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Synopsis The mangrove rivulus (Kryptolebias marmoratus) is a phenotypically plastic teleost fish that can spend considerable time on land and traverse the terrestrial realm through a behavior termed the tail-flip jump. The tail-flip jump is a transitional stage between fully aquatic and terrestrial lifestyles. Therefore, understanding this behavior can provide insight into how organisms adapt to new environments over evolutionary time. Studies of K. marmoratus show that terrestrial acclimation and exercise improve tail-flip jumping performance due to muscle remodeling, but the implications of these muscular changes on aquatic locomotion are unknown. In the present study, we hypothesized that (1) terrestrial acclimation and exercise lead to physiological changes, such as changes to muscle fiber type, muscle mass distribution, or body shape, that optimize tail-flip jump distance and endurance while negatively impacting swimming performance in K. marmoratus, and (2) plasticity of the brain (which has been demonstrated in response to a variety of stimuli in K. marmoratus) allows terrestrial emersion and exercise to cause behavioral changes that promote survival and long-term reproductive success. To test these hypotheses, we measured the critical swimming speed (Ucrit), tail-flip jump distance, terrestrial endurance, and undisturbed aquatic behavior of age- and size-matched K. marmoratus before and after a terrestrial exercise period. This period consisted of six 3-min exercise sessions spread over 12 days, during which the fish were prompted to jump continuously. To isolate the effects of air exposure, a separate group was exposed to air for an equivalent period but not allowed to jump. Air exposure improved maximum jump distance but negatively affected swimming performance (Ucrit). Terrestrial endurance (number of jumps) improved in the exercised group, but Ucrit showed no significant change. Contrary to our first hypothesis, a trade-off exists between jump distance and Ucrit but not between jump endurance and Ucrit. Exercised individuals were more active following exercise, resulting either from the onset of dispersion behavior or a heightened stress response.

This selection was originally to have been made by Professor Trevor Morris, but sadly Trevor passed away on 2 February 2009, and so I wish to dedicate this paper to him as an acknowledgement of the...

In the mammalian model of sex determination, embryos are considered to be sexually indifferent until the transient action of a sex-determining gene initiates gonadal differentiation. Although this model is thought to apply to all vertebrates, this has yet to be established. Here we have examined three lateral gynandromorph chickens (a rare, naturally occurring phenomenon in which one side of the animal appears male and the other female) to investigate the sex-determining mechanism in birds. These studies demonstrated that gynandromorph birds are genuine male:female chimaeras, and indicated that male and female avian somatic cells may have an inherent sex identity. To test this hypothesis, we transplanted presumptive mesoderm between embryos of reciprocal sexes to generate embryos containing male:female chimaeric gonads. In contrast to the outcome for mammalian mixed-sex chimaeras, in chicken mixed-sex chimaeras the donor cells were excluded from the functional structures of the host gonad. In an example where female tissue was transplanted into a male host, donor cells contributing to the developing testis retained a female identity and expressed a marker of female function. Our study demonstrates that avian somatic cells possess an inherent sex identity and that, in birds, sexual differentiation is substantively cell autonomous.

1. A total of 7960 Cobb and Ross broiler males were reared on various photoperiods or continuous illumination in two trials to 35 or 40 d. Tibial breaking strength was measured in both, and tibial ash content determined in the first of the two trials. 2. Tibial breaking strength was significantly affected by photoperiod, body weight, testicular weight, and genotype. Although peak bone strength occurred at about 7 h for Ross and at 12 h for Cobb, with reductions in strength for both shorter and longer photoperiods than these peaks, the removal of body weight effects showed that tibial breaking strength was negatively correlated with photoperiod per se. However, after removal of photoperiodic influences, breaking strength was positively correlated with both body weight and testicular weight. 3. Ross birds had greater tibial breaking strengths than Cobb, irrespective of whether the comparisons were made at the same photoperiod, the same body weight, or the same ash content. 4. Ash content increased according to the logarithm of photoperiod, but was unrelated to body weight. Tibial breaking strength increased with ash content. Ash contents were similar for Ross and Cobb birds. 5. Despite the significant differences in breaking strength and ash content, there were no broken bones or signs of leg abnormality in any of the 300 birds sampled. Tibial breaking strength data may therefore be of limited value in assessing the benefits of photoperiod to welfare in modern broilers.

