Effect of substitution of dietary fish meal by soybean meal on different sizes of gibel carp (Carassius auratus gibelio): digestive enzyme gene expressions and activities,and intestinal and hepatic histology

A 7‐week growth trial was conducted to evaluate the effects of dietary soybean meal (SBM) on digestive enzyme activity of intestinal mucosa, mRNA levels of digestive enzymes in hepatopancreas, and the mid‐intestinal and hepatopancreas histology of gibel carp CAS III (Carassius auratus gibelio). Four different growth phases of gibel carp (initial body weight: fry, 0.8 g; juvenile, 5.0 g; 1‐year‐old, 62.7 g; and broodstock, 135.6 g) were tested. Seven isonitrogenous and iso‐energetic diets were formulated to contain different SBM replacement levels (0%, 20%, 40%, 60%, 80% and 100% of dietary fish meal protein), and another diet (SBMAA) contained all SBM protein and supplied crystalline amino acids. The results showed that the activities of mid‐intestine trypsin, α‐amylase and gamma glutamyl transpeptidase reduced with increased dietary SBM, while the chymotrypsin activity increased first and then decreased. The ultrastructures of intestinal epithelial cells and hepatopancreas cells in fry and broodstock fish were distinctly affected by 200 g kg^‐1 dietary SBM. Supplementation of dietary amino acid to the highest replacement groups was not sufficient to improve digestive and absorptive capacities and growth performance. Gibel carp may be adapted to dietary SBM through increase in gene expression of hepatopancreas digestive enzymes and has potential to utilize proceeded SBM as feedstuffs.     

Effects of dietary coated protease on growth performance,feed utilization,nutrient apparent digestibility,intestinal and hepatopancreas structure in juvenile Gibel carp (Carassius auratus gibelio)

This study was conducted to investigate the effects of dietary protease on growth performance, feed utilization, whole‐body proximate composition, nutrient digestibility, intestinal and hepatopancreas structure of juvenile Gibel carp, Carassius auratus gibelio (mean weight 8.08 ± 0.18 g). Six diets were prepared, including a positive control diet (dietary protein 350 g/kg, PC), one negative control diet (dietary protein 33 g/kg, NC) and four protease supplementations diets, which were 75, 150, 300 and 600 mg/kg protease NC diet. After 12 weeks of diet feeding in indoor recycle aquarium tanks, no significant difference (p > .05) was found on growth performance between fish fed diet with 75–600 mg/kg protease and the PC group. Compared with the fish fed the NC diet, the specific growth rate of fish fed 300 mg/kg protease increased significantly (p < .05), as well as protein efficiency ratios (p < .05), while feed conversion was the opposite (p < .05). The nutrient digestibility of crude protein and lipid was higher (p < .05) in fish fed 150 mg/kg protease diet than the PC diet. Whole‐body proximate composition of fish was not affected (p > .05) by the dietary treatment. Serum alkaline phosphatase and albumin were significantly affected by dietary protease (p < .05), while the content of total protein, glucose, triglyceride, total cholesterol, aspartate aminotransferase and alanine aminotransferase activities in serum was not affected (p > .05). Foregut muscular thickness was thinner (p < .05), when the fish fed diets supplementation of protease in 150 or 600 mg/kg diet than the NC diet. Protease activities in hepatopancreas and foregut were higher (p < .05), in the fish fed 150 or 300 mg/kg protease diet than the fish fed the PC diet, but those in the mid‐ and hindgut were not significantly affected (p > .05) by the dietary treatments. Based on the regression analysis of weight gain rate, the optimal dietary inclusion level of protease was 400 mg/kg in the diet for juvenile Carassius auratus gibelio.     

