Dietary myo‐inositol requirement for juvenile gibel carp (Carassius auratus gibelio)

An 11‐week growth trial was conducted to determine dietary myo‐inositol (MI) requirement for juvenile gibel carp (Carassius auratus gibelio). Myo‐inositol was supplemented to the basal diet to formulate six purified diets containing 1, 56, 107, 146, 194 and 247 mg MI kg^?1 diet, respectively. Each diet was fed to triplicate groups of juvenile gibel carp (initial body weight 3.38 ± 0.27 g, mean ± SD) in a flow‐through system. The diets were randomly assigned to different fish tanks. Fish fed ≥ 107 mg MI kg^?1 diet had significantly higher weight gain (WG), feed efficiency (FE) and protein efficiency ratio than those fed 1 mg MI kg^?1 diet. Fish fed ≥ 56 mg MI kg^?1 diet had higher feeding rate and survival compared with fish fed 1 mg MI kg^?1 diet. Dietary supplemental inositol did not affect fish liver inositol concentration. Fish fed ≥ 56 mg MI kg^?1 diet had higher body dry matter, crude protein and gross energy and lower hepatosomatic index than fish fed 1 mg MI kg^?1 diet. Dietary inositol supplementation decreased fish body ash. Quadratic regression of weight gain indicated that the myo‐inositol requirement to maximum growth for juvenile gibel carp was 165.3 mg MI kg^?1 diet.     

Influence of dietary phosphorus levels on growth,body composition,metabolic response and antioxidant capacity of juvenile snakehead (Channa argus × Channa maculata)

A study was conducted to estimate the optimum requirement of dietary phosphorus (P) for Channa argus × Channa maculata. Effects of dietary P levels on the tissue composition, serum biochemical parameters and antioxidant status were also examined. Five practical diets were formulated to contain graded levels (4.8 g kg^?1, 6.4 g kg^?1, 7.9 g kg^?1, 9.4 g kg^?1 and 11.0 g kg^?1) of available P from dietary ingredients and monocalcium phosphate (MCP). Each diet was randomly assigned to triplicate groups of 30 juvenile fish (initial body weight, 20.50 ± 0.53 g) for 8 weeks. The results showed that the specific growth rate (SGR) and weight gain (WG) were all significantly improved by dietary P up to 9.4 g kg^?1 (P < 0.05) and then levelled off beyond this level. Broken‐line analysis showed maximum weight gain (WG) was obtained at dietary available P concentrations of 9.6 g kg^?1. With the increase in dietary P level, protein efficiency rate (PER) increased significantly and reached a plateau, while the feed conversion ratio (FCR), the mesenteric lipid somatic index (MSI) and the whole‐body lipid content significantly reduced (P < 0.05). Dietary P levels also affected the mineralization (ash and P) of whole body, vertebrae and scale (P < 0.05). Quadratic analysis based on P contents in whole body, vertebrae, scale and ash content in vertebra indicated that the available P requirements were 10.4, 9.8, 10.0 and 10.3 g kg^?1, respectively. However, no differences were found in the whole‐body moisture, crude protein, serum calcium (Ca) contents or Ca/P value, as well as the viscerosomatic index (VSI) and hepatosomatic index (HSI) among all the treatments (P > 0.05). Triglyceride (TG), total cholesterol (TC), high‐density lipoprotein cholesterol (HDL‐C) and low‐density lipoprotein cholesterol (LDL‐C) decreased significantly, while serum P content, HDL‐C/TC and HDL‐C/LDL‐C value increased significantly with dietary available P levels (P < 0.05). No significant changes in superoxide dismutase activity and malondialdehyde (MDA) content were observed (P > 0.05), but serum catalase (CAT) and glutathione peroxidase (GPx) activities and the ratio of CAT/SOD and GPx/SOD increased significantly with increasing dietary P levels (P < 0.05). In conclusion, the optimal P requirement of juvenile snakehead in practical feed was 9.6 g kg^?1. Signs of P deficiency were characterized by poor growth, slightly reduced mineralization and the antioxidant capacity and an increase in body lipid content.     

