Energy requirement of laying japanese quail

1. Two feeding experiments were conducted to determine the meta‐bolisable energy (ME) requirement of laying Japanese quail. Birds were fed to provide 5.5 g protein and 167, 209, 251 or 293 kJ ME/d.

2. As ME intake increased from 167 to 293 kJ egg production increased.

3. Quadratic relationships between ME intake and egg production, ME intake and egg weight, and ME intake and egg mass (g egg/ bird d) were derived and used to determine the energy required for an acceptable production rate.

4. To maintain a production of 8.3 g egg/bird d (90 eggs/100 bird d with a mean weight of 9.3 g) required 260 kJ ME/bird d.     

The effect of rapeseed meal on the energy metabolism of laying hens

1. The effect of 100 g rapeseed meal (RSM)/kg diet on the energy metabolism of hybrid laying hens was examined by indirect calorimetry. Thyroid hormone concentrations, thyroid weight, liver weight and body weight, egg production and food intake were also measured. 2. Fasting heat production was significantly lower in hens receiving RSM than in controls, but this difference disappeared when the birds were fed. 3. Thyroid hormone concentrations decreased, while thyroid and liver weights increased slightly; none of these effects was significant. Body weight, egg production and food intake were unaffected and no liver haemorrhages were noted. 4. The maintenance metabolisable energy (ME) requirement of control and treated birds, estimated from short-term energy balance measurements, was 474 kJ/kg0.75 d; net availability of ME in both treatments was 0.85.     

Influence of energy intake on growth and utilisation of dietary protein and energy in germ-free and conventional chicks

The effect of metabolisable energy (ME) intake on the growth and utilisation of dietary protein and energy in germ-free (GF) and conventional (CV) chicks was investigated in two experiments. In experiment 1 a high energy diet (HED, 14.8 kJ ME/g) and a marginally-adequate energy diet (AED, 11.7 kJ ME/g) were fed to the GF and CV chicks at 240 g/2 birds/10 d. In experiment 2 a diet with 13.7 kJ ME/g was fed at 118 g (low level, LL) or 128 g (high level, HL)/bird/10 d. Body weight gain, protein retention and protein retention rate were similar in GF and CV chicks on both AED and HED in the first experiment, but in the second were higher in GF than in CV chicks. The increased ME intake of the CV chicks in experiment 2 may be too small to compensate for the increased requirement. ME intake was significantly higher in the CV chicks than in the GF chicks, whereas energy retention was similar in both groups.     

Decreasing egg weight by energy or protein restriction and energy required for repletion 1

1. A diet containing 110 g crude protein/kg caused smaller losses in egg weight, numbers and body weight in Babcock B300 layers than diets containing 90 g protein/kg, 6.56 MJ ME/kg or 7.90 MJ/kg.

2. The sequence of repletion of depleted birds was body weight, egg weight and egg number. For the first alone more than 420 kJ/d was required, for body weight and egg weight more than 630 kJ/d and for all three more than 1170 kJ/d.     

Effect of Energy and Protein on Performance,Egg Components,Egg Solids,Egg Quality,and Profits in Molted Hy-Line W-36 Hens

An experiment was conducted to determine the influence of dietary energy on performance, egg composition, egg solids, egg quality, and profits of Hy-Line W-36 hens fed different protein levels. The experiment was designed as a 4 × 3 factorial arrangement with 4 added dietary energy levels (0, 79, 158, and 238 kcal of ME/kg) and 3 protein levels (14.89, 16.06, and 17.38%). The basal diets of 17.38, 16.06, and 14.89% protein contained 2,751, 2,784, and 2,815 kcal of ME/kg, respectively. This study lasted 12 wk. Molted Hy-Line W-36 hens (n = 1,440) in phase 1 (70 wk of age) were randomly divided into 12 treatments (8 replicates of 15 hens per treatment). Protein had a significant effect on egg production, egg mass, feed intake, feed conversion, egg weight, percentage of egg shell components, yolk color, and yolk and albumen weight. As dietary energy increased from 0 to 238 kcal of ME/kg by addition of poultry oil, feed intake linearly decreased. Increasing dietary energy also significantly increased BW and egg yolk color. As dietary energy increased, percentage yolk solids increased at the 2 greater dietary protein levels, whereas egg-specific gravity linearly decreased at the 17.38% protein level. Increasing dietary energy and protein significantly improved feed conversion. Increasing protein intake significantly increased albumen and yolk weight but had no influence on yolk, albumen, or whole egg solids. Because feed ingredient and egg prices vary, there can be no fixed ideal dietary energy level for optimal profits during molt phase 1 (70 to 81 wk).     

