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

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.

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.


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.


1970 ◽  
Vol 50 (2) ◽  
pp. 363-369 ◽  
Author(s):  
J. GUILLAUME ◽  
J. D. SUMMERS

Arnould’s method can be applied to the adult rooster to estimate the energy maintenance requirement, although estimation of the weight gain requirement is inaccurate with this method. The average value obtained of 117 kcal metabolizable energy per kg body weight per day for maintenance requirement agrees well with previously reported estimates but is higher than values reported for the laying hen. Maintenance requirement for energy appears to be very variable, the coefficient of variation being 13% which equals that found for basal metabolism. Maintenance requirement is correlated neither with body weight nor with endogenous N excretion. It is concluded that metabolic and endogenous energy should be taken into account for correcting metabolizable energy values when food intake is close to maintenance requirement, especially with adult birds.


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.


2020 ◽  
Vol 4 (2) ◽  
pp. 1182-1195
Author(s):  
Claire E Andresen ◽  
Aksel W Wiseman ◽  
Adam McGee ◽  
Carla Goad ◽  
Andrew P Foote ◽  
...  

Abstract The objective of this study was to investigate the impacts of cow breed type and age on maintenance requirements, feed energy utilization, and voluntary forage intake. The main effect of breed type included Angus (ANG; n = 32) and Hereford × Angus (HA; n = 27) lactating cows. The main effect of age included 2- and 3-yr-old (YOUNG; n = 29) and 4- to 8-yr-old (MATURE; n = 30) cows. Within breed type and age class, cows were randomly assigned to 1 of 2 pens for a total of 8 pens, each housing 7 to 9 cow/calf pairs. To determine maintenance energy requirements, cows and calves were limit-fed for 105 d to body weight (BW) and body condition score (BCS) stasis. There were no differences between breeds in cow hip height, BW, average milk yield (P > 0.31), diet digestibility, or cow maintenance energy requirement (P = 0.54). Crossbred cows had greater BCS (P < 0.05) throughout the experiment. Efficiency of calf growth was not different between breeds when expressed as feed intake of the cow/calf pair nor as energy intake of the pair per unit of calf BW gain (P ≥ 0.31). Young cows produced less milk per day and per unit of BW0.75 (P < 0.01); however, there was no effect of cow age on maintenance energy requirement, diet digestibility, or efficiency of calf growth (P > 0.10). Subsequently, a 45-d experiment was conducted to determine voluntary low-quality forage intake. Cows were housed in dry-lot pens equipped with shade, windbreaks, and feed bunks with free-choice access to clean water and a chopped hay ration was provided ad libitum to determine forage intake. Daily forage intake was lower (P = 0.05) for HA compared with ANG (123 vs. 132 g/kg BW0.75, respectively) although there was no difference in BW. However, HA cows sustained greater BCS (P < 0.01). There was no difference (P = 0.60) in forage intake per unit of BW0.75 due to cow age. Results indicate similar calf growth efficiency among breed types although crossbred cows maintained greater body energy stores and consumed less low-quality forage during the voluntary intake experiment. These differences could not be attributed to lower maintenance energy requirements. Neither maintenance energy requirement nor calf growth efficiency was different between young and mature cows.


1989 ◽  
Vol 61 (1) ◽  
pp. 59-65 ◽  
Author(s):  
J. S. Chrisp ◽  
A. R. Sykes ◽  
N. D. Grace

1. Two groups of eight 6–7-month-old wether lambs were offered either a frozen ryegrass (Lolium perenne L.)-white clover (Trifolium repens L.) pasture or a ryegrass-white clover hay, containing 12.1 and 6.4 g calcium/ kg dry matter (DM) respectively. Within groups the amounts offered to individual sheep ranged from 0.5 to 2.0 times the estimated maintenance energy requirements.2. A single intravenous injection of 150 μCi 45Ca as CaCl2. 2H2O, and stable balances were used to determine absorption, faecal endogenous loss and balance of Ca.3. Faecal endogenous loss of Ca increased by 1.2 mg/kg body-weight (W) per d with each g/kg W per d increase in DM intake regardless of the diet. At any DM intake the mean faecal endogenous loss was 5.5 mg/kg W per d higher in the sheep offered the frozen herbage diet when compared with those on the hay diet. At any Ca intake the mean faecal endogenous loss was 6.9 mg/kg W higher in sheep offered the hay diet compared with those on the frozen herbage.4. At feeding levels of about 1.5–2 times the estimated maintenance energy requirement the observed faecal endogenous loss of Ca ranged from 35 to 50 mg/kg W per d, which is two- to threefold greater than the present estimate of the Agricultural Research Council (1980) of 16 mg/kg W per d.5. A simple model to explain the variation in faecal endogenous loss of Ca between the present study with young sheep and that with lactating ewes (Chrisp et al. 1989) also offered herbage diets is developed, which incorporates the concept of a true endogenous loss related to DM intake and a net endogenous loss reflecting the extent of re-absorption of Ca endogenous losses within the gastrointestinal tract.


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.


2007 ◽  
Vol 137 (5) ◽  
pp. 1171-1175 ◽  
Author(s):  
Kwang S. Ko ◽  
Robert C. Backus ◽  
John R. Berg ◽  
Michael W. Lame ◽  
Quinton R. Rogers

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