Effect of diet energy density and season on voluntary dry-matter and energy intake in male red deer

2000 ◽  
Vol 70 (3) ◽  
pp. 547-554 ◽  
Author(s):  
J.R. Webster ◽  
I.D. Corson ◽  
R.P. Littlejohn ◽  
B.M. Masters ◽  
J.M. Suttie
Keyword(s):  
Food Intake ◽  
Energy Density ◽  
Growth Rates ◽  
Dry Matter ◽  
Red Deer ◽  
Energy Requirement ◽  
Live Weight ◽  
Metabolizable Energy ◽  
Wide Range ◽  
Pelleted Diet

AbstractFood intake and growth of red deer is lower in winter than in spring and this reduces the efficiency of venison production. Rumen capacity is also lower during winter and this may contribute to the reduced food intake and therefore growth. In the present study, we investigated the ability of deer to regulate food intake during winter and spring by feeding diets of differing energy densities.Six groups of eight male red deer calves were housed indoors in separate pens. Each group was given,ad libitum, a pelleted diet of a different energy density (8·5, 9·0, 9·5, 10·0, 10·5 and 11·0 MJ metabolizable energy (ME) per kg dry matter (DM) for groups 1 to 6 respectively) but the same amount of protein (156 g/kg DM). Food intake of each group was recorded every 2nd day and animals were weighed every 6 days from 17 May to 9 December. For seasonal comparisons, winter was defined as 24 May to 31 August and spring as 1 September to 9 December.There was no difference (P> 0·05) between the mean live weights of the groups at any time during the study. Live-weight gain (LWG) reached a minimum on 4 July and was lower in winter than spring (161 v. 308 g/day, s.e.d. = 10·0,P< 0·001). LWG was positively related (P< 0·001) to diet ME during winter. DM intake (g/kg M0·75per day) and ME intake (MJ ME per kg M0·75per day) decreased until 16 July and increased thereafter. Mean DM intake was lower in winter than spring (83·5 v. 97·2 g/kg M0·75per day, s.e.d. = 2·05,P< 0·001). DM intake increased as diet energy decreased (P< 0·001) in winter and spring with a steeper slope (P< 0·05) in spring than winter. ME intake was not related to diet ME (P> 0·005) and was lower in winter than spring (0·82 v. 0·95 MJ/kg M0·75per day, s.e.d. = 0·25,P< 0·001). Maintenance energy requirement (MEm) across groups and seasons was calculated to be 0·45 (s.e. 0·22) MJ ME per kg M0·75and the energy requirement for LWG (MEf) was 53 (s.e. 8·5) MJ/kg LWG. MEfwas related (P< 0·01) negatively to diet ME during winter.In summary, deer consuming diets with a wide range of energy densities, altered their DM intake, resulting in similar energy intakes and growth rates on all diets. Animals seemed less able to achieve this compensation in winter compared with spring when food intake increased to support the natural rise in growth rate at that time. These results indicate that deer have target growth rates and/or energy intakes that change with season, and are defended by adjusting food intake.

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.

Increased winter growth in male red deer calves under an extended photoperiod

1997 ◽  
Vol 65 (2) ◽  
pp. 305-310 ◽  
Author(s):  
J. R. Webster ◽  
I. D. Corsor ◽  
R. P. Littlejohn ◽  
J. M. Suttie
Keyword(s):  
Dry Matter ◽  
Red Deer ◽  
Live Weight ◽  
Natural Increase ◽  
Metabolizable Energy ◽  
The Other ◽  
Abrupt Increase ◽  
Winter Solstice ◽  
The Mean ◽  
Autumn And Winter

