungus species, including six new predator records. The linkage density, total number of trophic links, connectance, average chain length and predator–prey ratio were 1.617, 97, 0.0548, 2.267 and 0.694, respectively. Exclusion of any of the 15 species with four or more trophic links reduced the connectance of the food web. These 15 species included facultative mutualistic attendant ants and predators of S. divinus asonis, herbivores to So. flavescens, an omnivore feeding on S. divinus asonis and So. flavescens, and prey insects. Therefore, future studies should monitor these 15 species. 相似文献
Complex coevolutionary relationships among competitors, predators, and prey have shaped taxa diversity, life history strategies, and even the avian migratory patterns we see today. Consequently, accurate documentation of prey selection is often critical for understanding these ecological and evolutionary processes. Conventional diet study methods lack the ability to document the diet of inconspicuous or difficult‐to‐study predators, such as those with large home ranges and those that move vast distances over short amounts of time, leaving gaps in our knowledge of trophic interactions in many systems. Migratory raptors represent one such group of predators where detailed diet studies have been logistically challenging. To address knowledge gaps in the foraging ecology of migrant raptors and provide a broadly applicable tool for the study of enigmatic predators, we developed a minimally invasive method to collect dietary information by swabbing beaks and talons of raptors to collect trace prey DNA. Using previously published COI primers, we were able to isolate and reference gene sequences in an open‐access barcode database to identify prey to species. This method creates a novel avenue to use trace molecular evidence to study prey selection of migrating raptors and will ultimately lead to a better understanding of raptor migration ecology. In addition, this technique has broad applicability and can be used with any wildlife species where even trace amounts of prey debris remain on the exterior of the predator after feeding. 相似文献
Predation is an established cause of cycling in prey species. Here, the ability of predation to explain periodic travelling waves in prey populations, which have recently been found in a number of spatiotemporal field studies, is examined. The nature of periodic waves in these systems, and the way in which they can be generated by the invasion of predators into a prey population is discussed. A theoretical calculation that predicts, as a function of two parameter ratios, whether such an invasion will lead to a stable periodic travelling wave that would be observed in practice is presented ‐ the alternative outcome is spatiotemporal chaos. The calculation also predicts quantitative details of the periodic waves, such as speed and amplitude. The results give new insights into the types of predator‐prey systems in which one would expect to see periodic travelling waves following an invasion by predators. 相似文献
Characterization of energy flow in ecosystems is one of the primary goals of ecology, and the analysis of trophic interactions and food web dynamics is key to quantifying energy flow. Predator‐prey interactions define the majority of trophic interactions and food web dynamics, and visual analysis of stomach, gut or fecal content composition is the technique traditionally used to quantify predator‐prey interactions. Unfortunately such techniques may be biased and inaccurate due to variation in digestion rates ( Sheppard & Hardwood 2005 ); however, those limitations can be largely overcome with new technology. In the last 20 years, the use of molecular genetic techniques in ecology has exploded ( King et al. 2008 ). The growing availability of molecular genetic methods and data has fostered the use of PCR‐based techniques to accurately distinguish and identify prey items in stomach, gut and fecal samples. In this month’s issue of Molecular Ecology Resources, Corse et al. (2010) describe and apply a new approach to quantifying predator‐prey relationships using an ecosystem‐level genetic characterization of available and consumed prey in European freshwater habitats ( Fig. 1a ). In this issue of Molecular Ecology, Hardy et al. (2010) marry the molecular genetic analysis of prey with a stable isotope (SI) analysis of trophic interactions in an Australian reservoir community ( Fig. 1b ). Both papers demonstrate novel and innovative approaches to an old problem – how do we effectively explore food webs and energy movement in ecosystems? Figure 1 Open in figure viewer PowerPoint The aquatic habitats used for two studies of diet and trophic interactions that employed molecular genetic and stable isotope analyses. Panel a: Example of Rhone basin habitat (France) where fish diet was determined using PCR to classify prey to a series of ecological clades (photo by Emmanuel Corse). Panel b: A weir pool on the lower Murray River (Australia) where food web and prey use was evaluated using a combination of advanced molecular genetic and stable isotope analyses (photo credit: CSIRO). 相似文献
