Effect of esterification on the absorption of astaxanthin in rainbow trout, Oncorhynchus mykiss (Walbaum)

Gastrointestinal and serum absorption of astaxanthin was studied in rainbow trout, Oncorhynchus mykiss (Walbaum) (217 ± 2 g) fed diets supplemented with either esterified astaxanthin (from Haematococcus pluvialis) or free astaxanthin (synthetic, as 8% w/w beadlets) at similar levels (50 mg kg^?1). After 56 days of feeding, there was a significant difference (P = 0.0582) between steady‐state serum astaxanthin concentrations for fish fed free (2.0 ± 0.3 μg mL^?1) or esterified astaxanthin (1.3 ± 0.1 μg mL^?1) at the 90% confidence level. However, following ingestion of a single meal supplemented with free or esterified astaxanthin, the rates of astaxanthin absorption into serum were not significantly different (P > 0.1) (0.8 ± 0.2 µg mL^?1 h^?1 and 1.0 ± 0.4 µg mL^?1 h^?1 respectively). In fish fed both free or esterified astaxanthin, higher absorption (P < 0.05) of astaxanthin by the ileal (0.8 ± 0.14 μg g^?1 and 0.9 ± 0.15 μg g^?1 respectively) compared with the posterior (0.2 ± 0.01 μg g^?1 and 0.3 ± 0.14 μg g^?1 respectively) intestine was recorded. This confirmed the role of the anterior intestine in carotenoid absorption. Non‐detectable levels of esters in digesta taken from the hind intestine suggest the anterior intestine is also the primary region for ester hydrolysis.     

The pigmenting effect of different carotenoids on fancy carp (Cyprinus carpio)

The optimal concentration of a panel of individual and combined carotenoid sources on skin pigmentation in fancy carp was investigated by nine experimental diets that were formulated and supplemented with astaxanthin at 25 mg kg^?1, lutein at 25 and 50 mg kg^?1, β‐carotene at 25, 50 and 75 mg kg^?1, and lutein combined with β‐carotene at 25 : 25 and 50 : 50 mg kg^?1, while a diet without supplemented carotenoid served as a control. The results showed that serum TC of fish fed diets containing supplemented with lutein plus β‐carotene at 25 : 25; 50 : 50 mg kg^?1 and lutein 50 mg kg^?1 diet were higher than the other treatments (P ≤ 0.05). Serum TC of the respective treatments was 6.2 ± 2.0, 7.8 ± 3.3 and 7.3 ± 1.9 μg mL^?1 serum, respectively. Fish fed diets combined with lutein and β‐carotene at 25 : 25, 50 : 50 mg kg^?1 and lutein 50 mg kg^?1 diet had serum astaxanthin concentrations similar to fish fed the diet with astaxanthin alone at 25 mg kg^?1. Serum astaxanthin concentrations was 0.7 ± 0.01, 0.9 ± 0.01, 0.4 ± 0.02 and 1.7 ± 0.18 μg mL^?1 serum, respectively. The chromaticity of fish body skin of red and white position was assessed by colourimetry using the CIE L*a*b (CIELAB) system. Pigmentation response of skin redness of fancy carp fed with diets combined with lutein and β‐carotene at 25 : 25, 50 : 50 mg kg^?1 and lutein 50 mg kg^?1 were higher than other treatments (P ≤ 0.05) but they were similar to fish fed with 25 mg kg^?1 astaxanthin diet. The redness (a* values) of fish fed diets with diets combined with lutein and β‐carotene at 25 : 25, 50 : 50 mg kg^?1 and lutein 50 mg kg^?1 were 28.3 ± 0.53, 29.9 ± 1.38, 28.8 ± 3.95 and 28.5 ± 2.49, respectively. After 3 weeks of feeding the experimental diets, the fish fed on a diet without carotenoid supplement for one week demonstrated that the same three groups still retained their redness and had an overall tendency to improve skin colouring. Finally, concentrations 50 mg kg^?1 of lutein, or the combination of lutein and β‐carotene at 25 : 25 mg kg^?1 showed the highest efficiency for improving skin pigmentation and redness of skin.     

