Phosphorous (P) deficiency due to low P availability in fishmeal produced from blue whiting (Micromesistius poutassou) in feed for under-yearling Atlantic salmon (Salmo salar) smolt

Seawater transferred under-yearling Atlantic salmon (120 g) were fed a practical fishmeal formulated diet containing 57.4% blue whiting fishmeal and providing 15 g kg^− 1 total phosphorous (P) in the diet. The basal diet was supplemented with graded dietary levels of inorganic P (0, 3, 6, 9, 12 and 15 g kg^− 1) to total P levels of 15, 18, 21, 24, 27 and 30 g kg^− 1. Within a feeding period of 12 weeks, classical signs of P deficiency developed in Atlantic salmon fed the P un-supplemented diet containing 15 g kg^− 1 total P of natural origin. Deficiency signs included reduced growth and feed efficiency, reduced tissue mineral concentration (P, Ca, Mg, Zn), increased P:Ca ratio in the body, increased condition factor, metabolic disorder as indicated by lipid accumulation and impaired protein utilization, as well as reduced lipid, energy and Zn digestibility. Supplementation of inorganic P-salts in the diet at 3 g kg^− 1 (18 g kg^− 1 total P) significantly improved the production results with respect to growth and feed efficiency, and restored all other signs of P deficiency in fish. A higher supplementation level of 6 g kg^− 1 inorganic P (21 g kg^− 1 total P) was required for optimal mineralization in whole body and vertebrae. The highest supplementation levels of 15 g kg^− 1 added inorganic P (30 g kg^− 1 total P) seemed to increase P excretion and to have slightly negative impacts on growth and bone mineralization. Results suggest that P availability from blue whiting fishmeal is very low (3.2 g kg^− 1) and inadequate to meet dietary P requirement in rapidly growing under-yearling salmon immediately following seawater transfer, despite high natural P content in the blue whiting fishmeal.     

Sublethal effects and safe levels of carbon dioxide in seawater for Atlantic salmon postsmolts (Salmo salar L.): ion regulation and growth

Atlantic salmon (Salmo salar L.) postsmolts (0.17–0.26 kg) were exposed to four different levels of carbon dioxide partial pressure for 43 days in an open flow system: 0.6 mm Hg (control), 4.9 mm Hg (low), 12 mm Hg (medium), and 20 mm Hg (high). The water temperature was 15–16°C and the salinity 34‰. In the low carbon dioxide group (P_CO2=4.9 mm Hg; 10.6 mg/l), no significant differences were found in blood parameters (haematocrit, plasma chloride and plasma sodium) or in growth parameters (weight, length and condition factor) when compared to the control group. After 43 days, the mean plasma chloride concentration for the medium group (P_CO2=12 mm Hg; 26 mg/l) was significantly reduced, while weight and condition factor were slightly, although not significantly, lowered. For the high carbon dioxide group (P_CO2=20 mm Hg; 44 mg/l) plasma sodium and plasma pH were significantly increased and plasma chloride, oxygen consumption, weight, length and condition factor were significantly reduced at the end of exposure. There was no mortality in the control group or in the low carbon dioxide group. The mortalities in the medium and high carbon dioxide groups were 1.1 and 4.3%, respectively. Nephrocalsinosis was not observed in any of the groups. The results of the present investigation indicate that the CO₂ concentration of the low group may represent a safe level for Atlantic salmon postsmolts when the temperature is 15–16°C and the oxygen level is 6–7 mg/l. Further studies are required.     

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.     

Polyunsaturated fatty acid metabolism in cultured fish cells: Incorporation and metabolism of (n-3) and (n-6) series acids by Atlantic salmon (Salmo salar) cells

The incorporation and metabolism of (n-3) and (n-6) polyunsaturated fatty acids (PUFA) supplemented to growing cultures were studied in Atlantic salmon (AS) cells. A fatty acid concentration of 25 μM considerably altered the fatty acid composition of AS cells without increasing the neutral lipid content of the cells or inducing the production of cytoplasmic lipid droplets. Whereas Δ6 and Δ5 desaturase activities were significantly expressed in AS cells, Δ4 desaturase activity was very low. Both the Δ6 desaturase activity and the Δ5 desaturase activity showed some preference for (n-3) PUFA.     

