Yellow Body Color Research Articles

Structural basis of selective beta-carotene binding by a soluble protein

β-carotene (BCR) is the most abundant carotenoid, a colorant, antioxidant, and provitamin A. The extreme hydrophobicity of this hydrocarbon requires special mechanisms for distribution in aqueous media, including water-soluble carotenoproteins. However, all known carotenoproteins prefer oxygenated carotenoids and bind BCR inefficiently. Here, we present the crystal structure of the BCR-binding protein (BBP) from gregarious male locusts, which is responsible for their vivid yellow body coloration, in complex with its natural ligand, BCR. BBP forms an antiparallel tubular homodimer with α/β-wrap folded monomers, each forming a hydrophobic 47Å long, coaxial tunnel that opens outward and is occupied by one s-cisC6-C7, all-trans BCR molecule. In the BCR absence, BBP accepts a range of xanthophylls, with reduced efficiency depending on the position and number of oxygen atoms, but rejects lycopene. The structure captures a pigment complex with a Takeout 1 protein and inspires potential applications of BBP as a BCR solubilizer.

First record of Pipunculidae (Diptera) from Martinique, with a description of Eudorylas dumbardoni sp. nov.

ABSTRACT The family Pipunculidae is being recorded from Martinique for the first time. During a dipterological expedition on the island in January – February 2018, mainly based on the pan-trap method, four specimens of Eudorylas dumbardoni sp. nov. were collected. This species is described, illustrated, and compared with E. cressoni Johnson, a similar species based mainly on the yellow body coloration, originally described from the Bahamas and Jamaica, and also recorded from the Dominican Republic.

Four new saproxylic species of Paranura Axelson, 1902 (Collembola: Neanuridae: Neanurinae) from Japan.

Four new saproxylic species of the genus Paranura from Nagasaki, Nara, and Niigata provinces of Japan are described and illustrated in this paper. Paranura tsushimaensis sp. nov. is characterized by a dark blue body color, Abd. V four times as long as Abd. VI, 3+3 eyes, three ocular chaetae on the head, four ordinary chaetae De on Th. III, two ordinary chaetae Di on Abd. V, and all dorsal chaetae of Abd. VI in a unique reticulated plate. P. nakamurai sp. nov. is identified by its yellowish white body color, 2+2 eyes, tubercle Af on the head with two reticulated tubercles, and tubercles Di on Abd. V fused. P. alpicola sp. nov. is characterized by its yellow body color, 3+3 eyes, presence of complete chaetotaxy in the central area of the head, Th. IIIII with two and three ordinary chaetae De respectively, and tubercles Di on Abd. V separate. P. convallis sp. nov. is identified by its orange body color, 3+3 eyes, head without chaeta O, three mandibular teeth, and Th. IIIII with three and four ordinary chaetae De respectively. A key for all species of the genus Paranura is provided.

Redundant actions of neuropeptides encoded by the dh-pban gene for larval color pattern formation in the oriental armyworm Mythimnaseparata

The pyrokinin (PK)/pheromone biosynthesis-activating neuropeptide (PBAN) family, which is defined by a conserved C-terminal pentapeptide (FXPRLamide), is involved in many physiological processes in insects. In the oriental armyworm Mythimna separata, the larvae exhibit a variety of color patterns in response to changes in population density, which are caused by melanization and a reddish coloration hormone (MRCH), which is a member of the FXPRLamide neuropeptides. Interestingly, in some lepidopteran insects, MRCH is known as a PBAN, which activates the pheromone gland to produce sex pheromones. PBAN is encoded by a single gene, dh-pban, which encodes additional FXPRLamide neuropeptides, such as the diapause hormone (DH) and subesophageal ganglion neuropeptides (SGNPs). To determine the roles of the dh-pban gene, which produces multiple types of FXPRLamide neuropeptides after post-transcriptional cleavage of the precursor protein, we performed CRISPR/Cas9-mediated targeted mutagenesis in M. separata. We demonstrated that knockout armyworm larvae lost density-dependent cuticular melanization and retained yellow body color, even when reared under crowded conditions. Moreover, our rescue experiments using the synthetic peptides showed that not only PBAN but also β- and γ-SGNPs significantly induce the cuticular melanization in a dose dependent manner. Taken together, our results provide genetic evidence that neuropeptides encoded by the single dh-pban gene act redundantly to control density-dependent color pattern formation in M. separata.