Given the same dietary carotenoid inclusion, Atlantic salmon, Salmo salar (L.) display higher blood levels of canthaxanthin than astaxanthin

Atlantic salmon, Salmo salar, fitted with permanent dorsal aorta cannulae were fed diets containing either 0, 30, 60 mg kg^?1 or combinations of astaxanthin and canthaxanthin, with the aim of comparing the uptake efficiencies to blood of the two pigments and evaluating possible interactions during absorption when formulated in the same diet. Given either astaxanthin or canthaxanthin in separate diets, at dietary levels of <30 mg kg^?1, an identical linear relationship (R² = 0.97) between dietary levels and blood concentrations was observed for both carotenoids. At dietary astaxanthin inclusions above 30 mg kg^?1, blood astaxanthin concentration approached saturation at an average level of 1.2 ± 0.04 μg mL^?1 (arithmetic mean ± SD), whereas blood levels of canthaxanthin continued to increase linearly throughout the inclusion range tested (0–60 mg kg^?1). When both carotenoids were presented in the same diet, a reduction in the absorption efficiency of both pigments was observed (P < 0.05). This manifested itself as a lower level in blood than the level observed when each carotenoid was administered separately. The negative interaction was most prominent for astaxanthin, the maximum average blood saturation level of which fell (P < 0.05) to 0.73 ± 0.03 μg mL^?1 (arithmetic mean ± SD). Our data support the conclusion that at higher dietary inclusions, canthaxanthin is more efficiently absorbed from the digestive tract into the blood of S. salar than astaxanthin.     

The effect of synthetic and natural pigments on the colour of the cichlids (<Emphasis Type="Italic">Cichlasoma severum</Emphasis> sp., Heckel 1840)

In this study, we have investigated the effects of Porphyridium cruentum (Rodophyta) as a natural pigment source and astaxanthin and β-carotene as synthetic pigment sources on the skin colour of cichlid fish (Cichlasoma severum sp., Heckel 1840), which are generally light orange with white patches and becomes shiny orange in the reproductive phase. The fish were fed diets containing 50 mg kg⁻¹ astaxanthin and β-carotene, and P. cruentum powder. The amount of both natural and synthetic pigment sources given as feed was 50 mg kg⁻¹, and the experiment was continued for 50 days. Total carotenoid content of the fish was determined spectrophotometrically at the end of the experiment. As a result, while a visible change of colour in the skin of the fish fed on the feed containing astaxanthin was observed with 0.34 ± 0.2 mg g⁻¹ of pigment accumulation, a relatively small change of colour was observed in the skin of other fish that were fed on the feed containing P. cruentum and β-carotene with 0.22 ± 0.2 mg g⁻¹ and 0.26 ± 0.1 mg g⁻¹ of pigment accumulations, respectively. Therefore, it was determined that these pigment sources have an effect on the colour of cichlid fish.     

Dietary amino acid l-tryptophan requirement of fingerling Indian catfish, Heteropneustes fossilis (Bloch), estimated by growth and haemato-biochemical parameters

An 8-week feeding trial was conducted to determine the dietary tryptophan requirement of fingerling Indian catfish, Heteropneustes fossilis (6.10 ± 1.15 cm, 4.44 ± 0.50 g). Six isonitrogenous (40 g 100 g^?1) and isoenergetic (17.90 kJ g^?1) amino acid test diets were formulated with gradation of 0.1 g 100 g^?1 containing graded levels of l-tryptophan (0.04–0.54 g 100 g^?1, dry diet). Fish were stocked in triplicate groups, in 75-L circular trough with flow-through system and fed experimental diets at 4% BW/day twice daily. Maximum live weight gain (258%), best feed conversion ratio (FCR) (1.54) and protein efficiency ratio (PER) (1.62) were obtained in fish fed diet containing 0.34 g 100 g^?1 tryptophan. However, quadratic regression analysis of weight gain, FCR, PER and body protein deposition (BPD) data indicated requirements for dietary tryptophan at 0.37, 0.33, 0.32 and 0.33 g 100 g^?1 of dry diet, respectively. Significantly (P < 0.05) higher body protein, minimum moisture and intermediate fat contents were recorded at 0.34 g 100 g^?1 dietary tryptophan diet. Ash content was not significantly different (P > 0.05) among treatments except for diets 0.04 and 0.14 g 100 g^?1. Excellent somatic and haematological indices values were obtained at the requirement level. Based on above results, it is recommended that the diet for H. fossilis should contain tryptophan at 0.32 g 100 g^?1, dry diet, corresponding to 0.80 g 100 g^?1 dietary protein for optimum growth and efficient feed utilization.     

