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.     

Effect of autoclaved Ulva meal on growth performance, nutrient utilization and fatty acid profile of rainbow trout, Oncorhynchus mykiss

A feeding trial was conducted to investigate the effects of the dietary incorporation of autoclaved and raw (non-autoclaved) Ulva meal on juvenile rainbow trout (Oncorhynchus mykiss) growth, nutrient utilization, body composition, diet digestibility and fatty acid composition. An algae-free control diet and four experimental diets with either 5 or 10 % inclusion levels of raw Ulva meal (5 % = RU5; 10 % = RU10) or autoclaved Ulva meal (5 % = AU5; 10 % = AU10) were formulated. Fish were fed three times daily to apparent satiation for 12 weeks. The growth of fish fed RU10 (final weight = 76.7 ± 3.31 g; SGR = 2.8 ± 0.05 %) diet was significantly higher than that in fish fed the AU10 diet (67.5 ± 1.61 g; SGR = 2.6 ± 0.03 %). The feed conversion ratio (FCR) was significantly better in fish fed the RU10 diet (0.9 ± 0.06) compared with control diet (1.0 ± 0.06). Condition factor, viscerosomatic index and dress-out remained unaffected by dietary treatment. The hepatosomatic index (HSI) was significantly lower (P < 0.05) in fish fed the AU10 diet (1.2 ± 0.19) than fish fed the other diets (≥1.6). The level of eicosapentaenoic acid (20:5n-3—EPA) in muscle from fish fed the RU10, AU5 and AU10 diets was significantly higher than in fish fed control diet (P < 0.05). Dietary inclusion of Ulva meals resulted in a significant increase in muscle docosapentaenoic acid (22:5n-3—DPA) levels at the end of the feeding period. The results indicate that the dietary inclusion of raw Ulva meal at levels of up to 10 % can be used without significant negative effects on the growth performance, nutrient utilization, dietary digestibility and muscle fatty acid composition. In fact, the inclusion of dietary raw and autoclaved Ulva meal elevated n-3 fatty acids levels of rainbow trout muscle.     

Dietary biotin requirement determined for Indian catfish, Heteropneustes fossilis (Bloch), fingerlings

Triplicate groups of Indian catfish, Heteropneustes fossilis (Bloch), fingerlings (average wet weight 3.55 ± 0.03 g) were fed semi-purified diets containing six levels of biotin (0, 0.086, 0.26, 0.86, 2.5 and 4.3 mg kg⁻¹ diet) for 15 weeks. After 42 days of feeding, fish fed the control (no biotin) diet had developed severe deficiency signs characterized by convulsions, heavy mortality, listlessness, poor feed conversion and feed intake, dark skin colour, tetanus and weight loss. None of these signs was seen in fish fed biotin-supplemented diets. Among all the biotin-supplemented diets, percentage weight gain was significantly highest for fish fed the diet supplemented with 0.26 mg of biotin kg⁻¹ and significantly lowest for fish fed the diet supplemented with 0.086 mg of biotin kg⁻¹. Feed conversion ratio (FCR) and protein efficiency ratio (PER) patterns were similar to that of percentage weight gain. The carcass protein and lipid contents were influenced by the dietary biotin up to fish fed 0.26 mg of biotin kg⁻¹. Significantly higher body biotin content, liver pyruvate carboxylase and acetyl CoA carboxylase activities were observed in fish fed biotin-supplemented diets than in fish fed the control diet. Broken-line analyses showed that the optimum dietary requirement for biotin for maximal weight gain, body biotin content, liver pyruvate carboxylase and acetyl CoA carboxylase activities was about 0.25 mg kg⁻¹. Associated liver pyruvate carboxylase and acetyl CoA carboxylase activities for normal growth ranged from 105 to 120 units mg⁻¹ protein and from 9 to 11 units mg⁻¹ protein respectively.     