Growth,feed utilization,body composition and swimming performance of giant croaker,Nibea japonica Temminck and Schlegel,fed at different dietary protein and lipid levels

A 50‐day feeding trial was conducted to examine the effects of dietary protein and lipid levels on growth, feed utilization, body composition and swimming performance of giant croaker, Nibea japonica. Fish (initial body weight 44.6 g ind⁻¹) were fed ten test diets which were formulated at 5 crude protein levels (360, 400, 440, 480 and 520 g kg⁻¹) and 2 crude lipid levels (90 and 150 g kg⁻¹). In addition, a raw fish diet (fillet of small yellow croaker) served as the reference. The weight gain (WG) increased, whereas the feed intake (FI) and feed conversion ratio (FCR) decreased, with increasing dietary protein level from 360 to 520 g kg⁻¹. At the same dietary protein level, no significant difference was found in the WG between fish fed the diets containing 90 or 150 g kg⁻¹ crude lipid. Fish fed the diet containing 480 g kg⁻¹ crude protein and 90 g kg⁻¹ crude lipid exhibited higher WG, nitrogen retention efficiency (NRE) and energy retention efficiency (ERE) but lower nitrogen wastes output (TNW). At the end of the feeding trial, the hepatosomatic index (HSI) and viscerosomatic index (VSI) decreased, whereas the body protein content increased, with increase in dietary protein level. The body lipid content was higher in fish fed at the 150 g kg⁻¹ lipid level than in fish fed at the 90 g kg⁻¹ lipid level. No significant difference was found in the maximum sustained swimming speed (MSS) between fish fed at different dietary protein and lipid levels. The WG, NRE, ERE and condition factor (CF) were higher, whereas the FI, FCR, HSI, VSI and TNW were lower, in fish fed the raw fish diet than in fish fed the diet containing 480 g kg⁻¹ crude protein and 90 g kg⁻¹ crude lipid. No significant difference was detected in the MSS between fish fed the raw fish diet and diet containing 480 g kg⁻¹ crude protein and 90 g kg⁻¹ crude lipid. The results of this study suggest that the suitable dietary crude protein and crude lipid levels are 480 g kg⁻¹ and 90 g kg⁻¹ for giant croaker reared in net pens.     

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).     

Effect of dietary leucine on growth performance,hemolymph and hepatopancreas enzyme activities of swimming crab,Portunus trituberculatus

An 8‐week feeding trial was conducted to determine the dietary leucine requirement for juvenile swimming crabs reared in cement pools. Six isonitrogenous and isolipidic practical diets (430 g/kg crude protein and 70 g/kg crude lipid) were formulated to contain graded leucine levels which ranged from 16.7 to 26.7 g/kg (dry weight). Each diet was randomly assigned to triplicate groups of 60 juvenile swimming crabs (initial average weight 3.75 ± 0.12 g) that were stocked in rectangle plastic baskets. The results of the present study indicated that dietary leucine levels significantly influenced weight gain (WG) and specific growth ratio (SGR) (p < .05), crab fed the diet containing 22.7 g/kg leucine had significantly higher WG and SGR than those fed the other diets. Feed efficiency and protein efficiency ratio were not significantly affected by the dietary leucine levels (p > .05). Total protein, cholesterol, triglyceride and glucose in serum were significantly affected by the dietary leucine levels. Aspartate aminotransferase (AST) and alanine aminotransferase activities in hemolymph, AST and superoxide dismutase activities in hepatopancreas were significantly affected by dietary leucine levels; moreover, crab fed the 16.7 g/kg leucine diet had higher malondialdehyde in hemolymph and hepatopancreas than those fed the other diets. Crab fed the diet containing 24.9 g/kg leucine had higher phenoloxidase activity in hemolymph than those fed the other diets. Based on two‐slope broken‐line model of SGR against dietary leucine levels, the optimal dietary leucine requirement for growth was estimated to be 22.1 g/kg of the dry diet (corresponding to 51.4 g/kg of dietary protein on a dry weight basis). In summary, findings of this study indicated that dietary leucine could improve growth performance and antioxidant status.     

