The effects of plane of nutrition and environmental temperature on the energy metabolism of the growing pig

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.

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.


1978 ◽  
Vol 40 (3) ◽  
pp. 413-421 ◽  
Author(s):  
W. H. Close ◽  
L. E. Mount

1. The heat losses and energy balances of thirty-eight individually housed pigs (initial body-weights 21–38 kg) were measured continuously for periods of 14 d when they were maintained at environmental temperatures of 10, 15, 20, 25 or 30°. At each temperature four levels of feeding were given approximating to once, twice and three times the maintenance energy intake and the ad lib. level. The minimal maintenance energy requirement (M) was calculated to be 440 kJ metabolizable energy (me)/kg0.75 per d at 25°.2. me intake at the ad lib. level decreased from 1965 kJ/kg0.75 per d at 10° to 1202 at 30°.3. Heat loss calculated from multiple regression analysis decreased to minimum levels between 20 and 25° 30° was within the hyperthermic zone at each plane of nutrition.4. The partition of heat loss into its sensible and evaporative components showed that evaporation increased from 25% at 10° to 78% at 30°.5. Critical temperature was dependent upon food intake and decreased from 23.1° at M to 20.7° at 2M, 18.0° at 3M and 16.7° at 4M.6. The extra food required to meet extra thermoregulatory heat production per 1° below the effective critical temperature was 0.65 g/kg body-weight per d.


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.


1988 ◽  
Vol 110 (3) ◽  
pp. 531-541 ◽  
Author(s):  
A. R. Sykes ◽  
D. P. Poppi ◽  
D. C. Elliot

SummaryNinety 4-month-old wether lambs were allocated to an initial slaughter group (n =10) or to one cell (n= 5) of a 4 × 4 factorial treatment design involving four levels of infection with Ostertagia circumcincta (0, 1000, 2000 and 4000 larvae/day) and Trichostrongyluscolubriformis (0, 1000, 2000 and 3000 larvae/day). They were maintained indoors in individual pens and offered freshly cut ryegrass-white clover herbage during an 84-day period of infection after which they were slaughtered. Body protein, fat, water, Ca and P contents were determined. Feed digestibility was determined in all sheep during 5-day periods during weeks 2, 5, 8 and 11. Faecal egg counts were determined and blood samples obtained at intervals and total worm counts done at slaughter.The effects of mixed infection on feed intake and body-weight gain were multiplicative. Mean D.M. intake of sheep infected simply with 3000 larvae of T. colubriformis or with 4000 larvae of O. circtimcincta was reduced by 10 and 8% respectively, but in those infected simultaneously intake was reduced by 30%. Energy retention was depressed mainly by reduction in gross efficiency of use of metabolizable energy in infections with T. colubriformisand by reduction in feed intake in infections with O. circumcincta. The additional effect of mixed infection occurred mainly through further depression in feed intake.There was no interaction between infections in effect on deposition of Ca or P in the body, both species having significant effect. Infection with T. colubriformis caused hypophosphataemia and hypocalcaemia, but infection with O. circumcincta had no effect.The number of worms established by the infections was generally low compared with previous studies with conserved and concentrate feeds. This was associated with relatively low pathogenicity in infection with O. circumcincta and normal pathogenicity with T. colubriformis.Infection with T. colubriformis reduced the number of adult worms of O. circumcincta present at slaughter.


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.


1984 ◽  
Vol 38 (2) ◽  
pp. 221-231 ◽  
Author(s):  
W. H. Close ◽  
M. W. Stanier

ABSTRACT1. Measurements of heat loss, energy and nitrogen balance were made on 18 groups of piglets weaned at 2 weeks, at environmental temperatures of 18, 23 and 28°C, and at three levels of feeding at each temperature.2. From the experimental results, values of heat loss, energy retention, protein and fat deposition were derived for each temperature, at each of the three levels of metabolizable energy (kJ/kg M0·75 per day) intake: 550 (1·0MEm), 825 (1·5MEm) and 1100 (2·0MEm). The lowest of these levels was the calculated thermoneutral maintenance energy requirement (MEm).3. From the results the following deductions were made, (a) Heat loss varies with both environmental temperature and metabolizable energy intake, and at an intake of 2·0MEm is minimal between 23 and 28°C. Energy retention varies in an inverse manner to heat-loss, and at 1·0MEm is negative at all environmental temperatures below 28°C. (b) Protein and fat deposition increase significantly with increase in metabolizable energy intake (P < 0·05), with fat deposition being more dependent on temperature than protein deposition. The mean increase in protein deposition per 1°C increase in environmental temperature is 2·05 kJ/kg M0·75 per day. Fat deposition is negative at all temperatures at l·0MEm; at l·5MEm it is zero at 23°C and negative at temperatures below this.4. Critical temperature was calculated to decrease from 26·9°C at l·0MEm to 23·9°C at 2·0MEm.5. The efficiency of energy utilization (k) was 0·58 at 18°C, 0·81 at 23°C and 0·74 at 28°C. The corresponding values of the maintenance energy requirements were 739, 615 and 550 kJ/kg M0·75 per day. Estimates of the energetic efficiency of protein deposition (kp) of 0·60 to 0·65, and of fat deposition (k/) of 0·82 to 0·86, were determined at 23 and 28°C.