Poultry, unlike humans, have a fourth retinal cone that allows them to see in the UVA part of ultraviolet radiation. This ocular function is principally used by poultry to modify various behavioural functions such as feeding, peer recognition, mate selection, mating activity, and social encounters. Retinally perceived UVA controls the release of melatonin in the pineal gland of dark-adapted birds. Ultraviolet radiation has shorter wavelengths than visible light, and, as a result, is unable to penetrate to the hypothalamus to induce a photosexual response; UV is thus minimally involved in avian reproductive function. UVA and UVB have anti-rachitic properties which catalyse the synthesis of vitamin D3 from 7-dehydroxycholesterol in the skin of feet and legs, a function that prevents rickets, minimises the incidence of tibial dyschondroplasia, and normalises growth and bone ash in young birds fed diets deficient in vitamin D3; surprisingly, there is sufficient UVA in white fluorescent light to produce these benefits. UVC from the sun is filtered out by the atmosphere's ozone layer, so does not occur in sunlight, but artificially produced UVC has germicidal properties and has been shown to protect domestic fowl from aerogenic viral infections, however, vaccination has made this property superfluous to the modern poultry industry. Recently, the introduction of lamps that emit both visible light and UV has made the provision of UVA to poultry a practical proposition, and so it is opportune that the responses of poultry to UV radiation are reviewed and its relevance to modern poultry production assessed.

1. Ross broiler breeders were reared at a nominal illuminance of 15, 20 or 45 lux and transferred to a nominal illuminance of 25, 55 or 70 lux at 20 weeks. 2. There were no significant interactions between the response to illuminance during rearing and in lay. This means that it matters not whether illuminance is increased, decreased or held constant on transfer to the laying house, provided it equals or exceeds the biological optimum for satisfactory egg production. 3. Whilst there were no significant effects of illuminance in either the rearing period or laying periods on egg numbers, peak rate of lay, terminal rate of lay, egg mass output or liveability, meta-analyses of these and other data indicated biological optima of 15 lux during rearing and 7 lux in the laying period. Birds reared at 45 lux had a lower mean egg weight (and earlier sexual maturity) than birds reared at 15 lux, and hens illuminated at 25 lux in the laying period laid more eggs on the floor than at either 55 or 70 lux. 4. Typical primary breeder recommendations of 10-20 lux during rearing and 30-60 lux in lay are appropriate for floor-housed birds; however, an illuminance of 7 lux could be used for caged birds, subject to welfare-code compliance.

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.

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.

1. Cobb broiler breeders were fed to achieve typical body weight targets (2.1 kg at 20 weeks) on 6-, 8-, 10- or 16-h fully or intermittently illuminated (Biomittent) photoperiods in controlled-environment housing to 20 weeks, then moved to open-sided housing and 16-h photoperiods to 60 weeks. 2. At each photoperiod, birds given Biomittent lighting had heavier body weights up to 42 d, lighter body weights between 49 and 140 d, but similar body weights at sexual maturity. 3. Irrespective of lighting type, birds given 8-h photoperiods matured 3 to 4 d earlier than 6- or 10-h birds, but all matured=15 d before 16-h birds. 4. There were no significant differences between the 6-, 8- or 10-h groups for total eggs, mean egg weight or egg mass output, but all three produced=13 more, but =0.5 g smaller, eggs and =0.83 kg more egg mass to 60 weeks than 16-h birds. The proportion of abnormally large eggs was low (0.73/bird) and similar for all lighting groups. Egg production for a given period after sexual maturity was similar for all groups, and so differences among groups could be explained by the differences in age at sexual maturity.

