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.     

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

An 8‐week feeding trial was conducted to evaluate the effects of dietary tryptophan concentration on weight gain and feed efficiencies of fingerling Indian major carp, Cirrhinus mrigala. Six isonitrogenous (40% crude protein) and isocaloric (17.90 kJ g^?1) amino acid test diets containing casein, gelatin and l ‐crystalline amino acids with graded levels of l ‐tryptophan (0.06, 0.16, 0.26, 0.36, 0.46 and 0.56 g 100 g^?1 dry diet) were formulated. Fish (4.25±0.30 cm, 0.62±0.02 g) were randomly stocked in triplicate groups in 70 L (water volume 55 L) flow‐through (1–1.5 L min^?1) indoor circular tanks and fed experimental diets at 5% of their body weight/day in two feedings at 08:00 and 16:00 hours. Maximum live weight gain (277%), lowest feed conversion ratio (FCR) (1.50) and highest protein efficiency ratio (PER) (1.66) were measured at 0.36% dietary tryptophan. The relationship between dietary tryptophan levels and weight gain, FCR and PER data were described using second‐degree polynomial regression analysis indicating the tryptophan requirement at 0.42, 0.39 and 0.38 g 100 g^?1 of dry diet respectively. Whole body moisture decreased with increasing tryptophan up to 0.36%. Significantly (P<0.05) higher protein content was evident in fish fed diet containing 0.36% tryptophan. Body fat increased significantly (P<0.05) in fish fed with different tryptophan concentrations except those fed 0.36% tryptophan where a significantly lower fat content was noted. Significantly (P<0.05) higher ash content was reported at 0.06% and 0.16% tryptophan levels. Survival was 100% in fish fed all the diets except those fed 0.06% tryptophan. Based on the results, diets for fingerling C. mrigala should contain tryptophan at 0.38 g 100 g^?1 dry diet, corresponding to 0.95 g 100 g^?1 dietary protein for optimum growth and efficient feed utilization.     

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

An 8‐week feeding experiment was conducted to quantify the dietary isoleucine requirement of fingerling Indian major carp, Labeo rohita (3.50 ± 0.04 cm; 0.40 ± 0.02 g) using amino acid test diets (400 g kg⁻¹ crude protein; 17.90 kJ g⁻¹ gross energy) containing casein, gelatin and l ‐crystalline amino acids. Six dietary treatments supplemented with graded levels of isoleucine (7.5, 10.0, 12.5, 15.0, 17.5 and 20.0 g kg⁻¹), in gradations of 2.5 g kg⁻¹ diet, were fed to triplicate groups of fingerlings to apparent satiation divided over two feedings at 07:00 and 17:30 h. Performance of the fish was evaluated on the basis of live weight gain, feed conversion ratio (FCR), protein efficiency ratio (PER), specific growth rate (SGR) and protein productive value (PPV). Statistical analysis of live weight gain, FCR, PER, SGR and PPV reflected significant differences among treatments. Live weight gain and conversion efficiencies were best with isoleucine at 15.0 g kg⁻¹ of diet. Live weight gain, FCR, PER, SGR and PPV data were also analysed using second‐degree polynomial regression analysis to obtain more accurate isoleucine requirement estimate which was found to be at 15.9, 15.3, 15.2, 15.8 and 15.7 g kg⁻¹ of dry diet, corresponding to 39.8, 38.3, 38.0, 39.5 and 39.3 g kg⁻¹ of dietary protein respectively. Based on the quadratic regression analysis of the live weight gain, FCR, PER, SGR and PPV, the optimum level of isoleucine for fingerling L. rohita is in the range of 15.2–15.9 g kg⁻¹ of dry diet, corresponding to 38.0–39.8 g kg⁻¹ of dietary protein. Maximum body protein, minimum moisture and fat were noted at 15.0 g kg⁻¹ of dietary isoleucine while the body ash remained constant among all the treatment levels. No mortality was recorded during the duration of the experiment.     

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.     

