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).     

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.     

Response of fingerling stinging catfish,Heteropneustes fossilis (Bloch) to varying levels of dietary l‐leucine in relation to growth,feed conversion,protein utilization,leucine retention and blood parameters

Growth response of fingerling Heteropneustes fossilis (6.8 ± 0.2 g; 11.2 ± 0.3 cm) to dietary l ‐leucine levels was assessed by conducting 8‐week feeding trial in a flow‐through system (1–1.5 L min^?1) at 28 °C water temperature. Casein–gelatin‐based isonitrogenous (380 g kg^?1; crude protein) and isoenergetic [17.9 MJ kg^?1; gross energy (GE)] basal diet was supplemented with different levels of l ‐leucine to achieve desired leucine levels ranging between 10 and 22.5 g kg^?1 dry diet. Analysed values were 9.9 (Lc_9.9), 12.4 (Lc_12.4), 15.1 (Lc_15.1), 17.4 (Lc_17.4), 20.1 (Lc_20.1) and 22.4 (Lc_22.4) g leucine kg^?1 diet. Fishes were stocked randomly in quadruplicates and fed to satiation at 07:00 and 17:30 h. Maximum absolute weight gain (AWG g fish^?1), feed conversion ratio (FCR), protein utilization efficiency (PUE%), leucine retention efficiency (LRE%) and haematological parameters were found in fish fed diet Lc_17.4. For precise determination of dietary leucine requirement of Singhi, AWG g fish^?1, FCR, PUE% and LRE% were subjected to broken‐line and second‐degree polynomial regression analysis. Second‐degree polynomial regression analysis fitted the data more accurately (P > 0.05) exhibiting high R² values. Hence, based on this analysis, dietary leucine requirement of fingerling H. fossilis is recommended to be 16.5 g kg^?1 of the diet, corresponding to 43.4 g kg^?1 protein for developing leucine‐balanced commercial feeds.     

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.     

The effect of dietary methionine on growth,antioxidant capacity,innate immune response and disease resistance of juvenile yellow catfish (Pelteobagrus fulvidraco)

An 11‐week feeding trial was conducted to evaluate the effect of dietary methionine on the growth, antioxidant status, innate immune response and disease resistance to Aeromonas hydrophila of juvenile yellow catfish. Six isonitrogenous and isolipidic practical diets were formulated to contain different graded methionine levels ranging from 6.1 to 16.4 g kg^?1 of dry weight. The results indicated that growth performance and feed utilization were significantly influenced by the dietary methionine levels; fish fed the diet containing 6.1 g kg^?1 methionine level had lower specific growth rate, percentage weight gain (PWG), feed efficiency and protein efficiency ratio than those fed the other diets (P < 0.05). Fish fed the diet containing 16.4 g kg^?1 methionine level had lowest protein contents in whole body and muscle among all treatments. Triacylglycerols, cholesterol, aspartate aminotransferase, alanine aminotransferase and haemoglobin (Hb) in plasma or whole blood were significantly affected by dietary methionine levels. Fish fed the diet containing 6.1 g kg^?1 methionine level had higher superoxide dismutase, glutathione peroxidase activities and malondialdehyde values than those fed other diets. Fish fed diets containing 9.7 and 11.8 g kg^?1 methionine levels had higher lysozyme activity, total immune globulin, phagocytic activity and respiratory burst than those fed other diets. The lowest survival after A. hydrophila challenge was observed in fish fed a diet containing 6.1 g kg^?1 methionine. Quadratic regression analysis of PWG against dietary methionine levels indicated that the optimal dietary methionine requirement for the maximum growth of juvenile yellow catfish was estimated to be 11.5 g kg^?1 of the diet in the presence of 4.0 g kg^?1 cystine (corresponding to 23.5 g kg^?1 of dietary protein on a dry weight basis).     

