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 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 threonine requirement of fingerling Indian major carp,Catla catla (Hamilton) estimated by growth,protein retention efficiency,threonine deposition,haematological parameters and carcass composition

A 12‐week feeding trial was conducted to determine the dietary threonine requirement of fingerling Indian major carp, Catla catla (3.35 ± 0.11 cm; 0.59 ± 0.06 g). Six casein‐gelatin based (33% crude protein; 3.23 kcal g^?1 digestible energy) amino acid test diets with graded levels of analysed threonine (0.74%, 0.96%, 1.21%, 1.48%, 1.72% and 1.93% dry diet) were fed to satiation to triplicate groups of fish. Absolute weight gain (g per fish), feed conversion ratio, protein retention efficiency, threonine deposition, RNA/DNA ratio and carcass protein significantly improved with the increase in dietary threonine and peaked at 1.48% of the dry diet. Haematological indices were also found to be best in fish fed at 1.48% threonine diet. Quadratic regression analysis of absolute weight gain, feed conversion ratio, protein retention efficiency, threonine deposition, RNA/DNA ratio, carcass protein, haemoglobin (g dL^?1), haematocrit (%) and RBCs (10⁶ × mm^?3) at 95% of maximum and minimum response exhibited the threonine requirement of fingerling C. catla between 1.35% and 1.48% dry diet, corresponding to 4.09–4.48% dietary protein. Present finding would be useful in formulating threonine‐balanced feeds for the intensive culture of C. catla.     

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 amino acid l‐methionine requirement of fingerling Indian catfish,Heteropneustes fossilis (Bloch‐1974) estimated by growth and haemato‐biochemical parameters

An 8 weeks feeding trial was conducted to determine the dietary methionine requirement of fingerling Indian catfish, Heteropneustes fossilis (6.08 ± 0.95 cm; 4.33 ± 0.52 g). Six isonitrogenous (40%) and isoenergetic (17.90 kJ g^?1 GE) amino acid test diets were formulated with gradation of 0.25 g 100 g^?1containing graded levels of _L‐methionine (0.30, 0.55, 0.80, 1.05, 1.30 and 1.55 g 100 g^?1, dry diet) with 0.40 g 100 g^?1 constant level of cystine. Twenty fish were stocked in triplicate groups, in 75‐L circular trough with continuous flow‐through system and fed experimental diets at 4% BW/day twice daily, at 08:00 and 18:00 hours. Maximum live weight gain (296%), best feed conversion ratio (1.56) and protein efficiency ratio (1.60) were occurred at 1.05 g 100 g^?1 methionine, beyond which they showed declining tendency. However, quadratic regression analysis of weight gain, feed conversion ratio (FCR), protein efficiency ratio (PER) and body protein deposition (BPD) data indicated requirement for methionine at 1.15, 1.08, 1.06 and 1.05 g 100 g^?1 of dry diet respectively. Significantly (P < 0.05), higher whole body protein content, minimum moisture and intermediate fat contents were recorded at 1.05 g 100 g^?1 dietary methionine level. Ash content remained insignificantly (P > 0.05) low among all the treatments, excepting at diet I and diet II. Body protein deposition was also found to be significantly (P < 0.05) higher at 1.05 g 100 g^?1 methionine level. Best somatic and haematological indices values were also obtained at the requirement level. Based on above results, it is recommended that the diet for young H. fossilis should contain methionine at 1.09 g 100 g^?1 dry diet, corresponding to 2.73 g 100 g^?1 dietary protein with 0.40 g 100 g¹ cystine concentration for optimum growth and efficient feed utilization. Thus, the total sulphur amino acid requirement of H. fossilis would be (1.09 + 0.40) 1.49 g 100 g^?1 of dry diet, corresponding to 3.73 g 100 g^?1 of dietary protein.     

Dietary l‐lysine requirement of fingerling stinging catfish,Heteropneustes fossilis (Bloch) for optimizing growth,feed conversion,protein and lysine deposition

Dietary lysine requirement of fingerling Heteropneustes fossilis (6.96 ± 0.05 g) was quantified by conducting 12‐week feeding trial in a flow‐through system at 28°C. Casein–gelatin based isonitrogenous (38% CP) and isocaloric (14.7 kJ g^?1 DE) amino acid test diets with six levels of dietary lysine (1.5%, 1.75%, 2.0%, 2.25%, 2.5%, 3.0% dry diet) were fed to apparent satiation in triplicates. Broken‐line and second‐degree polynomial regression analyses at 95% plateau of absolute weight gain (AWG; g fish^?1), feed conversion ratio (FCR), protein deposition (PD; g fish^?1) and lysine deposition (LD; g fish^?1) exhibited lysine requirement between 2.0% to 2.3% of the dry diet, corresponding to 5.3–6.1% protein.     

