Feed intake, growth and feed utilization of offspring from wild and selected Atlantic salmon (Salmo salar)

The aim was to assess whether selection for increased growth rate in Atlantic salmon (Salmo salar) is associated with increased feed intake and/or better feed utilization. Growth responses of offspring from selected and wild lines of Atlantic salmon (initial weight 814±14 g and 533±12 g, respectively) were tested in a 14-week experiment. Selected and wild salmon increased body weight by 79 and 39%, respectively, during the experiment. Relative feed intake (DFI), thermal growth coefficient (TGC) and feed efficiency ratio (FER) were significantly higher in the selected (DFI: 0.67% BW d⁻¹, TGC: 2.96×10⁻³ and FER: 1.16), than in the wild, line (DFI: 0.48% BW d⁻¹, TGC: 1.39×10⁻³ and FER: 0.93). FER was positively correlated with mean growth rate (r=0.90, n=6, P<0.05), and differences between the lines indicated a 4.6% increase in FER per generation of selection. Fish of the selected line had a significantly lower intake of protein and energy per kilogram gain, so the higher growth rate of the selected line was the result of both greater feed consumption and more efficient feed utilization for growth. This implies that selection for increased growth rate in Atlantic salmon may improve both of these traits.     

Effects of continuous light and short-day photoperiod on smolting, seawater survival and growth in Atlantic salmon (Salmo salar)

Duplicate groups of 1-year-old Atlantic salmon were exposed to 5–7 weeks of short days (LD 8.15:15.45) with artificial light, followed by a period of continuous light (LL) for 3 months (A), 2 months (B) or 1 month (C) before transfer to sea cages. Duplicate groups were also exposed to a 2-week period of LD 8.15:15.45, followed by a period of continuous light for 2 months (D). Comparisons were made with fish that were reared under natural light conditions from October onwards (F) and continuous light (E) only. Fish from all groups were transferred to sea cages on 9 June and their survival and growth were monitored until 31 October. There was a significant (P < 0.001) interaction between light regime and time for all smolt characters measured. Development of smolt colouration, decrease in condition factor, increases in gill Na-K-ATPase activity and the ability to regulate plasma Na⁺ after 24 h in full-strength sea water, indicated that the fish in groups A, B and C completed smoltification 6–8 weeks after the end of the short-day periods. No decrease in the condition factor was recorded for fish in groups D and E. The mortality was 40% for group A and 34% for group B, and 15% or less for the other groups. Groups A and B had probably lost some of the smolt characters by the time of seawater transfer. The specific growth rate in sea water was 1.5% for group F and for the survivors of groups A and B, 1.4% for group C and 1.2% for groups D and E. In conclusion, a short-day regime of 5–7 weeks, followed by continuous artificial light, caused smolt-related changes similar to those found in outdoor-reared fish, whereas this was not so for fish exposed to either a short-day period of only 2 weeks or to continuous artificial light.     

Plasma levels of vitamin D3 metabolites during parr-smolt transformation of Atlantic salmon Salmo salar L.

Plasma vitamin D and vitamin D metabolites were measured in Atlantic salmon parr during smoltification and after transfer to seawater. The fish were fed commercial feed for 5 months under natural light, and Na⁺/K⁺ ATPase was measured as an indicator of the smoltification status. No significant differences were recorded in the level of plasma vitamin D metabolites. However, a tendency of increasing plasma concentration of 25OHD₃ and also a temporary increase in plasma 1,25(OH)₂D₃ and 24,25(OH)₂D₃ were recorded prior to seawater transfer. The minor changes in plasma levels of the metabolites indicate a role of the vitamin D metabolites during parr–smolt transformation, although we do not know whether the increased levels are caused by increased synthesis of the metabolites or by decreased binding to receptors or decreased excretion.     

