Disruptive coloration provides camouflage independent of background matching

Natural selection shapes the evolution of anti-predator defences, such as camouflage. It is currently contentious whether crypsis and disruptive coloration are alternative mechanisms of camouflage or whether they are interrelated anti-predator defences. Disruptively coloured prey is characterized by highly contrasting patterns to conceal the body shape, whereas cryptic prey minimizes the contrasts to background. Determining bird predation of artificial moths, we found that moths which were dissimilar from the background but sported disruptive patterns on the edge of their wings survived better in heterogeneous habitats than did moths with the same patterns inside of the wings and better than cryptic moths. Despite lower contrasts to background, crypsis did not provide fitness benefits over disruptive coloration on the body outline. We conclude that disruptive coloration on the edge camouflages its bearer independent of background matching. We suggest that this result is explainable because disruptive coloration is effective by exploiting predators' cognitive mechanisms of prey recognition and not their sensory mechanisms of signal detection. Relative to disruptive patterns on the body outline, disruptive markings on the body interior are less effective. Camouflage owing to disruptive coloration on the body interior is background-specific and is as effective as crypsis in heterogeneous habitats. Hence, we hypothesize that two proximate mechanisms explain the diversity of visual anti-predator defences. First, disruptive coloration on the body outline provides camouflage independent of the background. Second, background matching and disruptive coloration on the body interior provide camouflage, but their protection is background-specific.     

Cryptically Patterned Moths Perceive Bark Structure When Choosing Body Orientations That Match Wing Color Pattern to the Bark Pattern

Many moths have wing patterns that resemble bark of trees on which they rest. The wing patterns help moths to become camouflaged and to avoid predation because the moths are able to assume specific body orientations that produce a very good match between the pattern on the bark and the pattern on the wings. Furthermore, after landing on a bark moths are able to perceive stimuli that correlate with their crypticity and are able to re-position their bodies to new more cryptic locations and body orientations. However, the proximate mechanisms, i.e. how a moth finds an appropriate resting position and orientation, are poorly studied. Here, we used a geometrid moth Jankowskia fuscaria to examine i) whether a choice of resting orientation by moths depends on the properties of natural background, and ii) what sensory cues moths use. We studied moths’ behavior on natural (a tree log) and artificial backgrounds, each of which was designed to mimic one of the hypothetical cues that moths may perceive on a tree trunk (visual pattern, directional furrow structure, and curvature). We found that moths mainly used structural cues from the background when choosing their resting position and orientation. Our findings highlight the possibility that moths use information from one type of sensory modality (structure of furrows is probably detected through tactile channel) to achieve crypticity in another sensory modality (visual). This study extends our knowledge of how behavior, sensory systems and morphology of animals interact to produce crypsis.     

Can snakes hide in plain view? Chromatic and achromatic crypsis of two colour forms of the Western Terrestrial Garter Snake (Thamnophis elegans)

Colours influence numerous aspects of an animal's ecology. One possibility is that colour helps make an animal cryptic against the background on which it is resting. We test this hypothesis for two different, geographically separated colour forms (dark forms and light forms) of the Western Terrestrial Garter Snake, Thamnophis elegans. We quantified crypsis of snakes, in terms of colour (chromatic crypsis) and brightness (achromatic crypsis), by using objective measures of spectral reflectance of snakes and the surrounding habitat. These data were visually modelled from the perspective of potential snake predators and human researchers. Overall, snakes of both colour forms selected basking sites that increased chromatic crypsis over that which would have been achievable on random backgrounds. Both colour forms of T. elegans appear to exhibit similar achromatic and chromatic crypsis when viewed by potential predators, such as mammals and birds. From the perspective of the human visual model, dark T. elegans were generally more chromatically cryptic than light T. elegans, contrary to our a priori subjective impression. The main contribution of the present study is that we provide one of the first objective comparisons of snakes and their backgrounds as a measure of crypsis. Although we found some evidence for crypsis as a factor in choice of basking sites for snakes, other factors (e.g. thermoregulatory opportunities) undoubtedly play important roles as well. We also have not addressed whether snakes involved in other activities are cryptic or whether there are differences between the sexes or between reproductive and nonreproductive females. The adaptive significance of colour variation has been studied in diverse taxonomic groups. Although the mechanisms are not straightforward, the opportunities to carry out further work in this area are enhanced by the availability of objective approaches. © 2013 The Linnean Society of London,     