Growth and survival of Atlantic salmon, Salmo salar L. fed different dietary levels of astaxanthin. Juveniles

Atlantic salmon, Salmo salar L., juveniles, with a mean initial weight of 1.75 g, were fed casein-based purified diets which had been supplemented with different levels of astaxanthin for a 10-week period. The astaxanthin content of the diets ranged from 0 to 190 mg kg^?1 dry diet. The growth and survival of the juveniles were recorded throughout the experiment. The proximate composition, astaxanthin and vitamin A content were determined from whole-body samples at the start and termination of the experiment. The dietary treatment was found to affect growth significantly (P < 0.05). A reduction in the mean weight of the juveniles was observed in the groups fed the diets without astaxanthin supplementation. There was no difference in growth rate between the fish in the groups fed the diets containing 36 or 190 mg astaxanthin kg^?1 dry diet, whereas the fish in the group fed the diet containing 5.3 mg astaxanthin kg^?1 dry diet had a lower growth rate. There was a tendency to higher survival in the groups fed the diets containing astaxanthin when compared with the groups fed the non-supplemented diets. The moisture and ash contents were significantly lower and the lipid content was higher in the groups fed the astaxanthin-supplemented diets. The astaxanthin and the vitamin A concentrations in the fish were found to be dependent upon the dietary astaxanthin dose; the highest values were found in the fish fed the diet with the highest astaxanthin content. These results strongly indicate that astaxanthin functions as a provitamin A for juvenile Atlantic salmon. The body storage of vitamin A increased in the fish fed the diets containing astaxanthin. However, the increase was low in the fish fed the diet containing 5.3 mg astaxanthin kg^?1 dry diet.     

Dietary esterified astaxanthin effects on color, carotenoid concentrations, and compositions of clown anemonefish, Amphiprion ocellaris, skin

This study examined the effects of dietary esterified astaxanthin concentration on coloration, accumulation of carotenoids, and the composition of carotenoids over time in the skin of Amphiprion ocellaris. Juveniles of 30 days-post-hatch were fed 40, 60, 80, or 160 mg esterified astaxanthin per kg diet (mg kg^?1) for 90 days. Skin coloration was analyzed using the hue, saturation, and luminosity model. Increased astaxanthin concentrations and duration on diet lead to improvements in skin color, that is, lower hues (~27–29 to ~14–17; redder fish), higher saturation (~77 to ~87 %), and lower luminosity (~43 to ~35 %). Fish fed 80 and 160 mg kg^?1 astaxanthin feed showed significant coloration improvements over fish fed lower astaxanthin feeds. Increasing both dietary astaxanthin concentration and time on the feed resulted in significant increases in total skin carotenoid concentration (0.033–0.099 μg mm^?2). Furthermore, there was a significant linear relationship between hue and total skin carotenoid concentration. Compositionally, free astaxanthin and 4-hydroxyzeaxanthin were the major skin carotenoids. 4-hydroxyzeaxanthin was previously unreported for A. ocellaris. Carotenoid composition was affected by duration on diet. Fraction 4-hydroxyzeaxanthin increased by ~15 %, while free astaxanthin decreased equivalently. The transition from 4-hydroxyzeaxanthin to free astaxanthin appears to follow a reductive pathway. Results suggest that managing coloration in the production of A. ocellaris juveniles requires manipulation of both dietary astaxanthin concentration and period of exposure to astaxanthin containing diet. In order to achieve more orange–red-colored fish, feeding 80–160 mg kg^?1 esterified astaxanthin for an extended duration is recommended.     

