The effect of soybean oil containing stearidonic acid on growth performance,n‐3 fatty acid deposition and sensory characteristics of pacific white shrimp (Litopenaeus vannamei)

The ability of shrimp Litopenaeus vannamei to utilize soy oil (SO) modified to contain stearidonic acid (SDA) in replacement of fish oil (FO) by converting SDA to highly unsaturated fatty acids (HUFA) was examined. Six diets with either supplemental modified SO or FO and three levels of fishmeal (FM) replacement (0%, 50% and 100%) by soybean meal (SBM) were fed to shrimp (1.7 g) for 12 weeks. The effect of oil source at the three SBM levels on growth and fatty acid profiles was examined by contrast analysis and sensory attributes by t‐tests (5% error rate). At 0% SBM inclusion, there was no effect of dietary oil source, while at the highest SBM inclusion level, shrimp fed the FO diet outperformed those fed the corresponding SO diet. Oil source had no effect on sensory attributes. The fatty acid profiles of the shrimp reflected that of the diets. SDA SO can replace supplemental FO in diets for shrimp with no reduction in growth when there is sufficient oil present from FM. At low FM, however, replacing FO with SDA SO reduces shrimp performance and tissue n‐3 HUFA levels. It is concluded that SDA is unable to meet the essential fatty acid needs of shrimp.     

Replacement of fish oil with a DHA‐rich Schizochytrium meal on growth performance,activities of digestive enzyme and fatty acid profile of Pacific white shrimp (Litopenaeus vannamei) larvae

This trial was conducted to evaluate the effects of replacing dietary fish oil with Schizochytrium meal for Pacific white shrimp (Litopenaeus vannamei) larvae (initial body weight 4.21 ± 0.10 mg). Six test microdiets were formulated using Schizochytrium meal to replace 0 g/kg, 250 g/kg, 500 g/kg, 750 g/kg, 1000 g/kg or 1500 g/kg fish oil DHA. No significant differences were observed in survival, growth, final body length and activities of digestive enzyme among shrimp fed different diets (p > .05). No significant differences were observed in C20:5n‐3 (EPA) in muscle samples (p > .05). C18:3n‐3 and C20:4n‐6 in muscle increased as Schizochytrium meal replacement level increased (p < .05). No significant differences were observed in C22:6n‐3 (DHA) and n‐3 fatty acids among shrimp fed diets that algae meal replaced 0 g/kg ‐ 1000 g/kg of fish oil. Shrimp fed diet R150 had higher DHA content than other groups and had higher n‐3 fatty acids than that of shrimp fed diets R50, R75 and R100 (p < .05). C18:2n‐6, PUFA and n‐6 fatty acids in muscle increased, while n‐3/n‐6 ratio decreased with increasing algae meal replacement level from 0 g/kg to 1000 g/kg (p < .05). In conclusion, Schizochytrium meal could replace 1500 g/kg fish oil DHA in the microdiets without negatively affecting shrimp larvae survival, growth and activities of digestive enzyme.     

Nutritional evaluation of fatty acids for the open thelycum shrimp, Litopenaeus vannamei: I. Effect of dietary linoleic and linolenic acids at different concentrations and ratios on juvenile shrimp growth, survival and fatty acid composition

A 6‐week feeding trial was conducted to evaluate the nutritional value of dietary linoleic (18:2n‐6, LOA) and linolenic (18:3n‐3, LNA) acids for juvenile Litopenaeus vannamei by determining their effects on growth, survival and fatty acid composition of hepatopancreas and muscle tissue. Diets were formulated to contain 5% total lipid. A basal diet contained only palmitic and stearic acids, each at 2.5% of diet. Six diets contained one of three levels (0.25, 0.5 and 1%) of either LOA or LNA, and three diets had different ratios of LNA/LOA (1, 3, 9) at a combined inclusion level of 0.5% of diet. An additional diet contained 0.5% of a mixture of n‐3 highly unsaturated fatty acids (HUFA). The fatty acid profile of hepatopancreas and muscle of shrimp reflected the profile of the diets. HUFA of the n‐3 family showed higher nutritional value than LOA or LNA for juvenile L. vannamei by producing significantly (P < 0.05) higher final weight and weight gain. Neither LOA nor LNA, alone or in combination, improved growth significantly compared with shrimp fed the basal diet.Thus, dietary requirements for LOA and LNA were not demonstrated under these experimental conditions.     

