Effect of different light-dark schedules on survival from heart failure

Our earlier work showed that life in constant light prolonged life for hamsters with an inherited cardiomyopathy when compared to littermates spending their lives in 24 hour days (lights on 12 hr each day). This study was designed to begin evaluating the mechanism for this effect. 4-5.5 month old cardiomyopathic hamsters (CMHs) were placed on one of 5 different light-dark (LD) schedules for the remainder of their lives: (1) LD 12:12 (moderate total light exposure, short photoperiodic effect, 24 hr daylength); (2) LD 12:13 (same total light as LD 12:12, long photoperiodic effect, non-24 hr daylength); (3) LD 6:30 (less total light than LD 12:12, long photoperiodic effect, non-24 hr daylength); (4) LD 18:6 (more total light than LD 12:12, long photoperiodic effect, 24 hr daylength); (5) constant light (high total light exposure, long photoperiodic effect, non-24 hr daylength). CMHs living on the first two non-24 hr schedules lived longer than LD 12:12 controls. This study therefore suggests that manipulating the biological clock can have positive therapeutic consequences. However, in contrast to our earlier studies, hamsters living in constant light were not protected--perhaps because the hamsters began the treatment later in their lives or because their inherited disease was less severe than had been the case in hamsters used in previous studies. Defining the conditions that diminish or enhance the photobiological effect is an important challenge for future research.     

Untersuchungen zur Jahresperiodik von Laubs?ngern. II

Zusammenfassung 17 Fitisse und 20 Zilpzalpe aus Südwestdeutschland wurden im Alter zwischen 6 und 11 Tagen aus dem Nest genommen und unter konstanter Tageslichtdauer aufgezogen. Ein Teil der Vögel lebte in einem 12:12-Stunden-Tag, der andere Teil in einem 18:6-Stunden-Tag. Alle Vögel wurden auf Gefiederentwicklung, Jugendmauser, Gewichtsentwicklung und Zugunruhe untersucht.Viele der unter natürlichen Lichtbedingungen beobachteten Vorgänge (Gwinner 1969) traten auch in photoperiodisch konstanten Bedingungen auf. Unterschiede zwischen den beiden Arten blieben im wesentlichen erhalten. Bei beiden Arten waren die Bedingungen des 12:12-Stunden-Tages der artgemäßen Ausprägung des Musters der Jugendentwicklung günstiger als die Bedingungen des 18:6-Stunden-Tages.Die Tageslichtdauer beeinflußte sowohl den zeitlichen Ablauf der untersuchten Vorgänge als auch das Ausmaß mancher Änderungen. Bei beiden Arten begannen und endeten viele Vorgänge im Kurztag früher als unter natürlichen Lichtbedingungen und unter natürlichen Lichtbedingungen früher als im Langtag.Die Tageslichtdauer kann die Jugendentwicklung so modifizieren, daß das Muster der einen Art unter einer Bedingung dem der anderen Art unter einer anderen Bedingung weitgehend entspricht.Die Ergebnisse zeigen, daß die untersuchten Vorgänge sowohl von endogenen Mechanismen als auch von der Tageslichtdauer kontrolliert werden.

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Investigations on annual rhythms in Warblers. IIThe effects of photoperiod on the development of plumage, body weight and migratory restlessness inPhylloscopus trochilus andPh. collybita

Summary 17 Willow Warblers and 20 Chiffchaffs were taken from their nests in southwest Germany and raised under constant photoperiodic conditions. Approximately one half of the birds of each species was kept in a 12-hr photoperiod (LD 12:12), the other half in an 18-hr photoperiod (LD 18:6). Plumage development, postjuvenile molt, and changes in body weight and migratory restlessness were investigated.The typical sequence of processes observed under natural photoperiodic conditions (Gwinner 1969) was also observed under constant photoperiodic conditions. Differences in the pattern of development between the two species were essentially maintained. The behaviour of birds kept in LD 12:12 reflected the natural pattern of behaviour better than that of birds kept in LD 18:6.The photoperiodic conditions modified the age of onset and end of the events investigated as well as their duration. The birds of both species initiated and terminated many events earlier in LD 12:12 than under natural light conditions and under natural light conditions earlier than in LD 18:6.The photoperiodic conditions may modify the sequence of events in such a way that the general pattern representative for one species under one particular photoperiod may be almost identical with the pattern of the other species under another photoperiod.It is concluded that the processes investigated are controlled by endogenous mechanisms as well as by photoperiod.

