Observations on rodlet cells found in the vascular system and extravascular space of angelfish (Pterophyllum scalare scalare)

In the angelfish ( Pterophyllum scalare scalare ) numerous rodlet cells were found in the large post-orbital blood vessel caudal to the eye and in the surrounding extravascular space. Within the vessel the rodlet cells formed striking regular arrays, along the inner aspect of the wall. The rodlets within the cells were positive to PAS but negative to Sudan Black B, Masson's, and the Fuelgen stain. The capsule around the cells was negative for all these stains. These rodlet cells appeared to be traversing the vessel endothelium, and to be pushing the endothelium aside without damaging it. Some discharged their contents into the vessel, but we never observed the release of intact rodlets. The nuclei of rodlet cells in actual contact with the vessel were at the end of the cell more distant from the endothelial wall. Cell-to-cell adhesion structures or communications junctions between rodlet cells and the endothelium were not evident. A putative rodlet cell precursor in the extravascular space contained large electron-dense granules, and extended pseudopodia that contacted nearby rodlet cells. Based on their morphology, tissue distribution, and their behaviour, we conclude that the rodlet cell is an endogeneous teleost cell type, and possibly represents a form of matured granulocyte.     

Description of the digestive tract and feeding habits of the king angelfish and the Cortes angelfish

Morphologically, the digestive tracts of the king angelfish Holacunthus passer and the Cortes angelfish Pomacanthus zonipectus are similar, yet the king angelfish intestine is almost 30% longer than that of the Cortes angelfish. Both pomacanthids have a small mouth with villiform teeth, a short oesophagus, a well-defined stomach, and a terminal sac at the end of the digestive tract. The terminal sac, the acid pH in the stomach, and the long intestine may facilitate efficient use of seaweed nutrients. Stomach contents were analysed to determine diets and interspecific overlap. Seventy-one species were found in the stomachs of the king angelfish and 53 in the stomachs of the Cortes angelfish. Because of the wide range of species in their diets, both angelfish must be regarded as omnivorous. The most frequent foods were seaweed and sponges, but for the king angelfish, crustaceans were also important. A cluster analysis was done to determine whether the diets of these fish were similar by sex, size, or season. No similarities were found. Dietary overlap is high in relation to other pomacanthids.     

Alternative spawning tactics of female angelfish according to two different contexts of sex change

Social conditions for sex change and reproductive success werestudied in the haremic marine angelfish, Centropyge ferrugatus,in the coral reefs of southern Japan. In this species the largestfemale in a harem changed sex not only after disappearance ofthe dominant male but also occasionally in his presence. Inisolated harems containing two to three females, strict socialcontrol by the dominant male resulted in females changing sexonly after the male disappeared (takeover sex change). In haremsadjacent to each other, however, takeover sex change did notoccur even when one of the males disappeared. Instead, largeharems including more than four females were formed by fusionof two adjacent harems. In such large harems, the dominant malewas unable to socially prevent the largest female from changingsex later to acquire a portion of the harem (harem-fission sexchange). Females in adjacent harems spawned less frequentlyand tended to grow faster than those in isolated harems, probablyto gain an advantage in dominance status over neighbors of similarsize. Thus, females changed spawning frequencies according tothe two different contexts of sex change. The takeover tacticresults in higher fitness than the harem-fission tactic, whichshould be the best in the bad situation of adjacent harems.     

Do body and fin form affect the abilities of fish to stabilize swimming during maneuvers through vertical and horizontal tubes?

Goldfish, Carassius auratus, silver dollar, Metynnis hypsauchen, and angelfish, Pterophyllum scalare were induced to swim through narrow vertical and horizontal tubes ranging in length from 0 to 20 cm (approximately 0 to 3 times total fish length, FL). The ability to stabilize the body while negotiating these confined spaces was quantified as (1) the minimum width of vertical (w_v) and horizontal (w_h) tubes traversed, where width is the smaller cross-sectional dimension of the tube, (2) the ratio w_v/w_h, and (3) transit speed through the tubes. Tube width was expressed as relative width, obtained by dividing tube width by fish length. Minimum relative widths traversed increased from 0.15 to 0.19 in the order silver dollar > angelfish > goldfish for vertical tubes and from 0.17 to 0.18 in the order goldfish=silver dollar > angelfish for horizontal tubes. w_v/w_h increased from 0.91 to 1.10 in the order silver dollar=angelfish > goldfish. Minimum tube widths generally increased with tube length for vertical tubes. Although significant differences in relative minimum widths among species were found, these were small. In contrast, for horizontal tubes, there was no significant effect of tube length on minimum tube width for any species. Large differences were found in transit speed. Transit speed generally decreased as the tube length increased. The slope of the relationship between transit speed and tube length varied among species generally increasing from – 0.41 to – 1.16 for horizontal tubes in the order goldfish > silver dollar > angelfish and from – 0.42 to – 1.07 in the order silver dollar > goldfish > angelfish for vertical tubes. As a result, goldfish usually took longest to traverse tubes of zero length but the shortest time to traverse the longest tubes. In contrast, angelfish traversed short tubes in the least time and long tubes in the greatest time. Deeper bodied angelfish swam slowly and traversed tubes with difficulty because they required experience during each trial to replace median and paired fin with body and caudal fin swimming. According to our data, goldfish were best able to swim in confined spaces.     