Dietary threonine requirement of fingerling Indian major carp,Labeo rohita (Hamilton)

An 8‐week feeding experiment was conducted in a water flow‐through system (26–28 °C) to determine the dietary threonine requirement of fingerling Labeo rohita (3.90±0.03 cm; 0.58±0.02 g). Growth, feed utilization and body composition of fish fed test diets (40% crude protein; 17.9 kJ g^?1 gross energy) with graded levels of l ‐threonine (0.75%, 1.0%, 1.25%, 1.50%, 1.75% and 2.0% dry diet) to apparent satiation were response variables used to assess threonine adequacy. Diets were made isonitrogenous and isoenergetic by adjusting the levels of glycine and dextrin. The amino acid profiles of the test diets were formulated to that of 40% whole chicken egg protein except for threonine. The performance of fish fed experimental diets was evaluated using calculated values for weight gain (g fish^?1), feed conversion ratio (FCR), protein efficiency ratio (PER) and protein productive value (PPV) data. Maximum weight gain (g fish^?1) (1.79), lowest FCR (1.39), highest PER (1.76) and PPV (0.33) were recorded at 1.50 g per 100 g dietary threonine. Statistical analysis of weight gain, FCR, PER and PPV data reflected significant differences (P<0.05) among treatments. Except for reduced growth performance in fish fed threonine‐deficient diets, no deficiency signs were noted. Weight gain, FCR, PER and PPV data were also analysed using second‐degree polynomial regression analysis to obtain a more accurate threonine requirement estimate, which was found, using each response variable, to be at 1.70, 1.63, 1.65 and 1.51 g per 100 g of dry diet, corresponding to 4.2, 4.07, 4.12 and 3.77 g per 100 g of dietary protein respectively. Based on the second‐degree polynomial regression analysis of the live weight gain, FCR, PER and PPV data, the optimum dietary level of threonine for fingerling L. rohita was found to be in the range of 1.51–1.70 g per 100 g of the dry diet, corresponding to 3.77–4.2 g per 100 g of dietary protein.     

A study on dietary l‐lysine requirement of juvenile yellow catfish Pelteobagrus fulvidraco

An 8‐week feeding trial was conducted to determine lysine requirement of juvenile yellow catfish (Pelteobagrus fulvidraco) by feeding formulated diets containing crystalline l ‐lysine. Six isonitrogenous and isoenergetic diets (405 g kg^?1 protein, 18 kJ g^?1 gloss energy) containing fish meal together with soybean protein concentrate as protein sources and fish oil together with soybean oil as lipid sources were formulated. Crystalline l ‐lysine was added into the six diets to acquire lysine concentrations of 17.3, 21.8, 26.0, 31.3, 35.5 and 41.9 g kg^?1 dry diets, respectively. Mixture of crystalline amino acid was supplemented to simulate the amino acid profile in muscle of yellow catfish. The results indicated that final body weight (FBW), weight gain (WG), specific growth rate (SGR), feed efficiency (FE) and protein efficiency (PE) increased with the increase in dietary lysine level from 17.3 to 31.3 g kg^?1 of diet and then decreased as the dietary lysine levels further increased. No significant difference in survival rate was found among all the dietary treatments. One‐slope, quadratic broken‐line analysis on the basis of SGR showed that the dietary l ‐lysine requirement of juvenile yellow catfish was 33.1 g kg^?1 of dry diet (83.2 g kg^?1 of dietary protein).     

