Chromatophores Research Articles

A new insight into the pigmentation of the three-spined stickleback exposed to oxidative stress: day and night study

The diverse and changing pigmentation of the skin allows fish to adapt to environmental conditions for survival and communication with conspecifics. However, various physical and chemical environmental factors, including pollutants, affect fish coloration. Therefore, the implementation of an analysis of skin pigmentation has been considered in fish well-being and ecotoxicological studies. A physiological color change is achieved by the motility of melanin-containing organelles: they aggregate into the perikaryon or disperse throughout the cytoplasm of melanophores in response to various stimuli. In our study, we addressed the issue of implementing the analysis of pigment dispersion in melanophores in stickleback skin to assess the response of fish to oxidative stress. We examined pigment dispersion in day and night skin samples collected from the dorsal, lateral and ventral regions. The degree of pigment dispersion we assessed by the melanophore index. The total number of melanophores counted in the defined skin area was significantly higher in the night samples than in the day samples. Only in day samples of dorsal skin we observed the significant changes in pigment dispersion after exposure to stress: melanin was predominantly in the aggregated state. In the night samples, we did not report any response to stress in any part of the skin. Examination of pigment dispersion in melanophores in stickleback skin can be useful for assessing the welfare of fish and detecting toxic agents in the environment, but under specified conditions: in sticklebacks, it is analysis of dorsal skin during the day.

Preliminary estimate of a Gray Treefrog (<i>Hyla versicolor</i>) population at a protected site in New Brunswick using photo identification and community science

We provide a preliminary population estimate (n = 120, 95% CI 65–722) of (male) Gray Treefrog (Hyla versicolor) at the Hyla Park Nature Preserve, New Brunswick, Canada’s first amphibian conservation site. As proof of concept, we also demonstrate the efficacy of a minimally invasive photographic identification method (PIM) that uses pattern recognition software for estimating the population of a visually cryptic amphibian that is subject to physiological colour change. Finally, we validate the use of PIM data collected by community participants and the opportunity it provides to engage and educate the local community about amphibian conservation.

Colour change and colour phases in Lethrinidae with insights into ecology.

Colour change is used by a wide range of animals. It is used for intra- and interspecific communication and crypsis, and can occur on morphological and physiological levels. Bony fish employ rapid physiological colour change and display various types of patterns and colouration (colour phases) useful for aposematic and cryptic purposes. Using an existing database of benthic stereo-baited remote underwater video systems from two locations in Western Australia, we tested whether the frequency of colour phases of emperors, Lethrinidae, varied by species. We described colour phases and rapid physiological colour change in 16 species of lethrinids, and related occurrences of colour change to feeding activity and life stages. Dark and light colour phases were observed in nine of the 16 evaluated species of which seven also displayed physiological colour change. Frequency of colour phases varied between species, suggesting that the display of different dark patterns may be especially important for certain species. Both juveniles and adults showed the ability to change between different colour patterns. The change into a mottled pattern mainly occurred while feeding or when approaching to feed, suggesting that it may be triggered by feeding and the associated decrease in environmental awareness. Colour change is a commonly observed strategy in lethrinids and may have evolved as an adaptation for increased foraging success or to reduce aggression from conspecifics. Physiological colour change allows lethrinids to quickly adapt to various cues from the environment and can therefore be considered a versatile physiological mechanism in this family.

