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Results for “Photoperiod”

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At least 19 recordsLinked to original sources
PubMed1979

Photoperiodic effects in the Djungarian hamster: one minute of light during darktime mimics influence of long photoperiods on testicular recrudescence, body weight and pelage colour.

In male Djungarian hamsters (Phodopus sungorus) short photoperiods (L/D 8/16) with additional 1- or 5-min light-pulses 8 h after light-off were as effective as long photoperiods (L/D 16/8) in stimulating testicular recrudescence, increase in body weight and moult into summer pelage. The results are discussed with regard to the hypothesis that the pattern of melatonin release from the pineal gland is important in mediating photoperiodic effects in mammals.

Animals↗
PubMed1976

Effect of photoperiod upon age and maintenance of sexual development in female Coturnix coturnix japonica.

Coturnix kept in a 14L:10D photoperiod from hatch began to lay their first eggs at a mean age of 42.8 days (range 38-55). Approximately 2/3 of Coturnix held from hatch in photoperiods of 6L:16D light were laying at 165 days of age. Mean age at first egg was 112.7 days (range 68-162 days) in 8L:16D and 130.8 days (range 117-158 days) in 6L:18D photoperiod. Coturnix transferred from a non-stimulatory (8L:16D) photoperiod to a stimulatory one (14L:10D or 24L) begun laying in 15-20 days if less than 140 days old, and in about 5 days if greater than 140 days old, when trasferred. Birds which has spontaneously begun to lay in an 8L:16D photoperiod did not stop laying when the photoperiod was reduced to 6L:18D. Those which began laying under 14L:10D photoperiod ceased laying in about 15 days if 89 or fewer days old when switched to 8L:16D, or in about 6 days if 140 or more days old. Those switched from 14L:10D to 6L:18D ceased laying in about 13 days when 76 days old, and 7 days when 89 days old.

Age Factors↗
PubMed2025

Repeated evolution of photoperiodic plasticity by different genetic architectures during recurrent colonizations in a butterfly.

In cases of recurrent colonizations of similar habitats from the same base population, it is commonly expected that repeated phenotypic adaptation is caused by parallel changes in genetic variation. However, it is becoming increasingly clear that similar phenotypic variation may also evolve by alternative genetic pathways. Here, we explore the repeated evolution of photoperiodic plasticity for diapause induction across Swedish populations of the speckled wood butterfly, Pararge aegeria. This species has colonized Scandinavia at least twice, and population genomic results show that one of the candidate regions associated with spatial variation in photoperiodism is situated on the Z-chromosome. Here, we assay hybrid crosses between several populations that differ in photoperiodic plasticity for sex-linked inheritance of the photoperiodic reaction norm. We find that while a cross between more distantly related populations from the two different colonization events shows strong sex-dependent inheritance of photoperiodic plasticity, a cross between two more closely related populations within the oldest colonization range shows no such effect. We conclude that the genotype-phenotype map for photoperiodic plasticity varies across these populations and that similar local phenotypic adaptation has evolved during recurrent colonization events by partly non-parallel genetic changes.

Butterflies↗
PubMed1979

The effects of different photoperiods on circadian 5-HT rhythms in regional brain areas and their modulation by pinealectomy, melatonin and oestradiol.

Differential circadian rhythms in 5-HT levels were found in the hypothalamus and pineal (but not in the cortex, hippocampus or midbrain) in ferrets kept in either long (14 h light/10 h dark) or short (8 h light/16 h dark) photoperiods. 5-HT decreased during the first 6 h of illumination in all areas examined from animals kept in short photoperiods. In long photoperiods, 5-HT in the hypothalamus (particularly the anterior region) increased during the first 6 h after onset of light and levels in the pineal became arrhythmic. There were no differential effects of light on 5-HIAA/5-HT ratios. Removal of the pineal or the superior cervical ganglia abolished these differential rhythms, as did subcutaneous implants of oestradiol (releasing about 5 micrograms/day). Melatonin (1 mg/day) injected 8 h after the onset of light into animals kept in long photoperiods resulted in circadian 5-HT rhythms resembling those from animals exposed to short photoperiods, whereas melatonin given at 14 h after onset of light did not have this effect. It is suggested that 5-HT containing neural systems may play a role in the way the pineal transmits information about the duration of the photoperiod to the neural structures controlling the pituitary.

Animals↗
PubMed1977

Function and histology of testes from aged coturnix maintained on different photoperiods.

