Effect of age at starting biomittent lighting on performance of laying hens

1. Two experiments were conducted with brown‐egg laying hybrid pullets to determine the optimum age at which to begin Biomittent lighting (a system providing 15 min light and 45 min darkness in each hour for 16 h).

2. In the first experiment birds introduced to Biomittent lighting at 18, 24, 30 or 36 weeks of age all gave the same egg output. Use of Biomittent lighting between 22 and 34 weeks of age reduced food intake by 5.3% compared with normal lighting during this period.

3. In the second experiment, birds introduced to Biomittent lighting at 23 or 36 weeks of age gave essentially the same egg output and this was true even for half of the flock which had been severely restricted in food intake between 6 and 18 weeks of age.

4. It is concluded that Biomittent lighting can be safely introduced at point of lay as a means of saving food consumption without loss of output provided that an adequate diet is fed. The response is interpreted as a saving in energy expenditure rather than a restriction of feeding opportunity.

5. It is recommended that, to avoid the complication of combining weekly increments in photoperiod with intermittent lighting, Biomittent lighting can be introduced abruptly as a skeleton long day. However, if this follows rearing on short photoperiods and if egg size is important, the start should be delayed until about 22 weeks of age so as not to induce early sexual maturity.     

A test for photorefractoriness in high‐producing stocks of laying pullets

1. Pullets of 2 high‐producing commercial stocks (both brown‐egg layers) were exposed to 5 different lighting patterns between 18 and 72 weeks to test the hypothesis that photoperiods used in commercial lighting programmes early in the laying year may be unnecessarily long and, by accelerating the development of photorefractoriness, may contribute to the decline in egg production observed after the initial peak. Two rooms of 288 pullets were allocated to each treatment.

2. The rate of lay observed with a Step‐Up treatment which gave increases in photoperiod from 8L:16D at 18 weeks to 15L:9D at 27 weeks of age was not significantly different from that of treatments which held the birds on 11L:13D during peak egg production but gave increments up to 15L:9D later in the laying year.

3. A control group maintained on 11L:13D from 20 to 72 weeks laid 295 eggs per bird housed and a further group held on 8L:16D from 0 to 72 weeks laid 284 eggs per bird. These yields were lower than the Step‐Up treatment (299 eggs) but show the potential of modern hybrid stocks to lay prolifically even without light stimulation.

4. It is concluded that the stocks tested in this experiment showed no advantage when given lighting programmes in the first laying year which were designed to minimise the adverse effects of photorefractoriness.     

Lighting and mortality rates in domestic fowl

1. Data from intermittent and conventional lighting trials were analysed to investigate the effect of daily illumination upon mortality during the laying period and in 49‐d‐old broilers.

2. Iiveability in laying hens was improved by the use of intermittent lighting: the degree of improvement was proportional to the reduction in daily illumination achieved by the intermittent programme.

3. The reduction in mortality with intermittent lighting in laying hens was not the result of intermittent lighting per se. Intermittent regimens which did not reduce daily illumination did not reduce mortality.

4. Mortality in both conventionally‐lit laying hens and 49‐d old‐broiler chickens increased with photoperiod.     

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.     

Light intensity,intermittent lighting and feeding regimen during rearing as affecting egg production and egg quality

1. Four light treatments and two rearing regimens were imposed on 4 breeds of laying hen, using 6144 birds in an 8‐room climate house.

2. Room treatments were a standard lighting pattern with intensities of 0.5, 2 and 15 lux and an intermittent pattern (3 h light: 3 h dark) at 15 lux. Within room treatments were ad libitum or rationed feeding during rearing and 4 breeds: ISA Brown, Hisex Brown, Shaver Brown and Hisex White.

3. Rationing during rearing, by holding intake at its 6‐week level from 6 to 14 weeks of age, was associated with significantly higher egg production and lower egg weight, but no effect on food intake, or egg output.

4. Intermittent lighting, using a repeated 3L:3D regimen was associated with higher egg weight, but a lower rate of lay, food intake, and total egg output.

5. The absence of a consistent response to light intensity, over the range 0.75 to 12.4 lux was in contrast with earlier work, and it is possible that modern prolific hybrids are more tolerant of low intensity than were earlier stocks.

