Evaluation of tuna by‐product meal as a protein source in feeds for juvenile spotted rose snapper Lutjanus guttatus

This study evaluated the use of tuna by‐product meal (TBM), a locally produced feed ingredient, as a replacement for fish meal (FM) in diets for spotted rose snapper, Lutjanus guttatus. Six isonitrogenous compounds [480 kg^?1 crude protein (CP) and isoenergetic diets (21 kJ g^?1)] were formulated to replace 0 (D‐0%), 10 (D‐10%), 20 (D‐20%), 30 (D‐30%), 40 (D‐40% or 50% (D‐50%) of FM protein with TBM protein. Each diet was fed to four replicate groups of spotted rose snapper (initial weight 5.4 g ± 0.04 g) to apparent satiation three times a day. After 8 weeks of feeding, the fish gained 4–5 times their initial weight. Spotted rose snapper fed D‐30% had a significantly higher specific growth rate (2.7% day^?1) than fish fed the other diets containing lower or higher amounts of TBM. Haematological parameters and whole‐body proximate composition were unaffected by diet (P > 0.05). The ADC for protein and energy in D‐0%, D‐20% and D‐30% were significantly higher than those for the D‐40% and D‐50% groups. A broken line model indicated that 262 g kg^?1 TBM in the diet would yield maximum growth of the spotted rose snapper. The results of this study demonstrate that TBM is an acceptable ingredient for replacing 25–30% of dietary protein from FM in spotted rose snapper diets but that higher replacement levels reduce fish performance.     

Evaluation of apparent digestibility coefficients of individual feed ingredients in spotted rose snapper Lutjanus guttatus (Steindachner, 1869)

Apparent digestibility coefficients (ADCs) for dry matter, crude protein, energy and essential amino acids for five commonly used feed ingredients were determined for juvenile spotted rose snapper Lutjanus guttatus (average body weight 90.6 g). ADCs were determined using the stripping technique to collect faeces after fish were fed a reference diet and test diets composed of 700 g kg^?1 reference diet and 300 g kg^?1 test ingredient. Chromic oxide (Cr₂O₃) was used as an inert indicator. Ingredients tested included sardine fishmeal (FM), canola meal (CM), tuna by‐products meal (TBM), poultry by‐product meal pet grade (PBM‐PG) and solvent‐extracted soybean meal (SBM). In general, all ingredients showed high digestibility values for all essential amino acids, although differences were detected among ingredients. ADC values for dry matter, protein and energy ranged 77.0–80.4%, 84.3–82.5% and 89–88.8%, respectively, for marine ingredient and land‐based animal protein sources, and 75.0–74.2%, 81.5–80.9% and 87.4–86.8%, respectively, for the plant‐based protein source. SBM, TBM and PBM‐PG should be further evaluated in feeding trials as partial FM replacements in rose snapper L. guttatus diets. Knowledge of ADC values for these ingredients will allow feed producers to develop nutritionally balanced, low‐cost feed formulations for this species.     

Optimizing dietary protein sources for Japanese sea bass (Lateolabrax japonicus) with an emphasis on using poultry by‐product meal to substitute fish meal

This study evaluated the potential of using poultry by‐product meal (PBM) to replace fish meal in diets for Japanese sea bass, Lateolabrax japonicus. Fish (initial body weight 8.5 g fish^?1) were fed six isoproteic and isoenergetic diets in which fish meal level was reduced from 400 g kg^?1 (diet C) to 320 (diet PM1), 240 (diet PM2), 160 (diet PM3), 80 (diet PM4) or 0 g kg^?1 (diet PM5), using PBM as the fish meal substitute. The weight gain (WG), specific growth rate, nitrogen retention efficiency, energy retention efficiency and retention efficiency of indispensable amino acids were higher in fish fed PM1, PM2, PM3 and PM4 diets than in fish fed diets C or PM5. The phosphorus retention efficiency was lower in fish fed PM3, PM4 and PM5 diets than in fish fed C, PM1 or PM2 diets. Fish fed diet PM5 had the highest feed conversion ratio, total nitrogen waste output (TNW) and total phosphorus waste output (TPW) among the treatments. No significant differences were found in the hepatosomatic index or body contents of moisture, lipid and ash among the treatments. Fish fed diet C had lower condition factor and viscerosomatic index than those of fish fed PM1, PM3, PM4 and PM5 diets. The results of this study indicate that using fish meal and PBM in combination as the dietary protein source produced more benefits in the growth and feed utilization of Japanese sea bass than did using fish meal or PBM alone as the dietary protein source. The dietary fish meal level for Japanese sea bass can be reduced to 80 g kg^?1 if PBM is used as a fish meal substitute.     

