亚洲玉米螟越冬幼虫存活和滞育解除与水分摄入的关系

在22～28℃和16～22℃变温条件下研究了水分对亚洲玉米螟Ostrinia furnacalis (Guenée)越冬幼虫存活、滞育解除及成虫生殖潜力的影响。结果表明：在越冬幼虫复苏后至化蛹阶段,水分是影响越冬幼虫完成滞育发育的关键因子,只有满足其饮水需求,才能解除滞育而化蛹。幼虫的存活和化蛹率随幼虫饮水后体重的增加而增加。幼虫化蛹的早晚受温度和水分的综合影响,在22～28℃下越冬幼虫化蛹进度较快,在复苏后35天时为最佳饮水时间,比在16～22℃下早5～10天。此阶段如能满足幼虫的需水量,幼虫死亡率低,化蛹率高,而只在滞育发育早期或后期饮水时,死亡率高,化蛹率低。同一变温条件下,其滞育发育因饮水时间的推迟而延长。因此可以推测春季温度偏高、干旱的气候条件不利于亚洲玉米螟越冬代的大发生,反之亦然。     

温度对黑纹粉蝶越冬蛹滞育后发育的影响

为了探讨温度对黑纹粉蝶Pieris melete越冬蛹滞育后发育的影响, 系统调查了越冬蛹滞育解除后在不同恒温下的发育历期及其在自然条件下春后的羽化情况。结果表明: 黑纹粉蝶雄虫和雌虫越冬蛹滞育后发育的阈值温度分别为7.1±1.5℃ 和7.4±0.4℃, 滞育后发育的有效积温分别为133.4±3.3日·度和155.7±5.3日·度。根据连续7年黑纹粉蝶越冬蛹在田间的羽化情况, 结合当年春季滞育后发育阈值以上的温度, 推算出田间50%个体成虫羽化时雄虫和雌虫获得的有效积温分别为142.2±12.2日·度和149.2±13.8日·度, 与滞育后发育的理论有效积温接近。据此, 利用该理论上的发育阈值温度和有效积温, 参照当年2-4月的气温, 可预测田间越冬蛹50%个体成虫羽化的时间。     

意大利蝗的胚胎发育及卵滞育发生的胚胎发育阶段

【目的】明确意大利蝗Calliptamus italicus (L.)胚胎发育及卵滞育发生的胚胎发育阶段。【方法】2013-2014年间,通过室外胚胎发育进度检测和室内孵化培养观察,研究其胚胎发育等级、滞育和越冬的胚胎阶段及自然越冬滞育的解除。【结果】意大利蝗的胚胎发育可划分为18个阶段;意大利蝗胚胎有反向移转、转旋和顺向移动3种胚胎转动方式;意大利蝗卵滞育发生的胚胎发育阶段为第Ⅻ阶段。自然条件下,意大利蝗卵发育至次年1月21日,仅部分卵解除滞育,解除滞育卵的发育历期最长;随着越冬时间的延长,解除滞育的卵逐渐增多,其发育历期逐渐缩短;直至次年3月29日卵基本完全解除滞育。意大利蝗雌成虫所产的早中期卵（7月27日-8月16日所产卵）以胚胎发育第Ⅻ阶段（滞育发生的胚胎发育阶段）越冬,于翌年4月16日（侯地温平均值：7.59℃,最高温：15.95℃,最低温：2.67℃）继续发育;雌成虫所产的晚期卵（8月28日-9月4日所产卵）,自11月4日（侯地温平均值：7.32℃,最高温：9.00℃,最低温：5.18℃）开始以胚胎第Ⅹ阶段越冬,于翌年3月29日（侯地温平均值：3.78℃,最高温：10.27℃,最低温：0.14℃）继续发育。【结论】意大利蝗雌成虫所产的早中期和晚期卵,其越冬胚胎发育阶段、开始越冬时间及越冬后继续发育的时间均不同。     

越冬中华按蚊生理生态的研究

中华按蚊 Anopheles sinensis以成蚊越冬.在上海、无锡从11月至3月上旬当气温超过10℃时,于畜棚可诱捕到新饱血蚊.卵巢发育观察表明,71.5%为发育蚊,吸血蚊生殖营养协调.另外还捕到个别经产蚊(1.3%).采自户外草堆等处的越冬蚊人工喂血与卵巢发育观察表明,64%为滞育蚊,35%为静止的发育蚊.滞育蚊出现于11月份,持续2个月,到2月底及3月上旬滞育开始解除.本研究结果表明,中华按蚊在上海、无锡是以深滞育(3%)、浅滞育(41%)与静止(56%)的生理状态越冬.     

