Incorporating anthropogenic effects into trophic ecology: predator–prey interactions in a human-dominated landscape

Apex predators perform important functions that regulate ecosystems worldwide. However, little is known about how ecosystem regulation by predators is influenced by human activities. In particular, how important are top-down effects of predators relative to direct and indirect human-mediated bottom-up and top-down processes? Combining data on species'' occurrence from camera traps and hunting records, we aimed to quantify the relative effects of top-down and bottom-up processes in shaping predator and prey distributions in a human-dominated landscape in Transylvania, Romania. By global standards this system is diverse, including apex predators (brown bear and wolf), mesopredators (red fox) and large herbivores (roe and red deer). Humans and free-ranging dogs represent additional predators in the system. Using structural equation modelling, we found that apex predators suppress lower trophic levels, especially herbivores. However, direct and indirect top-down effects of humans affected the ecosystem more strongly, influencing species at all trophic levels. Our study highlights the need to explicitly embed humans and their influences within trophic cascade theory. This will greatly expand our understanding of species interactions in human-modified landscapes, which compose the majority of the Earth''s terrestrial surface.     

Non-additive effects of macrophyte cover and turbidity on predator–prey interactions involving an invertivorous fish and different prey types

Habitat complexity, turbidity and prey type availability affect trophic dynamics, and an improved understanding of how these three factors work together could facilitate interpretations of trophic dynamics in environments with regime shifts. We conducted an experiment to cross these three factors, hypothesising that increasing both turbidity and macrophyte cover reduce consumption of Chironomids more than they reduce consumption of Cypridids. Our results did not support our hypothesis, suggesting that the effect of macrophyte cover on predation depends on turbidity. However, the magnitude of this combined effect is the same as that of turbidity alone. Moreover, turbidity affected predation on both prey types similarly. In addition, the effect of macrophyte cover on predation also depended on prey type. We argue that visual and physical refuges may be as effective as shelter, but macrophyte cover may benefit smaller prey items. This may lead to higher predation rates by small-sized fish on invertebrates during periods of low turbidity devoid of macrophyte cover and to similar predation rates on invertebrates during periods of low turbidity and abundant macrophytes, high turbidity and scarce macrophytes or high turbidity and abundant macrophyte cover.     

The effect of learning and search images on predator–prey interactions

In dealing with the spatial and temporal variability of prey species, predators may be able to forage optimally if they have flexible and rapid behavioral plasticity rather than predetermined responses. For predators that learn to focus attention on the cryptic prey type most frequently encountered during recent searching (termed a “search image”), rare prey types may be overlooked because of a focus on more common prey. Search imaging reflects biased searching for one of a number of available prey types, and has been studied widely in birds and mammals. Here we discuss the significant implications of this phenomenon for insect predator–prey systems, particularly with respect to parasitic wasps searching for host species using learned olfactory cues. We (1) review studies about perceptual development through individual ontogeny, (2) define the term “search image” and discuss the cognitive mechanisms involved in search-image formation, (3) discuss the role of search images and frequency-dependent predation as a proximate mechanism in the maintenance of prey diversity, (4) examine data on host–parasitoid olfactory search imaging, and (5) conclude by identifying important research areas for future studies in the field of olfactory search images.     

Potential impact of temperature change on epibenthic predator–bivalve prey interactions in temperate estuaries

Temperate estuaries are indispensable as refuelling areas for long-distance shorebirds, where they depend on intertidal benthic fauna, such as bivalves, as food source. Bivalve recruitment is thought to be, at least partly, top-down regulated by epibenthic predators (the shrimp Crangon crangon and the crab Carcinus maenas) but this interaction is part of a complex predator–prey system since various fish species prey upon the crustaceans.     

Time optimal control of an additional food provided predator–prey system with applications to pest management and biological conservation

Use of additional food has been widely recognized by experimental scientists as one of the important tools for biological control such as species conservation and pest management. The quality and quantity of additional food supplied to the predators is known to play a vital role in the controllability of the system. The present study is continuation of a previous work that highlights the importance of quality and quantity of the additional food in the dynamics of a predator–prey system in the context of biological control. In this article the controllability of the predator–prey system is analyzed by considering inverse of quality of the additional food as the control variable. Control strategies are offered to steer the system from a given initial state to a required terminal state in a minimum time by formulating Mayer problem of optimal control. It is observed that an optimal strategy is a combination of bang-bang controls and could involve multiple switches. Properties of optimal paths are derived using necessary conditions for Mayer problem. In the light of the results evolved in this work it is possible to eradicate the prey from the eco-system in the minimum time by providing the predator with high quality additional food, which is relevant in the pest management. In the perspective of biological conservation this study highlights the possibilities to drive the state to an admissible interior equilibrium (irrespective of its stability nature) of the system in a minimum time.     

