Light intensity can influence plasma FSH and age at sexual maturity in domestic pullets

1. Shaver White and ISA Brown pullets were reared to 140 d in cage groups of 8 on a 10-h photoperiod of incandescent light and maintained at an illuminance of 3 or 25 lux, or transferred from 3 to 25 lux or from 25 to 3 lux at 63 or 112 d of age. 2. Plasma follicle stimulating hormone (FSH) concentration at 63 and 112 d was higher in both breeds for pullets maintained at an illuminance of 25 lux compared with 3 lux. After 2-4 d, and relative to constant-illuminance controls, plasma FSH increased significantly for ISA Brown transferred from 3 to 25 lux at 63 d and for Shaver White transferred at 112 d. Irrespective of genotype, plasma FSH for pullets given a decrease in illuminance at 63 or 112 d showed a tendency for less change than did constant-illuminance controls. 3. There was no significant difference in sexual maturity for ISA Brown maintained on 3 or 25 lux, but Shaver White pullets exposed to constant 3 lux matured later than those maintained on 25 lux. Shaver White matured later following an increase from 3 to 25 lux at 63 and 112 d, and earlier subsequent to a decrease from 25 to 3 lux at 112 d. ISA Brown pullets were not significantly affected by a change in illuminance at 63 or 112 d, though their responses were in the same direction as Shaver White. 4. Changes in plasma FSH in the 2- to 4-d period following a change in illuminance at 63 or 112 d were not significantly correlated with sexual maturity.     

Effect of age of release from light or food restriction on age at sexual maturity and egg production of laying pullets

1. Lohmann Brown pullets, in one trial, and Hyline Brown pullets in another, were reared from day 2 on short daylengths, and from week 8 in trial 1 (week 16 in trial 2) on food restriction. These restrictions were lifted at various times during the rearing period as a means of determining the relative importance of the day length and food restriction stimuli on the attainment of sexual maturity and subsequent laying performance. 2. A total of 2304 pullets were used in each trial. The birds were reared in light proof rooms, and subjected to 8L:16D until they were moved to a laying facility where a light stimulus of 16L:8D was applied. In trial 1 the six ages at which light stimulation was applied were 115, 122, 129, 136, 143 and 171 d. Within each light treatment, food restriction of pullets, which consisted of feeding 72 g of food/bird d, was lifted at six different ages, namely, 115, 129, 143, 157, 171 and 185 d. In trial 2 both the light stimulation and the lifting of food restriction occured at 111, 125, 139, 153, 167 and 181 d of age, producing 6x6=36 treatments in both trials. 3. The first trial was terminated when the pullets were 28 weeks old, soon after all the birds had commenced laying, because of an outbreak of Egg Drop Syndrome. However, because age at maturity was the variable of major interest, data from this experiment could be used in the analysis. The second trial ended when the birds reached 40 weeks of age. Variables measured were age at maturity, food intake and body weight gain subsequent to the lifting of restrictions and, in the second experiment, rate of lay, peak rate of lay and egg weight at various ages. 4. The mean age at sexual maturity was influenced by the date of release from light restriction (P<0.001) and from food restriction (P<0.001) in both trials. In addition, the interaction between the age at release from light and from food restriction was significant. Regression equations were produced for each trial to describe the relationships between the age at sexual maturity and the age at release from light restriction and food restriction. 5. There was an effect of both light restriction (P<0.001) and of food restriction (P<0.001) on the increase in food intake (g/bird d) in the week following release from food restriction in both experiments. These effects were not independent: the effect of the interaction of light and food restriction on this increase in food intake was also highly significant. The longer the birds were subjected to light restriction, the less dramatic the increase in food intake when food restriction was lifted. The more sustained the period of food restriction, the higher the increase in food intake in the week following release from the restriction. 6. Mean egg weight was 4 g heavier at 22 weeks of age in birds released from food restriction at 16 and 18 weeks, than from those released at 24 and 26 weeks of age. However, by 30 weeks of age, birds restricted for longer produced heavier eggs than their earlier-maturing counterparts. This effect continued to the end of the trial at 40 weeks of age, at which time there was a 2.3 g difference in egg weight between these treatments. 7. Both light and food restriction have an effect on the age of maturity in laying hens. The length of time between the release from light or from food restriction to the onset of laying depended on the age of the pullets when the release occurred. Egg weight at a given age was significantly affected by the age at release from food restriction, but not from light restriction.     

