Estimation of dietary vitamin K requirement of juvenile Chinese soft‐shelled turtle,Pelodiscus sinensis

A 10‐week feeding trial was conducted to estimate the dietary vitamin K requirements of juvenile Chinese soft‐shelled turtles, Pelodiscus sinensis, using menadione sodium bisulphite (MSB) as the vitamin K source. Juvenile soft‐shelled turtles with 6.1 ± 0.1 g body weight were individually reared and fed diets containing seven levels of MSB (0.0, 5.0, 8.9, 12.3, 16.6, 20.7 and 41.0 mg/kg). Turtles fed with an MSB‐free diet exhibited the lowest feed utilization, carapace Ca concentrations, carapace strength or liver menaquinone (MK‐4) concentrations among all dietary groups. Weight gain (WG) in the turtles tended to increase with increase in dietary MSB until a dietary MSB level of 16.6 mg/kg, where WG levelled off. Total plasma prothrombin concentrations, an indicator for blood clotting function, in the turtles fed on MSB supplemented diets were significantly (p < 0.05) lower than those in turtles fed on MSB supplemented diets. Liver MSB concentrations increased with increase in dietary MSB. Using broken‐line or sigmoidal regression model, the vitamin K requirements of juvenile Chinese soft‐shelled turtles based on WG, total plasma prothrombin concentrations and liver vitamin K were 21.5, 25.8 and 29.9 mg MSB per kg, respectively.     

Effects of dietary β‐carotene levels on growth and liver vitamin A concentrations of the soft‐shelled turtle,Pelodiscus sinensis (Wiegmann)

A feeding trial was conducted to evaluate the effect of dietary β‐carotene level on the growth and liver vitamin A concentrations in soft‐shelled turtles, Pelodiscus sinensis, fed a vitamin A‐free diet. Soft‐shelled turtles were fed diets containing 0, 14.5, 26.5, 47.5, 87.3, 112.8 and 163.8 mg β‐carotene kg^?1 for 10 weeks. Although it was not statistically significant due to high deviation within each group, mean weight gain of soft‐shelled turtles fed the diet without β‐carotene supplementation was the lowest among all test groups. Vitamin A concentrations in liver of turtles significantly (P<0.05) increased when dietary β‐carotene level reached 47.5 mg kg^?1 indicating that soft‐shelled turtles were capable of converting β‐carotene to vitamin A. Analysed by regression modelling, dietary β‐carotene levels for optimal growth and maximal liver vitamin A contents of juvenile soft‐shelled turtles fed the vitamin A‐free diets were 49.1 and 88.7 mg kg^?1 respectively.     

Effects of dietary magnesium on the growth,carapace strength and tissue magnesium concentrations of soft‐shelled turtle,Pelodiscus sinensis (Wiegmann)

A feeding trial was conducted to evaluate the effects of dietary magnesium on the growth, carapace strength, tissue and serum Mg concentration of soft‐shelled turtles, Pelodiscus sinensis (Wiegmann). Juvenile soft‐shelled turtles of approximate 5.4 g body weight were fed diets with seven levels of Mg (48, 206, 369, 670, 955, 1195 and 1500 mg Mg kg^?1) for eight weeks. No significant difference (P ≥ 0.05) was found in weight gain (WG), feed conversion ratio or protein efficiency ratio among treatments. However, the WG of turtles continued to increase with increasing dietary Mg levels up to 670 mg kg^?1, beyond which the WG levelled off. The plasma alkaline phosphatase activity and the muscle, bone Mg concentrations of the turtles increased with the increasing dietary Mg levels between 48 and 955 mg kg^?1, beyond which the tissue Mg concentrations remained relatively constant. Furthermore, the carapace strengths of turtles fed with the control diet of 48 mg Mg kg^?1 were significantly weaker (P < 0.05) than that of turtles fed with diets containing higher Mg levels. Based on a broken‐line modelling analysis, the required dietary Mg level for the optimal WG of juvenile soft‐shelled turtles was estimated to be approximately 650 mg kg^?1. By contrast, the required dietary Mg levels for turtles to reach the optimal muscle and bone Mg concentrations were 1050 and 1000 mg kg^?1 respectively. The required dietary Mg level for maximal alkaline phosphatase activity was approximately 980 mg kg^?1.     

