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.     

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.     

Comparative study on the effects of chelated or inorganic manganese in diets containing tricalcium phosphate and phytate on the growth performance and physiological responses of turbot Scophthalmus maximus

A growth trial was conducted to evaluate the effects of chelated (Mintrex^? Mn, Mn‐M) or inorganic (MnSO₄·H₂O, Mn‐S) manganese (Mn) on growth, feed utilization, tissue Mn deposition and liver superoxide dismutase (SOD) activity in turbot Scophthalmus maximus. A semi‐purified basal diet was formulated to be deficient in Mn (3.7 mg kg^?1) and contained tricalcium phosphate and sodium phytate at levels of 20 and 5 g kg^?1, respectively. Ten other diets were made by adding five levels (5, 10, 20, 35 and 55 mg Mn kg^?1 diet) of either the Mn‐M or Mn‐S to the basal diet, respectively. The 11 experimental diets were fed to groups of turbot (mean initial weight: 4.6 g) for 8 weeks. Results showed that the specific growth rate (SGR), feed intake, whole body Mn/vertebra Mn concentration and Mn‐SOD activity in liver were significantly improved by Mn supplementation (P < 0.05). On the basis of SGR, vertebra Mn concentration or liver Mn‐SOD activity data, dietary Mn requirement was estimated to be 10.5, 46.3 or 12.9 mg kg^?1 for turbot fed Mn‐S, and the same was estimated to be 7.6, 43.0 or 22.5 mg kg^?1 for turbot fed Mn‐M, respectively. There was no significant difference in growth, feed intake, whole body Mn concentration or vertebra Mn concentration between the two dietary Mn sources (P > 0.05).     

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 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.     

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.     

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.     

Dietary selenium requirement for juvenile cobia,Rachycentron canadum L.

A 10‐week feeding trial was conducted to estimate the optimum dietary selenium (Se) requirement for juvenile cobia, Rachycentron canadum L. The basal diet was formulated to contain 50.6% crude protein from vitamin‐free casein, gelatin. A control diet (no added seleno‐dl ‐methionine) and five experimental diets containing 0.20, 0.40, 0.60, 0.80 and 1.00 mg seleno‐dl ‐methionine kg^?1 were prepared. Each diet was randomly fed to triplicate groups of juvenile cobia with initial weight 6.27±0.03 g in a flow‐through system. The Se concentration in rearing water was monitored during the feeding period, and was not detectable. The dietary Se level significantly influenced the survival, specific growth rate (SGR), feed efficiency and the Se concentrations in the whole body and vertebra of cobia. The Se‐dependent glutathione peroxidase (EC 1.11.119) activity increased with an increase in the dietary Se levels (P<0.05). Hepatic glutathione reductase (EC 1.6.4.2) activity was the highest in fish fed the diet with 0.21 mg Se kg^?1, and declined with an increase in the dietary Se levels. Based on broke‐line regression of SGR, the Se concentration in the whole body and vertebra, the Se requirements of juvenile cobia were 0.788, 0.811 and 0.793 mg Se kg^?1 diet in the form of seleno‐dl ‐methionine respectively.     

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.     

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 available phosphorus requirement of juvenile walking catfish,Clarias leather

A feeding trial was conducted to evaluate the optimum requirement of dietary available phosphorus (AP) for juvenile walking catfish, Clarias leather. Six practical diets were formulated to contain graded levels (2.2, 3.9, 5.5, 7.1, 8.8 and 10.4 g kg^?1) of AP from dietary ingredients and monocalcium phosphate. Each diet was randomly fed to triplicate groups of fish with initial mean weight of 7.94 ± 0.08 g in floating cages (1.5 × 1.5 × 2.0 m) suspended in an earthen pond, and each cage was stocked initially with 60 fish. Fish were fed thrice daily (07:30, 13:00 and 17:30) to apparent satiation for 10 weeks. Both specific growth rate (SGR) and protein efficiency ratio significantly increased with increasing AP from 2.2 to 5.5 g kg^?1 (P < 0.05) and then levelled off. Dietary AP levels significantly influenced whole‐body protein, lipid and ash contents as well as condition factor and hepatosomatic index (P < 0.05). Whole‐body and vertebrae phosphorus contents showed similar patterns as SGR in response to dietary AP content. Broken‐line analyses based on SGR, phosphorus contents in the vertebrae and whole‐body indicated the AP requirements were 5.8, 7.2 and 7.5 g kg^?1, respectively.     

