An evaluation of the duration of efficacy of emamectin benzoate in the control of Caligus curtus Müller infestations in Atlantic cod, Gadus morhua L

The duration of efficacy of emamectin benzoate in the control of Caligus curtus infestations in Atlantic cod, Gadus morhua L., was studied following an administration of 50 μg kg^?1 for seven consecutive days. No lice were found on medicated fish when challenged 1 week (challenge 1) or 5 weeks (challenge 2) following termination of medication, whereas the mean abundance of lice among the unmedicated fish was 17.9 and 19.3 lice per fish in challenge 1 and 2, respectively. Muscle concentrations of 19.5 ± 8.2 ng g^?1 and 3.4 ± 0.9 ng g^?1, respectively, and skin concentrations of 23.1 ± 10.8 and 4.2 ± 1.0 ng g^?1, respectively, were found 27 and 55 days following the termination of medication. Tissue concentrations and the duration of efficacy indicate a dosing regime for emamectin in cod, similar to the regime used for Atlantic salmon, Salmo salar L.     

Bovine placental lactogen invokes rapid growth in chinook salmon

The effect of recombinant bovine placenta) lactogen (rbPL) treatment upon growth of juvenile chinook salmon, Oncorhynchus tshawytscha (Walbaum) (14.0 ± 0.31 g wet wt), was examined over a period of 6 weeks. Experimental animals were either injected (5 μg rbPL g^?1 week^?1), implanted with a cholesterol pellet containing 0.4 mg rbPL (approximately 4 μg g^?1 week^?1), or orally and rectally intubated with 7.5 μg rbPL g^?1 week^?1. Control animals were injected with bovine serum albumen (BSA), 5 μg g^?1 week^?1, implanted with a placebo or orally intubated (7.5 μg BSA g^?1 week^?1). Significant (P < 0.05) growth acceleration was recorded for rbPL-injected and pellet-implanted groups from week 2 onwards when compared against all other groups. Oral or rectal intubation of rbPL (7.5 μg rbPL g^?1 week^?1), however, was without effect. Condition factor decreased in all groups, but was significantly lower in rbPL-injected and pellet-implanted fish at trial end when compared against controls. No differences were recorded between groups for per cent body moisture or relative gut length. Hepatosomatic index was significantly (P < 0.05) higher in rbPL-injected and rbPL-implanted chinook salmon versus other fish.     

Ammonia production and oxidation during the culture of marine prawns and lobsters in laboratory recirculation systems

Data obtained during the culture of tropical prawns Penaeus sp. and European lobsters Homarus gammarus (L.) in 20 laboratory recirculation systems over a number of years were used to obtain gross estimates of (a) the rates and diurnal patterns of ammonia excretion, (b) food utilization and wastage, and (c) nitrification rates in biological filters. Ammonia excretion in Penaeus monodon decreased with increase in animal size from 0·93 to 0·30 mg N g^?1 day^?1 at 1·6 and 27 g live weight, respectively. Large lobsters (300 g) excreted 0·3 mg N g^?1 day^?1. Peak excretion times were approximately 3, 9 and 15 h after a single morning feed for prawns and after 6 and 12 h for lobsters. Uneaten food solids amounted to 11% (lobsters) and 32% (prawns) of the daily ration and, for 4 g animals, only 69% (lobsters) and 45% (prawns) of the food nitrogen in the daily ration was converted into crustacean flesh. Nitrification rates ranged from 0·03 to 0·43 g N oxidized per m² of filter media surface per day. Some evidence for periodicity in nitrifying activity was also found and is discussed in relation to the published literature.     

Effects of addition of a bird repellent to fish diets on their growth and bioaccumulation

The effects of adding the nonlethal bird repellent methyl anthranilate (MA), at levels of 100 and 1000 mg kg^?1, to fish feed on the bioaccumulation and growth of juvenile (10 g) hybrid striped bass (Morone chrysops×M. saxatilis) and juvenile (1 g) African cichlid fish Aulonocara jacobfreibergi were investigated under laboratory conditions. The bird repellent did not have any effect on the fish growth or survival over a period of 6 weeks. MA residues at low levels of 11.2±2.6 μg g^?1 were found in lipophilic tissues (liver) of MA‐fed fish. Control fish, which had no MA added to their diet, had a much lower level of 0.6±0.3 μg g^?1 MA in their liver. Fish muscle was found to contain negligible MA residues, while the outer body surface mucus did not contain any MA. Following a 6‐week depuration period, during which the previously MA‐fed hybrid striped bass were fed a feed to which no MA was added, the levels of MA residues detected were reduced by one order of magnitude.     