Growing pullets were maintained on 14-h photoperiods and given diets supplemented with 25 mg of melatonin (MEL)/kg during the final 7 h of the photo-period to investigate the role of MEL in sexual development. Melatonin diets were fed to 70 d (to mimic a transfer from 7 to 14 h at 70 d), from 105 d onward (to mimic a transfer from 14 to 7 h at 105 d), or throughout the trial (to mimic constant 7-h photoperiods). Control birds, which were fed normal diets, were maintained on 7 or 14 h, transferred from 7 to 14 h at 70 d, or transferred from 14 to 7 h at 105 d. The MEL groups matured 6 to 11 d later than the constant 14-h controls. The group mimicking a transfer from 7 to 14 h matured 35 d later than photostimulated controls, the group mimicking a 14 to 7-h change at 105 d matured 41 d earlier than birds given a decrease in day length; the third group matured 13 d earlier than constant 7-h controls. Although these data suggest that the birds did not perceive the final 7 h of the photoperiod as being part of the night, when given MEL diets, residual plasma MEL during the first 7 h of the photoperiod was atypically high, possibly preventing an interpretation of day and night. However, continuously high plasma MEL did not result in birds responding as if in constant darkness, because birds transferred from darkness to 14 h at 70 d would not have matured at a similar time to birds changed from 14 h to darkness at 105 d. Plasma LH concentrations for birds mimicking a 7 to 14 h change at 70 d were not significantly different from constant 7-h controls after the transfer to normal diets. The later maturity of the experimental groups, compared with constant 14-h controls, clearly indicated that MEL had some influence over hypothalamic activity and gonadal development.

It is frequently recommended that commercial laying pullets are reared on step-down lighting regimens, rather than on constant short photoperiods, to help achieve BW targets during rear and optimal performance in lay. To evaluate the effectiveness of this strategy, Shaver White pullets were maintained on 8-h day lengths or given a step-down lighting regimen from 23 to 8 h over periods of between 1 and 15 wk. Other pullets, which were initially maintained on 8 h of light, were given an abrupt increase in day length prior to transfer to step-down lighting at various ages between 1 and 13 wk. All birds were given abrupt increments to 14 h at 18 wk and to 16 h at 20 wk to stimulate appetite and optimize uniformity of sexual development. Body weights at 6 and 12 wk were generally heavier and cumulative feed intakes to 6 wk were greater for birds given step-down lighting from 1 wk of age than for constant 8-h controls or birds given an initial period on 8-h day lengths prior to step-down lighting. Sexual maturity for birds on step-down lighting from 1 wk and for those on < or =5 wk of 8-h day lengths before transfer to step-down lighting was delayed by about a week compared with the constant 8-h controls or birds on 9 wk or more of 8-h day lengths before step-down lighting. These delays in sexual maturity resulted in a lower BW at 18 wk. Body weight uniformity at 18 wk was improved by step-down lighting, whether it was given from 1 wk or after a period of 8-h day lengths. Despite step-down lighting resulting in larger initial feed intakes and improved early growth, there was no significant improvement in egg numbers, egg weight, egg mass, feed intake, shell deformation, or albumen height compared with constant 8-h controls. Differences in egg output were generally the consequence of photoperiodically induced changes in sexual maturity.