Seawater adaptation and growth of post-smolt Atlantic salmon (Salmo salar) of wild and farmed strains

Atlantic salmon smolts (Salmo salar L.) of wild (Namsen) and farmed (AquaGen) strains were transferred to full-strength seawater (33‰) for 0 (initial control group), 0.5, 1, 2, 4, 8, 14, 30, 42 and 60 days at three different temperatures (4.3, 9.4 and 14.3 °C). Freshwater temperature in each tank was adjusted to test conditions 10 days prior to transfer. Physiological adaptation was monitored as changes in plasma growth hormone levels, gill Na⁺,K⁺-ATPase activity, plasma chloride levels and survival in seawater. Overall, smolts from the wild strain were better able to tolerate transfer to seawater than smolts from the hatchery strain. A delay in the osmotic disturbance and a prolonged period of osmotic stress were observed at the low temperature. Circulating GH levels increased transiently in all groups during the first 12–48 h in seawater and long-term GH levels were positively correlated with seawater temperature. Growth rates were influenced by temperature and strain, with the farmed smolts showing a higher growth than the wild smolts. Food Conversion Efficiency (FCE) was higher in smolts from the farmed strain, whereas no differences in daily food consumption were observed. Optimum temperature for FCE was calculated to be 10.5 °C, whereas the optimal temperature for growth in seawater was calculated to be 13.0 °C. We suggest that the observed differences in seawater tolerance, growth and food conversion probably are genetic and may reflect the fact that the hatchery fish have been bred for rapid growth for several generations.     

A comparison of the swimming and cardiac performance of farmed and wild Atlantic salmon, Salmo salar, before and after gamete stripping

Farmed Atlantic salmon, Salmo salar, frequently escape from the aquaculture industry and interact with wild populations. The impact of these interactions on the wild populations will depend, in part, on differences in their performances. This study compared the swimming and cardiac performance of farmed salmon (Aquagen) with their founder population from the River Namsen both before and after gamete stripping. Cardiac output (CO), heart rate (HR), and stroke volume (SV), which were measured by placing Doppler flow probes around the ventral aorta of the fish, increased with exercise, but the response did not significantly differ between farmed and wild salmon. Similarly, the swimming performance of wild salmon never significantly differed from the farmed salmon. The overall similarity in swimming and cardiac performance between farmed and wild Atlantic salmon observed in the present study suggests that cultured salmon may have the ability to be competitive with the wild salmon in native waters.     

Seasonal variation in flesh quality, comparison between large and small Atlantic salmon (Salmo salar) transferred into seawater as 0+ or 1+ smolts

The aim of this study was to identify the effect of growth, size and season on the flesh quality of Atlantic salmon (Salmo salar). Following smoltification, two groups of size sorted 0+ and 1+ smolts (four treatment groups in all) were measured for body weight and length in January, June and October 2002. The fish were stored on ice for 4 days before filleted and samples taken for flesh colour, fat/dry content, end pH, gaping score and texture shear force. Large fish upon smoltification grew faster during the first year at sea, while smaller fish grew faster during the second year at sea, resulting in similar weight at slaughter. Season showed the main influence on quality, where fish slaughtered in October had harder texture, higher fat content and redder colour compared to previous samples (P < 0.05). There were only minor differences between the fish slaughtered in January and June (P > 0.15). No significant differences (P > 0.05) were detected as an effect of size or smoltification age when effects of season were accounted for in the statistical model. We conclude that the observed variation in quality was an effect of changes in growth with season. We recommend that actions aimed to halter growth prior to slaughter could be an effective control measure to reduce seasonal quality variations.     

Effect of hyperoxygenation and low water flow on the primary stress response and susceptibility of Atlantic salmon Salmo salar L. to experimental challenge with IPN virus

Intensive salmon smolt production normally includes reduced water flow and hyperoxygenation (added oxygen) of remaining water. There is little information on how different water quality parameters influence the fish health and the susceptibility to infectious diseases. The current experiment was carried out to evaluate if the combination of hyperoxygenation and reduced water flow (hyperoxic) can act as a chronic stressor to salmon in freshwater (FW) in such a way that it increases the susceptibility to IPN virus (IPNV) following seawater transfer. In FW, after 22 days of hyperoxic exposure plasma ion, TBARS and cortisol were measured. The cortisol levels were significantly (p = 0.011) higher in the hyperoxic group compared to controls maintained under normal oxygen saturation and water flow (normoxic), indicating chronic stress. Hyperoxygenation in FW caused decreased plasma [Cl⁻] compared to the normoxic group (p = 0.037), while [K⁺] tended to be higher in the hyperoxic group (p = 0.088). No significant differences were observed in plasma [Na⁺], total osmolality, TBARS or hematocrit, but there was a tendency towards a lower hct in the hyperoxic compared to the normoxic group. In SW the mortality was higher in the hyperoxic group challenged with IPNV (34%) compared to the normoxic group challenged with IPNV (20%) (p = 0.02), and no mortality was observed in the PBS injected fish. The challenged fish showed an overall increase in plasma cortisol day 8, 10, 12 and 14 post-challenge (p = 0.015, p = 0.000, p = 0.046 and p = 0.022 respectively). After SW transfer and challenge, plasma [K⁺] was elevated in both challenged groups, but no consistent trends were found for plasma [Cl⁻], [Na⁺] or total osmolality during the SW phase. There were no significant differences in the gene expression level of IFN 1, Mx and IL 1β prior to challenge, suggesting that the basic expression level of these genes were not affected by hyperoxygenation. IPNV was detected in kidney and pylorus, by immunohistochemistry, cell culture, and RT-PCR in head kidney. This experiment indicates that chronic stress induced by a combination of low water flow and hyperoxygenation increases the susceptibility to IPNV challenge.     