Dietary threonine requirement to optimize protein retention and fillet production of fast‐growing Nile tilapia

Threonine is the third‐limiting essential amino acid in diets based on cereal ingredients. A 4‐week trial was conducted to determine the threonine requirement of large Nile tilapia based on fish growth, feed efficiency, body composition, protein and amino acid retention. Six hundred fish (563.3 ± 15.1 g) were distributed into twenty 1.2‐m³ cages. Five diets containing 288 g kg^?1 of crude protein, 12.7 MJ kg^?1 of digestible energy and 8.9, 10.5, 12.2, 13.7 and 15.4 g kg^?1 of threonine were elaborated. Fish were hand‐fed five times a day to extruded diets. Significantly, differences in growth performance and amino acids retention among the treatments were observed. Fish fed 10.5 g kg^?1 of threonine showed higher daily weight gain, gutted weight and fillet weight (P < 0.05) compared to fish fed with other experimental diets. Diets containing 8.9–15.4 g kg^?1 of threonine did not affect whole body and muscle proximate composition. Based on second‐order regression analysis, the dietary threonine requirement estimated based on final gain, fillet weight and fillet yield was 12, 12.1 and 11.5 g kg^?1 diet, respectively. The dietary threonine requirement for maximum fillet yield of Nile tilapia was estimated to be 11.5 g kg^?1.     

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 leucine requirement of Juvenile Nile tilapia,Oreochromis niloticus

An 8‐week feeding trial was conducted to evaluate the effects of dietary leucine on growth performance, feed utilization, body composition and non‐specific immune responses of juvenile Nile tilapia. Five isonitrogenous and isoenergetic diets were formulated to contain graded levels of L‐leucine (5.3, 8.1, 10.9, 13.2, 15.6 and 18.1 g kg^?1 diet, respectively) from dietary ingredients and crystalline L‐leucine. Each diet was randomly assigned to triplicate groups of 20 juvenile fish (1.94 ± 0.01 g) three times daily to apparent satiation. Results showed that the weight gain (WG) and specific growth rate (SGR) increased as dietary leucine concentrations increased from 5.3 to 13.2 g kg^?1 and then decreased slightly with further increase in dietary leucine concentrations. Quadratic regression analysis (y = ?522.6x² + 1304.x + 132.6, R² = 0.684) on weight gain against dietary leucine levels indicated that the optimal dietary leucine requirement was estimated to be 12.5 g kg^?1 diet (corresponding to 43.1 g kg^?1 of dietary protein). Leucine supplementation had no impact on the survival and body composition of tilapia. Serum lysozyme activity of fish fed diet containing 13.2 g kg^?1 leucine significantly increased compared to fish fed diet containing 5.3 g kg^?1. Serum superoxide dismutase activity and immunoglobulin M (IgM) concentration were not significantly affected by dietary leucine supplementation.     

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.     

Utilization of gelatinized carbohydrate in diets of Labeo rohita fry

A total of 180 Labeo rohita fry (≈1 g) were distributed into six treatment groups with three replicates each. Six isoenergetic (15.8 kJ g^?1) diets were prepared with varying levels of protein (CP) and gelatinized carbohydrate (GC), viz. D₁: 450 g kg^?1 CP, 258 g kg^?1 GC; D₂: 400 g kg^?1 CP, 302 g kg^?1 GC; D₃: 350 g kg^?1 CP, 399 g kg^?1 GC; D₄: 301 g kg^?1 CP, 447 g kg^?1 GC; D₅: 249 g kg^?1 CP, 517 g kg^?1 GC and control diet, D₆: 400 g kg^?1 CP, 468 g kg^?1 GC and these were fed to fish at 40 g kg^?1 wet body weight per day for 60 days. Highest growth was recorded for fish fed D₄, decreasing for D₅. Protein utilization, amylase activity and carbohydrate digestibility were significantly positively correlated with GC (P < 0.05) and were highest in fish fed D₅. Hypertrophy of hepatic cells was only recorded for D₅. Lysine, which may be affected during gelatinization, was estimated in diets and found to be above the minimum level required. Survival rate was unaffected by diet. The results of the present study indicate that a diet containing 450 g kg^?1 GC and 300 g kg^?1 CP was efficiently utilized by L. rohita fry.     

