Effects of alternate phases of fish oil and vegetable oil-based diets in Murray cod

Fish oil (FO)- and canola oil (CO)-based diets were regularly alternated in a daily cycle (amCO: alternation of CO in the morning and FO in the afternoon, and pmCO: alternation of FO in the morning and CO in the afternoon) or in a series of weekly cycles (2W: alternation of 2 weeks on CO and 2 weeks on FO, 4W: alternation of 4 weeks on CO and 4 weeks on FO), over a 16-week period in juvenile Murray cod ( Maccullochella peelii peelii ). No significant differences were observed between any of the treatments in relation to the final weight. However, fish subjected to the 2W schedule were larger ( P >0.05) than all other treatments (37.2 ± 0.30 vs. 34.3 ± 0.58 in the control treatment). Fish receiving the 2W treatment had a significantly lower total net disappearance of eicosapentaenoic acid 20:5n-3 (EPA) and docosahexaenoic acid 22:6n-3 (62.1% and 24.0% respectively) compared with the control treatment (fish continuously fed a blend of 50% FO and 50% CO). Likewise, Murray cod receiving the amCO daily schedule had a significantly lower total net disappearance of EPA in comparison with the CD and pmCO treatments. These data point towards the existence of cyclical mechanisms relative to fatty acid utilization/retention.     

Finishing diets stimulate compensatory growth: results of a study on Murray cod, Maccullochella peelii peelii

The effective implementation of a finishing strategy (wash‐out) following a grow‐out phase on a vegetable oil‐based diet requires a period of several weeks. However, fish performance during this final stage has received little attention. As such, in the present study the growth performance during both, the initial grow‐out and the final wash‐out phases, were evaluated in Murray cod (Maccullochella peelii peelii). Prior to finishing on a fish oil‐based diet, fish were fed one of three diets that differed in the lipid source: fish oil, a low polyunsaturated fatty acid (PUFA) vegetable oil mix, and a high PUFA vegetable oil mix. At the end of the grow‐out period the fatty acid composition of Murray cod fillets were reflective of the respective diets; whilst, during the finishing period, those differences decreased in degree and occurrence. The restoration of original fatty acid make up was more rapid in fish previously fed with the low PUFA vegetable oil diet. During the final wash‐out period, fish previously fed the vegetable oil‐based diets grew significantly (P < 0.05) faster (1.45 ± 0.03 and 1.43 ± 0.05, specific growth rate, % day⁻¹) than fish continuously fed with the fish oil‐based diet (1.24 ± 0.04). This study suggests that the depauperated levels of highly unsaturated fatty acids in fish previously fed vegetable oil‐based diets can positively stimulate lipid metabolism and general fish metabolism, consequently promoting a growth enhancement in fish when reverted to a fish oil‐based diet. This effect could be termed ‘lipo‐compensatory growth’.     

Effect of dietary substitution of fish oil by Echium oil on growth, plasma parameters and body lipid composition in gilthead seabream (Sparus aurata L.)

Gilthead seabream juveniles were fed on either a fish oil (FO)-containing diet or a diet containing a 50 : 50 blend of FO and Echium oil (EO) to determine the effect of EO on growth, plasma parameters and tissue lipid compositions. After 4 months of feeding, there was a significant increase of 18 : 2 n -6 and a reduction of approximately 25% of 20 : 5 n -3 in the flesh of fish fed the EO diet. At this point, half of the fish that fed on EO were returned to the FO diet as a third treatment and the trial continued with the three groups for a further 3 months. At the end of the experiment, food intake, survival, growth and plasma parameters were not affected by the inclusion of dietary EO. However, hepatosomatic index (HSI), total lipid and triacylglycerol contents of muscle decreased in fish fed the EO diet. Feeding the EO diet resulted in significant increments of potentially health-promoting fatty acids such as 18 : 3 n -6, 18 : 4 n -3 and 20 : 3 n -6 but reduced n -3 highly unsaturated fatty acids, particularly 20 : 5 n -3. When EO-fed fish were returned to the FO diet, tissue lipid contents and HSI tended to increase, but 18 : 2 n -6 and 20 : 5 n -3 levels were not fully restored to the levels of fish fed the FO diet for the entire trial. Furthermore, the fatty acids present in EO, which may promote beneficial health effects, were reduced.     

