Utilisation of squilla meal (a novel animal protein source) by Broilers

1. The nutritive value of squilla meal, which contained 339 g crude protein, 18.6 g ether extract, 72.8 g calcium, 17.2 g phosphorus and 7.13 MJ of apparent metabolisable energy/kg, was examined in 5 experiments with broilers.

2. Squilla meal contained less lysine (3.45 vs 6.74 g/16g nitrogen) and methionine (1.02 vs 1.86/16 g nitrogen) dian fish meal, had a lower protein digestibility coefficient (0.66 vs 0.72) and a lower gross protein value (68% vs 74%).

3. By gradually replacing the fish meal with squilla meal in isocaloric, isonitrogenous broiler diets it was shown that there was a linear decrease in broiler weight gain; efficiencies of food utilisation were also lower at all squilla meal substitution rates. Inclusion of squilla meal in the diets increased intestinal lengths.

4. Addition of a proteolytic enzyme to the diets containing squilla meal restored broiler weight gain and efficiency of food utilisation to that of birds fed on the control diet.

5. Diets containing autoclaved squilla meal resulted in reduced weight gain although efficiency of food utilisation was not affected.     

Performance of broiler chicks fed on alkali‐treated neem (Azadirachta indica) kernel cake as a protein supplement

1. An experiment was conducted to evaluate growth and nutrient efficiency of broiler chicks from 3 to 42 d fed on diets containing alkali‐treated neem (Azadirachta indica A. juss) kernel cake (NKC) as a protein supplement in place of peanut meal (PNM).

2. NKC was treated with sodium hydroxide at 10 (ANKC 1) or 20 g (ANKC 2)/kg and incorporated into the test diets at 135 or 300 g/kg to replace 50 (low—L) or 100 (High—H) % of the PNM protein of the reference diet.

3. Despite comparable retentions of dry matter and total carbohydrate on L‐ANKC 1 and 2, fibre on L‐and H‐ANKC 2 and nitrogen, calcium and acid detergent fibre on all experimental diets compared to the retentions of chicks on the reference diet, only the chicks fed L‐ANKG 2 were found to grow and utilise food as well as those on the reference diet.

4. The activities of serum alkaline phosphatase on H‐ANKC 1 and alanine amino transferase on all test diets were depressed (P < 0.05), but the activity of serum aspartate amino transferase, total erythrocyte count and concentration of blood haemoglobin and urea were similar in all chicks.

5. No significant differences were noticed in the qualitative and quantitative characteristics of the meat of chicks fed on the reference diet and on diets incorporating ANKC at the lower concentrations. Feeding ANKC protein did not impart any untoward taste as evaluated in pressure cooked meat by a semitrained panel on a 7 point Hedonic scale.

6. Except for duodenal and jejunal inflammation in chicks on both reference and test diets, all the vital organs were normal, ruling out any adverse affects caused by residual neem bitters.

7. Comparable performance and cost of chicks fed on the reference and L‐ANKC 2 diets, warrants the utilisation of hitherto wasted protein‐rich NKC after alkali treatment in broiler chick diets to spare peanut meal for human consumption in developing countries.     

Utilisation of ambadi (hibiscus cannabinus) meal by growing chickens

1. Experiments were conducted to compare the utilisation of ambadi meal with that of peanut meal in WL chicks and broilers.

2. Ambadi meal, either expeller‐processed (135.5 g and 271 g/kg) or solvent‐extracted (130.5 g and 261 g/kg), was incorporated at the expense of the peanut meal protein used in the reference diet (180 g/ kg) into diets which were fed to WL pullets (experiment 1) from 1 to 56 d of age. The weight gains and food efficiencies of the chicks fed on the ambadi meal and reference diets were similar.

3. With broilers (experiment 2) the weight gains were also similar, at all dietary concentrations of ambadi meal (89 to 356 g/kg), to those on the reference diet (235 g/kg peanut meal) from 14 to 35 d of age. However, food intake was higher on the ambadi meal diets and this resulted in significantly poorer food efficiency when compared to the reference diet.

