A comparison of a new net energy system with the metabolisable energy system in broiler diet formulation,performance and profitability 1

Two trials were conducted with unsexed broilers to compare a net energy (NE) system and a metabolisable energy (ME) system on least‐cost broiler diet formulation, broiler performance and economic efficiency. Both energy systems were compared in the range of 3000 (2161) to 3400 kcal ME/kg (2560 kcal NE/kg) using rations with increasing energy concentration of about 100 kcal/kg food.

The two different energetic evaluation systems had considerable effect on dietary composition, the penalty cost of rejected ingredients, the marginal profit of some limiting constraints and the position of the least‐cost nutrient concentration. The starter and finisher rations, based on NE values, were on average 4.77 and 2.43 BF²/100 kg cheaper, respectively than those based on ME values. For equal NE contents, they contained 50 to 70 kcal less ME/kg and 1% less crude protein.

The broiler performances were on average better on the NE‐diets. The mean difference of 20 to 30 g in body weight was significant at 4 and 6 weeks (P < 0.01 and P < 0.05).

Regression analysis indicated no significant effect of rising energy concentration on food intake with the ME‐diets, but a significant (P < 0.05) linear decrease with the NE‐diets of 1.16 ± 0.34 and 1.72 ± 0.37 g/chick d at 6 and 8 weeks respectively for every 100 kcal/kg rise in the NE content of the ration. As a result body weight at 6 weeks improved linearly per increment of 100 kcal NE/kg with 37.2 ± 3.2 g (P < 0.05) on the ME‐diets and with 18.8 ± 6.8 g (P = 0.08) on the NE‐diets.

The efficiency of food utilisation, although slightly better on the NE‐diets, was not significantly affected by the energy systems. As expected, linear improvements (P < 0.001) of respectively 58 ± 6 and 62 ± 11 g food/kg weight gain at 6 and 8 weeks were noted for every increment of 100 kcal NE/kg diet.

Returns over food costs were for the whole energy range higher on the NE‐diets (average 0.66 BF/chick, variation 1.01 to 0.23 BF/chick). Gross profit increased with rising nutrient density from 16.33 to 17.97 BF/chick on the ME‐diets and from 17.34 to 18.23 BF/chick on the NE‐diets. The data illustrate that the economical efficiency of broiler production can be considerably improved by taking into account the effect of both energy content and energy system.     

A marginal income and cost analysis of the effect of nutrient density on the performance of white leghorn hens in battery cages 1

In an experiment lasting 40 weeks with 576 caged White Leghorn (WL) hens and using linearly programmed least‐cost rations, the influence of increasing the nutrient density by increments of 100 kcal metabolisable energy (ME)/kg food, within the range 2500 to 3200 kcal ME/kg, on production was studied.

Increasing the nutrient density was accompanied by increases in egg weight, body weight and ME intake/hen d but mortality and the number of eggs laid were not affected (P<0.01). From a regression analysis carried out on the combined results of this and of another similar experiment, it was found that with each 100 kcal/kg rise in the ME content, the mean ME intake/hen d increased by 3.14 ± 0.59 kcal, the body weight by 38.85 ± 10.7 g and the egg weight by 0.21 ± 0.04 g.

A marginal income and cost analysis, using the above data, was carried out for three price situations of raw materials in 1970 and for two price situations of eggs and carcasses. The rations had a marginal cost structure for each nutrient density. From the analyses it appeared that the effect of the increases in egg and body weight in determining the most profitable nutrient density were at least as important from the economic point of view as the influence of the increased ME intake caused by increasing nutrient density. In the price situations considered, they neutralised the effect of one another, so that the diets with the lowest cost per calorie were also the most profitable.

For every price situation of raw materials, eggs and hens, the economical optimal food composition can be quickly and accurately determined by making use of the marginal profit analysis. It is also possible to couple the regression analysis for the adaptation of the mathematical functions to the parametric computer program which calculates the least‐cost rations.     

An energy response curve for a commercial white leghorn laying‐strain cross

1. Individually‐caged White Leghorn hens, 235‐d‐old, were given daily metabolisable energy (ME) intakes ranging from 707 to 1321 kj for 8 two‐week periods. Energy was the first limiting nutrient, in those cases where the differences in egg output between treatments were sufficiently large.