     

Seasonal Prevalence of Lyme Disease Spirochetes in a Heterothermic Mammal,the Edible Dormouse (Glis glis)

In Europe, dormice serve as competent reservoir hosts for particular genospecies of the tick-borne agent of Lyme disease (LD) and seem to support them more efficiently than do mice or voles. The longevity of edible dormice (Glis glis) and their attractiveness for ticks may result in a predominance of LD spirochetes in ticks questing in dormouse habitats. To investigate the role of edible dormice in the transmission cycle of LD spirochetes, we sampled skin tissue from the ear pinnae of dormice inhabiting five different study sites in south western Germany. Of 501 edible dormice, 12.6% harbored DNA of LD spirochetes. Edible dormice were infected most frequently with the pathogenic LD spirochete Borrelia afzelii. The DNA of B. garinii and B. bavariensis was detected in ca. 0.5% of the examined individuals. No spirochetal DNA was detectable in the skin of edible dormice until July, 6 weeks after they generally start to emerge from their obligate hibernation. Thereafter, the prevalence of spirochetal DNA in edible dormice increased during the remaining period of their 4 to 5 months of activity, reaching nearly 40% in September. Males were more than four times more likely to harbor LD spirochetes than females, and yearlings were almost twice more likely to be infected than adults. The seasonality of the prevalence of LD spirochetes in edible dormice was pronounced and may affect their role as a reservoir host in respect to other hosts.     

Arylalkylamine N-acetyltransferase gene expression in retina and pineal gland of rats under various photoperiods

The present study examines how the circadian oscillators in the retina and the suprachiasmatic nucleus (SCN) respond to changes in photoperiod. Arylalkylamine N-acetyltransferase (aa-nat) gene expression studied by quantitative RT-PCR revealed that in adult Sprague-Dawley rats kept under different light-dark (LD) cycles for two weeks the temporal pattern of AA-NAT mRNA expression was identical in retina and pineal gland. In both tissues, the time span between the onset of darkness and the nocturnal rise in AA-NAT mRNA expression was 3 h under LD 20:4, 6 h under LD 12:12, and 15 h under LD 4:20. As aa-nat expression in the pineal gland is regulated by the circadian oscillator in SCN, the results suggest that the photoperiodic differences accompanying the seasons of the year are imprinted in more than one oscillator and that this may accentuate the important message regarding 'time of year.'     

Infradian cycles in dormice (Glis glis)

Summary Infradian cycles of body weight occur in captive dormice,Glis glis. The period of these cycles is often about 2 months but is highly variable both between and within individuals. These cycles can persist for at least 3 years. This paper describes a number of variables that change on an infradian basis along with body weight. These include: food and water intake, weight of the liver, adrenal and salivary gland weight, testes weight and spermatogenic condition, body temperature and wheel-running activity. Both the amount of running and its distribution over a 24 h period change. However, infradian cycles do not appear to be generated by the circadian system because they persist even in continuous bright light sufficiently intense to disrupt circadian organization. They also persist in LD 186, LD 1212, LD 618 and in naturally changing photoperiods. No evidence of photoperiodic effects on cycles was detected except that animals in long days have slightly higher moulting scores than those in short days. Moulting is more marked when body weight stays relatively stable. In dormice remaining stable in weight for several months testes have sperm present. The period of infradian cycles is temperature dependent: in a cool room animals that hibernate have longer cycles with periods varying from a few months to about a year. In a number of respects at least, infradian cycles appear to be accelerated circannual cycles. The adaptive value of a system that gives rise to infradian cycles probably relates to opportunism in an unpredictable environment. Infradian cycles in dormice may be a useful preparation for obtaining data on spontaneous physiological and behavioural changes in hibernators in less than a year.This work was supported by the Natural Sciences and Engineering Research Council of Canada and by an Ontario Graduate Scholarship to R.M. Many people have helped us in these experiments. We thank: Suzanne Hoy, Jenny Martin, Janice Farintosh, John Glover, Alex Joyner, Michael Juergensen, Harry Meyer, Yasmin Shah, Sara Shettleworth, Wendy Stewart, Vern Thiel, Patricia Williams, and Rae Weaver.     

