Utilisation of leucaena leaf meal by broilers

1. The effect of including Leucaena (Leucaena leucocephala) leaf meal (LLM) in broiler diets was investigated employing LLM at 0, 50, 100, 150 and 200 g/kg diet. Experiments were also conducted to investigate whether reduced food intake of diets containing LLM is responsible for the growth depression.

2. LLM appears to be a good source of protein and calcium.

3. Food intake was not significantly affected (P>0.05) with dietary LLM inclusion up to 200 g/kg.

4. Inclusion of LLM up to 150 g/kg diet did not influence significantly (P>0.05) the performance of broilers in terms of body weight gain and food efficiency. However, inclusion of LLM at 200 g/kg diet had an adverse effect on weight gain and food efficiency, when compared to other dietary treatments. The profitability over food costs was low with the 200 g LLM/kg diet compared to those of other diets.

5. It may be inferred from these experiments that LLM can safely be included in broiler diets up to 150 g/kg.

6. Studies using force‐feeding and restricted feeding techniques indicated that reduced food intake was not responsible for the growth depression in diets containing higher amounts of LLM.     

The effect of sodium sulphate and methionine on the utilisation of non‐protein nitrogen by laying hens

1. The response of layers to adding diammonium citrate (DAC), sodium sulphate or methionine to a basal diet containing 136–3 g protein/kg was determined.

2. Supplementing the diet with DAC equivalent to 25 g protein/kg did not improve egg production, the efficiency of food utilisation, egg weight, nitrogen retention or the apparent absorption of lysine and methionine; increases in food intake and in the concentration of methionine in the serum and liver were observed.

3. Adding sodium sulphate, alone or with DAC, did not affect the variables noted above.

4. Supplementation of the basal diet with methionine increased egg production, egg weight, food intake and the concentrations of lysine in the serum and liver.

5. It is concluded that the supplemental NPN was used only in serum protein synthesis.     

Effect of dietary inclusion of ascorbic acid and palm oil on the performance of laying hens in a hot tropical environment

1. Two experiments were conducted to evaluate the effects of including ascorbic acid (AA), palm oil or a combination of both in the diets of laying hens during the hot months in a tropical environment.

2. The inclusion of AA improved egg production, food intake and efficiency of utilisation, and decreased the cost of food per kg egg. The addition of 400 mg AA/kg diet gave the most efficient performance.

3. Palm oil inclusion reduced the effect of heat stress and increased egg production, egg weight, food intake and efficiency of utilisation.

4. When 200 mg AA and 50 g palm oil/kg were used, additive responses were obtained with further improvements in egg production, food cost and efficiency.

5. Ascorbic acid and palm oil when fed alone or in combination reduced the incidence of cracked eggs.

6. Thus, 400 mg ascorbic acid/kg of diet, 50 g palm oil or 200 mg AA plus 50 g palm oil/kg diet ameliorated the effects of heat stress in laying hens.     

Effects of short intermittent lighting on food consumption and performance of dwarf broiler breeders and progeny

1. Two hundred and sixty four dwarf broiler breeder hens were subjected to ad libitum or restricted feeding and to four lighting patterns: 15L (bright light):9D (dark), 15L:9d (dim light), 2L:10d: 1L:11d, (0.5L:3.5d) × 6.

2. Breeder hens fed ad libitum and subjected to either conventional or intermittent lighting ingested respectively, 25 g and 14 to 17 g more than hens restricted to 115 g/d.

3. Body weight was greater in hens fed ad libitum irrespective of the lighting pattern and of the amount of food intake.

4. Persistency of egg production was impaired by intermittent lighting.

5. Ad libitum feeding reduced egg fertility. The decrease was larger in breeder hens on intermittent lighting.

6. Hatchability was increased in hens submitted to the symmetrical lighting pattern (0.5L:3.5d).

7. Egg and chick weights were higher in hens fed ad libitum.

8. Shell index and shell breaking strength increased in restricted hens on the intermittent lighting pattern (0.5L:3.5d) × 6.

9. The best performance was obtained in restricted hens on the conventional lighting pattern.     

Effects of restricting the amounts of medium or low‐energy diets fed to laying hens in different colony sizes

1. Light hybrid hens between 32 and 68 weeks of age kept 4, 5 or 8 birds to the cage received one of three energy intakes, from a medium‐ or low‐energy diet.

