Effect of dietary DP/DE ratio on apparent digestibility, growth and nitrogen and phosphorus retention in rainbow trout, Oncorhynchus Mykiss (Walbaum)

The effect of DP/DE ratio in diets for rainbow trout, Oncorhynchus mykiss (Walbaum), was investigated. To evaluate growth and body composition, groups of trout were fed three experimental diets with a constant level of gross energy (25.4 ± 0.12 MJ kg^?1 dry matter (DM)) and different digestible protein/digestible energy (DP/DE) ratios (diet A, 16. 35; diet B, 17.21; dietC, 18.23 g Mr^?1). Fat, protein and energy digestibility coefficients were not affected by the DP/DE ratio of the diets. Growth and feed utilization improved markedly as dietary DP/DE ratio increased (P < .01). The efficiency of fat, protein and energy utilization tended to increase with increasing DP/DE ratio of the diets. Nitrogen discharge in effluent water per kg of weight gain was not affected by dietary treatments (mean values for: diet A, 29.9; diet B, 29.8; diet C, 29.1 g N kg^?1 weight gain) while phosphorus discharge in effluent water fell using diets with a higher DP/DE ratio (mean values for: diet A, 7.3; diet B, 6.7; diet C, 5.9 g P kg^?1 weight gain).     

Effect of different dietary protein and lipid levels on growth and survival of juvenile Australian redclaw crayfish, Cherax quadricarinatus (von Martens)

This study determined the effect of different dietary protein and lipid levels on growth and survival of juvenile redclaw Cherax quadricarinatus. Nine practical test diets were formulated to contain three crude protein (CP) levels [260, 310 and 360 g kg^?1, equivalent to 225, 260 and 296 g kg^?1 digestible protein (DP) respectively] at three crude lipid (CL) levels (40, 80 and 120 g kg^?1, equivalent to 38, 67 and 103 digestible lipids respectively), with digestible protein : digestible energy (DP : DE) ranging from 14.6 to 22.6 mg protein kJ g^?1. Three replicate groups of 15 crayfish (initial weight mean ± SD, 0.71 ± 0.13 g) per diet treatment were stocked in 40 L tanks, at 28 °C for 60 days. The highest mean weight, specific growth rate and biomass, with values of 7.0 g, 3.67% day^?1, and 370.2 g m^?2, respectively, were achieved by feeding a diet with P : L = 310 : 80 (P < 0.05). The treatments resulted in a survival rate of 80–91%, feed conversion ratio of 1.08–1.61 and protein efficiency ratio of 2.24–3.08. Results indicated that a diet containing 270 g kg^?1 DP (equivalent to 320 g kg^?1 CP), 75 g kg^?1 digestible lipid (DL) with a DP/DE of 18.4 mg protein kJ^?1, and 0.031 g protein per animal per day was optimum for juvenile C. quadricarinatus under the tested experimental conditions.     

The effects of dietary digestible protein and digestible energy content on protein retention efficiency of juvenile silver perch Bidyanus bidyanus (Mitchell)

Effects of varying dietary digestible protein (DP) and digestible energy (DE) on protein retention efficiency (PRE), weight gain, protein deposition and carcass composition for silver perch (Bidyanus bidyanus, Mitchell) were studied. Using digestibility data for silver perch, we formulated three series of diets with different DE contents (13, 15 or 17 MJ DE kg^?1). For each series, a ‘summit’ diet containing an excess of protein for silver perch (based on previous research) and a ‘diluent’ diet with only 10–13% DP were formulated. By blending the summit and diluent diets together in different ratios, five diets with different DP contents were produced for each DE series. A commercial diet was also included to give 16 experimental diets in total. Eight juvenile fish (mean initial weight 1.2 g) were stocked into each of 64 × 70‐L acrylic aquaria and then each of the 16 diets was randomly allocated to four replicate aquaria. Tanks were supplied with partially recirculated water (75%) at 25–27°C. Fish were fed restrictively, twice per day, based initially on 3.5% body weight day^?1 with 40% of the ration given at 08:30 hours and 60% given at 15:00 hours for 59 days. Quadratic functions were fitted to each energy series to describe the relationship between DP content of diets and PRE (the asymptote of these functions were used to predict maximum PRE). For low DE (13 MJ kg^?1), mid‐DE (15 MJ kg^?1) and high DE (17 MJ kg^?1), the dietary DP contents to give maximum PRE were 24.7%, 26.1% and 30.1% respectively. Carcass fat decreased with increasing DP and increasing DP:DE ratio. Varying the dietary protein and DE also influenced other indices of fish performance. ‘Optimum’ dietary protein therefore depends on several factors. For fish fed, restrictively, the protein content needed to maximize PRE is lower than the content needed to maximize weight gain or minimize carcass fat. For fish fed to satiation, the lowest protein content for maximum weight gain is lower than for fish fed restrictively.     