Response of the tropical spiny lobster Panulirus ornatus to protein content of pelleted feed and to a diet of mussel flesh

In an 8‐week growth experiment, juvenile spiny lobsters (Panulirus ornatus) grew best on a feed containing at least 610 g kg^?1 crude protein on a dry matter basis (DM) and a digestible protein to digestible energy ratio of 29.8 mg kJ^?1. The study entailed a six treatment by four replicate randomized block experiment with 222 wild‐caught P. ornatus of mean initial weight (±SD) of 2.5 ± 0.19 g. The lobsters were fed one of five isolipidic feeds (approximately 130 g kg^?1 DM) in which the crude protein was serially incremented between 330 and 610 g kg^?1 DM, or a reference diet comprising the flesh of frozen green‐lip mussels. Lobsters fed the pelleted feeds had high survival (79 ± 4.5%) and responded to increasing dietary crude protein content with progressively higher growth rates, with the daily growth coefficient improving from 0.72% day^?1 with 330 g kg^?1 crude protein to 1.38% day^?1 with 610 g kg^?1 crude protein. Both growth rate and survival were low with the mussel diet (0.80% day^?1and 41 ± 4.5%, respectively). These results demonstrate that tropical spiny lobsters grow well when fed high‐protein, high lipid, pelleted feeds, but feeding on a sole diet of freshly thawed green‐lip mussels was unsatisfactory.     

Retention of the synthetic antioxidant butylated hydroxyanisole in Atlantic salmon (Salmo salar) fillets

Butylated hydroxyanisole (BHA) is a phenolic antioxidant that is used as a food additive, particularly in fats and oils, and it is also authorized as a feed additive in the European Union for all animal species with a maximum concentration of 150 mg kg^?1 feed (alone or in combination with ethoxyquin and/or butylated hydroxytoluene). Information on the BHA levels in food of animal origin is scarce, as is literature on the transfer of BHA from feed to animal products. Consequently, the current feeding trial was conducted under realistic rearing conditions to determine the retention of BHA in Atlantic salmon (Salmo salar) fillets. Four different concentrations of BHA in feed were tested (0, 48.5, 92.5 and 225 mg BHA kg^?1 feed), and fish were sampled after 4, 8 and 12 weeks dietary exposure, and after a 2‐week starvation period, which is representative of commercial salmon farming in Norway. The levels of BHA in salmon fillets were fairly dose dependent during the feeding period. A steady state in fillet residues was reached after 4 weeks of administration of BHA. After the 2‐week withdrawal period, BHA was not detectable (<7 μg kg^?1) in either fish fillets or livers.     

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.     

Depletion of florfenicol amine in tilapia (Oreochromis sp.) maintained in a recirculating aquaculture system following Aquaflor®‐medicated feed therapy

Aquaflor^® [50% w w^?1 florfenicol (FFC)], is approved for use in freshwater‐reared warmwater finfish which include tilapia Oreochromis spp. in the United States to control mortality from Streptococcus iniae. The depletion of florfenicol amine (FFA), the marker residue of FFC, was evaluated after feeding FFC‐medicated feed to deliver a nominal 20 mg FFC kg^?1 BW d^?1 dose (1.33× the label use of 15 mg FFC kg^?1 BW d^?1) to Nile tilapia O. niloticus and hybrid tilapia O. niloticus × O. aureus held in a recirculating aquaculture system (RAS) at production‐scale holding densities. Florfenicol amine concentrations were determined in fillets taken from 10 fish before dosing and from 20 fish at nine time points after dosing (from 1 to 240 h post‐dosing). Water samples were assayed for FFC before, during and after the dosing period. Parameters monitored included daily feed consumption and biofilter function (levels of ammonia, nitrite and nitrate). Mean fillet FFA concentration decreased from 13.77 μg g^?1 at 1‐h post dosing to 0.39 μg g^?1 at 240‐h post dosing. Water FFC concentration decreased from a maximum of 1400 ng mL^?1 at 1 day post‐dosing to 847 ng mL^?1 at 240 h post‐dosing. There were no adverse effects noted on fish, feed consumption or biofilter function associated with FFC‐medicated feed administration to tilapia.     