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.     

Constant photoperiods and sexual maturity in broiler breeder pullets

1. Broiler breeder pullets were maintained on 10-, 11-, 12-, 13-, 14- or 16-h photoperiods to determine the effect of constant photoperiods on sexual development in broiler breeders. The birds were fed to achieve a 2100 g body weight at approximately 17 or 20 weeks to see if the photosexual response was modified by rate of growth. 2. In both body weight groups, pullets maintained on 10h were the first to reach sexual maturity (50 eggs/100 bird-d), and these and the 11-h pullets matured significantly earlier than any of the other photoperiod groups. Pullets maintained on 13 or 14 h matured latest, at about 3 weeks after the 10-h pullets, though both were only marginally later than the 12- or 16-h birds. These differences in maturation probably reflect the different rates at which photorefractoriness is dissipated in broiler breeders reared on photoperiods that vary in their degree of stimulatory competence. 3. There were no significant interactions among the photoperiods and the ages at 2100 g; faster-growing birds consistently matured about 10 d earlier than conventionally grown pullets.     

Effect of exogenous oestradiol and lighting regime on age at first egg in domestic pullets

1. Groups of ISA Brown pullets were transferred from 8- to 16-h photoperiods at 34, 44 or 54 d. In each group, 12 birds were injected on alternate days over a 12-d period starting 6 d before the change in photoperiod with beta-oestradiol-3-benzoate (1 mg/kg body weight) or with arachis oil vehicle (controls). Short-day controls were similarly injected from 28 to 40 d. Long-day (16 h) controls were also included in the trial but were not injected. Age at first egg (AFE) was recorded and plasma luteinising hormone (LH) concentrations were measured around the time of oestradiol treatment. 2. Mean AFE for birds photostimulated at 34 d was not significantly different from short-day controls. Birds photostimulated at 44 and 54 d matured at similar ages but 3 weeks earlier than short-day controls (P<0.05). 3. There was a tendency for oestradiol to advance AFE for birds photostimulated at 34 d (P=0.15) but to delay AFE following photostimulation at 44 d (P=0.23). Oestradiol significantly delayed AFE for the birds photostimulated at 54 d (P=0.01). 4. Plasma LH levels during 6 d of oestradiol injection but before transfer from 8- to 16-h photoperiods tended to fall between 28 and 34 d, were relatively constant between 38 and 44 d, but declined significantly between 48 and 54 d. Following photostimulation at 34 d, increases in plasma LH levels for oestradiol-injected birds were significantly greater than for controls. Oestradiol treatment had no significant effect on changes in plasma LH concentrations after photostimulation at 44 or 54 d. 5. This trial confirms previous work showing that pullets are unresponsive to photostimulation before 6 weeks of age. It also demonstrates that raising circulating oestrogen levels by injecting 0.5 mg/kg oestradiol benzoate on alternate days enhances the LH response to photostimulation at 34-d, but only very slightly sensitises a 34-d old bird to an increase in photoperiod which, 10 d later, is capable of advancing AFE in control birds by 24 d. Increased circulating oestrogen might be a factor which allows pullets to advance AFE in response to an increase in daylength.     

