Induction and termination of diapause inOrius predatory bugs

Photoperiodic induction of reproductive diapause at 18°C was investigated in fourOrius [Heteroptera: Anthocoridae] species.Orius insidiosus (Say) displayed a long-day response with a critical photoperiod between L11:D13 and L12:D12. Diapause in this species was terminated rapidly when the temperature and/or the daylength were increased.Orius majusculus (Reuter) also displayed a long-day response. The critical photoperiod fell between L14:D10 and L16:D8. Diapause in this species was not terminated within 14 days when both temperature and daylength were increased. InOrius albidipennis (Reuter) no diapause could be induced at photoperiods varying from L8:D16 to L16:D8. InOrius tristicolor (White) a high proportion of diapause was found at all photoperiods tested. The effect of temperature on photoperiodic induction of diapause was studied inO. insidiosus at L10:D14. Diapause occurred at 18°C, 21°C and 25°C, but not at 30°C. Again, diapause was terminated rapidly after transfer to 25°C/L16:D8. Exposing only the nymphal instars 1–5 to short daylength was not enough to induce diapause in the whole population ofO. majusculus. Orius predatory bugs are used as biocontrol agents against western flower thrips,Frankliniella occidentalis (Pergande) [Thysanoptera: Thripidael, in greenhouses. The consequences of photoperiodic induction of diapause for the success of early season releases ofOrius are discussed.     

Sexual difference in the photoperiodic induction of pupal diapause in the flesh fly Sarcophaga similis

The flesh fly Sarcophaga similis enters pupal diapause in response to short days, but averts diapause under long days. This species shows a sexual difference in the photoperiodic induction of diapause, with females having shorter critical daylength than males. Here, we proposed two hypotheses to explain this sexual difference. First, we proposed a sexual difference in the qualitative evaluation of photoperiods. This hypothesis assumes under the external coincidence model that although the photoinducible phase of both sexes locates at late scotophase, in males, it locates at a slightly earlier phase. However, the results of night interruption experiments clearly ruled out this hypothesis. Because we verified that S. similis evaluated photoperiods quantitatively, we next proposed a sexual difference in the quantitative evaluation of photoperiods. This hypothesis incorporates concepts of a hypothetical substance accumulation that shows a diapause‐inducing effect and an internal threshold that serves as a reference to determine the diapause/nondiapause developmental program. In long‐day exposure experiments and night interruption experiments, females consistently showed a lower incidence of diapause than males. Thus, the present study data satisfactorily meet the second hypothesis, that is a sexual difference in the quantitative evaluation of photoperiods exists in S. similis.     

温度和光周期对绿盲蝽滞育诱导的影响

为了阐明环境因子对绿盲蝽Apolygus lucorum Meyer-Dür卵滞育诱导作用,测定了3个温度和6个光周期组合处理对绿肓蝽的滞育诱导和绿盲蝽光周期感应的敏感虫态,系统调查了绿肓蝽在不同温度和不同光照组合下所产卵的孵化率.结果表明:绿盲蝽的敏感虫态为1龄若虫;在17℃,20℃和23℃3个不同温度下,光照时间小...     

Photoperiodic induction of larval diapause and temperature-dependent termination in a wild multivoltine bruchid,Kytorhinus sharpianus

A wild bean weevil,Kytorhinus sharpianus Bridwell (Coleoptera: Bruchidae), has a multivoltine life cycle and enters a hibernal larval diapause at the fourth instar under a short daylength (Shimada & Ishihara, 1991). Here, we investigated their diapause incidence under different photoperiods at 24°C and 27°C. The critical photoperiods for diapause induction were 14.5 h at 24°C and 14 h at 27°C. The stages susceptible to diapause-inducing stimuli were estimated by transferring larvae of various instars from long days to short days and vice versa. Then we investigated the incidence of larval diapause. The sensitive stage was estimated to be from the third to early fourth instar. Though larval diapause, which was induced under a short daylength, was terminated only by increasing the daylength, the termination was more synchronized by an exposure to a low temperature followed by increasing temperature, irrespective of photoperiod.     

