The intensive rearing of lambs 2. Voluntary food intake and performance on diets of varying oat husk and beef tallow content

1967 ◽  
Vol 9 (4) ◽  
pp. 509-520 ◽  
Author(s):  
J. B. Owen ◽  
D. A. R. Davies ◽  
E. L. Miller ◽  
W. J. Ridgman
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Beef Tallow ◽  
Live Weight ◽  
Physical Form ◽  
Intensive Rearing ◽  
Pelleted Diet ◽  
And Performance ◽  
Oat Husk ◽  
The Relationship

1. Two experiments concerned with the voluntary intake of food by artificially reared lambs are described and the results discussed.2. When the diets were pelleted the addition of finely ground oat husks to form as much as 40% of the diet had practically no effect on live weight gain since the lambs controlled their consumption to achieve the same energy intake on the various diets. When the diets were given as a meal, the addition of 20% oat husks caused food intake to increase, digestible dry-matter intake to remain the same and growth rate to be somewhat poorer; but the addition of 40% oat husks caused no further increase in intake so that digestible drymatter intake fell markedly and growth rate was much reduced. It is argued that the relationship between food intake and digestibility is dependent on the physical form of the diet.3. Addition of beef tallow to the meal diets had very little effect on the lambs' performance.4. Lambs which had received a restricted quantity of milk replacer from birth to 11·4 kg live weight had a slower growth rate and poorer food conversion efficiency during the subsequent feeding period (13·6–34·1 kg) than lambs which had received milk ad libitum. This effect was greater with meal diets containing 40% oat husks than with more concentrated diets.5. On a pelleted diet containing 85% barley a conversion ratio of 3·21 was achieved over the whole fattening period, indicating the commercial feasibility of intensive lamb production on cereal diets.

Milk-fed calves: 3. The milk intake, herbage intake and performance of suckled calves

1976 ◽  
Vol 87 (1) ◽  
pp. 205-211 ◽  
Author(s):  
Y. L. P. Le Du ◽  
R. D. Baker ◽  
J. M. Barker
Keyword(s):  
Growth Rate ◽  
Milk Production ◽  
Live Weight ◽  
Milk Intake ◽  
Milk Consumption ◽  
Herbage Intake ◽  
Consequent Effect ◽  
And Performance ◽  
The Relationship ◽  
Friesian Cows

SUMMARYTwo trials were conducted to measure the herbage intake of South Devon cross calves suckling Hereford × Friesian cows and to test the validity of applying the relationships established between milk and herbage intake and milk intake and live-weight gain for artificially fed calves to suckled calves. In Expt 1 the milk and herbage intakes of eight calves were monitored. Their average milk consumption was 2250 kg and their growth rate was 1·14 kg/day. Both milk consumption and growth rate were higher than those recorded in other studies with artificially-reared calves. Nevertheless, it was possible to predict the herbage intake and growth rate of the calves from the relationship previously established for artificially reared calves. The nutrition of cows in Expt 2 was manipulated to induce changes in milk production and the consequent effect on the herbage intake of their calves assessed. Milk consumption was at a lower level and herbage intakes fell within the expected range. Herbage intake also responded to changes in the milk production of the cows. The observed herbage intakes and live-weight gains were similar to those predicted from previously established relationships with artificially fed calves.

scholarly journals Effect of genotype, age of hens and K/k allele on eggshell quality

2011 ◽  
Vol 56 (No. 5) ◽  
pp. 242-249 ◽  
Author(s):  
Z. Ledvinka ◽  
L. Zita ◽  
M. Hubený ◽  
E. Tůmová ◽  
M. Tyller ◽  
...  
Keyword(s):  
Growth Rate ◽  
Egg Production ◽  
Statistical Significance ◽  
Live Weight ◽  
Shape Index ◽  
Feed Mixture ◽  
Eggshell Quality ◽  
Feather Growth ◽  
Two Factors ◽  
The Relationship

