Dietary protein requirement for fingerling Channa punctatus (Bloch), based on growth, feed conversion, protein retention and biochemical composition

An 8-week feeding trial was conducted in a flow-through system (1–1.5 L min⁻¹) at 27°C to determine dietary protein requirement for Channa punctatus fingerlings (4.58 ± 0.29 g) by feeding six isocaloric diets (18.39 kJ g⁻¹, gross energy). Diets containing graded levels of protein (300, 350, 400, 450, 500 and 550 g kg⁻¹) were fed to triplicate groups of fish to apparent satiation at 09:00 and 16:00 h. Maximum absolute weight gain (AWG; 8.11 g fish⁻¹), specific growth rate (SGR; 1.82%) and best feed conversion ratio (FCR; 1.48) were recorded in fish fed diet containing 450 g kg⁻¹ protein, whereas protein efficiency ratio (PER; 1.52), protein retention efficiency (PRE; 25%), energy retention efficiency (ERE; 78%) and RNA/DNA ratio (3.01) were maximum for the group fed dietary protein at 400 g kg⁻¹. Second-degree polynomial regression analysis of AWG, SGR and FCR data against varying levels of dietary protein yielded optimum dietary protein requirement of fingerling between 462.24 and 476.72 g kg⁻¹, whereas the regression analysis of PER, PRE, ERE and RNA/DNA ratio data showed a lower protein requirement of 438.28–444.43 g kg⁻¹ of the diet. Considering the PER, PRE, ERE and RNA/DNA ratio as more reliable indicators, this protein requirement is recommended for developing quality protein commercial feeds for C. punctatus fingerlings.     

Total sulphur amino acid requirement and cystine replacement value for fingerling rohu,Labeo rohita: effects on growth,nutrient retention and body composition

Two feeding experiments were conducted to quantify the total sulphur amino acid (TSAA) requirement and replacement value of cystine for methionine for fingerling Labeo rohita. In Experiment I, isonitrogenous (380 g kg^?1 CP) and isocaloric (17.90 kJ g^?1 GE) amino acid test diets with graded levels of methionine (4, 6, 8, 10, 12, 14 g kg^?1 dry diet) and 0.4 g kg^?1 cystine were fed to fish (4.62 ± 0.2 cm; 0.66 ± 0.1 g) and methionine requirement determined by analysing absolute weight gain (AWG) (5.48), feed conversion ratio (FCR) (1.26), protein retention efficiency (PRE%) (39%) and energy retention efficiency (ERE%) (85%) data which were best at 10 g kg^?1 methionine of dry diet. In Experiment II, six diets with different ratios of L‐cystine and L‐methionine on equimolar sulphur basis were fed to fish (4.71 ± 0.1 cm; 0.69 ± 0.2 g) under identical conditions. Maximum AWG (5.58), best FCR (1.24), PRE (41%) and ERE (86%) in fish fed Diet IV indicated cystine replacement value to be 40%. On the basis of the broken‐line and second‐degree polynomial regression analyses of results obtained in Experiments I and II, it is concluded that inclusion of TSAA in the range of 25.2–31.31 g kg^?1 of protein is optimum of which 33–39% could be spared by cystine.     

Dietary copper requirement of fingerling Channa punctatus (Bloch) based on growth,feed conversion,blood parameters and whole body copper concentration

A 12‐week feeding trial was conducted to estimate the dietary copper requirement of fingerling Channa punctatus. Six casein?gelatin‐based test diets (450 g kg^?1 crude protein; 18.81 kJ g^?1 gross energy) with graded levels of copper as copper sulphate (3.7, 4.7, 5.7, 6.7, 7.7 and 8.7 mg copper equivalent kg^?1 diet) were formulated and fed to triplicate groups of fish (7.25 ± 0.81 cm; 5.21 ± 0.27 g) near to satiation. Fish fed diet with 6.7 mg kg^?1 copper had highest absolute weight gain (AWG; 51.63 g fish^?1), protein efficiency ratio (PER; 1.42 g fish^?1), protein gain (PG; 8.34 g fish^?1), haemoglobin (Hb; 9.68 g dL^?1), haematocrit (Hct; 31.18%) and RBCs (3.24 × 10⁶ × mm^?3). Feed conversion ratio (FCR) was found to be best (1.57) at above level of dietary copper. Whole body copper concentration was found to increase with the increasing levels of dietary copper. Hepatic thiobarbituric acid‐reactive substances concentration was found to decrease with increasing dietary concentrations of copper up to 6.7 mg kg^?1 beyond which a reverse trend in this parameter was noted. Broken‐line regression analysis of AWG, FCR and PG concentrations against varying levels of dietary copper yielded the requirement in the range of 6.66–6.78 mg kg^?1. Data generated during this study would be useful in formulating copper‐balanced commercial feeds for the intensive culture of this fish.     