Factors governing the induction of diapause in Ephestia elutella and Plodia interpunctella (Lepidoptera)

Diapause in fully grown larvae of Ephestia elutella and Plodia inferpunctella was induced by low temperature and short photoperiods. Light intensities below 1 lx affected the induction of diapause in both species. At 20 and 25d?C, the critical photo-period for E.elutella was c. 14 h, and for P.interpunctella c. 13 h. The sensitive phase in both species occurred at about the time of the fourth larval moult. In E.elutella about seven short photoperiods were required for larvae to enter diapause. In P.interpunctella high population density during larval development increased the proportion of larvae entering diapause. The conditions inducing diapause in laboratory stocks, and in stocks collected from the field, were different. Laboratory stocks of both species did not enter diapause at 25d?C and required short photoperiods for diapause at 20d?C. Some larvae of the field stock of E.elutella entered diapause in constant darkness at 30d?C, the number being increased at low R.H., and almost all did in short photoperiods at 25°C. At 20T, most larvae of this stock entered diapause regardless of photoperiod, and at 15°C all did. In P.interpunctella up to one-third of larvae of the field stock entered diapause in short photoperiods at 25d?C, and all did if transferred to short photoperiods at 20d?C. In unheated premises, falling temperatures normally induce diapause in E.elutella each autumn, photoperiod only being important if temperatures are high. In P.interpunctella, photoperiod is a more important factor because it can override the effect of falling temperature to a greater extent than in E.elutella. In both species, however, different field populations may respond in different ways.     

Photoperiodic control of larval development in the semivoltine cockroachPeriplaneta japonica (Blattidae: Dictyoptera)

Periplaneta japonica is semivoltine, entering early diapause in any (except the first) larval instar before the last, and late diapause in the last instar. Early diapause was induced under a short day of 13 h or less at 28°C, and under both short and long daylength (12–16 h) at 20°C. The shorter the daylength and the lower the temperature, the younger the instar was entering early diapause. Early diapause was terminated by a long day (16 h) or a high temperature (28°C), after which larvae grew faster in short days than in long days until the last instar, when they again entered diapause, always in short days and frequently in long days. This late diapause was terminated also by an increase in daylength and was always followed by adult emergence. In this case, 13 and 14 h daylengths after exposure to 12 h daylength were as effective as 16 h daylength. Ourdoor samples collected in late autumn, winter and early spring at Hirosaki (40.5°N) comprised two distinct size groups, corresponding with the early and late diapause instars. Based on these results, the seasonal development strategy and intriguing aspects of the photoperiodic response in this cockroach are discussed.     

Some aspects of induction and termination of diapause in a Greek strain of the miteTetranychus cinnabarinus (Boisduval) Boudreaux, 1956 (Acari: Tetranychidae)

A Greek strain of the miteTetranychus cinnabarinus, collected from ivy (Hedera spec.) in Thessaloniki (41 °N), exhibits a facultative, imaginal diapause. Diapause is induced by photoperiod and the photoperiodic response is of the long-day type. The critical daylength is 12.5 h at 19 °C. A period of chilling is not necessary for the termination of diapause under long-day conditions. Diapausing females are sensitive to photoperiod at least during the first 11/2 month of diapause.     

Effects of photoperiod and low temperature on diapause termination in the yellow-spotted longicorn beetle (Psacothea hilaris)

Abstract. .The effects of photoperiod and low temperature on diapause termination in the yellow-spotted longicorn beetle, Psacothea hilaris (Pascoe) (Coleoptera: Cerambycidae), were examined using a population from Ino, Japan. Diapausing insects obtained by rearing larvae under short daylength (12 or 13 h) at 25^oC were subjected to various treatments. When the photoperiod was changed at the same temperature, diapausing larvae showed a long-day response with a critical daylength between 13.5 and 14h. The diapause was terminated and consequently pupation occurred if the daylength was longer than 13.5 h. Chilling the diapausing larvae at 10^oC for 30 or more days also terminated diapause in most larvae irrespective of the photoperiods during and after chilling treatment. In contrast, the post-chilling photoperiod had a critical effect on development of diapausing larvae chilled for only 15 days.     