2. Ad libitum fed birds laid more and heavier eggs than any of those restricted. A decrease in daily egg output of about 5 g was associated with each 100 kJ decrease in daily intake of metabolisable energy.

3. For the same energy intake, egg output of birds fed on the low‐energy diet was markedly greater than that associated with the medium‐energy diet.

4. The mortality of birds receiving restricted quantities of the medium‐energy diet was two to three times greater than that associated with similar rationing of the low‐energy diet.     

Lysine requirement of broiler chicks as affected by protein source and method of statistical evaluation 1

1. An experiment was designed to test if the lysine requirement, expressed as g lysine/kg CP, was the same for several protein sources.

2. Groundnut meal, groundnut meal adjusted with indispensable amino acids or sesame meal supplied the dietary CP at 180 g/kg diet. Increments of lysine (1.5 g/kg diet) were added to each of these diets.

3. The gain, food intake and food efficiency responses of broiler chicks were analysed using a quadratic equation and a two‐slope method. An estimate of lysine requirements was also obtained from a survey of college students.

4. The different methods produced widely different estimates of lysine requirement.

5. The average lysine requirement was estimated at 50.1 g lysine/kg CP for groundnut meal, 61.7 for adjusted groundnut meal and 54.9 for sesame meal.

6. Reasons for the effect of statistical analysis and protein source on lysine requirement are discussed.     

Studies on the incorporation of triticale in diets for growing chicks

1. The classical ME value of triticale varied from 12.305 to 13.778 kJ/g or 11.819 to 13.016 kJ/g corrected for N‐retention depending upon method of calculation.

2. Substituting triticale for maize, weight for weight, but not on a iso‐nitrogenous basis, in a groundnut oil cake (GNC) starter diet improved weight gain (P < 0.05) when the substitution exceeded 75% without affecting the protein efficiency ratio (PER).

3. A similar substitution in a soybean oil meal diet, improved weight gain (P < 0.05) at 50% or more but PER declined (P < 0.05).

4. The net protein utilisation and protein retention efficiency values of the diets in which maize protein was replaced by triticale protein were significantly reduced.

5. The maize‐GNC diet was equally limiting in methionine and lysine while the triticale‐GNC diet was not.

6. The growth and food efficiency obtained with a triticale‐GNC diet was higher (P < 0.01) than with the maize‐GNC diet but not with a maize‐GNC supplemented with fish meal and methionine.

7. It is concluded that triticale could quantitatively substitute maize in the starter diets.     

Effect of dietary protein and urea on in vitro caecal ammonia production from urea and uric acid in cockerels

1. Single Comb White Leghorn adult cockerels were fed on 50 g/kg protein diet, 200 g/kg protein diet or 50 g/kg protein diet plus urea and in vitro ammoniagenesis from urea and uric acid in the caeca was determined.

2. Four‐fold protein intake caused about 4.6‐fold increase in caecal ammonia production from urea (P < 0.05), and tended to increase it from uric acid as compared with 50 g/kg protein‐fed birds.

3. Dietary urea significantly increased caecal ammonia production from urea and uric acid by about 2 and 3 times as much as those of control birds, respectively (P < 0.05).

4. It is concluded that increased protein intake and the feeding of urea are able to induce ammoniagenesis from urea and uric acid in the caeca of fowls.     

Responses of laying hens to a low‐protein diet supplemented with essential amino acids,l‐glutamic acid and/or intact protein

1. Three sequential experiments, each lasting 8 weeks, were carried out on 576 singly‐caged light hybrids.

2. In experiment 1 egg production was 84% using a conventional control diet, 61% with a basal low‐protein diet, and 79% with the basal diet supplemented with 10 essential amino acids + L‐glutamic acid (GA).

3. In experiment 2 supplementation with lysine and methionine (L + M) alone increased egg production significantly from 54 to 72%, compared with 83% with the conventional diet.

4. In experiment 3 egg production was 55% with the basal diet, 71% with the basal diet + L + M, 75% with a diet containing 141 g protein/kg + L + M, and 73% with the conventional diet.

5. In all three experiments supplementation with GA alone either gave no significant response or a depression in production.