豆天蛾越冬幼虫滞育解除后生物学特性的研究

[目的]豆天蛾Clanis bilineata tsingtauica以老熟幼虫进入滞育越冬,为探明豆天蛾滞育解除的机制.[方法]本研究设置4个不同温度梯度,在恒湿条件下,研究不同温度处理下豆天蛾滞育持续时间、化蛹及羽化的差异.[结果]温度对豆天蛾滞育解除存在一定影响.随着温度升高,豆天蛾滞育持续时间和蛹期逐渐缩短,在35℃条件下滞育持续时间和蛹期最短,分别为(34.4±0.3)d和(6.7±1.2)d;而化蛹率、蛹重随温度的升高呈先升高后降低,在25 ℃时,化蛹率最高为(80.60±0.26)％,在30 ℃时,蛹重最大为(4.21±0.07)g/头.豆天蛾成虫羽化率随温度升高而显著降低;25℃条件下,单雌产卵量最大,达到(204±9)粒.本室内条件下,豆天蛾滞育解除的有效积温为111¨日·度.[结论]在温度为25 ℃的条件下最有利于豆天蛾滞育解除后的生长发育.     

枯叶蛱蝶越冬雌成虫的生殖休眠特征研究

【目的】为了开展枯叶蛱蝶Kallimainachus(Doyére,1840)野生种群保育、人工繁育与利用,研究了近自然实验种群越冬雌成虫生殖休眠的性质、自然休眠期及其进展过程。【方法】根据卵母细胞的成熟度,划分繁殖季直接发育雌成虫的生殖发育进度等级;主要根据越冬早期雌成虫是否即时响应适宜条件恢复发育,判定其休眠性质为滞育或静息;通过定期检查放养在近自然条件下的越冬雌成虫的生殖发育进度,阐明其自然休眠期;通过定期将越冬成虫转至25℃、光照L︰D=15︰9和RH70%条件下保育不同天数后解剖检查其生殖细胞的发育情况,判断其滞育期和后滞育静息期。【结果】(1)繁殖季雌成虫在2日龄即开始卵黄沉积,至14日龄均已发育出成熟卵母细胞,其生殖发育被划分为4个等级,日龄与发育等级呈显著线性相关。(2)将羽化于10月上旬、放养在近自然条件下的越冬雌成虫从其11日龄开始,保育在25℃条件下12 d,其生殖发育仍无启动迹象。(3)羽化于9月8日、放养于近自然条件下的雌成虫,在其10日龄时,绝大多数处于休眠状态,少量个体继续发育;羽化于10月1日的雌成虫,从10月中旬至12月下旬,几乎所有个体均处于休眠状态;次年1月上旬,部分个体的卵母细胞发育开始启动。(4)12月上旬,所有检查的近自然实验种群雌成虫均不能在25℃条件下迅速恢复生殖发育;12月下旬,大部分个体在25℃条件下恢复发育。但仍有少量个体未显示发育恢复迹象,体现了个体间存在滞育强度的差异。【结论】枯叶蛱蝶的越冬生殖休眠为典型的滞育;近自然条件下,绝大多数雌成虫从9月中旬到1月下旬处于休眠状态,部分个体在次年1月初开始生殖发育;越冬雌成虫在12月上旬前处于滞育维持阶段,自12月下旬开始逐渐进入后滞育静息期。     

低温和光周期对绿盲蝽越冬卵滞育解除和发育历期的影响

为了探讨温度和光周期对绿盲蝽Apolygus lucorum Meyer-Dür越冬卵滞育解除和发育历期的影响, 系统调查了绿盲蝽越冬卵在不同温度和不同光照组合下的孵化率和孵化时间, 结果显示：绿盲蝽的越冬卵均为滞育卵,低温和光周期对绿盲蝽越冬卵的滞育解除均有影响。2℃的低温处理能够显著促进其滞育解除,在0~65 d范围内,随着低温处理时间增长,其滞育解除时间缩短,未经低温处理的越冬卵T₅₀为68.5 d,低温处理65 d的T₅₀为12.25 d,绿盲蝽越冬卵在2℃低温处理65 d后完全解除滞育;在0~40 d范围内,低温处理时间越长,绿盲蝽越冬卵的孵化率越高,在25℃、全光照的条件下不经低温处理的孵化率为68.65%,低温处理40 d后在25℃的条件下的孵化率达到99.46%。在20~26℃范围内,绿盲蝽越冬卵的滞育后发育历期随着温度的上升而缩短, 随着光周期的延长而缩短。结果说明低温处理能够提高绿盲蝽越冬卵滞育解除率,但不是其滞育解除的必要条件,低温处理与自然变温对绿盲蝽滞育解除的作用相似;高温和长光照能够促进绿盲蝽的滞育解除,缩短发育历期。     