Design, loading, and water quality in recirculating systems for Atlantic Salmon (Salmo salar) at the USDA ARS National Cold Water Marine Aquaculture Center (Franklin, Maine)

The Northeastern U.S. has the ideal location and unique opportunity to be a leader in cold water marine finfish aquaculture. However, problems and regulations on environmental issues, mandatory stocking of 100% native North American salmon, and disease have impacted economic viability of the U.S. salmon industry. In response to these problems, the USDA ARS developed the National Cold Water Marine Aquaculture Center (NCWMAC) in Franklin, Maine. The NCWMAC is adjacent to the University of Maine Center for Cooperative Aquaculture Research on the shore of Taunton Bay and shares essential infrastructure to maximize efficiency. Facilities are used to conduct research on Atlantic salmon and other cold water marine finfish species. The initial research focus for the Franklin location is to develop a comprehensive Atlantic salmon breeding program from native North American fish stocks leading to the development and release of genetically improved salmon to commercial producers. The Franklin location has unique ground water resources to supply freshwater, brackish water, salt water or filtered seawater to fish culture tanks. Research facilities include office space, primary and secondary hygiene rooms, and research tank bays for culturing 200+ Atlantic salmon families with incubation, parr, smolt, on-grow, and broodstock tanks. Tank sizes are 0.14 m³ for parr, 9 m³ for smolts, and 36, 46 and 90 m³ for subadults and broodfish. Culture tanks are equipped with recirculating systems utilizing biological (fluidized sand) filtration, carbon dioxide stripping, supplemental oxygenation and ozonation, and ultraviolet sterilization. Water from the research facility discharges into a wastewater treatment building and passes through micro-screen drum filtration, an inclined traveling belt screen to exclude all eggs or fish from the discharge, and UV irradiation to disinfect the water. The facility was completed in June 2007, and all water used in the facility has been from groundwater sources. Mean facility discharge has been approximately 0.50 m³/min (130 gpm). The facility was designed for stocking densities of 20–47 kg/m³ and a maximum biomass of 26,000 kg. The maximum system density obtained from June 2007 through January 2008 has approached 40 kg/m³, maximum facility biomass was 11,021 kg, water exchange rates have typically been 2–3% of the recirculating system flow rate, and tank temperatures have ranged from a high of 15.4 °C in July to a low of 6.6 °C in January 2008 without supplemental heating or cooling.     

Protein and lysine requirements for maintenance and for tissue accretion in Atlantic salmon (Salmo salar) fry

Available data on the quantitative requirement for lysine (Lys) in different salmonids show much variability. So far, there are very limited data on the maintenance requirements of indispensable (I) amino acids (AA) in fish. In the present study, we determined simultaneously the Lys requirements for maintenance and for protein accretion in Atlantic salmon fry by adapting a protocol established for the piglet. Groups of fish having an initial body weight of 1.5 g were fed for 28 days on isoenergetic diets with increasing nitrogen (N) content supplied by cod meal and a mixture of crystalline AAs (50% of total dietary N). Except the protein-free diet (PF; 0.2% dry matter (DM)), the N content of the other diets was either low (2.9% DM), medium (6.2% DM) or high (8.5% DM). Two types of diets with the same N content were formulated. The AA pattern of three control diets was based on the AA pattern of the cod meal protein. For the other three diets, Lys·HCl was totally omitted from the low-N diet (LPD), and 50% of Lys·HCl was removed from the medium- and high-N diets. After a 28-day feeding trial, carcass N and Lys gains were estimated. N and Lys requirements for maintenance and for growth were calculated regressing daily N or Lys gain against N or Lys intakes. The daily N requirement for growth above maintenance was 3.05 g per g protein gain and for maintenance it was 54 mg kg body weight^− 0.75. From the regression between protein and Lys intake, we calculated that for the accretion of 1 g body protein, the dietary Lys requirement was 152 mg, and that the Lys maintenance requirement for zero N gain was 20 mg kg body weight^− 0.75/day. This last value is higher than the previous estimations obtained for rainbow trout and could be explained by the lower body weight or age of the fish used here.     

