Effect of diet and natural variations in climates on the performance of laying hens

1. Laying hens raised in 3 natural tropical environments were fed on 2 series of diets with a view to defining the optimum combination of climate and dietary energy.

2. A combination of 3 growing climates, 3 laying climates (temperate, hot dry, hot humid), and 2 dietary energy concentrations (10.03 and 11.70 MJ ME/kg with protein concentrations proportional to energy) were tested for 46 weeks using 432 point‐of‐lay pullets.

3. Both growing and laying climates significantly affected most traits measured during the laying period. The patterns of egg production showed good persistency in all environments and differences observed reduced with age.

4. The difference between the high and low energy intake reduced at high ambient temperatures. Feeding low energy diets did not affect mean age at first egg, rate of lay or the egg output in the hot dry environment, nor egg weight in either hot dry or hot humid climates. Rather, feeding low energy diets resulted in improved body weight change in all 3 laying environments.

5. The growing climate and diet interacted significandy on body weight change, while highly significant interactions between laying climate and diet occurred on rate of lay, food and energy intake and egg weight during the laying period.     

Effects of nutrient concentration and dietary presentation on performance of dwarf hens

1. Diets containing 170 or 190 g protein/kg and 10.9 or 11.7 MJ ME/kg in all combinations were offered to dwarf hens in two dietary presentations: a complete mash or a form in which part of the protein and calcium contents were presented as soyabean meal pellets and limestone grit respectively.

2. Egg production and egg mass output were higher with the 190 g protein/kg diets.

3. Lower‐energy diets gave better egg production, while higher‐energy diets containing 190 g protein/kg improved food conversion efficiency.

4. Separation of protein and calcium constituents tended to give better egg production, food conversion efficiency, shell thickness and egg mass output.     

Influence of activity and dietary energy on broiler performance,carcase yield and sensory quality

1. A total of 2560 male and female Ross broilers were raised to 42 days of age in a 2 × 2 treatment factorial arrangement experiment to investigate the influence of different degrees of physical activity and dietary energy on broiler performance, abdominal fat content, carcase yield and sensory quality.

2. Vertical fans were used to force the treatment birds to walk 3 to 4 times as far as the normal activity birds; birds were fed a normal and a high energy diet (12.55 compared with 13.81 MJ ME/kg) with the same energy/protein, energy/lysine and energy/methionine + cystine ratios.

3. High activity birds had greater body weight ( + 4.1%), food intake ( + 5.1%) and ME intake ( + 5.1%) than normal activity birds. Birds receiving high energy diet had a lower food conversion and food intake than birds receiving normal energy diet. There were no significant differences in body weight or ME intake between birds with different diets.

4. Slaughter yields, both absolute and relative to live body weight, were affected by activity or dietary energy to varying degrees. Breast meat was increased with more activity. The absolute weight of abdominal fat was independent of activity and in males the relative weight of abdominal fat was decreased in high activity birds.

5. Different degrees of activity and dietary energy had only minor influences on broilers' sensory quality.     

Energy requirement of laying japanese quail

1. Two feeding experiments were conducted to determine the meta‐bolisable energy (ME) requirement of laying Japanese quail. Birds were fed to provide 5.5 g protein and 167, 209, 251 or 293 kJ ME/d.

2. As ME intake increased from 167 to 293 kJ egg production increased.

3. Quadratic relationships between ME intake and egg production, ME intake and egg weight, and ME intake and egg mass (g egg/ bird d) were derived and used to determine the energy required for an acceptable production rate.

4. To maintain a production of 8.3 g egg/bird d (90 eggs/100 bird d with a mean weight of 9.3 g) required 260 kJ ME/bird d.     

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.     

Effect of dietary protein content on live and carcase performance of heterozygous naked neck and normally feathered broilers

1. An experiment was conducted to determine the effect of different dietary protein contents on the performance of naked neck (Na/na) and normally feathered (na/na) broilers.

2. Chicks from the two genotypes were reared in wire‐floored cages and divided at random into 3 groups. Birds were fed on high protein (HP, 12.99 MJ ME, 238 g crude protein/kg and 12.94 MJ ME, 216 g crude protein/kg from 0 to 3 and 3 to 7 weeks, respectively), medium protein (MP, 12.99 MJ ME, 219 g crude protein/kg and 12.87 MJ ME, 201 g crude protein/kg from 0 to 3 and 3 to 7 weeks), and low protein (LP, 12.94 MJ ME, 205 g crude protein/kg and 12.75 MJ ME, 184 g protein/kg from 0 to 3 and 3 to 7 weeks) diets.

3. The LP diets resulted in a significantly lower daily body weight gain of males from 0 to 3 weeks. Dietary protein content had no effect on body weight gain from 3 to 7 weeks, body weight at 7 weeks, and the food intake of birds. Carcase composition of birds from both genotypes was unaffected by dietary protein.

