Interactions between dietary docosahexaenoic acid and other long-chain polyunsaturated fatty acids on performance and fatty acid retention in post-smolt Atlantic salmon (Salmo salar)

A study with varying dietary inclusion levels (1, 5, 10, 15 and 20 g kg^?1) of docosahexaenoic acid (DHA; 22:6n-3) was conducted with post-smolt (111 ± 2.6 g; mean ± S.) Atlantic salmon (Salmo salar) over a 9-week period. In addition to the series of DHA inclusion levels, the study included further diets that had DHA at 10 g kg^?1 in combination with either eicosapentaenoic acid (EPA; 20:5n-3) or arachidonic acid (ARA; 20:4n-6), both also included at 10 g kg^?1. An additional treatment with both EPA and DHA included at 5 g kg^?1 (total of 10 g kg^?1 long-chain polyunsaturated fatty acids, LC-PUFA) was also included. After a 9-week feeding period, fish were weighed, and carcass, blood and tissue samples collected. A minor improvement in growth was seen with increasing inclusion of DHA. However, the addition of EPA further improved growth response while addition of ARA had no effect on growth. As with most lipid studies, the fatty acid composition of the whole body lipids generally reflected that of the diets. However, there were notable exceptions to this, and these implicate some interactions among the different LC-PUFA in terms of the fatty acid biochemistry in this species. At very low inclusion levels, DHA retention was substantially higher (~250 %) than that at all other inclusion levels (31–58 %). The inclusion of EPA in the diet also had a positive effect on the retention efficiency of DHA. However, EPA retention was highly variable and at low DHA inclusion levels there was a net loss of EPA as this fatty acid was most likely elongated to produce DHA, consistent with increased DHA retention with additional EPA in the diet. Retention of DPA (22:5n-3) was high at low levels of DHA, but diminished with increasing DHA inclusion, similar to that seen with DHA retention. The addition of EPA to the diet resulted in a substantial increase in the efficiency of DPA retention; the inclusion of ARA had the opposite effect. Retention of ARA was unaffected by DHA inclusion, but the addition of either EPA or ARA to the diet resulted in a substantial reduction in the efficiency of ARA retention. No effects of dietary treatment were noted on the retention of either linolenic (18:3n-3) or linoleic (18:2n-6) acids. When the total n-3 LC-PUFA content of the diet was the same but consisted of either DHA alone or as a combination of EPA plus DHA, the performance effects were similar.     

Effect of dietary arachidonic acid levels on growth performance,hepatic fatty acid profile,intermediary metabolism and antioxidant responses for juvenile Synechogobius hasta

An 8‐week feeding experiment was conducted to determine the effect of dietary arachidonic acid (ARA) levels on growth performance, hepatic intermediary metabolism and antioxidant responses for juvenile Synechogobius hasta. Five isonitrogenous and isolipidic diets were formulated with arachidonic oil (containing 400 g ARA kg^?1) at inclusion levels of 0, 2, 4, 8 and 16 g kg^?1 to replace corn oil. Dietary ARA levels were 0.6, 8.6, 16.7, 32.7 and 64.8 g kg^?1 total fatty acids (FAs), respectively. Fish fed the 8.6–32.7 g ARA kg^?1 total FAs showed the highest weight gain, specific growth rate (SGR) and feed intake. By contrast, feed conversion ratio was the lowest for fish fed the 8.6–32.7 g ARA kg^?1 total FAs. Increasing ARA and total n‐6 fatty acid contents and declining linoleic acid content in liver were observed in fish fed the diet containing increasing dietary ARA levels. As a consequence, ∑n‐6/∑n‐3 ratios increased with increasing dietary ARA levels. Dietary ARA levels significantly influenced several enzymatic activities involved in hepatic intermediary metabolism, such as succinate dehydrogenase, lactate dehydrogenase, lipoprotein lipase and hepatic lipase. Superoxide dismutase activity increased with increasing dietary ARA levels. Glutathione peroxidase and catalase activities and malondialdehyde levels in liver tended to increase with increasing dietary ARA levels from 0.6 to 32.7 g ARA kg^?1 total FAs then declined when dietary ARA levels further increased to 64.8 g ARA kg^?1 total FAs. Broken‐line regression analysis of SGR against dietary ARA level indicated that optimal dietary ARA requirement for juvenile S. hasta was 10.74 g kg^?1 total FAs.     

