Suprachiasmatic nucleus and photic entrainment of circannual rhythms in ground squirrels.

The efficacy of photoperiod as a zeitgeber for entrainment of circannual body weight and estrous rhythms was tested in female golden-mantled ground squirrels maintained for 3 or more years in either a simulated natural photoperiod (SNP) or a fixed LD 14:10 photoperiod (FP). The role of the retinohypothalamic tract--suprachiasmatic nucleus (RHT-SCN) projection in photic entrainment was assessed in animals that sustained destruction of the SCN (SCNX). Circannual rhythms were lengthened by the SNP as compared to the FP. Mean periods (tau's) for neurologically intact animals in the third year of testing were 49.6 +/- 0.3 weeks and 43.1 +/- 1.2 weeks (p less than 0.001) for the SNP and FP groups, respectively; furthermore, 56% and 7% of animals in these groups had tau's not significantly different from 365 days (p less than 0.005), and within-group variability was lower for SNP than for FP squirrels (p less than 0.01). SCNX squirrels differed from animals with the SCN intact (SCNC), as evidenced by higher within-group variability (p less than 0.001); only 29% of SCNX squirrels had tau's not different from 365 days (p less than 0.03 compared to the SCNC group). The coupling between estrous and body weight rhythms that was evident in SCN-intact SNP and FP squirrels was disrupted in SCNX animals. The RHT-SCN pathway is implicated in entrainment and in maintenance of normal phase relations among the several circannual rhythms. In a second experiment, female squirrels were maintained for 2.5 years in an accelerated SNP that compressed two normal annual photocycles into each calendar year. Of 12 squirrels, 3 had tau's that did not differ significantly from 6 months; 6 had tau's equivalent to 12 months; and 3 had tau's significantly different from both 6 months and 12 months. The data suggest that photoperiod is a major zeitgeber for entrainment of golden-mantled ground squirrels circannual rhythms.     

Photic entrainment of circannual rhythms in golden-mantled ground squirrels: role of the pineal gland

Entrainment of circannual rhythms of body mass and reproduction was monitored for 3 years in female golden-mantled ground squirrels maintained in a simulated natural photoperiod. Both pinealectomized and pineal-intact squirrels generated circannual rhythms of body mass and estrus, but only the intact animals entrained these rhythms to a period of 365 days. In the second and third years after treatment, the period of the body mass rhythm was significantly shorter than 365 days for pinealectomized squirrels, and variance in tau among these animals was significantly greater than for intact squirrels. A similar pattern was evident in the rhythm of reproduction, which was phase-disrupted in pinealectomized squirrels but entrained in intacts. Seasonal changes in duration of nocturnal melatonin secretion by the pineal appear to be necessary to produce phase-delays required to entrain the circannual clock to a period of 12 months.     

Circannual rhythms of ground squirrels: a test of the frequency demultiplication hypothesis

The frequency demultiplication hypothesis (FDH) posits that circannual rhythms are generated from circadian cycles by frequency transformation to the lower-frequency rhythm. To test the FDH, we determined the periods of the circannual body mass and estrous cycles of golden-mantled ground squirrels with circadian locomotor activity rhythms entrained to 23-, 24-, or 25-hr days (T-cycles). Circannual period length did not differ among squirrels entrained to the different T-cycles; intergroup ranges were 298-314 days and 303-312 days, respectively, for body mass and estrus. These results are not consistent with the FDH and suggest instead that separate mechanisms generate circadian and circannual rhythms. In ground squirrels the circannual system influences circadian organization, but a reciprocal influence of circadian on circannual rhythms has yet to be demonstrated.     