An experiment was conducted at the University of KwaZulu–Natal to assess the effect of constant photoperiods on sexual maturity and egg-laying performance in broiler breeders given two levels of control-feeding during the rearing phase. Cobb broiler breeder females were grown to reach 2·1 kg body weight at 17 or 21 weeks, and maintained on 10, 11, 12, 13, 14 or 16-h photoperiods from 2 days to 68 weeks of age. There were no significant interactions between photoperiod and growth rate for any production parameter. The time required reaching 2·1 kg increased proportionally with photoperiod but, because of delayed sexual development, birds on longer photoperiods consumed more feed to, and were heavier at, sexual maturity than shorter daylengths. The longer-photoperiod birds also had inferior rates of lay in the first half of the cycle, but superior in the second, which, together with the photoperiodic effects on maturity, resulted in birds on 11, 13 or 14 h producing most eggs to 68 weeks, and those on 16 h fewest. It is possible that the pattern of egg production was due to some of the birds on [ges ]13-h photoperiods becoming photorefractory, having a mid-cycle pause, and then spontaneously resuming egg production in the latter half of the cycle. However, a hinge-analysis of current and other data to the more usual depletion age of 60 weeks showed that the combined effects of photoperiod on sexual maturity and egg production resulted in constant 10-h birds producing the highest number of eggs, with numbers decreasing by 3·6 eggs/h of photoperiod above the hinge and 7·8 eggs/h of photoperiod below it. Mean egg weight increased by 0·4 g/h of photoperiod, but the proportion of abnormally large and floor eggs and the incidence of mortality were unaffected by daylength. For each photoperiod, accelerated growth resulted in body weights being heavier than controls at sexual maturity, despite the mean age at maturity being 10 days earlier for the faster-growing birds. Body weights for the two growth groups were not significantly different at 68 weeks. Faster-growth birds consumed 1 kg less feed to 2·1 kg body weight, but 1·3 kg more feed to sexual maturity and 2·7 kg more to 68 weeks, and produced 6 more eggs than, but had similar patterns of egg production to, the conventionally managed controls. Mean egg weight, the proportion of floor eggs and the incidence of mortality were similar for both groups. Notwithstanding that the overall production of abnormally large eggs was low (1·1 eggs per bird); the faster-growing birds produced significantly more than the controls. Egg weight was positively influenced by age at sexual maturity, body weight at sexual maturity and photoperiod, but was unaffected by rate of growth to 2·1 kg per se.These findings show that there are differences between broiler breeders and egg-type pullets in their response to constant photoperiods. It is likely that the factors responsible for these differences, particularly in terms of sexual development, are the exhibition of photorefractoriness by, and the retardational effects of controlled feeding on, broiler breeders.

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.

1. Shaver White and ISA Brown pullets were reared to 140 d in groups of 8 in cages 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. There was no significant difference in sexual maturity, measured as eggs per 100 bird.d at 139 and 140 d, for ISA Brown maintained on 3 or 25 lux, but Shaver White pullets exposed to constant 3 lux matured significantly later than those maintained on 25 lux. 3. In Shaver Whites, sexual maturity was significantly delayed by an increase from 3 to 25 lux at 63 and 112 d, and advanced by a decrease from 25 to 3 lux at 112 d. Sexual maturity of ISA Browns was not significantly affected by a change in illuminance at 63 or 112 d, though responses were in the same direction as for Shaver Whites. 4. In both breeds, total feed consumed to 112 d was higher for birds on 3 lux than 25 lux, but lower between 112 d and 140 d when birds on 25 lux underwent rapid sexual development. In both breeds, body weight at 63 d was higher for birds exposed to 3 lux than 25 lux, but body weight gain thereafter was similar for the two light intensities. 5. In both breeds, plasma luteinising hormone (LH) concentration at 63 and 112 d was lower in birds maintained on 3 lux than 25 lux. At 63 and 112 d, transfers from 25 to 3 lux depressed, whereas transfers from 3 to 25 lux at 63 d, but not at 112 d, increased plasma LH. 6. Advances or delays in sexual maturity induced by changes in illuminance were not correlated with differences in feed intake, body weight gain, or with changes in plasma LH. 7. One possible explanation for the inverse relationship between the direction of change in illuminance at 63 and 112 d in pullets exposed to a 10-h photoperiod and the age at which they became sexually mature is that changes in light intensity and/or spectral composition affect the entrainment of the circadian rhythm of photoinducibility, to effect a phase shift in the photoinducible phase and/or the responsiveness of phototransduction pathways.

