Rhinecanthus Aculeatus Research Articles

Triggerfish uses chromaticity and lightness for object segregation.

Humans group components of visual patterns according to their colour, and perceive colours separately from shape. This property of human visual perception is the basis behind the Ishihara test for colour deficiency, where an observer is asked to detect a pattern made up of dots of similar colour with variable lightness against a background of dots made from different colour(s) and lightness. To find out if fish use colour for object segregation in a similar manner to humans, we used stimuli inspired by the Ishihara test. Triggerfish (Rhinecanthus aculeatus) were trained to detect a cross constructed from similarly coloured dots against various backgrounds. Fish detected this cross even when it was camouflaged using either achromatic or chromatic noise, but fish relied more on chromatic cues for shape segregation. It remains unknown whether fish may switch to rely primarily on achromatic cues in scenarios where target objects have higher achromatic contrast and lower chromatic contrast. Fish were also able to generalize between stimuli of different colours, suggesting that colour and shape are processed by fish independently.

Stabilizing selection on individual pattern elements of aposematic signals.

Warning signal variation is ubiquitous but paradoxical: low variability should aid recognition and learning by predators. However, spatial variability in the direction and strength of selection for individual elements of the warning signal may allow phenotypic variation for some components, but not others. Variation in selection may occur if predators only learn particular colour pattern components rather than the entire signal. Here, we used a nudibranch mollusc, Goniobranchus splendidus, which exhibits a conspicuous red spot/white body/yellow rim colour pattern, to test this hypothesis. We first demonstrated that secondary metabolites stored within the nudibranch were unpalatable to a marine organism. Using pattern analysis, we demonstrated that the yellow rim remained invariable within and between populations; however, red spots varied significantly in both colour and pattern. In behavioural experiments, a potential fish predator, Rhinecanthus aculeatus, used the presence of the yellow rims to recognize and avoid warning signals. Yellow rims remained stable in the presence of high genetic divergence among populations. We therefore suggest that how predators learn warning signals may cause stabilizing selection on individual colour pattern elements, and will thus have important implications on the evolution of warning signals.

Fish use colour to learn compound visual signals

Colour patterns displayed by animals frequently comprise multiple elements, including hue, pattern, luminance and texture. Predators' perception of and learning about visual stimuli has important implications for the evolution of animal coloration, including aposematism and mimicry. This study investigated how a coral reef fish, the triggerfish Rhinecanthus aculeatus, learnt different elements of colour patterns. Fish trained to associate a food reward with blue, yellow and green patterns on a grey background selected novel stimuli by chromaticity, rather than pattern or luminance contrast. By comparison, when presented with small orange spots the fish appeared to learn luminance, which is consistent with findings in other animals, including bees, birds and humans, that for small objects the achromatic component of the signal is more salient than chromaticity. While internal pattern did not appear to be learnt in our first two experiments, a subsequent test showed that fish could distinguish between spotted and striped patterns over various sizes, up to the limits of their visual acuity. These results are discussed in relation to visual processing of colour patterns and the evolution of visual signals in the marine environment.

Correction: Unusual sound production mechanism in the triggerfish Rhinecanthus aculeatus (Balistidae).

There was an error published in J. Exp. Biol. 220 , [186-193][1]. The surname of Sam Van Wassenbergh was incorrectly displayed. This has been corrected in the online full-text and PDF versions. The authors apologise for any inconvenience this may have caused. [1]: /lookup/volpage/220/186?iss=2

Coral reef fish perceive lightness illusions

Visual illusions occur when information from images are perceived differently from the actual physical properties of the stimulus in terms of brightness, size, colour and/or motion. Illusions are therefore important tools for sensory perception research and from an ecological perspective, relevant for visually guided animals viewing signals in heterogeneous environments. Here, we tested whether fish perceived a lightness cube illusion in which identical coloured targets appear (for humans) to return different spectral outputs depending on the apparent amount of illumination they are perceived to be under. Triggerfish (Rhinecanthus aculeatus) were trained to peck at coloured targets to receive food rewards, and were shown to experience similar shifts in colour perception when targets were placed in illusory shadows. Fish therefore appear to experience similar simultaneous contrast mechanisms to humans, even when targets are embedded in complex, scene-type illusions. Studies such as these help unlock the fundamental principles of visual system mechanisms.

Colour thresholds in a coral reef fish.