Temperature-independence of circannual variations in circadian rhythms of golden-mantled ground squirrels

In golden-mantled ground squirrels, phase angles of entrainment of circadian locomotor activity to a fixed light-dark cycle differ markedly between subjective summer and winter. A change in ambient temperature affects entrainment only during subjective winter when it also produces pronounced effects on body temperature (Tb). It was previously proposed that variations in Tb are causally related to the circannual rhythm in circadian entrainment. To test this hypothesis, wheel-running activity and Tb were monitored for 12 to 14 months in castrated male ground squirrels housed in a 14:10 LD photocycle at 21 degrees C. Animals were treated with testosterone implants that eliminated hibernation and prevented the marked winter decline in Tb; these squirrels manifested circannual changes in circadian entrainment indistinguishable from those of untreated animals. Both groups exhibited pronounced changes in phase angle and alpha of circadian wheel-running and Tb rhythms. Seasonal variation in Tb is not necessary for circannual changes in circadian organization of golden-mantled ground squirrels.     

Circannual cycles in golden-mantled ground squirrels: fall and spring cold pulses

Summary Endogenous circannual rhythms of male golden-mantled ground squirrels (Spermophilus lateralis) exposed to low ambient temperature (6 °C) at various times were compared to the rhythms of a control group kept in a warm room (21 °C) throughout. A 20-week pulse of cold in the spring delayed the subsequent peak body weight and molt offset. However, in the second year after the spring cold pulse, a delay in the rhythm was evident only using peak weight as a phase marker. A 20-week cold pulse in the fall resulted in an earlier peak body weight and earlier onset of pigmented scrotum and descended testes, but there was no evidence from subsequent years that rhythms had been phase advanced. A third of the animals kept continuously at 6 °C remained with pigmented scrotum, descended testes and low body weight for more than a year. Circannual periodicities of animals that continued to display rhythms in the cold room were not significantly longer than those of controls in the warm room. The results suggest that low temperature in the fall can alter the expression of circannual rhythms without much affecting their phasing, while low temperature in the spring produces phase delays which last longer but have not been proved to be persistent.Abbreviation PRC phase response curve     

Circannual rhythms of ground squirrels: role of the hypothalamic paraventricular nucleus

Female golden-mantled ground squirrels, maintained in an LD 14:10 photoperiod at 23 degrees C, sustained lesions of the paraventricular nucleus (PVN) or sham operations. Body weight and reproductive status were recorded weekly pre- and postoperatively. Bilateral lesions of the PVN did not eliminate, phase-shift, or otherwise disrupt the circannual rhythms of body mass or reproduction. Absolute levels of body weight were unaffected by PVN ablation. The PVN is not an essential component of the oscillatory system that generates circannual cycles in ground squirrels.     

Circannual clocks in avian reproduction and migration

Many behavioural and physiological functions of organisms are adjusted to the periodic changes in their environment, particularly to those related to the natural day and year. This adjustment is often achieved through the action of endogenous daily (circadian) and annual (circannual) clocks. Studies of the control of avian moult, migration and reproduction have played a major role in understanding how biological clocks function and interact with rhythms in the environment. Investigations on tropical birds such as the East African subspecies of the Stonechat ( Saxicola torquata axillaris ) and long-distance migrants like the Garden Warbler ( Sylvia boriri ) have provided the longest records of circannual rhythms, some of them running for more than 12 years, with periods ranging from about 9 to 13 months. Avian circannual rhythms are organized in a characteristic way for a particular species or population, and cross-breeding experiments have shown that some of the differences found among them are genetically determined. In African Stonechats circannual rhythms guarantee that seasonal events occur at the appropriate times of the year and in the characteristic sequence. They also control a "reproductive window" that provides the temporal framework for breeding. The width of this window is rather inflexible but the performance of a bird within this framework (e.g. whether it breeds once or twice per season) is subject to modification by environmental conditions. In migratory birds circannual programs are involved in determining the time course, distance and direction of migration. Circannual rhythms are synchronized with and modified by environmental factors in a complex way, but the endogenous mechanisms usually respond to environmental cues such that an optimal adjustment to season and latitude is guaranteed.     