Effect of dietary calcium and phosphorus supplementation in fish meal-based diets on the growth of soft-shelled turtle Pelodiscus sinensis (Wiegmann)

A growth experiment was conducted to determine the effect of supplementing dietary calcium in fish meal‐based diets on the growth of cultured soft‐shelled turtle Pelodiscus sinensis. Juvenile soft‐shelled turtles of 4.1 g mean body weight were fed nine diets containing two levels of phosphorus (2.7% or 3.0%) and analysed calcium levels ranging from 4.7% to 6.6% for 10 weeks. The growth of the turtles was enhanced when inorganic calcium was added to the diets. The weight gain of the turtles fed the control diet containing calcium solely from fish meal was the lowest among the test groups, and was significantly lower than those fed the diet containing 5.7% calcium at the 3.0% phosphorus level (P<0.05). Feed conversion and protein efficiency ratios were not affected by different dietary treatments. Whole‐body moisture and crude protein contents of turtles were not affected by different dietary treatments. The body ash of turtles fed 3.0% phosphorus diets tended to be higher than turtles fed 2.7% phosphorus diets. The body calcium to phosphorus ratio of turtles fed 3.0% phosphorus diets was greater than that of turtles fed diets containing 2.7% phosphorus. Supplementation of Ca in a fish meal‐based practical diet is required for the optimum growth of soft‐shelled turtles.     

Effects of dietary zinc levels on growth,serum zinc,haematological parameters and tissue trace elements of soft‐shelled turtles,Pelodiscus sinensis

A 10‐week feeding trial was conducted to evaluate the effects of dietary zinc (Zn) contents on the growth, tissue trace element contents and serum Zn levels in soft‐shelled turtles, Pelodiscus sinensis. Juvenile soft‐shelled turtles approximately 4.8 g in body weight were fed casein‐based diets containing seven levels of Zn (14, 23, 32, 43, 58, 87 and 100 mg kg^?1) for 10 weeks. There were no significant differences (P > 0.05) in weight gain (WG), feed conversion ratio (FCR) or protein efficiency ratio (PER) among the dietary treatments. However, Zn concentrations in the liver, serum and carapace of turtles fed the basal diet containing 14 mg Zn kg^?1 were the lowest among all groups. Zn contents in the liver, serum and carapace increased when dietary Zn increased up to a dietary Zn level of approximately 43 mg kg^?1. Beyond this dietary level, tissue Zn contents were relatively constant. Carapace iron (Fe), selenium (Se) in hard tissues and haemoglobin concentrations decreased when dietary Zn increased. Dietary Zn requirements of juvenile soft‐shelled turtles derived from regression modelling using the liver, serum, carapace and bone Zn contents as indicators were 42, 39, 35 and 46 mg Zn kg^?1, respectively.     

Dietary lysine requirement of juvenile Pseudobagrus ussuriensis

An 8‐week feeding trial was conducted to determine dietary lysine requirement of juvenile Pseudobagrus ussuriensis (initial body weight: 0.60 g). Six isonitrogenous (crude protein, 400 g/kg) and isolipidic (crude lipid, 50 g/kg) diets were formulated to contain graded levels of dietary lysine (12.8, 19.9, 26.5, 34.0, 40.8 and 44.1 g/kg dry diets, respectively). The results indicated that weight gain, specific growth rate, productive protein value and protein efficiency ratio increased, while feed conversion ratio decreased with increasing dietary lysine level up to 34.0 g/kg dry diet and then levelled off. Fish fed diet with 12.8 g/kg lysine had the lowest lysine content (58.6 g/kg dry matter) in muscle, while fish fed diet with 34.0 g/kg lysine had the highest value (61.6 g/kg dry matter; p < .05). Broken‐line analysis on the basis of weight gain showed that the optimal dietary lysine requirement for maximum growth of juvenile Pseudobagras ussuriensis is 33.5 g/kg dry diet (82.4 g/kg dietary protein). Quadratic regression analysis of protein efficiency ratio against dietary lysine levels indicated that the optimal dietary lysine requirement of juvenile Pseudobagras ussuriensis is 36.4 g/kg dry diet (89.5 g/kg dietary protein).     