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.     

The effect of dietary carbohydrates on the growth response,digestive gland glycogen and digestive enzyme activities of early spiny lobster juveniles,Jasus edwardsii

The effect of various carbohydrate sources (glucose, sucrose, agar, wheat, tapioca, maize, potato and dextrin), and inclusion levels of gelatinized maize starch (0, 70, 170, 270 g kg^?1), incorporated in semi‐purified diets on the performance [growth, survival, food consumption (FC), enzyme activity and glycogen content of the digestive gland (DG)] of spiny lobster juveniles was investigated in a 12‐week culture experiment. There was no difference in specific FC among diets (1.1% BW day^?1), but lobsters fed with fresh mussel grew significantly faster (specific growth rate = 1.8% BW day^?1) than on the formulated diets (0.9–1.1% BW day^?1). None of the carbohydrate supplements tested produced a significant improvement in growth or survival over a basal control diet. However, the diet containing 270 g kg^?1 native wheat starch resulted in the highest moulting (mean = 2.1 moults per lobster), glycogen (3.3 mg g^?1) and free glucose (1.1 mg g^?1) concentrations among lobsters fed with the formulated diets, suggesting a superior utilization of this source of carbohydrate. The greater glycogen (8.0 mg g^?1 tissue) and free glucose (2.0 mg g^?1 tissue) concentrations, as well as higher specific activity of α‐amylase (2.3 versus <0.7 U mg^?1 for other diets), found in the DG of lobsters fed with fresh mussel indicated a metabolism strongly directed to the utilization of glycogen.     

Efficacy of bath and orally administered praziquantel and fenbendazole against Lepidotrema bidyana Murray,a monogenean parasite of silver perch,Bidyanus bidyanus (Mitchell)

We investigated the efficacy of praziquantel (PZQ) and fenbendazole (FBZ), each administered by bath and orally, against the monogenean Lepidotrema bidyana Murray, a gill parasite of the freshwater fish silver perch, Bidyanus bidyanus (Mitchell). PZQ and FBZ were each administered by bath at 10 mg L^?1 for 48 h and on surface‐coated feed pellets at 75 mg kg^?1 per body weight (BW) per day for 6 days. Bath treatments of PZQ and FBZ had an efficacy of 99% and 91%, respectively, against adult L. bidyana. Oral treatments of PZQ and FBZ had an efficacy of 79% and 95%, respectively, against adult L. bidyana. Fish rejected feed pellets surface‐coated with PZQ, suggesting that palatability of surface‐coated PZQ‐medicated feed is poor, which undermined efficacy. In all trials, some juvenile parasites were present on fish after treatment during efficacy assessment, indicating that efficacy may be lower against juvenile parasites or that recruitment occurred post‐treatment, demonstrating that repeat treatments are necessary to effectively control L. bidyana in aquaculture.     

Effects of feeding rate and frequency on growth performance,digestion and nutrients balances of Atlantic salmon (Salmo salar) in recirculating aquaculture systems (RAS)

A 10‐week study was conducted to investigate the effects of feeding rate and frequency on growth performance, digestion and nutrients balances of Atlantic salmon (Salmo salar) in replicated recirculating aquaculture systems (RAS). Replicated groups of juvenile salmon weighing 90 ± 2.5 g (mean ± SD) were fed a commercial feed (21.63 MJ kg^?1 gross energy) to designed feeding rate (1.4%, 1.6% and 1.8% body weight day^?1, BW day^?1) and feeding frequency (2 and 4 meals day^?1) combinations. Specific growth ratio varied between 1.15 ± 0.02 and 1.37 ± 0.16% day^?1, and feed conversion ratio ranged from 0.96 ± 0.03 to 1.16 ± 0.02. The nitrogen and phosphorus retention rates were from 36.50 ± 1.94 to 47.08 ± 5.23% and from 20.42 ± 1.05 to 38.59 ± 2.80%. Apparent digestibility coefficients (ADC) in dry matter, protein, lipid and energy showed no significant differences for all groups. However, fish fed at 1.6% BW day^?1 and 4 meal day^?1 groups had relatively better growth and nutrient retention efficiency compared to other groups. In addition, concentrations of nitrogenous and phosphorous compounds were also detected in this study. These results suggested that salmon of 100–200 g in RAS could in practice be fed at 1.6% BW day^?1 and 4 meals day^?1, taking environmental impacts into account.     

