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.     

Manganese supplementation of a practical, fish meal based diet for Atlantic salmon parr

This experiment was conducted to study whether practical fish meal based feeds for Atlantic salmon, Salmo salar L., require manganese (Mn) supplementation. Three thousand parr of initial weight 4.7 g were randomly distributed into 10 tanks and given a fish meal based diet, either unsupplemented or supplemented with 5, 10, 50 or 100 mg Mn kg^?1 (as MnSO₄*H₂O) for 12 weeks. The basal diet contained 4.8 mg Mn kg^?1. Mn concentration in vertebrae and whole fish responded linearly to supplemented Mn up to a level of 10 mg kg^?1 and then reached a plateau. Dietary Mn supplementation did not affect weight gain, liver Mn concentration, blood haemoglobin concentration or haematocrit. To the practical feed, a supplementary level of 10 mg Mn kg^?1, giving a total Mn concentration of 15 mg kg^?1 diet, was necessary to maintain normal Mn status as determined by Mn level in vertebrae and whole fish. However, taking into account the variable Mn content in fish meal and the uncertainty about availability, we recommend a general supplementation of 15 mg Mn kg^?1.     

Effect of dietary magnesium supplementation on the growth performance of juvenile gibel carp,Carassius auratus gibelio

Gibel carp (Carassius auratus gibelio) of mean initial weight 3.1 g were fed one of seven casein‐dextrin‐based diets containing graded levels of magnesium (Mg) (39, 120, 220, 380, 700, 1600 and 2900 mg kg^?1) for 3 months with the waterborne Mg concentration of 10.6–12.7 mg L^?1. Magnesium sulphate was used as the supplementation Mg source in the diets. The experiment was carried out in a flow‐through system. Growth, survival rate, Na⁺/K⁺‐ATPase, Mg²⁺‐ATPase and tissue mineral contents were measured to investigate the effect of dietary magnesium in gibel carp. At the end of the experiment, the hepatopancreas of fish were collected for enzyme determination. The hepatopancreas, vertebrae and whole body were collected for tissue magnesium content analysis. After 3 months, dietary magnesium supplementation did not improve the growth performance, including feed intake, weight gain and feed conversion efficiency of juvenile gibel carp. On the contrary, negative impacts on survival, reduced growth performance and dramatically decreased Na⁺/K⁺‐ATPase, Mg²⁺‐ATPase and superoxide dismutase activities were observed in gibel carp fed a high Mg diet of 2900 mg kg^?1. Although serum and hepatopancreas Mg and Ca contents were not affected by dietary Mg supplementation, vertebrae and whole‐body Mg contents increased significantly with the increasing dietary Mg concentrations. Based on the relationship between whole‐body Mg retention and dietary Mg concentration, a suitable dietary Mg level of 745 mg kg^?1 could be estimated for gibel carp. It could be concluded that dietary Mg supplementation did not improve the growth performance, but could increase vertebrae Mg contents of gibel carp. Considering the adverse effects, a dietary Mg concentration of above 2900 mg kg^?1 is not recommended and it should be careful to supplement magnesium in practical diets for gibel carp as most feed ingredients contain high magnesium concentrations.     

Dietary magnesium requirement and effects on growth and tissue magnesium content of juvenile grass carp (Ctenopharyngodon idella)

A growth trial was conducted to estimate the optimum concentration of dietary magnesium (Mg) for grass carp (Ctenopharyngodon idella). Triplicate groups of grass carp (5.56 ± 0.02 g) were fed diets containing graded levels (187, 331, 473, 637, 779 and 937 mg kg^?1) of Mg for 8 weeks. Weight gain, specific growth rate and feed efficiency were linearly increased up to 637 mg kg^?1 dietary Mg and then levelled off beyond this level. For body composition, dietary Mg levels higher than 473 mg kg^?1 significantly decreased the moisture content but increased the lipid content of whole body, muscle and liver. Dietary Mg levels higher than 473 mg kg^?1 significantly decreased the ash contents of vertebrae, scales and muscle. Mg contents in whole body, vertebrae, scales and plasma were increased up to 637 mg kg^?1 dietary Mg and then levelled off beyond this level. However, Ca and P contents seem to be inversely related to dietary Mg. Dietary Mg levels higher than 473 mg kg^?1 significantly decreased Zn and Fe contents in whole body and vertebrae. Broken‐line analysis indicated that 687 mg kg^?1 dietary Mg was required for maximal tissue Mg storage, as well as satisfied for the optimal growth.     

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.     

