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.     

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.     

Relationship between energy and protein intakes and laying characteristics in individually‐caged broiler breeder hens

1. Individually‐caged broiler hens, which had been reared on an advised rationing programme, were fed allowances of 1.88, 1.61, 1.32 or 1.13 MJ apparent metabolisable energy/bird d at four different protein intakes (27, 23, 19.5 or 16.5 g crude protein per bird d) from 21 to 60 weeks of age.

2. Age at first egg, body‐weight gain and egg production were affected by energy allowance. Birds on the lower energy allowances came into lay later than birds on the higher energy allowances and at a lower body weight.

3. Body‐weight gain decreased with decreasing energy allowance. The decrease in egg output in response to decreasing energy allowance resulted from more birds ceasing to lay and fewer birds laying on more than 3 d per week. Similar changes in the distribution of rates of lay were observed on each treatment as the flock aged.

4. The relationship between body‐weight gain and egg number on each treatment was negative from 21 to 36 weeks, but became less consistent with age.

5. Protein intake had little effect on body weight. At the lowest energy allowance, egg number and egg weight decreased with increasing protein allowance. This effect was not observed on the higher energy allowances.     

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.     

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.     

Sulphur amino acid requirement of laying hens and the effects of excess dietary methionine on laying performance

1. Individually‐caged laying hens were fed on maize‐soya bean meal diets containing 11.50 or 12.35 MJ ME/kg with sulphur amino acid (SAA) contents varying from 5.0 to 7.0 g/kg in period 1 (0 to 20 weeks); from 5.0 to 8.0 g/kg in period 2 (21 to 36 weeks) and from 5.0 to 10.0 g/kg in period 3 (37 to 52 weeks).

2. A SAA requirement of about 750 mg/hen d, of which about 425 mg was methionine, was found to be adequate for birds producing on average 51 g egg mass per hen d over 52 weeks. The SAA requirement was found to be higher for maximum efficiency of food utilisation than for maximum egg yield.

3. A diet containing 140 g protein/kg adequately supplemented with methionine and lysine, could sustain laying performance almost identical to that achieved on a diet containing 167 g protein/kg.

4. In diets with 140 g protein/kg the addition of 0.5 to 3.5 g dl‐methionine/kg diet in excess of the requirement did not affect egg production adversely, but food conversion efficiency was decreased.     

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.     

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.     

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.     

Diets for growing pullets containing unusual ingredients and varying concentrations of cereals,including no cereals

1. Growing pullets (Shaver 288) were fed on diets containing about 150 or 100 g protein/kg and 800, 600, 300 or 0 g of a mixture of equal parts of wheat and barley, from 12 to 20 weeks of age.

2. Varying mixtures of dried poultry manure, dried grass, dried potato meal, poultry offal meal and tallow were substituted for the cereal portion, so that calculated metabolisable energy values and methionine and lysine concentrations were constant within each protein series.

3. Within the 150 g protein/kg series, body weight at 20 weeks of age was similar for diets containing 800, 600 and 300 g/kg cereal whereas with the cereal‐free diet body weight was depressed by 10%; with the latter diet sexual maturity was also delayed by nearly 4 d though subsequent egg production was unimpaired.

4. Within the 100 g protein/kg series, body weight at 20 weeks of age and subsequent egg production, calculated either to a fixed age or for a given time spent laying, were depressed by diets containing 300 or 0 g cereal/kg, compared with diets containing 800 or 600 g/kg.

5. Dietary concentrations of dried poultry manure up to 250 g/kg had no effect on mortality.     

Comparison of wheats of high or conventional protein content with added lysine in diets for layers

1. High‐protein wheats (196 or 210 g/kg) were compared with conventional wheat (163 or 162 g/kg) in layers’ diets in three experiments.

2. In diets of 160 g protein/kg without added lysine, high‐protein wheats caused lower rates of production and egg size than conventional wheats in White Leghorns. Lysine supplementation of the former diets eliminated these differences.

3. The improvements in egg production and egg weight were significant with 1 g additional lysine/kg and egg production tended to improve further with 2 g additional lysine/kg, as did egg weight with all subsequent additions, but not significantly so.

4. With diets containing high‐protein wheats supplemented with lysine, high egg production and egg weight could be obtained without a protein supplement (e.g. soyabean meal).

5. In broiler‐breeders egg production was lower and food conversion poorer with high‐protein wheat despite added lysine.     

Effects of restricting the energy intake of laying hens

Light and medium hybrids were allowed to consume, from 24 to 52 weeks of age, ad libitum or approximately 1200, 1154, 1107 and 1062 kJ ME/bird d. A sixth treatment consisted of the lowest level of energy but with higher levels of protein calcium and phosphorus. From 52 to 58 weeks all the birds were fed ad libitum. Treatments were reimposed from 58 to 68 weeks of age.

