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Cognition and the evolution of camouflageVariation in cyanogenic compounds concentration within a Heliconius butterfly community: does mimicry explain everything?THE EFFECTS OF PREDATOR LEARNING, FORGETTING, AND RECOGNITION ERRORS ON THE EVOLUTION OF WARNING COLORATIONCommunity structure and the evolution of aposematic colorationThe benefits of being toxic to deter predators depends on prey body size.Warning color changes in response to food deprivation in the pipevine swallowtail butterfly, Battus philenorExperimental evidence suggests that specular reflectance and glossy appearance help amplify warning signals.Strong antiapostatic selection against novel rare aposematic prey.The evolution of inaccurate mimics.Rapid population divergence linked with co-variation between coloration and sexual display in strawberry poison frogs.Comparative tests of evolutionary trade-offs in a palinurid lobster acoustic system.The functional significance of aposematic signals: geographic variation in the responses of widespread lizard predators to colourful invertebrate prey.The signal environment is more important than diet or chemical specialization in the evolution of warning colorationWarning coloration can be disruptive: aposematic marginal wing patterning in the wood tiger moth.Artificial neural networks and the study of evolution of prey colorationImpact of Consuming 'Toxic' Monarch Caterpillars on Adult Chinese Mantid Mass Gain and Fecundity.Fearful symmetry in aposematic plants.Deimatism: a neglected component of antipredator defence.Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression.Müllerian mimicry in aposematic spiny plants.Conspicuous visual signals do not coevolve with increased body size in marine sea slugs.Global shape and pH stability of ovorubin, an oligomeric protein from the eggs of Pomacea canaliculata.Batesian mimics influence the evolution of conspicuousness in an aposematic salamander.Plant biological warfare: thorns inject pathogenic bacteria into herbivores.Color polymorphism in a land snail Cepaea nemoralis (Pulmonata: Helicidae) as viewed by potential avian predators.Toxin constraint explains diet choice, survival and population dynamics in a molluscivore shorebird.The importance of the ontogenetic niche in resource-associated divergence: evidence from a generalist grasshopper.ARE WARNING COLORS HANDICAPS?Aposematism and crypsis combined as a result of distance dependence: functional versatility of the colour pattern in the swallowtail butterfly larva.Trade-off between warning signal efficacy and mating success in the wood tiger moth.Higher survival of an aposematic than of a cryptic form of a distasteful bug.PERSPECTIVE: THE EVOLUTION OF WARNING COLORATION IS NOT PARADOXICALChinese mantids gut toxic monarch caterpillars: avoidance of prey defence?Can aposematic signals evolve by gradual change?The evolution of warning signalsINTEGRATING PREY DEFENSIVE TRAITS: CONTRASTS OF MARINE WORMS FROM TEMPERATE AND TROPICAL HABITATSBetter to be bimodal: the interaction of color and odor on learning and memoryDoes aggression and explorative behaviour decrease with lost warning coloration?Müllerian mimicry: an examination of Fisher's theory of gradual evolutionary changePost-attack Aposematic Display in Prey Facilitates Predator Avoidance Learning
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P2860
description
article publié dans la revue scientifique Nature
@fr
scientific article published in Nature
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в Nature в липні 1980
@uk
name
Why are distasteful prey not cryptic?
@en
Why are distasteful prey not cryptic?
@nl
type
label
Why are distasteful prey not cryptic?
@en
Why are distasteful prey not cryptic?
@nl
prefLabel
Why are distasteful prey not cryptic?
@en
Why are distasteful prey not cryptic?
@nl
P356
P1433
P1476
Why are distasteful prey not cryptic?
@en
P2093
John L. Gittleman
Paul H. Harvey
P2888
P304
P356
10.1038/286149A0
P407
P577
1980-07-01T00:00:00Z
P6179
1051881770