Metapopulation dynamics for spatially extended predator–prey interactions

Traditional metapopulation theory classifies a metapopulation as a spatially homogeneous population that persists on neighboring habitat patches. The fate of each population on a habitat patch is a function of a balance between births and deaths via establishment of new populations through migration to neighboring patches. In this study, we expand upon traditional metapopulation models by incorporating spatial heterogeneity into a previously studied two-patch nonlinear ordinary differential equation metapopulation model, in which the growth of a general prey species is logistic and growth of a general predator species displays a Holling type II functional response. The model described in this work assumes that migration by generalist predator and prey populations between habitat patches occurs via a migratory corridor. Thus, persistence of species is a function of local population dynamics and migration between spatially heterogeneous habitat patches. Numerical results generated by our model demonstrate that population densities exhibit periodic plane-wave phenomena, which appear to be functions of differences in migration rates between generalist predator and prey populations. We compare results generated from our model to results generated by similar, but less ecologically realistic work, and to observed population dynamics in natural metapopulations.     

Combined effects of environmental factors and predator–prey interactions on zooplankton assemblages in five high alpine lakes

The examination of a yearly cycle of plankton density (rotifer and microcrustacean) and of 419 stomach contents of four species of salmonid fishes, arctic charr, Salvelinus alpinus, brown trout, Salmo trutta, rainbow trout, Onchorynchus mykiss and lake trout, Salvelinus namaycush, living in five high altitude lakes in the French Alps, shows an impact of abiotic variates and the effects of predation on the composition of zooplankton assemblages. The lakes studied may be divided in two groups. The colder, Muzelle and Puy Vachier, are characterised by a low level of food resources, an important impact of predation, and the near absence of planktonic crustaceans. The second group, consisting of Lakes Les Pisses, Petarel and Palluel, is characterised by a low density rotifer assemblage and a more abundant crustacean population controlled by a low level of fish predation.     

A nonlocal kinetic model for predator–prey interactions

We extend the aggregation model from Fetecau (2011) by adding a field of vision to individuals and by including a second species. The two species, assumed to have a predator–prey relationship, have dynamics governed by nonlocal kinetic equations that include advection and turning. The latter is the main mechanism for aggregation and orientation, which results from interactions among individuals of the same species as well as predator–prey relationships. We illustrate numerically a diverse set of predator–prey behaviors that can be captured by this model. We show that a prey’s escape outcome depends on the social interactions between its group members, the prey’s field of vision and the sophistication of the predator’s hunting strategies.     

Assessing effects of radiation on abundance of mammals and predator–prey interactions in Chernobyl using tracks in the snow

To test whether radioactive contamination reduced the abundance of mammals, and whether species differed in susceptibility to radiation, we censused mammals by counting tracks in the snow along 161 100-m line transects around Chernobyl during February 2009. The abundance of mammal tracks was negatively related to level of background radiation, independent of the statistical model, with effects of radiation accounting for a third of the variance. The effect of radiation differed significantly among species. There was a positive relationship between abundance of predators and abundance of prey, modified by the level of background radiation because the number of predators increased disproportionately with the number of prey at high levels of radiation. These findings suggest that predatory mammals aggregate in areas with abundant prey, especially when prey are exposed to high levels of radiation. This study emphasizes the negative effects of level of background radiation on the abundance of mammals and predator–prey interactions.     