Effects of dietary L‐carnitine level on growth performance,body composition and antioxidant status in beluga (Huso huso L. 1758)

A 17‐week feeding trial was carried out to evaluate the effects of dietary L‐carnitine level in beluga, Huso huso. A total of fish averaging 1247 ± 15.6 g (mean ± SD) were randomly distributed into 18 fibreglass tanks, and each tank holding 10 fish was then randomly assigned to one of three replicates of six diets with 50, 150, 350, 650, 950 and 1250 mg L‐carnitine kg^?1 diet. At the end of 17 weeks of feeding trial, average weight gain (WG), feed efficiency (FE), protein efficiency ratio (PER) and condition factor (CF) of fish fed 350 mg kg^?1 diet were significantly (P < 0.05) higher than those of fish fed 50, 150, 950 and 1250 mg kg^?1 diets. WG, FE, PER and CF of beluga fed 650 mg kg^?1 diet were also significantly higher than those of fish fed 50, 950 and 1250 mg kg^?1 diets. Whole body and muscle protein were significantly improved by the elevation of dietary L‐carnitine level up to 350 mg kg^?1. Liver superoxide dismutase and glutathione peroxidase activities of fish fed 350 and 650 mg kg^?1 diets were significantly higher than those of fish fed 50, 950 and 1250 mg kg^?1 diets. The dietary L‐carnitine level of 350–650 mg kg^?1 diet could improve growth performance, feed utilization, protein‐sparing effects of lipid, antioxidant defence system and reproductive success. Polynomial regression of WG suggested that the optimum dietary L‐carnitine level was 480 mg kg^?1 diet. Therefore, these results may indicate that the optimum dietary L‐carnitine could be higher than 350 but <650 mg kg^?1 diet in beluga reared in intensive culture conditions.     

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 available phosphorus requirement for on‐growing gibel carp (Carassius auratus gibelio var. CAS III)

A nine‐week feeding experiment was conducted in flow‐through system with gibel carp (43.8 ± 0.2 g) to study the effects of dietary available phosphorus (P) on growth, phosphorous digestibility and intestinal enzyme activities. Seven semipurified diets were formulated to contain 0.8 (the basal), 2.4, 3.6, 6.1, 7.4, 10.1 and 15.8 g available phosphorus kg^?1 diet. The results showed that specific growth rate and feed efficiency increased with increasing dietary available P from 0.8 to 7.4 g P kg^?1. Fish body ash increased with increasing dietary available P, while moisture, protein content or energy content had no difference. Total phosphorus waste discharging (TPW) increased with increased dietary phosphorous. Plasma glucose was higher in the fish fed with 7.4 g kg^?1 P. Plasma triglycerides was lower in fish fed diets containing 6.1–10.1 g kg^?1 P. No significant effects were observed in plasma P and Ca (p > .05). The activities of intestinal amylase, lipase and trypsin showed no difference, while AKP and Na⁺, K⁺‐ATPase activities decreased with increasing dietary available P. In conclusion, based on the regression between specific growth rate (SGR), P retention efficiency, feed efficiency (FE) and dietary available P, the available P requirements for on‐growing gibel carp were 10.69, 8.22 and 6.72 g kg^?1, respectively.     

Effect of dietary zinc level on growth,enzyme activity and body trace elements of hybrid tilapia,Oreochromis niloticus × O. aureus,fed soya bean meal‐based diets

A feeding experiment was conducted to determine the dietary zinc (Zn) requirement of hybrid tilapia fed on a diet with soya bean meal as the sole protein source. The quantity of phytic acid in the experimental diet was 15.5 g kg^?1. Juvenile hybrid tilapia were fed on diets containing 31–227 mg Zn kg^?1 in triplicates for 6 weeks. Haematology of the fish was not affected by various dietary Zn levels. Fish fed on a diet containing 31 mg kg^?1 endogenous Zn showed the lowest growth rates, feed utilization, and body and plasma Zn levels. Weight gain (WG), plasma Zn level and superoxide dismutase (SOD) activity increased when a higher quantity of dietary Zn of 127 mg kg^?1 was administered to the experimental fish. Beyond this level, the values of these parameters were relatively stable. On the other hand, within the dietary Zn range tested, whole‐body Zn and ash increased with higher dietary Zn levels. Analysis using a broken‐line model showed that the dietary Zn requirements of hybrid tilapia fed on soya bean meal‐based diets containing 15.5 g kg^?1 endogenous phytic acid were 115, 115 and 105 mg kg^?1 based on WG, whole‐body Zn retention and plasma Zn level, respectively.     

Effects of dietary phosphorus and starch levels on growth performance,body composition and nutrient utilization of grass carp (Ctenopharyngodon idella Val.)

