Dietary phosphorus does not reduce the risk for spinal deformities in a model of adjuvant‐induced inflammation in Atlantic salmon (Salmo salar) postsmolts

Inflammation is a non‐specific protective mechanism towards injury known to affect bone remodelling. This study aimed to investigate the effect of Freund’s complete adjuvant (FCA) induced‐inflammation on the prevalence of spinal deformities of Atlantic salmon postsmolts fed with two different dietary P levels. Sextuple groups of salmon postsmolts were fed with either a low‐phosphorous (6 g kg^?1 available P, LP) or a high‐phosphorous (9 g kg^?1 available P) diet for a period of 101 days. On Day 102, individually tagged fish were subjected to (i) single injection with FCA (0.125 mg kg^?1 BW) dissolved in phosphate‐buffered saline (PBS) (ii) placebo injection with PBS or (iii) sham injection (insertion of needle only) or (iv) remained untreated. On Day 103, fish were given a common diet for 174 days in seawater. No significant differences in body weight were observed. Injected fish, particularly the FCA group, had more compressions in the injection site than untreated fish. No effect of diet and no interaction between treatment and diet were observed. Severe scoliosis was observed in ～7% of FCA‐injected individuals, corresponding to a mixture of bone malformations in the tail region. In conclusion, experimentally induced inflammation may be an independent risk factor for bone deformities in Atlantic salmon.     

Hypervitaminosis A in first‐feeding fry of the Atlantic salmon (Salmo salar L.)

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.     

Effects of various dietary factors on astaxanthin absorption in Atlantic salmon (Salmo salar)

The experiment was designed to investigate the dietary factors that might enhance or interfere with astaxanthin (Ax) absorption in salmon including potentially interfering factors such as certain carotenoids (zeaxanthin and lutein), plant sterols, fibre and enhancing compounds such as cholesterol and vitamin E. Two hundred and eighty‐eight salmon (778 ± 78 g) were reared in sea water under controlled conditions and fed practical experimental diets. The experimental diets were supplemented with 40 mg Ax kg^?1, in addition to various dietary factors, including cholesterol (2%), vitamin E (450 IU kg^?1), wheat bran (5%), lutein (40 mg kg^?1), zeaxanthin (40 mg kg^?1) and phytosterol (2%). After 26 days of feeding, blood was collected and plasma was separated to determine the plasma Ax concentration. Ax was not detected in the plasma of fish fed the non‐pigmented diet. Fish fed diet containing 2% cholesterol significantly improved Ax absorption, which was reflected in the higher Ax concentration in plasma of Atlantic salmon. Other supplements including vitamin E, wheat bran, lutein, zeaxanthin and phytosterols in diet had no significant effect on plasma Ax concentration . Fish fed diet containing 2% cholesterol significantly increased cholesterol concentration in fish plasma. Phytosterol had no benefit to lower cholesterol plasma level in fish fed 2% phytosterol‐supplemented diet.     

Antioxidant vitamins, minerals and lipid levels in diets for Atlantic salmon (Salmo salar, L.): effects on growth performance and fillet quality

An experiment with 2^{(7 ? 3)} reduced factorial design was conducted to study the biological effects of pro‐ and antioxidant micronutrients and lipid in Atlantic salmon. Vitamins C and E, astaxanthin, lipid, iron, copper and manganese were supplemented at high and low levels. For vitamins and minerals, high levels were chosen to be below the anticipated toxic level and the low levels were just above the requirement (vitamin C, 30 and 1000 mg kg^?1; vitamin E, 70 and 430 mg kg^?1; Fe, 70 and 1200 mg kg^?1; Cu, 8 and 110 mg kg^?1; Mn, 12 and 200 mg kg^?1). For astaxanthin, the dietary levels were 10 and 50 mg kg^?1 and for lipid, 150 and 330 g kg^?1. The experiment was started with postsmolts (148 ± 17 g) and lasted for 5 months. The variation in micronutrients had only minor effects on growth, feed conversion and fillet quality, measured as lipid and astaxanthin deposition. High dietary lipid had a profound positive effect on growth and feed conversion but gave fillets nearly two times the fat content that was found in fish fed the low lipid diet. Astaxanthin deposition in the fillet was primarily affected by dietary astaxanthin with a positive effect of high dietary lipid in week 14 but not in week 23. Vitamin E protected the fillet against iron ascorbate stimulated oxidation, with no effect of the other nutrient variables.     