Effects of dietary lipid sources on growth performance,lipid metabolism and antioxidant status of juvenile Russian sturgeon Acipenser gueldenstaedtii

Six isonitrogenous and isoenergetic diets were used to test the influence of lipid source on growth performance, antioxidant status and lipid metabolism of juvenile Russian sturgeon, Acipenser gueldenstaedtii. Each diet was supplemented with 90 g kg^?1 of lipid from each of six sources including fish oil (FO), beef tallow (BT), sunflower oil (SO), linseed oil (LO) and equal combinations of FO + SO + BT (FSB) or LO + SO + BT (LSB). After 56 days, fish fed LSB demonstrated highest weight gain, specific growth rate and lowest hepatosomatic index among all groups. The n‐6 polyunsaturated fatty acids (PUFAs) in the whole fish were highest in the SO group, and n‐3 PUFAs were highest in fish fed LO. The fish fed FO contained highest n‐3 highly unsaturated fatty acids. Triglyceride in the serum of fish fed LSB was lowest, but was not significantly different from that in the SO group. Triglyceride in the serum of fish fed FO and BT was highest among all groups. Lipase, malate dehydrogenase and lipoprotein lipase activities were highest in fish fed LSB. Serum malondialdehyde in fish fed LSB was significantly lower than in fish fed FO or SO, but no significant differences were found among fish fed LSB, BT, LO or FSB. Fish fed LSB showed higher catalase activity and total antioxidant capacity than fish fed FO or FSB. This study indicates that linseed, sunflower oil and BT mixed oil are a suitable lipid source and can benefit growth performance and antioxidation in juvenile sturgeon.     

Short‐term food deprivation before a fish oil finishing strategy improves the deposition of n‐3 LC‐PUFA,but not the washing‐out of C18 PUFA in rainbow trout

This study aimed to test the hypothesis that the efficiency of a finishing period can be improved by reducing the initial fat content of fish fillets, by means of a period of food deprivation. Two groups of rainbow trout (Oncorhynchus mykiss) were fed for an 18‐week grow‐out period on a vegetable oil‐based diet (VO) or a fish oil‐based diet (FO). VO fed fish were then split into two sub groups: one (VO/FO) was shifted to the FO diet for 8 weeks, whilst the other (UF/FO) was deprived of food (unfed) for 2 weeks and then fed the FO diet for the remaining 6 weeks. The control treatment (FO/FO) was represented by fish continuously fed FO. The subsequent reduction of total fat in the UF/FO treatment was then responsible for a much faster recovery towards a FO‐like fatty acid profile, validating the proposed hypothesis. However, the modification of the fatty acid composition of fish fillets during the feed withholding period, coupled with the postponement of the finishing diet, resulted in only minor beneficial effects of this strategy, and the loss of potential weight gain. However, the n‐3 LC‐PUFA content in UF/VO fish fillets was significantly higher than fish subjected to the VO/FO treatment.     