In the 24‐ to 68‐week period mean rate of lay decreased progressively with decreasing energy intake. Rate of lay of medium and light hybrids allowed 1200 kJ ME/d was, respectively, about 10 and 4 percentage points lower than controls. Initially differences in rate of lay in relation to energy intake were small, particularly in the case of light hybrids, but became more marked as restriction continued. During the 6‐week rehabilitation period previously restricted groups tended to lay more eggs than controls.

With both strains egg weight tended to decrease as energy intake was reduced. In the 6 weeks of rehabilitation most groups tended to lay slightly heavier eggs than controls. At 27 weeks eggs from birds allowed the 1062 kJ/bird d had thinner shells than those from other groups but treatment had no effect on Haugh units. At 48 weeks Haugh units were similar for each restricted group but significantly less for controls (P= 0.05).

Restricted groups lost between 6 and 12% of their body weight in the first 16 weeks but regained a little in the succeeding 12 weeks. During the 6 weeks of rehabilitation they gained weight rapidly but at 68 weeks restricted birds were lighter than they had been at 24 weeks of age. Least‐severely restricted birds were significantly lighter than controls (P = 0.001) and final body weight decreased slightly but progressively with severity of restriction.

Protein or minerals or both, as well as energy, limited egg weight and body weight at the lower level of food intake. The effect on egg weight was more marked in the early stages of lay. There was no evidence that rate of lay or egg quality were limited by nutrients other than energy. Mortality was generally low and there was no evidence of a treatment effect.     

The tryptophan requirements of young laying pullets

1. Two experiments were conducted with laying pullets between 32 and 47 weeks of age. In each trial 1 728 White Leghorn and 1 728 crossbred pullets were used.

2. A series of diets of increasing protein content was offered. Protein quality was identical in all diets and tryptophan was demonstrated to be the most limiting amino acid in the protein mixture used.

3. The daily tryptophan requirement of the individual pullet was estimated, by indirect methods, to be 2.25 mg/g egg output plus 10.25 mg/kg body weight. Response curves for flocks of pullets are illustrated. Calculated optimum intakes of tryptophan for various ratios of costs of input to value of output are tabulated.

4. It is estimated that for a flock of mean body weight 1.5 kg, producing 55 g egg mass/hen d and consuming 110 g food/hen d, the optimum dietary tryptophan concentration is 1.7 g/kg when the marginal cost of supplying 1 kg tryptophan is 20 times the marginal value of 1 kg egg output.     

Requirement of the hen for sulphur‐containing amino acids

1. The sulphur amino acid requirements of White Leghorn‐type laying hens were determined in two 52‐week experiments using diets based on maize and soyabean meal providing from 5.0 to 6.5 g sulphur amino acids/kg, 12.35 MJ ME/kg and 8.6 to 8.8 g lysine/kg. There were six replicates of 15 individually‐caged hens each per treatment.

2. A requirement of approximately 775 to 800 mg sulphur amino acids /hen d, of which about 390 to 440 mg was methionine, was found for a maximum of 80 to 83 eggs/100 hen d. There were indications that the requirement for maximum egg production was less than that for maximum efficiency of food utilisation.

3. Diets containing 138 g protein/kg supplemented with methionine and lysine supported production and food utilisation as effectively as a diet containing 167 g protein/kg.     

Growth rate and efficiency of food conversion of Italian and Landes broiler geese

Growth rate and efficiency of food conversion of Landes and Italian goslings, from hatching to 8 weeks of age, were measured. The goslings were fed on a starting ration containing 19.5% crude protein and 2877 kcal/kg (11.8 MJ/kg) for the first 3 weeks of age and then a growing ration containing 17.5% crude protein and 2877 kcal/kg (11.8 MJ/kg).

The mean body weight was similar in both breeds at 1 d of age, while at 8 weeks the Italian breed was slightly heavier than the Landes. The weekly percentage weight gain for the two breeds were similar, however.

The efficiency of food conversion was higher in the first 4 weeks than in the second 4 weeks in both breeds. The daily food consumption and the efficiency of food conversion of the Italian goslings were lower than those of the Landes throughout the period of the study.     

Growth related traits in body weight selected lines and their crosses reared under different nutritional regimens

1. Four populations—two that had undergone 37 generations of selection for high (HH) and low (LL) body weight, and reciprocal crosses between them (HL and LH) were fed two diets differing in protein and energy. Diet A, under which selection had been made, contained 200 g protein and 11.23 MJ/kg. Diet E contained 240 g protein and 13.16 MJ/kg.

