Consumer-food systems: why type I functional responses are exclusive to filter feeders.
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Merging resource availability with isotope mixing models: the role of neutral interaction assumptionsNumerical and functional responses of forest bats to a major insect pest in pine plantations.The allometry of prey preferences.Emergent effects of multiple predators on prey survival: the importance of depletion and the functional response.Estimating nonlinear interaction strengths: an observation-based method for species-rich food webs.Predator confusion is sufficient to evolve swarming behaviourModifying modifiers: what happens when interspecific interactions interact?Feeding on multiple sources: towards a universal parameterization of the functional response of a generalist predator allowing for switching.Dome-shaped functional response induced by nutrient imbalance of the prey.Functional Responses of Retaliatory Killing versus Recreational Sport Hunting of Leopards in South Africa.Eco-evolutionary experience in novel species interactions.Density-dependent adjustment of inducible defenses.On the context-dependent scaling of consumer feeding rates.Predator diversity and environmental change modify the strengths of trophic and nontrophic interactions.How patch size and refuge availability change interaction strength and population dynamics: a combined individual- and population-based modeling experiment.Non-linear feeding functional responses in the Greater Flamingo (Phoenicopterus roseus) predict immediate negative impact of wetland degradation on this flagship species.Habitat structure alters top-down control in litter communities.Combining indoor and outdoor methods for controlling malaria vectors: an ecological model of endectocide-treated livestock and insecticidal bed nets.Bayesian characterization of uncertainty in species interaction strengths.The numerical and functional responses of a granivorous rodent and the fate of Neotropical tree seeds.The adaptation of generalist predators' diet in a multi-prey context: insights from new functional responses.Network structural properties mediate the stability of mutualistic communities.How do biting disease vectors behaviourally respond to host availability?When is a type III functional response stabilizing? Theory and practice of predicting plankton dynamics under enrichment.Linear functional response by two pupal Drosophila parasitoids foraging within single or multiple patch environments.Intermittency in processing explains the diversity and shape of functional grazing responses.Improving the assessment of predator functional responses by considering alternate prey and predator interactions.Hydra effects in stable communities and their implications for system dynamics.The functional response predicts the effect of resource distribution on the optimal movement rate of consumers.Predator-dependent functional response in wolves: from food limitation to surplus killing.Increasing temperature decreases the predatory effect of the intertidal shanny Lipophrys pholis on an amphipod prey.Body size, body size ratio, and prey type influence the functional response of damselfly nymphs.Delousing efficiency of farmed ballan wrasse (Labrus bergylta) against Lepeophtheirus salmonis infecting Atlantic salmon (Salmo salar) post-smolts.The functional response of a hoarding seed predator to mast seeding.Tracking and forecasting ecosystem interactions in real time.Harvesting creates ecological traps: consequences of invisible mortality risks in predator-prey metacommunities.Meta-ecosystem dynamics and functioning on finite spatial networks.Estimating interaction strengths in nature: experimental support for an observational approach.Type III functional response in Daphnia.The top-down mechanism for body-mass-abundance scaling.
P2860
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P2860
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
@ast
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
@en
type
label
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
@ast
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
@en
prefLabel
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
@ast
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
@en
P2860
P1433
P1476
Consumer-food systems: why type I functional responses are exclusive to filter feeders.
@en
P2093
Michael Kopp
Ralph Tollrian
P2860
P304
P356
10.1017/S1464793103006286
P577
2004-05-01T00:00:00Z