Six iso‐nitrogenous (410 g kg^?1) diets with three levels of total phosphorus (P4, P10 and P18 g kg^?1) and two levels of starch (S200 and S350 g kg^?1) were fed to triplicate groups of 30 fish to evaluate whether the high level of dietary phosphorus could improve the utilization of starch. Over 8‐week‐growth trial, best weight gain (WG) and specific growth rate (SGR) (P < 0.05) were observed in fish fed the P10/S200 and P18/S200 diets. WG and SGR significantly decreased as starch levels increased whereas for P4, while lipid contents of liver and whole body, hepatosomatic index and intraperitoneal fat ratio (IPF) significantly increased. These results suggested that high dietary starch will depress the growth performance and cause lipid accumulation. Within both starch levels, fish fed diet with P4 tended to produce lower (P < 0.05) WG and SGR, and had higher (P < 0.05) values of IPF. The whole body lipid, ash, calcium, phosphorus and iron contents were significantly affected by dietary phosphorus levels. Supplied phosphorus could improve the growth and decrease the whole body lipid, but there is no more effect after the phosphorus requirement was met at 10 g kg^?1.     

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.     

Dietary isoleucine requirement of juvenile blunt snout bream,Megalobrama amblycephala

A 9‐week feeding trial was conducted to estimate the dietary isoleucine requirement of juvenile blunt snout bream. Six isonitrogenous and isoenergetic experimental diets were formulated to contain graded isoleucine levels ranging from 5.3 to 20.1 g kg^?1 dry diet. At the end of the experiment, weight gain (WG), specific growth rate (SGR), feed efficiency ratio (FER) and protein efficiency ratio (PER) increased with increasing dietary isoleucine level up to 11.1 g kg^?1 dry diet, and dietary isoleucine level above 14.2 g kg^?1 dry diet declined these performances. Dietary isoleucine levels (14.2 and 17.3 g kg^?1 dry diet) significantly improved whole‐body protein content, but decreased whole‐body lipid, plasma triglyceride and cholesterol contents. Significantly lower visceral fat index (VFI) in fish fed with 14.2 g kg^?1 dietary isoleucine was observed compared to those fed with deficient or excessive isoleucine. Dietary isoleucine supplementation significantly increased plasma isoleucine concentration, while plasma valine and leucine concentrations showed a reversed trend. Dietary isoleucine levels regulated the target of rapamycin (TOR) gene expression and improved plasma superoxide dismutase (SOD) activity in juvenile blunt snout bream. Based on second‐order polynomial regression model analysis of SGR and FER, the optimum dietary isoleucine requirement was estimated to be 13.8 g kg^?1 dry diet (40.6 g kg^?1 dietary protein) and 14.0 g kg^?1 dry diet (41.2 g kg^?1 dietary protein), respectively.     

Supplementations of poultry by‐product meal and selenium yeast increase fish meal replacement by soybean meal in golden pompano (Trachinotus ovatus) diet

The effects of poultry by‐product meal (PBM) and selenium yeast (Se‐yeast) supplementations on fish meal replacement by soybean meal (SBM) in the diet of golden pompano (Trachinotus ovatus) were examined. In trial I, a 2 × 3 layout including two PBM levels (100 and 170 g kg^?1) and three levels of fish meal replacement (0, 40 or 60%) was used. At 100 g kg^?1 PBM, fish fed the basal diet exhibited the highest weight gain (WG) and nitrogen retention efficiency (NRE) and the lowest feed conversion ratio (FCR). At 170 g kg^?1 PBM, no significant differences were found in WG and NRE between fish fed the basal diet and diet with 40% of fish meal replaced by SBM. In trial II, the basal diet containing 170 g kg^?1 PBM (trial I) served as a reference. A 2 × 2 layout included two levels of fish meal replacement (40 or 60%) and two levels of Se‐yeast addition (0 and 1 g kg^?1). No significant differences were found in WG, feed intake, FCR and NRE between fish fed the reference diet and diet with 40 or 60% fish meal replacement plus 1 g kg^?1 Se‐yeast addition. This study indicates that supplementations of PBM and Se‐yeast can enhance the level of fish meal replacement by SBM in golden pompano diet. Dietary fish meal level can be reduced to 140 g kg^?1 by optimizing inclusion of SBM, PBM and Se‐yeast.     