Reduced fishmeal allowance with constant protein input for juvenile channel catfish Ictalurus punctatus

In this study, we evaluated different dietary fishmeal and protein levels on growth performance, intestinal structure and intestinal microbial community of juvenile channel catfish, Ictalurus punctatus. A total of 1800 fish distributed into 36 tanks were fed with nine different diets containing three protein levels (300, 330 and 360 g/kg) with three fishmeal (FM) levels (0, 30 and 60 g/kg) for 90 days. The results showed that significant interactions between the protein level and FM level were observed in final weight (FW), weight gain (WG), Na⁺, K⁺‐ATPase and alkaline phosphatase (AKP) activities. The significant lowest FW, WG, Na⁺, K⁺‐ATPase and AKP activities were observed in fish fed with no fishmeal and 300 g/kg protein dietary while the highest were shown in 60 g/kg fishmeal and 330 g/kg protein treatment. Additionally, the microvillar length of the mid‐intestine in catfish was significantly affected by the interaction between dietary protein level and fishmeal level. The intestinal samples were dominated by three major phyla, Firmicutes, Proteobacteria and Fusobacteria. Genera Romboutsia and Turicibacter accounted for probably 800 g/kg of the phylum Firmicutes; meanwhile, genus Cetobacterium represented more than 900 g/kg of the phylum Fusobacteria. In conclusion, this study indicated that channel catfish juveniles can be fed with a practical diet without fishmeal as long as the protein level increased to 360 g/kg; however, if the percentage of dietary protein was 300 g/kg, it seemed that fishmeal need to be supplied as a protein source.     

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 potassium requirement of fingerling Indian major carp,Labeo rohita (Hamilton), based on growth parameters,gill Na+‐K+ ATPase activity,tissue mineralization and antioxidant activities

To quantify the dietary potassium requirement of fingerling Labeo rohita (6.2 ± 0.12 cm; 1.98 ± 0.06 g), seven purified experimental diets (350 g/kg crude protein and 16.72 kJ/g gross energy) with graded levels of potassium (0.32, 1.35, 2.41, 3.46, 6.48, 9.47 and 12.39 g/kg diet) were fed to triplicate groups of fishes at 08:00, 12:00 and 16:00 hr to apparent satiation for 8 weeks. Live weight gain (LWG; 671.46%), specific growth rate (3.65%/day), protein efficiency ratio (2.16), protein gain (PG; 2.41 g/fish) and feed conversion ratio (1.32) were found to be best in fish fed diet containing 3.46 g/kg potassium. Gill Na⁺‐K⁺ ATPase activity was also highest in fish fed diet with 3.46 g/kg potassium. Potassium content of whole‐body, vertebrae and scales increased significantly with the increase in dietary potassium level up to 6.48 g/kg. Significant changes were also noted in serum malondialdehyde content, superoxide dismutase, catalase, glutathione peroxidase and alkaline phosphatase activity. Based on the maximum live weight and protein gain observed in the present study, the inclusion of 3.55 g/kg potassium is recommended for developing potassium‐balanced commercial feeds for intensive culture of fingerling L. rohita.     

Effect of dietary valine levels on the growth performance,feed utilization and immune function of juvenile golden pompano,Trachinotus ovatus

This experiment was designed to investigate the effects of dietary valine on the growth performance, feed utilization, digestive enzymes, serum antioxidant and immune indices of juvenile Trachinotus ovatus and determine its valine requirement. Six diets with different concentrations of L‐valine (15.0, 16.6, 18.6, 20.7, 23.5 and 25.4 g/kg dry diet, defined as diet Val‐1 to Val‐6.), were formulated to contain 430 g/kg crude protein with fish meal, soybean meal, peanut meal and precoated crystalline amino acids. Each diet was randomly assigned to triplicate treatments of 20 fish (the initial body weight was 5.34 ± 0.03 g) for 8 weeks. The results indicated that the final body weight and percent weight gain (PWG) increased with increasing valine concentration up to 18.6 g/kg (diet Val‐3), whereas the diets containing higher valine concentration reduced the growth performance significantly (p < .05). Moreover, the protein efficiency ratio, body protein deposition (BPD), muscle protein content, intestinal amylase and pepsin activities, serum T‐AOC, LZM activities, IgM, complement 3 and complement 4 concentration had a similar trend with PWG, and the trend of feed conversion ratio, serum AST, ALT activities, urea and MDA content was opposite. Meanwhile, the lipid contents of whole fish and muscle in diet Val‐6 were particularly lower than other diets (p < .05). The survival rate of diet Val‐1 was lowest in this study and was significantly lower than diet Val‐2 (p < .05). The results of polynomial regression based on PWG and BPD indicated that the optimal dietary valine requirement for Trachinotus ovatus reared in seawater‐floating net cages was 19.87–20.17 g/kg valine of dry diet, correspondingly 46.22–46.91 g/kg of dietary protein.     