6. Daily intakes of 1.24 g nitrogen as non‐essential amino acids and 13 to 14 g total crude protein per bird resulted in good egg production. Supplementation of the basal diet with L + M resulted in a daily intake of 413 mg methionine/bird day which was considered adequate, and a daily intake of 710 mg lysine which was considered slightly inadequate.     

Responses in growth,food intake and food conversion efficiency to different dietary protein concentrations in meat‐type lines of Japanese quail

1. A total of 360 Japanese quail of 4 commercial meat‐type lines and two diet treatments (260 and 216 g/kg or 238 and 195 g/kg of crude protein (CP) in the starter and grower diet, respectively) were used.

2. The positive effect of a high CP diet on body weight was significant only for the first 4 weeks after hatching.

3. The mean age at inflection point of the growth curve (t ⁺) across lines and sexes was 1.4 d (0.6 to 2.8 d within line/sex groups) earlier for quail fed on a high CP diet than in quail receiving a low CP diet. The inflection (y ⁺) and asymptotic (A) weights were similar under both dietary protein concentrations. Nevertheless, the shape of the growth curve, characterised by the ratio y⁺1A and parameter of the maturing rate k, was significantly influenced by diet.

4. A higher food intake and less efficient food conversion were found for quail fed on a high CP diet in the period from 15 to 28 d of age.

5. The fattening traits such as body weight, cumulative food intake and food conversion, were not affected by dietary CP content at the age of 5 weeks.

6. The effects of line on body weight, food intake and food conversion are discussed.     

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.     

Incorporation of triticale in layer diets

1. Diets containing either maize or triticale were fed unsupplemented or supplemented with meat meal or groundnut oil to White Leghorn pullets for two periods of 11 weeks each.

2. The egg production of birds fed on the unsupplemented triticale diet was significantly higher than that of the birds fed on the unsupplemented maize diet, but was not significantly different from that of the birds fed on the maize plus meat meal diet.

3. Protein quality of the unsupplemented triticale diet as judged by efficiency of nitrogen retention was similar or inferior to that of the unsupplemented maize diet.

4. The higher protein content of triticale and the increased intake of these diets seemed to be responsible for the better performance observed.

5. Addition of groundnut oil to the triticale diet did not improve either egg weight or production.

6. It is concluded that the quantitative substitution for triticale of maize does not adversely affect egg production and egg weight.     

Hydrolysed feather protein as a source of amino acids for broilers

1. The inclusion of 25 g hydrolysed feather meal (HFM) in each kilogram of diet (floor experiment) and 60 g/kg (cage experiment) did not depress performance.

2. Chemical tests indicated 72.5% of the total lysine in HFM was available.

3. Total lysine concentration of 11.3 g/kg diet maximised performance during the period 0 to 34 d.

4. Reduction in dietary methionine content during the period 0 to 34 d from 4.2 g/kg to 3.2 g/kg did not depress performance on diets containing 60 g HFM/kg.

5. The results indicate that at least 57% by weight of the total sulphur amino acid requirement of broilers can be provided by cystine.     

The response of egg weight to the inclusion of different amounts of vegetable oil and linoleic acid in the diet of laying hens

1. Four diets containing different amounts of vegetable oil and linoleic acid were fed to White Leghorn hens throughout a full laying year.

2. Egg weight was poor with the low fat basal diet but increased in relation to the amounts of maize oil (4 and 30 g/kg) included in the diet.

3. With a diet containing 30 g olive oil/kg, egg weight was similar to that obtained with the diet containing the same amount of maize oil.

4. Rearing the birds on diets containing low or moderate amounts of linoleic acid did not affect the response to fatty acid content of the layer's diet.

5. It is concluded that the requirement of the laying hen for linoleic add is not higher than 9 g/kg but that egg weight does respond to higher dietary amounts of readily absorbable fatty acids.     

The effect of delaying the onset of laying in pullets with a low‐calcium diet on subsequent egg production

1. A low‐calcium diet (0.5 g calcium/kg) was used to prevent the onset of laying in young pullets.

2. It was fed at 16 weeks of age to five separate groups (groups 2 to 6) each of 50 to 60 birds.

3. Group 2 was fed on a normal layers’ diet at 23 weeks of age, group 3 at 27 weeks, group 4 at 31 weeks, group 5 at 35 weeks and group 6 at 55 weeks while the control group (group 1) of similar size to groups 2 to 6 was subjected to a normal commercial treatment for laying stock.