温度在柑橘凤蝶蛹滞育解除中的作用

调查温度在柑橘凤蝶Papillio xuthus L.滞育蛹解除中的作用。结果显示,羽化温度在15,20,25和30℃时,滞育蛹最早羽化分别在第45,16,11和第5天,发育历期分别为60.3,26.0,15.2和11.6d,羽化持续时间分别为35,19,14和15d。同时低温处理(10℃)显示,25℃时,低温处理0,20和40d后,滞育蛹分别在处理后第38,第14和第13天开始羽化,羽化时间持续分别为40,71和16d,发育历期分别为60.9,28.5和19.0d。结果表明,随着羽化温度升高和低温处理时间延长,滞育蛹羽化时间提前,发育历期缩短。但当羽化温度超过25℃后,滞育蛹发育历期差异已不显著。     

低温对麦红吸浆虫滞育解除及蜕皮激素受体基因EcR和热激蛋白基因Hsp70和Hsp90表达水平的影响

【目的】本研究旨在明确破茧率和破茧所需时间作为典型的专性幼虫期滞育昆虫麦红吸浆虫Sitodiplosis mosellana滞育解除指标的可行性,探讨蜕皮激素受体基因EcR和热激蛋白基因Hsp70和Hsp90在低温解除滞育中的作用。【方法】9月上旬采自田间的麦红吸浆虫滞育幼虫在低温(4℃)和自然变温处理不同时间(0~90 d)后转移至24℃化蛹,调查幼虫的破茧率、化蛹率及破茧和化蛹所需时间;采用qPCR技术分析4℃低温终止滞育并在24℃下恢复发育的幼虫EcR, Hsp70和Hsp90的mRNA水平。【结果】不同时间低温(4℃)和自然变温处理的麦红吸浆虫滞育幼虫破茧率和化蛹率以及破茧和化蛹所需时间均存在显著差异。未经低温(4℃)处理的幼虫在水分满足的条件下破茧率为71.3%,但均不能化蛹;低温(4℃)处理60 d内,随着处理时间的延长破茧率和化蛹率逐渐升高,破茧和化蛹所需时间逐渐缩短;与4℃低温处理30~60 d相比,自然变温处理30~60 d的幼虫化蛹率显著较低;4℃低温处理60 d和自然变温处理90 d后幼虫的化蛹率均超过91%。低温(4℃)处理显著提高了麦红吸浆虫幼虫EcR, Hsp70和Hsp90的表达量,其中处理30 d时其表达量最高,随着低温(4℃)处理时间的延长,表达量逐渐降低,大部分幼虫滞育解除后表达量趋于恒定。【结论】低温能显著促进麦红吸浆虫的滞育解除,效果优于9-10月自然变温;破茧率及破茧所需时间可作为评判麦红吸浆虫幼虫滞育强度的参考,但不能独立作为滞育解除的指标;EcR,Hsp70和Hsp90的表达水平与滞育强度密切相关,在麦红吸浆虫滞育解除中发挥潜在作用。     

烟夜蛾滞育蛹和非滞育蛹的耐寒性

对烟夜蛾Helicoverpa assultaGuen?e不同日龄滞育蛹和非滞育蛹的过冷却点和结冰点测定结果表明,在预蛹至5日龄蛹期,过冷却点和结冰点均逐渐下降。在预蛹期和3日龄蛹期,滞育蛹的过冷却点与非滞育蛹差异不显著;5日龄蛹时,滞育蛹和非滞育蛹的过冷却点分别下降至(-15.7±1.8)℃和(-13.5±1.2)℃,结冰点分别降至(-12.7±2.7)℃和(-9.5±1.3)℃,两类蛹间的差异均达极显著水平。自然越冬后,滞育蛹的存活率显著高于非滞育蛹,在土壤不同深处越冬的蛹的存活率存在差异,距土表15cm深的蛹存活率最高。     

