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.     

Effect of size and timing of photoperiod increase on age at first egg and subsequent performance of two breeds of laying hen

1. ISA Brown and Shaver 238 pullets were changed from 8 h to 8, 10, 13 or 16 h photoperiods at 42, 63, 84, 105, 126 or 142 d of age.

2. Age at first egg (AFE) was curvilinearly affected by the size and timing of the change in photoperiod. AFE was advanced most by a photoperiod change from 8 to 13 h made at 63 or 84 d. ISA birds were generally more responsive than Shaver to the photoperiod changes.

3. Longer photoperiods significandy increased survivors' egg production, but decreased liveability to 504 d, so that eggs per hen housed were unaffected. Retarding AFE by 10 d reduced survivors' egg numbers by 7.0, but increased mean egg weight by 1.26 g. Egg output by Shaver birds was unaffected by AFE, but that of ISA was curvilinearly affected, with an apogee at an AFE of 135 d. In both breeds, egg weight and egg output were greater following an early or late, rather than a mid‐term photostimulation.

4. Photoperiod significandy increased mean daily food intake during lay by 1.26 g/h. A 10 d retardation in AFE resulted in a reduction in food intake of 1 g/d. Efficiency of food conversion deteriorated according to the square of the photoperiod, and changed curvilinearly according to age at photostimulation. Food conversion efficiency improved by 0.05 g/g for each 10 d delay in AFE.

5. Shell quality was unaffected by AFE, but deteriorated with increasing photoperiod and was curvilinearly affected by age at photostimulation with the smallest shell weights associated with photostimulation at 63 d. The incidence of double‐yolked (DY) egg production increased with photoperiod and decreased with delayed photostimulation. There was an exponential regression of DY eggs on AFE.

6. Body weight at first egg increased by 75 g/d delay in AFE, but body weight at 504 d of age was unaffected by AFE, photoperiod or age at photostimulation. Body weight gain during lay increased by 15 g/h increase in photoperiod, decreased by 6 g per 10 d delay in photostimulation and by 40 g per 10 d delay in AFE. Fat content at 504 d increased by about 10 g/kg and by 23 g/bird for each 10 d delay in AFE.

7. Mortality in lay increased by 0.8%/h increase in photoperiod, but was unaffected by either age at photostimulation or AFE.     

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 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.     

Effect of constant and of changing photoperiods on age at first egg and related traits in pullets

1. The effects of constant photoperiods and of single (5 h) changes in photoperiod applied at 12 or 17 weeks of age upon age at first egg (AFE) were studied using ISA Brown and Shaver 288 pullets.

2. Birds reared from 2 d of age until after maturity on constant 10 h photoperiods matured 8 d earlier than birds reared on constant 8 h and 5 d earlier than the average for 13 or 18 h photoperiods.

3. A single increment in photoperiod from 8 to 13 h advanced AFE by 23 d (compared to 8 h constant day controls) when applied at 84 d, but by only 6 d when given at 119 d. An increase in photoperiod from 13 to 18 h advanced AFE by only 4 d, averaged across breeds and age at increase. A reduction in photoperiod from 13 to 8 h delayed AFE by 22 d when given at 84 d and by 16 d at 119 d. A similar 5 h reduction in photoperiod, but from 18 to 13 h, retarded maturity by 11 d in ISA Brown pullets, but only when given at 84 d, and delayed AFE in Shaver 288 by 12 d, but only when given at 119 d. This interaction may be partly explained by the different physiological stages reached by the two breeds when the photoperiod was changed.

4. Under constant daylengths cumulative food intake before first egg was positively correlated with photoperiod, but the early AFE for birds on 10 h photoperiods resulted in this group having the lowest cumulative food intake to first egg.

5. A 5 h increase in photoperiod at 84 d significantly reduced the food consumed to first egg, but had no effect when given at 119 d. A 5 h decrease in photoperiod generally increased the food consumed to first egg, but the effect was only significant when the daylength was reduced from 13 to 8 h at 119 d. Food intake to first egg in birds subjected to a change in photoperiod was highly correlated with AFE.

6. The data confirm that sexual development in growing pullets responds more to changes in photoperiod than to the absolute daylength, that changes made at different daylengths are not equivalent and that sensitivity changes with age.     

The clutch patterns of hens in constant illumination

1. Although flocks of hens under constant illumination lay eggs by night and day, it has not yet been demonstrated that the number of eggs laid by night is equal to the numbers expected on a hypothesis of random distribution around the clock.