Experiments on resting site selection by nocturnal moths

When different species of moths are presented with a choice between black and white resting backgrounds, there is a strong correlation between the colour selected and the reflectance of the forewings. Under more natural conditions, light-coloured moths usually rest on fresh vegetation whilst dark-winged species select tree bark or rest upon the ground, and different defensive strategies appear to have been adopted by species in these two latter situations. Studies on the mechanism of background selection, and on background selection in polymorphic species, are reviewed.     

Behaviourally mediated crypsis in two nocturnal moths with contrasting appearance

The natural resting orientations of several species of nocturnal moth on tree trunks were recorded over a three-month period in eastern Ontario, Canada. Moths from certain genera exhibited resting orientation distributions that differed significantly from random, whereas others did not. In particular, Catocala spp. collectively tended to orient vertically, whereas subfamily Larentiinae representatives showed a variety of orientations that did not differ significantly from random. To understand why different moth species adopted different orientations, we presented human subjects with a computer-based detection task of finding and ‘attacking’ Catocala cerogama and Euphyia intermediata target images at different orientations when superimposed on images of sugar maple (Acer saccharum) trees. For both C. cerogama and E. intermediata, orientation had a significant effect on survivorship, although the effect was more pronounced in C. cerogama. When the tree background images were flipped horizontally the optimal orientation changed accordingly, indicating that the detection rates were dependent on the interaction between certain directional appearance features of the moth and its background. Collectively, our results suggest that the contrasting wing patterns of the moths are involved in background matching, and that the moths are able to improve their crypsis through appropriate behavioural orientation.     

Crypsis in a heterogeneous environment: relationships between changeable polymorphic colour patterns and behaviour in a galaxiid fish

1. The ability to achieve optimal camouflage varies between microhabitats in heterogeneous environments, potentially restricting individuals to a single habitat or imposing a compromise on crypsis to match several habitats. However, animals may exhibit morphological and behavioural attributes that enhance crypsis in different habitats. 2. We used an undescribed fish species, Galaxias‘nebula’, to investigate two objectives. First, we examined two potential methods of enhancing crypsis: change in colour pattern and selection of a suitable background. Second, we characterised the colour pattern of this unstudied fish and assessed its capacity for crypsis. 3. No background selection was apparent but the area of dark pigment expressed varied between backgrounds, which may negate the requirement to be choosy about habitats. The capacity to change colour and selection of a background that maximises crypsis are most likely separate, non‐mutually exclusive strategies. 4. Galaxias‘nebula’ exhibits polymorphic, non‐interchangeable colour patterns that have elements of both background pattern matching and disruptive colouration. This, coupled with habitat characteristics, suggests a combination of generalist and specialist strategies of habitat use. The fish’s camouflage strategy and air‐breathing ability may be key to survival under increasing pressure from habitat degradation and invasive predators.     

Substrate colour-matching cues in the cryptic grasshopper Circotettix rabula rabula (Rehn & Hebard)

Experiments with two sympatric colour morphs of the cryptic grasshopper Circotettix rabula rabula suggest that substrate colour-matching may be achieved by a visual comparison between body colour and those backgrounds which provide crypsis. The significance of this mechanism of background matching to polymorphic species in heterogeneous environments is discussed.     

Evolution of color variation in dragon lizards: quantitative tests of the role of crypsis and local adaptation