High feeding and growth rates in common octopus (Octopus vulgaris) fed formulated feeds with an improved amino acid profile and mixture of binders

Four semi‐moist formulated feeds were supplied to Octopus vulgaris subadults (664 ± 70 g; 18.4 ± 0.7°C) in two different experiments. In the experiment #1, two diets were prepared with a new mixture of binders (gelatine 150 g kg^?1, starch 100 g kg^?1 and gum 50 g kg^?1). The GEL15‐Squid and GEL15‐Hake feeds included 100 g kg^?1 freeze‐dried squid (Todarodes sagittatus) or hake (Merluccius sp.) respectively. Both feeds showed low water disintegration rates at 24 h (13.6–15.0% dry weight). The specific feeding rate was higher in animals fed GEL15‐Hake (2.7%BW day^?1), but the growth and feed efficiency were significantly better in animals fed GEL15‐Squid (1.4%BW day^?1 and 61.2% respectively; P < 0.05). The proximate composition of the digestive gland, carcass and whole animals was similar. In the experiment #2, the GEL15‐Squid amino acid profile was improved by replacing 50 g kg^?1 gelatine by 50 g kg^?1 freeze‐dried squid (GEL10‐Squid) or freeze‐dried fish (GEL10‐Fish). These feeds showed higher water disintegration rates (31.7–36.3% dry weight). The feeding rates (2.2–2.3%BW day^?1), growth (1.5%BW day^?1) and feed efficiency were similar for both diets. Total lipids were higher in the digestive gland and whole animals fed GEL10‐Fish diet (P < 0.05). Future effort could be directed towards alternative binders that allow improve amino acid balance with a minimum gelatine content or even supplementation trials including essential amino acids.     

Temperature-dependent pharmacokinetics and tissue distribution of oxolinic acid in sea bass, Dicentrarchus labrax L., after a single intravascular injection

The pharmacokinetics and tissue distribution of oxolinic acid following an intravascular administration (15 mg kg^?1 fish) were determined in sea bass, Dicentrarchus labrax L. (110 g), at 13 °C and 22 °C water temperature. The kinetic profile of the drug was found to be temperature dependent, with increased temperature having a greater effect on distribution after equilibrium and the elimination phase than on the distribution process. The distibution half‐life of oxolinic acid was 1.15 and 2.76 h at 22 °C and 13 °C respectively, whereas the elimination half‐life of the drug was 55 h at 22 °C and 315 h at 13 °C. The values of the apparent volume of distribution (1.44 L kg^?1 at 22 °C and 3.31 L kg^?1 at 13 °C) and the volume of distribution at steady state (5.2 and 14.7 L kg^?1 at the high and low temperature respectively) were considerably different between the two tested temperatures. The total body clearance of the antibiotic was found to be low (1.47 L kg^?1 day^?1 at 22 °C and 0.80 L kg^?1 day^?1 at 13 °C). Lower rates of elimination were found for the liver compared with muscle, the difference increasing with increasing temperature, while elimination rates from the serum were higher than those of other tissues, especially at the high temperature.     

