Effects of dietary chitosan oligosaccharide complex with rare earth on growth performance and innate immune response of turbot,Scophthalmus maximus L.

An 8‐week‐feeding trial was conducted to investigate the effect of dietary chitosan oligosaccharide complex with rare earth (COS‐REE) on growth performance and innate immune response of turbot, Scophthalmus maximus L. (Initial average weight was (12.1 ± 0.1) g) as well as disease resistance against Edwardsiella tarda. Six practical diets (approximately 53.01% protein and 12.57% lipid) were formulated to contain graded levels (0, 75, 150, 300, 600 and 1200 mg kg^?1) of COS‐REE. Results of the present study showed that, compared to the control group (0 mg kg^?1), the specific growth rate (SGR) was significantly higher in fish fed the diet with 300 mg kg^?1 COS‐REE (P < 0.05), while the feed conversion ratio (FCR) significantly decreased (P < 0.05). The phagocytic index (PI) and the activity of super oxide dismutase (SOD) of serum in fish fed the diet with 300 mg kg^?1 COS‐REE was significantly higher than fish fed the control diet (P < 0.05), but no significant differences were observed in malondialdehyde (MDA) and hepatic metallothionein (MT) concentrations. After 8 weeks, fish were challenged by intraperitoneal injection with E. tarda, and COS‐REE‐treated fish demonstrated increased protection capability. These results suggested that COS‐REE could enhance growth, innate immunity and disease resistance in turbot, and the optimum dose was approximately 300 mg kg^?1.     

Dietary manganese requirement for juvenile cobia,Rachycentron canadum L

A 10‐week feeding trial was conducted to estimate the optimum dietary manganese requirement for juvenile cobia, Rachycentron canadum L. The basal diet was formulated to contain 501 g kg^?1 crude protein from vitamin‐free casein, gelatin and fish protein concentrate. Manganese sulphate was added to the basal diet at 0 (control group), 6, 12, 18, 24 and 36 mg Mn kg^?1 diet providing 5.98, 7.23, 16.05, 23.87, 28.87 and 41.29 mg Mn kg^?1 diet, respectively. Each diet was randomly fed to three replicate groups of cobia for 10 weeks, and each tank was stocked with 30 fish (initial weight, 6.27 ± 0.03 g). The manganese concentration in rearing water was monitored during the feeding period and was < 0.01 mg L^?1. Dietary manganese level significantly influenced survival ratio (SR), specific growth ratio (SGR), feed efficiency ratio (FER) and the manganese concentrations in the whole body, vertebra and liver of cobia. When the dietary manganese level rose from 5.98 mg kg^?1 to 23.87 mg kg^?1, the superoxide dismutase (SOD; EC 1.15.1.1) activities in liver also increased (P < 0.05). But there was no significant change in SOD activities for the groups fed with diets containing manganese level higher than 23.87 mg kg^?1. On the basis of broken‐line regression of SGR, manganese concentration in whole body and vertebra the manganese requirements of juvenile cobia were 21.72 mg kg^?1, 22.38 mg kg^?1 and 24.93 mg kg^?1 diet in the form of manganese sulphate, respectively.     

Effects of dietary manganese source and supplemental levels on growth performance,antioxidant enzymes activities,tissue Mn concentrations and cytosolic manganese superoxide dismutase (cMnSOD) mRNA expression level of juvenile Litopenaeus vannamei