Effect of varying dietary energy level on feed intake, feed conversion, whole-body composition and growth of Malawian tilapia, Oreochromis shiranus– Boulenger

Four isonitrogenous [30% crude protein (CP)] diets containing different gross energy levels (13.39, 16.74, 20.50 and 23.85 kJ g⁻¹) were evaluated to determine the optimum energy for the Malawian tilapia Oreochromis shiranus. Each tank (120 L) was stocked with 18 juvenile tilapia (average weight 7.32±0.25 g) and they were fed the experimental diets for 10 weeks. The final average weight of the fish was approximately twofold higher (range: 12.64–16.77 g) than the initial weight. The dietary energy significantly (P<0.05) influenced growth. The average weight of fish fed dietary energy level 20.50 kJ g⁻¹ was significantly higher (P<0.05) than the weight of the fish fed any of the other experimental diets. There was no significant difference in growth of fish fed 13.39 and 16.74 kJ g⁻¹ energy levels, but 23.85 kJ g⁻¹ produced the lowest growth rates. There were no significant differences (P>0.05) between feed intake across the treatments. Feed conversion ratio (range: 2.2–3.0) and protein efficiency ratio (range: 1.10–1.50) among the dietary treatment groups were in agreement with trends for weight gain. Dietary energy level significantly (P<0.05) influenced the body composition of O. shiranus. Whole‐body moisture (range: 64.27–67.15%) and ash (range: 13.21–14.73%) decreased in all treatments. Whole‐body protein (range: 63.57–66.16%) increased only in groups fed on the diet containing 20.50 kJ g⁻¹. Whole‐body fat (range: 13.58–17.27%) and gross energy (range: 28.411–33.210 kJ g⁻¹) increased significantly (P<0.05). Fish survival was 100% in all treatments. The results demonstrated that to maximize growth at a temperature of 23°C, O. shiranus should be fed diets containing 20.50 kJ g⁻¹ gross energy.     

Growth and survival of Atlantic salmon, Salmo salar L., fed different dietary levels of astaxanthin. First-feeding fry

Atlantic salmon fry hatched from pigment-free eggs and from eggs containing the pigment astaxanthin were fed eleven casein/gelatine-based purified diets with varying levels of astaxanthin, ranging from 0 to 317 mg kg^?1, to determine the optimum dietary astaxanthin level for satisfactory growth and survival during the start-feeding period. The fish were fed the experimental diets for a period of 11 weeks. No difference in performance was found between the two types of fry originating from the pigment-free eggs and those containing pigment. However, the dietary astaxanthin concentration was found to have a significant effect on both the growth and the survival of fry. Fish fed diets with astaxanthin concentrations below 5.3 mg kg^?1 were found to have marginal growth. In addition, mortality was high in the groups fed diets with astaxanthin concentrations below 1.0 mg kg^?1. The specific growth rate (SGR) was also affected by the dietary treatment. The lipid content was higher and the moisture content was lower in the fish fed the diets containing astaxanthin concentrations above 5.3 mg kg^?1. The vitamin A and astaxanthin concentrations in whole-body samples of the fry were significantly affected by the dietary level of astaxanthin. A plateau level in whole-body vitamin A concentration was observed at dietary levels of approximately 80 mg astaxanthin kg^?1 and higher, while no maximum astaxanthin concentration in whole-body samples was observed within the dietary levels used. The results suggest the need for a minimum dietary astaxanthin concentration of 5.1 mg kg^?1 to achieve maximum growth and survival during the start-feeding period. The results indicate a low bioavailability of vitamin A palmitate and acetate and the results also suggest a provitamin A function for astaxanthin during the same period.     