Dietary arginine requirement of Heteropneustes fossilis fry (Bloch) based on growth,nutrient retention and haematological parameters

Dietary arginine requirement of Heteropneustes fossilis fry (3.0 ± 0.5 cm; 5.1 ± 0.3 g) was determined by feeding casein‐gelatin‐based isonitrogenous (400 g kg^?1 crude protein) and isocaloric (17.97 kJ g^?1) amino acid test diets containing graded levels of l ‐arginine (15, 17, 19, 21, 23 and 25 g kg^?1 dry diet) for 12 weeks. Maximum absolute weight gain (AWG) (44.4), best feed conversion ratio (FCR) (1.22), highest protein retention efficiency (PRE%) (41%), energy retention efficiency (ERE%) (75%), best condition factor, hepatosomatic index and viscerosomatic index were noted at 21 g kg^?1 arginine of the dry diet. Maximum body protein (189.8 g kg^?1) was also obtained in fish fed above diet. Highest haematocrit value (35%), Hb concentration (9.54 g dL^?1), RBC count (3.44 × 10⁹ mL^?1) and lowest Erythrocyte sedimentation rate (ESR) (1.93 mm h^?1) were obtained at the above level of arginine in the diet. AWG, FCR, PRE% and ERE% data were analysed using broken‐line and an exponential fit to obtain more precise dietary arginine requirement. On the basis of broken‐line and exponential analyses of AWG, FCR, PRE and ERE data, inclusion of dietary arginine in the range of 20.4–22.6 g kg^?1 dry diet, corresponding to 51–56.5 g kg^?1 dietary protein, is recommended for formulating arginine‐balanced feeds for rearing H. fossilis fry.     

Dietary Vitamin C Requirement of Fingerling,Cirrhinus mrigala (Hamilton), Based on Growth,Feed Conversion,Protein Retention,Hematological Indices,and Liver Vitamin C Concentration

This study was conducted to quantify dietary vitamin C requirement of fingerling, Cirrhinus mrigala, (0.79 ± 0.07 g; 3.51 ± 0.15 cm) by feeding casein‐gelatin based purified diets (400 g/kg crude protein; 3.45 kcal/g digestible energy) containing nine levels of vitamin C as l‐ascorbyl‐2‐polyphosphate (0.0, 5, 15, 25, 35, 45, 55, 75, and 95 mg vitamin C equivalent/kg diet) to triplicate groups of fish to apparent satiation for 16 wk. Absolute weight gain (AWG, g/fish), feed conversion ratio (FCR), protein retention efficiency (PRE%), RNA/DNA ratio, hemoglobin (Hb, g/dL), and hematocrit value (Hct%) were taken as the response criteria to determine vitamin C requirement of mrigal. Fish fed diet with 35 mg/kg vitamin C had significantly higher AWG (9.94 g/fish), FCR (1.39), PRE (27.72%), RNA/DNA ratio (4.18), Hb (11.15 g/dL), and Hct (34.44%) values. However, liver vitamin C concentration was found to be higher (64.92 µg/g wet tissue) in diet containing 45 mg vitamin C/kg. Broken‐line regression analysis of AWG data estimated the requirement of 35.65 mg/kg, whereas that of the liver vitamin C concentration data projected the requirement to 41.99 mg/kg.     

