A model of egg production

1. A quantitative literature review has been used as the basis of an empirical simulation model of the responses in food intake and egg output of laying hens to temperature, light pattern, light intensity, feeding system type, crude protein, methionine, lysine and metabolisable energy. The financial consequences are considered, by the calculation of gross margin of egg value minus food cost.

2. Response to protein intake in an optimal environment is taken as the first limiting factor. Depressions below the maximum are calculated for sub‐optimal environments.

3. The model was tested against a sample of flocks for which detailed records were available, and found to give realistic answers. A FORTRAN program was written which calculates egg output and food intake by 4‐week production periods, permitting the user to examine the effects of management changes made during lay. Shortened versions of the model, based on annual values have been written for a programmable calculator.

     

Changes in dietary protein level during the pullet year

A “High” protein diet (14 per cent crude protein, 2490 k cal. ME/kg.) and a “Low” protein diet (10.5 per cent protein, 2420 k cal. ME/kg.) were fed to two types of laying pullet. One type was a small commercial hybrid weighing about 1.6 kg. and the other was a large first cross weighing about 2.4 kg. at 20 weeks. After 12 weeks and 24 weeks of lay, groups were transferred from the High to the Low protein diet and vice versa.

In the heavy strain birds the High and Low protein diets both supported good egg production throughout the trial and changing from High to Low protein had no effect on rate of lay. The opposite change from Low to High, made after 12 weeks of lay, stimulated an increase in rate of lay above the level of birds which had received the High protein diet throughout.

In the small hybrid pullets the low protein diet did not support a normal rate of lay. Attempts to reduce dietary protein by switching from High to Low after 12 or 24 weeks caused a fall in rate of lay. Groups transferred from Low to High increased their rate of lay to a level comparable with controls kept on High protein throughout.

Egg weight and body weight were affected by dietary protein level in both strains. Changes in the diet caused corresponding changes in both egg weight and body weight.

It is concluded that there is little scope for reducing the level of protein in the diet during the laying year. If a diet is inadequate in the early stages of production it is likely to remain inadequate for any later stage. On the other hand, some unexpected benefit was obtained in one strain by increasing the dietary protein beyond the level which was adequate for maximum egg production in the first 3 months of lay.     

Effects of low dietary protein and different allocations of food during rearing and restricted feeding after peak rate of lay on egg production,fertility and hatchability in female broiler breeders

1. A 3x2x2 factorial experiment was conducted with boiler breeder females to determine the effects of body weight gain (three levels) and conventional or lower crude protein concentrations in the rations during rearing, and restricted or ad libitum feeding after the peak rate of lay on egg production, fertility, hatchability, mortality and food consumption. 2. Compared with ad libitum feeding, conventional food restriction resulted in a decrease in average daily food consumption of 0.6 during rearing, 0.2 during early lay and an increase of 0.4 after the peak rate of egg production. Mortality was decreased by more than half. 3. Restricted birds had higher total and settable egg production, fewer defective or damaged eggshells and higher fertility and hatchability than those fed ad libitum. The modified (more generous) rearing programme resulted in lower rates of egg production and higher rates of mortality compared with the conventional food restriction programme. 4. Low-protein rearing rations were associated with higher rates of food intake, higher mortalities and lower rates of egg production than the conventional protein rations. There were no differences in the fertility or hatchability of eggs between birds fed on the two concentrations of dietary crude protein. 5. Ad libitum feeding post-peak was associated with higher rates of mortality to 60 weeks of age. Post-peak feeding had little effect on the rate of lay or egg weight in conventionally restricted birds fed high protein rations or in birds fed ad libitum. Restricted feeding post-peak decreased the rate of lay and egg weight in birds on the modified restriction programme and in conventionally restricted birds fed on the low protein rations. There was no effect of post-peak feeding on fertility or hatchability of eggs. 6. The total numbers of saleable chicks per kg food consumed were 1.83, 1.72 and 0.52 for conventional, modified and ad libitum feeding during rearing; 1.56 and 1.15 for restricted and ad libitum feeding post-peak: there were no differences associated with protein concentrations of rations fed during rearing.     