Dietary fat type affects lipid metabolism in Atlantic salmon (Salmo salar L.) and differentially regulates glucose transporter GLUT4 expression in muscle

An experiment was conducted to study dietary fat type (fish oil (FO) vs. vegetable oil) effect on lipid and glucose metabolism in post-smolt Atlantic salmon. Duplicate groups of salmon were fed one of eight diets in which the two fat sources FO (long chain n-3 fatty acids, FA) or linseed oil (LO) (short chain n-3 FA) were combined in a 2 × 4 factorial design with sunflower oil (SO) (rich in n-6 FA) at inclusion levels of 0, 25, 50 and 75% of total added fat. The effects of the diets on plasma metabolites, the activity of selected enzymes involved in lipid metabolism, biometric indices and muscle glucose transporter GLUT4 expression were determined after 12 weeks of feeding. Lower viscero-somatic indices (VSI) and fatty livers were observed in fish fed LO based diets. Increasing inclusion levels of SO affected plasma glucose concentration in fish fed FO based diets, and plasma triglycerides, which decreased in a linear and quadratic pattern in fish fed FO based diets, but increased linearly in fish fed LO based diets. Specific activity of liver carnitine palmitoyl transferase I (CPT I) and glucose-6-phosphate dehydrogenase (G6PD) and plasma nonesterified fatty acids (NEFA) concentration was higher in fish fed LO based diets. Two GLUT4 isoforms I and II have been described in muscle and proved to be differentially expressed related to dietary fatty acids. In summary, dietary fat type affects lipid metabolism in post-smolted Atlantic salmon. In addition, a possibility to interfere on glucose metabolism by means of dietary fat type is discussed.     

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.     

Decreased concentration of hemoglobin,accumulation of lipid oxidation products and unchanged skeletal muscle in Atlantic salmon (Salmo salar) fed low dietary vitamin E

Atlantic salmon (Salmo salar) fry, initial weight 0.16 g, were fed a semipurified diet with 0, 15, 30, 60 or 120 mg dl-α-tocopheryl acetate/kg. After 24 weeks, the first two of these groups were extinct, and the fish receiving 30 mg/kg were clearly vitamin E deficient. Vitamin E deficient fish had low hemoglobin levels, characterized by a combination of reduced cellular hemoglobin concentration, red cell volume and red cell number, and an increased number and fraction of immature red blood cells. The hemoglobin concentration decreased over the decreasing range of experimental dl-ga-tocopheryl acetate levels. Therefore, even if 60 mg dl-α-tocopheryl acetate/kg gave good survival, this level was clearly physiologically suboptimal. Ceroid accumulated in the liver of fish fed 30 mg vitamin E/kg, and autofluorescent inclusions were found in the red blood cells of fish fed 30 and 60 mg vitamin E/kg. Degeneration of skeletal muscle was not observed in the present study.     

Influence of dietary blends of menhaden oil and canola oil on growth, muscle lipid composition, and thyroidal status of Atlantic salmon (Salmo salar) in sea water

