Digestibility and performance of pacu (Piaractus mesopotamicus) juveniles — fed diets containing different protein, lipid and carbohydrate levels

Due to lack of information on the use of non‐protein energy sources in diets for pacu (Piaractus mesopotamicus), a 2 × 2 × 3 factorial experiment was conducted to evaluate the performance and digestibility of 12 diets containing approximately two crude protein (CP; 220 and 250 g kg⁻¹), two lipid (40 and 80 g kg⁻¹) and three carbohydrate levels (410, 460 and 500 g kg⁻¹). The pacu juveniles‐fed diets containing 220 g kg⁻¹ CP did not respond (P > 0.05) to increased dietary lipid and carbohydrate levels, but the fish‐fed diets containing 250 g kg⁻¹ CP showed a better feed conversion ratio. There were interactions in weight gain (WG), specific growth rate (SGR), crude protein intake (CPI) and feed conversion rate (FCR) dependent on dietary carbohydrate and lipid levels, showing positive effects of increasing carbohydrate levels only for fish‐fed diets containing 80 g kg⁻¹ lipid level. However, when the diets contained 40 g kg⁻¹ lipid, the best energy productive value (EPV) results were obtained at 460 g kg⁻¹ carbohydrate. A higher usage of lipids (80 g kg⁻¹) reduced CPI and was detrimental to protein [apparent digestibility coefficient (ADC)_CP] and energy (ADC_GE), but did not affect growth. The ADC_GE improved proportionally as dietary carbohydrate levels increased (P < 0.05), increasing the concentration of digestible energy. In addition, the WG, CPI, ADC_GE results showed best use of the energy from carbohydrates when dietary protein level was 250 g kg⁻¹ CP. The utilization of 250 g kg⁻¹ CP in feeds for juvenile pacu for optimal growth is suggested. Therefore, the optimum dietary lipid and carbohydrate levels depend on their combinations. It can be stated that pacu uses carbohydrates as effectively as lipids in the maximization of protein usage, as long as it is not lower than 250 g kg⁻¹ CP or approximately 230 g kg⁻¹ digestible protein.     

Optimum digestible protein and energy levels and ratio for greater amberjack Seriola dumerili (Risso) fingerling

A study was conducted to determine optimum dietary digestible protein (DP) and digestible energy (DE) levels and DP DE⁻¹ ratio for growth of greater amberjack Seriola dumerili fingerlings. A 3 × 3 factorial design with duplication was used in this study. Nine experimental diets were formulated to contain three levels of crude protein (CP; 420, 470 and 530 g kg⁻¹) and three levels of crude lipid (CL; 130, 180 and 230 g kg⁻¹). Nine groups of fingerling (initial weight 51.8 g) were fed each experimental diet for 40 days. Final body weight, feed efficiency, specific growth rate and energy efficiency were significantly affected by dietary protein and lipid level. These parameters tended to improve with increasing dietary protein level. Conversely, an increase of lipid level negatively affected these parameters. High growth rate and feed efficiency were obtained from fish fed the diet containing 393 g kg⁻¹ DP and 14.2 MJ kg⁻¹ DE (27.7 g MJ⁻¹ DP DE⁻¹). The high DP DE⁻¹ (27.7 g MJ⁻¹) indicates that greater amberjack fingerling are highly dependent on dietary protein as an energy source.     

Effect of dietary protein and lipid levels and protein to energy ratios on growth, survival and body composition of the mangrove red snapper, Lutjanus argentimaculatus (Forsskal 1775)