Dietary methionine requirement of juvenile Pseudobagrus ussuriensis

An 8‐week feeding trial was conducted to determine the optimum dietary methionine (Met) requirement of juvenile Pseudobagrus ussuriensis with an initial average weight of 0.60 g reared in indoor flow‐through and aerated aquaria. Six isonitrogenous (430 g kg^?1 protein) and isolipidic (50 g kg^?1 lipid) test diets were formulated to contain graded levels of crystalline L‐methionine (4.9, 9.0, 11.8, 14.2, 18.1 and 20.8 g kg^?1 dry diets, respectively) at a constant dietary cystine level of 2.5 g kg^?1 dry diets. Equal amino acid nitrogen was maintained by replacing methionine with non‐essential amino acid mixture. Fish were randomly allotted to 18 aquaria (1.0 × 0.5 × 0.8 m) with 50 fish to each glass aquarium. Fish were fed twice daily (08:00 and 16:00) to apparent satiation. No significant difference was observed in survival of fish (84.67–91.33%). Specific growth rate (SGR), weight gain (WG), feed conversion ratio (FCR), protein productive value (PPV) and protein efficiency ratio (PER) were significantly affected by different dietary methionine levels (P < 0.05). WG, SGR PPV and PER increased, while FCR decreased with increasing dietary methionine level from 4.9 to 11.8 g kg^?1 (P < 0.05). However, with further increase from 11.8 to 20.8 g kg^?1, WG, SGR PPV and PER significantly decreased, FCR increased (P < 0.05). The whole body and muscle composition were affected by different dietary methionine levels (P < 0.05). Condition factor (CF) increased with increasing dietary methionine levels up to 11.8 g kg^?1 (P < 0.05) and after 11.8 g kg^?1 methionine diet, but not significant, declines were observed (P > 0.05). Hepatosomatic index (HSI) of the 4.9, 9.0, 11.8 and 14.2 g kg^?1 Met diets was significantly higher than that of fish fed diets 18.1 and 20.8 g kg^?1 Met diets (P < 0.05). Viscerosomatic index (VSI) of the 4.9, 9.0 and 11.8 g kg^?1 Met diets was significantly higher than that of fish fed diets 14.2, 18.1 and 20.8 g kg^?1 Met diets (P < 0.05). Quadratic regression analysis of WG and PER against dietary methionine levels indicated that the optimal dietary methionine requirement for maximum growth and feed utilization of juvenile Pseudobagrus ussuriensis was 14.3 and 14.1 g kg^?1 dry diet (35.3 and 34.8 g kg^?1 dietary protein), respectively, in the presence of 2.5 g kg^?1 dry diets cystine.     

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.     

Relative efficacy of dietary administration of 3,5,3'-triiodothyronine (T3) to different stages of an Indian major carp, Cirrhina mrigala (Hamilton): growth and economics

Different stages of an Indian major carp, Cirrhina mrigala (Hamilton), i.e. hatchling, fry and fingerling, were fed diets supplemented with 3,5,3′-triiodothyronine (T₃) at doses of 0, 1, 5 and 10 mg kg^?1 diet for 60 days, and then reared on a hormone-free diet for 120 days to study the growth performance of fish during the treatment period (TP) and post-treatment period (PTP). Oral administration of T₃ at all the stages resulted in a significantly higher specific growth rate (SGR) and better food conversion ratio (FCR) in comparison to the control group (P<0.05). However, the growth response of C. mrigala towards T₃ administration appeared to be stage-specific. At the end of the experimental period of 180days (60days TP+120days PTP), the optimum dosage of T₃ appeared to be 5.0 mg kg^?1 diet for both hatchlings and fry, and 1.0 mg kg^?1 diet for fingerlings, resulting in 62.08%, 30.22% and 13.33% higher weights than in the control group, respectively. The cost of hormone for production of 1 kg of fish was lowest in the case of hatchlings (Rs 0.54), followed by fry (Rs 7.00) and fingerlings (Rs 16.07). Hence, based on the degree of growth response of the fish towards T₃ administration in addition to its economics, only incorporation of T₃ in the diet of hatchlings appeared to be economical.     