Digestible lysine requirement for growing Japanese quails

A total of 1,000 one-day-old Japanese quails were distributed at random, with 5 digestible lysine levels, in 10 replicates and with 20 birds per experimental unit. The basal diet was formulated based on corn and soybean, with 200.6 g CP/kg, 2900.00 kcal/kg ME, and 8.8 g digestible lysine/kg. This basal diet was supplemented with L-lysine HCl (784 g/kg), replacing glutamic acid, and corresponding to digestible lysine levels of 8.8 g/kg, 9.8 g/kg, 10.8 g/kg, 11.8 g/kg, and 12.8 g/kg. The increase in the levels of digestible lysine produced a greater weight gain in birds with up to 12.2 and 12.1 g of lysine/kg at 40 d of age. Carcass weight increased as levels were increased to up to 11.85 g of lysine/kg, and, similarly, egg production per bird housed increased up to 12.03 g of lysine/kg. A linear increase took place in the growing phase for feathering, fat, and crude protein deposits in the carcass, feed intake, and lysine intake. Egg production and egg mass per bird per d increased linearly in the laying phase with the weight gain of birds decreasing linearly until 100 d of age, and, similarly, the feed conversion per egg mass linearly improved in function of the lysine levels. A level of 11.85 g of digestible lysine/kg in the diet, which corresponded to a lysine intake of 120.5 mg/bird/d, provided better carcass weight at the end of the growing phase and better performance at the beginning of the laying phase for the Japanese quails.     

Self-selection of dietary protein and energy by turkey breeder hens

1. An experiment was conducted to determine the effects of self-selection of dietary protein and energy by turkey hens on reproductive performance in a warm environment. 2. Dietary self-selection had no significant effect on egg production, egg weight, or body weight of turkey hens. 3. Fertility and hatchability of eggs produced by self-selecting hens were significantly reduced compared to eggs from control hens fed on a complete diet. 4. Protein intake was significantly reduced among self-selecting hens when compared to control hens fed on a complete diet (P less than or equal to 0.001). 5. Food and energy intake decreased as the ambient temperature increased. Nevertheless, protein intake of self-selecting hens increased over the course of egg production despite decreasing food intake. Therefore, self-selecting hens preferred a diet with a greater protein content (g protein/kg diet) in the last 10 weeks of egg production than during the first 10 weeks of egg production.     

Model for predicting egg output and metabolisable energy intake of laying pullets.

1. The data compiled by Marsden and Morris (1987) to examine the relationships between environmental temperature and the long-term, adapted responses of laying pullets were divided at random into two subsets of 99 and 113 observations. The first subset was used to estimate regression coefficients for an econometric model, and the second subset to validate the model. 2. Equations to predict inputs (costs) and outputs (returns) were estimated with a three-stage least-squares regression model. Three stage least-squares estimation is a technique which corrects for the simultaneity of variables within the model and correlation across equations of the model. This results in more efficient estimates of the regression coefficients. 3. The final output and output equations were: MEI = 253.86-190.31EM+5.766EM2-0.546EM3 + 0.7034T-0.004388T3 + 695.08BW-120.23BW2 + 397.37ME-13.132ME2-1.06MEXT; R2 = 0.86; EO = 119 + 0.025MEI -0.0000045MEI2-1.462T-0.0791T2-135.3BW + 38.31BW2-1.483T X BW + 0.0288T2 X BW + 0.673 delta BW; R2 = 0.59 where MEI = daily metabolisable energy intake (kJ/bird d), T = environmental temperature (degree C), EO = egg output (g/bird d), BW = body weight, and ME = metabolisable energy concentration (kJ/g). The values for R2 indicate very good fits considering that the data were recorded over a 26-year period in 14 different laboratories. 4. This statistical model can serve as the basis for an econometric model of egg production to determine the environmental temperature that maximises profits from laying pullets of different body weights.     

