The Otolithes ruber is considered a valuable fish in the Indo-West Pacific. Estimates of the Q/B ratio and parameters of equations to ‘predict’ Q/B values for O. ruber in northwestern part of the Persian Gulf and the effects of different age-groups (age 1 to 6 year) on prey are presented. The age and food item of O. ruber were recorded on data collected from monthly samplings by bottom tra...

The predation and searching efficiency of fourth instar of predatory C. septempunctata at various densities of mustard aphid, Lipaphis erysimi (Kaltenbach) and predator was investigated under laboratory conditions. The feeding rate of predatory stage decreased at increased prey- and predator densities. Highest percent (92.80%) prey consumption was observed at initial prey density and lowest per...

Scavenging (feeding on dead prey) has been demonstrated across a number of spider families, yet the implications of feeding on dead prey for the growth and development of individuals and population is unknown. In this study we compare the growth, development, and predatory activity of two species of spiders that were fed on live and dead prey. Pardosa astrigera (Lycosidae) and Hylyphantes grami...

Prey selection is a key factor shaping animal populations and evolutionary dynamics. An optimal forager should target prey that offers the highest benefits in terms of energy content at the lowest costs. Predators are therefore expected to select for prey of optimal size. Stalking predators do not pursue their prey long, which may lead to a more random choice of prey individuals. Due to difficu...

A predator’s per capita feeding rate on prey, or its functional response, provides a foundation for predator–prey theory. Since 1959, Holling’s prey-dependent Type II functional response, a model that is a function of prey abundance only, has served as the basis for a large literature on predator–prey theory. We present statistical evidence from 19 predator–prey systems that three predator-depe...

Traditionally, predator switching has been assumed to be a stabilizing force in ecological systems. Recent work, however, has shown that predator switching can be either stabilizing or destabilizing. Most models of predator switching, to date, assume that prey are behaviorally passive and do not respond to predators. We allowed prey to respond behaviorally to predators, so as to avoid capture, ...

Predator-prey relationships are a central component of community dynamics. Classic approaches have tried to understand and predict these relationships in terms of consumptive interactions between predator and prey species, but characterizing the interaction this way is insufficient to predict the complexity and context dependency inherent in predator-prey relationships. Recent approaches have b...

Predators can have remote effects on prey populations that are connected by migration (i.e. prey metapopulations) because predator-mediated changes in prey behavior and abundance effectively transmit the impact of predators into predator-free prey populations. Behavioral changes in prey that might give rise to remote effects are altered rates of migration or activity in the presence of predatio...

Spider orb-webs are the ultimate anti-ballistic devices, capable of dissipating the relatively massive kinetic energy of flying prey. Increased web size and prey stopping capacity have co-evolved in a number orb-web taxa, but the selective forces driving web size and performance increases are under debate. The rare, large prey hypothesis maintains that the energetic benefits of rare, very large...