Effect of one or two pre-pubertal long days on age at first egg in domestic pullets

1. Two trials were conducted, using 288 brown-egg hybrid pullets in each, to determine the effect on age at first egg (AFE) of exposure to one or two 'long days' during the rearing period. In the first trial, birds were given a single 'long day' of 10, 12 or 14 h at 75, 89 or 103 d of age, with controls maintained on 8-h photoperiods. All treatment groups were transferred to cages at 110 d, and half the birds from each treatment combination given a 6-h increment in photoperiod at 116 d, with the remainder held on 8-h photoperiods. In the other trial, birds were given one or two long days of 14 or 16 h at 96, 107, 117 or 128 d of age; controls were again held on 8-h photoperiods. All groups were moved to cages at 130 d but maintained on 8-h photoperiods. 2. AFE was not significantly affected by one or two pre-pubertal long days, irrespective of when the long day was given or its length. AFE was advanced by 2 to 3 weeks following a transfer from 8 to 14 h at 116 d, independently of whether or not the birds had received a previous long day exposure. 3. It appears that a full-fed egg-type hybrid requires more than two cycles of long days to initiate rapid gonadal development, and that exposure to a single long day during the rearing period will have minimal effect on the timing of sexual maturation and no influence on the response to a subsequent permanent transfer to long days.     

Effect of constant and of changing photoperiod on plasma LH and FSH concentrations and age at first egg in layer strains of domestic pullets

1. ISA Brown pullets were transferred from 8 to 14 h or from 14 to 8 h photoperiods at 35 or 56 d of age. Controls were maintained on constant 8 or 14 h photoperiods from day 1. 2. Blood samples were obtained immediately before each daylength change and subsequently at 7 d intervals until 1st egg in the treated groups and at 70 d of age and then at 14 d intervals until 1st egg in the constant photoperiod controls. Plasma luteinising hormone (LH) and follicle stimulating hormone (FSH) concentrations were determined using homologous radioimmunoassays. 3. Prior to 16 weeks, LH was consistently higher in birds on constant 14 h photoperiods than in those on constant 8 h, but was down-regulated as birds approached maturity so that LH concentrations in the 2 groups were similar during the final 10 d before the first egg was laid. FSH concentrations rose steadily with age but with a tendency for concentrations to be higher in the 8 h than in the 14 h treatment. Birds on constant 8 h daylengths matured 18.3 d later than those on constant 14 h photoperiods. 4. A 6 h increment in photoperiod given at 35 d or 56 d, resulted in an increase in LH within 7 d in both cases. FSH concentration did not respond to an increase in photoperiod at 35 d but rose following the same increase at 56 d. This was associated with a 3-week advance in sexual maturity, whilst age at 1st egg in birds photostimulated at 35 d was similar to the age with a constant 14 h photoperiod. 5. LH concentration fell when photoperiod was reduced from 14 to 8 h at either 35 or 56 d and remained below the constant 8 h controls for many weeks before rising to a concentration not significantly different from other groups in the final 10 d before 1st egg. FSH concentrations in birds exposed to a decreased daylength at 35 d, although more oscillatory, were similar to the constant 8 h photoperiod controls. In birds exposed to the same decrease at 56 d, FSH concentration initially tumbled but was similar in the 2 groups during the latter stages of rearing; neither differed significantly from the constant daylength controls during the 60 d before 1st egg. Sexual maturity in both groups given a reduction in photoperiod was delayed by about 2 weeks compared with constant 8 h controls. 6. Change in FSH concentration following an increase in daylength was a better predictor of age at 1st egg than change in LH. However, FSH concentrations after 14 weeks of age were rather similar in short day and long day controls and in the 2 groups given reductions in photoperiod at 35 d and 56 d, despite differences of nearly 5 weeks in mean age at 1st egg amongst these 4 treatments.     