Effects of temperature on feed intake,growth and oxygen consumption in adult male king crab Paralithodes camtschaticus held in captivity and fed manufactured diets

The current study investigates whether it is possible to increase the meat content of captive male king crab (Paralithodes camtschaticus) (average = 2.2 kg) by feeding manufactured diets at different temperatures (4°C, 8°C and 12°C). A 110 days trial was undertaken with groups of male king crabs held in 12 land‐based holding tanks. All crabs survival in the lowest temperature treatment, one animal died in the medium‐temperature group (8°C) and four animals in the highest temperature treatment (12°C). The results showed that feed intake increased with increasing temperature from an average of 1.0 g kg^?1 day^?1 at 4°C to 2.8 g kg^?1 day^?1 crab at 12°C. The percentage meat content was significantly higher at the final census (60.0%) compared with the initial census (37.5%) in all temperature groups, but there were no significant differences in the percentage meat content of the king crabs held in the different temperature treatments at the conclusion of the experiment. Oxygen consumption was also significantly affected by temperature and increased with increasing temperature. The results of the experiment show that the optimal temperature to maintain, and enhance, the meat content of king crab is close to 4°C.     

Optimum dietary ratio of digestible protein and energy for juvenile American eel, Anguilla rostrata, fed practical diets

Triplicate groups of juvenile American eel, Anguilla rostrata, initial weight 8.2 ± 0.24 g, were fed to satiation herring meal based diets formulated with digestible protein/digestible energy (DP/DE) ratios of 19, 20, 21, 22 and 23 g DP MJ DE^?1 (as‐fed basis) for 84 days. Data were collected to determine the effect of dietary DP/DE ratio on feed intake (FI), mean weight (MW), specific growth rate (SGR), feed conversion ratio (FCR), apparent digestibility (AD) of major nutrients, rate of phosphate excretion (RPE) and nutrient retention efficiency (RE). Highest MW, SGR and lowest FCR (P < 0.05) were achieved by feeding 22 g DP MJ DE^?1 with values (mean ± SE) of 22.9 ± 0.07 g fish^?1, 1.23 ± 0.033% day^?1 and 0.91 ± 0.075 g feed g gain^?1, respectively. With exception of lipid, digestibility of all nutrients were the same (P > 0.05) with mean AD coefficients for organic matter, protein, energy and phosphorous of 86.3, 94.1, 89.2 and 34.7%, respectively. Lipid AD was significantly higher (P < 0.05) when DP/DE ratio was 21, 22 or 23 g DP MJ DE^?1 at 92.3% as opposed to when DP/DE ratio was 19 or 20 g DP MJ DE^?1 at 90.3%. The DP/DE ratio had no significant effect (P > 0.05) on RPE and it averaged 0.05 ± 0.002 g phosphate kg fish^?1 day^?1. Nitrogen retention efficiency (NRE) significantly (P < 0.05) increased as DP/DE ratio increased to 21 g DP MJ DE^?1 and was similar thereafter (P > 0.05) at an average of 31.6 ± 0.67%. Energy retention efficiency (ERE) significantly (P < 0.05) increased to 42.9 ± 1.24% as DP/DE ratio increased to 22 g DP MJ DE^?1 and thereafter significantly (P < 0.05) decreased. Lipid retention efficiency (LRE) increased significantly (P < 0.05) to 75.7 ± 0.85% as dietary DP/DE ratio increased to 23 g DP MJ DE^?1. Non‐linear quadratic regression of ERE against dietary DP/DE ratio yielded an estimated optimum DP/DE ratio for juvenile American eel of 22.1 g DP MJ DE^?1.     