Replacing fish meal with a blend of poultry by‐product meal and feather meal in diets for giant croaker (Nibea japonica)

An 8‐week feeding trial was conducted to evaluate the potential of replacing fish meal with poultry by‐product meal (PBM) and feather meal (FEM) in giant croaker (Nibea japonica) diet. The control diet (C) contained 400 g/kg fish meal, and 20%, 40%, 60% and 80% of the fish meal in diet C was replaced by a blend of PBM and FEM (PBM: FEM = 7:3) in diets B20, B40, B60 and B80, respectively. The weight gain and feed intake of fish fed diet C did not differ from those of fish fed diets B20 and B40 (p > .05), but were higher than those of fish fed diets B60 and B80 (p < .05). Phosphorus retention efficiency was lower in fish fed diets C, B20 and B40 than in fish fed diets R60 and R80 (p < .05). No significant differences were found in feed conversion ratio, nitrogen retention efficiency, condition factor, hepatosomatic index, body composition and nitrogen waste among the treatments (p > .05). Ratio of fish meal consumption to fish production linearly declined with the decrease in dietary fish meal level. This study indicates that dietary fish meal for giant croaker could be reduced to 240 g/kg by inclusion of the blend of PBM and FEM.     

In vitro protein digestibility of different grow‐out stages of spotted rose snapper (Lutjanus guttatus,Steindachner, 1869)

The aim of this study was to compare in vitro protein digestibility between two groups of fish, at early (21 g) and late stages (400 g) of spotted rose snapper Lutjanus guttatus, to evaluate the degree of hydrolysis (DH) and total amino acid release (TAAR) using crude extracts from stomach, pyloric caeca and intestine of 13 protein ingredients including marine, animal and plant meals. Degree of hydrolysis and TAAR were measured by a pH‐Stat method, and the PAGE‐Zymogram was also used as complementary technique. Differences in DH were found between both grow‐out stages mainly in the alkaline hydrolysis phase. Fish and squid meals (marine sources) had the highest DH and TAAR, followed by porcine meat and poultry meal by‐products from recycling sources, and soybean and canola meals (plant sources), which represent better protein sources for use in practical diets. Stomach zymograms showed two pepsin isoforms in both grow‐out stages. Pyloric caeca and intestine zymograms showed five bands with proteolytic activity in the early grow‐out stage, whereas four additional bands were found in late grow‐out stage. Alkaline proteases were identified as serine and metalloproteases. Thus, L. guttatus presents an ontogenetically differentiated digestive enzyme pattern that modifies the DH and TAAR of different protein sources.     

Ascorbic acid requirement and histopathological changes due to its deficiency in juvenile spotted rose snapper Lutjanus guttatus (Steindachner, 1869)

