亚洲玉米螟两个不同地理种群对暗期干扰的滞育反应

为了探明亚洲玉米螟Ostrinia furnacalis (Guenée)不同地理种群对暗期干扰的滞育反应, 本文在研究了亚洲玉米螟南昌种群（28°41′N, 115°53′E）和哈尔滨种群（44°56′N, 127°10′E）光周期反应的基础上, 在室内分别测试了25℃和28℃温度下1 h的光脉冲干扰光周期L9∶D15和L12∶D12对这两个不同地理种群幼虫滞育抑制的影响。结果表明： 在25℃和28℃下, 哈尔滨种群的临界日长分别比南昌种群延长了1 h 40 min和2 h; 在所有测试的暗期干扰实验中, 除了极少数光脉冲干扰点外, 南昌种群幼虫滞育的发生率显著低于哈尔滨种群; 1 h光脉冲干扰光周期L9∶D15的滞育发生率明显低于干扰光周期L12∶D12, 且前者表现了暗期的中间对光脉冲最敏感, 而后者显示了暗期的初期对光脉冲最敏感; 28℃下光脉冲对滞育的抑制效果强于25℃。这些结果进一步提示, 即使在同种昆虫中, 如果地理种群和实验条件不同, 暗期干扰对滞育抑制的效果也可能不同。     

暗期干扰对环带锦斑蛾滞育诱导的影响

在短日照条件下,环带锦斑蛾Pseudopidorus fasciata以4龄幼虫进入冬季滞育,其滞育诱导的临界暗长为10.5 h。本文系统测试了暗期干扰实验［即在暗期采用单一的光（亦称光脉冲）干扰光周期反应的实验］对环带锦斑蛾幼虫滞育的抑制影响。幼虫孵化后在25℃,短日照L9∶D15(光9 h∶暗15 h),L10∶D14、L11∶D13及L12∶D12暗期的不同时段给予1 h或30 min光脉冲干扰。结果表明： 滞育是否被抑制主要取决于暗期的长度,当光脉冲干扰前的暗长（D₁）或光脉冲干扰后的暗长（D₂）超过临界暗长（10.5 h）时,100%的幼虫被诱导进入滞育;当D₁和D₂都短于（或等于）临界暗长时,滞育不同程度被抑制,抑制的效果则取决于所干扰的光周期、光脉冲的长度和光脉冲落入的位点。结果说明该虫滞育诱导的暗期干扰反应是基于临界暗长的时间测量。     

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。     

高温对环带锦斑蛾幼虫滞育的抑制作用

本文报道了高温（31℃）对环带锦斑蛾幼虫滞育发生的抑制作用。当幼虫暴露于31℃ 时,所有个体都继续发育,与光周期无关。在诱导滞育的光周期条件(L12∶D12)下,光期的高温配合不同的暗期低温（15～28℃）,导致几乎所有个体滞育,但当暗期为5℃时,滞育率反而下降;相反,当光期的低温配合不同持续时间的暗期高温（31℃）时,则几乎所有的个体都继续发育,这说明高温在暗期发挥着重要的作用。在暗期给予不同时间长度（2、4、 6、8、10、12 h）的高温处理,结果表明一个2 h的高温处理就能有效地抑制滞育的发生。在暗期的不同时间给予4 h高温处理,显示了幼虫在暗期开始后的第一个4 h (18:00～22:00 )对高温最敏感,完全抑制了滞育的发生。最后讨论了高温调节滞育机制在该虫生活史上的适应意义。     

光周期和温度对大猿叶虫泰安种群滞育诱导的影响

为了明确光周期和温度对大猿叶虫泰安种群滞育诱导的影响,在实验室恒温和变温条件下,观察了该虫滞育诱导的光温反应。滞育诱导的光周期反应表明,大猿叶虫泰安种群滞育的发生与光周期无关,主要取决于日平均温度。当温度20℃时,全部个体进入滞育;在温度25℃时,仅有极少数个体发育;在温度28℃时,发育的个体也没有达到40%。对温度的敏感虫态包括幼虫期、蛹期和成虫期。在缺乏光信号的条件下,温度本身也能诱导滞育发生。在平均温度24℃、26℃下,温周期变化幅度对滞育的诱导有显著影响。在相同的温度下,有光参与的温周期的滞育率比全暗的温周期的滞育率明显低。结果表明,温度是大猿叶虫泰安种群滞育诱导的主要因素。     