Development of a pelleted feed for juvenile tropical spiny lobster (Panulirus ornatus): response to dietary protein and lipid

Critical to the development of a cost‐effective feed for the tropical spiny lobster Panulirus ornatus is knowledge of its response to the protein and lipid (or energy) content of the feed. An experiment of 12 weeks duration was carried out to examine growth responses of juvenile lobsters to pelleted diets that provided six crude protein (CP) levels [320–600 g kg^?1 dry matter (DM)] and two lipid levels (nominally 60 and 100 g kg^?1 DM). Lobsters (mean initial weight of 1.8 g) were held in groups of nine or 10 animals in 24 × 350 L tanks, fed twice daily at a restricted level, and maintained at 28 °C. Maximal growth responses occurred at dietary CP contents of 474 g kg^?1 for the 60 g kg^?1 lipid series and 533 g kg^?1 for the 100 g kg^?1 lipid series. A second experiment, of 4 weeks duration, compared two dietary treatments: a mixture of two of the best diets from the first experiment, and a commercial shrimp (Penaeus japonicus) feed. Lobsters were held under the same experimental conditions as in the first experiment, but were fed to excess twice daily. Their growth was significantly greater (P < 0.05) on the shrimp feed (0.68 g week^?1) than on the laboratory‐pelleted diets used in the main study (0.32 g week^?1). The results indicate that the optimal dietary protein and lipid content of the diet for P. ornatus is about 530 and 100 g kg^?1, respectively.     

A screening of medicinal compounds for their effect on egg strings and nauplii of the salmon louse Lepeophtheirus salmonis (Krøyer)

Egg strings and nauplii of the salmon louse Lepeophtheirus salmonis were exposed to a variety of medicinal compounds at 50 mg L^?1 for 30 min in two experiment series. This medicine concentration was selected as a starting point for a screening series. Hatching of egg strings and development to copepodid larvae were monitored in one experiment, and the survival and development of nauplii were monitored in the other. Two compounds, emamectin benzoate and cypermethrin, inhibited hatching effectively. Several compounds affected nauplii, either directly or through inhibiting development to the infective stage. A total of 50 mg L^?1 of azamethiphos, cypermethrin, emamectin benzoate and propoxur was lethal to >70% of the larvae. Diflubenzuron, fenoxycarb, pymetrozine, pyriprole and tebufenozide diminished the ability of nauplii developing to copepodids.     

Digestible dietary protein and energy requirements of juvenile Asian horseshoe crabs,Tachypleus tridentatus and Carcinoscorpius rotundicauda

A 84‐day feeding experiment of two juvenile horseshoe crab species, including nine formulated diets with three digestible protein (DP) levels (36%, 40% and 44%) and three digestible energy (DE) levels (14, 16 and 18 kJ g^?1) versus the control, fed on frozen brine shrimp (Artemia salina), was conducted. The results showed that the survival rate of Tachypleus tridentatus ranged from 67% to 100%, while that of Carcinoscorpius rotundicauda varied from 44% to 100%. The results also indicated that the formulated diet containing 40% DP with 14 kJ g^?1 DE was the best, in terms of growth and feed utilization, for the two juvenile horseshoe crab species. Final body weight (FBW), thermal‐unit growth coefficient (TGC), feed efficiency (FE), nitrogen retention efficiency (NRE) and energy retention efficiency (ERE) of T. tridentatus fed 40% DP and 14 kJ g^?1 DE were significantly higher than that of T. tridentatus fed the control diet. However, for C. rotundicauda, only significantly higher FE, NRE and ERE were found in juveniles fed 40% DP and 14 kJ g^?1 DE than the control diet. The present findings revealed that the optimum DP/DE ratio for the two species was 28 g protein MJ^?1.     