The approximate levels of dietary protein and energy that would sustain good growth and survival of the mangrove red snapper Lutjanus argentimaculatus (Forsskal) were determined in two feeding experiments. In the preliminary experiment, six fish meal‐based diets were formulated to contain three protein levels (35%, 42.5% and 50%) and two lipid levels (6% and 12%) for each protein, with dietary energy ranging from 14.6 MJ kg^?1 to 20.5 MJ kg^?1. The protein to energy (P/E) ratios of diets ranged from 20.6 mg protein kJ^?1 to 27.5 mg protein kJ^?1. Diets were fed for 100 days to triplicate groups of snappers with an average initial weight of 24.8 ± 0.4 g. No significant interaction between different levels of protein and lipid was observed. Survival rates (93.8% to 100%), feed conversion ratios (FCR) (2.61–3.06) and condition factors (K) were not affected by different dietary treatments. Regardless of lipid level, fish fed 50% protein diets had a significantly higher specific growth rate (SGR) than fish fed the 35% protein diets, but not compared with the 42.5% diets (P < 0.05). Increasing lipid to 12% in all protein levels resulted in no improvement in growth over the 6% level. Fish body moisture did not vary while lipid levels based on dry matter were high (27.9% to 33.7%). Snapper appear to require more than 40% dietary protein and a high dietary energy level for good growth. In the second experiment, fish (21.1 ± 0.1 g) in four replicate groups were fed for 94 days with three diets (39%, 44% and 49% protein with P/E ratios of 21.1, 23.3 and 25.5 mg protein kJ^?1 respectively) containing similar dietary energy levels of about 19 MJ kg^?1. Average final weight, SGR and FCR were significantly higher in diets containing 44% and 49% protein diets (P > 0.05). There were no differences in survival rates, protein efficiency ratio (PER) and nutrient composition of snapper flesh. All fish had fatty livers. Results indicated that the diet containing 44% protein with a P/E ratio of 23.3 mg protein kJ^?1 was optimum for snapper growth under the experimental conditions used in the study.     

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.     

Effects of dietary protein and lipid levels and DP DE−1 ratio on growth, feed utilization and hepatosomatic index of juvenile haddock, Melanogrammus aeglefinus L.

Juvenile haddock, Melanogrammus aeglefinus L. (initial weight, 13.5 ± 0.1 g) were fed practical diets containing digestible protein to digestible energy (DP DE^?1) ratios of 25–30 g DP MJ DE^?1as‐fed using three protein levels (450, 500 and 550 g kg^?1) each at two lipid levels (110 and 160 g kg^?1) for 63 days. The results showed mean weight gain and feed conversion ratio were highest for diets containing 28.5 and 30.2 g DP MJ DE^?1. DP DE^?1 ratio had no significant effect on protein efficiency ratio except at the lowest level (24.7 g DP MJ DE^?1) indicating a protein sparing effect of higher lipid when dietary protein is below the requirement. Haddock appears to preferentially use protein as the prime source of DE. DP DE^?1 ratio had little effect on apparent digestibility (AD) of protein while AD of lipid was significantly affected. Significant differences in AD of energy and organic matter were found to be inversely related to the carbohydrate level of the diet. DP DE^?1 ratios of 28.5 g DP MJ DE^?1 or lower resulted in significantly higher hepatosomatic indexes. The highest whole‐body nitrogen gains and energy retention efficiencies were achieved at 28.5 and 30.2 g DP MJ DE^?1, whereas only slight differences in nitrogen retention efficiencies were observed. The highest levels of energy retained in the form of protein were achieved at 28.5 and 30.2 g DP MJ DE^?1. The diet that provided the best growth, feed utilization and digestibility with minimal HSI contained 546 g kg^?1 protein (513 g kg^?1 DP), 114 g kg^?1 lipid, 164 g kg^?1 carbohydrate, 17.0 MJ kg DE^?1 and a DP DE^?1 ratio of 30.2 g DP MJ DE^?1.     

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).     

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.     

The influence of dietary protein and energy levels on growth, survival and thyroid hormone (T3 and T4) composition of Lates calcarifer larvae

Two growth trials were conducted to determine the effects of different dietary protein (450–550 g kg^?1) and energy contents (18–22 MJ kg^?1) on growth, survival and carcass thyroid hormone (T3 and T4) levels of barramundi (Lates calcarifer) larvae. Larvae fed diets containing 21 and 22 MJ kg^?1 dietary energy performed consistently better than those fed diets containing 18 and 19 MJ kg^?1 dietary energy in terms of final dry weight and total length, while those fed 20 MJ kg^?1 had intermediate values for both the parameters. No effects of dietary protein level were discernable from the physical parameters measured; however, larvae fed diets containing the lowest protein and energy combination (450 g kg^?1 protein/18 MJ kg^?1 energy) had significantly lower carcass T4 levels than larvae in all other treatments, except for those fed the 500 g kg^?1 protein/18 MJ kg^?1 diet, which had an intermediate value. The results indicate that the optimum diet for L. calcarifer larvae from 14 to 28 days after hatch should contain 500 g kg^?1 protein and a minimum of 21 MJ kg^?1 dietary energy. Carcass T4 content was influenced by macronutrient inclusion level, and correlated significantly with growth, described by the total length. Reduced T4 levels may indicate a depressed larval status in this species.     

