Influence of metabolizable energy content of the diet and of feeding level on lamb performances. I. growth and body composition

1982 ◽  
Vol 9 (4) ◽  
pp. 471-485 ◽  
Author(s):  
M Theriez ◽  
Y Villette ◽  
C Castrillo
1977 ◽  
Vol 89 (3) ◽  
pp. 759-765 ◽  
Author(s):  
V. K. Cilly ◽  
G. N. Lodhi ◽  
J. S. Ichhponani

SummaryExperiments were made to assess the nutritive value of expeller-proeessed mustard cake (MS) for egg-type and meat-type chicks. Eight samples of MS on average contained 37·2% crude protein, 27·5% true protein, 12·6% available carbohydrate and 2·09 % tannins. The average metabolizable energy content (ME) of eight samples of MS for egg-type and meat-type chicks were 2350 and 2300 kcal/kg respectively. MS in the diet replacing groundnut cake (GN) which formed 30–32 % of the control diets was found to have no effect on growth rate of the chicks of either breed although there was thyroid enlargement. MS was also found not to affect the body composition of the chicks.


1985 ◽  
Vol 53 (2) ◽  
pp. 251-265 ◽  
Author(s):  
J. Noblet ◽  
W. H. Close ◽  
R. P. Heavens ◽  
D. Brown

1. Twenty-six gilts were used in an experiment to study the effects of level of feed intake on the growth and chemical composition of the gravid uterus and mammary tissue at several stages of gestation. The animals were given either 1.8 or 2.5 kg feed/d (20 or 30 MJ metabolizable energy (ME) respectively) and were slaughtered at intervals between days 40 and 110 of gestation. The gravid uterus was dissected into fetal, placental, fluid and empty uterus components. From day 70 of gestation the mammary tissue was also dissected. The fresh weight and dry matter (DM), energy and nitrogen contents of the various tissues were determined.2. (a) With the exception of the fluid component, there was a significant increase (P < 0.01) in the fresh weight of each tissue with both stage of gestation and level of feeding. At comparable litter sizes the total weight of the fetuses in late gestation was 16% higher with the higher feed intake. (b) The DM content of the individual uterine tissues increased significantly (P < 0.01) with increase in stage of gestation so that the mean DM content of the gravid uterus increased from 74.6g/kg at day 50 to 103.1 and 159, 0g/kg at days 90 and 110 of gestation respectively. (c) Neither stage of gestation nor feeding level influenced the respective energy contents of the individual uterine tissues, when expressed per g DM. The mean energy content of the total gravid uterus was 19.5 kJ/g DM. (d) The N content (g/g fresh weight) of the tissues increased with stage of gestation and was generally higher at the higher feeding level. The mean N contents (g/g DM) of the fetal, placental, fluid and empty uterine tissues were 0.090, 0, 101, 0.098 and 0.128 respectively.3. The mammary tissue was the most variable of all the tissues investigated. Whereas the fresh weight and N content increased with stage of gestation, both the DM and energy content decreased.4. Gompertz equations were fitted to describe the effects of stage of gestation, level of feed intake and litter size on the fresh weight and chemical content of the individual uterine tissues, total gravid uterus and mammary tissue. The use of these equations for calculating the nutrient requirements of pregnancy is demonstrated.5. It was calculated that between days 50 and 110 of gestation the ME requirement for reproduction increased from 3 to 12% of maternal energy intake. The calculated requirement for protein was from 7 to 41 % of maternal dietary protein intake respectively.


1976 ◽  
Vol 86 (2) ◽  
pp. 411-423 ◽  
Author(s):  
E. R. Ørskov ◽  
I. McDonald ◽  
D. A. Grubb ◽  
K. Pennie

SummaryAbout sixty male lambs were fed ad libitum from 6 weeks of age on low- or highprotein diets based on barley or barley and fishmeal and containing respectively 120 and 200 g crude protein/kg dry matter. Some lambs were changed from one diet to the other when they reached 28 kg live weight. All were slaughtered as they attained a predetermined series of live weights ranging from 20 to 75 kg.Throughout the experiment, rates of live-weight gain were substantially higher with the high-protein (HP) than with the low-protein (LP) diet, but were highest after a change from low to high protein (LHP). The feed consumption of the LHP lambs did not exceed that of the HP lambs, but the former showed a substantial superiority in feed conversion ratio at the same live weight.At similar empty body weights, the LP lambs contained more fat and less water in the empty body than the HP lambs. Although the percentage differences decreased at higher weights, differences were still apparent at 70 kg live weight.The LHP lambs showed dramatic and rapid changes in body composition, particularly in water and fat content. By 40 kg live weight, their composition approached that of the HP lambs.The ratio of water to protein was consistently lower for the LP lambs. The ratio of protein to ash also differed between LP and HP lambs. It was initially highest for the HP lambs, at about 40 kg live weight it was the same, and at 70 kg live weight it was highest for the LP lambs.The ash content of the LHP lambs remained virtually constant during the period of rapid growth and rapid deposition of water, protein and fat which took place immediately after the change of diet, and only showed compensatory increases after 35 kg live weight. This finding was supported by the pattern of changes in weight and specific gravity of the femur and tibia + fibula.Use was made of separate relationships between live weight and body composition for the LP, HP and LHP lambs to estimate rates of accretion of crude protein, fat and water in the empty body. There was a particularly striking increase in the rate of accretion of water immediately following the change of diet. There was an increase in the water content of empty-body gain and a reduction in the ratio of gain in fat to gain in protein.Derived estimates of the ratio of metabolizable energy intake above maintenance to the energy content of empty-body gain gave some suggestion of an improvement in efficiency of utilization of metabolizable energy for gain following the change from low to high protein. It is concluded however that the improvement in food conversion ratio following the change is attributable mostly to difference in the composition of gain.


