Some effects of temperature on the hour glass photoperiod timer in the aphid Megoura viciae

“Resonance” experiments conducted at 3 temperatures do not support the view that the Megoura photoperiod (scotophase) timer has an oscillatory component. The main effects of temperature, which are consistent with an hour glass model, have been examined by exposing the aphids to temperatures ranging from −3 to 30°C for the first 4 h of the scotophase, subsequently returning them in each cycle to 15°C for measurement of the critical night length. During the temperature treatments the insects were removed from the plant to avoid indirect effects resulting from changes in the rate of development (this procedure causes a slight shift in the critical night length from 9.5 to 9.0 h). The timer was found to be almost perfectly compensated between 6 and 20°C, but at lower temperatures it runs slow, only one quarter the normal elapsed time being measured at −3°C. At higher temperatures (25 and 30°C) considerable irregularities appear, eventually resulting in the elimination of the critical night length. The results suggest that the timer may sometimes be stopped.Light perception was assessed by cooling the aphids in light. Photoreception was impaired in some individuals at temperatures as high as +6°C and became negligible at −3°C. The illuminated phase was then accepted as a dark interval of equal duration. Yet at this temperature the timer was still operating, albeit slowly. Their differing temperature thresholds point to some degree of separation in these two functions.High-temperature (25°C) experiments with continously feeding aphids showed that although scotophase heating was more effective, there was a distinct response when high temperatures were synchronized with the photophase. This was attributed to the operation of a “photoperiod counter” mechanism.     

Effects of thermoperiods on the reproductive activity of females and on the maternal induction of larval diapause in the blowfly, <Emphasis Type="Italic">Calliphora vicina</Emphasis> R.-D. (Diptera,Calliphoridae)

The interaction of thermoperiod and photoperiod in their influence on the reproductive maturation of females and on the induction of the maternal effect determining larval diapause of the progeny of the blowfly, Calliphora vicina, was first investigated under laboratory conditions. Under the combination of a day length of 12 h with a thermoperiod (the alternation of 12 h long periods with temperatures of 10 and 20°C) the reproductive maturation of females was faster than at the corresponding mean constant temperature of 15°C. Under the “natural” thermoperiod, when the period with a temperature of 10°C coincided with “night-time” (the dark phase of the diurnal light-dark cycle) the maturation of females was slower than that under the “inverted” thermoperiod, when the period with a temperature of 10°C coincided with “day-time” (the light phase of the diurnal light-dark cycle). The proportion of diapausing individuals was maximal in the progeny of females kept at 20°C and decreased with the increase in temperature. Under thermoperiods (the alternations of 12 h long periods with temperatures of 20 and 26°C) the proportion of diapausing progeny was lower than that under the corresponding mean constant temperature of 23°C, but under the inverted thermoperiod with a high night temperature this effect was much stronger. In combination with the results of our previous studies, these data support the hypothesis that the effects of “night” and “day” temperatures are substantially different only when the thermal response interacts with a strong photoperiodic response.     

The photoperiodic control of wing development in the black bean aphid,Aphis fabae

Newly born presumptive gynoparae of Aphis fabae were transferred from their prenatal short-day rearing conditions (light-dark 12:12, 15°C) to a variety of postnatal photoperiodic regimes. Long days prevented wing formation and the majority of aphids developed into apterous or alate-apterous intermediate adults. Continued short days resulted, almost exclusively, in winged adults. The photoperiodic-response curve (T = 24) revealed a critical photoperiod of light-dark 13.5:10.5 and further investigations showed that morphogenesis depended more upon night- than day-length. Maximal apterization occurred with 8 or 9 h dark regardless of the length of the photophase but at photophases of 12 h or less the critical night length was reduced to 8.5 h. Night-interruption experiments revealed two peaks of photosensitivity when the scotophase was 12–14 h long but only a single peak was seen with longer dark periods. A series of experiments using early night interruptions followed by extended dark revealed apparent critical night lengths which decreased as the interruption was placed later in the scotophase. Resonance experiments involving 12 or 16 h photophases and extended scotophases at 15°C revealed long-day effects with scotophases shorter than critical and short-day effects with longer dark periods. However, similar regimes at 20°C produced three peaks of apterization 24 and 20 h apart indicating the possibility of a circadian element involved in the photoperiodic response. The results are compared with the photoperiodic responses of other insects.     