Dietary magnesium requirements of juvenile grass carp,Ctenopharyngodon idella

To determine dietary magnesium (Mg) requirements of juvenile grass carp, Ctenopharyngodon idella, magnesium sulphate was added to the basal diet at 0, 150, 300, 600, 1200, 2400 mg Mg kg⁻¹ diet. Each diet was fed to three replicate groups of juvenile grass carp (initial weight: 7.69 ± 0.13 g) in a closed, recirculating rearing system for 76 days. No mortality or nutritional deficiency signs were observed except the growth depression in fish fed the Mg‐deficient diet. Growth performance and activities of serum superoxide dismutase (SOD), glutathione peroxidase (GPx) and lysozyme (LSZ) were highest (P <0.05) in fish fed the diet supplemented with 600 mg Mg kg⁻¹. The serum malondialdehyde (MDA) content was higher (P <0.05) in fish fed the diets supplemented with 0 and 150 mg Mg kg⁻¹ than that in fish fed the diets with ≥300 mg Mg kg⁻¹. Mg concentrations both in whole‐body and vertebrae increased with the increase in dietary Mg level up to 300 mg kg⁻¹, whereupon the response reached a plateau. Analysis by second‐order polynomial regression of weight gain, by broken‐line regression of vertebrae Mg concentration and by linear regression of whole‐body Mg retention of fish indicated that the adequate dietary Mg concentration for juvenile grass carp was 713.5, 627.7 and 469.8 mg kg⁻¹ diet, respectively.     

Magnesium requirement of Atlantic salmon (Salmo salar L.) parr in seawater-treated fresh water1

This experiment was undertaken to establish the magnesium (Mg) requirement in young Atlantic salmon, Salmo salar L., in seawater-treated fresh water. In Norwegian hatcheries it is a common practice to add sodium hydroxide and/or sea water (1–2%) to improve pH and conductivity of the natural fresh water. Parr with initial weight of 8 g, were divided in six triplicate groups in brackish water containing 54 mg Mg L^?1 and fed a basal casein-gelatine diet supplemented with minor amounts of krill and fish meal (containing 200 mg Mg kg^?1) for an initial period of 3 weeks. Thereafter the fish were fed this diet supplemented with either 0, 100, 200, 300, 400 or 500 mg Mg kg^?1 (as MgSO₄) for 12 weeks. Growth and feed efficiency were recorded. Concentrations of Mg and other divalent cations (Ca and Zn) were measured in whole fish, serum and vertebrae. Sodium concentration in vertebrae was also measured. Growth and feed efficiency were unaffected by the levels of dietary magnesium used in the experiment. Magnesium concentrations in the whole body, serum and vertebrae Mg appeared to be more sensitive than growth and feed efficiency to differences in dietary Mg intake. The group fed the unsupplemented diet showed significantly lower Mg concentration in these tissues than the other groups. Whole-body calcium concentration was negatively correlated with dietary Mg and Ca:Mg ratios in the vertebrae were significantly affected by the dietary Mg levels. Zinc concentration in whole body, serum and vertebrae was not altered by the dietary Mg levels. Further, vertebral Na concentration did not vary between the dietary treatments. In conclusion, a minimum Mg supplementation level of 100 mg kg^?1 dry diet (in total, 326 mg kg^?1) was needed to maintain Mg concentration in the whole body and serum and for proper bone mineralization.     

Dietary phosphorus requirement of juvenile Chinese sucker,Myxocyprinus asiaticus

A growth trial was conducted to estimate the optimum requirement of dietary available phosphorus (P) for Chinese sucker juveniles. Triplicate groups of juveniles Chinese sucker (initial mean weight: 1.77 ± 0.02 g, mean ± SD) were fed diets containing graded levels (3.1, 5.3, 7.5, 9.6 and 11.8 g kg^?1) of available phosphorus. The basal diet (diet 1), containing 3.1 g kg^?1 available P, was supplemented with graded levels of monocalcium phosphate to formulate four experimental diets. The fish were fed twice daily (08:00 and 17:00 h) to satiation for 8 weeks. During the experimental period, the water temperature fluctuated from 27.5 to 30.5 °C and dissolved oxygen was more than 6 mg L^?1. The specific growth rate, protein efficiency ratio were all significantly increased by dietary available phosphorus up to 7.5 g kg^?1 (P < 0.05) and then levelled off beyond this level. Feed conversion ratio significantly decreased with dietary available phosphorus level up to 7.5 g kg^?1 (P < 0.05). Dietary treatments did not significantly affect feed intake (P > 0.05). Efficiency of phosphorus (P) utilization significantly decreased with dietary available phosphorus level (P < 0.05). Body composition analysis showed that the whole‐body lipid, ash, calcium, phosphorus, magnesium (Mg), zinc (Zn) and copper (Cu) contents were all significantly affected by dietary available P concentration (P < 0.05); however, no significance were found for manganese (Mn) concentration and calcium/phosphorus (Ca/P) ratios in whole‐body among all the treatments (P > 0.05). Dietary phosphorus levels also significantly affected the mineralization of vertebrae and scale (P < 0.05), and Ca/P ratios in scale were not influenced by dietary P supplementation, while vertebrae Ca/P ratio decreased with dietary available P levels (P < 0.05) (quadratic effect, P < 0.001). Signs of phosphorus deficiency were characterized by poor growth, slightly reduced mineralization and an increase in body lipid content. The blood chemistry analysis showed that dietary available P had distinct effects on enzyme activities of alkaline phosphatase, as well as contents of triacyglycerol and total cholesterol (P < 0.05). Broken‐line analysis based on weight gain indicated the minimum available phosphorus requirement for the optimal growth of juvenile Chinese sucker was 7.4 g kg^?1. Based on the phosphorus content in whole body, vertebrae or scale indicated that the requirements were 8.3, 8.8 and 8.6 g kg^?1 respectively.     