6. Despite this result it is suggested that current recommendations of 10 to 20 lux in laying houses need not be changed, because such intensities are advisable on the grounds of welfare, staff working conditions and aesthetics.     

Dietary rapeseed meal and the incidence of tainted eggs

1. Incorporating 0, 3, 6 or 9% rapeseed meal in the diet of brown‐egg laying birds for 28 d resulted in the production of 0, 1.2, 19.3 and 20.9% tainted eggs respectively, the first tainted eggs being laid on the fifth day.

2. During the second and third weeks the incidence of tainted eggs exceeded 20% but fell to 11.4% during the final week.

3. Omission of the rapeseed meal from the diets halted the production of tainted eggs.

4. Neither egg production nor the health of the birds was adversely affected by the treatments.

5. The taint was described as “ fishy ” or “ crabby ” and was distinctive, but the source was not identified.     

Effect of photoperiod on the mean oviposition time of two breeds of laying hen

1. Oviposition times were recorded for brown and white egg‐laying hybrids under 8, 10, 13 and 18 h photoperiods.

2. Mean oviposition time for both breeds was advanced relative to dusk by approximately 0.5 h for each 1 h extension of photoperiod.

3. Mean oviposition time for the brown egg hybrid was 1.2 to 1.4 h earlier than that of the white egg hybrid under each lighting regimen.

4. A genetic difference in phase setting of the Open Period for Luteinising Hormone (LH) release is the likely reason for the difference in mean time of lay of the two breeds. The difference is possibly one between brown and white hybrids generally, rather than between the particular varieties of hen used in this trial.

5. The proportion of the day in which eggs are laid is shorter under long photoperiods presumably because light at the end of the photoperiod inhibits the pre‐ovulatory surge of LH.     

The effect of 6‐ and 8‐hour light‐dark cycles on egg production and pattern of ovipositions

1. Two flocks of 60 laying hens were transferred from 14 h light (L): 10 h dark (D), to repeated 3L:3Dor4L:4D lighting schedules at 37 weeks of age. Egg production decreased slightly but egg weight and shell quality improved.

2. The intake of low‐calcium diet and of oyster shell were similar for each light period of each lighting regimen.

3. Ovipositions were distributed virtually at random throughout the day and the mean interval between successive eggs within a clutch was increased.

4. Reducing the total daily photoperiod from 12 to 6 h decreased daily food consumption.     

Genetic evaluation of laying performance in the Zatorska goose: contribution to the conservation programme

1. The aim of the study was to estimate the heritability of the laying performance in the cumulative and partial production of eggs and predict the breeding values of native Zatorska geese in a conservation programme using Best Linear Unbiased Prediction (BLUP) methodology. Second, the trajectory of the egg production curve was examined.

2. The data contain information about the laying performance of 1831 individuals in the first year of laying. To describe the trajectory of the laying performance, 10 mathematical models were tested. For the genetic parameter estimation of egg production, data from 1038 birds were used with a production higher than 20 eggs during the first season of laying.

3. The analysis of egg production was based on single and multi-trait models. Heritability, genetic and phenotypic correlations between phases of the laying performance as well as breeding values were estimated.

4. The best adaptation to the goose egg laying curve was the Ali and Schaeffer model. The estimates of heritability were 0.20 (0.06 SE) using the single-trait model and ranged from 0.12 to 0.24 using the multi-trait model.

5. The results suggest that the BLUP method can support the conservation programme.     

Whitening of brown shelled eggs: Individual variation and relationships with age,fearfulness, oviposition interval and stress

1. Fearfulness, shell colour, incidence and degree of shell whitening and the interval between ovipositions were studied in two populations of 30 brown egg laying hens with family histories of a low or a high incidence of egg shell whitening.

2. Hens of the population with the high incidence of whitening appeared to be more fearful than hens of the population with the low incidence of whitening.

3. Brown colouration of the egg shell and the incidence and degree of shell whitening declined as the hens aged.

4. Brown colouration and egg shell whitening were most pronounced on the blunt ends of the eggs.

5. A large part of the variation in egg shell whitening was attributable to the individual (hen) component of variance.

6. Differences in egg shell whitening, between the two populations, were detectable throughout the 26 weeks of the experiment.