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

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

Optimal dietary protein levels in juvenile Senegalese sole (Solea senegalensis)

A study was undertaken to determine the dietary protein level for optimal growth performance and body composition of juvenile Senegalese sole. Five experimental extruded diets were formulated to contain increasing levels of protein [430, 480, 530, 570 and 600 g kg^?1 dry matter (DM)] and a constant lipid level, ranging from 100 to 130 g kg^?1 DM. Triplicate groups of 35 sole (initial body weight: 11.9 ± 0.5 g) were grown over 84 days in 60‐L tanks supplied with recirculated seawater. Fish were fed by means of automatic feeders in eight meals per day. At the start and end of the trial, whole‐body samples were withdrawn for proximate composition analysis. At the end of 84 days of experimental feeding, daily weight gain and specific growth rate in fish fed diets P43 and P48 were significantly lower than those found in fish fed higher protein level diets (P53, P57 and P59). Similarly, feed efficiency was also significantly lower in fish fed diet P43 than in fish fed all other dietary treatments. Sole juveniles fed lower protein level diets (P43 and P48) showed a significantly lower protein content than fish fed the higher dietary protein level treatments (P53, P57 and P60). Changes within the tested dietary protein levels did not affect significantly protein productive value or total nitrogen (N) losses in fish. However, daily N gain was significantly higher (P < 0.05) in fish fed diets P53 and P60 than in fish fed the lowest protein level diet (P43). Data from the present study indicate that diets for juvenile Senegalese sole should include at least 53% crude protein to maintain a good overall growth performance. Based on a second‐order polynomial regression model, the daily crude protein requirement for maximum whole‐body N gain as estimated here for Senegalese sole juveniles was 6.43 g kg^?1 body weight day^?1 which corresponds to a value of 1.03 g N intake kg^?1 body weight day^?1. If the present data are expressed on a dietary crude protein concentration basis, the allowance for maximum protein accretion (N gain) would be met by a diet containing a crude protein level of 600 g kg^?1.     

Effects of dietary protein and lipid levels on growth,feed utilization and body composition in red‐tailed catfish juveniles (Hemibagrus wyckioides,Chaux & Fang 1949)

A feeding trial was conducted in a recycling water system during 10 weeks to determine the optimal protein to lipid ratio in Asian red‐tailed catfish (Hemibagrus wyckioides). Six diets of two protein levels (390 and 440 g kg^?1) with three lipid levels (60, 90 and 120 g kg^?1) were formulated. Fish (1.96 g) were fed six diets with four replicates to apparent satiation at a stocking density of 50 fish per tank (500 L). Faeces were collected in cultured tanks at the end of the feeding trial for digestibility measurement. Significantly, improved growth performances (P < 0.01) and higher feed utilization (P < 0.001) were observed in fish fed with higher lipid diets. However, higher protein diets did not significantly improve fish growth but they reduced FCR (P < 0.001) and protein efficiency ratio (P < 0.01). Higher lipid diets also resulted in significantly increased adipose‐somatic index, carcass fat and reduced moisture of the fish. The study revealed the protein sparing effect of dietary lipid in the catfish and highest growth performance was found by fish fed 390 g kg^?1 protein and 120 g kg^?1 lipid diet with P/E ratio of 20.48 mg protein kJ^?1. DP/DE ratio for maximal growth rate in diets was 21.48 mg protein kJ^?1.     

Dietary potassium requirement of juvenile grass carp (Ctenopharyngodon idella Val.) based on growth and tissue potassium content

A growth trial was conducted to estimate the optimum concentration of dietary potassium (K) for grass carp (Ctenopharyngodon idella). Triplicate groups of grass carp (3.96 ± 0.06 g) were fed diets containing graded levels (0.87, 2.90, 5.37, 7.54, 9.87 and 12.4 g kg^?1) of K for 8 weeks. Final body weight, weight gain and feed efficiency and gill Na⁺‐K⁺ ATPase activity were highest in fish fed with 9.87 g kg^?1 dietary K and lowest in fish fed the basal diet (P < 0.05). The K contents in whole body and muscle were linearly increased up to the 9.87 g kg^?1 dietary K and then levelled off beyond this level, whereas in scales and vertebrae up to the 7.54 g kg^?1 dietary K (P < 0.05). However, dietary K levels had no significant effect on ash, Ca, P and Mg contents in whole body, scales, vertebrae or muscle. Analysis using polynomial regression of weight gain and gill Na⁺‐K⁺ ATPase activity and using the broken‐line regression of whole body K concentrations indicated that the adequate dietary K concentration for grass carp is about 9.45–9.99 g kg^?1 diet.     