The effect of photoperiod on the calling behaviour of virgin females of the true armyworm,Pseudaletia unipuncta (Haw.) (Lepidoptera: Noctuidae)

The effect of photoperiod on the calling behaviour of Pseudaletia unipuncta virgin females was examined under five different photoperiodic regimes at 25°C, 65% r.h. The age at which females called for the first time following emergence varied with photoperiod; generally calling was later under long-scotophase conditions. However under a 6 h scotophase there was also a delay in calling and >63% of the females tested never called. There was a considerable variability in the daily calling patterns between the different photoperiods, and the mean onset time of calling was not constant with either “lights on” or “light off”. There was however a constancy of the mean onset time of calling relative to the mid-point of both the photo- and scotophase at all photoperiods tested, indicating that females could measure the absolute duration of either the photo- or scotophase. Transferring females from one photoperiodic condition to another once calling had been initiated, determined that it was the “lights off” signal that P. unipuncta females used to phase set the clock governing circadian calling behaviour.Females subjected to a decrease of 4 or 6 h in the length of the scotophase following the initiation of calling required several days to adjust to the new photoperiodic regime and a high proportion of females did not call during the night following the transfer. A 4 or 6 h increase in the scotophase did not inhibit calling on the night following the transfer but females still required several days to adjust completely. However, females experiencing a 2 h increase or decrease in the duration of the scotophase were able to maintain normal calling behaviour. The results of these experiments are discussed in relation to the seasonal biology of the true armyworm and the hypothesis that this is a migrant species.     

Role of phytochrome B in the development of cold tolerance in cucumber plants under light and in darkness

Cold tolerance of cucumber (Cucumis sativus L.) seedlings was investigated using wild-type plants and the phytochrome B-deficient mutant (lh-mutant). Plants were subjected for 6 days to intermittent short-term cooling (12°C for 2 h per day) and to continuous chilling under conditions of 16-h photoperiod (day/night = 16/8 h) and permanent illumination. “Dehardening” process was initiated by the transfer of plants to either light or dark conditions at 23°C. It was concluded that phytochrome B participates in the development of cold tolerance in cucumber plants under stress conditions, i.e., under short-term intermittent chilling at nights and during dehardening in continuous darkness.     

The effects of photoperiod and temperature on calling behaviour and egg development of the bertha armyworm,Mamestra configurata (Lepidoptera: Noctuidae)

The effects of photoperiod and temperature on calling behaviour and the effects of temperature on the relationship between egg development and calling of virgin females of Mamestra configurata Walker were examined at 3 photoperiodic regimes and seven constant temperatures. Photoperiod affected the diel periodicity of calling and length of the daily calling period. The mean onset calling times were similar if the preceding scotophase(s) was 6–10 h long, but the onset of calling was delayed by 1–5 h if the preceding scotophase(s) was 12–18 h long. Long-term, constant temperature (from emergence until death) affected 4 aspects of calling: age at first calling, diel periodicity, length of the daily calling period, and percentage of females calling. Short-term temperature changes (during a single scotophase) affected calling in 3 ways: diel periodicity, length of the daily calling period, and percentage of females calling. The optimal temperature range for calling was, at least, 10–25°C; the upper limit and threshold were near 35 and < 5°C. The time of first calling was synchronized closely with the appearance of the first chorionated eggs in the ovaries at 10–35°C. Egg development and calling were adversely affected at 30 and 35°C. The physiological and ecological significance of the data are discussed.     

Pre-treating paclobutrazol enhanced chilling tolerance of sweetpotato

The objective of this work was to study changes in low molecular weight antioxidants and antioxidative enzymes in chilling-stressed sweetpotato, as affected by paclobutrazol (PBZ) pre-treatment 24 h prior to exposure to chilling conditions. Sweetpotato ‘TN71’ and ‘TN65’ were treated with 300 mg PBZ/5 ml/plant, after which plants were subjected to 7°C/7°C (day/night) for periods of 1, 3 and 5 days, followed by a 3-day recovery period at 24°C/20°C (day/night). A factorial experiment in completely randomized design with four replications was used in this study. Young fully expanded leaves at each temperature and period of time were clipped for antioxidative system measurement. We concluded that different varieties displayed variations in their oxidative system, and the differential expressions of each genotype were associated with chilling stress response. Plants with various antioxidative systems responded differently to chilling stress according to the duration of the chilling period and subsequent re-warming period. ASA, GSH and GSSG contents were enhanced in TN71 prior to chilling stress. Increased APX, GR, ASA and MDA activities accounted for chilling tolerance in TN65. Furthermore, our results indicate that the elevated levels of the antioxidative system observed after PBZ pre-treatments afforded the sweetpotato leaf improved chilling-stress tolerance. The levels of ASA and GSSG of both TN71 and TN65 under chilling were significantly raised by pre-treating with PBZ. PBZ pre-treatment exhibited the important function of enhancing the restoration of leaf oxidative damage under chilling stress and increasing the chilling tolerance of plants to mitigate chilling stress effects.     