Nutritional evaluation of fatty acids for the open thelycum shrimp, Litopenaeus vannamei: II. Effect of dietary n-3 and n-6 polyunsaturated and highly unsaturated fatty acids on juvenile shrimp growth, survival, and fatty acid composition

This study evaluated the nutritional value of dietary n‐3 and n‐6 polyunsaturated fatty acids (PUFA) such as linoleic (LOA) and linolenic (LNA) acids, and highly unsaturated fatty acids (HUFA) such as arachidonic (AA), eicosapentaenoic (EPA), and docosahexaenoic (DHA) acids for juvenile Litopenaeus vannamei, based on their effects on growth, survival, and fatty acid composition of hepatopancreas and muscle tissue. Diets contained 5% total lipid. A basal diet contained palmitic and stearic acids each at 2.5% of diet. Five diets contained 0.5% dry weight of LOA, LNA, AA, EPA, or DHA. An additional diet evaluated HUFA in combination by supplementing at 0.5% of diet, a mixture of n‐3 HUFA. All HUFA showed higher nutritional value than PUFA for shrimp and produced significantly (P < 0.05) higher final weight, weight gain, and total lipid in shrimp muscle. Fatty acid profiles of shrimp tissues reflected the composition of the dietary lipids. In general, saturated fatty acids were more abundant in the neutral factions, while PUFA and HUFA were more abundant in the polar fractions of tissues. Under these experimental conditions, HUFA had much greater nutritional value than PUFA for juvenile L. vannamei; moreover, dietary requirements for PUFA were not demonstrated.     

Effects of dietary n‐3HUFA on different growth stages of the white shrimp,Litopenaeus vannamei: Growth,haematological characteristics,enzyme activities and fatty acid profiles

This study investigated the effects of n‐3 high unsaturated fatty acid (n‐3HUFA) levels on the growth performance, antioxidant enzyme activities and fatty acid profiles of both subadult and adult Litopenaeus vannamei (L. vannamei). Seven iso‐nitrogenous and iso‐lipidic diets were used, containing n‐3HUFA concentrations of 1.6 (control), 4.8, 7.4, 13.9, 23.9, 29.2 and 34.4 g/kg, respectively. Two 8‐week feeding trials were conducted to determine the dietary n‐3HUFA requirements of L. vannamei with an initial body weight of 4.25 ± 0.00 g (subadults) and 8.50 ± 0.01 g (adults). The results showed that the dietary n‐3HUFA level significantly affected the weight gain rate (WGR), specific growth rate, the feed conversion ratio and the hepatosomatic index (HSI) (p < 0.05), but did not significantly affect the survival rate (p > 0.05). At appropriate level, dietary n‐3HUFA improved growth performance and HSI of both subadult and adult L. vannamei. Both subadults and adults showed significant differences in body composition (p < 0.05), except for moisture and crude ash (p > 0.05). Cholesterol and low‐density lipoprotein significantly decreased with increasing dietary n‐3HUFA both in subadults and adults (p < 0.05); however, triglyceride showed no significant change (p > 0.05). High‐density lipoprotein (HDL) in subadults was significantly affected by dietary n‐3HUFA (p < 0.05), but followed no apparent regularity; HDL significantly changed in adults and showed an upward trend followed by a downward trend (p < 0.05). There was no significant effect on aspartate transaminase (AST) activity in subadults, but AST in adults and alanine transaminase (ALT) in subadults and adults were significantly affected (p < 0.05). Dietary n‐3HUFA significantly affected serum polyphend oxidase, malic dehydrogenase, alkaline phosphatase, superoxide dismutase and sodium‐potassium adenosine triphosphatase enzyme activities in gills (p < 0.05). The fatty acid composition of the shrimp tissue was associated with the fatty acid composition of the diet. Dietary n‐3HUFA supplementation significantly improved the contents of tissue ∑HUFA and n‐3HUFA, increased the n‐3/n‐6 ratio in the tail muscle and decreased the contents of tissue polyunsaturated fatty acid and saturated fatty acid (p < 0.05). Based on the WGR, the broken‐line equations indicated that the optimum requirements of dietary n‐3HUFA were determined to be 9.0 and 5.1 g/kg for subadult and adult L. vannamei, respectively.     