2. Body weight, egg number and egg weight all responded (P < 0–001) to energy intake, and as judged by regression analyses, these responses had stabilised by the fifth period.

3. For a near‐maximum egg output of 48 g/bird d, the difference between the ME requirement of the average bird and of the flock, estimated from linear and curvilinear models respectively, was 20–5%.

4. The ME requirement (Y, kj/bird d) of the average bird for egg production (E, g/bird d) and maintenance of metabolic body size (kg W°. ⁷⁵ ) corrected to an ambient temperature of 22 °C is given by the equation, Y = 440W ^0.75 + 8.96 E     

Effects of dietary supplementation of choline and carnitine on growth performance,meat oxidative stability and carcass composition of broiler chickens fed diets with different metabolisable energy levels

1. This study was conducted to investigate the effects of two lipotropic factors (choline and carnitine) on growth performance, oxidative stability of leg and breast muscles and carcass characteristics in broiler chickens fed diets differing in metabolisable energy (ME) levels.

2. A total of 540 one-d-old Ross 308 broiler chicks were allotted to 9 experimental diets, including three ME levels (control, or 0.42 or 0.84 MJ/kg higher ME) and three types of supplemental lipotropic factors (control, 1000 mg/kg of choline or 100 mg/kg of carnitine) as a 3 × 3 factorial arrangement of treatments. Average daily feed intake (ADFI), average daily gain (ADG) and feed conversion ratio (FCR) were recorded during the starter (1–14 d of age), grower (15–28 d of age) and finisher (29–42 d of age) periods.

3. Results showed that the increase in dietary ME level had no impact on ADFI during the starter and grower periods. In the finisher period, increasing dietary ME decreased (P < 0.001) ADFI. Raising dietary ME level by 0.84 MJ/kg resulted in the greater ADG during the grower (P < 0.05) and finisher (P < 0.001) periods. Moreover, an improvement in FCR was observed with feeding the +0.84 MJ/kg diet. Dietary supplementation of lipotropic factors improved FCR values in birds fed the control and +0.84 MJ/kg diets during the grower and finisher periods (P < 0.01).

4. Dietary supplementation of both choline and carnitine increased (P < 0.05) moisture content of leg muscle, although malondialdehyde content of leg muscle was decreased (P < 0.01) in the presence of both lipotropic factors. Dietary supplementation of carnitine decreased (P < 0.01) leg fat content, and this effect was more obvious with higher ME levels, giving a significant ME × lipotrope interaction (P < 0.05). Higher dietary ME level (+0.84 MJ/kg) reduced (P < 0.05) protein content of breast muscle, but this factor was increased (P < 0.05) by dietary supplementation of choline.

5. Although dietary ME level had no marked effect on carcass yield and internal organ weight, supplemental choline increased (P < 0.01) carcass yield.

6. The results from this trial indicated that dietary supplementation with lipotropic factors can improve feed efficiency in high energy diets. In addition, oxidative stability of leg/breast muscles was improved as a result of dietary supplementation with choline or carnitine.     

Guanidinoacetic acid supplementation in broiler chickens fed on corn-soybean diets affects performance in the finisher period and energy metabolites in breast muscle independent of diet nutrient density

(1) Guanidinoacetic acid (GAA) is the single immediate endogenous precursor of creatine (Cr). It was hypothesised that dietary GAA would have different effects on performance and energy metabolites in breast muscle depending on the nutrient density (ND) of corn-soybean-based diets.

(2) A total of 540 one-day-old male Ross 308 broilers were allocated to 9 dietary treatments with 6 replicates (10 birds each) in a 3 × 3 factorial arrangement with three levels of ND (low, 2800; medium, 2950 and high, 3100 kcal metabolizable energy (ME)/kg; and with the other nutrients being constant relative to ME) and supplemented with three levels of GAA (0, 0.6 and 1.2 g/kg) in a 42-d feeding trial.