Formal properties of the circadian and photoperiodic systems of Japanese quail: phase response curve and effects of T-cycles.

A role for the circadian system in photoperiodic time measurement in Japanese quail is controversial. The authors undertook studies of the circadian and photoperiodic system of Japanese quail to try to identify a role for the circadian system in photoperiodic time measurement. The circadian studies showed that the circadian system acts like a low-amplitude oscillator: It is readily reset by light without significant transients, has a Type 0 phase response curve (PRC), and has a large range of entrainment. In fact, a cycle length that is often used in resonance protocols (LD 6:30) is within the range of entrainment. The authors employed T-cycle experiments; that is, LD cycles with 6- and 14-h photoperiods and period lengths ranging from 18 to 36 h to test for circadian involvement in photoperiodic time measurement. The results did not give evidence for circadian involvement in photoperiodic time measurement: T-cycles utilizing 6-h photoperiods were uniformly noninductive (that is, did not stimulate the reproductive system), whereas T-cycles utilizing 14-h photoperiods were inductive (stimulatory). A good match was observed between the phase-angles exhibited on the T-cycles employing 6-h photoperiods and the predicted phase-angles calculated from a PRC generated from 6-h light pulses.     

The effect of temperature on the photoperiodic 'clock' and 'counter' of a Scottish clone of the vetch aphid, Megoura viciae

Photoperiodic response curves were determined for a Scottish clone of the vetch aphid, Megoura viciae Buckton, at three temperatures: 12.5, 15, and 17.5 degrees C. Critical night lengths (CNLs) for ovipara (sexual female) induction were 6 h, 7 h and 8 h, respectively. High incidences of ovipara production were observed in all night lengths longer than the CNL including continuous darkness (DD), as well as in continuous light (LL) at 12.5 and 15 degrees C. At the same three temperatures, the number of long- or short-night cycles required for half of the experimental aphids to be ovipara producers (i.e. the required day number, RDN) was determined. The RDN for long-night cycles (LD12:12) could not be determined at 12.5 degrees C, but was temperature compensated between 15 and 17.5 degrees C. The RDN for short-night cycles (LD20:4) could not be determined at any temperature. However, as induction of oviparae was always 100% in 12.5 degrees C, 94-100% in 15 degrees C and dropped from 100% to between 47 and 71% in 17.5 degrees C, it seems that short-night accumulation was temperature dependent. When fourth-stadium larvae were transferred from LD20:4 at 20 degrees C to the same light-dark cycle at 15 degrees C, the aphids, when adult, switched to the production of oviparae after about 4 weeks. First-born progeny kept in LD20:4 and 15 degrees C switched to the production of oviparae about 7 days after the moult to adult. Thus, the photoperiodic response can be directly affected by temperature, irrespective of photoperiod. Model-generated response curves using the 'double circadian oscillator model' for photoperiodic time measurement (Vaz Nunes, M., 1998. A double circadian oscillator model for quantitative photoperiodic time measurement in insects and mites. Journal of Theoretical Biology 194, 299-311) closely resembled the observations. Differences between these data and the results of previous experiments with an English clone of M. viciae could be accounted for by differences in the photoperiodic clocks (damping rate and period) as well as the photoperiodic counters.     