The prolonged effects of short, medium, and long photoperiods on longevity, cloacal gland size and function, and the testicular morphology of the aged coturnix were studied. In all testes, the effects of aging were characterized histologically by decreased tubular sperm concentration, increased abnormal sperm and cellular debris, as well as dislodgement of maturing sperm from Sertoli cells. However, testicular abnormality in the long photoperiod quail was more pronounced than in the short photoperiod quail whose testes were judged to be morpholoigcally in better condition, thus indicating an aging-photoperiod relationship. Aging had little or no effect on the cloacal gland function, although its size similar to the testicular histology, was affected by different photoperiods. Cloacal gland size and function can indicate sexual potency, but not necessarily the reproductive capabilities of aged coturnix. Also, an increased incidence of cataract formation was recorded in aged coturnix, unrelated to photoperiods.

Aging↗
PubMed1977

Interaction between photoperiod, temperature, and chilling in dormant larvae of the tree-hole mosquito, Toxorhynchites rutilus Coq.

1. Unchilled, diapausing larvae of Toxorhynchites rutilus rely on photoperiod for the maintenance of diapause. The photoperiodic clock is temperature-compensated between 16.5 degrees and 25 degrees C, maintaining both a similar set-joint and inherent accuracy over this range. The rates of development among larvae terminating diapause are dependent upon both temperature and photoperiod. 2. Chilling of dormant Toxorhynchites rutilus can promote response to progressively shorter daylengths, thus decreasing the critical photoperiod. Chilling can also accelerate response to long days, thereby decreasing the depth of diapause and, after prolonged exposure, can eventually terminate diapause directly, leaving subsequent morphogenesis independent of photoperiod. 3. The optimal temperature for these effects of chilling is above 4 degrees C, below 16.5 degrees C, and may lie around 7 degrees C. 4. Temperatures between 5 degrees and 15 degrees C are vernal and autumnal rather than hibernal. The interaction between chilling and photoperiod may then represent an adaptive compromise between selection due to long-term climatic trends and the vagaries of spring weather.

Acclimatization↗
PubMed1976

Circadian rhythms and photoperiodic time measurement in mammals.

Many mammalian species display seasonal breeding patterns correlated with annual cycles of change in the physiology and morphology of the reproductive system. Such annual reproductive cycles are often photoperiodically controlled (i.e, the annual change in day length determines when reproductive activity begins and when it ends within the annual cycle). Photoperiodic control of seasonally appropriate changes in reproductive activity is dependent on an endogenous time measuring process. Among mammals the physiological basis of photoperiodic time measurement has been studied most extensively in the golden hamster. Studies with this species indicate that photoperiodic time measurement is executed by the circadian system. The time measuring process depends on a circadian oscillation of responsiveness to light with properties similar to those of the hypothetical rhythm originally proposed by Bünning to explain photoperiodic phenomena in plants. The available evidence strongly suggests the participation of the pineal gland and the suprachiasmatic nucleus (SCN) in the photoperiodic regulation of mammalian reproductive cycles. However, little is known regarding concrete physiological mechanisms, and the extent to which the SCN and the pineal gland may participate in the time measuring process per se remains to be determined.

Animals↗
PubMed1976

Photoperiodic control of antler cycles in deer. III. Decreasing versus increasing day lengths.

Deer were exposed for three years to photoperiods which increased or decreased two hours every four months, starting at 4L/20D or 20L/4D, respectively. Under both sets of conditions, antlers were repeatedly shed and replaced, usually in synchrony with every other time the day lengths were changed. On decreasing days, antler cycles were omitted as the photoperiod passed the equinox (12L/12D). On increasing days, the equinoctial photoperiod induced prolonged episodes of antler growth. The tendency for the antler replacement cycle to lock onto alternate changes in artificial photoperiods is consistent with the seasonal growth of antlers every other time the day lengths change in the natural environment. It is suggested that antler replacement is triggered neither by shortening nor lengthening days, but by the alternation of such changes irrespective of the direction of the shift in the photoperiod.

Animals↗
PubMed1977

Effect of photoperiod on gonadotrophin concentrations in domestic turkeys.

1. Circulating immunoreactive luteinising hormone (LH) and follicle stimulating hormone (FSH) concentrations have been measured during photoperiodically-induced changes in the reproductive state of turkeys. 2. In a period of sexual quiescence on short photoperiods (6L: 18D) LH concentrations were higher during the hours of darkness in both sexes. 3. Transfer to long photoperiods (16L: 8D) stimulated a rapid increase in LH and FSH concentrations. This was maintained for between 2 to 3 months when the concentrations of both gonadotrophins decreased as the birds became photorefractory. 4. Return to short photoperiods had no immediate effect on the concentrations of LH and FSH in females. The concentration of LH was increased during the 3rd week of short photoperiods when the hens were moulting. 5. LH concentrations fluctuated during the ovulatory cycle and were highest about 6 h before ovulation.

Animals↗
PubMed1976

Regulation of serum gonadotropins by photoperiod and testicular hormone in the Syrian hamster.