Effects of dietary immunostimulant combination on the growth performance,non‐specific immunity and disease resistance of cobia,Rachycentron canadum (Linnaeus)

The aim of this study was to examine the effects of the immunostimulant combination (IC) containing β‐glucan, A3α‐peptidoglycan, vitamin C and vitamin E on the growth performance, non‐specific immunity and protection against Vibrio harveyi infection in cobia (Rachycentron canadum). Fish were fed diets containing six graded levels of IC (0, 1, 2, 3, 4 and 5 g kg^?1 diet) for 8 weeks. The results showed that the survival rate ranged from 81.1 to 84.4% with no significant difference among all the groups (P > 0.05) after the feeding experiment. Dietary IC significantly increased the specific growth rate (SGR), serum lysozyme, alternative complement pathway (ACH50) activity, phagocytosis percentage (PP) and respiratory burst activity of head kidney macrophages of cobia. Moreover, feeding of supplemented diets containing 3.0 g kg^?1 IC resulted in significantly lower mortality against the pathogens, V. harveyi compared with the control group. To elevate the growth and immune resistance ability of cobia, the optimal dose of dietary IC administration, determined by second‐order polynomial regression analysis was 3.43 and 2.71 g kg^?1 diet, respectively, on the basis of the SGR and mortality after challenge with V. harveyi.     

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.     

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.     

Growth performance and tissue mineral content of juvenile grouper (Epinephelus coioides) fed diets supplemented with various levels of manganese

This study was conducted to investigate the effect of dietary manganese (Mn) on growth, vertebrae and whole‐body Mn content of juvenile grouper, and to examine the effect of dietary Mn on copper (Cu), iron (Fe), zinc (Zn), calcium (Ca), phosphorus (P) and magnesium (Mg) content of vertebrae and whole body. Seven casein‐gelatin‐based diets were supplemented with 0, 5, 10, 15, 20, 50 and 1000 mg kg^?1 of Mn from MnSO₄·H₂O. Grouper with an initial weight of 12.9 ± 0.4 g were fed to satiation with one of the seven diets for 8 weeks. Growth was not significantly affected by dietary Mn supplements. Vertebrae Mn increased from 31.7 to 118.1 mg kg^?1 dry weight with dietary Mn supplement increasing from 0 to 50 mg kg^?1 (y = ?0.0002x³ + 0.0162x² + 1.3903x + 26.27, R² = 0.9561, where y is the vertebrae Mn content and x is the dietary Mn content). Whole‐body Mn increased from 2.5 to 7.8 mg kg^?1 wet weight with dietary Mn supplement increasing from 0 to 50 mg kg^?1 (y = 0.00001x³ ? 0.00107x² + 0.11054x + 2.24615, R² = 0.9080, where y is the whole‐body Mn content and x is the dietary Mn content). Dietary Mn had no significant effect on vertebrae Fe, Ca, P and Mg content, and whole‐body Cu, Zn and Mg content. However, vertebrae Zn and whole body Ca, P were highest in fish fed diet supplemented with 15 mg kg^?1 of Mn. Based on this, Mn supplement of 15 mg kg^?1 might be the optimum when the basal diet contained 4 mg kg^?1 of Mn. Fish fed diet supplemented with 1000 mg kg^?1 of Mn did not show any gross abnormality or change in feeding behaviour, but Mn contents of vertebrae and whole body were as high as 695.1 mg kg^?1 dry weight and 42.5 mg kg^?1 wet weight, respectively. Also, whole body Fe decreased significantly when Mn supplement was up to 1000 mg kg^?1.     

Effects of temperature and dietary protein on the growth performance and IGF‐I mRNA expression of juvenile mirror carp (Cyprinus carpio)

