scholarly journals Energy and nitrogen intake, expenditure and retention at 20° in growing fowl given diets with a wide range of energy and protein contents

1990 ◽  
Vol 64 (3) ◽  
pp. 625-637 ◽  
Author(s):  
M. G. Macleod

Heat production (HP) and the intake and retention of energy and nitrogen were measured at 20° in growing female broiler fowl given diets with metabolizable energy (ME) contents ranging from 8 to 15 MJ/kg at each of two crude protein (nitrogen × 6.25; CP) contents (130 and 210 g/kg). ME intake was partially controlled by the birds, but increased by 30% over the range of dietary ME concentration. CP intake varied directly with dietary CP:ME ratio, indicating that control of energy intake took priority and that food intake did not increase in order to enhance amino acid intake on low-CP diets. Maintenance energy requirement and fasting HP were not affected by diet. Although the HP of fed birds was significantly affected by dietary energy source, there was no evidence for regulatory diet-induced thermogenesis as energy intake increased. Total energy retention doubled on the higher-energy diets as a result of increased intake and retention efficiency in the absence of any compensation by diet-induced thermogenesis. The proportion of energy retained as fat was negatively correlated with dietary CP:ME ratio. It was concluded that the growing female broiler fowl responded to large differences in energy intake and dietary CP concentration not by changes in rate of energy dissipation as heat but by changes in the quantity of energy retained and in the partition of retained energy between body protein and body fat.

1976 ◽  
Vol 35 (2) ◽  
pp. 201-209 ◽  
Author(s):  
P. I. Wilke ◽  
F. J. Van Der Merwe

1. Two diets, an all-roughage diet and a high-concentrate diet, were fed at two levels, a low level of estimated 1.5 times maintenance energy requirement and a higher level of estimated two times maintenance energy requirement, to South African Mutton Merino castrated male sheep, aged 13 months and in fairly lean condition at the start of the 93 d experimental period..2. Body composition and energy retention were determined using the comparative slaughter technique and two series of digestibility and balance studies were done during the course of the experiment. Metabolizability of each diet was estimated and corrected for fermentation heat using the fermentation balance approach..3. Although there were significantly different rates of energy gain on different diets and feeding levels, fat energy gained (% total energy gained) was similar for the four groups, i.e. 78–80..4. Regression of energy gain v. corrected metabolizable energy (ME) intake indicated that the maintenance energy requirements of sheep used in this experiment were 310.2 and 302.3 kJ ME/kg body-weight0.75 per d and the values for net utilization of ME for body energy gain were 0.411 and 0.479 with the roughage and concentrate diets respectively..5. It was concluded that the estimated maintenance energy requirements of sheep obtained in this study are realistic values and that the efficiency of utilization of surplus ME for the two diets did not differ significantly.


2003 ◽  
Vol 140 (4) ◽  
pp. 451-459 ◽  
Author(s):  
H. DARMANI KUHI ◽  
E. KEBREAB ◽  
S. LOPEZ ◽  
J. FRANCE

Data from six studies with male broilers fed diets covering a wide range of energy and protein were used in the current two analyses. In the first analysis, five models, specifically re-parameterized for analysing energy balance data, were evaluated for their ability to determine metabolizable energy intake at maintenance and efficiency of utilization of metabolizable energy intake for producing gain. In addition to the straight line, two types of functional form were used. They were forms describing (i) diminishing returns behaviour (monomolecular and rectangular hyperbola) and (ii) sigmoidal behaviour with a fixed point of inflection (Gompertz and logistic). These models determined metabolizable energy requirement for maintenance to be in the range 437–573 kJ/kg of body weight/day depending on the model. The values determined for average net energy requirement for body weight gain varied from 7·9 to 11·2 kJ/g of body weight. These values show good agreement with previous studies. In the second analysis, three types of function were assessed as candidates for describing the relationship between body weight and cumulative metabolizable energy intake. The functions used were: (a) monomolecular (diminishing returns behaviour), (b) Gompertz (smooth sigmoidal behaviour with a fixed point of inflection) and (c) Lopez, France and Richards (diminishing returns and sigmoidal behaviour with a variable point of inflection). The results of this analysis demonstrated that equations capable of mimicking the law of diminishing returns describe accurately the relationship between body weight and cumulative metabolizable energy intake in broilers.