Male hamsters were maintained on long (14L:10D) or short (10L:14D) photoperiods. The serum concentrations of LH and FSH were reduced in the animals kept on the short photoperiod, and these animals had atrophied testes and sex accessories. Serum gonadotropin concentrations increased following castration in both long and short photoperiods, but gonadotropin secretion was inhibited by much smaller doses of testosterone in the males maintained on the short photoperiod as compared to males kept on a long photoperiod. The levels of testosterone required to suppress serum gonadotropin levels in castrated animals corresponded reasonably well with the serum androgen levels observed in intact males, suggesting that serum androgen is a major regulator of gonadotropin secretion in the male hamster.

Androgens↗
PubMed1978

Rate of testicular maturation, in relation to gonadotrophin and testosterone levels, in quail exposed to various artificial photoperiods and to natural daylengths.

Rates of testicular growth and plasma levels of FSH, LH and testosterone were determined in Japanese quail exposed to various fixed photoperiods (number of hours of light: number of hours of darkness): 12L : 12D, 13L : 11D, 14L : 10D, 16L : 8D and 20L : 4D and to natural daylengths. All five artificial photoperiods stimulated spermatogenesis, with the testes reaching maturity after 30-40 days. Maximum rates of testicular growth occurred with 14L : 10D, 16L : 8D or 20L : 4D but the rate was reduced by 50% in birds exposed to 12L : 12D.. This reduction was due to decreased growth in the seminiferous tubule epithelium (and hence in tubule diameter); the duration of spermatogenesis hardly being affected. Near maximum growth rates occurred with 13L : 11D. The hormone profiles offer an explanation for the differential rates of testicular growth. In the three longest photoperiods, FSH rose from 20 ng/ml to peak levels of 300-400 ng/ml after 10 days. As the testes matured, so the level of FSH decreased to 50-100 ng/ml. This pattern was not seen under 12L : 12D ; the level of FSH rose slowly to about 100 ng/ml and showed no peak of secretion. With 13L : 11D a small peak was found, which decreased at maturity. In quail with testes is greater than 1500 mg, the level of FSH was invariably about 100 ng/ml. Patterns of LH secretion were rather similar with all treatments, but testosterone was affected by photoperiod; lower levels were found under 12L : 12D than 20L : 4D. The rate of photoperiodically induced testicular growth was proportional to the levels of FSH, and possibly also testosterone, in the circulation. Outdoors, testicular growth began when daylengths reached about 12 h. Maturity occurred within the next 40 days. The levels of FSH rose steadily but did not show a peak of secretion. In general, the highest levels of hormone were found in July just before gonadal regression which occurred when the daylengths were still quite long.

Animals↗
PubMed1979

Influence of the pineal gland, olfactory bulbs and photoperiod on surges of plasma prolactin in the female rat.

The role of the pineal gland, olfactory bulbs and photoperiod in the regulation of the two daily surges of plasma prolactin in the pseudopregnant rat has been investigated. Pinealectomy had no effect on the surges of prolactin in pseudopregnant rats maintained on either a long (14 h light : 10 h darkness; 14L : 10D) or a short (2L : 22D) photoperiod, but olfactory bulbectomy decreased the nocturnal surge in animals maintained on 14L : 10D. This effect of bulbectomy was eliminated if the rats maintained on 14L : 10D were also pinealectomized. After cervical stimulation, bulbectomized rats maintained on a 2L : 22D photoperiod had nocturnal-type prolactin surges similar to those of intact rats maintained on the same photoperiod. These results indicate that the pineal gland andlength of photoperiod are not involved in the regulation of the surges of plasma prolactin in pseudopregnant rats but that the olfactory bulbs may enhance the nocturnal surge.

Animals↗
PubMed1979

Variables associated with peripartum traits in dairy cows. IV. Seasonal relationships among temperature, photoperiod, and blood plasma prolactin.

Concentrations of prolactin in plasma were measured in 176 dairy cows and heifers from 13 days before calving to 2.5 days after calving over 21 mo. Prolactin averaged 35.1, 115.0, and 34.4 ng/ml prepartum (days -13 to -2), peripartum (days -1.0 to +.5), and postpartum (days +1.5 and +2.5). Season of the year affected prolactin in all periods. The linear covariate of daily photoperiod (hours of daylight per 24 h) accounted for as much variation in prolactin prepartum and postpartum as did linear covariates of both photoperiod and average daily temperature. However, it was possible to account for additional seasonal variation in prolactin peripartum by addition of the temperature covariate to the photoperiod covariate. Although photoperiod was related either directly or indirectly more than temperature to factors affecting prolactin seasonally, these statistical inferences cannot prove that prolactin is more dependent on photoperiod than on temperature because the two metereorological measures were correlated (r = .84). When the data were grouped for correlation analysis by months, correlations between temperature and prolactin among prepartum samples collected in the spring and in the fall were positive, small but significant.