Effects of dietary fatty acids on the production and quality of eggs and larvae of Atlantic cod (Gadus morhua L.)

Cultivated Atlantic cod (Gadus morhua) entering their first year of gamete maturation were fed diets with different levels of arachidonic acid (ARA) and eicosapentaenoic acid (EPA) for 6.5 months prior to commencement of spawning. Gravid females were stripped three times: at the beginning, peak and end of spawning. Lipid composition and egg and larval quality of 34 family crosses were investigated. Results indicated that ARA uptake into eggs from broodstock diet was highly efficient achieving proportions of ARA up to 84% higher in eggs than in the diet. EPA was 42–76% higher, and DHA was 155–173% higher in eggs than in diets. Cod fed the diet with the lowest EPA/ARA ratio had the greatest egg production. Eggs from fish on a diet with high ARA level had significantly higher fertilization and hatching success than those fed low levels of ARA. This diet produced on average 71 viable eggs g^?1 female compared with 32.5 and 4 eggs in diet B and C, respectively. Furthermore, larval survival until 8 days posthatch was higher in diets with lower ARA levels. The combined results showed that ARA dietary supplementation and low EPA/ARA ratio yielded a greater number of viable larvae kg^?1 female.     

No significant effect of additive ratios of docosahexaenoic acid to eicosapentaenoic acid on the survival and growth of cobia (Rachycentron canadum) juvenile

An experiment was conducted in the laboratory to investigate the effects of additive ratios of docosahexaenoic acid (DHA) to eicosapentaenoic acid (EPA) on the growth and survival of cobia (Rachycentron canadum) juveniles from August to October 2005. Three hundred and eighty cobia juveniles (56 days of age, body weight 6.9 ± 0.1 g, body length 9.2 ± 0.1 cm) were selected and 20 of them were freely taken for initial sample analysis in the week 0. Additional 360 juveniles were randomly assigned into eight groups with triplicate, total 24 tanks with 15 fish each. Cobia juveniles were reared in glass‐steel tanks (200‐L volume per tank) using filtered seawater with temperature 26–30.5 °C, salinity 25.4–33.0 g L^?1 and pH 7.8–8.0. Cobia juveniles were fed for 8 weeks using seven treatment diets (D‐1 to D‐7) with the same amount of DHA and EPA (15.0 ± 1.2 g kg^?1 of dried diet), but varying ratios of DHA to EPA (0.9, 1.1, 1.3, 1.5, 1.7, 1.9, 2.1, respectively) and a control diet (D‐0, DHA + EPA = 8.0 g kg^?1 of dried diet, DHA/EPA = 1.3). Five juveniles per tank were randomly taken for sample analysis at the end of weeks 4 and 8, respectively. The highest protein efficiency rate (PER; 1.5 in mean), average body weight (BW; 73.3 g per fish in mean) and the lowest feed conversion ratio (FCR; 1.6 in mean) were obtained in cobia juveniles fed the control diet at the end of week 8. These parameters were significantly different (P < 0.05) among juveniles fed the control and treatment diets; however, no significant difference (P > 0.05) was found among juveniles fed the treatment diets evaluated in this study. It was concluded that the survival and growth of cobia juveniles were not greatly influenced by additive ratios of DHA to EPA in our experimental conditions.     