1978 ◽  
Vol 40 (3) ◽  
pp. 423-431 ◽  
Author(s):  
W. H. Close ◽  
L. E. Mount ◽  
D. Brown

1. Measurements of energy and nitrogen balances were made on thirty-eight individually housed pigs (initial body-weights 21–38 kg) at environmental temperatures of 10, 15, 20, 25 and 30° with four levels of feeding at each temperature. Values for energy retention (ER), protein (P) and fat (F) deposition and body weight gain (δW) were calculated at each temperature at metabolizable energy (me) intakes equivalent to once (M; 440 kJ/kg0.75 per d), twice (2M), three (3M) and four (4M) times the thermoneutral maintenance energy requirement.2. ER at each plane of nutrition increased with temperature to maximal values between approximately 20 and 25° ER was negative at four of the five environmental temperatures at M.3. P increased significantly with increase in me intake but was dependent on environmental temperatures only at intakes of M and 2M. The increase in P per unit increment in me intake decreased from 0.16 at 10° to 0.12 at 30°. The net efficiency of protein utilization also decreased with increase in environmental temperature from 0.54 at 10° to 0.39 at 30°.4. F increased significantly with increase in me intake, but was more temperature-dependent than P, increasing to maximum values estimated to be between 20 and 25° at each level of intake; F at 30° was less than that at 25°. The increase in F per unit increment in me intake decreased from 0.63 at 10° to 0.51 at 30°.5. The optimum temperature for ΔW was dependent upon me intake, varying from above 30° at M to less than 20° at 4M. The reduction in ΔW per 1° at 15° was also dependent upon the level of intake decreasing from 1.63 g/kg0.75 per d at M to -0.09 at 4M.6. For a 35 kg pig the reduction in P, as a result of a 1° decrease in temperature at 15° at an intake corresponding to 2.5M, was equivalent to a 4 g/d reduction in food intake; the corresponding equivalent for F was 28 g/d.


1992 ◽  
Vol 67 (2) ◽  
pp. 195-206 ◽  
Author(s):  
M. G. Macleod

Heat production (HP) and the intake and retention of energy and nitrogen were measured in growing broiler fowl kept at 32° and given diets with metabolizable energy contents from 8 to 15 MJ/kg and crude protein (N × 6·25; CP) contents of 130 and 210 g/kg. The temperature of 32° was chosen for comparison with earlier measurements at 20° to minimize heat produced for the maintenance of body temperature. The effects of diet composition were observed when the same birds were taken from 20 to 32°. The tendency for energy intake to increase with dietary energy concentration was less at 32 than at 20°. The lower heat increments measured for the high-fat diets did not, therefore, confer an increased ability to sustain higher energy intake at 32°. HP was about 17% lower at 32 than at 20°; the change in HP between 20 and 32° was not significantly influenced by diet composition. The absence of significant effects of diet composition on HP, combined with the significant trend in energy intake, produced significant differences (related both to dietary energy and dietary protein concentrations) in total energy retention and in the partition of retained energy between protein and fat. As at 20°, variation in energy retention and in the composition of retained energy were the main responses to variation in dietary CP concentration and energy intake; a significantly higher energy cost of unit protein accretion on the low-CP diets was insufficient to produce an elevation in total HP because the higher unit energy cost was balanced by a lower absolute rate of protein accretion.


1984 ◽  
Vol 51 (3) ◽  
pp. 379-387 ◽  
Author(s):  
H. Gillian Barr ◽  
K. J. Mccracken

1. Male, Sprague-Dawley (Charles-River) rats, of initial weight 272 g, were given a powdered stock diet (T1) ad lib. force-fed a synthetic diet (T2) or offered a range of palatable foods in conjunction with the powdered stock diet (T3) or a similar diet supplemented with certain minerals and vitamins (T4).2. Metabolizable energy (ME) intake (kJ/d) averaged 303, 453, 402 and 383 for T1, T2, T3 and T4 respectively and corresponding weight gains were 5.5, 6.9, 8.2 and 7.9 g/d and were significantly different (P < 0.001).3. The intakes of T3 and T4 rats ranged from 10 to 60% above the mean value for T1.4. Crude protein (CP; nitrogen × 6.25) retentions were similar for T1, T3 and T4 rats and significantly lower (P < 0.01) for T2 rats. Fat retentions were 1.1, 4.1, 2.9 and 2.4 g/d for T1 to T4 respectively (P < 0.001).5. The energy contents of the gain (MJ/kg) were 12.7, 26.0, 16.7 and 14.9 for T1 to T4 respectively (P < 0.001) and energy retentions (kJ/d) were 70, 179, 139 and 117 respectively (P < 0.001).6. A linear regression of energy retention (ER) on ME yielded a slope of 0.78 and a mean energy requirement for zero balance of 510 kJ/kg body-weight0.75.7. These results are in conflict with reports of ‘diet-induced thermogenesis’ in ‘cafeteria’-fed rats.