Influence of feeding intensity on corporeal development, body composition and sexual maturity in female rabbits

Twenty-six 6-week old female New Zealand White rabbits were divided into two groups: ad libitum (AL) and 70% restricted (RS) feeding. At the beginning of the experiment the liveweights were practically the same: 0.99 +/- 0.08 vs. 1.01 +/- 0.08 kg in group AL and RS, respectively. At 18 weeks of age the body weight of Group RS rabbits was 84.7% (3.14 +/- 0.24 kg) of the group AL (3.71 +/- 0.31 kg). The apparent digestibility of crude protein was significantly (p < 0.001) higher in Group RS than in Group AL (76.5 +/- 1.4 vs. 73.0 +/- 2.7%). The daily water consumption was significantly (p < 0.05) higher (3.5 ml/g DM intake) in Group RS as compared to Group AL (1.9 ml/g DM). Since the average body weight in Group RS at 18 weeks was the same as that of Group AL at 14 weeks of age (3.14 kg), the comparison of the live body measures and indices was based on these ages. Animals fed ad libitum or restricted show no differences at the defined age in most live body measurements except in heart girth and rump width, which were significantly (p < 0.05) shorter in Group AL than in Group RS (29.3 +/- 0.8, 5.7 +/- 0.5 and 30.7 +/- 1.0, 6.2 +/- 0.3 cm, respectively). Body capacity was significantly (p < 0.05) smaller in Group AL, as the head capacity-body capacity proportion was significantly (p < 0.05) higher in Group AL than in Group RS (1653.1 +/- 134.5, 22.0 +/- 2.5 and 1913.7 +/- 168.7, 17.7 +/- 1.9, respectively). Due to restricted feeding the growth of the head proved to be less intensive than that of the body at the same body weight. The body in these does tended to be wider. Since the head in comparison to length or capacity of the body was smaller in does fed 70% of ad libitum, it could be concluded that the development of body parts of restricted-fed does was unequal (allometric growth). The effect of feed restriction reflected in lower dry matter and fat, and a higher ash and protein content both in total body and in dry matter composition of rabbits at 18 weeks of age. Restricted feeding delayed sexual maturity (69 vs. 92% of rabbits) with later starting ovarian activity, weaker ovarian responsiveness, and a smaller number of tertiary follicles on the ovarian surface.     

Bone mineral density QTL at sexual maturity and end of lay

1. An F₂ cross of a broiler male line and a White Leghorn layer line was used to identify quantitative trait loci (QTL) for bone density at the onset of lay and at the end of the laying period. A total of 686 measures of humeral bone density were available for analysis.

2. There was no evidence for epistasis.

3. Genome-wide significant QTL for bone density at the onset of lay were identified on chromosomes 1 (311?cM) and 8 (2?cM) and on chromosomes 1 (311?cM), 3 (57?cM) and 8 (2?cM) with a covariate for the number of yellow follicles (a proxy for the concentration of circulating oestrogen).

4. Evidence for only 4 chromosome-wide suggestive QTL were detected at the end of lay (72 weeks).

5. Analysis of the combined data confirmed two genome-wide suggestive QTL on chromosome 1 (137 and 266?cM) and on chromosomes 8 (2?cM) and 9 (10?cM) in analyses with or without the covariate.

6. Positive QTL alleles came from the broiler line with the exception of 2 suggestive QTL at the onset of lay on chromosomes 3 and 5 in an analysis with the covariate.

7. In general, QTL acted additively, except that dominant effects were identified for three suggestive QTL at the onset of lay on chromosomes 3 (57 and 187?cM) and 5 (9?cM).

8. The significant QTL in this study were at similar locations to QTL identified in a range of crosses in other publications, suggesting that they are prime candidates for the search for genes and mutations that could be used as selection criteria to improve bone strength and decrease fractures in commercial laying hens.     

Genetic and environmental control of ovarian function in turkeys at sexual maturity.

1. The relationships between the numbers of ovarian yellow follicles and body weight was investigated in four strains of turkeys photostimulated at 24 or 30 weeks of age. The birds were fed ad libitum or control fed to reach 0.8 or 0.6 of the body weight of ad libitum-fed birds at 24 weeks of age. 2. There were more yellow follicles at 24 compared with 30 weeks of age. 3. The number of yellow follicles was higher in bigger strains. 4. Body weight control reduced the number and the proportion of similar sized yellow follicles. The effect decreased with increasing strain body weight. 5. There was a linear relationship of 0.633 between log yellow follicle number and log body weight. The intercept was higher in turkeys photostimulated at 24 compared with 30 weeks of age.     