Optimum dietary protein and lipid specifications for grow-out of humpback grouper Cromileptes altivelis (Valenciennes)

Fingerling Cromileptes altivelis of less than 50 g have been shown to require feeds of 50–56% crude protein (CP) and 9–15% lipid. The requirements of larger, market‐size fish have not been reported. A total of 324 hatchery‐produced C. altivelis were weight sorted into three groups of 136, 175 and 225 g start weight and equally (12 seacage^?1) and randomly distributed to floating net seacages in accordance with a 3 × 3 factorial arrangement of CP (42%, 47% or 53%; estimated digestible CP of 40%, 46% or 52%) and lipid (8%, 12% or 16%; equivalent to estimated digestible energy (DE) contents of 14.0, 15.8 or 17.5 MJ kg^?1). Changes in dietary CP and lipid content were achieved at the cost of wheat flour by proportionally varying the protein mixture (essentially a 0.62:0.22:0.16 ratio of fish meal, mysid meal and casein respectively) and oil mixture (a 2:1 ratio of fish oil and soybean oil respectively). Fish were fed twice daily to satiation for 180 days. There was no significant (P>0.05) interaction between the main effects of dietary protein and lipid for any growth, nutrient retention or whole‐body composition measurements. Increasing dietary CP significantly improved the survival rate (80.6%, 88.9% and 87.0%), specific growth rate (SGR; 0.24%, 0.28% and 0.31% day^?1), feed conversion ratio (FCR; 2.77, 2.21 and 2.00) and DE retention (18.2, 21.3 and 23.2%), respectively, but did not significantly affect digestible protein retention. Increasing dietary lipid increased SGR (0.25, 0.29 and 0.29% day^?1) and the whole‐body lipid (and energy) composition, and reduced the survival rate (87.0%, 88.9% and 80.6%), respectively, but FCR and retentions of digestible protein and DE were not significantly affected. These results indicate that humpback grouper of 150–400 g require a dietary specification of not less than 51% digestible protein (～53% CP), 10–12% lipid and digestible protein:DE of 31–32 g MJ^?1 for optimal growth.     

Growth and haematology of pacu, Piaractus mesopotamicus, fed diets with varying protein to energy ratio

Haematopoiesis and blood cells' functions can be influenced by dietary concentration of nutrients. This paper studied the effects of dietary protein:energy ratio on the growth and haematology of pacu, Piaractus mesopotamicus . Fingerling pacu (15.5±0.4 g) were fed twice a day for 10 weeks until apparent saciety with diets containing 220, 260, 300, 340 or 380 g kg⁻¹ crude protein (CP) and 10.88, 11.72, 12.55, 13.39, 14.22 MJ kg⁻¹ digestible energy (DE) in a totally randomized experimental design, 5 × 5 factorial scheme ( n =3). Weight gain and specific growth rate were affected ( P <0.05) by protein level only. Protein efficiency ratio decreased ( P <0.05) with increasing dietary protein at all levels of dietary energy. Daily feed intake decreased ( P <0.05) with increasing dietary energy. Mean corpuscular haemoglobin concentration was affected ( P <0.05) by DE and interaction between dietary CP and DE. Total plasma protein increased ( P <0.05) with dietary protein and energy levels. Plasma glucose decreased ( P <0.05) with increasing dietary protein. The CP requirement and optimum protein:energy ratio for weight gain of pacu fingerlings, determined using broken-line model, were 271 g kg⁻¹ and 22.18 g CP MJ⁻¹ DE respectively. All dietary CP and DE levels studied did not pose damages to fish health.     