Functional relation of agouti signaling proteins (ASIPs) to pigmentation and color change in the starry flounder, Platichthys stellatus

We investigated the involvement of agouti-signaling proteins (ASIPs) in morphological pigmentation and physiological color change in flatfishes. We isolated ASIP1 and 2 mRNAs from the skin of starry flounder (Platichthys stellatus), and compared their amino acid (aa) structures to those of other animals. Then, we examined the mRNA expression levels of two ASIPs (Sf-ASIPs) in the pigmented ocular body and in the unpigmented blind body, as well as in the ordinary skin and in albino skin, in flatfishes. To investigate the role of Sf-ASIPs in physiological color change (color camouflage), we compared the expression of the two genes in two background colors (dark-green and white). Sf-ASIP1 cDNA had a 375-bp open reading frame (ORF) that encoded a protein consisting of 125 aa residues, and Sf-ASIP2 cDNA had a 402-bp ORF that encoded a protein consisting of 132 aa residues. RT-PCR revealed that the strongest Sf-ASIP1 and Sf-ASIP2 expression levels were observed in the eye and blind-skin, respectively. In Sf-ASIP1, the gene expression did not differ between the ocular-side skin and blind-side skin, nor between ordinary skin and abnormal skin of the fish. However, in Sf-ASIP2, the expression level was significantly higher in blind-side skin, compared to ocular-side skin, suggesting that the ASIP2 gene is related to the countershading body pigment pattern of the fish. In addition, the Sf-ASIP2 gene expression level was lower in the pigmented spot regions than in the unpigmented spot regions of the malpigmented pseudo-albino skins on the ocular side, implying that ASIP2 is responsible for the ocular-side pseudo-albino. Additionally, ASIP2 gene expression in the blind-side skin of ordinary fish was enhanced by a white tank, implying that a bright background color could inhibit hypermelanosis in the blind-side skin of cultured flounder by increasing the activity of the Sf-ASIP2 gene. However, we did not find any relationship of ASIPs with camouflage color changes. In conclusion, the ASIP2 gene is related to the morphological pigmentation (countershading and malpigmentation) of the skin in starry flounder, but not with physiological color changes (color camouflage) in the ocular-side skin.

Light-specific wavelengths differentially affect the exploration rate, opercular beat, skin color change, opsin transcripts, and the oxi-redox system of the longsnout seahorse Hippocampus reidi

Light is a strong stimulus for the sensory and endocrine systems. The opsins constitute a large family of proteins that can respond to specific light wavelengths. Hippocampus reidi is a near-threatened seahorse that has a diverse color pattern and sexual dimorphism. Over the years, H. reidi's unique characteristics, coupled with its high demand and over-exploitation for the aquarium trade, have raised concerns about its conservation, primarily due to their significant impact on wild populations. Here, we characterized chromatophore types in juvenile and adult H. reidi in captivity, and the effects of specific light wavelengths with the same irradiance (1.20 mW/cm2) on color change, growth, and survival rate. The xanthophores and melanophores were the major components of H. reidi pigmentation with differences in density and distribution between life stages and sexes. In the eye and skin of juveniles, the yellow (585 nm) wavelength induced a substantial increase in melanin levels compared to the individuals kept under white light (WL), blue (442 nm), or red (650 nm) wavelengths. In addition, blue and yellow wavelengths led to a higher juvenile mortality rate in comparison to the other treatments. Adult seahorses showed a rhythmic color change over 24 h, the highest reflectance values were obtained in the light phase, representing a daytime skin lightening for individuals under WL, blue and yellow wavelength, with changes in the acrophase. The yellow wavelength was more effective on juvenile seahorse pigmentation, while the blue wavelength exerted a stronger effect on the regulation of adult physiological color change. Dramatic changes in the opsin mRNA levels were life stage-dependent, which may infer ontogenetic opsin functions throughout seahorses' development. Exposure to specific wavelengths differentially affected the opsins mRNA levels in the skin and eyes of juveniles. In the juveniles, skin transcripts of visual (rh1, rh2, and lws) and non-visual opsins (opn3 and opn4x) were higher in individuals under yellow light. While in the juvenile's eyes, only rh1 and rh2 had increased transcripts influenced by yellow light; the lws and opn3 mRNA levels were higher in juveniles' eyes under WL. Prolonged exposure to yellow wavelength stimulates a robust increase in the antioxidant enzymes sod1 and sod2 mRNA levels. Our findings indicate that changes in the visible light spectrum alter physiological processes at different stages of life in H. reidi and may serve as the basis for a broader discussion about the implications of artificial light for aquatic species in captivity.