The growth performance of southern catfish fed diets with raw, precooked cornstarch and glucose at two levels

The ability of juvenile carnivorous southern catfish (Silurus meridionalis Chen) to use different levels, kinds and physic state (glucose, raw cornstarch and precooked cornstarch) of dietary carbohydrate was evaluated in term of growth performance. All diets contained 100 g kg^?1 lipid and 16 kJ metabolizable energy. Three isonitrogeneus (400 g kg^?1) diets were formulated to contain 150 g kg^?1 raw cornstarch, precooked cornstarch and glucose. Another three isonitrogeneus (300 g kg^?1) diets were formulated to contain 300 g kg^?1 raw cornstarch, precooked cornstarch and glucose. A control diet was formulated with no carbohydrate containing 500 g kg^?1 protein. Each experimental diet was fed to four tanks of 10 fish (28.3 ± 0.5 g) for 8 weeks at 27.5 °C. Specific growth rate (SGR) of 300 g kg^?1 glucose diet was significantly lower than those of other diets (P < 0.05). Feeding rates (FR) of 300 g kg^?1 glucose and control diets were significantly lower than those of the other diets (P < 0.05). Feed efficiency (FE) was significantly decreased with increased dietary carbohydrate level (P < 0.05). Feed efficiency of the 300 g kg^?1 glucose diet was significantly lower than those of the 300 g kg^?1 raw and precooked cornstarch diets (P < 0.05). The protein efficiency ratio (PER) was significantly increased with dietary carbohydrate level except that of the 300 g kg^?1 glucose diet, which was lowest among all diets (P < 0.05). The results suggested that both dietary starch and glucose were utilized for energy in southern catfish and had a protein‐sparing effect. At 150 g kg^?1 inclusion level, the utilization of raw and precooked cornstarch and glucose did not vary significantly, but a higher dietary glucose level (300 g kg^?1) had a markedly detrimental effect on growth in southern catfish.     

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

An 8-week feeding experiment was conducted to evaluate the dietary leucine requirement of fingerling Indian major carp, Labeo rohita (3.50±0.04 cm; 0.40±0.02 g) using amino acid test diets (40% crude protein; 17.90 kJ g⁻¹ gross energy) containing casein and gelatin as intact protein sources and l -crystalline amino acids. Growth performance and biochemical parameters were assessed by feeding six amino acid test diets supplemented with graded concentrations of leucine (0.75, 1.0, 1.25, 1.50, 1.75 and 2.0 g per 100 g) to triplicate groups of fingerlings to apparent satiation divided over two feedings at 07:00 and 17:30 hours. Performance of the fish was evaluated on the basis of live weight gain, feed conversion ratio (FCR), protein efficiency ratio (PER) and body protein deposition (BPD) data. Maximum live weight gain (315%), best FCR (1.35), highest PER (1.86) and BPD (33.9) were recorded at 1.50 g per 100 g dietary leucine. Statistical analysis of live weight gain, FCR, PER and BPD data reflected significant differences (P<0.05) among treatments. Live weight gain, FCR, PER and BPD data were also analysed using second-degree polynomial regression analysis to obtain more accurate leucine requirement estimate which was found to be at 1.57, 1.55, 1.52 and 1.50 g per 100 g of dry diet, corresponding to 3.92, 3.87, 3.80 and 3.75 g per 100 g of dietary protein respectively. Based on the quadratic regression analysis of the live weight gain, FCR, PER and BPD data, the optimum requirement of fingerling L. rohita for leucine is estimated to be in the range of 1.50–1.57 g per 100 g of the dry diet, corresponding to 3.75–3.92 g per 100 g of dietary protein.     