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

Indian major carp fingerling, Cirrhinus mrigala (3.85±0.75 cm, 0.52±0.21 g), were fed isonitrogenous and isocaloric diets (40% crude protein, 4.28 kcal g^?1, gross energy) containing casein, gelatin and crystalline amino acids with graded levels of l ‐threonine (1.00, 1.25, 1.50, 1.75, 2.00 and 2.25 g 100 g^?1, dry diet) to determine the dietary threonine requirement. The feeding trial was conducted in triplicate for 8 weeks. Diets were fed twice a day at 08:00 and 16:00 hours at 5% body weight day^?1. The ration size and feeding schedule were worked out before the start of the feeding trial. Highest weight gain (304%) and best feed conversion ratio (1.43) were evident in fish fed diet containing 1.75% dietary threonine. Second‐degree polynomial regression analysis of weight gain, feed conversion ratio and protein efficiency ratio data indicated the dietary threonine requirement to be at 1.84%, 1.81% and 1.78%, respectively, corresponding to 4.60%, 4.52% and 4.45% of dietary protein. Minimum carcass moisture, fat and maximum carcass protein were evident in fish fed 1.75% threonine level. However, ash content did not affect body composition, except the 1.00% threonine level, which showed a significantly higher ash content value. Based on the above results, it is recommended that the diet for C. mrigala should contain threonine at 1.80 g 100 g^?1 dry diet, corresponding to 4.50 g 100 g^?1 dietary protein for optimum growth and efficient feed utilization.     

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.     

Dietary thiamin could improve growth performance,feed utilization and non‐specific immune response for juvenile Pacific white shrimp (Litopenaeus vannamei)

This study evaluated the effect of dietary thiamin on growth performance, feed utilization and non‐specific immune response for juvenile Pacific white shrimp, Litopenaeus vannamei. Six isonitrogenous and isolipidic practical diets were formulated with graded thiamin levels of 6.9, 32.7, 54.2, 78.1, 145.1 and 301.5 mg kg^?1 of dry diet, respectively. Each diet was randomly assigned to triplicate groups of 30 juvenile shrimp and provided four times each day to apparent satiation. Weight gain (WG) and specific growth rate (SGR) of the shrimp were significantly influenced by the dietary thiamin levels, the maximal WG and SGR occurred at 54.2 mg kg^?1 dietary thiamin level. However, with further increase in dietary thiamin level from 54.2 to 301.5 mg kg^?1, the WG and SGR significantly decreased. Shrimp fed the 54.2 mg kg^?1 thiamin diet exhibited higher feed efficiency, protein efficiency ratio and protein productive value than those fed the other diets. Dry matter and protein content in whole body were significantly affected by the dietary thiamin levels. Thiamin concentration in hepatopancreas significantly increased when the dietary thiamin level increased from 6.9 to 145.1 mg kg^?1. The total protein, glucose, triacylglycerol and cholesterol contents in hemolymph were not significantly affected by the dietary thiamin levels. Dietary thiamin had significantly influenced superoxide dismutase, catalase and lysozyme activities in hemolymph. Results of this study indicated that the optimal dietary thiamin requirements estimated using a two‐slope broken‐line model based on WG and thiamin concentration in hepatopancreas were 44.66 and 152.83 mg kg^?1, respectively.     

The effect of dietary methionine concentrations on growth performance of juvenile Nile tilapia (Oreochromis niloticus) fed diets with two different digestible energy levels

A growth trial was conducted to examine the effect of dietary digestible energy (DE) content on methionine (Met) utilization and requirement in juvenile Nile tilapia (Oreochromis niloticus). Ten iso‐nitrogenous (288 g kg^?1 protein) practical diets, with two DE levels (10.9 MJ kg^?1; 12.4 MJ kg^?1) and five methionine supplementation levels (0, 1, 2, 4 and 6 g kg^?1), were hand‐fed twice daily to triplicate groups of Nile tilapia (initial body weight 8.95 ± 0.06 g) for 8 weeks. Weight gain (WG) and specific growth rate (SGR) increased significantly with increasing dietary methionine concentration at the same DE content (P < 0.001). At the same dietary methionine level, WG and SGR of fish fed high‐DE diets were significantly higher than that of fish fed low‐DE diets (P = 0.0001), although no interaction was found between dietary DE and methionine supplementation. Based on quadratic regression analysis between dietary methionine concentration and weight gain, optimal methionine requirement for maximum growth, expressed as g Met required kg^?1 diet (low‐ versus high‐DE diets), increased as diet DE concentration increased (7.34 versus 9.90 g kg^?1 diet, respectively; with cysteine 4.70 g kg^?1 diet). The results indicated that diet DE content affects methionine utilization and requirement in juvenile Nile tilapia, fish fed high‐DE diets required more methionine for maximum growth.     

