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Notes: A 56-day growth trial was conducted to study the utilization of hydrolysed potato starch by juvenile Atlantic salmon Salmo salar L. using a restricted feeding regime. Two diets supplemented with either 15% or 30% hydrolysed potato starch and a control diet without carbohydrate supplementation were each fed to triplicate groups of salmon. Feeding rate varied from 1.4% to 2.0% of body weight per day, so that fish were fed similar amounts of protein and lipid. In spite of the restricted feeding used, no growth stimulation was measured as a consequence of the additional starch intake. No variation was found in protein utilization, measured as protein efficiency ratio values (PER), while feed utilization showed decreased values as starch intake increased. Plasma glucose concentrations did not vary as a consequence of increased starch intake when measured 24 h after feeding, indicating efficient regulation of plasma glucose. In fish fed the 30% starch, the plasma triacylglycerol concentration was significantly increased, which may point to de novo lipid synthesis from the high starch intake. No variation was found in plasma cholesterol or protein concentrations, or asparagine aminotransferase, alanine aminotransferase and lactate dehydrogenase activities. This shows that the fish health status and liver function were normal (no mortality was registered). Liver and muscle showed increased glycogen levels as a function of increased starch intake. The same diets were also fed to juvenile white sturgeon Acipencer transmontanus and hybrid tilapia Oreochromis niloticus×O. aureus. These results are presented separately.

Notes: To determine seasonal variation in growth and feed conversion ratio (FCR), Atlantic salmon postsmolts (Salmo salar L.) were exposed to either simulated natural photoperiod (SNP) for 12 months or continuous light (LL) from January to June followed by SNP until December. Feed was given to excess and uneaten feed pellets were collected after every meal for estimation of feed intake and calculation of FCR. Body weight increased from 1086 ± 9 g (mean ± SEM) in January to 4970 ± 7 g (SNP) and 5190 ± 23 g (LL) in December. Specific growth rate (SGR), condition factor and feed intake displayed strong seasonal variation in both groups. Measurements of the thermal growth coefficient correlated highly with SGR (r = 0.98, P 〈 0.05), indicating that the seasonal variation in SGR was independent of temperature and fish size. Continuous light treatment resulted in increased growth from spring, while the fish exposed to simulated natural light had increased growth rate in late summer. Furthermore, LL improved FCR. Periods of high SGR were concurrent with periods of low FCR in both groups.

Notes: Accumulation of 14C in various tissues and organs was studied in three different groups of 0.8-kg Atlantic salmon Salmo salar force-fed with 14C1-glucose in order to evaluate if metabolism of glucose depended on adaptation to dietary carbohydrate level. The salmon had been fed diets supplemented with 0, 100 and 200 g maize dextrin kg−1 for 10 months before the experiment. The fish were force-fed 6.65 × 104 Bq of 14C1 glucose kg−1 BW, in gelatin capsules. Fish for analysis were obtained 16 h later. 14C was measured in blood plasma, gill, kidney, liver and white muscle, and in lipid extract of liver.The liver contained most 14C, followed by heart, blood plasma, gill and liver lipid extract, while kidney and muscle contained the least 14C per gram or millilitre tissue. The muscle contained most radioactivity, on an estimated total tissue basis, followed by liver, blood plasma, gill, liver lipid extract, kidney and heart tissue. Thirty-eight per cent of the orally administered 14C was recovered in the salmon adapted to the diet without dextrin after 16 h. This was significantly (P 〈 0.05) higher than the 30% and 32% recovered in the salmon adapted to diets with 10% and 20% dextrin. This effect on adaptation to dietary dextrin level in glucose uptake or metabolism was supported by a trend (P 〈 0.10) toward higher radioactivity per gram or millilitre of each individual tissue in the fish adapted to the diet without dextrin, when compared with the other two adaptation regimes.

Notes: The utilisation of dietary carbohydrates and their effects on fish metabolism are reviewed. Details on how dietary carbohydrates affect growth, feed utilisation and deposition of nutrients are discussed. Variations in plasma glucose concentrations emphasizing results from glucose tolerance tests, and the impact of adaptation diets are interpreted in the context of secondary carbohydrate metabolism. Our focus then shifts to selected aspects of hormonal regulation of carbohydrate metabolism and dietary carbohydrates and their variable effects on glycogen and glucose turnover. We analyse the interaction of carbohydrates with other nutrients, especially protein and protein sparing, and de novo synthesis of lipids, and finish by discussing the correlation of dietary carbohydrates with fish health.

Notes: The present study evaluated how different photoperiods, carbohydrate sources and inclusion levels influenced growth, plasma, organ and body compositions in Atlantic salmon (Salmo salar). Four different diets were used, containing 10 or 20% starch on a dry matter basis, using gelatinized corn (C10 and C20) or wheat (W10 and W20). Two different photoperiods were used, Continuous (Con) light throughout the study, Winter (Wi) two initial weeks of continuous light, thereafter 6 weeks of short day, ending with 6 weeks of continuous light. The winter regime resulted in reduced growth rate compared with continuous light. All Wi groups were smaller than Con groups when the experiment was terminated, except for fish given diet C10. Diet W10 resulted in better growth compared with all other groups when exposed to Con. regime. Atlantic salmon fed with diets containing 20% starch had lower growth rates than fish fed diets containing 10% starch, when the same starch source and light regime were compared. All fish belonging to the Con group exhibited similar and higher condition factors compared with fish from groups Wi. Condition factor was not influenced by dietary starch source. Higher whole body lipid concentrations were found when fish were given the corn compared with the wheat diets, without any responses to starch level or light regime. Whole body protein showed increased values in fish exposed to regime Wi compared with Con, without any influence from dietary manipulation. Liver glycogen values and hepatosomatic index reflected dietary starch levels and were significantly influenced by light regime, whilst muscle glycogen levels varied only as a response to light regime with lower values in fish from the Wi compared with the Con groups. Light regime influenced plasma glucose levels, except in groups fed with diet W10. All measured plasma nutrient concentrations were within normal ranges.At the end of the feeding period, all fish were evaluated for glucose and salt water tolerance to ascertain whether diet and/or light regime influenced glucose regulation capacity and/or smolt quality. Fish fed with 20% starch had reduced osmoregulatory ability measured as plasma chloride after a seawater challenge test. Fish from the Wi regime, but not from the Con regime developed characteristics associated with smoltification. Glucose tolerance in Atlantic salmon was substantially influenced by both photoperiod regime and diet. Fish reared under the Wi photoperiod showed reduced glucose regulation capacity compared with fish held under continuous light. Glucose regulation capacity was also reduced in fish adapted to the highest starch levels.