Knockout of microphthalmia-associated transcription factor (mitf) confers a red and yellow tilapia with few pigmented melanophores

As the most important genetic factor for melanophore differentiation and melanogenesis, mitf has been studied for over 30 years. The phenotypes of mitf mutants have also received continuous attention for nearly a century. Due to the third round of genome duplication, teleosts have two mitf genes. Mutation analysis demonstrates that mitfa plays an important role in zebrafish pigmentation. However, there have been no functional studies on body color regulation by mitfb or studies of mitfa;mitfb double mutants. In the present study, we mutated both mitf genes in tilapia using CRISPR/Cas9. Disruption of mitfa resulted in light yellow body color with weak gray vertical bars due to significantly reduced numbers of melanophores and increased sizes of xanthophores, while disruption of mitfb led to slight hypo-pigmentation. Double mutation of mitfa and mitfb resulted in dramatic hypo-pigmentation in trunk and fins due to loss of additional melanophores and increase in the number of iridophores compared to the single mutants, but had no influence on retinal pigment epithelium (RPE) pigmentation. The mitfa−/−;mitfb−/− mutants were yellow with black spots at early juvenile stage (60 dpf), yellow-reddish at late juvenile stage (120 dpf) and red and yellow (including iris) at adult stage (180 dpf), due to increased erythrophores and enlarged xanthophores. Our results demonstrated that both mitf genes are important for body color formation in tilapia, but mitfa plays a more important role than mitfb. Additionally, by comparing the phenotypes of the mitfa−/−;mitfb−/−, pmela−/−;pmelb−/− and hps4−/− mutants, we found that disruption of genes with different functions in different aspects of melanogenesis could lead to different body colors in tilapia. Mitf is the most important gene for melanophore differentiation and is probably also critical for differentiation of erythrophores, xanthophores and iridophores. To our knowledge, this is the first report showing that both mitf genes are involved in body color formation by loss of function study, and the first report showing that erythrophore numbers and xanthophore sizes were affected by mitf. Our research not only serves as a model for studying mitf function in tilapia and the closely related cichlids, but also provides new strategies for breeding red and yellow tilapia for aquaculture.

First report of the genera Paralobella and Blasconura (Collembola: Neanuridae: Neanurinae) from Japan with the description of three new species.

This study reports the first record of the genera Paralobella Cassagnau Deharveng, 1984 and Blasconura Cassagnau, 1983, three new species from Kuchinoerabu-jima and Miyako-jima of Japan, respectively. Paralobella kuchierabu sp. nov. can be distinguished from all known genus members by distinct morphological characteristics: yellow body color, mandible with 3 teeth, presence of chaeta O on head, and tubercle De of Th. IIIII with 5 (4+s) chaetae, tubercle Di of Th. I with 1 chaeta, tubercles De and Dl of Abd. V separated. Blasconura triangulum sp. nov. is characterized by a tubercle Fr fused to An, unguis without an inner tooth, and 2 very closely placed tubercles Di on head. Blasconura cordis sp. nov. is unique in the genus, with a tubercle An fused to Cl. Other characteristic features of the species are the absence of chaeta O on head, tubercle Oc with 3 chaetae, Ant. I with 7 chaetae, and tubercle De of Th. III with 5 (4+s) chaetae. A key to all species of the genus Paralobella and Blasconura is provided.

A novel symbiotic relationship between ascidians and a new tunic-boring polychaete (Annelida: Spionidae: Polydora).