The effect of dietary vitamin A on the immunocompetence of Atlantic salmon (Salmo salar L.)

Atlantic salmon, Salmo salar L. were maintained on diets containing low (0.37 mg kg^–1 diet), normal (1.95 mg kg^–1 diet) and high (15 mg kg^–1 diet) levels of vitamin A fed at 1.5% body weight per day. After 4 months, liver vitamin A levels reflected dietary intake and growth rates of all three groups were similar. Kidney leucocyte migration and serum bactericidal activity were found to be significantly reduced in fish fed low levels of vitamin A. On the other hand, high levels of vitamin A in the diet were found to augment serum antiprotease activity relative to the levels found in the other dietary groups. However, phagocyte respiratory burst activity, bactericidal activity and eicosanoid production were unaffected by the dietary vitamin A regime, as were lymphocyte functions (lymphokine and antibody production) and both serum lysozyme and classical complement activity. That the overall immunomodulatory effect of vitamin A was small was reflected in the resistance to Aeromonas salmonicida. No significant differences were found between the different vitamin A intake groups despite a trend to decreased resistance in the low vitamin A diet group.     

Growth and survival of Atlantic salmon, Salmo salar L. fed different dietary levels of astaxanthin. Juveniles

Atlantic salmon, Salmo salar L., juveniles, with a mean initial weight of 1.75 g, were fed casein-based purified diets which had been supplemented with different levels of astaxanthin for a 10-week period. The astaxanthin content of the diets ranged from 0 to 190 mg kg^?1 dry diet. The growth and survival of the juveniles were recorded throughout the experiment. The proximate composition, astaxanthin and vitamin A content were determined from whole-body samples at the start and termination of the experiment. The dietary treatment was found to affect growth significantly (P < 0.05). A reduction in the mean weight of the juveniles was observed in the groups fed the diets without astaxanthin supplementation. There was no difference in growth rate between the fish in the groups fed the diets containing 36 or 190 mg astaxanthin kg^?1 dry diet, whereas the fish in the group fed the diet containing 5.3 mg astaxanthin kg^?1 dry diet had a lower growth rate. There was a tendency to higher survival in the groups fed the diets containing astaxanthin when compared with the groups fed the non-supplemented diets. The moisture and ash contents were significantly lower and the lipid content was higher in the groups fed the astaxanthin-supplemented diets. The astaxanthin and the vitamin A concentrations in the fish were found to be dependent upon the dietary astaxanthin dose; the highest values were found in the fish fed the diet with the highest astaxanthin content. These results strongly indicate that astaxanthin functions as a provitamin A for juvenile Atlantic salmon. The body storage of vitamin A increased in the fish fed the diets containing astaxanthin. However, the increase was low in the fish fed the diet containing 5.3 mg astaxanthin kg^?1 dry diet.     

Evaluation of iron methionine and iron sulphate as dietary iron sources for juvenile cobia (Rachycentron canadum)