Effect of arachidonic acid supplementation on reproductive performance of tank‐domesticated Penaeus monodon

The reproductive performance of domesticated Penaeus monodon was assessed when fed on two experimental semi‐moist maturation diets varying in their arachidonic acid content for 21 days before ablation and throughout a 17‐day reproductive assessment. The biochemical composition of the two semi‐moist two diets was similar with the exception of arachidonic acid (ARA) content; the basal diet (BAS) consisting of 0.9 g kg^?1 DM ARA (1.1% of total fatty acids) and the supplemented diet (ARA‐SUP) consisting of 5.0 g kg^?1 DM ARA (5.8% of total fatty acids). ARA/EPA and ARA/DPA ratios were 0.1 in the BAS diet and 0.5 in the ARA‐SUP diet. Fatty acid composition of the spawned eggs was comparable between diets with the exception of ARA concentration, which was higher in the ARA‐SUP (8.95 ± 0.44 g kg^?1 DM) than the BAS (3.23 ± 0.17 g kg^?1 DM) (P < 0.0001). The cumulative percentage of females spawning (mean ± SE after 17 days) (31.9 ± 7.0%; 24.1 ± 1.3%), number of spawnings per female (0.48 ± 0.1; 0.29 ± 0.02), and eggs per female (62 520 ± 16 935; 44 521 ± 9914) was significantly (P < 0.0001) higher for the ARA‐SUP than the BAS. Results of this study suggest that arachidonic acid plays a key role in promoting egg development and spawning in P. monodon.     

Effect of lipid supplementation on reproductive performance of female channel catfish,Ictalurus punctatus,induced and strip‐spawned for hybridization

The influence of different lipid sources and n3:n6 ratios on reproductive performance of female channel catfish, Ictalurus punctatus was evaluated. A commercial catfish feed was top coated with 2% oil and offered to brood stock females fish during 70–85 days before spawning season. Four dietary treatments were formulated using the following top coating ratios: diet 1, soybean oil 9.5 g kg^?1 and linseed oil 10.5 g kg^?1; diet 2, soybean oil 17.5 g kg^?1 and linseed oil 2.5 g kg^?1; diet 3, 20.0 g kg^?1 linseed oil, and diet 4, 10.0 g kg^?1 menhaden fish oil, supplemented with 5.0 g kg^?1 arachidonic acid (ARA), and 5.0 g kg^?1 docosahexaenoic acid (DHA). Fatty acid composition of the eggs reflected the effect of dietary treatment offered during spring season. Supplementation of ARA, EPA and DHA in commercial catfish feed in the form of menhaden fish oil with purified liquid algae extracts of ARA and DHA produced from two to five times the number of fry per female body weight when compared to the effect of fed top coated with vegetable oils. Although, this effect was not statistically significant it may represent an economical improvement for the industry.     

Partial substitution of fish oil with rapeseed, linseed and olive oils in diets for European sea bass (Dicentrarchus labrax L.): effects on flesh fatty acid composition, plasma prostaglandins E2 and F2α, immune function and effectiveness of a fish oil finishing diet

Triplicate groups of European sea bass (Dicentrarchus labrax L.), of initial weight 90 g, were fed four practical‐type diets in which the added oil was 1000 g kg^?1 fish oil (FO) (control diet), 600 g kg^?1 rapeseed oil (RO) and 400 g kg^?1 FO, 600 g kg^?1 linseed oil (LO) and 400 g kg^?1 FO, and 600 g kg^?1 olive oil (OO) and 400 g kg^?1 FO for 34 weeks. After sampling, the remaining fish were switched to the 1000 g kg^?1 FO diet for a further 14 weeks. Fatty acid composition of flesh total lipid was influenced by dietary fatty acid input but specific fatty acids were selectively retained or utilized. There was selective deposition and retention of docosahexaenoic acid (DHA; 22:6n‐3). Eicosapentaenoic acid (EPA; 20:5n‐3) and DHA were significantly reduced and linolenic (LNA; 18:3n‐3), linoleic (LA; 18:2n‐6) and oleic (OA; 18:1n‐9) acids significantly increased in flesh lipids following the inclusion of 600 g kg^?1 RO, LO and OO in the diets. No significant differences were found among different treatments on plasma concentrations of prostaglandin E₂ and prostaglandin F_2α. Evaluation of non‐specific immune function, showed that the number of circulating leucocytes was significantly affected (P < 0.001), as was macrophage respiratory burst activity (P < 0.006) in fish fed vegetable oil diets. Accumulation of large amounts of lipid droplets were observed within the hepatocytes in relation to decreased levels of dietary n‐3 HUFA, although no signs of cellular necrosis was evident. After feeding a FO finishing diet for 14 weeks, DHA and total n‐3 HUFA levels were restored to values in control fish although EPA remained 18% higher in control than in the other treatments. This study suggests that vegetable oils such as RO, LO and OO can potentially be used as partial substitutes for dietary FO in European sea bass culture, during the grow out phase, without compromising growth rates but may alter some immune parameters.     

