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1.
A 12-week feeding trial was conducted to evaluate the effects of varying levels of dietary arginine on growth, feed conversion, protein productive value and carcass composition of fingerling Heteropneustes fossilis (10.11?±?0.14?cm; 5.87?±?0.07?g). Casein and gelatin-based isonitrogenous (38% crude protein) and isocaloric (14.72 kJ?g?1 digestible energy) amino acid test diets with varying levels of l-arginine (1.00, 1.25, 1.50, 1.75, 2.00 and 2.25?g 100?g?1 of dry diet) were fed to randomly assigned triplicate groups of fish to apparent satiation twice daily at two feeding schedules (08.00 and 17.30?h). Thermal growth coefficient (TGC; 0.86), feed conversion ratio (FCR; 1.97) and protein productive value (PPV; 0.25) were best attained by the group fed diet containing 1.75?g arginine 100?g?1 of dry diet (D4). Carcass protein content also peaked at the above level of dietary arginine whereas carcass lipid showed consistent drop with the increase in dietary arginine level up to 1.75?g 100?g?1 of dry diet. Second-degree polynomial regression analysis at 95% maximum and minimum response of thermal growth coefficient, feed conversion, protein productive value, carcass protein and lipid productive value against varying levels of dietary arginine yielded that dietary arginine in the range of 1.51–1.66?g 100?g?1 of dry diet, corresponding to 3.97–4.37?g 100?g?1 protein is adequate to optimize growth, feed conversion, protein productive value and improve carcass quality in fingerling H. fossilis.  相似文献   

2.
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.  相似文献   

3.
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.  相似文献   

4.
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.  相似文献   

5.
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.  相似文献   

6.
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.  相似文献   

7.
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.  相似文献   

8.
Indian major carp, Cirrhinus mrigala fingerling (3.85 ± 0.50 cm, 0.50 ± 0.02 g) were fed isonitrogenous and isocaloric diets (40% CP, 4.28 kcal g−1, GE) containing casein, gelatin and crystalline amino acids with graded levels of L- methionine (0.50, 0.75, 1.00, 1.25, 1.50 and 2.00 g/ 100 g, dry diet) with 1.00% cystine fixed, to determine its dietary methionine requirement. A feeding trial was conducted in triplicate for six weeks. Diets were fed twice a day at 0800 and 1600 h at 5% of body weight/day. The ration size and feeding regime were worked out prior to the start of the feeding trial. Weight gain (158%) and food conversion ratio (1.45) were significantly (P < 0.05) higher in fish fed diet containing 1.00% methionine with 1.00% cystine fixed. Second degree polynomial regression analysis of the weight gain data indicated the dietary methionine requirement to be 1.20 g/100 g of dry diet, corresponding to 3.00% of dietary protein. Second degree polynomial regression analysis was also employed to determine the relationship between food conversion ratio (FCR) and dietary methionine levels which indicated that the best FCR occurred at approximately 1.20% dietary methionine level. Carcass composition of fish fed diet containing graded levels of methionine varied significantly (P < 0.05) except carcass ash content which showed insignificant (P > 0.05) differences among the dietary methionine levels. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

9.
The dietary arginine requirement of fingerling hybrid Clarias (Clarias gariepinus×Clarias macrocephalus) (4.2±0.03 cm, 0.56±0.04 g) was determined by feeding six isonitrogenous (400 g kg−1 crude protein) and isocaloric (17.9 kJ g−1) amino acid test diets containing casein, gelatin and l ‐crystalline amino acids with graded levels of arginine (10.0, 12.5, 15.0, 17.5, 20.0 and 22.5 g kg−1) for 4 weeks to triplicate groups. Diets were fed twice a day at 09:00 and 16:00 hours at 8% body weight day−1. Maximum weight gain (523%), best feed conversion ratio (FCR, 1.41), protein efficiency ratio (1.78) and specific growth rate (6.53%) were recorded in fish fed the diet containing arginine at 20.0gkg−1 of the diet. Second‐degree polynomial regression analysis of live weight gain and FCR values indicated the dietary arginine requirement at 17.8 and 20.0 g kg−1 of dry diet respectively. Significantly higher carcass protein and protein deposition values were recorded at the requirement level (20.0 g kg−1). Higher fat and lower moisture values were obtained in carcass of fish fed the diet with 15.0g kg−1 arginine. The maximum carcass ash value was noticed in the fish fed at 20.0 g kg−1 dietary arginine. We recommend that the diet for hybrid Clarias (C. gariepinus×C. macrocephalus) should contain arginine in the range of 17.8–20.0 g kg−1 of the dry diet, corresponding to 44.5 and 50 g kg−1 of dietary protein respectively.  相似文献   