This experiment was conducted to study the effects of different forms and levels of manganese (Mn) on the growth performance, antioxidant activities, tissue Mn content and cytosolic manganese superoxide dismutase (cMnSOD) gene expression of Litopenaeus vannamei. Treatments consisted of 0, 10, 20, 30, 40 and 60 mg Mn kg^?1 from manganese sulphate (Mn‐S) and manganese methionine (Mn‐Met), providing the actual dietary value of 5.17, 15.62, 25.55, 34.22, 44.48 and 67.90 mg Mn kg^?1 Mn‐S, and 5.17, 15.71, 25.36, 35.86, 45.16 and 65.06 mg Mn kg^?1 Mn‐Met, respectively. Each diet was fed to triplicate groups of L. vannamei (initial body weight: 1.925 ± 0.002 g) in a recirculated fresh water rearing system for 8 weeks. Weight gain rate (WGR) increased in prawns provided with from 25.55 to 44.48 mg Mn kg^?1 Mn‐S and 15.71 to 45.16 mg Mn kg^?1 Mn‐Met and then declined above these levels. The lowest protein efficiency ratio (PER) and the highest feed conversion rate (FCR) were observed in prawns fed the control diet (P < 0.05) and showed no significant differences among other treatments (P > 0.05). Survival rate (SR) was not affected by the dietary treatments (P > 0.05). Total SOD and Mn‐SOD activities were higher in the hepatopancreas of prawns fed with Mn‐supplemented diets from 15.71 to 44.48 mg Mn kg^?1 (P < 0.05). On the contrary, malondialdehyde (MDA) content was lower in the hepatopancreas of prawns fed the basal diet (P < 0.05). Mn concentrations in the hepatopancreas and muscles increased with increasing levels of dietary Mn supplementation. Moreover, Mn accumulation was lower in the muscle than in the hepatopancreas of the prawns. The mRNA expression of cMnSOD gene in the hepatopancreas of prawns was upregulated with increasing dietary Mn levels of Mn‐S from 25.55 to 44.48 mg Mn kg^?1, Mn‐Met from 15.71 to 45.16 mg Mn kg^?1 and then plateaued above these levels. Broken‐line regression analysis of WGR indicated that the optimal dietary Mn requirements for juvenile L. vannamei were 32.26 mg Mn kg^?1 Mn‐S and 23.90 mg Mn kg^?1 Mn‐Met, respectively.     

Effects of dietary ethoxyquin on growth,feed utilization and residue in the muscle of juvenile Japanese seabass,Lateolabrax japonicus

Ethoxyquin (EQ) is the most common synthetic antioxidant used for preventing rancidity in fish foodstuffs. However, literature related to the effects of dietary EQ on performance of fish was limited. The present study was conducted to investigate the effects of EQ on performance and EQ residue in muscle of juvenile Japanese seabass Lateolabrax japonicus and to estimate the optimal EQ concentration in the diet. Graded levels [0 (control), 50, 150, 450 and 1350 mg EQ kg^?1 diet] of EQ were added to the basal diet, resulting in five dietary treatments in the experiment. Each diet was fed to triplicate groups of seabass (initial body weight 8.01 ± 0.76 g) for 12 weeks in floating sea cages (1.5 × 1.5 × 2.0 m, 30 fish per cage). Survival ranged from 78.9 to 86.7%, and was irrespective of dietary EQ levels. The specific growth rate (SGR) of fish fed diets supplemented with ≤50 mg kg^?1 EQ had significantly (P < 0.05) higher SGR than fish fed diets supplemented with ≥150 mg kg^?1 EQ, the highest SGR was observed in fish fed diet with 50 mg kg^?1 EQ supplementation. Feed intake (FI) and feed efficiency (FE) were not significantly (P > 0.05) different among dietary treatments. Fish fed diets with 50 and 1350 mg kg^?1 EQ had a significant (P < 0.05) lower body lipid content than fish in the control group. Muscle EQ level significantly increased when dietary EQ increased. Optimal EQ concentration estimated by polynomial regression based on maximum growth of juvenile Japanese seabass was 13.78 mg kg^?1 diet.     

Dietary nucleotides improve the growth performance,antioxidative capacity and intestinal morphology of turbot (Scophthalmus maximus)

A growth trial was conducted to evaluate the effects and safety of nucleotides in low fish meal diets on the growth performance, antioxidative capacity and intestinal morphology of turbot (Scophthalmus maximus). High fish meal control diet was formulated with 500 g kg^?1 fish meal. Seven levels (0.075, 0.15, 0.225, 0.300, 1.5 and 3.0 g kg^?1, respectively) of nucleotides were added to a low fish meal basal diet, which was formulated with 400 g kg^?1 fish meal. The eight experimental diets were fed to groups of juvenile turbot (initial weight: 6.0 ± 0.03 g) for 60 days. Results showed that compared with high fish meal control diet, low fish meal basal diet treatment had lower total antioxidative capacity (T‐AOC), glutathione peroxidase activity, fold height of proximal and distal intestine, enterocyte height of all evaluated enteric section and microvillus height of mid‐intestine and distal intestine (P < 0.05). However, supplemented nucleotides in diets could significantly improve growth (specific growth rate, SGR), feed utilization, antioxidative capacity and intestinal morphology of turbot (P < 0.05). Broken‐line regression analysis of SGR and T‐AOC showed that the optimal supplemental levels of dietary nucleotide for juvenile turbot were 0.366 and 0.188 g kg^?1, respectively. In summary, 0.300 g kg^?1 of dietary nucleotides was helpful in improving growth, feed utilization, antioxidative capacity and intestinal morphology of turbot fed with low fish meal diet. Excessive dietary nucleotides (3.0 g kg^?1) might cause oxidative stress and morphological damage in intestine and then reduce the growth of turbot.     

