scholarly journals Changes of Growth Rate and Energy Retention Related to Metabolizable Energy Intake in Weaned Piglets

1993 ◽  
Vol 64 (7) ◽  
pp. 741-747
Author(s):  
Hiroshi HATA ◽  
Tooru KOIZUMI
1997 ◽  
Vol 64 (3) ◽  
pp. 485-492 ◽  
Author(s):  
M. R. Sanz Sampelayo ◽  
I. Ruiz Mariscal ◽  
F. Gil Extremera ◽  
J. Boza

AbstractThe efficiency of utilization of protein for retention was analysed in pre-ruminant kid goats of the Granadina breed. Sixty male kids were used. Six were slaughtered at birth and the remaining 54 were offered different protein and fat intakes using nine different milk replacers. The protein concentrations were 200, 240 and 280g/kg dry matter (DM) and those of fat were 200, 240 and 280 g/kg DM. Animals were maintained on experiment until they were 60 days old. All were slaughtered on day 61. Nitrogen (N) balance trials were performed during the last 8 days of the 1st and 2nd months. Body composition of the animals slaughtered at birth and at 61 days were determined. Rates of energy retained as protein and as fat were determined (kJ/kg M0·75 per day) and the corresponding rates of metabolizable energy intake as protein and as fat (kJ/kg M0·75 per day) estimated.Once the relationships between the rates ofN retained and those of digestible N ingested had been established, it was evident that by increasing the protein content of the diet the efficiency of protein retention was decreased. In contrast, increasing the fat content of the milk replacer increased the efficiency of protein retention. The latter effect was noted for the milk replacers containing the high and medium levels of protein but not for those that contained the lowest level of protein, indicating that the level of protein was then the limiting factor. Having recorded this protein-sparing effect of the fat, the results obtained from the slaughter trials were used to develop generalized equations expressing the rates of energy retention in the form of protein or fat as a function of the rates of metabolizable energy intake achieved as both protein and fat. From the analysis of these equations conclusions are drawn about the variable contribution to protein retention in these animals of energy ingested as fat. This contribution depended on the energy intake achieved both in the form of protein and in the form of fat.


1998 ◽  
Vol 131 (4) ◽  
pp. 477-485 ◽  
Author(s):  
L. E. R. DAWSON ◽  
R. W. J. STEEN

Metabolizable energy intake and heat production were measured in a series of calorimetry experiments carried out at the Agricultural Research Institute of Northern Ireland, Hillsborough, between 1993 and 1996 with beef cattle and sheep. A total of 75 estimates were made with cattle: 23 with Charolais cross steers; 16 with Simmental cross steers and 36 with Angus cross steers (450–628 kg liveweight). Fifty-six estimates were made with lambs: 24 with Blackface cross, eight with Suffolk cross and 24 with Texel cross (23–53 kg liveweight). The diets offered to both cattle and sheep contained proportionately 0·0–0·8 cereal-based concentrates, the remainder being grass silage. Linear regressions of energy retention (measured by calorimetry) against metabolizable energy intake were produced for the cattle and sheep studies. From these linear regressions an estimate of metabolizable energy required for maintenance (MEm) was obtained. For cattle, the derived MEm was 0·614 MJ/kg LW0·75 per day, and for sheep the derived MEm was 0·460 MJ/kg LW/kg LW0·75 per day. The estimates were proportionately 0·34 higher in cattle and 0·32 higher in sheep than the 1990 values of the UK Agricultural and Food Research Council.


The Auk ◽  
2001 ◽  
Vol 118 (2) ◽  
pp. 519-524 ◽  
Author(s):  
Avner Anava ◽  
Michael Kam ◽  
Amiram Shkolnik ◽  
A. Allan Degen

Abstract Arabian Babblers (Turdoides squamiceps) are territorial, cooperative breeding passerines that inhabit extreme deserts and live in groups all year round. All members of the group feed nestlings in a single nest, and all group members provision at similar rates. Nestlings are altricial and fledge at about 12 to 14 days, which is short for a passerine of its body mass. Because parents and helpers feed nestlings, we hypothesized that the growth rate of nestlings is fast and that they fledge at a body mass similar to other passerine fledglings. Using a logistic growth curve, the growth rate constant (k) of nestlings was 0.450, which was 18% higher than that predicted for a passerine of its body mass. Asymptotic body mass of fledglings was 46 g, which was only 63% of adult body mass, a low percentage compared to other passerines. Energy intake retained as energy accumulated in tissue decreased with age in babbler nestlings and amounted to 0.29 of the total metabolizable energy intake over the nestling period. However, energy content per gram of body mass increased with age and averaged 4.48 kJ/g body mass. We concluded that our hypothesis was partially confirmed. Growth rate of babbler nestlings was relatively fast compared to other passerine species, but fledgling mass was relatively low.