The effects of various dietary blends of menhaden oil (MO) with canola oil (CO) on the growth performance, whole body proximate composition, flesh quality (muscle proximate and lipid composition) and thyroidal status of immature Atlantic salmon in sea water were studied.Atlantic salmon (initial weight, 145.2–181.3 g), held on a natural photoperiod and in 1100 L fibreglass tanks that were supplied with running, aerated (D.O., 9–10.5 p.p.m.), ambient temperature (8–10.5 °C) sea water (salinity, 28–30), were fed twice daily to satiation one of four isonitrogenous (36% digestible protein) and isoenergetic (18.8 MJ of digestible energy kg^-1) extruded high-energy diets for 112 days. All diets contained omega –3 (n-3) fatty acids in excess of requirements and differed only with respect to the source of the supplemental lipid which was either, 25% MO; 20.75% MO and 4.25% CO; 16.5% MO and 8.5% CO; or 12.25% MO and 12.75% CO. Thus, CO comprised, respectively, 0, 15.5, 31.2, or 47.0% of the total dietary lipid content (28% on an air-dry basis).Dissimilar percentages of saturated fatty acids in the dietary lipids were not found to be consistently related to the apparent gross energy digestibility coefficients of the diets. Atlantic salmon growth, dry feed intake, feed and protein utilization, percent survival, thyroidal status, and whole body and muscle proximate compositions were generally not influenced by the different sources of supplemental lipid. Therefore, our results suggest that canola oil may comprise as much as 47% of the lipid in high-energy grower diets for Atlantic salmon without compromising performance.The muscle lipid compositions generally mirrored those of the dietary lipids which, in turn, were influenced strongly by the concentrations and compositions of the CO and MO in the diet. Hence, as the dietary CO level was increased there were attendant increases in percentages of oleic acid (18:1(n-9)), linoleic acid (18:2(n-6)), total omega-6 (n-6) fatty acid content, and ratios of (n-6) to (n-3) and decreases of eicosapentaenoic acid (EPA; 20:5(n-3)), docosahexaenoic acid (DHA; 22:6(n-3)) and n-3 HUFAs (EPA & DHA) in the flesh lipids. The ranges for percentages of saturated and unsaturated fatty acids in the flesh lipids were, however, much less than those noted respectively in the dietary lipids probably because of selective metabolism of many of the former acids and some of the 18 carbon unsaturates for energy purposes.     

The mineral content affects vertebral morphology in underyearling smolt of Atlantic salmon (Salmo salar L.)

This study investigated the individual variation in vertebral morphology and mineral content (as % of bone dry weight) in rapid growing underyearling smolt (n = 33) twelve weeks after transfer to seawater. The smolt, which were reared in triplicate tanks, had a large individual variation in vertebral bone mineral content (Tank A: 36.2% min, 45.2% max, 39.6% mean. Tank B: 32.6% min, 46.6% max, 40.0% mean. Tank C: 38.5% min, 47.9% max, 42.4% mean), and were subdivided into two groups based on mean within each tank: high mineral content (HMC, above tank mean, n = 15) and low mineral content (LMC, below tank mean, n = 18). Vertebrae of smolt with a low mineral content were more compressed in the anterior–posterior direction (HMC vertebral length/dorso-ventral diameter ratio 0.83, LMC 0.80). This was related to a change in the growth direction of the vertebral cone. This change occurred around transfer to seawater and was characterised by an increased angle between the wall of the cone of the vertebrae and the cranial–caudal axis, and gave the vertebrae a compressed appearance. Smolt with a high mineral content were significantly longer (HMC 28.1 cm, LMC 26.5 cm) and heavier (HMC 270 g, LMC 210 g) twelve weeks after transfer to seawater.     

Effects of salinity on the growth and lipid composition of Atlantic salmon (Salmo salar) and turbot (Scophthalmus maximus) cells in culture

The direct effects of osmotic pressure (salinity) on growth performance and lipid composition were investigated in fish cells in culture. Cell lines from a relatively stenohaline marine species, turbot (Scophthalmus maximus) (TF) and an anadromous species, Atlantic salmon (AS) were cultured in media supplemented with NaCl to produce osmotic pressures varying from 300 to 500 mOsm kg⁻¹. The growth rates of the two cell lines were affected in a similar manner by the salinity of the media with the rank order for both peak cell numbers and growth rates up to the day of peak cell number being 300 > 350 > 400 > 450 > 500 mOsm kg⁻¹. Cell death occurred in both cell lines in older cultures at all salinities with the greatest loss of viable cells in media of 300 and 350 kg⁻¹. However, there were quantitative and qualitative differences between the cell lines in their lipid metabolism in response to the salinity of the media. The lipid content expressed per cell showed a positive correlation between lipid per cell and salinity in TF cells, but this was less apparent in AS cells. The percentage of total polar lipid classes increased with increasing salinity in TF cells due mainly to graded increases in the percentages of choline phospholipids. In contrast, there were no significant differences in the proportions of polar and neutral lipid classes with salinity in AS cells. The only significant effect of salinity in AS cells was a decreased proportion of dimethylacetals in total lipid at the highest salinity. The same significant effect of salinity on dimethylacetal content of total lipid was observed in TF cells. However, in addition there was a graded decrease in the percentage of 18:2n-9 in TF cell total lipid with increasing salinity. This was accompanied by increased percentages of total n-3 and n-6 PUFA with higher proportions of both groups of PUFA at 450 and 500 compared with 300 mOsm kg⁻¹. The results show that environmental salinity, in the absence of hormonal or other physiological stimuli, has direct effects on the growth and lipid metabolism of fish cells and that these effects differ in cells from different fish species.     