An 8‐week experiment was designed to determine the optimum dietary iron requirement of juvenile cobia Rachycentron canadum (mean initial weight, 15.89 ± 0.84 g) with iron sulphate (FeSO₄•7H₂O) and iron methionine (FeMet) as iron sources, using a semi‐purified diet based on casein and white fish meal as the protein sources. The basal diet was supplemented with 0, 30, 60, 120, 240 and 480 mg iron kg⁻¹ dry diet from either FeSO₄ or FeMet, respectively. Survival was not significantly affected by the all dietary treatment. Weight gain (WG), feed efficiency (FE), serum catalase activity (SCAT), and haemoglobin were significantly affected by any of the dietary treatments from both of two iron sources. Based on broken‐line regression analysis of WG, FE and SCAT, a minimum requirement for dietary iron was recommended to be 80.5–94.7 mg kg⁻¹ from FeSO₄ and 71.3–75.1 mg kg⁻¹ from FeMet. Iron supplement to the basal diet had no significant effect on haematocrit, erythrocyte count, iron concentration in whole body and fillet. Our experiment also showed that the bioavailability of FeMet and FeSO₄ to juvenile cobia was similar for WG and FE, and the relative bioavailability of FeMet and FeSO₄ to juvenile cobia was 275% for maximum SCAT.     

Adult triploid Atlantic salmon (Salmo salar) have higher dietary histidine requirements to prevent cataract development in seawater

The study investigated cataract preventive effects of dietary histidine (His) supplementation in triploid Atlantic salmon during seawater grow‐out. Groups of individually PIT tagged diploid (2N) and triploid (3N) postsmolts were fed one of two supplemented dietary histidine levels; low (L, 12.6 g kg^?1 diet) or high (H, 17.4 g kg^?1 diet) from March to September following their first sea winter. Low severity cataracts were detected in both ploidy prior to supplemented His diet application. Thereafter, 3N‐L showed progression of cataract development in the second spring‐summer period, while development was inhibited in 3N‐H. Severity of cataract showed a strong family effect. A positive correlation between initial triploid seawater growth (weight and TGC) under increasing water temperature and cataract severity was identified as a major risk factor. The relationship was reversed at harvest, where triploids were on average 7.5% smaller than their diploid siblings. Lens N‐acetyl‐histidine content reflected dietary His inclusion level and cataract severity, although no significant differences in lens His content were evident between ploidy or dietary groups. Results indicate that triploid Atlantic salmon appear to have a higher dietary histidine requirement than diploids and that preventative measures can be taken to mitigate further cataract development.     

Determination of the threonine requirement for maintenance in Atlantic salmon (Salmo salar L.) fry with the diet dilution procedure

A study was conducted to evaluate the threonine (Thr) requirement for maintenance in Atlantic salmon using the diet dilution procedure (DDP). Fourteen groups of 60 salmon fry [1.46 g initial body weight (BW)] were fed on seven semi‐purified diets containing graded levels of N (3–64 g kg⁻¹ dry matter) and L‐Thr (1–39 g kg⁻¹ dry matter). Seven doses of Thr represented 1–31% of its ideal level for optimum protein deposition. Indispensable amino acids (AA) other than Thr were included in the same proportion as in the Atlantic salmon fry whole‐body carcass. Protein deposition and Thr accretion were linear functions of Thr intake. At zero Thr intake fry lost 4.4 mg Thr kg BW^−0.75 day⁻¹ and the Thr requirement for maintenance was 5.8 mg kg BW^−0.75 day⁻¹, which represented 11% of the total need for Thr. Increasing doses of Thr did not show any effect on AA concentrations in whole‐body protein, except for cystine. The linear relationship between Thr gain and Thr intake indicates a constant Thr cumulative efficiency (77%) at marginal Thr intake. Finally, our results suggest that (1) both the DDP and the graded supplementation technique can be used in Atlantic salmon fry for the determination of AA maintenance requirement and utilization efficiency, at least for Thr; (2) the dietary protein level has only a minor effect on the Thr maintenance requirement determination.     