Polydora tunicola Abe, Hoshino Yamada, sp. nov., a new spionid species currently considered an obligate symbiont of styelid ascidians, is described based on materials collected from Polycarpa cf. cryptocarpa kroboja (Oka, 1906) and Cnemidocarpa sp. in Izu-Oshima Island and Polycarpa sp. in Wakayama Prefecture, Japan. Polychaeteascidian symbiotic relationships are known only in two syllid species: Myrianida pinnigera (Montagu, 1808) and Proceraea exoryxae Martin, Nygren Cruz-Rivera, 2017. The latter has been the only polychaete known to bore into the tunic of an ascidian. Polydora tunicola sp. nov. is the second known example of a tunic-boring polychaete, which constructs U-shaped burrows in the tunic of the host ascidians. Worms were often concentrated near the host siphons and assumed to use water currents created by the filter-feeding host for suspension feeding. Although the boring mechanism into ascidian tunica is unknown, the plate assay and zymography results consistently detected cellulase activities, suggesting that cellulose digestion may enable the worms to bore into the cellulose-rich ascidian tunics. Polydora tunicola sp. nov. is morphologically similar to P. aura Sato-Okoshi, 1998, P. cornuta Bosc, 1802, P. fusca Radashevsky Hsieh, 2000, P. glycymerica Radashevsky, 1993, P. latispinosa Blake Kudenov, 1978, P. lingulicola Abe Sato-Okoshi, 2020, P. nanomon Orensky Williams, 2009, P. robi Williams, 2000, and P. vulgaris Mohammad, 1972 in having a single median antenna on the caruncle and chaetiger 5 without dorsal superior capillaries but with ventral capillaries. The new species is unique in having a black-rimmed pygidium, distinguishing it from these species. The phylogenetic analyses of the concatenated 18S, 28S, and 16S sequences recovered P. tunicola sp. nov. as the sister species to P. aura within a well-supported clade also including P. lingulicola and P. cf. glycymerica. The bright yellow body color of P. tunicola sp. nov. in life is similar to that of P. aura, however, these two species are distinguished by the former not having modified posterior notochaetae. The symbiotic nature of the association between P. tunicola sp. nov. and styelid ascidians is discussed.

Yellow–green color polymorphism in males of a pea aphid clone and its genetic pattern

AbstractAlthough most aphid species living on leaves have a green body color, little is known regarding the biosynthetic pathways of green pigments. We found that a clone of the pea aphid, Acyrthosiphon pisum (Harris) produced both green‐ and yellow‐colored males. The females of this clone were green in color, while 8.4% of the males produced were yellow. To date, yellow body color has been reported only in a single mutant clone in A. pisum. To explore the genetic pattern of yellow body color, green or yellow males were mated with green females of the same clone. The hatchability of the eggs sired by yellow males (26.2%) was less than half that of the eggs sired by green males (79.0%). The hatched foundresses of both groups were all green, with no yellow foundresses. Because aphids have an XX‐XO sex determination system, color polymorphism in males suggests that male body color may be governed by an X‐linked locus. If females possess heterozygosity at the putative locus, they can produce alternative phenotypes in males. The small proportion of yellow males and absence of yellow foundresses imply that the allele responsible for yellow body color has a deleterious effect. The present study suggests that this clone could be used to elucidate the biosynthetic pathways and underlying genetics of green pigments in aphids.

Yellow-b, -c, -d, and -h are required for normal body coloration of Henosepilachna vigintioctopunctata.

The involvement of yellow genes y-b, y-c, y-e, and y-h in cuticle tanning has poorly been clarified. In the present paper, six putative yellow (y-y, y-b, y-c, y-e y-f, and y-h) genes were identified in Henosepilachna vigintioctopunctata. Hvy-b, Hvy-c, Hvy-e, and Hvy-h were abundantly transcribed at early larval and late pupal stages, especially in the epidermis. Accordingly, RNA interference (RNAi) experiments were performed by an injection of dsy-b, dsy-c, dsy-e, or dsy-h into the second instar larvae and 1-day-old pupae. The head capsule, scoli and strumae, and legs in the fourth-instar larvae became blacker; the blackish spots in the pupae were darkened and widened after RNAi of Hvy-b, compared with those of dsegfp-treated controls. Depletion of Hvy-b at the 1-day-old pupal stage expanded two pair of black markings on the sternum of the metathorax, and darkened the black patched on the sterna of the abdomen segments I-VI in the resultant adults. Depletion of Hvy-e caused darker pigmented adult body and elytral cuticles than those of dsegfp-introduced controls. However, there was no obvious difference in pigmentation of the black markings. Hvy-h-deficient larvae displayed dark yellow body color, whereas the body color of the dsegfp-injected control was pale yellow. There was no obvious difference in coloration of larval specific-black markings or pupal cuticle between dsHvy-h- and dsegfp-treated animals. Moreover, silence of Hvy-c at the second instar larval stage lightened black markings in the resulting larvae and pupae, but had no influence on pale yellow body color. Our results demonstrated their different roles of the four yellow genes during body pigmentation: HvY-b and HvY-c, respectively, inhibit and facilitate the coloration within dark markings, whereas HvY-e and HvY-h, respectively, repress the pigmentation in adult and larval body cuticles outside the black patches in H. vigintioctopunctata.