Dietary pyridoxine requirement of fingerling Channa punctatus (Bloch) based on growth performance,liver pyridoxine concentration,and carcass composition

Seven casein gelatin-based diets containing 450 g/kg CP and 18.39 kJ/g GE with different levels of pyridoxine (0, 2, 4, 6, 8, 10, and 12 mg/kg diet) were fed to fingerling Channa punctatus (4.66 ± 0.46 g) for 12 weeks to determine pyridoxine requirement. Highest absolute weight gain (AWG; 25.81 g/fish, P < 0.05), protein retention (PRE; 23.69%, P < 0.05), energy retention efficiencies (ERE; 69.63%, P < 0.05), and minimum feed conversion ratio (FCR; 1.48) were noted at 8 mg pyridoxine/kg diet. However, liver pyridoxine content achieved the positive correlation as the dietary pyridoxine increased up to 10mg/kg. On the basis of broken-line analysis of AWG, PRE, FCR, and liver pyridoxine data, pyridoxine requirement is recommended between 7.6 and 10.4 mg/kg of dry diet.     

Dietary L‐tryptophan requirement of fingerling stinging catfish,Heteropneustes fossilis (Bloch)

To quantify dietary L‐tryptophan requirement of fingerling Heteropneustes fossilis (6.66 ± 0.08 g), casein–gelatin‐based isonitrogenous (38% CP) and isoenergetic (14.72 kJ g^?1 DE) purified diets with eight levels of L‐tryptophan (0.12%, 0.16%, 0.20%, 0.24%, 0.28%, 0.32%, 0.36%, 0.40% dry diet) were fed to triplicate groups of fish twice daily to apparent satiation for 12 weeks. Incremental levels of dietary tryptophan from 0.12 to 0.28% significantly (P < 0.05) improved absolute weight gain (AWG; 14.3–65.9 g fish^?1), feed conversion ratio (FCR; 5.9–1.5), protein retention efficiency (PRE; 6.2–32.2%), haemoglobin (Hb; 6.5 to 11.9 g dL^?1) and haematocrit (Hct; 23.5–33.8%). To determine the precise information on tryptophan requirement, data were subjected to broken‐line and second‐degree polynomial regression analysis. Broken‐line regression analysis reflected highest R² values for AWG g fish^?1 (0.999), PRE% (0.993), Hb g dL^?1 (0.995) and Hct% (0.993) compared with R² values obtained using second‐degree polynomial regression analysis of AWG g fish^?1(0.949), PRE% (0.890), Hb g dL^?1(0.969) and Hct% (0.943), indicating that data were better fit to broken‐line regression analysis. Hence, based on broken‐line regression analysis at 95% maximum response, tryptophan requirement of fingerling H. fossilis is recommended between 0.24% and 0.27% dry diet (0.63–0.71% protein).     

Synergistic effects of dietary vitamin E and selenomethionine on growth performance and tissue methylmercury accumulation on mercury‐induced toxicity in juvenile olive flounder,Paralichthys olivaceus (Temminck et Schlegel)

An 8‐week feeding trial was conducted to evaluate the synergistic effects of dietary vitamin E and selenomethionine (SeMet) on induced methylmercury (MeHg) toxicity in juvenile olive flounder Paralichthys olivaceus. Nine semi‐purified diets were formulated to contain three different vitamin E levels as DL‐α‐tocopheryl acetate (0, 100 and 200 mg TAkg^?1 diet) and three different selenium (Se) levels (0, 2 and 4 SeMet mg kg^?1 diet) on the constant mercury toxicity level (20 mg MeHgkg^?1 diet). Nine experimental diets, in a 3² factorial design (E₀Se₀, E₀Se₂, E₀Se₄, E₁₀₀Se₀, E₁₀₀Se₂, E₁₀₀Se₄, E₂₀₀Se₀, E₂₀₀Se₂ and E₂₀₀Se₄), were fed to triplicate groups of fish averaging 2.3 ± 0.04 g (mean ± SD) in the semi‐recirculation system. After 8 weeks of feeding trial, vitamin E and Se showed significant effects on weight gain (WG) of fish (P < 0.05). We found that there was a clear trend of increasing WG with elevating vitamin E and Se levels in the diets. Feed efficiency (FE), specific growth rate (SGR), protein efficiency ratio (PER) and survivability exhibited a similar trend with WG. Both antioxidants had significant interaction effects on FE and PER (P < 0.05). Methylmercury concentrations in fish muscle, liver and kidney decreases in a dose‐dependent manner as dietary vitamin E and Se levels increase. Interestingly, the most significant interactive effects of vitamin E and Se were found in liver tissue for depleting Hg concentrations (P < 0.05). These findings suggest that dietary vitamin E more than 100 mg TA kg^?1 diet with 2 or 4 mg SeMet kg^?1‐supplemented diets could have synergistic effects on growth and liver mercury bioaccumulation on MeHg‐induced toxicity in juvenile olive flounder.     