Effect of inclusion of sugar beet pulp,pelleting and season on laying hen performance

1. The effect of three metabolisable energy (ME) concentrations 12.2, 11.3 and 10.5 MJ ME/kg and two forms of diet (mash and pellet) on egg production in summer and winter were studied. The different ME values were obtained by diluting the 12.2 MJ ME/kg diet with sugar beet pulp of 2.88 MJ/kg DM. In a 3rd summer experiment the water intake of hens on these diets was examined. Data were analysed by factorial analysis of variance, and the relationship between performance and dietary energy concentration was examined by regression analysis.

2. The use of low energy diets (10.5 to 11.3 MJ ME/kg) decreased egg production in both seasons, but pelleting diets improved egg production and egg weight in summer. Egg weight was not affected by energy density in winter, but decreased in the summer when energy density increased.

3. In winter, food consumption was not affected by the dietary ME, while in summer food consumption increased when the dietary ME increased. Therefore, energy intake was not the same at all energy densities, but tended to increase as the energy density increased.

4. In summer, pelleting improved food efficiency and egg production and increased water consumption and the ratio of water to food intake. Water intake and water: food ratio decreased with increasing dietary energy concentration.     

Dietary methionine requirement of the Chinese egg-laying duck

1. The dietary methionine requirement of egg-laying ducks was assessed by feeding diets supplemented with graded levels of DL-methionine (0, 4, 8, 12, 16 g/kg dietary protein) for 8 weeks. The basal diet contained 175 g protein and 2.6 g methionine per kg feed (or 14.9 g/kg protein) and an estimated ME of 11.5 MJ/kg. 2. A total of 800 Shaoxin laying ducks (420 d old) were randomly divided into 5 groups of 160 each and fed in 4 separate pens. 3. Dietary supplementation of methionine significantly increased egg production and feed conversion efficiency. 4. Dietary methionine requirement for optimum egg production was estimated to be 25.7 g/kg of dietary protein or 4.5 g/kg of the diet or 380 mg/bird-d. 5. Methionine supplementation increased the methionine level in plasma, and the free glutamic acid and aspartic acid concentrations in plasma were quadratically related to dietary methionine levels. Increasing dietary methionine had little effect on egg quality characteristics.     

Food intake of normal and internal layers: a question of energy balance

1. Normal adult laying hens, which produced 41 g egg/hen d, ate 30 g/hen d more of a pelleted diet than did hens of the same age which were induced to lay eggs internally by surgical treatment of their oviducts. This implied that 0.336 MJ metabolised energy was required to produce 0.251 MJ egg, or 75% efficiency of utilisation of ME. 2. This may not have represented the true cost of egg production because both normal and internal layers gained weight during testing, at slightly different rates, suggesting that they did not regulate energy balance precisely. 3. The internal layers were less active and also saved energy by resorbing egg material. Their greater body weight was due to unresorbed eggs and to heavier fat deposits, which were accompanied by higher concentrations of lipid in the blood. 4. It was estimated that internal layers ate 4 to 5% more per day than was required to maintain the same lipid status as normal layers; these data provide further evidence that poultry do not regulate their food intake precisely by energostatic or lipostatic means.     

Use of limited daily access to food in measuring the heat production associated with food intake in laying hens

1. Two experiments were carried out to determine the heat production associated with food intake in laying hens allowed access to food for one (experiment 2) or two hours (experiment 1) daily. 2. In experiment 1, heat production in the fed state was measured for two successive days after 46 h of food deprivation. The rate of heat production in the fasting state was measured from 47 to 69 h after feeding. 3. In experiment 2, heat production was measured at 4 fixed food intakes: 100, 70, 40 and 0 g/bird. Heat production associated with food intake, eating activity, net availability of ME and maintenance ME requirement was estimated. 4. Heat production after 46 h of food deprivation did not differ from that after 22 h of deprivation. In the hens receiving 100 g of food, heat production reached the pre-feeding level by 20 h after eating; the hens with lower food intakes reached the pre-feeding level more rapidly. It is suggested that the heat production associated with feeding had been eliminated by 22 h after eating. 5. Heat production associated with feeding was 16% of ME intake. Because the total energy cost of eating activity was only 0.8% of ME intake, the heat production associated with food intake in the limited-access hens came mainly from the effects of digestion, absorption and metabolism of the ingesta. 6. The net availability of ME was estimated to be 0.84. The estimated maintenance ME requirement was 569.6 kJ/kgW0.75 d.     