Influence of edge on predator–prey distribution and abundance

I investigated the effect of spatial configuration on distribution and abundance of invertebrate trophic groups by counting soil arthropods under boxes (21 × 9.5 cm) arranged in six different patterns that varied in the amount of edge (137–305 cm). I predicted fewer individuals from the consumer trophic group (Collembola) in box groups with greater amount of edge. This prediction was based on the assumption that predators (mites, ants, spiders, centipedes) select edge during foraging and thereby reduce abundance of the less mobile consumer group under box patterns with greater edge. Consumer abundance (Collembola) was not correlated with amount of edge. Among the predator groups, mite, ant and centipede abundance related to the amount of edge of box groups. However, in contrast to predictions, abundance of these predators was negatively correlated with amount of edge in box patterns. All Collembola predators, with the exception of ants, were less clumped in distribution than Collembola. The results are inconsistent with the view that predators used box edges to predate the less mobile consumer trophic group. Alternative explanations for the spatial patterns other than predator–prey relations include (1) a negative relationship between edge and moisture, (2) a positive relationship between edge and detritus decomposition (i.e. mycelium as food for the consumer group), and (3) a negative relationship between edge and the interstices between adjacent boxes. Landscape patterns likely affect microclimate, food, and predator–prey relations and, therefore, future experimental designs need to control these factors individually to distinguish among alternative hypotheses.     

The challenge of predicting temperature effects on short-term predator–prey dynamics

Understanding how interacting species respond to changing temperatures is complicated because both inter- and intraspecific processes can be temperature-dependent, and because the dynamics of interest often occur over short time scales. While efforts to document and integrate inter- and intraspecific effects are ongoing, few broad conclusions have emerged. Here, we use a simple structured predator–prey model to explore whether some such conclusions can be reached with incomplete knowledge about initial population sizes or about how temperature alters predation rates. We find that, despite strong sensitivity of quantitative predictions to the model’s details, qualitative predictions for how predator–prey communities respond to temperature may still be possible. As a case study, we ask whether biological control of the herbivorous insect pea aphid will be strengthened or weakened by increasing temperatures. Our empirically derived parameter estimates suggest biological control will be strengthened, but we caution that this result is not inevitable given what we currently know about the effects of temperature in this system. Our work highlights the complex interaction between inter- and intraspecific effects of temperature in ecological communities.     

Effect of prey type and inorganic turbidity on littoral predator–prey interactions in a shallow lake: an experimental approach

Predation often represents the prevailing process shaping aquatic ecosystems. As foraging and antipredatory behaviour frequently relate to vision, turbidity may often impair the interactions between the predator and its prey, depending on prey type and source and level of turbidity. We studied the effect of inorganic turbidity (0–30 NTU) on the effectiveness of fish feeding on two types of prey in different habitats: free-swimming cladoceran (Daphnia pulex) in open water and plant-associated cladoceran (Sida crystallina) attached to Nuphar lutea leaves. For the planktivore, we used vision-oriented perch (Perca fluviatilis) common in the littoral zone of temperate lakes. In our study, increasing inorganic turbidity did not appear to initiate any significant change in the feeding efficiency of perch on free-swimming Daphnia pulex. However, we saw a markedly different feeding efficiency when perch targeted plant-attached Sida crystallina. Our results substantiate that floating-leaved macrophytes in turbid lakes may provide a favourable habitat for plant-attached cladocerans.     

Effects of rapid prey evolution on predator–prey cycles

We study the qualitative properties of population cycles in a predator-prey system where genetic variability allows contemporary rapid evolution of the prey. Previous numerical studies have found that prey evolution in response to changing predation risk can have major quantitative and qualitative effects on predator-prey cycles, including: (1) large increases in cycle period, (2) changes in phase relations (so that predator and prey are cycling exactly out of phase, rather than the classical quarter-period phase lag), and (3) "cryptic" cycles in which total prey density remains nearly constant while predator density and prey traits cycle. Here we focus on a chemostat model motivated by our experimental system (Fussmann et al. in Science 290:1358-1360, 2000; Yoshida et al. in Proc roy Soc Lond B 424:303-306, 2003) with algae (prey) and rotifers (predators), in which the prey exhibit rapid evolution in their level of defense against predation. We show that the effects of rapid prey evolution are robust and general, and furthermore that they occur in a specific but biologically relevant region of parameter space: when traits that greatly reduce predation risk are relatively cheap (in terms of reductions in other fitness components), when there is coexistence between the two prey types and the predator, and when the interaction between predators and undefended prey alone would produce cycles. Because defense has been shown to be inexpensive, even cost-free, in a number of systems (Andersson et al. in Curr Opin Microbiol 2:489-493, 1999: Gagneux et al. in Science 312:1944-1946, 2006; Yoshida et al. in Proc Roy Soc Lond B 271:1947-1953, 2004), our discoveries may well be reproduced in other model systems, and in nature. Finally, some of our key results are extended to a general model in which functional forms for the predation rate and prey birth rate are not specified.     