Circannual clocks in avian reproduction and migration

Many behavioural and physiological functions of organisms are adjusted to the periodic changes in their environment, particularly to those related to the natural day and year. This adjustment is often achieved through the action of endogenous daily (circadian) and annual (circannual) clocks. Studies of the control of avian moult, migration and reproduction have played a major role in understanding how biological clocks function and interact with rhythms in the environment. Investigations on tropical birds such as the East African subspecies of the Stonechat ( Saxicola torquata axillaris ). and long-distance migrants like the Garden Warbler ( Sylvia borin ). have provided the longest records of circannual rhythms, some of them running for more than 12 years, with periods ranging from about 9 to 13 months. Avian circannual rhythms are organized in a characteristic way for a particular species or population, and cross-breeding experiments have shown that some of the differences found among them are genetically determined. In African Stonechats circannual rhythms guarantee that seasonal events occur at the appropriate times of the year and in the characteristic sequence. They also control a "reproductive window" that provides the temporal framework for breeding. The width of this window is rather inflexible but the performance of a bird within this framework (e.g. whether it breeds once or twice per season) is subject to modification by environmental conditions. In migratory birds circannual programs are involved in determining the time course, distance and direction of migration. Circannual rhythms are synchronized with and modified by environmental factors in a complex way, but the endogenous mechanisms usually respond to environmental cues such that an optimal adjustment to season and latitude is guaranteed.     

Effect of winter high temperatures on reproduction and circannual rhythms in hibernating ground squirrels

We tested whether prevention of hibernation in ground squirrels by midwinter exposure to high ambient temperatures influenced timing of the spring phase of reproductive maturation and the phase and period of subsequent circannual rhythms of reproduction and body mass. Exposing hibernating adult male Spermophilus lateralis to 30 degrees C for 6 weeks beginning December 4 advanced the timing of testicular recrudescence by 4-5 weeks, compared to controls left at 4 degrees C. Males exposed to 30 degrees C for 6 weeks beginning at the average time of spontaneous end of hibernation (January 15) reached reproductive maturation at a time intermediate to those of controls and of the December 4 experimental group. However, neither the date of the subsequent fall's body mass peak, the date of the next year's reproductive maturation, nor the periods of circannual rhythms of body mass and reproduction differed among groups. Premature interruption of hibernation appears to allow early expression of reproduction, but does not affect the underlying timing mechanism.     

Daily body temperature rhythms persist under the midnight sun but are absent during hibernation in free-living arctic ground squirrels

In indigenous arctic reindeer and ptarmigan, circadian rhythms are not expressed during the constant light of summer or constant dark of winter, and it has been hypothesized that a seasonal absence of circadian rhythms is common to all vertebrate residents of polar regions. Here, we show that, while free-living arctic ground squirrels do not express circadian rhythms during the heterothermic and pre-emergent euthermic intervals of hibernation, they display entrained daily rhythms of body temperature (T(b)) throughout their active season, which includes six weeks of constant sun. In winter, ground squirrels are arrhythmic and regulate core body temperatures to within ±0.2°C for up to 18 days during steady-state torpor. In spring, after the use of torpor ends, male but not female ground squirrels, resume euthermic levels of T(b) in their dark burrows but remain arrhythmic for up to 27 days. However, once activity on the surface begins, both sexes exhibit robust 24 h cycles of body temperature. We suggest that persistence of nycthemeral rhythms through the polar summer enables ground squirrels to minimize thermoregulatory costs. However, the environmental cues (zeitgebers) used to entrain rhythms during the constant light of the arctic summer in these semi-fossorial rodents are unknown.     

Circannual rhythms in birds

In many birds, reproduction, molt, migration and other seasonal activities are controlled by endogenous circannual rhythmicity. Under constant conditions, this rhythm persists for many cycles with a period deviating from 12 months. Whether or not the rhythm is expressed depends on day length (photoperiod), which thus represents an important permissive factor in the process of rhythm generation. In nature, circannual rhythms are usually synchronized by the seasonal changes in photoperiod. However, equatorial birds may use daytime light intensity, which changes with the annual cycle of dry and rainy seasons, as a synchronizing zeitgeber. Photoperiod also modulates the rate of progress of the successive phases of the rhythmicity, such that an optimal adjustment to the annual environmental cycle is guaranteed. Populations of a given species may differ in their responsiveness to photoperiod in a manner that can be described as 'adaptive population-specific reaction norms'. In young migratory songbirds a circannual program determines changes in migratory direction and, at least partly, the time course and distance of migration. This circannual mechanism is replaced or supplemented in older birds by mechanisms formed on the basis of learning and memory. In general, circannual rhythms are intimately involved in the seasonal organization of a bird's behavior, providing the substrate onto which seasonal environmental factors act.     