1. Urban environments are fragmented habitats characterised by the presence of physical barriers, which may negatively affect dispersal and colonisation by insect herbivores and their natural enemies. Conversely, plants growing along pavements may function as dispersal corridors, helping to moderate the harmful effects of resource patch isolation on organism movement and population persistence. 2. We experimentally tested the effects of walls as physical barriers to the dispersal of the leaf miner Liriomyza commelinae Frost and colonisation of its host plant, Commelina erecta L., in urban habitats. We also evaluated whether plants along pavements could act as corridors for this species. 3. We exposed experimental host plants to the leaf miner in houses with front gardens and back yards, the latter being completely surrounded by walls. The front gardens had walls but none separating them from the pavement. Previously mined plants were also exposed to parasitoids in the yards to determine parasitoid attack. 4. Liriomyza commelinae took longer to colonise back yards with higher walls, and the abundance of mined plants along pavements reduced the colonisation time. Leaf‐miner abundance was marginally affected by the yard type, and was lower in back yards. Cumulative parasitism rates decreased with increasing distance at which mined plants were placed from pavements. 5. Constructions act as physical barriers, having a negative impact on colonisation of host plants by leaf miners. The function of pavements as corridors seems to depend on the abundance of mined plants. Parasitism may be affected by distance from the corridor rather than physical barriers or other potential hosts. 相似文献
Migration is expected to benefit individuals through exposure to higher quality forage and reducing predation rates more than non‐migratory conspecifics. Previous studies of partially migratory ungulates (with migrant and resident individuals) have focused on bottom–up factors regulating resident and migrant segments, yet differential predation between strategies could also be a density‐dependent regulatory mechanism. Our study tested for density‐dependence in mortality, as well as mechanisms of bottom–up or top–down regulation in the resident and migrant portions of the partially migratory Ya Ha Tinda elk population. We tested for density dependence in adult female and juvenile survival rates, and then discriminated between predator‐ and food‐regulation hypotheses by testing for density‐dependence amongst mortality causes for adult female elk. Notably, the population declined almost 70% from near previously published estimates of carrying capacity over 10 years, providing ideal conditions to test for density dependence. In contrast to predictions, we found only weak support for density dependence in adult survival and juvenile survival. We also found few differences between migrant and resident elk in adult or juvenile survival, though juvenile survival differences were biologically significant. Predation by humans and grizzly bears was density dependent, but similar between migratory strategies. Predation by wolves was the leading known cause of mortality, yet remained constant with declining elk density equally for both migrant and resident elk, indicating wolf predation was density‐independent. Instead of being strongly regulated by food or predation, we found adult female survival was driven by density‐independent predation and climatic factors. The few differences between migratory strategies suggest equivalent fitness payoffs for migrants and residents. This population is being limited by density‐independent predation leading to declines of both migratory strategies. Our results challenge classical predator–prey theory, and call for better integration between predator–prey and migration theory. 相似文献
Light is a central driver of biological processes and systems. Receding sea ice changes the lightscape of high‐latitude oceans and more light will penetrate into the sea. This affects bottom‐up control through primary productivity and top‐down control through vision‐based foraging. We model effects of sea‐ice shading on visual search to develop a mechanistic understanding of how climate‐driven sea‐ice retreat affects predator–prey interactions. We adapt a prey encounter model for ice‐covered waters, where prey‐detection performance of planktivorous fish depends on the light cycle. We use hindcast sea‐ice concentrations (past 35 years) and compare with a future no‐ice scenario to project visual range along two south–north transects with different sea‐ice distributions and seasonality, one through the Bering Sea and one through the Barents Sea. The transect approach captures the transition from sub‐Arctic to Arctic ecosystems and allows for comparison of latitudinal differences between longitudes. We find that past sea‐ice retreat has increased visual search at a rate of 2.7% to 4.2% per decade from the long‐term mean; and for high latitudes, we predict a 16‐fold increase in clearance rate. Top‐down control is therefore predicted to intensify. Ecological and evolutionary consequences for polar marine communities and energy flows would follow, possibly also as tipping points and regime shifts. We expect species distributions to track the receding ice‐edge, and in particular expect species with large migratory capacity to make foraging forays into high‐latitude oceans. However, the extreme seasonality in photoperiod of high‐latitude oceans may counteract such shifts and rather act as a zoogeographical filter limiting poleward range expansion. The provided mechanistic insights are relevant for pelagic ecosystems globally, including lakes where shifted distributions are seldom possible but where predator–prey consequences would be much related. As part of the discussion on photoperiodic implications for high‐latitude range shifts, we provide a short review of studies linking physical drivers to latitudinal extent. 相似文献