Effects of the probability of a predator catching prey on predator–prey system stability

To understand the effect of the probability of a predator catching prey, P_catch, on the stability of the predator–prey system, a spatially explicit lattice model consisting of predators, prey, and grass was constructed. The predators and prey randomly move on the lattice space, and the grass grows according to its growth probability. When a predator encounters prey, the predator eats the prey in accordance with the probability P_catch. When a prey encounters grass, the prey eats the grass. The predator and prey give birth to offspring according to a birth probability after eating prey or grass, respectively. When a predator or prey is initially introduced or newly born, its health state is set at a high given value. This health state decreases by one with every time step. When the state of an animal decreases to less than zero, the individual dies and is removed from the system. Population densities for predator and prey fluctuated significantly according to P_catch. System stability was characterized by the standard deviation ? of the fluctuation. The simulation results showed that ? for predators increased with an increase of P_catch; ? for prey reached a maximum at P_catch = 0.4; and ? for grass fluctuated little regardless of P_catch. These results were due to the tradeoff between P_catch and the predator–prey encounter rate, which represents the degree of interaction between predator and prey and the average population density, respectively.     

Reciprocity in predator–prey interactions: exposure to defended prey and predation risk affects intermediate predator life history and morphology

A vast body of literature exists documenting the morphological, behavioural and life history changes that predators induce in prey. However, little attention has been paid to how these induced changes feed back and affect the predators’ life history and morphology. Larvae of the phantom midge Chaoborus flavicans are intermediate predators in a food web with Daphnia pulex as the basal resource and planktivorous fish as the top predator. C. flavicans prey on D. pulex and are themselves prey for fish; as D. pulex induce morphological defences in the presence of C. flavicans this is an ideal system in which to evaluate the effects of defended prey and top predators on an intermediate consumer. We assessed the impact on C. flavicans life history and morphology of foraging on defended prey while also being exposed to the non-lethal presence of a top fish predator. We tested the basic hypothesis that the effects of defended prey will depend on the presence or absence of top predator predation risk. Feeding rate was significantly reduced and time to pupation was significantly increased by defended morph prey. Gut size, development time, fecundity, egg size and reproductive effort respond to fish chemical cues directly or significantly alter the relationship between a trait and body size. We found no significant interactions between prey morph and the non-lethal presence of a top predator, suggesting that the effects of these two biological factors were additive or singularly independent. Overall it appears that C. flavicans is able to substantially modify several aspects of its biology, and while some changes appear mere consequences of resource limitation others appear facultative in nature.     

In hot water: effects of climate change on Vibrio–human interactions

Sea level rise and the anthropogenic warming of the world's oceans is not only an environmental tragedy, but these changes also result in a significant threat to public health. Along with coastal flooding and the encroachment of saltwater farther inland comes an increased risk of human interaction with pathogenic Vibrio species, such as Vibrio cholerae, V. vulnificus and V. parahaemolyticus. This minireview examines the current literature for updates on the climatic changes and practices that impact the location and duration of the presence of Vibrio spp., as well as the infection routes, trends and virulence factors of these highly successful pathogens. Finally, an overview of current treatments and methods for the mitigation of both oral and cutaneous exposures are presented.     

Effects of epibiosis on consumer–prey interactions

In many benthic communities predators play a crucialrole in the population dynamics of their prey. Surfacecharacteristics of the prey are important forrecognition and handling by the predator. Because theestablishment of an epibiotic assemblage on thesurface of a basibiont species creates a new interfacebetween the epibiotized organism and its environment,we hypothesised that epibiosis should have an impacton consumer–prey interactions. In separateinvestigations, we assessed how epibionts onmacroalgae affected the susceptibility of the latterto herbivory by the urchin Arbacia punctulataand how epibionts on the blue mussel Mytilusedulis affected its susceptibility to predation bythe shore crab Carcinus maenas.Some epibionts strongly affected consumer feedingbehavior. When epibionts were more attractive thantheir host, consumer pressure increased. Whenepibionts were less attractive than their host or whenthey were repellent, consumer pressure decreased. Insystems that are controlled from the top-down,epibiosis can strongly influence community dynamics.For the Carcinus/Mytilus system that westudied, the in situ distribution of epibiontson mussels reflected the epibiosis-determinedpreferences of the predator. Both direct and indirecteffects are involved in determining theseepibiont-prey–consumer interactions.