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

A 12‐week growth trial was conducted in a flow‐through system to determine dietary selenium (Se) requirement for on‐growing gibel carp (initial body weight: 76.2 ± 0.05 g, mean ± SEM). Selenomethionine was supplemented to the basal diet to formulate seven semi‐purified diets containing 0.26, 0.58, 0.72, 1.14, 1.34, 1.73 and 2.09 mg Se kg^?1 diet. The results showed that plasma superoxide dismutase (SOD) activity significantly increased when fish were fed with 0.58 mg Se kg^?1 diet (P < 0.05) and then decreased at 2.09 mg Se kg^?1 diet (P < 0.05). Plasma T‐AOC activity was higher in fish fed with 0.72 mg Se kg^?1 diet (P < 0.05) and plasma malondialdehyde (MDA) was higher in fish fed with 0.26 mg Se kg^?1 diet (P < 0.05). When fish were fed 1.14 mg Se kg^?1 diet, hepatic GSH‐Px, T‐AOC, GSH and CAT activities were significantly higher than those fed with 0.26 mg Se kg^?1 diet (P < 0.05). Hepatic superoxide dismutase (SOD) activity was higher at 1.34 mg Se kg^?1 diet (P < 0.05). Fish liver Se concentrations were significantly higher when fed with 0.72 mg Se kg^?1 diet (P < 0.05) and then kept constant when Se ≥ 0.72 mg kg^?1 (P > 0.05). Whole‐body and muscle Se concentrations were higher when fed with 1.34 mg Se kg^?1 diet (P < 0.05) and kept a plateau when Se ≥ 1.34 mg kg^?1 (P > 0.05). In conclusion, based on broken‐line regression of hepatic Se concentrations, hepatic SOD activity and hepatic T‐AOC activity, dietary Se requirements for on‐growing gibel carp was 0.73 mg kg^?1, 1.12 mg kg^?1 and 1.19 mg kg^?1 diet respectively.     

Effect of graded levels of dietary thiamine on the growth performance,body composition and haemato‐biochemical parameters of juvenile Sclizothorax prenanti

This study was conducted to determine dietary thiamine requirement of juvenile Sclizothorax prenanti and evaluate the effect of dietary thiamine levels on growth performance, body composition and haemato‐biochemical parameters for this fish species. The seven experimental diets were formulated to contain the graded levels of thiamine (0, 10, 20, 30, 40, 60 and 100 mg kg^?1 diet, respectively), providing the actual dietary thiamine values of 0.31 (control), 9.82, 21.49, 29.83, 41.66, 62.24 and 114.58 mg kg^?1 diet, respectively. Each diet was assigned to three replicate groups of S. prenanti (initial body weight: 13.46 ± 0.28 g, means ± SD) for 60 days. Increasing dietary thiamine level up to 21.49 mg kg^?1 diet increased weight gain rate (WGR), specific growth rate (SGR), feed efficiency (FE) and protein efficiency ratio (PER) (P < 0.05), beyond which they remained nearly unchanged. Similarly, hepatic thiamine concentration and several serum biochemical parameters (transketolase activity, triglyceride and total cholesterol contents) increased with increasing levels of thiamine up to 21.49 mg kg^?1 diet (P < 0.05) and, thereafter, remained almost constant. However, no significant differences in body composition (moisture, protein, lipid and ash contents) were found among dietary thiamine treatments (P > 0.05). Analysis by the broken‐line regression of WGR, SGR, FE, PER, hepatic thiamine concentration and serum transketolase activity indicated that dietary thiamine requirements in juvenile S. prenanti were 18.45–25.91 mg kg^?1 diet.     

Effects of dietary manganese sources and levels on growth performance,relative manganese bioavailability,antioxidant activities and tissue mineral content of juvenile cobia (Rachycentron canadum L)