Dietary biotin requirement of fingerling Channa punctatus (Bloch)

ABSTRACT

Dietary biotin requirement of fingerling Channa punctatus (4.52 ± 0.46 g) was estimated by conducting a 16-week growth trial. Fish were fed casein gelatin-based purified diets (450 g/kg crude protein, 18.39 kJ/g gross energy) with seven levels of dietary biotin (0, 0.04, 0.09, 0.47, 1.02, 1.43, and 1.96 mg/kg diet) to triplicate groups near to satiation. Significantly higher absolute weight gain (P = 0.0018), specific growth rate (P = 0.0027), protein gain (P = 0.0016), protein deposition (P = 0.0038), and lower feed conversion ratio (P = 0.0003) were shown in fish fed diet containing 0.47 mg/kg biotin, whereas liver biotin concentration showed a significant improvement (P = 0.0021) with increasing levels of dietary biotin up to 1.02 mg/kg. Broken-line analysis of absolute weight gain, protein gain, and liver biotin concentrations indicated that fingerling C. punctatus require biotin at 0.46, 0.44, and 0.97 mg/kg diet. Based on protein gain, optimum pyridoxine requirement for fingerling C. punctatus is recommended at 0.44 mg/kg diet.     

Meat and bone meal as a potential source of phosphorus in plant-protein-based diets for Nile tilapia (Oreochromis niloticus)

A growth trial was conducted to evaluate meat and bone meal (MBM) as a source of Phosphorus (P) for Nile tilapia fed with plant-based diets on growth, and the efficiency of P utilization. Four isonitrogenous and isoenergetic diets were formulated. A plant-based diet, deficient in P (0.45 % diet, no P added), was used as the basal diet. Three levels of MBM were substituted for cornstarch in the base diet to produce experimental diets containing MBM_0.56, MBM_0.67, or MBM_0.78% P. These diets were fed (to apparent satiation) to Nile tilapia (initial body weight = 1.53 ± 0.01 g) for eight weeks. Weight gain (WG), specific growth rate (SGR), feed conversion ratio (FCR, feed:gain), whole-body P concentration (WBPC), protein retention (PR), and retained phosphorus (RP) increased significantly (P ≤ 0.05), with the increasing dietary P levels coming from MBM. Diets containing MBM_0.78 produced significantly greater WG, SGR, WBPC, PR, and RP compared to other experimental diets (P ≤ 0.05). The linear regression analysis revealed a positive correlation between the WG, WBPC, RP, and dietary P levels coming from MBM of Nile tilapia. These results indicate that MBM has an additional value as a source of P and can serve as a potential source of supplemental P for Nile tilapia fed plant-protein-based diets.     

Juvenile tilapia (Oreochromis niloticus×Oreochromis aureus) requires dietary myo-inositol for maximal growth

An 8-week growth experiment was conducted to estimate the dietary requirement of myo-inositol (MI) for juvenile hybrid tilapia. MI was supplemented at 0, 150, 250, 350, 450, 600, and 1200 mg/kg diet in the basal diet providing 0, 167, 259, 367, 479, 612, and 1253 mg MI/kg diet. Basal diet without MI but with succinylsulfathiazole to suppress MI synthesis by intestinal bacteria was included for comparison. Each diet was fed to triplicate groups of tilapia (mean initial weight 0.51±0.01 g, n=3). Fish fed ≥367 mg MI/kg diet had significantly (P<0.05) higher weight gain, followed by fish fed 259 mg MI/kg diet, and lowest for fish fed the unsupplemented basal diet. Fish fed ≥367 mg MI/kg diet had higher feed efficiency than fish fed the basal diet. Supplementation of dietary inositol did not affect survival of tilapia. The MI concentrations in liver were highest in fish fed the ≥479 mg MI/kg diet, followed by fish fed the 259 and 167 mg MI/kg diets, and lowest in fish fed the basal diet. Hepatic lipid concentrations were higher in fish fed 367 mg MI/kg diet than fish fed ≤259 mg MI/kg diet. Weight gain percentage and MI concentrations in the liver for the different treatments were analyzed by broken-line regression and indicated that the requirement for dietary MI in growing tilapia is about 400 mg/kg diet. Addition of an antibiotic to basal diet did not affect the growth and hepatic inositol concentration of tilapia, suggesting that the intestinal microbial synthesis was not a significant source of inositol for tilapia.     