高温条件下棉铃虫化蛹率、夏滞育率和蛹重的变化

在预蛹期,高温处理能诱导棉铃虫蛹进入夏滞育。本实验着重就33～39℃的变温下滞育蛹和未滞育蛹的失重动态进行了对比研究,同时以常温（27℃）下蛹作为参照。研究发现： 在33～39℃的变温条件下,棉铃虫化蛹率显著低于其在常温下的化蛹率,且所化蛹中有63.2%的雄性和10.9%的雌性进入高温夏滞育,其中高温滞育蛹和未滞育蛹分别都轻于正常发育蛹。化蛹后第2日至第5日期间,高温滞育蛹失重量显著低于高温未滞育蛹和正常发育蛹的失重量,分别为3.62、13.30和5.49 mg;蛹期总失重量结果与化蛹后第2～5日间蛹失重量趋势一致,高温滞育蛹、未滞育蛹和正常发育蛹失重量分别为15.60、49.35和26.30 mg。蛹失重动态研究发现高温滞育蛹在夏滞育期间其失重曲线平缓,显著低于高温未滞育蛹和正常发育蛹;高温滞育蛹滞育解除后,其失重曲线与正常发育蛹的失重趋势基本一致。结果表明,棉铃虫夏滞育蛹能通过维持低的代谢水平来度过不利环境,具有一定的生态适应意义。     

Physiology of diapause and cold hardiness in overwintering pupae of the apple leaf miner Phyllonorycter ringoniella in Japan

Abstract The apple leaf miner Phyllonorycter ringoniella (Matsumura) (Lepidoptera: Gracillariidae) overwinters as a diapausing pupa. The diapause rate reaches 100% in early October. Diapause intensity decreases gradually from early October and diapause terminates in early February. The fresh body weight of diapausing pupae is 1.6 times that of non-diapausing pupae. The main cryoprotectant in P. ringoniella pupae is trehalose. Three stages are distinguishable as indicated by the correlations between diapause intensity, levels of cold hardiness and the trehalose content: diapause induction occurred in October, diapause development from November to December, and post-diapause quiescence from January to April. During diapause induction, the pupae accumulate low levels of trehalose and do not survive exposure to −15 °C. During diapause development, the pupae gradually accumulate more trehalose and show some ability to survive exposure to −15 °C, but not to −20 °C. During post-diapause quiescence, the pupae accumulate relatively more trehalose and cold hardiness fully develops, but decreases quickly in April. The trehalose content in pupae sampled in December is unaffected by acclimation temperatures in the range 0–30 °C, but decreases in pupae sampled in March after acclimation at temperatures from 5 to 15 °C. These results suggest that overwintering pupae of P. ringoniella have the ability to accumulate trehalose and develop a high level of cold hardiness during diapause development.     

Completion of diapause in field populations of the cabbage root fly (Delia radicum)

The various diapause and post-diapause stages entered by cabbage root fly pupae during the overwintering period are shown schematically. Although diapause induction started in mid-Aug., the early-pupating insects did not develop further but were maintained in diapause by the warm autumn temperatures. Therefore, diapause development was simultaneous in all Wellesbourne pupae, whether of second or third generation origin. Diapause development started only in mid-Oct., when mean soil temperatures fell below 10°. In the field, 90% of the overwintering population of cabbage root fly pupae had completed pleted diapause by 5 March 1980, 17 Feb. 1981 and 18 Feb. 1982. This was equivalent to a duration of 19 weeks from mid-Oct. onwards, during the winters of 1979–80, 1980–81 and 1981–82 respectively. A further break between the completion of diapause and the warm conditions required to start post-diapause development also helps to condense the emergence of flies in the spring. Hence, an accurate forecast of the time of spring attack by populations of flies similar to those at Wellesbourne should be possible.This study was financed partly by the Commission of the European Communities as CEC Contract No. 0771.     