This study was conducted to compare the effects of manganese sulphate (Mn‐S), glycine manganese(Mn‐Gly) and manganese 2‐hydroxy‐4‐(methylthio)butyrate (Mn‐HMB) on juvenile cobia, Rachycentron canadum L. Treatments consisted of 0, 2, 4, 8, 16 or 32 mg supplemental Mn kg^?1 from Mn‐S, Mn‐Gly or Mn‐MHB. Growth performance, manganese status, antioxidant activities and tissue mineral content were analysed after a 70‐day feeding period. Specific growth rate (SGR) increased with feeding 6.29 to 12.65 mg Mn kg^?1 diet from the Mn‐S or 6.86 to 12.39 mg Mn kg^?1 from the Mn‐Gly or 6.50 to 8.33 mg Mn kg^?1 from the Mn‐HMB and then plateaued above these levels. Feed conversion ratio (FCR) show decreasing first and then increased trend. Survival rate (SR) were not affected by the dietary treatments (P > 0.05). Fish fed diets supplemented with manganese at levels of 4–32 mg Mn kg^?1 had obviously higher hepatic Mn‐SOD activity (P < 0.05); on the contrary, hepatic has lower malondialdehyde (MDA) content (P < 0.05) than fish fed the basal diet. The manganese concentrations of whole body and vertebrae increased with increasing dietary Mn levels from 2–32 mg Mn kg^?1 (independent on manganese sources). Dietary Mn supplementation did not significantly influence the copper concentrations of whole body and vertebrae, the zinc concentrations of whole body and liver. Analysis by the broken‐line regression of SGR indicated that the optimal dietary Mn requirements in juvenile cobia were 15.42, 11.22 and 10.50 mg Mn kg^?1 diet from Mn‐S, Mn‐Gly or Mn‐HMB respectively.     

Effects of dietary choline on growth performance,lipid deposition and hepatic lipid transport of grouper (Epinephelus coioides)

The number of 360 individuals with an average initial weight of 87.8 ± 0.04 g was fed six diets containing graded levels of choline at 8.1 (control group), 602.5, 1119.0, 1511.5, 1970.0 and 4029.0 mg choline kg^?1 diet, respectively, to investigate the effects of dietary choline on growth performance, lipid deposition and hepatic lipid transport for grouper, Epinephelus coioides. Dietary methionine was estimated to be 10.02 g kg^?1, less than the requirement (13.10 g kg^?1). The results of 10‐week study period indicated that the best values of specific growth rate (SGR), feed conversion rate (FCR) and protein efficiency rate (PER) all occurred in 1119.0 mg choline kg^?1 diet (P < 0.05). The survival range increased from 8.1 to 1511.5 mg choline kg^?1 diet and then plateaued. Dietary choline supplementation significantly decreased the liver lipid content of grouper (P < 0.05), but the lipid content of the muscle tended to be increased firstly and then decreased (P < 0.05). Liver choline concentration reached a plateau in 1511.5 mg choline kg^?1 diet and then levelled off (P < 0.05). Serum high density lipoprotein‐cholesterol (HDL‐C) and total cholesterol (TCHO) levels were firstly decreased and then increased with dietary choline supplementation. A reversed tendency, however, was found in triglyceride. Broken‐line regression analysis of SGR and liver choline content indicated that choline requirement of grouper was 1093.7 and 1579.7 mg kg^?1 diet, 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 vitamin C on the growth performance,antioxidant ability and innate immunity of juvenile yellow catfish (Pelteobagrus fulvidraco Richardson)

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

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

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

Dietary choline requirement in slight methionine‐deficient diet for juvenile gibel carp (Carassius auratus gibelio)

A 10‐week feeding trial was conducted in a flow‐through system to determine dietary choline requirement for juvenile gibel carp (Carassius auratus gibelio) (5.5 ± 0.1 g). Purified basal diet was formulated using vitamin‐free casein as protein source. Choline chloride was supplemented to the basal diet to formulate seven diets containing 76.1, 163, 356, 969, 1457, 2024 and 4400 mg kg^?1 choline. Dietary methionine was 0.58%, less than the requirement (0.69%). The results indicated that specific growth rate (SGR) was higher in the fish fed 2024 mg kg^?1 diet than the control group. Feeding rate and feed efficiency were not significantly affected. Protein productive value increased as dietary choline increased from 76.1 to 2024 mg kg^?1 diet and was lower in the fish fed the diet containing 4400 mg choline kg^?1 diet. Serum high‐density lipoprotein cholesterol (HDL‐C) and total cholesterol significantly increased with increasing dietary choline up to 1457 mg kg^?1, and no differences were found with further increase. Fish carcass fat contents decreased significantly with increased dietary choline. Hepatic lipid contents increased with dietary choline up to 1457 mg kg^?1 and then decreased. Quadric regression of SGR and plasma HDL‐C indicted dietary choline requirement was 2500 and 2667 mg kg^?1 diet, respectively.     