Cuttlefish color change as an emerging proxy for ecotoxicology.

Lately, behavioral ecotoxicology has flourished because of increasing standardization of analyses of endpoints like movement. However, research tends to focus on a few model species, which limits possibilities of extrapolating and predicting toxicological effects and adverse outcomes at the population and ecosystem level. In this regard, it is recommended to assess critical species-specific behavioral responses in taxa playing key roles in trophic food webs, such as cephalopods. These latter, known as masters of camouflage, display rapid physiological color changes to conceal themselves and adapt to their surrounding environments. The efficiency of this process depends on visual abilities and acuity, information processing, and control of chromatophores dynamics through nervous and hormonal regulation with which many contaminants can interfere. Therefore, the quantitative measurement of color change in cephalopod species could be developed as a powerful endpoint for toxicological risk assessment. Based on a wide body of research having assessed the effect of various environmental stressors (pharmaceutical residues, metals, carbon dioxide, anti-fouling agents) on the camouflage abilities of juvenile common cuttlefish, we discuss the relevance of this species as a toxicological model and address the challenge of color change quantification and standardization through a comparative review of the available measurement techniques.

Sexual dimorphism in dynamic body color in the green anole lizard

Animals capable of rapid (i.e., physiological) body color change may use color to respond quickly to changing social or physical environments. Because males and females often differ in their environments, the sexes may use changes in body color differently, reflecting sexual dimorphism in ecological, behavioral, or morphological traits. Green anole lizards, Anolis carolinensis, frequently switch their dorsal body color between bright green and dark brown, a change that requires only seconds, but little is known regarding sexual dimorphism in their color change. We tested three hypotheses for the function of body color (thermoregulation, camouflage via background-matching, and social communication) to determine the ecological role(s) of physiological color change in anoles. First, we examined instantaneous body color to determine relationships between body color and body temperature, substrate color and type, and whether these varied between the sexes. Next, we examined the association between color change and behavioral displays. Altogether, we found that males were more likely to be green than females, and larger lizards were more often green than smaller ones, but there was no evidence that anole body color was associated with body temperature or background color during the summer breeding season. Instead, our results show that although the sexes change their color at approximately the same rates, males changed color more frequently during social displays, while females remained green when displaying. In sum, social communication appears to be the primary function of anole color change, although the functions of body color may differ in the nonbreeding season.Significance statementMany animals can change their body color in response to their environments, and in many species, males and females experience different environments. In this study, we examined whether the sexes of green anole lizards use the ability to rapidly change their body color between green and brown for different functions. We found that, when a lizard was first sighted, its body color did not appear to match its background color in either sex (suggesting that color change does not contribute to avoidance of detection by potential predators), and body color was not associated with temperature for either sex (i.e., color was unlikely to influence body temperature). Yet, males changed color more often when performing social displays to other lizards, while females remained green during social displays. Thus, rapid color change plays an important role in social communication in both sexes, highlighting how males and females may use the same behavior to convey different messages.

Melatonin modulates the hypothalamic-pituitary neuroendocrine axis to regulate physiological color change in teleost fish.