7. Oviposition intervals were similar for normal and coated eggs when birds were not exposed to disturbance.

8. Disturbance of hens increased oviposition intervals and the incidence and degree of shell whitening, to a similar extent, in both populations.

9. It is concluded that stress‐related egg retention is not the sole factor responsible for abnormal egg shell whitening. Shell whitening may occur as a consequence of the premature termination of shell pigmentation as well as a consequence of the retardation of oviposition which occurs when hens are disturbed.     

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.     

Comparisons of frequencies and egg shell characteristics of broken and intact eggs within diverse populations of chickens

1. Differences were found among eight populations of White Plymouth Rock pullets in the frequency of broken eggs.

2. The shells of such eggs were thinner than those of intact eggs in seven of the populations.

3. The number of defective eggs, the specific gravity of the eggs, and the percentage hen‐day egg production of normal eggs were significantly correlated within populations with the incidence of broken eggs.

4. No significant correlations were found within populations between the incidence of egg breakage and either egg weight, body weight, or shank length.     

The use of rapeseed meals and a mustard seed meal as a protein source in diets for laying pullets

1. Three experiments with laying pullets were carried out in which rapeseed meals (B. napus and B. campestris) and a mustard seed meal (B. juncea) formed 12% of the diet.

2. Dietary rapeseed had no effect on the onset of lay when fed from 17 weeks of age but caused a delay when fed from 10 weeks of age: changing to a control soyabean diet for the laying period resulted in normal egg production.

3. Diets containing B. napus but not B. campestris consistently depressed egg production and reduced egg weight in one experiment. Mustard seed meal did not affect performance.

4. Significant number of eggs with a “fishy” taint were laid by brown‐egged birds fed on a diet containing rapeseed.

5. Thyroids of birds fed on rapeseed meal diets during the laying period were significantly heavier than those of birds fed on diets containing mustard seed or soyabean.

6. The enlargement of the thyroid gland is probably related to the oxazolidinethione content of the rapeseed.     

Egg‐shell deposition and blood plasma inorganic phosphorus concentration in individual laying hens

1. The relationship between plasma inorganic phosphorus measured at the end of the dark period and the weight of the next egg shell produced was investigated in 30 Hisex Brown hens.

2. Hens received an adequate conventional layers’ diet and the lighting pattern was conventional (17 L:7 D). Observations were made early (31 to 40 weeks) and late (62 to 68 weeks of age) in the laying period.

3. Eggs were classified by position in the clutch sequence and significant negative correlations were found between shell weights of early eggs in the sequence and plasma phosphate at the end of the dark period.

4. No significant trends were found in plasma total calcium.

5. No significant differences were found in bone compositions of birds producing consistently more or less than average shell weight during the laying period.

6. The negative correlations between plasma phosphate and shell weight are consistent with the observations of Sauveur and Mongin (1983) and show that impairment of shell deposition is associated with skeletal mobilisation as indicated by increase in plasma phosphate. This is consistent with the observations on bone composition and indicates that selection for shell quality will tend to select birds which are not dependent on excessive skeletal mobilisation during shell formation.     

Responses of modern hybrid laying stocks to changes in photoperiod

Two replicates of each of 4 light patterns were imposed on 4 breeds of laying hen. The light patterns were designed to induce sexual maturity, defined as 50% production, at a range of ages. Within‐room treatments were ad libitum or rationed feeding during rearing and 4 breeds, namely ISA Brown, Hisex Brown, Ross G‐Link Brown and Shaver Brown. A total of 6144 birds were used to test the 32 treatments.

2. Age at 50% production was significantly affected by both lighting treatment and rearing regimen.

3. The light pattern treatments had no significant effect on any cumulative performance variable measured from 20 to 80 weeks of age.

4. Breed had a significant effect on eggs/hen housed, rate of lay, egg weight, egg output and food intake.

5. Rationing feeding during rearing, by holding intake at its 6‐week level from 6 to 14 weeks of age, was associated with significantly lower egg production, but had no effect on egg weight or food intake during lay.

6. Although both rearing and light treatments influenced age at 50% production, this character was not correlated with egg weight or egg production.

7. It is suggested that modern hybrid laying stocks are so genetically predisposed to ovulate that they are becoming refractory towards treatments hitherto regarded as influential.     