Protein and energy self-selection by turkey hens: reproductive performance

1. The influence of protein and energy self-selection on the reproductive performance of turkey hens was investigated. Large White turkey hens were fed on either a complete diet (185 g CP/kg, 11.30 MJ ME/kg) or were provided with a choice between a high protein-low energy diet (348 g CP/kg, 7.74 MJ ME/kg) and a high energy-low protein diet (81 g CP/kg, 13.39 MJ ME/kg). 2. Egg production, egg weight, and the fertility and hatchability of eggs produced were not significantly affected by the dietary treatments (P greater than 0.05). 3. While energy intake was not significantly different between groups, protein consumption decreased by approximately 40% (P less than or equal to 0.001) among self-selecting hens compared to hens fed on the complete diet. This resulted in a 10% (P less than or equal to 0.05) reduction in the food intake in the self-selecting birds.     

Comparison between concentrated complete diets and self‐selection for feeding sexually‐maturing pullets at hot and cold temperatures

1. Pullets in late growth and early lay were maintained at hot (25° to 35°C) or cold (6° to 16°C) ambient temperatures and either fed complete diets or allowed to self‐select nutrients from separate energy‐ and protein‐rich foods.

2. Manipulating the metabolisable energy (ME) and/or nutrient density (ND) of complete layer diets failed to improve egg output at hot temperatures to that obtained at cold temperatures.

3. At both temperatures self‐selection increased protein, but not ME, intake. This increased egg output and body weight gain at the hot, but not cold, temperatures. At the hot temperatures pullets fed by self‐selection were the only ones to gain weight between sexual maturity and 28 weeks of age.

4. Nutrient intake patterns, related to each pullet's physiological age of sexual maturity, identified distinctive changes in protein intake and the selected protein: ME intake ratio of pullets fed by self‐selection. Pullets attempted to maintain a preferred protein:ME intake ratio, irrespective of the markedly different intakes of ME and protein at the two temperatures.

5. Pullets trained to self‐select nutrients from separate energy‐ and protein‐rich foods are better able to sustain egg output and body weight at sexual maturity when food intake is limited by high ambient temperatures.     

Influence of dietary energy, supplemental fat and linoleic acid concentration on performance of laying hens at two ages

1. The aim of this study was to investigate the influence of metabolisable energy (ME), supplemental fat (SFAT) and linoleic acid (LIN) content of the diet on the productive performance and weight of eggs and egg components of Isabrown hens of 22 or 74 weeks of age. 2. Six diets were formulated to contain the following concentrations of ME (MJ/kg), SFAT (g/kg) and LIN (g/kg), respectively: A) 11.8, 0 and 11.5; B) 11.8, 40 and 11.5; C) 11.8, 40 and 16.5; D) 11.2, 40 and 16.5; E) 11.2, 40 and 11.5; and F) 11.2, 0 and 11.5. Data were collected for 28 d and analysed using linear contrasts to test the effect of SFAT, LIN, ME and their interactions. 3. When the LIN content of the diets was maintained constant at 11.5 g/kg, an increase in the SFAT from 0 to 40 g/kg increased egg weight (63.8 vs 64.5 g; P<0.05), food intake (119 vs 124 g; P<0.01) and energy intake (1.36 vs. 1.42 MJ/d; P<0.01) and body weight change of the hens (-85 vs. 27 g; P<0.001). Supplemental fat also increased yolk (15.8 vs. 16.3 g; P<0.001) and albumen weight (40.8 vs. 42.3 g; P<0.01) but yolk to albumen ratio was not modified. 4. Egg and albumen weights were improved by SFAT in early but not in late producing hens. As a result, yolk to albumen ratio decreased in the younger hens, from 0.371 to 0.357, but increased in the older hens, from 0.408 to 0.415; P<0.01) with fat addition. 5. An increase in the LIN content of the diets from 11.5 to 16.5 g/kg did not modify any of the traits studied. 6. It was concluded that the LIN requirement of the hens for maximal productivity and weight of eggs is 11.5 g/kg or less. Supplemental fat increased the weight of eggs and albumen in the younger but not in older hens and the beneficial effect was independent of its LIN content.     