Typically, poultry diets contain 1–2 mg I/kg, but higher concentrations are sometimes used to enhance the I content of eggs. In addition to an increased deposition of I in the yolk, other often adverse responses occur, especially at exceptionally high concentrations. Excess I in grower diets can prevent sexual maturation in male and female fowl, and in layer diets will progressively reduce egg production until, by about 2500 mg I/kg diet, ovulation is inhibited and egg production ceases. Most I accumulates in the thyroid gland, and it is likely that the mechanism responsible for these reproductive disorders involves a modification of thyroid hormone activity. Simultaneous with the declining rate of lay, feed intake declines, egg weight and yolk-cholesterol contents decrease and body weight increases. Whereas fertility is unaffected in female breeders, hatch of fertile eggs is reduced, hatch time extended and embryonic mortality and dead-in-shell proportions increased. In contrast, male fertility is decreased because of an increased incidence of dead spermatozoa, although hatchability of eggs from normally fed hens is unaffected. All reproductive variables, together with feed intake and body weight, are normalised within about 7 d of returning to a diet with normal I levels. Excess I suppresses growth in meat-type chickens, but does not affect feed conversion efficiency. There are transient increases in plasma I and cholesterol concentration during excess I intake in all types of bird. The evidence for varying responses to different I sources is equivocal, but the consensus is that source is probably not important.

An experiment was designed to test the response of growing pullets to two changes in photoperiod (an increase from 8 to 14 h followed 5 weeks later by the reverse change, or a decrease from 14 to 8 h followed by an increase). The first change was made either at 35 days or at 56 days of age, to test the influence of age on the responses observed. Control groups were kept on constant 8-h and constant 14-h photoperiods and the responses to appropriate single changes were also tested. Mean age at first egg varied from 111 days for birds given a single increment at 56 days to 166 days for pullets given an increase in photoperiod at 35 days followed by a reduction at 70 days. Responses to the single changes confirmed earlier reports that sensitivity to change in photoperiod varies with age in a manner that is quantitatively predictable. Responses to the double changes could be explained by postulating that the initial change altered the ‘physiological age’ of the bird to an extent that was also quantitatively predictable. An early increase in photoperiod advances sexual development and makes the bird more sensitive to a subsequent decrease than would be expected by reference to its chronological age. An early decrease in photoperiod delays sexual development, which can have the effect of making the bird more or less sensitive to a subsequent increase since, in layer-strain pullets, sensitivity to an increment in photoperiod normally increases up to about 9 weeks of age but decreases thereafter. Mean age at first egg predicted using these concepts was very highly correlated with observed age at first egg. The results provide a rational basis for constructing a model to predict age at first egg for any combination of increases and decreases in photoperiod applied to growing pullets.

A model is presented which will predict mean age at first egg (AFE) for pullets of laying strains reared under non-limiting environmental conditions but exposed to a single change in photoperiod during the rearing stage. An initial analysis of 12 previously reported trials involving a wide range of genotypes showed that the response to an increase in photoperiod is not simply the inverse of the response to an equal decrease in photoperiod applied at the same age. Maximum sensitivity to a reduction in photoperiod was found shortly before onset of lay, whereas maximum sensitivity to an increment in photoperiod was observed at around 10 weeks of age. Two experiments were conducted to provide further data. The first compared the effect of 3-h increases in photoperiod from 8 h to 11 h or from 11 h to 14 h with the double increment from 8 h to 14 h and also tested a reduction from 11 h to 8 h, all imposed at 17 weeks of age. AFE was advanced to a similar extent by the changes from 8 to 11 h and from 11 to 14 h (9.8 and 10.9 days respectively). Response to the double increment was not additive: AFE on this treatment was 13.3 days earlier than for constant 8 h controls. Reduction in photoperiod from 11 to 8 h at 17 weeks delayed AFE by 18.7 days compared with constant 11-h controls. In the second experiment, pullets of two strains were transferred from 8 to 16-h photoperiods and from 16 to 8 h at 5, 7, 9, 15, 17 and 19 weeks of age. Controls were kept on constant 8 and constant 16-h days. Transfer from 8 to 16-h photoperiods at 5 weeks of age had no effect on AFE. At 7 weeks there was a bimodal response with some pullets subsequently showing advanced maturity and others not. Maximum stimulation of early maturity (31 days on average for the two genotypes) was obtained at 9 weeks of age and response to stimulation declined linearly with age thereafter. The delay in AFE resulting from a reduction in photoperiod (16 to 8 h) increased linearly between 0 and 15 weeks. At 17 and 19 weeks, the response was bimodal, with some pullets maturing at the same age as long-day controls and others showing delayed maturity. Using all this evidence and some other unpublished data, a model is developed to predict AFE as a function of mean photoperiod and change in photoperiod during the rearing phase. Elements are incorporated to allow for the insensitivity of pullets younger than 50 days to an increase in photoperiod and the effect observed late in rearing when a change in photoperiod comes too late to alter AFE for the most precocious individuals in a flock. Two coefficients are required to adjust for genotype. One describes mean AFE for the genotype when reared on constant daylength and the other defines the rate at which age effects the response to a single change in photoperiod.