Effect of dietary energy,protein, and a versatile enzyme on hen performance,egg solids,egg composition,and egg quality of Hy-Line W-36 hens during second cycle,phase two

This study was conducted to evaluate the effect of Rovabio, dietary energy, and protein on performance, egg composition, egg solids, and egg quality of commercial Leghorns in phase 2, second cycle. A 4 × 2 × 2 factorial arrangement of treatments comprising 4 dietary energy levels (2,791, 2,857, 2,923, and 2,989 kcal of ME/kg) and 2 protein levels (15.5 and 16.1%) with and without Rovabio was used. Hy-Line W-36 hens (n = 1,920, 87 wk old) were randomly divided into 16 dietary treatments (8 replicates of 15 hens per treatment). The trial lasted 12 wk. Dietary protein significantly increased feed consumption but decreased yolk color. As dietary energy increased from 2,791 to 2,989 kcal of ME/kg, feed consumption decreased from 98.0 to 94.9 g per hen daily, and yolk color increased from 5.27 to 5.56. There was a significant interaction among dietary protein, energy, and Rovabio on egg production, BW, egg mass, feed conversion, and yolk solids. Egg weight of hens fed the diets supplemented with Rovabio was significantly greater than that of hens fed the diets without Rovabio during wk 3 and 4. However, Rovabio did not significantly influence average egg weight (87 to 98 wk of age). Rovabio supplementation significantly increased BW of hens. These results suggest Rovabio had a small but significant influence on nutrient utilization of commercial Leghorns during phase 2 of the second cycle.     

Genetic variation for egg production,egg quality and bone strength in selected and traditional breeds of laying fowl

1. A multi-breed experiment was conducted with 25 commercial and traditional lines of laying fowl to determine the extent of between-breed genetic variation for adult body weight, sexual maturity, rate of lay, egg weight and egg composition to 55 weeks of age. The genetic variability for bone strength and eggshell strength was determined at 55 weeks of age and a comparison of commercially selected and traditional breeds was performed. 2. The proportion of the total variation that was associated with breed or line of origin was high (> 0.8) for body weight, sexual maturity and shell colour; moderately high (0.4 to 0.7) for rate of lay, early and late egg weight, weights of egg yolk, albumen and shell at 55 weeks; and low (< 0.4) for egg weight at 42 to 45 weeks, albumen quality and the number of egg inclusions. 3. There were no detectable differences between breed within category (traditional and commercial lines) for rate of lay, and estimates of breed variation for egg weight and egg components were substantially decreased within category compared with the overall analysis. 4. Commercial lines displayed earlier sexual maturity, greater rates and persistency of lay, and higher egg weights at earlier (32 to 35 weeks) and later (52 to 55 weeks) ages. At 55 weeks, the larger eggs from commercial birds contained more albumen of higher quality and paler yolks of similar weight to those from traditional breeds. The relative weight of the eggshell was similar in both categories. 5. There was considerable genetic variation between commercial lines for bone density and a moderate proportion of genetic variability for bone strength. Commercial lines had very weak bones compared with traditional lines but there was relatively little genetic variation for eggshell strength. The results suggest that eggshell quality is maintained in genetically selected lines at the expense of bone strength and bone radiographic density.     

Effects of constant environmental temperatures on the performance of laying pullets

1. Two experiments are described in which laying pullets maintained at constant temperatures were fed a range of diets with a view to defining optimum combinations of temperature and nutrient intake. 2. In the first experiment, all combinations of 6 temperatures (15 degrees, 18 degrees, 21 degrees, 24 degrees, 27 degrees and 30 degrees C) 9 diets (three protein concentrations and three energy contents) and two stocks were tested for 34 weeks using 4320 pullets. In experiment 2, all combinations of three rearing temperatures, three laying temperatures (18 degrees, 22.5 degrees and 27 degrees C) three diets (protein concentration) and two stocks were tested for 61 weeks using 2160 pullets. 3. As anticipated, higher dietary protein concentrations were needed to maintain egg output at higher temperatures. If diets suplying adequate amino acid intakes were provided, egg output was unaffected by temperatures in the range 15 degrees to 27 degrees C although, at the highest temperature, egg weight was slightly reduced and rate of lay (particularly in the later part of the laying year) was increased. At 30 degrees C, egg output was depressed whichever diet was fed. 4. Dietary energy content had small but significant effects on egg weight and egg output but did not interact with temperature. It was not possible to maintain egg weight or egg output at 30 degrees C by feeding a high energy, high protein diet. 5. Estimated heat output of the birds increased during the course of the experiment at the lower temperatures but decreased with time at 30 degrees C. Feather loss occurred earlier at the lower temperatures and this is interpreted as an effect of temperature on the timing of the annual moult, which also accounts for the better persistency of lay observed at 27 degrees C.     