(3) In the starter and grower periods, increasing levels of ND improved body weight (BW), average daily gain (ADG), average daily feed intake (ADFI) and feed conversion ratio (FCR), with the exception of ADFI in the starter period. GAA supplementation did not affect performance characteristics. All performance indicators responded markedly to increasing ND in the finisher period, whereas the highest GAA level reduced ADFI compared to the unsupplemented control (156 vs. 162 g/d) and concomitantly FCR (1.81 vs. 1.93). No interactive effects were noted for any performance trait. The high ND diet resulted in more breast meat yield on d42, associated with higher fat content and darker colour compared to the other ND levels. The GAA supplementation did not affect carcass and breast traits. At the end of the experiment, Cr was elevated when feeding GAA at 1.2 g/kg (5455 vs. 4338 mg/kg fresh muscle).

(4) To conclude, ND had a substantial effect on performance and carcass traits, whereas any effect of GAA was limited to FCR in the finisher period and independent of diet ND level.     

The effect of restricting the individual daily energy intake of caged layers on the efficiency of egg production

Two experiments are described in which the daily metabolisable energy intake of laying hens fed a concentrated diet (ME = 3550 kcal/kg) was restricted on an individual hen basis. Performance on this diet was compared with that of hens fed a high‐energy diet (ME = 2690 kcal/kg). In experiment 1 medium‐weight hybrid pullets were used and in experiment 2 two light‐weight hybrid strains were used.

In both experiments maximum egg production was obtained from the birds fed the high‐energy diet ad libitum. Restriction of the concentrated diet caused a significant reduction of body weight gain and a statistically insignificant fall in the total weight of egg product and in percentage production in both experiments.

Restriction of the concentrated diet caused improvements of 22 and 18 per cent in the efficiency of utilisation of metabolisable energy in experiments 1 and 2 respectively.

The data are discussed in relation to the relevant literature and the current cost of concentrated sources of energy.     

Effect of different concentrations of metabolisable energy and protein on performance of White Leghorn layers in a tropical climate

1. An experiment was conducted to study the effects of feeding graded concentrations of metabolisable energy (ME) and crude protein (CP) on the performance of layers. Nine diets with three concentrations each of ME (10.04, 10.67 and 11.30 MJ/kg) and CP (150, 165 and 180 g/kg) in a 3 × 3 factorial arrangement of treatments were formulated.

2. A total of 5544 White Leghorn (WL) pullets (20 weeks of age) were housed in 4-bird colony cages and 22 adjacent cages constituted a replicate. Each diet was fed ad libitum to 7 replicates from 21 to 72 weeks of age. Production variables were recorded in 13 laying periods of 28 d each, and the data were pooled into three production phases, namely initial (21–32 weeks), peak (33–52 weeks) and post-peak (53–72 weeks).

3. No interaction was observed between ME and CP for egg production (EP), food intake (FI), food efficiency (FE), egg weight (EW), egg mass (EM) and body weight gain.

4. The EP, EW and EM during the initial phase of production were not affected by dietary ME concentrations, while the EW and EM improved with increasing concentrations of dietary CP from 150 to 165 g/kg.

5. During the peak production phase, improvements in EP (ME and CP), FI (ME), FE (ME, CP), EW (ME) and EM (ME, CP) were observed with increasing concentrations of energy and protein to 11.30 and 180 g/kg diet, respectively.

6. EP, EW and EM were unaffected by dietary variation in concentrations of ME and CP during post-peak production phase, but the FE improved and FI reduced with increasing dietary concentrations of these nutrients.

7. It is concluded that the optimum concentrations of ME for WL layers during the 21–32, 33–52 and 53–72 weeks of age are 11.30, 11.30 and 10.04 MJ/kg diet, respectively. The corresponding values for CP in diets are 180, 180 and 150 g/kg.     

Evaluation of probiotics in diets with different nutrient densities on growth performance,blood characteristics,relative organ weight and breast meat characteristics in broilers

1. A total of 720 1-d-old broilers were used in a 28 d experiment to determine the effects of probiotic supplementation in diets with different dietary nutrient densities.

2. Birds were randomly allotted to one of the 4 treatments in a 2 × 2 factorial arrangement (12 replicateswith 15 broilers per replicate) with two levels of nutrient density [high nutrient density (metabolisable energy (ME) 12.7 MJ/kg and crude protein (CP) 230.3 g/kg for 1–7 d; ME 13.2 MJ/kg and CP 220.3 g/kg for 8–28 d) or low nutrient density (ME 12.1 MJ/kg and CP 220.2 g/kg for 0–7 d; ME 12.6 MJ/kg and CP 209.8 g/kg for 8–28 d)] and 0 or 2 g/kg probiotics (1.0 × 10¹⁰ viable spores/g of Bacillus subtilis endospores and 1.0 × 10⁹ viable spores/g of Clostridium butyricum).

