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1.
Three lighting treatments were given to laying hens, for which the bright and dim light of 28-h ahemeral light cycles was provided by incandescent (tungsten filament) lamps only or by combinations of tubular fluorescent or compact gas-discharge lamps with incandescent lamps. There were no differences in entrainment (the proportion of eggs laid in 4, 6 or 8 h modal periods) between the three bright:dim treatments. A fourth ahemeral lighting treatment in which the dim lights were extinguished except during a designated work period (09.00 h to 12.00 h daily) was termed bright:dim:dark. Hens given the bright:dim:dark treatment showed an increased entrainment compared with the three bright:dim light treatments. There were no differences (P greater than 0.05) in egg numbers or mean egg weight between all 4 lighting treatments. Birds given the bright:dim:dark treatment tended to have a lower (P greater than 0.05) food intake compared to the three bright:dim treatments.  相似文献   

2.
Seven hundred and twenty laying hens housed in 8 environmentally-controlled rooms were changed from a 24 h light:dark cycle to a 28 h ahemeral bright:dim cycle. The ahemeral cycles consisted of periods of bright and dim light in ratios of intensity: 5:1, 10:1 and 30:1. The last regimen was applied either at a constant 21 degrees C or with a 24 h alternating temperature varying between 21 and 31 degrees C. Eggs were collected hourly from each bird for 5 d immediately before the introduction of ahemeral cycles and then over the same period 2 weeks after introduction. The interval between successive eggs within sequences lengthened with increasing bright:dim ratios. The increase in egg weight and decrease in deformation score were not significant. Total egg mass output was not altered. The cycling temperature regimen did not alter the entrainment of the birds, although intra-sequence interval decreased. The decrease in egg weight and increase in deformation score were not significant.  相似文献   

3.
1. Nine short trial, involving 96 different treatments, were used to investigate the critical intensities and duration of bright and dim periods of lighting needed to entrain oviposition in cycles ranging from 21 to 30 h. 2. Entrainment was shown to depend upon the contrast between bright and dim lighting, and to be independent of the absolute light intensity. 3. A bright: dim ratio of 13:1 fully entrained oviposition in cycles of 25 h and 27 h. For 23-h and 28-h cycles a 30:1 ratio was required. Twenty-one-hour cycles required a ratio of 300:1 and with 30-h cycles a ratio of 1000:1 was needed to achieve full entrainment of oviposition. 4. In 24-h cycles, 1 h of bright lighting at 02.00 h was sufficient to override other environmental signals and cause eggs to be laid in the late evening, but a minimum bright period of 6 h was needed to cause full phase setting with 21-h cycles. 5. Circadian periodicity can easily be imposed on hens by providing a short exposure to bright light with a background of continuous dim light; but the signal must be increased (by providing a greater contrast between bright and dim lights and/or a longer period of bright lighting) to entrain oviposition when the cycle deviates markedly from the natural period of 24 h.  相似文献   

4.
1. Two short-term trials are described in which laying hens were exposed to 8 h light followed by 8 one-min pulses of light at hourly intervals followed by 8 h darkness (8L:8i:8D). The effect of varying the intensity of illumination during the one-min pulses and the effect of placing the intermittent lighting before the 8 h photoperiod (8i:8L:8D), were studied. 2. Normal egg production was maintained by the 8L:8i:8D system when the light pulses were at 20 lux, but not at 5 lux. This suggests a minimum threshold for illumination with short light pulses higher than that needed for continuous lighting. 3. Time of lay under 8L:8i:8D was the same as with 8L:16D in relation to the beginning and ending of the 8 h main photoperiod, but with 8i:8L:8D mean time of lay was 2 to 3 h earlier. Thus the hourly pulses caused a phase advance when placed before the normal photoperiod but did not cause a phase delay when placed after the normal photoperiod.  相似文献   

