Academic literature on the topic 'Ontogenetic colour change'

Ontogenetic colour change is typically associated with changes in size, vulnerability or habitat, but assessment of its functional significance requires quantification of the colour signals from the receivers' perspective. The tropical python, Morelia viridis , is an ideal species to establish the functional significance of ontogenetic colour change. Neonates hatch either yellow or red and both the morphs change to green with age. Here, we show that colour change from red or yellow to green provides camouflage from visually oriented avian predators in the different habitats used by juveniles and adults. This reflects changes in foraging behaviour and vulnerability as individuals mature and provides a rare demonstration of the adaptive value of ontogenetic colour change.

Phenotypic plasticity, particularly during development, allows organisms to rapidly adjust to different environmental conditions. Yet, it is often unclear whether the extent and direction of plastic changes are restricted by an individual's ontogeny. Many species of cichlid fishes go through ontogenetic changes in visual sensitivity, from short to long wavelengths, by switching expression of cone opsin genes crucial for colour vision. During this progression, individuals often exhibit phenotypic plasticity to the ambient light conditions. However, it is commonly assumed that once an adult visual phenotype is reached, reverting to an earlier ontogenetic state with higher sensitivity at shorter wavelengths is not common. In this study, we experimentally demonstrate that four-month-old Midas cichlid fish ( Amphilophus astorquii ) show plasticity in single cone opsin expression after experiencing drastic changes in light conditions. Resulting shifts of visual sensitivity occurred presumably in an adaptive direction—towards shorter or longer wavelengths when exposed to short- or long-wavelength light, respectively. Single cone opsin expression changed within only a few days and went through a transitional phase of co-expression. When the environment was experimentally enriched in long-wavelength light, the corresponding change occurred gradually along a dorsoventral gradient within the retina. This plasticity allowed individuals to revert earlier ontogenetic changes and return to a more juvenile visual phenotype demonstrating previously unrecognized insights into temporal and spatial dynamics of phenotypic plasticity of the visual system in response to ambient light.

Abstract Ontogenetic colour change (OCC) is defined as the progressive and non-reversible process of changes in colouration of organisms associated with their development. Among the many vertebrate groups, amphibians are particularly impressive for their strikingly wide variety of colours, colour patterns, and signals, whose evolutionary and ecological significance have been poorly studied. Elachistocleis comprises 18 species currently separated into two main groups based on their ventral colour pattern: one immaculate and the other with specks and/or colour patches. Elachistocleis haroi is a small-sized species within the immaculate venter group, distributed in the Yungas and Dry Chaco ecoregions from which little information is known. In a comprehensive sampling of post-metamorphic individuals of E. haroi at different stages of development we identified a significant variation in ventral colour pattern, which could denote a progressive filling of yellow colour according to an ontogenetic pattern. To test this hypothesis, we analysed 39 post-metamorphic individuals of E. haroi at different stages of development with imaging procedures. We found that yellow spots and their intensity are significantly related to snout-vent length, as major expansion of colour on the sides, gular region and male chest, as almost no development on the belly. We briefly discuss our findings in relation to sexual display and predation avoidance. To our knowledge, this is the first analysis of post-metamorphic OCC in ventral colouration in the genus Elachistocleis.