Effects of dietary protein level on growth,feed utilization and digestive enzyme activity of the Chinese mitten crab,Eriocheir sinensis

A feeding trial was conducted using isoenergetic practical diets to evaluate the effects of the dietary protein level on growth performance, feed utilization and digestive enzyme activity of the Chinese mitten crab, Eriocheir sinensis. Four experimental diets were formulated containing 250, 300, 350 and 400 g kg^?1 protein and 16 kJ g^?1 gross energy. Each diet was randomly assigned to triplicate groups of juvenile crab with mean initial body weight 3.56 ± 0.16 g and mean shell width 15.31 ± 0.06 mm. Juvenile crab were reared in indoor flow‐through system consisting of 12 plastic tanks (1.0 m × 0.6 m × 0.5 m) and fed diets twice daily at 6–8% of body weight for 12 weeks. Performance was judged on the basis of growth (specific growth rate of weight, SGR_G; specific growth rate of shell width, SGR_SW), feed conversion ratio (FCR) and protein efficiency ratio (PER). A decreased FCR was observed with increasing dietary protein levels. Both SGR_G and SGR_SW significantly increased with increasing dietary protein levels up to 350 g kg^?1, whereas there were no significant differences for protein levels from 350–400 g kg^?1. Application of broken line regression analysis to SGR_G provided an estimate of 347.8 g kg^?1 dietary protein for maximal growth. The highest PER was observed in crab fed the diet containing 350 g kg^?1 protein (P < 0.05). The percent survival was not affected (P > 0.05) by the different dietary treatments. No significant differences were observed in the apparent digestibility coefficients of crude lipid and dry matter among dietary treatments (P > 0.05). However, the apparent digestibility coefficients of crude protein and energy in crab fed different protein levels significantly increased with increasing dietary protein level (P < 0.05). Both amylase and protease activities in the intestine of E. sinensis were studied. The amylase activity decreased significantly (P < 0.05) with increased dietary protein level and protease activity increased. Regression analysis showed a negative effect of inclusion of dietary protein level on amylase activity (P < 0.05). However, protease activities were found to be positively correlated (P < 0.05) with dietary protein level. The protein content of the crab significantly increased with dietary protein levels up to 350 g kg^?1 (P < 0.05), but no significant differences (P > 0.05) were founded with protein levels higher than 350 g kg^?1.     

Effect of soybean-meal-based diets on the growth and survival rate of the Indian major carp, Cirrhinus mrigala (Ham.)

The effect of varying dietary levels of defatted soybean meal on the growth and survival of mrigal, Cirrhinus mrigala (Hamilton) was investigated. In a feeding trial of 90 days, three experimental diets containing soybean meal at 200, 300 and 400 g kg^?1 level of incorporation were fed to quadruplicate groups of 10 fish each. The conventional feed used in India, consisting of a mixture of groundnut oil cake and rice bran in 1 : 1 ratio served as the control. Best growth in terms of percentage weight gain, specific growth rate, protein efficiency ratio (PER), feed conversion ratio and survival rate was obtained for the test diet with 354 g kg^?1 crude protein and with 400 g kg^?1 soybean meal inclusion level. However, no statistical significant difference was observed between the three soybean‐based diets, except for PER and survival rate. Soybean meal is an easily available, acceptable and cost‐effective protein source in formulated feeds for Indian major carps. The results of the present study indicate that a diet of 350 g kg^?1 overall protein with soybean meal included at 400 g kg^?1 can elicit good growth response and survival in mrigal.     

Effect of dietary cornstarch levels on growth performance, digestibility and microscopic structure in the white shrimp, Litopenaeus vannamei reared in brackish water

The ability of Litopenaeus vannamei (initial mean weight: 0.96 ± 0.02 g) to utilize different levels of cornstarch was examined in terms of growth indices, body composition, digestibility and microscopic structure of the hepatopancreas. Six isonitrogenous semipurified diets were fed to satiation to shrimp for 8 weeks in triplicate tanks (30 shrimps per tank) connected to a natural brackish water (6–8 g L^?1) recirculating system. Diets contained different levels of cornstarch (100, 150, 200, 250, 300 and 350 g kg^?1) as the source of carbohydrate and were balanced using cellulose. Weight gain (WG), survival rate and feed conversion rate (FCR) were considerably affected by cornstarch levels of diets. The highest WG (453.6 g kg^?1) and best FCR was observed in shrimp fed the 150 g kg^?1 (cornstarch level) diet and was significantly (P < 0.05) higher than those fed diets containing 250–350 g kg^?1 cornstarch. However, the survival rate reached maximum in shrimp fed the 100 g kg^?1 diet (96.7), some 30% higher than the lowest rate, which was found in shrimp fed the 250 g kg^?1 diet. Body lipid tended to be higher in shrimp fed diets with higher cornstarch levels. The apparent digestibility of dry matter and crude fat increased with increasing levels of cornstarch and, hence, decreasing levels of cellulose. In addition, histological study on shrimp fed 10–350 g kg^?1 diets exhibited histological changes. The overall conclusion was that the optimum cornstarch level may be set at 100–200 g kg^?1 when the diets contain 380 g kg^?1 protein.     