2020 ◽  
Vol 33 (10) ◽  
pp. 1624-1632
Author(s):  
Ting Yang ◽  
Lexiao Yu ◽  
Min Wen ◽  
Hua Zhao ◽  
Xiaoling Chen ◽  
...  

Objective: A total of three hundred unsexed ducks were utilized to estimate net energy requirements of maintenance (NEm) and weight gain (NEg) for 2 to 3-week-old Cherry Valley ducks and to establish a model equation to predict NE requirements using the factorial method.Methods: To determine the apparent metabolizable energy (AME) of the diet, fifty 7-day-old ducks at approximately equal body weights (BWs) were randomly assigned into five groups that were fed at different levels (ad libitum, 85%, 75%, 65%, and 55% of ad libitum intake), and the endogenous acid-insoluble ash as indigestible marker. The two hundred and fifty 7-day-old ducks were used for a comparative slaughter experiment. At the beginning of the experiment, ten ducks were sacrificed to determine the initial body composition and energy content. The remaining ducks were randomly assigned into five groups (same as metabolic experiment). Ducks of the ad libitum group were slaughtered at 14 and 21-dayold. At the end of the experiment, two ducks were selected from each replicate and slaughtered to determine the body composition and energy content.Results: The results of the metabolizable experiment showed AME values of 13.43 to 13.77 MJ/kg for ducks at different feed intakes. The results of the comparative slaughter experiment showed the NEm value for 2 to 3-week-old Cherry Valley ducks was 549.54 kJ/kg of BW0.75/d, and the NEg value was 10.41 kJ/g. The deposition efficiency values of fat (Kf) and crude protein (Kp) were 0.96 and 0.60, respectively, and the values of efficiency of energy utilization (Kg) and maintenance efficiency (Km) were 0.75 and 0.88, respectively.Conclusion: The equation for the prediction of NE requirements for 2 to 3-week-old Cherry Valley ducks was the following: NE = 549.54 BW0.75+10.41 ΔW, where ΔW is the weight gain (g).


1962 ◽  
Vol 41 (2) ◽  
pp. 445-456 ◽  
Author(s):  
J.I. McIntosh ◽  
S.J. Slinger ◽  
I.R. Sibbald ◽  
G.C. Ashton

2011 ◽  
Vol 169 (1-2) ◽  
pp. 140-145 ◽  
Author(s):  
E. Loyra-Tzab ◽  
L.A. Sarmiento-Franco ◽  
C.A. Sandoval-Castro ◽  
R.H. Santos-Ricalde

1997 ◽  
Vol 127 (4) ◽  
pp. 579-586 ◽  
Author(s):  
David J. Baer ◽  
William V. Rumpler ◽  
Carolyn W. Miles ◽  
George C. Fahey

2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 84-85
Author(s):  
Luis O Tedeschi

Abstract The understanding of how nutrition influences the body composition of growing animals has fascinated researchers for centuries. It involves the expertise of scientists with different areas of knowledge, encompassing the composition of the diet and its nutritive value to the fermentation and digestion of substrates to the absorption and metabolism of nutrients, and finally, to the deposition of fat, protein, and minerals in body tissues. The comparative slaughter technique is the preferred method to assess the body composition of growing and finishing animals. However, the methodological procedures are labor-intensive, expensive, and time-consuming, facilitating the incidence of errors and inconsistencies of the measurements that are collected, including the initial animal’s body composition. First, retained fat and protein (RP) are used to compute retained energy (RE). Then, RP and RE are used to compute protein and energy requirements for growth. Heat production, calculated from the metabolizable energy (ME) intake for animals at maintenance, is used to compute maintenance requirements. Three areas of concern exist for this approach: 1) the efficiencies of possible mobilization of fat and protein tissues during the feeding period are unaccounted for, especially for the animals fed near the maintenance level of intake; 2) the correlation between observed and predicted RP when using predicted RE is higher than when using observed RE (0.939 vs. 0.679); and 3) the disconnection when predicting partial efficiency of use of ME for growth using the proportion of RE deposited as protein — carcass approach — versus using the concentration of ME of the diet — diet approach. These concerns raised questions about the interdependency between predicted RP and RE and the existence of internal offsetting errors that may prevent overall adequacy in predicting energy and protein requirements of beef cattle.


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