4. Naked neck birds had significandy higher body weights at 7 weeks. Yields of carcase and breast of Na/na males were significantly higher than those of na/na males. There were no significant differences between females from the two genotypes as regards carcase yield.

5. It was concluded that the dietary protein requirements of naked neck birds were similar to those for normally feathered birds.     

Effects of energy and protein allowances during lay on the reproductive performance of broiler breeder hens

1. Broiler parent stock were fed daily allowances of 1.88, 1.73 or 1.52 MJ apparent metabolisable energy (AME) per bird at two different daily protein intakes (27, 21.3 g crude protein (CP) per bird) or daily protein intakes of 24.6 and 19.4 g CP per bird at a daily energy intake of 1.88 MJ AME per bird from 21 to 64 weeks of age.

2. Body‐weight gain and carcass fat and water content increased and fertility decreased with increasing energy allowance. Maximum egg production occurred at an energy intake of 1.73 MJ AME/bird d.

3. Differences in egg weight and hatchability were related to differences in both energy and protein intake. The highest egg weight occurred at the highest allowance of energy and protein. Hatchability was depressed where the daily allowances of protein and energy were in a ratio of more than 15 g protein: 1 MJ AME.

4. Apart from egg size no significant effects on reproductive performance were observed when dietary protein intake was varied from 27 to 19.5 g/bird d.

5. Requirements of broiler breeder hens for protein during lay may be lower than previously thought. For the strain used a protein intake of 19.5 g/bird d appeared adequate provided essential amino acid concentrations were maintained.

6. The close relationships between body weight and energy allowance and the latter and egg production make body‐weight gain a useful guide to management. A body‐weight gain of about 1.1 kg from 21 to 36 weeks of age was associated with optimum performance in this study.     

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.     

Fat deposition and heat production as responses to surplus dietary energy in fowls given a wide range of metabolisable energy: Protein ratios

1. Female broiler fowl between 21 and 42 d of age were given diets with apparent metabolisable energy (AME) contents ranging from 8 to 15 MJ/kg at each of two crude protein (nitrogen x 6.25; CP) contents (130 and 210 g/kg).

2. Food intake was measured daily for 21 d. Body composition was determined at 42 d and gains in body mass, protein, fat and gross energy calculated by comparison with a group analysed at 21 d. Heat production was calculated by difference between AME intake and energy gain.

3. Decrease of food mass intake with increased dietary AME concentration limited the increase in AME intake to about 25%, despite the near 2‐fold range of AME concentrations.

4. There was no effect of CP concentration on food mass intake. CP intake was directly related to CP: AME ratio.

5. When body weight differences were taken into account, heat production was independent of dietary AME concentration, but increased by about 8% on the higher‐protein diets.

6. There were strong linear correlations between dietary CP:AME ratio and carcase protein: energy ratio, carcase fat content and carcase protein content.

7. It was concluded that the growing fowl responded to dietary nutrient: energy ratio, and the associated differences in nutrient and energy intakes, by varying the rate of energy deposition as fat, without regulatory variation of energy dissipation as heat.     

The nutritional value of salseed (Shorea robusta) meal for growing chicks

1. Salseed meal contains 98 g crude protein, 22 g ether extractives, 450 g available carbohydrate and 117 g tannins per kg.

2. From the chemical analysis the metabolisable energy (ME) content of salseed meal would be expected to be 11.22 MJ/kg. In vivo assay with chicks yielded values considerably less than this, 7.1 MJ/kg being found at an inclusion rate of 150 g/kg diet.

3. As the inclusion rate of salseed meal was increased to 300 g/kg, dietary ME and the digestion and retention of dietary protein decreased.

4. More than 50 g salseed meal/kg in the diet of chicks resulted in poor growth rate and food conversion.     

The nutrient intake of laying hens given a choice of diets,in relation to their production requirements

1. Sixty individually‐caged birds, each of two stocks, were offered either a complete diet (11.2 MJ ME, 173 g crude protein and 32 g Ca per kilogram) or a choice between the same diet and ground barley. All diets were offered ad libitum from 41 to 56 weeks of age.

2. Weight gain, rate of lay, mean egg weight, egg output, shell thickness and total food intake were unaffected by the treatments in either stock.

3. The mean intake of the complete diet was 825 and 845 g/kg of total intake with standard deviations between individuals of 73 and 61 g/kg respectively in the two stocks.

4. In birds given a choice of diet the one selected was related to output (P < 0.01).     

Comparison between concentrated complete diets and self‐selection for feeding sexually‐maturing pullets at hot and cold temperatures

1. Pullets in late growth and early lay were maintained at hot (25° to 35°C) or cold (6° to 16°C) ambient temperatures and either fed complete diets or allowed to self‐select nutrients from separate energy‐ and protein‐rich foods.

2. Manipulating the metabolisable energy (ME) and/or nutrient density (ND) of complete layer diets failed to improve egg output at hot temperatures to that obtained at cold temperatures.