Protein‐to‐energy ratio of 21.43 g MJ−1 improves growth performance of Nile tilapia at the final rearing stage under commercially intensive rearing conditions

This study evaluated the effect of ratio of dietary digestible protein (DP) to digestible energy (DE) on growth performance, fillet chemical composition and haematological profile of Nile tilapia subjected to transport‐induced stress at the final rearing stage (450 to 800 g) under commercial conditions. The trial was conducted using a 5 × 2 factorial layout (DP: 200, 230, 260, 290 and 320 g kg^?1) and (DE: 12.6 and 13.8 MJ kg^?1). Energy levels did not influence any analysed parameters in this research. Final weight and biomass gain were increased up to the ratio of 269 and 270 g PD kg^?1, respectively, and feed conversion ratio was reduced down to a 275 g DP kg^?1. Protein efficiency ratio linearly decreased from 200 g DP kg^?1 diet to 320 g DP kg^?1. There was no statistical difference in fillet chemical composition. Red blood cell count (RBC), haemoglobin (Hb), mean corpuscular volume (MCV) and mean corpuscular haemoglobin concentration (MCHC) were different before and after transport‐induced stress. Leucocyte differentiation after transport‐induced stress revealed lymphocytopenia and neutrophilia. We conclude that for tilapia weighing 450–800 g reared under commercially intensive conditions, a diet with 270 g DP kg^?1 and 12.6 MJ DE kg^?1 (21.43 g DP MJ^?1 DE) can improve the growth performance and ensure the fish health.     

Dietary methionine requirement of Indian major carp fry,Cirrhinus mrigala (Hamilton) based on growth,feed conversion and nitrogen retention efficiency

This study was aimed at quantifying methionine requirement of Indian major carp fry, Cirrhinus mrigala (2.2 ± 0.2 cm; 0.19 ± 0.02 g) by conducting a 12‐week feeding trial. Casein–gelatine‐based isonitrogenous (40 g 100 g^?1 crude protein) and isoenergetic (15.42 kJ g^?1 DE) amino acid test diets were prepared to contain six levels of l ‐methionine (1.1, 1.3, 1.5, 1.7, 1.9 and 2.1 g 100 g^?1 dry diet) at a fixed level of cysteine (0.85 g 100 g^?1 dry diet) and fed to apparent satiation thrice daily to triplicate groups of fish. When absolute weight gain (g per fish), feed conversion ratio, protein deposition (g per fish) and nitrogen retention efficiency data were subjected to broken‐line and second‐degree polynomial regression analysis, 95% of the plateau of above parameters was achieved at dietary methionine concentrations between 1.60 and 1.69 g 100 g^?1 dry diet or 0.10 to 0.11 g methionine kJ^?1 DE, corresponding to 4.1–4.22 g 100 g^?1 protein or 0.44–0.47 g methionine kJ^?1 DE. Based on these results, dietary methionine requirement of fry C. mrigala is recommended 1.60–1.69 g 100 g^?1 diet or 0.10–0.11 g methionine kJ^?1 DE.     

Growth,feed utilization and body composition of juvenile Manchurian trout,Brachymystax lenok (Pallas) fed different dietary protein and lipid levels