Aging and photoperiod affect the daily rhythm pattern of atrial natriuretic peptide in the rat atrium

This study investigates the release characteristics of atrial natriuretic peptide (ANP) from young (10 weeks) and old (22 months) rat atrium. Levels of ANP release from samples of atrium were studied by organ perifusion. Rats were exposed to light:dark (LD) cycles of 12:12 or 18:6 and sacrificed at different zeitgeber time (ZT) points: ZT0, ZT6, ZT8, ZT12, ZT16, and ZT19 for LD 12:12 or ZT0, ZT9, ZT16, ZT18, ZT20, and ZT 21.5 for LD 18:6. The heart was collected, and the right atrium was removed, weighed, and perifused with Krebs-bicarbonate buffer for 100 min, including a period of 50 min for stabilization of secretion rate. ANP concentrations released by atrium did not differ between the two age groups either under LD 12:12 or under LD 18:6, except at the light:dark transition under LD 12:12 conditions where ANP levels were significantly (P < 0.05) lower in young compared to old rats. ANP exhibited daily variations in concentrations under LD 12:12, with a peak during the beginning of photophase (ZT0) in young rats and a peak at the beginning of scotophase (ZT12) in old animals. These variations were strongly modified under LD 18:6, where the pattern of the release exhibited a peak during the light phase at ZT16 in both young and old rats. This strongly suggests that the atrial ANP rhythm is dependent on the environmental light:dark cycle. Moreover, the total ANP levels released by atria in old rats were significantly increased under LD 18:6 compared to standard LD 12:12. This observation strongly suggests that old animals are more sensitive to a photoperiodic change. In conclusion, our results show that ANP concentrations in the rat atrium exhibit daily variations which are significantly affected by the daylength (photoperiod) change in aged rats.     

Photoperiodic induction of diapause in the spider mite Tetranychus urticae: qualitative or quantitative time measurement?

Abstract. Insects and mites may measure photoperiods eitfier by classifying them as long or short relative to a critical value (qualitative time measurement) or by using the absolute value (quantitative time measurement). The spider mite Tetranychus urticae is thought to use a qualitative mechanism of time measurement. In this paper we present the results of experiments with an inbred line of the spider mite (to keep genetic variation in photoperiodic responses small), to test whether quantitative aspects also play a role. Differences in diapause incidence in different long-night photoperiods at different temperatures may be an indication of quantitative responses to photoperiod. The effect of temperature on the photoperiodic response curve was studied at 16^oC, 19^oC and 22^oC. The response curves appeared to be similar at 16^oC and 19^oC, with a critical nightlength between 10 and 11 h. At 22^oC, diapause induction was less than 100% in all long-night regimens and die critical nightlength had shifted to 12 h. Maximum diapause induction (93%) occurred in a light-dark cycle with a 16 h dark phase (LD 8:16 h). Diapause induction was lowest in long-night photoperiods with dark phases of 20 h and longer. The number of light-dark cycles needed for 50% diapause induction at 19^oC varied. between 12.1 and 14.7 for LD 6:18 h, between 10.9 and 12.5 for LD 8:16 h, between 10.6 and 11.6 for LD 10:14 h, and between 10.1 and 10.7 for LD 12:12 h. Independent of die light-dark regimen, diapause induction took place in some individuals after receiving 8 cycles and virtually all individuals entered diapause after 16 cycles. No effect was found of the photoperiodic treatment during prediapause development (LD 6:18 h, LD 8:16 h, LD 10:14 h, LD 12:12 h) on diapause duration. The average diapause duration at LD 10:14 h and 19^oC was 61 days over all four treatments. We explained the results by hypothesising that nightlengths are assessed qualitatively and mat the photoperiodic clock operates more accurately near the critical nightlength.     