We assessed the influence of the particular genotype, age of layers, feather growth-rate gene, and their mutual interactions on selected indicators of eggshell quality in six groups of hens of the laying type Dominant. The following genotypes were examined in the experiment: Barred Plymouth Rock, Dominant BPR 951 (K) strain, slow-feathering; Barred Plymouth Rock, Dominant BPR 901 (k) strain, fast-feathering; Blue Plymouth Rock, Dominant BLPR 954 (K) strain, slow-feathering; Blue Plymouth Rock, Dominant BLPR 894 (k) strain, fast-feathering; crossbreds of the above strains in the F<sub>1</sub> generation Dominant D 107 blue (K), slow-feathering and Dominant D 107 blue (k), fast-feathering. The layers were fed a feed mixture NP1 (16.64 % CP) from the 20<sup>th</sup> week of age and a feed mixture NP2 (15.02% CP) from the 42<sup>nd</sup> week. Husbandry conditions met the regular requirements of laying hens. Egg production and live weight of hens were monitored for the duration of the experiment (12 months). Eggshell quality was examined at the layers' age of 27, 35 and 56 weeks. The average hen-day egg production for the duration of the experiment (12 months) was not significantly influenced by the particular genotype or the feather growth-rate gene. The varying representation of the feather growth-rate gene significantly (P &le; 0.001) influenced the live weight; similarly, the relationship between the genotype and the representation of K/k alleles was significant. The average egg weight was influenced statistically significantly (P &le; 0.001) by the age of hens, their genotype (P &le; 0.05), feather growth-rate gene (P &le; 0.001), and the relationship between the age and genotype (P &le; 0.001). The age of hens, genotype, and the interaction of these two factors affected the egg shape index, as did the incidence of the feather growth-rate gene within the population (with a statistical significance of P &le; 0.001). The age, genotype and the feather growth-rate gene incidence within the population also significantly affected the eggshell quality indicators. In the eggshell to egg ratio, eggshell thickness and strength, an interaction was determined between the age of hens and their particular genotype. The eggshell colour was also significantly (P &le; 0.001) affected by hens' age, genotype (P &le; 0.001), as well as by the feather growth-rate gene (P &le; 0.001). No significant interaction between the age and the genotype was found for this indicator.

Selection on ram 18-month weight to improve lamb growth rate

1983 ◽  
Vol 36 (2) ◽  
pp. 159-164
Author(s):  
D. Croston ◽  
J. L. Read ◽  
D. W. Jones ◽  
D. E. Steane ◽  
C. Smith
Keyword(s):  
Growth Rate ◽  
Live Weight ◽  
Indirect Selection ◽  
Direct Selection ◽  
Selection For ◽  
The Relationship ◽  
Lamb Growth

ABSTRACTThirteen pairs of Suffolk rams were selected on high and low 18-month adjusted live weight from six farms over 2 years, to establish the relationship between 18-month weight and early lamb growth. Progeny were first produced in recorded crossbred flocks (618 lambs) and then in an experimental flock of crossbred ewes (1083 lambs). Different results were obtained from the recorded and experimental flocks. The regressions of lamb 12- to 13-week weight on ram 18-month weight (within farm deviation) were 0·053 ± 0·022 kg and –0·004 ± 0·020 kg, respectively. These regressions for indirect selection correspond to ‘effective’ heritabilities for direct selection for lamb growth of 0·18 ± 0·07 and 0·02 ± 0·06 respectively. Improvement of early Iamb growth is discussed and it is concluded that selection for 18-month weight is unlikely to be a useful method.

A note on the response of pigs weaned at 28 days to dietary protein

1986 ◽  
Vol 42 (3) ◽  
pp. 427-429 ◽  
Author(s):  
R. G. Campbell ◽  
M. R. Taverner
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Dietary Protein ◽  
Live Weight ◽  
Gain Ratio ◽  
Digestible Energy ◽  
Voluntary Food Intake

ABSTRACTThirty-six piglets were used to investigate the effect of six concentrations of dietary protein ranging from 155 to 235 g/kg, and corresponding dietary lysine concentrations from 10·1 to 15·4 g/kg, on the performance of pigs weaned at 28 days of age and growing between 7·5 and 20 kg live weight. Voluntary food intake was not significantly affected by dietary protein, and growth rate increased with increase in dietary protein and lysine up to 167 and 10·9 g/kg respectively (0·75 g lysine per MJ digestible energy (DE)). Food: gain ratio improved significantly with each increase in dietary protein and lysine up to 177 and 11·6 g/kg (0·79 g lysine per MJ DE) respectively.

