Effect of dietary carbohydrate‐to‐lipid ratios on growth performance,body composition,nutrient utilization and hepatic enzymes activities of herbivorous grass carp (Ctenopharyngodon idella)

Six isonitrogenous (390 g kg^?1) and isoenergetic (16.2 kJ g^?1) diets with varying carbohydrate : lipid (CHO : L) ratios (202.5–1.74), were fed to triplicate groups of 25 fish in indoor recirculation system. Over 8‐week‐growth trial, best weight gain (WG), specific growth rate, feed conversion ratio, protein efficiency ratio and protein production value (P < 0.05) were observed in fish‐fed diets with CHO : L ratio of 7.5. Fish fed either the lowest (1.7) or highest (202.5) CHO : L ratio tended to produce lower (P < 0.05) growth and feed conversion efficiencies. The values of viscerosomatic index, hepatosomatic index and intraperitoneal fat ratio increased as dietary CHO : L ratios decreased. There were no significant differences in whole body and liver crude protein among dietary treatments. Whole body and liver lipid increased as CHO : L ratios decreased. Plasma cholesterol and triacylglyceride levels increased linearly as dietary CHO : L ratios decreased. Activities of glucokinase and pyruvate kinase were stimulated by elevated levels of dietary carbohydrate; however, activities of lipase (LPS) and alkaline phosphatase were stimulated by elevated levels of dietary lipid. Based on a second‐order polynomial regression analysis of WG against dietary carbohydrate and lipid levels, 275 g kg^?1 of carbohydrate and 59 g kg^?1 of lipid, corresponding to a CHO : L ratio of 4.7, in a diet holding 390 g kg^?1 of crude protein and 16.3 kJ g^?1 of gross energy, proved to be optimal for grass carp. These results indicated that utilization of dietary lipid and carbohydrate was moderate in grass carp, but the fish were a little more capable of utilizing lipid compared with carbohydrate.     

Effect of dietary protein-energy levels and fish initial sizes on growth rate, development and production of Nile tilapia, Oreochromis niloticus L.

The effects of dietary protein‐energy levels on the growth rate, proximate composition and production were examined in Nile tilapia, Oreochromis niloticus, at two starting weights (22.9 and 39.8 g) reared in concrete ponds for 180 days. The highest weight gain (183.1 g) was obtained with fish fed a 30% protein and 10.5 kJ g^?1 diet for the small initial size and 180.2 g for a diet containing 25% protein and 12.6 kJ g^?1 for the large initial size. Dressed yields (edible mass) and fillets increased to 56.9% and 52.5% in fish fed diet with 25% protein and 10.5 kJ g^?1 at the initial size of 22.9 g, while fish started at 39.8 g exhibited the best values (56.5% and 52.1%) when fed the 30% protein and 10.5 kJ g^?1 diet. Proximate composition of soft tissue (wet weight basis) in small fish was significantly influenced by dietary protein‐energy levels. Protein was 26.1±0.3% in fish fed the high protein (30%) and low energy (10.5 kJ g^?1 diet), while lipid content was 6.4±0.3% at diet containing 20% protein and 14.7 kJ g^?1 diet. Large initial size fish fed the diet with 25% protein and 14.7 kJ g^?1 had the highest body protein (32.0±0.4%) and lowest lipid content (2.2±0.3%). Feed conversion ratio (FCR) and protein efficiency ratio varied with different dietary protein‐energy levels and initial fish sizes. Feed conversion ratio increased with increasing protein and decreasing energy level in the diet, and values in small fish were higher than values in large fish. Protein efficiency ratio decreased with increasing dietary protein level and decreasing energy level. The maximum total production (7.6 tons feddan^?1) was with dietary high protein (30%) and low energy (10.5 kJ g^?1) for small‐sized fish, while large initial fish had the highest production (3.7 tons feddan^?1) when fed the 25% protein and 12.6 kJ g^?1 diet energy. Starting with 22.9 g fish was more advantageous than the initial size of 39.8 g for rearing Nile tilapia. Small fish required a high‐protein and low‐energy diet, whereas large fish required a low‐protein and high‐energy diet to achieve highest production.     

