Effect of timing and size of photoperiod change on plasma FSH concentration and the correlation between FSH and age at first egg in pullets.

1. ISA Brown pullets were transferred at 6, 9, 12, 15, 18 or 20.3 weeks of age from an 8 h photoperiod to an 8, 10, 13 or 16 h photoperiod. Plasma follicle stimulating hormone (FSH) concentration was measured at transfer at 7 and 14 d afterwards, and age at first egg (AFE) was recorded. 2. Plasma FSH concentration in pullets reared on constant 8 h photoperiods generally increased with age but with a trough at 12 weeks. Plasma FSH increased during the first 14 d of photostimulation to a significantly higher concentration, compared with constant 8 h controls, when the photoperiod was increased to 13 or 16 h at 9, 12 or 15 weeks; but for the increase from 8 h to 10 h photoperiods FSH was only significantly higher than controls when the change was made at 12 weeks. 3. The change in plasma FSH concentration 14 d after photostimulation was significantly correlated with mean AFE (reported in Lewis et al., 1997) and appears to be a better predictor of gonadal development than concurrent changes in plasma LH concentration previously reported (Lewis et al., 1994).     

Lighting regimens and plasma LH and FSH in broiler breeders

Egg production by meat-type fowl is markedly inferior to that from commercial laying hens, and so, to assess the degree to which photorefractoriness might be a contributing factor, male- and female-line broiler breeders were maintained on 8-, 11- or 16-h photoperiods. In addition, to determine the age-related rate of change in response to an increment in photoperiod, other birds were transferred from 8- to 16-h photoperiods at 67 or 124 d. Blood samples were taken from all groups, except those on constant 11-h photoperiods, in both genotypes at 67, 69, 124 and 126 d, and from all lighting groups in the female line at 58 weeks (end of trial), and the plasma was assayed for plasma luteinising hormone (LH) and follicle stimulating hormone (FSH) concentration to investigate possible correlations with rate of sexual maturity, total egg numbers and terminal rates of lay. Prepubertal LH was consistently higher for the female line than for the male line, and higher for 16-h birds than for 8-h birds. At 69 and 126 d, LH values were not significantly different from those 2 d earlier for 8-h birds, but significantly reduced for 16-h birds. There was an increase in LH following photostimulation at 67 d, but no significant change after the 124-d light increase. There were no significant differences in FSH between the two genetic lines, nor any effect of photostimulation at 67 or 124 d. There was a tendency for FSH in 8-h birds to be higher than for 16-h birds, and this difference became significant for male-line birds at 67 d. At 58 weeks, LH was higher for constant 11- and 16-h birds and for birds photostimulated at 67 d than for constant 8-h controls or birds transferred from 8 to 16h at 124 d. Neither baseline nor photoinduced prepubertal changes in plasma LH nor FSH were found to be of value for predicting age at sexual maturity or subsequent rates of egg production. At 58 weeks, LH was not generally correlated with sexual maturity, total eggs or terminal rates of lay, however, there was a negative correlation with age at first egg in birds photostimulated at 124 d. It must be concluded that plasma LH and FSH concentrations are of minimal value to the broiler breeder industry for predicting the degree of photorefractoriness, the age at sexual maturity, or subsequent egg production.     

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.     

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.     

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.     

A model for the effect of constant photoperiods on the rate of sexual maturation in pullets

1. This paper reviews evidence from 15 experiments, reported over a span of 44 years, in which pullets were reared from hatching to sexual maturity on 2 or more constant photoperiods. 2. The evidence strongly indicates that earliest age at first egg (AFE) was observed when pullets were held on constant 10 h days (though earlier maturity is easily induced by increasing the photoperiod during rearing). The pair of equations which best describe the relationship between AFE (y,d) and photoperiod (x,h) are for x < 10 h, y = 175.8- 1.731x; for x > 10 h, y=155.5 + 0.301x. 3. This 2-straight-line model, hinged at 10 h, should be used in preference to curvilinear models published earlier, which wrongly predict that pullets reared on long days (14h to 17h) mature faster than birds reared on constant 10 h.     

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.     

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.     