The effect of total replacement of fish oil with DHA‐Gold® and plant oils on growth and fillet quality of rainbow trout (Oncorhynchus mykiss) fed a plant‐based diet

This study investigated the effect of the replacement of fish oil (FO) with DHA‐Gold (DHA‐G)‐supplemented plant oils (PO) in rainbow trout fed plant‐protein‐based diets. Five diets (450 mg g^?1 digestible protein and 150 mg g^?1 crude lipid) were fed to rainbow trout (initial weight 37 ± 0.5 g) for 12 weeks in a 15 °C recirculating water system. The lipid inclusion types and levels were FO, PO and PO with DHA‐G supplemented at 30 mg g^?1, 60 mg g^?1 or 90 mg g^?1 of the diet replacement for corn oil. Fish fed 90 mg g^?1 DHA‐G were significantly larger and consumed more feed than fish‐fed PO or FO (218 g and 2.6% bwd^?1 versus 181 g and 2.4% and 190 g and 2.3%, respectively). Feed conversion ratio was significantly increased in fish fed 90 mg g^?1 DHA‐G (0.99) as compared to fish‐fed FO (0.90) and 30 mg g^?1 DHA‐G (0.91). Panellists found trout fillets from fish fed the 90 mg g^?1 DHA‐G diet to have significantly fishier aroma and flavour than fish fed the FO diet. Fatty acid analysis demonstrated that 60 mg g^?1 or 90 mg g^?1 DHA‐G supplementation increased PO fed fish fillet DHA to fatty acid levels equivalent or higher than those fish fed a FO diet.     

Efficacy of an equal blend of canola oil and poultry fat as an alternate dietary lipid source for Atlantic salmon (Salmo salar L.) in sea water. I: effects on growth performance, and whole body and fillet proximate and lipid composition

This study assessed the suitability and cost efficacy of an equal blend of canola oil (CO) and poultry fat (PF) as a supplemental dietary lipid source for juvenile Atlantic salmon. Quadruplicate groups of Atlantic salmon (～400 g) held in 4000 L outdoor fibreglass tanks supplied with running (35–40 L min^?1), aerated (dissolved oxygen, 7.88–10.4 mg L^?1), ambient temperature (8.6–10.9°C) sea water (salinity, 26–35 g L^?1) were fed twice daily to satiation one of three extruded dry pelleted diets of equivalent protein (488–493 g kg^?1 dry matter) and lipid (267–274 g kg^?1 dry matter) content for 84 days. The diets were identical in composition except for the supplemental lipid (234.7 g kg^?1) source viz., 100% anchovy oil (AO; diet COPF‐0), 70.2% AO and 29.8% CO and PF (diet COPF‐30), and 40.3% AO and 59.7% CO and PF (diet COPF‐60). Atlantic salmon growth rate, feed intake, feed efficiency, protein and gross energy utilization, percent survival and whole body and fillet proximate compositions were not affected by diet treatment. Cost per kilogram weight gain was about 10% less for fish fed diet COPF‐60 than for diet COPF‐0. Percentages of saturated fatty acids in dietary and fillet lipids varied narrowly. Moreover, percentages of 18:1n‐9, monounsaturated fatty acids, 18:2n‐6, n‐6 fatty acids, 18:3n‐3, and ratios of n‐6 to n‐3 fatty acids in the flesh lipids were directly related to the dietary level of CO and PF whereas 22:6n‐3, the total of 20:5n‐3 (eicosapentaenoic acid; EPA) and 22:6n‐3 (docosahexaenoic acid; DHA), and n‐3 fatty acids revealed the opposite trend. Percentages of 22:6n‐3, EPA and DHA, and n‐3 fatty acids were significantly depressed in fish fed diet COPF‐60 versus diet COPF‐0. We conclude that a 1:1 blend of CO and PF is an excellent cost‐effective dietary source of supplemental lipid for Atlantic salmon in sea water.     

