| scholarly article | Q13442814 |
| P50 | author | Johanna Mappes | Q6216397 |
| Ossi Nokelainen | Q57019581 | ||
| Carita Lindstedt | Q87929022 | ||
| Janne K Valkonen | Q89877962 | ||
| P2860 | cites work | Predation, apparent competition, and the structure of prey communities | Q28248676 |
| Fluctuating selection: the perpetual renewal of adaptation in variable environments | Q28748404 | ||
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| Predator learning favours mimicry of a less-toxic model in poison frogs | Q33993997 | ||
| Warning signals, receiver psychology and predator memory | Q34046995 | ||
| Wright's shifting balance theory and the diversification of aposematic signals | Q34217640 | ||
| Spatial heterogeneity, predator cognition, and the evolution of color polymorphism in virtual prey | Q34480153 | ||
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| Probing the adaptive landscape using experimental islands: density-dependent natural selection on lizard body size | Q34627041 | ||
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| Disruptive selection and then what? | Q36477493 | ||
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| Biases in signal evolution: learning makes a difference. | Q36767245 | ||
| The role of predator selection on polymorphic aposematic poison frogs | Q37133609 | ||
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| Positive frequency-dependent selection on warning color in Alpine leaf beetles. | Q46437173 | ||
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| Evolution of Diversity in Warning Color and Mimicry: Polymorphisms, Shifting Balance, and Speciation | Q55952590 | ||
| Reactions of passerine birds to aposematic and non-aposematic firebugs (Pyrrhocoris apterus ; Heteroptera) | Q56168434 | ||
| Can aposematic signals evolve by gradual change? | Q56432061 | ||
| Specific Hypotheses on the Geographic Mosaic of Coevolution | Q56602294 | ||
| Receiver psychology and the evolution of animal signals | Q56608232 | ||
| The spatial pattern of natural selection when selection depends on experience | Q57893137 | ||
| Tracking the evolution of warning signals | Q59099071 | ||
| Shift happens! Shifting balance and the evolution of diversity in warning colour and mimicry | Q59321283 | ||
| P433 | issue | 3 | |
| P921 | main subject | warning signal | Q2549582 |
| predation | Q170430 | ||
| Arctiidae | Q15043775 | ||
| P304 | page(s) | 598-605 | |
| P577 | publication date | 2014-01-24 | |
| P1433 | published in | Journal of Animal Ecology | Q1709829 |
| P1476 | title | Changes in predator community structure shifts the efficacy of two warning signals in arctiid moths | |
| P478 | volume | 83 |
| Q59141428 | Abrupt Geographical Transition between Aposematic Color Forms in the SpittlebugProsapia ignipectus(Fitch) (Hemiptera: Cercopidae) |
| Q46851005 | Antagonistic evolution in an aposematic predator-prey signaling system |
| Q59024293 | Aposematism in the burying beetle? Dual function of anal fluid in parental care and chemical defense |
| Q41032877 | Aposematism: balancing salience and camouflage. |
| Q38969409 | Avoidance of an aposematically coloured butterfly by wild birds in a tropical forest |
| Q38791378 | Behavioural, ecological, and evolutionary aspects of diversity in frog colour patterns |
| Q40793600 | Colour polymorphism torn apart by opposing positive frequency-dependent selection, yet maintained in space. |
| Q91252814 | Correlates of color polymorphism in coconut crabs Birgus latro |
| Q40619161 | Costs and benefits of plant allelochemicals in herbivore diet in a multi enemy world. |
| Q35803042 | Diversity in Müllerian mimicry: The optimal predator sampling strategy explains both local and regional polymorphism in prey |
| Q57167333 | Diversity in warning coloration: selective paradox or the norm? |
| Q41695959 | Does spatial variation in predation pressure modulate selection for aposematism? |
| Q57486036 | Environment-dependent attack rates of cryptic and aposematic butterflies |
| Q92786084 | Evaluating responses to temperature during pre-metamorphosis and carry-over effects at post-metamorphosis in the wood tiger moth (Arctia plantaginis) |
| Q41989341 | Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression |
| Q33669819 | Experimental evidence suggests that specular reflectance and glossy appearance help amplify warning signals. |
| Q90014206 | Gray plumage color is more cryptic than brown in snowy landscapes in a resident color polymorphic bird |
| Q89763207 | How do predators generalize warning signals in simple and complex prey communities? Insights from a videogame |
| Q52486607 | How to fight multiple enemies: target-specific chemical defences in an aposematic moth. |
| Q97533390 | Interactions in multi-pattern Müllerian communities support origins of new patterns, false structures, imperfect resemblance and mimetic sexual dimorphism |
| Q52868934 | Maintaining mimicry diversity: optimal warning colour patterns differ among microhabitats in Amazonian clearwing butterflies. |
| Q64252655 | Mimicry in viceroy butterflies is dependent on abundance of the model queen butterfly |
| Q57467426 | No evidence of quantitative signal honesty across species of aposematic burnet moths (Lepidoptera: Zygaenidae) |
| Q98224109 | Out in the open: behavior's effect on predation risk and thermoregulation by aposematic caterpillars |
| Q57248117 | Phenology of Predation on Insects in a Tropical Forest: Temporal Variation in Attack Rate on Dummy Caterpillars |
| Q34348676 | Seasonal changes in predator community switch the direction of selection for prey defences. |
| Q35687513 | Signal honesty and predation risk among a closely related group of aposematic species |
| Q89796045 | Social learning within and across predator species reduces attacks on novel aposematic prey |
| Q57551786 | Social transmission of avoidance among predators facilitates the spread of novel prey |
| Q42001669 | Temporal relationship between genetic and warning signal variation in the aposematic wood tiger moth (Parasemia plantaginis). |
| Q38680479 | The current and future state of animal coloration research |
| Q46366273 | The role of rare morph advantage and conspicuousness in the stable gold-dark colour polymorphism of a crater lake Midas cichlid fish. |
| Q53515426 | Visual illusions in predator-prey interactions: birds find moving patterned prey harder to catch. |
| Q36325850 | Warning coloration can be disruptive: aposematic marginal wing patterning in the wood tiger moth |
| Q93086423 | Weak warning signals can persist in the absence of gene flow |
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