Fluoride retention of Atlantic salmon (Salmo salar) fed krill meal

The present experiment was performed to study how fluoride from krill meal enriched muscle, whole fish and bone of adult Atlantic salmon (Salmo salar) reared in sea water. Atlantic salmon (mean weight 0.5 kg) were divided into four triplicate groups and fed a commercial fish meal based diets with 0, 100, 200 and 300 g krill kg^?1 feed, respectively, for 12 weeks. The fluoride concentrations in the experimental feeds were analysed to be 18, 132, 235 and 358 mg kg^?1, respectively. Growth, mortality and feed efficiency were recorded through the experiment. Fluoride concentration was measured in muscle, whole‐body, and bone initially and after 12 weeks of feeding. The fluoride concentrations in the samples were determined by alkali fusion and fluoride ion‐selective electrode. Growth, mortality and feed efficiency ratio were not affected by the dietary treatments. The results showed that fluoride concentration in muscle, whole body and bone were not affected by the dietary fluoride level. The fluoride concentration in the tissues showed great variation among replicates of the group given the same diet. Fillets of the fish varied between 0.3 and 1.4 mg fluoride kg^?1 wet weight, whereas the whole‐body concentration of fluoride varied between 3.3 and 6.1 mg kg^?1 wet weight and the fluoride bone concentration varied between 5.8 and 7.2 mg kg^?1 fresh weight. These results suggest that Atlantic salmon are highly tolerant of dietary fluoride given as krill meal with concentration of fluoride up to 350 mg kg^?1 diet, and that accumulation of fluoride from feeding diets containing krill meal does not lead to tissue accumulation in the fish, at least over a short period of time.     

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.     

Growth,feed utilization,body composition and swimming performance of giant croaker,Nibea japonica Temminck and Schlegel,fed at different dietary protein and lipid levels

A 50‐day feeding trial was conducted to examine the effects of dietary protein and lipid levels on growth, feed utilization, body composition and swimming performance of giant croaker, Nibea japonica. Fish (initial body weight 44.6 g ind⁻¹) were fed ten test diets which were formulated at 5 crude protein levels (360, 400, 440, 480 and 520 g kg⁻¹) and 2 crude lipid levels (90 and 150 g kg⁻¹). In addition, a raw fish diet (fillet of small yellow croaker) served as the reference. The weight gain (WG) increased, whereas the feed intake (FI) and feed conversion ratio (FCR) decreased, with increasing dietary protein level from 360 to 520 g kg⁻¹. At the same dietary protein level, no significant difference was found in the WG between fish fed the diets containing 90 or 150 g kg⁻¹ crude lipid. Fish fed the diet containing 480 g kg⁻¹ crude protein and 90 g kg⁻¹ crude lipid exhibited higher WG, nitrogen retention efficiency (NRE) and energy retention efficiency (ERE) but lower nitrogen wastes output (TNW). At the end of the feeding trial, the hepatosomatic index (HSI) and viscerosomatic index (VSI) decreased, whereas the body protein content increased, with increase in dietary protein level. The body lipid content was higher in fish fed at the 150 g kg⁻¹ lipid level than in fish fed at the 90 g kg⁻¹ lipid level. No significant difference was found in the maximum sustained swimming speed (MSS) between fish fed at different dietary protein and lipid levels. The WG, NRE, ERE and condition factor (CF) were higher, whereas the FI, FCR, HSI, VSI and TNW were lower, in fish fed the raw fish diet than in fish fed the diet containing 480 g kg⁻¹ crude protein and 90 g kg⁻¹ crude lipid. No significant difference was detected in the MSS between fish fed the raw fish diet and diet containing 480 g kg⁻¹ crude protein and 90 g kg⁻¹ crude lipid. The results of this study suggest that the suitable dietary crude protein and crude lipid levels are 480 g kg⁻¹ and 90 g kg⁻¹ for giant croaker reared in net pens.     