Histologic changes in channel catfish,Ictalurus punctatus Rafinesque,fed diets containing graded levels of gossypol–acetic acid

A study was performed to evaluate the histologic changes among fingerling channel catfish, Ictalurus punctatus Rafinesque, fed purified diets containing gossypol from gossypol–acetic acid. The catfish were maintained on diets with 0, 300, 600, 900, 1200 or 1500 mg gossypol kg^?1 diet for 12 weeks, and histologic samples from the stomach, proximal and distal intestines, pancreas, liver, and spleen were obtained from fish in all groups. Stomach sections exhibited significant gastric gland necrosis in fish fed 600 mg gossypol kg^?1 diet or higher. Non‐existent‐to‐mild enterocyte vacuolization loss, inflammatory cell infiltration, and hyperplastic lamina propria were noted in the intestinal sections from gossypol‐fed fish, but no significant differences in severity scores were noted. The pancreas from fish fed doses of gossypol above 600 mg gossypol kg^?1 diet exhibited significant mild‐to‐severe necrosis, and livers from fish fed 900 and 1500 mg gossypol kg^?1 diet exhibited significantly higher pigment deposition. No other significant histologic differences were observed in the fish fed diets containing gossypol–acetic acid. The data in this study indicates that at least 600–900 mg gossypol kg^?1 purified diet can cause statistically significant histologic changes in fingerling channel catfish, suggesting that gossypol should remain at concentrations below 600 mg gossypol kg^?1 diet.     

Dietary thiamin and pyridoxine requirements of fingerling Indian major carp,Cirrhinus mrigala (Hamilton)

Two experiments were conducted to quantify the dietary thiamin (experiment I) and pyridoxine (experiment II) requirements of fingerling Cirrhinus mrigala for 16 weeks. In experiment I, dietary thiamin requirement was determined by feeding seven casein–gelatin‐based diets (400 g kg^?1 CP; 18.69 kJ g^?1 GE) with graded levels of thiamin (0, 0.5, 1, 2, 4, 8 and 16 mg kg^?1 diet) to triplicate groups of fish (6.15 ± 0.37 cm; 1.89 ± 0.12 g). Fish fed diet with 2 mg kg^?1 thiamin had highest specific growth rate (SGR), protein retention (PR), RNA/DNA ratio, haemoglobin (Hb), haematocrit (Hct), RBCs and best feed conversion ratio (FCR). However, highest liver thiamin concentration was recorded in fish fed 4 mg thiamin kg^?1 diet. Broken‐line analysis of SGR, PR and liver thiamin concentrations exhibited the thiamin requirement in the range of 1.79–3.34 mg kg^?1 diet (0.096–0.179 μg thiamin kJ^?1 gross energy). In experiment II, six casein–gelatin‐based diets (400 g kg^?1 CP; 18.69 kJ g^?1 GE) containing graded levels of pyridoxine (0, 2, 4, 6, 8 and 10 mg kg^?1 diet) were fed to triplicate groups of fish (6.35 ± 0.37 cm; 1.97 ± 0.12 g). Fish fed diet containing 6 mg kg^?1 pyridoxine showed best SGR, FCR, PR, RNA/DNA ratio, Hb, Hct and RBCs, whereas maximum liver pyridoxine concentration was recorded in fish fed 8 mg kg^?1 dietary pyridoxine. Broken‐line analysis of SGR, PR and liver pyridoxine concentrations reflected the pyridoxine requirement from 5.63 to 8.61 mg kg^?1 diet. Data generated during this study would be useful in formulating thiamin‐ and pyridoxine‐balanced feeds for the intensive culture of this fish.     