Influence of dietary lipid sources on growth,reproductive performance and fatty acid compositions of muscle and egg in three‐spot gourami (Trichopodus trichopterus) (Pallas, 1770)

Five isonitrogenous (420 g kg^?1 crude protein) and isoenergetic (16.3 kJ g^?1) practical diets were formulated to contain fish oil (FO), Kilka fish oil (KFO), linseed (LO), canola (CO) and soybean (SBO) oils fed to juveniles of three‐spot gourami (Trichopodus trichopterus) (initial weight 1 ± 0.03 g) three times per day to apparent satiation for 14 weeks. Results showed the mean final weight of brooders was not significantly affected by dietary oil sources. Specific growth rate for fish fed in SBO and CO diets was statistically higher than for fish fed diet LO. Fish fed diets CO and KFO showed in significantly higher GSI value compared with other diets. Absolute fecundity was greatest in fish fed diets KFO and CO, which significantly differ with other treatments. Except for KFO diet, high fertilization percentages (87.3–93.45%) were observed in other treatments. Fatty acid composition of muscle and egg was found to be positively correlated with their respective dietary lipid sources. High levels of EPA, DHA and n‐3 HUFA in brooders fed diet FO negatively affect egg quality parameters. Therefore, the results demonstrated that vegetable oil‐based diets (CO, SBO and LO, respectively) can positively affect on growth performance of juveniles compared with fish oil‐based diets. Furthermore, CO and LO diets, respectively, showed positive effects on reproductive performance in T. trichopterus compared with fish oil diets during experimental period under controlled conditions.     

Finishing feeding strategy as an instrument for modification of fatty acid composition of brook char (<Emphasis Type="Italic">Salvelinus fontinalis</Emphasis>)

This study investigated the possibility of using a finishing feeding strategy and to apply a dilution model for the calculation of the content of fatty acids (FA) in farmed brook char (Salvelinus fontinalis). Four duplicate groups of fish with an initial weight 153.3 ± 4.9 g^?1 were kept in a flow-through system for 135 days, during which they more than triplicated their weight. Control groups were fed the same unmodified commercial diet with 100 % fish oil (FO) or with 60 % fish oil and 40 % rapeseed oil (RO) mixture. Two groups were fed by RO diet followed by 45 (RO:45FO) and 90 (RO:90FO) days of FO diet, respectively, at the end of the growing period. The fillet FA composition at the end of the experiment corresponded with the FA composition of the lipid source in the diet for the tested groups. A significant (p < 0.05) impact on FA composition with a decreasing tendency in the representation of n-3 HUFA with a prolonged feeding period with the RO diet was observed. The application of a dilution model enabling the prediction of the content of a given fatty acid in a given time was successfully performed.     

Alternative vegetable lipid sources in diets for grouper, Epinephelus coioides (Hamilton): effects on growth, and muscle and liver fatty acid composition

The aim of this study was to investigate the effects of different oils on growth performance and lipid metabolism of the grouper, Epinephelus coioides. Five experimental fish meal‐based isonitrogenous and isolipidic diets were formulated containing either 5.5%‐added fish oil (FO), soybean oil (SBO), corn oil (CO), sunflower oil (SFO) or peanut oil (PO). Each diet was fed to triplicate groups of 20 fish (initial body weight 13.2±0.02 g) grown in seawater at 28.0–30.5 °C for 8 weeks. Fish were fed twice a day to visual satiety. No significant differences in the survival, weight gain, specific growth rate, feed conversion ratio, protein efficiency ratio or hepatosomatic index were found between fish fed the FO or vegetable oils (VO) diets. Dietary lipid sources did not affect whole‐body composition among grouper fed the various diets. Muscle of fish fed the FO diet had significantly higher levels of 14:0, 16:0, 16:1n‐7, 20:5n‐3[eicosapentaenoic acid (EPA)] and docosahexaenoic acid (DHA)+EPA (except for PO fed fish) compared with those of fish fed VO diets. However, the levels of 18:1n‐9, 18:2n‐6 and DHA/EPA ratios in the muscle of fish fed FO diet were significantly lower than those of fish fed the VO diets. The liver of fish fed the FO diet had significantly higher levels of 18:0, 20:5n‐3, 22:6n‐3, n‐3 highly unsaturated fatty acids and DHA+EPA than those of fish fed the VO diets, whereas increases in 18:1n‐9, 18:2n‐6 and mono‐unsaturated fatty acid levels were observed in the liver of fish fed the VO diets.     