Effects of dietary vitamin E and astaxanthin on growth,skin colour and antioxidative capacity of large yellow croaker Larimichthys crocea

A 10‐week feeding trial was conducted to evaluate the effect of dietary vitamin E and astaxanthin on growth performance, skin colour and antioxidative capacity of large yellow croaker Larimichthys crocea. Six practical diets were formulated in a 2 × 3 factorial design to supplement with two levels of astaxanthin (25 and 50 mg/kg) and three levels of vitamin E (0, 120 and 800 mg/kg). The results showed that both the highest final body weight and specific growth rate were found in fish fed diets with 120 mg/kg vitamin E supplementation. No significant differences were found in survival rate, feed conversion ratio and protein efficiency ratio among all the treatments (p > .05). Skin lightness (L*) was not significantly affected by dietary treatments (p > .05). Ventral skin redness (a*) of fish fed diet with 25 mg/kg astaxanthin and 0 mg/kg vitamin E supplementation was significantly lower than that of fish fed with other diets. Yellowness (b*) and carotenoid contents both in the dorsal and in the ventral skin were found to be significantly increased with increasing dietary astaxanthin or vitamin E (p < .05), but no significant interactions were found (p > .05). The vitamin E content in liver reflected the dietary vitamin E content. Level of vitamin E content in fish fed diets with 800 mg/kg vitamin E supplementation was significantly higher than that in fish fed with the other diets (p < .05). Liver superoxide dismutase activity and thiobarbituric acid reactive substance levels were found to be decreased with increasing dietary astaxanthin and vitamin E levels, respectively. Levels of reduced glutathione in the liver were found to be increased with increasing dietary vitamin E contents. The total antioxidative capacity in the liver was found to be decreased with increasing dietary vitamin E or astaxanthin contents. In conclusion, adequate dietary vitamin E can improve the growth of large yellow croaker, and the supplementation of astaxanthin and vitamin E benefited the skin coloration and antioxidative capacity of large yellow croaker.     

Effect of microalgal biomass concentration and temperature on ornamental goldfish (Carassius auratus) skin pigmentation

The aim of this work was to investigate the effect of different carotenoid sources/concentrations and temperature on goldfish (Carassius auratus) skin pigmentation. In the first trial (trial A), the effect of carotenoid source (natural – microalgae Chlorella vulgaris and synthetic – Carophyll Pink) and carotenoid concentration (45, 80 and 120 mg pigment kg^?1 diet) was tested. Six homogeneous duplicate groups of juvenile goldfish (7.4 g) were fed, for 5 weeks, one of the diets containing 45, 80 or 120 mg of total pigments of C. vulgaris biomass or synthetic astaxanthin per kg of diet (Cv45, Cv80, Cv120, Ax45, Ax80, Ax120), respectively. In trial B, the effect of water temperature on skin pigmentation was studied. Five homogeneous duplicate groups of 25 goldfish each (5.2 g) were fed diet Ax45 over 9 weeks, to test the following temperatures: 22, 24, 26, 28 and 30 °C. At the end of both trials, samples of skin along the dorsal fin were withdrawn for subsequent analysis of total carotenoid content, intensity of colour, red and yellow hue and visual observation. The best carotenoid concentrations were achieved with astaxanthin diets. There was a tendency to an overall improvement of colour parameters (L and b) in fish fed diets with high levels of C. vulgaris. The results indicated that the best temperature range to maximize skin pigmentation was 26–30 °C.     

Physiological, metabolic and haematological responses in white shrimp Litopenaeus vannamei (Boone) juveniles fed diets supplemented with astaxanthin acclimated to low-salinity water

The effects of dietary astaxanthin supplemented at 0, 40, 80 or 150 mg astaxanthin kg⁻¹ on growth, survival, moult frequency, osmoregulatory capacity (OC) and selected metabolic and haematological variables in Litopenaeus vannamei acclimated to low‐salinity water (3 g L⁻¹) were evaluated. Supplemented astaxanthin at 80 mg kg⁻¹ improved growth, survival and moult frequency in shrimp. The lowest OC was also exhibited in shrimp fed with dietary astaxanthin at 80 mg kg⁻¹. Shrimp haemolymph concentrations of glucose, lactate, haemocyanin and total haemocyte count were all significantly enhanced by feeding the diet supplemented with 80 mg astaxanthin kg⁻¹ compared with shrimp fed with the other diets. On the basis of these results, dietary astaxanthin supplementation of 80 mg kg⁻¹ is recommended for juvenile L. vannamei cultured in low‐salinity water.     