The effect of variation in egg numbers,body weight and egg weight upon shell thickness

It is expected that when birds consume a diet with a fixed calcium content variation in the rate of egg production, in body weight or in egg weight will lead to variation in calcium consumption. This analysis investigated whether, in a particular experiment, this also led to variation in egg shell thickness. Data from 67 birds over ten consecutive 28‐d periods were considered. Within birds and within periods it was found that the relationships between shell thickness and these production characters varied at different dietary calcium levels and in some cases the partial regression coefficients calculated were different in sign from those expected. However, only comparatively small amounts of variation in shell thickness could be ascribed to yariation in egg numbers, body weight or egg weight and, after regression, significant (P<0.001) differences still existed in shell thickness between birds. In this investigation there was little tendency for the egg shells to become thinner as the birds aged and hence the correlation coefficients between shell thickness and each of the three production characters due to common seasonal or ageing effects were small. The correlation between the angular transformation of the percentage cracked egg shells produced by each bird and its'mean shell thickness was — 0.357.     

Genetic basis of the increase in egg weight with pullet age in a White Leghorn flock

1. In a closed White Leghorn flock over a 6-year period the average increase in egg weight from the start of lay to 37 weeks of age was 12.6 g. 2. The heritability of this egg weight increase was estimated at 0.36 +/- 0.06. 3. The genetic correlations of egg weight increase with other characteristics were: age at first egg -0.50, early egg weight -0.51, 37 week egg weight 0.42 and egg production to 273 d 0.44. 4. It is predicted that with unit selection intensity the direct response in egg weight increase will be -1.30 g, with correlated responses in age at first egg of 2.1 d, early egg weight 0.64 g, 37 week egg weight -0.51 g and egg production to 273 d -1.83 eggs.     

Effect of daily feed intake in laying period on laying performance, egg quality and egg composition of genetically fat and lean lines of chickens

1. The objectives of this study were to evaluate the effects of feed intake on laying performance, egg quality and egg composition in a Fat line and a Lean line during the laying period (34 to 54 weeks of age). 2. The experiment was a 2 × 2 factorial design with two dietary intake levels (nutrition recommendation and 75% of recommendation) and two broiler genotypes (Fat line and Lean line). Hens (384 of each line) were randomly divided at 23 weeks of age into 4 treatments, with each treatment represented by 12 replicates of 16 birds each. The experiment started when the rate of lay reached 5% and continued until 54 weeks of age. 3. The results indicated that there was a significant interaction between daily feed intake and genotype on egg production, egg weight, percentage yolk, yolk/albumen ratio and yolk cholesterol content. Fat line hens produced significantly more eggs and had a lower incidence of cracked eggs than the Lean line hens. The reduction in feed intake decreased egg weight and increased egg production, egg-shape index and cholesterol content of yolk significantly.     

Selection for increased egg mass under ahemeral light-dark cycles

Selection for an increased rate of egg mass production under a 21-h light-dark regime was successful in reversing the decline in egg weight which had occurred throughout the previous history of this experiment, while retaining the ability of the flock to lay eggs at an acceptable rate under this abnormal regime.     

The effects of a protein deficiency on egg composition

Eggs were collected from groups of pullets receiving 9, 14 or 20 per cent dietary protein and the component parts were separated and weighed. The reduction in egg weight associated with protein deficiency was found to be due to reductions in all components, but yolk and shell weight changed proportionately less than total weight and albumen weight proportionately more. The resulting increase in percentage yolk was found to be of similar magnitude to that expected from a consideration of the relationship between egg size and yolk size in birds receiving adequate protein. In a similar way the increased proportion of shell apparently reflected only the relationship between egg size and surface area in eggs collected when the birds were 52 weeks of age but at 67 weeks a real increase in shell thickness on the deficient diet was also indicated.     