Incorporation of a mixture of meat and bone meal,poultry by‐product meal,blood meal and corn gluten meal as a replacement for fish meal in practical diets of Pacific white shrimp Litopenaeus vannamei at two dietary protein levels

A 6‐week feeding trial was carried out in glass tanks to determine the effects of partial replacement of fish meal (FM) with a combination of meat and bone meal (MBM), poultry by‐product meal (PBM), blood meal (BM) and corn gluten meal (CGM) in practical diets on the growth, nutrient digestibility and body composition of Pacific white shrimp. Six practical diets were formulated, containing two levels of crude protein (CP) (330 and 380 g kg^?1) and similar crude lipid (CL) levels. For the 330 g kg^?1 dietary protein level, 0, 357 and 714 g kg^?1 FM were replaced by the mixture in Diets 1–3, respectively; while 0, 514 and 784 g kg^?1 FM were replaced in Diets 4–6, respectively, for 380 g kg^?1 dietary protein level. White shrimp‐fed diets containing 330 g kg^?1 CP had significantly lower weight gain compared with white shrimp fed diets containing 380 g kg^?1 CP. Increasing the mixture and dietary protein level significantly raised the body ash content of white shrimp. White shrimp fed a low‐protein diet obtained better nutrient digestibility compared with those fed a high‐protein diet.     

Polka dot grouper Cromileptes altivelis fingerlings require high protein and moderate lipid diets for optimal growth and nutrient retention

An 8‐week comparative slaughter experiment was carried out to determine the effect of dietary protein and lipid on growth, apparent digestibility (AD) and nutrient retention of polka dot grouper Cromileptes altivelis. Fingerlings were fed diets that varied in crude protein (CP) at 55 g kg^?1 increments between 410 and 630 g kg^?1 dry matter (DM) and at either a moderate (150 g kg^?1 DM) or high (240 g kg^?1DM) lipid concentration. Each diet was fed to satiety twice daily to four replicate tanks (110 L) of fish. One replicate block of tanks comprised 150 fish of mean (±SD) initial weight of 9.6 ± 0.29 g, which were distributed equally to 10 tanks. The other three replicate blocks of tanks comprised 300 fish of 12.6 ± 0.45 g, which were distributed equally to 30 tanks. Tanks were provided with filtered and heated (29 ± 0.5 °C) seawater in a flow‐through system within a laboratory where photoperiod was maintained at 12 : 12 h light–dark cycle. Voluntary food intake was not significantly affected by either the CP or lipid concentration of the diet (mean ± SD of 1.93 ± 0.146 g week^?1) but there was a trend for intake to be higher on the moderate compared with the high lipid diets (mean ± SEM of 1.97 versus 1.89 ± 0.033 gweek^?1, respectively). Daily growth coefficient (DGC) and food conversion ratio (FCR) improved linearly (P < 0.01) with increasing dietary CP (from 0.94 to 1.35% day^?1 for DGC and 1.58 to 1.00 g DM g^?1 wet gain for FCR) and these responses were almost coincident for each of the lipid series. The AD of CP increased linearly with increasing dietary CP (from 46.8 to 74.1%) and was independent of dietary lipid. Apparent digestibility of energy increased curvilinearly with increasing dietary CP, with the quadratic component being more prominent for the high‐lipid series. Increasing the amount of lipid in the diet markedly increased the lipid content of the fish from an initial composition (mean ± SD) of 173 ± 7.3 g kg^?1 to a final composition (mean ± SEM) of either 217 or 250 ± 5.9 g kg^?1 for moderate and high‐lipid series, respectively. Total body lipid content tended to increase linearly with increasing dietary CP for the high‐lipid series but with an opposite effect for the moderate‐lipid series. The retention of digestible nitrogen decreased linearly with increasing dietary CP but at a steeper rate for the moderate, compared with the high, lipid series (from 62.7 to 35.7%, slope ?0.115 for moderate‐lipid and 54.6 to 41.9%, slope ?0.050 for high‐lipid). A quadratic function of dietary CP concentration best explained the retention of digestible energy with the curvilinearity being more marked for the high, compared with the moderate, lipid diet series. While there was some indication that ingested lipid spared dietary protein, the results showed a far greater propensity of polka dot grouper fingerlings to use protein as the prime dietary energy source. Diets for juvenile polka dot grouper should contain not less than 440 g digestible protein kg^?1 DM and at least 150 g lipid kg^?1 DM.     