Optimal dietary carbohydrate to lipid ratio for juvenile yellowfin seabream (Sparus latus)

A growth experiment was conducted to determine the optimal carbohydrate‐to‐lipid (CHO: L) ratio for juvenile yellowfin seabream cultured in 340‐L indoor recirculating tanks. Seven isonitrogenous (450 g kg⁻¹ dietary protein) and isoenergetic (14.1 MJ kg⁻¹) diets with increasing CHO: L ratios (0.03–5.09 g: g) were fed to triplicate groups of 30 fish with an initial weight of 4.91 g for 56 days. Fish were fed to satiation twice a day and the water temperature ranged between 28 and 31.7 °C during the experimental period. Survival was high in all the groups and was not affected by dietary treatments. Best weight gain (WG) and specific growth rate (SGR) were observed in fish fed diets with CHO: L ratios of 0.29 and 0.72, which were not significantly different from that of 0.03, 1.26 and 1.92, but apparently higher than that of 3.22 and 5.09. Feed efficiency (FE), protein efficiency ratio (PER) and protein production value (PPV) followed the same general pattern as WG and SGR. Highest level of energy production value (EPV) was found in fish fed diets with CHO: L ratio of 0.72. Proximate compositions of fish whole body and tissues were markedly affected by dietary CHO: L ratios. Whole body, muscle and liver lipid increased as CHO: L ratios decreased, whereas moisture contents were reduced. Dietary CHO: L ratios had no significant effect on protein content in whole body and muscle. Plasma total cholesterol levels of fish fed diets with CHO: L ratios less than 0.72 were significantly higher than those of the other groups. Triacylglyceride levels decreased linearly as dietary CHO: L ratios increased. Viscerosomatic index (VSI) significantly increased as dietary CHO: L ratios decreased. Intraperitoneal fat ratio (IPF) of fish fed diets with CHO: L ratios less than 1.92 were significantly higher than those fed CHO: L ratios of 3.22 and 5.09. Hepatosomatic index (HSI) did not vary between the test diets. Based on second‐order polynomial regression analysis of WG against dietary carbohydrate and lipid levels, 84.1 g kg⁻¹ of carbohydrate and 136.3 g kg⁻¹ of lipid, corresponding to a CHO: L ratio of 0.62, in a diet holding 450 g kg⁻¹ of crude protein and 14 KJ g⁻¹ of metabolizable energy, proved to be optimal for juvenile yellowfin seabream.     

Effects of dietary carbohydrate to lipid ratios on growth and body composition of juvenile and grower rockfish, Sebastes schlegeli

Two feeding trials were conducted to determine the optimal dietary carbohydrate to lipid (CHO:L) ratio for juvenile and grower rockfish. Triplicate groups of juvenile (initial mean weight 3.6 g) and duplicate groups of grower (initial mean weight 166 g) were fed the five isonitrogenous (51% CP) and isoenergetic (4.0 kcal g^?1) diets with the different CHO:L ratios (0.4–5.6 g:g) for 8 weeks respectively. The survival of juvenile and grower was above 93% and was not affected by the dietary CHO:L ratios. Weight gain of juvenile fed the diets with CHO:L ratios of 0.8 and 1.6 was significantly higher than that of the fish fed diets with CHO:L ratios of 2.8 and 5.6 (P<0.05). The feed efficiency and protein efficiency ratio of juvenile fed the diet with CHO:L ratio of 5.6 were the lowest among all groups (P<0.05). The daily feed intake of juvenile fed the diet with a CHO:L ratio of 5.6 was significantly higher than that of the other groups (P<0.05). The condition factors of juvenile fed the diets with CHO:L ratios of 0.8 and 1.6 were significantly higher than that of 5.6 (P<0.05). The crude lipid content of whole body, liver and viscera of juvenile decreased as the dietary CHO:L ratio increased, and the opposite was found for the moisture content. Weight gain, feed efficiency, daily feed intake, protein efficiency ratio and condition factor of grower were not affected by the dietary CHO:L ratio. Hepatosomatic and viscerasomatic indexes of grower were significantly influenced by dietary CHO:L ratio (P<0.05). Significant differences were observed in the lipid content of whole body and viscera of grower. Dietary CHO:L ratios significantly affected the major fatty acid composition of whole body in both juvenile and grower. The contents of 18:2n‐6 and 18:3n‐3 linearly decreased as the dietary CHO:L ratio increased, whereas the 20:4n‐6, 20:5n‐3 and 22:6n‐3 contents increased. Based on growth, feed efficiency and body composition, the optimal dietary CHO:L ratio was 1.6 for juvenile rockfish fed isonitrogenous (51% CP) and isoenergetic (4.0 kcal g^?1) diets, and starch could partially replace lipids in the diets with CHO:L ratios ranging from 0.4 to 5.6 for grower.     