Seasonal Changes in Reproductive Activity in the Potter's angelfish (Centropyge potteri) in Kaneohe Bay, Hawaii

Potter's angelfish, Centropyge potteri, is a protogynous hermaphrodite, with the alpha female of a harem becoming male under the proper social conditions. Gonads and plasma samples were collected from females every 6–9 days for 1 year, and then for every 4–6 weeks for another year. The gonadosomatic index (GSI) of females remained below 1% from July until December. Starting from the first week of December, large spikes occurred in the GSI, fluctuating from 1.4% to 4.1% and falling below 1% in June. Plasma concentrations of estradiol-17 were relatively low (1–2ngml^–1) between July and November. Beginning in the third week of November, large spikes of plasma estradiol-17 were observed, fluctuating from 0.5 to 5ngml^–1. This pattern continued until the third week of May, and then estradiol-17 levels remained low for the rest of the year. Estradiol-17 levels showed a highly significant correlation with GSI. Estradiol-17 levels during late vitellogenesis and final maturation were significantly greater than those of the other stages. These results suggest that the spawning season of the Potter's angelfish is from December to June. One of the causes of the large fluctuations in GSI and plasma estradiol-17 within the spawning season appears to be due to the fact that Potter's angelfish is an asynchronous daily spawner.     

Modeling spawning strategy for sex change under social control in haremic angelfishes

In haremic angelfishes where protogynous (female to male) sexchange is favored, females have been reported to adopt severaltactics for earlier sex change on the basis of a trade-offbetween reproduction and growth, or survivorship. A recentfield study on Centropyge ferrugatus revealed that femalesreduce spawning frequency in competition with similar-sized neighbors for social dominance. To evaluate the optimal spawningstrategy taken by haremic fishes, we developed an evolutionarilystable strategy model that focuses on their life history andsocial structure based on field data of C. ferrugatus. Theresults of the analysis predict that the spawning frequencywill be low when the mortality rate of females is high comparedwith males, the harem size is large, and there is a moderatedegree of social control. Our model further predicts conditionsunder which females completely stop spawning, as if they havebecome bachelors. Thus, the regulated spawning frequency maybe taken as a strategy to optimize the reproductive successof an individual in response to the available choices for sexchange, social control, and environmental conditions. Socialcontrol would also play an important role in sex change inmany other haremic species.     

Understanding behaviour to improve the welfare of an ornamental fish

Some common practices in aquaculture, ornamental trade and fish facilities may disturb the behavioural repertoire of fish and its natural adaptive value, reducing welfare and impairing fish production. Hence, it is necessary to understand fish behaviour, as well as the factors affecting it, to improve the quality of fish's life under artificial environment. Here, we reviewed the behaviour of the angelfish Pterophyllum scalare, an Amazonian cichlid used worldwide both as an ornamental fish and as a fish model in scientific research. We characterized social, reproductive and feeding behaviour, as well as the amazing cognitive ability of the angelfish. In addition, we reviewed the effects of environmental enrichment and suggested some important variables that need to be considered for rearing P. scalare. In this review, we show for the first time a synthesis on behaviour and a best practice overview to improve the welfare of angelfish as a target species. Nonetheless, most topics reviewed fit a broader set of fish species, particularly ornamental ones. This synthesis can therefore open a path for further behavioural research applied to the welfare of angelfish and bring insights to other fish species.     

Density-dependent protogynous sex change in territorial-haremic fishes: models and evidence

Several hypotheses of the proximate control of protogynous (female-to-male)sex change propose that social group composition triggers sexchange, but they do not address how proximate cues are alteredby population density. I present three mutually exclusive encounter-ratethreshold hypotheses that assume that population density determinesrates of contact between social group members and that ratesof contact are cues for sex change. Different densities arepredicted to induce sex change, depending on the encountersassumed to be important in the sex change process (e.g., encounterswith smaller and larger individuals). Tests of the models usea pomacanthid angelfish(Centropyge potten) to show that continuedpresence of a smaller (female) conspecific is needed for sexchange, and that continued presence of a larger (male) conspecificcan either inhibit sex change or prevent its behavioral stimulation.Using constant social group composition, sex change is preventedat higher density but not at a lower density. The absolute encounter-ratethreshold hypothesis, which predicts sex change under intermediate-densityconditions, is the most probable model of the social controlof sex change in C.potteri