Photoperiodic requirements for rapid growth in young male red deer

1998 ◽  
Vol 67 (2) ◽  
pp. 363-370 ◽  
Author(s):  
J. R. Webster ◽  
I. D. Corson ◽  
R. P. Littlejohn ◽  
S. K. Stuart ◽  
J. M. Suttie
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Rapid Growth ◽  
Red Deer ◽  
Young Male ◽  
Live Weight ◽  
Reproductive Development ◽  
The Other ◽  
Plasma Prolactin ◽  
Lower Amplitude

AbstractWinter growth of young male red deer can be increased by exposure to 16 h of light (L) and 8 h of dark (D) per day (16L: 8D). This study tested the duration of photoperiod required for this growth response, determined if the time to reach slaughter weight can be reduced and monitored plasma IGF-1, prolactin and reproductive development. Fifty male calves were allocated to five equal groups. Four groups were housed indoors and for 33 weeks from the winter solstice (22 June, southern hemisphere) until 11 February were placed under either 16L: 8D (16L), 13·25L: 10·75D (13L), 10·751:13·25D (111) or 8L: 16D (8L) photoperiods. The fifth group of deer (OC) remained outside in a gravelled enclosure. All groups were given a pelleted diet ad libitum. Group food intake was recorded daily, individual live weight was measured weekly and testes diameter and blood samples taken at weekly or 2-week intervals.Plasma prolactin concentrations in 16L increased within 4 weeks of treatment and were different (P < 0·001) between groups from 14 August to 4 September. IGF-1 increased in both 16L and 13L 4 weeks after treatments and then increased further in 16L above that of 13L (P < 0·01). All groups grew at the same rate for the first 7 weeks. 16L then gained more weight (P < 0·001) than the other groups over the next 19 weeks (50·7 kg v. 38·5 for 13L, 35·7 for 11L, 37·0 for 8L and 37·4 for OC; s.e.d. 3·76). Food intake was positively related to growth rate in a similar way among the inside groups (P < 0·001), however there was a higher energy requirement outdoors (P < 0·05). A target live weight for slaughter of 95 kg was reached 7 weeks earlier for 16L than the other groups (P < 0·01). Testes diameter of 16L was larger than in the other groups from 13 November until 24 December (P < 0·001). The growth oflSL slowed from 1 January while that of OC increased and the live weight ofOC was equal to 16L by the end of the experiment. OC also had the largest testes diameter from 5 February onwards (P < 0·01). The live-weight increase in OC was associated with increases in both prolactin and IGF-1 levels.This study confirmed that 16L: 8D stimulates rapid growth of young male red deer during winter for sufficient time to achieve an earlier slaughter date. The live-weight advantage was lost by late summer however. The increased growth rate was mediated by food intake and associated with increases in IGF-1 and prolactin and earlier reproductive development. Photoperiods of 13 h of light per day or less did not stimulate growth and increases in IGF-1 and prolactin were of a lower amplitude than under 16L: 8D.

The effect of pellet size on the voluntary food intake and performance of young pigs

2001 ◽  
Vol 2001 ◽  
pp. 167-167
Author(s):  
H.L. Edge ◽  
J.A. Dalby ◽  
P. Rowlinson ◽  
M.A. Varley
Keyword(s):  
Food Intake ◽  
Adverse Effects ◽  
Physical Performance ◽  
Digestive Efficiency ◽  
Pellet Size ◽  
Popular Belief ◽  
Young Pigs ◽  
Physical Form ◽  
And Performance ◽  
Voluntary Food Intake

Immediately following weaning, voluntary food intake in the young pig is low and very variable. This can lead to reduced digestive efficiency and poor physical performance. One approach to try to stimulate intake is to manipulate the physical form of the diet. Previously it has been shown that, contrary to popular belief, young pigs are very adaptable with regards to diet presentation and in particular with respect to pellet size(Edge et al., 2000). Pigs from 10 to 56 days of age would consume a 5.0mm pellet as readily as a 1.8mm pellet with no adverse effects on production variables.