Prey organisms reduce predation risk by altering their behavior, morphology, or life history. Avoiding or deterring predators often incurs costs, such as reductions in growth or fecundity. Prey minimize costs by limiting predator avoidance or deterrence to situations that pose significant risk of injury or death, requiring them to gather information regarding the relative threat potential predators pose. Chemical cues are often used for risk evaluation, and we investigated morphological responses of oysters (Crassostrea virginica) to chemical cues from injured conspecifics, from heterospecifics, and from predatory blue crabs (Callinectes sapidus) reared on different diets. Previous studies found newly settled oysters reacted to crab predators by growing heavier, stronger shells, but that adult oysters did not. We exposed oysters at two size classes (newly settled oyster spat and juveniles ~2.0 cm) to predation risk cue treatments including predator or injured prey exudates and to seawater controls. Since both of the size classes tested can be eaten by blue crabs, we hypothesized that both would react to crab exudates by producing heavier, stronger shells. Oyster spat grew heavier shells that required significantly more force to break, an effective measure against predatory crabs, when exposed to chemical exudates from blue crabs as compared to controls. When exposed to chemical cues from injured conspecifics or from injured clams (Mercenaria mercenaria), a sympatric bivalve, shell mass and force were intermediate between predator treatments and controls, indicating that oysters react to injured prey cues but not as strongly as to cues released by predators. Juvenile oysters of ~ 2.0 cm did not significantly alter their shell morphology in any of the treatments. Thus, newly settled oysters can differentiate between predatory threats and adjust their responses accordingly, with the strongest responses being to exudates released by predators, but oysters of 2.0 cm and larger do not react morphologically to predatory threats. 相似文献
Environmental changes such as global warming can affect ecological communities by altering individual life histories and species interactions. Recent studies focusing on the consequences of environmental change on species interactions highlighted the need for a wider, multi‐species context including both trophic and non‐trophic interactions (e.g. predator interference). However, the effects of biotic and abiotic factors on trophic and non‐trophic interactions remain largely unexplored.
To fill this gap, we combined laboratory experiments and functional response modelling to investigate how temperature and prey density influence trophic and non‐trophic interactions in multiple predator communities.
The system under study consisted of predatory dragonfly larvae (Aeshna cyanea) and omnivorous marbled crayfish (Procambarus virginalis) preying on common carp fry (Cyprinus carpio). We estimated the functional response of each predator in single‐predator experiments and used this information to disentangle the trophic and non‐trophic interactions and their dependence on environmental conditions in multiple predator trials.
We found that consumer identity, prey density, and temperature all affect the magnitude of trophic and non‐trophic interactions. Non‐trophic interactions mostly decreased predator feeding rates, corroborating previous observations that interference prevails in aquatic communities. Moreover, trophic interactions depended primarily on the environmental variables whereas non‐trophic interactions depended mainly on consumer identity.
Our results indicate that non‐trophic interactions among true predators and omnivores can be substantial and that biotic and abiotic conditions further modify the magnitude and direction of these interactions, which can affect food web dynamics and stability.
In New Zealand and Australia, rural landowners believe that local predator control to protect indigenous biota exacerbates European rabbit Oryctolagus cuniculus problems on their land. We assess the validity of their concerns by reviewing the published literature on effects of predators on rabbit abundance.
In New Zealand, where rabbits and their predators are introduced, predators appear to have relatively little effect on rabbit numbers compared with other factors leading to mortality, such as disease, flooding of burrows and burrow collapse. Similarly, in Australia, rabbit numbers are driven primarily by climate and its effects on food abundance and quality, and by disease. However, where rabbit numbers are low following drought or major epizootics, predation can limit population recovery. In the Iberian Peninsula, where rabbits and their predators are indigenous, the effects of predators are unknown, as they are often confounded by other factors. Rabbit numbers are influenced mostly by habitat, food, disease and rainfall. Elsewhere in Europe, predators have their strongest effect when rabbit numbers have been reduced by other factors, but have little effect on high‐density rabbit populations.
In Australasia, abundance of predators (especially rabbit specialists) can usually be predicted from rabbit abundance, not vice versa. Although predation effects can be limiting under certain conditions, they are minor compared to the roles of climate, food, disease and habitat.
A key unresolved question is whether those circumstances where predator control might lead to increases in rabbit populations can be identified with enough certainty to allow reliable predictions to be generated. One approach is to implement robust rabbit, predator and disease monitoring programmes at sites with predator control operations. Data on changes in rabbits, predators, and disease prevalence could be combined with local data on other key factors to facilitate reasonable inference about effects of predators on rabbits. The inclusion of carefully matched non‐treatment areas is crucial if such programmes are to succeed.