The optimum dietary docosahexaenoic acid level based on growth and non‐specific immune responses in juvenile rock bream,Oplegnathus fasciatus

A feeding trial was conducted to determine the optimum level and effect of incremental dietary levels of docosahexaenoic acid (DHA, 22:6n‐3) on growth and non‐specific immune responses in juvenile rock bream, Oplegnathus fasciatus. A basal diet without DHA supplementation was used as a control, and six other diets were prepared by supplementing with 4, 8, 12, 16, 20 or 40 g kg^?1 DHA. These diets included no eicosapentaenoic acid and/or arachidonic acid contents. The actual DHA concentrations of the diets were 1, 4.8, 8.9, 13.1, 17.6, 21.2 and 41.4 g kg^?1 diet (DHA_1.0, DHA_4.8, DHA_8.9, DHA_13.1, DHA_17.6, DHA_21.2 and DHA_41.4 respectively). At the end of feeding trial, final body weight, weight gain, specific growth rate and feed efficiency of fish fed the DHA_13.1, DHA_17.6, DHA_21.2 and DHA_41.4 diets were significantly higher than those fed the other diets (P < 0.05). The broken‐line analysis of weight gain indicates that the optimum dietary DHA level is 11.9 g kg^?1. Fish fed DHA_1.0 had the highest hepatosomatic index, an increase in plasma cholesterol, triglyceride, low‐density lipoprotein and aspartate aminotransferase levels, as well as a decrease in high‐density lipoprotein. Superoxide dismutase activity of fish fed DHA_13.1 and DHA_17.6 diets was significantly higher than that of fish fed DHA_1.0, DHA_4.8 and DHA_8.9 diets. Fish fed the DHA_17.6, DHA_21.2 and DHA_41.4 diets showed significantly higher lysozyme activity than those fish fed DHA_1.0, DHA_4.8 and DHA_8.9 diets. Therefore, the optimum dietary DHA level could be greater than 11.9 g kg^?1 but less than 13.1 g kg^?1 in diet.     

Evaluation of Cassia fistula meal as a replacement for soybean meal in practical diets of Oreochromis niloticus fingerlings

This study was undertaken to determine the replacement value of Cassia fistula seed meal (CFM) for soybean meal (SBM) in practical diets of Oreochromis niloticus fingerlings. Five practical diets (350 g kg^?1 crude protein) containing 0 g kg^?1 (control), 170 g kg^?1 (diet II), 340 g kg^?1 (diet III), 509 g kg^?1 (diet IV) and 670 g kg^?1 (diet V) substitution levels of CFM for SBM were formulated and fed to triplicate groups of O. niloticus fingerlings (mean initial weight of 10.22 ± 0.03 g) for 70 days. Fish mortality increased linearly with increase in inclusion levels of CFM in the diet. Growth and diet utilization efficiency were depressed in fish fed diets containing CFM at varying inclusion levels. Feed conversion ratio, specific growth rate and protein efficiency ratio of O. niloticus fed on diet containing 170 g kg^?1 substitution level of CFM were similar (P > 0.05) to the control diet. Digestibility of the different diets decreased with increase in inclusion levels of CFM. Fish fed diet containing 670 g kg^?1 CFM had significantly lower carcass protein. However, no significant differences were observed in carcass protein and lipid contents between fish fed the control diets and diet containing 170 g kg^?1 CFM. The most efficient diet in terms of cost per unit weight gain of fish was obtained in 170 g kg^?1 CFM dietary substitution.     