Protein‐sparing effects and LPL gene expressions of dietary lipids in the juvenile soft‐shelled turtle,Pelodiscussinensis

The aim of this study was to evaluate the effects of dietary lipids on protein‐sparing and lipoprotein lipase (LPL) mRNA expression in culture using 360 juvenile soft‐shelled turtles (Pelodiscussinensis) (initial weight 4.26 ± 0.14 g). The turtles were allotted to six diets with three duplicates for 60 days. A control diet with 46% protein and 55% fishmeal (CD) and five isonitrogenous diets with 41.3% protein and 45% fishmeal (F, S, L1, L2 and L3) were used, containing the following three lipid types: fish oil, soybean oil and mixed oils (soybean oil: fish oil = 1:1). The results showed that the survival rate was not affected by dietary lipids (P > 0.05). The highest weight gain and lowest feed coefficient ratio were seen in the L3 diets (P < 0.05). Turtles fed with L2 and L3 diets had lower superoxide dismutase activities, higher alanine aminotransferase activities and higher cholesterol concentrations than those exposed to other diets (P < 0.05). Hepatic LPL activity and LPL mRNA expression were higher in the L3 diets than in the other diets (P < 0.05). Overall, there were obvious protein‐sparing effects of dietary lipids and LPL mRNA expression was stimulated by high dietary lipids in soft‐shelled turtles in this study.     

Dietary copper requirement of fingerling Heteropneustes fossilis for formulating copper‐balanced commercial feeds

Dietary copper requirement of Heteropneustes fossilis (6.74 ± 0.03 g) was determined by feeding purified diets containing same protein (400 g/kg) and gross energy (17.89 kJ/g) but different levels of copper for 12 weeks. Graded amount of CuSO₄.5H₂O (0, 1.96, 3.93, 5.89, 7.86, 9.82, 11.79 mg/kg) was supplemented to basal diet to attain desired dietary copper levels (0, 0.5, 1.0, 1.5, 2.0, 2.5 and 3.0 mg/kg). Analysed dietary copper concentrations were 4.28, 4.63, 5.28, 5.70, 6.19 and 6.69 mg/kg. Absolute weight gain, feed conversion ratio and protein gain improved with the increasing levels of dietary copper up to 5.28 mg/kg. Further inclusion of copper at a level of 5.70 mg/kg did not improve the above parameters. Significantly higher (p < .05) plasma ceruloplasmin, liver copper‐zinc superoxide dismutase, catalase activities and lower thiobarbituric acid reactive substances were evident in fish receiving diets with 5.28 and 5.70 mg/kg copper compared to other groups. Whole body and liver copper concentrations increased significantly (p < .05) with increasing dietary copper levels. Quadratic regression analysis of absolute weight gain, feed conversion ratio, protein gain and broken‐line regression analysis of plasma ceruloplasmin activity and liver TBARS value against the variable dietary copper levels depicted the dietary copper requirements for fingerling H. fossilis in the range of 5.24–5.68 mg/kg.     

Estimation of dietary copper requirement of juvenile soft-shelled turtles, Pelodiscus sinensis

Juvenile soft-shelled turtles (Pelodiscus sinensis) were fed diets containing 10 levels (0.8, 3.0, 5.0, 7.8, 9.0, 10.9, 20.4, 41.8, 78.6, 158 mg/kg diet) of copper (Cu) for 16 weeks. Turtles fed 5.0 mg Cu/kg achieved the best growth performance and the highest hematological values among all dietary groups. Growth was reduced significantly when dietary copper exceeded 20 mg/kg. Using the broken-line model with growth and hematological parameters as the dependent variables, the dietary Cu requirement of soft-shelled turtle was estimated to be 4.4–4.8 mg Cu/kg diet. Copper, iron, zinc and selenium concentrations in turtle liver were found to be influenced by dietary Cu level. Thiobarbituric acid-reactive substances in liver tissue of turtles fed diets containing 78.6–158 mg Cu/kg were higher (P < 0.05) than those fed diets containing less copper. Furthermore, diets containing more than 20 mg Cu/kg significantly impaired growth and hematology of soft-shelled turtles, indicating the dietary Cu tolerance above the requirement may be as low as 4 fold (20 vs. 5 mg/kg). Based on the results of this study, a dietary Cu level of 4–5 mg/kg is recommended for soft-shelled turtles.     