Animals↗
PubMed1979

Photoperiodic control of rat pineal serotonin N-acetyl-transferase activity.

Adult male albino rats were acclimated to constant light (light:dark-LD-24:0) or to darkness interrupted with brief periods of light at 6 h intervals (LD 1/4:5 3/4 X 4) concurrently with rats maintained in a LD 14:10 photoperiodic cycle. The activity and rhythmicity of pineal serotonin N-acetyltransferase (NAT) was examined at regular intervals for 24 hours in rats maintained in the experimental photoperiods and compared to pineal NAT activity and rhythmicity in rats maintained in the LD 14:10 photoperiod. The results indicate that constant light is capable of depressing nocturnal levels of rat pineal NAT and obliterating the pineal NAT rhythm. Likewise, rats subjected to darkness interrupted with brief periods of light at 6 h intervals experienced a similar response in pineal NAT activity to animals subjected to constant light, i.e., pineal NAT activity was persistently low and the rhythmicity was obliterated. The results are discussed relative to the hypothesis that the pineal NAT activity responds to an endogenous rhythm in photoperiodic time measurement. The evidence herein suggests that the time of occurrence of environmental light in the photoperiod is more important in determining pineal NAT activity and/or rhythmicity than is the total amount of darkness or the dark to light ratio to which animals may be subjected.

Acetyltransferases↗
PubMed2026

Long-day photoperiod promotes growth of pea (Pisum sativum L.) via auxin biosynthesis and polar transport.

Photoperiodic sensitivity is an essential factor that may affect agricultural practices under current climate scenarios. This study used pea (Pisum sativum) to examine effects of varying photoperiods on growth and photosynthetic parameters and then reveal the mechanistic basis of this process by linking them with tissue-specific distribution of auxin and regulation of related genes. This was achieved by transcriptome sequencing, genome-wide gene family identification, and expression pattern analysis. Best results in terms of growth and yield were obtained with a 20 h/4 h light/dark photoperiod and these plants had the highest content of endogenous indole-3-acetic acid (IAA) in both the shoot apex and the root. Genes consistently upregulated with prolonged light exposure were significantly enriched in pathways related to light signal transduction, photosynthetic carbon metabolism, and phytohormone signal transduction. Through genome-wide identification, we characterized the TAA/TAR and YUCCA families (key gene families involved in auxin biosynthesis) as well as the PIN family (responsible for auxin polar transport) in pea. Extending the light duration positively affected expression of several genes related to auxin biosynthesis and transport, among them members of the Elongated Hypocotyl (HY) and Phytochrome-Interacting Factor (PIF) families being key light-induced transcription factors, PsTAR2, the principal gene regulating auxin biosynthesis, as well as PsPIN4, PsPIN5, PsPIN11, and PsPIN13 which mediate polar auxin transport. By elucidating mechanisms underlying the coordinated regulation of pea growth by light and auxin, this work provides a significant reference for photoperiod research on long-day crops for both protected- and field-based horticulture.

Auxin↗
PubMed1977

Effect of extended photoperiod on the spermatogenic activity of chicken-pheasant hybrids.

1. Males of chicken-pheasant hybrids and non-breeding pheasants were exposed to photoperiods of 10 or 20 h/d to test the effect of light on spermatogenic activity. 2. Testicular weights of hybrids and pheasants exposed to 10 h/d were similar and extending the photoperiod did not increase this in hybrids, although it caused a 48-fold increase, and complete recovery of spermatogenic activity, in pheasant. 3. Extending the photoperiod caused an increase in the number of primary spermatocytes and a corresponding decrease in the number of spermatogonia in hybrids, however, stages beyond primary spermatocytes were not present. This suggests that the stimulus of extending the photoperiod, while sufficient to induce meiosis in existing germ cells, is not enough to effect proliferative bursts or to overcome the meiotic arrest in the hybrids.

Animals↗
PubMed1978

The photoperiodic effect of ahemeral light-dark cycles which entrain circadian rhythms.

1. A 27-h cycle of light and dark provides a greater gonadotrophic stimulus to the laying fowl, as judged by sexual maturity and rate of lay, than a 24-h cycle incorporating the same photoperiod. 2. An hypothesis put forward to account for these effects states that Effective Photoperiod equal p + c - b, where p = actual photoperiod, c = cycle length and b = the period of the endogenous biological clock. 3. Two experiments designed to test this hypothesis have yielded results which are consistent with it. 4. A poultryman who use an ahemeral cycle to alter egg weight or shell thickness and then whishes to transfer his flock back to a 24-h cycle should calculate the difference between the two cycle lengths and then add this quantity to the prevailing photoperiod to find the appropriate amount of light to be used in the 24-h cycle.

Animals↗