Antioxidant status of serum,muscle, intestine and hepatopancreas for fish fed graded levels of biotin

Lipid peroxidation, protein oxidation and antioxidant activities of muscle, intestine, hepatopancreas and serum in juvenile Jian carp (Cyprinus carpio var. Jian) were investigated after feeding graded levels of biotin (0.010, 0.028, 0.054, 0.151, 0.330, 1.540 and 2.680 mg kg^?1 diet) for 63 days. Both malondialdehyde and protein carbonyl content in all studied tissues and serum were the lowest in fish fed diets containing 0.151–0.330 mg biotin kg^?1 diet and then increased in fish fed the diet with 2.680 mg biotin kg^?1 diet (P < 0.05). Similarly, glutamate–oxaloacetate transaminase and glutamate–pyruvate transaminase activities in serum significantly decreased with biotin levels up to 0.151 mg kg^?1 diet (P < 0.05). Conversely, capacities of anti-hydroxyl radical (AHR) and anti-superoxide anion (ASA) in the detected tissues and serum significantly improved with biotin levels up to 0.054–1.540 mg kg^?1 diet and then decreased in 2.680 mg biotin kg^?1 diet group for muscle and intestinal AHR as well as hepatopancreas ASA (P < 0.05). Activities of superoxide dismutase in all studied tissues and serum significantly elevated with biotin levels up to 0.330 mg kg^?1 diet and then decreased when fish fed the diet with 2.680 mg biotin kg^?1 diet, except intestine (P < 0.05). Meanwhile, activities of catalase, glutathione peroxidase, glutathione-S-transferase and glutathione reductase and total thiol content in all studied tissues and serum showed the upward trend with biotin supplementations (P < 0.05). These results indicated that biotin improved antioxidant status and depressed lipid peroxidation and protein oxidation in all studied tissues and serum.     

Dietary Biotin Requirement of Fingerling Catla catla (Hamilton) Based on Growth,Feed Conversion Efficiency,and Liver Biotin Concentration

A 12‐wk experiment was conducted to determine the dietary biotin requirement of the fingerling Catla catla (7.9 ± 0.37 cm; 3.5 ± 0.12 g). Eight diets (35% crude protein, 16.72 kJ/g gross energy) with different levels of biotin (0, 0.05, 0.1, 0.5, 1.0, 1.5, 2.0, and 2.5 mg/kg diet) were fed to triplicate groups of fish to apparent satiation. Highest percent weight gain, protein retention efficiency, and best feed conversion ratio were observed in fish fed 0.5 mg biotin per kg diet. However, fish fed diets containing dietary biotin of 1.0, 1.5, 2.0, and 2.5 mg/kg did not show significant (P > 0.05) differences compared to those fed on dietary biotin of 0.5 mg/kg. Hematological indices, including hematocrit value, hemoglobin content, and red blood cell counts were found to be directly proportional (P < 0.05) to the dietary biotin levels up to 0.5 mg/kg, beyond which a plateau was recorded. Pyruvate carboxylase activity (PCA) was also found to increase with the incremental levels of dietary biotin up to 0.5 mg/kg and further increasing dietary biotin concentration led to stagnation in PCA of fish. Liver biotin concentrations responded positively (P < 0.05) until saturation, which occurred at 1.0 mg/kg diet. Broken‐line analysis of percent weight gain, protein retention efficiency, PCA, and liver biotin concentrations demonstrated that fingerling C. catla require biotin in the range of 0.41–0.87 mg/kg diet.     

Effects of dietary Biogen and sodium butyrate on hematological parameters,immune response,and histological characteristics of Nile tilapia (<Emphasis Type="Italic">Oreochromis niloticus</Emphasis>) fingerlings