Effect of partial and total replacement of fish, shrimp head, and soybean meals with red crab meal Pleuroncodes planipes (Stimpson) on growth of white shrimp Litopenaeus vannamei (Boone)

Red crab meal (RCM), as a potential protein source in diets for juvenile shrimp Litopenaeus vannamei, was evaluated over a 45‐day growth trial under laboratory conditions. Eight experimental diets were tested. The basal diet contained fish (tuna by‐product), shrimp head and soybean (solvent extracted) meals as primary protein sources. Fish or soybean meals were substituted, on an equal‐protein basis, at 33%, 66% and 100% by RCM, whereas shrimp head meal (SHM) was substituted at 100%. A commercial diet was included as a reference. Final weight ranged between 2.23 and 3.36 g and growth rates (GRs) between 0.048 and 0.073 g day⁻¹. Where 66% or 100% of the protein from fish or soybean meals was substituted by RCM, the diets produced significantly higher final weights and GRs than other diets. Regression analysis showed that final weight of shrimp depended significantly on the percentage of substitution, and that the maximum weight gain would be obtained when substituting RCM for 80.2% of fish meal and 81.2% of soybean meal. Feed conversion ratio was below 1.8 for all treatments and there was no apparent relationship with other aspects of the diet. Red crab meal served as a suitable protein source for partial or total replacement of tuna by‐product, soybean and SHMs for cultivated juvenile shrimp L. vannamei.     

Replacement of fish meal by meat and bone meal in practical diets for the white shrimp Litopenaeus vannamai (Boone)

The use of meat and bone meal (MBM) was evaluated as a replacement for fish meal in a practical diet formulated to contain 41% protein and 8% lipid. Anchovy meal was replaced by 0%, 20%, 30%, 40%, 50%, 60% and 80% of MBM (diets 1–7) respectively. Healthy post larvae of Litopenaeus vannamei were reared in an indoor, semi‐closed recirculating system. Each dietary treatment was fed to triplicate groups of 40 shrimp per tank (260 L) arranged in a completely randomized design. The shrimp were hand‐fed to near‐satiation three times daily between 07:00 and 18:00 hours for 56 days. There were no significant differences (P>0.05) in growth performance among shrimp fed diets 1–6. However, shrimp fed diet 7 had significantly lower (P<0.05) growth than those fed diet 2 or diet 4. Survival ranged from 95% to 100% and did not significantly (P>0.05) differ. Feed conversion ratio (FCR) and carcass composition of the shrimp were not significantly (P>0.05) affected by dietary treatments. No significant differences (P>0.05) in protein efficiency ratio (PER) were found among shrimp fed diets 1‐6. However, shrimp fed diet 7 had significantly lower (P<0.05) PER than those fed diet 1 or diet 4. Results showed that up to 60% of fish meal protein can be replaced by MBM with no adverse effects on growth, survival, FCR, PER and body composition of L. vannamei.     

The use of HUFA-rich algal meals in diets for Litopenaeus vannamei

A 15‐week growth trial was conducted with juvenile, Pacific white shrimp Litopenaeus vannamei to study the efficacy of using algal meals as a source of highly unsaturated fatty acids in practical diets that are designed to contain no marine protein or oil sources. Based on previous study, a practical diet was designed containing co‐extruded soybean poultry by‐product meal with egg supplement and soybean meal as the primary protein sources for formulations containing 350 g kg^?1 crude protein and 100 g kg^?1 lipid. To further refine the diets, the fish oil in two of the diets was completely substituted with plant oils and oil originating from microbial fermentation products rich in docosahexanoic acid (DHA) and arachidonic acid (ArA). A commercial shrimp feed was also included in the trial for comparison. The mean values for shrimp final weight (17.8 g), yield (537.7 g m^?2 or 703.2 g m^?3), survival (98.5%) and feed conversion ratio (1.4 : 1) showed no statistically significant differences between diets. The results suggest that co‐extruded soybean poultry by‐product meal and oil from heterotrophic microalgal fermentation sources can be potential candidates for fish meal and marine oil replacement in shrimp diets.     

