How evolution may mitigate the effects of global warming and pesticide exposure on predator-prey interactions is directly relevant for vector control. Using a space-for-time substitution approach, we addressed how 4°C warming and exposure to the pesticide endosulfan shape the predation on Culex pipiens mosquitoes by damselfly predators from replicated low- and high-latitude populations. Althoug...

Predation on planktonic larval stages is frequently a major source of mortality for the offspring of benthic marine invertebrates. Mortality rate likely varies with larval size and developmental stage, but few experiments have measured how these factors affect predation rates. I used experimental reductions in egg size to test how variation in larval size affects the likelihood of predation dur...

John J. Meyer* and James E. Byers Department of Zoology, University of New Hampshire, 46 College Road, Durham, NH 03824, USA *Corresponding: E-mail: [email protected] Abstract Although ecologists have speculated that sublethal predation can impact prey dynamics, consequences of these predator effects have seldom been experimentally tested. In softsediment marine communities, fishes crop extended ...

Initially, aposematism, which is an unprofitable trait, e.g. noxiousness conspicuously advertised to predators, appears to be a paradox since conspicuousness should increase predation by naive predators. However, reluctance of predators for eating novel prey (e.g. neophobia) might balance the initial predation caused by inexperienced predators. We tested the novelty effects on initial predation...

Ecological character displacement is common in nature but the mechanisms causing divergence are not well understood. The contributions of ecological interactions other than competition have received little attention. We conducted a pond experiment to explore the contribution of both competition and predation to character divergence in threespine stickleback species. We estimated the strength of...

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 ph...

http://dx.doi.org/10.1016/j.anbehav.2017.03.020 0003-3472/© 2017 The Association for the Study of A Predator mimicry occurs when prey resemble their predator to gain protection. We explored the relative importance of the morphological and locomotor signals that spider-mimicking moths use to deceive their jumping spider predators. Two hypotheses explain why animals use multicomponent signals for...

Anti-predator responses by ungulates can be based on habitat features or on the near-imminent threat of predators. In dense forest, cues that ungulates use to assess predation risk likely differ from half-open landscapes, as scent relative to sight is predicted to be more important. We studied, in the Białowieża Primeval Forest (Poland), whether perceived predation risk in red deer (Cervus elap...

Refugia can affect predator-prey dynamics via movements between refuge and non-refuge areas. We examine the influence of a refuge on population dynamics in a large mammal predator-prey system. Wolves (Canis lupus) have recolonized much of their former range in North America, and as a result, ungulate prey have exploited refugia to reduce predation risk with unknown impacts on wolf-prey dynamics...

The life history and predation rate were determined for all stages of female and male of Phytoseiulus persimilis Athias-Henriot fed on the eggs of Tetranychus urticae Koch ˗ as the preferred prey-stage ˗ on rose (cv ‘blarodje’) leaf discs under laboratory conditions at 25±1°C, 75±5% RH, and 16 L: 8 D hour photoperiod. According to the age-stage, two-sex life table model, the intrinsic rate of i...