Increasing food intake in late gestation improved sow condition throughout lactation but did not affect piglet viability or growth rate

2000 ◽  
Vol 71 (1) ◽  
pp. 141-148 ◽  
Author(s):  
H. M. Miller ◽  
G. R. Foxcroft ◽  
F. X. Aherne
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Growth Rates ◽  
Live Weight ◽  
Late Gestation ◽  
Backfat Thickness ◽  
Maintenance Energy ◽  
Early Lactation ◽  
Treatment Groups ◽  
Food Intake Level

AbstractIncreasing sow food intake in late gestation prevents loss of sow fatness prior to farrowing. However, this may result in reduced food intake and greater overall fat loss during lactation and has also been associated with increased incidence of agalactia. In this experiment 78 Camborough sows (parities 1 to 3) were given food at one of two levels: either 1·15 × maintenance energy (normal-N sows, 2·3 (s.e. 0·03) kg/day) or 2·00 × maintenance energy (high-H sows, 3·9 (s.e. 0·04) kg/day) from day 100 of gestation until farrowing. Lactation food intake, changes in sow live weight and backfat thickness and piglet growth rates were then measured. Diet digestibility in early lactation was measured using a chromium III oxide marker in the food. There was no change in backfat thickness in late gestation in H sows (0·2 (s.e. 0·25) mm), whereas N sows lost backfat during this period (1·6 (s.e. 0·23) mm, P <; 0·001). There was no difference in lactation food intake between the two groups (6·5 (s.e. 0·13) kg/day) and differences in backfat thickness at parturition were maintained through to weaning. H sows did not show increased incidence of agalactia compared with N sows. There was no difference in diet digestibility between the two treatment groups. Food intake level in late gestation did not affect piglet birth weights, growth rates or mortality. It is concluded that the main benefit of increasing sow food intake in late gestation was to reduce sow backfat loss during the reproductive cycle.

Effects of ardacin supplementation on food intake and growth rate of growing and finishing steers

1995 ◽  
Vol 60 (3) ◽  
pp. 409-417 ◽  
Author(s):  
M. G. Keane ◽  
M. P. Read ◽  
A. P. Moloney
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Live Weight ◽  
Basal Diet ◽  
Initial Weight ◽  
Grazing Season ◽  
Treatment Groups ◽  
Grass Silage ◽  
Finishing Steers ◽  
Ad Libitum

AbstractArdacin is an antibacterial glycopeptide with ruminal activity. The objective of this study was to measure its effects on food intake and growth rate of growing and finishing steers. Two experiments were carried out simultaneously using the same foods and the same ardacin supplementation levels. In experiment 1, 72 growing steers (8 months old and 240 kg initial weight) in four treatment groups were individually offered a basal diet of grass silage ad libitum. In experiment 2, 44 finishing steers (19 months old and 463 kg initial weight), also in four treatment groups were individually offered a basal diet of grass silage ad libitum plus 3 kg (5 kg for the final 28 days) concentrates per head daily. The four treatments were 0, 50, 125 and 210 mg ardacin per head daily incorporated into 1 kg ground barley. This was offered in addition to the basal diet. The duration of the experimental period was 154 days after which 48 of the growing steers were put to pasture for a 196-day grazing season. The finishing steers were slaughtered following a withdrawal period of 7 days. Mean daily silage dry-matter intakes, and mean daily total metabolizable energy intakes for the treatments as listed above were 4·91, 5·15, 5·10 and 5·03 (s.e. 0·083) kg and 63, 66, 65 and 65 (s.e. 0·7) MJ (experiment 1), and 5·63, 5·62, 5·51 and 5·54 (s.e. 0·059) kg and 108, 108, 107 and 107 (s.e. 0·4) MJ (experiment 2), respectively. In the same order, mean daily live-weight gains during the treatment period were 612, 758, 784 and 798 (s.e. 25·2) g (experiment 1) and 911, 942, 851 and 860 (s.e. 40·0) g (experiment 2). In the growing steers proportionately 0·64 of the weight response to ardacin was retained to the end of the following grazing season. It is concluded that ardacin supplementation increased live-weight gain and improved the efficiency of conversion of food to live weight in growing steers but had no significant effect on finishing steers in this study.