Effects of dietary n‐3HUFA on juvenile white shrimp,Litopenaeus vannamei: Growth,feed utilization,antioxidant enzymes activities and fatty acid compositions

Present study investigates the effects of n‐3 high‐unsaturated fatty acid (n‐3HUFA) levels on growth performance, antioxidant enzymes activities and fatty acid compositions of juvenile Litopenaeus vannamei. These represented seven iso‐nitrogenous and iso‐lipidic diets. Analysed n‐3HUFA concentrations were 0.16% (control), 0.48%, 0.74%, 1.39%, 2.39%, 2.92% and 3.44% respectively. A total of 840 juvenile L. vannamei were randomly stocked into 21 0.5 m³ tanks for 56 days. A significant increase (p < 0.05) was observed from 0.16% to 0.74% n‐3HUFA and a decrease when n‐3HUFA was above these levels in weight gain rate (WGR) and specific growth rate. Total cholesterol, triglyceride and low‐density lipoprotein in serum showed a significant decrease, high‐density lipoprotein showed a significant increase (p < 0.05). Phenoloxidase activity in serum and sodium‐potassium adenosine triphosphatase activity in gill were significantly affected by dietary n‐3HUFA (p < 0.05), both of them showing a downward trend after upward. Malic dehydrogenase and superoxide dismutase activities in serum were also significantly affected by dietary n‐3HUFA (p < 0.05), which rose first and then decreased in general, both of them have a maximum in 2.39% group. No significant differences of the activities of aspartate transaminase and alanine transaminase were observed among all groups (p > 0.05). With dietary n‐3HUFA increase, both ∑HUFA and n‐3HUFA contents gradually increased in hepatopancreas and tail muscles (p < 0.05). Based on broken‐line regression analysis of WGR, the optimal n‐3HUFA requirement is 0.89% for juvenile L. vannamei with initial weight of 0.50 ± 0.01 g.     

Estimation of Arachidonic Acid Requirement for Improvement of Pre‐maturation Growth and Egg and Larval Quality in the Female Blue Gourami (Trichopodus trichopterus; Pallas, 1770): A Model for the Anabantidae Family

This study investigates the dietary arachidonic acid (ARA) requirement from juvenile to maturation stage in an anabantid model fish, the blue gourami, Trichopodus trichopterus. Specifically we determined the optimum dietary ARA content to maximize juvenile growth and subsequent sexual maturation and to improve the quality of their eggs and offspring. Five experimental diets containing 0.02, 0.53, 1.05, 1.60, and 2.12% ARA (of dry weight) were fed to juveniles over 5 mo. The results showed that whole‐body fatty acid profile of broodstock significantly changed in fish fed diets of different ARA content (ANOVA, P < 0.003). The highest contents of 18:2n‐6 and Σn‐6 were obtained in fish fed 0.53% ARA, and a decreasing trend was observed with elevated dietary ARA levels. Monthly specific growth rate (SGR) measurements revealed significant differences in the juvenile stage, but the SGR of broodstock was unaffected by dietary ARA. Protein and ash content of whole‐body broodstock showed no differences among groups, while lipid content decreased as ARA levels increased. Maximum volume of the oocyte was obtained in the 1.05% ARA group, while the yolk sac size increased as dietary ARA increased. The optimum growth and survival of the larvae produced by broodstock were recorded in the 2.12 and 1.6% ARA groups, respectively. It was concluded that despite the presumed ability of freshwater fish to synthesize and meet their highly unsaturated fatty acid requirements, dietary ARA higher than 1.05% had significant stimulatory effects on growth of juveniles but no obvious influence on the growth of matured fish. Also, higher ARA levels (1.6–2.12%) were found to improve the quality of eggs and offspring.     