Body coloration as a dynamic signal during intrasexual communication in a cichlid fish

BackgroundIntrasexual competition over access to resources can lead to aggression between individuals. Because overt aggression, i.e. fights, can be costly for contestants, the communication of aggressive motivation prior to engagement in a physical fight is often mediated by conventional signals. Animals of various taxa, including fishes, display visual signals such as body coloration that can dynamically be adjusted depending on the individual’s motivation. Male individuals of the West African cichlid Pelvicachromis taeniatus express a yellow body coloration displayed during courtship but also in an intrasexual competition context.ResultsWithin-individual variation in male yellow body coloration, as quantified with standardized digital photography and representation in a CIELab color space, was examined in a mating context by exposing males to a female and in a competitive intrasexual context, i.e. in a dyadic contest. Additionally, spectrometric reflectance measurements were taken to obtain color representations in a physiological color space based on spectral sensitivities of our model species. Exposure to females did not significantly affect male color expression. However, analysis of body coloration revealed a change in within-individual color intensity and colored area after interaction with a male competitor. In dominant males, extension of coloration was positively correlated with restrained aggression, i.e. displays, which in turn explained dominance established between the two contestants.ConclusionBody coloration in male P. taeniatus is a dynamic signal that is used in concert with display behavior in communication during intrasexual competition.

Revision of the Empis (Enoplempis) mira species group (Diptera: Empididae).

The Empis (Enoplempis) mira species group is revised and includes the type species of Enoplempis and four new species (E. macdonaldi sp. nov., E. submira sp. nov., E. williamturneri sp. nov., E. winkleri sp. nov.). A lectotype is designated for Enoplempis mira Bigot. The species group is defined by the yellow body colour, directionally asymmetrical male hindlegs and geniculate hindlegs in both males and females. The group has not been found outside of western North America and is known from California, Oregon, Idaho and Washington.

Ebony affects pigmentation divergence and cuticular hydrocarbons in Drosophila americana and D. novamexicana.

Drosophila pigmentation has been a fruitful model system for understanding the genetic and developmental mechanisms underlying phenotypic evolution. For example, prior work has shown that divergence of the tan gene contributes to pigmentation differences between two members of the virilis group: Drosophila novamexicana, which has a light yellow body color, and D. americana, which has a dark brown body color. Quantitative trait locus (QTL) mapping and expression analysis has suggested that divergence of the ebony gene might also contribute to pigmentation differences between these two species. Here, we directly test this hypothesis by using CRISPR/Cas9 genome editing to generate ebony null mutants in D. americana and D. novamexicana and then using reciprocal hemizygosity testing to compare the effects of each species' ebony allele on pigmentation. We find that divergence of ebony does indeed contribute to the pigmentation divergence between species, with effects on both the overall body color as well as a difference in pigmentation along the dorsal abdominal midline. Motivated by recent work in D. melanogaster, we also used the ebony null mutants to test for effects of ebony on cuticular hydrocarbon (CHC) profiles. We found that ebony affects CHC abundance in both species, but does not contribute to qualitative differences in the CHC profiles between these two species. Additional transgenic resources for working with D. americana and D. novamexicana, such as white mutants of both species and yellow mutants in D. novamexicana, were generated in the course of this work and are also described. Taken together, this study advances our understanding of loci contributing to phenotypic divergence and illustrates how the latest genome editing tools can be used for functional testing in non-model species.

Yellowing and YPT gene expression in the desert locust, Schistocerca gregaria: Effects of developmental stages and fasting.