Dietary amino acid <Emphasis Type="SmallCaps">l</Emphasis>-threonine requirement of fingerling Indian catfish, <Emphasis Type="Italic">Heteropneustes fossilis</Emphasis> (Bloch) estimated by growth and biochemical parameters

An eight-week feeding experiment was conducted to quantify the dietary threonine requirement of young catfish, Heteropneustes fossilis (9.20 ± 0.85 cm, 3.60 ± 0.45 g) using isonitrogenous and isoenergetic diets [40% crude protein (CP); 4.28 kcal g/100 g, gross energy (GE)] containing casein, gelatin and l-crystalline amino acids. Six dietary treatments supplemented with graded levels of l-threonine (0.50, 0.75, 1.00, 1.25, 1.50 and 1.75 g per 100 g, dry diet), in gradations of 0.25 g per 100 g dry diet were formulated. Fish were randomly stocked, in triplicate groups, in 55-l indoor polyvinyl flow-through circular tanks and fed experimental diets at 4% of their body weight divided over two equal feedings at 08:00 and 16:00 hours. Feeding schedule and ration size were worked out prior to the start of the feeding trial. Live weight gain (263%), feed conversion ratio (FCR) (1.35) and protein efficiency ratio (PER) (1.85) were significantly higher (P < 0.05) in fish fed a diet containing 1.25% dietary threonine. However, second-degree polynomial regression analysis of live weight gain, FCR, PER and body protein deposition data indicated the dietary threonine requirement to be 1.37, 1.26, 1.23 and 1.24 g per 100 g of dry diet, respectively. Whole-body moisture decreased significantly (P < 0.05) with the increase of dietary concentration up to 1.25%. A significantly (P < 0.05) higher protein content was evident in fish fed a diet containing 1.25% threonine. Body fat increased significantly (P < 0.05) with the increase of dietary concentration and was found to be highest at a 1.75% threonine concentration. A significantly (P < 0.05) higher ash content was reported at the 0.50 and 0.75% threonine levels. Body protein deposition was also found to be significantly (P < 0.05) higher at the 1.25% threonine level, followed by the 1.50% threonine level. Based on these results, it is recommended that the diet for fingerling H. fossilis should contain threonine at a level of 1.27 g per 100 g of dry diet, corresponding to 3.17 g per 100 g of dietary protein for optimum growth and efficient feed utilization. No mortality was observed during the experiment.     

Effect of dietary vitamin C on the growth performance,antioxidant ability and innate immunity of juvenile yellow catfish (Pelteobagrus fulvidraco Richardson)

A 12‐week feeding trial was conducted to evaluate the effects of dietary vitamin C on growth performance, antioxidant status and innate immune responses in juvenile yellow catfish, Pelteobagrus fulvidraco. Six isonitrogenous and isolipidic diets (44% crude protein and 7% lipid) were formulated to contain six graded dietary vitamin C (ascorbate‐2‐poly‐ phosphate, ROVIMIX^® STAY‐C^® 35) levels ranging from 1.9 to 316.0 mg kg^?1 diet. The results of present study indicated that fish fed the lowest vitamin C diet had lower weight gain (WG) and specific growth rate (SGR) than those fed the diets supplemented vitamin C. WG and SGR did significantly increase with dietary vitamin C levels increasing from 1.9 to 156.5 mg kg^?1. However, no significant increase was observed with further dietary vitamin C levels increasing from 156.5 to 316 mg kg^?1. Survival, protein efficiency ratio and feed efficiency were not significantly affected by the dietary vitamin C levels. The activities of serum superoxide dismutase, catalase and glutathione peroxidase significantly increased when dietary vitamin C levels increased from 1.9 to 156.5 mg kg^?1, fish fed the lowest vitamin C diet had higher serum malondialdehyde content than those fed the diets supplemented with vitamin C. Fish fed the diet containing 156.5 mg kg^?1 vitamin C had the highest lysozyme, total complement activity, phagocytosis index and respiratory burst of head kidney among all treatments. The challenge test with Aeromonas hydrophila indicated that lower cumulative survival was observed in fish fed the lowest vitamin C diet. Analysis by broken‐line regression of SGR and lysozyme activity indicated that the dietary vitamin C requirement of juvenile yellow catfish was estimated to be 114.5 and 102.5 mg kg^?1 diet, respectively.     

