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Sami Merilaita

Publications and source records attributed to Sami Merilaita.

5 recordsLinked to original sources

Aposematic signals and the relationship between conspicuousness and distinctiveness.

It has long been recognized that prey that invest in toxic or other defenses often advertise these defenses by means of conspicuously coloured signals. One question that remains unanswered is why conspicuousness is such a universal trait of aposematic signals. Conspicuousness may allow more rapid avoidance learning by predators or improved retention of such learning. An alternative or complementary explanation is that defended species should adopt a conspicuous signal of their defence to make them visually distinct from inconspicuous undefended prey. Here, we use a neural network model of prey detection and attack decision making by a predator in combination with evolving, virtual prey to shed light on the relative importance of conspicuousness against the background and distinctiveness from other species as mechanisms underlying aposematic signalling. Our model suggests that prey conspicuousness may result from selection for distinctiveness, but that selection for distinctiveness does not result in maximization of conspicuousness. On the other hand, our model does not justify the exclusion of the possibility that conspicuousness as such may be a beneficial attribute of warning coloration. It is likely that the relative importance of the two selective forces (for conspicuousness and for distinctiveness) will differ on a case-by-case basis, however there is no empirical or logical reason for the current neglect of evolutionary pressure for distinctiveness. Thus, we suggest that description of aposematism as the teaming of a secondary defence with a conspicuous signal may be overly simplistic; we would rather that the signal were described as conspicuous and/or distinctive.

Animals↗

Aposematism and crypsis combined as a result of distance dependence: functional versatility of the colour pattern in the swallowtail butterfly larva.

The idea that an aposematic prey combines crypsis at a distance with conspicuousness close up was tested in an experiment using human subjects. We estimated detectability of the aposematic larva of the swallowtail butterfly, Papilio machaon, in two habitats, by presenting, on a touch screen, photographs taken at four different distances and measuring the time elapsed to discovery. The detectability of larvae in these images was compared with images that were manipulated, using existing colours either to increase or decrease conspicuousness. Detection time increased with distance for all colourations. However, at the closest distance, detection time was longer for the larvae manipulated to be more cryptic than for the natural and more conspicuous forms. This indicates that the natural colouration is not maximally cryptic at a short distance. Further, smaller increments in distance were needed to increase detection time for the natural than for the conspicuous larva. This indicates that the natural colouration is not maximally conspicuous at longer distances. Taken together, we present the first empirical support for the idea that some colour patterns may combine warning colouration at a close range with crypsis at a longer range. The implications of this result for the evolution of aposematism are discussed.

Adaptation, Biological↗

Background-matching and disruptive coloration, and the evolution of cryptic coloration.

Cryptic prey coloration typically bears a resemblance to the habitat the prey uses. It has been suggested that coloration which visually matches a random sample of the background maximizes background matching. We studied this previously untested hypothesis, as well as another, little studied principle of concealment, disruptive coloration, and whether it could, acting in addition to background matching, provide another plausible means of achieving camouflage. We presented great tits (Parus major) with artificial background-matching and disruptive prey (DP), and measured detection times. First, we studied whether any random sample of a background produces equally good crypsis. This turned out to not be the case. Next, we compared the DP and the best background-matching prey and found that they were equally cryptic. We repeated the tests using prey with all the coloration elements being whole, instead of some of them being broken by the prey outline, but this did not change the result. We conclude that resemblance of the background is an important aspect of concealment, but that coloration matching a random visual sample of the background is neither sufficient nor necessary to minimize the probability of detection. Further, our study lends empirical support to the principle of disruptive coloration.

Adaptation, Physiological↗

Constrained camouflage facilitates the evolution of conspicuous warning coloration.

The initial evolution of aposematic and mimetic antipredator signals is thought to be paradoxical because such coloration is expected to increase the risk of predation before reaching a stage when predators associate it effectively with a defense. We propose, however, that constraints associated with the alternative strategy, cryptic coloration, may facilitate the evolution of antipredator signals and thus provide a solution for the apparent paradox. We tested this hypothesis first using an evolutionary simulation to study the effect of a constraint due to habitat heterogeneity, and second using a phylogenetic comparison of the Lepidoptera to investigate the effect of a constraint due to prey motility. In the evolutionary simulation, antipredator warning coloration had an increased probability to invade the prey population when the evolution of camouflage was constrained by visual difference between microhabitats. The comparative study was done between day-active lepidopteran taxa, in which camouflage is constrained by motility, and night-active taxa, which rest during the day and are thus able to rely on camouflage. We compared each of seven phylogenetically independent day-active groups with a closely related nocturnal group and found that antipredator signals have evolved at least once in all the diurnal groups but in none of their nocturnal matches. Both studies lend support to our idea that constraints on crypsis may favor the evolution of antipredator warning signals.

Animals↗

Visual background complexity facilitates the evolution of camouflage.

Cryptic animal coloration or camouflage is an adaptation that decreases the risk of detection. The study of the evolution of camouflage has strongly emphasized the minimization of visual information that predators receive from prey, by means of background matching. However, the evolutionary effects of information processing after its reception have been virtually ignored. I constructed a model that employs an artificial neural network and simulates the evolution of prey coloration in a visually complex and simple habitat. The model suggests: (1) the difficulty of a detection task is related to the visual complexity of the habitat; (2) it is easier to decrease the risk of detection by the means of camouflage in a visually complex habitat; (3) selection on camouflage can exploit limitations in predators information processing; and (4) there are shortcomings in using the degree of background matching as the measure of camouflage.

Adaptation, Physiological↗