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 (P0.05). 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.

It has been shown that, in small groups of intact male domestic turkeys, supplementary ultraviolet (UV-A) radiation, visual barriers, and added straw (environmental enrichment) minimize the incidence of injurious pecking under incandescent light at 5 lux. This paper describes two experiments, each involving eight groups of 100 non beak-trimmed birds up to 5 weeks of age, that assessed the effectiveness of these procedures at higher light intensities and with fluorescent light. Experiment 1 examined 5 or 10 lux of incandescent or fluorescent light. Experiment 2 studied responses to 5, 10, 36 or 70 lux of fluorescent light. Individual inspections of the birds, for wing, tail and head injuries due to pecking, were conducted daily.Fluorescent light significantly reduced the incidence of tail injuries (P = 0.03), and tended to reduce those to the wings (P = 0.08), compared with incandescent light. No difference was observed between 5 and 10 lux for either tail or wing injuries. In Experiment 2, the incidence of tail and wing injuries was significantly and positively correlated with light intensity (tail, P = 0.05; wing, P = 0.02). Injuries to the head were minimal in all treatments. These results suggest that turkey poults may be kept with minimal injurious pecking, under fluorescent light at an intensity of 10 lux, with appropriate environmental enrichment.

Poultry have four types of cone in the retina of the eye, and this means that they probably see colour differently from trichromatic humans. Notwithstanding the fact that humans and birds have maxi...

Ultraviolet (UV) sensitivity in birds has been shown to be intrinsically involved in the selection of mates; UV may, therefore, also play a role in the establishment and maintenance of social hierarchies in intensively housed turkeys. Cereal seeds and straw are known to reflect UV, and turkeys may use these cues for foraging and exploratory behaviors. A series of trials was conducted to see if supplementation of the photoperiod (12 h at various white light intensities) with UV radiation (0.06 to 0.16 W/m2 at floor level) and regular supplies of straw to the litter allow a better recognition of individuals within a flock, enrich the environment by the provision of new pecking material and of radiation across the whole range of avian sensitivity, and, as a consequence, reduce the incidence of injurious pecking in male turkeys that have not been beak-trimmed, detoed, or desnooded. Body weight gain, feed intake, feed conversion efficiency, and leg integrity were generally not significantly affected by UV supplementation and environmental enrichment. In contrast, the provision of UV radiation, simultaneous with a 12-h photoperiod of white light at intensities of70 lx to 5 wk and of 10 lx to 20 wk, and the regular addition of straw to the litter, significantly reduced the incidence of culling because of injurious pecking. However, complex interactions among UV supplementation, white light intensity, and material environmental enrichment precluded a simple recommendation to solve the problem of injurious pecking.

1. Responses to ultraviolet (UV) radiation were studied in two trials. In one trial, sexually mature pullets, that had been maintained on an 8L:16D regimen from 2 d of age, were exposed sequentially, for periods of 9 to 12 d, to a further 8 h of very dim visible light (VDV), to 8 h of UV radiation and, finally, to an extra 8 h of normal light (conventional 16L:8D). Individual ovipositions were recorded during the last 48 h of each treatment. In the second trial, sexually mature pullets which had been allowed to 'free-run' for 14 d under continuous normal illumination (LL), were given, in addition to the normal light, a 12-h period of UV radiation commencing at midday or midnight for a further 15 d. During the final 48 h oviposition times were recorded and 4 food intakes for each 12-h period were determined. 2. In trial 1, mean oviposition time under VDV and UV supplementation was not significantly different from that under the 8L:16D regimen. Transfer to a 16L:8D regimen altered mean time of oviposition by about 4 h. In trial 2, eggs continued to be laid almost at random in all groups. 3. Food intake was suppressed during the 12-h period of UV supplementation compared with that when the birds were not receiving UV. 4. It is concluded that the addition of 8 h of UV radiation (at the intensity used in these studies) to 8 h of normal light does not cause a phase shift in the timing of the 'open-period' for pre-ovulatory luteinising hormone release which determines the time of oviposition. Furthermore, the insertion of 12-h periods of UV into continuous illumination does not entrain egg laying. 5. The suppressing effect of UV on food intake but lack of influence on the timing of the ovulatory cycle suggests that UV (at the intensity used in this study) acts principally at the retinal level and, as a result, stimulates only behavioural responses in laying birds.