Diapause development in early and late emerging phenotypes of Delia floralis

The turnip fly, Delia floralis Fall6n （Diptera： Anthomyiidae） is an important insect pest of brassica vegetable crops in the holarctic region. Different populations have strongly varying temperature requirements for fly emergence, a challenge for accurate prediction of activity. This study focused on diapause development in one early and one late emerging phenotype. The physiological state after various treatments was deduced from emergence data. Our results showed a slow diapause progression at chilling conditions for both populations and diapause ended about 7 months after pupae were formed for the early population. For the late population held at 4℃ diapause did not end, no matter how long the duration of chilling. These pupae required a period with elevated temperatures above 6~C to continue development. At constant non-chilling conditions （18℃） from the time pupae were formed both populations completed diapause most rapidly. These results indicate that chilling delayed, rather than accelerated development and was not a prerequisite for diapause development. For post-diapause, results indicated a linear relationship between rate of development and temperature within the range of 6-18℃and a theoretical base temperature for development of about 2℃ for both populations. In conclusion, D. floralis pupae are in diapause throughout a long winter period, and delayed emergence of the late population appears to be caused by prolonged diapause regulated by a developmental temperature threshold. The study has added information on the biology of turnip fly populations, a prerequisite for improved pest control.     

Embryonic stage of obligatory diapause and effects of abiotic conditions on egg hatching in the balsam twig aphid,Mindarus abietinus

Diapause‐mediated dormancy in overwintering insect eggs has rarely been studied with regard to the ecological factors controlling postdiapause development. In insects of temperate latitudes, water availability at the end of winter, in interaction with temperature, could control the resumption of development for insect stages in postdiapause quiescence. The balsam twig aphid, Mindarus abietinus Koch (Hemiptera: Aphididae), overwinters as eggs in southern Québec, Canada, on balsam fir, Abies balsamea (L.) Miller (Pinaceae), in Christmas tree plantations, where it is known as a pest. Previous work has shown that eggs of this aphid maintain low water content during winter, presumably to survive sub‐zero temperatures. Conversely, in late winter and early spring, they passively or actively absorb surrounding moisture, which is accompanied by notable changes in size, shape, and fresh mass. The primary objective here was to determine the embryonic stage at which winter diapause starts and is maintained in M. abietinus, a relatively primitive aphid. Secondly, we tested the hypothesis that free water availability to postdiapause eggs, in combination with temperatures above developmental threshold, is essential for embryonic development and hatching, by experimentally soaking field‐collected eggs in water at controlled frequencies. We observed that embryogenesis starts at the time of egg laying and stops after a few days, before the anatrepsis stage of blastokinesis is complete, when the germ band has not yet entirely immersed itself into the yolk. We also found that water surrounding overwintered eggs on fir shoots, in interaction with temperature regime, significantly increases M. abietinus egg hatching rates. Potential impacts of environmental factors such as precipitation are discussed in relation to M. abietinus egg hatching rates and potential for population growth in spring.     

Regulation of heat shock proteins in the apple maggot Rhagoletis pomonella during hot summer days and overwintering diapause

Abstract Developing larvae of the apple maggot Rhagoletis pomonella are frequently exposed to summertime apple temperatures that exceed 40 °C and, during their overwintering diapause, pupae are exposed to sub‐zero soil temperatures for prolonged periods. To investigate the potential involvement of heat shock proteins (Hsps) in response to these environmental extremes, the genes encoding Hsp70 and Hsp90 in R. pomonella are cloned and expression monitored during larval feeding within the apple and during overwintering pupal diapause. Larvae reared in the laboratory at constant temperatures of 25, 28 or 35 °C express Hsp90 but very little Hsp70. Larvae do not survive rearing at 40 °C. The temperature cycles to which larvae were exposed inside apples in the field, ranging 16–46.9 °C over a 24‐h period, elicit strong Hsp70 and Hsp90 expression, which begins at mid‐day and reaches a peak in late afternoon, coinciding with peak air and apple temperatures. Heat shock proteins are also expressed strongly by pupae during their overwintering diapause. Hsp70 is not expressed in nondiapausing pupae but is highly expressed throughout diapause. Hsp90 is constitutively expressed in both diapausing and nondiapausing pupae. Rhagoletis pomonella thus strongly expresses its Hsps during pupal diapause, presumably as a protection against low temperature injury, and during larval development to cope with natural temperature cycles prevailing in late summer.     