4. In all the experimental groups the onset of sexual maturity occurred normally, but only one or two eggs were laid before laying ceased under the influence of the treatment.

5. Laying re‐started when the hens were fed on a normal diet and production rapidly rose to a high level.

6. Groups 1, 2 and 3 differed little in the total number of eggs produced up to 72 weeks of age.

7. In all experimental groups there were fewer very small, small and medium eggs than in the control group.

8. It is suggested that the use of a low‐calcium diet before the onset of lay may have advantages which could be exploited on a commercial scale.     

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.     

Performance of laying hens fed on low sulphur amino acids diets supplemented with choline and methionine

1. Two experiments were carried out to examine the possibility of replacing a part of the methionine content with choline in a layers’ diet.

2. In the first a low methionine diet with 2.6 g methionine/kg was supplemented with 0.3, 0.6, 0.9 and 1.2 g DL‐methionine/kg. Choline at 1.12 g/kg was added to the diets, which contained 5.4, 6.0 and 6.6 g TSAA.

3. In the second diets with 3.02, 3.80, 4.53, 5.30, 6.04 and 6.51 g TSAA/kg were used and 0.94 g choline/kg was added to these diets.

4. Supplemental methionine increased egg production but not egg weight in the first experiment. When the low TSAA diet was supplemented with choline, egg output increased slightly but not significantly.

5. When supplemental methionine was added to the low protein and TSAA diets in experiment 2 it increased egg production and egg weight. Added choline did not increase egg production or egg weight, even with the diet very low in protein and TSAA. Body weight gain, food intake and feed conversion efficiency of food utilisation were improved by supplemental methionine but not choline.     

Protein and energy metabolism in two lines of chickens selected for growth on high or low protein diets

1. Genetic adaptation was investigated in broilers selected for seven generations on a normal (A) or a low (B) protein diet.

2. Protein and energy metabolism were studied in males from these selected lines fed on a diet of intermediate protein content.

3. All selected birds retained more nitrogen than those studied 10 years previously.

4. There was no difference in nitrogen retention between groups, although relative growth rate of group B birds was higher.

5. Heat productions relative to gross energy intake were 0.38 (group B) and 045 (group A). Energy retentions relative to gross energy intake were 0.39 (group B) and 0.35 (group A); the difference being primarily due to higher fat retention in group B.

6. Using a common maintenance requirement for metabolisable energy, group B utilised metabolisable energy for growth (0.78) better than did group A (0.71).

7. At 53 d of age plasma glucose (10%) and insulin (50%) were higher in group B than in group A.     

Restricting energy intake of laying hens: Effects of different patterns of restriction and rehabilitation

1. Light hybrids were subjected to ten treatments, consisting of different timing, length and severity of energy restriction alternating with periods of unrestricted feeding, between 24 and 68 weeks of age.

2. The pattern of restriction had no direct effect but affected egg production indirectly through its influence on overall energy intake.

3. Groups fed ad libitum throughout laid more and heavier eggs than any restricted group.

4. A decrease in daily egg output of about 4 g was associated with each 100 kJ reduction in daily metabolisable energy intake.     

Diet selection by Japanese quail (Coturnix coturnix japonica) in relation to ambient temperature and metabolic rate

1. A choice between a high‐energy, wheat‐based, low protein mixture and a lower‐energy, soya‐based, high protein mixture was offered to growing Japanese quail at ambient temperatures of 20°, 25°, 30° and 35°C.

2. The quail were kept in open‐circuit respiration calorimeters, so that diet selection could be related to energy requirement.

3. Increasing ambient temperature had no significant effect on food intake by weight, but the proportion of the high energy choice decreased and, conversely, the proportion of the lower‐energy but higher‐protein choice increased.

4. Energy intake was therefore negatively correlated with ambient temperature, but protein intake per unit of energy intake increased, allowing the birds to gain weight at about the same rate at all temperatures.

5. Heat production decreased as ambient temperature increased. Respiratory quotient decreased with increasing temperature, which indicates a reduced utilisation of carbohydrate as an energy source.

6. Water intake increased with temperature but there were no overt signs of heat stress and there was no significant change in body temperature.

7. Japanese quail selected a dietary mixture which maintained similar growth rates over a wide range of ambient temperature, by sustaining protein intake but altering energy intake in line with thermoregulatory energy demands.