Abstract Many animal species display striking color differences with respect to geographic location, sex, and body region. Traditional adaptive explanations for such complex patterns invoke an interaction between selection for conspicuous signals and natural selection for crypsis. Although there is now a substantial body of evidence supporting the role of sexual selection for signaling functions, quantitative studies of crypsis remain comparatively rare. Here, we combine objective measures of coloration with information on predator visual sensitivities to study the role of crypsis in the evolution of color variation in an Australian lizard species complex (Ctenophorus decresii). We apply a model that allows us to quantify crypsis in terms of the visual contrast of the lizards against their natural backgrounds, as perceived by potential avian predators. We then use these quantitative estimates of crypsis to answer the following questions. Are there significant differences in crypsis conspicuousness among populations? Are there significant differences in crypsis conspicuousness between the sexes? Are body regions “exposed” to visual predators more cryptic than “hidden” body regions? Is there evidence for local adaptation with respect to crypsis against different substrates? In general, our results confirmed that there are real differences in crypsis conspicuousness both between populations and between sexes; that exposed body regions were significantly more cryptic than hidden ones, particularly in females; and that females, but not males, are more cryptic against their own local background than against the background of other populations. Body regions that varied most in contrast between the sexes and between populations were also most conspicuous and are emphasized by males during social and sexual signaling. However, results varied with respect to the aspect of coloration studied. Results based on chromatic contrast (“hue’ of color) provided better support for the crypsis hypothesis than did results based on achromatic contrast (“brightness’ of color). Taken together, these results support the view that crypsis plays a substantial role in the evolution of color variation and that color patterns represent a balance between the need for conspicuousness for signaling and the need for crypsis to avoid predation.     

Warning coloration can be disruptive: aposematic marginal wing patterning in the wood tiger moth

Warning (aposematic) and cryptic colorations appear to be mutually incompatible because the primary function of the former is to increase detectability, whereas the function of the latter is to decrease it. Disruptive coloration is a type of crypsis in which the color pattern breaks up the outline of the prey, thus hindering its detection. This delusion can work even when the prey's pattern elements are highly contrasting; thus, it is possible for an animal's coloration to combine both warning and disruptive functions. The coloration of the wood tiger moth (Parasemia plantaginis) is such that the moth is conspicuous when it rests on vegetation, but when it feigns death and drops to the grass‐ and litter‐covered ground, it is hard to detect. This death‐feigning behavior therefore immediately switches the function of its coloration from signaling to camouflage. We experimentally tested whether the forewing patterning of wood tiger moths could function as disruptive coloration against certain backgrounds. Using actual forewing patterns of wood tiger moths, we crafted artificial paper moths and placed them on a background image resembling a natural litter and grass background. We manipulated the disruptiveness of the wing pattern so that all (marginal pattern) or none (nonmarginal pattern) of the markings extended to the edge of the wing. Paper moths, each with a hidden palatable food item, were offered to great tits (Parus major) in a large aviary where the birds could search for and attack the “moths” according to their detectability. The results showed that prey items with the disruptive marginal pattern were attacked less often than prey without it. However, the disruptive function was apparent only when the prey was brighter than the background. These results suggest that warning coloration and disruptive coloration can work in concert and that the moth, by feigning death, can switch the function of its coloration from warning to disruptive.     

Colour plasticity and background matching in a threespine stickleback species pair

Examining differences in colour plasticity between closely‐related species in relation to the heterogeneity of background colours found in their respective habitats may offer important insight into how cryptic colour change evolves in natural populations. In the present study, we examined whether nonbreeding dorsal body coloration has diverged between sympatric species of stickleback along with changes in habitat‐specific background colours. The small, limnetic species primarily occupies the pelagic zone and the large, benthic species inhabits the littoral zone. We placed benthic and limnetic sticklebacks against extremes of habitat background colours and measured their degree of background matching and colour plasticity. Benthics matched the littoral background colour more closely than did the limnetics, although there was no difference between species in their resemblance to the pelagic background colour. Benthics were able to resemble both background colours by exhibiting greater directional colour plasticity in their dorsal body coloration than limnetics, which may be an adaptive response to the greater spectral heterogeneity of the littoral zone. The present study highlights how habitat‐specific spectral characteristics may shape cryptic coloration differences between stickleback species. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 902–914.     