Relationships between circadian rhythm of chilling resistance and acclimation to chilling in cotton seedlings

Cotton (Gossypium hirsutum L. cv. Deltapine 50) seedlings grown under light-dark cycles of 12:12h at 35°C showed rhythmic daily changes in chilling resistance. Chilling treatment (5°C, 48h) started at the beginning or middle of the daily light period resulted in a substantial growth inhibition of the seedlings upon return to 35°C whereas when chilling was started at the beginning or middle of the dark period the subsequent growth of the seedlings was much less inhibited. This rhythm in chilling resistance persisted under continuous light for three 24-h periods, indicating that it is of an endogenous nature. Seedlings grown under continuous light from germination showed no daily changes in resistance, but a rhythm was initiated by introduction of a dark period of 6h or longer. In 24-h cycles with different light and dark periods, maximal resistance was reached just before the start of dark period. Seedlings grown at 35°C could be acclimated to chilling by exposure to low, non-damaging temperatures (25–15°C). A short-term (6h) exposure to 25°C started at the resistant phase resulted in a large increase in resistance during the following otherwise sensitive phase. The resistance induced by the low temperature matched or slightly exceeded the maximal resistance reached during the resistant phase of the daily rhythm of chilling. The low-temperature-induced resistance and the daily rhythmic increase in resistance were not additive, indicating a common mechanism for the two kinds of resistances. An adaptive advantage of a combination of a rapid temperature-induced acclimation and the daily rhythmic increase in resistance is suggested.     

Photoperiodic time measurement in the aphid Megoura viciae

Megoura produces parthenogenetic virginoparae in long day conditions, gamic oviparae in short days. The nature of this photoperiodic response has been analysed by rearing parent apterae in a wide range of circadian and non-circadian light cycles. By varying the light and dark components independently in a two-component cycle it has been established that the time measuring function is associated primarily with the dark period. There is no evidence that an endogenous circadian oscillation is implicated: thus (a) the ‘short day’ response is abolished by ‘night interruptions’ positioned in the early or late night. But this bimodal response pattern remains unchanged when the duration of the ‘main’ photoperiod is varied from ca. 6 hr to at least 25·5 hr. The stability of the maxima within the scotophase is inconsistent with the ‘coincidence’ models of photoperiodic timing that have been proposed. It is suggested that the essential timing process operates on the hour-glass principle, beginning anew with the onset of each period of darkness; (b) night interruption experiments employing very long (up to 72 hr) scanned dark periods yielded response maxima explicable in terms of the hour-glass hypothesis but did not reveal any circadian relationship between the maxima.The ‘dark reaction’ comprises a sequence of four stages, definable by the effects of light. Stage 1, extending from dark hr 0 to ca. 2·5, is fully photoreversible: at the next dark period the entire timing sequence is repeated up to the 9·5 hr critical night length. Towards the end of stage 1 reversibility is gradually lost and after a light interruption the reaction is resumed from a later time equivalent than dark hr 0; the subsequent critical night length is therefore reduced. The extent of the photoreversal is related to light duration. The period of maximum light insensitivity (stage 2) is attained at the end of the fourth hour. From ca. dark hr 5 to just short of the critical night length light exerts an increasingly promotive action which favours the production of virginoparae. This dark process is not photoreversible. Stage 4, which begins at hr 9·5, marks the end of the timing sequence. Light will not then annul the non-promotive action of the previous long night.Light has three effects which are determined by its duration and position within the cycle. The two terminal effects, mentioned above, are associated with the interception of dark stages 1 and 3 by either short (1 hr) or longer photoperiods. Light also prepares or primes the dark period timer. Thus the critical length is increased, and timing accuracy lost, if the preceding photoperiod is less than ca. 6 hr. Light during stage 4 has a priming action but no terminal function. Repeated cycles are ‘read’ in various ways, depending on the cycle structure. For example, if light intercepts stage 3, a two-component cycle is interpreted as the overlapping sequence light/dark/light. One and the same photoperiod then acts terminally in respect of the preceding dark period and as a primer for the next dark period.There is also a mechanism for summing the promotive effects produced by repeated interruption of dark stage 3. With complex (four-component) cycles both halves of the same cycle may contribute. ‘Product accumulation’ falls below threshold if the frequency of presentation of a given promotive cycle is too low. This occurs if there are very long, relatively non-promotive dark components. Such cycles are accepted as ‘continuous darkness’.     