Effects of dietary n‐3 long‐chain unsaturated fatty acid on growth performance,lipid deposition,hepatic fatty acid composition and health‐related serum enzyme activity of juvenile Japanese seabass Lateolabrax japonicus

Studies were conducted to investigate the effects of dietary n‐3 long‐chain polyunsaturated fatty acid (n‐3 LC‐PUFA) on growth performance, lipid deposition, hepatic fatty acid composition and serum enzyme activities of juvenile Japanese seabass Lateolabrax japonicus (initial mean weight 29.2 ± 1.34 g). Triplicate groups of 30 Japanese seabass were fed with six diets containing grade levels of n‐3 LC‐PUFA (1.30, 2.98, 5.64, 10.31, 14.51, 24.13 g kg^–1 of dry weight) to apparent satiation twice daily for 9 weeks. The specific growth rate (SGR) was the highest in 10.31 g kg^–1 dietary n‐3 LC‐PUFA group. Crude lipid content of the fish decreased significantly with increasing dietary n‐3 LC‐PUFA. Meanwhile, the hepatic lipid content increased significantly in the 24.13 g kg^–1 group. Hepatic n‐3 LC‐PUFA content of total fatty acids was closely correlated with that in diet. No significant difference was observed in serum alanine transaminase (ALT) and aspartate aminotransferase (AST) activities. Moderate n‐3 LC‐PUFA level (10.31 g kg^–1 of dry weight) in the diet was beneficial to enhance the activity of lysozyme in serum. Based on SGR, the optimum dietary n‐3 LC‐PUFA content was estimated to be around 10.94 g kg^–1 of dry weight by second‐order polynomial regression method.     

First step of non‐fish meal,non‐fish oil diet development for red seabream, (Pagrus major), with plant protein sources and microalgae Schizochytrium sp

A feeding experiment was conducted to develop non‐fish meal and non‐fish oil diet for red seabream by using plant protein source and Schizochytrium meal which is rich in 22:6n‐3 (DHA). Three iso‐nitrogenous and iso‐lipidic experimental diets were prepared (CP 41.2% ± 0.4%, CL 16.4% ± 1%). Control diet contained both fish meal (40%) and fish oil (6%). In the second diet, fish meal was replaced by plant meals (soy protein concentrate, soybean meal, corn gluten meal) [FO]. In the third diet, fish meal and fish oil were replaced by algae meal (Schizochytrium sp. powder) and plant proteins [AO]. Duplicated groups of juvenile red seabream (8.8 g ± 1.5) were fed the experimental diets for 12 weeks to near satiation. There was no statistical difference among treatment in specific growth rate. Feed conversion ratio of AO diet group was higher than that of control. In wet basis, whole body protein level was significantly higher in AO diet than FO group while lipid content was lower than control group. In fatty acid profile, AO group had significantly lower 18:4n‐3, 20:4n‐3, 22:5n‐3 and 20:5n‐3 (EPA) level, but significantly higher 18:3n‐3 and DHA level than the other two diet fed fish. The results might suggest that further developments in microalgae diet offer a promising lipid source of n‐3 PUFA as essential fatty acid on marine fish. And it showed possibility to develop non‐fish meal and non‐fish oil feed for marine aquaculture fish by using microalgae.     

Influence of 18:2n‐6/20:5n‐3 ratio in diets on growth and fatty acid composition of juvenile abalone,Haliotis discus hannai Ino