The necessity of supplementing laying hen diets with linoleic acid

Results from four experiments with laying hens have been re‐examined using the means of individual 28‐d periods during egg production to investigate the influence of the developing ovary and linoleate storage during growth on the linoleic acid requirement of the laying hen.

Apart from a possible beneficial effect during the first few weeks of production, little increase in egg weight occurs when birds are fed on conventional rearing diets and then fed on laying diets containing linoleic acid in excess of requirement.

After depletion of linoleate reserves, dietary supplementation with linoleic acid significantly increases egg weight at any age.

The necessity of supplementing diets for laying hens with linoleic acid is discussed.     

Food consumption records for the genetic improvement of income over food costs in laying flocks of white leghorns

1. A study of genetic parameters of egg mass based on the weights of all eggs laid, individual food consumption, body weight and age at first egg was made. Data from three populations differing in average egg weight were available over two production periods, from 20 to 40 and from 40 to 60 weeks of age, respectively.

2. Selection indexes designed to maximise income over food costs (IOFC) were used to evaluate the usefulness of food consumption data for the genetic improvement of laying flocks.

3. Given reliable estimates correlating food consumption to egg mass, body weights and age at first egg it is possible to construct highly efficient selection indexes for genetic improvement of IOFC without the direct use of food consumption data.

4. Selection for genetic gains in egg mass appears to be the most important factor for genetic improvement of IOFC. Correlated increases in egg weight were observed for two of the populations.

5. Body weights showed very small and inconsistent genetic responses under index selection suggesting that a reduction in body weight need not be necessary for more efficient egg production.

6. Indexes which showed greatest genetic improvement also resulted in an increase of food consumption. Thus genetic efficiency in egg laying flocks would be achieved by increasing egg mass through earlier sexual maturity, larger eggs and higher production rates with increased food consumption and only slight, if any, reduction in body size.

7. Estimates of heritabilities and genetic correlations indicate that food consumption measurements can be based on partial records; high heritabilities were found for egg mass and food consumption measurements in both early (20 to 40 weeks) as well as late (40 to 60 weeks) production periods.     

Genotypic differences in speed and magnitude of response to ahemeral lighting

1. The paper compares between three genetically different lines in their egg weight and shell thickness response to a 28‐h cycle.

2. The response in shell thickness to ahemeral lighting was more rapid (2.2 d) than for egg weight (4.2 d).

3. Differences between genotypes were evident in both the speed and magnitude of response.

4. Overall, egg weight and shell thickness on the 28‐h cycle were 7% and 8% greater than on 24 h.

5. The allometric increase indicates that the increase in shell weight was on average 14% more than the increase in egg weight.     

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.     

Effect of egg composition on hatchability and on growth and slaughter characteristics of meat-type chicks

1.?Using the so-called TOBEC (Total Body Electrical Conductivity) method, which allows the determination of egg composition in vivo, correlations between egg composition, hatchability and hatched chicks’ development were studied.

2.?A total of 1500 hen eggs (Ross-308) were measured by TOBEC, and eggs with extremely high (10%, n = 150), extremely low (10%, n = 150) and average (10%, n = 150) electrical conductivity values were chosen for further investigation.

3.?During the incubation period, it was observed that eggs with high electrical conductivity had a significantly higher mortality than eggs with low electrical conductivity.

4.?It was observed that both the increase in electrical conductivity at the same egg weight, and the increase in egg weight at the same electrical conductivity resulted in an increase in the hatching weight.

5.?It was found that the dry matter, protein and fat content of the chicks hatched from eggs with low electrical conductivity was higher at hatching than that of the chicks hatched from eggs with high electrical conductivity.

6.?At 42 d of age the liveweight of cocks and pullets hatched from eggs with low electrical conductivity was 3·2 and 8·2% higher than the liveweight of cocks and pullets hatched from eggs with high electrical conductivity.

7.?Because of the higher liveweight at slaughter, there was a significant superiority of the chicks hatched from eggs with low electrical conductivity in the case of the examined carcase traits at slaughter.

8.?Similar tendencies were found also in the ratios of carcase variables to liveweight, but the between group differences were not statistically significant in this case.

9.?Based on the results it was concluded that TOBEC seems to be a useful method for separating eggs with different composition.

10.?This could be a good starting point for further in vivo investigations in order to clarify the effect of egg composition on hatchability and further development.