Thermoperiod-photoperiod interactions in the determination of diapause in Ostrinia nubilalis

Photoperiodic determination of larval diapause in Ostrinia nubilalis is shown to be strongly influenced by superimposed thermoperiods, here termed “thermophotoperiods.” Thermoperiodic cryophase temperatures (0–25°C) exert effects that are markedly different from responses evoked by thermophotoperiodic cryoscotophases of the same temperatures. The differences are attributed to the presence or absence of light (thermophotophase or thermophase). Perturbations of 12 h dark: 12 h light and 10 h dark: 14 h light photoperiods by low-temperature pulses of 4 h duration demonstrated that the biological clock reactions associated with both the scotophase and photophase are sensitive to temperature. Statistically significant thermoperiod-photoperiod interactions have been demonstrated.     

Photoperiodic and thermoperiodic interactions in the regulation of the larval diapause of Diatraea grandiosella

The effect of various combinations of photoperiod and temperature on the induction and termination of the mature larval diapause of a Missouri strain of the southwestern corn borer. Diatraea grandiosella, was examined. Larval exposure to regimes in which the low phase of a 30°:23°C thermoperiod coincided with a scotophase of 10 to 14 hr duration led to high incidence of diapause. Larval exposure to 30°:24°C, 33°:21°C, and 36°:18°C thermoperiods with half cycles of 12 hr in continuous darkness yielded a diapause incidence of 16%, 22%, and 59%, respectively, whereas exposure to a 30°:24°C thermoperiod in continuous illumination yielded a completely nondiapause generation. Larval exposure to one of a series of 36°:18°C thermoperiods in which the duration of the high phase was increased in 2 hr increments from 0 to 24 hr in continuous darkness showed that “short-day” thermoperiods yielded a high incidence of diapause. However, no clearly defined critical thermoperiod was observed. An examination of photoperiodic and thermoperiodic effects on diapause development showed that, in general, those combinations of temperature and light cycles which were diapause inductive also retarded diapause development. The relationship between seasonal photoperiods and thermoperiods in southeastern Missouri was examined.     

THE EFFECT OF SHORT PERIODS OF HIGH TEMPERATURE DURING DAY AND NIGHT PERIODS ON PEA YIELDS

Karr , E. J. (Ohio State U., Columbus), A. J. Linck , and C. A. Swanson . The effect of short periods of high temperature during day and night periods on pea yields. Amer. Jour. Bot. 46(2) : 91-93. Illus. 1959.—The effect of high temperatures during periods of relatively short duration (3-4 days) at various stages following anthesis at the first bloom node was studied in relation to yield of peas at this node. Except for the periods of differential temperature treatments, the plants were maintained in a standard environment room (24°C., light, 12 hr.; 15°C., darkness, 12 hr.). Three different temperature regimes during the treatment periods were studied: high day temperature—standard night temperature (32°—15°C.) ; standard day temperature—high night temperature (24°—30°C.) ; and high day and night temperatures combined (32°—30°C.). The data reveal the existence of a relatively well-defined thermal-sensitive period, with maximal sensitivity to high day temperatures occurring at about 9-11 days from full bloom, and maximal sensitivity to high night temperatures occurring about 6-9 days from full bloom. High night temperatures proved more critical, resulting in a maximal reduction of 25% in yield, as opposed to about 8% for high day temperatures. The effect of high day and night temperatures combined tended to be roughly additive.     