1970 ◽  
Vol 37 (3) ◽  
pp. 481-491 ◽  
Author(s):  
F. J. Gordon ◽  
T. J. Forbes

SummaryEight lactating cows were used in a Latin square experiment, to study the associative effects of level of energy and protein intake on milk yield and composition. Four diets were used, supplying 80 and 120% of estimated energy requirements and 80 and 120% of estimated protein requirements. The level of energy intake significantly affected milk yield, milk energy output, percentage butterfat, ash and non-protein nitrogen. The level of protein intake only significantly affected milk energy output and the non-protein nitrogen content of the milk. Although only the interaction of the effects of energy and protein intake on the milk content of solidsnot-fat (SNF) and ash was significant, it was evident that the effect of each of these factors on milk yield or composition was related to the level of the other in the diet.Input-output relationships within each protein level were used to compute the response in milk energy output and bodyweight change to a change in energy intake. These showed a greater partitioning of additional energy toward milk energy output with the high than with the low protein level. Multiple regression analysis within each level of protein intake was used to partition energy intake between that used for maintenance, milk energy output and liveweight change. The results showed efficiencies of utilization of metabolizable energy for milk output of 63 and 50% on the high- and low-protein diets, respectively.Nitrogen balance data are presented.


1999 ◽  
Vol 133 (4) ◽  
pp. 409-417
Author(s):  
D. E. KIRKPATRICK ◽  
R. W. J. STEEN

An experiment was carried out in 1994 to examine energy and nitrogen utilization of lambs offered two contrasting grass-based diets. The two forages, which were from the same parent herbage, were grass silage and grass which was conserved by freezing. They were offered as sole diets or supplemented with either 250 or 500 g concentrates per kg total dry matter intake (DMI) to give a total of six experimental treatments. Seventy-two Dutch Texel × Greyface (Border Leicester × Blackface) lambs, consisting of 36 males which were initially 36 (S.D. 4·9) kg liveweight and 36 females which were initially 34 (S.D. 2·5) kg liveweight were used. Ensiling significantly increased apparent digestibility of dry matter, energy and nitrogen (P<0·001), but had no significant effect on methane energy loss as a proportion of gross energy intake, metabolizable energy intake (MEI), heat production, energy retained, efficiency of utilization of energy for growth (kg) or nitrogen retention. Supplementation of forage with concentrates resulted in a curvilinear decrease in heat production expressed as a proportion of MEI (P<0·05) and a linear increase in energy retention, expressed as an absolute value or as a proportion of MEI (P<0·05). Supplementation of forage tended to increase kg when calculated using Agricultural Research Council estimates of maintenance energy requirements, but had no significant effect when alternative estimates of maintenance were used. It is concluded that ensiling had no effect on efficiency of utilization of energy or nitrogen as measured by indirect calorimetry.


1978 ◽  
Vol 40 (3) ◽  
pp. 433-438 ◽  
Author(s):  
W. H. Close

1. From the relation between metabolizable energy (me) intake and heat loss (H), energy retention (ER), protein (P) and fat (F) deposition the energy costs of maintenance (MEm) and the partial efficiencies of energy retention (k) and protein (kp) and fat (kf) retention were determined in growing pigs at environmental temperatures of 10, 15, 20, 25 or 30°.2. k decreased with increase in environmental temperature from 0.79 at 10° to 0.63 at 30° with 0.67 at the thermally-neutral temperature of 25°. Each 0.04 decrease in k was associated with a 100 kJ/kg0.75 per d decrease in mem Analysis, within several ranges of environmental temperature, suggested a curvilinear relation between ER and me intake indicating a decrease in k with increase in level of feeding, particularly at thermally-neutral temperatures.3. Both kp and kf were similar at each environmental temperature and decreased from 0.78 at 10° to 0.63 at 30°. These values are discussed in relation to those predicted from experimentation and it is suggested that the wide range of predicted estimates of kp could be attributed to differences in the rate of protein turnover.


1972 ◽  
Vol 23 (1) ◽  
pp. 57 ◽  
Author(s):  
BA Young ◽  
JL Corbett

Grazing pressure on three pastures was adjusted so that the mean liveweights (W) of three groups of 10 Merino wethers, initially uniform, were kept at nominally 45, 35, and 25 kg. Daily rates of energy expenditure were calculated by measuring the respiratory gaseous exchanges of tracheostomized sheep in each group, and from estimates of CO2 entry rate determined during constant infusion with NaH14CO3. These measurements were made during a period of 3 weeks when the sheep had been at constant W for 9 months, and during a further 3 weeks beginning 30 days after the sheep were shorn. Further measurements were made in two periods of 7 days after animals had been interchanged between groups so that W was increasing in some animals and decreasing in others. Maintenance requirements of all sheep, indicated by the energy expenditures during the periods at constant W, were described by the equation M = 45.1 W + 256, where M is the estimated metabolizable energy requirement in kilocalories per 24 hr. Similar results were obtained during the two periods when W was changing. The requirements were in general 60–70% greater than those for housed sheep of similar W and are discussed in relation to the climatic environment, the condition of the sheep, and the availability of herbage.


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