The dietary zinc requirement of a benthic fish Paramisgurnus dabryanus

This study was conducted to assess the dietary zinc (Zn) on growth and antioxidant capacity of adult Paramisgurnus dabryanus. Zinc methionine (ZnM) of grade levels (0, 20, 40, 80, 120 and 160 mg/kg diet respectively) was supplemented, providing actual dietary Zn concentrations of 24.38, 28.03, 31.68, 38.98, 46.28 and 53.58 mg/kg diet respectively. P. dabryanus with an initial body weight of 5.21 ± 0.15 g were fed these Zn supplemented diets for 8 weeks. Results showed that the weight gain (WG) and specific growth rate (SGR) increased with increasing dietary Zn levels from 24.38 to 31.68 mg/kg, and then decreased above these levels. The hepatopancreas index (HIS) was the highest at 31.68 mg/kg, followed by 38.98 mg/kg. The enzymatic antioxidants in plasma and hepatopancreas firstly increased, and reached the peak at 31.68 or 38.98 mg/kg, then kept stable with the increase of dietary Zn levels. On the contrary, the content of MDA firstly decreased, and then increased. According to WG and T‐AOC in plasma, the Zn requirement was determined to be 32.02 and 32.24 mg/kg, respectively, based on regression analysis. The relatively low dietary Zn requirement of P. dabryanus may involve in the evolutional adaption of metal absorption and utilization to their habitat.     

Optimum selenium requirement of juvenile Nile tilapia,Oreochromis niloticus

A feeding experiment was conducted to determine the optimum selenium requirement in juvenile Nile tilapia. Each of six purified diets with Se‐methionine levels at 0.05, 0.21, 0.41, 0.57, 0.79 and 1.00 mg/kg was assayed in triplicate with initial body weight of 3.00 ± 0.01 g for 8 weeks. The growth of fish was obviously increased when the dietary Se was less than 0.57 mg/kg diet and reached a plateau when the dietary Se was ≥0.57 mg/kg. Serum and hepatopancreatic glutathione peroxidase (GPx) activity increased markedly when the dietary Se was less than 0.57 mg/kg, but then decreased when the dietary Se was higher than 0.57 mg/kg. The malondialdehyde contents in hepatopancreas were significantly decreased when the dietary Se was higher than 0.79 mg/kg. No significant differences were observed in hepatopancreatic total antioxidant capability (T‐AOC) among the groups (p > .05). The results of this study indicated that Se addition as Se‐methionine was essential, while both the deficiency and excess levels of dietary Se would cause negative effects on growth or antioxidant capability in juvenile Nile tilapia. Based on broken‐line regression of WG and piecewise regression of liver GPx, the optimum requirement of Se for juvenile Nile tilapia is 0.57 mg/kg diet.     

Effects of dietary starch levels on the growth,plasma metabolites and expression of genes involved in glucose transport and metabolism in Pelodiscus sinensis juveniles

A 10‐week feeding trial was conducted to evaluate the growth performance, glucose transport and metabolism of Chinese soft‐shelled turtles (Pelodiscus sinensis) exposure to graded levels of dietary starch (0.52%, 7.43%, 14.74%, 22.99% and 31.38%). The 360 turtles (initial body weight, 12.94 ± 0.50 g) with 12 replicates were randomly assigned to five experimental diets. The highest weight gain and specific growth rate (SGR) were observed in 7.43% group and the lowest in 31.38% group. The protein efficiency ratio, whole‐body lipid contents, hepatic glycogen contents and the 4‐hr postprandial plasma glucose levels were significantly increased with the increment of starch levels (p < .05). In contrast, the daily feed intake and feed conversion ration were significantly declined (p < .05). The mRNA levels of glucose transporter 2, glucokinase, pyruvate kinase, malic enzyme and acetyl‐CoA carboxylase alpha genes in the liver significantly increased as the increase in starch levels at 4‐hr and 24‐hr post feeding (p < .05). No significant differences were observed in the expression of gluconeogenesis genes at each time point (p > .05). These results suggested that dietary addition of starch up‐regulated hepatic glycolysis, glycogenesis and lipogenesis genes expression, but the deficient response of gluconeogenesis to dietary starch might be part of the causes limited the starch utilization. Based on the secondary polynomial regression of SGR, y = ?0.0011x² + 0.028x + 1.63 (R² = 0.9292), the 12.73% inclusion level of dietary starch was recommended in juvenile turtles.     