4. High food intake and consequently low food efficiency was still evident in birds given ambadi meal diets even when ambadi meal replaced peanut meal on a digestible protein basis (experiment 4) or when ambadi meal (expeller or solvent‐extracted) was subjected to physical treatments such as soaking, autoclaving and pelleting (experiment 5).

5. The transit time of food through the gastro‐intestinal tract of broilers was faster when the diet contained ambadi meal than peanut meal. The higher food intake seen in broilers given diets containing ambadi meal could be the consequence of the fast rate of food passage.

6. Ambadi meal in diets for broilers resulted in significant increase (P<0.05) in the lengths of jejunum plus ileum and caecum. Fibre from the ambadi meal might have influenced the changes in the dimensions of gastro‐intestinal tract as well as in the transit time of food.     

Studies on the toxic effects of crambe meal and two of its constituents, 1‐cyano‐2‐hydroxy‐3‐butene (GHB) and epiprogoitrin,in broiler chick diets

1. Studies were undertaken to determine a safe inclusion rate for crambe (Crambe abyssinica) meal in broiler chick diets, and to determine the mechanism for adverse effects by investigating its constituents; l‐cyano‐2‐hydroxy‐3‐butene (CHB) and 3‐butenyl glucosinolate (epi‐progoitrin, E‐PG).

2. Crambe meals were prepared to differ in E‐PG (19, 36 and 40 g/kg) and CHB contents (0.1, 0.7 and 1.9 g/kg), and with either active or inactive thioglucosidase.

3. Meals were fed to 7‐d‐old broiler chicks at 50 or 100 g/kg of the diet for 12 or 13 d. In separate studies, isolated E‐PG or CHB were mixed into the diet or administered by gavage to 7‐d‐old broiler chicks in amounts equivalent to 50 or 100 g/kg crambe meal diets for 10 and 12 d, respectively.

4. Weight gain decreased (P<0.05) in chicks fed on the high glucosinolate crambe diets or isolated E‐PG. Food consumption decreased (P<0.05) in chicks fed on the diet containing the high E‐PG meal with active enzyme.

5. Mild liver lesions and increased serum aspartate aminotransferase were found in chicks fed on the diet containing the high glucosinolate meal with active enzyme. Other organs, including thyroids, were normal.

6. Commercially‐processed crambe meal appeared safe at an inclusion rate of 50 or 100 g/kg diet, but could not be recommended at this point for long term feeding.     

Phosphorus requirements of poultry. V. The effects during the subsequent laying year of feeding growing diets containing no animal protein or supplementary phosphorus

Pullets reared to 18 weeks of age on diets containing no feeding stuffs of animal origin and without phosphorus supplementation showed no significant difference in egg yield compared with similar pullets fed rearing diets containing animal protein and added phosphorus.

During the laying stage, diets in commercial use at this centre gave significantly higher egg yields, better average egg prices due to superior grading results and a higher margin over food cost than the same diets modified to conform with the nutrient recommendations of the National Research Council of America (1960).

Where the supplementary protein in both types of layers' diet was of vegetable origin, egg yield, food cost and margin of income over food cost were all significantly inferior to groups fed comparable diets containing supplementary protein of both vegetable and animal origin.

Soyabean meal and sunflower seed meal gave significantly poorer results when used in combination as the sole protein supplement compared with soyabean meal plus methionine.     

Food intake adjustments of chicks: Short term reactions to deficiencies in lysine,methionine and tryptophan

1. Two experiments were conducted to compare food intake responses of broiler chicks fed diets varying in lysine, methionine, and tryptophan. Diet D was formulated to create simultaneous deficiencies of lysine, methionine, and tryptophan. Diet A matched National Research Council (1984) recommendations for broilers, and diets B and C were, respectively, 2:1 and 1:2 mixes of diets A and D.