A 13-week feeding trial was conducted to determine the optimal dietary ascorbic acid (AA) requirement of juvenile spotted rose snapper (Lutjanus guttatus). Six experimental diets containing 0, 7, 19, 29, 62 and 250 mg AA equivalent kg^?1 diet, supplied as l-ascorbyl-2-polyphosphate designated as VC0, VC7, VC19, VC29, VC62 and VC250, were fed ad libitum to triplicate groups of 20 juveniles [initial weight (IW) of 8 ± 1.85 g]. Nutrient deficiency resulting in fin erosion, dark skin, desquamation and erratic swimming was observed after 8 weeks in fish fed diets from 0 to 29 mg AA kg^?1. Fish that were fed all diets showed gill, kidney and brain alterations. The degree of tissue change values indicates that increasing vitamin C (VC) levels reduces these alterations. Fish fed diets VC29, VC62 and VC 250 showed a significantly higher growth rate in comparison with those fed the diets VC0, VC7 and VC17 (P > 0.05). The dietary requirement of VC in L. guttatus was estimated to be 29 mg kg^?1 of AA based on weight gain and specific growth rate, but more than 250 mg kg^?1 of AA is required to eliminate clinical signs and histopathological lesions.     

Evaluation of poultry by‐product meal as partial replacement of fish meal in practical diets for juvenile tench (Tinca tinca L.)

The aim of this study was to evaluate different replacement levels of fish meal (FM) by poultry by‐product meal (PBM) on survival, growth performance and body composition of juvenile tench (Tinca tinca). A 90‐day experiment was conducted with 5 month‐old juveniles (31.95 mm total length, 0.396 g weight). Eight practical diets (50% crude protein) differing in the level of replacement of FM protein by PMB protein were tested: 0% (control), 25%, 31%, 37%, 43%, 49%, 55% and 61% corresponding to 0, 184.8, 229.2, 273.5, 317.8, 362.1, 406.5 or 450.8 g PBM kg^?1 diet respectively. Significant differences were not found (P > 0.05) between 25% replacement of FM protein by PBM protein (184.8 g kg^?1 PBM in diet) and control diet. At higher replacement levels, fish had significantly lower growth, higher feed conversion ratio and lower protein productive value (P < 0.05). Fish with externally visible deformities ranged from 1.1% to 3.3%. The relation among amino acid profiles of the diets, body composition, growth performance of juveniles and amino acid requirements of other fish species is discussed. Up to 184.8 g PBM kg^?1 diet can be included in diets for juvenile tench without impairing growth performance.     

Effect of fishmeal replacement by poultry by‐product meal on growth performance,proximate composition,digestive enzyme activity,haematological parameters and gene expression of gilthead seabream (Sparus aurata)

Two feeding trials examined the replacement of fishmeal (FM) with poultry by‐product meal (PBM) in the diet of juvenile Sparus aurata. In Feeding trial I (100 days), three diets were formulated, where FM protein was replaced by 50% (PBM50) and 100% (PBM100) PBM, while in Feeding trial II (110 days), four diets were formulated using the same FM control diet, but FM was replaced at lower levels: 25% (PBM25), and 25% (PBM25 + ) and 50% (PBM50 + ) with the supplementation of lysine and methionine amino acids. PBM protein can successfully replace 50% of FM protein in the diet of S. aurata without adverse effects on survival, feed intake, growth performance and feed utilization, given that the diet is balanced with lysine and methionine. The proximate composition of body and muscle was unaffected by the diet, but the total FM replacement resulted in reduced lipid and energy contents in fish. A fifty per cent FM replacement by PBM did not affect haematological parameters indicating a good fish health. Similarities in trypsin and chymotrypsin activities with FM‐fed fish suggest a high digestibility of PBM. High dietary levels of PBM reduced the liver gene expression of GH/IGF axis and of cathepsin D suppressing fish growth and modulating the protein turnover.     

Effect of the dusk photoperiod change from light to dark on the incubation period of eggs of the spotted rose snapper, Lutjanus guttatus (Steindachner)