Egg crypsis and clutch survival in three species of blackbirds (Icteridae)

For most open-nesting passerine birds, the primary function of egg pigmentation is crypsis. Interspecific variation for egg coloration is quite high, even among species that nest in the same locale. This variation might be maintained by selection to blend into species-specific nest cups, which vary in pattern because they are constructed from different materials. To test this hypothesis we photographed 30 clutches of Brewer's blackbirds ( Euphagus cyanocephalus ), 26 clutches of red-winged blackbirds ( Agelaius phoeniceus ), and 24 clutches of yellow-headed blackbirds ( Xanthocephalus xanthocephalus ), and quantified crypsis in terms of pattern (PD crypsis), brightness (MB crypsis) and brightness disparity (BD crypsis). The species were equally cryptic in terms of pattern crypsis, but differed significantly ( P < 0.01) in MB and BD crypsis. Intraspecific variation in pattern crypsis was surprisingly high. Mean clutch pattern disparity was highly correlated with mean background pattern disparity ( r = 0.999); this suggests selection for disparity matching, rather than for crypsis. We also monitored 25 clutches (7 Brewer's, 9 red-winged, and 9 yellow-headed blackbirds) for a 9-day period to determine if survival was related to crypsis. For Brewer's and yellow-headed blackbirds, successful nests were no more cryptic than failed nests. For red-winged blackbirds, there was a tendency ( P = 0.1) for less cryptic clutches to have higher survival; in addition, successful red-winged blackbird clutches had significantly ( P < 0.05) higher egg pattern disparity and background pattern disparity. Red-winged blackbird clutches are not concealed by overhanging vegetation, and high pattern disparity may enable them to blend into a large-scale heterogeneous background.     

Camouflage through an active choice of a resting spot and body orientation in moths

Cryptic colour patterns in prey are classical examples of adaptations to avoid predation, but we still know little about behaviours that reinforce the match between animal body and the background. For example, moths avoid predators by matching their colour patterns with the background. Active choice of a species‐specific body orientation has been suggested as an important function of body positioning behaviour performed by moths after landing on the bark. However, the contribution of this behaviour to moths’ crypticity has not been directly measured. From observations of geometrid moths, Hypomecis roboraria and Jankowskia fuscaria, we determined that the positioning behaviour, which consists of walking and turning the body while repeatedly lifting and lowering the wings, resulted in new resting spots and body orientations in J. fuscaria and in new resting spots in H. roboraria. The body positioning behaviour of the two species significantly decreased the probability of visual detection by humans, who viewed photographs of the moths taken before and after the positioning behaviour. This implies that body positioning significantly increases the camouflage effect provided by moth’s cryptic colour pattern regardless of whether the behaviour involves a new body orientation or not. Our study demonstrates that the evolution of morphological adaptations, such as colour pattern of moths, cannot be fully understood without taking into account a behavioural phenotype that coevolved with the morphology for increasing the adaptive value of the morphological trait.     

Crypsis, conspicuousness, mimicry and polyphenism as antipredator defences of foraging octopuses on Indo-Pacific coral reefs, with a method of quantifying crypsis from video tapes

We tested the hypothesis that soft-bodied octopuses, which spend most of their lives in dens, remain highly cryptic as their primary defence against predation while they forage. We videotaped foraging octopuses on two widely dispersed Pacific coral reefs and developed a rigorous method to analyse the degree of crypsis from videotapes. Five ranks were assigned (two of‘ highly cryptic’, one of ‘moderately cryptic’, and two of ‘conspicuous’) to assess each octopus's body pattern match to its background, using the criteria of brightness, colour, shape and skin patterning. The data do not support the hypothesis. In Tahiti, octopuses were highly cryptic only 54%, moderately cryptic 24% and conspicuous 22% of the time. In Palau, the respective calculations were 31 %, 19% and 50%. A major feature of their behaviour was their remarkable ability to instantly change their body pattern, or phenotype, by direct neural control of the skin. Six chronic and nine acute categories of body patterns were observed. On average, octopuses changed their phenotype 2.95 times/minute, or 177 times per hour, based upon 7.5 hours of videotaped foraging. This rapid neurally controlled polyphenism was used most often to adjust their appearance as they foraged slowly across highly diverse substrates, thus implementing appropriate mechanisms of crypsis over each (e.g. general background resemblance, deceptive resemblance, disruptive coloration). However, when crawling rapidly, or swimming for short distances, octopuses often engaged a second antipredator lactic that was conspicuous: mimicking fishes or showing bold disruptive patterns that rendered them visibly different from an octopus. Nevertheless, sometimes they were simply conspicuous even when moving slowly, particularly in Palau, where the octopuses were larger, there was a high degree of mating“, and fewer signs of predation were evident. The results suggest that, while foraging, the overall strategy is to use polyphenism to produce ‘apparent rarity’ of any single phenotype (or search image) through mechanisms of crypsis, conspicuousness and mimicry, all of which are guided by keen vision in this marine invertebrate.     