Circannual distribution of glioblastoma and anaplastic astrocytoma diagnoses in men and women

Background: circannual variations of incidence may influence human tumors. For example, seasonal distribution of breast cancers suggests an influence of circannual hormonal rhythms. Periodicity of brain tumors has not yet been investigated. The aim of this study was to assess the seasonal variation in glioblastomas and anaplastic astrocytomas. Methods: a large dataset of high-grade gliomas (n = 697) was evaluated with the month of diagnosis as key criterion for time series and seasonal analysis. Circannual and ultra-annual cosinor models were calculated. Results: women suffering from glioblastoma show a peak incidence in fall. No suitable circannual or ultra-annual cosinor model months could be fitted to the data. In women with anaplastic astrocytoma, a peak incidence was detected in summer and fall with a nadir in spring. Here, a significant cosinor model with a period of 8.5 months could be calculated. Conclusion: our data strongly suggest seasonality of diagnosis of high-grade gliomas in women. As gliomas express hormonal receptors, an underlying endocrinal or cell proliferation rhythms may be a possible explanation.     

Avian circannual clocks: adaptive significance and possible involvement of energy turnover in their proximate control

Endogenous circannual clocks are found in many long-lived organisms, but are best studied in mammal and bird species. Circannual clocks are synchronized with the environment by changes in photoperiod, light intensity and possibly temperature and seasonal rainfall patterns. Annual timing mechanisms are presumed to have important ultimate functions in seasonally regulating reproduction, moult, hibernation, migration, body weight and fat deposition/stores. Birds that live in habitats where environmental cues such as photoperiod are poor predictors of seasons (e.g. equatorial residents, migrants to equatorial/tropical latitudes) rely more on their endogenous clocks than birds living in environments that show a tight correlation between photoperiod and seasonal events. Such population-specific/interspecific variation in reliance on endogenous clocks may indicate that annual timing mechanisms are adaptive. However, despite the apparent adaptive importance of circannual clocks, (i) what specific adaptive value they have in the wild and (ii) how they function are still largely untested. Whereas circadian clocks are hypothesized to be generated by molecular feedback loops, it has been suggested that circannual clocks are either based upon (i) a de-multiplication ('counting') of circadian days, (ii) a sequence of interdependent physiological states, or (iii) one or more endogenous oscillators, similar to circadian rhythms. We tested the de-multiplication of days (i) versus endogenous regulation hypotheses (ii) and (iii) in captive male and female house sparrows (Passer domesticus). We assessed the period of reproductive (testicular and follicular) cycles in four groups of birds kept either under photoperiods of LD 12L:12D (period length: 24h), 13.5L:13.5D (27 h), 10.5L:10.5D (23 h) or 12D:8L:3D:1L (24-h skeleton photoperiod), respectively, for 15 months. Contrary to predictions from the de-multiplication hypothesis, individuals experiencing 27-h days did not differ (i.e. did not have longer) annual reproductive rhythms than individuals from the 21- or 24-h day groups. However, in line with predictions from endogenous regulation, birds in the skeleton group had significantly longer circannual period lengths than all other groups. Birds exposed to skeleton photoperiods experienced fewer light hours per year than all other groups (3285 versus 4380) and had a lower daily energy expenditure, as tested during one point of the annual cycle using respirometry. Although our results are tantalizing, they are still preliminary as birds were only studied over a period of 15 months. Nevertheless, the present data fail to support a 'counting of circadian days' and instead support hypotheses proposing whole-organism processes as the mechanistic basis for circannual rhythms. We propose a novel energy turnover hypothesis which predicts a dependence of the speed of the circannual clock on the overall energy expenditure of an organism.     