Dietary arginine requirement of fingerling Indian major carp, Cirrhinus mrigala (Hamilton)

Dietary arginine requirement of fingerling Indian major carp, Cirrhinus mrigala (4.20 ± 0.05 cm; 0.60 ± 0.02 g) was determined by conducting a 8‐week feeding trial with casein–gelatine‐based diets (400 g kg^?1 crude protein; 17.90 kJ g^?1, gross energy), containing crystalline amino acids with graded levels of l ‐arginine (10, 12.5, 15, 17.5, 20 and 22.5 g kg^?1, dry diet). Fish were randomly stocked, in triplicate groups, in 55‐L indoor polyvinyl flow through circular tanks and fed experimental diets at 5% of their body weight divided into two feedings at 08.00 and 16.00 hours. Live weight gain (321%) and feed conversion ratio (FCR 1.40) were significantly (P < 0.05) higher in fish fed diet containing 17.5 g kg^?1dietary arginine compared with other diets. Second‐degree polynomial regression analysis of live weight gain, FCR and protein efficiency ratio data indicated requirements for dietary arginine at 18.7, 18.4 and 18.3 g kg^?1 of the dry diet, respectively. Maximum carcass protein, and minimum moisture and fat contents were noticed at the requirement level. Carcass ash content remained insignificantly different among the treatments except at 17.5 g kg^?1 dietary arginine showing significantly higher ash content. Based on the above results, it is recommended that the diet for fingerling C. mrigala should contain arginine at 18.4 g kg^?1, dry diet, corresponding to 46 g kg^?1 dietary protein for optimum growth and efficient feed utilization.     

Effect of dietary l‐lysine levels on growth,feed conversion,lysine retention efficiency and haematological indices of Heteropneustes fossilis (Bloch) fry

Effect of varying dietary lysine levels on growth, feed conversion, nutrient retention, lysine retention efficiency and haematological indices of Heteropneustes fossilis fry (2.97 ± 0.11 cm; 4.78 ± 0.31 g) was studied by conducting a 12‐week feeding trial. Isonitrogenous (450 g kg^?1 CP) and isocaloric (17.97 kJ g^?1 GE) amino acid test diets with graded concentrations of l ‐lysine (18, 20, 22, 24, 26, 28 g kg^?1 dry diet) were fed to triplicate groups of fish to apparent satiation twice daily at 17 and 17:30 h. Maximum thermal growth coefficient (TGC, 0.82), best feed conversion ratio (FCR, 1.28) highest protein retention efficiency (PRE, 36%), energy retention efficiency (ERE, 79%) and lysine retention efficiency (LRE, 75%) were noted at 24 g kg^?1 lysine of dry diet. Body protein was also found to be in line with growth data and peaked at 24 g kg^?1 lysine of dry diet. Similarly, superior somatic and haematological indices were exhibited by the groups fed dietary lysine at 24 g kg^?1 of the dry diet. However, exponential analysis of dietary lysine intake against TGC, lysine retention and protein retention indicated that inclusion of dietary lysine in the range of 13.24–14.14 g kg^?1 dry diet, corresponding to 29.42–31.42 g kg^?1 dietary protein, is essential for faster growth of this fish.     

Dietary histidine requirement of Singhi,Heteropneustes fossilis fry (Bloch)

Amino acids are vital for all living organisms including fish and histidine is an essential amino acid for fish. In view of this, dietary histidine requirement of fry Heteropneustes fossilis was determined by feeding casein–gelatin‐based isonitrogenous (430 g kg^?1 CP) and isocaloric (17.9 MJ kg^?1 GE; 15.5 MJ kg^?1 DE) amino acid test diets (10 to 20 g histidine kg^?1 dry diet) to quadruplicate groups of randomly assigned fish to apparent satiety for 12 weeks. Maximum absolute weight gain (AWG; 44 g fish^?1), protein retention efficiency (PRE; 20%), protein efficiency ratio (PER; 1.04), haemoglobin (Hb; 11.24 g dL^?1), haematocrit (Hct; 35.11%), red blood count (RBCs; 2.98 × 10⁹ mL^?1) and lowest erythrocyte sedimentation rate (ESR; 1.92 mm h^?1) were obtained at 16 g histidine kg^?1 dry diet. The 95% maximum quadratic response of above data exhibited the requirement to be at 15.2, 15.1, 15.6 and 15.5 g histidine kg^?1 diet. As histidine is found in higher concentration in haemoglobin, requirement obtained for Hct% and Hb is 4% greater than that required for maximizing weight gain and protein retention. Based on these results, dietary histidine requirement of H. fossilis fry is recommended between 15.1 and 15.6 g kg^?1, corresponding to 35.1–36.3 g kg^?1 protein.     