Fish oil replacement by different microalgal products in microdiets for early weaning of gilthead sea bream (Sparus aurata,L.)

The aim of this study was to determine if algal products rich in DHA or ARA are able to completely replace fish oil in microdiets for marine fish larvae, gilthead seabream and if extra supplementation with EPA may further enhance larval performance. For that purpose, 20 day‐old gilthead seabream larvae of 5.97 ± 0.4 mm mean total length and 0.12 ± 0.001 mg mean dry body weight were fed with five microdiets tested by triplicate: a control diet based on sardine oil; a diet containing AquaGrow^® DHA (diet DHA) to completely substitute the sardine oil; a diet containing AquaGrow^® ARA (diet ARA); a diet containing both products, AquaGrow^® DHA and AquaGrow^® ARA to completely substitute the fish oil; and, a diet containing both products, AquaGrow^® DHA and AquaGrow^® ARA, together with an EPA source. Temperature, air and salinity activity tests were also performed to detect larval resistance to stress. At the end of the experiment, final survivals did not differ among groups. The microorganism produced DHA was able to completely replace fish oil in weaning diets for gilthead seabream without affecting survival, growth or stress resistance, whereas the inclusion of microorganism produced ARA did not improve larval performance. Moreover, addition of EPA to diets with total replacement of fish oil by microorganism produced DHA and ARA, significantly improved growth in terms of body weight and total length. The results of this study denoted the good nutritional value of microorganisms produced DHA as a replacement of fish oil in weaning diets for gilthead seabream, without a complementary addition of ARA. However, dietary supplementation of EPA seems to be necessary to further promote larval performance.     

Effect of green and clear water and lipid source on survival, growth and biochemical composition of Pacific white shrimp Litopenaeus vannamei

Despite the shrimp ability to obtain additional nutrients from food organisms endogenously produced within the ‘green water’ system has been suggested as one of the causes for the better performance of Pacific white shrimp reared in ‘green water’ in comparison with ‘clear water’, the nutritional components responsible for these effects have yet to be determined. The present study aims to understand the importance of natural food organisms in zero‐water exchange systems as source of essential fatty acids for the Pacific white shrimp Litopenaeus vannamei. Five treatments were tested: two conducted in mesocosms systems with shrimp‐fed diets containing either fish oil (FO) or olive oil, and another three conducted in clear water with shrimp‐fed diets containing either olive oil, a docosahexaenoic acid (DHA)‐rich oil or an arachidonic acid (ARA)‐rich oil. The presence of higher levels of fatty acids 16:1n‐7, 17:1, 20:4n‐6, 20:3n‐3 and 22:5n‐6, characteristic of floc lipids, in shrimp reared in mesocosms denoted their assimilation from the floc. Substitution of FO by olive oil in diets for shrimp reared in mesocosms did not affect growth or survival. Survival and growth of shrimp reared in mesocosms was better than those reared in clear water and fed an olive oil diet, whereas DHA or ARA enrichment of non‐fish oil (NFO) diet improved survival of shrimp reared in clear water. Higher survival rate, triglyceride and DHA content in whole body and eyes of shrimp fed a DHA‐rich diet suggests that under these conditions, in clear water, it is necessary to include at least 4.8 g kg^?1 DHA in diet dry weight. ARA enrichment seemed to negatively affect growth. The nutritional contribution of the floc to shrimp in mesocosm culture reduces or eliminates the need for a dietary source of FO and illustrates the importance of DHA and ARA to enhance shrimp survival in clear water conditions.     