The degree of carotenoid esterification influences the absorption of astaxanthin in rainbow trout, Oncorhynchus mykiss (Walbaum)

The absorption of astaxanthin from diets (30 mg kg^?1 inclusion) supplemented with either unesterified astaxanthin; isolated astaxanthin monoesters, diesters or a cell‐free carotenoid extract from Haematococcus pluvialis were studied in rainbow trout (>200 g). No significant differences (P > 0.05) were recorded in the apparent digestibility coefficients (ADC) (≈60–65%) between astaxanthin sources. However, following consumption of a single meal, peak serum astaxanthin levels at 32 h (≈1.0–1.6 μg mL^?1) were significantly higher (P < 0.05) in fish fed unesterified astaxanthin and astaxanthin monoester, compared to fish fed astaxanthin diester and the cell free extract. However, no significant differences (P > 0.05) were recorded in serum astaxanthin uptake rates between sources of astaxanthin. Results suggest that the extent of carotenoid esterification negatively influences the peak serum levels of astaxanthin in rainbow trout.     

A preliminary study on growth of Crassostrea gigas larvae and spat in relation to dietary protein

Diets of Chaetoceros calcitrans (Paulsen) Takano and Tetraselmis suecica (Kylin) Butch containing high or low levels of protein were fed to Crassostrea gigas Thunberg larvae and spat. The 4-day increment in D-larvae shell length was not related to differences in the ash-free dry weight or protein content of the diets at cell concentrations of 75–125 Chaetoceros μl⁻¹. At concentrations of 2–100 Chaetoceros μl⁻¹ the largest growth increment was found when 0.267 μg ash-free dry weight larva⁻¹ d⁻¹ (equivalent to 3.35 Joules · 10⁻³ larva⁻¹ d⁻¹) was filtered at a temperature of 28.1°C.Percentage settlement of C. gigas increased as protein in Chaetoceros, fed at 75–125 cells μl⁻¹ (P < 0.001), and in Tetraselmis, fed at 5–15 cells μl⁻¹ (P < 0.05), increased. Growth of spat during the 14 days immediately after settlement was better on a low-protein than a high-protein Tetraselmis diet (P < 0.001) but differences between Chaetoceros diets were not significant.     

Effects of dietary astaxanthin concentration and feeding period on the skin pigmentation of Australian snapper Pagrus auratus (Bloch & Schneider, 1801)

A single‐factor experiment was conducted to investigate the effects of dietary astaxanthin concentration on the skin colour of snapper. Snapper (mean weight=129 g) were held in white cages and fed one of seven dietary levels of unesterified astaxanthin (0, 13, 26, 39, 52, 65 or 78 mg astaxanthin kg^?1) for 63 days. Treatments comprised four replicate cages, each containing five fish. The skin colour of all fish was quantified using the CIE L^*, a^*, b^* colour scale after 21, 42 and 63 days. In addition, total carotenoid concentrations of the skin of two fish cage^?1 were determined after 63 days. Supplementing diets with astaxanthin strongly affected redness (a^*) and yellowness (b^*) values of the skin at all sampling times. After 21 days, the a^* values increased linearly as the dietary astaxanthin concentration was increased before a plateau was attained between 39 and 78 mg kg^?1. The b^* values similarly increased above basal levels in all astaxanthin diets. By 42 days, a^* and b^* values increased in magnitude while a plateau remained between 39 and 78 mg kg^?1. After 63 days, there were no further increases in measured colour values, suggesting that maximum pigmentation was imparted in the skin of snapper fed diets >39 mg kg^?1 after 42 days. Similarly, there were no differences in total carotenoid concentrations of the skin of snapper fed diets >39 mg kg^?1 after 63 days. The plateaus that occurred in a^* and b^* values, while still increasing in magnitude between 21 and 42 days, indicate that the rate of astaxanthin deposition in snapper is limited and astaxanthin in diets containing >39 mg astaxanthin kg^?1 is not efficiently utilized. Astaxanthin retention after 63 days was greatest from the 13 mg kg^?1 diet; however, skin pigmentation was not adequate. An astaxanthin concentration of 39 mg kg^?1 provided the second greatest retention in the skin while obtaining maximum pigmentation. To efficiently maximize skin pigmentation, snapper growers should commence feeding diets containing a minimum of 39 mg unesterified astaxanthin kg^?1 at least 42 days before sale.     

