茧蜂滞育的研究进展

滞育现象在多种茧蜂类天敌昆虫中存在, 通过调控茧蜂滞育, 可达到延长产品货架期、延长防控作用时间、提高产品的抗逆性和繁殖力的目标, 对茧蜂的扩繁和应用具有重要意义。本文通过总结1910年以来的2 545篇国内外滞育文献, 统计得出有明确滞育诱导或滞育解除报道的茧蜂有37种, 分属7亚科16属, 其中对滞育特征有详细描述的有23种。茧蜂大多以预蛹进入滞育, 其次为幼虫滞育, 少数为成虫滞育, 其滞育敏感阶段因种不同而异。滞育持续期相对较长, 大多可维持数月, 最长的可达14个月。光周期、温度和寄主是影响茧蜂滞育的主要因子, 湿度、亲代和寄主植物也可在一定程度上影响滞育进程。目前, 茧蜂滞育的研究仅限于生物学观察阶段, 对茧蜂滞育的生理学特征、激素调控和分子调控等尚未有研究报道, 有许多问题有待进一步探讨。     

为害黄芪种子的广肩种子小蜂属四新种(膜翅目:广肩小蜂科)

据我们在北京和内蒙古等地多年研究表明,黄芪的植食性种子小蜂包括广肩小蜂科Bruchophagus属5种和金小蜂科Habrocytus属1种,为多种混合群体。我们通过大量标本的形态比较以及交配行为的观察,结合其生物学特性研究以及应用扫描电镜对其并胸腹节花纹的超微结构观察,鉴定出黄芪种子里有5种广肩种子小蜂,即黄芪种子小蜂Bruchophagus huonchi Liao et Fan及本文的4新种。     

稻螟蛉的寄生蜂(三)——小蜂和细蜂

巳知寄生于稻螟蛉的小蜂和细蜂有14种,其中有6种是完全重寄生的种类。按分类系统,隶属于小蜂总科的小蜂科3种,广肩小蜂科1种,金小蜂科1种,寡节小蜂科(姬小蜂科)3种,扁股小蜂科1种,纹翅小蜂科(赤眼蜂科)3种;细蜂总科的分盾细蜂科2种。这些寄生蜂的绝大部分,都是稻田中常见的种类,与其他害虫或其寄生蜂有广泛的食物连锁关系。各蜂形态、生物学及分布情况简述如下。     

丽蝇蛹集金小蜂的生物学及其滞育调控机制研究进展

丽蝇蛹集金小蜂可以蛹外寄生多种双翅目蝇科害虫,在防治卫生害虫及牲畜害虫方面效果显著。该蜂是实验室内研究寄生蜂的理想模式昆虫,其发育学、行为学、生态学以及遗传学等的研究已有70多年的历史,近年来,随着金小蜂基因组测序的完成,系统的RNAi方法和CRISPR-Cas9技术在丽蝇蛹集金小蜂中的成功应用,该蜂现已成为优良的新型遗传学研究模式昆虫。丽蝇蛹集金小蜂以末龄幼虫进行兼性滞育,其滞育由母代经历的短光照和低温决定,研究该蜂的滞育,不仅有助于揭示昆虫滞育的分子机制,也可帮助解决有益昆虫实际应用中的贮存、运输和适时防治等问题,为提高天敌昆虫的应用效果提供技术支撑。本文总结了近年来丽蝇蛹集金小蜂的研究文献,主要介绍了该蜂的基本生物学特征,概括了现代分子生物学前沿技术在金小蜂研究中的应用情况,并重点讨论了丽蝇蛹集金小蜂滞育的最新研究进展,以期为深入金小蜂的滞育研究和促进该蜂其他研究领域的发展提供参考。     