AbstractThe growth of male red deer slows during the first winter of life before increasing again during spring. This study aimed to determine if this period of slow growth could be minimized using artificial photoperiods during autumn and winter (10 April (week 1) to 11 September (week 23), southern hemisphere). Four groups of deer (no. = 10) were housed indoors as follows. Two groups were placed on a winter solstice photoperiod (8·5 light (L): 15·5 dark (D)) and given either a natural increase in photoperiod to 11·25L: 12·75D (WSN) or held on 8·5L: 15·5D for 7 weeks followed by an abrupt increase to 11·25L: 12·75D (WSH). One group was exposed to a summer solstice photoperiod of 16L: 8D (SS) and one group exposed to a natural photoperiodic pattern (IC). A fifth group of deer (no. = 10) was maintained outside on a gravelled enclosure under natural changes in photoperiod (OC). All groups were given a diet containing 160 g protein per kg and 11·0 MJ metabolizable energy per kg dry matter (DM) ad libitum. All animals were weighed weekly and group food intake recorded daily. Metatarsal length was measured at weeks 3,17 and 22 from the start of treatments.The major differences occurred between SS and the other groups. After a period of slower growth (weeks 1 to 5, SS = 88 g/day v. 168 g/day other groups, s.e.d. 31·2, P < 0·05), SS grew more rapidly from week 10 (P < 0·01). As a result, SS was heaviest from week 17 (P < 0·05) until the end of the experiment (P < 0·01). The mean growth rate of SS animals from weeks 10 to 23 was 346 g/day compared with 173 g/day (s.e.d. 15·3; P < 0·001) for the other groups. Over the whole experiment, SS animals gained 42·3 kg live weight, compared with 31·1 kg for WSN, 26·6 kg for WSH, 25·1 kg for OC and 23·7 kg for IC (s.e.d. 2·08 kg P < 0·01). The DM intake of SS from week 9 until the end of the experiment averaged 2·04 kg DM per head per day compared with 1·48 (s.e. 0·041) kg DM per head per day for the mean of the other groups. Metatarsal length increased more in SS than the other groups (P < 0·001) between weeks 3 and 17 and was longest in SS at weeks 17 and 22 (P < 0·01). Exposure to a 16L: 8D photoperiod during winter advanced the rapid growth of red deer calves normally associated with spring and summer. This response may be used to advance slaughter dates for venison production.

Complete diets for dairy cows: comparisons of feeding to appetite with rationing according to milk yield

1980 ◽  
Vol 94 (3) ◽  
pp. 715-726 ◽  
Author(s):  
J. F. D. Greenhalgh ◽  
G. W. Reid
Keyword(s):  
Milk Yield ◽  
Dry Matter ◽  
Energy Content ◽  
Energy Requirement ◽  
Live Weight ◽  
Metabolizable Energy ◽  
Dry Matter Intake ◽  
Late Winter ◽  
Early Lactation ◽  
Under Nutrition

SummaryTwo experiments were made, each with 35 autumn-calving cows fed on complete diets containing 40–70% hay and 60–30% concentrates. In both experiments, cows fed to appetite on a diet containing 11 MJ metabolizable energy/kg D.M. for weeks 7–24 of lactation ate about 20% more than cows rationed according to yield, but produced only about 3% more milk. The cows fed to appetite gained more in live weight, but lost their weight advantage during the subsequent grazing season.In Expt 1, a further group of cows were fed to appetite on diets progressively reduced in metabolizable energy content from 11·0 to 9·2 MJ/kg. Dry-matter intake decreased by about 1·2 kg/day per 1 MJ reduction in energy content. The lower dry-matter and energy intakes of cows on this treatment did not significantly reduce their milk yield, but their response when turned out to grass suggested under-nutrition in late winter. In Expt 2, increasing the energy content of the diet in early lactation (weeks 7–12) and reducing it thereafter had no significant effect on milk yield.Within each treatment group there were reasonably close relationships between energy intake and energy requirement. Nevertheless, it seems likely that the efficiency of feed utilization of cows fed on complete diets will be low unless intake is controlled by energy dilution.

Growth and reproductive development of red deer calves (Cervus elaphus) born out-of-season

1992 ◽  
Vol 55 (2) ◽  
pp. 265-270 ◽  
Author(s):  
C. L. Adam ◽  
C. E. Kyle ◽  
P. Young
Keyword(s):  
Food Intake ◽  
Cervus Elaphus ◽  
Dry Matter ◽  
Red Deer ◽  
Plasma Concentrations ◽  
Live Weight ◽  
Reproductive Development ◽  
Normal Birth ◽  
Melatonin Administration ◽  
Voluntary Food Intake

