Insect Color Research Articles

Adaptive change in protective coloration in adult striated shieldbugs Graphosoma lineatum (Heteroptera: Pentatomidae): test of detectability of two colour forms by avian predators

1. Protective coloration in insects may be aposematic or cryptic, and some species change defensive strategy between instars. In Sweden, the adult striated shieldbugs Graphosoma lineatum (Heteropte ...

A Fungal Past to Insect Color

Gene transfer from a fungus to an ancestral aphid is responsible for the insect's red and green coloration.

Wing Patterns in the Mist

Wing Patterns in the Mist

Predation on heliconia bugs, Leptoscelis tricolor: examining the influences of crypsis and predator color preferences

Individuals in natural populations commonly vary in color, and such color variation can be important for survival under predation pressure. Potential prey may be more likely to survive when they are cryptic against their backgrounds. Alternatively, individual coloration, regardless of background, may itself best predict predation events. Few studies have simultaneously tested the importance of crypsis and predator color preferences in explaining predation events. In this study we used objective measures of coloration to examine whether heliconia bugs, Leptoscelis tricolor Westwood, 1842 (Hemiptera: Coreidae), resembling their background were less likely to be eaten by avian predators (crypsis hypothesis). Next, we evaluated whether insect color, irrespective of background, best explains predation events (color preference hypothesis). We found the strongest evidence for the crypsis hypothesis; predators chose prey that differed most from their background in color saturation. Some evidence was also found for the color preference hypothesis; predators avoided brightly colored prey. These results suggest that crypsis can be effective in detouring predation. However, when potential prey are detected, predator color preferences may best explain predation events.

Book review: Iridescences - The Physical Colors of Insects

Book review: Iridescences - The Physical Colors of Insects

Fast geometry deformable insect's color image segmentation algorithm

Most of the existing geometric deformable model methods can not be directly used for color image segmentation. Therefore, fast geometry deformable color image segmentation algorithm was proposed to solve the problem and be applied to insect color image. The experimental results show that the algorithm can segment target insect in the image successfully. However, the results with channel by channel fast geometry deformable algorithm are different edges of the same insect in different channels.

Role of different colours of aposematic insects in learning, memory and generalization of naïve bird predators

Among the various properties of visual warning signals, colour seems to be especially important for avian predators. We tested the role of particular colours of an aposematic insect (firebug, Pyrrhocoris apterus; Heteroptera: Pyrrhocoridae) in unlearned avoidance, learning, memory and generalization of a naive avian predator (great tit, Parus major). The wild type of the firebug is aposematic, red-and-black, and its colour mutants (white, yellow, orange) retain the same black pattern; the bug can be made artificially nonaposematic (painted uniformly brown). Wild-caught great tits avoid the firebug depending on colour, and their reaction to variously coloured prey is a result of avoidance learning and may vary according to their experience. We trained naive great tits to avoid firebugs of different colours, and then gave some birds a memory test with firebugs of the same colour and other birds a generalization test with firebugs of a different colour. Naive, hand-reared great tits showed no initial avoidance and attacked firebugs irrespective of colour. They learned to avoid all the colour forms at a similar rate. The generalization was asymmetric: birds that learned to avoid red firebugs did not generalize their experience to yellow or white mutants whereas birds that learned to avoid yellow mutants generalized their experience to red firebugs. The red colour thus represents a more effective signal than the yellow; predation by birds could have played a crucial role in selectively favoured evolutionary transitions from yellow to red coloration in pyrrhocorids.

Juvenile Hormone Regulates Butterfly Larval Pattern Switches

Insect color patterns can be very diverse. This variation is also seen among many larval instar stages, which can take on vastly different phenotypes. Young caterpillars of the swallowtail butterfly, Papilio xuthus, are mimics of bird droppings, whereas the fifth larval instar is camouflaged among the leaves of host plants (cryptic pattern). We find that juvenile hormone (JH) titers decrease during the fourth larval instar. Furthermore, treatment with JH analog at the beginning of the fourth instar stage resulted in reproducing the mimetic pattern instead of the usual cryptic one and likewise altered gene expression patterns to that associated with the mimetic pattern. These findings suggest that JH regulates the progressive larval pattern switch of this insect.