Dietary leucine requirement of Juvenile Nile tilapia,Oreochromis niloticus

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

Dietary 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.     

Comparative studies on dietary protein requirements of juvenile and on‐growing gibel carp (Carassius auratus gibelio) based on fishmeal‐free diets

Two trials were conducted to investigate protein requirements of juvenile (3.18 g in Trial 1) and on‐growing (87.1 g in Trial 2) gibel carp, Carassius auratus gibelio var. CAS III. Six isoenergetic diets containing 250–500 g kg^?1 dietary protein were formulated using soy protein concentrate (SPC) and casein as protein sources. The results showed that weight gain (WG) increased when dietary protein increased from 250 to 400 g kg^?1 and decreased at 400 to 500 g kg^?1 CP in Trial 1, while WG increased when dietary protein increased from 250 to 350 g kg^?1 and kept constant at 350 to 500 g kg^?1 CP in Trial 2. With increasing dietary protein, feed conversion ratio (FCR) decreased, while protein retention efficiency (PRE) decreased in Trial 1 and was not affected in Trial 2. Apparent digestibility coefficient of protein (ADC_p) increased with increasing dietary protein in two trails. Trypsin activity increased with dietary protein in the juveniles and was not affected in on‐growing fish. Hepatic alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities increased with dietary protein. Broken‐line and quadratic regression of WG estimated that dietary protein requirements for maximum growth were about 402–427 g kg^?1 for the juvenile and 337–418 g kg^?1 for on‐growing gibel carp.     

Combined effects of dietary mannan‐ and fructo‐oligosaccharide on growth indices,body composition,intestinal bacterial flora and digestive enzymes activity of regal peacock (Aulonocara stuartgranti)

A 56‐d feeding trial was conducted to investigate the effect of dietary mannan‐oligosaccharides (MOS) and fructo‐oligosaccharide (FOS) on growth indices, body composition, intestinal bacterial community and digestive enzymes activity of regal peacock. A total of 240 fish were randomly distributed to 15 experimental units (40‐L aquariums) of 16 fish each. These replicates were randomly assigned to one of five treatments in a 2 × 2 + 1 factorial arrangement. The treatments were control diet (no MOS and FOS), diet A (2 gkg^?1 MOS + 1.5 g kg^?1 FOS), diet B (2 g kg^?1 MOS + 3 g kg^?1 FOS), diet C (4 g kg^?1 MOS + 1.5 g kg^?1 FOS) or diet D (4 g kg^?1 MOS + 3 g kg^?1 FOS). The results showed that feeding diet C increased specific growth rate and protein efficiency ratio and decreased feed conversion ratio compared with control diet. Higher intestinal trypsin activity and increased Lactobacillus counts were observed in fish fed diets B and C. All diets significantly elevated body protein deposition and intestinal amylase activity compared to the control diet. In conclusion, the diet supplemented with 4 g kg^?1 MOS + 1.5 g kg^?1 FOS was advantageous over other MOS + FOS‐supplemented diets, with respect to growth performance and health benefits of regal peacock.     

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.     

Optimum dietary crude protein level for growth in South African abalone (Haliotis midae L.)

A 95‐day feeding trial was conducted to evaluate the effects of dietary crude protein level on total body weight gain and protein gain of juvenile (4.89 ± 0.57 g) South African abalone (Haliotis midae). Six semi‐purified diets containing casein, fish meal and cottonseed meal as protein sources, and with crude protein levels ranging from 54.8 to 479.2 g kg^?1 dry matter (DM), were fed to four tanks containing 30 abalone each in a continuous flow system. No differences (P > 0.05) were found in moisture, ash or lipid content of soft‐body tissue as dietary crude protein level increased, indicating that differences (P < 0.05) in soft‐body protein content were solely due to dietary crude protein level. The relationships between dietary crude protein level and total body weight gain and protein gain were analysed by broken‐line and second‐order polynomial regression models. Based on total body weight gain, 358.7 g kg^?1 DM dietary protein from good quality sources is recommended for maximum growth of juvenile H. midae, while, if dietary protein is reduced to 280.7 g kg^?1 DM, growth will be depressed with 5 g kg^?1.