Search results for "APOSEMATISM"
showing 10 items of 124 documents
An aposematic colour‐polymorphic moth seen through the eyes of conspecifics and predators – Sensitivity and colour discrimination in a tiger moth
2018
Although predation is commonly thought to exert the strongest selective pressure on coloration in aposematic species, sexual selection may also influence coloration. Specifically, polymorphism in aposematic species cannot be explained by natural selection alone. Males of the aposematic wood tiger moth (Arctia plantaginis) are polymorphic for hindwing coloration throughout most of their range. In Scandinavia, they display either white or yellow hindwings. Female hindwing coloration varies continuously from bright orange to red. Redder females and yellow males suffer least from bird predation. White males often have higher mating success than yellow males. Therefore, we ask whether females ca…
Multimodal Aposematic Defenses Through the Predation Sequence
2021
Aposematic organisms warn predators of their unprofitability using a combination of defenses, including visual warning signals, startling sounds, noxious odors, or aversive tastes. Using multiple lines of defense can help prey avoid predators by stimulating multiple senses and/or by acting at different stages of predation. We tested the efficacy of three lines of defense (color, smell, taste) during the predation sequence of aposematic wood tiger moths (Arctia plantaginis) using blue tit (Cyanistes caeruleus) predators. Moths with two hindwing phenotypes (genotypes: WW/Wy = white, yy = yellow) were manipulated to have defense fluid with aversive smell (methoxypyrazines), body tissues with a…
Multiple modalities in insect warning displays have additive effects against wild avian predators
2019
Allocation to different components of defence has been suggested as an explanation for the existence of multiple aposematic morphs in a single population. We tested whether there are trade-offs between warning colouration and chemical defence or whether these have an additive effect when combined, using blue tits (Cyanistes caeruleus) as predators and the polymorphic wood tiger moth (Arctia plantaginis) as prey. We used artificial edible models (with and without the moths’ defensive fluids) with paper wings whose colour and pattern properties matched those of real moths. When the models were presented sans defensive fluids or when the fluids were presented without colour cues, we detected n…
Transparency reduces predator detection in mimetic clearwing butterflies
2019
International audience; Predation is an important selective pressure and some prey have evolved conspicuous warning signals that advertise unpalatability (i.e. aposematism) as an antipredator defence. Conspicuous colour patterns have been shown effective as warning signals, by promoting predator learning and memory. Unexpectedly, some butterfly species from the unpalatable tribe Ithomiini possess transparent wings, a feature rare on land but common in water, known to reduce predator detection.We tested if transparency of butterfly wings was associated with decreased detectability by predators, by comparing four butterfly species exhibiting different degrees of transparency, ranging from ful…
Safety in Numbers: How Color Morph Frequency Affects Predation Risk in an Aposematic Moth
2021
Polymorphic warning signals in aposematic systems are enigmatic because predator learning should favor the most common form, creating positive frequency-dependent survival. However, many populations exhibit variation in warning signals. There are various selective mechanisms that can counter positive frequency-dependent selection and lead to temporal or spatial warning signal diversification. Examining these mechanisms and their effects requires first confirming whether the most common morphs are favored at both local and regional scales. Empirical examples of this are uncommon and often include potentially confounding factors, such as a lack of knowledge of predator identity and behavior. …
The Effect of Predator Population Dynamics on Batesian Mimicry Complexes.
2022
Understanding Batesian mimicry is a classic problem in evolutionary biology. In Batesian mimicry, a defended species (the model) is mimicked by an undefended species (the mimic). Prior theories have emphasized the role of predator behavior and learning as well as evolution in model-mimic complexes but have not examined the role of population dynamics in potentially governing the relative abundances and even persistence of model-mimic systems. Here, we examined the effect of the population dynamics of predators and alternative prey on the prevalence of warning-signaling prey composed of models and mimics. Using optimal foraging theory and signal detection theory, we found that the inclusion …
Predator-Induced Plasticity on Warning Signal and Larval Life-History Traits of the Aposematic Wood Tiger Moth, Arctia plantaginis
2021
Correction Frontiers in Ecology and Evolution Volume 9 Article Number 737651 DOI 10.3389/fevo.2021.737651 Published JUL 29 2021 Predator-induced plasticity in life-history and antipredator traits during the larval period has been extensively studied in organisms with complex life-histories. However, it is unclear whether different levels of predation could induce warning signals in aposematic organisms. Here, we investigated whether predator-simulated handling affects warning coloration and life-history traits in the aposematic wood tiger moth larva, Arctia plantaginis. As juveniles, a larger orange patch on an otherwise black body signifies a more efficient warning signal against predators…
Can warning signals be honest? : wing colouration and the strength of chemical defence in the female wood tiger moth (Parasemia plataginis)
2016
The warning displays of aposematic organisms signal to predators that they possess a secondary defence and are unprofitable. Within species variation exists in the strength of the signal and defence. As natural selection is expected to favour higher levels of defence, variation in such traits requires explanation. One hypothesis is that the strength of primary and secondary defences are correlated as they reflect the condition of the signaller. This study explores if variation in individual conspicuousness is an honest signal of the level of defence in the wood tiger moth (Parasemia plantaginis). P. plantaginis has conspicuous hind wing warning colouration, which in females varies from yell…
Weak warning signals can persist in the absence of gene flow
2019
Aposematic organisms couple conspicuous warning signals with a secondary defense to deter predators from attacking. Novel signals of aposematic prey are expected to be selected against due to positive frequency-dependent selection. How, then, can novel phenotypes persist after they arise, and why do so many aposematic species exhibit intrapopulation signal variability? Using a polytypic poison frog (Dendrobates tinctorius), we explored the forces of selection on variable aposematic signals using 2 phenotypically distinct (white, yellow) populations. Contrary to expectations, local phenotype was not always better protected compared to novel phenotypes in either population; in the white popul…
Evolution of signal diversity: predator-prey interactions and the maintenance of warning colour polymorphism in the wood tiger moth Arctia plantaginis
2017
Aposematic organisms avoid predation by advertising defences with warning signals. The theory of aposematism predicts warning signal uniformity, yet variation in warning coloration is widespread. The chemically defended wood tiger moth Arctia plantaginis shows both geographic variation and local polymorphism in warning coloration. In this thesis, I studied whether predation by local avian predators is driving the evolution of wood tiger moth warning colours. The close relatives of the wood tiger moth designated here to genus Arctia do not show similar colour polymorphism. The wood tiger moth is thus apparently under evolutionary radiation and provides a natural laboratory for observing curr…