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.     

Anisakid larva in the viscera of a farmed Atlantic salmon (Salmo salar)

Parasitic nematodes of the family Anisakidae occur in the visceral cavity and surrounding tissues of many marine fish species at a prevalence as high as 100% in wild salmon samples. Human consumption of fish products containing these parasites can result in the zoonotic disease anisakiasis, and Anisakis simplex is most commonly associated with human disease. Previous studies of farmed salmon have found no anisakids in viscera or muscle, presumably because formulated feed production renders parasite larvae nonviable. However, among farmed Atlantic salmon (Salmo salar) examined by histopathology as part of a provincial government auditing program in British Columbia, Canada, 1 of 894 (0.11%) had an anisakid larva partly embedded in the wall of an intestinal cecum. Skeletal muscle is not examined as part of the government's program, but other studies have correlated anisakids in the viscera and muscle. Using anisakid prevalence in viscera as an estimate of its prevalence in muscle, the risk ratio of anisakid parasites in commercial product is 570 times less in farmed than in wild Atlantic salmon.     

Duration and method of fixation affects the sensitivity of a digoxygenin-labelled DNA probe in detecting Kudoa thyrsites in Atlantic salmon skeletal muscle

The effect of fixative and duration of fixation on the sensitivity of a non-radioactive in situ hybridisation (ISH) protocol to detect Kudoa thyrsites small subunit ribosomal deoxyribonucleic acid (DNA) was investigated. Strong ISH reactions were detected in 5-μm sections of paraffin-embedded Atlantic salmon muscle after fixation for 1 day in Davidson's solution (DS). Reactions were weak following 3 or 5 days fixation and absent after 17 or 28 days fixation. Strong ISH reactions were observed after 1, 3 or 5 days fixation in neutral buffered formalin (NBF). The reactions were weak after 17 days and weak to nonexistent after 28 days of fixation. Reactions were consistently strong after fixation in 95% ethanol for up to 28 days. Some mature spores reacted weakly or not at all by ISH. Parasite DNA was weakly amplified by polymerase chain reaction (PCR) from paraffin-embedded muscle after 1 day of fixation in DS but not after fixation for 3, 5, 17 or 28 days. Amplified DNA was detected after fixation in NBF for 1, 3 and 5 days, but not after 17 or 28 days. In contrast, PCR consistently amplified DNA from paraffin-embedded, ethanol-fixed muscle. Caution should be used in the choice of fixative and duration of fixation when preserving Atlantic salmon tissues for molecular diagnosis of K. thyrsites.     

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.     

Effects of salinity on the fatty acid compositions of total lipid and individual glycerophospholipid classes of Atlantic salmon (Salmo salar) and turbot (Scophthalmus maximus) cells in culture