3. The high-nutrient-density diet increased body weight gain (BWG), feed conversion ratio (FCR), serum cholesterol and triglyceride concentration relative to the low-nutrient-density diet. High-nutrient-density diet reduced water loss ratio of breast muscle, liver and fat relative to body weight compared to low-nutrient density-diet. The inclusion of probiotics increased BWG and feed intake throughout the experiment. Dietary probiotics increased the percentage of blood lymphocytes and relative weight of spleen and bursa of Fabricius when compared to the non-probiotic treatment. The inclusion of probiotics decreased serum cholesterol and triglyceride concentrations and lightness (L*) value of breast meat compared to the non-probiotic-supplemented diet.

4. In conclusion, high dietary nutrient density increased growth performance and serum cholesterol and triglyceride concentrations in broiler chickens. The inclusion of probiotics increased growth performance but reduced serum cholesterol and triglyceride concentrations. The positive effect of probiotic supplementation on growth performance was reduced by the high-nutrient-density diet during the first week of life.     

The effects of dietary calcium concentration on pheasant breeder performance

1. Thirteen pens of breeding pheasants (Phasianus colchicus) were fed ad libitum on diets containing 20, 23 or 27 g calcium/kg.

2. All diets were formulated to contain 10.6 MJ ME/kg.

3. Three pens of birds receiving the diet containing 23 g calcium/kg were also offered grit free choice containing 280 g calcium/kg.

4. There were no effects of treatment on food consumption or reproductive performance.     

Comparison of nutritive values of groundnut oil cake and Niger oil cake for laying pullets

1. The nutritive value of Niger oil cake (Guizotia abyssinica, Cass.) as a protein supplement for layers’ diets has been assessed.

2. Replacing groundnut oil cake (GNC) by Niger oil cake (NC) on an isonitrogenous basis, did not affect egg production, egg weight or the amount of food required per dozen eggs.

3. The percentage retention of nitrogen from diets containing 30% GNC or 30% NC was similar.

4. The ME value of NC used was 3025 kcal/kg.

5. It is concluded that NC can replace GNC in layers’ diets.     

Metabolisable energy and digestible nutrient contents of brewers grains and glucose for the young Turkey

1. The metabolisable energy (ME) contents of dried brewers grains and of dried brewers grains with yeast were 5.51 +0.69 and 7.20 ±0.69 MJ/kg dry matter or 0.25 + 0.03 and 0.34 + 0.03 of their respective gross energy contents.

2. In these respective ingredients, the apparent digestibility coefficients of protein were, 0.66 + 0.08 and 0.69 + 0.08; of fat, 0.49 + 0.16 and 0.64 + 0.16; of dry matter 0.14 + 0.05 and 0.24 + 0.05, while fibre and nitrogen‐free extract (NFE) were not digested.

3. In balanced low‐protein diets formed by adding glucose to a high‐protein diet, the ME content of glucose was 15.12 + 0.44 MJ/kg dry matter or 0.97 ± 0.03 of its gross energy content, while the apparent digestibility coefficient of its NFE was 0–99 + 0–02, and that of its dry matter was 1.02 + 0.04.

4. Imbalancing diets greatly by removing or adding glucose to a balanced diet did not affect the nutrient digestibility or the ME of glucose, indicating that the basic assumption of linearity of these measurements with dietary content of the test ingredient was valid.     

A comparison of the energy and nitrogen metabolism of broilers selected for increased growth rate,food consumption and conversion of food to gain

1. Calorimetric measurements were made on 5‐week‐old male chickens sampled from the third generation of three lines selected for either increased live‐weight gain (W), food consumption (F), or food conversion efficiency (E). A control line (C) was also measured.

2. Food intake and food conversion ratio were greater (P<0.05) in the F line than in the E and C lines.

3. Metabolisability of the diet was 0.8% higher in the E line than in the other lines.

4. Metabolisable energy (ME) intake and heat production were greater (P<0.05) in the F line than in the E and C lines, and energy balance was greater (P<0.05) in the F than in the W and E lines.