Melatonin (MT) is a crucial neuroendocrine regulator of various physiological activities in vertebrates, especially in circadian or seasonal rhythm control. In the present study, the large yellow croaker (Larimichthys crocea), a marine bony fish with circadian body color change behavior, is chosen for functional investigation on teleost MT signaling systems that remain uncharacterized. All five melatonin receptors (LcMtnr1a1, LcMtnr1a2, LcMtnr1b1, LcMtnr1b2, and LcMtnr1c) were significantly activated by MT, triggering extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation through different G protein coupling signaling pathways, with exclusive Gαi-dependency for LcMtnr1a2 and LcMtnr1c, and Gαq-dependency for two LcMtnr1b paralogs, whereas LcMtnr1a1 activated Gαi and Gαs dual-dependent signaling pathways. A comprehensive model of the MT signaling system in the hypothalamic-pituitary neuroendocrine axis was further constructed based on ligand-receptor interaction analysis using single-cell RNA-seq data, as well as spatial expression patterns of Mtnrs and related neuropeptides in central neuroendocrine tissues. A novel regulatory pathway of MT/melanin-concentrating hormone (MCH) and MT/(tachykinin precursor 1 (TAC1)+corticotropin-releasing hormone (CRH))/melanocyte-stimulating hormone (MSH) was discovered that functions in chromatophore mobilization and physiological color change and was further validated by pharmacological experiments. Together, our findings define multiple intracellular signaling pathways mediated by L. crocea melatonin receptors and provide the first in-depth evidence that uncover the upstream modulating roles of the MT signaling system in the hypothalamic-pituitary neuroendocrine axis of a marine teleost species, particularly in chromatophore mobilization and physiological color change.

Sex-specific effects of inbreeding on body colouration and physiological colour change in the cichlid fish Pelvicachromis taeniatus

BackgroundColour expression is highly variable in animals. In fishes, rapid colour change, i.e. physiological colour change, can be observed in multiple contexts, e.g. in camouflage or communication, and is affected by various factors, such as stress. Pelvicachromis taeniatus is a cichlid fish from West Africa with sexual dichromatism and both sexes being brightly coloured and flexible in ornament expression. In the present study, inbred and outbred P. taeniatus were photographed before and after a stress situation to investigate the stress response regarding colour expression in both sexes.ResultsThe chromaticity and the colour patch size (relative coloured area at the abdomen) were determined at both timepoints and the changes were analysed. Additionally, the coefficients of variation within family groups for the chromaticity (CVchromaticity) and colour patch size (CVarea) were calculated. Chromaticity as well as the extent of colouration increased significantly following handling stress. The change in chromaticity was not significantly different between in- and outbred individuals in females and males. Inbred males showed more intense yellow colouration than outbred males. Independent from inbreeding, the CVchromaticity decreased following the handling stress. The change in CVarea of females and males differed between in- and outbred individuals. In females, the decrease was significantly stronger in inbred individuals and in males the decrease was stronger in the outbred group.ConclusionThe results show that short-term stress can increase colouration, potentially advertising individual’s stress tolerance. Furthermore, this study shows positive inbreeding effects on a sexually selected trait.

Colours of stress in male Indian rock agamas predict testosterone levels but not performance

Rapid physiological colour change offers dynamic signalling opportunities that can reveal distinct information to receivers in different contexts. Information content in dynamic colours, however, is largely unexplored. In males of the Indian rock agama (Psammophilus dorsalis), stressful events, including male-male agonistic interactions, induce a colour change, wherein the dorsal band turns yellow and the lateral bands turn orange. We aimed to determine whether these pigment-based dynamic colours convey information about individual quality. Using an agamid-specific visual model, we first quantified the chromatic and achromatic contrasts of each colour component displayed by males during handling stress, which induces the maximal response of aggression-typical colours. We then measured baseline testosterone levels, morphology (body mass and size), and performance measures (bite force and sprint speed) of these lizards. Chromatic contrasts of the dorsal yellow and lateral orange bands, individually and relative to each other (internal pair), were negatively correlated with testosterone levels, while the chromatic contrast of the internal pair was positively correlated with body condition. The lack of an association between colour contrasts and both bite force and sprint speed indicate that the conspicuousness of colours expressed during stressful events, such as agonistic interactions, do not reveal male performance ability. Despite our expectations of a positive relationship with testosterone, morphology (body condition), and performance (bite force, sprint speed), we find that for P. dorsalis, the conspicuousness of stress-induced colours provide only some information about individual quality. We speculate that the dynamicity of physiological colours may influence their function as content-containing signals in social interactions.