AbstractSince the productivity of farmed red deer is constrained by their inherent seasonal biology, the potential advantages of breeding out-of-season following melatonin administration were investigated. Calves born in February (F; no. = 8) were heavier at weaning in September of the same year than calves born with normal birth dates in June (}; no. = 8) (73·2 v. 441 (s.e.d. 3·59) kg; P < 0·001) and at the end of April of the next year (88·0 v. 67·6 (s.e.d. 6·44) kg; P < 0·02) although their suckled live-weight gain to 100 days of age was lower (304 v. 361 (s.e.d. 21·4) g/day; P < 0·05). After weaning, F calves had higher voluntary food intake than / calves (g dry matter per head per day) from September to November (1643 v. 2224 (s.e.d. 92·6); P < 0·002), November to February (1435 v. 926 (s.e.d. 67·9); P < 0·002), and February to April (1487 v. 2059 (s.e.d. 115·5); P < 0·02).Unlike J calves, F calves showed puberty in their first autumn. F male calves (no. = 3) grew antlers which hardened in November, whereas J males (no. = 3) did not, and F males, aged 8 months, had significantly higher mean plasma concentrations of testosterone than J males, aged 4 months (1·35 v. 0·28 (s.e.d. 0·154) fj.g/1, P < 0·001). Oestrous cyclicity was observed in 3/5 group F females, aged 9 months, but in 0/5 group ] females, aged 5 months. Although the dams of F and ] calves had similar live weights at mating, birth and 100 days pos t partum, F dams were heavier (P < 0·05) at weaning. Following parturition, F dams had a mean voluntary food intake of 2700 (s.e. 110) g dry matter per head per day from February to April.

scholarly journals The effects of protein degradability and food intake on milk yield and composition in cows in early lactation

1981 ◽  
Vol 45 (3) ◽  
pp. 547-555 ◽  
Author(s):  
E. R. Ørskov ◽  
G. W. Reid ◽  
I. McDonald
Keyword(s):  
Food Intake ◽  
Milk Yield ◽  
Fish Meal ◽  
Energy Requirement ◽  
Live Weight ◽  
Milk Composition ◽  
Metabolizable Energy ◽  
Early Lactation ◽  
Groundnut Meal ◽  
Protein Degradability

1. In two experiments measurements were made of food intake, live-weight change, milk yield and milk composition in early lactation when dairy cows were given diets containing varying proportions of protein as fish meal (low rumen degradability) or as groundnut meal (high rumen degradability). In a preliminary trial measurements were also made with cows given supplements of either fish meal or barley and fed at a restricted level of feeding.2. When metabolizable energy (ME) intake exceeded 160 MJ/d there was no evidence of responses to changes in protein degradability, but at ME intakes below 135 MJ/d increases in the supply of undegradable protein led to increases in fat-corrected milk yield, protein content and live-weight loss.3. The interaction between energy intake and protein degradability is unexpected because net protein:net energy requirement increases as milk yield increases, but may be explained in terms of differential effects of changing rumen outflow rates on degradabilities.

scholarly journals Energy Requirement and Food Intake Behaviour in Young Adult Intact Male Cats with and without Predisposition to Overweight

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Brigitta Wichert ◽  
Julia Trossen ◽  
Daniel Uebelhart ◽  
Marcel Wanner ◽  
Sonja Hartnack
Keyword(s):  
Body Weight ◽  
Food Intake ◽  
Dry Matter ◽  
Body Condition Score ◽  
Energy Requirement ◽  
Fat Free Mass ◽  
Energy Requirements ◽  
Intact Male ◽  
Feeding Station ◽  
Condition Score

Obesity is a common problem in cats. In the experimental cat family of the institute of animal nutrition besides a “normal” lean phenotype, cats with predisposition to an overweight phenotype are present. To investigate energy requirements and food intake behaviour of intact male cats of different phenotypes, six “normal” lean cats (GL) and six cats disposed to overweight (GO) were used. At the beginning of the experiment, all cats had an ideal body condition score of 5. To reach this the GO cats had to pass a weight-loss program. Energy requirements of the cats were determined using respiration chambers, whereas the amount and frequency of food intake was measured with a feeding station recording the data automatically. Energy requirement at weight constancy of the GO cats was even on fat-free mass (FFM) significantly (P=0.02) lower (162.6 kJ/kg FFM/d) than that of the “normal” lean cats (246 kJ/kg FFM/d). The GO cats also showed a higher food intake34.5±1.5 g dry matter/kg body weight0.67compared to the GL cats (24.0±2.1 g dry matter/kg body weight0.67)(P=0.001). In conclusion quantifiable differences in food intake and behaviour in cats predisposed to overweight compared to “normal” lean cats were found.