5. During starvation, excreta energy and heat production were greater (P < 0.05) in the F than the other lines.

6. Availability of ME (net energy) was the same (85%) for all lines but calculated daily maintenance energy requirements (kJ ME/kgW) were W, 860; F, 937; E, 796 and C, 810.

7. By 9 weeks the F line contained more fat and less water than lines E and C.     

Growth rate of different sexes of the European quail (Coturnix coturnix)

1. The Gompertz equation was used to described the growth of the European quail (Coturnix coturnix) from hatching until 107 d of age.

2. Differences (P < 0.05) in growth existed between sexes. Mature mass values of 148.0 ±3.00 and 191.9 ±5.35 g respectively were found for males and females. Males reached maximum growth at 13.4 ± 0.33 d while a value of 16.4 ± 0.46 d was found for females.

3. A plateau in daily food intake was reached when the time of mature mass was approached.     

The performance of male ducklings given starter diets with different concentrations of energy and protein

1. Male ducklings were fed for 14, 21 or 28 d on diets containing 180, 200, 220 or 240 g of protein and 10.88 or 12.55 MJ of metabolisable energy (ME) per kg, followed by a common finisher diet until 56 d of age.

2. Birds given starter diets with 220 or 240 g of protein per kg were significantly heavier at 14 d than those given diets with 180 or 200 g protein per kg.

3. There was no significant benefit in feeding diets with protein levels greater than 180 g/kg for more than 14 d.

4. Diets with only 10.88 MJ of ME per kg produced significantly lighter birds at 28 and 56 d of age and significantly reduced food conversion efficiency up to 14 d.     

Effects of lighting regimen and grower diet energy concentration on energy expenditure,fat deposition and body weight gain of laying hens

1. Mean metabolisable energy (ME) intakes and heat productions over a laying year were calculated for laying hens which had been submitted to one of various lighting regimens and given either a normal or a high energy ration during the rearing period.

2. Daily ME intake and heat production per hen in the laying period were unaffected by either lighting regimen or grower diet. ME intake per kg W ^0.75 and heat production per kg W ^0.75 during lay increased significantly with laying photoperiod, was non‐significantly higher following an 8‐h rather than an 11‐h rearing photoperiod, but was unaffected by dietary energy concentration. The increase in heat production (/kgW°‘⁷⁵) associated with a 1‐h increment in photoperiod was similar to predictions made from calorimetric measurements of diurnal variation.

3. Efficiency of conversion of food to egg was unaffected by either lighting regimen or dietary energy concentration.

4. Fat weight gain in lay was not influenced by lighting regimen, but was significantly lower in birds reared on the high, compared to the normal, energy grower ration. Fat‐free weight gain in lay was unaffected by grower diet, but was significantly increased by photoperiods longer than 8 h.

5. ME intake and heat production per kgW^⁰⁷⁵ were negatively correlated with age at first egg, but ME intake and heat production per bird d were not related to age at sexual maturity.     

Effects of environmental temperature,dietary energy,sex and age on nitrogen and energy retention in the edible carcase of broilers

1. Two environmentally‐controlled houses, one set at constant 21°C (low temperature, LT) and the other set at diurnally cycling 21°C to 30°C (high temperature, HT), and two dietary energy concentrations of 13 MJ ME/kg (low energy, LE) and 13.8 MJ ME/kg (high energy, HE) were used to study nitrogen and energy retention in the edible carcase of male and female broilers slaughtered at 34 and 54 days.

2. Carcase nitrogen was higher in males than in females, and in birds reared at LT than in those reared at HT.

3. Birds at LT and on HE diet, regardless of sex, retained more energy as fat in their carcases than those at HT and on LE diet respectively.

4. Maintenance energy requirement averaged 6.70, 7.67, 7.43 and 9.01 kJ per g metabolic body size (kJ/gW 0.66) for broilers at HT and LT up to 34 d and at HT and LT up to 54 d, respectively.

5. There was a similar increase with age in the energy requirement for growth but with requirements of broilers at LT consistently lower than for those at HT.     

Immune-modulatory effects of dietary Saccharomyces cerevisiae cell wall in broiler chickens inoculated with Escherichia coli lipopolysaccharide

1. An experiment was conducted to study the effect of yeast (Saccharomyces cerevisiae) cell wall (YCW) supplemented in diets of broiler chickens challenged with Escherichia coli lipopolysaccharide (LPS).