Growth,digestive and absorptive abilities and antioxidative capacity in the hepatopancreas and intestine of young grass carp (Ctenopharyngodon idellus Val.) fed graded levels of dietary manganese

To study the effects of manganese on growth performance, digestive and absorptive abilities, as well as the antioxidative capacity in the hepatopancreas and intestine, young grass carp (Ctenopharyngodon idellus Val.) (264 ± 1 g) were fed diets containing graded levels of manganese at 3.65 (control), 8.62, 13.48, 18.24, 22.97 and 27.86 mg kg^?1 diet for 8 weeks. Per cent weight gain (PWG) and feed intake were the poorest in fish fed the basal diet (P < 0.05). The activities of trypsin, lipase and alkaline phosphatase in the intestine were significantly enhanced with dietary manganese level at 13.48 mg kg^?1 diet (P < 0.05). Additionally, in the hepatopancreas and intestine, the protein carbonyl and malondialdehyde contents were the lowest in fish fed the diet with dietary manganese level at 13.48 mg kg^?1 diet (P < 0.05), while the anti‐hydroxyl radical capacities, manganese superoxide dismutase (MnSOD), glutathione peroxidase and glutathione‐S‐transferase activities were significantly enhanced with dietary manganese level at 13.48 mg kg^?1 diet (P < 0.05). Moreover, the catalase activity and glutathione content in the intestine were the highest in fish fed the diet with dietary manganese level at 18.24 mg kg^?1 diet (P < 0.05). These results indicated that optimum dietary manganese promoted growth, enhanced the digestive and absorptive abilities, and improved the antioxidative capacity in young grass carp. Based on the quadratic regression analysis for PWG and intestinal MnSOD activity, the manganese requirements for young grass carp with the initial body weight of 264 g were 16.91 and 18.21 mg kg^?1 diet respectively.     

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.     

Effect of dietary selenium level on growth performance,body composition and hepatic glutathione peroxidase activities of largemouth bass Micropterus salmoide

An 8‐week growth trial was conducted to determine the effect of dietary selenium (Se) level on growth performance, body composition and hepatic glutathione peroxidase (GPx) activities of largemouth bass. Sodium selenite was added to the fish meal basal diet at 0, 0.2, 0.4, 0.6, 0.8 and 1.0 mg kg^?1 Se providing 0.97, 1.17, 1.42, 1.60, 1.85 and 2.06 mg Se kg^?1 diet respectively. Each diet was fed to triplicate groups of fish (initial mean body weight: 4.95 ± 0.03 g) in a closed indoor recirculating system. The Se concentration in the rearing water was not detectable during the whole experimental period. The highest weight gain was obtained in fish fed diets with 1.60 mg Se kg^?1, which was significant higher (P < 0.05) than the basal diet with 0.97 mg Se kg^?1 and did not differ significantly (P > 0.05) with the other treatments. Feed conversion ratio, protein efficiency ratio, protein productive value, apparent digestibility coefficients of dry matter and muscle composition were not significantly impacted (P > 0.05) by dietary treatments. Fish fed diets with ≥1.42 mg Se kg^?1 obtained higher liver lipid contents than treatments with lower dietary Se levels. Hepatic malondialdehyde (MDA) was unchanged (P > 0.05) in relation to dietary Se concentration. Hepatic GPx and glutathione reductase (GR) activities markedly increased and decreased (P < 0.05) with increasing dietary Se concentration, respectively, and both reached a plateau with ≥1.85 mg Se kg^?1. Based on growth performance, hepatic MDA and enzymatic responses of GPx and GR, the highest Se concentration (2.06 mg kg^?1) employed in our study was not harmful for largemouth bass, and the optimal dietary level should be 1.60–1.85 mg Se kg^?1 from sodium selenite, at a dietary vitamin E level of 400 IU kg^?1.     

The impaired flesh quality by iron deficiency and excess is associated with increasing oxidative damage and decreasing antioxidant capacity in the muscle of young grass carp (Ctenopharyngodon idellus)