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 31 (3) ◽  
pp. 279-289 ◽  
Author(s):  
C. W. Holmes ◽  
J. R. Carr ◽  
G. Pearson

ABSTRACTFour diets which varied in crude protein concentration from 140 to 240 g crude protein per kg dry matter were given to gilts in experiment 1, and two diets containing 140 and 200 g crude protein per kg dry matter were given t o boars and barrows in experiment 2. Two levels of feeding were offered in both experiments and energy and nitrogen balances were measured at 30 and 90 kg live weight in both experiments, and also at 50 kg in experiment 1. Nitrogen intake had a small negative influence on energy retention by pigs of all sexes, an effect which was independent of the large positive effect of metabolizable energy intake. The ratio of metabolizable energy concentration to digestible energy concentration decreased in association with increases in crude protein concentration of the diets. The results show that comparisons of feeds on the basis of their digestible energy concentrations would lead to overestimation of the energy values of those containing high protein concentrations. Live weight (or age) and metabolizable energy intake exerted positive influences on the amount of energy retained per kg live-weight gain, whereas nitrogen intake exerted a negative influence. Values for energy retained per kg live-weight gain predicted from multiple regression equations, together with calculated values for maintenance and net efficiency, were used to predict the energy retention and growth rate of pigs in various circumstances.Nitrogen retention increased in association with increases in nitrogen intake for pigs of all sexes at 30 kg live weight; there was also a corresponding increase for boars at 90kg live weight, but not for gilts or barrows at this weight. Boars retained more nitrogen than did barrows at 30 and 90 kg live weight only if given the diet with the higher concentration of protein.Metabolizable energy intake appeared to exert a small positive influence on the nitrogen retention by pigs of all sexes at 90kg live weight; however, it appeared to have no influence on nitrogen retention by pigs at 30kg live weight.


1979 ◽  
Vol 29 (2) ◽  
pp. 245-255 ◽  
Author(s):  
D. J. Thomson ◽  
S. B. Cammell

ABSTRACTA primary growth crop of perennial ryegrass (cv. S24), containing 17% crude protein and 9·9 MJ metabolizable energy/kg dry matter, was artificially dried, ground through a 3·0 mm screen and pelleted either without further treatment (C), or after the application of formaldehyde (T) at a rate of 1 g/100 g crude protein. The C and T diets were each fed to 20 lambs for 77 days. Diets C and T were given ad libitum and at three lower planes of nutrition. Similar amounts of dry matter, nitrogen and digestible energy were consumed at each of the four planes of nutrition by lambs fed diets C and T. Carcass energy, fat and protein retention, and total body energy retention were measured by the comparative slaughter technique and did not differ between the diets (P> 0·05). Metabolizable energy intake was calculated from digestible energy intake using the factor 0·81. The efficiency of utilization of the metabolizable energy for growth and fattening (kf) and the net energy value were calculated by linear regression analysis from the total body energy retention, the calculated metabolizable energy intake and dry-matter intake data scaled to M0·75. They did not differ between the diets (P > 0·05), and were 0·370 (C) and 0·431 (T) for kf, and 2·09 (C) and 1·97 MJ/kg dry matter (T) for net energy.


2015 ◽  
Vol 99 (6) ◽  
pp. 1025-1030 ◽  
Author(s):  
M. Thes ◽  
N. Koeber ◽  
J. Fritz ◽  
F. Wendel ◽  
B. Dobenecker ◽  
...  

2002 ◽  
Vol 138 (2) ◽  
pp. 221-226 ◽  
Author(s):  
A. ALLAN DEGEN ◽  
B. A. YOUNG

Body mass was measured and body composition and energy requirements were estimated in sheep at four air temperatures (0 °C to 30 °C) and at four levels of energy offered (4715 to 11785 kJ/day) at a time when the sheep reached a constant body mass. Final body mass was affected mainly by metabolizable energy intake and, to a lesser extent, by air temperature, whereas maintenance requirements were affected mainly by air temperature. Mean energy requirements were similar and lowest at 20 °C and 30 °C (407·5 and 410·5 kJ/kg0·75, respectively) and increased with a decrease in air temperature (528·8 kJ/kg0·75 at 10 °C and 713·3 kJ/kg0·75 at 0 °C). Absolute total body water volume was related positively to metabolizable energy intake and to air temperature. Absolute fat, protein and ash contents were all affected positively by metabolizable energy intake and tended to be related positively to air temperature. In proportion to body mass, total body water volume decreased with an increase in metabolizable energy intake and with an increase in air temperature. Proportionate fat content increased with an increase in metabolizable energy intake and tended to increase with an increase in air temperature. In contrast, proportionate protein content decreased with an increase in metabolizable energy intake and tended to decrease with an increase in air temperature. In all cases, the multiple linear regression using both air temperature and metabolizable energy intake improved the fit over the simple linear regressions of either air temperature or metabolizable energy intake and lowered the standard error of the estimate. The fit was further improved and the standard error of the estimate was further lowered using a polynomial model with both independent variables to fit the data, since there was little change in the measurements between 20 °C and 30 °C, as both air temperatures were most likely within the thermal neutral zone of the sheep. It was concluded that total body energy content, total body water volume, fat and protein content of sheep of the same body mass differed or tended to differ when kept at different air temperatures.


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