The effects of dietary fat and bird age on the weights of eggs and egg components in the laying hen

1. A low-fat diet or an isoenergetic and isonitrogenous high-fat diet containing 55 g maize oil/kg were fed to laying hens at different stages during the laying year in two experiments. 2. Feeding the high-fat diet to young hens resulted in a rapid increase of 2.5 g in egg weight, made up of increases in both yolk and albumen weights. 3. Switching the diets at 50 weeks caused changes in egg weight that were accounted for entirely by changes in egg albumen weight. 4. Feeding the high-fat diet from 46 weeks in a second experiment increased egg and egg albumen weights by 1.26 and 1.34 g respectively. 5. The increase in egg weight with age was associated with a greater increase in the proportion of yolk, at the expense of albumen, compared to egg weight increases related to dietary fat. 6. It is concluded that dietary fatty acids increase egg weight by a mechanism different from that causing age-related increases in weight and that the mechanism involves a stimulation of oviduct protein synthesis.     

Changes in light intensity during the rearing period can influence egg production in domestic fowl

1. A total of 240 Shaver White and 240 ISA Brown pullets that had been reared in multi-bird cages on a 10-h photoperiod, and maintained at a light intensity of 3 or 25 lux, or changed from 3 to 25 lux or from 25 to 3 lux at 9 or 16 weeks of age, were moved into individual-bird cages at 20 weeks and transferred to 15-h photoperiods at 25 lux. 2. In both breeds, birds transferred from 3 to 25 lux at 16 or 20 weeks laid significantly more eggs than birds maintained on the brighter intensity from one day or increased to it at 9 weeks. 3. Mean egg weight, shell deformation, albumen height, feed intake and body weight gain in lay were not significantly affected by the light intensity treatments during the rearing period. There was, however, a small, but significant, negative correlation of egg numbers with mean egg weight, although this only partially explained the difference in egg numbers. The differences in egg production were unrelated to rate of sexual maturation.     

Parental diet effects on egg component weights and shell quality

An experiment was conducted to investigate the effects of feeding laying hens a low protein and energy diet (LPE), a high protein and energy diet (HPE), and a commercial protein and energy diet (control) on whole egg components, egg weight, and shell quality. The hens were fed their respective diets from 15 to 30 wk of age. At 30 wk of age, egg component weight and percentages were measured along with eggshell quality. The results demonstrated that birds fed the LPE diet had significantly lower albumen, yolk, and total egg weights that the control and HPE groups. The LPE group had significantly lower levels of total albumen protein than the control group. The HPE hens had significantly lower shell thickness and pore concentration than the LPE group, demonstrating that dietary levels of CP and ME can alter not only shell quality component but also albumen protein levels.     

Effect of 1 alpha,25-dihydroxycholecalciferol on egg shell quality and egg production

1. The effect of replacing dietary cholecalciferol (D3) by 1 alpha,25-dihydroxycholecalciferol (1,25-(OH)2D3) on egg shell quality and egg production was tested on 32-week-old White Leghorn laying hens over 9 weeks. 2. Hens fed on a diet supplemented with 5 micrograms 1,25-(OH)2D3/kg diet, tended to lay more eggs, and the eggs had significantly higher specific gravity and percentage shell than eggs from control hens fed on a diet supplemented with 27.5 micrograms D3/kg diet. 3. The effect became apparent after about 4 weeks of treatment and persisted until the end of the test. 4. Hens fed on a diet without D3 supplement started to lay very thin or soft shelled eggs within 4 weeks, suggesting that the birds' reserves of D3 or its metabolites were depleted within this period. 5. The results suggest that 1,25-(OH)2D3 can be substituted for D3 in layer diets to improve egg shell quality.     

Increment of egg weight with hen age in various commercial avian species

1. The present study indicates that a common biological pattern exists for egg weight increase with hen age for the various commercial avian species, breeds and strains at their first laying cycle. Therefore, one common equation can be used for the estimation of egg weight increase.

2. The parameters estimated for this equation are based on (a) egg weights in terms of percentage of seasonal mean egg weight, and (b) age as percentage of maximum age of the hen. Therefore, if the season's mean egg weight is known for any species, breed or strain, the increase in egg weight can be easily predicted for the whole season, or for any particular hen age. For early prediction, egg weight expressed as a percentage of initial egg weight can be used, although such prediction will be somewhat less accurate.