Variation in growth and efficiency in twin cattle with live weight and food intake controlled

1966 ◽  
Vol 66 (1) ◽  
pp. 67-85 ◽  
Author(s):  
ST C. S. Taylor ◽  
G. B. Young
Keyword(s):  
Growth Rate ◽  
Food Intake ◽  
Control Systems ◽  
Food Consumption ◽  
Growth Rates ◽  
Live Weight ◽  
Feeding System ◽  
Similar Growth

In an experiment to investigate the interrelationships of genetics and nutrition in the growth of cattle up to 2 years of age, five monozygotic and six dizygotic Ayrshire twin heifers were reared under close nutritional control on an all cubed diet.Two control systems were used. Some animals were fed similar amounts of food, and differences in growth rate and efficiency examined while others were made to grow alike and differences in food consumption and efficiency examined. Overall, similarly fed animals had similar growth rates and efficiencies and similarly grown animals similar food intakes and efficiencies. Variation in growth, food consumption and efficiency was much less than in an ad lib. feeding system.

The effects of food intake in gestation on sows lactating for 14 days

1983 ◽  
Vol 37 (1) ◽  
pp. 25-31 ◽  
Author(s):  
N. Walker
Keyword(s):  
Growth Rate ◽  
Birth Weight ◽  
Food Intake ◽  
Growth Rates ◽  
Subcutaneous Fat ◽  
Live Weight ◽  
Weaning Weight ◽  
Subcutaneous Fat Thickness ◽  
Fat Thickness

ABSTRACTNinety-two gilts in replicates of four littermates were mated at puberty at a mean live weight and age of 95 kg and 191 days respectively. The littermates were allocated at random to one of four food allowances (kg/day) during four successive gestations: (A) 1·5, (B) 2·0 in parity 1 followed by 1·5 in subsequent parities, (C) 20 and (D) 2·5. A diet calculated to contain 12·7 MJ digestible energy per kg was fed throughout gestation, the 2-week lactation and from weaning to conception.The numbers of sows which conceived at parity 5 when the experiment terminated were 10, 12, 13 and 16 for treatments A to D respectively. Sow live weight at conception differed significantly (P < 0·01) from parity 2 onwards: the maximum live weights of sows on treatments A and B did not exceed 130 to 135 kg, but the live weights of sows on treatment D continued to increase to reach 195 kg at the end of the experiment. The in vivo skin plus subcutaneous fat thickness at the P2 location differed significantly (P < 0·001) between treatments from parity 2 onwards, decreasing by 3 mm in treatment A and increasing by 6 mm in treatment D from the start of the experiment to conception at parity 4. The interval from weaning to conception was significantly (P < 0·05) lower in treatment B in parity 2. This was the only significant effect and was contrary to the tendency for the interval to increase as the food allowance in gestation was decreased. The numbers of pigs born alive, stillborn or weaned (including fostered pigs) were not significantly affected by treatment. Birth weight and post-natal growth rates were significantly (P < 0·05) increased after parity 1 as gestation food allowance increased, with the exception of the post-natal growth rate in parity 3. Overall birth weight was increased by 018 kg per pig and weaning weight by 0·93 kg per pig on treatment D compared with treatment A.

scholarly journals Mammary Gland Structures Are Not Affected by an Increased Growth Rate of Yearling Ewes Post-Weaning but Are Associated with Growth Rates of Singletons

Animals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 884
Author(s):  
Emmanuelle Haslin ◽  
Rene A. Corner-Thomas ◽  
Paul R. Kenyon ◽  
Adrian J. Molenaar ◽  
Stephen T. Morris ◽  
...  
Keyword(s):  
Growth Rate ◽  
Mammary Gland ◽  
Live Weight ◽  
Late Pregnancy ◽  
Control Group ◽  
Early Lactation ◽  
Fat Pad ◽  
Negative Effects ◽  
Lamb Growth ◽  
Heavy Group