5.
1. In experiment 1, 10 laying hens were given the choice to eat food pellets from any of 4 food bowls illuminated by overhead, incandescent luminaires at <1, 6, 20 or 200 lux. During a trial hens were allowed to eat for 5 min. After each minute had elapsed (from the start of eating) the light sources were extinguished and the illuminances re-assigned to the food bowls in a random manner. Each hen received two trials, one where the food was freely available and another where it was hidden in a sand and gravel mix. 2. The hens chose to eat for most time in the brightest (200 lux) and least in the dimmest (<1 lux) environments for both free and hidden food (free: 5.9, 10.5, 10.4, 15.7s for increasing illuminance; Hidden: 5.5, 9.8, 9.1 and 15.7s. 3. In experiment 2, 9 hens were trained to peck at either an illuminated or unilluminated panel to access a food reward behind a guillotine door for 3 s. Five hens were trained to peck the illuminated panel to access food brightly lit (200 lux) or the unilluminated panel to access food dimly lit (<1 lux); 4 hens were trained vice versa. The flock was then divided into three groups of three, and three treatments imposed on each group in a Latin-square arrangement. In treatment 1, one peck at either panel allowed access to the chosen light environment (F1:F1). In treatment 2, 5 pecks were required to access food brightly lit on a variable ratio, but only one to access food dimly lit (ratio V5:F1). In treatment 3, the variable ratio was increased to V10:F1 to access food in the light. 4. Over 40 trials for each hen, the mean number of attempts to eat food in the light (where the panel which allowed access to food brightly lit was pecked at least once) was 34.5 for F1:F1, 12.1 for V5:F1 and 8.5 for V10:F1. The mean number of food rewards taken in bright light was 34.5, 3.1 and 1.8, respectively. For both variables, the difference between F1:F1 and V5:F1 was significant but not between V5:F1 and V10:F1. By interpolation of the 'attempts' data, it was estimated that hens would work 2.3 times harder to gain access to food brightly lit than for food dimly lit. 5. In experiment 3, the influence of the same illuminances applied over a food bowl as in experiment 1 (<1, 6, 20 or 200 lux) on the number of pecks/min, food consumed/min, food consumed/peck and the force of pecks was examined. 6. The amount of food consumed was lowest in the dimmest environment (3.1 vs 7.5, 7.4 and 7.1 g/ min for increasing illuminance, respectively); as was the number of pecks (35.6 vs. 125.0, 123.1, and 125.4 pecks/min respectively for increasing illuminance). The amount consumed per peck did not vary significantly with illuminance. The mean peck force showed a trend to be lowest in the dimmest environment (5.3 vs. 6.6, 7.0 and 6.6 N respectively, for increasing illuminance). 7. Overall, the hens showed a preference and appeared motivated to eat in bright as opposed to dim light. The hens were unwilling to eat at low illuminances although the 'efficiency' of eating (g/peck) was not impaired significantly. These data may have implications for novel lighting systems and those where hens are required to eat in the dark or in very dim light.  相似文献   

6.
1. Fourteen experiments were performed to determine the minimum photoperiod and minimum scotoperiod needed for entrainment of oviposition in hens exposed to 21-h, 24-h and 30-h cycles. Entrainment was measured by the proportion of total eggs laid in a modal 8-h segment of each cycle. 2. In a 24-h light and dark cycle, a 15-min photoperiod or a 5-h scotoperiod produced essentially the same degree of entrainment as 6 h light, 18 h darkness (6L : 18D) or 14L : 10D, which were used as control treatments. Under 21-h light and dark cycles a minimum 3-h photoperiod or a minimum 9-h scotoperiod was needed to achieve full phase setting. When the cycle length was increased to 30 h a minimum 8-h photoperiod or a minimum 12-h scotoperiod was required for full entrainment. 3. This study demonstrates that photoperiod is a stronger signal than scotoperiod for the purpose of phase setting oviposition. It also shows that a stronger signal is required to achieve entrainment when the length of the light-dark cycle is several hours shorter or longer than the natural period of 24 h.  相似文献   

7.
A study was conducted to assess the effects of photoperiod length (constant 23L:1D vs. a photoperiod program going from decreasing to increasing quantity of light), light intensity (bright vs. a dim, reducing intensity), and feed ME levels (low vs. high) on performance and carcass characteristics of female broilers grown to 56 d. Use of a treatment with early decreasing photoperiod followed by an increasing photoperiod reduced feed consumption and subsequent BW early. However, growth compensation occurred and feed consumption and BW were similar across photoperiod treatments by study end. Likewise, reducing light intensity (from 1 to 0.25 fc) stimulated feed consumption and a subsequent BW improvement early, as compared with high-intensity (2 fc) lighting maintained at a constant level. However, the disparity in feed consumption and BW, as influenced by light intensity, did not persist throughout the growing period. Feed conversion was not noticeably affected by photoperiod or light intensity treatments. Minimal effects of lighting were observed for carcass or part yields; however, there appeared to be a subtle substitution effect between leg, wing, and breast yield influenced by lighting program. Birds exposed to the decreasing–increasing photoperiod and dim, reducing light treatments yielded more leg and wing at the expense of breast. Feeding a low ME diet resulted in increased feed consumption and feed conversion. However, birds consuming a low ME diet were more uniform. No effects of treatment on mortality were measured. These data indicate that a decreasing–increasing photoperiod can be used effectively to reduce early growth, yet allow birds to compensate as they approach market age. Low intensity lighting, however, appears to stimulate early feed consumption and growth, although this effect is transitory. Furthermore, the increased feed conversion of birds grown on the low energy diet may make its use less desirable.  相似文献   

8.
1. Under continuous lighting, time of oviposition was controlled by a temperature cycle (12 h at 30 °C and 12 h at 20 °C). The peak of egg laying occurred 15 h after the beginning of the cool period, which is the same interval as the interval observed between lights‐out and peak egg laying under a 12L : 12D lighting schedule.