2. Hens under continuous illumination lay eggs at quite regular intervals. With highly productive pullets and a limited period of observation (e.g. 10 weeks), many birds lay unbroken sequences (i.e. intervals between consecutive ovipositions do not exceed 33 h).

3. Some birds under continuous light lay eggs in clutches (i.e. one observes characteristic inter‐clutch intervals of 35 to 41 h between ovipositions). However, the first egg of a new clutch has a high probability of being laid between 05.00 h and 16.00 h and this is taken as evidence that the timing of clutches is dependent on diurnal environmental influences which persist in spite of attempts to provide a non‐varying environment.

4. The evidence available neither supports nor refutes the hypothesis that under constant environmental conditions an internal “ clock “ with a fixed period is responsible for timing the open periods during which release of luteinising hormone may occur.

5. Further experiments are needed with hens having a lower rate of lay, and therefore more likely to lay in clutches, maintained in a better‐controlled constant environment.     

Influence of sequence length on the response to ahemeral lighting late in lay

1. An experiment is described in which 96 individually‐caged SCWL hens in two rooms were used to investigate the response to changing to a 28‐h cycle using a reverse treatment design.

2. The application of the 28‐h cycle did not affect mean rate of lay but increased mean egg weight and egg output.

3. Grouping the birds according to their preliminary sequence length yielded an interesting outcome. In both rooms, birds with short sequences (≤ 6 eggs) produced significantly more eggs under the 28‐h cycle, while those with long sequences (> 6 eggs) produced marginally fewer eggs. The same trend was also evident with egg output.

4. Changing from 24‐h to 28‐h increased yolk and albumen weights as well as shell quality. However, relative to egg weight, no measurable effect was detected due to light cycle, age or sequence length on yolk and albumen weights.

5. The paper provides new evidence suggesting that long ahemeral cycles could be used to improve egg production as well as shell thickness in flocks with modest rates of lay.     

Studies on effects of nutritional factors on bone structure and osteoporosis in laying hens

1. A modern hybrid strain of laying hen (Hisex) was fed from point of lay to 68 weeks on a control diet and diets containing oystershell, fluoride, 1,25‐dihydroxycholecalciferol, ascorbic acid, a lower concentration of phosphorus and a combination of a lower concentration of crude protein and higher concentration of vitamin K. Hens from a much older strain (Brown Leghorn J‐line) were fed on the control diet.

2. Plasma variables were measured during lay. End‐of‐lay trabecular and medullary bone volumes in the proximal tarsometatarsus and free thoracic vertebra were measured by histomorphometry.

3. The majority of Hisex hens were considered to be osteoporotic by the end of lay. In contrast, none of the J‐line were osteoporotic.

4. None of the nutritional treatments affected trabecular bone volumes. Medullary bone volumes were increased significantly by feeding oystershell or fluoride.

5. There was no phenotypic correlation between egg production and trabecular bone volume in the Hisex hens.

6. The experiment provided evidence that osteoporosis in laying hens, as assessed by trabecular bone volumes, is not caused by calcium deficiency and could not be prevented by any of the nutritional treatments studied.     

Ovarian morphology and rates of ovarian follicular development in laying broiler breeders and commercial egg‐producing hens

1. Ovaries from a light‐bodied egg laying strain and a broiler breeder strain were compared at 26 and 82 weeks of age.

2. The rate of lay in both strains was lower in the older hens. The 82‐week‐old hens were subdivided into good and poor layers: the poor layers produced eggs at about half the rate of the good layers.

3. The yellow‐yolky ovarian follicles in both strains were smaller, more numerous and more closely ranked in hierarchies in 26‐week‐old hens than in 82‐week‐old hens.

4. No marked differences were seen between the strains at 26 or 82 weeks of age in the sizes, numbers or hierarchical arrangements of yellow‐yolky ovarian follicles.

5. The ovaries from 82‐week‐old good and poor layers from both strains contained similar numbers of yellow‐yolky follicles.

6. After feeding a fat‐soluble dye, the number of days over which eggs containing dye were laid did not differ between 26‐, 52‐ and 113‐week‐old hens from an egg laying strain. However, fewer eggs with dyed yolks were laid by the older hens.

7. These observations suggest that the decrease in egg production with age is due initially to a reduction in the rate of recruitment of yellow‐yolky follicles. Towards the end of the laying year it may also be due to an increased incidence of follicular atresia, internal ovulation and the production of membraneous or soft shelled eggs.     