Maintenance of Larval Color Polymorphism in <I>Orgyia antiqua</I> (Lepidoptera: Lymantriidae): Evaluating the Role of Thermal Adaptation

Intraspecific color polymorphism is widespread in insects, and various mechanisms have been proposed to explain its maintenance. Some explanations rely on the effect of body color on the organism's thermal physiology. Darker individuals accumulate solar energy more efficiently, and therefore, dark body coloration in insects is frequently presumed to be an adaptation to low temperature conditions. However, it is largely unclear what is the importance of the thermal biology in comparison to other potential selective forces on body coloration. In this study, we evaluated the role of temperature as a potential selective factor maintaining color polymorphism in aposematic larvae of the moth Orgyia antiqua L. It was found that darker, and thus less aposematic, larvae accumulated solar energy more efficiently. However, in a set of laboratory and outdoor experiments, we found no evidence of temperature-dependent performance of different color morphs or in development of different morphs induced by rearing temperature. We conclude that the effects related to thermal physiology are not likely important determinants of optimal coloration in O. antiqua. The reasons may lie in high mobility of the larvae, which allows for effective behavioral thermoregulation, which is also shown in this study. Our results caution against an uncritical extrapolation of results obtained for model organisms and indicate the need for giving more attention to the species-specific ecological background in ecophysiological studies.

Iridescences: the physical colors of insects

Iridescence.- Why Colors.- Lepidoptera Description and Scales of Observation.- Coleoptera Description and Observation Scales.- Changing Colors: Structures or Pigments?.- Physical Colors, Chemical Colors Basics of Solid State Optics.- 1-Dimensional Structures: Interferences.- 2-Dimensional Structures: Interferences and Diffraction.- 3-Dimensional Structures: Crystalline Diffraction.- Amorphous Structures: Scattering.- Pigments and Pigmentary Colors.- Thermoregulation and Spectral Selectivity.- Vision and Colorimetry.

Mimicry in hoverflies (Diptera: Syrphidae): a field test of the competitive mimicry hypothesis

Although most studies on the evolution of mimicry and warning coloration in insects have considered predators as the major selective force, it is possible that competition for food resources could also facilitate selection for these conspicuous signals. For example, when warningly colored social wasps visit flowers, then they frequently behave aggressively toward heterospecifics, and they also attack and feed on other flying insects. Under these conditions, a resemblance to a wasp might provide a mimetic hoverfly with improved access to floral resources by reducing the frequency with which it is disturbed by other pollinators. We experimentally evaluated whether wasp-like colors and patterns were important in preventing other flower visitors from sharing the same flower resource, using pairwise presentations of both natural and artificial prey in the field. Flower visitors were more likely to visit unoccupied flowers compared with the flowers pinned with either natural or artificial specimens in 2 plant species with different inflorescences. However, flower visitors did not show a significantly reduced rate of visitation to flowers pinned with specimens bearing wasp-like colors and patterns compared with the flowers occupied by similar-sized specimens that were nonmimetic. Overall, we found no compelling evidence in this study to support the contention that wasp-like warning signals of hoverflies prevent other flower visitors from sharing flower resources, although insects showed a greater tendency to avoid visiting flowers pinned with a wasp compared with flowers pinned with a nonmimetic fly.

Analysis of Insect and Plant Colors in Digital Images Using Java Software on the Internet

Description of colors of insects and plants in biological research is often subjective and imprecise. A quantitative, statistical, and standardized method for describing colors by software analysis of digital images would be useful to researchers if readily available. An Internet Web page with JavaScript and Java applet was made that loads a digital image and analyzes the red, green, and blue (RGB) intensity components of the pixels in any rectangular area of relatively uniform color. A mean, standard deviation (SD), coefficient of variation, and percentage of each of the three color components in the area is calculated. Thus, a colored area in an image can be depicted objectively as R ± SD, G ± SD, and B ± SD, or percentages thereof, allowing mean color to be reproduced elsewhere by paint programs. For each analysis, the software uses the RGB component colors to make a bar graph with each RGB value and SD. The software was used to analyze colors of flowers and leaves of two cotton species, white and red varieties of upland, Gossypium hirsutum L., and Pima, Gossypium barbadense L. (Malvaceae); western tarnished plant bug, Lygus hesperus Knight (Heteroptera: Miridae); yellow plastic used in insect traps; and eight other insect species. Three two-dimensional (2D) color-space diagrams (hexagon, 2D-cube, and ternary percentages) are described and used to plot colors from analyses. Statistical tests are presented that compare whether two groups of color-space points in three dimensions are significantly separated. Differences in color vision are compared in humans, insects, digital cameras, and spectroradiometers.