Protein and energy utilization and the requirements for maintenance in juvenile mulloway (<Emphasis Type="Italic">Argyrosomus japonicus</Emphasis>)

This study describes the digestible protein (DP) and digestible energy (DE) utilization in juvenile mulloway, and determined the requirements for maintenance. This was achieved by feeding triplicate groups of fish weighing 40 or 129 g held at two temperatures (20 or 26°C), on a commercial diet (21.4 g DP mJ DE⁻¹) at four different ration levels ranging from 0.25% of its initial body weight to apparent satiation over 8 weeks. Weight gain and protein and energy retention increased linearly with increasing feed intake. However, energy retention efficiency (ERE) and protein retention efficiency (PRE) responses were curvilinear with optimal values, depending on fish size, approaching or occurring at satiated feeding levels. Maximum predicted PRE was affected by body size, but not temperature; PRE values were 0.50 and 0.50 for small mulloway, and 0.41 and 0.43 for large mulloway, at 20 and 26°C respectively. ERE demonstrated a similar response, with values of 0.42 and 0.43 for small, and 0.32 and 0.34 for large mulloway at 20 and 26°C respectively. Utilization efficiencies for growth based on linear regression for DP (0.58) and DE (0.60) were independent of fish size and temperature. The partial utilization efficiencies of DE for protein (k _p) and lipid (k _l) deposition estimated using a factorial multiple regression approach were 0.49 and 0.75 respectively. Maintenance requirements estimated using linear regression were independent of temperature for DP (0.47 g DP kg^−0.7 day⁻¹) while maintenance requirements for DE increased with increasing temperature (44.2–49.6 kJ DE kg^−0.8 day⁻¹). Relative feed intake was greatest for small mulloway fed to satiation at 26°C and this corresponded to a greater increase in growth. Large mulloway fed to satiation ate significantly more at 26°C, but did not perform better than the corresponding satiated group held at 20°C. Mulloway should be fed to satiation to maximize growth potential if diets contain 21.4 g DP mJ DE⁻¹.     

Protein‐to‐energy ratio of 21.43 g MJ−1 improves growth performance of Nile tilapia at the final rearing stage under commercially intensive rearing conditions

This study evaluated the effect of ratio of dietary digestible protein (DP) to digestible energy (DE) on growth performance, fillet chemical composition and haematological profile of Nile tilapia subjected to transport‐induced stress at the final rearing stage (450 to 800 g) under commercial conditions. The trial was conducted using a 5 × 2 factorial layout (DP: 200, 230, 260, 290 and 320 g kg^?1) and (DE: 12.6 and 13.8 MJ kg^?1). Energy levels did not influence any analysed parameters in this research. Final weight and biomass gain were increased up to the ratio of 269 and 270 g PD kg^?1, respectively, and feed conversion ratio was reduced down to a 275 g DP kg^?1. Protein efficiency ratio linearly decreased from 200 g DP kg^?1 diet to 320 g DP kg^?1. There was no statistical difference in fillet chemical composition. Red blood cell count (RBC), haemoglobin (Hb), mean corpuscular volume (MCV) and mean corpuscular haemoglobin concentration (MCHC) were different before and after transport‐induced stress. Leucocyte differentiation after transport‐induced stress revealed lymphocytopenia and neutrophilia. We conclude that for tilapia weighing 450–800 g reared under commercially intensive conditions, a diet with 270 g DP kg^?1 and 12.6 MJ DE kg^?1 (21.43 g DP MJ^?1 DE) can improve the growth performance and ensure the fish health.     

Investigation of the nutritional requirements of Australian snapper Pagrus auratus (Bloch & Schneider, 1801): effects of digestible energy content on utilization of digestible protein

This study used a curvilinear model to investigate the effects of different digestible energy (DE) levels on the digestible protein (DP) requirements of juvenile snapper Pagrus auratus. For each DE level (15, 18 or 21 MJ kg⁻¹), DP content was increased from about 210–560 g kg⁻¹ in seven evenly spaced increments by formulating a summit diet (highest DP content) and a diluent diet (lowest DP content) at the desired DE level and combining the summit and diluent diets in various ratios to achieve the desired DP content. This ensured the DE level remained relatively stable. Each of the 21 dietary treatments was fed to three replicate groups of snapper twice daily to apparent satiation for 57 days. At the completion of the trial, fish were weighed and killed for chemical analysis. Results indicated that the rapid growth of snapper weighing 30–90 g was highly dependent on the ratio of DP to DE and that optimum protein deposition did not occur until snapper were offered feeds with at least 350 g DPkg⁻¹, irrespective of DE level. According to the fitted models, diets formulated for snapper reared at temperatures from 20–25°C should contain approximately 23 g DP MJ DE⁻¹ to promote optimal weight gain and protein deposition. Based on the feeding regime used in this study, this could be achieved with practical diets containing a DP:DE ratio of 460:20, 420:18 or 350:15.     