Dietary Thiamin Requirement of Juvenile Grass Carp,Ctenopharyngodon idella

Dietary thiamin requirement of juvenile grass carp, Ctenopharyngodon idella, was to investigate in this experiment. Eight purified diets were formulated with graded levels of thiamin (0.1, 0.6, 1.1, 2.1, 5.5, 9.8, 21.2, and 41.8 mg/kg, respectively). Each diet was fed to triplicate groups of 40 fish (initial average weight 10.7 ± 0.2 g) for 12 wk in 400‐L aquaria (R = 1 m, h = 0.6 m). Results showed that weight gain rate, specific growth rate, feed efficiency, protein efficiency ratio, and hepatosomatic indice of fish increased before dietary thiamin increased to the optimum level, then remained similar thereafter (P > 0.05). Thiamin concentration in fish liver was positively correlated with dietary thiamin and it stayed in stable when dietary thiamin level exceed 5.0 mg/kg. The serum biochemical indices analysis showed that dietary thiamin had significant effects on serum triglycerides, total cholesterol, glucose, pyruvate contents, and lactate dehydrogenase activity. Body composition was unaffected by dietary thiamin. Broken‐line regression analysis showed that, a dietary thiamin level of 1.3 mg/kg diet was adequate for optimum growth, and 5.0 mg/kg for maximum liver thiamin accumulation.     

Dietary manganese requirement of juvenile hybrid grouper,Epinephelus lanceolatus × E. fuscoguttatus

An 8‐week feeding trial was conducted to estimate the optimum dietary manganese (Mn) requirement for juvenile hybrid grouper, Epinephelus lanceolatus × E. fuscoguttatus. The basal diet was formulated to contain 520 g/kg crude protein from casein and fishmeal. Manganese methionine was added to the basal diet at 0 (control group), 2.5, 5, 10, 20 and 40 mg Mn/kg diet providing 7.48, 10.34, 13.76, 19.72, 31.00 and 53.91 mg Mn/kg diet, respectively. Each diet was randomly fed to triplicate groups of juveniles, and each tank was stocked with 20 fish (initial weight, 60.06 ± 0.68 g). The manganese content in rearing water was monitored and kept below 0.01 mg/L. Results showed that the weight gain ratio (WGR), protein efficiency ratio (PER), specific growth rate (SGR), Mn contents in whole body, liver and vertebra, and activities of hepatic Mn superoxide dismutase (Mn‐SOD), total SOD (T‐SOD) and glutathione peroxidase (GSH‐PX) were significantly improved by dietary Mn supplementation (p < .05). However, dietary Mn did not affect arginase (DArg) activity. The highest feed conversion ratio (FCR) was observed in fish fed the basal diet (p < .05). No significant differences were found on the Cu and Zn contents in whole body by supplementing dietary Mn. Supplemented Mn in diets had significantly effect on liver and vertebral trace element deposition (p < .05). Fish fed the basal diet had the highest Fe and Zn contents in vertebra (p < .05). There were no significant differences on hepatic pyruvate decarboxylase (PDC) activity with supplemented Mn levels below 13.76 mg/kg. As biomarker of oxidative stress, malondialdehyde (MDA) content in liver was significantly higher in fish fed the basal diet (p < .05). Using the broken‐line models based on SGR, dietary Mn requirement of the juvenile hybrid grouper was estimated to be 12.70 mg/kg diet.     