Reassessment of riboflavin requirement for single comb White Leghorn pullets from 0 to 6 weeks of age fed on maize-soyabean meal diets and its subsequent effect on sexual maturity and egg production

1. Two experiments were conducted using a total of 228 Hyline W-26 1-d-old pullets in each experiment. The purpose of the study was to reassess the riboflavin requirement from 0 to 6 weeks of age (WOA) and its subsequent effect on sexual maturity and egg production using a maize-soybean meal diet. 2. Approximately 10% incidence of curly toe paralysis was observed among birds fed on the diet with no added riboflavin (1.5 mg total riboflavin/kg diet). 3. Applying the non-linear regression model to the body weight gain data at 3 and 6 WOA in both the experiments, it was found that the minimum total riboflavin required to achieve maximum body weight gain for the two age periods was 2.3 and 2.0 mg/kg of the total diet. This is equivalent to 5.0 and 5.7 micrograms riboflavin/g of body weight gain from 0 to 3 and 3 to 6 WOA respectively. 4. Birds fed on the diet containing no added (1.5 mg total/kg) riboflavin laid fewer eggs and had lower body weights at 24 weeks. 5. We conclude that, from 0 to 6 WOA, at least 2.3 mg total riboflavin/kg should be present in the diet to prevent curly toe paralysis, obtain the maximum body weight gain and sustain the subsequent performance at sexual maturity.     

Changes in the protein requirements of pullets during the first laying year

A range of protein intakes (5 to 20 g protein/d) was achieved by feeding six diets containing 7 to 14½% protein to a total of 400 pullets for 10 weeks from 28 weeks of age. The same six diets and an additional diet with 16% protein were fed again for 10 weeks from 62 weeks of age. The resulting patterns of egg output were different at the two ages. The birds required more protein at the end of the laying year than at the beginning to sustain any given level of output. This difference in protein requirement was not accounted for by changes in body weight.

It is concluded that measurements of protein input‐output relationships made at one stage in the laying year do not form a satisfactory basis for predicting protein requirement at another stage.     

Influence of feeding intensity on the growth, body composition and sexual maturity of male New Zealand White rabbits

An experiment was carried out with young male New Zealand White (NZW) rabbits to establish live body weight changes, body measurements, body composition and sexual maturity as a function of feeding intensity. Animals in Group 1 ('AL', n = 10) were fed ad libitum, while those in Group 2 ('RS', n = 10) received restricted feeding corresponding to 70% of the ad libitum level. The starting liveweights were practically the same (0.907 +/- 0.146 and 0.911 +/- 0.147 kg in Group AL and Group RS, respectively). The feeding trial lasted from 6 to 22 weeks of age. The average body weight was significantly higher in Group AL from 7 to 22 weeks of age. At 22 weeks of age the body weight of RS rabbits was 85.64% of the weight of AL animals (3.22 +/- 0.52 kg and 3.76 +/- 0.33 kg, respectively). Average body weights of RS males at 8, 9, 11, 19 and 21 weeks of age were similar to those of ad libitum fed (AL) animals at 7, 8, 10, 15 and 16 weeks of age, respectively. The growth of bucks fed restricted tended to be allometric. The most significant difference was found at 16 and 18 weeks of age, while the lowest difference occurred at 6, 12, 15 and 19 weeks of age. It can be stated that low-intensity feeding up to slaughtering weight causes backwardness in rear cannon length and this backwardness remains also after the 15th week, which is well over the optimal slaughtering age. Based on the present data, the 70% restricted feeding cannot be recommended either for the future breeding bucks or for broiler males reared for slaughter. To determine the major chemical components of the body, rabbits were euthanised. Original dry matter and crude fat content of the body significantly (P < 0.05) decreased under restricted feeding (41.42%; 32.48% and 16.73%; 7.35%) while the percentage of protein within the dry matter increased (49.6%; 65.0%) and fat decreased (40.17%; 22.1%) significantly. Libido unambiguously decreases as a consequence of feed deprivation. The most conspicuous difference was found in the level of blood testosterone. Although a few RS bucks produced semen but only much later than the rabbits fed ad libitum. On the other hand, there was no difference in the motility of spermatozoa and ejaculate volume in comparison with AL animals. There was no relationship between the body fat content and the reproductive status of bucks in the present trial.     