Emergence of the overwintering generation of peach fruit moth (Carposina sasakii) depends on diapause and spring soil temperatures

Survival rate and emergence timing of the overwintering generation of many temperate agricultural pests is expected to affect their population dynamics and damage potential. However the impact of fluctuating winter and spring conditions on the successful emergence of insects post-diapause is generally poorly known. Here we characterize diapause responses in the peach fruit moth (PFM) pest, Carposina sasakii Matsumura, which overwinters at the larval stage in soil. Temperatures at a depth of 5 cm fluctuated markedly in early spring during the critical PFM post-diapause period (late December to mid-April). By removing outdoor larval samples over this period, we show that the completion of diapause for PFM in northern China starts from late January and continues until March. This extended developmental period is accompanied by an ongoing loss of cold resistance. Temperature conditions experienced in the field were associated with cold tolerance and emergence times, and reduced cold tolerance was associated with shorter emergence time. Cryoprotectants declined from late December, and levels were associated with changes in the supercooling point (SCP) of the larvae, but both correlated weakly to survival under cold stress during the post-diapause period. These findings suggest that diapause stage and soil temperatures should be taken into account when predicting field dynamics of soil-dwelling overwintering insects based on degree day accumulation models and other approaches.     

Diapause termination and thermal requirements for postdiapause development inAphelinus mali at constant and fluctuating temperatures

Diapause termination under natural and simulated overwintering conditions, the effect of subzero temperature on postdiapause development and the relationship between postdiapause development rate and constant and fluctuating temperatures was studied in a Dutch population ofAphelinus mali Hald. (Hymenoptera: Aphelinidae).The rate of diapause termination was similar in larvae overwintering under natural and simulated conditions. Most larvae had terminated diapause by the last week of February. Some female larvae may have remained in diapause until the end of March. The exposure of postdiapause larvae to –10°C for two weeks did not affect their survival or postdiapause development rate.PostdiapauseA. mali larvae could complete development and the adults emerge from their mummified aphid hosts at constant temperatures from 12 to 24°C. Although some larvae completed postdiapause development at 10°C, few emerged. The theoretical threshold temperature (t_o) for postdiapause development was 9.4°C and the thermal constant (K) 136.4 degree-days. K was 121.4 and 134.8 for first and 50% emergence, respectively.The number of heat units accumulating above 9.4°C to 1st and 50% emergence was similar under constant and fluctuating temperatures.

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Fin de la diapause et exigences thermiques pour le développement après la diapause d'Aphelinus mali soumis à des températures constantes ou à des thermopériodes

Résumé L'achèvement de la diapause en conditions naturelles ou simulant l'hiver, les effets des températures inférieures à zéro sur le développement après la diapause et les relations entre la vitesse de développement après la diapause et les températures constantes ou en thermopériodes ont été examinés sur des populations néerlandaises d'A. mali (Hymenop.; Aphélinidae).Les taux d'achèvement de la diapause de larves hivernantes étaient semblables en conditions naturelles ou simulées. La plupart des larves ont terminé leur diapause la dernière semaine de février. Quelques larves femelles sont restées en diapause jusqu'à fin mars. L'exposition pendant 2 semaines des larves sorties de diapause à –10 °C ne compromet pas leur survie ou leur taux de développement après la diapause.Les larves ayant diapause peuvent terminer leur développement et les adultes émerger des pucerons momifiés aux températures constantes comprises entre 12 et 24 °C. Bien que quelques larves achèvent leur développement à 10 °C, peu émergent. La température seuil théorique de développement après la diapause (t_o) a été de 9,4 °C et la constante thermique (K), 136,5 degrés-jours. Pour la première émergence et pour 50% d'émergences, les valeurs de K étaient respectivement: 121,4 et 134,8.Le nombre d'unités thermiques pour la première émergence et pour 50% d'émergences était le même à température constante ou avec une thermopériode.

     

粟穗螟滞育的形成和解除与环境条件的关系

粟穗螟Manpava bipunctella Ragonot在川南地区为二化性兼性滞育的昆虫。光周期是诱发滞育的主导因素,在中位温度下,滞育与否主要取决于幼虫发育期间的每日光照时数。在2s℃恒温下,临界光周期为14小时38分。幼虫对光照刺激反应的敏感期为低龄期。 温度和食料效应只发生在每天14小时以上的长光照下,低温有抵销长光照抑制滞育的作用,高温影响不显著;取食玉米的幼虫滞育率比高粱的高,并随寄主生育阶段的发展而增高。该虫滞育解除必需每天14-15小时的长光照;不利于滞育发育和解除,适宜温度为10一25℃。本文最后讨论了该虫滞育形成和解除的特点对发生规律的作用及在测报上的意义。