The present study was carried out to evaluate the use of Biogen and sodium butyrate (SB) as feed additives in the diet of Nile tilapia (Oreochromis niloticus) fingerlings, in two parallel experiments. Biogen was incorporated in isonitrogenous (35% crude protein) and isocaloric (19 MJ kg^?1) diets at four levels (0.0 (control), 0.5, 1.0, and 2.0%), while SB was included at five levels (0.0 (control), 0.5, 1.0, 2.0, or 3.0%). The diets were fed to fingerling Nile tilapia (10.5 ± 0.5 g) at a daily rate of 4% of their body weight, three times a day, for 60 days. Except the lymphocytes and monocyte numbers in fish fed SB, hematological parameters, including red blood cell (RBC) hematocrit (Ht), hemoglobin (Hb), and white blood cells (WBC) were not significantly (P > 0.05) affected by dietary Biogen and SB. The lymphocytes number in Nile tilapia fed on SB increased with increasing SB up to 2% level, and decreased afterwards. Monocyte numbers showed irregular patterns. The activities of serum enzymes alanine aminotransferase (ALT) and aspartate aminotransferase (AST) of fish fed diets containing Biogen or SB were not significantly affected by dietary treatments (P > 0.05). No structural differences of tilapia liver were detected between all Biogen treatments and sodium butyrate concentrations up to 1% with control. At concentrations of 2 and 3% sodium butyrate, liver steatosis increased leading to shrinked acentric nuclei. At a concentration of 2% Biogen, some glomerulus cells had fading cytoplasm. Concerning fish fed SB diets, the structure of kidney was the same as in control except at concentration of 3% SB, where the septum between cells disappeared. No changes in gill structure were noticed at all concentrations of Biogen and SB.     

Dietary calcium requirements of juvenile tilapia, Oreochromis niloticus × O. aureus, reared in fresh water

A feeding experiment was conducted to determine the dietary calcium (Ca) requirement for juvenile hybrid tilapia, Oreochromis niloticus × O. aureus reared in nature water. Purified diet supplemented with 0, 1, 2, 3, 4, 5, 7 and 10 g Ca kg⁻¹ diet providing of 0.6, 1.6, 2.6, 3.7, 4.7, 5.5, 7.5 and 10.7 g Ca kg⁻¹ diet, respectively, were fed to tilapia (mean initial weight: 0.52 ± 0.01 g, n = 3) for 8 weeks. Each diet was fed to three replicate groups of fish in a closed, recirculating fresh water rearing system. The rearing water contained 27.1–33.3 mg L⁻¹ Ca. The tilapia fed the diets supplemented with ≥3.7 g Ca kg⁻¹ had significantly (P < 0.05) higher weight gain, when compared with fish fed the diet with ≤1.6 g Ca kg⁻¹. Fish fed the unsupplemented control showed significantly lower weight gain when compared with the other groups (P < 0.05). Bone Ca concentration was highest in fish fed the diets with ≥4.7 g Ca kg⁻¹, intermediate in fish fed the diet with 2.6 g Ca kg⁻¹ and lowest in fish fed the control diet. Scale Ca concentration was higher in fish fed the diets with ≥3.7 g Ca kg⁻¹ than in fish fed the diets with ≤2.6 g Ca kg⁻¹. Serum alkaline phosphatase activity was 36% increased in fish fed the diets with ≥2.6 g Ca kg⁻¹ than fish fed the diets with <1.6 g Ca kg⁻¹. Analysis by broken‐line regression of weight gain, bone and scale Ca concentrations indicated that the adequate dietary Ca concentration for tilapia in water containing 27.1–33.3 mg Ca L⁻¹ was 3.5, 4.3 and 4.2 g Ca kg⁻¹ diet, respectively, supplied as Ca‐lactate.     

Ascorbic acid requirement and histopathological changes due to its deficiency in juvenile spotted rose snapper Lutjanus guttatus (Steindachner, 1869)

A 13-week feeding trial was conducted to determine the optimal dietary ascorbic acid (AA) requirement of juvenile spotted rose snapper (Lutjanus guttatus). Six experimental diets containing 0, 7, 19, 29, 62 and 250 mg AA equivalent kg^?1 diet, supplied as l-ascorbyl-2-polyphosphate designated as VC0, VC7, VC19, VC29, VC62 and VC250, were fed ad libitum to triplicate groups of 20 juveniles [initial weight (IW) of 8 ± 1.85 g]. Nutrient deficiency resulting in fin erosion, dark skin, desquamation and erratic swimming was observed after 8 weeks in fish fed diets from 0 to 29 mg AA kg^?1. Fish that were fed all diets showed gill, kidney and brain alterations. The degree of tissue change values indicates that increasing vitamin C (VC) levels reduces these alterations. Fish fed diets VC29, VC62 and VC 250 showed a significantly higher growth rate in comparison with those fed the diets VC0, VC7 and VC17 (P > 0.05). The dietary requirement of VC in L. guttatus was estimated to be 29 mg kg^?1 of AA based on weight gain and specific growth rate, but more than 250 mg kg^?1 of AA is required to eliminate clinical signs and histopathological lesions.     