Juvenile mirror carp were fed with five different diets containing 303, 322, 341, 361 and 379 g kg^?1 protein and reared at three different water temperatures (18, 23 and 28 °C) for 60 days. We investigated the insulin‐like growth factor I (IGF‐I) mRNA expression, growth performance and the relationship between IGF‐I mRNA expression and the growth performance. The results indicated that the IGF‐I mRNA expression, final body weight, specific growth rate (SGR) and feed efficiency (FE) were enhanced significantly with increasing dietary protein levels (P < 0.05), whereas the protein efficiency ratio, hepatosomatic index (HSI) and viscerosomatic index (VSI) were decreased. Moreover, the IGF‐I mRNA expression, final body weight and SGR were increased significantly with temperature, whereas the HSI and VSI indices were decreased significantly with temperature. Correlation analysis showed that the IGF‐I mRNA expression levels in the brain and liver were positively related to the SGR and FE growth indices (P < 0.01). Finally, the optimal protein requirements for fish growth in different seasons were determined based on the values of SGR and FE, that is 343–348 g kg^?1 protein at 18 °C, 354–352 g kg^?1 at 23 °C and 371–362 g kg^?1 at 28 °C. In this way, we can adjust the dietary protein levels according to culture temperature to reduce any negative impacts on dietary costs and environmental pollution.     

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 manganese requirement of juvenile grass carp (Ctenopharyngodon idella Val.) based on growth and tissue manganese concentration

A growth trial was conducted to estimate the optimum concentration of dietary Manganese (Mn) for grass carp (Ctenopharyngodon idella). Triplicate groups of grass carp (3.97 ± 0.05 g) were fed diets containing graded levels (4.0, 8.9, 13.8, 18.7, 23.6 and 33.3 mg kg^?1) of Mn for 8 weeks. Weight gain, specific growth rate and feed efficiency were linearly increased up to the 18.7 mg kg^?1 dietary Mn and then levelled off beyond this level. For body composition, lipid contents in whole body, muscle and liver decreased significantly with increasing dietary Mn level. Grass carp fed with dietary Mn levels higher than 19.7 mg kg^?1 significantly decreased condition factor. Whole body, vertebrae and scales mineralization were all affected significantly by dietary Mn levels. Mn contents in whole body, vertebrae and scales were linearly increased up to the 18.7 mg kg^?1 dietary Mn and then levelled off beyond this level. Contrarily, Ca and P contents seem to be inversely related to dietary Mn. However, dietary Mn levels had no significant effect on body Fe contents. Broken‐line analysis indicated that 20.6 mg kg^?1 dietary Mn was required for maximal tissue Mn storage, as well as satisfied for the optimal growth of juvenile grass carp.     

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.     

Combined effects of dietary fructooligosaccharide and Bacillus licheniformis on growth performance,body composition,intestinal enzymes activities and gut histology of triangular bream (Megalobrama terminalis)

This study was conducted to investigate the effects of fructooligosaccharide (FOS) and Bacillus licheniformis (B. licheniformis) on growth performance, body composition, intestinal enzymes activities and gut histology of Megalobrama terminalis. Nine experimental diets were formulated to contain three FOS levels (0, 3 and 6 g kg^?1) and three B. licheniformis levels (0, 1 and 5 × 10⁷ CFU g^?1) following a 3 × 3 factorial design. Accordingly, diets were named as 0/0, 0/3, 0/6, 1/0, 1/3, 1/6, 5/0, 5/3 and 5/6 (B. licheniformis/FOS). At the end of the 8‐week feeding trial, weight gain (WG) and specific growth rate (SGR) of fish fed 6 g kg^?1 FOS were both significantly (P < 0.01 and P < 0.05) higher than that of the other groups in terms of dietary FOS levels. Besides, WG and SGR of fish fed 1 × 10⁷ CFU g^?1 B. licheniformis were significantly (P < 0.05) higher than that of the control group in terms of dietary B. licheniformis levels. In addition, a significant interaction (P < 0.05) between dietary FOS and B. licheniformis was observed in finial weight, WG, SGR as well as the survival rate with the highest values all observed in fish fed diet 1/3. Hepatosomatic index, carcass lipid content, lipase activities as well as microvilli length increased significantly (P < 0.05) from 0 to 1 × 10⁷ CFU g^?1, but no significant difference (P > 0.05) was observed in terms of dietary FOS levels. In addition, a significant (P < 0.05) interaction of FOS and B. licheniformis was observed in both protease and Na⁺, K⁺‐ATPase activities with the highest value obtained in fish fed diet 1/3. The results indicated that the dietary applications of dietary FOS and B. licheniformis alone or in combination can significantly improve the growth performance, survival rate, intestinal enzymes activities as well as microvilli length of triangular bream. In addition, there is a significant interaction between dietary FOS and B. licheniformis. The best combination for this species is 3 g kg^?1 FOS with 1 × 10⁷ CFU g^?1 B. licheniformis.