Effect of carotenoids and background colour on the skin pigmentation of Australian snapper Pagrus auratus (Bloch & Schneider, 1801)

Three 2‐factor experiments were conducted to determine the effects of background colour and synthetic carotenoids on the skin colour of Australian snapper Pagrus auratus. Initially, we evaluated the effects on skin colour of supplementing diets for 50 days with 60 mg kg^?1 of either astaxanthin (LP; Lucantin^® Pink), canthaxanthin (LR; Lucantin^® Red), apocarotenoic acid ethyl ester (LY; Lucantin^® Yellow), selected combinations of the above or no carotenoids and holding snapper (mean weight=88 g) in either white or black cages. In a second experiment, all snapper (mean weight=142 g) from Experiment 1 were transferred from black to white, or white to white cages to measure the short‐term effects of cage colour on skin L^*, a^* and b^* colour values. Skin colour was measured after 7 and 14 days, and total carotenoid concentrations were determined after 14 days. Cage colour was the dominant factor affecting the skin lightness of snapper with fish from white cages much lighter than fish from black cages. Diets containing astaxanthin conferred greatest skin pigmentation and there were no differences in redness (a^*) and yellowness (b^*) values between snapper fed 30 or 60 mg astaxanthin kg^?1. Snapper fed astaxanthin in white cages displayed greater skin yellowness than those in black cages. Transferring snapper from black to white cages increased skin lightness but was not as effective as growing snapper in white cages for the entire duration. Snapper fed astaxanthin diets and transferred from black to white cages were less yellow than those transferred from white to white cages despite the improvement in skin lightness (L^*), and the total carotenoid concentration of the skin of fish fed astaxanthin diets was lower in white cages. Diets containing canthaxanthin led to a low level of deposition in the skin while apocarotenoic acid ethyl ester did not alter total skin carotenoid content or skin colour values in snapper. In a third experiment, we examined the effects of dietary astaxanthin (diets had 60 mg astaxanthin kg^?1 or no added carotenoids) and cage colour (black, white, red or blue) on skin colour of snapper (mean weight=88 g) after 50 days. Snapper fed the astaxanthin diet were more yellow when held in red or white cages compared with fish held in black or blue cages despite similar feed intake and growth. The skin lightness (L^* values) was correlated with cage L^* values, with the lightest fish obtained from white cages. The results of this study suggest that snapper should be fed 30 mg astaxanthin kg^?1 in white cages for 50 days to increase lightness and the red colouration prized in Australian markets.     

An evaluation of techniques for the administration of 17β-extradiol to teleosts

Goldfish (Carassius auratus) were treated with 17β-estradiol in saline, peanut oil, cocoa butter or silastic pellet, and the resulting elevation in serum estradiol was measured by radioimmunoassay. Injection of estradiol in saline or oil at 2 or 20 μg·g⁻¹ body weight produced a large elevation in steroid levels (up to 400 ng·ml⁻¹ in 1 h) followed by a rapid fall to basal levels over the next 3–4 days. Estradiol in cocoa butter at the same doses maintained elevated serum estradiol levels for up to 8 days, while estradiol administered in a silastic pellet (50 μg·g⁻¹ body weight) was still producing a stable elevation 9 days after implant. The results indicate that injected steroid is rapidly absorbed and cleared whereas release from pellets is lower but of longer duration. The choice of method for treatment with steroids therefore depends upon the degree and duration of elevation which is required by the experimental protocol. The appropriateness of steroid doses and methods of administration used by other workers is discussed.     