The green python Morelia viridis is a most striking animal. Individuals are born either brick red or bright yellow and both colours change to green as adults. These colours and the remarkable colour change have long made them of interest to biologists and in demand for the pet trade. Despite this interest nothing is known of their distribution, biology or ecology in the wild. Here I address this knowledge gap by presenting results from the first detailed study of the species, at Iron Range on eastern Cape York Peninsula, Australia.¶ Individual growth was described by the von Bertalanffy growth curve, with a maximum predicted size of 1.35 metres snout-vent length. Males matured at 2.4 years and females at 3.6 years, and growth was indeterminate after approximately 12 years. The colour change from yellow to green occurs at 55 centimetres, which corresponds to individuals approximately a year old. There was no sexual dimorphism in adults, however juvenile females had larger heads than juvenile males. Adult sized individuals comprised ~50% of the population.¶ Females had a home range of 6.2 ± 1.9 ha (mean ± SE), which was positively correlated with their snout-vent length. Males adopted a roaming strategy through suitable habitat while juveniles were restricted to areas where more light reached the ground. There was overlap between multiple female home ranges, and between female home ranges and the movement paths of males. There were no differences in the distances moved by males and females of any size, although the variation in movement distances was greater in the dry season than the wet season.¶ Green pythons are obligate ambush predators which eat a variety of prey. They show an ontogenetic shift from invertebrates and terrestrial, diurnal reptiles to birds and terrestrial, nocturnal mammals. This diet change is concurrent with a shift in the time of hunting, and the location and characteristics of ambush sites. Yellow individuals were usually found within ten metres of the ground, while green individuals used the full vegetation strata and were often found in the canopy.¶ The three colour morphs of the green python appear to be adaptive for camouflage rather than intraspecific communication, as conspicuousness of each morph was always greater to a predator than to that of a conspecific. Using advanced light analysis techniques I show that each colour morph is adaptive for camouflage from visually orientated avian predators under different environmental conditions. Yellow and red morphs are half as conspicuous as green individuals would be in locations near the ground where juveniles hunt during the day. Green was the least conspicuous morph in only the canopy, where it was half as conspicuous as either the red or yellow morph. In both leafy and non-leafy sub-canopy environments green individuals were more conspicuous than both yellow and red morphs. Red morphs were least conspicuous in only the non-leafy sub-canopy environment. The conspicuousness of green males decreased with age, but this was not the case with green females. Predation of plasticine models of the three colour morphs showed that red models were ten times more likely to be predated than either green or yellow morphs, however the model colours did not always match the real morph colours.¶ There is a large predicted global distribution in Papua New Guinea, including some offshore islands, however the Australian range is restricted to small areas of eastern Cape York Peninsula. In Australia green pythons occurred in nine regional ecosystems, with most records for the closed semi-deciduous mesophyll vine forest ecosystem. A mark-recapture study at Iron Range captured 101 individuals 147 times over two wet seasons, which equates to a population size of 227 ± 81 individuals in the study area of 51 hectares. Based on the known population structure at this site only 114 (or 50%) of these individuals are adult. Although green pythons have a high density at the one intensely studied site and are predicted to occur over a large geographic area, my data are insufficient to conclude that the species is not vulnerable.

The green python Morelia viridis is a most striking animal. Individuals are born either brick red or bright yellow and both colours change to green as adults. These colours and the remarkable colour change have long made them of interest to biologists and in demand for the pet trade. Despite this interest nothing is known of their distribution, biology or ecology in the wild. Here I address this knowledge gap by presenting results from the first detailed study of the species, at Iron Range on eastern Cape York Peninsula, Australia.¶...

碩士
東海大學
生物學系
89
In giant wood spider (Nephila maculata Fabricius 1793) populations in western Taiwan, some individuals are almost morphologically indistinguishable from the typical females except their brown body color. In this study, I investigated the color polymorphism by the following questions: (1) is there significant genetic differentiation between these two color morphs; (2) how brown morphs obtain their melanic coloration during development; (3) will the difference in body color be associated with a change in body surface reflection property and (4) will individuals of different colors differ in foraging success and thus reproductive output. Intra-population genetic structure was estimated by allozyme electrophoresis using 12 enzymes. An examination on allele frequencies and distribution patterns showed that genetic differentiation between typical and brown morphs was low ( = 0.0233). This result suggests that the genetic structuring between two morphs is congruent with that estimated from a highly-interbreeding population. Monthly field census conducted in Foyan Shan, Miauli County from July 1999 to July 2000 showed that no brown morphs were found in spiders smaller than 7 mm, indicating that color transformation occurred when spiders reached certain developmental stage. Among juveniles kept in laboratory under identical conditions, some became darker and darker after successive molts. This result suggests that color variation in N. maculata may not be induced by environments. An examination of body-surface reflection properties showed that typical morphs reflected significantly more visible and ultra-violet light than brown morphs. To understand whether this reflectance variation affects spiders’ foraging success, prey interception rates were examined in a population in Foyan Shan in July 2000. No significant difference in prey-interception rates was found between two morphs. A comparison of body weight and egg sac mass of pregnant females collected in fall of 2000 also showed no significant difference. These results showed that although N. maculata of different colors differ in reflection properties, this phenotypic variation does not seem to affect foraging success and reproductive output of the population in Foyan Shan.