Pharmacokinetics and tissue residues of marbofloxacin in crucian carp (Carassius auratus) after oral administration

Pharmacokinetics and residue elimination of marbofloxacin (MBF) were studied in crucian carp (Carassius auratus, 250±30 g) kept at two water temperatures of 15 and 25 °C. Marbofloxacin concentrations in plasma and tissues were analysed by means of high‐performance liquid chromatography using an ultraviolet detector. The limits of detection were 0.02 μg mL^?1, 0.02 μg g^?1, 0.025 μg g^?1, 0.02 μg g^?1 and 0.025 μg g^?1 in plasma and muscle, skin, liver and kidney respectively. Fish were administered orally at a single dosage of 10 mg kg^?1 body weight in the PK group. The data were fitted to two‐compartment open models at both temperatures. At 15 °C, the absorption half‐life () and distribution half‐life (t_1/2α) of the drug were 0.36 and 4.48 h respectively. The corresponding values at 25 °C were 0.23 and 0.87 h respectively. The elimination half‐life (t_1/2β) was 50.75 h at 15 °C and 25.05 h at 25 °C. The maximum MBF concentration (C_max) differed little between 15 (6.43 μg mL^?1) and 25 °C (8.36 μg mL^?1). The time to peak concentration was 1.74 h at 15 °C and 0.78 h at 25 °C. The apparent volume of distribution (V_d/F) of MBF was estimated to be 1.36 and 0.87 L kg^?1 at 15 and 25 °C respectively. The area under the concentration–time curve (AUC) was 301.80 μg mL^?1 h at 15 °C and 182.80 μg mL^?1 h at 25 °C. The total clearance of MBF was computed as 0.03 and 0.05 L h^?1 kg^?1 at 15 and 25 °C respectively. After repeated oral administration at a dosage of 10 mg kg^?1 body weight per day for 3 days, the results showed that the elimination half‐lives () of MBF from all tissues at 15 °C were longer than that at 25 °C. Therefore, water temperature is an important factor to be considered when deciding a reasonable withdrawal time.     

Dietary amino acid l‐methionine requirement of fingerling Indian catfish,Heteropneustes fossilis (Bloch‐1974) estimated by growth and haemato‐biochemical parameters

An 8 weeks feeding trial was conducted to determine the dietary methionine requirement of fingerling Indian catfish, Heteropneustes fossilis (6.08 ± 0.95 cm; 4.33 ± 0.52 g). Six isonitrogenous (40%) and isoenergetic (17.90 kJ g^?1 GE) amino acid test diets were formulated with gradation of 0.25 g 100 g^?1containing graded levels of _L‐methionine (0.30, 0.55, 0.80, 1.05, 1.30 and 1.55 g 100 g^?1, dry diet) with 0.40 g 100 g^?1 constant level of cystine. Twenty fish were stocked in triplicate groups, in 75‐L circular trough with continuous flow‐through system and fed experimental diets at 4% BW/day twice daily, at 08:00 and 18:00 hours. Maximum live weight gain (296%), best feed conversion ratio (1.56) and protein efficiency ratio (1.60) were occurred at 1.05 g 100 g^?1 methionine, beyond which they showed declining tendency. However, quadratic regression analysis of weight gain, feed conversion ratio (FCR), protein efficiency ratio (PER) and body protein deposition (BPD) data indicated requirement for methionine at 1.15, 1.08, 1.06 and 1.05 g 100 g^?1 of dry diet respectively. Significantly (P < 0.05), higher whole body protein content, minimum moisture and intermediate fat contents were recorded at 1.05 g 100 g^?1 dietary methionine level. Ash content remained insignificantly (P > 0.05) low among all the treatments, excepting at diet I and diet II. Body protein deposition was also found to be significantly (P < 0.05) higher at 1.05 g 100 g^?1 methionine level. Best somatic and haematological indices values were also obtained at the requirement level. Based on above results, it is recommended that the diet for young H. fossilis should contain methionine at 1.09 g 100 g^?1 dry diet, corresponding to 2.73 g 100 g^?1 dietary protein with 0.40 g 100 g¹ cystine concentration for optimum growth and efficient feed utilization. Thus, the total sulphur amino acid requirement of H. fossilis would be (1.09 + 0.40) 1.49 g 100 g^?1 of dry diet, corresponding to 3.73 g 100 g^?1 of dietary protein.     