The yellow protein of the takeout family (YPT) controls the development of yellow body color in the desert locust. This study focused on two aspects related to YPT in the locust. We first examined the expression pattern of YPT during nymphal stages because yellowing was not obvious during the early instars. YPT expression levels were extremely low in the second and third instars compared with the last two nymphal instars. Warm rearing temperature and juvenile hormone (JH) injection, which stimulated YPT expression in the late instars, had little effect in the second instar, suggesting that YPT expression during the early instars was suppressed and could not be stimulated by either of these factors. We also investigated delayed yellowing in fasting male adults, under the hypothesis that fasting decreased the JH titers and delayed the onset of YPT expression. Yellowing was delayed in fasting adults compared with well-fed adults and YPT expression was stimulated by JH injections at Day 15. However, we failed to obtain evidence that fasting significantly influenced the expression levels of YPT and the JH early-inducible gene Krüppel homolog 1 at Days 15 and 20 post-adult emergence. Results suggest that a YPT-independent mechanism possibly induces delayed yellowing in fasting males.

Expanding the genetic toolkit of Tribolium castaneum.

The red flour beetle, Tribolium castaneum, is an important model insect and agricultural pest. However, many standard genetic tools are lacking or underdeveloped in this system. Here, we present a set of new reagents to augment existing Tribolium genetic tools. We demonstrate a new GAL4 driver line that employs the promoter of a ribosomal protein gene to drive expression of a UAS responder in the fat body. We also present a novel dual fluorescent reporter that labels cell membranes and nuclei with different fluorophores for the analysis of cellular morphology. This approach also demonstrates the functionality of the viral T2A peptide for bicistronic gene expression in Tribolium. To facilitate classical genetic analysis, we created lines with visible genetic markers by CRISPR-mediated disruption of the yellow and ebony body color loci with a cassette carrying an attP site, enabling future φC31-mediated integration. Together, the reagents presented here will facilitate more robust genetic analysis in Tribolium and serve as a blueprint for the further development of this powerful model’s genetic toolkit.

Genetic Basis of Body Color and Spotting Pattern in Redheaded Pine Sawfly Larvae (Neodiprion lecontei).

Pigmentation has emerged as a premier model for understanding the genetic basis of phenotypic evolution, and a growing catalog of color loci is starting to reveal biases in the mutations, genes, and genetic architectures underlying color variation in the wild. However, existing studies have sampled a limited subset of taxa, color traits, and developmental stages. To expand the existing sample of color loci, we performed QTL mapping analyses on two types of larval pigmentation traits that vary among populations of the redheaded pine sawfly (Neodiprion lecontei): carotenoid-based yellow body color and melanin-based spotting pattern. For both traits, our QTL models explained a substantial proportion of phenotypic variation and suggested a genetic architecture that is neither monogenic nor highly polygenic. Additionally, we used our linkage map to anchor the current N. lecontei genome assembly. With these data, we identified promising candidate genes underlying (1) a loss of yellow pigmentation in populations in the mid-Atlantic/northeastern United States [C locus-associated membrane protein homologous to a mammalian HDL receptor-2 gene (Cameo2) and lipid transfer particle apolipoproteins II and I gene (apoLTP-II/I)], and (2) a pronounced reduction in black spotting in Great Lakes populations [members of the yellow gene family, tyrosine hydroxylase gene (pale), and dopamine N-acetyltransferase gene (Dat)]. Several of these genes also contribute to color variation in other wild and domesticated taxa. Overall, our findings are consistent with the hypothesis that predictable genes of large effect contribute to color evolution in nature.

Environmental and hormonal control of body color polyphenism in late-instar desert locust nymphs: Role of the yellow protein