亚洲玉米螟南昌种群滞育的解除

【目的】为了探明滞育诱导期和滞育期间的光周期和温度如何影响亚洲玉米螟Ostrinia furnacalis滞育的强度。【方法】采用不同条件下诱导的亚洲玉米螟滞育幼虫转到不同条件下解除滞育的方法,测试了亚洲玉米螟南昌种群滞育幼虫滞育解除的光周期反应、滞育诱导期和滞育期间的光周期和温度对滞育持续时间的影响及田间越冬幼虫滞育解除的时间进程。【结果】滞育解除是由光周期控制的,临界日长为14.5 h。在25℃和28℃,光周期13L︰11D诱导的滞育个体的滞育强度显著弱于11L︰13D和12L︰12D。滞育幼虫在长光周期15L︰9D和22,25和28℃解除滞育,显示了其滞育持续时间随温度的升高显著缩短,从22℃下的72 d降到28℃下的34 d。5℃的低温处理没有缩短滞育持续时间,但低温处理同步了滞育个体的化蛹时间。越冬幼虫不同时期从自然条件下转入恒温25℃,长光周期15L︰9D和短光周期12L︰12D的条件下解除滞育,显示了越冬幼虫滞育初期对光周期仍然敏感,但这种光敏感性在1月份后丧失。3年的田间观察揭示了50%滞育幼虫的化蛹时间出现在4月末至5月上旬,50%羽化时间出现在5月中旬。【结论】亚洲玉米螟滞育幼虫的滞育强度受到滞育诱导期和滞育期间的光周期和温度的显著影响。     

光周期对梨小食心虫滞育诱导的影响

在实验室条件下对梨小食心虫滞育诱导的光周期反应和不同日龄幼虫对滞育诱导光周期的敏感性进行了研究。结果表明:梨小食心虫属于典型的短日照滞育型,在20℃条件下,当光周期为8L ∶ 16D,10L ∶ 14D和12L ∶ 12D时,梨小食心虫的滞育率均达95%以上,诱导滞育的临界光周期为13.75L ∶ 10.25D;在24℃条件下,当光周期为10L ∶ 14D和12L ∶ 12D时,滞育率均达95%以上,诱导滞育的临界光周期为13.68L ∶ 10.32D。在幼虫期,分别给不同日龄幼虫以12L ∶ 12D和16L ∶ 8D光照处理后,在不同发育时间内幼虫对滞育诱导光周期反应均显示出一定程度的敏感性,无明显的临界时间点,但仍以第5-8日龄幼虫接受滞育诱导光周期反应更为敏感。     

大猿叶虫夏滞育的诱导：基于定量的光周期反应

为了探明大猿叶虫Colaphellus bowringi Baly夏滞育诱导的光周期时间测量特性, 我们通过室内实验系统比较了该虫在25℃、 不同长光照条件下,夏滞育的发生以及诱导50%个体进入夏滞育所需求的光 暗循环数。结果表明：不同长光照诱导的夏滞育比率有显著差异, 其中15 h或16 h光照诱导的滞育比率最高, 短于或长于这两个光照其滞育率均明显下降。在不同光 暗循环实验中, 14 h诱导的滞育比率均低于50%, 诱导50%个体进入夏滞育所需求的光 暗循环数在L15∶D9, L16∶D8, L17∶ D7和L18∶D6分别为2.61, 3.72, 4.64和5.92 d, 处理间存在显著差异。这些结果提示该虫夏滞育的诱导是基于定量的光周期反应。     