生物因子对寄生蜂滞育的影响

在影响寄生蜂滞育的生物因子中,寄主及亲代是主要影响因子。寄主可以从种类、类型、生理状态及丰富度等方面影响寄生蜂的滞育:寄生不同种类的寄主,寄生蜂的滞育反应、滞育进度、滞育比例以及光周期反应表现等均有不同;寄主类型的影响在蚜茧蜂类群中表现最为突出,不同寄主类型能对蚜茧蜂的滞育诱导产生不同影响;此外,寄主生理状态和寄主丰富度也是影响寄生蜂滞育的重要因子。亲代对寄生蜂滞育的影响则通过其所经历的环境条件以及自身因素等方面来表现:亲代经历的光周期和温度等能显著影响子代的滞育,甚至起完全决定作用;在亲代自身因素的影响中,亲代虫龄差异是主要因素。本文同时对寄生蜂滞育的研究及应用前景也一并作了展望。     

元宝枫籽象的重要天敌昆虫——元宝枫刺胫广肩小蜂线粒体全基因组的测定与分析

【目的】元宝枫刺胫广肩小蜂Eurytoma acutibialis Yang, Liu et Cao是我国元宝枫种实Acer truncatum的主要害虫元宝枫籽象Bradybatus sp.的寄生蜂，是调查元宝枫籽象时发现的一个新种，在控制元宝枫籽象上可发挥重要作用。为进一步了解该新寄生蜂，测定和分析元宝枫刺胫广肩小蜂的线粒体全基因组序列，从而为膜翅目(Hymenoptera)小蜂总科(Chalcidoidea)广肩小蜂科(Eurytomidae)昆虫系统分类和发育系统关系等研究提供分子生物学证据。【方法】采用Illumina HiSeq^TM4000测序平台测定元宝枫刺胫广肩小蜂线粒体全基因组序列，并进行拼接、注释和分析。基于膜翅目小蜂总科40种昆虫线粒体的13个蛋白质编码基因(protein-coding genes, PCGs)的核苷酸序列，应用贝叶斯法(Bayesian inference, BI)和最大似然法(maximum likelihood, ML)构建系统发育树，分析元宝枫刺胫广肩小蜂与小蜂总科其他昆虫的系统发育关系。【结果】元宝枫刺胫广肩小蜂线...     

福州大叶榕隐头果内榕小蜂的分类

通过对福州两个样地大叶榕雄花期隐头果进行定时、定点采集,观察与鉴定,从546个花序果内共收集到榕小蜂33641头,隶属于小蜂总科中的7个科(亚科)7个属的11个种,其中传粉小蜂为榕小蜂科的Platyscapa coronata,其余10种非传粉小蜂分别隶属于隐针榕小蜂亚科Epichrysomallinae,金小蜂科Pteromalidae的锥尾榕小蜂亚科Otitesellinae和延腹榕小蜂亚科Sycoryctinae,广肩小蜂科Eurytomidae,刻腹小蜂科Ormyridae和姬小蜂科Eulophidae。传粉小蜂和非传粉小蜂的种类和数量呈现明显的季节性。冬-春季(12-翌年5月)榕果内小蜂的种类和数量较多,传粉榕小蜂是优势种;夏-秋季(6-11月间)小蜂种类和数量略少,Camarothorax bismasculinus和Sycophila sp.1是优势种。在非传粉小蜂中,Camarothorax、Sycophila、Otitesella、Sycoscapter等4个属的榕小蜂为常见种,而Ormyrus和Aprostocetus等2个属的榕小蜂为偶见种。根据小蜂的形态特征制定大叶榕隐头果中榕小蜂种类检索表,本实验为榕小蜂分类、榕-蜂协同进化研究,以及非传粉小蜂对榕-蜂共生体系的影响等研究提供科学依据。     

昆虫滞育持续时间的影响因子及其对滞育后生物学的影响

滞育持续时间(diapause duration)是昆虫的一种生理特性,它主要由特定环境条件下的滞育强度或滞育发育速率来决定,滞育强度或滞育发育速率通常以将滞育状态的昆虫转移至解除滞育的条件(如低温处理、光周期的转换)后,滞育消除所需时间的长短来衡量。文章系统综述昆虫滞育持续时间的影响因子及其对滞育后生物学的影响。     