Inclusion of camelina meal as a protein source in diets for farmed salmonids

Camelina meal (Camelina sativa) (CM) is a potential protein source for aquaculture feeds, on account of its crude protein level (380 g kg^?1) and inclusion of most indispensable amino acids. Two experiments were conducted with rainbow trout (Oncorhynchus mykiss) and Atlantic salmon (Salmo salar). Rainbow trout (44.9 g fish^?1) were fed diets with CM at 0 g kg^?1 (0% CM), 70 g kg^?1 (7% CM), 140 g kg^?1 (14% CM) or 210 g kg^?1 (21% CM) for 12 weeks at 14 °C in freshwater, and salmon (241.8 g fish^?1) were fed diets with CM at 0 g kg^?1 (0% CM), 80 g kg^?1 (8% CM), 160 g kg^?1 (16% CM) or 240 g kg^?1 (24% CM) for 16 weeks at 14 °C in sea water. Growth, lipid and amino acid tissue compositions were compared between species. Trout could tolerate up to 14% CM diets without affecting the growth compared to the control, while salmon fed ≥8% CM gained less weight than the control (P = 0.008). The feed conversion ratio in trout fed 21% CM was higher than the control (P = 0.002), and feed intake in salmon fed ≥8% CM was lower than the control (P = 0.006). Trout fatty acid and amino acid composition showed minimal differences between CM‐fed and control‐fed fish, while salmon showed significant alterations after feeding CM diets. Multivariate analyses emphasized differences in tissue composition between species fed CM diets.     

Evaluation of feeding rate based on growth,feed conversion,protein gain and carcass quality of fingerling Indian major carp,Catla catla (Hamilton)

The effects of feeding rates on growth, feed conversion, protein deposition and carcass quality of fingerling Catla catla (3.61 ± 0.03 cm; 0.71 ± 0.04 g) were worked out by conducting a 16‐week feeding trial. Fingerlings were fed with a casein‐gelatin‐based purified diet (40% crude protein CP; 14.95 MJ kg^?1 digestible energy; DE) at 1%, 2%, 3%, 4%, 5%, 6% and 7% body weight per day. The absolute weight gain (AWG; 10.50 g fish^?1) and feed conversion ratio (FCR; 1.41) were highest at the feeding rate of 5% body weight per day. However, protein gain (PG; 0.36 g fish^?1) and carcass protein content attained the maximum values at 4% BW day^?1. Quadratic regression analyses of AWG g fish^?1 and PG g fish^?1 at 95% maximum response indicated that these parameters attained the best values at 4.19% and 3.81% BW day^?1. On the basis of the above results it is recommended that the feeding rate in the range of 3.81–4.19% BW day^?1 with a P:E ratio of 26.69–27.74 mg protein MJ^?1 DE is optimum for maximum growth, efficient feed conversion and best carcass quality in fingerling C. catla.     

Growth performance and expression of immune‐regulatory genes in rainbow trout (Oncorhynchus mykiss) juveniles fed extruded diets with varying levels of lupin (Lupinus albus), peas (Pisum sativum) and rapeseed (Brassica napus)

