The maintenance requirement of the adult sheep

1926 ◽  
Vol 16 (2) ◽  
pp. 325-333 ◽  
Author(s):  
T. B. Wood ◽  
J. W. Capstick

In attempting to interpret the results of two series of sheep feeding experiments, we have been confronted with the fact that the sum of the accepted figure for maintenance requirement and the allowance for the live weight increase produced does not account for the whole of the ration consumed. Sheep averaging 100 lb. live weight folded on swedes in the winter usually eat per week at least 100 lb. of swedes, 7 lb. of hay and 3½ lb. of cake and corn. Such a ration supplies per week about 11½ lb. of starch equivalent.Sheep fed in this way normally put on per week about 2 lb. of live weight increase, starting from store condition. It is true that figures for the composition of the live weight increase put on by store sheep are somewhat scanty, being practically confined to a series of analyses by Kern and Wattenberg (Journ. Landw. 1880) which give the composition of the live weight increase of store sheep as 44 per cent, water, 45 per cent. fat and 11 per cent, protein, which corresponds to 2200 calories or 2 lb. of starch equivalent per lb.The requirement for producing 2 lb. of such increase would therefore be 4 lb. of starch equivalent per week.Measurements of the maintenance requirement of sheep are likewise scanty. There are no recent measurements, but Armsby has recalculated the experiments of Henneberg, Kellner, Hagemann and Wolff, the most recent of which were made in 1893. These workers used two methods. The more scientific method of estimating by respiration experiments the storage of fat on a known ration and arriving at the maintenance requirement by deduction was used by Henneberg, Kellner and Hagemann. Recalculating and averaging their results, which differ widely, Armsby arrives at an average figure of 719 calories per day of net energy for the maintenance requirement of the 100 lb. sheep.

1926 ◽  
Vol 16 (3) ◽  
pp. 425-442 ◽  
Author(s):  
T. B Wood

The facts and considerations set out above provide the information necessary to enable an intelligent pig-keeper to compute on a logical and scientific basis a series of rations which from the energy point of view will produce any desired rate of live weight increase within the capacity of his animals. It is however necessary to make the reservation that the data apply strictly only to pigs of the Large White breed kept under good conditions and liberally fed.It should also be noted that the method can only be applied to animals of known age and weight.The method is applied as follows:1. From the age of the animals read off from the basal metabolism chart, Fig. 1, the intensity of the basal metabolism per square metre per hour.2. From the live weight—surface chart, Fig. 2—read off the surface area in square metres corresponding to the animal's live weight.3. Multiply the basal metabolism per square metre per hour by the area of the animal's surface in square metres. The product multiplied by 24 gives the basal metabolism of the animal per day.4. To get the practical maintenance requirement add to the basal metabolism per day 1000 calories to allow for an average amount of muscular effort.5. Decide the growth rate in pounds of live weight increase per day at which it is desired to aim. The growth rate curve, Fig. 4, will help in assessing this figure.6. Read off from Fig. 3 the calorie value per lb. of live weight increase corresponding to the live weight of the animals under consideration, and multiply the figure there found by the desired live weight increase in lb. per day. This will give the productive ration in calories per day.7. The total ration is then found by adding together the maintenance requirement estimated in 4 above and the productive ration estimated in 6 above. This gives the total ration in calories of net energy.8. Transform calories of net energy into lb. of meal on the assumption that 1 lb. of meal supplies to the pig 1000 calories, or preferably that 1 lb. of starch equivalent supplies 1500 calories.


1915 ◽  
Vol 7 (2) ◽  
pp. 137-141
Author(s):  
Charles Crowther

In an earlier issue of this Journal, Robinson and Halnan have communicated the results of a statistical analysis of three sets of pig-feeding experiments from which they conclude that “the probable error of one animal in a pig-feeding experiment is in the region of 10 per cent, of the average live-weight increase.”