3. At both temperatures self‐selection increased protein, but not ME, intake. This increased egg output and body weight gain at the hot, but not cold, temperatures. At the hot temperatures pullets fed by self‐selection were the only ones to gain weight between sexual maturity and 28 weeks of age.

4. Nutrient intake patterns, related to each pullet's physiological age of sexual maturity, identified distinctive changes in protein intake and the selected protein: ME intake ratio of pullets fed by self‐selection. Pullets attempted to maintain a preferred protein:ME intake ratio, irrespective of the markedly different intakes of ME and protein at the two temperatures.

5. Pullets trained to self‐select nutrients from separate energy‐ and protein‐rich foods are better able to sustain egg output and body weight at sexual maturity when food intake is limited by high ambient temperatures.     

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.     

Voluntary food restriction by laying hens mediated through dietary self‐selection

1. Individually caged Single Comb White Leghorn hens simultaneously received two diets which allowed selection of certain nutrients: these “ split‐diets “, essentially provided concentrated sources of either protein and energy (191 g crude protein, 12.82 MJ ME and 4.7 g Ca/kg diet), or calcium (107 g CP, 7.28 MJ ME and 131 g Ca/kg).

2. During four, 28‐d periods of lay, birds offered these split‐diets consumed some 7% less food in total than did control birds receiving a conventional diet ad libitum.

3. Calculation of nutrient intakes showed that birds on the split‐diets consumed significantly less protein, energy and calcium than the control birds.

4. Giving split‐diets also resulted in superior shell quality; treatment differences were also noted in the timing of oviposition.

5. It is suggested that the voluntary reduction in food intake noted for birds offered split‐diets is associated with an appetite for calcium.     

Effect of dietary energy concentration on the response of laying hens to amino acids

1. A hypothesis, that the optimum amino acid concentration in the diet is not directly proportional to the dietary energy concentration, but changes in inverse proportion to the change in food intake resulting from a change in energy concentration, was tested in three experiments.

2. Response experiments involving the amino acids methionine, lysine and isoleucine were conducted, in each case at three dietary energy concentrations, using a diet dilution and blending technique, thereby ensuring a constant ratio between background amino acids and the first‐limiting amino acid in all diets, and also keeping the ratio of amino acids to energy constant as energy varied.

3. A common response curve relating egg output (g/bird d) to amino acid intake (mg/bird d) for each amino acid, fitted by means of the Reading Model, adequately described the response at each of the dietary energy contents. This implies that energy does not influence egg output directly, but only indirectly through its effect on food intake and hence on amino acid intake.

4. Both amino acid and energy concentration significantly influenced food intake. Energy intake was not constant over all dietary energy concentrations, being lower at low energy levels and higher at high energy concentrations.

5. It is concluded that amino acid requirements should not be stated either as percentages or as ratios with energy. Optimum amino acid intakes and energy concentrations should be calculated; the expected food intake should then be predicted, after which the appropriate concentration of nutrients in the diet can be determined.     

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.     

Influence of dietary calcium and phosphorus on metabolism and production in laying hens

1. The effects of different dietary concentrations of calcium (24 to 56.9 g/kg) and phosphorus (4.5 to 14.2 g/kg) on production and some aspects of metabolism were studied in laying hens.

2. Treatments did not affect egg numbers, food consumption, conversion efficiency of food to egg, bodyweight gain or mortality.

3. Increasing dietary calcium (Ca) significantly increased plasma Ca and inorganic phosphorus (P), breaking strength at the radius and egg specific gravity and significantly decreased plasma alkaline phosphatase and egg weight.

4. Increasing dietary phosphorus increased plasma P and decreased egg specific gravity significantly.

5. Plasma Ca, P and alkaline phosphatase and radius breaking strength were suitable indices of the Ca status of the hens.     

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.     

Effects of cultivar,pelleting and enzyme addition on nutritive value of barley in poultry diets

1. The effect of pelleting process and Trichoderma viride enzymes (TVE) addition on apparent metabolisable energy, corrected for nitrogen balance (AMEn) and on productive value of practical diets containing 40 and 45% of three different barley cultivars and one wheat were studied in poultry.

2. The effect of the pelleting process on AMEn was inconsistent and was dependent on the cereal included and the addition of enzyme.

3. The growth trial showed a significant effect of enzyme addition to pelleted diets over the whole growth period (0 to 42 d). Addition of TVE improved weight gain and food efficiency by 1.3% and 2.9%, respectively and decreased food intake by 1.6% between 0 and 22 d. In the finisher period (23 to 42 d) TVE improved efficiency by 2.8% and reduced food intake by 2.9%.

4. The incidence of sticky droppings was related to the viscosity of barley used, and enzyme supplementation reduced it. Both pelleting and enzyme addition increased dry matter content of excreta.

5. At the end of the experiment, 14 animals per treatment were slaughtered and carcass yield, viscera weight and abdominal fat were determined.     

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.