Coral reef fishes are among the most colourful animals in the world. Given the diversity of lifestyles and habitats on the reef, it is probable that in many instances coloration is a compromise between crypsis and communication. However, human observation of this coloration is biased by our primate visual system. Most animals have visual systems that are ‘tuned’ differently to humans; optimized for different parts of the visible spectrum. To understand reef fish colours, we need to reconstruct the appearance of colourful patterns and backgrounds as they are seen through the eyes of fish. Here, the coral reef associated triggerfish, Rhinecanthus aculeatus, was tested behaviourally to determine the limits of its colour vision. This is the first demonstration of behavioural colour discrimination thresholds in a coral reef species and is a critical step in our understanding of communication and speciation in this vibrant colourful habitat. Fish were trained to discriminate between a reward colour stimulus and series of non-reward colour stimuli and the discrimination thresholds were found to correspond well with predictions based on the receptor noise limited visual model and anatomy of the eye. Colour discrimination abilities of both reef fish and a variety of animals can therefore now be predicted using the parameters described here.

Circling and touching: two new behaviours in the courtship of the Picasso triggerfish Rhinecanthus aculeatus (Linnaeus, 1758)

The reproduction of Rhinecanthus aculeatus (Linnaeus, 1758), a tropical Indo-Pacific reef fish, occurs around the full and new moon (Kuwamura 1997). Spawning begins 16 to 45 min before the sunrise. The courtships begin 7 to 27 min before the spawning. A specific behaviour of the courtships is when the male places its rostrum against the caudal peduncle of the female (Kuwamura 1997). Observations have been recorded in the lagoon of Tiahura [shallow sandy area (0.5 - 2 m deep) with algae Hypnea spinella (C.Agardh) Kutzing, 1847 - Moorea, French Polynesia; 17°29′27′ S, 149°53′32″O] in March and April 2015. Fifteen R. aculeatus (five males and ten females) lived in this area where the males have territories, which included the subterritories of the females. During video-recorded courtships, in addition to the behaviour described by Kuwamura (the nuzzling), two new behaviours have been observed: circling and touching. During the circling, the male and the female swim to the surface in progressively larger circles (Fig. 1). The circling behaviour has been observed in other Balistidae such as Pseudobalistes flavimarginatus (Ruppell, 1829) and Balistapus undulatus (Park, 1797) (Lobel and Johannes 1980). During the touching, the abdomens of the male and the female’s touch each other without gametes emission (Fig. 2). The touching has been reported for Xanthichthys mento (Jordan and Gilbert 1882) (Kawase 2003). Although Balistidae present different reproductive strategies, they have common reproduction features, such as the time and the day of hatching and spawning (Kawase 2003). Our observations are innovative because the courtship of R. aculeatus is more complicated than previously described. This result suggests, thus, that Balistidae have also some common courtship behaviour features. These behaviours may facilitate the release of gametes, as with the nuzzling (Kuwamura 1997) or can convince the partner to mate. We do not know if these patterns are phylogenetically related. But as the egg care strategy of Balistidae (biparental vs maternal) appears to be related to the distribution of food and breeding sites, more than by the phylogeny (Kuwamura 1997), more studies on this topic will be useful to better understand the establishement of these behaviours.

Female defence polygyny and plasticity in the mating system of the demersal triggerfish Rhinecanthus aculeatus (Pisces: Balistidae) from Okinawa Island

The prevalence of a haremic mating system type with parental care is one of the main characteristics of the modern triggerfish family (Balistidae). In addition, intraspecific modifications of the mating system in relation to environmental conditions have been recognized. Thirteen months of observation of mating units in a natural population of Rhinecanthus aculeatus from Okinawa Island, Japan, revealed that the mating system in this species involved a mixture of polygyny, monogamy, and potential promiscuity in solitary females. Females defended individual, multi-purpose territories, while males engaged in female defence (“female defence polygyny”) using displays and overt aggressions that advertised that territories were occupied. Male size was strongly linked to access to multiple females (i.e. polygyny). Plasticity in the mating system was related to male–male competition and the ability of females to reject males. An increase in the proportion of monogamous pair territories over the course of the reproductive season was positively correlated with the adult sex ratio (increased male density relative to females), and facultative monogamy was enhanced under a less female-biased sex ratio. A comparison between female and male mating success (number of matings) and the adjustment of the mating status over time revealed that polygyny was advantageous and the optimal mating system for males. Females achieved higher number of matings when pairing with larger males, but mating success was not negatively affected by the actual mating status, and females did not attempt to escape polygyny. Polygyny is therefore considered as the primary mating system in R. aculeatus.

Unusual sound production mechanism in the triggerfish Rhinecanthus aculeatus (Balistidae).