Influence of dietary menadione nicotinamide bisulphite (vitamin K3) and phylloquinone (vitamin K1) on Atlantic salmon (Salmo salar L.) tissue levels,determined by high‐performance liquid chromatography with fluorescence detection

The aim of the present study was to investigate the retention of menadione nicotinamide bisulphite (MNB; vitamin K₃) and phylloquinone (vitamin K₁) in Atlantic salmon (Salmo salar L.). Another objective was to find a reliable method for determination of menadione in fish feed, and to include and validate more matrices in the methods for phylloquinone and menaquinones (vitamin K₂). Duplicate tanks of Atlantic salmon (～93 g) were fed four levels (0–1000 mg menadione kg^?1 feed) of MNB for 9 weeks. The concentration of menadione and phylloquinone in the feed and the concentration of phylloquinone and menaquinone‐4 (MK‐4) in the tissues were determined. The analysed concentration of dietary menadione found in feed indicated a substantial loss of MNB during feed production. This assumption was supported by screening 15 commercial fish feed samples which also revealed menadione concentrations far below the recommended level. MNB fed salmon showed only a minor increase in liver MK‐4 concentration, compared to salmon fed phylloquinone which had a considerably higher level of liver phylloquinone, indicating a higher retention of phylloquinone compared to menadione in Atlantic salmon. Due to highly varying stability and bioavailability of the different vitamin K derivatives, vitamin K supplementation in fish feed needs a revision.     

Effects of selenium dietary enhancement on hatchery-reared coho salmon, Oncorhynchus kisutch (Walbaum), when compared with wild coho: hepatic enzymes and seawater adaptation evaluated

Hatchery-reared coho salmon, Oncorhynchus kisutch (Walbaum), were fed elevated levels of selenium (as Na₂SeO₃) to raise eviscerated body burdens to the level measured in wild counterparts. The goal was to find a dietary concentration that would achieve the desired effect without causing damage to growth and normal development. To measure some indices of health, the detoxifying enzymes chosen were hepatic glutathione peroxidase (GSH-Px) and hepatic superoxide dismutase (SOD). Eviscerated body selenium (Se) concentration, GSH-Px and SOD levels were measured during and at the end of the 9 month freshwater feeding trial. Selenium retention and enzyme activity were also measured during 6 months’residence in sea water (SW). Selenium supplements were added to a commercial ration to give final concentrations of 1.1, 8.6, 11.1, 13.6 μg g^-1 Se in the four respective diets. The results indicated that a dietary concentration of 8.6 μg g^-1 selenium was capable of inducing eviscerated body burdens similar to those found in wild fish. The elevated selenium levels persisted throughout the freshwater (FW) rearing phase, but declined when the fish were fed an unsupplemented ration upon SW entry. Superoxide dismutase levels did not increase above control levels. Glutathione peroxidase levels increased in fish fed the supplemented diets. GSH-Px activity declined in the higher supplemented dietary groups when all groups were reduced to the control group level of 1.1 μg g^-1. Cumulative mortality in SW was 20% in fish fed either the 1.1 or the 8.6 μg g^-1 Se diets. The 8.6 μg g^-1 Se supplemented diets did produce healthy coho, comparable to their wild counterparts.     

Effect of esterification on the absorption of astaxanthin in rainbow trout, Oncorhynchus mykiss (Walbaum)

Gastrointestinal and serum absorption of astaxanthin was studied in rainbow trout, Oncorhynchus mykiss (Walbaum) (217 ± 2 g) fed diets supplemented with either esterified astaxanthin (from Haematococcus pluvialis) or free astaxanthin (synthetic, as 8% w/w beadlets) at similar levels (50 mg kg^?1). After 56 days of feeding, there was a significant difference (P = 0.0582) between steady‐state serum astaxanthin concentrations for fish fed free (2.0 ± 0.3 μg mL^?1) or esterified astaxanthin (1.3 ± 0.1 μg mL^?1) at the 90% confidence level. However, following ingestion of a single meal supplemented with free or esterified astaxanthin, the rates of astaxanthin absorption into serum were not significantly different (P > 0.1) (0.8 ± 0.2 µg mL^?1 h^?1 and 1.0 ± 0.4 µg mL^?1 h^?1 respectively). In fish fed both free or esterified astaxanthin, higher absorption (P < 0.05) of astaxanthin by the ileal (0.8 ± 0.14 μg g^?1 and 0.9 ± 0.15 μg g^?1 respectively) compared with the posterior (0.2 ± 0.01 μg g^?1 and 0.3 ± 0.14 μg g^?1 respectively) intestine was recorded. This confirmed the role of the anterior intestine in carotenoid absorption. Non‐detectable levels of esters in digesta taken from the hind intestine suggest the anterior intestine is also the primary region for ester hydrolysis.