Importance of colour in the reaction of passerine predators to aposematic prey: experiments with mutants of Pyrrhocoris apterus (Heteroptera)

Persistent questions concerning the warning coloration of unpalatable insects address whether the bright aposematic colour itself or its combination with a species-specific dark pattern is the key factor in their protection against insectivorous birds, and how chromatic polymorphism originates and is maintained in aposematics. In the present study, these questions were tested experimentally, using the birds Parus major, Parus caeruleus, Erithacus rubecula, and Sylvia atricapilla as predators, and chromatically polymorphic firebug Pyrrhocoris apterus: red wild form, white, yellow, and orange mutants (all four of them with the same black melanin pattern, the mutants differing in colour of pteridine pigments only) and the nonaposematic brown-painted wild form as prey. The results show that a specific colour is essential for the birds to recognize the specific aposematic prey; the melanin pattern is not sufficient. White mutants were no better protected than nonaposematic firebugs; red wild-type and orange mutants were equally well protected against all bird species; and the reaction of birds to yellow mutants was species-specific. An evolutionary scenario of ‘recurrent recessive mutations’ is formulated to explain the origin of colour polymorphism in some aposematics.

The predation costs of symmetrical cryptic coloration

In psychological studies of visual perception, symmetry is accepted as a potent cue in visual search for cryptic objects, yet its importance for non-human animals has been assumed rather than tested. Furthermore, while the salience of bilateral symmetry has been established in laboratory-based search tasks using human subjects, its role in more natural settings, closer to those for which such perceptual mechanisms evolved, has not, to our knowledge, been investigated previously. That said, the salience of symmetry in visual search has a plausible adaptive rationale, because biologically important objects, such as prey, predators or conspecifics, usually have a plane of symmetry that is not present in their surroundings. We tested the conspicuousness to avian predators of cryptic artificial, moth-like targets, with or without bilateral symmetry in background-matching coloration, against oak trees in the field. In two independent experiments, symmetrical targets were predated at a higher rate than otherwise identical asymmetrical targets. There was a small, but significant, fitness cost to symmetry in camouflage patterns. Given that birds are the most commonly invoked predators shaping the evolution of defensive coloration in insects, this raises the question of why bilateral asymmetry is not more common in cryptic insects.

Know Thyself: Stable Cell Fate Decisions in Insect Colour Vision

The retina provides an example of a fundamental property of developing cells: cell fate decisions are stable. A recent paper reports a double negative feedback loop that leads to bistable fate decisions in the colour-detecting photoreceptors of Drosophila.

Insect colour preference compared to flower colours in the Australian Alps

An apparent predominance of plant taxa with pale flowers in the alpine floras of Australia and New Zealand may be due to the prevalence of insects, such as flies, that prefer pale colours and the absence of other types of potential pollinators that are attracted to bright colours such as social bees and birds. In this study, the diversity of flower colours, and the preference of insects for different colours were examined for the largest contiguous alpine area in Australia, around Mt Kosciuszko. Out of an alpine flora of 204 taxa, 127 species were found to have large showy flowers. The most common flower colour among these taxa was white (53.5%), then yellow (21.3%), followed by pink (6.3%), and cream (6.3%). Only a handful of taxa had red, blue, brown, green, orange or purple flowers. When the colour preference of insects was tested using five different coloured traps (white, yellow, orange, red and purple), the most successful traps were white then yellow, with these two colours accounting for 66% of all individual insects collected. Diptera were the most common insects caught (576 insects greater than 4 mm in length, 31 morphotaxa) showing an apparent preference for white and yellow coloured traps over others. Therefore, the results add some support to the proposition that the ‘white’ flora of the Australian Alps may be associated with the colour preference of flies, which have previously been found to be the most common type of pollinators in the Kosciuszko alpine zone.