A 10‐week feeding trial with four dietary protein levels (400, 450, 500 and 550 g kg^?1 crude protein) and two dietary lipid levels (80 and 160 g kg^?1 crude lipid) was conducted to assess optimum dietary protein and lipid levels for the growth, feed utilization and body composition of juvenile Manchurian trout (initial weight 11.80 ± 0.15 g). Fish were fed twice daily (08:30 and 16:30 h) to apparent satiation. The results showed that fish fed the diet with 500 g kg^?1 protein and 80 g kg^?1 lipid had the highest growth and feed efficiency. However, fish fed the diet with 450 g kg^?1 protein and 160 g kg^?1 lipid showed comparable growth to that of the fish fed diet 5 (500/80) and had higher protein efficiency ratio (PER), nitrogen retention (NR) and energy retention (ER) than other groups (P < 0.05). Growth, PER, NR and ER of fish fed the 160 g kg^?1 lipid diet was significantly higher (P < 0.05) than that of fish fed the 80 g kg^?1 lipid diet at 400 and 450 g kg^?1 protein diet, whereas these values showed an opposite trend at 500 and 550 g kg^?1 protein diet, and the lowest PER, NR and ER was found by fish fed the 400 g kg^?1 protein diet with 80 g kg^?1 lipid. Fish fed diets with 400 g kg^?1 protein had lower feed intake (FI) than that of other groups. Feed intake of fish fed 80 g kg^?1 lipid level was significantly lower than that of fish fed 160 g kg^?1 lipid diet at 400 g kg^?1 protein (P < 0.05), while no significant differences were observed at 450, 500 and 550 g kg^?1 protein‐based diets. Contrary to moisture content, lipid content of whole body and muscle increased significantly (P < 0.05) with increasing lipid levels. The results of this study indicated that the diet containing 450 g kg^?1 protein and 160 g kg^?1 lipid, with a P/E ratio of 23.68 g protein MJ^?1 would be suitable for better growth and feed utilization of juvenile Manchurian trout under the experimental conditions and design level used in this study.     

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

A 12‐week feeding trial was conducted in eighteen 70 L indoor polyvinyl circular troughs provided with a water flow‐through system (1–1.5 L min^?1) at 28 ± 1 °C to evaluate the dietary tryptophan requirement of fingerling Catla catla (3.45 ± 0.24 cm; 0.60 ± 0.13 g). Six casein‐gelatin‐based amino acid test diets (330 g kg^?1 crude protein; 13.6 kJ g^?1 digestible energy) containing graded levels of L‐tryptophan (1.0, 1.4, 1.9, 2.3, 2.8, 3.4 g kg^?1 dry diet) were fed to triplicate groups of fish near to satiation at 08:00, 12:30 and 17:30 h. Absolute weight gain, feed conversion ratio, protein gain, RNA/DNA ratio, hepatosomatic index, viscerosomatic index, condition factor and haematological indices improved with the increasing levels of tryptophan from 1.0 to 2.3 g kg^?1 of dry diet. Significantly higher carcass protein was obtained at 2.3 g tryptophan per kilogram of the dry diet. Exponential analysis of absolute weight gain, feed conversion ratio, protein gain and RNA/DNA ratio against dietary tryptophan levels at 95% maximum and minimum responses displayed the tryptophan requirement at 2.5, 2.3, 2.5 and 2.1 g kg^?1 dry diet, respectively. Inclusion of dietary tryptophan in the range of 2.1–2.5 g kg^?1 dry diet, equivalent to 6.4–7.6 g kg^?1 dietary protein, is recommended in formulating tryptophan‐balanced feed for the culture of this fish species.     

Optimal dietary methionine requirement of juvenile Chinese sucker,Myxocyprinus asiaticus