The effect of spectral composition and light intensity on melatonin, stress and retinal damage in post-smolt Atlantic salmon, Salmo salar

Metal halide lights are currently used as standard in commercial Atlantic salmon sea cages as a means of enhancing productivity through grilse inhibition. However, such systems create bright point light sources that are neither environment specific nor species specific and could potentially compromise fish welfare. Light emitting diodes (LEDs) are a new form of lighting technology currently being developed for the fish farming industry that can be tuned to environment and species sensitivities through narrow bandwidth outputs. However, prior to implementing these new high energy alternatives, any potential adverse effects must be determined in fish. The objectives of this study were thus (1) to determine the effect of increasing intensities of blue LED light (0.199–2.7 W m^− 2, at 0.1 m from the light source) on light perception and stress response, and (2) to examine potential retinal damage under these conditions in post-smolt Atlantic salmon, Salmo salar. A white LED light was also tested, as well as a very high intensity metal halide positive control. Results demonstrated firstly that salmon perceived blue LED light (basal melatonin levels maintained) irrespective of intensity. Secondly, fish exposed to high intensity blue LED light showed an increase in plasma cortisol and glucose levels within 3 h, returning to a basal state 24 h post-light onset. This typical acute stress response was not observed in fish exposed to the white LED light and lower blue light intensities which could indicate differential sensitivities to spectral content of the light. No effects on the non-specific immune system (lysozyme activity) were observed. Finally, extensive histological examination of the retina from fish exposed to these various light treatments revealed no signs of damage. This demonstrates the efficiency of the adaptive mechanisms to light developed in fish.     

Microsatellite analysis in domesticated and wild Atlantic salmon (Salmo salar L.): allelic diversity and identification of individuals

Samples of wild and domesticated salmon in Norway were genotyped at 12 microsatellite loci to compare allelic variability and investigate the potential of microsatellite markers for identification of individuals. The following loci were amplified: Ssa20, Ssa62NVH, Ssa71NVH, Ssa90NVH, Ssa103NVH, Ssa105NVH, SsaF43; Ssa20.19; Ssa13.37; SsOSL85; Ssa197; Ssa28. All domesticated strain samples displayed reduced variability compared to wild salmon. On average 58% of the allelic richness observed within the four wild stocks were present in the samples taken from domesticated strains. No systematic differences in heterozygosity were observed between samples representing the two groups.

Pairwise genetic distances, as estimated by Fst values and Nei [1978] was 2–8 times higher among domesticated strains than among wild strains. Among the wild stocks, the highest genetic distances were observed between the river Neiden, located in northern Norway, and the other wild stocks located in the southwest of Norway.

Assignment tests indicated that the wild and domesticated salmon could be distinguished with high precision. Less than 4% of domesticated salmon were misassigned as wild salmon, and less than 3% of wild fish were misassigned as domesticated salmon. Fish from individual domesticated strains were identified with similarly high precision. Assignment to wild salmon stocks was less accurate, with the exception of the sample taken from the river Neiden, for which 93% of the individuals were correctly assigned.     

A model for oxygen consumption of Atlantic salmon (Salmo salar) based on measurements of individual fish in a tunnel respirometer

A model for oxygen consumption of Atlantic salmon (Salmo salar) including body-weight (BW, kg), temperature (T, °C) and swimming speed (U, bodylengths s⁻¹) was developed. A multiregression analysis of 157 measurement periods on six different fish gave the model:

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(mg kg⁻¹ h⁻¹)=61.6(±6.6) BW^{−0.33(±0.11)} 1.03(±0.10)^T1.79(±0.10)^U. The model is compared with earlier work on oxygen consumption of salmonids.     