Effects of dietary amylose/amylopectin ratio on growth performance,feed utilization,digestive enzymes,and postprandial metabolic responses in juvenile obscure puffer Takifugu obscurus

The effect of dietary amylose/amylopectin (AM/AP) ratio on growth, feed utilization, digestive enzyme activities, plasma parameters, and postprandial blood glucose responses was evaluated in juvenile obscure puffer, Takifugu obscurus. Five isonitrogenous (430 g kg^?1 crude protein) and isolipidic (90 g kg^?1 crude lipid) diets containing an equal starch level (250 g kg^?1 starch) with different AM/AP ratio diets of 0/25, 3/22, 6/19, 9/16 and 12/13 were formulated. Each experimental diet was fed to triplicate groups (25 fish per tank), twice daily during a period of 60 days. After the growth trial, a postprandial blood response test was carried out. Fish fed diet 6/19 showed best growth, feed efficiency and protein efficiency ratio. Hepatosomatic index, plasma total cholesterol concentration, liver glycogen and lipid content, and gluconokinase, pyruvate kinase and fructose-1,6-bisphosphatase activities were lower in fish fed highest AM/AP diet (12/13) than in fish fed the low-amylose diets. Activities of liver and intestinal trypsin in fish fed diet 3/22 and diet 6/19 were higher than in fish fed diet 9/16 and diet 12/13. Activities of liver and intestinal amylase and intestinal lipase, and starch digestibility were negatively correlated with dietary AM/AP ratio. Fish fed diet 3/22 and diet 6/19 showed higher plasma total amino acid concentration than fish fed the other diets, while plasma urea nitrogen concentration and activities of alanine aminotransferase and aspartate aminotransferase showed the opposite trend. Equal values were found for viscerosomatic index and condition factor, whole body and muscle composition, plasma high-density and low-density lipoprotein cholesterol concentrations, and activities of lipase and hexokinase and glucose-6-phosphatase in liver. Postprandial plasma glucose and triglyceride peak value of fish fed diet 12/13 were lower than in fish fed the low-amylose diets, and the peak time of plasma glucose was later than in fish fed the other diets. Plasma glucose and triglyceride concentrations showed a significant difference at 2 and 4 h after a meal and varied between dietary treatments. According to regression analysis of weight gain against dietary AM/AP ratio, the optimum dietary AM/AP ratio for maximum growth of obscure puffer was 0.25. The present result indicates that dietary AM/AP ratio could affect growth performance and feed utilization, some plasma parameters, digestive enzyme as well as hepatic glucose metabolic enzyme activities in juvenile obscure puffer.     

Dietary threonine requirement of juvenile Nile tilapia,Oreochromis niloticus

An 8-week feeding trial was conducted to determine the dietary threonine requirement of juvenile Nile tilapia Oreochromis niloticus. Six isonitrogenous and isoenergetic diets were formulated to contain graded levels of threonine, 0.73, 0.91, 1.14, 1.31, 1.56 and 1.72 % of dry weight, respectively. Each diet was randomly assigned to triplicate groups of 25 juvenile fish (2.97 ± 0.02 g), which were fed three times daily (8:30, 12:30 and 17:00) to apparent satiation. By the end of the feeding trial, weight gain (WG) was found to have increased with increasing dietary threonine levels up to 1.31 %, but WG then decreased in fish fed higher dietary threonine concentrations. Threonine concentration had no significant impact on survival, body composition or the measured haematological and immune parameters. There were, for example, no significant differences in serum lysozyme activity, superoxide dismutase activity, immune globulin M concentration and C-reactive protein content among dietary treatments. Using quadratic regression analysis of WG data, the optimal dietary threonine inclusion for juvenile tilapia was estimated to be 1.33 % of the diet (4.74 % of dietary protein).     