The optimal dietary protein level of large‐size grouper Epinephelus coioides

An 8‐week feeding trial was conducted to determine the requirement of protein for large‐size grouper Epinephelus coioides (initial body weight: 275.07 ± 1.56 g). Six iso‐lipidic (124 g/kg) diets were formulated containing graded levels of protein (350, 400, 450, 500, 550 and 600 g/kg). Grouper was hand‐fed twice daily to apparent satiation with triplicate. The results showed that significantly high weight gain, specific growth rate and significantly low feed conversion ratio were observed in fish fed 450 g/kg protein group. High‐protein level diets significantly increased protein content and significantly decreased lipid content of fish body and muscle. Total protein and cholesterol content in serum of 600 g/kg group were significantly higher than those of 350 g/kg group. However, serum glucose and triglyceride contents of fish fed low‐protein diets were significantly higher than those of fish fed high‐protein diets. Meanwhile, liver glutamic‐pyruvic transaminase and glutamic‐oxaloacetic transaminase in high‐protein diet groups were significantly higher than those of low‐protein diet groups. The intestinal protease activity in high‐protein diet groups was significantly higher that of low‐protein diet groups, but lipase and amylase showed opposite trend. With the increasing of dietary protein level, the activities of alkaline phosphatase, superoxide dismutase and lysozyme in liver of grouper increased significantly compared with 350 g/kg group, while the activities of acid phosphatase decreased significantly. With specific growth rate as the evaluation index, the optimum dietary protein level of large‐size grouper Epinephelus coioides was 438.39 g/kg by fitting the broken‐line regression analysis.     

Effects of dietary inulin and Jerusalem artichoke (Helianthus tuberosus) on intestinal microbiota community and morphology of Nile tilapia (Oreochromis niloticus) fingerlings

This study investigated the effects of dietary inulin and Jerusalem artichoke (JA) on intestinal microbiota and morphometry of Nile tilapia fingerlings. Five treatment diets were designed to supplement inulin at 0 (basal diet), 2.5 and 5.0 g/kg, and JA at 5.0 and 10.0 g/kg. Nile tilapia larvae were fed experimental diets from the first feeding through the fingerling stage (84 days). The cultivation‐dependent technique showed that dietary inulin at 5.0 g/kg and JA (at both levels) increased lactic acid bacteria and Bifidobacterium spp., but decreased Vibrio spp. (p < .05). PCR‐DGGE targeting 16S ribosomal RNA gene revealed that dietary inulin and JA generated different profiles of microbial community compared with fish fed a basal diet. Compared with fish fed the basal diet, a greater intestinal villi height was observed in fish fed 5.0 g/kg inulin and JA at both levels (p < .05). A larger relative goblet cell number were observed in the anterior intestine of fish fed 5.0 g/kg inulin or JA (p < .05). Overall, dietary inulin (5.0 g/kg) and JA (5 and 10.0 g/kg) since the first feeding had effects on modulating the intestinal microbiota and morphology of Nile tilapia fingerlings.     

Dietary supplementation of autolysed yeast enhances growth,liver functionality and intestinal morphology in African catfish

A feeding trial was conducted to evaluate the potential of dietary supplementation of autolysed brewer's yeast (AY) on African catfish. The catfish (22.5 ± 1.15 g/fish, 20 fish 33 L/tank) were fed with either of diets (390 g/kg crude protein, 140 g/kg lipid) supplemented with 0, 3, 6 or 10 g/kg AY (n = 3). After 49 days of feeding, the final body weight and metabolic growth rate of the catfish fed 3 g/kg AY (3‐AY) diet were higher than those fed the control diet (p < .05). The lowest level (p < .05) of alanine transaminase was detected in the blood of the catfish fed 3‐AY diet. The mid‐intestinal histology of the catfish revealed no significant difference (p > .05) in intestinal perimeter ratio. However, an elevated (p < .05) abundance of goblet cells and intraepithelial leucocytes were found in the intestine of catfish fed 3, 6 and 10 g/kg AY diets, with the highest level of abundance recorded in the mid‐intestine of the catfish fed 3‐AY diet. The results suggest that dietary 3 g/kg autolysed brewer's yeast supplementation improves growth performance of African catfish without deleterious effect on liver functionality and gut morphology.     