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 protein requirement of juvenile obscure puffer,Takifugu obscurus

A 10‐week feeding experiment was conducted to determine the optimum dietary protein requirement of juvenile obscure puffer (Takifugu obscurus). Six isoenergetic (20 MJ kg^?1 gross energy) diets were formulated to contain graded levels of 34%, 38%, 42%, 46%, 50% or 54% crude protein (as dry matter basis). The results showed final body weight, weight gain and specific growth rate (SGR) increased significantly with increasing protein levels up to 42% and then decreased thereafer. Second‐order polynomial regression analysis (y = ?0.0024x² + 0.1788x ? 1.3196, R² = 0.9032) indicated a maximum SGR at protein level of 37%. Feed conversion ratio (FCR) decreased with increasing levels of dietary protein up to 42% and increased thereafter. Second‐order polynomial regression analysis (y = 0.0054x² ? 0.4351x + 10.391, R² = 0.753) indicated a minimum FCR at protein level of 40%. Protein efficiency ratio (PER) of fish fed the 34%, 38% and 42% diets was significantly higher than that of fish fed the 46%, 50% and 54% diets, and broken‐line analysis indicated PER tended to decrease when dietary protein level was higher than 40%. Generally, whole body lipid content, total cholesterol, low‐density lipoprotein cholesterol and triacylglycerol decreased with increasing levels of dietary protein. Fish fed the 42% protein diet showed the highest essential amino acids (histidine, isoleucine, leucine, lysine and threonine) and non‐essential amino acids (aspartic acid and glutamic acid) in muscle. Based on the second‐degree polynomial regression analysis of SGR and FCR and broken‐line analysis of PER, the optimal dietary protein level of obscure puffer is estimated to be between 37% and 40% (% as dry matter basis).     

Dietary arginine requirement of juvenile swimming crab,Portunus trituberculatus

An 8‐week feeding trial was conducted to determine the optimal dietary arginine requirement for juvenile swimming crab Portunus trituberculatus. Six isonitrogenous and isolipidic experimental diets were formulated to contain graded arginine levels which ranged from 15.9 to 33.0 g kg^?1. Each diet was randomly assigned to triplicate groups of 60 juvenile swimming crabs (4.72 ± 0.12 g). The results indicated that dietary arginine had significant effects on weight gain (WG), specific growth rate (SGR), protein productive value, feed efficiency and protein efficiency ratio. Weight gain and SGR significantly increased with the dietary arginine increasing from 15.9 to 27.4 g kg^?1, while with the further increasing from 27.4 to 33.0 g kg^?1, WG and SGR did not increase significantly. Maximum arginine, proline and total essential amino acid contents in muscle were observed in 27.4 g kg^?1 group diet. The swimming crab fed the diet with lower dietary arginine level showed higher AST and lower ALT in the serum. Crab fed with the lower dietary arginine level had significantly lower ALT in the serum than the other groups. Haemolymph indexes were significantly affected by the dietary arginine level except for the cholesterol concentration, and the highest values were all found in 27.4 g kg^?1 group diet. The two slope broken‐line model using SGR showed that the optimal dietary arginine requirement was 27.7 g kg^?1 of the dry matter (56.0 g kg^?1 dietary protein) for juvenile swimming crab.     

Total sulphur amino acid requirement and maximum cysteine replacement value for methionine for fingerling Catla catla (Hamilton)

Two separate 12 weeks feeding trials were performed to quantify the total sulphur amino acid (TSAA) requirement (experiment I) and cysteine replacement value for methionine (experiment II) of fingerling Catla catla. In experiment I, six casein–gelatin based (33% crude protein; 16.72 kJ g^?1 gross energy) diets with graded levels of TSAA (0.56%, 0.81%, 1.06%, 1.31%, 1.56%, 1.81% dry diet) were fed to triplicate groups of fish (3.55 ± 0.06 cm; 0.65 ± 0.02 g) near to satiation. The TSAA requirement was determined by quadratic regression analysis of absolute weight gain (AWG), protein efficiency ratio (PER), feed efficiency (FE), protein gain (PG) and TSAA gain (TSAAG) against dietary TSAA concentrations at 95% maximum response. Above analysis revealed that inclusion of TSAA at 1.28% dry diet (1.22% methionine + 0.06% cysteine), corresponding to 3.87% of dietary protein is optimum. In experiment II, to determine the replacement value of cysteine for methionine, six diets containing 1.28% TSAA determined in experiment I with different ratios of l ‐methionine and l ‐cysteine (80:20, 70:30, 60:40, 50:50, 40:60, 30:70) on equimolar sulphur basis were fed to fish (3.65 ± 0.08 cm; 0.67 ± 0.04 g). Broken‐line regression analysis of AWG, PER, FE, PG and TSAAG against varying methionine to cysteine ratios yielded the optimum cysteine replacement value at 40.3%. Based on above analysis, it is recommended that inclusion of 1.28% dietary TSAA, corresponding to 3.87% of dietary protein is optimum of which 40.3% could be spared by cysteine. Data generated during this study would be useful in formulating TSAA balanced, cost‐effective feeds for the intensive culture of this fish.     