2. Body weight and feed efficiency were measured weekly from hatch to 56 d of age at which time oesophagus, abdominal fat pad, heart, liver and lungs were removed and weighed. At 35 d of age chicks were inoculated with sheep erythrocytes (SRBC) and antibody titre was measured 6 d later.

3. Chicks fed diet E were heavier than those fed diet A. HH chicks were heavier dian LL chicks wim HL and LH chicks intermediate to the parental lines. LH chicks were heavier than HL ones reflecting large maternal effects.

4. Food efficiencies among stocks and diets were consistent with those for body weight, with HH > LH > HL > LL and E > A. Relative differences between diets were similar across ages and heterosis for food efficiency was about 15%.

5. Relative to body weight, oesophagus and liver weights were heavier in chickens fed diet A than fed diet E. The pattern reversed for abdominal fat pad.

6. Antibody to SRBC antigen was greater in the crosses than in line HH and in cross HL than line LL, with heterosis of 70%.     

Effect of added soyabean oil and dietary energy on metabolisable and net energy of broiler diets

1. The ‘extra caloric’ effect of added soyabean oil, as reflected in improved body weight gain, food utilisation, metabolisable energy or net energy deposition in the body was determined.

2. Two diets were formulated to contain 12.1 MJ/kg, one with no added fat and the second with 30 g/kg soyabean oil. Addition of oil improved body weight gain by 6.9% (P< 0.05). Two other diets were formulated to contain 13.0 MJ/kg, one with 30 and one with 60 g/kg added soyabean oil bringing the total fat in the high energy, high fat diet to 84 g/kg. Addition of oil in this case improved weight gain by only 3^.4% (ns). Addition of soyabean oil increased the apparent digestibility of total dietary fat and reduced that of starch.

3. The effect of soyabean oil supplementation on mash diets at both energy concentrations or to the pelleted diet (formulated to contain 12.1MJ) on AME_n was consistently positive although not significant. Addition of soyabean oil improved net energy deposition in the body by 17% within the 12.1 MJ/kg diets, (30 g/kg soyabean oil addition) (P< 0.05), but was reduced by 2% (ns) within the 13.0 MJ/kg diets (60 g/kg soyabean oil addition).

4. Supplementing a pelleted diet formulated to contain 12.1 MJ/kg, with 30 g/kg soyabean oil, improved food utilisation (P< 0.05). The ‘extra caloric’ effect of added soyabean oil, defined as the beneficial effect of the oil above that predicted from its energy value, varied according to the parameter chosen to express this effect and was influenced by the concentration of added soyabean oil and the dietary energy.     

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.     

A comparison of the energy and nitrogen metabolism of starved ducklings and chickens

1. Respiration chambers were used to measure, over 24 h, the heat production of groups of starved ducklings from two batches and of starved broiler chickens from one batch up to 28 and 39 d of age, respectively. Duration of starvation prior to measurements and ambient temperature were adjusted according to the age of the birds.

2. Respiratory quotient of 0.705 for chickens was significantly lower than that of 0.713 for ducklings.

3. Starvation heat production (kJ/d) of ducklings was 804 kgW^0.70 compared with 675 kgW⁰‘⁷⁴ for chickens. There were differences in heat production between the two batches of ducklings used when expressed per kg body weight (W).

4. Ducklings lost more body weight, body fat and protein than chickens during starvation. Gaseous ammonia‐N was on average 9% of N excreted by ducklings and 4% of N excreted by chickens.     

Evaluation of rabbit excreta as an ingredient in broiler diets

1. Dry rabbit excreta were found to contain 188.1 g crude protein, 6.6 g non‐protein nitrogen, 0.3 g ammonia, 89.8 g moisture, 8.0 g ether extractives, 135.2 g crude fibre, 266.9 g ash and 19.18 MJ gross energy/kg. Methionine and lysine contents were 3.95 and 4.29 g/100 g protein, respectively.

2. In one experiment, 0, 50, 100 or 200 g rabbit excreta/kg were substituted for maize in a broiler diet. Chickens receiving the diet containing 200 g rabbit excreta/kg gained significantly less weight to 8 weeks of age than those receiving other diets.

3. In a second experiment, 0, 100, 150 or 200 g rabbit excreta/kg were substituted primarily for maize in a broiler diet to provide equal energy and protein contents. Weight gains to 8 weeks of birds receiving these diets did not differ significantly. The uncorrected metabolisable energy content of the excreta was 9.15 MJ/kg.

4. There were no gross pathological changes in the birds fed on the experimental diets.