Developmental requirements of the univoltine species Chrysopa downesi: Photoperiodic stimuli and sensitive stages

Chrysopa downesi reproduces only in the spring and the resulting adults enter an aestival-autumnal-hibernal diapause which is primarily controlled by photoperiod. In the laboratory, constant photoperiods result in diapause induction and maintenance, whereas a series of short days followed by long days prevents or terminates diapause and promotes reproduction. The stages most sensitive to the diapause-averting stimulus are the free-living third instar, the third instar within the cocoon, and the pupa.C. downesi responds in different ways to three aspects of photoperiod: (a) an all-or-none response (diapause prevention or induction) to a sequence of two critical photoperiods, (b) an all-or-none response (diapause prevention or induction) to the difference between the long and short daylengths (a 4 hr difference is sufficient to avert diapause but a 2 hr difference is not), and (c) a quantitative response to the absolute duration of day (or night) length (after the short day requirement is fulfilled the rate of diapause termination is related to daylength).Differences and similarities in phenological adaptations and in photoperiodic responses of C. downesi, C. carnea, and C. harrisii reflect the degree of phylogenetic relationship between these closely related species.     

Effect of photoperiod on a winter and on a summer diapause in two species of cranefly (Tipulidae)

Two craneflies, Tipula subnodicornis and Tipula pagana, both undergo diapause in the final larval instar. The species showed differences in the intensity of diapause and in the timing of the photoperiodic reaction during diapause, that could be related to season. Tipula subnodicornis undergoes a winter diapause that is induced and maintained in its early stages by short photoperiod (L:D:6:18). In the laboratory individuals in the early stages of diapause terminated diapause and pupated earlier when they were exposed to daylengths of, or greater than, 12 hr. However, it is suggested that in the field diapause is broken before the natural daylength is long enough to have any accelerating effect on development. Tipula pagana has a summer diapause which is of greater intensity than that of Tipula subnodicornis and some larvae were maintained for 197 days in the laboratory, without pupating, on an 18 hr daylength. Diapause was broken by a L:D;16:8 photoperiod and development was accelerated by a further decrease in daylength. The acceleration in development rate was attended by a decrease in the variance about the mean date of emergence and resulted in a highly synchronised emergence period. It is suggested that this quantitative response to daylength is particularly important to a species that emerges in the autumn when the temperature in the field is falling.     

Photoperiodism and control of summer diapause in the Mediterranean tiger moth Cymbalophora pudica

Photoperiodic responses to both constant and changing photoperiods were studied in the Mediterranean tiger moth Cymbalophora pudica. Embryos, larval instars and prepupae were all sensitive to photoperiod, and the responses of larvae and prepupae to changing photoperiods were similar. At 23+/-2 degrees C, constant 24-h photoperiods with short photophases (11, 12h) induced a long diapause (mean 88days) whereas long photophases (14, 16h) induced a short diapause (mean 52days). A change to a longer or shorter photophase during larval development or during diapause caused a significant extension (up to a maximum of 138days) or shortening (down to a minimum of 10days) of diapause, respectively, but only when at least one of the photophases was longer than 14h. Thus, shortening and prolongation of photophase had an opposite effect than constant short and long photophases, respectively. Changes within the range of photophases of 10-14h did not cause a significant change in diapause duration.Experimental results enabled us to outline the mechanisms regulating voltinism and the duration of summer diapause. For the monovoltine cycle, cold autumn/winter temperatures slow down larval development, and prepupal aestivation starts relatively late (March, April). Prepupae are then kept in diapause by the increasing daylength (>14h after late April). Pupation is synchronized by decreasing daylength after summer solstice, and imagoes emerge in September/October. For the bivoltine cycle, when the autumn/winter temperatures are relatively warm, a certain portion of the population (depending on the individual rate of growth) may be diverted to a bivoltine life-cycle. In such a case, larval development is fast and short enough to allow an early start of diapause (prior to or during February). The duration of such early diapause is not influenced by changes in daylength (<14h); pupation occurs very early (April/May), and spring generation imagoes fly and oviposit in May/June. Summer larvae and prepupae live under decreasing daylength (>14h), which shortens their diapause to 20-30days. Imagoes of the autumnal generation thus occur in September/October, together with the univoltine portion of the population.     

Diapause termination in the spotted stem borer, Chilo partellus (Lepidoptera: Pyralidae) in the laboratory

The effect of temperature, photoperiod, artificial diet and water on the termination of diapause by larvae of the stem borer, Chilo partellus (Lepidoptera: Pyralidae), was studied in the laboratory. Termination of diapause as indicated by pupation was affected mainly by a combination of high temperature and a long day photoperiod. Total darkness did not prevent termination of diapause and pupation occurred also in larvae which were never exposed to water. Long days accelerated pupation, but, under 16 h daylength, termination of diapause was faster than under constant illumination. Provision of artificial diet had no effect or slowed down pupation but water decreased the time to pupation. Under 28°C, 16 h daylength and availability of water, C. partellus diapausing larvae terminated diapause and pupated in about 9 days.     