稻螟赤眼蜂诱导滞育条件的优化

应用滞育技术是延长赤眼蜂货架期的可行性措施之一。为实现工厂化生产稻螟赤眼蜂滞育蜂,本研究以在3种光周期(16 L∶8 D、12 L∶12 D和8 L∶16 D)下繁育的稻螟赤眼蜂种群为材料,考察了诱导始期(寄生后发育12 h、24 h、36 h、48 h、60 h和72 h)、诱导温度(10℃和13℃)和诱导历期(14 d、21 d、28 d和35 d)对稻螟赤眼蜂滞育的影响。研究结果表明短光照下繁育的种群更容易进入滞育状态;寄生后发育24 h和12 h为最敏感的诱导始期,随着诱导始期虫龄的增长,滞育效果也随之下降;诱导温度对滞育也有显著影响,其中8 L∶16 D的种群在13℃下诱导的滞育率要显著高于10℃,但其他两个种群在10℃下诱导的滞育率要显著高于13℃;诱导历期的增加可以显著提高稻螟赤眼蜂的滞育率。供试稻螟赤眼蜂种群的较适宜滞育条件为8 L∶16 D下繁育的赤眼蜂种群寄生后发育12 h于13℃下诱导滞育28 d或35 d,以及寄生后发育24 h于10℃或13℃下诱导滞育35 d,滞育率可超过95%。     

光周期和温度对亚洲玉米螟滞育诱导的影响

亚洲玉米螟Ostrinia furnacalis (Guenée)属兼性滞育昆虫, 其滞育特性与种群利用适生境的最大化和季节性活动密切相关。解析季节性因素如光周期和温度对其滞育的诱导作用可为预测种群发生动态提供科学依据。本实验在HPS 500型和HPG-320H型自动控制环境气候箱中, 测定了RH 80%下温度20℃, 27℃和30℃与11个光周期组合对吉林农安（NA）、 河北衡水（HS）、 广东惠州（HZ）和海南海口（HK）等4个地理种群的滞育诱导作用。结果表明： 光周期、 温度及其交互作用均对亚洲玉米螟滞育诱导具有重要影响, 其中光周期在滞育诱导中起主导作用。在20℃条件下, 其光周期反应曲线属典型的长日照反应型, 临界光周期随种群分布的地理纬度降低而缩短, 4个地理种群NA, HS, HZ和HK的临界日昼长依次为14 h 3 min, 13 h 59 min, 13 h 32 min和13 h 7 min, 最有效的滞育诱导光周期是日昼长12 h。另一方面, 随种群分布纬度升高, 其对光周期诱导滞育的敏感性降低。温度为27℃时, 其光周期反应曲线为短日照 长日照反应型, 各种群有两个临界光周期, 临界日昼长依次为12 h 50 min和13 h 32 min, 11 h 35 min和13 h 8 min, 12 h 58 min和13 h 1 min, 以及11 h 50 min和12 h 26 min, 且最有效的滞育诱导光周期范围的滞育率明显低于20℃。一定温度范围内（20℃～27℃）, 随温度升高, 临界光周期缩短; 温度达到30℃时则滞育显著被抑制, 滞育率仅为4.3%或更低。这些结果说明温度对亚洲玉米螟滞育的光周期诱导具有很强的补偿作用。因此, 在自然界亚洲玉米螟的滞育属具有温度补偿作用的长日照反应型昆虫, 临界光周期随地理纬度北移而增长; 种群滞育的短日照 长日照反应型特性可能是产生局部世代种群的重要内因。     

Determination of effective light pulse and classical Bünsow experiment in the larval diapause of the Indian meal moth Plodia interpunctella