2. Short‐term food intake can provide information on the sequences of adaptation of chicks to a diet deficient in essential amino acids.

3. Chicks consumed 26% less of diet D than A during the first 24 h posthatch. When chicks fed diet A or D to 7 d of age were then fed one of 4 diets singly, within 24 h intake was lowest for chicks fed diet D. Within 48 h, food intake of diet C was more than that of diet D and less than that of diet A, while for diet B intake was more than of diet D but not different from diet A.

4. In the second experiment, chicks were fed diet A to 8 d and then diets A or D alone or given a choice of diets A and D from 8 to 20 d of age. Within 4 to 8 h, food intake of chicks fed diet D alone decreased markedly followed by partial recovery within 24 h. In a choice setting, consistent preference of Diet A over Diet D was observed within 7 h followed by stabilisation at about 65% diet A to 35% diet D.

5. Chicks fed diet D alone from 8 to 20 d of age, then placed in the same choice situation preferred diet A to D with a delay of less than one h and stabilisation at about 85%. Chicks provided a choice of diets A and D from 8 to 20 d, and then diet D alone reduced their food intake more quickly than those not given a choice initially.

6. Broiler chicks appear to react to amino acid deficiencies within a short period (hours) by adjusting their feed intake and/or selection. The response is influenced by age and prior experience.     

Calcium and phosphorus levels in the diet of laying birds

Two hatches of crossbred pullet chicks were brooded and reared to 18 weeks of age on diets which conformed to the recommendations of the National Research Council (N.R.C.) of America for calcium and phosphorus. The pullets of each hatch were then divided at random into six laying groups. Three groups were fed diets containing 2.25, 3.14 and 5.0 per cent respectively of calcium without supplementary phosphorus and the other three groups were fed diets of the same graded calcium levels but with supplementary phosphorus to give a total inorganic phosphorus content of 0.45 per cent. When the rate of egg production in the groups receiving 2.25 per cent calcium exceeded 70 per cent an ad libitum supply of limestone grit was provided and the intake recorded. Over the twelve months of lay this resulted in an average total dietary intake level of nearly 2.65 per cent calcium.

Egg yield was not significantly influenced by the diets, except that the production of birds fed on the diet containing 5 per cent calcium without supplementary phosphorus was significantly depressed. Food intake was not adversely affected by the higher levels of ground limestone; in fact, there was a positive regression of food consumption on the percentage of calcium in the diet. Because of the greater food intake and the lower egg production, food consumed per dozen eggs and cost of food per dozen eggs were higher in the groups receiving 5 per cent dietary calcium without phosphorus supplementation, compared with groups which received lower dietary levels of calcium. There were, however, no significant differences between the various groups in income or in the margin of income over costs, per bird or per dozen eggs.

The data on egg grading showed that over the two experiments and at all levels of calcium there was no evidence of any influence of phosphorus on the combined percentage of large and standard eggs. The average percentage for the two diets with the 5 per cent level of calcium was significantly greater than the combined average for all the other diets.

The average percentage of cracked eggs for the groups with diets containing 5 per cent calcium was 9.4 per cent compared with an average of 11.1 per cent for all the other diets, but the difference was not significant.

The results suggest that there is no economic advantage in raising the calcium content of the basal diet used in these experiments beyond the level of 3.14 per cent and that at this level there appears to be no need with this basal diet to supplement the phosphorus content.     

Response of broiler chicks to threonine‐supplemented diets to 4 weeks of age

1. Two experiments were carried out to determine the response of broiler chicks to threonine‐supplemented diets between 10 and 28 d and 7 and 21 d of age, respectively.

2. In the first experiment female broiler chicks were fed on 11 experimental diets. Two iso‐energetic basal diets (diets 1 and 2) were prepared with 200 and 160 g CP/kg and 7·6 and 6·0 g threonine/kg respectively. Both diets contained 11·5 g lysine and 8·7 g sulphur‐containing amino acids/kg. Diet 3 was composed of diet 2, supplemented with all essential and non‐essential amino acids (EAA and NEAA, respectively) except threonine, to the concentrations of the amino acids in diet 1. The NEAA were added as a combination of glutamic acid and glycine. Diets 4 to 11 had the same compositions as diet 3, but contained increasing amounts of threonine.