10.
An 8‐week feeding trial was conducted to assess the effects of dietary l ‐threonine on growth, protein utilization, threonine retention efficiencies, nucleic acid indices and body composition of fingerling Heteropneustes fossilis (6.6 ± 0.1 g; 10.9 ± 0.2 cm). Casein–gelatin based isonitrogenous (38% crude protein; CP) and isocaloric (15.3 kJ g?1 digestible energy; DE) amino acid test diets with six levels of dietary l ‐threonine (0.75%; 1.0%; 1.25%; 1.5%; 1.75%; 2.0% dry diet) were prepared and hand‐fed to quadruplicate groups of fingerling to apparent visual satiation twice daily. Weight gain (WG; 46.3 g fish?1), feed conversion ratio (FCR; 1.98), protein utilization efficiency (PUE; 0.25), threonine retention efficiency (TRE; 0.69), lipid productive value (LPV; 0.45), body protein (18.2%) and RNA/DNA ratio (3.6) of fish fed graded levels of dietary threonine increased significantly (P < 0.05) up to 1.49% threonine of dry diet. To generate precise information, the WG, RNA/DNA and LPV data were subjected to broken‐line and quadratic regression analyses. The two models were superimposed and requirement was determined by establishing the point, where the quadratic curve first intersected the plateau of broken‐line. Based on the above mathematical analyses, optimum dietary threonine requirement of fingerling H. fossilis was estimated to range between 1.62% and 1.69% of the diet, corresponding to 4.26–4.44% protein.  相似文献   

11.
An 8‐week growth trial was conducted to determine the dietary histidine requirement of the Indian major carp, Cirrhinus mrigala fingerling (length 4.22 ± 0.45 cm; weight 0.61 ± 0.08 g; n = 40). Isonitrogenous (400 g kg?1 crude protein) and isoenergetic (17.90 kJ g?1 gross energy) diets with graded levels of l ‐histidine (2.5, 5.0, 7.5, 10.0, 12.5 and 15.0 g kg?1 dry diet) were formulated using casein and gelatin as a source of intact protein, supplemented with l ‐crystalline amino acids. Twenty fish were randomly stocked in 70‐L indoor polyvinyl circular fish tank (water volume 55‐L, water exchange rate 1–1.5 L min?1) and fed experimental diets at the rate of 5% of their body weight/day divided over two feedings at 08:00 and 16:00 h. Maximum live weight gain (295%), best feed conversion ratio (FCR) (1.48) and protein efficiency ratio (PER) (1.69) occurred at 7.5 g kg?1 of dietary histidine level. When live weight gain, FCR and PER data were analysed using second‐degree polynomial regression, the break points indicated histidine requirements at 9.4, 8.6 and 8.5 g kg?1 of dry diet respectively. Significantly (P < 0.05) higher whole body protein and low moisture values were recorded at 7.5 g kg?1 histidine level. Body fat increased significantly (P < 0.05) with increasing histidine levels. However, at 7.5 and 10 g kg?1 histidine diets body fat did not differ (P > 0.05) to each other. Ash content of fish fed diets containing various levels of histidine did not differ except at 2.5 and 5.0 g kg?1 inclusion levels where significantly (P < 0.05) higher ash was recorded. Protein deposition was also found to be significantly (P < 0.05) higher in the 7.5 g kg?1 histidine diet. Based on the polynomial regression analysis of FCR and PER data, it is recommended that the diet for fingerling C. mrigala should contain histidine at 8.5 g kg?1 of dry diet, corresponding to 21.25 g kg?1 of dietary protein for optimum growth and efficient utilization of feed.  相似文献   