The ability to produce sound has been known for decades in Balistidae. Sounds of many species have been recorded and a variety of sound-producing mechanisms have been proposed, including teeth stridulation, collision of the buccal teeth and movements of the fins. The best-supported hypothesis involves movements of the pectoral fin against the lateral part of the swimbladder, called a drumming membrane. In this study, we describe for the first time the sounds made by the blackbar triggerfish Rhinecanthus aculeatus, which are like short drum rolls with an average duration of 85 ms, 193 Hz dominant frequency and 136 dB SPL level at 3 cm distance. The sounds are a series of pulses that result from alternate sweeping movements of the right and left pectoral fins, which push a system of three scutes that are forced against the swimbladder wall. Pulses from each fin occur in consecutive pairs. High-speed videos indicate that each pulse consists of two cycles. The first part of each cycle corresponds to the inward buckling of the scutes, whereas the second part of the cycle corresponds to an apparent passive recoil of the scutes and swimbladder wall. This novel sound production mechanism is probably found in many members of Balistidae because these peculiar scutes occur in other species in the family. Comparison of sound characteristics from fishes of different sizes shows that dominant frequency decreases with size in juveniles but not in adults.

Integrating and Utilizing Citizen Biodiversity Data on the Web for Science: An Example of a Rare Triggerfish Hybrid Image Provided by a Sport Fisherman

ABSTRACT Miyazaki, Y.; Murase, A.; Shiina, M.; Masui, R., and Senou, H., 2015. Integrating and utilizing citizen biodiversity data on the Web for science: An example of a rare triggerfish hybrid image provided by a sport fisherman. We report a photograph of the rare triggerfish hybrid, Rhinecanthus aculeatus × R. rectangulus (order Tetraodontiformes; family Balistidae), from Miyako-jima Island, Ryukyu Islands, southern Japan, that was provided by a sport fisherman via WEB sakana-zukan (an online photographic database of fish in Japan). The image was registered in the Fish Image Database of the Kanagawa Prefectural Museum of Natural History to make it available for scientific scrutiny. Here we emphasize the importance of communication between citizens, such as fishermen, scuba divers, and others, and experts via the Internet, to make possible the processing of biodiversity information provided by citizens into museum collections. This communication contributes Global Biodiversity Information Facility data ...

Visual Acuity in a Species of Coral Reef Fish: Rhinecanthus aculeatus

Coral reef fish present the human observer with an array of bold and contrasting patterns; however, the ability of such fish to perceive these patterns is largely unexamined. To understand this, the visual acuity of these animals - the degree to which they can resolve fine detail - must be ascertained. Behavioural studies are few in number and anatomical analysis has largely focused on estimates of ganglion cell density to predict the visual acuity in coral reef fish. Here, we report visual acuity measures for the triggerfish Rhinecanthus aculeatus. Acuity was first assessed using a series of behavioural paradigms and the figures were then contrasted with those obtained anatomically, based on photoreceptor and ganglion cell counts. Behavioural testing indicated an upper behavioural acuity of 1.75 cycles·degree^-1, which is approximately the same level of acuity as that of the goldfish (Carassiusauratus). Anatomical estimates were then calculated from wholemount analysis of the photoreceptor layer and Nissl staining of cells within the ganglion cell layer. Both of these anatomical measures gave estimates that were substantially larger (7.75 and 3.4 cycles·degree^-1 for the photoreceptor cells and ganglion cells, respectively) than the level of acuity indicated by the behavioural tests. This indicates that in this teleost species spatial resolution is poor compared to humans (30-70 cycles·degree^-1) and it is also not well indicated by anatomical estimates.

Pathological Findings of Tenacibaculum maritimus Infection in Black Damselfish, Neoglyphieodon melas and Picasso Triggerfish, Rhinecanthus assasi in Red Sea, Egypt