3. For birds fed on diet 2, gain was significantly lower and food/gain ratio was significantly higher than for birds fed on diet 1. Supplementation with EAA, NEAA and threonine to the same concentrations in diet 1 resulted in a performance similar to that found on diet 1.

4. In experiment 2, male and female broiler chicks both received 10 experimental diets. Diet 1 contained 220 g CP/kg and 8.5 g threonine/kg, diet 2 contained 160 g CP/kg from natural raw materials and 6 g threonine/kg. Both diets contained 12·4 g lysine and 9·3 g sulphur‐containing amino acids/kg. Basal diet 2 was supplemented with all EAA and NEAA to the concentrations of basal diet 1, except for threonine. Diets 3 to 10 had the same compositions as the supplemented diet 2, but contained increasing amounts of threonine.

5. For male and female chicks on diet 2, gain was significantly lower and food/gain ratio significantly higher than those on diet 1. Diet 10 (160 g CP/kg plus all EAA, including threonine, and NEAA supplemented to the concentrations of diet 1) resulted in the same performance as diet 1.

6. The results indicate that, when low protein maize‐soyabean meal diets supplemented with EAA and NEAA with 13·31 MJ ME/kg were fed to male and female broiler chicks until 21 d of age, improvements in gain and food/gain ratio were obtained when the dietary threonine content was increased to 7·25 g/kg. When female chicks were fed threonine‐supplemented diets to 28 d of age, improvement in gain and food/gain ratio was obtained when the threonine concentrations were increased to 6·32 g/kg diet.

7. Curves have been fitted to the data, from which a cost‐benefit analyses can be made and an optimum threonine dose calculated, using local prices.     

Dietary chloride requirement of broiler chicks fed on a wheat‐soyabean diet

1. A diet based on soyabean meal and wheat contained insufficient chloride to support normal growth in chicks.

2. Ammonium chloride and sodium chloride were equally good sources of supplementary chloride for the chick.

3. When seven diets providing increasing proportions of chloride from 608 to 1808 mg/kg, were fed to chicks, maximal growth at 21 d was obtained at about 1200 mg chloride/kg diet.     

The use of n‐paraffin‐grown yeast as the main source of protein in diets for chicks

1. n‐Paraffin‐grown yeast and a mixture of soyabean meal and fish meal were compared in the net protein utilisation (NPU) test, and as protein supplements in diets for broilers up to 4 weeks of age.

2. The difference between the NPU values, 0.66 for yeast and 0.80 for the soyabean meal and fish meal mixture, could largely be attributed to the high nucleic acid content of the yeast.

3. Chicks given the diet containing yeast (190 g/kg) did not grow as rapidly as those given the soyabean meal and fish meal reference diet, and the reduced growth could only partly be explained by a marginal deficiency of methionine.

4. Food conversion efficiency with the yeast diet was improved by maize oil while responses to α‐tocopheryl acetate and sodium selenite were inconsistent.

5. Chicks grew well when yeast replaced fish meal in the mixture of soyabean meal and fish meal, and when fish meal (194 g/kg diet) was the sole protein supplement.     

Lupin and rapeseed meals in poultry diets: Effect on broiler performance and sensory evaluation of carcasses

1. The effect of including lupin meal (Lupinus angustifolius), with or without rapeseed meal, in computer‐formulated, least‐cost diets for broilers has, been determined.

2. In the first experiment the diets contained 0, 8 (with and without supplementary methionine, lysine, or methionine and lysine) or 16% lupin meal: addition of the lupin meal required a concomitant addition of 5 % rapeseed meal (by computer selection).