Modification of tissue fatty acid composition in Murray cod (Maccullochella peelii peelii, Mitchell) resulting from a shift from vegetable oil diets to a fish oil diet

The dynamics of fatty acid composition modifications were examined in tissues of Murray cod fed diets containing fish oil (FO), canola oil (CO) and linseed oil (LO) for a 25‐week period and subsequently transferred to a FO (finishing/wash‐out) diet for a further 16 weeks. At the commencement of the wash‐out period, following 25 weeks of vegetable oil substitution diets, the fatty acid compositions of Murray cod fillets were reflective of the respective diets. After transfer to the FO diet, differences decreased in quantity and in numerousness, resulting in a revert to the FO fatty acid composition. Changes in percentages of the fatty acids and total accumulation in the fillet could be described by exponential equations and demonstrated that major modifications occurred in the first days of the finishing period. A dilution model was tested to predict fatty acid composition. In spite of a general reliability of the model (Y=0.9234X+0.4260, R²=0.957, P<0.001, where X is the predicted percentage of fatty acid; Y the observed percentage of fatty acid), in some instances the regression comparing observed and predicted values was markedly different from the line of equity, indicating that the rate of change was higher than predicted (i.e. Y=0.4205X+1.191, R²=0.974, P<0.001, where X is the predicted percentage of α‐linolenic acid; Y the observed percentage of α‐linolenic acid). Ultimately, using the coefficient of distance (D), it was shown that the fatty acid composition of fish previously fed the vegetable oil diets returned to the average variability of the fillet fatty acid composition of Murray cod after 70 or 97 days (LO and CO respectively).     

Effects of different dietary lipid sources in the diet for Pangasius nasutus (Bleeker, 1863) juveniles on growth performance,feed efficiency,body indices and muscle and liver fatty acid compositions

Four isonitrogenous (300 g kg^?1 crude protein), isoenergetic (21 kJ g^?1) experimental diets were formulated to contain fish oil (FO), soybean oil (SBO), crude palm oil (CPO) and linseed oil (LO), respectively, as the lipid sources, added at 120 g kg^?1 of crude lipid each. The diets were fed by hand to triplicate groups of Pangasius nasutus (Bleeker, 1863) juveniles (mean weight 10.66 ± 0.04 g), to apparent satiation twice daily for 12 weeks. Fish survival rate was 100% among all the treatments. Growth performance (DGR) was similar among fish fed the SBO, CPO and LO diets, but was significantly (P < 0.05) higher in the CPO compared to fish fed the control (FO) diet. Fish fed SBO and CPO diets also recorded significantly (P < 0.05) higher intraperitoneal fat compared to fish fed the control, whereas fish fed the LO diet did not significantly differ from the other treatments. Muscle and liver fatty acid profile of fish from all the treatments generally mirrored the composition of the diets fed and the major fatty acids recorded were 18:3n‐3 and 18:2n‐6 in the tissues of fish fed the LO and SBO treatments, respectively. Results of this study suggests that P. nasutus fed diets containing vegetable oils (especially CPO and SBO) produce better growth performance, without compromising fish survival and feed efficiency compared with those fed a diet containing only FO.     

Cottonseed oil as a complementary lipid source in diets for gilthead seabream Sparus aurata juveniles