The effect of dietary methionine concentrations on growth performance of juvenile Nile tilapia (Oreochromis niloticus) fed diets with two different digestible energy levels

A growth trial was conducted to examine the effect of dietary digestible energy (DE) content on methionine (Met) utilization and requirement in juvenile Nile tilapia (Oreochromis niloticus). Ten iso‐nitrogenous (288 g kg^?1 protein) practical diets, with two DE levels (10.9 MJ kg^?1; 12.4 MJ kg^?1) and five methionine supplementation levels (0, 1, 2, 4 and 6 g kg^?1), were hand‐fed twice daily to triplicate groups of Nile tilapia (initial body weight 8.95 ± 0.06 g) for 8 weeks. Weight gain (WG) and specific growth rate (SGR) increased significantly with increasing dietary methionine concentration at the same DE content (P < 0.001). At the same dietary methionine level, WG and SGR of fish fed high‐DE diets were significantly higher than that of fish fed low‐DE diets (P = 0.0001), although no interaction was found between dietary DE and methionine supplementation. Based on quadratic regression analysis between dietary methionine concentration and weight gain, optimal methionine requirement for maximum growth, expressed as g Met required kg^?1 diet (low‐ versus high‐DE diets), increased as diet DE concentration increased (7.34 versus 9.90 g kg^?1 diet, respectively; with cysteine 4.70 g kg^?1 diet). The results indicated that diet DE content affects methionine utilization and requirement in juvenile Nile tilapia, fish fed high‐DE diets required more methionine for maximum growth.     

Dietary digestible lysine requirement and essential amino acid to lysine ratio for pacu Piaractus mesopotamicus

To determine the digestible lysine requirement for pacu juveniles, a dose–response feeding trial was carried out. The fish (8.66 ± 1.13 g) were fed six diets containing the digestible lysine levels: 6.8, 9.1, 11.4, 13.2, 16.1 and 19.6 g kg^?1 dry diet. The gradual increase of dietary digestible lysine levels from 6.8 to 13.2 g kg^?1 did not influence the average values of the parameters evaluated (P > 0.05). The increase of dietary digestible lysine level to 16.1 g kg^?1 significantly improved weight gain (WG), specific growth rate (SGR), protein productive value (PPV), protein efficiency rate (PER), and apparent feed conversion rate (FCR), but was not different from fish fed diets containing 19.6 g kg^?1 lysine. Fish fed diets containing 16.1 and 19.6 g kg^?1 digestible lysine showed lower body lipid contents than fish in the other treatments. The digestible lysine requirement as determined by the broken‐line model, based on average WG values, was 16.4 g kg^?1. The other essential amino acid requirements were estimated based on the ideal protein concept and the value determined for lysine.     

Effects of dietary protein and lipid levels on growth and energy productive value of pacific white shrimp,Litopenaeus vannamei,at different salinities

A 8‐week feeding experiment was conducted to evaluate the effect of different dietary protein and lipid levels on growth and energy productive value of juvenile Litopenaeus vannamei, at 30 and 2 ppt, respectively. Nine practical diets were formulated to contain three protein levels (380, 410 and 440 g kg^?1) and three lipid levels (60, 80 and 100 g kg^?1). Each diet was randomly fed to triplicate groups of 30 shrimps per tank (260 L). The effects of salinity and an interaction between dietary protein level and lipid level on growth and energy productive value of shrimp were observed under the experimental conditions of this study. At 30 ppt seawater, shrimp fed with 440 g kg^?1protein diets had significantly higher weight gain (WG) than those fed with 380 g kg^?1 protein diets at the same dietary lipid level, and the 60 g kg^?1 lipid group showed higher growth than 80 g kg^?1and 100 g kg^?1 lipid groups at the same dietary protein level. At 2 ppt seawater, the growth of shrimp was little affected by dietary protein treatments when shrimp fed the 80 and 100 g kg^?1 lipid, shrimp fed the 80 g kg^?1 lipid diets had only slightly higher growth than that fed 60and 100 g kg^?1 lipid diets when fed 380 and 410 g kg^?1 dietary protein diets. A significant effect of salinity on growth of shrimp was detected with the growth responses at 30 ppt > 2ppt (P < 0.05). Final body lipid content, body protein content and energy productive value of shrimp was significantly higher in animals exposed to 30 ppt than in shrimp held at 2 ppt.     