1921 ◽  
Vol 11 (3) ◽  
pp. 275-286 ◽  
Author(s):  
Reginald Arthur Berry ◽  
Daniel Grant O'Brien

The probable error on one pig calculated on the average daily live weight increase was found to be for cross-bred pigs about 7 per cent.; for pure-bred pigs from the same litter and each of similar live weight about 3 per cent.; for cross-bred pigs each of similar live weight but from different parents about 4 per cent.The error is greatest in experiments of short duration and it decreases as the period of the experiment is lengthened. The decrease is slight if the experiment is prolonged beyond seven weeks.The errors on 18 separate pens containing four pigs to each pen (the total initial live weight of each pen being similar) varied from 2·3 per cent, to 12·08 per cent., the average being 6·21 per cent.The percentage probable error is relatively low when the pigs are fattening rapidly and high when the pigs are fattening slowly. The average daily increase of the quicker fattening female pigs when un-speyed appears to be depressed as a result of periodic sexual disturbances.The stage of fattening does not appear to influence the probable error. Animals in the later stages of fattening show a greater range in their rate of fattening than animals in the early stages, see Fig. 2, p. 284.Weekly weighing of individual pigs is recommended as it gives an indication of the health of each pig. It also enables each experimenter to discriminate between differences in the rate of fattening due to individuality and differences due to ill health, etc.The rate of fattening of pigs is very variable, periods of rapid fattening are followed by periods of depression.


1933 ◽  
Vol 23 (4) ◽  
pp. 580-614 ◽  
Author(s):  
George Dunlop

The unsatisfactory nature of the methods adopted in feeding experiments at Animal Nutrition Research Institutes has been shown to be due to the neglect of the worker to control variable factors, other than those being investigated, which affect the growth rate of his animals.It has been proved that age, sex (females and castrated males), condition and previous growth rate have no effect on the rate of live-weight increase of swine in the Cambridge University herd, and the basis on which animals are allotted to groups to ensure homogeneity is fallacious.


1958 ◽  
Vol 195 (3) ◽  
pp. 654-658 ◽  
Author(s):  
F. W. Hill ◽  
L. B. Carew ◽  
A. van Tienhoven

Increased fat production in diethylstilbestrol-treated chicks was found to be due primarily to increased energy consumption and to a lesser extent to preferential synthesis of fat at the expense of protein tissue. This was shown in experiments comparing normal and estrogen-treated male chicks with respect to gains in live weight, fat and protein at two planes of nutrition, and the yield of metabolizable and productive (net) energy which they obtained from the diet. It was found that the fattening effect could not be due to increased digestibility, increased net energy yield from absorbed nutrients, or lowered heat production. Under the influence of estrogen, total tissue gain expressed in Calories was increased, and was composed of greater fat gain and lower protein gain. Tissue energy gains were a linear function of metabolizable energy consumption. This relationship predicted equal tissue energy gains under pair-feeding conditions, which was confirmed experimentally.


1963 ◽  
Vol 5 (1) ◽  
pp. 11-16 ◽  
Author(s):  
J. P. Langlands ◽  
J. L. Corbett ◽  
I. McDonald ◽  
G. W. Reid

SUMMARYThe mean daily digestible organic matter intake (D) of each of 47 adult sheep during a grazing period of mean length 48 days was estimated by the chromium sesquioxide/faecal nitrogen technique. Mean live-weights (W) and mean daily weight gains (G) were also measured.The regression of D on W and G, and the underlying or functional relationship between D, W and G were both estimated. From the underlying relationship, the preferred equation, the maintenance requirement of a 100 lb. sheep at pasture is estimated to be 1·02 lb. digestible organic matter daily. This value is 24% higher than the corresponding value for housed sheep obtained previously by us.This result is compared with other estimates of the energy cost of grazing and it is concluded that further work is needed in order to define those circumstances which elevate the maintenance requirements of grazing animals.


2002 ◽  
Vol 75 (3) ◽  
pp. 459-468 ◽  
Author(s):  
L. E. R. Dawson ◽  
A. F. Carson ◽  
L. O. W. McClinton