Secretion of inhibin in male Japanese quail (Coturnix japonica) from one week of age to sexual maturity

The objective of this study was to investigate the changes in secretion of inhibin and cellular localization of the inhibin alpha and inhibin/activin (beta(A) and beta(B)) subunits in male Japanese quail from 1 to 7 weeks after hatching. The post-hatch profile of plasma luteinizing hormone (LH), immunoreactive (ir) inhibin and testosterone were measured by radioimmunoassay. Testes were immunostained by the avidin-biotin-peroxidase complex method (ABC) using polyclonal antisera raised against inhibin alpha, inhibin/activin beta(A) and inhibin/activin beta(B) from one week of age to sexual maturity. Testicular weight increased gradually until 4 weeks and abruptly increased from 5 weeks of age onwards. The plasma concentrations of LH and ir-inhibin increased significantly at 5 weeks of age, and the plasma concentration of testosterone increased significantly at 6 weeks of age. Pituitary contents of LH showed a steady increase until 6 weeks of age and then abruptly increased at 7 weeks of age. Coincident to the increase in plasma testosterone, the testicular contents of testosterone significantly increased from 5 weeks through sexual maturity. Immunohistochemically, localization of the inhibin/activin alpha, beta(A) and beta(B) subunits was found in the Sertoli and Leydig cells at all ages of development from one week of age to sexual maturity. These results suggest that Sertoli and Leydig cells are the major source of inhibin secretion during development in male Japanese quail.     

Effect of age and body weight at photostimulation on the sexual maturation of broiler breeder pullets transferred from 8L:16D to 16L:8D

1. In two trials, broiler breeders were grown to a mean body weight of 2.0 to 2.2 kg at 20 weeks on 8L:16D and transferred to 16L:8D at various ages between 69 and 175 d of age at mean body weights varying between 1.0 and 2.7 kg. Other groups were grown to have a mean 20-week body weight 0.87, 1.15, 1.25 or 1.37 of the normal birds and photostimulated simultaneously with the normal weight birds. Controls were held on 8L:16D in each weight group. In a third trial, broiler breeders were transferred from 8L:16D to 16L:8D at 45 (ad libitum fed), 75 or 90 d (mild feed control), when the mean body weight of each group had reached 2.1 kg. Controls weighing 2.0 kg at 20 weeks were held on 8L:16D or 16L:8D. 2. In trial 1, photostimulating normal weight birds at 69, 76, 83 or 97 d delayed maturity and widened the spread of individual maturities, whilst transferring to 16L:8D at 111 or 125 d advanced maturity. Increasing the mean 20-week body weight to 2.8 kg advanced maturity in birds transferred to 16L:8D at 97, 111 or 125 d. Birds photostimulated at 69, 76 and 83 d matured at a similar age to controls held on 8L:16D. 3. In trial 2, transferring normal weight birds to 16L:8D at 91, 112, 133, 147, 161 or 175 d advanced maturity. Reducing the 20-week mean body weight to 1.91 kg delayed maturity in birds photostimulated at 91 or 112 d, but advanced it in birds photostimulated at 112, 133, 147, 161 or 175 d. Sexual maturity was similar for birds with a 20-week mean body weight of 2.54 or 2.74 kg, with advances for all groups photostimulated between 91 and 175 d. 4. In trial 3, birds maintained on 16L:8D matured later than birds held on 8L:16D, but maturity was advanced when birds were transferred to 16L:8D at 45, 75 or 90 d at a common body weight of 2.1 kg.     