The effect of protein levels on growth,postprandial excretion and tryptic activity of juvenile mullet Mugil platanus (Günther)

The objective of the present work was to determine the optimum dietary protein level for juvenile mullets. Five isocaloric diets were formulated to contain increasing levels (300, 350, 400, 450 and 500 g kg^?1) of crude protein (CP) corresponding to 18.7 MJ metabolizable energy kg^?1. All diets were tested in triplicate. Each experimental unit was composed of a 50 L tank with 50 juveniles (mean ± SE initial weight and length equal to 1.17 ± 0.02 g and 4.34 ± 0.03 cm respectively). Diets were offered five times a day until apparent satiation for 35 days. No significant difference (P>0.05) was observed in survival rate, feed efficiency and body composition between treatments. However, weight gain, feed consumption and specific growth rate were higher in fish fed the 350 g kg^?1 CP level than those fed the highest protein content diet (500 g kg^?1 CP). The amount of postprandial ammonia excreted by mullet was linearly related to protein intake. Intestinal tryptic activity was inversely proportional to the percentage of dietary CP. It is likely that diets containing <350 g kg^?1 CP will be needed for on‐growing mullet, especially when reared in ponds with abundant natural food.     

Optimal dietary protein requirement of grouper Epinephelus coioides juveniles fed isoenergetic diets in floating net cages

An experiment to determine the optimal protein requirement of grouper Epinephelus coioides juveniles was conducted in floating net cages (1.5 m × 1 m × 1.5 m). Six isoenergetic fishmeal–casein‐based experimental diets containing 350–600 g kg^?1 crude protein (CP) were fed to triplicate groups of 20 fish (10.7 ± 0.2 g) for 56 days. Weight gain (WG) and specific growth rate (SGR) increased with increasing dietary protein level from 350 to 450 g kg^?1 and then plateaued above these levels. Feed intake (FI) showed no significant difference among fish fed more than 350 g kg^?1 CP. Lowest feed conversion ratio (FCR) was found for fish fed 500 g kg^?1 CP but this was not significantly different from that of fish fed the 450 and 600 g kg^?1 CP. Lowest protein efficiency ratio (PER) was found for fish fed 550 and 600 g kg^?1 CP. Fish fed the 600 g kg^?1 CP had the highest body protein and moisture contents but the lowest body lipid content. Body ash content was unaffected by protein level for fish fed >400 g kg^?1 CP. Dietary protein level had no significant effect on hepatosomatic index (HSI). Fish fed the 350 g kg^?1 CP had significantly lower condition factor (CF) and viscerosomatic index (VSI). Based on broken‐line regression analysis of SGR the optimal dietary protein requirement for E. coioides juveniles was determined to be close to 480 g kg^?1.     

Effect of dietary protein and lipid levels on growth and feed utilization of white sea bream (Diplodus sargus) juveniles

In this study, two growth trials were conducted to evaluate the effect of dietary protein and lipid levels on growth and feed utilization of white sea bream (Diplodus sargus) juveniles. For the first trial, five diets were formulated to contain 120 g kg^?1 lipid and increasing levels of protein, ranging from 400 to 600 g kg^?1. Two additional diets were formulated with 400 and 600 g kg^?1 protein and 180 g kg^?1 lipids. The diets were fed to apparent visual satiety to duplicate groups of fish with a mean weight of 1.5 g for 10 weeks. For the second growth trial, four diets were formulated to contain 120 g kg^?1 lipid and 380–520 g kg^?1 protein. Two additional diets were formulated with 380 and 520 g kg^?1 protein and 180 g kg^?1 lipids. The diets were fed to apparent visual satiety to triplicate groups of fish with a mean weight of 41 g for 12 weeks. At the end of both trials, there were no growth differences among groups independent of the dietary protein content. In the first trial, growth was negatively correlated to dietary lipid levels. No significant differences of feed intake were detected among groups in both trials, but a direct correlation between feed efficiency and dietary protein level was observed. Protein efficiency ratio and nitrogen (N) retention (% N intake) significantly decreased with the increase of dietary protein levels. In both trials, energy retention (% energy intake) was highest in groups fed on diets with the highest protein‐to‐energy (P/E) ratio. At the end of both trials, no significant differences in whole‐body composition were observed among groups. Specific activity of enzymes involved in amino acid catabolism [aspartate aminotransferase (AST), alanine aminotransferase (ALT) and glutamate dehydrogenase (GDH)] showed no significant differences with dietary protein level in both trials. Nevertheless, in the first trial, a significantly lower GDH activity was observed in fish fed with higher dietary lipid levels. No differences were found for specific activity of the lipogenic enzymes, fatty aid synthetase and glucose‐6‐phosphate dehydrogenase, in the second trial. Results of this study indicate that a diet with a protein level of 380–420 g kg^?1 and a P/E ratio of 20 g protein MJ^?1 satisfies the growth requirements of D. sargus juveniles. Also, within the range tested, no evidence of protein sparing by dietary lipids seems to occur.     