Selection for early response to photostimulation in broiler breeders

1. To determine if selection for early response to photostimulation could be successful, 150 male broiler breeders were photostimulated at 8 weeks of age. The first 20 to produce a semen sample and have a reddened comb with an area > 10 cm2 were selected as responders (R) and 20 birds that did not show these signs of sexual development were chosen as non-responders (NR). Once sexually mature, 8 birds from each group that consistently produced a semen sample were mated with both egg-type hybrids and broiler breeder females to observe the response to 8-week photostimulation in the as-hatched offspring. 2. The AFE of the F1 females with NR or R paternity and egg-type hybrid layer maternity (F1L) were similar, but AFE was advanced in birds from R relative to NR paternity when they had broiler breeder maternity (F1B). 3. Date following a normal distribution of AFE were extracted from the overall data set. This group included offspring from both NR and R paternity, but AFE in F1L and F1B females with R paternity was advanced compared to those with NR paternity. 4. Mean testis weights, or age at most rapid testis growth predicted using parameters from Tyler and Gous (2009), of F1 males were not significantly different in birds with NR or R paternity. A strong correlation was found between predicted age at most rapid growth and AFE of full sibs and so it is likely that an advance in AFE in female offspring would also result in an advance in age of testis development of males. 5. There was no significant difference in 21-d body weight of F1B females of NR or R paternity, but the 21-d body weights of F1L females were higher from R than from NR sires, suggesting that although fertility and meat-type traits are often negatively correlated, there was no adverse effect of selection for responsiveness to early photostimulation and broiler growth rates to 21 d. 6. These findings showed that the response to early stimulation is heritable, and should be useful to the broiler breeder industry, where a reduction in photorefractoriness would improve egg production and fertility.     

Model to predict age at sexual maturity in broiler breeders given a single increment in photoperiod

1. Data from 9 experiments in which broiler breeder pullets had been photostimulated at two or more ages were integrated to produce a model to predict age at 50% egg production following a single increase in photoperiod during rearing. 2. It was clear that the photosexual response in broiler breeders was strongly influenced by the feed allowance and hence the rate of prepubertal growth. Regressions for birds given either a constant photoperiod or a single increase indicated that mean age at 50% lay advances by 2 d for every 100-g increase in body weight at 20 weeks. 3. The general response of broiler breeders was similar to that previously reported for egg-type pullets, but with important changes in the ages at which the birds progressed from one physiological state to the next, depending on body weight. 4. Broiler breeders, unlike modern egg-type pullets, exhibit juvenile photorefractoriness and, depending on their body weight, require up to 20 weeks to dissipate this (faster growth allows quicker dissipation). As a consequence, a group of birds grown to a typical weight of 2.1 kg at 20 weeks do not start to be photoresponsive until about 10 weeks and are not uniformly responsive until 19 or 20 weeks. A transfer to a stimulatory photoperiod before a bird has dissipated photorefractoriness causes a delay of about 3 weeks in its sexual development, and this results in a bimodal distribution of ages at maturity when a flock is photostimulated between 10 and 20 weeks. 5. Once photosensitive, the response of broiler breeders to an increment in photoperiod is between 0.50 and 0.65 of that observed in ISA Brown egg-type pullets. However, a flock of broiler breeders with typical feed restriction starts to mature spontaneously under the influence of the initial photoperiod from about 25 weeks. 6. There is a difference of only 1 to 3 d in age at 50% egg production between a flock transferred to 11 or 12 h followed by further increases to 15 or 16 h and one increased abruptly to one of these photoperiods, and so this model can be used to predict maturity in a commercial flock of birds even though they are likely to be given a stepped, rather than a single, increase in photoperiod.     

Effect of 5 hour increases in photoperiod and in feeding opportunity on age at first egg

1. ISA Brown pullets were given an 8‐h photoperiod and fed ad libitum to 63 d of age. At 63 d the photoperiod was either kept at 8 h or increased to 13 h, and the photostimulated birds were subjected to 1 of 3 feeding systems: ad libitum, 8 h daily access to food or a daily individual allocation of food equal to that given to the 8 h control group.

2. Mean age at first egg (AFE) of the groups given the photoperiod increase was on average 33 d earlier than that of the 8 h controls. Within the photostimulated groups, limiting daily feeding opportunity to 8 h delayed maturity by 4 d compared with ad libitum feeding. The mean AFE of the birds which were given allocated quantities of food was intermediate and not significantly different from either of the other groups.

3. Light was the principal factor which determined AFE, but moderate food restriction had a small modifying influence, consistent with earlier evidence.

4. The 3 groups given a 5‐h increase in photoperiod consumed similar quantities of food to first egg, which was laid around 15 weeks of age. The 8 h control group ate a similar amount of food to this age, but needed more than 40% extra food to reach their first egg at 20 weeks.     