Photoperiod and seasonal influences on the growth of turkey hens

1. The influence of photoperiod and time of year on the growth of hen turkeys was investigated.

2. Photoperiod treatments consisted of computer simulations of day lengths which occur naturally in the spring and autumn of the year. Both photoperiod treatments were given to hens in the autumn and spring.

3. Data were collected for growth evaluations at 2‐ to 4‐week intervals to 16 weeks of age. No significant season × photoperiod interactions occurred.

4. The spring trial resulted in greater body weights and better food conversions (food/gain) than the autumn trial.

5. Simulated autumn daylengths resulted in greater body weights and improved food efficiency at 16 weeks of age compared with simulated spring daylengths.

6. The pattern of growth (period changes) was influenced by season, but not photoperiod.

7. Season and photoperiod both have important and independent influences on the growth of the turkey hen.     

Day‐length during rearing and the subsequent egg production of meat‐strain pullets

1. The effects of lighting pattern on production to 399 d in caged, female, meat‐strain chickens was investigated. Energy intake was controlled from 56 to 399 d.

2. Four different rearing treatments with a subsequent constant 16‐h photoperiod during laying were used.

3. A 15‐h rearing photoperiod resulted in delayed sexual maturity, increased mature body weight and decreases in both total egg numbers and the proportion of smaller eggs, compared with a 6‐h photoperiod.

4. Continuous light to 56 d, although associated with a high incidence of subsequent blindness, resulted in satisfactory egg production.

5. Abrupt reduction in the photoperiod from 15 to 6 h for the 112 to 167 d period resulted in unsatisfactory subsequent performance, especially when the day‐length was only slowly increased to 16 h during laying.

6. In the two laying treatments, in which the photoperiod was increased gradually from 6 to 16 h during the 168 to 238‐d period, a decrease in the number of smaller eggs occurred, compared with the treatments in which a single abrupt increase in photoperiod was used.     

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.     

Behavioural adaptation of laying hens to dilution of diets under mash and pellet form

1. Two laying diets, control (A) and a low‐energy (B) diet diluted by adding 450 g/kg wheat bran, were fed to semi‐heavy hens in three different forms: mash, small pellets and large pellets. The behavioural adaptations and the production characteristics for these six regimens were studied on 72 individually caged hens, between 19 and 29 weeks of age, subjected to a lighting pattern of 14 h light/24 h.

2. Diet B, as mash, showed a lower apparent physical density than the others. The hardness and durability of the pelleted diets were similar.

3. Hens fed the mash diet B could not completely adjust their food intake to compensate for the dilution and showed reduced egg output and body weight gain compared to the other groups.

4. Video observation of each hen for 14 consecutive hours showed that mash‐fed hens ate for longer periods than pellet‐fed hens during the first 11 h (proportion of time spent eating: 41.3% mash B, 32.5% mash A and 20% to 25% for all the pelleted diets). These differences were less pronounced during the last 3 h of the photoperiod.

5. Trough‐oriented stereotypies were noted in 14 out of 22 mash‐fed hens and in 12 out of 47 pellet‐fed hens. Dilution of the diet did not appear to exacerbate stereotyped behaviours under the conditions of the study.

6. This experiment demonstrates that the feeding behaviour of laying hens is affected by the physical characteristics of the diet and that this may lower their productivity.

7. Low‐energy pelleted diets might be used to feed hens efficiently in tropical countries where cereal by‐products are abundant.     

Relationship between body fatness,ovarian structure and reproduction in mature females from lines of genetically lean or fat broilers given different food allowances

1. Reproductive and other characteristics were measured at 34 and 60 weeks of age in broiler breeder hens on 6 different feeding regimes. The hens came from genetically lean and fat lines selected on the basis of low or high 7‐week plasma very low density lipoprotein (VLDL) concentration.

2. Plasma VLDL concentrations were consistently higher at all ages in fat line hens but were not affected by dietary treatment.

3. Mature body weight did not differ between the lines in birds fed ad libitum but with food restriction throughout life, fat line birds were lighter at 34 weeks.

4. There was little difference between the lines in abdominal fatness of birds fed ad libitum up to 60 weeks. Fat line birds were always fatter than lean line counterparts under food restriction.

5. Egg production was higher in lean line birds fed ad libitum but food restriction improved egg production in both lines. Peak egg productions were similar in both lines but there was evidence that the optimal food allowances for egg production was higher in the lean compared with the fat line.