Growth,feed utilization,and liver histology of juvenile Nile tilapia (Oreochromis niloticus) fed diets containing increasing levels of swine fat

Due to predictions that the expanding aquaculture sector cannot continue to rely on finite marine stocks for fish oil, there have been several research works within the aquafeed industry to find sustainable alternatives for dietary lipid sources. This study was conducted to evaluate the effects of a range of inclusion levels of rendered swine fat on the growth performance and liver histology of juvenile Nile tilapia, Oreochromis niloticus. Fish (initial weight ~ 20 g) were randomly stocked into twelve 1 m³ nylon mesh hapas and fed isoenergetic and isonitrogenous diets containing rendered swine fat at varying inclusion levels of 0% (Control), 5% (SF5), 7% (SF7), or 10% (SF10) for 84 days. The control diet contained 5% fish oil as the lipid source. At the end of the trial, there were no significant differences between the final weights of the fish that were fed the control (38.01 ± 0.76) and SF5 diets (37.85 ± 0.68), and both groups recorded significantly higher (P < 0.05) specific growth rates relative to the SF7 and SF10 groups. Specific growth rates ranged from 0.59% day^?1 (SF10) to 0.75% day^?1 (Control and SF5). The fish that were fed the SF7 and SF10 diets had significantly (P < 0.05) larger livers relative to the control and SF5 fish. Histological examination further revealed significant liver alterations in the SF7 and SF10 fish, as evidenced by hepatocyte nuclei migration, hepatic vacuolation, and varying degrees of steatosis. Calculations of profit indices showed that the SF5 diet offers the best economic viability, taking into consideration both the monetary values of fish produced and cost of feed fed over the trial period. The results of this study indicate that rendered swine as a sole lipid source in juvenile Nile tilapia diets can be included at 5% without depressing fish growth.     

Protein: energy ratio in practical diets for Nile tilapia Oreochromis niloticus

The present study was conducted to evaluate the interaction of protein and energy ratio in low protein (20, 25 and 30 %) diets for juvenile Nile tilapia (Oreochromis niloticus) (initial weight 7.44 ± 0.03 g). Dietary protein to energy (P/E) ratio of nine practical diets ranged from 66.84 to 115.14 mg protein/kcal energy. Each diet was randomly assigned to four replicate groups of fifteen fish. After 10 weeks, Fish fed the lowest dietary protein (20 %) and lowest energy (2,600 kcal/kg) diets were significantly smaller than fish maintained on D5 (25/2800) and D6 (30/2800), However, there were no significant differences among all the treatments except D1. The whole body moisture and protein levels were significantly influenced by dietary protein and energy content. Whole body energy content and digestible energy retention were significantly influenced by energy content of the diet. Conversely, dietary protein level significantly influenced protein retention but it did not influence digestible energy retention. Under the reported conditions, the response of tilapia to dietary energy or protein was seen only at the lower levels of inclusion and tilapia demonstrated limited protein sparing as dietary energy was increased. However, this did modify the carcass composition through higher dietary energy.     

Palm oil-laden spent bleaching clay as a substitute for marine fish oil in the diets of Nile tilapia, Oreochromis niloticus