A 120‐day feeding trial was conducted to examine the effects of the ratio of dietary linoleic acid (LA, 18:2n‐6) to eicosapentaenoic acid (EPA, 20:5n‐3) on the growth and fatty acid composition of juvenile Haliotis discus hannai (initial shell length 10.23 ± 1.48 mm; initial body weight 0.13 ± 0.05 g) in a recirculation water system. Five semipurified diets with 35 g kg^?1 total lipid were formulated to contain graded LA/EPA ratios (1 : 0, 0.75 : 0.25, 0.5 : 0.5, 0.25 : 0.75, and 0 : 1, respectively). Twenty‐five juveniles were stocked in a rearing unit, a plastic basket (20 × 20 × 10 cm), as a replicate, and there were three replicates for each dietary treatment. The results showed that abalone survival rates were generally high (90.1–98.3%) and independent of the dietary treatments. However, abalone growth was significantly affected by LA/EPA ratio (P < 0.05). The LA/EPA ratio of 0.25 : 0.75 (Diet 4) produced the highest weight gain rate (WGR, 416.3%), closely followed by the ratio of 0 : 1 (Diet 5, 412.9%), the ratio of 0.5 : 0.5 (Diet 3, 399.7%) and the ratio of 0.75 : 0.25 (Diet 2, 372.1%), but no significant differences were observed among these treatments. The abalone fed the diet without 20:5n‐3 (Diet 1) had the lowest WGR (Diet 1, 363.8%), which was significantly lower than that of Diet 4. Fatty acid profiles in abalone body reflected those of dietary lipids, especially for the polyunsaturated fatty acids. The contents of arachidonic acid (AA; 20:4n‐6) in abalone tissues were positively correlated with dietary level of 18:2n‐6 (P < 0.05). Similar correlation was also observed between the level of docosahexaenoic acid (DHA, 22:6n‐3) in abalone tissues and the level of dietary EPA. It is suggested that abalone, H. discus hannai, have the capacity to synthesize 20:4n‐6 from 18:2n‐6, and maybe 22:6n‐3 from 20:5n‐3.     

Replacement of fish oil with alternative lipid sources in plant‐based practical feed formulations for marine shrimp (Litopenaeus vannamei) reared in outdoor ponds and tanks

The objective of this study was to demonstrate the feasibility of partial substitution of menhaden fish oil by alternative lipid sources (soybean oil, poultry grease and flaxseed oil) in non‐marine protein‐based shrimp production diet, its influence on fatty acid profile and its final product flavour. Results for the pond study (17 weeks) showed no differences (P ≥ 0.05) in shrimp production among different test diets. Production ranged from 5070 to 5363 kg ha^?1; mean final weight, 18.0 to 21.6 g; weekly growth, 1.04 to 1.25 g; survival, 65.6 to 75.4%; and FCR, 1.37 to 1.45. Results from the tank trial (12 weeks) confirmed these findings, final weight, 13.8–14.8 g; weekly growth, 1.1–1.2 g; survival, 92.5–98.3%; FCR, 1.05–1.11; and final standing crop, 4738–5024 kg ha^?1. The fatty acids profiles of edible tail muscle reared on the various diets displayed a similar fatty acid profile to that of the diets. The sensory test showed no statistical differences in texture, appearance, aroma and flavour between the shrimp fed diets containing menhaden fish oil and soybean oil. These studies demonstrated that practical shrimp feeds containing non‐marine protein ingredients and a percentage of fish oil replaced by alternative lipid sources had no negative impact on mean final weight, weekly growth, survival, FCR, final standing crop, fatty acids profile and organoleptic properties of Litopenaeus vannamei.     

Supplementation with 2‐hydroxy‐4‐(methylthio)butanoic acid (HMTBa) in low fish meal diets for the white shrimp,Litopenaeus vannamei

This work evaluated the performance of Litopenaeus vannamei to low fish meal diets supplemented with 2‐hydroxy‐4‐(methylthio)butanoic acid (HMTBa). A basal diet with 150.0 g kg^?1 of anchovy fish meal was designed. Two positive control diets were formulated to reduce fish meal at 50% and 100% with 1.0 and 2.0 g kg^?1 of MERA? Met_Ca (calcium salt with 84% HMTBa activity), respectively. Two nearly equivalent diets acted as negative controls, without HMTBa supplementation. A total of 50 clear‐water tanks of 500 L were stocked with 2.22 ± 0.19 g shrimp under 70 animals m^?2. Shrimp survival (92.3 ± 5.1% and 81.4 ± 8.0%), yield (808 ± 12 and 946 ± 17 g m^?2) and FCR (2.17 ± 0.19 and 3.12 ± 0.37) showed no differences among diets after 72 or 96 days, respectively. A significantly higher shrimp body weight and weekly growth were observed for those fed with the basal diet or diets supplemented with HMTBa compared with non‐supplemented ones. This study has shown that L. vannamei growth, body weight, survival, yield and FCR were supported by HMTBa supplementation when 150.0 g kg^?1 of fish meal was replaced by soybean meal and other ingredients, at 50% and 100%.     