Growth,feed utilization and body composition of African bonytongue,Heterotis niloticus,fingerlings fed diets containing various protein and lipid levels

In order to evaluate the effects of dietary protein and lipid levels on the growth, feed utilization and body composition of Heterotis niloticus fingerlings, a factorial experiment with three replicates was conducted. Six experimental diets containing three crude protein levels (28%, 32% and 36%) and two crude lipid levels (6% and 13%) were tested. Heterotis niloticus (2.34 g) were fed with the diets to apparent satiation, twice a day. For 56 days, weight gain (WG), specific growth rate (SGR), feed efficiency (FE) and protein retention (PR) were significantly affected by dietary protein and dietary lipid levels respectively (P<0.01). The highest WG, SGR and FE were observed for fingerlings fed the diet containing 36% protein and 6% lipid, but no significance difference was found between groups fed with the following diets: P28L13 (28% protein and 13% lipid), P32L6, P32L13 and P36L13. A significant interaction between dietary protein and lipid was observed for WG, SGR, FE and PR. The whole‐body protein, lipid, moisture and ash content were not significantly affected by dietary lipid levels, but body protein and lipid content were significantly affected by dietary protein. The dietary protein‐sparing effect was clearly demonstrated when the dietary energy of lipid increased from 17 to 19.6 kJ g^?1 at 28% crude protein on H. niloticus.     

Optimum protein-to-energy ratio for two size groups of rabbitfish, Siganus canaliculatus (Park)

Three approximately isoenergetic (17 kJ g^?1) diets were formulated with dietary protein levels of 270, 360 and 480 g kg^?1 (DM basis) providing protein-to-energy ratios of 15.69, 20.48 and 27.16 mg crude protein (CP) kJ^?1, respectively. The effects of these diets on several growth and nutritional parameters were evaluated for the fry (2.50 ± 0.184 g) and fingerlings (11.53 ± 0.023 g) of Siganus canaliculatus (Park). Maximum growth and best feed utilization efficiency of fry were obtained using the diet containing 480 g kg^?1 protein and P:E ratio of 27.16 mg CP kJ^?1. For fingerlings the best results were obtained with the diet containing 360 g kg^?1 protein and P:E ratio of 20.48 mg CP kJ. Body composition of the fry was not affected by the feeding regime whilst the effect was evident in the fingerling groups. The carcass protein content of the fingerling was observed to increase with increasing P:E ratios while lipid content decreased as P:E increased.     

Interacting effects of dietary lipid level and temperature on growth, body composition and fatty acid profile of rohu, Labeo rohita (Hamilton)

Three isonitrogenous (320 g kg^?1 crude protein, casein and gelatine) semi‐purified diets with 80 (L8), 130 (L13) and 180 (L18) g kg^?1 lipid (sunflower oil at increasing levels and cod liver oil fixed at 50 g kg^?1) at three digestible energy levels (12 096, 13 986 and 15 876 kJ kg^?1 dry weight) and were tested, in triplicate, on rohu fingerlings (3.2 ± 0.08 g) at two different temperatures (21 and 32 °C). Fish were fed to apparent satiation, twice daily, at 09.00 and 15.00 h, 7 days a week for 56 days. Maximum growth was obtained at a lipid level of 80 g kg^?1 (L8) at 21 °C (439.37%) and 130 g kg^?1 (L13) at 32 °C (481.8%). In general growth rate was higher at 32 °C than at 21 °C at all lipid levels. Tissue monounsaturated fatty acid (MUFA) contents decreased with increasing lipid level at 32 °C, but the reverse occurred at 21 °C. At 21 °C, Polyunsaturated fatty acid (PUFA) level increased significantly (P > 0.05) over initial values, but was affected insignificantly by dietary lipid level. At 32 °C, fish fed diet L13 had more n‐3 fatty acid (FA) in liver and muscle than the other two dietary groups while at 21 °C, both liver and muscle FA profiles exhibited significant change (P > 0.05) in n‐3 and n‐6 FA content which corresponded to variation in percent addition of dietary lipid. However, n‐3/n‐6 ratio was higher for fish fed diet L13 at 32 °C and diet L8 at 21 °C and may be correlated with fish growth.     