An estimation of dietary iron requirement of Atlantic salmon, Salmo salar L., parr

A study was conducted to determine the dietary iron requirement of fingerling Atlantic salmon Salmo salar L. During the first 4 weeks of the experiment, fish with an initial weight of 5 g were fed a casein–gelatine-based purified diet which contained 11 mg iron kg^?1. Thereafter duplicate tanks (200 fish in each) were fed the casein–gelatine purified diets containing supplemental iron levels of 0, 10, 20, 30, 40, 60, 100, 200 or 400 mg iron kg^?1 (added as FeSO_?4* 7H₂O) for 12 weeks. Weight gain, body length and mortality were monitored. Liver iron and ascorbic acid concentration were analysed in addition to whole-body iron, manganese and zinc concentration. Several haematological parameters were also measured. There were no significant differences in weight gain and survival of salmon fed diets containing different iron levels. Haematological values, hepatic and whole-body iron concentrations were, however, significantly affected by the dietary iron content. Liver vitamin C concentration decreased with increasing dietary iron levels. Dietary supplementation with iron significantly reduced whole-body manganese, but no effect of dietary iron on whole-body zinc was found. Based on haematology and hepatic iron concentration, the iron requirement of Atlantic salmon was determined to be between 60 and 100 mg iron kg¹.     

A multivariate study on the effects of dietary vitamin K, vitamin D3 and calcium, and dissolved carbon dioxide on growth, bone minerals, vitamin status and health performance in smolting Atlantic salmon Salmo salar L.

Bone deformities represent an increasing, unsolved problem for intensive farming of Atlantic salmon, Salmo salar L. To increase insight into nutritional and environmental impacts on bone mineralization, 16 groups of Atlantic salmon parr were fed diets with different levels of menadione sodium bisulphite (MSB), vitamin D₃, and calcium (Ca), and exposed to different levels of dissolved carbon dioxide (CO₂) based on a multivariate factorial design (2⁴). The composition of the experimental diets was either a high or low level of each of the design variables. In addition, four groups (centre points) were fed a diet with intermediate levels of all dietary parameters and exposed to an intermediate level of dissolved CO₂ to record the variation among tanks. After 6 weeks in fresh water, fish were marked according to group, transferred to a common net pen in sea water and fed commercial feed for another 11 weeks. High levels of CO₂ decreased fish growth both in fresh water and sea water. No visible bone deformities were recorded at any time. Dry matter, protein and ash compositions of bone and concentrations of Ca, phosphorus (P) and magnesium (Mg) in bone were not significantly affected by any of the design variables. Minor effects were observed in clinical parameters recording health performance, stress and plasma Ca homeostasis. The mean level of vitamin D₃ measured as cholecalciferol in fish organs increased significantly during the freshwater period and reflected dietary vitamin D₃, whereas the level decreased when fish were fed commercial feed in sea water. The level of menaquinone in liver increased significantly in response to high dietary levels of MSB, indicating that dietary MSB was converted to menaquinone in salmon.     

Nutritive value of partially dehulled and extruded sunflower meal for post-smolt Atlantic salmon (Salmo salar L.) in sea water

This study determined the digestibility of protein in partially dehulled sunflower meal (SFM) and then, as the main goal, the nutritive value of high‐temperature extruded (≤149°C) partially dehulled SFM (SFM_EX) for post‐smolt Atlantic salmon Salmo salar in sea water. The digestibility study was conducted using the settling column approach (‘Guelph system’) for faeces collection as described by Hajen, Higgs, Beames and Dosanjh. In the nutritive value study, triplicate groups of 50 salmon (mean weight ～116 g) in 4000‐L outdoor fibreglass tanks supplied with 25–40 L min^?1, filtered, oxygenated (dissolved oxygen, 7.0–8.5 mg L^?1), 11–12°C sea water (salinity, 29–31 g L^?1), were fed twice daily to satiation one of five steam‐pelleted dry diets that contained 422 g of digestible protein (DP) kg^?1 and ～16.4 MJ of digestible energy (DE) kg^?1 on a dry weight basis for 84 days. Low‐temperature‐dried anchovy meal (LT‐AM) comprised 68.2% of the basal diet protein whereas in four test diets, SFM_EX progressively replaced up to 33.0% of the DP provided by LT‐AM in the basal diet (SFM_EX≤271 g kg^?1 of dry matter). Sunflower meal had 87.9% DP. Diet treatment did not significantly affect specific growth rate (1.39–1.45% day^?1), feed efficiency (1.19–1.26), percentage of dietary protein retained (45.8–47.5), gross energy utilization (46.5–49.4%), per cent survival (96.0–99.3) or terminal whole body and muscle proximate compositions. We conclude that SFM_EX can comprise ≥271 g kg^?1 of the dry diet or ≥22.7% of the digestible dietary protein of post‐smolt Atlantic salmon in seawater without any adverse effects on their performance.     