First person – Kun Guo

ABSTRACTFirst Person is a series of interviews with the first authors of a selection of papers published in Biology Open, helping early-career researchers promote themselves alongside their papers. Kun Guo is first author on ‘The thermal dependence and molecular basis of physiological color change in Takydromus septentrionalis (Lacertidae)’, published in BiO. Kun conducted the research described in this article while a PhD student in Xiang Ji's lab at Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Jiangsu, China. They are now research assistant in the lab of Xiang Ji at College of Life and Environmental Sciences, Wenzhou University, Zhejiang, China, and Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, Jiangsu, China.

The thermal dependence and molecular basis of physiological color change in Takydromus septentrionalis (Lacertidae).

ABSTRACTOne of the main functions of physiological color change is thermoregulation. This change occurs much more rapidly than morphological color change, but the underlying mechanism remains poorly understood. Here, we studied the thermal dependence and molecular basis of physiological color change in lizards using Takydromus septentrionalis (Lacertidae) as the model system. Body color was thermally sensitive, becoming increasingly light as body temperatures deviated from the level (∼30°C) preferred by this species. We identified 3389 differentially expressed genes (DEGs) between lizards at 24°C and 30°C, and 1,097 DEGs between lizards at 36°C and 30°C. Temperature affected the cAMP signal pathway, motor proteins, cytoskeleton, and the expression of genes related to melanocyte-stimulating hormone (MSH) and melanocyte-concentrating hormone (MCH). Our data suggest that the role of physiological color change in thermoregulation is achieved in T. septentrionalis by altering the arrangement of pigments and thus the amount of solar radiation absorbed and reflected. G protein-coupling system inhibits adenylate cyclase activity to transform ATP into cAMP and thereby causes rapid pigment aggregation. MCH deactivates the G proteins and thereby initiates pigment dispersion. This mechanism differs from that reported for teleost fish where MCH activates the G proteins and thereby causes pigment aggregation.This article has an associated First Person interview with the first author of the paper.

From extraocular photoreception to pigment movement regulation: a new control mechanism of the lanternshark luminescence

The velvet belly lanternshark, Etmopterus spinax, uses counterillumination to disappear in the surrounding blue light of its marine environment. This shark displays hormonally controlled bioluminescence in which melatonin (MT) and prolactin (PRL) trigger light emission, while α-melanocyte-stimulating hormone (α-MSH) and adrenocorticotropic hormone (ACTH) play an inhibitory role. The extraocular encephalopsin (Es-Opn3) was also hypothesized to act as a luminescence regulator. The majority of these compounds (MT, α-MSH, ACTH, opsin) are members of the rapid physiological colour change that regulates the pigment motion within chromatophores in metazoans. Interestingly, the lanternshark photophore comprises a specific iris-like structure (ILS), partially composed of melanophore-like cells, serving as a photophore shutter. Here, we investigated the role of (i) Es-Opn3 and (ii) actors involved in both MT and α-MSH/ACTH pathways on the shark bioluminescence and ILS cell pigment motions. Our results reveal the implication of Es-Opn3, MT, inositol triphosphate (IP3), intracellular calcium, calcium-dependent calmodulin and dynein in the ILS cell pigment aggregation. Conversely, our results highlighted the implication of the α-MSH/ACTH pathway, involving kinesin, in the dispersion of the ILS cell pigment. The lanternshark luminescence then appears to be controlled by the balanced bidirectional motion of ILS cell pigments within the photophore. This suggests a functional link between photoreception and photoemission in the photogenic tissue of lanternsharks and gives precious insights into the bioluminescence control of these organisms.