Effects of dietary magnesium on the growth,carapace strength and tissue magnesium concentrations of soft‐shelled turtle,Pelodiscus sinensis (Wiegmann)

A feeding trial was conducted to evaluate the effects of dietary magnesium on the growth, carapace strength, tissue and serum Mg concentration of soft‐shelled turtles, Pelodiscus sinensis (Wiegmann). Juvenile soft‐shelled turtles of approximate 5.4 g body weight were fed diets with seven levels of Mg (48, 206, 369, 670, 955, 1195 and 1500 mg Mg kg^?1) for eight weeks. No significant difference (P ≥ 0.05) was found in weight gain (WG), feed conversion ratio or protein efficiency ratio among treatments. However, the WG of turtles continued to increase with increasing dietary Mg levels up to 670 mg kg^?1, beyond which the WG levelled off. The plasma alkaline phosphatase activity and the muscle, bone Mg concentrations of the turtles increased with the increasing dietary Mg levels between 48 and 955 mg kg^?1, beyond which the tissue Mg concentrations remained relatively constant. Furthermore, the carapace strengths of turtles fed with the control diet of 48 mg Mg kg^?1 were significantly weaker (P < 0.05) than that of turtles fed with diets containing higher Mg levels. Based on a broken‐line modelling analysis, the required dietary Mg level for the optimal WG of juvenile soft‐shelled turtles was estimated to be approximately 650 mg kg^?1. By contrast, the required dietary Mg levels for turtles to reach the optimal muscle and bone Mg concentrations were 1050 and 1000 mg kg^?1 respectively. The required dietary Mg level for maximal alkaline phosphatase activity was approximately 980 mg kg^?1.     

Effect of dietary l‐methionine concentrations on growth performance,serum immune and antioxidative responses of juvenile Nile tilapia,Oreochromis niloticus

An 8‐week feeding trial was conducted to determine the effect of dietary l ‐methionine supplementation on growth performance, serum immune and antioxidative responses of juvenile Nile tilapia Oreochromis niloticus. Six iso‐nitrogenous (282 g kg^?1 crude protein) diets were formulated to contain graded levels of methionine (0.32%, 0.54%, 0.75%, 0.93%, 1.14% and 1.33% of dry weight) at a constant dietary cysteine level of 0.83 g kg^?1. Each diet was randomly assigned to triplicate groups of 25 juvenile fish (2.3 ± 0.0 g), which were fed three times daily (8:30, 12:30 and 17:00 hours). The results showed that growth performance and feed utilization significantly improved when dietary methionine levels increased (P < 0.05). Using quadratic regression analysis of weight gain against dietary methionine levels indicated that, the optimal dietary methionine requirement for maximum growth of juvenile tilapia was 9.12 g kg^?1 of the dry diet in the presence of 0.83 g kg^?1 cystine. In addition, maximum C4 content and lysozyme activity were observed in fish fed 7.50 g kg^?1 methionine diet; maximum C3 content and superoxide dismutase activity were obtained in fish fed 9.30 g kg^?1 dietary methionine level. While there was no significant difference in serum glutathione peroxidase activity among all methionine supplemented treatments (P > 0.05). Methionine supplementation decreased malondialdehyde content in serum significantly (P < 0.05) when compared with the control diet, while there was no significant difference among supplemented treatments. These data suggested that l ‐methionine affected antioxidant status and promoted serum immune response in juvenile Nile tilapia, and at non‐stressed status, the requirement of dietary methionine in maintaining normal immunity and physiology is lower than that for maximum growth.