Growth and body composition of juvenile white shrimp,Litopenaeus vannamei,fed different ratios of dietary protein to energy

A 10‐week feeding experiment was conducted to evaluate the effect of different protein to energy ratios on growth and body composition of juvenile Litopenaeus vannamei (initial average weight of 0.09 ± 0.002 g, mean ± SE). Twelve practical test diets were formulated to contain four protein levels (300, 340, 380 and 420 g kg^?1) and three lipid levels (50, 75 and 100 g kg^?1). Each diet was randomly fed to triplicate groups of 30 shrimps per tank (260 L). The water temperature was 28.5 ± 2 °C and the salinity was 28 ± 1 g L^?1 during the experimental period. The results showed that the growth was significantly (P < 0.05) affected by dietary treatments. Shrimps fed the diets containing 300 g kg^?1 protein showed the poorest growth. However, shrimp fed the 75 g kg^?1 lipid diets had only slightly higher growth than that fed 50 g kg^?1 lipid diets at the same dietary protein level, and even a little decline in growth with the further increase of dietary lipid to 100 g kg^?1. Shrimp fed the diet with 420 g kg^?1protein and 75 g kg^?1 lipid had the highest specific growth rate. However, shrimp fed the diet with 340 g kg^?1 protein and 75 g kg^?1 lipid showed comparable growth, and had the highest protein efficiency ratio, energy retention and feed efficiency ratio among dietary treatments. Triglycerides and total cholesterol in the serum of shrimp increased with increasing dietary lipid level at the same dietary protein level. Body lipid and energy increased with increasing dietary lipid level irrespective of dietary protein. Results of the present study showed that the diet containing 340 g kg^?1 protein and 75 g kg^?1 lipid with digestible protein/digestible energy of 21.1 mg kJ^?1 is optimum for L. vannamei, and the increase of dietary lipid level has not efficient protein‐sparing effect.     

Growth and metabolism of pacu (Piaractus mesopotamicus Holmberg 1887) juveniles fed diets containing different protein, lipid and carbohydrate levels

To verify the potential of lipids and carbohydrates to spare dietary protein and to understand the intermediary metabolism of interaction of these nutrients in pacu juveniles, an experiment was carried out to evaluate pacu physiological and performance parameters. The experimental design was completely randomized with 12 treatments in a 2 × 2 × 3 factorial arrangement, consisting of diets containing two digestible protein levels (200 and 230 g kg⁻¹ PD), two lipid levels (40 and 80 g kg⁻¹) and three carbohydrate levels (410, 460 and 500 g kg⁻¹). Fish‐fed 230 g kg⁻¹ digestable protein (DP) showed increased glycaemia, decreased hepatic glycogen, as well as a smaller intake index and better feed conversion ratio. The higher dietary lipid level (80 g kg⁻¹) reduced protein intake and serum protein concentration, increased liver and body fat content, but did not affect growth. At a lipid level of 80 g kg⁻¹, the increase in dietary carbohydrate levels promoted greater weight gain (WG), crude protein intake (CPI) and better feed conversion ratio (FCR). For fish fed diets containing 40 g kg⁻¹ lipid, the best energy‐productive values (EPV) were obtained at 460 g kg⁻¹ carbohydrate. Increased levels of the main nutrients in the diets reduced the levels of serum triglycerides, while the increase in energy concentration increased the hepatosomatic (HSI) and glycaemia index values. Pacu used lipids as effectively as carbohydrates in the maximization of protein usage, as long as dietary protein was at a level of 230 g kg⁻¹ DP. The physiological parameters indicated that the best balance between the DP, dietary lipid and carbohydrate levels within the ranged this trial was obtained at 230, 40 and 460 g kg⁻¹, respectively, without lower growth.