3. The diets were fed from 38 to 65 d and did not affect live‐weight but the efficiency of food utilisation was significantly worse on the 16 % lupin, 5% rapeseed meal diet than it was on the control diet.

4. The second experiment was designed as a 2 x 4 factorial to separate any effect due to rapeseed meal from that due to lupin meal, the treatments, which were applied from 1 to 62 d, being 0, 8, 16 and 24% lupin meal with and without 5 % rapeseed meal.

5. Birds gained more rapidly in the second experiment on diets containing 16 or 24% lupin meal whereas live‐weight was depressed when 5% rapeseed meal was included in the diets containing 0 or 8% lupin.

6. The 16 and 24% lupin treatments also had added dietary fat from 6 to 9 weeks of age and this may have ameliorated the adverse effect of rapeseed meal.

7. Up to 16% lupin meal and 5% rapeseed meal had no detectable effect on the colour, appearance, flavour or texture of roasted chicken meat when evaluated by a trained taste panel.     

Use of khesari (lathyrus sativus) in chick diets

1. Broiler chicks, reared for 14 d in battery brooders, were given diets containing 100, 222 or 367 g/kg of khesari meal (Lathyrus sativus) in three different experiments.

2. Birds receiving raw khesari consumed less food and grew more slowly than birds receiving a maize‐soya diet. Supplementation with DL‐methionine did not improve the nutritive value of khesari diets, but the inclusion of L‐tryptophan produced a positive response.

3. When khesari was either autoclaved or heated in a commercial “ micronisation “ process and then incorporated at 367 g/kg in a balanced chick diet, growth and efficiency of food utilisation were at least equal to those obtained with a maize‐soya diet.

4. Khesari depresses chick growth when fed raw, but is an excellent protein source for growing chicks if fed after a suitable heat treatment. Since the component in raw khesari which is toxic to chickens is heat‐labile, it is probably not the same factor that is responsible for human lathyrism.     

Effect of diets containing raw and extrusion‐cooked rice bran on growth and efficiency of food utilization of broilers

1. Meat strain chicks were fed on diets containing 600 g rice bran/kg for the 7 to 8 week period required to reach broiler weight.

2. Extrusion cooking of rice bran resulted, in improved chick weight gain and food efficiency for the first two weeks of feeding, but this advantage was lost by the end of the feeding period.

3. Addition of 10 g calcium/kg to the stabilised rice bran diet prevented the decline in performance after two weeks of age, and birds fed on this diet continued to gain at an increasing rate until the end of the experiment.

4. Calcium supplementation of stabilised rice bran diets produced significantly greater gains and superior food utilisation compared to stabilised rice bran diets without added calcium.

5. Calcium supplementation did not affect weight gain of chicks fed on diets containing raw rice bran.

6. Taste panel evaluation of meat from birds fed on diets containing raw rice bran, stabilised rice bran, or no rice bran indicated a significant preference in only one combination tested. Any ‘off flavour could not be related to dietary treatment.     

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%.     

Biological availability of selenium and phosphorus in fish meal as affected by condition of fish and type of meal

1. Experiments were conducted to determine the effects of the condition of the fish and of processing procedures on the biological availability of selenium and phosphorus in fish meals.

2. In fresh fish processed to whole fish meal the biological availability of selenium was estimated as 77%, in fresh fish processed to pressed‐cake fish meal it was 59% and in partly‐decomposed fish processed to whole fish meal it was 51%.

3. When the phosphorus content of the test diet was 2–51 g/kg the biological availability was 88% and unaffected by the condition of the fish and the method of processing.     

Nutritive content of house fly pupae and manure residue 1

The metabolisable energy value of pupae of Musca domestica L. and digested poultry manure was determined to be 10.6 and 2.4 MJ/g (2528 and 580 kcal/g), respectively. Chemical analyses showed that pupae contained 61.4% protein and 9.3% fat: their amino acid composition was comparable with that of meat‐and‐bone meal or fish meal and was better than soybean oil meal.