Effect of restricted food intake, before and/or after mating, on the reproductive performance of Greyface ewes

1989 ◽  
Vol 48 (1) ◽  
pp. 149-155 ◽  
Author(s):  
S. M. Rhind ◽  
W. A. C. McKelvey ◽  
S. McMillen ◽  
R. G. Gunn ◽  
D. A. Eiston
Keyword(s):  
Food Intake ◽  
Reproductive Performance ◽  
Live Weight ◽  
Experimental Period ◽  
Metabolizable Energy ◽  
Ovulation Rate ◽  
Daily Ration ◽  
The Mean ◽  
Low Levels ◽  
Lambing Rate

ABSTRACTThe effect on the reproductive performance of Greyface (Border Leicester × Scottish Blackface) ewes of a low level food intake and associated loss of live weight from either 14 days before mating, or from the time of mating, until 11 to 26 days after mating, was investigated. Ewes (252) were allocated to one of three treatments with ewes within each treatment divided into two flocks (flock A: 16 ewes per treatment; flock B: 68 ewes per treatment). Ewes of treatment LL were given a ration providing proportionately 0·5 estimated metabolizable energy (ME) requirements for maintenance from 2 weeks before mating. Those of treatment HL were given a daily ration providing 1·5 estimated ME requirements for maintenance until mating and the restricted ration thereafter. Ewes of treatment HH were given the higher ration throughout the experimental period. Flock A ewes were slaughtered at 11 days post mating and flock B ewes at between 18 and 26 days post mating. Treatment differences in the ovulation rates of flock A ewes were not statistically significant but in flock B, ewes of treatment LL had a lower mean ovulation rate (1·81) than those of treatments HL (2·23) and HH (2·09) (P < 0·001). The lower ovulation rate of LL ewes relative to HL ewes in flock B was reflected in a lower mean potential lambing rate per ewe pregnant than in the HL treatment (1·58 v. 1·79; P < 0·01) and per ewe put to the ram (1·37 v. 1·65; P < 0·01). HL ewes had a slightly lower mean potential lambing rate per ewe pregnant (1·79 v. 1·97; P < 01) and per ewe put to the ram (1·65 v. 1·82; P < 0·05) than HH ewes. Ova wastage rates of LL + HL and HH ewes were 0·26 and 014 (P < 001) respectively at 24 days post mating. Values for LL and HL ewes (0·27 and 0·25 respectively) were not significantly different.Estimated mean conceptus lengths were 370, 500 and 1400 μin for LL, HL and HH ewes respectively (P < 0·05).It is concluded that low food intake before mating reduced the mean ovulation rate and low intakes after mating compromised embryo growth rate and induced a higher rate of ova wastage; this increase in the incidence of ova wastage was not significantly exacerbated by the low levels of intake prior to mating.

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 effects of liveweight at weaning, date of weaning and winter nutrition on the subsequent performance of red deer

1986 ◽  
Vol 1986 ◽  
pp. 140-140
Author(s):  
J A Milne ◽  
Angela M Sibbald
Keyword(s):  
Birth Weight ◽  
Growth Rates ◽  
Red Deer ◽  
Live Weight ◽  
Meat Production ◽  
Weaning Weight ◽  
Calf Growth ◽  
Subsequent Performance ◽  
Number Of Factors

A desirable liveweight for red deer at 15 months of age is approximately 80 kg. This will provide a saleable carcase and a liveweight at which yearling hinds will successfully breed. Live-weight at 15 months will be influenced by a large number of factors including date of birth, birth-weight, liveweight gain to weaning, date of weaning, liveweight gain during the first winter and subsequent summer, and the interactions between weaning weight and subsequent levels of nutrition and between winter levels of nutrition and liveweight gain at pasture in the following summer. These latter two aspects were examined in two experiments and the effect of date of weaning on contemporary calf growth rates and on hind calving date in the following year were studied in a third experiment. The objective was to provide information which would allow the development of effective systems of deer meat production based on slaughter at 15 months of age.

Sign in / Sign up

Export Citation Format

Share Document