The effect of increasing photoperiod and food restriction in sexed broiler-type birds. I. Growth and abdominal fat cellularity.

1. Sexed broiler-type chicks were raised either under a continuous (CON) 23 h Light (L) and 1 h Dark (D) schedule or an increasing photoperiod (INC) consisting of an initial 6 h L and 18 h D which increased by 4 h L per week from 14 to 35 d of age after which a 23 L:1D was maintained to 49 d of age. 2. From 5 to 11 d of age birds were fed either: ad libitum (AL), energy intake (kJ ME) restricted to 9.414 x gBW0.67 (R1) or energy intake (kJ ME) restricted to 6.276 x gBW0.67 (R2). Food intake was ad libitum at all other times. 3. Food restriction reduced growth to 49 d of age although some compensatory growth did occur. Food efficiency was not significantly affected by restriction. 4. Although abdominal fat pad weight was significantly reduced for R2 compared to AL, this was not significant on a percentage body weight basis. 5. Adipocyte number in the abdominal fat pad was similar for AL, R1 and R2, but concomitant with a smaller fat pad weight, R2 showed reduced adipocyte volume compared to AL. 6. INC birds were lighter at 21 d of age, but body weights were equivalent to CON by 42 d of age. 7. Abdominal fat pad weight was some 10% larger at 49 d of age for INC birds. Adipocyte volume was unaffected, the increase in adipocyte being entirely caused by an increase in adipocyte number in INC birds.     

Feed intake and weight gain of growing goats fed diets of various energy and protein levels

Growing goats, 45 Alpine and 45 Nubian, were used in a 3 x 3 factorial arrangement to quantify the influence of dietary energy and protein levels on daily DM intake and nutrient utilization for growth. Goats had ad libitum access to complete mixed diets containing either 2.46, 2.77 or 3.05 Mcal/kg ME plus 11.2, 12.7 or 15.1% CP for 16 wk. Dry matter intake decreased curvilinearly as dietary ME density increased (P less than .001). Dry matter intake increased linearly (P less than .05) as dietary CP level increased during all growth intervals except wk 25 to 28 of age. Average daily gain was 115, 113 and 99 g/d for goats fed diets containing 2.46, 2.77 and 3.05 Mcal/kg ME, respectively. Average daily gain was 104, 106 and 117 g/d for goats fed diets with 11.2, 12.7 and 15.1% CP, respectively. Dry matter intake was higher (P less than .01) for Alpine than for Nubian goats, whereas ADG was similar between breeds. Intake of ME was 248, 260 and 198 kcal/(kg.75.d) for goats fed the low- medium- and high-energy diets, respectively. Intake of CP was 9.1, 10.7 and 13.2 g/(kg.75.d) for goats fed low-, medium- and high-protein diets, respectively. Average requirements for growth derived from regression analysis of all data points were 4.6 kcal ME and .26 g CP/g ADG. The prediction equation for intake of growing goats of 4 to 8 mo of age was: DMI, g/d = 1,749 - 496 DE, kcal/g + 18 live weight, kg + 3 ADG, g/d; r2 = .73 (Sy.x = 127, P less than .0001, n = 90). The requirement of ME for growth was 33% lower than the value recommended in 1981 by the National Research Council.     