2. One-day-old broiler chicks were randomly distributed into 24 cages (6 replicate cages; 8 birds/cage) and were inoculated with 0 or 1 mg/kg body weight E. coli-LPS (d 4 and 9) and 0 or 500 mg YCW/kg feed, resulting in a 2 × 2 factorial arrangement of treatments. Experimental diets did not include coccidiostats, in-feed antibiotics or enzymes.

3. On d 21, the inoculation of E. coli-LPS reduced weight gain and feed intake and increased feed conversion ratio (FCR) of birds, an effect maintained until 28 d. In contrast, chickens given diets with YCW improved the FCR at both 21 and 28 d of age.

4. E. coli-LPS challenge reduced the relative weight of bursa of Fabricius, except when chickens were given YCW, which resulted in an interaction. Supplementation of broiler diets with YCW exacerbated the cellular immune response as measured by the delayed cutaneous hypersensitivity response test.

5. The results of this study suggested a benefit on feed efficiency when YCW was added to diets fed to broiler chickens challenged with E. coli-LPS. Part of the mode of action of YCW might be related to better maintenance of immune status in response to microbial challenge.     

A comparison of methods for estimating the metabolisable energy of a sample of grass meal

1. The inclusion of grass meal in the diets of broilers and laying hens reduced food intake and, as a consequence, the apparent metabolisable energy (AME) and nitrogen‐corrected AME (AME_N) values estimated for the grass meal were artificially low.

2. With young broilers the AME and AME_N values of a sample of grass meal were estimated to be 5.97 ± 0.45 and 6.05 + 0.46 MJ/kg dry matter respectively.

3. With adult laying hens the AME and AME_N values of the sample of grass meal were estimated to be 5.36 ± 1.04 and 6.26 ± 0.96 MJ/kg dry matter respectively and the corresponding true metabolisable energy (TME) and nitrogen‐corrected TME (TME_N) values were shown to be 9.12 ± 1.25 and 8.66 ± 1.33 MJ/kg dry matter.

4. It was further illustrated that if the dietary intake of the adult birds had been 100 g/d, the AME value of the grass meal would have been estimated as 8.33 MJ/kg dry matter.     

The effects of temperature on broilers: A simulation model of the responses to temperature

1. The effects of post‐brooding temperature (15 to 27 °C), age (42 to 56 d) and dietary nutrient and concentration energy (11.7 to 13.3 MJ/kg for the finisher diet) on the cumulative food intake and body weight responses of broilers were combined in a predictive simulation model, using multiple regression techniques.

2. An economic model of these responses was developed in which the temperature and age at slaughter are optimised, given food and live body weight prices.

3. If a finisher diet of 13.3 MJ ME and 199 g protein/kg costing 150 £/tonne is fed, and provided the grower diet contains 13.5 MJ and 221 g protein/kg, the optimum temperature is 21 to 22 °C for male and female broilers slaughtered at 61 and 54 d respectively with a live body weight value of £0.50/kg.     

Energy requirements of laying hens in a semi‐arid continental climate 1

A total of 1260 Single Comb White Leghorn layers were used in three experiments, each of 12 months duration. The experimental site was inland, at an elevation of 995 m above sea level and received a mean annual rainfall of 450 mm. The metabolisable energy (ME) contents of the diets used ranged from 2582 to 2918 kcal/kg, lower energies being achieved by the substitution of barley for maize and higher energies by the use of beef tallow.

Differences in dietary energy caused significant differences in egg production and weight in two of the experiments. Increasing ME of the diet caused significant decreases in food intake in two experiments and significant improvements in the efficiency of food conversion in all experiments. Dietary energy was found to affect body weight gains significantly in only one experiment. Energy intake during the summer was 10 to 15% lower than during the winter or spring.

It is concluded from this study that hens of the strain used, laying at a rate of 70 to 75% and weighing about 1·65 kg in a semi‐arid continental climate, require approximately 300 kcal (1·25 MJ) per bird‐days. This requirement varies with the season, being approximately 20 kcal (84 kJ) higher during the winter and 20 kcal lower during the summer.