Effects of dietary mulberry leaf extract on the growth,gastrointestinal, hepatic functions of Chinese giant salamander (Andrias davidianus)

Mulberry leaf extract (MLE), an active substance extracted from mulberry leaves, is known to have a positive effect on several physiological functions. The current study examined the effects of dietary MLE in feed at concentrations 0, 3.0, 6.0, 9.0, 12.0 and 15.0 g/kg on the growth performance and gastrointestinal and hepatic functions of Andrias davidianus for 12 weeks. Results indicated that the final body weight, weight gain rate (WGR), specific growth rate and feed intake (FI) of A. davidianus increased with the increase in the dietary MLE up to 9.0 g/kg and declined thereafter, while the feed conversion ratio (FCR) exhibited an opposite trend. Meanwhile, A. davidianus with a dietary intake of 9.0 g/kg MLE showed higher levels of crude protein in muscles and lower levels of moisture and crude lipid levels in the liver and muscles when compared with the control. In addition, dietary MLE increased the density and length of the villi and decreased the cavity rate in the foregut, enhancing the activities of carbonic anhydrase, H⁺‐K⁺‐ATPase, pepsin, intestinal trypsin, lipase and Na⁺‐K⁺‐ATPase (p < .05) in the stomach. Furthermore, dietary MLE increased the intestinal and hepatic superoxide dismutase activities and total antioxidative capacities but decreased their malondialdehyde contents in A. davidianus. Dietary MLE also significantly increased the immune parameters, and the plasma total protein, albumin and immunoglobulin M contents but significantly decreased the aspartate aminotr‐ansferase, alanine aminotransferase and diamine oxidase activities, and the total bilirubin, direct bilirubin, cholesterol, triglyceride and endotoxin contents (p < .05). In conclusion, a quadratic regression analysis of WGR and FCR indicated that the optimum level of MLE for A. davidianus was between 8.21 and 8.30 g/kg of the diet.     

Dietary lysine requirement of juvenile dusky kob,Argyrosomus japonicus

To determine dietary lysine requirement of dusky kob, Argyrosomus japonicus, six isonitrogenous and isoenergetic diets (431 g/kg crude protein, 141 g/kg lipid and 20 kJ/kg) were formulated with graded levels of crystalline L‐lysine (18–42 g/kg of the dry diet). The protein source in the basal diet comprised fishmeal and soya, where a combination of L‐aspartic and L‐glutamic acids was maintained at a ratio of 1:1, and all diets were supplemented with a mixture of crystalline essential amino acids to simulate the amino acid profile in dusky kob. Dietary treatments were randomly assigned to triplicate groups of 12 fish (4.5 ± 0.2 g, mean weight; 66.5 ± 1.1 mm, total length ± SD), which were fed to apparent satiation three times daily for 12 weeks. The fish fed dietary L‐lysine at 21, 29 and 33 g/kg dry diet showed the highest specific growth rates (SGR) and the lowest feed conversion ratio. For most amino acids, retention in the body of the fish increased with an increase in dietary lysine from 18 to 21 g/kg, and it reached a maximum somewhere between 21 and 33 g/kg, where after amino acid retention decreased with increasing dietary lysine. Based on SGR and using segmented broken‐line analysis, the dietary L‐lysine requirement of juvenile dusky kob was estimated at 31.7 ± 1.6 g/kg dry diet corresponding to 73.5 g lysine per kg protein.     