The experiment aimed to examine the impacts of an increased growth rate of ewes between three and seven months of age on udder development using ultrasound and to establish whether ultrasonography could be used to identify ewe mammary structures that may be indirect indicators of singleton growth to weaning. Udder dimensions, depths of gland cistern (GC), parenchyma (PAR) and fat pad (FP) were measured in late pregnancy (P107), early lactation (L29), and at weaning (L100) in 59 single-bearing yearling ewes selected from two treatments. The ‘heavy’ group (n = 31) was preferentially fed prior to breeding achieving an average breeding live-weight of 47.9 ± 0.38 kg at seven months of age. The ‘control’ group (n = 28) had an average breeding live-weight of 44.9 ± 0.49 kg. Udder dimensions, GC, PAR and FP did not differ between treatments. Lamb growth to L100 was positively associated (p < 0.05) with PAR at P107 and GC at L29. There was no evidence of negative effects of the live-weight gain treatments on udder development of yearling ewes as measured by ultrasonography. The results suggest that this ultrasound method has the potential to identify pregnant yearling ewes which would wean heavier singletons.

Influence of energy and protein concentration in the diet on the performance of growing pigs 2. Differing nutrient density at a constant energy: protein ratio

1972 ◽  
Vol 14 (1) ◽  
pp. 47-55 ◽  
Author(s):  
G. A. Lodge ◽  
M. E. Cundy ◽  
R. Cooke ◽  
D. Lewis
Keyword(s):  
Growth Rate ◽  
Live Weight ◽  
Fat Content ◽  
Growing Pigs ◽  
Feed Conversion ◽  
Large White ◽  
Protein Ratio ◽  
Treatment Groups ◽  
Nutrient Density ◽  
Amino Acid Balance

SUMMARYForty-eight gilts by Landrace sires on Large White × Landrace females were randomly allocated to eight pens and within pens to six treatment groups involving three diets and two levels of feeding from 23 to 59 kg live weight. All diets were formulated to have approximately the same ratio of digestible energy to crude protein (160 kcal DE/unit % CP) but different energy and protein concentrations: (A) 3500 kcal/kg DE and 21 % CP, (B) 3150 kcal/kg DE and 19% CP, and (C) 2800 kcal/kg DE and 17% CP. Amino acid balance was maintained relatively constant with synthetic lysine, methionine and tryptophan. The levels of feeding were such that the lower level of diet A allowed an intake of energy and protein similar to the higher level of diet B, and the lower level of B was similar to the higher level of C.On the lower level of feeding, growth rate, efficiency of feed conversion and carcass fat content increased linearly with each increment in nutrient concentration; on the higher level of feeding growth rate and EFC increased from diet C to B but not from B to A, whereas carcass fat content increased linearly with diet from the lowest to the highest concentration. There was a non-significant tendency for the higher density diets at a similar level of nutrient intake to give better EFC and fatter carcasses than the lower density diets.

The rôles of photoperiod and nutrition in the seasonal increases in growth and insulin-like growth factor-1 secretion in male red deer

2001 ◽  
Vol 73 (2) ◽  
pp. 305-311 ◽  
Author(s):  
J. R. Webster ◽  
I. D. Corson ◽  
R. P. Littlejohn ◽  
S. K. Martin ◽  
J. M. Suttie
Keyword(s):  
Growth Factor ◽  
Food Intake ◽  
Growth Rates ◽  
Energy Demand ◽  
Red Deer ◽  
Young Male ◽  
Live Weight ◽  
Metabolizable Energy ◽  
Plasma Prolactin ◽  
Insulin Like Growth Factor