Efficacy of bithionol as an oral treatment for amoebic gill disease in Atlantic salmon Salmo salar (L.)

This study examined the efficacy of bithionol as an oral treatment for Atlantic salmon Salmo salar affected by amoebic gill disease (AGD). The current commercial management strategy of AGD is a costly 3 h freshwater bath. It is labour intensive and the number of baths needed appears to be increasing; hence, there is an effort to identify alternative treatments. Efficacy was examined by feeding AGD-affected Atlantic salmon twice daily to satiation with bithionol, an antiprotozoal, at 25 mg kg^− 1 feed. Three seawater (35‰, 17 °C) re-circulation systems were used each consisting of three tanks containing 32 Atlantic salmon smolts with an average (± SEM) mass of 90.4 g (± 5.2). Three feeds were examined in the trial including bithionol, plain commercial control and oil coated commercial control. Feeding commenced 2 weeks prior to exposure to Neoparamoeba spp. at 300 cells L^− 1 and continued for 28 days post-exposure. Efficacy was determined by examining gross gill score and identifying percent lesioned gill filaments twice weekly for 4 weeks post-exposure. Bithionol when fed as a two-week prophylactic treatment at 25 mg kg^− 1 feed delayed the onset of AGD pathology and reduced the percent lesioned gill filaments by 53% and halved the gill score from 2 to 1 when compared with both the plain and oil controls during an experimental challenge. There were no palatability problems observed with mean feed intake of bithionol over the trial duration with fish consuming higher levels of the bithionol diet compared to both the oil and plain controls. This study demonstrated that bithionol at 25 mg kg^− 1 feed, when fed as a two-week prophylactic treatment for Neoparamoeba spp. exposure, delayed and reduced the intensity of AGD pathology and warrants further investigation as an alternative to the current freshwater bath treatment for AGD-affected Atlantic salmon.     

Effect of low temperature on feed intake, growth rate and body composition of juvenile Baltic salmon

Feed intake, specific growth rate and changes in body composition were studied in juvenile (140-170 g) Baltic salmon, Salmo salar, reared at three temperatures (2, 4 and 6 °C) under continuous light conditions. Feed intake increased from 20.4 kJ kg-1 day-1 at 2 °C to 63.8 kJ kg-1 day-1 at 6 °C, and growth rate increased from 0.10% day-1 to 0.37% day-1 over the same temperature interval. The estimated lower temperature limits for feeding and growth were approximately 0.35 °C and 0.6 °C, respectively. Amongst fish reared at 2 °C the majority (86%) of the weight gain consisted of water and protein, and these fish deposited very little lipid. Lipid deposition increased amongst the groups of fish held at the higher temperatures, and amongst the salmon reared at 6 °C lipid accounted for 43% of the body energy gain.     

Production performance of Atlantic salmon (Salmo salar L.) postsmolts in cyclic hypoxia,and following compensatory growth

This study investigated the production performance of the Atlantic salmon postsmolt (Salmo salar L.) subjected to cyclic oxygen reductions (hypoxia) of varying severity. Triplicate groups (N = 955) were kept at constant 80% O₂ (control) or subjected to 1 h and 45 min of hypoxia (50, 60 or 70% O₂, termed 80:70, 80:60 and 80:50 groups) every 6 h at 16°C for 69 days. Feed was provided in normoxia. One third of the fish were kept further for 30 days in normoxia to study possible compensatory growth. Cyclic hypoxia did not alter the oxygen uptake rates of fish, measured in night‐time. Fish subjected to 50% and 60% O₂ reduced feeding by 13% and 6% compared with the controls, respectively, with corresponding reductions in specific growth rates. Feed utilization was not reduced. Compensatory growth was observed in fish from the 80:50 group, but full compensation was not achieved. The main conclusions were that feeding in normoxia does not fully alleviate negative effects of cyclic hypoxia on feeding and growth, when oxygen is reduced to 60% or below in hypoxic periods, that feed utilization is maintained, and that compensatory growth may lessen negative effects.     