Effects of dietary protein to energy ratios on growth and body composition of juvenile Chinese sucker,Myxocyprinus asiaticus

A growth experiment was conducted to investigate effect of dietary protein to energy ratios on growth and body composition of juvenile Myxocyprinus asiaticus (initial mean weight: 10.04 ± 0.53 g, mean ± SD). Nine practical diets were formulated to contain three protein levels (340, 390 and 440 g kg^?1), each with three lipid levels (60, 100 and 140 g kg^?1), in order to produce a range of P/E ratios (from 22.4 to 32.8 mg protein kJ^?1). Each diet was randomly assigned to triplicate groups of 20 fish in 400‐L indoors flow‐through circular fibre glass tanks provided with sand‐filtered aerated freshwater. The results showed that the growth was significantly affected by dietary P/E ratio (P < 0.05). Fish fed the diets with 440 g kg^?1 protein (100 and 140 g kg^?1 lipid, P/E ratio of 31.43 and 29.22 mg protein kJ^?1) had the highest specific growth rates (SGR) (2.16 and 2.27% day^?1, respectively). However, fish fed the diet with 390 g kg^?1 protein and 140 g kg^?1 lipid showed comparable growth (2.01% day^?1), and had higher protein efficiency ratio (PER), protein productive value (PPV) and energy retention (ER) than other groups (P < 0.05). No significant differences in survival were found among dietary treatments. Carcass lipid content was positively correlated with dietary lipid level, but irrespective of protein level and inversely correlated with carcass moisture content. Carcass protein contents increased with increasing dietary lipid at each protein level. The white muscle and liver composition showed that lipid increased with increasing dietary lipid level (P < 0.05). Dietary protein concentrations had significant effect on condition factor (CF), hepatosomatic index (HSI) and viscerosomatic index (VSI) (P < 0.05). However, dietary lipid concentrations had no significant effect on CF, HSI (P > 0.05). Based on these observations, 440 g kg^?1 protein with lipid from 100 to 140 g kg^?1 (P/E ratio of 29.22 to 31.43 mg protein kJ^?1) seemed to meet minimum requirement for optimal growth and feed utilization, and lipid could cause protein‐sparing effect in diets for juvenile Chinese sucker.     

Effects of dietary non‐protein energy source levels on growth performance,body composition and lipid metabolism in herbivorous grass carp (Ctenopharyngodon idella Val.)

A study was conducted to determine the effects of dietary non‐protein energy sources on growth, tissue lipid accumulation and lipid metabolism‐related genes expression of grass carp. Triplicate groups of fish were fed for 9 weeks on four isonitrogenous (300 g kg^?1) experimental diets with four levels of non‐protein energy (6.52 kJ g^?1 control diet, 5.32 kJ g^?1 high‐CEL diet, 8.46 kJ g^?1 high‐CHO diet and 8.53 kJ g^?1 high‐LIP diet respectively). Increasing dietary non‐protein energy source levels did not improve the growth, and the high‐CEL diet reduced the growth of grass carp. The high‐CHO diet tended to induce high hepatosomatic index, with high fat and glycogen content of liver. However, the high‐LIP diet caused the high mesenteric fat index, but did not increase liver fat. The mRNA abundance and activities of hepatic lipogenic enzymes were significantly increased in the high‐CHO diet group, whereas the opposite tendencies were observed in the high‐LIP diet group. Peroxisome proliferator‐actived receptor‐α (PPARα) in liver and PPARγ in mesenteric adipose tissue were up‐regulated in the high‐CEL diet group. Lipoprotein lipase (LPL) gene expression was significantly increased both in liver and mesenteric adipose tissue of fish fed the high‐LIP diet, while the LPL gene expression was up‐regulated in liver but down‐regulated in mesenteric adipose tissue of fish fed the high‐CEL diet. These findings suggest that an increase in dietary non‐protein energy sources alters the genes expression of lipid metabolism and increased lipid deposition.     