Locusts show body color polyphenism that is considered to be an adaptation to various biotic and abiotic environmental changes. In Schistocerca gregaria, wild-type late-instar nymphs growing under crowded conditions (gregarious form) develop yellow and black body coloration, whereas they assume various body colors under isolated conditions (solitarious form). Black and green body colorations are induced by the neuropeptide corazonin (Crz) and juvenile hormone (JH), respectively. To characterize the molecular mechanisms controlling body color polyphenism, we investigated factors influencing body coloration in S. gregaria. We report here that yellow body coloration in the last nymphal instar is caused by the yellow protein of the takeout family (YPT) in this locust. YPT transcription was enhanced under high-temperature conditions during which the nymphs turned bright yellow and had little black patterning. RNAi-mediated YPT knockdown suppressed the appearance of yellow individuals and yellow staining in the exuviae. In albino nymphs, injection of JH induced yellow and green coloration and enhanced the YPT expression levels in both yellow and green individuals. YPT knockdown also suppressed yellow staining in the exuviae but did not prevent the appearance of yellow individuals. Therefore, another factor or pigment may contribute to the observed yellow body color. Injection of Crz into wild-type nymphs caused darkening and suppressed yellowing and YPT expression at high temperatures. Thus, Crz signaling could inhibit yellowing by suppressing YPT expression. Rearing cup substrate color significantly influenced YPT expression in albino nymphs both under isolated and crowded conditions. In contrast, substrate color affected YPT expression in wild-type nymphs only under isolated conditions. From these results, we conclude that YPT is an important factor in the control of body color polyphenism in S. gregaria, and its expression is influenced by temperature, JH, Crz, and substrate color of the growing environment.

First record of abnormal body coloration in a rockfish Sebastes trivittatus (Scorpaenoidei: Sebastidae)

Abnormal body coloration (malpigmentation) in teleost fishes usually occurs as either a deficiency (albinism or hypomelanosis) or an excess (melanism or hypermelanosis) of pigmentation (e.g., Simon et al. 2009; Jawad et al. 2013). A particular form of the former, phenotypically expressed as bright yellow or orange body coloration, has been referred to as xanthism or xanthochroism (e.g., Amaoka 1995; Carson 2011; Lewand et al. 2013). Although malpigmentation in teleosts has been extensively studied in the context of aquaculture, especially in Pleuronectiform fishes in relation to developing asymmetry (e.g., Matsumoto and Seikai 1992; Venizelos and Benetti 1999; Burton 2010), it has been largely overlooked in natural populations. Abnormal coloration in rockfishes of the genus Sebastes has occasionally been reported, mostly from the eastern North Pacific (e.g., Phillips 1957, 1964; reviewed in Love et al. 2002). However, most of these were considered to have been caused by skin tumors, resulting in black patches on the body, with other color abnormalities having been relatively rarely documented [Love et al. 2002; but see Muto et al. (2013) for partial albinism; Lewand et al. (2013) for xanthochroism]. On 7 July 2014, a single individual of Sebastes trivittatus, exhibiting a rare example of abnormal body coloration, was captured by gill net at a depth of 17 m, near Daikokujima Island, off Muroran, Hokkaido, Japan (Fig. 1a). A brief description of the specimen is given below. Morphological characters were examined following Muto et al. (2011). The terminology of the head spines followed Randall and Eschmeyer (2001). The specimen was deposited in the Kyoto University Fish Collection (FAKU). Description (based on FAKU 137112, male, 189.5 mm in standard length). The following measurements are expressed as percentage of standard length: head length 38.2; snout length 9.3; orbit diameter 9.4; interorbital width 4.9; postorbital length 19.9; upper-jaw length 19.5; body width 17.1; body depth 1 35.0; body depth 2 26.9; caudal-peduncle depth 9.6; upper-peduncle length 10.8; lower-peduncle length 18.6; dorsal-fin base length 60.9; spinous dorsal-fin base length 37.2; soft dorsal-fin base length 24.2; anal-fin base length 15.3; preanal length 65.4; predorsal length 34.7; prepelvic length 41.7; first dorsal-fin spine length 7.1; second dorsal-fin spine length 11.6; third dorsal-fin spine length 17.0; fourth dorsal-fin spine length 19.5; fifth dorsal-fin spine length 19.9; antepenultimate dorsal-fin spine length 11.8; penultimate dorsal-fin spine length 9.9; last dorsal-fin spine length 12.2; first anal-fin spine length 8.2; second anal-fin spine length 16.5; third anal-fin spine length 15.3; longest (second) anal-fin soft ray length 19.9; pectoral-fin length 30.1; pelvic-fin length 25.2; pelvic-fin spine length 14.7. Dorsal-fin rays XIII, 13; anal-fin rays III, 6; pectoral-fin rays 18, uppermost ray unbranched, second to ninth Electronic supplementary material The online version of this article (doi:10.1007/s10228-015-0471-x) contains supplementary material, which is available to authorized users.