An outbreak of a disease with external body lesions in Picasso triggerfish (Rhinecanthus assasi) and black damselfish (Neoglyphieodon melas) has been observed in the indoor aquarium of NIOF, Hurghada, Egypt. Thirty Picasso triggerfish and thirty-five black damselfish were clinically affected with gross skin lesions. The affected fishes were euthanized for gross, histological and bacteriological examinations. The disease onset started after exposing the fish to catching and indoor rearing stress. Anorexia, erratic swimming and hemorrhagic skin and mouth ulcers and fin rot were the main symptoms and lesions among Picasso triggerfish and black damselfish. Single species of bacteria was isolated from skin ulcer, liver and spleen and was diagnosed as Tenacibaculum maritimus. The gross lesions were irregular shallow erosions and deep ulcers on the dorsal and lateral skin, sometimes on the head, mouth and fins, and occasionally, on the cornea. Histological findings, the hepatic tissue revealed fatty degeneration and focal liquefactive necrosis. Congestion, hemorrhage, hemosidrosis and lymphoid depletion was observed in spleen. The deep skin ulcers characterized by epidermal and muscular necrosis. Picasso triggerfish and black damselfish had lesions similar to those of natural infection and mortality rates of 50 and 60%, respectively in experimental reproduction of the disease. The natural T. maritimus infection in Picasso triggerfish and black damselfish in Red Sea is not only a superficial skin lesion but also a systemic infection.

Gnathia aureamaculosa, a likely definitive host of Haemogregarina balistapi and potential vector for Haemogregarina bigemina between fishes of the Great Barrier Reef, Australia

Investigations to determine whether juvenile gnathiid isopods are vectors of haemogregarines between coral reef fishes were undertaken at Lizard Island, Australia. Haemogregarina balistapi parasitaemias in triggerfish, Rhinecanthus aculeatus, decreased under gnathiid-free, laboratory conditions, compared with those in tagged R. aculeatus returned to the reef. Gnathia aureamaculosa juveniles were common ectoparasites of reef R. aculeatus and laboratory reared specimens of this gnathiid were fed on R. aculeatus infected with H. balistapi. Subsequent squashes of this gnathiid contained haemogregarine gamonts similar to those seen in blood films of R. aculeatus, and haemogregarine developmental stages, including oocysts, sporozoites, meronts and merozoites. Biological transmission of H. balistapi and a second haemogregarine species, Haemogregarina bigemina, using laboratory reared gnathiids to several species of triggerfishes and surgeonfishes raised from larvae was then attempted. Investigations involved recipient fish ingesting, or being bitten by, G. aureamaculosa juveniles fed on donor fish with haemogregarines; control fish were exposed to gnathiids fed on uninfected donor fish. Subsequently, no haemogregarines were detected in recipient triggerfishes and controls were negative. However, a recipient surgeonfish, Acanthurus xanthopterus, which had ingested gnathiids likely infected with donor fish H. balistapi, carried H. bigemina-like stages. A second recipient surgeonfish, which had ingested gnathiids presumed to be infected with H. bigemina, also carried haemogregarine stages. Finally, a third surgeonfish apparently carried haemogregarines after gnathiids presumed to be infected with H. bigemina had bitten this fish, although not all gnathiids were recovered during the trials and the third infected surgeonfish may have also ingested gnathiids. The study provides strong evidence that G. aureamaculosa is the definitive host of H. balistapi, to our knowledge the first such observation from a coral reef environment. Although transmission of H. balistapi has not yet been demonstrated, laboratory trials tend to support the view that G. aureamaculosa is also a potential vector of H. bigemina between surgeonfish.

Colour vision and response bias in a coral reef fish

Animals use coloured signals for a variety of communication purposes, including to attract potential mates, recognize individuals, defend territories and warn predators of secondary defences (aposematism). To understand the mechanisms that drive the evolution and design of such visual signals, it is important to understand the visual systems and potential response biases of signal receivers. Here, we provide raw data on the spectral capabilities of a coral reef fish, the Picasso triggerfish Rhinecanthus aculeatus, which is potentially trichromatic with three cone sensitivities of 413 nm (single cone), 480 nm (double cone, medium sensitivity) and 528 nm (double cone, long sensitivity), and a rod sensitivity of 498 nm. The ocular media have a 50% transmission cut off at 405 nm. Behavioural experiments confirmed colour vision over their spectral range; triggerfish were significantly more likely to choose coloured stimuli over grey distractors, irrespective of luminance. We then examined whether response biases existed towards coloured and patterned stimuli to provide insight into how visual signals - in particular, aposematic colouration - may evolve. Triggerfish showed a preferential foraging response bias to red and green stimuli, in contrast to blue and yellow, irrespective of pattern. There was no response bias to patterned over monochromatic non-patterned stimuli. A foraging response bias towards red in fish differs from that of avian predators, who often avoid red food items. Red is frequently associated with warning colouration in terrestrial environments (ladybirds, snakes, frogs), whilst blue is used in aquatic environments (blue-ringed octopus, nudibranchs); whether the design of warning (aposematic) displays is a cause or consequence of response biases is unclear.