Plodia interpunctella Hübner (Lepidoptera: Pyralidae) comprises a model insect to analyse the photoperiodic time‐measuring system controlling its larval diapause. In the present study, the effective length of light pulse in night interruption experiments is determined at 25 °C. Various lengths of light pulse are tested by inserting them at the midnight of an LD 12 : 12 h photoperiod. When the light pulse is 15 or 30 min, the incidence of diapause is 86%. To inhibit the induction of diapause effectively, a light pulse of 1.75–2 h is needed. The incidence of diapause is 12% under an LD 12 : 5 : 2 : 5 h photoperiod. To determine the precise role of the light pulse, 2‐h light pulses placed at the midnight of an LD 12 : 12 h photoperiod are disrupted systematically by darkness. When a 2‐h light pulse is disrupted by 15 min of darkness, diapause is generally prevented (< 29%) regardless of the temporal position of darkness. Longer disruption by darkness induces diapause moderately (37–67%). A Bünsow experiment is also conducted at 25 and 20 °C, in which the main photophase of 12 h of light is combined with 24–72‐h scotophases scanned by a 2‐h light pulse. The photoperiodic cycle length tested, therefore, varies in the range 36–84 h. In each cycle length, the incidence of diapause fluctuates as the light pulse moves toward dawn. However, no regular and circadian changes in the percentage diapause are observed in relation to diapause determination.     

Photoperiodic counter of diapause induction in Pseudopidorus fasciata (Lepidoptera: Zygaenidae)

Induction of larval diapause is a photoperiodically controlled event in the life history of the moth Pseudopidorus fasciata. In the present study, the photoperiodic counter of diapause induction has been systematically investigated. The required day number (RDN) for a 50% response was determined by transferring from a short night (LD 16:8) to a long night (LD 12:12) or vice versa at different times after hatching, The RND differed significantly between short- and long-night cycles at different temperatures. The RDN for long-night cycles at 20, 22, 25 and 28 degrees C was 11.5, 9.5, 7.5 and 8.5 days, respectively. The RDN for short-night cycles was 3 days at 22 degrees C and 5 days at 20 degrees C indicating that the effect of one short night was equivalent to the effect of 2-3 long nights effect. Night-interruption experiments of 24h photoperiods by a 1 h light pulse showed that the most crucial event for the photoperiodic time measurement in this moth was whether the length of pre-interruption (D(1)) or the post-interruption (D(2)) scotophases exceeded the critical night length (10.5 h). If D(1) or D(2) exceeded 10.5 h diapause was induced. The diapause-averting effect of a single short-night cycle (LD 16:8) against a background of long nights (LD 12:12) showed that the photoperiodic sensitivity was greatest during the first 7 days of the larval period and the highest sensitivity was on the fourth day. Both non-24 and 24 h light-dark cycle experiments revealed that the photoperiodic counter in P. fasciata is able to accumulate both long and short nights during the photosensitive period, but in different ways. The information from short-night cycles seems to be accumulated one by one in contrast to long-night cycles where six successive cycles were necessary for about 50% diapause induction and eight cycles for about 90% diapause. These results suggest the accumulation of long-night and short-night cycles may be based on different mechanisms.     

An “hourglass-like” feature in the photoperiodic time measurement in Diatraea grandiosella (Pyralidae)

Photoperiodic time measurement of Diatraea grandiosella, a Pyralid moth, was investigated for its role in the determination of diapause by using various night-interruption protocols. The photoperiodic-response curve showed a temperature dependence under short days, whereas at long days it was stable in the range between 20 and 30°C. A light pulse averted diapause most effectively when it was placed 6 h after lights-off. Earlier pulses were less effective but gradually increased in effectiveness as the time of the pulse approached the critical time, i.e. 6 h after lights-off. A strong conversion in response appeared as the pulse passed the critical time. The same response pattern was observed both in diapause induction and termination. The species required a long light pulse to avert diapause completely, even if the light pulse was placed during the critical time; 45 min was required to reverse diapause in 50% of the individuals. The most crucial event for photoperiodic time measurement in this species was whether a night phase 6–7.5 h after lights-off was illuminated or not. This hourglass-like feature was also shown in more complex night-interruption protocols with 2–3 light pulses. A possible relation of this phenomenon to the cricadian pacemaker was sought. The Dual System Theory failed to account for most of the features for the photoperiodic time measurements of D. grandiosella found in this study.     

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.     

