Changes in olfactory-mediated behaviour caused by elevated CO(2) levels in the ocean could affect recruitment to reef fish populations because larval fish become more vulnerable to predation. However, it is currently unclear how elevated CO(2) will impact the other key part of the predator-prey interaction--the predators. We investigated the effects of elevated CO(2) and reduced pH on olfactory...

Plant resistance and predation have strong independent and interacting eff ects on herbivore survival, behavior, and patterns of herbivory. Historically, research has emphasized variation in the consumption of herbivores by enemies. Recent work, however, demonstrates that predators also elicit important changes in the traits of their prey, but we do not know how this is infl uenced by plant qua...

Discussions of intraguild predation (IGP) have assumed that the nutritional quality of intraguild (IG) prey is similar to that of any other prey available to the IG predator. It has been suggested therefore that generalist predators do not distinguish between healthy and parasitized aphids and thus function as facultative predators of parasitoids. More recent studies have shown that predators m...

Heteropteran predators constitute an important component of predatory guilds in terrestrial and aquatic ecosystems. Most heteropteran species have generalist diets, and intraguild predation has been documented in most heteropteran families. Zoophytophagous species also frequently engage in intraguild interactions. An increase in extraguild prey density is often predicted to reduce intraguild pr...

Paradigms of sustainable exploitation focus on population dynamics of prey and yields to humanity but ignore the behavior of humans as predators. We compared patterns of predation by contemporary hunters and fishers with those of other predators that compete over shared prey (terrestrial mammals and marine fishes). Our global survey (2125 estimates of annual finite exploitation rate) revealed t...

Anticoagulant rodenticides may pose a secondary poisoning hazard to non-target predators and scavengers because of the time-delay between ingestion of a lethal dose and death of a target rodent. We investigated some pre-lethal effects of an anticoagulant rodenticide on the behaviour of wild rats in cages and in enclosures. We found that social interactions shortened time to death, that most rat...

In this paper we consider a prey population that gathers in herds, together with its interactions with predators. The latter are affected by a disease, and only the healthy individuals hunt. The defensive attitude of the prey is reflected in the fact that mostly the individuals at the border of the herd suffer from the attacks of the predators. Equilibria and their stability are fully analysed....

Aim: To detect the induction of morphological and populational alterations on Ceriodaphnia cornuta concerning cyclomorphosis and population dynamic parameters as densities, fecundity rates, juveniles percentage, males presence and ephippia presence in the presence of predators; Methods: Two experiments were performed: Experiments with fishes fed on Ceriodaphnia cornuta – Experiment 1 – and “Fis...

The escape response of an organism is generally its last line of defense against a predator. Because the effectiveness of an escape varies with the approach behaviour of the predator, it should be advantageous for prey to alter their escape trajectories depending on the mode of predator attack. To test this hypothesis we examined the escape responses of a single prey species, the ground-dwellin...

This article examines the interaction between prey populations, juvenile predators, and adult predators. A mathematical model that considers adding food anti-predators was developed. The equilibria of existing system are has four points with conditions suitable for locale. Numerical simulations were carried out to describe dynamics solution. Based on numerical simulations, varying parameter cau...