Photoperiod as a modifying and limiting factor in the expression of avian circannual rhythms

In three species of birds that migrate long distances, the annual rhythms of gonadal activity, molt, and migratory restlessness (Zugunruhe) persist for more than 1 year under certain constant conditions. The most important zeitgeber for these circannual rhythms is the annual cycle of photoperiod, which adjusts the overall period of circannual rhythms to exactly 1 year and also provides for the appropriate adjustment of seasonal activities to the temporal structure of the environment. This is illustrated by results on garden warblers (Sylvia borin) indicating that the longer photoperiods experienced by individuals wintering far south in the African wintering area phase-advance spring migration and the accompanying gonadal development, relative to those of individuals wintering further north. The rate of acceleration is, however, slow enough to prevent a reproductive cycle during the Southern Hemisphere summer. Hence, endogenous circannual components and zeitgeber stimuli constitute a functional entity that provides as a whole for adaptive temporal programming. This idea is further supported by findings in the pied flycatcher (Ficedula hypoleuca), in which a circannual rhythmicity persists only if photoperiod in winter is at least as short as that normally encountered by the species in its wintering grounds slightly north of the equator. In collared flycatchers (Ficedula albicollis), in contrast, rhythmicity continues under much longer photoperiods, consistent with the fact that the wintering area of this species extends to latitudes far south of the equator. It is proposed that the adaptive function of circannual rhythms can be properly understood only if their interactions with environmental factors, particularly those that play a role as zeitgebers, are analyzed in sufficient detail. The biological significance of circannual rhythms may be more apparent in the context of the environmental constraints limiting their expression than in the often rather restricted set of conditions sustaining spontaneous annual cyclicity.     

季节、环境温度与黄鼠冬眠的关系

观察了达乌尔黄鼠在实验室内冬眠的一般情况。常温黄鼠的体温有着规律性的年周期,与环境温度的年周期变动不完全呈依从关系。出眠初期(4月下旬),动物体温高而稳定。4月至6月常温黄鼠的平均体温(皮温)为35.6℃,波动菹围32—37.5℃。随着体重达到顶峰,体温逐渐降低。8月份部分黄鼠出现低于32℃的低常体温,表明部分黄鼠自8月盛夏开始冬眠。但就整个种群而言,北京地区实验室内黄鼠冬眠季自9月下半月开始。3月底止,共6.5个月。秋季室温下降,动物入眠趋势增长。浅低体温(31.9—15℃)的比数逐渐升高。9月至12月,低体温(低于31.9℃)的百分比从47％增至84.8％,反映了动物从浅冬眠向深冬眠过渡。1月至2月份,低体温占85％以上,深低体温(低于15℃)占绝对优势。标志着动物种群的深眠月份。秋季动物从常温期向冬眠期转化的界线是不清的,而春季从冬眠期向常温相转化的界限却比较明显。     

Pinealectomy and LL Abolished Circadian Perching Rhythms but Did Not Alter Circannual Reproductive or Fattening Rhythms in Finches

In the subtropical finch, spotted munia (Lonchura punctulata) circannual rhythms (of gonads, fattening, feeding) have been demonstrated in an information-free environment of continuous illumination (LL), rendering it an ideal model for research on the physiology of the circannual clock. In an attempt to understand the involvement, if any, of the circadian system in the genesis of circannual rhythms, we studied the effect of pinealectomy (LL 15 lux) and strong continuous illumination (LL 300 lux), both known to abolish circadian rhythms, on the circadian perch-hopping rhythm and on the circannual rhythm of reproduction and fattening in the same birds. While both pinealectomy and LL 300 lux treatments abolished the circadian rhythm of motor activity, they had no effect on the circannual rhythms of gonadal size and fattening. If the endogenous circadian rhythm in perch-hopping can be taken to reflect the circadian clock mechanism associated with gonadal functioning, present results suggest that circannual rhythm of reproduction in spotted munia is independent of circadian events.     