Effect of dietary protein and lipid levels and protein–energy ratio on growth indices, feed utilization and body composition of freshwater prawn, Macrobrachium rosenbergii (de Man 1879) post larvae

A grow‐out experiment was designed to determine the effect of different dietary protein, lipid levels and protein–energy (P:E) ratio on growth performance and feed utilization of the freshwater prawn, Macrobrachium rosenbergii post larvae (PL) culture in pond net enclosures (hapa, 3.75 m^?3 each) for 12 weeks (84 days). The experimental treatments were assigned in triplicate. Six test diets were formulated to contain three different protein levels (300, 350 and 400 g kg^?1 diet) and two lipid levels (100 and 140 g kg^?1 diet) in a factorial manner (3 × 2) to provided six different dietary P:E ratio: 16, 17, 18, 19, 20 and 21 mg CP kJ^?1 g^?1). The result showed that the highest significant (P≤0.05) survival rate, growth indices and feed utilization were observed for M. rosenbergii PL fed a diet with a P:E ratio of 17 mg CP kJ^?1 g¹, whereas, the lowest value was recorded for prawns fed a diet with a P:E ratio of 20 mg CP kJ^?1 g^?1. Whole body contents of protein and lipid were highest (P≤0.05) when fed diets with 21 and 17 mg CP kJ^?1 g^?1 respectively. Concerning dietary protein levels, the highest (P≤0.05) values for survival and growth indices were observed for PL fed a diet containing 300 g kg^?1 diet protein. The same trend was observed for PL fed a diet with 100 g kg^?1 diet lipid level, irrespective of dietary protein levels. A diet containing 300 g kg^?1 protein and 100 g kg^?1 lipid with a dietary P:E ratio of 17 mg CP kJ g^?1 is recommended to stimulate growth performance and nutrients utilization efficiency of M. rosenbergii PL.     

Predicting dietary essential amino acid requirements for hybrid striped bass

Three experiments were conducted that were designed to evaluate our ability to predict essential amino acid (EAA) needs of hybrid striped bass using the quantified lysine requirement and whole‐body amino acid concentrations. In the first experiment, six diets containing various amino acid profiles were fed to triplicate groups of fish initially weighing 7.7 g per fish. At the end of the 8‐week experiment, no significant differences were detected in growth rates or feed efficiencies (FE) between fish fed a practical diet containing 510 g kg^?1 herring fish meal (FM) and fish fed a purified diet containing the amino acid profile of herring fish meal (CAA‐FM). Growth responses of fish fed purified diets containing 100 (HSB), 110 (HSB110), 120 (HSB120) or 140 g 100 g^?1 (HSB140) of the amino acid profile of hybrid striped bass whole‐bodies were significantly lower than those of fish fed diet FM. In the second experiment, triplicate groups of fish (5.6 g per fish) were fed diets containing various energy : protein (E : P) ratios (34.8, 41.2, 47.5 and 53.9 kJ g^?1 protein) and one of two amino acid profiles (CAA‐FM and HSB120) in a 4 × 2 factorial design. Carbohydrate concentration was varied to achieve the desired energy concentrations. At the end of the 8‐week experiment, weight gain and FE were significantly higher in fish fed diets formulated to simulate the amino acid profile of herring fish meal (CAA‐FM) compared with fish fed diets formulated to contain 120 g 100 g^?1 of the amino acid profile of hybrid striped bass whole‐bodies (HSB120). Weight gain, FE and survival data indicated the optimum dietary E : P was 41.2 kJ g^?1 protein. Dietary treatments in the final experiment included three amino acid profiles and four levels of lipid in a 3 × 4 incomplete factorial design. Dietary amino acid treatments included the amino acid profile of herring fish meal (CAA‐FM) or 120 g 100 g^?1 of the predicted EAA requirement profile for hybrid striped bass (HSB120). The amino acid profile of the remaining dietary treatment (PRED+) was similar to that of the HSB120 treatment, but contained additional threonine, isoleucine and tryptophan. Diets CAA‐FM and HSB120 contained either 90, 130, 170 or 210 g kg^?1 lipid, whereas diet PRED+ contained 130 g kg^?1 lipid. Dietary treatments were fed for 10 weeks to triplicate groups of fish initially weighing 81.0 g per fish. Weight gain and FE were not significantly affected by dietary amino acid profile. Feed efficiency was significantly reduced in fish fed diets containing 210 g kg^?1 lipid compared with fish fed diets containing 90–170 g kg^?1 lipid. Intraperitoneal fat (IPF) ratio and hepatosomatic index (HSI) values generally increased as dietary lipid concentrations increased. Total liver lipid concentrations were significantly reduced in fish fed diets containing 210 g kg^?1 lipid compared with those of fish fed 90–130 g kg^?1 lipid. Results of this study indicate an appropriate dietary amino acid profile can be predicted for hybrid striped bass using the quantified lysine requirement and whole‐body amino acid concentrations. Further, the optimum E : P appears to be 40 kJ g^?1 protein.     