3. The use of egg weight as a percentage of seasonal mean egg weight, and age as a percentage of maximum age, was found to overcome the differences between strains, breeds and even species, by applying the same denominators for egg weights and periods of lay.

4. At each point of hen age (mean egg weight), the egg weight grades can be easily estimated by employing the computerised Burr's (1967) equation. These values showed excellent fit with extensive field data, provided that only normal eggs and those originating from a single flock and from no more than two weeks of collection are counted.     

北京鸭蛋重与受精率、孵化率、蛋形指数及出雏重的关系

本研究将北京鸭Z1系种蛋分为小蛋组(82～92g)、中蛋组(92～105g)和大蛋组(106～124g),分别研究蛋重与受精率、孵化率、蛋形指数及初出重等性状的关系.结果表明蛋重对受精率的影响差异不显著(P＞0.05),但随着蛋重增大,受精率有增大的趋势;孵化率随蛋重的增加而显著减小(P＜0.05或P＜0.01);蛋重对蛋形指数的影响不显著(P＞0.05);雏鸭出生重受蛋重的正向影响差异极显著(P＜0.01).综合以上结果,本文得出北京鸭Z1系适宜孵化的蛋重范围是82～105g.     

Some effects of changing protein levels during the pullet laying year

Three diets containing 12, 14 and 16 per cent crude protein were fed to laying pullets from 23 to 63 weeks of age. The laying year was divided into three periods of 10, 15 and 15 weeks to examine the effect of feeding these diets at different stages of lay. Eighteen treatments were used, representing all possible combinations of three diets in the first period, three diets in the second period and two diets (16 and 12 per cent) in the third period. Two groups of 75 pullets were allocated to each treatment.

In each period the diet had a significant effect on the rate of lay, egg output (g./day) showed a linear regression on protein intake. There was no indication that the amount of protein needed to maximise egg output was any less in one period than another, although the level of maximum output varied substantially as the year progressed.

Where the feeding of an inadequate level of protein in one period was followed by a higher level in the next, liveweight showed a marked recovery but there was little evidence of compensatory egg production. When the protein of the diet was reduced from 16 to 12 per cent, rate of lay fell sharply to a level below that of birds which had received the 12 per cent protein diet throughout.     

The effects of early and late maturity on the protein requirements of pullets

Growing pullets were exposed to two light patterns which caused a difference in sexual maturity of 5 weeks. From 28 to 38 weeks of age they were fed diets containing crude protein levels of 7.0, 8.5, 10.0, 11.5, 13.0 and 14.5 per cent. Yellow maize provided 45 per cent and soyabean meal 55 per cent of the protein in all six diets.

Rate of lay, egg weight and body weight were greater in the late maturing flock than in the early flock at the start of the assay and throughout the assay period. The late maturing pullets required more protein to reach and maintain their maximum potential than the early birds, presumably because their potential output was greater. The late birds showed a diminishing but continued response to protein up to the highest level fed (14.5 per cent corresponding to 23 g. protein per bird day). The early maturing pullets showed no response to dietary protein levels beyond 11.5 per cent and their estimated protein requirement was about 16 g. per bird day.

When limiting amounts of protein were fed (7.0–10.0 per cent of the diet) the two flocks achieved similar levels of egg output. In both flocks and throughout the assay, body weight and egg weight fell at the two lowest levels and increased at the three highest levels of protein.

It is concluded that the protein requirements of early maturing and late maturing flocks of pullets may differ, but only in a way which corresponds directly with their different potential outputs. In the late flock, which had the higher protein requirement, excellent production was obtained with a diet containing 14½ per cent crude protein all of which came from vegetable sources.     

The control of egg production using a low‐sodium diet

Experiments have shown that egg production can be controlled by using a low‐sodium diet. When a diet containing 0.038% sodium was fed to birds prior to point of lay, egg production was severely restricted. When this diet was fed to hens already in lay, production ceased but the subsequent feeding of an adequate diet resulted in rapid re‐attainment of production to a level higher than that of normally‐fed birds. There were also improvements in egg and shell quality. Birds fed on the low‐sodium diet remained in good condition and mortality did not increase.