Determination of dietary phosphorus requirement of stinging catfish Heteropneustes fossilis based on feed conversion,growth, vertebrae phosphorus,whole body phosphorus,haematology and antioxidant status

A 12‐week feeding trial was conducted to determine the dietary phosphorus requirement of Heteropneustes fossilis fingerlings (7.7 ± 0.04 g). Fish were fed casein–gelatine‐based purified diets in triplicate groups near satiation with seven different levels of dietary phosphorus (3.2, 5.2, 7.2, 9.2, 11.2, 13.2 and 15.2 g/kg dry diet). All diets were formulated to be isoproteic (400 g/kg) and isoenergetic (17.89 kJ/g). Highest absolute weight gain (68.38 g/fish), best feed conversion ratio (1.48), protein retention efficiency (30.74%), protein gain (12.44 g/fish), haemoglobin (11.19 g/dL), RBCs (3.12 x10⁶/mm³), haematocrit (33.44%) and serum phosphate (2.82 mg/L) were found at 9.2 g/kg phosphorus. Hepatic superoxide dismutase and catalase activity were also significantly influenced by the dietary phosphorus levels. Whole body and vertebrae phosphorus concentrations increased significantly as the amount of dietary phosphorus increased from 3.2 to 11.2 g/kg dry diet and then plateaued. More accurate information on dietary phosphorus requirement was obtained by subjecting the AWG, FCR, vertebrae phosphorus and whole body phosphorus concentrations data against various levels of dietary phosphorus to broken‐line analysis, which yielded the requirement in the range of 9.0–11.0 g/kg for optimum growth and mineralization of H. fossilis.     

Effects of phospholipid addition to diets with different inclusion levels of fish oil on growth and fatty acid body composition of juvenile swimming crab Portunus trituberculatus

Six experimental diets were designed with two phospholipid (PL; 0% and 1.5%) and three fish oil levels (0%, 1% and 3%) to evaluate the effects of dietary fish oil and PL levels on growth, survival and fatty acid composition of juvenile swimming crab, Portunus trituberculatus. Diets were iso‐energetic and iso‐nitrogenous and each diet was fed to triplicate groups (initially weight, 24.88 ± 0.04 g per crab) for 59 days. Weight gain (WG) and specific growth rate (SGR) increased with dietary PL addition to 0% fish oil‐supplemented diets (P < 0.05). On the other hand, WG and SGR decreased with dietary PL addition to 3% fish oil diets (P < 0.05). Crabs fed PL supplemented diets had higher haemolymph low‐density lipoprotein cholesterol concentrations and muscle crude lipid levels (P < 0.05) than crabs fed a none PL supplemented diet. The percentage of highly unsaturated fatty acids (HUFA; % total FA) in both polar and neutral lipids fractions of muscle tissue only increased in case of PL addition to 0% and 1% fish oil‐supplemented diets (P < 0.05). HUFA levels in the neutral lipids fraction of the hepatopancreas increased by dietary PL addition at each dietary fish oil level (P < 0.05). In this study, both dietary fish oil and PL addition contributed to a high n‐3/n‐6 ratio in muscle and hepatopancreas of P. trituberculatus. In conclusion, PL addition is only meaningful with fish oil‐deficient diets, in which case it enhanced lipid transport and HUFA absorption efficiency, hence improving the nutritional value of the diet.     

Effects of dietary protein levels on the growth performance, digestive capacity and amino acid metabolism of juvenile Jian carp (Cyprinus carpio var. Jian)

This experiment was conducted to evaluate the effects of protein levels on the growth performance, digestive capacity and amino acid metabolism of juvenile Jian carp. Brown fish meal was used as the sole protein source in the present study. Six isoenergetic experimental diets containing 14.4 MJ kg^?1 of digestible energy and 220–495 g crude protein kg^?1 diets were fed to triplicate groups of 50 fish with a mean initial weight of 16.67 ± 0.01 g for 45 days. Per cent weight gain (PWG) and feed efficiency ratio (FER) improved with an increase in the dietary protein levels up to 330 g kg^?1 diet. The condition factor, relative gut length, intestinal folds height, hepatopancreas and intestine protein content improved with an increase in the protein levels up to 330–385 g kg^?1 diet. Trypsin, creatinkinase, Na⁺, K⁺‐ATPase and alkaline phosphatase activities generally followed the same tendency as that of growth parameters. Amylase and γ‐glutamyl transpeptidase (γ‐GT) activities were negatively correlated with increasing protein levels from 220 to 330 g kg^?1 diet, and no differences were found thereafter. Lipase activity was unaffected by protein levels. Lactobacillus amount was increased with protein levels up to 275 g kg^?1 diet, while Aeromonas amount followed the opposite pattern. Escherichia coli amount was not influenced by dietary protein levels. Glutamate–oxaloacetate transaminase (GOT) activities in the hepatopancreas and plasma ammonia concentration (PAC) were not influenced by protein levels between 220 and 275 g kg^?1 diet, but significantly increased with increasing protein levels from 275 to 440 g kg^?1 diet, and remained similar thereafter. Glutamate–pyruvate transaminase (GPT) activities significantly increased with protein levels >275 g kg^?1 diet. Based on the broken‐line model, the dietary protein requirement for PWG of Jian carp (16.7–55.0 g) was estimated to be 341 g kg^?1 diet with a digestible energy of 14.4 MJ kg^?1 diet.     