Feed intake, growth rate and body composition of juvenile Baltic salmon exposed to different constant temperatures

Feed intake, specific growth rate and changes in body composition of age 1+ and 2+ Baltic salmon, Salmo salar L, were studied for fish held under constant temperature conditions. The 1+ fish (60 g) were reared for 6 weeks at 11, 15, 17, 19 or 23 °C and 2+ fish (250 g) were held at 15 °C. Feed intake of 1+ salmon increased from 176 kJ kg-1 day-1 at 11 °C to 275 kJ kg-1 day-1 at 17 °C and decreased to 229 kJ kg-1 day-1 at 23 °C. Specific growth rate increased from 1.18% day-1 at 11 °C to 1.59% day-1 at 15 °C and decreased to 0.56% day-1 at 23 °C. Optimum temperatures for feed intake and growth were estimated at 17.8 °C and 15.6 °C, respectively, and estimated upper thermal limits for feeding and growth were 29.0 °C and 24.1 °C, respectively. Models for feed intake and growth rate in relation to temperature and fish size are presented. The utilization efficiency of ingested energy decreased from 57% at 11 °C to 22% at 23 °C. For all groups of 1+ fish, most (approximately 86%) of the weight gain consisted of water. Lipid deposition accounted for about 52% of the body energy gain irrespective of rearing temperature.     

The effect of artificial light treatment and depth on the infestation of the sea louse Lepeophtheirus salmonis on Atlantic salmon (Salmo salar L.) culture

Two field studies were carried out with farmed Atlantic salmon (Salmo salarL.) in sea cages to examine various effects of artificial light (AL) and the vertical distribution of salmon on lice infestation.

The use of AL light caused an overall increase in lice infestation in both experiments. The first study showed that salmon held at 0–4 m depth in cages developed higher infestation than salmon held at greater depths (4–8 and 8–12 m) under both natural light (NL) and AL. In the second study, salmon maintained in 14-m deep sea cages that were exposed to AL with different light intensities. The AL treatments resulted directly in different diel and seasonal patterns of vertical distribution of the salmon and also different temporal patterns in lice infestations. So indirectly the infestation pattern appeared to be correlated with median day-time swimming depth of the salmon.     

Safety and efficacy of emamectin benzoate administered in-feed to Atlantic salmon, Salmo salar L., smolts in freshwater, as a preventative treatment against infestations of sea lice, Lepeophtheirus salmonis (Krøyer)

The safety and efficacy of emamectin benzoate, administered in-feed to Atlantic salmon smolts, Salmo salar L., held in freshwater, was evaluated as a preventative treatment against sea lice, Lepeophtheirus salmonis, following transfer of fish to seawater.

In the safety study, salmon smolts held in freshwater were fed with diets containing emamectin benzoate at nominal doses of 0 (control), 50 (recommended dose) and 250 (5× recommended dose) μg kg⁻¹ fish day⁻¹ for 7 days (days 0–6). Actual dose rates, based on measured concentrations of emamectin benzoate in feed, differences in fish weight, and feed consumed, were 0, 54, and 272 μg kg⁻¹ day⁻¹, respectively. On day 9, fish were transferred to seawater and observed for 14 days. No differences in feeding response, coordination, behaviour, gross and histological appearance were observed between control fish and those that received 54 μg kg⁻¹ day⁻¹. Among smolts that received 272 μg kg⁻¹ day⁻¹, approximately 50% exhibited darker coloration, and one fish (1%) exhibited uncoordinated swimming behaviour. No pathognomonic signs of emamectin benzoate toxicity were identified.

In the efficacy study, smolts held in freshwater were fed an unmedicated ration (control group) or emamectin benzoate at 50 μg kg⁻¹ day⁻¹ (treated group) for 7 days (days 0–6). On day 9, fish were re-distributed to eight seawater tanks, each holding 30 control and 30 treated fish. On days 28, 56, 77 and 109, respectively, control and treated fish in two tanks were challenged with L. salmonis copepodites. When lice in each group reached chalimus stage IV, fish were sampled and the numbers of lice were recorded. Fish challenged at day 109 were sampled for the second time when lice were at the adult stage. Efficacy was calculated as the reduction in the mean number of lice on treated fish relative to the mean on control fish. Treatment with emamectin benzoate resulted in an efficacy of 85.0–99.8% in fish challenged at days 28–77, from the start of treatment, and lice counts were significantly lower (P<0.001) on treated fish than on controls. When fish challenged at day 109 were sampled at day 128, efficacy was 44.3%, but survival of chalimus to adult lice on treated fish was lower, and at day 159, efficacy had increased to 73%. These results demonstrate that treatment of salmon smolts with emamectin benzoate in freshwater was well tolerated and highly effective in preventing sea lice infestation following transfer of fish to seawater.     