Influence of dietary vitamin B6 on tissue vitamin B6 contents and immunity in Atlantic salmon, Salmo salar L.

Atlantic salmon, Salmo salar L., (14 g) were fed a practical fish-meal-based diet supplemented with 0. 10, 20. 40, 80 and 160 mg pyridoxine (PN) per kg feed for 20 weeks. Tissue vitamin B₆ contents were significantly reduced in fish fed the non-supplemented diet compared with fish fed PN-supplemented diets. Serum haemolytic complement activity and head kidney lysozyme activity, and the specific antibody response following immunization with Vibrio salmonicida. were not influenced by the dietary regimes. Challenge with Aeromonas salmonicida showed that increasing the dietary levels of vitamin B₆ did not improve the resistance to furunculosis. Growth, mortality and haematology were not affected by supplementing a practical diet with vitamin B₆ In conclusion, feed levels of vitamin B₆ higher than the minimum dietary requirement did not enhance immune functions and disease resistance in Atlantic salmon.     

Effect of dietary vitamin B6 on growth,feed utilization,health and non‐specific immune of juvenile Pacific white shrimp,Litopenaeus vannamei

Six diets were formulated with vitamin B₆ levels (2.6, 32.7, 54.8, 90.7, 119.6 and 247.4 mg kg⁻¹, dry diet) to determine the requirement for juvenile Pacific white shrimp, Litopenaeus vannamei. Triplicate groups of 40 juvenile shrimp (approximately 1.0 g) were provided four times each day to apparent satiation (8 weeks). Weight gain (WG), specific growth rate, feeding efficiency, protein efficiency ratio (PER) and protein productive value of the shrimp were significantly influenced by the vitamin B₆ levels. No significant differences in whole‐body and muscle composition, except for dry matter and protein contents in whole body. Vitamin B₆ concentration in the hepatopancreas significantly increased with the dietary vitamin B₆ level increasing from 2.6 to 32.7 mg kg⁻¹. High‐density lipoprotein cholesterol in the haemolymph improved with the dietary vitamin B₆ levels increasing from 2.6 to 90.7 mg kg⁻¹ diet and no significant differences in low‐density lipoprotein cholesterol, cholesterol, glucose and total protein concentrations. Aspartate aminotransferase, alanine aminotransferase, superoxide dismutase, catalase and lysozyme in the haemolymph were significantly influenced by dietary vitamin B₆ levels. The optimal dietary vitamin B₆ requirements estimated using a two‐slope broken‐line model based on WG and SGR and an exponential model based on the vitamin B₆ concentration in the hepatopancreas were 110.39, 110.08 and 167.5 mg kg⁻¹, respectively.     

Effects of dietary cadmium on calcium homeostasis, Ca mobilization and bone deformities in Atlantic salmon (Salmo salar L.) parr