AbstractAn experiment was undertaken to compare the productivity of crossbred ewes, produced by crossing Texel sires with Rouge de l’Ouest (Rouge) dams and Rouge sires with Texel dams, relative to purebred Texel and Rouge ewes. The purebred and crossbred ewes were crossed with Rouge and Texel sires. The proportion of productive ewes was similar in the purebred and crossbred ewes with an average figure of 0·92. Irrespective of crossing sire, Rouge ewes produced 0·48 more lambs per ewe lambed than Texel ewes (P < 0·001). The two crossbred ewe types (Texel ✕ Rouge and Rouge ✕ Texel) each produced similar numbers of lambs (on average 1·92 lambs per ewe lambed). Individual heterosis values for ewe fertility and prolificacy were small and not significant (–1·67 for the proportion of productive ewes and –3·14 for the number of lambs born per ewe lambed). Maternal heterosis values were also not significant but were of larger magnitude (6·26 for ewe fertility and 3·12 for prolificacy). Lamb mortality (number of lambs born dead per ewe lambed) at birth was similar for purebred Rouge (0·44) and Texel (0·30) ewes and was significantly reduced by crossbred matings and mating the crossbred ewes (individual heterosis –30·68, P < 0·10; maternal heterosis –80·23, P < 0·001). Individual and maternal heterosis values for lamb growth rate from birth to six weeks were 8 (P < 0·05) and 4 (P > 0·05) respectively. Lamb growth rate from birth to weaning was significantly lower in lambs from Texel ewes compared with those from the other genotypes (P < 0·05). Individual and maternal heterosis values for live-weight gain from birth to weaning were 5 (P < 0·10) and 5 (P < 0·01). The results of the current study demonstrate the superior performance of purebred Rouge ewes compared with purebred Texel ewes in terms of prolificacy and lamb growth rate from birth to weaning. However, both breeds had high lamb mortality at birth. Crossbreeding led to the production of hybrid ewes which had relatively high prolificacy with low levels of dystocia and lamb mortality.


1998 ◽  
Vol 7 (3) ◽  
pp. 381-390 ◽  
Author(s):  
Jarmo Valaja ◽  
Hilkka Siljander-Rasi

A digestibility and balance trial was carried out with four intact castrated male pigs (live weight 33-82 kg) to study the effects of dietary crude protein and energy content on nutrient digestibility, nitrogen metabolism, water intake and urinary output. In a 4 x 4 Latin square design, four barley-oats-soya bean meal based diets were arranged 2x2 factorially. The corresponding factors were dietary crude protein (CP) content: high (180 g/kg CP) or low protein diet (140 g/kg CP) supplemented with free lysine, methionine and threonine; and dietary net energy content; high (1.05 feed units (FU)/kg) (feed unit=9.3 MJ net energy) or low net energy content (0.95 FU/kg). Lowering dietary CP content (mean values of 189 to 152 g/kg dry matter, respectively) by supplementation of free amino acids decreased urinary nitrogen (N) excretion by 6.9 g/day (32%) (P


1996 ◽  
Vol 1996 ◽  
pp. 149-149
Author(s):  
P.H. Simmins ◽  
J.P. Braund ◽  
A. Laurie ◽  
J. Pinasseau ◽  
J. Weigel

The potential reduction in nitrogenous excretion by growing pigs, through the reduction of protein levels in diets, has not been consistently achieved without compromising performance. This may have been due to inadequate formulation of the diets. Formulation on the basis of the total amino acid content of feed ingredients may limit the nitrogen retention, and hence the rate of protein accretion (Lee et al., 1993). Therefore, the objective of the experiment reported here was to evaluate the nitrogen balance of pigs fed diets at two levels of protein, formulated on the basis of true ileal digestibility of the essential amino acids (Rhône-Poulenc Animal Nutrition, 1993) and the net energy available from the raw materials (Noblet et al., 1994).


1964 ◽  
Vol 6 (3) ◽  
pp. 357-362 ◽  
Author(s):  
F. X. Vanschoubroek ◽  
R. L. Van Spaendonk ◽  
W. Nauwynck

Six comparable groups, each of 4 castrate pigs, were used to compare the feed value of maize and sorghum as estimated by live-weight gain, food conversion efficiency, slaughter quality and ham composition.The maize ration contained 40% yellow maize and the sorghum ration 40% Sorghum vulgare subglabrescens, all other ingredients being the same for both diets.No statistically significant differences were found between the maize and sorghum pigs with regard to the criteria mentioned.It is concluded that no difference exists between the feed value of the maize and the sorghum used. This result is in better agreement with the net energy values of maize and sorghum as calculated by the formula of Hoff-mann and digestion coefficients for pigs, than with “classical” starch equivalents.


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