Dietary ratios of n‐3/n‐6 fatty acids do not affect growth of Nile tilapia at optimal temperatures (28°C) nor at temperatures that simulate the onset of winter (22°C)

Nile tilapia (Oreochromis niloticus) juveniles were fed diets containing 13 g/kg total polyunsaturated fatty acids (PUFAs) at different n‐3/n‐6 dietary ratios (0.2, 0.5, 0.8, 1.3 and 2.9) for 56 days, at 28°C. Subsequently, fish were submitted to a winter‐onset simulation (22°C) for 33 days. PUFA n‐3/n‐6 dietary ratios did not affect fish growth at either temperature. At 28°C, tilapia body fat composition increased with decreasing dietary PUFA n‐3/n‐6. Winter‐onset simulation significantly changed feed intake. The lowest dietary n‐3/n‐6 ratio resulted in the highest feed intake. At both temperatures, body concentrations of α‐linolenic acid, docosahexaenoic acid, eicosatrienoic acid and docosapentaenoic acid decreased as dietary n‐3/n‐6 decreased. Body concentrations of eicosapentaenoic acid (EPA, 20:5 n‐3) increased with decreasing concentrations of dietary EPA. The n‐6 fatty acids with the highest concentrations in tilapia bodies were linoleic acid and arachidonic acid (ARA, 20:4 n‐6). At 28°C, SREBP1 gene expression was upregulated in tilapia fed the lowest n‐3/n‐6 diet compared to tilapia fed the highest n‐3/n‐6 ratio diet. Our results demonstrate that a dietary PUFA of 13 g/kg, regardless of the n‐3/n‐6 ratio, can promote weight gains of 2.65 g/fish per day at 28°C and 2.35 g/fish per day at 22°C.     

Effects of dietary lipid level and n‐3/n‐6 fatty acid ratio on growth,fatty acid composition and lipid peroxidation in Russian sturgeon Acipenser gueldenstaedtii

The growth performance, fatty acid composition, hepatic lipid content, hepatic somatic index and lipid peroxidation in Russian sturgeon were investigated using diets containing three lipid levels 50 g kg^?1 (L5), 150 g kg^?1 (L15) and 250 g kg^?1 (L25) and three n‐3/n‐6 fatty acid ratios (1 : 3, 1 : 1 and 3 : 1) for 8 weeks. Weight gain significantly increased with the increase in dietary lipid levels at n‐3/n‐6 fatty acid ratios of 1 : 3 and 1 : 1, but not at the 3 : 1 ratio. Correspondingly, fish survival gradually decreased with the increase in dietary lipid at the 3 : 1 n‐3/n‐6 fatty acid ratio. The dietary lipid level significantly affected the composition of whole‐body fatty acid. The retention of highly unsaturated fatty acid dramatically decreased at the level of 250 g kg^?1 dietary lipid. The liver malondialdehyde increased with the increase in dietary lipid levels and the n‐3/n‐6 fatty acid ratios. The contents of lipid and triglyceride in the liver and the hepatic somatic index also increased with the increase in dietary lipid. The diet combination of L25 + 3 : 1 showed the highest aspartate transaminase and alanine transaminase, indicatives of hepatic injury. This study indicates that the L25 + 1 : 3 diet can improve fish growth performance, whereas the L25 + 3 : 1 diet may lead to poor growth performance due to high lipid peroxidation.     

Aurantiochytrium sp. meal can replace fish oil in practical diets for the juvenile Pacific white shrimp

This study evaluated the use of microalgae (Aurantiochytrium sp.) meal as a substitute for fish oil in the diet of juvenile Pacific white shrimp (Litopenaeus vannamei) reared in a clear‐water system. Dietary treatments at five replacement levels (0%, 25%, 50%, 75%, 100%) were performed in triplicate. After 46 days, only a slight difference in shrimp final weight was observed among treatments (0.61 g). An increase in final weight was observed with replacement of up to 50% fish oil for microalgae meal, while the optimal percentage of replacement estimated was 44.7%. Feed conversion rate (FCR) of animals fed a diet of Aurantiochytrium sp.meal to replace up to 50% fish oil decreased, and the optimal percentage of replacement estimated was 49.3%. The fatty acids profile in shrimp muscle tissue demonstrated an increase in docosahexaenoic acid (DHA) from 10.03% to 14.28% with increased replacement of fish oil by microalgae meal in the diet. Therefore, the partial replacement of fish oil by microalgae meal resulted in improved shrimp growth and FCR, and total replacement of dietary fish oil had no negative effects on these parameters. In addition, inclusion of microalgae meal raises the level of DHA in shrimp muscle.     