The efficacy of using cottonseed oil (CSO) as a fish oil (FO) substitute in gilthead seabream (Sparus aurata) juveniles feed was evaluated. Fish (BW_i 4.0 ± 2.9 g) were fed one of four isoproteic (~48% CP) and isolipidic (~18% L) diets for 9 weeks. Added oil was either FO (control diet, CTRL) or CSO, replacing 50% (CSO50 diet), 60% (CSO60 diet) and 70% (CSO70 diet) of dietary FO. Results indicated that FO replacement by CSO up to 60% level had no detrimental effects on growth or nutritive utilization and composition in fish muscles. Higher CSO intake (CSO70 diet, 56 g kg^?1) led to a 16% reduction in weight gain, 14% in feed utilization (FCR) and 57% in muscle n‐3 long‐chain polyunsaturated fatty acids (lc PUFA) as compared with CTRL and to abundant accumulation of lipid within the hepatocytes. Use of CSO altered fatty acid (FA) profiles of muscle and liver. Data suggested utilization of linoleic acid (LOA) by fish and retain of docosahexaenoic acid (DHA) in muscles. Therefore, limits of CSO inclusion as the main source of supplementary dietary lipid, with no negative effects on fish performance or nutritive composition and utilization in muscles, are: 40–48 g kg^?1 feed for gilthead seabream juveniles.     

Fish oil–based finishing diets strongly increase long‐chain polyunsaturated fatty acid concentrations in farm‐raised common carp (Cyprinus carpio L.)

This study investigated effects of linseed or fish oil–enriched finishing diets on the polyunsaturated fatty acids (PUFA) composition in dorsal muscle tissues of pond‐cultured common carp (Cyprinus carpio). After 180 days of dietary exposure to cereal diet containing vegetable oil (1%), carp were exposed to 7% linseed (LO) or 7% fish oil–enriched (FO) finishing diets for 30 days. FO supplied 17 and 20 mg fish^?1 day^?1, respectively, of the long‐chain n‐3 fatty acids eicosapentaenoic and docosahexaenoic acid for 30 days and doubled long‐chain PUFA concentrations in carp of the FO pond. The increased supply of short‐chain PUFA in LO resulted in higher short chain, but not long‐chain PUFA, showing that there was very little PUFA conversion. Thus, dietary short‐chain PUFA could not compensate for the low levels of dietary long‐chain PUFA in LO. However, moderate supply of dietary long‐chain PUFA in finishing diets for 30 days is very efficient in increasing nutritionally important long‐chain PUFA concentrations in carp.     

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.     

The effect of temperature and dietary fat level on tissue lipid composition in Atlantic salmon (Salmo salar) fed wax ester‐rich oil from Calanus finmarchicus

Copepod oil (CO) from the marine zooplankton, Calanus finmarchicus, is a potential alternative to fish oils (FOs) for inclusion in aquafeeds. The oil is composed mainly of wax esters (WE) containing high levels of saturated fatty acids (SFAs) and monounsaturated fatty alcohols that are poorly digested by fish at low temperatures. Consequently, tissue lipid compositions may be adversely affected in salmon‐fed CO at low temperatures. This study examined the lipid and FA compositions of muscle and liver of Atlantic salmon reared at two temperatures (3 and 12 °C) and fed diets containing either FO or CO, supplying 50% of dietary lipid as WE, at two fat levels (～330 g kg^?1, high; ～180 g kg^?1, low). Fish were acclimatized to rearing temperature for 1 month and then fed one of four diets: high‐fat fish oil (HFFO), high‐fat Calanus oil (HFCO), low‐fat fish oil (LFFO) and low‐fat Calanus oil (LFCO). The fish were grown to produce an approximate doubling of initial weight at harvest (220 days at 3 °C and 67 days at 12 °C), and lipid content, lipid class composition and FA composition of liver and muscle were determined. The differences in tissue lipid composition between dietary groups were relatively small. The majority of FA in triacylglycerols (TAG) in both tissues were monounsaturated, and their levels were generally higher at 3 °C than 12 °C. Polyunsaturated fatty acids (PUFA), particularly (n‐3) PUFA, predominated in the polar lipids, and their level was not significantly affected by temperature. The PUFA content of TAG was highest (～26%) in the muscle of fish fed the HFCO diet at both temperatures. Tissue levels of SFAs were lower in fish‐fed diets containing HFCO than those fed HFFO, LFFO or LFCO, particularly at 3 °C. The results are consistent with Atlantic salmon being able to incorporate both the FA and fatty alcohol components of WE into tissue lipids but, overall, the effects of environmental temperature on tissue lipids were more pronounced in fish fed the CO diets than FO diets.     