The effect of different carotenoid sources on skin coloration of cultured red porgy (Pagrus pagrus)

This study presents data on the effect of carotenoid sources on skin coloration of red porgy (Pagrus pagrus). Three experiments were conducted: in the first, fish were fed an astaxanthin (Naturose^®)‐supplemented diet, while the second fish received diets supplemented with β‐carotene (Rovimix β‐caroten^®) or lycopene (Lyc‐O‐Mato^®): Carotenoids were added to the level of 100 ppm in each diet, while a non‐carotenoid‐supplemented diet served as a control. In the third experiment, the effect of dietary protein/carbohydrate ratio on melanin content in the skin was investigated. For this experimentation, four diets were formulated to contain 50/23, 40/32, 30/48 and 20/59 protein/carbohydrate ratio. Naturose^® astaxanthin increased total carotenoid content in the dorsal skin area while β‐carotene and lycopene seem to have had no significant effect. Naturose^® was the only carotenoid source that had a significant effect on skin hue, promoting a reddish coloration to the dorsal skin area and a ventral hue similar to wild red porgy. No apparent effect of carotenoid source on skin melanin content was observed. In contrast, dietary protein/carbohydrate ratio affected melanin content in the skin. The fish fed the 50/23 diet showed significantly higher values. Farmed red porgy had eight times higher dorsal‐skin melanin content than wild ones.     

Growth performance and color enhancement of goldfish,Carassius auratus,fed diets containing natural dyes extracted from annatto (Bixa orellana) seeds

ABSTRACT

The present study was conducted to evaluate growth performance and color enhancement of goldfish, Carassius auratus, fed diets containing 0, 50, 100, 200, and 250 mg kg^?1 diet of annatto dye (AD) for 60 days. The survival rate was significantly higher in fish fed 100, 200, and 250 mg AD kg^?1 diet over than these fed control and 50 mg AD kg^?1 diet (p < 0.05). AD significantly (p <0 .05) increased the pigmentation in the skin and caudal fin of goldfish in a concentration dependent manner (R² = 0.995, 0.997). The highest amount of total carotenoid deposition in fish skin and fins were given by diets containing 200–250 mg AD kg^?1 diet. The highest redness (a*) of 43.21 and yellowness (b*) of 12.53 were obtained by 250 and 50 mg AD kg^?1, respectively. The present results show that AD can be successfully used as an alternative natural carotenoid source in goldfish diets at levels of 200–250 mg AD kg^?1 diet.     

Dietary arginine requirement of fingerling hybrid Clarias (Clarias gariepinus×Clarias macrocephalus)

The dietary arginine requirement of fingerling hybrid Clarias (Clarias gariepinus×Clarias macrocephalus) (4.2±0.03 cm, 0.56±0.04 g) was determined by feeding six isonitrogenous (400 g kg⁻¹ crude protein) and isocaloric (17.9 kJ g⁻¹) amino acid test diets containing casein, gelatin and l ‐crystalline amino acids with graded levels of arginine (10.0, 12.5, 15.0, 17.5, 20.0 and 22.5 g kg⁻¹) for 4 weeks to triplicate groups. Diets were fed twice a day at 09:00 and 16:00 hours at 8% body weight day⁻¹. Maximum weight gain (523%), best feed conversion ratio (FCR, 1.41), protein efficiency ratio (1.78) and specific growth rate (6.53%) were recorded in fish fed the diet containing arginine at 20.0gkg⁻¹ of the diet. Second‐degree polynomial regression analysis of live weight gain and FCR values indicated the dietary arginine requirement at 17.8 and 20.0 g kg⁻¹ of dry diet respectively. Significantly higher carcass protein and protein deposition values were recorded at the requirement level (20.0 g kg⁻¹). Higher fat and lower moisture values were obtained in carcass of fish fed the diet with 15.0g kg⁻¹ arginine. The maximum carcass ash value was noticed in the fish fed at 20.0 g kg⁻¹ dietary arginine. We recommend that the diet for hybrid Clarias (C. gariepinus×C. macrocephalus) should contain arginine in the range of 17.8–20.0 g kg⁻¹ of the dry diet, corresponding to 44.5 and 50 g kg⁻¹ of dietary protein respectively.