Changes in plasma luteinizing hormone concentration in Turkey hens after switching from short-day to long-day photoperiods

Luteinizing hormone (LH) has been reported to increase in plasma shortly after switching photosensitive turkey hens from short-day (SD) photoperiods (6 hr light: 18 hr dark) to long-day (LD) photoperiods (14 hr light: 10 hr dark). An experiment was conducted to determine the timing and nature of these changes in plasma LH concentrations after the photostimulation of photosensitive turkey hens. The turkey hens were cannulated (jugular vein) to allow serial bleeding every 15 min for 48 hr. One group (controls) was continued under the SD photoperiod, and one group (treated) was switched to the LD photoperiod by the addition of 8 hr of light to the end of the photoperiod. In the control hens, no changes were seen in the observed or calculated baseline concentrations of LH or in the frequency and amplitude of LH peaks during the 48 hr of serial bleeding. In the treated hens, the observed and baseline concentrations of LH increased during the first LD scotoperiod, with a further increase during the second LD scotoperiod. This rapid increase was due to an increase in the baseline LH concentration, whereas no consistent changes were detected in the frequency and amplitude of LH peaks.     

Effect of temporary transfers to 14 h on age at first egg in domestic pullets reared on 8-h photoperiods

1. Brown-egg pullets were reared on 8-h photoperiods and temporarily transferred at 80 d of age to 14-h photoperiods for 2, 4, 6, 8, 10 or 12 d. Controls were either maintained on 8 h or permanently transferred to 14 h at 80 d. 2. Pullets given 8 or 12 long days matured 8-9 d earlier than constant 8-h controls, but 22-23 d later than pullets transferred permanently to long days. Mean age at first egg for the groups given 2, 4, 6 or 10 d of 14-h days were not significantly different from the 8-h controls. The mean weight of first egg and body weight at first egg for the temporarily-photostimulated groups were not significantly different from constant 8-h controls, but egg weights were > or = 5.1 g and body weights at first egg > or = 200 g heavier than the birds transferred permanently to 14 h. 3. It is concluded that up to 6 temporary long days may be given (from 80 d of age) without affecting the timing of sexual maturity, but that the provision of 8 or more long days will accelerate sexual development, thought not to the extent of a permanent transfer, in most birds within a flock. A regression analysis of the ages at which the first and last birds in the groups given 6, 8, 10 or 12 long days matured suggested that about 20 d of photostimulation are required to achieve a mean age at first egg similar to that of birds permanently transferred to long days.     

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.     

Effects of exogenous melatonin and photoperiod on sexual maturation in pullets

Hy‐Line Gray commercial pullets were maintained under 8‐h photoperiods, 16‐h photoperiods and 16‐h photoperiods supplemented with a diet containing 20 or 200 mg/kg melatonin (MEL) to investigate the role of MEL in sexual development. A total of 256 Hy‐Line Gray commercial pullets were placed, four birds to a cage, in four similar light‐proof rooms (8‐h photoperiod) at 6 weeks of age. At 70 day, three rooms containing a total of 192 birds were transferred to a 16‐h photoperiod, whereas 64 birds were maintained under the 8‐h photoperiod. Diets containing MEL at 20 and 200 mg/kg were fed to birds in two of the rooms under 16‐h photoperiods. Birds maintained under an 8‐h photoperiod matured 11.25 day later than those maintained under a 16‐h photoperiod (p < 0.05). The group of birds receiving 20 mg/kg MEL matured 1.19 day later than those maintained under the 16‐h photoperiod and 10.06 day earlier than those maintained under the 8‐h photoperiod. The group of birds receiving 200 mg/kg MEL matured 3.13 day later than those maintained under a 16‐h photoperiod and 8.12 day earlier than those maintained under an 8‐h photoperiod. The average body weight of birds maintained under the 8‐h photoperiod was greater than that of birds maintained under the 16‐h photoperiod (p < 0.05) and was similar between the different MEL groups. The abdominal fat weight was lower in 16L:8D group compared with 8L:16D group (p < 0.05). The concentrations of follicle‐stimulating hormone, luteinizing hormone, oestrogen and insulin did not differ significantly among the groups. The melatonin concentration in 200 mg/kg melatonin group was higher than that observed in the other groups; however, this concentration did not differ significantly (p > 0.05). These data suggest that the birds did not perceive the final 8‐h photoperiod as being part of the night when they were given the MEL diets; continuously high plasma MEL was not observed in birds that responded as if they were in constant darkness. However, the later maturity of the groups administered MEL diets compared with the groups maintained under a constant 16‐h photoperiod clearly indicated that MEL has some influence on the sexual maturity of pullets.     