Effect of dietary carbohydrate to lipid ratios on growth,digestive enzyme and blood metabolites of juvenile Brazilian sardines,Sardinella brasiliensis (Steindachner, 1879)

The limited availability of live bait for capturing skipjack tuna, Katsuwonus pelamis, is a bottleneck to increasing tuna production in many parts of the world. Therefore, a nutrition trial was performed to contribute to the production of the Brazilian sardine, Sardinella brasiliensis, for use as live bait. This study determined the best dietary carbohydrate to lipid ratio (CHO:L) for juvenile Brazilian sardines based on growth performance, feed utilisation, body composition, blood metabolites and digestive enzyme activity. Six isoenergetic and isonitrogenous diets were formulated with increased CHO:L ratios (2.05, 3.41, 4.15, 5.11, 5.80 and 6.72). Each diet was randomly assigned to triplicate groups of 100 fish with mean initial body weight of 2.97 ± 0.51 g, which were fed four times a day to apparent satiation. Survival was not affected by differences in diet, however, a low CHO:L ratio stimulated growth. Juveniles fed with a rich‐carbohydrate diet inhibit feed intake and protein intake. Body lipid increased as dietary lipid increased and was inversely correlated to body moisture. The diets did not affect the juvenile's blood metabolites. Alkaline and acid protease activities were not significantly different, but lipase and amylase responded positively to the dietary lipids and carbohydrates. Using segmented regression, the optimum CHO:L ratio for maximum weight gain of juvenile Brazilian sardines was estimated to be 3.41, which contain approximately 300 g kg^?1 carbohydrate and 88 g kg^?1 lipid.     

Effect of dietary calcium on growth and survival of silver catfish fingerlings, Rhamdia quelen (Heptapteridae), exposed to different water pH

The purpose of this study was to verify the effect of dietary Ca²⁺ on the growth and survival of silver catfish fingerlings (Rhamdia quelen) exposed to different water pH (5.5, 7.5 and 9.0). Silver catfish fingerlings were randomly placed in a thermoregulated water re‐use system with twelve 250 L‐tanks, two 1000 L‐biofilters and a 2000 L‐reservoir with a medium flow of 3.84 L min^?1 tank. Stocking density was 0.16 fingerlings L^?1. To prepare the treatment diets, the control diet (0.8 g kg^?1 Ca²⁺) was supplemented with CaCO₃ to yield experimental diets with 6.4, 9.5 and 23.9 g kg^?1 Ca²⁺. There were three replicates/treatments. Survival was more than 93.9% in all treatments. Exposure of silver catfish fingerlings to alkaline or acid water reduced growth, and this effect was not ameliorated by dietary Ca²⁺ supplementation. Moreover, when fingerlings were maintained in water with pH 7.5, the best dietary Ca²⁺ range for silver catfish fingerling growth was 0.8–6.4 g kg^?1.     

Evaluation of optimum dietary protein-to-energy ratio in juvenile olive flounder Paralichthys olivaceus (Temminck et Schlegel)