Notes: Atlantic salmon fry were reared on a fishmeal based diet with increasing levels of vitamin A (VA) (6, 122 and 938 mg retinol kg–1 dry feed) from startfeeding and for 14 weeks. Signs of VA stress, such as reduced fat stores, liver size and growth, were found for groups receiving 122 and 938 mg retinol kg–1. Signs of vitamin A toxicity, such as increased mortality, abnormal vertebral growth, and reduced growth, were found for groups receiving 938 mg retinol kg–1. These results suggest that excess VA in the early life stages of Atlantic salmon is deleterious for normal development.

Notes: Atlantic halibut larvae were fed docosohexanoic acid- (DHA) selco enriched Artemia (RH-cysts) or wild zooplankton in duplicate tanks from first-feeding and 60 days onward. The zooplankton were collected from a fertilized sea water pond and consisted mainly of different stages of Eurytemora affinis and Centropages hamatus. There were no differences in survival, or in growth during the first 45 days of feeding, between larvae fed the two prey items, but the larvae fed Artemia showed much higher incidence of malpigmentation and impaired eye migration than larvae fed zooplankton. The prey organisms contained similar amounts of dry matter and protein, but Artemia was higher in lipid and glycogen than the zooplankton. Larvae fed Artemia were higher in both glycogen and lipid than the zooplankton-fed larvae towards the end of the feeding period. There were large differences between the prey organisms in the concentrations of essential fatty acids (% of total fatty acids) which was reflected in the fatty acid composition of the larval body. It is concluded that the macronutrient composition of Artemia in the present study was probably within the optimal range for promotion of growth and survival in young Atlantic halibut. The concentration of n-3 HUFA, and especially DHA, is however, very much lower in enriched Artemia than in copepods, and may be one of the factors triggering developmental errors in Atlantic halibut.

Notes: With the aim of elucidating seasonally changing lipid metabolism in immature Atlantic salmon (Salmo salar L.) in sea water, one group was reared under simulated natural light, while one group was reared under continuous light. Fatty acid profile in plasma lipoproteins did not vary during the experiment, while β-oxidation capacity increased during spring, concurrent with decreasing temperatures. Simultaneously, the relative level of monounsaturated fatty acids (MUFA) in muscle tissue decreased (42–36%). Muscle levels of saturated fatty acids were low during early spring (19%), but then increased slowly, and muscle levels of polyunsaturated fatty acids increased during spring (from 36% to 39%). It is suggested that increased spring growth and the concomitant energy demand was met by increased lipid oxidation, where MUFA were preferred as energy substrate.

Notes: Juvenile Atlantic cod (Gadus morhua) were fed extruded feeds formulated to contain 360–660 g kg−1 protein, 80–280 g kg−1 lipid and 80–180 g kg−1 starch at feeding frequencies of either once per day or every second day to satiation. The trial was conducted at 8 °C and lasted for 28 weeks during which fish were weighed five times at regular intervals. Sampling for proximate analysis was performed at the start, after 12 weeks and at the end of the trial. Fish grew from an average weight of 192 g to between 750 and 866 g, with growth being negatively affected by low dietary protein concentration. High dietary starch concentrations had some negative effects on growth, whereas changes in dietary fat concentration had no significant effect on growth. Liver indices (at the end of the experiment) varied between 80 and 170 g kg−1, and there was a negative correlation between the ratio of protein to fat and liver index. Feed conversion ratio (FCR) ranged between 0.74 and 0.88, and feed utilization improved with increasing concentrations of dietary protein and fat. Increasing dietary starch concentrations resulted in poorer feed utilization. To achieve good growth and protein retention, and avoid excessive liver size in juvenile cod, feeds should contain 500–600 g kg−1 crude protein, 130–200 g kg−1 lipid and 〈150 g kg−1 starch.

Notes: In order to investigate how seasonal variation in growth affects selected fillet quality parameters, immature Atlantic salmon (Salmo salar L.) were reared under simulated natural photoperiod (SNP) for 12 months or continuous light (LL) from January to June followed by SNP until December. Photoperiod treatments advanced the growth rate pattern of the LL group compared with the SNP group and influenced macronutrient metabolism, evaluated both as trends in protein and lipid retention and in fillet lipid and protein levels. Good growth was associated with low fillet lipid and protein level, in addition to reduced levels of fillet tocopherol and astaxanthin, indicating increased oxidative stress. Elevated levels of thiobarbituric reactive substances (TBARs) further supported this. Slaughtering during periods of high growth may therefore reduce postmortem quality, both because of increased susceptibility to fillet lipid peroxidation and reduced astaxanthin levels, which were lowered in vivo and might consequently be depleted further after slaughter. Specialized use of antioxidant-rich feed prior to slaughter is suggested if slaughtering is expected to occur during periods of high growth rate.