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.     

Diapause and seasonal life cycle strategy in the house spider, Achaearanea tepidariorum (Araneae, Theridiidae)

Abstract In order to elucidate the mechanism regulating its seasonal life cycle, the photoperiodic response of Achaearanea tepidariorum has been analysed. Nymphal development was faster in long-day and slower in short-day photoperiods. The combined action of low temperature, poor food supply and short daylength induced diapause at an earlier developmental stage than short days alone. Thus, photoperiod is a primary factor inducing nymphal diapause, but the diapausing instar is influenced by both temperature and food supply. Hibernating nymphs became unresponsive to photoperiod in late December. After hibernation, however, sensitivity was restored and the nymphs remained sensitive to photoperiod throughout their life. This spider could also enter an imaginal or reproductive diapause. Photoperiod was again a primary inducing factor and temperature modified the photoperiodic response to some extent. The induction of the reproductive diapause was almost temperature-compensated whereas development was not. So the involvement of a photoperiodic counter system was suggested. Irrespective of whether the nymph had experienced diapause or not, the imaginal diapause was induced in response to a short-day photoperiod after adult moult. Based on these observations, the seasonal life cycle and the adaptive significance of nymphal and imaginal diapause are discussed.     

The role of photoperiod and temperature in determination of summer and winter diapause in the cabbage beetle,Colaphellus bowringi (Coleoptera: Chrysomelidae)

The cabbage beetle, Colaphellus bowringi, is a short-day species undergoing an imaginal summer and winter diapause. Its photoperiodic response highly depends on temperature. All adults entered diapause at ≤ 20 °C regardless of photoperiods. High temperatures strongly weakened the diapause-inducing effects of long daylengths. The diapause-averting influence of short daylengths was expressed only at high temperatures (above 20 °C). This indicates that the beetle has a cryptic ability to reproduce in summer. In fact, summer and winter diapause were induced principally by relatively low temperatures in the field, whereas photoperiod had less influence on diapause induction. The critical daylength for the autumnal population was between 12 h and 13 h. By transferring from a long day to a short day or vice versa at different times after hatching, it was shown that the sensitive stage with regard to photoperiod was the larva, whereas a long day was photoperiodically more potent than a short day. The sensitive stage to temperature encompassed the larval, pupal and adult stages. This different response pattern serves to ensure that the beetle enters summer and winter diapause in time. The selections for non-diapause trait under laboratory (at 25 °C) and natural conditions (at >24 °C) showed that the beetle could lose its sensitivity to photoperiod very rapidly.     

Repeated larval diapause and diapause-free development in geographic strains of the burnet moth Zygaena trifolii Esp. (Insecta,Lepidoptera)

Summary Zygaena trifolii is a long-day insect with temperature-dependent photoperiodic responses. All larval instars are sensitive to photoperiod; however, diapause may occur at the third larval stage or any subsequent larval instars. There were quantitative differences within populations in the threshold photoperiod for diapause induction. The diapause response was polymorphic, so that larvae might enter diapause at different instars under the same culture conditions. Furthermore, decreasing photoperiods below a critical daylength shifted the diapausing instar towards earlier stages. Geographic strains of Z. trifolii showed discontinuous clinal variation. Near the northern edge of the distribution [Cologne (Köln), FRG], there is first an obligatory diapause, mainly during early instars, and additional facultative (repeat) diapauses during later larval instars in subsequent years. In the southern part of its distribution, this burnet moth is partially bivoltine in the field with a facultative first developmental arrest and a decreased capacity for repeated diapause (Valencia, Spain; Marseille, France). Further experiments indicated that the photoperiodically controlled diapause reaction is also influenced by the number of photoperiodic cycles experienced during the period spent in each larval instar, which depends on temperature. The adaptive significance of obligatory and facultative repeated diapause, varying even among the offspring of a single female, may be to buffer the populations against the more extreme and, from year to year, unpredictable fluctuations in climatic conditions at the northern edge of the distribution.Abbreviations L₃ feeding 3rd larval instar - L₄D diapausing 4th larval instar - L₅D2 repeat-diapausing larval instar with second diapause at the 5th larval stage - LD light-dark cycle - KT shortday conditions (e.g. LD 8:16) - LT long-day conditions (e.g. LD 16:8)     