Tests of two theories of food intake using growing pigs 2. The effect of a period of reduced growth rate on the subsequent intake of foods of differing bulk content

2001 ◽  
Vol 72 (2) ◽  
pp. 361-373 ◽  
Author(s):  
E.C. Whittemore ◽  
G.C. Emmans ◽  
B.J. Tolkamp ◽  
I. Kyriazakis
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Sugar Beet ◽  
Live Weight ◽  
Growing Pigs ◽  
Sugar Beet Pulp ◽  
Beet Pulp ◽  
Bulk Content ◽  
High Bulk ◽  
Subsequent Intake

AbstractThe effect of a period of feeding on a high bulk food, upon the subsequent intake of foods of differing bulk content, was investigated in two experiments of the same design. The intention was to provide a severe test of the two current conceptual frameworks available for the prediction and understanding of food intake. In each experiment 40 male Manor Meishan pigs were randomly allocated to one of four treatment groups at weaning. Each experiment was split into two periods, P1 (12 to 18 kg) and P2 (18 to 32 kg). The treatments, all with ad libitum feeding, were: a control food (C) given throughout (treatment CC); a medium bulk food (M) given throughout (treatment MM); a high bulk food (H) given in P1 and then C in P2 (treatment HC); H given in P1 and M in P2 (treatment HM). C was based on micronized wheat with 13·4 MJ digestible energy and 243 g crude protein per kg fresh food. In experiment 1 M contained 350 g/kg and H 560 g/kg of unmolassed sugar-beet pulp and in experiment 2 M contained 500 g/kg and H 700 g/kg of unmolassed sugar-beet pulp. Framework 1 predicted that food intake on the medium bulk food (M) would not be increased, whereas framework 2 predicted that intake on M would be increased after a period of feeding on H, compared with when M was offered continuously.In P1, both food intake (P < 0·01) and growth (P < 0·001) were severely limited on H compared with C. In experiment 1 growth was limited on M compared with C during the first 7 days of P1 (P < 0·01) only. In experiment 2 intake (P < 0·001) and growth (P < 0·001) on M were limited throughout P1, compared with C but not thereafter. Therefore, in neither experiment did M cause a lower growth rate than C from 18 to 32 kg. In experiment 1 there was full adaptation to M after about 10 days from 12 kg. In experiment 2 adaptation was complete by the end of the first 7 days from 18 kg.In P2, food intake (P < 0·001) and live-weight gain (P < 0·05 and P < 0·001 in experiments 1 and 2, respectively) were increased on HC compared with CC. By the last 7 days of P2 intake was still higher (P < 0·01) but growth rate was no longer different to CC. Intake and gain were increased in P2 on HM compared with MM but, in general, these differences were small and not significant. In the first 7 days of P2, in experiment 1 pigs on HM had higher intakes (P < 0·001) and gains (P < 0·05) than those on MM, but in experiment 2 only intake was higher (P < 0·01) with no difference in gain. By the last 7 days of P2 there was no difference in either intake or gain between these two groups in either experiment. Pigs on HC increased intake by more than those on HM. There was, therefore, a significant interaction for food intake (P < 0·05, in experiment 1 and P < 0·001, in experiment 2) between prior and present food.The unexpected failure of either M food to limit growth throughout the experimental period meant that the results of these experiments could not be used as a strong test to reject either one of the frameworks. However, the ability of the pigs to compensate on M was less than that on C. The data provide some evidence that under conditions of compensation foods such as M may be limiting. This is in closer agreement with the framework that predicted that consumption of a limiting food will not increase after a period of feeding on a high bulk food (framework 1).

Predicting the effects of body fatness on food intake and performance of sheep

2005 ◽  
Vol 2005 ◽  
pp. 16-16
Author(s):  
B. J. Tolkamp ◽  
J. M. Yearsley ◽  
I. Kyriazakis
Keyword(s):  
Food Intake ◽  
Energy Expenditure ◽  
Live Weight ◽  
Body Lipid ◽  
Body Fatness ◽  
Ewe Lambs ◽  
Test Models ◽  
Condition Score ◽  
And Performance ◽  
Using Data

Food intake (FI) can be predicted on the basis of variables that describe food quality and the animal. Live weight (LW) is usually the only variable that is used to describe the animal. Animal fatness, as estimated by condition score (CS), can affect FI at a given LW. Body lipid produces signals (leptin) that affect energy intake and energy expenditure. If fatness acts on intake via its effect on energy expenditure, the effects of body lipid content on food intake can be incorporated into an existing intake model. Our objectives were to construct and test models that predict effects of fatness on intake and performance, using data obtained with ewe lambs to parameterise and test the models.