Diapause Induction and Termination in Hyphantria cunea (Drury) (Lepidoptera: Arctiinae)

The fall webworm, Hyphantria cunea (Drury), enters facultative diapause as a pupa in response to short-day conditions during autumn. Photoperiodic response curves showed that the critical day length for diapause induction was 14 h 30 min, 14 h 25 min and 13 h 30 min at 22, 25 and 28°C, respectively. The photoperiodic responses under non-24 h light–dark cycles demonstrated that night length played an essential role in the determination of diapause. Experiments using a short day length interrupted by a 1-h light pulse exhibited two troughs of diapause inhibition and the effect of diapause inhibition was greater in the early scotophase than in the late scotophase. The diapause-inducing short day lengths of 8, 10 and 12 h evoked greater intensities of diapause than did 13 and 14 h. Diapause can be terminated without exposure to chilling, but chilling at 5°C for 90 and 120 d significantly accelerated diapause development, reduced mortality, and synchronized adult emergence. Additionally, the potential for H. cunea from the temperate region (Qingdao) to emerge and overwinter under field conditions in subtropical regions (Nanchang) of China was evaluated. Pupae that were transferred to Nanchang in early July showed a 60% survival rate and extremely dispersed pupal period (from 12 to 82 days), suggesting that some pupae may undergo summer diapause. Diapausing temperate region pupae that were moved out-of-doors in Nanchang during October showed approximately 20% overwintering survival; moreover, those pupae that overwintered successfully emerged the next spring during a period when their host plants would be available. The results indicate that this moth has the potential to expand its range into subtropical regions of China.     

Membranes of Tetrahymena: III. The effect of temperature on membrane core structures and fatty acid composition of Tetrahymena cells

Membrane core structures as revealed by the freeze-etch electron microscopy and the fatty acid composition measured by gas-liquid chromatography have been analyzed in Tetrahymena cells exposed to low temperature for varying periods.When cells were grown to mid-log phase at the optimal growth temperature of 28 °C and then chilled to 10 °C, cell division was inhibited. However, within 16 h the cells adapted to the low temperature.Chilling effected drastic structural alterations in the cores of different membrane types (membranes of the pellicula, the alveolar sacs, the endoplasmic reticulum and the nuclei). In all cases, there was a segregation of smooth faces from particle-rich faces in the fracture planes. However, the native membrane state, i.e. like that of cells grown at 28 °C, reappeared when the cells adapted to the low temperature.The total lipids of Tetrahymena cells contained primarily even-numbered fatty acids ranging from C₁₂ to C₁₈, but we also detected appreciable amounts of C₂₀ acids; this has not been reported before. During the initial phase of chilling, when cell division is inhibited, about 50% of the saturated fatty acids were replaced by unsaturated fatty acids, primarily monoenoic, dienoic and trienoic acids.We conclude that the structural recovery of the membranes in chilled Tetrahymena cells is accomplished by a desaturation of membrane fatty acids. This is discussed with respect to membrane “fluidity”.     

Effects of lipid-phase separation on the filipin action on membranes of ergosterol-replaced Tetrahymena cells,as studied by freeze-fracture electron microscopy

The effects of lipid-phase separation on the filipin action on pellicle membranes of ergosterol-replaced Tetrahymena pyriformis cells were studied by freeze-fracture electron microscopy. The pellicle membranes with phase separations induced by chilling from 34°C (growth temperature) to lower temperatures (30, 22 and 15°C) were treated with filipin. This produced filipin-induced lesions (“pits”) only in the particulated (liquid) regions along the margin between solid and liquid domains, while they were produced in the particle-free (solid) areas when membranes were chilled to 15°C. The pellicle membranes with lesions induced by filipin at 34°C were chilled to 22°C. This chilling raised larger particle-free areas and more condensed particle-aggregations on the membranes than on the membranes without the filipin treatment. These results suggest that the membrane fluidity affects induction and development of the ergosterol-filipin complex in the membrane.     

Stomatal conductance in Cucumis sativus upon short-term and long-term exposures to low temperatures

We studied stomatal conductance (g_s) in leaves of cucumber plants (Cucumis sativus L., cv. Zozulya) subjected at early developmental stages to either short-term daily cooling (2 h at the end of night periods) or continuous chilling (12°C throughout the day and night). Irrespective of the irradiance during measurements, continuous chilling either lowered g_s or had no effect, as compared to g_s of control plants (23°C). In plants subjected to periodic short-term cooling, the g_s was found to increase at low temperatures both at moderate and high irradiance; it also increased at high temperature (33°C) but only at photosynthetically active irradiance of 800 ??mol/(m² s). It is supposed that heat-loving plants, subjected to different types of low-temperature treatment, mobilize different mechanisms of stomatal regulation and employ different strategies of adaptation in response to low- and high-temperature treatments. The unusual behavior of stomata, manifested in stomatal opening at both low and high temperatures, extends the adaptive potential of plants subjected daily to short-term low-temperature treatments. This leads to a high level of photosynthesis, biomass accumulation, and supports high physiological activity in plants.     