A 8‐week feeding trial was conducted to determine the effect of substituting fish oil with palm oil‐laden spent bleaching clay (SBC), a by‐product from crude palm oil (CPO) refining, on growth, feed utilization, fatty acid composition and heavy metal accumulation in the muscle of Nile tilapia, Oreochromis niloticus. Four isonitrogenous and isolipidic practical diets were formulated to contain 0, 100, 200 or 300 g kg^?1 SBC. Growth performance of Nile tilapia was significantly better in fish fed the 100 g kg^?1 SBC diet compared with fish fed the 0, 200 or 300 g kg^?1 SBC diet. Growth and feed utilization efficiency of fish fed 200 or 300 g kg^?1 SBC were similar to fish fed the control diet without added SBC. Whole‐body composition, body‐organ indices and haematocrit of tilapia were not affected by dietary treatments. Fatty acid compositions in the muscle lipid of Nile tilapia were strongly influenced by dietary treatments with progressively elevated levels of total saturates and n‐6 PUFA because of the dietary influence of these fatty acids from residual CPO adsorbed onto SBC. A gradual decrease in total n‐3 PUFA concentrations were also observed with the ratio of n‐3 to n‐6 fatty acids in muscle lipids decreasing from 4.75 to 4.41, 3.23 or 2.37 after 8 weeks on the 0, 100, 200 or 300 g kg^?1 SBC diet, respectively. The arsenic, cadmium and lead concentrations in the experimental diets increased with increasing dietary levels of SBC but the concentrations of these heavy metals in the whole body and bone of Nile tilapia were not significantly different among fish fed the various diets. The present 8‐week study showed that in fishmeal‐based diets for Nile tilapia, palm oil‐laden SBC can totally replace added fish oil. The use of this presently discarded waste product from palm oil refining in tilapia diets will greatly contribute to reducing the impact of rising feed costs in the culture of tilapia in many tropical countries. Other potential benefits may include acting as a feed binder, removal of mycotoxins in fish feeds as well as adsorbing toxic substances present in the culture water.     

The optimal dietary level of ascorbic acid for juvenile Pacific bluefin tuna, Thunnus orientalis

A feeding experiment was conducted to evaluate the efficacy of, and determine the requirements for dietary AsA (l-ascorbic acid) using its popular derivative l-ascorbyl-2-monophosphate-Mg (APM) for juvenile Pacific bluefin tuna (PBT). The five test diets (with APM-0, -400, -800, -1200 and -1600) were prepared by adding 0, 400, 800, 1200 and 1600 mg of APM kg diet^?1, respectively. These diets, together with chopped sand lance (the control diet), were administered, in duplicate to 0.27 g PBT at 25 days after hatching (300 juveniles per 15 m³ tank). The PBT were fed to apparent satiety 6 times a day for 2 weeks. While final body weight, feed conversion and survival showed no differences among diets APM 400–1600, PBT fed APM-0 indicated lower growth performance together with anorexia, dark pigmentation and ataxia from 5 days and reached 80 % mortality at 12 days after the start of the feeding trial. In addition, liver and brain ascorbic acid (AsA) concentrations increased with increasing dietary APM levels, the values were similar in PBT fed diets with APM-1200 and APM-1600, and liver and brain concentrations of AsA were significantly higher in these fish than in the PBT fed the other diets (P < 0.05). The PBT responded to increasing dietary APM, and the fish fed APM-1200 had the highest weight gain, protein and lipid content. The data indicate that PBT can utilize APM as an AsA source and suggest that dietary supplementation with APM-1200 (454 mg AsA kg^?1 diet) would result in satisfactory growth.     

Dietary green tea extract improves growth performance, body composition, and stress recovery in the juvenile black rockfish, Sebastes schlegeli

In this study, we evaluated the effects of dietary green tea ethanol extract (GTE) supplementation on growth performance, body composition, and stress recovery of the juvenile black rockfish, Sebastes schlegeli. The fish (mean body weight, 8.1 ± 2.0 g) were fed fish meal diets that included 0 % (control), 1, 3, and 5 % GTE for 8 weeks. Weight gain, specific growth rate, feed efficiency, and protein efficiency rate were measured and compared among the fish in the different groups. The whole body and liver lipid compositions of fish fed the control diet were higher than those of the fish fed the GTE diets. Lysozyme activity in the plasma samples of fish fed the GTE diet showed an increasing trend in a dose-dependent manner. After administrating anesthesia (2-phenoxyethanol), the stress recovery time differed significantly between the control and the 3 and 5 % GTE diet groups and the mortality of fish fed on the GTE diet was significantly lower than that of the control group. In addition, plasma glucose levels in the fish fed the 3 % GTE diet showed a rapid recovery. Our results showed that the addition of GTE to the fish diet improved lipid utilization, lysozyme activity and stress recovery, and reduced total cholesterol levels in a dose-dependent manner.     