Effect of Dietary n‐3 highly unsaturated fatty acids on Growth,Body Composition and Fatty Acid Profiles of Juvenile Black Seabream,Acanthopagrus schlegeli (Bleeker)

An 8‐wk feeding trial was conducted to investigate the effects of dietary n‐3 highly unsaturated fatty acids (n‐3 HUFA) on growth, body composition, and fatty acid profiles of juvenile Acanthopagrus schlegeli. Three replicate groups of fish (initial mean weight: 8.08 ± 0.09 g, mean ± SD) were fed diets with different levels of n‐3 HUFA (0.76%, HUFA_0.76; 0.83%, HUFA_0.83; 0.90%, HUFA_0.90; 0.97%, HUFA_0.97; 1.04%, HUFA_1.04; 1.12%, HUFA_1.12) at 12.9% of total lipid, with a constant eicosapentaenoic acid (EPA, 20:5n‐3) to docosahexaenoic acid (DHA, 22:6n‐3) ratio of about 2.1. Hepatosomatic index (HSI) and intraperitoneal fat (IPF) ratio were all linearly depressed by dietary n‐3 HUFA levels (P < 0.05), and condition factor (CF) was not affected. Adipocyte diameter in IPF decreased with the elevation of dietary n‐3 HUFA and significance occurred between group HUFA_0.90 and HUFA_1.12. Lipid content in dorsal muscle was significantly lowered by dietary n‐3 HUFA compared to fish fed diet HUFA_0.76. No significance was found in whole fish proximate composition. In liver, dorsal muscle and IPF, ∑SFA, 16:0 or ∑n‐3 HUFA were all positively correlated with dietary n‐3 HUFA, while DHA to EPA ratios remained constant in 2.68, 2.86, and 3.60, respectively. Fatty acid synthase (FAS, EC 2.3.1.85) activities of all treatments remained constant at first and then were significantly elevated by dietary n‐3 HUFA higher than 0.97% (P < 0.05). In contrast, hormone sensitive lipase (HSL, EC 3.1.1.3) changed following an opposite tendency. Quadratic analysis based on weight gain rate (WGR) indicated that dietary n‐3 HUFA requirement for juvenile black seabream was 0.94% of the diet in 12.9% lipid diets .     

Effects of freeze‐dried powder of the Antarctic krill Euphausia superba on the growth performance,molting and fatty acid composition of the Pacific white shrimp Litopenaeus vannamei

This study was designed to evaluate the effect of dietary replacement fish meal supplemented with freeze‐dried powder of the Antarctic krill Euphausia superba (FDPE) on the growth performance, molting, and fatty acid composition of the Pacific white shrimp Litopenaeus vannamei (initial weight 1.27 ± 0.09 g). Four diets containing 0% (S0 group), 10% (S10 group), 20% (S20 group), and 30% (S20 group) FDPE were used in the present study. At the end of growth trial, the final body weight, weight gain rate, and specific growth rate in the S10, S20, and S30 groups were higher than those in the S0 group. The shrimp in the S10 and S20 groups exhibited better molting synchronism than those in the S0 group. The astaxanthin content in the hepatopancreas from the shrimp in the groups supplemented with FDPE was significantly higher than that in the S0 group (p < 0.05) and increased as the FDPE content in the feed increased. The shrimp in the S10, S20, and S30 groups had a higher monounsaturated fatty acid (MUFA) content in the hepatopancreas than those in the S0 group. The sum of EPA and DHA in the muscles from the shrimp in the S0 group was lower than that in the other groups. These results indicate that the dietary inclusion of 10%–20% FDPE can be used as practical diets in L. vannamei farmed under a clear water system.