A feeding trial was conducted to evaluate house fly pupae and catabolised poultry residue as alternative protein sources to soybean meal for growing chickens.

No significant difference (P>0.05) in weight gain was observed between the control and chicks fed pupae in their diet from 1 d to 4 weeks of age. Food conversion of the chicks fed digested poultry manure was significantly (P<0.05) inferior to that of the controls.     

Effects of high inclusion rates of salseed meal in the diet of chicks

1. Starter diets containing either maize or salseed meal to replace the maize were fed to chicks over a period of 2 weeks.

2. Growth rate, food intake, food utilisation and proportion of dietary nitrogen retained were much poorer in chicks receiving salseed meal.

3. The chicks receiving salseed meal developed pathological lesions in liver and kidney.

4. The red blood cell count, white blood cell count, haemoglobin concentration and packed cell volume of the chicks receiving salseed meal were lower than those of chicks receiving maize.

5. The apparent metabolisable energy value of salseed meal was determined as 6.83 MJ/kg.     

A comparison of phosphorus assay techniques with chicks. 4. Evaluation of a proposed calcium standard curve for calcium phosphate, soft phosphate and defluorinated phosphate

Two experiments were conducted to determine whether previously suggested calcium levels were adequate for use in assaying phosphorus availability from soft phosphate, defluorinated phosphate, and calcium phosphate. Results indicate that the levels were capable of producing maximum growth rate and maximum bone ash.

The tibia ash data indicated that all sources of phosphorus were equal in biological availability. However, only defluorinated and calcium phosphate produced maximum growth. No explanation is given for the ability of soft phosphate to produce high bone mineralisation without maximum growth rate.     

Studies on the effect of lysine and methionine supplementation of a high‐protein maize‐soyabean diet and of a low‐protein barley‐white fish meal diet on the performance of caged layers

Selected literature relating to the amino acid supplementation of layers’ diets is reviewed and the results of two experiments are presented.

In the first experiment a basal soyabean meal diet (14.3 per cent crude protein) was supplemented with L‐lysine and DL‐methionine, singly and together. Supplementation of the basal soyabean diet with the amino acids caused no significant effects on egg production, mean and total egg weight or food conversion efficiency. None of the soyabean diets proved as satisfactory for egg production or food conversion efficiency as a fish meal control diet (16.9 per cent crude protein).

In the second experiment the effect of adding 0.1 per cent each of L‐lysine and DL‐methionine or 0.2 per cent each of l‐lysine and DL‐methionine to a low fish meal diet (2.5 per cent fish meal) was examined. The addition of 0.2 per cent of each amino acid caused an increase in egg production.

Mean egg weight was improved by the addition of amino acids at both levels although this effect was not statistically significant. Comparison of the low fish meal diets with a fishmeal control diet (10 per cent fishmeal) showed that at the 0.2 per cent addition of amino acids, egg production, total egg weight and food conversion efficiency were better than on the 10 per cent fish meal control diet.

Two breeds, light and medium hybrids were used in both experiments.

The results are discussed with reference to their practical significance.     

Effect of urea on growth,food utilisation and body composition of chicks

1. A study was made of the effect of urea, added to chick diets of different protein contents with or without added methionine, on growth and body composition.

2. In chicks fed on diets containing urea, concentrations of urea were higher in the blood and digestive tract but not in the excreta, as compared with chicks fed on diets containing soyabean as the only source of protein.

3. Urea‐nitrogen was utilised better for growth when the diets were supplemented with methionine rather than unsupplemented.

4. Body fat content was decreased with the increase in protein content of the diet. Addition of urea decreased body fat less than an equivalent amount of protein.

5. There was no correlation between body fat and body weight in groups fed on diets containing 189 or 216 g protein/kg, but there was a significant correlation between these variables in groups fed on diets containing 292 g protein/kg or either concentration of urea. This phenomenon was much more pronounced in diets not supplemented with methionine.