Spotted rose snapper, Lutjanus guttatus (Steindachner), eggs were incubated under different photoperiods to examine the effect of photoperiod on incubation. The eggs from two fish were incubated under five artificial photoperiods: constant dark (D), constant light (L) from 06:00 hours and 6, 10 and 14 h of light from 06:00 hours. The eggs from seven other fish were incubated under a natural photoperiod. Different spawning times (21:00 – 01:00 hours) and different photoperiods combined to give the start of the dusk photoperiod change after 11–23 h of incubation. Constant light or applying the dusk photoperiod change after ≥20 h of incubation appeared to extend the hatching period. The mean hatching period for groups of eggs incubated in darkness or that received the dusk photoperiod change after ≤19 h of incubation (n=8 different groups) was 2 h 15±10 min, which was significantly lower (P<0.05) than the mean hatching period of 4 h±37 min for groups that did not receive the dusk photoperiod change or that received the dusk photoperiod change after ≥20 h of incubation (n=9 groups). However, despite these differences, the majority of the eggs hatched during a 2–3 h period from 17 to 20 h of incubation, and a sigmoid regression (r²=0.9) explained the relationship between percentage hatch and hours of incubation for all photoperiod groups.     

The effect of substituting fishmeal with poultry by‐product meal in diets for Totoaba macdonaldi juveniles

Four diets were formulated to evaluate the partial to total substitution of fishmeal with poultry by‐product meal (PBM) (0, 33, 67 and 100PBM) in diets for totoaba juveniles (Totoaba macdonaldi). Amino acid profiles from diets and fatty acid content in diets and muscle tissue were used to assess the fish performance using PBM as fishmeal replacement. Stable isotopes of nitrogen (δ¹⁵N) were measured in muscle and liver tissue to quantify the retention of each protein source. At the end of the experimental period, the fish fed the 67PBM diet had a significantly higher growth gain increase compared to the other treatments (almost 2000% over an 86 days period; TGC of 1.06). The total replacement of fishmeal with PBM led to low growth gain increase (ca. 220% over 72 days; TGC of 0.52) and increased mortality. Both fish performance and tissues' fatty acid composition suggest that the 100PBM diet was deficient in essential fatty acids. An isotope‐mixing model applied to isotope ratios of muscle and liver tissues of fish fed the 67PBM tissues indicated that PBM was retained into muscle and liver tissue in a higher proportion than its level of inclusion in the diet. We conclude that PBM is a good source of nutrients for totoaba juveniles when used in up to 67% fishmeal replacement level in diets containing 52% protein leading to adequate growth rate and survival.     

Growth,feed utilization and endocrine responses in Atlantic salmon (Salmo salar) fed diets added poultry by‐product meal and blood meal in combination with poultry oil

The suitability of land animal by‐products (ABPs) in feed for Atlantic salmon postsmolts (initial weight 372 g) in sea water was studied in a feeding experiment, using poultry by‐product meal (PBM) and porcine blood meal (BM) as protein sources and poultry oil as fat source. Four extruded feeds were tested in a 2 * 2 factorial model, with or without ABP protein sources and with or without poultry oil. The control feed contained a mix of marine and plant ingredients. Initial feed intake was highest in the ABP protein‐based diets, whereas poultry oil had a weak opposite effect. No differences were seen in growth rate or body weight. Addition of PBM and BM led to increased FCR, and lower retention of crude protein and energy. This could be explained by lower digestibility of amino acids and crude protein, and a slightly lower energy level in these diets. Reduced igf1 mRNA levels in liver and muscle were seen in fish fed dietary ABP protein and oil. Despite lower protein digestibility of ABP protein, this study confirms the suitability of ABP protein and lipid in combination with plant ingredients in feed for Atlantic salmon growers.     

Supplementations of poultry by‐product meal and selenium yeast increase fish meal replacement by soybean meal in golden pompano (Trachinotus ovatus) diet