A total of 630 juvenile Chinese sucker, with an average initial weight of 1.72 ± 0.05 g, were fed seven diets for 56 days to study the effect of dietary methionine levels on growth, feed utilization, body composition and haematological parameters on juvenile Chinese sucker. Diet 1 using fish meal as the sole protein source and diets 2–7 using fish meal and fermented soybean meal as intact protein sources supplemented with crystalline amino acids contained six levels of l ‐methionine ranging from 6.4 to 18.9 g kg^?1 of dry diet at a constant dietary cystine level of 3.7 g kg^?1. Each diet was randomly assigned to three aquaria. Results indicated that the highest weight gain, specific growth rate (SGR), feed efficiency ratio, protein efficiency ratio and protein productive value occurred at 13.9 g methionine kg^?1 diet among the methionine supplemented dietary groups, beyond which they showed declining tendency. The whole body and muscle protein contents of juvenile Chinese sucker were positively correlated with dietary methionine level, while muscle lipid content was negatively correlated with it. The total essential amino acids content of muscle was increased significantly with increasing dietary methionine level from 6.4 to 13.9 g kg^?1 (P < 0.05). Apparent digestibility coefficients of dietary protein were significantly affected by dietary treatments. Serum protein, cholesterol and triacylglycerol increased with increasing dietary methionine levels, but showed a relatively lower value for fish fed the 18.9 g methionine kg^?1 diet. Quadratic regression analysis of SGR against dietary methionine level indicated that optimal dietary methionine requirement for juvenile Chinese sucker was 14.1 g kg^?1 of the diet in the presence of 3.7 g kg^?1 cystine (corresponding to 32.0 g kg^?1 of dietary protein on a dry‐weight basis).     

Dietary protein requirement of zebra sea bream (Diplodus cervinus,Lowe 1838) juveniles

A 14 weeks growth trial was performed to estimate the protein requirement for growth and maintenance of zebra sea bream (Diplodus cervinus) juveniles. For that purpose, nine isolipidic diets were formulated to contain increasing protein levels (from 50 to 550 g kg^?1) at the expense of carbohydrate. Each diet was assigned to duplicate groups of 20 fish, with an average body weight of 7.7 g. Feed efficiency improved with dietary protein up to 400 g kg^?1, no further differences being noticed at higher protein levels. Fish fed the 50 g kg^?1 protein diet lost weight during the trial. In the other groups, weight gain improved as dietary protein increased up to 350–400 g kg^?1. Fish fed diets with 250 g kg^?1 protein or lower had lower whole‐body protein content than the other groups. A curvilinear‐plateau model was used to adjust weight gain and protein gain (g kg ABW^?1 day^?1) to dietary protein levels. Based on that model, the optimum dietary protein requirement for maximum weight gain was estimated to be 437.6 g kg^?1 and for maximum protein gain 461.9 g kg^?1, corresponding to a protein intake of 7.63 g kg ABW^?1 day^?1. Protein requirement for maintenance was estimated to be 1.01 g kg ABW^?1 day^?1.     

Evaluation of dietary inclusion of housefly maggot (Musca domestica) meal on growth,fillet composition and physiological responses for barramundi,Lates calcarifer

The study was to evaluate the effects of dietary fish meal (FM) partially replaced by housefly maggot meal (HMM) on growth, fillet composition and physiological responses of juvenile barramundi, Lates calcarifera. HMM at 100, 150, 200 and 300 g kg^?1 was supplemented in the basal diet to replace dietary FM protein. Basal diet without HMM supplementation was used as control. Total of five experimental diets were fed to triplicate groups of juvenile barramundi (initial weight: 9.66 ± 0.22 g) in a flow‐through rearing system for 8 weeks. Fish fed all experimental diets showed no effects (P > 0.05) on weight gain and whole body protein, lipid and moisture content. Fish fed control diet and 100 g kg^?1 HMM diet had the highest (P < 0.05) hepatic superoxide dismutase (SOD) activity, followed by 150 g kg^?1 HMM group, the lowest in 200 and 200 g kg^?1 HMM groups. Hepatic thiobarbituric acid reactive substance (TBARS) value was the highest in fish fed 150–300 g kg^?1 HMM diets, followed by 100 g kg^?1 HMM group and the lowest in fish fed the control diet. Fish fed the 300 g kg^?1 HMM diet had lower plasma lysozyme activity than fish fed other diets. The results indicated that up to 300 g kg^?1 HMM can be used to substitute dietary FM protein without negative effect on growth. Although physiological responses were also considered, up to 100 g kg^?1 HMM in barramundi diet was recommended.     