12.
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.  相似文献   

13.
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.  相似文献   

14.
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.  相似文献   

15.
An 8‐week feeding trial was conducted to estimate the optimum dietary protein to energy (P/E) ratio in juvenile olive flounder Paralichthys olivaceus. Eight experimental diets were formulated with two energy levels and four protein levels at each energy level. Two energy levels of 12.5 and 16.7 kJ g?1 diets were included at crude protein (CP) levels of 25%, 30%, 35% and 45% with 12.5 kJ g?1, and CP levels of 35%, 45%, 50% and 60% with 16.7 kJ g?1. After 1 week of the conditioning period, fish initially averaging 8.1±0.08 g (mean±SD) were randomly distributed into the aquarium as groups of 15 fish. Each diet was fed on a dry‐matter basis to fish in three randomly selected aquariums at a rate of 3–5% of total wet body weight per day for 8 weeks. After 8 weeks of the feeding trial, weight gain (WG), feed efficiency ratio and specific growth rate of fish fed 45% CP with 16.7 kJ g?1 energy diet were significantly higher than those from the other dietary treatments (P<0.05). WG of fish fed 12.5 kJ g?1 energy diets increased with the increase of dietary protein levels. However, WG of fish fed 16.7 kJ g?1 energy diets increased with the increase of dietary protein levels up to 45% CP and then decreased when fish fed 50% and 60% CP diets. Both dietary protein and energy affected protein retention efficiency and energy retention efficiency. Haemoglobin (Hb) of fish fed 35% and 45% CP diets with 12.5 kJ g?1 energy were significantly high and not different from Hb of fish fed 45% and 50% CP diets with 16.7 kJ g?1 energy. Haematocrit of fish fed 45% CP diet with 16.7 kJ g?1 energy was significantly higher than those from fish fed 25% and 30% CP diets with 12.5 kJ g?1 energy (P< 0.05). Based on the results of this experiment, we concluded that the optimum dietary P/E ratio was 27.5 mg protein kJ?1 with diet containing 45% CP and 16.7 kJ g?1 energy in juvenile olive flounder.  相似文献   

16.
Cherax albidus (A) and Cherax destructor (D) male juveniles (mean weight 0.95 ± 0.03 g) were reared for 20 weeks on isoenergetic diets containing 150 g kg?1 protein (A 15, D15) or 300 g kg?1 protein (A30, D30). Mean weight, percentage weight gain, and specific growth rate (%) were substantially higher for both species on the 300 g kg?1 protein diet. Mean percentage weight gain ranged from 2.39% day?1 (D15) to 17.59% day?1 (A30). A maximum weight of 33.81 g was attained by C. albidus on the higher protein diet. The most effective utilization of food was observed in C. albidus when fed the higher protein diet (food conversion ratio, 0.79; protein efficiency ratio, 4.21; apparent net protein utilization, 44.64%). Carcass composition was influenced by feed type. The higher protein diet resulted in an increase in carcass protein and ash and a decrease in carcass lipid and energy relative to the low-protein diet (150 g kg?1 protein diet –C. albidus: 37.15% protein, 15.00% lipid, 25.20% ash, 15.55kJ g?1 energy; C. destructor: 38.10% protein, 15.43% lipid, 25.70% ash, 15.65kJ g?1 energy; 300 g kg?1 protein diet –C. albidus: 46.10% protein, 8.71% lipid, 27.36% ash, 14.94kJ g?1 energy; C. destructor: 42.99% protein, 8.56% lipid, 26.44% ash, 14.71kJ g?1 energy). Carcass moisture and calcium were not affected by feed type. The time spent in the intermoult phase of growth was highly dependent on the premoult weight and varied according to diet and to species. A comparison of animals of similar weight (< 8 g) revealed that elevated dietary protein caused a reduction in the intermoult period by 11 days in C. albidus and 7 days in C. destructor. The moult increment, however, was independent of animal weight, and the highest percentage weight increment occurred for C. albidus fed the 300 g kg?1 protein diet (per cent weight increase; A15, 33.1%; A30, 61.3%; D15, 31.2%; D30, 56.5%). Dietary induced morphological changes were also recorded. Animals of a standard carapace length had significantly larger abdomens (both species) and larger claws (C. albidus) when fed the higher protein diet.  相似文献   