Growth and herbage consumption of grazing Merino and Border Leicester lambs reared by their mothers or fostered by ewes of the other breed

1972 ◽  
Vol 14 (3) ◽  
pp. 317-322 ◽  
Author(s):  
J. P. Langlands
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Milk Production ◽  
Live Weight ◽  
The Other ◽  
Weight Gains ◽  
Ad Libitum ◽  
Voluntary Food Intake

SUMMARYEight Border Leicester castrated male lambs (wethers) were fostered on to 8 Merino ewes (MB) at birth, and 10 Merino wethers were fostered on to Border Leicester ewes (BM). Two additional groups of 10 wethers consisted of Border Leicester lambs (BB) and Merino lambs (MM) reared by their natural mothers. The lambs and ewes grazed together and growth rate, and milk and herbage consumption of the lambs were recorded.Live-weight gains to weaning at 74 days were 275, 245, 204 and 184 g/day for groups BB, MB, BM and MM respectively. Lambs reared by Border Leicester ewes received more milk and consumed less grass than lambs of similar genotype reared by Merinos, but BM lambs consumed less milk than BB lambs. Merino lambs also consumed less grass than Border Leicester lambs.It was concluded that Merinos grew more slowly than Border Leicester lambs primarily because of their lower voluntary food intake. The lower milk production of Merino ewes was considered to be of secondary significance since if herbage is available ad libitum, lambs with high voluntary intakes will compensate for the lack of milk by consuming more forage.

Diet selection in pigs: choices made by growing pigs given foods of different protein concentrations

1990 ◽  
Vol 51 (1) ◽  
pp. 189-199 ◽  
Author(s):  
I. Kyriazakis ◽  
G. C. Emmans ◽  
C. T. Whittemore
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Protein Concentration ◽  
Live Weight ◽  
Diet Selection ◽  
Growing Pigs ◽  
Growth Potential ◽  
Feeding Method ◽  
Total Food Intake ◽  
Total Food

ABSTRACTTo test the proposition that growing pigs, when given a choice between two foods, are able to select a diet that meets their requirements, and to investigate the rules of diet selection, four foods (L, A, B and H) with similar energy yields, but different concentrations of crude protein (CP) (125, 174, 213 and 267 g CP per kg fresh food respectively) were formulated. The four foods were offeredad libitumeither singly, or as a two-way choice using all the six possible pairs, to 40 individually caged pigs from 12 to 30 kg live weight. On the single foods the rate of food intake fell from 1001 to 971 to 961 to 868 (s.e.d. 40) g/day (F < 0·05) as the protein concentration of the foods increased from L to H; the growth rate followed an opposite trend (492, 627, 743 and 693 (s.e.d. 31) g/day respectively;P< 0·01). When the pigs had to select between two foods limiting in protein (L and A) the less limiting one was preferred (710 (s.e. 200) g A per kg total food intake; the protein concentration of the selected diet was 160 (s.e. 10) g CP per kg). On the choice between B and H (a choice between a food with protein concentration close to requirements and a food with protein excess) the lower food was markedly preferred (928 (s.e. 4) g B per kg total food intake; the protein concentration of the selected diet was 218 (s.e. 1) g CP per kg). When the animals were given a choice between two foods, a combination of which was non-limiting (pairs LB, LH, AB and AH), the protein concentrations of the selected diets were not different between treatments (208, 204, 202 and 205 (s.e.d. 13) g CP per kg respectively) and they also declined systematically with time and weight. The growth rate of the animals on these pairs were 752, 768, 769 and 763 (s.e.d. 54) g/day (P > 0·05), which were not significantly different from the highest growth rate achieved on a single food. The results suggest that pigs, when given a choice between a suitable pair of foods, are able to choose a balanced diet and to change its composition to reflect their changing requirements. The choice-feeding method may well be useful as an effective and economic way of estimating and meeting requirements, and of measuring the growth potential of pigs.

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