Total aromatic amino acid requirement of juvenile grass carp (Ctenopharyngodon idella)

This experiment was conducted to investigate total aromatic amino acid requirement of juvenile grass carp Ctenopharyngodon idella. Six isonitrogenous and isoenergetic semipurified diets containing casein and gelatin with graded level of phenylalanine (7.8, 11.1, 14.4, 17.6, 21.7, 24.9 g kg^?1 DM) were formulated. Each diet was randomly assigned to triplicate group of 30 fish (3.58 ± 0.002 g, mean ± SEM) each tank for 8 weeks. The highest weight gain (WG, %), final body weight (g) and specific growth rate were recorded when phenylalanine level was 17.6 g kg^?1 of the diet. Fish muscle protein content, protein efficiency ratio (PER), feed conversion ratio and alanine aminotransferase were significantly affected by dietary phenylalanine level. The polynomial regression calculated using WG and PER indicated that the optimal dietary total aromatic amino acid (phenylalanine + tyrosine) requirement for juvenile grass carp was 24.4 g kg^?1 of the diet, corresponding to 65.9 g kg^?1 of dietary protein.     

Effect of different feeds on the growth,survival and reproductive performance of zebrafish,Danio rerio (Hamilton, 1822)

Present experiment was conducted to determine the effect of different feeds with varying protein levels on the growth, survival and reproductive performance of zebrafish, Danio rerio. The control diet (T1) was wild‐collected zooplankton from local fish ponds, while test diets with 350 g kg^?1 protein (T2), 400 g kg^?1 protein (T3) and 450 g kg^?1 protein (T4) were formulated and fed to fish for a period of 210 days. The significantly (P < 0.05) highest mean weight gain and specific growth rate were observed in T1, which were similar with T3 and T4. The significantly (P < 0.05) highest number of egg production per female and relative fecundity were found in T1, followed by T4 and T3 while T2 produced lowest number of eggs. No significant (P > 0.05) differences were observed in brood survival rate, fertilization and hatching rate among the dietary treatments. The highest (P < 0.05) fry survival rate was recorded in T1, followed by T3 and T4. Thus, it is suggested that control diet i.e. mixed zooplankton exhibited better growth, reproductive performance and fry survival rate. However, diet containing 400 g kg^?1 crude protein also gave comparable results in terms of growth, survival and reproductive performance of zebrafish.     

A comparison of the effect of dietary fungal phytase and dicalcium phosphate supplementation on growth performances,feed and phosphorus utilization of tra catfish juveniles (Pangasianodon hypophthalmus Sauvage, 1878)

Six isonitrogenous (320 g kg^?1) and isolipidic (60 g kg^?1) diets were formulated with graded levels (0, 5, 10 and 15 g kg^?1) of dicalcium phosphate (DCP) and fungal phytase (750 and 1500 FTU kg^?1 diet). Tra catfish (Pangasianodon hypophthalmus), 9.6 g, were fed the diets for 12 weeks. Each experimental diet was fed to eight replicates of fish to apparent satiation. At the end of the trial, fish fed the diets containing 15 g kg^?1 DCP, 750 and 1500 FTU kg^?1 phytase had higher growth performances, protein efficiency ratio and phosphorus retention than those fed the control diet, 5 g kg^?1 DCP and 10 g kg^?1 DCP diets (P < 0.05). Whole body ash and phosphorus concentration of fish fed the 10 g kg^?1 DCP and 15 g kg^?1 DCP diets were significantly higher than those of fish fed the control diet. Higher apparent digestibility coefficient of phosphorus was observed in fish fed the phytase supplemented diets. The present results indicate that supplementation of phytase at 750 FTU kg^?1 and 1500 FTU kg^?1 improves growth performances, feed and phosphorus utilization. The supplementation can completely replace dicalcium phosphate or other phosphorus sources in tra catfish feed and reduce the phosphorus discharge into environment.