Observation on rapid physiological color change in Giant tree frog Rhacophorus smaragdinus (Blyth, 1852) from Namdapha Tiger Reserve, Arunachal Pradesh, India

Many poikilotherms have the ability to change body color for homeostatic regulation, conspecific communication or predator deterrence. Physiological color change is a rapid, reversible mode of color change regulated by neuromuscular or neuroendocrine system and has been observed in several anuran species. Here we report the occurrence of physiological color change in the tree frog Rhacophorussmaragdinus (Blyth, 1852) (Amphibia, Anura, Rhacophoridae) for the first time from Namdapha Tiger Reserve, Arunachal Pradesh, India. Probable proximate causes of the behavior are discussed along with an overview of physiological color change in species of the family Rhacophoridae and nature of color change observed.

First Report of Physiological Color Change in a Crocodilian

Physiological color change in animals is a rapid process involving the redistribution of pigments within chromatophores, and may have roles in camouflage, communication, or thermoregulation. Although observed in other ectotherms, it has not previously been documented in crocodilians. Using wild and captive Sunda gharials (Tomistoma schlegelii), we confirm rapid ventral color change in juveniles, as evidenced by significantly darker ventral scales in illuminated vs. dark environments. We also found that color varied significantly with body size, with larger individuals losing the ability to change color, and by testing environmental factors potentially triggering color change—temperature, ambient light, background color, or stress—we report that illumination was the only factor observed to explain the change. Our results reveal an unusual trait not corresponding to established countershading patterns, which provides a basis for further research not only into crocodilian behavioral ecology and physiology, but also into animal camouflage and convergent evolution. These results add further evidence to Tomistoma being an evolutionarily distinct lineage of crocodilian, confined to the threatened peat swamp habitats of Southeast Asia.

Regulation of eye and jaw colouration in three-spined stickleback Gasterosteus aculeatus.

Fish can change their skin and eye colour for background matching and signalling. Males of Gasterosteus aculeatus develop ornamental blue eyes and a red jaw during the reproductive season, colours that are further enhanced during courtship. Here, the effects of different hormones on physiological colour changes in the eyes and jaws of male and female G. aculeatus were investigated in vitro. In an in vivo experiment, G. aculeatus were injected with a receptor blocker of a pivotal hormone (noradrenaline) that controls colour change. In males, noradrenaline had aggregating effects on melanophore and erythrophore pigments resulting in blue eyes and a pale jaw, whereas melanocyte-concentrating hormone (MCH) and melatonin resulted in a pale jaw only. When noradrenalin was combined with melanocyte stimulating hormone (MSH) or prolactin, the jaw became red, while the eyes remained blue. In vivo injection of yohimbine, an alpha-2 adrenoreceptor blocker, resulted in dispersion of melanophore pigment in the eyes and inhibited the blue colouration. Altogether, the data suggest that noradrenalin has a pivotal role in the short-term enhancement of the ornamental colouration of male G. aculeatus, potentially together with MSH or prolactin. This study also found a sex difference in the response to MCH, prolactin and melatonin, which may result from different appearance strategies in males, versus the more cryptic females.

MONITORING OF SUBLETHAL EFFECT OF CHROMIUM ON MELANOPHORES

Some heavy metals are essential for normal physiological functioning of fish but become toxic when they accumulate in their body tissues and are not metabolized, dyes. Chromium is dangerous as it can accumulate in fish body as much as 4000 times greater than that of their surroundings. The present investigation deals with sublethal effects of chromium sulphate (10 ppm. 10% of 96 h LC50) on the melanophores of Catla catla was investigated to understand its toxicity on Melanophores morphology. Observed toxic pathological alterations include statistically significant variations in the number, size and shape of the Melanophores. Due to the lysis of the Melanophores, the melanin contents were poured into the surrounding matrix of the connective tissue, between 20 and 30 days of exposure. The chromium induced morphological changes in the melanophores protected the delicate epidermis from the toxic medium. In addition to the physiological colour changes, there was slow morphological colour changes by the gradual regeneration of the chromatophores. The density of chromatophores was maximum after 45 days. These generated pigment cells were smaller in size and more in number when compared with the normal melanophores. The study show that higher concentrations of metals in fish can alter its physiological functioning that could lead to high mortality and ultimately loss of indigenous fish biota.