Hypothesis: cyclical histogenesis is the basis of circannual timing

Circannual rhythms are innately timed long-term (tau ≈ 12 months) cycles of physiology and behavior, crucial for life in habitats ranging from the equator to the Poles. Here the authors propose that circannual rhythm generation depends on tissue-autonomous, reiterated cycles of cell division, functional differentiation, and cell death. They see the feedback control influencing localized stem cell niches as crucial to this cyclical histogenesis hypothesis. Analogous to multi-oscillator circadian organization, circannual rhythm generation occurs in multiple tissues with hypothalamic and pituitary sites serving as central pacemakers. Signals including day length, nutrition, and social factors can synchronize circannual rhythms through hormonal influences, notably via the thyroid and glucocorticoid axes, which have profound effects on histogenesis. The authors offer 4 arguments in support of this hypothesis: (1) Cyclical histogenesis is a prevalent process in seasonal remodeling of physiology. It operates over long time domains and exhibits tissue autonomy in its regulation. (2) Experiments in which selected peripheral endocrine signals are held constant indicate that circannual rhythms are not primarily the product of interacting hormonal feedback loops. (3) Hormones known to control cell proliferation, differentiation, and organogenesis profoundly affect circannual rhythm expression. (4) The convergence point between photoperiodic input pathways and circannual rhythm expression occurs in histogenic regions of the hypothalamus and pituitary. In this review, the authors discuss how testing this hypothesis will depend on the use of cellular/molecular tools and animal models borrowed from developmental biology and neural stem cell research.     

Pinealectomy and LL Abolished Circadian Perching Rhythms but Did Not Alter Circannual Reproductive or Fattening Rhythms in Finches

In the subtropical finch, spotted munia (Lonchura punctulata) circannual rhythms (of gonads, fattening, feeding) have been demonstrated in an information-free environment of continuous illumination (LL), rendering it an ideal model for research on the physiology of the circannual clock. In an attempt to understand the involvement, if any, of the circadian system in the genesis of circannual rhythms, we studied the effect of pinealectomy (LL 15 lux) and strong continuous illumination (LL 300 lux), both known to abolish circadian rhythms, on the circadian perch-hopping rhythm and on the circannual rhythm of reproduction and fattening in the same birds. While both pinealectomy and LL 300 lux treatments abolished the circadian rhythm of motor activity, they had no effect on the circannual rhythms of gonadal size and fattening. If the endogenous circadian rhythm in perch-hopping can be taken to reflect the circadian clock mechanism associated with gonadal functioning, present results suggest that circannual rhythm of reproduction in spotted munia is independent of circadian events.     

Synchronization of circannual cycles: a cold spring delays the cycles of thirteen-lined ground squirrels

Summary Ground squirrels, show circannual cycles with periods normally less than a year when kept under laboratory conditions. The way in which environmental factors synchronize these cycles with the geophysical year under natural conditions is not known. We tested the possibility that cold temperatures can cause long-term phase delays in circannual cycles of thirteen-lined ground squirrels.Two groups of animals were kept in the cold (4 °C) for either 8.5 or 13 months, after which they were returned to the warm (21 °C) and kept there until they had completed at least one additional cycle. A third group was kept in the warm for the entire experiment. Most of the males in the cold room groups became arrested in the spring phase of their cycles while they were in cold. When returned to the warm, these males resumed cycling. When animals showed prolonged spring phases, their cycles were phase-delayed and continued to reflect this delay even after they were returned to the warm. Both body weight cycles and molt cycles were delayed. In contrast to the males in the cold room, none of the females in the cold room groups and none of the warm room animals of either sex showed this response.Our results demonstrate that cold temperatures can phase-delay both body weight and molt cycles and that the spring phase is a critical stage in this effect. We suggest that spring temperatures are largely responsible for the seasonal synchronization of circannual cycles in ground squirrels and are, therefore, a possible Zeitgeber for these cycles.