Colour change ability and its effect on prey capture success in female Misumenoides formosipes crab spiders

1. Changing between white and yellow body colour in certain crab spider species has been interpreted as an adaptation for matching the background colour where they hunt and thereby remaining cryptic to prey and/or their own predators. The potential costs and benefits of colour change in female Misumenoides formosipes Walckenaer were investigated via assessment of prey opportunities and capture success, in conjunction with the tendency for and rate of colour change on different backgrounds.2. It was tested whether being matched or mismatched to their background affected foraging by moving females between white and yellow inflorescences. Female colour was quantified in digital photos using the Lab colour space component of Adobe photoshop, providing the first empirical assessment of the rate of colour change for a crab spider species.3. Insect visits (potential prey) on inflorescences with and without spiders and prey capture success with females matched and mismatched to their background were quantified.4. Yellow females abandoned white inflorescences, whereas white females remained on and underwent colour change on yellow inflorescences. This difference supported the notion that the costs of colour change differ depending on the starting colour. Female departures from white flowers were apparently not due to a lack of insect visitation, as white inflorescences had higher visitation rates than did yellow inflorescences, even in the presence of spiders.5. An increase in the prey capture success of females who transitioned from white to yellow body colour on a yellow background supported the hypothesis that colour matching functions to deceive prey.

The hormonal regulation of color changes in the sexually dichromatic frog Buergeria robusta.

During the breeding season, dynamic changes in body coloration are regularly observed in the male brown tree frog Buergeria robusta. This study investigated the hypothesis that this sexual dichromatism in male B. robusta is mediated through hormonal regulation. Frogs were exogenously injected with testosterone (T) or estradiol (E2). This manipulation revealed that the body coloration (hue, brightness, and saturation) of the male frog increased significantly (i.e., the brilliant yellow color developed) in response to T but not in response to E2. Concurrently, the levels of expression of brain-derived neurotrophic factor (BDNF) and pituitary adenylate cyclase-activating polypeptide (PACAP) in the pituitary gland were reduced in frogs whose coloration was pale brown on a yellow background. In particular, the weakest expressions of BDNF, PACAP, and PACAP type II receptors (VPAC-1R) were found in male frogs with a brilliant yellow body color during the breeding season regardless of background color. These changes may decrease α-melanocyte-stimulating hormone production associated with the PACAP receptors (VPAC-1R), resulting in the aggregation of black pigment in melanophores and the production of a brilliant yellow body color. The effects of hormones on skin coloration were further examined in isolated skin in vitro. The results of this investigation showed that the dispersion of xanthophores was stimulated by T or prolactin (PRL) and that the melanophores were aggregated by melatonin (MEL) but not by E2. Furthermore, yellow pigments in the xanthophores were significantly dispersed following the PRL+T treatment. In the T+MEL, PRL+MEL, and T+PRL+MEL treatments, xanthophores were dispersed, and melanophores were aggregated and subsequently moved to the low spongiosum layer of the dorsal skin, causing the increase in yellow coloration. These results reveal that multiple hormones play major roles in the regulation of the brilliant yellow coloration of male B. robusta by high plasma T during the breeding season.

A taxonomic review of the genus Minettiella Malloch (Diptera: Lauxaniidae) in Palearctic Region

The genus Minettiella (Diptera: Lauxaniidae) in Palearctic Region is reviewed. This genus currently includes two Palearctic and three Oriental species. We here provide a key to the five known Minettiella species and detailed redescriptions of the two Palearctic species (M. coracina and M. dolabriformis) based on the specimens discovered for the first time in South Korea. We also clarified some taxonomic confusion involving these two species. Currently, Minettiella can only be distinguished from the closely resembling genera, Melinomyia and Minettia, by the combination of the yellow body coloration and single katepisternal seta. These characters, however, do not seem to justify their generic differentiation, because body coloration and chaetotaxy of thorax tend to vary within a single genus in Lauxaniidae. Therefore, we believe that the genera Minettiella (five species), Melinomyia (single species) and the large genus Minettia (over 100 known species) should be more carefully revised based on a comprehensive phylogenetic analysis involving them as well as related taxa.