Reactions of passerine birds to aposematic and non-aposematic firebugs (Pyrrhocoris apterus ; Heteroptera)

In spite of the existence of many experimental studies on the function of warning coloration in insects, little is known about the universality of reactions of different predators towards a particular warning signal. Reactions of nine passerine bird species, namely Parus major , Parus caeruleus , Aegithalos caudatus , Erithacus rubecula , Turdus merula , Sylvia atricapilla , Fringilla coelebs , Carduelis chloris and Emberiza citrinella , to the firebug Pyrrhocoris apterus wildtype (brachypterous adults) and its artificially obtained (painted) brown non-aposematic variant were compared. Most insectivorous birds (great tits, blue tits, robins and blackcaps) distinguished between aposematic and non-aposematic bugs, attacking the former less often. Partly granivorous buntings and finches did not distinguish between them, and attacked both variants equally. As all the birds were caught in the wild, the results can be interpreted in terms of the presence of a higher proportion of experienced individuals among insectivorous than among omnivorous species. Two insectivorous species differed from others. The heaviest blackbird attacked and killed aposematic as well as non-aposematic firebugs, and, in contrast, the lightest long-tailed tit avoided both variants. © 2003 The Linnean Society of London, Biological Journal of the Linnean Society , 2003, 78, 517–525.

Colour in the eyes of insects.

Many insect species have darkly coloured eyes, but distinct colours or patterns are frequently featured. A number of exemplary cases of flies and butterflies are discussed to illustrate our present knowledge of the physical basis of eye colours, their functional background, and the implications for insect colour vision. The screening pigments in the pigment cells commonly determine the eye colour. The red screening pigments of fly eyes and the dorsal eye regions of dragonflies allow stray light to photochemically restore photoconverted visual pigments. A similar role is played by yellow pigment granules inside the photoreceptor cells which function as a light-controlling pupil. Most insect eyes contain black screening pigments which prevent stray light to produce background noise in the photoreceptors. The eyes of tabanid flies are marked by strong metallic colours, due to multilayers in the corneal facet lenses. The corneal multilayers in the gold-green eyes of the deer fly Chrysops relictus reduce the lens transmission in the orange-green, thus narrowing the sensitivity spectrum of photoreceptors having a green absorbing rhodopsin. The tapetum in the eyes of butterflies probably enhances the spectral sensitivity of proximal long-wavelength photoreceptors. Pigment granules lining the rhabdom fine-tune the sensitivity spectra.

The relationship between mimetic imperfection and phenotypic variation in insect colour patterns.

Many hoverflies (Syrphidae) mimic wasps or bees through colour or behavioural adaptations. The relationship between phenotypic variation in colour pattern and mimetic perfection (as determined by pigeons) was investigated in three species of Müllerian mimics (Vespula spp.) and 10 Batesian hoverfly mimics, plus two non-mimetic species of flies. Four predictions were tested: (i) Batesian mimics might be imperfect because they are in the process of evolving towards perfection, hence there should be a positive relationship between variation and imperfection; (ii) some Batesian mimics are imperfect because they do not have the appropriate genetic variation to improve and have evolved to be as good as possible, hence there should be no differences between species, all displaying a low level of variation; (iii) very common hoverflies should show the highest levels of variation because they outnumber their models, resulting in high predation and a breakdown in the mimetic relationship; and (iv) social wasps (Vespula) have such a powerful defence that anything resembling a wasp, both Müllerian and perfect Batesian mimics, would be avoided, resulting in relaxed selection and high variance. Poor mimics may still evolve to resemble wasps as well as possible and display lower levels of variation. The data only provided support for the fourth prediction. The Müllerian mimics, one of the most perfect Batesian mimics, and the non-mimetic flies displayed much higher levels of variation than the other species of Batesian mimics.

Aposematic Coloration of Gregarious Insects Can Delay Predation by an Ambush Predator: Fig. 1.

An important hypothesis concerning the role of aggregation in the antipredator defense of aposematic insects is that a group projects a larger aposematic signal to a predator. The nearly exclusive use of birds as model predators may be leading us to over-emphasize the importance of signal amplification as an explanation for the gregarious behavior of aposematic insects. Ambush (sit-and-wait) predators such as amphibians and praying mantids make predatory decisions relying primarily on prey movement, and secondarily on prey size, with prey color being less important. Therefore, we tested the interaction of aposematic coloration and gregarious behavior in insect defense from frogs. We offered frogs four types of mealworm prey: (1) cryptic and solitary, (2) cryptic and gregarious, (3) aposematic and solitary, and (4) aposematic and gregarious. The frogs ate aposematic and gregarious prey significantly later than they ate cryptic and gregarious prey and cryptic and solitary prey. Our results support the hypothesis that aposematic coloration in gregarious prey, but not in solitary prey, can function to produce a sufficient aposematic signal to delay attack by an ambush predator. This result was not due to predator learning. Hence, the antipredator benefits of aposematic coloration in aggregated prey may function in encounters with a wide range of predators, including frogs.