白蛾周氏啮小蜂滞育诱导及滞育后发育

本研究针对人工繁育白蛾周氏啮小蜂Chouioia cunea Yang过程中出现的小蜂滞育现象, 对其滞育诱导的光周期反应及敏感光照虫态进行了调查。结果表明: 沈阳地区的白蛾周氏啮小蜂属长日照型昆虫, 以老熟幼虫进入滞育状态, 但在不同的温度条件下诱导滞育的临界光周期不同, 在18℃时诱导滞育的临界光周期处于13L∶11D和14L∶10D之间; 在21℃和24℃时诱导滞育的临界光周期变短, 处于12L∶12D和13L∶11D之间。白蛾周氏啮小蜂滞育诱导的敏感光照虫态为幼虫期, 且以幼虫的后期最为敏感, 但整个幼虫期接受短光照对滞育的形成更为有利。通过观察白蛾周氏啮小蜂滞育后在18℃, 21℃, 24℃和30℃的恒温条件下的发育历期, 由最小二乘法计算出白蛾周氏啮小蜂老熟幼虫滞育后发育起点温度和有效积温分别为14.60±0.31℃和209.38±8.72日·度。这些结果可为进一步研究白蛾周氏啮小蜂的种蜂长期保存技术和指导商品蜂生产, 正确把握放蜂时机提供理论依据。     

中国广肩小蜂科二新纪录属及二新纪录种(膜翅目,小蜂总科)

记述了广肩小蜂科中国2新纪录属:普氏广肩小蜂属Plutarchia Girault,1925和拉氏广肩小蜂属Ramdasoma Narendran,1994,及2个新纪录种:凹纹普氏广肩小蜂Plutarchia indefensa Walker,1860和简拉氏广肩小蜂Ramdasoma simplexus Narendran,1994.提供了其形态描述、形态特征图,首次报道并描述了简拉氏广肩小蜂Ramdasoma simplexus Narendran,1994的雄虫.研究标本保存于中国科学院动物研究所动物标本馆.     

Meeting the energetic demands of insect diapause: nutrient storage and utilization

Insects in diapause characteristically feed very little or not at all, thus they are largely or totally dependent on energy reserves sequestered prior to the entry into diapause. Fats are the dominant reserve used during this period, but non-fat reserves are also important for some species, especially during certain phases of diapause. Metabolic depression, coupled with the low temperatures of winter, facilitates the economic utilization of reserves during the many months typical of most diapauses. Though many insects store additional lipid prior to the entry into diapause, our review of the literature indicates that this is not always the case. We provide evidence that interactions between nutrient storage and metabolism can influence the decision to enter diapause and determine how long to remain in diapause. In addition, the energy reserves expended during diapause have a profound effect on post-diapause fitness. Though the physiological and biochemical mechanisms that regulate nutrient homeostasis prior to and during diapause remain poorly known, we propose several mechanisms that have the potential to contribute to diapause-associated nutrient homeostasis. Potential players include insulin signaling, neuropeptide F, cGMP-kinase, AMP-activated protein kinase, and adipokinetic hormone.     

Dormancy, dispersal and the survival of cyclopoid copepods (Cyclopoida, Copepoda) in a lowland floodplain

1. The survival of cyclopoid copepods was investigated in a floodplain for 2 years where flooding occurred during the cold season. The cyclopoid community was studied in three waterbodies with distinct hydroperiods: a permanent pond connected to the flooded area during inundation, a temporary pool that is part of the flooded area and an isolated temporary pool.
2. Field studies, including data obtained from samples of water, sediment and soil, showed the overall predominance of species with a summer diapause over those with a winter diapause or without diapause. Emergence of cyclopoid copepods at the onset of flooding, examined using emergence traps and data from recently filled or still isolated temporary pools, showed that some species can survive several months of drying.
3. The ability of the diapausing fourth copepodid stages of Cyclops strenuus and C. insignis , the two cyclopoids most abundant during winter and spring flooding, to survive terrestrial conditions was tested in laboratory experiments. Both species survived for several months, but rates differed among the species. A higher percentage of C. strenuus survived for a longer period, possibly explaining why this species was relatively more abundant in more temporary habitats.
4. Both dormancy and dispersal facilitated survival of cyclopoid copepods in transient habitats connected to each other during flood periods. Dormancy was the most important survival strategy, whereas dispersal could be more important following prolonged periods without flooding.     