Varying levels of lupin (Lupinus albus), peas (Pisum sativum) and rapeseed (Brassica napus) meals were evaluated as partial replacements for fishmeal in extruded diets for rainbow trout, with particular emphasis on the effect on growth performance and the expression of three genes associated with immune response. A series of 10 isonitrogenous (450 g kg^?1 crude protein) and isolipidic (17 g kg^?1 crude lipid) diets were formulated to contain different levels of lupin (150 g kg^?1, 250 g kg^?1 and 350 g kg^?1), rapeseed cake (100 g kg^?1, 200 g kg^?1 and 300 g kg^?1) and pea (50 g kg^?1, 150 g kg^?1 and 250 g kg^?1) meals. The control diet was prepared with fish meal as the sole source of protein. Triplicate groups of fish (37.08 ± 3.58 g) were assigned to each experimental diet. The feeding experiment was conducted for 9 weeks at 14.3 ± 0.4 °C. The fish were hand fed three times per day, 6 days per week to apparent satiation level. Growth performance, feed utilization and immunological response were significantly affected by the type of plant protein as well as level of inclusion. Hepatosomatic index (HSI) increased in all groups of fish fed diets with pea and rapeseed cake meal. Dietary inclusion of lupin did not affect the expression of Mx‐1 gene. Our results suggest that fish meal can be replaced by lupin in the diet of rainbow trout without any apparent adverse effects on key innate immunological genes.     

Optimizing zinc supplementation levels of rainbow trout (Oncorhynchus mykiss) fed practical type fishmeal‐ and plant‐based diets

Rainbow trout (23.1 ± 0.4 g) were fed either a fishmeal‐ or plant‐based diet supplemented with various levels of zinc (0, 15, 30, 60 or 120 mg kg^?1) for 12 weeks. Trout fed the fishmeal diet had significantly higher weight gain than with the plant‐based diet. Zinc supplementation in the fishmeal diet had no effect on growth performance, suggesting that additional dietary supplementation of zinc is not required. However, in trout fed the plant‐based diet, growth increased significantly up to 30 mg kg^?1 zinc after which growth was not affected. Trout fed the plant‐based diet containing no zinc exhibited severe growth retardation, and in fish fed the 0 and 15 mg kg^?1 zinc diets, cataracts were present. Use of broken‐line quadratic modelling suggests that dietary supplementation of zinc needed to prevent deficiency and promote adequate growth in rainbow trout fed the plant‐based diet in this study was 30.1 mg kg^?1 (80 mg kg^?1 total dietary zinc). This is higher than the NRC (2011, Nutrient Requirements of Fish and Shrimp) dietary recommended level of 15 mg kg^?1 for rainbow trout. Following the NRC recommendation could lead to zinc deficiency in rainbow trout fed a plant‐based diet.     

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 digestible protein levels on growth and feed utilization of juvenile meagre Argyrosomus regius

This study investigates the effect of digestible protein levels in experimental diets for meagre (Argyrosomus regius). A group of 253 fish, 52 g of mean weight, was distributed in 12 tanks, three replicates per treatment. Four isolipidic diets (170 g kg^?1 crude lipid) with different digestible protein levels (350 g kg^?1, 430 g kg^?1, 490 g kg^?1 and 530 g kg^?1) were formulated using commercial ingredients. The trial lasted 62 days. Meagre fed diets 430, 490 and 530 g kg^?1 obtained higher TGC (2.47, 2.57, 2.69 × 10^?3, respectively) than fish fed diet 350 g kg^?1 (2.14 × 10^?3). Group of fish fed diet with 350 g kg^?1 DP showed the lowest ammonia excretion level. According to the in vitro digestibility trial diets with 350 and 430 g kg^?1 DP released less amino acids in comparison with diet with 49% DP, although in vivo digestibility test did not show significant differences among diets 430, 490 and 530 g kg^?1 DP. Using the quadratic regression, optimal digestible protein intake according to the ECR for rearing juvenile meagre was recorded in 0.8 g DP/100 g fish and day.     