Circadian participation in the photoregulation of testis activity and prolactin secretion in the mink, a short-day breeder

It has been demonstrated that an endogenous mechanism is involved in photoperiodic time measurement in the mink, a short-day-breeding mannal. A study of testicular activity (testicular volume, plasma testosterone concentration) and plasma prolactin level was carried out in sexually resting minks (the experiment began in November). Groups of minks were kept in the natural photoperiod or subjected to different resonance light-dark (LD) cycles (LD 4:8, LD 4:20, LD 4:32, LD 4:44); an additional group of animals was reared in an ahemeral photoperiod (LD 4:16). A rapid increase of testicular activity was observed in control animals or those kept in LD 4:20 (T 24) and LD 4:44 (T 48). In the other groups of animals, those kept in LD 4:8 (T 12), LD 4:32 (T 36), and LD 4:16 (T 20), testicular function remained at rest. Prolactin secretion was, in contrast, stimulated in the groups kept in LD 4:8 (T 12). LD 4:32 (T 36), and LD 4:16 (T 20), and remained low in the groups kept in LD 4:20 (T 24) and LD 4:44 (T 48). These results show that the effects of the different photoperiodic regimens do not depend on the duration of the photophase, but rather on the period of the LD cycles. The LD cycles that allow an increase of testicular function are those that are inhibitory to reproduction in birds and long-day-breeding mammals. To explain these results, it is suggested that in the mink exposure to light during the circadian photosensitive phase induces inhibition of testicular activity and stimulation of prolactin secretion. To explain the opposite effects of a single photoperiod on testicular function and secretion of prolactin, the hypothesis has been advanced that, in the mink, long days might simultaneously inhibit hypothalamic luteinizing-hormone-releasing hormone (LH-RH) activity and prolactin-inhibiting factor (PIF) activity.     

Responsiveness to photoperiodic changes in the circannual rhythm of the varied carpet beetle, <Emphasis Type="Italic">Anthrenus verbasci</Emphasis>

The circannual pupation rhythm of Anthrenus verbasci is entrained to an environmental cycle by changes in photoperiod. Exposure of larvae reared under short-day conditions to 4 weeks of long days can induce phase-dependent phase shifts. In the present study, we examined the range of photoperiodic changes effective for phase shifts at 20°C. For larvae under light/dark (LD) 12:12 conditions, 4-week exposure to LD 14:10 caused a clear phase delay, as great an extent as that brought about by exposure to LD 15:9 and LD 16:8. In contrast, the delay brought about by exposure to LD 13:9 was slight. For larvae under LD 10:14, exposure to LD 14:10 and LD 16:8 for 4 weeks induced a phase delay, but exposure to LD 12:12 did not. These results indicate that a clear phase delay is induced when the photoperiodic change exceeds a critical value in the photophase between 13 and 14 h, regardless of the amplitude of the change. Although phase advances were smaller than phase delays, they depended on the amplitude of photoperiodic changes rather than the absolute photophase duration in contrast to the case of the phase delay.     

A comparison of photoperiodic control of diapause between aestivation and hibernation in the cabbage butterfly Pieris melete

In the cabbage butterfly, Pieris melete, summer and winter diapause are induced principally by long and short daylengths, respectively; the intermediate daylengths (12-13 h) permit pupae to develop without diapause. In this study, photoperiodic control of summer and winter diapause was systematically investigated in this butterfly by examining the photoperiodic response, the number of days required to induce 50% summer and winter diapause and the duration of diapausing pupae induced under different photoperiods. Photoperiodic response curves at 18 and 20 degrees C showed that all pupae entered winter diapause at short daylengths (8-11 h), the incidence of diapause dropped to 82.3-85.5% at 22 degrees C without showing a significant difference between short daylengths, whereas the incidence of summer diapause induced by different long daylengths (14-18 h) was varied and was obviously affected by temperature. By transferring from various short daylengths (LD 8:16, LD 9:15, LD 10:14 and LD 11:13) to an intermediate daylength (LD 12.5:11.5) at different times after hatching, the number of cycles required to induce 50% winter diapause (7.28 at LD 8:16, 7.16 at LD 9:15, 7.60 at LD 10:14 and 6.94 at LD 11:13) showed no significant difference, whereas by transferring from various long daylengths (LD 14:10, LD 15:9, LD 16:8 and LD 17:7) to an intermediate daylength (LD 12.5:11.5) at different times, the number of cycles required to induce 50% summer diapause (5.95 at LD 14:10, 8.02 at LD 15:9, 6.80 at LD 16:8, 7.64 at LD 17:7) were significantly different. The intensity of winter diapause induced under different short daylengths (LD 8:16, LD 9:15, LD 10:14 and LD 11:13) was not significantly different with an average diapause duration of 87 days at a constant temperature of 20 degrees C and 92 days at a mean daily temperature of 19.0 degrees C, whereas the intensity of summer diapause induced under different long daylengths (LD 14:10, LD 15:9, LD 16:8 and LD 17:7) was significantly different (the diapause duration ranged from 75 to 86 days at a constant temperature of 20 degrees C and from 76 to 88 days at a mean daily temperature of 19.0 degrees C). All results suggested that photoperiodic control of diapause induction and termination is significantly different between aestivation and hibernation.     