Physiology of larval diapause: a tool for insect pest management

Summary

Two major pests cause damage of economic importance to maize crops in France: the European corn borer (Ostrinia nubilalis), which has a worldwide distribution, and the pink maize stalk borer (Sesamia nonagrioides), which is present all around the Mediterranean. During winter, last instar larvae of these species exhibit a facultative diapause. Early forecasting of the field emergence period and a good knowledge of the overwintering survival (both strongly dependent on conditions controlling diapause maintenance and termination) are key features for effective management of these pests. In this connection physiological studies of diapause provide us with useful information. Special emphasis is given to variations of carbohydrate metabolism, particularly glycogen, trehalose and glycerol in both species. In the European corn borer the presence of glycerol and trehalose makes it possible to forecast diapause termination 2–3 months before the first field pupal molts. These data are used for the construction of a model of the population dynamics, developed by the National Institute of Agronomic Research. In the pink maize stalk borer we demonstrate the great sensibility of this pest to low temperatures, and we propose a novel cultural pest-suppressing method which is now being tested in collaboration with the General Association of Maize Producers.     

Eco-physiological phases of insect diapause

Insect diapause is a dynamic process consisting of several successive phases. The conception and naming of the phases is unsettled and, sometimes, ambiguous in the literature. In this paper, the ontogeny of diapause was reviewed and the most often used terms and the best substantiated phases were highlighted, explained and re-defined. The aim was to propose relatively simple and generally applicable terminological system. The phases of diapause induction, preparation, initiation, maintenance, termination and post-diapause quiescence were distinguished. The specific progression through diapause phases in each species, population (genotype), or even individual, is based on (thus far largely unknown) physiological processes, the actual expression of which is significantly modified by diverse environmental factors. Thus, such phases are eco-physiological in their nature.     

Effect of photoperiod experienced by parents on diapause induction in Trichogramma cacoeciae

In the genus Trichogramma, the prepupal stage can survive the cold season in diapause. However, optimal conditions for the induction of this cessation of development during the process of mass production of the parasitoid in a biological control program depend on the species. In Trichogramma cacoeciae Marchal (Hymenoptera: Trichogrammatidae), diapause is induced more easily if the parents are reared under short‐day conditions (L10:D14), and if the temperature is 10 °C rather than 13 °C. However, the effect of parental photoperiod on diapause induction is weaker at lower temperatures (10 °C). Following diapause induction, individuals can be stored at 3 °C for several months, up to 1 year. Non‐optimal conditions led to the establishment of a quiescent state in some or all individuals. In such cases, it was necessary to reduce the storage period to 1 or 2 months only, to prevent high mortality rates and low fecundity.     