Dietary valine requirement of juvenile Nile tilapia,Oreochromis niloticus

An 8‐week feeding trial was conducted to quantify the dietary valine requirement of cultured juvenile Nile tilapia, Oreochromis niloticus. Six isonitrogenous (280 g/kg crude protein) and isoenergetic (16.06 MJ/kg gross energy) diets with graded levels of valine (amounting to 4.1, 7.2, 9.9, 12.7, 15.6 and 18.8 g/kg of dry diet) were formulated. Each diet was randomly assigned to triplicate groups of 20 fish (6.48 ± 0.06 g). Results showed that the weight gain, specific growth rate, protein efficiency ratio and protein retention efficiency all increased with an increasing level of dietary valine up to 12.7 g/kg, but remained relatively constant for fish fed higher levels of dietary valine. In addition, the total protein concentration and aspirate aminotransferase activity in plasma, hepatic lysozyme and catalase activities were all significantly (p < .05) improved by dietary valine supplementation. Based on the broken‐line regression analysis of weight gain and protein retention efficiency, the optimal dietary valine requirement for juvenile Nile tilapia occurred between a level of 11.5 g/kg of diet (equivalent to 41.1 g/kg of dietary protein) and 12.7 g/kg of diet (equivalent to 45.3 g/kg of dietary protein).     

Dietary vitamin E requirement of sub‐adult genetically improved farmed tilapia strain of Nile tilapia (Oreochromis niloticus) reared in freshwater

A two‐factor orthogonal test was conducted to determine the dietary vitamin E (VE, dl ‐α‐tocopheryl acetate) requirement for sub‐adult GIFT strain of Nile tilapia (Oreochromis niloticus) at two lipid levels, and evaluate its effect on antioxidant responses. A basal diet containing 60 or 130 g/kg of soybean oil was supplemented with 0, 20, 40, 60, 120 and 240 mg VE/kg, respectively. Each diet was fed to three replicate groups of tilapia with initial weight (80.3 ± 0.7) g for 10 weeks. Results showed that the weight gain, feed efficiency and hepatic VE retention of fish were significantly increased by the increased VE in diets. In groups with 60 and 130 g/kg lipid, fish fed diets supplemented with VE had higher serum superoxide dismutase (SOD) and catalase activity, and lower malondialdehyde content than fish fed the VE un‐supplemented diet (p < .05). The proximate composition of fish had no significant difference in the group with 130 g/kg lipid, whereas crude lipid and ash content were significantly affected by dietary VE in the group with 60 g/kg lipid. Based on broken‐line regression analysis, dietary VE requirement to support the maximum weight gain and serum SOD were 43.2–45.8 and 66.0–76.1 mg/kg in diets with 60 and 130 g/kg lipid, respectively.     

Dietary thiamin requirement of fingerling Channa punctatus (Bloch) based on growth,protein gain,liver thiamin storage,RNA/DNA ratio and biochemical composition

Dietary thiamin requirement of fingerling Channa punctatus was quantified by feeding casein/gelatin‐based diets (450 g/kg CP; 18.39 kJ/g GE) with seven graded levels of thiamin (0, 0.5, 1, 1.5, 2, 2.5 and 5 mg/kg diet) to triplicate groups of fish (6.9 ± 0.93 cm; 4.91 ± 0.62 g) for 16 weeks. Fish fed diet with 2.5 mg/kg thiamin reflected highest absolute weight gain (AWG), protein gain (PG), RNA/DNA ratio and lowest feed conversion ratio. Similarly, highest liver thiamin concentration was also recorded in fish fed 2.5 mg/kg thiamin diet. Hepatic thiobarbituric acid reactive substance (TBARS) concentration responded negatively with increasing concentrations of dietary thiamin up to 2.5 mg/kg, whereas superoxide dismutase and catalase activities were found to improve with the increasing levels of dietary thiamin from 0 to 2.5 mg/kg. Transketolase activity also improved as the thiamin concentrations increased up to 2.5 mg/kg. Broken‐line regression analysis of AWG, PG, RNA/DNA ratio, liver thiamin concentrations, transketolase and TBARS activities exhibited the thiamin requirement in the range of 2.34–2.59 mg/kg diet. Data generated during this study would be useful in formulating thiamin‐balanced feeds for the intensive culture of this fish.     