The effects of poultry by‐product meal (PBM) and selenium yeast (Se‐yeast) supplementations on fish meal replacement by soybean meal (SBM) in the diet of golden pompano (Trachinotus ovatus) were examined. In trial I, a 2 × 3 layout including two PBM levels (100 and 170 g kg^?1) and three levels of fish meal replacement (0, 40 or 60%) was used. At 100 g kg^?1 PBM, fish fed the basal diet exhibited the highest weight gain (WG) and nitrogen retention efficiency (NRE) and the lowest feed conversion ratio (FCR). At 170 g kg^?1 PBM, no significant differences were found in WG and NRE between fish fed the basal diet and diet with 40% of fish meal replaced by SBM. In trial II, the basal diet containing 170 g kg^?1 PBM (trial I) served as a reference. A 2 × 2 layout included two levels of fish meal replacement (40 or 60%) and two levels of Se‐yeast addition (0 and 1 g kg^?1). No significant differences were found in WG, feed intake, FCR and NRE between fish fed the reference diet and diet with 40 or 60% fish meal replacement plus 1 g kg^?1 Se‐yeast addition. This study indicates that supplementations of PBM and Se‐yeast can enhance the level of fish meal replacement by SBM in golden pompano diet. Dietary fish meal level can be reduced to 140 g kg^?1 by optimizing inclusion of SBM, PBM and Se‐yeast.     

Bio‐Ag reutilization of distiller's dried grains with solubles (DDGS) as a substrate for black soldier fly larvae,Hermetia illucens,along with poultry by‐product meal and soybean meal,as total replacement of fish meal in diets for Nile tilapia,Oreochromis niloticus

A feeding trial was conducted in a closed system with Nile tilapia, Oreochromis niloticus, juveniles (mean initial weight, 2.66 g) to examine total replacement of menhaden fish meal (FM) with distiller's dried grains with solubles (DDGS), which had been used as substrate for the production of black soldier fly larvae, Hermetia illucens, in combination with soybean meal (SBM) and poultry by‐product meal (PBM), with or without supplementation of the amino acids (AA) DL‐methionine (Met), L‐lysine (Lys) and a commercial non‐amylaceous polysaccharide enzyme (Enz) product. Fish were fed seven isoenergetic [available energy (AE) = 4.0 kcal g^?1 of diet] and isonitrogenous (350 g kg^?1 protein as‐fed basis) practical diets formulated with equivalent digestible protein levels. Diet 1 was formulated to be similar to a commercial, high‐quality, tilapia diet containing 200 g kg^?1 FM. Diets 2–5 were formulated as a 2 × 2 factorial to replace FM with similar contributions from DDGS (45%), PBM (25%) and SBM (2.1–2.9%), but to differ in supplementation of AA and/or Enz preparation. Diets 6 and 7 were formulated to investigate the effects of a 2/3 and 1/3 reduction, respectively, in DDGS contribution to the replacement protein mix, with concomitant increases in SBM, with respect to diet 3, and were balanced with Lys and Met. After 6 weeks, growth responses were slightly attenuated (P ≤ 0.05) and average daily intake (ADI) and feed conversion ratio (FCR) were slightly higher in tilapia fed DDGS diets 2–5 compared to those of fish fed the FM control diet 1. Growth responses were not significantly affected by the presence or absence of AA or Enz (diets 2–5), or the level of DDGS (diets 3, 7 and 6). Whole‐body proximate composition was not different among treatments. Amino acid profiles of fish fed DDGS diets were not significantly different from those of fish fed the FM control. Evidence of interaction between AA and Enz supplementation was detected in whole‐body amino acid concentrations such that AA content was higher with AA or Enz addition alone, but lower when both were added to the diet. Results suggest that DDGS replacement of FM in tilapia diets can be substantial when diets are formulated on a digestible protein basis and DDGS is combined with highly digestible animal (PBM) and plant proteins (SBM).     