Long life cycles in insects

Long life cycles covering more than one year are known for all orders of insects. There are different mechanisms of prolongation of the life cycle: (1) slow larval development; (2) prolongation of the adult stage with several reproduction periods; (3) prolongation of diapause; (4) combination of these mechanisms in one life cycle. Lasting suboptimal conditions (such as low temperature, low quality of food or instability of food resources, natural enemies, etc.) tend to prolong life cycles of all individuals in a population. In this case, the larvae feed and develop for longer than a year, and the active periods are interrupted by dormancy periods. The nature of this dormancy is unknown: in some cases it appears to be simple quiescence, in others it has been experimentally shown to be a true diapause. Induction and termination of these repeated dormancy states are controlled by different environmental cues, the day-length being the principal one as in the case of the annual diapause. The long life cycles resulting from prolonged adult lifespan were experimentally studied mainly in beetles and true bugs. The possibility of repeated diapause and several periods of reproductive activity is related to the fact that the adults remain sensitive to day length, which is the main environmental cue controlling their alternative physiological states (reproduction vs. diapause). Habitats with unpredictable environmental changes stimulate some individuals in a population to extend their life cycles by prolonged diapause. The properties of this diapause are poorly understood, but results of studies of a few species suggest that this physiological state differs from the true annual diapause in deeper suppression of metabolism. Induction and intensity of prolonged diapause in some species appear to be genetically controlled, so that the duration of prolonged diapause varies among individuals in a group, even that of sibles reared under identical conditions. Thus, long life cycles are realized due to the ability of insects to interrupt activity repeatedly and enter dormancy. This provides high resistance to various environmental factors. Regardless of the nature of this dormancy (quiescence, annual or prolonged diapause, or other forms) and the life cycle duration, the adults always appear synchronously after dormancy in the nature. The only feasible explanation of this is the presence of a special synchronizing mechanism, most likely both exo- and endogenous, since the adults appear not only synchronously but also in the period best suited for reproduction. As a whole, the long life cycles resulting from various structural modifications of the annual life cycle, are typical of the species living under stable suboptimal conditions when the pressure of individual environmental factors is close to the tolerance limits of the species, even though it represents its norm of existence. Such life cycles are also typical of the insects living in unstable environments with unpredictable variability of conditions, those developing in cones and galls, feeding on flowers, seeds, or fruits with limited periods of availability, those associated with the plant species with irregular patterns of blossoming and fruiting, and those consuming low-quality food or depending on unpredictable food sources (e.g., predators or parasites). Long cycles are more common in: (1) insect species at high latitudes and mountain landscapes where the vegetation season is short and unstable; (2) species living in deserts or arid areas where precipitation is unstable and often insufficient for survival of food plants; (3) inhabitants of cold and temporary water bodies that are not filled with water every year. At the same time, long life cycles sometimes occur in insects from other climatic zones as well. It is also important to note that while there is a large body of literature dealing with the long life cycles in insects, it mostly focuses on external aspects of the phenomenon. Experimental studies are needed to understand this phenomenon, first of all the nature of dormancy and mechanisms of synchronization of adult emergence.     

The plurennial life cycles of the European Tettigoniidae (Insecta: Orthoptera)

Summary The effect of drought on embryonic development and on hatching was studied in 13 European Tettigoniidae species. Drought can affect development in three different ways: (1) Embryonic development proceeds slower than if the eggs are in contact with water; (2) it stops (for final diapause) in an earlier embryonic stage; (3) it affects maintenance and termination of the initial embryonic diapause.In many Tettigoniidae species, the initial diapause is prolonged, and may last several years. Without draught stress, between 1 and 7 cold treatments in the laboratory, and with eggs of the Tettigonia-species between 1 and 6 winters in the field were necessary to enable all eggs to complete initial diapause. In Central European species, the number of eggs maintaining initial diapause significantly increased when the eggs had no contact with water at the time when they should recover from diapause. In contrast, termination of initial diapause in Tettigonia caudata from Greece, when the environment became favorable for growth again, was highest in that group of eggs that had lost most water in a preceding period of drought. The importance of the prolonged initial diapause for the survival of unpredictable adverse conditions is discussed.     

Effects of temperature on free‐embryonic diapause in the autumn‐spawning bitterling Acheilognathus rhombeus(Teleostei: Cyprinidae)

In bitterling Acheilognathus rhombeus , developmental arrest always occurred at stage D of the free‐embryonic phase, regardless of incubation temperature. Developmental arrest was terminated only by a cold treatment at 4° C for 60–90 days, initiated 10 days post‐hatching. After the termination of developmental arrest, free‐embryos became larvae c . 6 months after hatching, regardless of the time of initiation and duration of the cold treatment. In hybridization experiments between A. rhombeus and several species of spring‐spawning bitterlings, free‐embryos became free‐swimming larvae within 60 days after hatching in all experiments. Developmental arrest was not observed in any of the hybrids, regardless of parental sex. These results suggest that free‐embryonic diapause in A. rhombeus is not induced by environmental factors, such as cold, but by genetic factors, which are recessive to those in spring‐spawning bitterlings. Free‐embryonic diapause in A. rhombeus appears to be an adaptation to winter, which might have evolved with reproduction in autumn among autumn‐spawning bitterling species. This is the only report of free‐embryonic diapause after hatching in fishes, and only the second example of diapause in fishes, along with annual killifishes (Rivulidae).