We measured maximal oxygen consumption (VO(2max)) and burst speed in populations of Trinidadian guppies (Poecilia reticulata) from contrasting high- and low-predation habitats but reared in "common garden" conditions. We tested two hypothesis: first, that predation, which causes rapid life-history evolution in guppies, also impacts locomotor physiology, and second, that trade-offs would occur b...

Predation is a major factor driving evolution, and organisms have evolved adaptations increasing their survival chances. However, most defenses incur trade-offs between benefits and costs. Many organisms save costs by employing inducible defenses as responses to fluctuating predation risk. The level of defense often increases with predator densities. However, individual predation risk should no...

Questions: Are prey animals’ behavioural responses against predation associated with their ability to resist parasites and pathogens, and if so, how is this adjusted in different populations? Methods: We studied the association between anti-predator behaviour and immune defence (encapsulation response and lytic activities of the haemolymph) using laboratory-reared male field crickets originatin...

The hypothesis that size-selective predation and species-specific prey behaviours facilitate the coexistence between larvae of invasive Aedes albopictus (Skuse) and U.S.A.-native Ochlerotatus triseriatus (Say) was tested experimentally with the predator Corethrella appendiculata (Grabham).Larval behaviours associated with a higher risk of predation were identified, and prey behavioural response...

Limitations of phenotypic plasticity affect the success of individuals and populations in changing environments. We assessed the plasticity-history limitation on predator-induced defenses in anurans (Wood Frogs, Lithobates sylvaticus (LeConte, 1825), and Northern Leopard Frogs, Lithobates pipiens (Schreber, 1782)), predicting that plastic responses to predation risk by dragonfly larvae (family ...

Indirect effects of insect control strategies on weed populations are important to consider when developing robust integrated pest management strategies. Weed seed predation rates were investigated in corn managed under three contrasting treatments based on control practices for corn rootworm: (1) the transgenic crop Cry3Bb Bt corn, (2) the broad-spectrum insecticide tefluthrin, and (3) no inse...

Risk of predation is an evolutionary force that affects behaviors of virtually all animals. In this study, we examined how habitat selection by roe deer was affected by risk of predation by Eurasian lynx - the main predator of roe deer in Scandinavia. Specifically, we compared how habitat selection by roe deer varied (1) before and after lynx re-established in the study area and (2) in relation...

To begin identifying what behavioral details might be needed to characterize community dynamics and stability, we examined the effect of prey behavioral responses to predation risk on community dynamics and stability. We considered the case of prey altering their foraging effort to trade off energy gain and predation risk. We used state-dependent dynamic optimization to calculate the optimal tr...

Nest predation is the principal cause of mortaliv for many grassland birds. Predation rates may be higher on prairie dog colonies because they may have less available nesting cover and may increase predator abundance. We compared 14-day nest predation rates for 1,764 artificial nests on 102 black-tailed prairie dog (Cynovnys ludovicianus) colonies and their paired off-colony sites (similar habi...

This paper studies the practice of semi-domestic reindeer (Rangifer t. tarandus) herding in Finnmark county in northern Norway. In this area, the Saami reindeer herders compete for space and grazing areas and keep large herds, while at the same time, the reindeer population is heavily exposed to carnivore predation by the lynx (Lynx lynx), the wolverine (Gulo gulo), and the golden eagle (Aquila...