Dietary histidine requirement of fingerling Indian major carp, Cirrhinus mrigala (Hamilton)

An 8‐week growth trial was conducted to determine the dietary histidine requirement of the Indian major carp, Cirrhinus mrigala fingerling (length 4.22 ± 0.45 cm; weight 0.61 ± 0.08 g; n = 40). Isonitrogenous (400 g kg^?1 crude protein) and isoenergetic (17.90 kJ g^?1 gross energy) diets with graded levels of l ‐histidine (2.5, 5.0, 7.5, 10.0, 12.5 and 15.0 g kg^?1 dry diet) were formulated using casein and gelatin as a source of intact protein, supplemented with l ‐crystalline amino acids. Twenty fish were randomly stocked in 70‐L indoor polyvinyl circular fish tank (water volume 55‐L, water exchange rate 1–1.5 L min^?1) and fed experimental diets at the rate of 5% of their body weight/day divided over two feedings at 08:00 and 16:00 h. Maximum live weight gain (295%), best feed conversion ratio (FCR) (1.48) and protein efficiency ratio (PER) (1.69) occurred at 7.5 g kg^?1 of dietary histidine level. When live weight gain, FCR and PER data were analysed using second‐degree polynomial regression, the break points indicated histidine requirements at 9.4, 8.6 and 8.5 g kg^?1 of dry diet respectively. Significantly (P < 0.05) higher whole body protein and low moisture values were recorded at 7.5 g kg^?1 histidine level. Body fat increased significantly (P < 0.05) with increasing histidine levels. However, at 7.5 and 10 g kg^?1 histidine diets body fat did not differ (P > 0.05) to each other. Ash content of fish fed diets containing various levels of histidine did not differ except at 2.5 and 5.0 g kg^?1 inclusion levels where significantly (P < 0.05) higher ash was recorded. Protein deposition was also found to be significantly (P < 0.05) higher in the 7.5 g kg^?1 histidine diet. Based on the polynomial regression analysis of FCR and PER data, it is recommended that the diet for fingerling C. mrigala should contain histidine at 8.5 g kg^?1 of dry diet, corresponding to 21.25 g kg^?1 of dietary protein for optimum growth and efficient utilization of feed.     

Dietary histidine requirement of fingerling Catla Catla (Hamilton) based on growth,protein gain,histidine gain,RNA/DNA ratio,haematological indices and carcass composition

To investigate the histidine requirement of fingerling Catla catla (3.65 ± 0.15 cm; 0.65 ± 0.36 g), six casein‐gelatin based diets (33% CP; 13.58 kJ g^?1 DE) containing graded levels of L‐histidine (0.25%, 0.39%, 0.53%, 0.67%, 0.83%, 0.96% of the dry diet) were fed near to satiation thrice a day for 12 weeks. Maximum absolute weight gain (AWG; 8.63 g fish^?1), protein gain (PG; 1.45 g fish^?1), histidine gain (HG, 48.19 mg fish^?1), RNA/DNA ratio (4.15), best feed conversion ratio (FCR; 1.31), highest haemoglobin (Hb, 9.61 g dL^?1), RBCs (2.84 × 10⁶ mm^?3) and haematocrit (Ht, 30.12%) were recorded in fish fed diet containing 0.67% histidine. However, broken‐line regression analysis of AWG, PG, HG, RNA/DNA ratio, FCR, Hb, Ht and RBCs against dietary histidine reflected the histidine requirement at 0.65%, 0.64%, 0.63%, 0.68%, 0.63%, 0.66%, 0.68% and 0.65% dry diet respectively. Carcass protein was found to improve significantly (P < 0.05) from 13.36% to 16.42% with the increase in dietary histidine from 0.25% to 0.67%. Based on regression analysis of AWG, PG, HG, RNA/DNA ratio, FCR, Hb, Ht and RBCs, it is recommended that the diet for fingerling catla should contain histidine in the range of 0.63–0.68% dry diet, equivalent to 1.91–2.06% of the dietary protein for optimum growth, feed utilization, blood profile and carcass composition.     