Further demonstration of the ambient temperature dependence of the annual biological cycles in the edible dormouse,Glis glis

Summary In the male edible dormouse, it has been proposed that the annual temperature cycle is the major external factor triggering annual biological rhythms in this hibernating species. The present study was designed to explore (i) the effects of suppression of the annual thermoperiodic cycle under natural photoperiodic conditions, and (ii) the effects of acute exposure to a warm environment on basal plasma T4 levels observed during hibernation. The results of the first experiment demonstrate an absence of circannual cycles of hibernation, body weight, and endocrine thyroid and gonadal functions in the absence of annual fluctuations of temperature (constant warm environment at 24°C) despite the maintenance of a normal photoperiodic cycle. On the other hand, acute exposure to 24°C during the late stage of hibernation stimulated thyroid function as expressed by a consistent transitory rise in plasma T4 concentrations, which was maximal within 7 days and restored to basal levels after 14 days. These findings are in close agreement with the concept that in the edible dormouse, the annual thyroid cycle is synchronized with the annual temperature cycle. Moreover, the present study, combined with prior data indicating that the thyroid cycle induces the testis cycle, suggests that the ambient temperature cycle may be intricately involved in the control of neuroendocrine cycles in dormice, although the mechanism is still unknown.     

The effect of allatectomy and photoperiod on the supercooling point in Pyrrhocoris apterus adults

Abstract Adults of Pyrrhocoris apterus (L.) (Heteroptera: Pyrrhocoridae) reared at 26°C had a considerably lower supercooling point (SCP) in diapause-inducing (LD 12:12 h) than in diapause-inhibiting (LD 18:6 h) photoperiodic regimes. Exposure of the insects to diapause-inducing acclimation conditions (LD 8:16 h and a temperature of 20°C during photophase and 5°C during scotophase) for 2–3 weeks had very little effect on the SCP, irrespective of the rearing photoperiod. Allatectomized adults kept continuously at LD 18:6 h and 26°C had high SCP similar to intact or sham-operated insects. In contrast to non-allatectomized insects, the SCP of allatectomized insects decreased after an exposure of from 2 to 3 weeks to diapause-inducing acclimation conditions (see above) almost to the level found in the intact diapausing insects. The relationship between the decrease of SCP and ‘diapause syndrome’ (de Wilde, 1970) is discussed.     

Induction and termination of prepupal summer diapause in Pseudopidorus fasciata (Lepidoptera: Zygaenidae)