Apparent digestibility coefficient of poultry by‐product meal (PBM) in diets of Penaeus monodon (Fabricius) and Litopenaeus vannamei (Boone), and replacement of fishmeal with PBM in diets of P. monodon

Nutrient apparent digestibility coefficients (ADCs) of pet food grade poultry by‐product meal (PBM) were determined for black tiger prawn, Penaeus monodon and Pacific white shrimp, Litopenaeus vannamei by the indirect method (reference diet and test diet at 7:3 ratio). Subsequently, an 8‐week growth trial was conducted to evaluate the effects of substitution of fishmeal (FM) with PBM in diets of P. monodon (initial weight = 0.21 ± 0.01 g). In the growth trial, six isonitrogenous and isoenergetic diets PBM0, PBM25, PBM50, PBM75, PBM100 and PBMA100, containing a gradient of PBM 0, 88.7, 177.4, 266, 354.7 and 354 g kg^?1 to replace 0, 92.5, 185, 277.5, 370 and 370 g kg^?1 FM were fed to four replicate groups respectively. The diet PBMA100 was supplemented with DL‐Met to be similar to PBM0. The results showed that both P. monodon and L. vannamei had relatively high ADC of crude protein (77.6% and 84.2% respectively) and gross energy (72.8% and 84.0% respectively) for PBM. Litopenaeus vannamei showed significantly higher digestion ability for PBM than P. monodon (P < 0.05). In growth trial, no significant difference in growth performance was observed among shrimp fed the experimental diets. DL‐Met supplementation did not improve the growth of P. monodon. PBM is a suitable protein ingredient for P. monodon feeds and can be used up to 354.7 g kg^?1 to totally replaced FM.     

The effect of the dietary substitution of fishmeal with tuna by‐product meal on growth,body composition,plasma chemistry and amino acid profiles of juvenile Korean rockfish (Sebastes schlegeli)

The effect of the substitution of fishmeal with tuna by‐product meal (TBM) in the diet of Korean rockfish on growth, body composition, plasma chemistry and amino acid profiles was determined. Nine experimental diets were prepared. The control (Con) diet consisted of 550 g kg^?1 fishmeal. The 10, 20, 30, 40, 60, 80 and 100 % fishmeal diets were substituted with tuna by‐product meal (TBM), referred to as the TBM10, TBM20, TBM30, TBM40, TBM60, TBM80 and TBM100 diets, respectively. Finally, the fishmeal and soybean meal was completely replaced with TBM in the diet TBM100‐S. There was no significant difference in weight gain and SGR of the fish that were fed the TBM40 and Con diets. The feed conversion ratio (FCR) of the fish that were fed the Con, TBM10, TBM20 and TBM30 diets was lower than that of the fish that were fed all of the other diets. The protein efficiency ratio (PER) of fish that were fed the TBM10, TBM20 and TBM300 diets was higher than that of fish that were fed the TBM40, TBM60, TBM80, TBM100 and TBM100‐S diets. It can be concluded that the substitution of fishmeal with up to 40 and 30 % TBM in the diet of juvenile Korean rockfish could be made without exerting a detrimental effect on their growth (SGR) and feed utilization (FCR and PER), respectively.     

Animal by‐products with or without enzymatic hydrolysis completely replacement of fish meal in genetically improved farmed tilapia diets (Oreochromis niloticus)