AbstractYoung male red deer follow a seasonal growth pattern that can be shifted by altering the photoperiod they experience. An increase in photoperiod to 16 h of light per day (16L : 8D) during winter advances the onset of rapid growth and high food intake that normally commences in spring. These changes are associated with increased growth hormone (GH) and insulin-like growth factor-1 (IGF-1) secretion. The GH/IGF-1 axis is acutely sensitive to the level of nutrition and the relative rôles of photoperiod and nutrition in determining the spring IGF-1 rise is unknown. The present experiment set out to examine this by exposing two groups of deer (no. = 8 per group) to a photoperiod shift during their 1st year of life (16L : 8D from 2 June), designed to cause accelerated growth and increased food intake after approximately 7 weeks. However, after 6 weeks the food intake (pellets containing 11 MJ metabolizable energy and 160 g crude protein per kg dry matter (DM)) of one group (LDRES) was clamped, thereby preventing the intake component of the response. The intake of the other group (LDAL) remained ad libitum for a further 12 weeks until 6 October, when the experiment concluded.During the first 6 weeks of 16L : 8D, growth rate (118 (s.e. 15·4) g/day) and food intake (1·37 (s.e. 0·031) kg DM per head per day) did not differ between the groups. Food intake following the clamp in LDRES averaged 1·40 (s.e. 0·015) kg per head per day. The intake of LDAL increased 2 weeks after the clamp and thereafter was higher than LDRES (P < 0·001). Food intake of LDAL averaged 2·13 (s.e. 0·051) kg during the nutritional clamp period. Growth rates increased in both groups during the first 3 weeks of the clamp, averaging 237 (s.e. 25·0) g/day, then growth slowed in LDRES and live weights diverged. Growth rates until the end of the experiment (147 (s.e.23·0) g/ day v. 299 (s.e. 12·5) g/day, P < 0·001) and mean live weight over the last 5 weeks of the experiment were lower (P < 0·05) in LDRES than LDAL, weights reaching 88·3 (s.e. 1·86) kg and 97·9 (s.e. 2·74) kg respectively on the final sampling date. Metatarsal bone length grew more in LDAL than in LDRES (3·1 v. 2·2 cm, s.e.d. = 0·23, P < 0·01). Prior to the nutritional clamp, mean plasma prolactin and IGF-1 concentrations increased at 3 and 6 weeks after 16L : 8D respectively, in both groups. Prolactin concentrations were lower in LDRES than LDAL on two occasions, at weeks 3 and 7 after the onset of the nutritional clamp, and IGF-1 concentrations were lower in LDRES than LDAL (676 v. 872 ng/ml, s.e.d. = 73·8, P < 0·05) over the last 7 weeks of sampling.In summary, a photoperiodically driven increase in IGF-1 occurred even when the usual associated increase in food intake was prevented. This indicates that the seasonal IGF-1 rise in red deer is not a consequence of the increased food intake, although the latter appears necessary to maintain elevated IGF-1 concentrations. The rise in IGF-1 may therefore be considered as a component of the photoperiodically entrained seasonal drive to grow, and the increase in food intake a response to satisfy the increased energy demand.

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.

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).

An analysis of growth of different cattle genotypes reared in different environments

1984 ◽  
Vol 103 (1) ◽  
pp. 137-153 ◽  
Author(s):  
J. E. Frisch ◽  
T. E. Vercoe
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
High Growth ◽  
Environmental Stresses ◽  
Growth Potential ◽  
Gastrointestinal Helminths ◽  
Treatment Groups ◽  
Survival And Growth ◽  
Different Levels ◽  
High Growth Potential

SummaryCalves from three breeds, Brahman, Hereford × Shorthorn (HS) and Brahman × HS (BX), were divided equally into two groups, one of which was treated every 3 weeks from birth onwards to control ticks and gastrointestinal helminths, and one of which was untreated. Mortalities, growth rates and levels of resistance to environmental stresses that affected both mortality and growth under grazing conditions were recorded for all animals up to weaning (6 months) and for all males up to 15 months of age. The Brahmans were the most and the HS were the least resistant to environmental stresses, each of which was shown to depress growth in proportion to its magnitude and to contribute to the high mortalities of the HS. All breeds responded positively to parasite control with the greatest response in both survival and growth in the HS breed and the least response in the Brahman breed.Samples of males from the various breed-treatment groups were taken into pens where they were protected from environmental stresses and fed both low-quality pasture hay and high-quality lucerne hay ad libitum. Measurements were made of fasting metabolism, maintenance requirement, voluntary food intake and gain, variables related to the growth potential of each animal. The HS animals had the highest whilst the Brahmans had the lowest values for each variable.However, despite their low growth potential, the Brahmans had the highest growtli rate, and the HS, despite their high growth potential, had the lowest growth rate, when growth was measured in the presence of all environmental stresses. When parasites were controlled, growth rates were highest for the BX, the breed with intermediate growtli potential, and did not differ between the HS and Brahmans. These interactions arose because of the different contributions of resistance to environmental stresses and growth potential to growth rate measured at the different levels of environmental stresses. The relevance of these interactions to breed evaluation and cross-breeding is considered.Growth potential and resistance to environmental stresses were negatively correlated both between and within breeds, though the latter was biased by the effects of compensation. The influence of these relationships on the likely outcome of selection for increased growth rate, both between and within breeds, is discussed.

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