The seasonal life cycle of the zygaenid moth, Pseudopidorus fasciata is complicated by two different developmental arrests: a winter diapause as a fourth larval instar and a summer diapause as a prepupa in a cocoon. Both larval diapause induction and termination are under photoperiodic control. Short days induce larval diapause with a critical daylength of 13.5h and long days terminate diapause with a critical daylength of 14h. In the present study photoperiodic control of summer diapause was investigated in Pseudopidorus fasciata. Under long photoperiods ranging from LD 14:10 to LD 18:6, only part of the population entered summer diapause, the rest continued to develop. The lowest number of prepupae entered diapause at LD 14:10, followed by LD 16:8 and LD 17:7. The highest incidence of diapause occurred with photoperiods of LD 15:9 and LD 18:6. By transferring the diapausing prepupae induced by various long photoperiods (LD 14:10, LD 15:9, LD 16:8, LD 17:7, LD 18:6) to LD 13:11, 25 degrees C, the duration of diapause induced by LD 14:10 was significantly shorter than those induced by longer photoperiods. By keeping aestivating prepupae induced by LD 15:9, 28 degrees C or by natural conditions at short photoperiods (LD 11:13 and LD 13:11) and at a long photoperiod (LD 15:9), the duration of diapause at LD 15:9 was more than twice as long as than those at LD 11:13 and LD 13:11. Moreover, adult emergence was highly dispersed with a high mortality at LD 15:9 but was synchronized with low mortality at LD 11:13 and LD 13:11. When the naturally induced aestivating prepupae were kept under natural conditions, the early aestivating prepupae formed in May exhibited a long duration of diapause (mean 126 days), whereas the later-aestivating prepupae formed in July exhibited a short duration of diapause (mean 69 days). These results indicate that aestivating prepupae require short or shortening photoperiod to terminate their diapause successfully. By transferring naturally induced aestivating prepupae to 25, 28 and 30 degrees C, the duration of diapause at the high temperature of 30 degrees C was significantly longer than those at 25 and 28 degrees C, suggesting that high temperature during summer also plays an important role in the maintenance of summer diapause in Pseudopidorus fasciata. All results reveal that summer diapause can serve as a "bet hedging" against unpredictable risks due to fluctuating environments or as a feedback mechanism to synchronize the period of autumn emergence.     

The effect of temperature and light pulses on the induction of diapause in the Toyama strain of the Indian meal moth, Plodia interpunctella

Abstract.The photoperiodic response in Plodia interpunctella collected at Toyama (36.7°N) was of long-day type and highly sensitive to temperature. The critical photoperiod giving 50% diapause was between 14 and 16 h at 20°C, between 12 and 14 h at 25°C and between 6 and 8 h at 30°C. Effects of night interruption by a 2-h light pulse on the diapause response were examined at 25°C on different background photoperiods ranging from LD 12:12 h to LD 2:22 h. Percentage diapause was very low when the middle portion of dark period was interrupted, so that U- or V-shaped response curves were obtained with background scotophases longer than 12 h. In these curves, the descending slopes were less steep than the ascending slopes. The critical dark period measured from dusk to an interrupting light pulse was about 1.5 h longer than the critical dark period ( c . 10 h) in the normal photoperiodic response. The critical dark period from the interrupting light pulse to dawn, on the other hand, was not parallel to dawn but shorter than the normal critical period in LD 12:12 h and LD 10:14 h and longer than that in LD 7:17 h to LD 4:20 h, indicating that the priming effects of the light pulse might be under the influence of the photophase.     

Description of the Photoperiodic Control of Larval Burrowing in the Blowfly Lucilia Cuprina: a Novel Index for Photoperiodic Research

The photoperiodic control of larval burrowing depth in the Australian sheep blowfly Lucilia cuprina (Wiedemann) (Diptera: Calliphoridae) was investigated by measuring burrowing depth under controlled laboratory photo-periods. The results demonstrated that larvae exposed to long photoperiods (LD 18:6) burrowed to deeper depths than those in shorter photoperiods (LD 12:12), and that this behavior was induced during the third instar stage. The ecological significance of this behavior is discussed, as are the ways in which daylength is measured and depth assessed. The use of burrowing depth could prove to be a novel index of a photoperiodic response and provide a far simpler approach to the study of photoperiodism in certain insect species. (Chronobiology International, 14(3), 247–252, 1997)     

Life cycle regulation in the heather psyllid Strophingia ericae : responses to temperature and photoperiod