To investigate effects of iron (Fe) on growth, haematological parameters, flesh quality and antioxidant status in muscle, young grass carp (Ctenopharyngodon idella) (292.0 ± 3.2 g) were fed graded levels of Fe (20.7, 38.4, 52.8, 79.3, 98.0 and 120.0 mg kg^?1 diet) for 8 weeks. Per cent weight gain (PWG) and feed intake were improved with Fe levels up to 52.8 mg kg^?1 diet. Serum Fe, erythrocyte counts, haemoglobin (Hb), haematocrit and mean cell haemoglobin increased with optimal Fe levels (38.4–79.3 mg kg^?1 diet) (P < 0.05). The muscle protein and lipid contents were increased by dietary Fe, whereas moisture, liquid loss, shear force and hydroxyproline contents followed opposite trends. Malondialdehyde and protein carbonyl contents in muscle were the lowest in fish fed the 52.8 or 79.3 mg Fe kg^?1 diet, respectively, while superoxide dismutase, catalase, glutathione‐S‐transferase, glutathione peroxidase and glutathione reductase activities, and glutathione content were increased by Fe levels up to 52.8–79.3 mg kg^?1 diet. Results indicated that the optimal Fe improved growth, flesh quality and muscle antioxidant defence of young grass carp. Dietary Fe requirements for PWG, serum Fe and Hb of young grass carp (292–695 g) were 73.5, 72.8 and 69.0 mg kg^?1 diet, respectively.     

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

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

Quantifying the dietary potassium requirement of subadult grass carp (Ctenopharyngodon idellus)

A growth trial lasting for 12 weeks was conducted in 21 net cages to determine the dietary potassium (K) requirement of subadult grass carp (Ctenopharyngodon idellus) (Average weight: 331.3 g). Seven isonitrogenous and isoenergetic semi‐purified diets were compounded with different dietary K level. The specific growth rate (SGR) of fish was significantly (P < 0.05) improved by dietary K supplementation, SGR and the gill Na⁺‐K⁺ ATPase activity increased first and then decreased (P < 0.05) as dietary K level increased. The highest SGR and gill Na⁺‐K⁺ ATPase activity values were both observed at 6.38 g kg^?1 group. Dietary K level showed significant (P < 0.05) effect on serum superoxide dismutase (SOD) and glucose (GLU), the maximum values of SOD and GLU were in 8.42 and 6.38 g kg^?1 group, respectively. The body lipid content of the 6.38 g kg^?1 group was significantly (P < 0.05) lower than that of the control. However, the ash content in the 8.42 g kg^?1 group was significantly higher than those in the 1.21, 2.21, 4.41 and 6.38 g kg^?1 group. When dietary protein was 320 g kg^?1 and the waterborne potassium ranged from 6.86 to 9.10 mg L^?1, the dietary K requirement for subadult grass carp judged from SGR and gill Na⁺‐K⁺ ATPase activity is 5.38 and 7.41 g kg^?1 diet, respectively.     

Effects of dietary protein and lipid levels on growth,feed utilization and body composition in Pseudobagrus ussuriensis fingerlings

An 8‐week feeding trial was conducted to investigate the optimum dietary protein and lipid levels for growth, feed utilization and body composition of Pseudobagrus ussuriensis fingerlings (initial weight: 3.40 ± 0.01 g). Twelve diets containing four protein levels (350, 400, 450 and 500 g kg^?1 crude protein) and three lipid levels (50, 100 and 150 g kg^?1 crude lipid) were formulated. Fish were randomly allotted to 36 aquaria (1.0 × 0.5 × 0.8 m) with 25 fish to each glass aquarium. Fish were fed twice daily (08:00 and 16:00) to apparent satiation. The results showed that weight gain and specific growth rate (SGR) decreased with increasing dietary lipid level from 50 to 150 g kg^?1 at the same dietary protein level. Fish fed the diets containing 150 g kg^?1 lipid exhibited higher feed conversion ratio (P < 0.05), lower protein efficiency ratio (PER) and nitrogen retention efficiency (NRE) relative to fish fed the diet containing 50 and 100 g kg^?1 lipid. Weight gain and SGR significantly increased with increasing dietary protein from 350 to 450 g kg^?1 at the same dietary lipid level, and even a little decline in growth with the further increase in dietary protein to 500 g kg^?1. Daily feed intake, NRE and PER were significantly affected by both dietary protein and lipid levels (P < 0.05) and tended to decrease with increasing dietary protein and lipid levels. Whole‐body protein content increased as protein levels increased and lipid levels decreased. Whole‐body lipid and muscle lipid content increased with increasing dietary lipid level, and decreased with increasing dietary protein at each lipid level. There was no significant difference in condition factor and viscerosomatic index among fish fed the diets. Hepatosomatic index was affected by dietary lipid level (P < 0.05), and increased with increasing dietary lipid level at the same protein level. These results suggest that the diet containing 450 g kg^?1 protein and 50 g kg^?1 lipid with a P/E ratio of 29.1 mg protein kJ^?1 is optimal for growth and feed utilization of P. ussuriensis fingerlings under the experimental conditions used in the study.