Effects of extruded and pelleted diets with differing lipid levels on growth,nutrient retention and serum biochemical indices of tilapia (Oreochromis aureus × Tilapia nilotica)

This study was conducted to evaluate the effects of extruded diets and pelleted diets with varying dietary lipid levels on growth performance and nutrient utilization of tilapia. Six diets, containing three levels of lipid at 40, 60 or 80 g kg^?1 (with the supplemental lipid of 0, 20 or 40 g kg^?1, respectively), were prepared by extruding or pelleting and then fed to tilapia juveniles (8.0 ± 0.1 g) in cages (in indoor pools) for 8 weeks. The results indicated that the fish that were fed the diet with 60 g kg^?1 of lipid had a higher weight gain (WG), specific growth rate (SGR), protein efficiency ratio (PER), lipid retention (LRE), energy retention (ERE), apparent protein digestibility, apparent dry matter digestibility and a lower feed conversion ratio (FCR) than those fed the diet with 40 g kg^?1 lipid in both the extruded diet and pelleted diet (P < 0.05). As the dietary lipid level increased from 60 to 80 g kg^?1, these parameters were not further improved, even digestibilities of the crude protein and dry matter decreased (P < 0.05). With the dietary lipid level increased, whole‐body lipid content significantly increased (P < 0.05), serum aspartate aminotransferase, alkaline phosphatase, total cholesterol and low‐density lipoprotein cholesterol (LDL‐C) tended to increase (P > 0.05), whereas whole‐body protein content, serum triglyceride (TG), high‐density lipoprotein cholesterol (HDL‐C) and HDL‐C/LDL‐C tended to decrease (P > 0.05). Fish fed with the extruded diets had a higher WG, SGR, hepatosomatic index (HSI), PER, protein retention (PRE), LRE, ERE, TG, apparent digestibility of protein and dry matter, as well as a lower FCR, than those fed with the pelleted diets at the same dietary lipid level (P < 0.05). These results suggested that tilapia fed with the extruded diets had a better growth and higher nutrient utilization than fish fed with the pelleted diets, when dietary lipid level ranged from 40 to 80 g kg^?1 and at dietary crude protein level was 280 g kg^?1. The optimum dietary lipid level was 60 g kg^?1 in both the pelleted and extruded diets, and extrusion did not affect dietary lipid requirement of the tilapia.     

Dietary pantothenic acid requirement of fingerling Channa punctatus (Bloch) based on growth,feed conversion,liver pantothenic acid concentration and carcass composition

A 16‐week feeding trial was conducted to determine the dietary pantothenic acid requirement of fingerling Channa punctatus. Six casein–gelatin‐based diets (450 g/kg CP; 18.39 kJ/g GE) with graded levels of pantothenic acid (0, 10, 20, 30, 40 and 50 mg/kg diet) were fed to triplicate groups of fish (6.2 ± 0.71 cm; 4.26 ± 0.37 g) near to apparent satiation. The growth evaluation in terms of absolute weight gain (AWG), feed conversion ratio (FCR) and protein retention efficiency (PRE) indicated the best performance (p < .05) in fish fed diet containing 30 mg/kg pantothenic acid. Highest haemoglobin, haematocrit and RBCs counts were also obtained in fish fed diet with 30 mg/kg pantothenic acid. Mean cell haemoglobin and mean cell volume were found to be lowest in fish fed pantothenic acid‐free diet indicating the anaemia in this group of fish. Superoxidase dismutase and catalase activities of liver tissue were found to improve (p < .05) with the increasing levels of dietary pantothenic acid from 0 to 30 mg/kg. However, liver pantothenic acid concentration responded positively with the increasing levels of pantothenic acid up to 40 mg/kg diet and then stagnation in liver pantothenic acid concentration with the further inclusion of pantothenic acid was recorded. Second‐degree polynomial regression analysis of AWG, FCR and PRE exhibited the pantothenic acid requirement at 36.4, 32.8 and 34.7 mg/kg diet, respectively. Data generated during this study would be useful in formulating pantothenic acid‐balanced commercial feeds for the intensive culture of this fish.     

Growth,Feed Conversion,and Nutrient Retention Efficiency of African Catfish,Clarias gariepinus, (Burchell) Fingerling Fed Diets with Varying Levels of Protein

Growth, feed conversion, and nutrient retention efficiencies of African catfish fingerling, Clarias gariepinus (5.22 ± .07 cm; 8.22 ± 0.03 g), fed diets with varying levels of protein were assessed by feeding seven casein/gelatin based isocaloric (17.62 kJ/g GE) experimental diets with graded levels of dietary protein (20%, 25%, 30%, 35%, 40%, 45%, and 50% of the diet) to triplicate groups of fish to apparent satiation for eight weeks. Effects of feeding these diets on live weight gain (LWG%), feed conversion ratio (FCR), protein efficiency ratio (PER), protein retention efficiency (PRE%), and energy retention efficiency (ERE%) were assessed. Maximum LWG% (867%), PER (2.01), highest PRE (32%), ERE (69%), best FCR (1.39), and maximum body protein were recorded in fish fed diet containing 35% protein. On the basis of the second-degree polynomial regression analysis of the above response variables, it is recommended that the inclusion of protein in the range of 34.4%–39.6% is optimum for maximizing growth potential, feed conversion, and nutrient retention in African catfish fingerling, Clarias gariepinus.     