Effects of body weight at sexual maturity and the degree and age of restriction during rearing on the ovarian follicular hierarchy of broiler breeder females

1. Groups of 18 birds were reared to 10 different body weight targets in a randomised block experiment to assess the effect of body weight and the degree and age of restriction on ovarian function at first egg.

2. There was no effect of age at restriction (15 to 18 compared with 19 to 22 weeks) on the number of yellow follicles.

3. The treatment with the larger body weight of two groups given the same degree of restriction (maintenance) had more follicles than the treatment which had a smaller body weight.

4. There was a positive linear relationship between the number of yellow follicles and body weight and food intake. Addition of the weight of fat or age at first egg to the model increased the residual mean squares.

5. The proportion of atresia among yellow follicles and the incidence of internal ovulation increased with body weight at first egg.

6. It was concluded that the physiological processes occurring during rearing which underlie ovarian function are reflected solely in the body weight and food intake of broiler breeders at first egg.     

Photorefractoriness in broiler breeders: sexual maturity and egg production evidence

1. Photorefractoriness was assessed in two lines of broiler breeders. In one trial, male-line and female-line pullets were reared on the floor and transferred to individual cages at 15 weeks. Birds were either maintained on 8-, 11- or 16-h photoperiods or transferred from 8- to 16-h photoperiods at 67 or 124 d. In the second trial, female-line pullets were concurrently housed in the same rearing facilities as trial 1 and transferred to adult floor-pens at 12 weeks. These birds were either maintained on 11- or 16-h photoperiods or transferred from 8- to 11-h or from 8- to 16-h photoperiods at 140 d. 2. In the cages, male-line and female-line birds responded similarly to the lighting treatments, but with the male-line maturing 1 to 2 weeks later than the female-line in each case. Birds on constant 11-h photoperiods matured 3 to 8 d earlier than constant 8-h birds, but 3 weeks earlier than constant 16-h birds. Birds photostimulated at 67 d matured at a similar time to constant 16-h birds, but almost 7 weeks later than those transferred from 8 to 16 h at 124 d. In the floor facilities, constant 11-h birds matured 3 weeks earlier than constant 16-h birds, but almost 2 weeks later than either of the photostimulated groups. Birds transferred from 8 to 16 h matured 4d earlier than those transferred from 8 to 11 h. 3. Caged birds maintained on 16 h or transferred from 8 to 16 h at 67 d laid at least 24 fewer eggs, and had more hens not laying at 58 weeks, than birds maintained on 11-h days or those transferred from 8 to 16 h at 124 d. In the floor-pens, constant 11-h and both photostimulated groups produced about 20 more eggs to 56 weeks of age than the constant 16-h controls. 4. Collectively, these findings indicate that conventionally managed broiler breeders exhibit photorefractoriness. Additionally, a combination of photorefractoriness and controlled feeding appears to prevent broiler breeders from being photoresponsive until at least 10 weeks of age, and to cause some individuals still to be photoperiodically non-responsive at 18 weeks.     

Effects of timing and size of daylength change on brown egg laying domestic hens: Plasma luteinising hormone concentration and sexual maturity

1. Brown egg laying pullets were transferred from an 8‐h photoperiod to an 8‐, 10‐, 13‐ or 16‐h photoperiod at 6, 9, 12, 15, 18 or 20–3 weeks of age. Plasma luteinising hormone (LH) concentrations were measured at transfer and 7 and 14 d afterwards.

2. Significant increases in plasma LH occurred following light stimulations at 6, 9 and 12 weeks of age.

3. Changes in LH concentration 7 d after a light increase from 8 h to 8, 10, 13, 16 h were highly correlated with photoperiod length at 9 and 12 weeks of age.

4. Changes in LH were generally poorly correlated with age at sexual maturity, although the reduced influence on age at first egg of a light increase given close to sexual maturity was reflected in minimal LH responses at 18 and 20.3 weeks.