Selenium Modifies the Effect of Short-Term Chilling Stress on Cucumber Plants

The objective of this study was to investigate the effect of selenium (Se) supply (0, control; 2.5, 5, 10, or 20 μM) on cucumber (Cucumis sativus L.) cv. Polan F1 plants grown under short-term low temperature stress. About 14–16 day-old seedlings, grown at an optimal temperature (25/20°C; day/night), were exposed to short-term chilling stress with a day/night temperature of 10°C/5°C for 24 h, for a further 24 h at 20°C/15°C, and then transferred to 25/20°C (re-warming) for 7 days. Se did not affect the fresh weight (FW) of plants at a concentration of 2.5–10 μM, but in the presence of 20 μM Se, the biomass of shoots significantly decreased. The contents of chlorophylls and carotenoids witnessed no significant change after Se supplementation. Compared with the control, the Se-treated plants showed an increase of proline content in leaves, once after chilling and again after 7 days of re-warming. However, proline levels were much higher immediately after chilling than after re-warming. The malondialdehyde (MDA) content in the root of plants treated with 2.5–10 μM Se decreased directly after stress. This was in comparison with the plants grown without Se, whereas it increased in roots and leaves of plants exposed to 20 μM Se. Seven days later, the MDA level in the root of plants grown in the presence of Se was still lower than those of plants not treated with Se and generally witnessed no significant change in leaves. Although Se at concentrations of 2.5–10 μM modified the physiological response of cucumber to short-term chilling stress, causing an increase in proline content in leaves and diminishing lipid peroxidation in roots, the resistance of plants to low temperature was not clearly enhanced, as concluded on the basis of FW and photosynthetic pigments accumulation.     

Effects of growth temperature and winter duration on leaf phenology of a spring ephemeral (Gagea lutea) and a summergreen forb (Maianthemum dilatatum)

Effects of growth temperature and winter duration on leaf longevity were compared between a spring ephemeral, Gagea lutea, and a forest summergreen forb, Maianthemum dilatatum. The plants were grown at day/night temperatures of 25/20°C and 15/10°C after a chilling treatment for variable periods at 2°C. The temperature regime of 25/20°C was much higher than the mean air temperatures for both species in their native habitats. Warm temperature of 25/20°C and/or long chilling treatment shortened leaf longevity in G. lutea, but not in M. dilatatum. The response of G. lutea was consistent with that reported for other spring ephemerals. Air temperature increases as the vegetative season progresses. The decrease in leaf longevity in G. lutea under warm temperature condition ensures leaf senescence in summer, an unfavorable season for its growth. This also implies that early leaf senescence could occur in years with early summers. Warm spring temperatures have been shown to accelerate the leafing-out of forest trees. The decrease in leaf longevity due to warm temperature helps synchronize the period of leaf senescence roughly with the time of the forest canopy leaf-out. Prolonged winter due to late snowmelt has been shown to shorten the vegetative period for spring ephemerals. The decrease in leaf longevity due to long chilling treatment would correspond with this shortened vegetative period.     

Diapause induction and photoperiodic clock in Chilo suppressalis (Walker) (Lepidoptera: Crambidae)

The mature larvae of the rice stem borer, Chilo suppressalis Walker (Lepidoptera: Crambidae) enters facultative diapause in response to short‐day conditions in the autumn (August–September). Diapause induction and photoperiodic clock mechanism were investigated in C. suppressalis larvae reared on an artificial diet in the present study. The critical night length for diapause induction was about 9 h 53 min to 10 h 39 min at 22 to 28°C. The third‐instar larvae were found to be relatively sensitive to diapause induction. Photoperiodic response under non‐24‐h light–dark cycles showed that scotophase length played an essential role in the induction of larval diapause in C. suppressalis, and consecutive exposure to long‐night cycles was necessary for a high diapause incidence. In the Nanda–Hamner experiment, diapause incidence peaked at scotophase of 12 h and dropped rapidly at scotophases > 24 h. In the Bünsow experiment, diapause incidence was clearly suppressed, especially at the light pulse located 8 h in the scotophase. Both the Nanda–Hamner and Bünsow experiments showed no rhythmic fluctuations with a period of about 24 h; thus the photoperiodic clock in C. suppressalis is a non‐oscillatory hourglass timer or a rapidly damping circadian oscillator.