2. When the temperature cycle was set 12 h out of phase with a light‐dark cycle (12L : 12D; temperature reduced when the lights came on), oviposition was entrained by the light‐dark cycle.

3. When a temperature cycle was set 6 h in advance or 6 h in arrears of a 12L : 12D cycle there was a difference of 1.4 h in mean time of lay between the two treatments, indicating that temperature can have a significant, though subsidiary, effect on oviposition time in the presence of a clear light‐dark signal.

4. When the light‐dark signal was reduced to 22L : 2D, oviposition time was controlled by the temperature cycle. With 20L : 4D oviposition time was determined principally by the photoperiod, but with a subsidiary effect due to temperature.  相似文献   


9.
The cerebral epiphysis of twelve gilts, aged 6.5 months, was histologically, histochemically, and histometrically tested, after the animals had been kept permanently under artificial light, 100 lux, or in darkness, interrupted twice a day by two hours of lighting, over ten weeks altogether. The parenchymal cells of the epiphyses of the animals kept in darkness changed clearly from those of the other group with constant exposure to light. Changes in the darkness animals included significant enlargement of the cell nuclear volume by 33 per cent, increase in nucleoli count as well as increases of lipids and ribonucleic acid in cytoplasm.  相似文献   

10.
1. New lighting programmes were designed to change the pattern of goose reproduction, based on the response of predictable avian photoperiodic stimulation. The objective of this study was to evaluate the efficiency of a long photoperiod of 20L on shifting goose reproduction to the non-breeding season in an open housing system. 2. Eighty mature White Roman geese were randomly allocated into 4 groups (male:female = 1:4). The supplemental lighting programmes with a daily photoperiod of 20 h were initiated on 22 November and withdrawn when 90% of geese were moulting in the treatment groups. Artificial light intensities of 220, 120 and 20 lux were provided to experimental groups A, B and C, respectively. In contrast, the geese in control group D were kept under natural lighting conditions throughout this study. 3. The annual reproductive curves of all the experimental groups consisted of two separate laying periods. The first period was induced by the supplemental lighting programme while the second was induced by the naturally increasing photoperiod in this subtropical region. The first laying period of the experimental groups occurred in the breeding season, and the second was relocated to the non-breeding season. 4. The supplemental lighting could shift the laying periods of geese to the non-breeding season and had no significant effect on annual reproductive performance. The supplemental light programmes described here were able to manipulate the reproductive season of geese reared in open houses, which would be of practical value.  相似文献   

11.
The pattern of oviposition in continuous illumination or continuous darkness was investigated. In continuous darkness the mean time of all ovipositions was at 05.00 h and the mean time of the first oviposition of a sequence (C1) was 01.00 h. There was considerable variation and some ovipositions occurred throughout the 24 h. In contrast, the mean time of all ovipositions under continuous illumination was at 15.00 h and the mean time of C1 ovipositions was 12.30 h. When a diurnal rhythm of bird noise was audible during the light period (photoperiod 06.00 to 18.00 h or 18.00 to 06.00 h) in adjoining rooms, the birds in continuous illumination showed a mean time of oviposition at 09.30 h with mean time of C1 ovipositions at 06.30 h. For birds in continuous dark the corresponding mean values for the two treatments were 04.00 and 03.00 h for all ovipositions and 00.30 and 23.00 h for the first oviposition of a sequence. When continuous illumination was changed to continuous darkness and vice versa and the 12L:12D lighting treatments in the adjoining rooms were correspondingly reversed, the mean times of oviposition under continuous darkness occurred at 05.00 and 06.30 h, which was earlier by 3 and 4.5 h than the mean time of oviposition at 09.30 h under continuous lighting. The tendency of birds kept in constant darkness to lay eggs in the early morning hours was found to be persistent and repeatable. It is concluded that the findings are best explained by the entrainment of the circadian rhythm to an unidentified synchronising Zeitgeber, but only in continuous darkness.  相似文献   

12.
1. Diurnal food intake rhythms of laying hens were studied under 21, 24 and 30‐h cycles, using either a constant 12‐h photoperiod or a 10‐h scotoperiod in each cycle. The feeding patterns essentially followed a circadian periodicity under all experimental situations. The peak in food intake which normally occurs before “sunset” in a 24‐h cycle was consistently observed to be timed from the onset of the previous dark period in each light and dark cycle, regardless of cycle length.