Effects of dietary palm oil source on growth,tissue fatty acid composition and nutrient digestibility of red hybrid tilapia,Oreochromis sp., raised from stocking to marketable size

A 20-week feeding trial was carried out to investigate the influence of three palm oil products as the principal dietary lipid source on the growth performance, proximate composition, tissue fatty acid composition and nutrient digestibility of red hybrid tilapia (Oreochromis sp.) fed these diets from stocking to marketable size. Four isonitrogenous (30% crude protein) and isoenergetic (16.5 kJ g^− 1) practical diets were formulated with 8% of added fish oil (FO), crude palm oil (CPO), palm fatty acid distillate (PFAD) or refined, bleached and deodorized palm olein (RBDPO), respectively. Each diet was fed to triplicate groups of 30 fish of 31.24 ± 0.05 g mean initial body weight. The tilapia were raised at 29 ± 1 °C in 12 round 1000 L fiberglass tanks with a continuous water flow rate of about 1.8 L/min.Results showed that the source of added lipid did not significantly influence (P > 0.05) final body weight, specific growth rate, feed conversion ratio, survival, body indices, hematocrit and production yield of tilapia. There was no significant difference in the fillet proximate composition of fish fed the various diets, except that fish fed the PFAD diet showed lower lipid deposition. The deposition of fatty acids in fish tissues was generally influenced by the fatty acid profile of the diets. Fillet fatty acid profiles of tilapia fed palm oil-based diets had significantly higher concentrations of saturated and monounsaturated fatty acids, but lower levels of polyunsaturated fatty acids (PUFA) compared to the fish fed the FO diet. Fillet of fish fed the FO diet had significantly higher concentrations of EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid) compared with fish fed palm oil-based diets. Dietary lipid source did not significantly affect dry matter and protein digestibility (62.1–64.8% and 83.5–85.0%, respectively). The inclusion of dietary palm-origin oils significantly reduced the total lipid digestibility of the diets due mainly to the decreased digestibility of the saturated fatty acids. In all treatments, the apparent digestibilities of both n − 3 and n − 6 PUFA were the highest, followed by monoenes, while the lowest were the saturated fatty acids. Despite the high free fatty acid content of PFAD (92.2%) compared to CPO (4.8%) and RBDPO (0.1%), the different free fatty acid content did not significantly affect the nutrient digestibility of the palm oil-based diets. Results obtained confirmed the feasibility of feeding tilapia with palm oil-based diets with a 100% substitution of added dietary fish oil throughout the grow-out cycle until marketable size.     

吉富罗非鱼对饲料中维生素B1的需要量

采用维生素B1(VB1)含量为0.08(对照组)、0.57、1.13、2.09、4.11和8.09 mg/kg的6种纯化饲料,分别饲养初始体质量为(64.4±1.5)g的吉富罗非鱼12周,研究VB1对其生长性能、部分血清生化指标、肝脏VB1蓄积量及转酮醇酶基因表达量的影响,以确定其对饲料VB1的需要量.结果显示,随着饲料中VB1含量增加,吉富罗非鱼增重率先呈线性增加后趋于稳定,当饲料中VB1含量为1.13、2.09、4.11、8.09 mg/kg时增重率达最大.吉富罗非鱼肝脏VB1含量随着饲料VB1含量增加不断增大,当增加到2.09 mg/kg后趋于稳定.饲料中缺乏VB1显著提高血清丙酮酸含量(P＜0.05),但对全鱼水分、粗脂肪、粗蛋白、灰分无显著性影响(P＞0.05).饲料中添加VB1显著提高血清高密度脂蛋白胆固醇和肝脏转酮醇酶基因表达量(P＜0.05).饲料中VB1含量大于1.13 mg/kg各组的肝脏转酮醇酶活性显著高于VB1含量小于0.57 mg/kg组(P＜0.05).折线回归分析表明,吉富罗非鱼(64 ～325 g)获得最佳生长时对饲料VB1需要量为1.16 mg/kg;肝脏VB1蓄积量达到最大时,对VB1的需要量为2.06mg/kg.