Atlantic salmon parr were reared for 4 months on experimental fish‐meal‐based diets supplemented with 0 (control), 0.5, 5, 25, 125 or 250 mg Cd kg^?1 feed to assess the effects of dietary Cd on active Ca uptake, mobilization of Ca from internal reservoirs, and development of bone malformations. The accumulation of dietary Cd in tissues was, in decreasing order, intestine > kidney >> gill > bone. No significant accumulation of Cd in the scales was observed. Strongest inhibition of ATP dependent Ca uptake (measured as Ca²⁺‐ and Na⁺/K⁺‐ATPase) was observed in the intestine of salmon fed 25 mg Cd kg^?1. This suppression in active intestinal Ca uptake did not lead to disturbed plasma Ca levels. Significant reduction of Ca from the scales in salmon fed 25 mg Cd kg^?1, indicates remobilization of Ca to maintain Ca homeostasis. At the end of the experiment no significant differences were observed in bone Ca levels, nor were any bone malformations observed in any of the dietary Cd‐exposed salmon. This indicates that bone as an endogenous Ca reservoir is spared compared with scales. It was concluded that dietary Cd‐induced disturbance of Ca homeostasis did not lead to bone deformities, even when Atlantic salmon were fed high amounts of cadmium. This indicates a low risk of spinal deformations being developed in Atlantic salmon sub‐chronically exposed to high Cd concentrations in the feed.     

Energy and nutrient utilization of Atlantic cod, Atlantic salmon and rainbow trout fed diets differing in energy content

The growth and feed utilization of Atlantic cod (Gadus morhua) (437 g), Atlantic salmon (Salmo salar) (485 g) and rainbow trout (Oncorhynchus mykiss) (413 g) fed a diet (170 g kg⁻¹ fat, 600 g kg⁻¹ crude protein; LE) similar to that used in commercial cod production or one that was top dressed with additional fat (280 g kg⁻¹ fat, 530 g kg⁻¹ crude protein; HE), were compared in an 11‐week trial. In the cod, relative feed intake was 41–58% and thermal growth coefficient 63% of that in the salmonids, but the feed efficiency ratio (FER) was 38% better (P ≤ 0.05). In contrast to the cod where there was no effect of diet on feed intake, growth or FER, both the salmon and trout fed the HE diet had greater feed intake than those fed the LE diet, but the effect of this was only positive for growth in the salmon. The cod retained more of the digested nitrogen (44.9 ± 2.7%) than the salmon (39.4 ± 0.8%), and both of these species retained more than the trout (33.6 ± 1.1%) (P ≤ 0.05). The retention of digested energy was significantly higher in the salmon (52.2 ± 0.9%) than in the trout (44.8 ± 1.1%), with the cod (44.9 ± 4.9%) not different from either of the other species. There were no differences between the species in the retention of absorbed phosphorus (65.9 ± 3.6%). There were very few dietary effects on nutrient utilization in this trial and, for the cod, this indicates that higher energy diets may be feasible for use in production.     

Comparative effects of dietary supplementation with maggot meal and soybean meal in gibel carp (Carassius auratus gibelio) and darkbarbel catfish (Pelteobagrus vachelli): growth performance and antioxidant responses

A 6‐week growth trial was conducted to investigate the effect of dietary supplementation with maggot meal (MGM) and soybean meal (SBM) on the growth performance and antioxidant responses of gibel carp (GC) and darkbarbel catfish (DC). The basal diet was formulated to contain 114 g kg⁻¹ fish meal (FM) and 200 g kg⁻¹ SBM. The basal diet was supplemented with either 280 g kg⁻¹ FM (Control), 390 g kg⁻¹ MGM or 450 g kg⁻¹ SBM to obtain three isonitrogenous (crude protein: 380 g kg⁻¹) and isocaloric (gross energy: 16 kJ g⁻¹) diets. For GC, a significant decrease in specific growth rate (SGR) was only observed in fish fed the SBM diet compared with the control (P < 0.05). Principal components analysis (PCA) of GC showed a higher similarity in antioxidant response to dietary supplementation with MGM and SBM proteins between liver and intestine, but the DC did not. The present results suggest that supplementing 390 g kg⁻¹ MGM protein to basal diet cause an enhancement of the antioxidant capacity in GC, but supplementing 390 g kg⁻¹ MGM and 450 g kg⁻¹ SBM proteins to basal diets resulted in a significant attenuation of the antioxidant capacity in DC.