Abstract .The response of overwintering nymphs of Strophingia ericae (Curtis) (Homoptera: Psylloidea) to long and short photoperiods over a range of temperatures was investigated to determine the interaction between these factors and winter development as a regulatory mechanism of their life cycle. Strophingia ericae was successfully reared from egg to adult in a long photoperiod (LD 18:6 h) at 10, 15 and 20°C on its host plant Calluna vulgaris. Although development time was longer at 10 than at 15 or 20°C (≈ 263 days compared with ≈ 155 and ≈ 159 days, respectively), there was no interruption in development at any of these temperatures, indicating that there was no obligatory diapause. However, short photoperiod (LD 12:12 h) inhibited development of overwintering fifth instars collected from the field in early winter. Those collected in September and kept at 15°C developed to adult in ≈ 120 days in a short photoperiod (LD 12:12 h) compared with ≈ 40 days in a long photoperiod (LD 18:6 h). Inhibition became weaker in December and disappeared by January, when fifth instars developed to adult at the same rate in both long and short photoperiods (≈ 30 days). A similar photoperiodic response was observed when the experiment was repeated at 10°C, although development times were consistently longer. The observation that insects collected from the field in early winter were able to resume development immediately on transfer to favourable conditions (15°C and LD 18:6 h photocycle) suggests that there is a photoperiodically induced quiescence (rather than a true diapause) in overwintering S. ericae, which becomes progressively reduced as winter proceeds. It was concluded that the life cycle of the upland and possibly the lowland form of S. ericae is regulated by a winter-active photoperiodic inhibition of development, which effectively synchronizes the emergence of the adult stage with higher spring temperatures and renewed host plant growth.     

Circadian rhythm of locomotor activity in the Japanese honeybee, Apis cerana japonica

Abstract.  To reveal circadian characteristics and entrainment mechanisms in the Japanese honeybee Apis cerana japonica , the locomotor-activity rhythm of foragers is investigated under programmed light and temperature conditions. After entrainment to an LD 12 : 12 h photoperiodic regime, free-running rhythms are released in constant dark (DD) or light (LL) conditions with different free-running periods. Under the LD 12 : 12 h regime, activity offset occurs approximately 0.4 h after lights-off transition, assigned to circadian time (Ct) 12.4 h. The phase of activity onset, peak and offset, and activity duration depends on the photoperiodic regimes. The circadian rhythm can be entrained to a 24-h period by exposure to submultiple cycles of LD 6 : 6 h, as if the locomotive rhythm is entrained to LD 18 : 6 h. Phase shifts of delay and advance are observed when perturbing single light pulses are presented during free-running under DD conditions. Temperature compensation of the free-running period is demonstrated under DD and LL conditions. Steady-state entrainment of the locomotor rhythm is achieved with square-wave temperature cycles of 10 °C amplitude, but a 5 °C amplitude fails to entrain.     

Effect of light pulses in early scotophase on resetting of the night-measuring diapause clock of the Indian meal moth, Plodia interpunctella

Abstract.  The Indian meal moth, Plodia interpunctella Hübner (Lepidoptera: Pyralidae) may enter diapause in the last larval instar in response to the photoperiod during the preceding instars. An hourglass-type photoperiodic clock may measure night length for this purpose. The present study describes the resetting of the hourglass by light pulse(s) in the early scotophase and by scanning the subsequent clock phase by another light pulse (P). When the lights-off time of a first light pulse is fixed at 4 h after dusk under LD 4 : 20 h and LD 6 : 18 h photoperiods and its duration is increased from 1 to 3 h, the critical night length (CNL) from dawn is decreased, but that from dusk to P increases. A 3-h first light pulse efficiently resets the time measuring system. If this 3-h light pulse is split into two 1-h light pulses (L₁ and L₂) by 1 h of darkness, the dark-time measuring function appears to be impeded and CNL from P to dawn disappears, but that from L₂ to P is expressed. This indicates that the receptivity to light pulses varies among individual insects.