Effects of dietary lipid levels on growth,feed utilization,digestive tract enzyme activity and lipid deposition of juvenile Manchurian trout,Brachymystax lenok (Pallas)

Six isoproteic diets were designated to evaluate the effects of dietary lipid levels (from 70 to 270 g/kg) on the growth performance, feed utilization, digestive tract enzyme activity and lipid deposition of juvenile Brachymystax lenok (average initial weight 0.54 ± 0.04 g). Each diet was fed to triplicate tanks (30 fish per tank) in an indoor closed recirculating system for 9 weeks. Final body weight and weight gain were highest in fish fed 190 g/kg diet and lowest in fish fed the 70 g/kg diet. Specific growth rate of fish fed with 190 g/kg diet was significantly higher than those fed with 70 and 270 g/kg diets (p < .05). Protein efficiency ratio of fish fed with 70 g/kg diet was significantly lower than the 110–230 g/kg treatments and was not significantly different from the 270 g/kg treatment. Fish fed with 270 g/kg diet had significantly higher hepatosomatic index and viscerosomatic index than those fed with 70–190 g/kg diets (p < .05). Intraperitoneal fat ratio and the whole‐body lipid content had a trend to increase with increase in dietary lipid level. Muscle crude lipid content increased up to 190 g/kg with increase in dietary lipid level. Lipid retention decreased with increase in dietary lipid level, while no significant differences in protein intake and retention levels were observed in fish among all treatments. Lipase activity of the mixture of pyloric caeca and foregut in fish fed 190 and 230 g/kg diets was significantly higher than those fed 70 and 110 g/kg diets. Midgut and hindgut lipase activities of fish were significantly higher than those fed the 190 and 230 g/kg diets. In conclusion, based on the second‐order polynomial model of WG and FCR, this study suggested that 173.8–195.0 g/kg dietary lipid levels were appropriated for B. lenok.     

Dietary folic acid requirement of fingerling Catla,Catla catla (Hamilton)

The dietary folic acid requirement of fingerling Catla catla (3.4 ± 0.17 g; 7.6 ± 0.41 cm) was evaluated by feeding casein–gelatin‐based isonitrogenous (350 g/kg crude protein) and isocaloric (16.72 kJ/g GE) diets containing different concentrations of folic acid (0, 0.2, 0.4, 0.6, 0.8, 1.0, 2.0 mg/kg) to triplicate groups to apparent satiation at 08:00, 12:30 and 17:30 hr for 16 weeks. Absolute weight gain (AWG; 40.07 g/fish), specific growth rate (SGR; 2.25%), feed conversion ratio (FCR; 1.53), protein retention efficiency (PRE; 31.42%) and protein gain (PG; 6.74) improved significantly (p < .05) with increasing folic acid levels up to 0.4 mg/kg diet and then reached a plateau. However, maximum liver folic acid concentration increased up to 0.6 mg/kg diet. Dietary folic acid levels also significantly affected (p < .05) body composition of fish. No significant change (p > .05) in haematological parameters except in fish fed folic acid‐free diet was noted. Antioxidant and immune parameters increased with increasing concentration of dietary folic acid up to 0.4 mg/kg diet. Broken‐line regression analysis of AWG, FCR, PRE, PG, HCT and liver folic acid concentrations of fingerling C. catla against dietary folic acid levels indicated optimum growth, FCR, PRE, PG, HCT and liver folic acid saturation ranging between 0.22 and 0.56 mg/kg diet, respectively.