Dietary available phosphorus requirement of juvenile grass carp (Ctenopharyngodon idella)

A growth trial was conducted to estimate the optimum concentration of dietary available phosphorus (P) for grass carp (Ctenopharyngodon idella). Triplicate groups of grass carp (5.59 ± 0.02 g) were fed diets containing graded levels (2.36, 4.27, 6.31, 8.36, 10.4 and 14.8 g kg^?1) of available P for 8 weeks. Grass carp fed with the P‐supplemented diets had significantly higher specific growth rate, weight gain, protein efficiency ratio and feed efficiency than fish fed with the basal diet. In whole‐body composition, protein content increased, while lipid content decreased with the increase in P level in diet (P < 0.05). Fish fed with the P‐supplemented diets had significantly higher whole body, vertebrae and scales mineralization (P < 0.05), but Ca/P ratios were not influenced. The blood chemistry analysis showed that dietary available P had distinct effects on P, Ca and Mg contents, as well as on the contents of triacylglycerol and total cholesterol. Broken‐line analysis indicated that 8.49 g kg^?1 dietary available P was required for maximal tissue storage and mineralization as well as optimal growth.     

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 choline requirement for juvenile blunt snout bream,Megalobrama amblycephala

A 12‐week feeding trial was conducted to determine dietary choline requirement for juvenile Megalobrama amblycephala. The basal diet was formulated to contain 310 g kg^?1 diet from vitamin‐free casein and gelatine. Choline chloride was supplemented to the basal diet to formulate six purified diets containing 0, 250, 500, 1000, 2000 and 4000 mg kg^?1, respectively. Each diet was randomly fed to quadrupled groups of Megalobrama amblycephala with initial average weight 1.84 ± 0.04 g in a flow‐through system. Results showed weight gain was increased significantly with increasing dietary choline levels (P < 0.01). Lipid content of liver decreased significantly as dietary choline concentration increased (P < 0.01), whereas lipid content of dressed carcass showed opposite trend (P < 0.01), and lipid content of whole‐body was unaffected by dietary choline supplementation. Broken‐ line regression of weight gain, liver and muscle choline concentration showed choline requirements of Megalobrama amblycephala of 1198, 1525 and 1365 mg kg^?1, respectively. In addition, dietary choline supplementation significantly improved lipid content of dressed carcass but not the content of whole body of blunt snout bream.     

Dietary biotin requirement for growth of juvenile zebrafish Danio rerio (Hamilton‐Buchanan)

This study was conducted to estimate the dietary biotin requirement for maximum growth of zebrafish Danio rerio. Six isonitrogenous and isocaloric purified diets containing 0.031 (biotin‐unsupplemented diet), 0.061, 0.263, 0.514, 1.741 and 2.640 mg biotin kg^?1 diet were fed in triplicate tanks for a total of 12 weeks to juvenile zebrafish (initial mean body mass 0.13 ± 0.001 g). From 4 weeks of feeding, fish fed diets with ≤0.061 mg biotin kg^?1 showed biotin deficiency signs, such as retarded growth and skeletal deformity, was observed on some dead fish. At the end of the study, gill disorders were observed on some fish and liver glycogen accumulation were also observed in fish fed these diets. Fish fed the biotin‐unsupplemented diet exhibited a lower final body weight, protein efficiency ratio and feed utilization than the fish fed the biotin‐supplemented diets, whereas the highest values were observed with the diet containing 0.51 mg biotin kg^?1 diet (P < 0.05). A linear relationship (r² = 0.77; P < 0.0001) was observed between whole‐body biotin content and dietary biotin level. A broken‐line analysis indicated that the optimum dietary biotin content for maximal growth expressed as final body weight is 0.51 mg kg^?1 diet.     