Evidence from published trials is reviewed to investigate whether there is any need to change the recommended optimal light intensity for laying fowls from 5 lux. Although some recent trials have r...

Layer strain pullets were reared on litter and given an 8-h photoperiod to 10 wk of age. They were then transferred to cages in which light intensity at the feed trough varied from 5 to 14 lx. Thirty birds continued on 8 h light (L):16 h dark (D) (negative controls), and another 30 birds were given 14L:10D (positive controls). Two other groups of 30 birds were given a regimen of 3 dim:8 L:3 dim:10 D with intensity during the dim phase ranging from 0.03 to 0.42 lx (very dim) or from 0.6 to 3.0 lx (marginal). Mean age at first egg (AFE) differed by 30 d between the positive and negative controls. Birds receiving very dim lighting matured 10 d earlier than the negative controls but 20 d later than positive controls. It is concluded that either the very dim light was itself nonstimulatory but had a phase shifting effect upon the biological clock that caused the 8-h normal light to fall partly in the photoinducible phase, or the first 3 h of very dim light was added to the bright phase to form an 11-h photoperiod. Birds in the top tier of the room with marginal supplementary lighting received 1.7 to 3.0 lx and matured at the same age as the positive controls, whereas those in the bottom tier received 0.6 to 0.9 lx and matured at the same age as the negative controls. Birds in the middle tier showed an intermediate AFE. It is concluded that the threshold intensity at the feed trough for white light stimulation of the photoperiodic mechanism in caged pullets lies between 0.9 and 1.7 lx. However, very dim lighting, below the threshold required for stimulation of a photoperiodic response, may shift the biological clock with unexpected consequences and, as a result, there is no known intensity of dim light that can be equated with darkness for all purposes.

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).

To illustrate the importance of black people in American history, specific individuals are identified who played major roles in the American Revolution, the War of 1812, exploration and pioneering, and science and technology. (AV)

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. FISH 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.

More energy efficient and longer lasting lamps are being used to replace incandescent lighting in poultry houses. This paper reviews the responses of domestic fowl, turkeys and geese to various sou...

1. ISA Brown and Shaver 288 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 significantly 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 significantly 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.

1. Data for modern egg-type hybrids reared on constant daylengths show that, as expected, they mature more quickly than earlier genotypes. However, the constant photoperiod which gives earliest sexual maturity has not changed as a result of selection and is 10 h for both early and modern genotypes. 2. Further analysis showed that the rate of delay in sexual maturity for constant photoperiods above 10 h is similar for modern and for early hybrids (+0.29 d for each incremental one hour of photoperiod), the response of modern hybrids below 10 h (+4.22 d for each one-hour reduction in photoperiod) is more than double that of early hybrids (+1.71 d/h).

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.

1. Data from intermittent and conventional lighting trials were analysed to investigate the effect of daily illumination upon mortality during the laying period and in 49‐d‐old broilers. 2. Iiveability in laying hens was improved by the use of intermittent lighting: the degree of improvement was proportional to the reduction in daily illumination achieved by the intermittent programme. 3. The reduction in mortality with intermittent lighting in laying hens was not the result of intermittent lighting per se. Intermittent regimens which did not reduce daily illumination did not reduce mortality. 4. Mortality in both conventionally‐lit laying hens and 49‐d old‐broiler chickens increased with photoperiod.