Despite nearly a century of research, the causes of population cycles in Arvicoline rodents (voles and lemmings) in northern latitudes are not yet fully understood. Theory tells us that delayed density‐dependent feedback mechanisms are essential for rodent population cycles, suggesting vegetation–rodent, rodent–parasite or rodent–predator interactions as the most likely drivers of population cycles.
However, food provisioning, carried out either indirectly through fertilisation treatments of the habitat or directly through food supplementation, has failed to alter population cycles substantially, suggesting that variation in food supply by itself is not necessary or sufficient to cause cyclic fluctuations in abundance.
Predator exclusion experiments conducted in Fennoscandia have succeeded in slowing population crashes and increasing autumn densities, implicating predation as the most likely cause of rodent cycles in this region. However, experimental removal of specialist predators in northern England had no discernible effect on a cyclic vole population, casting doubt on the notion that predation is a necessary explanation of rodent population cycles.
Population cycle research has contributed substantially to our current understanding of the dynamics, regulation and persistence of biological populations, but we do not yet know with certainty what factors or processes cause multiannual population fluctuations or if population cycles are driven by the same mechanisms everywhere. Recent theoretical and empirical studies suggest that extrinsic factors (primarily food supply and predator abundance) may interact with population intrinsic processes (e.g. dispersal, social behaviour, stress response) to cause multiannual population fluctuations and to explain biological attributes of rodent population cycles.
Solving the enigma of population cycles may necessitate identifying factors and processes that cause phase‐specific demographic changes and performing conclusive experiments to ascertain the mechanisms that generate multiannual density fluctuations.
Both theoretical and laboratory research suggests that many prey animals should live in a solitary, dispersed distribution unless they lack repellent defences such as toxins, venoms and stings. Chemically defended prey may, by contrast, benefit substantially from aggregation because spatial localization may cause rapid predator satiation on prey toxins, protecting many individuals from attack. If repellent defences promote aggregation of prey, they also provide opportunities for new social interactions; hence the consequences of defence may be far reaching for the behavioural biology of the animal species. There is an absence of field data to support predictions about the relative costs and benefits of aggregation. We show here for the first time using wild predators that edible, undefended artificial prey do indeed suffer heightened death rates if they are aggregated; whereas chemically defended prey may benefit substantially by grouping. We argue that since many chemical defences are costly to prey, aggregation may be favoured because it makes expensive defences much more effective, and perhaps allows grouped individuals to invest less in chemical defences. 相似文献
For the present study, we investigated the prey of Polistes rothneyi koreanus, which is the most common social wasp in South Korea, and the relationship between prey diversity and vegetation cover around their nests. Prey was collected over two 6‐hr sampling from seven nests between July and mid‐August 2015 in Daegu, Gyeongsan and Gunwi in South Korea. To analyse the prey spectrum, we identified species using DNA barcodes; to analyse vegetation cover, we used the normalized difference vegetation index in a 200 m radius around the nests. A total of 338 prey samples were collected, and eight orders, 24 families, and 65 species were identified, demonstrating a much broader prey spectrum than those previously recorded for Polistes spp. Lepidoptera were the most prevalent, with 158 samples and 47 species. Nest 7, located in a rural area, had the highest numbers of samples and species per worker (5.2 and 1.9, respectively). Lepidoptera accounted for over half of the prey spectrum for all nests, and the families Noctuidae and Geometridae accounted for 60% of all Lepidoptera. Tenodera sinensis (Mantodea) and Gabala argentata (Noctuidae) were the most ubiquitous species, collected at five locations. Six species and some genera of prey are designated as pests in South Korea, indicating that P. r. koreanus also has a beneficial role in pest control. A higher vegetation cover was associated with significantly higher prey species diversity (R2 = .4597, p < .1) and abundance (R2 = .5986, p < .05), indicating that vegetation cover is an important factor for maintaining colonies. Therefore, the recent increase in green spaces in South Korean cities is probably a major contributor to the increased density of social wasps. 相似文献
In birds, little is known about how the presence of predators alters parental food distribution decisions among nestlings. We found that experimentally increasing perceived predation risk changed parental care in female but not in male Great Tits Parus major. Females fed the lightest and average nestlings at similar rates under control conditions when predation risk was not manipulated but ignored the lightest nestling under increased perceived predation risk. Moreover, females reduced the duration of nest visits greatly after encountering a model predator, suggesting that the perception of predators may facilitate brood reduction mechanisms. 相似文献