Residue levels of enrofloxacin and ciprofloxacin in processed animal by‐products used in Atlantic salmon feeds and their long‐term carry‐over to the edible part of the fish

Residue levels of the antibacterials enrofloxacin and ciprofloxacin were analysed in 15 commercially relevant animal by‐products (ABPs). Enrofloxacin was detected in all ABPs, and ciprofloxacin was detected in 11 of 15 ABP samples. Feed to muscle and skin carry –over of low background enro‐ and ciprofloxacin levels were assessed by applying a simple toxicokinetic model. The muscle and skin uptake and elimination rates were established in Atlantic salmon (Salmo salar L.) fed enrofloxacin enriched diets (100 μg kg^?1 ‘low’ and 4000 μg kg^?1 ‘high’) in triplicate for 41 days followed by a 90 days depuration period. The terminal half‐lives were 17 ± 0.4 and 18 ± 0.7 days, and uptake rates were 9.3 ± 3.3 and 11 ± 3.1 (day^?1) for the ‘low’ and ‘high’ groups, respectively. Only fish fed high background levels had quantifiable levels of the metabolite ciprofloxacin with a formation of 0.25 ± 0.01% day^?1. The toxicokinetic carry‐over model predicted muscle and skin steady state levels of 1.8 μg kg^?1 when fed theoretically high enrofloxacin levels (158 μg kg^?1), which is below the EU limit of 100 μg kg^?1 for enrofloxacin in finfish food products. The antibacterial residue levels could however be detected in EU food surveillance programmes.     

Influence of dietary fat level and whole-body adiposity on voluntary energy intake by juvenile rainbow trout Oncorhynchus mykiss (Walbaum) under self-feeding conditions

The influence of dietary fat level and whole‐body adiposity on voluntary energy intake of juvenile rainbow trout Oncorhynchus mykiss (Walbaum) was examined using self‐feeders. Groups of lean fish [crude fat (CF) = 7%] and fat fish (CF = 11%), pretreated with a commercial diet with or without supplemental pollock oil, were self‐fed one of three fat level diets (CF = 8%, 13.5% and 19%) for 48 days at 17 °C. Final body weight (BW) and total digestible energy (DE) intake (kJ per fish) were positively affected by the initial BW. Relative to the initial BW, however, fat fish consumed less DE than lean fish. Although the effect of dietary fat level was not significant, percentage weight gain and daily DE intake per BW (kJ kg^?1 BW day^?1) of fat fish were significantly lower than those of lean fish (ancova with initial BW as a covariate, P < 0.05). Energy digestibility, feed efficiency and protein retention were improved with the dietary fat level; however, there was no difference resulting from body fat level. The whole‐body fat levels at the end of the experiment increased with the dietary fat level. Between groups self‐fed the same diet, fat levels of the initially fat fish were still higher than those of the lean fish. The results of the present medium‐term study suggest that rainbow trout adjust DE intake from diets with fat levels ranging from 8% to 19%. Although body fat level affects neither energy digestibility nor protein utilization, a high body fat level may reduce DE intake and consequently depress growth.     

Utilization of diets with different fish oil content in common octopus (Octopus vulgaris Cuvier, 1797) and resulting changes in its biochemical composition

The aim of the present work was to obtain the lipid utilization of Octopus vulgaris supplying formulated semi‐moist diets with different contents in cod oil (reduced from water content): 0 g kg^?1 (A0, 138 g kg^?1 lipids DW; N = 4), 100 g kg^?1 (A100, 286 g kg^?1 lipids DW; N = 6) and 200 g kg^?1 (A200, 388 g kg^?1 lipids DW; N = 6). The rest of the ingredients were constant in the three diets: 200 g kg^?1 gelatin, 100 g kg^?1 egg yolk powder, 150 g kg^?1 freeze‐dried Todarodes sagittatus and 50 g kg^?1 freeze‐dried Sardinella aurita). Survival was 100% with the three diets. The highest absolute feeding (15.8 ± 1.2 g day^?1), growth (9.6 ± 1.4 g day^?1; 0.91% BW day^?1) and feed efficiency rates (60.3%) were obtained with diet A0. This diet also showed greater retention of lipid and protein than A100 and A200. Protein digestibility was above 95% in all of the diets. Only diet A0 led to a high lipid digestibility coefficient (81.25%), which fell drastically to 12.3% in A200. It was notable the high polar lipid digestibility rates (83–89%) respect to neutral lipids (2–87%) in all diets. The best results were obtained with lipid feeding rates of around 1 g day^?1 and a suitable lipid content on 130–140 g kg^?1 DW in formulated diets for O. vulgaris.