Dietary ascorbic acid requirement for growth of striped catfish,Pangasianodon hypophthalmus (Sauvage, 1878) juveniles

A sixty‐day feeding trial was conducted to determine the ascorbic acid (AA) requirement for growth of striped catfish, Pangasianodon hypophthalmus juveniles. Seven iso‐nitrogenous and iso‐energetic (370 g protein per kg and 19.6 MJ/kg) purified diets were prepared with different levels of ascorbic acid such as control (0), T₁ (17.5), T₂ (35), T₃ (70), T₄ (175), T₅ (350) and T₆ (700) mg ascorbic acid (L‐ascorbyl‐2‐polyphosphate) equivalent per kg diet. Fish with a mean body weight of 3.2–3.4 g were stocked (fifteen fish per tank) in triplicates following a completely randomized design. Each group was fed to satiation twice a day for 60 days. Significant differences were observed in growth, survival, body composition and metabolic enzymes activities with different dietary ascorbic acid levels. Maximum weight gain, specific growth rate (SGR) and protein efficiency ratio (PER) were found in fishes fed with 35 mg AA per kg diet, supported by best feed conversion. Fish fed a diet containing vitamin C had the highest activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) compared to those fed with vitamin C‐depleted diets. In this study, based on using broken‐line regression analysis, the dietary vitamin C requirement for growth of P. hypophthalmus juveniles was estimated to be in the range of 46–76 mg AA per kg, depending on the criterion used, growth and liver storage. Our results will be helpful for the formulation of cost‐effective ascorbic acid incorporated diets for striped catfish, P. hypophthalmus.     

Effects of dietary vitamin E level on growth and tissue lipid peroxidation of soft-shelled turtle, Pelodiscus sinensis (Wiegmann)

A feeding trial was conducted to determine the effect of dietary vitamin E supplementation on growth, liver lipid peroxidation and liver and muscle vitamin E level of soft‐shelled turtle, Pelodiscus sinensis. Eight experimental diets analysed to contain 0–457 IU vitamin E kg^?1 were fed to juvenile soft‐shelled turtle of 4.8 g initial body weight for 12 weeks. Weight gain (WG) of the turtles fed the diet containing no vitamin E was significantly lower than those fed diets containing 83–457 IU vitamin E kg^?1 (P<0.05). Feed conversion ratio and protein efficiency ratio showed similar trends to that of WG. No significant difference (P>0.05) was found in whole‐body composition among turtles fed the different diets. Dietary vitamin E requirement using WG as the response and estimated using the broken‐line regression model is approximately 88 IU kg^?1. Liver and muscle vitamin E content increased when dietary vitamin E level increased. Ascorbate‐induced lipid peroxidation in liver tissue of turtles fed diets containing 0 and 17 IU vitamin E kg^?1 was significantly (P<0.05) greater than those fed diets containing high vitamin E (≥35 IU kg^?1).     

Effects of dietary selenium on growth performance and oxidative stress in juvenile grass carp Ctenopharyngodon idellus

An 8‐week feeding trial was conducted to investigate the effect of dietary selenium (Se) on feed intake, weight gain and antioxidant activity in juvenile grass carp (11.2 ± 0.03 g). Six Se levels (0.13, 0.41, 0.56, 1.12, 2.18 and 4.31 mg/kg) of semi‐purified diets were assayed in triplicate. The maximum weight gain, specific growth rate and feed intake were obtained in fish fed with 1.12 mg Se/kg diet. Hepatic glutathione peroxidase activity was markedly increased when dietary Se ≤1.12 mg/kg diet and reached a plateau when dietary Se ≥1.12 mg/kg diet. Hepatic superoxide dismutase and serum catalase activities in juvenile grass carp fed with 0.56, 1.12 and 2.18 mg Se/kg diets were all significantly higher than those in the other groups. The malondialdehyde content in liver and serum was firstly decreased and then increased with increasing dietary Se content, and the lowest content was observed in fish fed with 1.12 mg Se/kg diet. With the increase in Se level, the activities of serum alanine aminotransferase and aspartate aminotransferase were reduced. In addition, serum alkaline phosphatase activity and albumin content were highest in fish fed with 1.12 mg Se/kg diet. This study indicated that both the Se deficiency and excess of Se caused negative effect on the oxidative stress in juvenile grass carp and suggested that the health‐giving concentration of dietary inorganic Se was 1.12 mg/kg diet. Moreover, based on the broken‐line regression analysis of weight gain, the optimal concentration of dietary inorganic Se was 0.83 mg/kg for juvenile grass carp.