Validation of age and growth of the Picasso triggerfish (Balistidae: Rhinecanthus aculeatus) from Okinawa Island, Japan, using sectioned vertebrae and dorsal spines

To understand age and growth of the Picasso triggerfish, Rhinecanthus aculeatus, monthly sampling was conducted from February 2010 to October 2011 on the subtropical Okinawa Island, Japan, using trammel net and speargun. Fish were measured by weight (W) and standard length (SL) and age was determined by examining thin-sections of the first dorsal spine and the second abdominal vertebra. A total of 352 fish were caught ranging from 20.9 mm to 209.5 mm (SL). Marginal increment analysis indicated that translucent rings were deposited annually during the colder season from October to January. The relationship of observed SL and age was described by the original form of the von Bertalanffy growth equation. Male and female growth models were significantly different. Overall growth was rapid during the first 2.5 years for both sexes, thereafter growth curves diverged. Males consequently reached larger sizes and greater ages. Maximum age for males and females was 13.5 and 9.5 years, respectively. Regression models of somatic growth (SL) as a function of vertebral and spine radii were significantly correlated (r = 0.98 and r = 0.96, respectively). According to the weight–length relationship, growth in R. aculeatus was negative allometric. Small recruits (SL < 40 mm) appeared in high numbers in shallow coastal areas starting from August. This is the first record of age and growth for R. aculeatus. Our data suggest that the Picasso triggerfish is a moderately long-lived balistid and that the observed sex-specific growth pattern is driven by the fish’s polygynous mating system and different reproduction strategies of males and females.

Morphological characterization of retinal bipolar cells in the marine teleost Rhinecanthus aculeatus

The marine teleost Rhinecanthus aculeatus (Balistidae) has recently been shown to possess trichromatic color vision supported by a retinal combination of double and single cones. Double cones are composed of two members with different spectral sensitivity. It is not known whether a correlation exists between the chromatic wiring of double cones to the inner retina and trichromacy, nor how unmixed, chromatic information is extracted from the two members of the couple. In mammalians, bipolar cells determine color segregation by means of the midget system, central to trichromatic color vision; however, midget bipolar cells have never been described in teleosts. On the basis of its likely importance in transferring chromatic photoreceptor signals to the inner retina, we have morphologically characterized the retinal bipolar cell types of R. aculeatus using DiOlistic staining techniques to verify if an anatomical specialization of this group of cells is required to support trichromatic color vision. Thirteen cell types are described: eight putative OFF types and five putative ON types. Of these, four had axonal boutons ramifying in both sublayers (ON and OFF) of the inner plexiform layer, six had terminals restricted to the OFF layer, and three cell types had terminals restricted to the ON layer. Dendritic arbors of bipolar cells had narrower diameters (5-40 microm) in comparison to bipolar cells of other teleost species; this supports the idea that a low degree of photoreceptor to bipolar convergence is correlated with trichromacy in this retina and possibly with the function of double cones as color receptors.

Suspected viral erythrocytic necrosis (VEN) in a juvenile blackbar triggerfish, Rhinecanthus aculeatus, from Lizard Island, Great Barrier Reef, Australia

Suspected viral erythrocytic necrosis (VEN) was detected in blood films from an immature blackbar triggerfish, Rhinecanthus aculeatus, captured on a patch reef at Lizard Island, Great Barrier Reef in November 2005, probably the first record of such an infection from Australia. The fish was kept in captivity and sampled intermittently until December 2007. Giemsa-stained blood films showed initially 18% of mature erythrocytes affected by the VEN-like condition, but accompanying erythroblasts appeared free from infection. Erythrocytes with VEN-like bodies were smooth or crenated in outline, while the inclusion bodies were intracytoplasmic, single or paired, round in outline, stained deep magenta and were between 0.5–1.7 mm across. Bodies associated with clouds of granular material, fine eosinophilic haloes, and distinct pink-stained comet-tails, were also observed. The DNA content of the VEN-like bodies was confirmed by their green fluorescence following acridine orange staining. Infection levels in this fish fell to 0.4% of mature erythrocytes by May 2006 and persisted at this level until December 2007, when the fish died after just over two years in captivity. Squashes of haematophagous, juvenile gnathiid isopods taken from this fish on initial capture, also contained eosinophilic VEN-like bodies within digesting erythrocytes, suggesting that these crustaceans may be vectors of the condition observed.