Great tits (Parus major) searching for artificial prey: implications for cryptic coloration and symmetry

It has been suggested that bilateral symmetry may impose a costfor animals relying on camouflage because symmetric color patternsmight increase the risk of detection. We tested the effect ofsymmetry on crypsis, carrying out a predation experiment withgreat tits (Parus major) and black-and-white–patterned,artificial prey items and background. First, we found that detectiontime was significantly longer for a highly cryptic, asymmetricpattern based on a random sample of the background than forits symmetric variants. Second, we were able to arrange theelements of a prey pattern in a way that the resulting asymmetricpattern was highly cryptic and, furthermore, its symmetric variantwas highly cryptic as well. We conclude that symmetry may imposea substantial cost on cryptic patterns, but this cost variesamong patterns. This suggests that for prey, which predatorstypically view from an angle exposing their symmetry, selectionfor pattern asymmetry may be less important and selection fordecreased detectability cost of symmetry may be more importantthan previously thought. This may help to understand the existenceof so many prey with cryptic, symmetric color patterns.     

Threatened tadpoles of Bokermannohyla alvarengai (Anura: Hylidae) choose backgrounds that enhance crypsis potential

Crypsis results from a complex interaction among prey coloration, background matching, behaviour and predator visual perception. Tadpoles are known to have varied adaptations to escape predation, but the use of crypsis is little explored, although it is likely for certain species. We investigated potential escape mechanisms related to active escape (fleeing) and crypsis improvement in Bokermannohyla alvarengai tadpoles, proposing a new method to measure cryptic potential. We studied the range of distances covered by threatened and fleeing tadpoles and the proportion of tadpoles that seek shelter or remain exposed after fleeing. We hypothesized that tadpoles that remain exposed may use alternative strategies to avoid detection, such as reaching deeper microhabitats or positioning themselves on substrates that confer greater crypsis than the ones they were on before disturbance. A significantly greater proportion of tadpoles remained exposed after disturbance and positioned themselves on backgrounds that offered greater cryptic potential, but did not differ in depth. Tadpoles may respond to a trade‐off between sheltering and being cryptic. On the one hand, they may remain close to retreat sites or they may escape to microhabitats that provide appropriate background matching as a means to achieve crypsis. On the other hand, the absence of matching backgrounds in the tadpoles' vicinities may induce them to seek shelter. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 101 , 437–446.     

The interrelationship between crypsis and colour polymorphism

The mechanisms behind the evolution and maintenance of conspicuous visible polymorphisms comprising tens of morphs present a challenge to evolutionary theory. However, for cryptic forms Endler (Evol. Biol., 11, 1978, 319) conjectured that complex backgrounds facilitate polymorphism because in such habitats there are several ways to resemble the resting surface. We use computer simulation to explore the evolution of cryptic morphs on increasingly complex backgrounds under regimes that include selection for crypsis, apostatic predation and dietary wariness. We show that there is a monotonic increase in the number of morphs evolving in a population as the potential number of cryptic morphs increases. The relationship is very weak with selection for crypsis alone, but much stronger with the addition of apostatic selection. In contrast, when dietary wariness is added to the model the plot of number of morphs maintained, as a function of the potential number of cryptic forms available, is minimized at an intermediate number of cryptic forms, i.e. is V-shaped. These counter-intuitive patterns are robust to varying strengths of apostatic selection and different implementations of dietary wariness, and are more pronounced when predator and prey generation lengths are similar.     

