The effects of the expected predation rate on population dynamics have been studied intensively, but little is known about the effects of predation rate variability (i.e., predator individuals having variable foraging success) on population dynamics. In this study, variation in foraging success among predators was quantified by observing the predation of the wolf spider Pardosa pseudoannulata o...

I studied the population structure and dynamics of the collared lemming, Dicrostonyx groenlandicus Traill, on Traill Island (NE Greenland) in 1998 to 2000. This is the first comprehensive study of a Greenlandic collared lemming population. During this period, population density continuously declined ( 100 fold-decrease) from more than 10 ind/ha (peak year 1998) to less than 0.1 ind/ha (low year...

To effectively balance investment in predator defenses versus other traits, organisms must accurately assess predation risk. Chemical cues caused by predation events are indicators of risk for prey in a wide variety of systems, but the relationship between how prey perceive risk in relation to the amount of prey consumed by predators is poorly understood. While per capita predation rate is ofte...

Foraging parasitoids often must estimate local risk of predation just as they must estimate local patch value. Here, we investigate the effects a generalist predator Chlaenius bioculatus (Coleoptera: Carabidae), has on the oviposition behavior and the patch residence decisions of a solitary parasitoid Meteorus pulchricornis (Hymenoptera: Braconidae) in response to the varying host quality of Sp...

It is widely held that herbivore growth and production is limited by dietary nitrogen (N) that in turn constrains ecosystem elemental cycling. Yet, emerging evidence suggests that this conception of limitation may be incomplete, because chronic predation risk heightens herbivore metabolic rate and shifts demand from N-rich proteins to soluble carbohydrate-carbon (C). Because soluble C can be li...

Predation is thought to shape the macroscopic properties of animal groups, making moving groups more cohesive and coordinated. Precisely how predation has shaped individuals' fine-scale social interactions in natural populations, however, is unknown. Using high-resolution tracking data of shoaling fish (Poecilia reticulata) from populations differing in natural predation pressure, we show how p...

The grapsid crabs Chasmagnathus granulata and Cyrtograpsus angulatus are considered as key species within the benthic communities of estuaries and brackish coastal lagoons in the southwestern Atlantic region. In controlled laboratory experiments, we studied the intensity of interspecific predation as well as intraand intercohort cannibalism in setllers in relation to refuge Ž . availability, pr...

We investigated predation rates of small copepods, primarily species of Oithona, on microprotozooplankton and net growth rates of these prey at several locations in the Ross Sea, Antarctica, during an austral summer (January 1997; US JGOFS Process Study II). Ciliates, particularly non-loricate ciliates, contributed substantially to the carbon ration of Oithona spp., averaging 90% body Cd~1, whi...

Signaling individuals must effectively capture and hold the attention of intended conspecific receivers while limiting eavesdropping by potential predators. A possible mechanism for achieving this balance is for individuals to modulate the physical properties of their signals or to alter the proportion of time spent signaling, depending upon local levels of predation pressure. We test the hypot...

Many air-breathing aquatic foragers may be killed by aerial or subsurface predators while recovering oxygen at the surface; yet the influence of predation risk on time allocation during dive cycles is little known in spite of numerous studies on optimal diving. We modeled diving behavior under the risk of predation at the surface. The relationship between time spent at the surface and the risk ...