2. This study demonstrates that the laying fowl makes use of an endogenous biological rhythm to regulate its feeding behaviour. A light to dark transition in a light and dark cycle is the primary signal for phase‐setting the pattern of food intake.  相似文献   


13.
In two experiments, 17-wk-old Holstein bulls exposed to 16 (Exp. 1) or 24 h (Exp. 2) of light daily were compared with bulls given 8 h of light. Blood was sampled at 30-min or 120-min intervals for 48 h at the beginning and again after 4 wk of light treatment. Melatonin concentrations varied episodically in serum, and means were 1.6-fold to 5.1-fold greater during darkness than during light periods. Continuous lighting abolished the nocturnal increase in concentrations of melatonin in three of four calves. Prolactin (PRL) was greater (P less than .05) in calves receiving 16 h (30.9 ng/ml of serum) than in calves receiving 8 h (7.0 ng/ml) of light daily. Prolactin was not different between calves receiving 24 or 8 h of light daily. In a third experiment, one pinealectomized (PX) and two sham PX (SPX) calves were exposed to continuous lighting and infused with melatonin for 16 h/d for 5 wk, and one PX and two SPX calves were infused for 8 h daily. Melatonin infusion increased average concentrations of melatonin in serum 7.2-fold to 18-fold above baseline concentrations. Duration of melatonin infusion did not affect PRL (21.0 vs 20.8 ng/ml of serum). Also, surgical treatment did not affect PRL concentrations. Similarly, in a fourth experiment, PRL in postpubertal heifers fed melatonin to mimic and 8L:16D photoperiod averaged 27.1 ng/ml of serum, which was not different from PRL in heifers receiving 16L:8D and fed vehicle (32.6 ng/ml). We conclude that PRL and melatonin are each affected by photoperiod but are not casually related in cattle.  相似文献   

14.
1. Under a symmetric skeleton photoperiod of 2 h light, 10 h dark, 2 h light and 10 h dark (2L : 10D : 2L : 10D), most ovippositions occurred in the first 10‐h dark period with an important mode during the first hour of darkness.

2. With a gradual increase of the first dark period (the period of activity), the ovipositions become increasingly spread throughout the 24‐h cycle; a complete phase shift for the timing of oviposition was observed with the programme 2 h light, 11 h 15 min dark, 2 h light and 8 h 45 min dark (2L : 11.15D : 2L : 8.45D).

3. With the photoperiod 2L : 10D : 2L : 10D, the servicing of the birds during either 2‐h light period, and the withdrawal of calcium source during either the second 2‐h light period or during the first 10‐h dark and second 2‐h light periods did not change the timing of ovipositions.  相似文献   


15.
短周期间歇光照对肉用仔鸡生产性能的影响   总被引：2，自引：0，他引：2  
在７日龄时，肉服仔鸡由接近全日制光照改变为１ｈ光照，３ｈ黑暗的短周期简歇光照。结果表明，短周期间歇光照的肉仔鸡饲料报酬和饲料利用率提高，氮平衡试验表明，增加肉用仔鸡的光周期，粪氮分泌量减少，饲料氮在鸡体内的沉积增加，而饲料氮的摄入量并未增加，因而使得饲料氮的利用率和到提高。  相似文献   

16.
1. Two experiments are described in which a system of intermittent lighting (15 min light followed by 45 min dark for 15 h, then 15 min light, 30 min dark, 15 min light and 8 h dark) was applied to laying pullets from 37 to 72 weeks of age. A step-up lighting programme was used as a control treatment (8L:16D from 0 to 18 weeks, photoperiod increased by 20 min each week from 18 to 41 weeks, 16L:8D from 41 to 72 weeks of age). 2. Food consumption was reduced by about 5% when intermittent lighting was in use and by 3.8% for the period from 18 to 72 weeks. 3. Rate of lay and egg weight were similar for intermittent lighting and the control treatment, provided that protein content of the diet was adjusted to maintain an adequate amino acid intake. 4. In the second trial 2 stocks, 2 stocking densities confounded with 2 temperatures and 2 types of food trough were used. Each of these factors affected food intake and it was found that more food was saved by intermittent lighting when intake was high and less when it was low. The proportion saved was approximately 5%. 5. Mortality was slightly but not significantly lower in both experiments where intermittent lighting was used. This may indicate that caged pullets are under less stress when intermittent lighting is used.  相似文献   