The effects of five dietary lipid sources on growth,body composition and antioxidant parameters of the clamworm,Perinereis aibuhitensis

The clamworm Perinereis aibuhitensis is a commercially important polychaete in China, but knowledge about the nutritional demands of this species is limited. In this study, the effects of five lipid sources in the diet, namely fish oil (FO), soyabean oil (SO), rapeseed oil (RO), cottonseed oil (CO) and mixed vegetable oil (MO), on growth, whole‐body composition and antioxidant parameters of juvenile P. aibuhitensis were evaluated. The results showed that clamworms fed the CO diet had higher specific growth rate (SGR) and protein efficiency ratio (PER) than the other treatments. The accumulation of longer‐chain polyunsaturated fatty acids (PUFAs) was observed in P. aibuhitensis, suggesting that P. aibuhitensis had the ability to elongate and desaturate PUFAs with 18C to form longer‐chain PUFAs. The values of n‐3/n‐6 in clamworms fed vegetable oil diets (ranged from 0.20 to 0.31) were much closer to the recommended values for human food compared with FO diet (2.47). Analysis of the antioxidant parameters revealed that clamworms fed the CO diet suffered lower peroxidation burden than those fed FO diet. These results suggested that cottonseed oil is a suitable lipid source for P. aibuhitensis feeds.     

Vegetable oil blend as alternative lipid resources in diets for gilthead seabream, Sparus aurata

The recent decreasing worldwide supplies of marine oils have forced the aquaculture industry to investigate alternative lipid sources for use in marine fish feeds. The aim of this study was to determine the impact of dietary replacement of fish oil by vegetable oils on gilthead seabream (Sparus aurata) growth performance, nutritive utilization, body composition, and fatty acid profile as well as feed cost. Two dietary vegetable oil (VO) mix blends (VO1 and VO2) in which: sunflower (SO), cottonseed (CO) and linseed (LO) for VO1 or soybean oil (SBO) for VO2, were tested as 60% fish oil (FO) substitutes versus the 100% FO control or reference diet (FO). Three iso-proteic (46% CP) and iso-lipidic (18%) experimental diets were hand fed, twice a day, 6 days a week to apparent visual satiety to triplicate groups of seabream growers (average initial weight, 130.9 ± 3.44 g), until fish reached market size (300–400 g/fish) after 20 weeks at mean ambient temperature 27.0 ± 1.8°C. All experimental diets were well accepted by seabream growers regardless of the different lipid sources used, as overall mean feed intake (FI) and daily intake (DFI) were not significantly different (P > 0.05) among dietary treatments. In terms of growth performance, fish fed VO1 diet (with LO) exhibited a relatively lower, but significant (P < 0.05), total weight gain (WG) than fish fed all FO diet (FO). However, mean value of WG of fish fed either vegetable oil-tested diet was nonsignificantly different. Feeding seabream growers vegetable oil (VO) diets (VO1 or VO2) had no significant effect on specific growth rate (SGR), daily weight index (DWI), or feed conversion ratio (FCR) among dietary treatments. Consumption of VO for 20 weeks did not significantly alter the major nutrient composition of fish, but the muscle fatty acid (FA) profile was significantly altered compared to the reference FO diet. Comparatively reduced levels of eicosapentaenoic acid (EPA) and docosahexaenoic acids (DHA), as well as elevated levels of linoleic and linolenic acids (LA and LNA) compared with fish fed the FO were noticed. In terms of economics, 17 or 20% reduction in Kg feed cost was obtained for diets VO1 or VO2, respectively. In terms of growth performance and cost, VO2 diet showed slight relative superiority over VO1 diet. However, in terms of liver structure morphology, VO1 diet (with LO) has resulted in less fat-infiltration and altered hepatic cells than VO2 (with SBO). As these traits do not affect yield or the price paid for the fish, VO2 diet has therefore been considered better than VO1 as complementary lipid sources for gilthead seabream grower diets.     