1980 ◽  
Vol 44 (3) ◽  
pp. 313-323 ◽  
Author(s):  
J. Le Dividich ◽  
M. Vermorel ◽  
J. Noblet ◽  
J. C. Bouvier ◽  
A. Aumaitre

1. Six experiments each involving two groups of six piglets, were designed to study the influence of environmental temperature on heat production, energy retention and protein and fat gain in early weaned piglets. Immediately after weaning, at a mean age of 25 d, the animals were raised in two open circuit respiratory chambers. Each chamber was equipped with a totally wired cage. The piglets were paired-fed and maintained at environmental temperatures of 20, 24 or 28°. Four replicates were used for each temperature. Metabolizable energy, heat production and nitrogen balance were measured during two consecutive periods (A and B), each of 6 d duration.2. Heat production was higher at 20° than at 24 and 28° during periods A and B. Energy retention was negative during period A, it was positive during period B and increased with temperature.3. Protein deposition was always positive and independent of environmental temperature. The net efficiency of protein utilization was 0.77.4. Body fat was mobilized during period A at a higher rate at 20° than 28°. During period B, fat gain increased with increase in temperature.5. The calculated ME requirement for maintenance amounted to 411 kJ/kg body-weight0.75 per d at 28°.6. The critical temperature of early weaned piglets raised in intensive modern housing and fed at about 90% of the ad lib. intake is close to 28° during the first 12 d after weaning.


1987 ◽  
Vol 45 (3) ◽  
pp. 345-348 ◽  
Author(s):  
E. R. Ørskov ◽  
G. W. Reid ◽  
C. A. G. Tait

ABSTRACTThirty-two Friesian cows in early lactation were divided into four treatment groups to receive ad libitum a mixed diet consisting of silage (0·70) and grain-based concentrate (0·30). Fish meal was subsequently mixed into the diet at levels of 0, 40, 80 and 120 g/kg to provide crude protein concentration (g/kg dry matter) in the complete diets of 156, 181, 200 and 212 respectively. In the 2nd week after calving the yields of fat-corrected milk (FCM) were 28·5, 29·2, 32·0 and 34·9 kg/day for the four levels respectively; at this time, food intake was sufficient only to meet the calculated energy requirement for 15 kg FCM per day. Due to recurring problems with ketosis on the diet containing 120 g fish meal per kg, this treatment was terminated and the experiment continued for 15 weeks with the groups receiving 0, 40 and 80 g/kg fish meal supplements. During this time average yields of FCM were 23·5, 25·6 and 28-0 kg FCM per day respectively and energy intakes were calculated to be sufficient to meet the requirement for 18 kg FCM per day.It appeared possible to increase milk yield by stimulating fat mobilization through giving undegraded protein supplements to underfed cows in early lactation. However, when an excessive mobilization occurred with a high supplement, and when the animals were yielding 15 to 20 kg FCM more than their metabolizable energy intake was calculated to sustain, some cows became ketotic.


1969 ◽  
Vol 72 (3) ◽  
pp. 479-489 ◽  
Author(s):  
D. W. F. Shannon ◽  
W. O. Brown

SUMMARYExperiments to determine the net availabilities of the metabolizable energy (NAME) of a cereal-based diet and a maize-oil diet for maintenance and lipogenesis and the effect of environmental temperature on the NAME of the cereal-based diet are described. Four 1- to 2-year-old Light Sussex cockerels were used.The relationship between ME intake and energy retention was linear for each diet. The NAME'S of the cereal-based diet given at 22° and 28 °C (70.6 ± 1.83 % and 73.6 ± 3.54%, respectively) were significantly (P < 0.05) lower than the NAME of the maize-oil diet (84.1 ± 1.85%). It is concluded that the beneficial effect of maize oil on the efficiency of energy utilization is due to a reduced heat increment rather than a reduction in the basal component of the heat production. The higher efficiency from the maize-oil diet led to an increase in the energy retained as fat.The mean fasting heat production at 28 °C was 15 % lower than at 22 °C (43.2 ± 1.45 and 51.2 ± 1.09 kcal/kg/day, respectively). The NAME of the cereal-based diet was not significantly different when the birds were kept at 22° or 28 °C. The lower metabolic rate at 28 °C was reflected in a lower maintenance requirement and in an increase in the deposition of body fat.


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.


Sign in / Sign up

Export Citation Format

Share Document