Long-term separate and combined effects of environmental hypercapnia and hyperoxia in Atlantic salmon (Salmo salar L.) smolts

Atlantic salmon (Salmo salar L.) parr (mean start weight 50 g) were reared in freshwater (FW) and exposed to three levels of oxygen saturation measured in effluent water; control group (93% O₂, LO₂), medium (111% O₂, MO₂) and high (123% O₂, HO₂). Further three groups were exposed to similar water oxygen levels in combination with elevated carbon dioxide levels (17–18 mg L^– 1 CO₂), named LO₂–CO₂, MO₂–CO₂ and HO₂–CO₂, respectively. The experiment was run in duplicate tanks for 42 days, and the fish were subsequently transferred to the same seawater (SW) regime for 45 days for an assessment of post-smolt growth. As a consequence of the CO₂ addition, tank pH levels in the FW period were reduced from 6.7 to 5.9 for the hypercapnia groups compared to for the normcapnia groups. Water temperature in FW ranged between 6.4 and 9.0 °C. Citrate was added to the water to complex labile aluminium.In the CO₂ groups observed ventilation frequencies were significantly increased compared to the control (p < 0.05). This difference declined towards the end of the FW period, suggesting acclimation to elevated CO₂. The degree of oxygenation appeared to contribute to the acclimation as the lowest mean ventilation frequency on day 36 was found in the HO₂–CO₂ group and the highest in the LO₂–CO₂ group. Lower plasma chloride and sodium levels were observed in the CO₂ groups relative to the respective oxygenation groups during the FW period, while plasma chloride and sodium levels were normalised to equal levels for all groups after 44 days in SW. No significant differences were found among treatments for blood concentrations of red blood cells, haemoglobin, potassium and glucose during the experiment.By termination of the FW period, the HO₂ group had significantly higher body weight than all other groups (p < 0.05), with specific growth rate significantly higher than the CO₂ groups (p < 0.05). Further, the condition factor was significantly lower in all the CO₂ groups at the end of the FW period compared to the control and normcapnia groups (p < 0.05). Although variable among replicates, occurrence of nephrocalcinosis was 10 times higher in the hypercapnia groups than in the control and normcapnia groups. Mortality was negligible (< 2.0%) during the trial, and most of the mortality occurred following SW transfer.     

Cholesterol and short-chain fatty acids in diets for Atlantic salmon Salmo salar (L.): effects on growth, organ indices, macronutrient digestibility, and fatty acid composition

The influence of dietary cholesterol (CHOL) and short-chain fatty acids (SCFA; sodium salts of acetic, propionic and butyric acid, 5:5:2 w/w/w) on growth, organ indices, macronutrient digestibility, and fatty acid composition of Atlantic salmon Salmo salar was investigated. Salmon (initial average weight 0.7 kg) held in seawater (7°C) for 175 days were fed one of six diets: 1, without CHOL/SCFA supplement; 2, with 0.5% SCFA; 3, with 2.0% SCFA; 4, with 1.0% CHOL; 5, with 1.0% CHOL and 0.5% SCFA; 6, with 1.0% CHOL and 2.0% SCFA.
Neither SCFA nor CHOL supplements had any significant effects on specific growth rate (SGR), mortality, apparent digestibility coefficients (ADC) of macronutrients, total lipid content. Hepatosomatic index (HSI) was slightly increased in salmon fed the CHOL supplement ( P  < 0.05). Hepatic CHOL concentration, but not the hepatic CHOL pool, was significantly increased ( P  < 0.001) by dietary CHOL supplementation.
The fatty acid compositions of fillet and gut tissues were not influenced by dietary treatment, while significant effects of CHOL supplements were observed in faeces and liver. Less saturated fatty acids and more mono- and poly-unsaturated fatty acids were excreted with faeces in salmon fed CHOL supplements. Salmon fed CHOL supplements significantly reduced the relative concentration of hepatic palmitic acid (C16 : 0), arachidonic acid (C20 : 4 n-6) and docosahexaenoic acid (C22 : 6 n-3), while the contents of oleic acid (C18 : 1 n-9) and eicosenoic acid (C20 : 1 n-9) were significantly increased. SCFA did not influence the observed effects of dietary CHOL.
The present study shows that dietary CHOL supplements profoundly altered excretion and liver metabolism of individual fatty acids in salmon. The impact of this alteration on physiological performance has not been elucidated.     

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.