Effect of replacement of fish oil with camelina (Camelina sativa) oil on growth, lipid class and fatty acid composition of farmed juvenile Atlantic cod (Gadus morhua)

Camelina (Camelina sativa) oil was tested as a replacement for fish oil in diets for farmed Atlantic cod (Gadus morhua). Camelina differs from other plant oilseeds previously used in aquaculture with high lipid (40 %), α-linolenic acid (40 %), antioxidants and low proportions of saturated fats. Dietary treatments were fed to cod (19 g fish^?1 initial weight) for 9 weeks and included a fish oil control (FO), 40 % (CO40) and 80 % (CO80) replacement of fish oil with camelina oil. There was no effect of replacing fish oil with camelina oil included at levels up to 80 % on the growth performance. Cod fed CO80 stored more lipid in the liver (p < 0.01), including more neutral lipid (p < 0.05) and triacylglycerol (p < 0.05). Cod fed CO80 decreased in total polyunsaturated fatty acids (PUFAs) in muscle compared to CO40 and FO (p < 0.05), increased in monounsaturated fatty acids (p < 0.01), decreased in total ω3 fatty acids (FO > CO40 > CO80; p < 0.01) and increased in total ω6 fatty acids (FO < CO40 < CO80; p < 0.01). In the liver, long-chain (LC) PUFA such as 20:4ω6, 20:5ω3, 22:5ω3 and 22:6ω3 decreased when fish oil was removed from the diet (p < 0.05), and increased in 18-carbon fatty acids (p < 0.01). Camelina oil can reduce the amount of fish oil needed to meet lipid requirements, although replacing 80 % of fish oil reduced LC PUFAs in both tissues. A comparison of BF₃ and H₂SO₄ as catalysts to transmethylate cod liver and muscle lipids revealed small but significant differences in some fatty acid proportions.     

Effects of Different Dietary Lipid Sources on Growth Performance,Fatty Acid Composition,and Antioxidant Enzyme Activity of Juvenile Rockfish,Sebastes schlegeli

This study was carried out to investigate and compare the effects of various dietary lipid sources on growth performance, body composition, fatty acid profiles, and hepatic and plasma antioxidant enzyme activities of juvenile rockfish, Sebastes schlegeli. Three replicate groups of fish (initial mean weight, 1.7 ± 0.04 g) were fed four isonitrogenous and isolipidic diets containing either fish oil (FO), soybean oil (SO), linseed oil (LO), or a mixture of SO and LO (SO + LO) for 8 wk. There were no significant differences in survival, weight gain, feed efficiency, and protein efficiency ratios of fish fed the diets containing different lipid sources (P > 0.05). The fatty acids compositions of the liver and muscle tissues reflected the dietary fatty acid compositions. Liver and muscle of fish fed the SO diet had high concentration of linoleic acid, whereas those of fish fed the LO diet were rich in linolenic acid. Liver and muscle of fish fed the FO diet had significantly (P < 0.05) higher levels of eicosapentaenoic acid and docosahexaenoic acid than those of fish fed the SO and LO diets. Dietary lipid source had no significant effect on the hepatic and plasma enzyme activities of superoxide dismutase and glutathione peroxidase. The results of this study suggest that SO and LO can be used as a replacement for FO in the diets of juvenile rockfish without incurring any negative effects on growth, feed utilization, and antioxidant enzyme activity, when the dietary essential fatty acid requirements are satisfied for rockfish.     

Comparison of effects of vegetable oils blended with southern hemisphere fish oil and decontaminated northern hemisphere fish oil on growth performance, composition and gene expression in Atlantic salmon (Salmo salar L.)