Effects of cellulase addition to canola meal in tilapia (Oreochromis niloticus L.) diets

The effects of commercial cellulase enzyme products on the nutritive value of canola meal (CM) were determined in tilapia fry. Nine diets were prepared by adding cellulase enzyme (1–5 g kg^?1) to control diet (containing no canola), low canola (41.7 g kg^?1 CM) and high canola (208.3 g kg^?1 CM). Tilapia fry was fed for 90 days, and growth, feed conversion ratio (FCR), body composition and nutrient digestibility were determined. Fish fed the diets containing the lowest levels of canola meal (41.7 g kg^?1) had similar final weight and FCR relative to the group fed the control diet, and high canola diet showed significantly lower growth than other groups (P < 0.05), irrespective of cellulase enzyme. The addition of canola meal to tilapia diets resulted in lower protein digestibility and cellulose digestibility. There were no significant differences in body compositions in all treatments. Addition of enzymes to canola meal diets had no significant effects on growth performance, body compositions and nutrient digestibility. The results of this study indicate that use in higher level of canola meal in tilapia diet was adversely affected growth parameters and FCR. Adding dietary cellulase enzyme in different rations to diets showed no significant differences in growth parameter.     

Effect of dietary niacin on growth and body composition of two Indian major carps rohu, <Emphasis Type="Italic">Labeo rohita</Emphasis>, and mrigal, <Emphasis Type="Italic">Cirrhinus mrigala</Emphasis> (Hamilton), fingerlings based on dose–response study

An 15 week two set of feeding experiments were conducted to determine the dietary niacin requirement of Indian major carp fingerlings Labeo rohita and Cirrhinus mrigala, using casein gelatin–based diet. In both experiments, six isonitrogenous (40%) and isoenergetic (15.35 kJ g⁻¹) test diet, with graded levels of niacin (0–50 mg kg⁻¹ dry diet) in gradation of 10 mg kg⁻¹ dry diet, were formulated. In first experiment, fingerling of L. rohita (4.20 ± 1.22 cm; 0.632 ± 0.67 gm) were randomly stocked, in triplicate groups, in 55-L indoor polyvinyl flow-through system (1.5 L min⁻¹) and fed experimental diet at 0800 and 1600 h. Maximum live weight gain (1214%), feed conversion ratio (1.55) and protein efficiency ratio (1.60) were recorded at 30 mg dietary niacin diet. In second experiment, C. mrigala (4.50 ± 1.25 cm, 0.665 ± 0.88) were stocked in same setup. At the end of experiments, maximum live weight gain (1248%), FCR (1.47) and PER (1.70) occurred at 30 mg dietary niacin diet. However, the weight gain, FCR and PER data were analyzed by polynomial regression analysis indicating the requirement of niacin for L. rohita at 36.69, 33.06 and 32.0 mg kg⁻¹, respectively, and for C. mrigala at 35.19, 28.69 and 27.70 mg kg⁻¹ of dry diet, respectively. Whole body composition also showed significant (P < 0.05) differences among each other. On the basis of regression analysis of growth data, it is recommended that the diet for fingerlings should contain niacin at 33 and 30 mg kg⁻¹ dry diet for L. rohita and C. mrigala, respectively.     

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.     