光温条件明显影响棉铃虫的滞育强度

为了探明不同地理种群棉铃虫Helicoverpa armigera滞育强度的地理变异, 本研究系统地比较了光温条件（光照时数 11～16 h, 恒温20, 22, 25, 28和31℃及变温）对来自中国的4个地理种群（广东广州、 江西永修、 山东泰安和辽宁喀佐）棉铃虫滞育强度的影响。结果表明： 滞育诱导的光周期对继后棉铃虫的滞育强度有明显影响。在光照时数11～14 h范围内, 各地理种群的滞育持续期均随着光照时数的增加而延长。滞育强度也受到滞育诱导的温周期影响, 当光期温度相同时, 低纬度的GZ种群温周期比恒温有更强的诱导效应; 中纬度的YX种群温周期与恒温具有相同的滞育诱导强度; 高纬度的KZ和TA种群温周期所诱导的滞育强度一般低于恒温。滞育解除过程中的温度也显著影响到滞育的解除, 在20~31℃下, 温度愈高滞育解除愈快; 滞育持续期同时受到滞育诱导温度的影响, 对于北方的泰安种群和喀佐种群, 较高的滞育诱导温度能诱导更强的滞育。     

Existence of a light-sensitive phase in the photoperiodic termination of diapause inPieris brassicae L. (Insecta:Lepidoptera) and comparison with diapause induction

Summary Pupal diapause ofPieris brassicae can be terminated experimentally by the sole action of photoperiod. Curves gave evidence of similar effect of photoperiod within a broad range of regimes in both diapause induction and termination. However, they showed opposite responses to ultra-short and ultra-long days and to continuous light and darkness. In diapause termination, the critical daylength is longer than in diapause induction by about 1.20 h.Results of night interruption experiments (asymmetrical skeleton photoperiods) provided the first reliable evidence of the involvement of a particular light-sensitive phase in photoperiodic diapause termination. A light pulse delivered at this moment elicited a complete long-day effect (i.e. diapause termination). Only one single point of long-day effect (lying in the early night) was disclosed in diapause termination whereas two points (A and B) characterize diapause induction in this species. Results of experimental designs where the period of the photoperiodic cycles differed from 24 h indicated that photoperiodic clock likely makes a nightlength measurement in both diapause induction and termination. This is discussed in relation to the formal properties of the clock, especially those derived from the time distribution of points of long-day effect.     

Diapause Induction and Termination in the Small Brown Planthopper,Laodelphax striatellus (Hemiptera: Delphacidae)

The small brown planthopper, Laodelphax striatellus (Fallén) enters the photoperiodic induction of diapause as 3rd or 4th instar nymphs. The photoperiodic response curves in this planthopper showed a typical long-day response type with a critical daylength of approximately 11 h at 25°C, 12 h at 22 and 20°C and 12.5 h at 18°C, and diapause induction was almost abrogated at 28°C. The third stage was the most sensitive stage to photoperiod. The photoperiodic response curve at 20°C showed a gradual decline in diapause incidence in ultra-long nights, and continuous darkness resulted in 100% development. The required number of days for a 50% response was distinctly different between the short- and long-night cycles, showing that the effect of one short night was equivalent to the effect of three long nights at 18°C. The rearing day length of 12 h evoked a weaker intensity of diapause than did 10 and 11 h. The duration of diapause was significantly longer under the short daylength of 11 h than it was under the long daylength of 15 h. The optimal temperature for diapause termination was 26 and 28°C. Chilling at 5°C for different times did not shorten the duration of diapause but significantly lengthened it when chilling period was included. In autumn, 50% of the nymphs that hatched from late September to mid-October entered diapause in response to temperatures below 20°C. The critical daylength in the field was between 12 h 10 min and 12 h 32 min (including twilight), which was nearly identical to the critical daylength of 12.5 h at 18°C. In spring, overwintering nymphs began to emerge in early March-late March when the mean daily temperature rose to 10°C or higher.     

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)