An 8‐week feeding trial was conducted to estimate the optimum dietary protein to energy (P/E) ratio in juvenile olive flounder Paralichthys olivaceus. Eight experimental diets were formulated with two energy levels and four protein levels at each energy level. Two energy levels of 12.5 and 16.7 kJ g^?1 diets were included at crude protein (CP) levels of 25%, 30%, 35% and 45% with 12.5 kJ g^?1, and CP levels of 35%, 45%, 50% and 60% with 16.7 kJ g^?1. After 1 week of the conditioning period, fish initially averaging 8.1±0.08 g (mean±SD) were randomly distributed into the aquarium as groups of 15 fish. Each diet was fed on a dry‐matter basis to fish in three randomly selected aquariums at a rate of 3–5% of total wet body weight per day for 8 weeks. After 8 weeks of the feeding trial, weight gain (WG), feed efficiency ratio and specific growth rate of fish fed 45% CP with 16.7 kJ g^?1 energy diet were significantly higher than those from the other dietary treatments (P<0.05). WG of fish fed 12.5 kJ g^?1 energy diets increased with the increase of dietary protein levels. However, WG of fish fed 16.7 kJ g^?1 energy diets increased with the increase of dietary protein levels up to 45% CP and then decreased when fish fed 50% and 60% CP diets. Both dietary protein and energy affected protein retention efficiency and energy retention efficiency. Haemoglobin (Hb) of fish fed 35% and 45% CP diets with 12.5 kJ g^?1 energy were significantly high and not different from Hb of fish fed 45% and 50% CP diets with 16.7 kJ g^?1 energy. Haematocrit of fish fed 45% CP diet with 16.7 kJ g^?1 energy was significantly higher than those from fish fed 25% and 30% CP diets with 12.5 kJ g^?1 energy (P< 0.05). Based on the results of this experiment, we concluded that the optimum dietary P/E ratio was 27.5 mg protein kJ^?1 with diet containing 45% CP and 16.7 kJ g^?1 energy in juvenile olive flounder.     

Effects of different dietary protein and lipid levels on growth, feed utilization and body composition of red porgy (Pagrus pagrus) fingerlings

Two feeding trials were conducted to determine the minimum dietary protein level producing maximum growth, and the optimum protein to energy ratio in diets for red porgy (Pagrus pagrus) fingerlings, respectively. In the first trial, six isoenergetic diets were formulated with protein levels ranging from 400 to 650 g kg^?1 in increments of 50 g kg^?1, and fed for 11 weeks to 2.8 g average initial weight fish. Weight gain, specific growth rate and feed efficiency were significantly higher with diets containing higher protein levels, when compared with dietary levels below 500 g kg^?1. The highest protein efficiency ratios were obtained in fish fed 500 g kg^?1 dietary protein. The minimum dietary protein level producing maximum fish growth was found to be 500 g kg^?1. In the second trial, 15 g average initial weight fish were fed for 12 weeks, six diets containing three different lipid levels (100, 150 and 200 g kg^?1) combined with two protein levels (450 and 500 g kg^?1). Weight gain values increased when dietary lipids increased from 100 to 150 g kg^?1, with a further decrease for 200 g kg^?1 lipids in diets; the lowest fish growth being supported by 200 g kg^?1 dietary lipids. Fish growth was significantly higher when dietary protein increased from 450 to 500 g kg^?1. There was no evidence of a protein‐sparing effect of dietary lipids. Liver protein and lipid contents were low when compared with other fish species. All diet assayed produced high liver glycogen accumulation. The recommended protein and lipid levels in diets for red porgy fingerlings were 500 and 150 g kg^?1, respectively.     

Effect of dietary protein levels on growth,feed utilization and carcass composition of endangered bagrid catfish Horabagrus brachysoma (Gunther 1864) fingerlings

An 84‐day feeding trial was conducted to study the effect of different levels of dietary protein, 250 (P25), 300 (P30), 350 (P35), 400 (P40) and 450 g (P45) kg^?1 dry matter (DM) on growth, feed intake, feed utilization and carcass composition of bagrid catfish Horabagrus brachysoma fingerlings. Triplicate groups of fingerlings with mean initial body weight of 2.2 g were fed the experimental diets twice daily, till satiation, in 150‐L tanks supplied with flow‐through freshwater. Daily dry matter intake by the fingerlings decreased significantly (P < 0.05) when fed P25 diet, containing 250 g protein kg^?1. The highest body weight gain, specific growth rate (SGR) and protein efficiency ratio (PER), and the lowest feed conversion ratio (FCR) were observed in fish fed 350 g protein kg^?1 diet. The fish fed with P45 diet had the lowest (P < 0.05) carcass lipid content. The polynomial regression analysis indicates that H. brachysoma fingerlings require 391 g dietary crude protein kg^?1 diet.     