Effect of dietary protein levels on growth,feed utilization and carcass composition of endangered bagrid catfish Horabagrus brachysoma (Gunther 1864) fingerlings

An 84‐day feeding trial was conducted to study the effect of different levels of dietary protein, 250 (P25), 300 (P30), 350 (P35), 400 (P40) and 450 g (P45) kg^?1 dry matter (DM) on growth, feed intake, feed utilization and carcass composition of bagrid catfish Horabagrus brachysoma fingerlings. Triplicate groups of fingerlings with mean initial body weight of 2.2 g were fed the experimental diets twice daily, till satiation, in 150‐L tanks supplied with flow‐through freshwater. Daily dry matter intake by the fingerlings decreased significantly (P < 0.05) when fed P25 diet, containing 250 g protein kg^?1. The highest body weight gain, specific growth rate (SGR) and protein efficiency ratio (PER), and the lowest feed conversion ratio (FCR) were observed in fish fed 350 g protein kg^?1 diet. The fish fed with P45 diet had the lowest (P < 0.05) carcass lipid content. The polynomial regression analysis indicates that H. brachysoma fingerlings require 391 g dietary crude protein kg^?1 diet.     

Dietary digestible lysine requirement and essential amino acid to lysine ratio for pacu Piaractus mesopotamicus

To determine the digestible lysine requirement for pacu juveniles, a dose–response feeding trial was carried out. The fish (8.66 ± 1.13 g) were fed six diets containing the digestible lysine levels: 6.8, 9.1, 11.4, 13.2, 16.1 and 19.6 g kg^?1 dry diet. The gradual increase of dietary digestible lysine levels from 6.8 to 13.2 g kg^?1 did not influence the average values of the parameters evaluated (P > 0.05). The increase of dietary digestible lysine level to 16.1 g kg^?1 significantly improved weight gain (WG), specific growth rate (SGR), protein productive value (PPV), protein efficiency rate (PER), and apparent feed conversion rate (FCR), but was not different from fish fed diets containing 19.6 g kg^?1 lysine. Fish fed diets containing 16.1 and 19.6 g kg^?1 digestible lysine showed lower body lipid contents than fish in the other treatments. The digestible lysine requirement as determined by the broken‐line model, based on average WG values, was 16.4 g kg^?1. The other essential amino acid requirements were estimated based on the ideal protein concept and the value determined for lysine.     

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.     

Quantifying the dietary niacin requirement of the Indian catfish, Heteropneustes fossilis (Bloch), fingerlings

A growth study was conducted to determine the dietary niacin requirement of the Indian catfish, Heteropneustes fossilis (Bloch), fingerlings (Mean weight 9.41 ± 0.18 g). Semi‐purified diets with five levels (0, 5, 10, 20 and 40 mg kg^?1 diet) of supplemental niacin were fed to H. fossilis for 15 weeks. Each diet was fed to three replicate groups of fish. Results indicated that the highest (P < 0.05) weight gain was for the fish fed the diet supplemented with 20 mg niacin kg^?1, followed by fish fed the diets with 40, 10 and 5 mg niacin kg^?1, and the lowest in fish fed the unsupplemented control diet. Patterns of specific growth rate (SGR) and protein efficiency ratio (PER) were similar to those of the weight gain. Survival of fish fed the control diet and niacin‐supplemented diet was 58% and 91–100% respectively. Niacin deficiency signs such as anaemia, anorexia, lethargy and skin haemorrhage were observed in fish fed the control diet. The haematocrit values (Ht) were higher (P < 0.05) in fish fed the diets supplemented with niacin than in fish fed the control diet. The hepatosomatic indexes (HSI) of fish fed with or without niacin‐supplemented diets were not significantly (P > 0.05) different from each other. Both body protein and lipid content were higher (P < 0.05) in fish fed the diet supplemented with 20 and 40 mg niacin kg^?1, respectively, than those fish fed other diets. The niacin content in liver significantly (P < 0.05) reflected the supplementation level in the diet and ranged from 29.11 to 40.31 mg g^?1 tissue. The associated liver niacin content for growth was about 47 μg g^?1 tissue. Quadratic regression analysis showed that the dietary niacin requirement for maximal growth of H. fossilis under these experimental conditions was about 25 mg kg^?1 diet.