Effects of dietary α‐lipoic acid on the growth and antioxidative responses of juvenile abalone Haliotis discus hannai Ino

A feeding experiment was conducted to determine the effects of α‐lipoic acid (LA) on the growth and antioxidative responses of juvenile abalone Haliotis discus hannai Ino. Six purified diets supplemented with 0, 200, 400, 800, 1600 and 3200 mg kg^?1 of LA, respectively, were fed to abalone for 16 weeks in a flow‐through water system. The results showed that the weight gain ratio (WGR) increased with the dietary LA levels, and reached the highest value in the group with 800 mg kg^?1 dietary LA supplement. Glutathione peroxidase activity in the 800 mg kg^?1 dietary LA group was significantly higher than that in the dietary LA‐deficient (0 mg kg^?1) group. Superoxide dismutase activities in the 200, 400 and 800 mg kg^?1 groups were significantly increased. Supplements of 200, 400 and 800 mg kg^?1 dietary LA elevated the total antioxidative capacity significantly. The glutathione level in the hepatopancreas increased significantly with the dietary LA supplements in a dose‐dependent manner (except for the 200 mg kg^?1 group). Catalase and malondialdehyde in the hepatopancreas were not significantly affected by dietary LA. In conclusion, dietary LA promoted the growth and stimulated the antioxidative defence capacity of abalone. Based on the data of WGR, the optimal dietary LA supplement for juvenile abalone was found to be 709 mg kg^?1 using piece‐wise linear analysis.     

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.     

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).     

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 zinc requirement of juvenile grass carp (Ctenopharyngodon idella) based on growth and mineralization

A growth trial was conducted to estimate the optimum requirement of dietary zinc (Zn) for grass carp (Ctenopharyngodon idella). Triplicate groups of grass carp (3.97 ± 0.05 g) were fed diets containing graded levels (13, 25, 34, 53, 89 and 135 mg kg^?1) of Zn for 8 weeks. Grass carp fed with dietary Zn levels higher than 34 mg kg^?1 significantly increased final body weight, weight gain and specific growth rate (P < 0.05). For body composition, fish fed with dietary Zn levels higher than 53 mg kg^?1 significantly decreased the moisture contents but increased the lipid contents of whole body and liver. Whole body, scales, vertebrae and liver mineralization were all affected significantly (P < 0.05) by dietary Zn levels. Zn contents in whole body, scales, vertebrae and plasma were linearly increased up to the 53 mg kg^?1 dietary Zn and then remained stable beyond this level. Grass carp fed with dietary Zn levels higher than 53 mg kg^?1 significantly increased triacyglyceride and total cholesterol contents and plasma alkaline phosphatase activity in plasma (P < 0.05). Broken‐line analysis indicated that 55.1 mg kg^?1 dietary Zn was required for maximal tissue storage and mineralization as well as optimal growth of grass carp.     

Effect of dietary iron supplement on growth, haematology and microelements of juvenile grouper, Epinephelus coioides

An experiment was conducted to investigate the effect of dietary iron supplement on growth, haematology and microelements of juvenile grouper, Epinephelus coioides. Casein–gelatine‐based diets supplemented with 0, 50, 100, 150, 200 and 250 mg kg⁻¹ iron from ferrous sulphate were fed to grouper (mean initial weight: 21.0 ± 0.2 g) for 8 weeks. Weight gain was highest in fish fed the diet supplemented with 100 mg kg⁻¹ iron, intermediate in fish fed diets with 50, 150, 200 and 250 mg kg⁻¹ iron and lowest in fish fed the basal diet. Feed efficiency followed a similar trend except that the lowest value was in fish fed the basal diet and the diet supplemented with 250 mg kg⁻¹ iron. Hepatic iron was highest in fish fed diets supplemented with iron ≥100 mg kg⁻¹, followed by fish fed diet with 50 mg kg⁻¹ iron and lowest in fish fed the basal diet. The whole‐body iron was lowest in fish fed the basal diet but not significantly different from other groups, as judged by anova . Iron supplement to the basal diet had no significant effect on haematological parameters (red blood cell count, haematocrit and haemoglobin), hepatic copper concentration or manganese, zinc concentration in liver and whole body. Broken‐line analysis of hepatic iron indicated that iron supplementation of 100 mg kg⁻¹ satisfied the hepatic iron storage and that further supplementation did not expand the iron status.     

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 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.