Effects of photostimulation at 18, 24 and 30 weeks of age on the productivity of female turkeys fed ad libitum or restricted until point of lay.

1. Turkey females were fed ad libitum or restricted from 6 weeks of age to achieve mean body weights of 0.6 of ad libitum fed birds on photostimulation at 18, 24 or 30 weeks of age. Body weight, food intake, egg production and hatchability were recorded to 54 weeks of age. 2. Restricted turkeys were fed ad libitum after first egg or 36 weeks of age. Food intake after 30 weeks of age averaged 170 g/bird/d and was similar for all treatments. At 54 weeks of age, restricted turkeys photostimulated at 24 and 30 weeks were not as heavy as turkeys photostimulated at 18 weeks and ad libitum fed turkeys. 3. A large proportion of restricted turkeys photostimulated at 18 weeks of age did not commence lay until 30 to 40 weeks and a significant number of restricted birds photostimulated at 24 weeks had short laying cycles. Restricted birds photostimulated at 30 weeks came into lay and showed similar persistency of lay to ad libitum fed turkeys. 4. Ad libitum fed turkeys laid 115.0, 122.0 and 101.0 and restricted turkeys 92.4, 99.5 and 103.4 eggs when photostimulated at 18, 24 and 30 weeks, respectively. The number of non-settable eggs was lower in restricted compared with ad libitum fed turkeys and declined with age at photostimulation. 5. Egg size at the end of the experiment was similar for ad libitum fed turkeys and restricted birds photostimulated at 18 weeks but was 2.3 g lower for restricted birds photostimulated at 24 and 30 weeks of age. 6. Hatchability was higher, and the proportion of second quality poults was lower with eggs from restricted turkeys. The mean numbers of poults hatched were 59.9, 75.1 and 66.0 for ad libitum fed and 71.7, 65.7 and 79.4 for restricted turkeys photostimulated at 18, 24 and 30 weeks of age.     

Effect of age and body weight on plasma concentrations of luteinizing hormone in turkey hens before and after photostimulation

The independent effects of age and body weight (BW) on photostimulatory response in turkey breeder hens were studied by measuring changes in plasma luteinizing hormone (LH; ng/mL) before and 3 d after photostimulation. The study was conducted with hens from two BW groups at 24–25, 27–28, and 31–32 wk of age. There was approximately a 1-kg difference in BW between groups within an age. Six hens per BW and age group were cannulated (jugular vein) and serially sampled during each of two 6-hr periods. Samples were collected at 10-min intervals. The two sampling periods were the last 6 hr of the short-day photoperiod (SD) and the same period during the third long day after photostimulation (LD). The photostimulatory response (PR) or difference between the SD and LD baseline LH concentrations was greatest in the 24–25-wk-old hens. The PR was unaffected by hen BW at any age. The baseline LH concentration during the SD photoperiod declined as hens aged. After photostimulation, baseline LH and LH peak amplitude concentrations were higher in 24–25-wk-old hens compared with the older ages. The number of LH peaks increased after photostimulation, but there were no significant effects attributable to age or BW within an age. In conclusion, the PR was affected by hen age but not hen BW or BW within a particular age.     

Rearing photoperiod and abrupt versus gradual photostimulation for egg-type pullets

1. Lohmann White and Lohmann Brown egg-type hybrids were reared on 6-, 8-, 10- or 12-h photoperiods, transferred to 12.5 h at 18 weeks and then given weekly increments to reach 14 h at 21 weeks. In a second experiment, Lohmann White pullets from the same rearing facility were transferred abruptly to 14 h at 18 weeks. 2. Body weight gain and feed intake to 6 and 18 weeks were positively correlated with rearing photoperiod in both breeds. Mortality to 18 weeks was unaffected. 3. Whether the photoperiod was increased abruptly or in a series of increments, Lohmann White pullets reared on 6 or 8 h matured 4 to 6 d later than pullets reared on 10 or 12 h. Rearing day-length had little effect on sexual maturity in Lohmann Brown pullets. 4. In both genotypes and each experiment, egg numbers, egg weight and shell strength increased with rearing photoperiod. Feed intake in the laying period was not significantly affected by rearing day-length, but a meta-analysis of all data showed a significant, though small, increase in adult feed intake with rearing photoperiod. Despite Lohmann White birds reared on 6 and 8 h having lower body weights throughout the laying period, they had larger body weight gains between 18 and 70 weeks than those reared on 10 or 12 h. There were no clear effects of rearing photoperiod on albumen height or mortality. 5. The heavier eggs and stronger shells of the birds reared on the longer day-lengths were correlated with heavier body weights at 18 weeks, and the superior egg numbers and higher feed intake were associated with age at sexual maturity.     