Replacement of fishmeal by soy protein concentrate with taurine supplementation in diets for golden pompano (Trachinotus ovatus)

Two 7‐week feeding trials were conducted to evaluate the capacity of golden pompano (Trachinotus ovatus) to use soy protein concentrate (SPC) as a dietary fish meal substitute. In trial I, fish were fed with a control diet (C) containing 400 g kg^?1 fish meal and other four diets in which the fish meal in diet C was replaced by SPC at 20 (R20), 40 (R40), 60 (R60) and 80% (R80). In trial II, a 3 × 2 design was used, and 40 and 80% of the fish meal in diet C were replaced by SPC, with or without 5 g kg^?1 taurine supplementation (six diets, C + T, R40 + T, R80 + T, C, R40 and R80, were formulated). In trial I, no significant difference was found in the feed intake between feeding treatments. The weight gain and nitrogen retention efficiency (NRE) decreased, whereas the feed conversion ratio (FCR) and phosphorus retention efficiency (PRE) increased, with decreasing dietary levels of fish meal. No significant differences were found in the weight gain, FCR and NRE between fish fed diets C and R20, whereas fish fed diets C and R20 had higher weight gain than those fed diets R40, R60 and R80. In trial II, no significant differences were found in the feed intake, weight gain, FCR, NRE and PRE between fish fed diets C + T and C. No significant differences were found in the feed intake, weight gain and NRE between fish fed diets R40 and R40 + T or between fish fed diets R80 and R80 + T. At the end of trial II, no significant differences were found in the condition factor, hepatosomatic index and body composition between fish fed diets C and C + T, or between fish diets R40 and R40 + T, or between fish fed diets R80 and R80 + T, except that fish fed diet R40 had lower body protein content than that of fish fed diet R40 + T. The present study reveals that taurine supplementation can elevate fish meal replacement level by SPC in the golden pompano diets. Fish meal can be reduced from 400 to 320 g kg^?1, if fish meal is substituted by SPC without taurine supplementation, and can be further reduced to 240 g kg^?1, if fish meal is substituted by SPC with 5 g kg^?1 taurine supplementation.     

Dietary folic acid requirement of fingerling Catla,Catla catla (Hamilton)

The dietary folic acid requirement of fingerling Catla catla (3.4 ± 0.17 g; 7.6 ± 0.41 cm) was evaluated by feeding casein–gelatin‐based isonitrogenous (350 g/kg crude protein) and isocaloric (16.72 kJ/g GE) diets containing different concentrations of folic acid (0, 0.2, 0.4, 0.6, 0.8, 1.0, 2.0 mg/kg) to triplicate groups to apparent satiation at 08:00, 12:30 and 17:30 hr for 16 weeks. Absolute weight gain (AWG; 40.07 g/fish), specific growth rate (SGR; 2.25%), feed conversion ratio (FCR; 1.53), protein retention efficiency (PRE; 31.42%) and protein gain (PG; 6.74) improved significantly (p < .05) with increasing folic acid levels up to 0.4 mg/kg diet and then reached a plateau. However, maximum liver folic acid concentration increased up to 0.6 mg/kg diet. Dietary folic acid levels also significantly affected (p < .05) body composition of fish. No significant change (p > .05) in haematological parameters except in fish fed folic acid‐free diet was noted. Antioxidant and immune parameters increased with increasing concentration of dietary folic acid up to 0.4 mg/kg diet. Broken‐line regression analysis of AWG, FCR, PRE, PG, HCT and liver folic acid concentrations of fingerling C. catla against dietary folic acid levels indicated optimum growth, FCR, PRE, PG, HCT and liver folic acid saturation ranging between 0.22 and 0.56 mg/kg diet, respectively.