Cells from a relatively stenohaline marine species, turbot (Scophthalmus maximus) (TF) and an anadromous species, Atlantic salmon (AS) were cultured in media supplemented with NaCl to produce OPs varying from 300 to 500 mOsm kg^–1 and the direct effects of OP (salinity) on the fatty acid compositions of the main glycerophospholipid classes were determined. The most dramatic effects of salinity on total lipid fatty acids were observed in polyunsaturated fatty acids (PUFA) in TF cells. There was a graded decrease in the percentage of 18:2n-9, and consequently total n-9 PUFA, and concomitantly increased percentages of both total n-3 and n-6 PUFA with increasing salinity. The increased n-3 and n-6 PUFA was due to significantly increased percentages of the major fatty acids in each of these groups, namely 22:6n-3 and 20:4n-6, respectively. The reciprocal changes in n-9 PUFA and n-3/n-6 PUFA in TF cell total lipid resulted in the percentage of total PUFA not being significantly affected by changes in salinity. The graded decrease in 18:2n-9 with increasing salinity in TF cells was observed in all the major glycerophospholipids but especially PE, PI and PS. Increasing salinity resulted in graded increases in the percentages of 22:6n-3 in PE and PS in TF cells. The quantitatively greatest increase in the percentage of n-6 PUFA in TF cells occurred with 20:4n-6 in PC, PE and PL. There were less significant changes in the fatty acid compositions of glycerophospholipids in AS cells. However, the proportion of total n-3 + n-6 PUFA in PE varied reciprocally with the proportion of dimethylacetals in response to salinity. Similar reciprocal changes between fatty acids in response to salinity were also evident in the quantitatively more minor glycerophospholipids PS and Pl. In PS, the percentage of 22:6n-3 was significantly lower at 400 mOsm kg^–1 whereas the proportion of total monoenes was significantly higher at that salinity. A similar inverse relationship between total monoenes and 20:4n-6 (and, to a lesser extent total saturates) in response to salinity was noted in PI. The results show that environmental salinity, without whole-body physiological stimuli, has direct effects on the fatty acid composition of major glycerophospholipid classes in fish cells and that these effects differ in cells from different fish speciesAbbreviations ANOVA analysis of variance - BHT butylated hydroxytoluene - BSA bovine serum albumin - DMA dimethylacetals - EMEM Eagle's minimal essential medium - FCS fetal calf serum - GC gas chromatography - HBSS Hank's balanced salt solution (without Ca²⁺ and Mg²⁺) - OP osmotic pressure - PC phosphatidylcholine - PE phosphatidylethanolamine - PI phosphatidylinositol - PS phosphatidylserine - PUFA polyunsaturated fatty acid - TLC thin-layer chromatography     

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.     

Dietary uptake of dioxins (PCDD/PCDFs) and dioxin-like PCBs in Atlantic salmon (Salmo salar)

Atlantic salmon (Salmo salar) were fed graded levels of dioxins (polychlorinated dibenzo‐p‐dioxins and polychlorinated dibenzofurans) and dioxin‐like polychlorinated biphenyls (DLPCBs) in their diets for 7 months. The dioxin and DLPCB concentrations in both fillet and whole body of salmon increased with increasing dietary exposure. DLPCBs transferred more efficiently from the feed to edible flesh of salmon than dioxins, and contributed a higher proportion to the total toxic equivalents (TEQ). At the end of the trial, the maximum concentrations of dioxins in fillet and whole fish were 1.9 and 2.3 pg WHO‐TEQ g^?1 fresh weight, respectively. Hence with this feeding period even with the most contaminated feed (4.9 pg WHO‐TEQ g^?1 dw) the dioxin concentrations in salmon did not exceed the maximum level set by the European Commission [4 pg WHO‐TEQ g^?1 (EC 2375/2001)]. The inclusion of DLPCBs in this study provides valuable information for forthcoming risk assessments and the future establishment of maximum limits for these compounds in feed and fish.     

Dietary phytase supplementation and the utilisation of phosphorus by Atlantic salmon (Salmo salar L.) fed a canola-meal-based diet

The effect of phytase supplementation to a canola-meal-based diet on phosphorus utilisation in Atlantic salmon was studied in a two-by-two factorial design. Diets were prepared without phytase or inorganic phosphorus supplementation, with phytase, with supplemental inorganic phosphorus and with both phytase and supplemental inorganic phosphorus. Available phosphorus was set below requirement and the total phosphorus set to meet requirements for salmonids. After 12 weeks, there were no significant differences in survival, feed intake and weight gain between diets. There was an interaction effect between supplements on bone ash, bone phosphorus and whole-body phosphorus so that adding phytase, inorganic phosphorus, or both resulted in significantly (P<0.05) higher values for these parameters. An interaction effect was also observed for phosphorus digestibility, phosphorus retention efficiency and phosphorus load. Phosphorus digestibility and retention efficiency were significantly (P<0.05) higher, and phosphorus load was significantly (P<0.05) lower in fish fed the phytase supplemented diet compared with diets containing supplemental inorganic phosphorus. In conclusion, phytase increased phosphorus availability, therefore reducing the need to add inorganic phosphorus and reducing phosphorus waste from plant-meal-based diets for Atlantic salmon.