6. Ovarian yellow follicle numbers were highest at 34 weeks in ad libitum fed lean line birds and declined linearly with decreasing body weight caused by food restriction but there was no such relationship in fat line birds.

7. White follicle numbers were higher and follicular atresia was lower in the lean line.

8. It is concluded that poor reproduction in fat line birds was associated with inhibition of follicular development and atresia rather than by high plasma VLDL concentrations promoting excessive yolk formation.     

Influence of dietary calcium and phosphorus on metabolism and production in laying hens

1. The effects of different dietary concentrations of calcium (24 to 56.9 g/kg) and phosphorus (4.5 to 14.2 g/kg) on production and some aspects of metabolism were studied in laying hens.

2. Treatments did not affect egg numbers, food consumption, conversion efficiency of food to egg, bodyweight gain or mortality.

3. Increasing dietary calcium (Ca) significantly increased plasma Ca and inorganic phosphorus (P), breaking strength at the radius and egg specific gravity and significantly decreased plasma alkaline phosphatase and egg weight.

4. Increasing dietary phosphorus increased plasma P and decreased egg specific gravity significantly.

5. Plasma Ca, P and alkaline phosphatase and radius breaking strength were suitable indices of the Ca status of the hens.     

Responses of immature pullets to repeated cycles of gradual increases and abrupt decreases in photoperiod

1. Growing pullets were reared on constant 8, 11 or 14 h photoperiods or given 12 daily increments of 30 min followed by an abrupt 6 h decrease in photoperiod in 14 d cycles from 2 d of age to sexual maturity.

2. Birds on the experimental lighting programme matured earlier than constant 8‐h controls, later than 11‐h controls but at the same age and body weight as constant 14‐h controls.

3. Weight of the first egg was correlated with age at first egg.

4. It is assumed that potential advances in maturity for the experimental birds from the 30 min increments in photoperiod were cancelled by the retarding influences of 6 h decreases in photoperiod, resulting in their maturity being similar to that of birds reared on a constant daylength equal to the longest photoperiod reached during the cycle.     

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.     

Effects of lighting regimen and grower diet energy concentration on energy expenditure,fat deposition and body weight gain of laying hens

1. Mean metabolisable energy (ME) intakes and heat productions over a laying year were calculated for laying hens which had been submitted to one of various lighting regimens and given either a normal or a high energy ration during the rearing period.

2. Daily ME intake and heat production per hen in the laying period were unaffected by either lighting regimen or grower diet. ME intake per kg W ^0.75 and heat production per kg W ^0.75 during lay increased significantly with laying photoperiod, was non‐significantly higher following an 8‐h rather than an 11‐h rearing photoperiod, but was unaffected by dietary energy concentration. The increase in heat production (/kgW°‘⁷⁵) associated with a 1‐h increment in photoperiod was similar to predictions made from calorimetric measurements of diurnal variation.

3. Efficiency of conversion of food to egg was unaffected by either lighting regimen or dietary energy concentration.

4. Fat weight gain in lay was not influenced by lighting regimen, but was significantly lower in birds reared on the high, compared to the normal, energy grower ration. Fat‐free weight gain in lay was unaffected by grower diet, but was significantly increased by photoperiods longer than 8 h.

5. ME intake and heat production per kgW^⁰⁷⁵ were negatively correlated with age at first egg, but ME intake and heat production per bird d were not related to age at sexual maturity.     

Individual variation in prelaying behaviour and the incidence of floor eggs

1. Floor eggs are a problem in non‐cage systems for laying hens, as they require secondary egg collecting. Failure to lay in a well‐defined nest site may also be a welfare problem for the hens, but only if their nesting motivation has been thwarted.

2. We investigated the relationships between a hen's prelaying behaviour and its tendency to lay on the floor by recording the behaviour of 20 hens housed individually in wire cages with single littered nest boxes.

3. Most floor eggs (80%) were laid by the same 6 hens. These 6 “floor‐layers” performed more nest seeking behaviour, less nest‐building behaviour and less sitting prior to oviposition than the 14 hens that consistently laid in nest boxes.

4. The incidence of floor eggs declined with age. Both nest and floor laying hens performed less nest seeking behaviour with age. Floor layers, however, increased their performance of nesting behaviour, whilst nest layers performed less nesting behaviour with age.

5. Floor laying hens behaved as if they found the nest box less attractive than nest‐laying hens; perhaps because they had lower nesting motivation, or perhaps because their nesting motivation was as high, but they less readily perceived the nest box as an appropriate nest site.     

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.