Effects of dietary highly unsaturated fatty acids and astaxanthin on the fecundity and lipid content of pond-reared Penaeus monodon (Fabricius) broodstock

Five diets that contained fresh squid meat as the basic constituent and were supplemented with different amounts of highly unsaturated fatty acids (HUFA) and astaxanthin were fed to pond‐reared Penaeus monodon broodstock. Diet A was sole squid meat. Diets B and C were supplemented with astaxanthin 50 and 100 mg kg^?1 respectively. Diets D and E were supplemented with HUFA 5 and 10 g kg^?1 and astaxanthin 50 mg kg^?1 respectively. The result showed that the group fed diet E had the best reproductive performance in all experimental groups. It had a higher proportion of spawns (71.5%), spawning rate (0.047), a shorter latency period (7.7±0.3 d), higher absolute fecundity (× 10³) (361.6±5.5) and egg production/female (× 10³) (597.0±18.0) than all the other experimental groups. The fatty acid composition in broodstock diets strongly affected the tissue and fecundity of broodstock. Good correlations between the content of 20:4n‐6 in eggs and the fecundity (r²=0.6109) and egg production (r²=0.9876) of broodstock were found. On the other hand, 22:6n‐3 and DHA/EPA ratio was negatively correlated with the fecundity of broodstock (r²=0.5362, 0.8702 respectively). The result also showed that the balance between n‐3 and n‐6 fatty acid families, total polyunsaturated fatty acids and total saturated fatty acid and 20:5n‐3 (EPA) and 22:6n‐3 (DHA) may play vital roles in maturation and reproductive performance of P. monodon broodstock.     

Effects of diet supplementation of soya‐saponins,isoflavones and phytosterols on Atlantic salmon (Salmo salar,L) fry fed from start‐feeding

A 14‐week trial was conducted to investigate the effects of antinutritional factors (ANFs) commonly present in soybean ingredients, singly and in combination, on Atlantic salmon (Salmo salar L.) fed from start‐feeding. The experimental diets consisted of a negative control fish meal diet (FM), and a positive control diet with 167 g kg^?1 soybean meal inclusion (SBM) and four diets based on the FM diet supplemented with 2 g kg^?1 soya‐saponins (SAP), 1.5 g kg^?1 isoflavones (IFL), 0.3 g kg^?1 phytosterols (PHS) or a mixture of these (MIX). Fish fed the SAP diet showed significantly higher growth performance than those fed FM, while the IFL treatment significantly decreased growth performance of salmon fry. Fish fed the IFL diet had significantly lower maltase activity and higher trypsin activity in proximal intestine than fish fed the FM diet. Histological differences were observed in the liver of fish fed the IFL diet, characterized by reduced size of the hepatocytes. Fish fed the PHS and IFL diets showed the highest frequencies of skeletal deformities among the six treatments. In conclusion, the results indicate that purified isoflavones may negatively affect growth performance, intestinal function, liver metabolism and bone formation of salmon fry.     

Effect of lipid levels on the reproductive performance of Snakehead murrel,Channa striatus

Present study aimed to determine the optimum dietary lipid level in snakehead murrel channa striatus broodstocks. Triplicate groups of fish were fed for 240 days with isonitrogenous experimental diets with increasing lipid levels (100, 140, and 180 g kg^?1), using fish oil and soybean oil as the lipid sources with the ratio of (1:1). Weight gain, GSI, fecundity, oocyte diameter and number of mature oocyte were found to be significantly higher in the group fed with diet containing 180 g kg^?1 lipid level. Muscle fatty acid profile showed a significant increase in LA (18:2n‐6), LNA (18:3n3), total PUFA, n‐6 and ArA (20:4n‐6) in fish fed with diet containing 180 g kg^?1 lipid. Increasing lipid level up to 180 g kg^?1 resulted in significant increase in PUFA (LA & LNA), lc‐PUFA (EPA, DHA, ArA), total PUFA, n‐3 and n‐6 series in ovary and liver of female C. striatus.     