17.
Two artificial lighting regimens were studied in a commercial unit of 800 sows. The aim was to develop a simplified lighting regimen to overdrive the effects of season on reproduction. A long-day group had a constant 16 hours light and eight hours dark photoperiod in all units during a production cycle. A short-day group had eight hours of light and 16 hours darkness in a farrowing unit for four weeks and in a mating unit for four weeks. After one month of pregnancy the short-day group was transferred to 16 hours light and eight hours dark for the rest of the dry-sow period. Production data were collected for eight months, and the farrowing rate, weaning to oestrus interval, culling rate for fertility problems and the number of live-born piglets were analysed. Seasonal infertility, which had previously affected the herd, was not detected in either group during the follow-up period. The farrowing rate was 90 per cent for both groups. The median weaning to oestrus interval was five days in both lighting regimens with ranges from four to 74 days in the short-day group and three to 55 days in the long-day group. The long-day programme had a positive effect on the weaning to oestrus interval. When the sows were classified as either "normal", with a weaning to oestrus interval of up to 10 days, or "problem" animals, with a weaning to oestrus interval of over 10 days, the short-day programme also had a positive effect. The culling rate for fertility problems was 2.4 per cent for the short-day group and 3.2 per cent for the long-day group (P=0.027). The only significant predictor for the number of live-born piglets was parity (P=0.027).  相似文献   

18.
In a 2-wk experiment, the effect of photoperiod on performance and energy metabolism of newly weaned pigs was studied. Forty 4-wk-old crossbred weanling barrows weighing 8.0 kg (SE = 0.13) were assigned to one of eight groups (five pigs per group) based on BW and litter. Groups were allotted to one of two lighting schedules: 8 h light:16 h darkness or 23 h light:1 h darkness. Each group was housed in a climate respiration chamber. Piglets had ad libitum access to feed and water. Energy and nitrogen balances, heat production, ADFI, and ADG were measured weekly. Heat production, energy metabolism, and performance were unaffected (P > 0.10) by photoperiod during wk 1. However, in the 2nd wk ADFI (418 vs 302 g/d) and ADG (381 vs 240 g/d) were higher (P < 0.05 and P = 0.05, respectively) for pigs on the 23:1 h lighting schedule than for those on the 8:16 h schedule. Furthermore, heat production (P < 0.10), total energy retention, and energy retained as protein and as fat were higher (P < 0.05) during wk 2 in pigs on the 23:1 h lighting schedule (8, 125, 41, and 350%, respectively) than in those on the 8:16 h schedule. Moreover, metabolizability of energy tended to be higher (P < 0.10) and energy requirements for maintenance were lower (P < 0.05) during wk 2 for pigs on the 23:1 h schedule compared with those on the 8:16 h schedule (P < 0.10). In conclusion, exposing pigs to a longer period of light after weaning stimulated ADFI and ADG. In addition to the feed intake, the high ADG is due to an improved metabolizability of energy and a reduced energy requirement for maintenance. This study suggests that lighting schedule can be used as a tool to stimulate feed intake after weaning.  相似文献   

19.
Horses are transported for a variety of purposes. Loading the horse onto a trailer or horsebox can be a source of stress and injury for both the horse and handler. This study investigated whether lighting conditions either inside or outside the trailer influence the welfare of horses during loading. Eight horses were initially trained to enter a trailer for a food reward, and were then loaded into an enclosed trailer either from a dark or lit arena and into a dark or lit trailer, in a replicated Latin Square design. Heart rate increased from the start to the end of each test in all treatments, suggesting that the horses experienced some fear of the loading process. However, there was no effect of lighting treatment on the increase in heart rate or the maximum or mean heart rates. Neither was there any effect of treatment on the speed of loading or number of refusals, which when examined with the heart rate data, suggests that there was no effect of lighting treatment on the horses’ fear of loading. However, horses loading from a lit arena were more likely to turn away from the trailer or lower their head than horses loading from a dark arena. In addition, those loading from a lit arena to a dark trailer sniffed the ground more, showing increased exploration of their environment. It is concluded that the amount of fear shown by horses was not affected by lighting conditions inside or outside the trailer, but there was some evidence of negative emotions when they loaded from a lit arena, particularly when they were entering a dark trailer.  相似文献   

20.
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.  相似文献   

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