Possible involvement of distinct photoreceptors in the photoperiodic induction of diapause in the flesh fly Sarcophaga similis

Physiological characteristics of the photoreceptors involved in the photoperiodic induction of diapause were investigated in the flesh fly Sarcophaga similis. Both the early and late phases of scotophase were sensitive to light and a light pulse during each of these phases prevented diapause. Certain physiological differences between the phases were, nevertheless, detected. Compared with early scotophase, late scotophase required a light pulse with a long period and a large number of night interruption photoperiodic cycles in order to effectively prevent diapause. The diapause-averting effects of a light pulse during early scotophase were canceled by an additional long dark period, but those during late scotophase were not. Thus, the diapause-averting effects produced during early scotophase are different to those produced during late scotophase. The early scotophase was sensitive to light at wavelengths of 470 nm or shorter, but not to light of 583 nm or longer. In contrast, the late scotophase was sensitive to light of a broad range of wavelengths, ranging from 395 to 660 nm. Furthermore, the early scotophase was considerably more sensitive to monochromatic light with low photon flux density than the late scotophase. These results suggest that different types of photoreceptor are involved in the photoperiodic response.     

Diapause induction and clock mechanism in the cabbage beetle, Colaphellus bowringi (Coleoptera: Chrysomelidae)

Photoperiodic control of diapause induction was investigated in the short-day species, Colaphellus bowringi, which enters summer and winter diapause as adult in the soil. Photoperiodic responses at 25 and 28 degrees C revealed a critical night length between 10 and 12 h; night lengths > or =12 h prevented diapause, whereas night lengths <12 h induced summer diapause in different degree. Experiments using non-24-h light-dark cycles showed that the duration of scotophase played an essential role in the determination of diapause. Night-interruption experiments with T=24 h showed that diapause was effectively induced by a 2-h light pulse in most scotophases; whereas day-interruption experiments by a 2-h dark break had a little effect on the incidence of diapause. The experiments of alternating short-night cycles (LD 16:8) and long-night cycles (LD 12:12) during the sensitive larval period showed that the information of short nights as well as long nights could be accumulated. Nanda-Hamner experiments showed three declining peaks of diapause at 24 h circadian intervals. Bünsow experiments showed two very weak peaks for diapause induction, one being 8 h after lights-off, and another 8 h before lights-on, but it did not show peaks of diapause at a 24 h interval. These results suggest that the circadian oscillatory system constitutes a part of the photoperiodic clock of this beetle but plays a limited role in its photoperiodic time measurement.     

Photoperiodic clock of diapause induction in Pseudopidorus fasciata (Lepidoptera: Zygaenidae)

Pseudopidorus fasciata enters diapause as fourth instar larvae at short day lengths. Using 24-h light-dark cycles, the photoperiodic response curves in this species appeared to be similar with a critical night length of 10.5h at temperatures below 30 degrees C. At an average temperature of 30.5 degrees C, the critical night length had shifted to between 15 and 17h. In experiments using non-24-h light-dark cycles, it was clearly demonstrated that the dark period (scotophase) was the decisive phase for a diapause determination. In night interruption experiments using 24-h light-dark cycles, a 1-h light pulse at LD12:12 completely reversed the long night effect and averted diapause in all treatments. At LD 9:15 light pulses of 1-h, 30- or 15-min also averted diapause effectively when both the pre-interruption (D(1)) or the post-interruption scotophases (D(2)) did not exceed the critical night length. If D(1) or D(2) exceeded the critical night length diapause was induced. The most crucial event for the photoperiodic time measurement in this species is the length of the scotophase. A 10-min light pulse placed in the most photosensitive phase reversed diapause in over 50% of the individuals. Night interruption experiments under non-24-h light-dark cycles indicated that the photoperiodic clock measured only D(1) regardless of the length of D(2), suggesting that the most inductive cycles are often those in which L+D are close to 24h. In resonance experiments, this species showed a circadian periodicity at temperatures of 24.5 or 26 degrees C, but not at 30.5 and 23.3 degrees C. On the other hand, Bünsow and skeleton photoperiod experiments failed to reveal the involvement of a circadian system in this photoperiodic clock. These results suggest the photoperiodic clock in this species is a long-night measuring hourglass and the circadian effect found in the final expression of the photoperiodic response in the resonance experiments may be caused by a disturbing effect of the circadian system in unnatural regimes.