Partial replacement of fish meal with peanut meal in practical diets for the Pacific white shrimp,Litopenaeus vannamei

In this study, we replaced fish meal with peanut meal (PM) in isonitrogenous and isolipidic diets for Pacific white shrimp at inclusion levels of 0, 70, 140, 210, 280 and 350 g kg^?1. The diets were hand‐fed to three independent groups of shrimp three times a day over a 6‐week period. Shrimp fed PM diets at a level of 280 g kg^?1 or higher had lower per cent weight gain compared with those fed the basal diet, whereas shrimp fed PM diets at 140 g kg^?1 or higher had a lower feed utilization and protein efficiency ratio compared with shrimp fed the basal diet. The feeding rate in shrimp fed PM diets at 350 g kg^?1 and the survival and protease activity in shrimp fed PM diets at 210 g kg^?1 or higher were lower than that in shrimp fed the basal diet. Diets containing 280 g kg^?1 or higher of PM caused an increase in the whole‐body moisture content of the shrimp, but decreased whole‐body protein and ash contents compared with the basal diet. Nutrient digestibility was lower or tended to be lower in shrimp fed a PM diet compared with those fed the basal diet. The activities of peroxidase and acid and alkaline phosphatases in plasma decreased with increasing levels of PM inclusion up to 210 g kg^?1. Superoxide dismutase activity decreased at dietary PM levels of 280 g kg^?1 or higher. Aflatoxin B₁ residue in the muscle was not affected by any of the treatments and remained low. The data suggest that up to 140 g kg^?1 of PM could be included in practical diets for Pacific white shrimp.     

Effect of different sources and levels of dietary phospholipids on performances and fatty acid composition of pikeperch (Sander lucioperca) larvae

The aim of this study was to evaluate the effects of dietary phospholipids (PL) sources (fish gonad G‐PL and soybean lecithin S‐PL) and levels (50 and 90 g kg^?1 dry matter) on the performances and fatty acid (FA) composition of pikeperch larvae. From day 10 to day 34 posthatching (p.h.), larvae were fed with three isoproteic and isolipidic microdiets. The best results of growth and skeletal development were related to a high phospholipid level regardless of their origin and FA profile. Jaw deformities seemed associated with high dietary highly unsaturated FA (HUFA) level. The optimal level of eicosapentaenoic acid and docosahexaenoic acid (EPA + DHA) for pikeperch larvae appeared to be around 12 g kg^?1 (dry matter) associated with a PL level around 90 g kg^?1. FA composition of diets and larvae revealed a better incorporation of arachidonic acid, EPA and DHA into PL fraction especially in larvae fed with soybean PL. Moreover, 34‐day‐old pikeperch larvae may have capability of converting 18 carbon n‐3 FA into the n‐3 HUFA. Hence, for pikeperch larvae, PL from plant origin were as efficient as those from marine fish origin.     

Effects of various corn distillers by‐products on growth,feed efficiency,and body composition of channel catfish,Ictalurus punctatus

A study was conducted to examine the use of corn distillers’ by‐products in diets and the effects of additional dietary fat on channel catfish, Ictalurus punctatus, performance. Juvenile channel catfish (initial weight: 12.6 g per fish) were stocked in flow‐through aquaria and fed one of six practical diets for 9 weeks. Fish fed the control + fat diet consumed more diet and had higher feed efficiency ratio (FER) than fish fed the control diet, but weight gain was not significantly different between fish fed these two diets. Fish fed the diet containing 300 g kg^?1 distillers dried grains with solubles (DDGS) consumed more diet and gained more weight, but had similar FER compared with fish fed the control + fat diet. The diet containing 200 g kg^?1 high‐protein distillers grains (HPDDG) resulted in similar diet consumption, weight gain and FER as the control + fat diet. Fish fed the diet containing 100 g kg^?1 distillers solubles (DS) consumed more diet, but had similar weight gain and FER compared with fish fed the 300 g kg^?1 DDGS diet. The presence of distillers solubles in the diet (300 g kg^?1 DDGS, 100 g kg^?1 DS, 100 g kg^?1 EDS diets) appears to increase diet consumption, weight gain, and FER over the control diets with or without additional fat.