Cableia balistidicola n. sp. (Digenea, Monorchiidae) from Pacific Ocean balistids (Tetraodontiformes) and new reports of Cableia pudica Bray, Cribb and Barker, 1996 in temperate Australian monacanthids

Cableia balistidicola n. sp. is described from Abalistes stellatus (type-host) off New Caledonia (type-locality) and the Great Barrier Reef and Pseudobalistes fuscus off New Caledonia and Rhinecanthus aculeatus off Moorea, French Polynesia. It is distinguishable by its large ventral sucker with a highly developed sphincter around the aperture. Cableia pudica is reported from Meuschenia freycineti off northern Tasmania, M. hippocrepis off south-western Western Australia and northern Tasmania and Acanthaluteres spilomelanurus off Kangaroo Island, South Australia. Measurements of C. pudica are given and the distinguishing features of the three known species of Cableia are discussed and summarised in a key. C. balistidicola is reported only in balistid fishes in the tropical Pacific Ocean and C. pudica is reported only in monacanthid fishes in Australian coastal waters. RésuméCableia balistidicola n. sp. est décrit de Abalistes stellatus (hôte type) de Nouvelle-Calédonie (localité type) et de la Grande Barrière de Corail, de Pseudobalistes fuscus en Nouvelle-Calédonie et de Rhinecanthus aculeatus à Moorea, Polynésie Française. L'espèce se distingue par une grande ventouse ventrale avec un sphincter très développé autour de l'ouverture. Cableia pudica est signalé de Meuschenia freycineti du nord de la Tasmanie, M. hippocrepis de l'Australie du sud-ouest et du nord de la Tasmanie et de Acanthaluteres spilomelanurus de Kangaroo Island, au sud de l'Australie. Des mesures de C. pudica sont données et les caractères distinctifs des trois espèces connues de Cableia sont discutés et résumés dans une clé. C. balistidicola est signalé seulement de poissons Balistidae dans l'Océan Pacifique tropical et C. pudica est signalé seulement de poissons Monacanthidae des eaux côtières de l'Australie.

Spatial repartition and ontogenetic shifts in habitat use by coral reef fishes (Moorea, French Polynesia)

This study explores the extent to which ontogenetic habitat shifts modify spatial patterns of fish established at settlement in the Moorea Island lagoon (French Polynesia). The lagoon of Moorea Island was divided into 12 habitat zones (i.e. coral seascapes), which were distinct in terms of depth, wave exposure, and substratum composition. Eighty-two species of recently settled juveniles were recorded from March to June 2001. Visual censuses documented changes in the distribution of juveniles of each species over time among the 12 habitats. Two patterns of juvenile habitat use were found among species. Firstly, some species settled and remained in the same habitat until the adoption of the adult habitats (i.e. recruitment; e.g. Chaetodon citrinellus, Halichoeres hortulanus, Rhinecanthus aculeatus). Secondly, others settled to several habitats and then disappeared from some habitats through differential mortality and/or post-settlement movement (e.g. 65–70 mm size class for Ctenochaetus striatus, 40–45 mm size class for Epinephelus merra, 50–55 mm size class for Scarus sordidus). A comparison of the spatial distribution of juveniles to that of adults (61 species recorded at both stages) illustrated four patterns of subsequent recruitment in habitat use: (1) an increase in the number of habitats used during the adult stage (e.g. H. hortulanus, Mulloidichthys flavolineatus); (2) a decrease in the number of habitats adults used compared to recently settled juveniles (e.g. Chrysiptera leucopoma, Stethojulis bandanensis); (3) the use of different habitat types (e.g. Acanthurus triostegus, Caranx melampygus); and (4) no change in habitat use (e.g. Naso litturatus, Stegastes nigricans). Of the 20 most abundant species recorded in Moorea lagoon, 12 species modified the spatial patterns established at settlement by an ontogenetic habitat shift.

Receptor noise as a determinant of colour thresholds.

Inferences about mechanisms at one particular stage of a visual pathway may be made from psychophysical thresholds only if the noise at the stage in question dominates that in the others. Spectral sensitivities, measured under bright conditions, for di-, tri-, and tetrachromatic eyes from a range of animals can be modelled by assuming that thresholds are set by colour opponency mechanisms whose performance is limited by photoreceptor noise, the achromatic signal being disregarded. Noise in the opponency channels themselves is therefore not statistically independent, and it is not possible to infer anything more about the channels from psychophysical thresholds. As well as giving insight into mechanisms of vision, the model predicts the performance of colour vision in animals where physiological and anatomical data on the eye are available, but there are no direct measurements of perceptual thresholds. The model, therefore, is widely applicable to comparative studies of eye design and visual ecology.