Effect of dietary protein content on growth performance, feed utilization and carcass composition in the Australian freshwater crayfish, Cherax albidus Clark and Cherax destructor Clark (Decapoda, Parastacidae)

Cherax albidus (A) and Cherax destructor (D) male juveniles (mean weight 0.95 ± 0.03 g) were reared for 20 weeks on isoenergetic diets containing 150 g kg^?1 protein (A 15, D15) or 300 g kg^?1 protein (A30, D30). Mean weight, percentage weight gain, and specific growth rate (%) were substantially higher for both species on the 300 g kg^?1 protein diet. Mean percentage weight gain ranged from 2.39% day^?1 (D15) to 17.59% day^?1 (A30). A maximum weight of 33.81 g was attained by C. albidus on the higher protein diet. The most effective utilization of food was observed in C. albidus when fed the higher protein diet (food conversion ratio, 0.79; protein efficiency ratio, 4.21; apparent net protein utilization, 44.64%). Carcass composition was influenced by feed type. The higher protein diet resulted in an increase in carcass protein and ash and a decrease in carcass lipid and energy relative to the low-protein diet (150 g kg^?1 protein diet –C. albidus: 37.15% protein, 15.00% lipid, 25.20% ash, 15.55kJ g^?1 energy; C. destructor: 38.10% protein, 15.43% lipid, 25.70% ash, 15.65kJ g^?1 energy; 300 g kg^?1 protein diet –C. albidus: 46.10% protein, 8.71% lipid, 27.36% ash, 14.94kJ g^?1 energy; C. destructor: 42.99% protein, 8.56% lipid, 26.44% ash, 14.71kJ g^?1 energy). Carcass moisture and calcium were not affected by feed type. The time spent in the intermoult phase of growth was highly dependent on the premoult weight and varied according to diet and to species. A comparison of animals of similar weight (< 8 g) revealed that elevated dietary protein caused a reduction in the intermoult period by 11 days in C. albidus and 7 days in C. destructor. The moult increment, however, was independent of animal weight, and the highest percentage weight increment occurred for C. albidus fed the 300 g kg^?1 protein diet (per cent weight increase; A15, 33.1%; A30, 61.3%; D15, 31.2%; D30, 56.5%). Dietary induced morphological changes were also recorded. Animals of a standard carapace length had significantly larger abdomens (both species) and larger claws (C. albidus) when fed the higher 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.     

Effect of varying dietary energy level on feed intake, feed conversion, whole-body composition and growth of Malawian tilapia, Oreochromis shiranus– Boulenger

Four isonitrogenous [30% crude protein (CP)] diets containing different gross energy levels (13.39, 16.74, 20.50 and 23.85 kJ g⁻¹) were evaluated to determine the optimum energy for the Malawian tilapia Oreochromis shiranus. Each tank (120 L) was stocked with 18 juvenile tilapia (average weight 7.32±0.25 g) and they were fed the experimental diets for 10 weeks. The final average weight of the fish was approximately twofold higher (range: 12.64–16.77 g) than the initial weight. The dietary energy significantly (P<0.05) influenced growth. The average weight of fish fed dietary energy level 20.50 kJ g⁻¹ was significantly higher (P<0.05) than the weight of the fish fed any of the other experimental diets. There was no significant difference in growth of fish fed 13.39 and 16.74 kJ g⁻¹ energy levels, but 23.85 kJ g⁻¹ produced the lowest growth rates. There were no significant differences (P>0.05) between feed intake across the treatments. Feed conversion ratio (range: 2.2–3.0) and protein efficiency ratio (range: 1.10–1.50) among the dietary treatment groups were in agreement with trends for weight gain. Dietary energy level significantly (P<0.05) influenced the body composition of O. shiranus. Whole‐body moisture (range: 64.27–67.15%) and ash (range: 13.21–14.73%) decreased in all treatments. Whole‐body protein (range: 63.57–66.16%) increased only in groups fed on the diet containing 20.50 kJ g⁻¹. Whole‐body fat (range: 13.58–17.27%) and gross energy (range: 28.411–33.210 kJ g⁻¹) increased significantly (P<0.05). Fish survival was 100% in all treatments. The results demonstrated that to maximize growth at a temperature of 23°C, O. shiranus should be fed diets containing 20.50 kJ g⁻¹ gross energy.     

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.