Lake Erie water snakes revisited: Morph- and age-specific variation in relative crypsis

Summary Populations of water snakes (Nerodia sipedon insularum) on islands in western Lake Erie are variable in colour pattern, consisting of unbanded, intermediate, and banded morphs. In contrast, mainland populations (N. s. sipedon) consist solely of banded morphs. Previous investigators hypothesized that natural selection favoured unbanded morphs on exposed island shorelines and banded morphs in overgrown mainland habitats and that gene flow from mainland populations was responsible for the persistence of banded morphs on islands. To clarify the potential role of natural selection, I quantified relative crypsis among morphs and age classes of water snakes by comparing the size of patches making up their colour patterns with the size of patches in island and mainland backgrounds. This analysis reveals that if unbanded morphs are more cryptic than intermediate and banded morphs on islands, it is only in the young-of-the-year age class. For older snakes on islands and for all snakes on the mainland, unbanded morphs are consistently less cryptic than intermediate and banded morphs. Given these results, the net direction of selection in island populations should depend on the intensity of predation on different age classes of snakes. Overall, selection may favour unbanded morphs (e.g. if predation occurs primarily on young-of-the-year), intermediate and banded morphs (e.g. if predation occurs primarily on older snakes), or be weak or absent (e.g. certain combinations of predation on young-of-the-year and older snakes). Using estimates of relative crypsis to guide reanalysis of morph frequency data, I find support for the hypothesis that unbanded morphs are favoured by natural selection in island populations.     

Local adaptation and divergence in colour signal conspicuousness between monomorphic and polymorphic lineages in a lizard

Population differences in visual environment can lead to divergence in multiple components of animal coloration including signalling traits and colour patterns important for camouflage. Divergence may reflect selection imposed by different receivers (conspecifics, predators), which depends in turn on the location of the colour patch. We tested for local adaptation of two genetically and phenotypically divergent lineages of a rock‐inhabiting lizard, Ctenophorus decresii, by comparing the visual contrast of colour patches to different receivers in native and non‐native environments. The lineages differ most notably in male throat coloration, which is polymorphic in the northern lineage and monomorphic in the southern lineage, but also differ in dorsal and lateral coloration, which is visible to both conspecifics and potential predators. Using models of animal colour vision, we assessed whether lineage‐specific throat, dorsal and lateral coloration enhanced conspicuousness to conspecifics, increased crypsis to birds or both, respectively, when viewed against the predominant backgrounds from each lineage. Throat colours were no more conspicuous against native than non‐native rock but contrasted more strongly with native lichen, which occurs patchily on rocks inhabited by C. decresii. Conversely, neck coloration (lateral) more closely matched native lichen. Furthermore, although dorsal coloration of southern males was consistently more conspicuous to birds than that of northern males, both lineages had similar absolute conspicuousness against their native backgrounds. Combined, our results are consistent with local adaptation of multiple colour traits in relation to multiple receivers, suggesting that geographic variation in background colour has influenced the evolution of lineage‐specific coloration in C. decresii.     

Resting site selection in the geometrid moth Phigalia pilosaria (Lepidoptera: Geometridae)

When tested in a cylindrical apparatus, males of both typical and melanic morphs of the nocturnal moth Phigalia pilosaria (Schiffermueller) prefer to rest on light backgrounds. This preference is more pronounced when the moths have a rough surface on which to rest than when it is smooth. The two morphs show a distinct tendency to adopt resting positions close to the boundary between the shades presented in the experiments; this is interpreted as being a result of walking moths stopping at or close to the boundary when approaching it from the light side. The surface texture of the background influences the resting attitude of the moths in relation to vertical.     

Physiological colour change in the Moorish gecko,Tarentola mauritanica (Squamata: Gekkonidae): effects of background,light, and temperature

Colour has many different functions in animals, such as an involvement in thermoregulation, crypsis, and social interactions. Species capable of physiological colour change may alter their coloration in response to ecological conditions. The Moorish gecko, Tarentola mauritanica, is capable of actively changing its body coloration. In the present study, we investigated colour change in this gecko as a function of background, temperature, and light. Our results demonstrate that the Moorish gecko indeed changes its dorsal colour in response to changes in environmental conditions. By contrast to several other reptilian species, this rapid colour change does not appear to be associated with thermoregulation. Background matching, however, did appear to be a prominent function, although illumination appears to be an essential trigger. Future research should concentrate on individual variation and its effectiveness with respect to antipredatory mechanisms. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ?? , ??–??.