An 8‐week feeding trial was performed to examine the potential of total replacement of fish meal with animal by‐products with or without enzymatic components in juvenile genetically improved farmed tilapia (GIFT) diets, Oreochromis niloticus, (mean initial weight, 19.71 ± 0.28 g), reared in RAS system. Five isonitrogenous and isoenergetic diets were formulated with fish meal for the diets with total replacement of the isonitrogenous amounts of enzymatic fish meal (E‐FM), chicken liver meal (CLM), enzymatic chicken liver meal (E‐CLM), dried porcine solubles (DPS) and enzymatic dried porcine solubles (E‐DPS) respectively. The results indicated that the weight gain rate (WGR) and specific growth rate (SGR) in the FM group were significantly higher than the E‐FM and E‐CLM groups (p < .05), but the specific growth rate (SGR) in the E‐CLM group lower than the E‐FM group. The feed conversion ratio (FCR) in FM and CLM was significantly lower than the E‐FM, E‐CLM and E‐DPS groups (p < .05), and no significant difference was observed among the FM, CLM and DPS groups (p > .05). The values of the protein retention efficiency (PRE) and protein efficiency ratio (PER) in FM, CLM and DPS groups were significantly higher than the E‐CLM group (p < .05). The values of feed intake ratio (FIR) in FM and CLM groups were significantly lower than the E‐FM, E‐CLM and E‐DPS groups (p < .05). There was no significant difference in the whole body contents of moisture, crude lipid and crude ash among the FM and E‐CLM groups (p > .05). The whole body contents of crude protein in the FM group were significantly higher than the E‐FM, CLM, E‐CLM DPS and E‐DPS groups (p < .05). The apparent digestibility coefficients (ADC) of dry matter, crude protein and crude lipid in the FM, E‐FM, E‐CLM and E‐DPS groups were not significantly different (p > .05). The serum glucose(GLU), total cholesterol (TCHO) and triglycerides (TG), or the activities of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were not affected by the different treatments (p > .05). There was no significant difference in serum total protein (TP) or albumin (ALB) and between the FM group and other groups (p > .05). There was no significant difference in the serum urea nitrogen (BUN) content in the FM, CLM, E‐CLM and DPS groups (p > .05). Fish fed with the CLM and DPS diets had significantly lower hepatic GHR1, IGF1 and IGF2 gene mRNA expression levels than in fish fed the FM diet (p < .05). The present data showed that 6% of dietary fish meal can be totally replaced by the chicken liver meal and dried porcine solubles with no effect on the growth performance of GIFT strain tilapia.     

Use of salmon by‐product meals as a replacement for anchovy meal in practical diets for the Pacific white shrimp (Litopenaeus vannamei)

A series of trials were conducted with Pacific white shrimp Litopenaeus vannamei, to evaluate the efficiency of two salmon meals as compared to anchovy meal. The basal diet contained 200 g/kg anchovy meal, which was systematically replaced (0%, 50%, 75% and 100%) with salmon meal on an isonitrogenous basis. Another two diets were formulated with a hydrolysed salmon meal to replace 50% and 100% anchovy meal. Each diet was randomly fed to four replicate groups of 25 and 30 shrimp per tank in clear (indoor) and green (outdoor) water trials, respectively. The results showed that growth performance and feed conversion ratio were not statistically different when salmon meal replaced anchovy meal in both trials. However, when hydrolysed salmon meal was used to replace 100% of the anchovy meal, growth performance of the shrimp significantly decreased. The four kinds of fish meal (anchovy, salmon by‐product meals and menhaden) were evaluated in an ingredient digestibility trial using the 70:30 replacement technique. In general, dry matter, energy, protein and individual amino acids digestibility of salmon meal were significantly higher than those of menhaden and anchovy meal. Results of this study demonstrated that salmon meals are a good protein sources which can replace anchovy meal.     

Partial to total replacement of fishmeal by poultry by‐product meal in diets for juvenile rainbow trout (Oncorhynchus mykiss) and their effect on fatty acids from muscle tissue and the time required to retrieve the effect

Triplicate groups of rainbow trout (Oncorhynchus mykiss) (1.4 ± 0.1 g) were fed experimental diets containing four levels of protein substitution to totally replace fishmeal with poultry by‐product meal (0, 33, 67 and 100%). Fishmeal (FM) from tuna fish by‐products and poultry by‐product meal ‘pet food grade' (PBM) were used. Diets were formulated to be isonitrogenous (43.5% crude protein) and isolipidic (12.5% crude fat). After 80 days of feeding, no significant differences were found in terms of thermal unit growth coefficient (TGC). However, the EPA levels in muscle tissue among treatments 0PBM, 24PBM and 44PBM were found to be significantly higher than those for the 59PBM diet. Nevertheless, a re‐feeding period with the control diet showed that 28 days was long enough to regain the FA profile needed. We concluded that PBM used up to 44% in diets for juvenile rainbow trout can be used without a significantly decrease in EPA and DHA under the present conditions. The use of a whole fishmeal diet could be an important strategy to recuperate the fatty acid profile obtained when trout is feed on PBM basis. It will be important to perform longer experiments with larger fish to confirm these results.