17.
A feeding trial was conducted to determine the dietary threonine requirement of juvenile large yellow croaker (Larmichthys crocea). Six diets were formulated containing 45% crude protein with six graded levels of threonine (0.71–2.46% in about 0.35% increment). Each diet was randomly assigned to triplicate groups of 60 juvenile fish (initial body weight 6.00 ± 0.10 g). Fish were fed twice daily (05:00 and 16:30) to apparent satiation for 8 weeks. The result indicated that significant difference was observed in the weight gain among all treatments. Specific growth rate (SGR), feed efficiency (FE), protein efficiency ratio (PER) and nitrogen retention (NR) increased with increasing levels of threonine up to 1.75% diet (P < 0.05), and thereafter, declined. No significant differences in body dry matter, crude protein, crude lipid or ash content were found among dietary treatments. Theronine contents of fish muscle were significantly affected by dietary threonine levels (P < 0.05). Fish fed the diet with 0.71% threonine showed the lowest threonine content (2.94%) in fish muscle, while fish fed the diet with 1.75% threonine had the highest value (3.16%). Other essential amino acid contents of muscle were not significantly different among the dietary treatments. On the basis of SGR, FE or NR, the optimum dietary threonine requirements of juvenile L. crocea were estimated to be 1.86% of diet (4.13% of dietary protein), 1.90% of diet (4.22% of dietary protein) and 2.06% of diet (4.58% of dietary protein), respectively, using second‐order polynomial regression analysis.  相似文献   

18.
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.  相似文献   

19.
Effect of varying dietary lysine levels on growth, feed conversion, nutrient retention, lysine retention efficiency and haematological indices of Heteropneustes fossilis fry (2.97 ± 0.11 cm; 4.78 ± 0.31 g) was studied by conducting a 12‐week feeding trial. Isonitrogenous (450 g kg?1 CP) and isocaloric (17.97 kJ g?1 GE) amino acid test diets with graded concentrations of l ‐lysine (18, 20, 22, 24, 26, 28 g kg?1 dry diet) were fed to triplicate groups of fish to apparent satiation twice daily at 17 and 17:30 h. Maximum thermal growth coefficient (TGC, 0.82), best feed conversion ratio (FCR, 1.28) highest protein retention efficiency (PRE, 36%), energy retention efficiency (ERE, 79%) and lysine retention efficiency (LRE, 75%) were noted at 24 g kg?1 lysine of dry diet. Body protein was also found to be in line with growth data and peaked at 24 g kg?1 lysine of dry diet. Similarly, superior somatic and haematological indices were exhibited by the groups fed dietary lysine at 24 g kg?1 of the dry diet. However, exponential analysis of dietary lysine intake against TGC, lysine retention and protein retention indicated that inclusion of dietary lysine in the range of 13.24–14.14 g kg?1 dry diet, corresponding to 29.42–31.42 g kg?1 dietary protein, is essential for faster growth of this fish.  相似文献   

20.
This study aimed to assess the effect of soybean meal (SBM) and cottonseed meal (CSM), as partial replacement of dietary fish meal on growth, feed efficiency (FE) and body mineral composition of juvenile vundu (Heterobranchus longifilis). Five iso‐nitrogenous (390 g kg?1 crude protein) and iso‐caloric (18 kJ g?1, gross energy) diets (Control, SBM30, SBM60, CSM30 and CSM60) were fed to triplicate groups of 40 fish (initial mean weight: 12 g) in each tank (0.9 m3). Over a 7‐week feeding period, significant differences (P < 0.05) were observed on growth, FE and body mineral composition between treatments. Fish‐fed CSM‐based diets and 600 g kg?1 SBM‐based diet had reduced growth and reduced feed and protein efficiencies when compared with those fed diet containing 300 g kg?1 SBM or the control diet. Data from body mineral composition in response to dietary treatment could be divided into two groups. The first group refers to elements such as Mg and Fe for which carcass and fillet composition did not show significant differences with dietary level of SBM or CSM. Ca, P, K, Zn and Mn composed the second group of minerals whose concentrations in fish body were significantly reduced in fish‐fed SBM60. In conclusion, the results of this study indicate that although solvent‐extracted SBM and CSM are often reported safe for fish, they can only partially replace fish meal as a source of protein in compound feed for vundu at a limited amount between 300 and 600 g kg?1 for SBM and <300 g kg?1 for CSM.  相似文献   

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