Wound healing in Piaractus mesopotamicus supplemented with chromium carbochelate and Saccharomyces cerevisiae

A cicatrização e reparação de tecidos são mecanismos essenciais para garantir a sobrevivência e saúde de qualquer indivíduo. O objetivo deste trabalho foi avaliar o impacto da suplementação com carboquelato de cromo (CC) e Saccharomyces cerevisiae (SC) sobre a cicatrização no peixe tropical Piaractus mesopotamicus. Para isto, os peixes foram distribuídos em quatro grupos: controle (sem tratamento), suplementados com 18 mg/kg de carboquelato de cromo, 0,3% de S. cerevisiae e associação de ambos os suplementos. Após 105 dias de alimentação, foram realizadas incisões na pele de espessura completa (2,0 x 1,0 x 0,25 cm) removendo epiderme e derme. Avaliações macroscópicas e microscópicas foram realizadas 1, 3, 7, 14, 21, 28 e 35 dias após a indução das feridas, para monitorar a taxa de cicatrização. As bordas opostas das feridas avançaram gradualmente a cada dia, demonstrando o aumento progressivo do processo de cicatrização ao longo do tempo. O processo inflamatório foi exacerbado e expansivo, com aumento no número de células mucosas e cromatóforos. Apesar deste processo, não foram observadas diferenças significativas na retração das feridas e nos parâmetros microscópicos entre os grupos. Peixes suplementados com CC ou Sc apresentaram rápida reepitelização, maior grau de organização de fibras colágenas e de neovascularização inicial. Concluiu-se que a suplementação com S. cerevisiae ou carboquelato de cromo melhora aspectos específicos do processo cicatricial no pacu.

Signalling with physiological colours: high contrast for courtship but speed for competition

Dynamic physiological colour change allows animals to alter colours and patterns for communication, camouflage and thermoregulation. Using reflectance spectrometry and digital photography, we found that males of the Indian rock agama, Psammophilus dorsalis, can rapidly express intense colours that are different from the neutral state and specific to the social context. The distinct bands on males shifted between yellow and red (dorsal) and between orange and black (lateral) within seconds, and the resulting colour pattern was diametrically different depending on whether males were in courtship or aggressive interactions. Although males showed higher chromatic contrast when courting females, the colour change was faster during competitive encounters with other males. The nature of this social colour communication also differed across populations in anthropogenically disturbed landscapes. Compared to males from rural areas, suburban males were slower to change colour and showed duller and paler colours during staged social encounters. Consistent with other disturbance-induced shifts in phenotypic traits seen in numerous taxa, we provide the first evidence that social signalling through dynamic colour change in terrestrial vertebrates is also affected by urbanization. (C) 2017 The Association for the Study of Animal Behaviour. Published by Elsevier Ltd. All rights reserved.

Geographic Color Variation and Physiological Color Change in Eastern Collared Lizards (Crotaphytus collaris) from Southern New Mexico, USA

Abstract: Many factors can contribute to geographic color variation, including natural selection, sexual selection, and genetic drift. In squamates, phenotypic plasticity can also play an important role in color variation because color can change during maturation, across seasons, and over short time scales in response to environmental stimuli. Here, we quantify geographic color variation and assess the contribution of physiological plasticity (rapid color change) in populations of Eastern Collared Lizards (Crotaphytus collaris). First, we quantified the dorsal coloration of four geographically distinct populations of C. collaris: two putatively melanistic populations on lava flows, and two typically colored populations from the surrounding desert. Second, we quantified the degree of physiological color change occurring in response to stress and temperature, two factors known to affect reptile coloration over short time scales. We found that populations differed in overall coloration, but that only one of...