Replacement of fish oil with sustainable alternatives, such as vegetable oil, in aquaculture diets has to be achieved without compromising the nutritional quality, in terms of n-3 highly unsaturated fatty acid (HUFA) content, of the product. This may be possible if the level of replacement is not too high and oil blends are chosen carefully but, if high levels of fish oil are substituted, a fish oil finishing diet prior to harvest would be required to restore n-3HUFA. However, a decontaminated fish oil would be required to avoid increasing undesirable contaminants. Here we test the hypotheses that blending of rapeseed and soybean oils with southern hemisphere fish oil will have a low impact upon tissue n-3HUFA levels, and that decontamination of fish oil will have no major effect on the nutritional quality of fish oil as a feed ingredient for Atlantic salmon. Salmon (initial weight ~ 0.8 kg) were fed for 10 weeks with diets in which 60% of fish oil was replaced with blends of soybean, rapeseed and southern hemisphere fish oil (SVO) or 100% decontaminated northern fish oil (DFO) in comparison with a standard northern fish oil diet (FO). Decontamination of the oil was a two-step procedure that included treatment with activated carbon followed by thin film deodorisation. Growth performance and feed efficiency were unaffected by either the SVO or DFO diets despite these having lower gross nutrient and fatty acid digestibilities than the FO diet. There were also no effects on the gross composition of the fish. Liver and, to a lesser extent flesh, lipid levels were lower in fish fed the SVO blends, due to lower proportions of neutral lipids, specifically triacylglycerol. Tissue lipid levels were not affected in fish fed the DFO diet. Reflecting the diet, flesh eicosapentaenoic acid (EPA) and total n-3 fatty acids were higher, and 18:1n-9 lower, in fish fed DFO than FO, whereas there were no differences in liver fatty acid compositions. Flesh EPA levels were only slightly reduced from about 6% to 5% although docosahexaenoic acid (DHA) was reduced more severely from around 13% to about 7% in fish fed the SVO diets. In contrast, the liver fatty acid compositions showed higher levels of n-3 HUFA, with DHA only reduced from 21% to about 18% and EPA increased from under 8% to 9–10% in fish fed the SVO diets. The evidence suggested that increased liver EPA (and arachidonic acid) was not simply retention, but also conversion of dietary 18:3n-3 and 18:2n-6. Increased HUFA synthesis was supported by increased hepatic expression of fatty acyl desaturases in fish fed the SVO diets. Flesh n-3HUFA levels and desaturase expression was significantly higher in fish fed soybean oil than in fish fed rapeseed oil. In conclusion, partial replacement of fish oil with blends of vegetable oils and southern hemisphere fish oil had minimal impact on HUFA levels in liver, but a greater effect on flesh HUFA levels. Despite lower apparent digestibility, decontamination of fish oil did not significantly impact its nutritional quality for salmon.     

Effect of Replacing Menhaden Oil with Catfish Oil on the Fatty Acid Composition of Juvenile Channel Catfish, Ictalurus punctatus

The effect of using a finishing diet containing menhaden fish oil on the fatty acid composition of fingerling channel catfish, Ictalurus punctatus, was evaluated in a 12‐wk growth trial. Three isocaloric, isonitrogenous practical diets with three different sources of lipids (menhaden oil [MO], catfish oil [CO], or beef tallow [BT]) were formulated (35% crude protein). No differences in eicosapentaenoic acid, docosahexaenoic acid, or arachidonic acid were observed to occur in catfish fed MO or CO diets; however, these fatty acids were significantly lower in fish fed BT diet. No differences were observed for unsaturated fatty acid content in channel catfish fed a diet containing MO for 8 or 12 wk. In addition, no differences in production characteristics were observed to occur when catfish were fed diets containing CO, MO, or BT as the dietary lipid source, which indicates that BT, CO, and MO are equally effective as sources of energy. It is apparent from these results that CO may be successfully substituted for MO in formulated diets without adversely affecting n‐3 highly unsaturated fatty acid content in channel catfish.