Effect of dietary energy,protein, and a versatile enzyme on hen performance,egg solids,egg composition,and egg quality of Hy-Line W-36 hens during second cycle,phase two

This study was conducted to evaluate the effect of Rovabio, dietary energy, and protein on performance, egg composition, egg solids, and egg quality of commercial Leghorns in phase 2, second cycle. A 4 × 2 × 2 factorial arrangement of treatments comprising 4 dietary energy levels (2,791, 2,857, 2,923, and 2,989 kcal of ME/kg) and 2 protein levels (15.5 and 16.1%) with and without Rovabio was used. Hy-Line W-36 hens (n = 1,920, 87 wk old) were randomly divided into 16 dietary treatments (8 replicates of 15 hens per treatment). The trial lasted 12 wk. Dietary protein significantly increased feed consumption but decreased yolk color. As dietary energy increased from 2,791 to 2,989 kcal of ME/kg, feed consumption decreased from 98.0 to 94.9 g per hen daily, and yolk color increased from 5.27 to 5.56. There was a significant interaction among dietary protein, energy, and Rovabio on egg production, BW, egg mass, feed conversion, and yolk solids. Egg weight of hens fed the diets supplemented with Rovabio was significantly greater than that of hens fed the diets without Rovabio during wk 3 and 4. However, Rovabio did not significantly influence average egg weight (87 to 98 wk of age). Rovabio supplementation significantly increased BW of hens. These results suggest Rovabio had a small but significant influence on nutrient utilization of commercial Leghorns during phase 2 of the second cycle.     

Energy intake and milk production in mink (Mustela vison)--effect of litter size.

Energy intake and milk production were measured in 12 mink dams raising litters of 3, 6 and 9 kits one to four weeks post partum by means of balance experiments and measurements of milk intake of the kits by the water isotope dilution technique. The dams were fed ad libitum on a conventional wet mink diet (DM: 323 g/kg; CP: 173 g/kg; ME: 4.4 MJ/kg). Milk samples collected from dams with corresponding litter sizes and lactation weeks, and body composition of kits nursed by these dams, were analysed for content of DM, ash, N and fat. The ME and drinking water consumption were higher in dams nursing 9 kits than in dams nursing 3 kits. The N and water balances as well as the live weight of dams were not affected by litter size. Daily milk production was higher in dams nursing 9 kits than in dams nursing 3 kits. The DM, N and fat content of the milk increased during lactation, but were not affected by litter size. Individual kit live weight was higher in litters of 3 than in litters of 6 and 9 kits four weeks post partum. The DM and fat content of the kits were lowest in kits from litters of 9 kits, whereas these kits had the highest protein content. Daily ME for maintenance of kits and the efficiency of utilisation of ME in milk for body gain were estimated to 356 kJ/kg0.75, kp approximately 0.53 and kf approximately 0.71, respectively. In conclusion, daily milk production increased with increasing litter size, but not in proportion to the number of kits, indicating that milk production limits the growth rate of the young. In the fourth week of lactation, milk production was not different between dams nursing 6 or 9 kits, indicating a maximum capacity.     

Quantitative influence of lysine and energy intake on yield of milk components in the primiparous sow.

A regression approach was used to assess quantitatively the influence of lysine and ME intake during lactation on yield of milk components and to determine whether this influence was mediated through precursor metabolite concentrations in the blood. The influence of lysine and energy intake on sow weight and backfat loss also was analyzed by linear regression. Twenty-three primiparous Landrace x Yorkshire sows were fed one of nine corn-soybean meal diets to achieve a matrix of lysine (15, 30, or 45 g/d) and ME (6.5, 11.5, or 16.5 Mcal/d) intakes. Sow BW and backfat losses were found to be predominantly controlled by ME intake (P less than .02), with no response to lysine intake (P greater than .92). Lysine and ME intake explained a smaller portion of the variability in milk component yield on d 8 (R2 less than .34) than on d 22 (R2 = .64 to .78), evidence that dietary effects of milk production increased as lactation progressed. Lysine and ME intake had an interactive influence (P less than .05) on yield of all milk components except lactose, demonstrating that the amount of lysine required to maximize milk production increased as ME intake increased. Strong relationships between diet and most blood precursor metabolite concentrations (R2 = .5 to .7) were detected on d 22. No obvious relationships between precursor metabolite concentrations and milk component yield (R2 = .05 to .2) were observed. These results describe quantitatively the prominent interactive effects of lysine and ME intake on yield of milk components and demonstrate that these effects are not directly associated with changes in precursor pool concentrations.