Effect of moving dawn, dusk, or both on oviposition time in domestic laying hens

1. Lohmann Brown pullets were reared on 8-h photoperiods and transferred to 12 h at 15 weeks by either advancing dawn or delaying dusk by 4 h. At 25 weeks, half of each group was transferred to 16 h by advancing dawn or delaying dusk and, 10 d later, each photoperiod-group was advanced or delayed 4 h by moving both dawn and dusk. Individual oviposition times were recorded over 48 h at 25 weeks and 8-10 d after each lighting change. 2. At 25 weeks, there were no differences in mean time of oviposition, eggs laid in the modal 8 h, or in the proportion of eggs laid before dawn between pullets that had been given a 4-h increase in daylength at 15 weeks by advancing dawn and those photostimulated by delaying dusk. 3. Extensions of the daylength from 12 to 16 h at 25 weeks, whether by advancing dawn or by delaying dusk, delayed mean oviposition time by 2 h and virtually eliminated egg-laying before dawn. All groups laid > or = 94% of eggs in the modal 8 h. 4. Moving the complete 12- or 16-h photoperiod forwards by 4 h delayed egg-laying by 0.5 h (relative to dawn), whilst moving them backwards advanced it by 0.7 h. Pullets given 16 h of light laid very few eggs before lights-on, but the divergent movements in oviposition time, relative to dawn, resulted in more eggs being laid before lights-on when the 12-h photoperiod was moved backwards and fewer eggs when it was moved forwards. However, a slower adjustment to the new times of dawn and dusk by the pullets whose day had been moved forward, as indicated by fewer eggs being laid in the modal 8 h and poorer rates of lay compared with pullets that had their photoperiod moved backwards, may explain these differences. It is doubtful that the differences would have persisted after all birds had adjusted their ovulatory cycle, and so any reduction in pre-dawn egg-laying is likely to have been transitory. 5. The only permanent way to minimise pre-dawn egg-laying in brown-egg hybrids is to provide a photoperiod of at least 16 h, though 14-15 h may be long enough for white-egg hybrids and 12-13 h sufficient for broiler breeders.     

Effects of body weight at, and lighting regimen and growth curve to, 20 weeks on laying performance in broiler breeders

1. A total of 4000 Ross broiler breeders were reared to a 20-week target body weight of 1.55, 2.16 (standard), 2.50 or 2.84 kg, using either a convex or concave growth curve. Each treatment group was either exposed to a conventional broiler breeder lighting regimen, with a series of weekly one-hour increments in photoperiod from 8h at 19 weeks to a 16-h maximum, or maintained from 4d on a 17-h photoperiod. 2. Each 100 g increment in body weight at 20 weeks was associated with a significant increase of 0.55 kg in cumulative food intake, and a 1.5-d advance in sexual maturity. However, leaner body weights at 20 weeks resulted in smaller body weight gains between 20 and 60 weeks (-2.4 g/d/kg body weight at 20 weeks), and an increased production of double-yolked eggs. Neither egg production nor mean egg weight was affected by 20-week body weight. 3. Birds fed to produce more rapid early growth had higher feed intakes to 20 weeks, but reached sexual maturity 7 d later than birds permitted accelerated growth from 15 weeks. Growth curve did not influence body weight gain in lay, egg production or mean egg weight. 4. Birds maintained on 17-h photoperiods reached sexual maturity 27 d later, produced 7 fewer eggs to 60 weeks, and had a mean egg weight 1.2 g heavier than birds photostimulated at 19 weeks. Lighting treatment did not affect food intake to 20 weeks, the proportion of double-yolked eggs or body weight gain between 20 and 60 weeks. 5. Birds fed to have a faster growth early in the rearing phase and maintained on 17-h photoperiods produced 11 fewer eggs than those fed to have accelerated growth at the end of the rearing phase, yet there was only one egg difference between the growth-curve groups for the conventionally lighted birds, which was not significant. 6. The earlier sexual maturity of the conventionally lighted birds compared with those maintained on 17-h photoperiods either indicates that broiler breeders require an increment in photoperiod to stimulate rapid gonadal development or that broiler breeders exhibit juvenile photorefractoriness that takes longer to be dissipated when birds are not given a period of short days. 7. The findings suggest that a nutritional stimulus late in rearing is only necessary for satisfactory egg production if birds have not received a concurrent increment in photoperiod.