昆虫耐寒性研究

昆虫是变温动物,气候变化是造成种群季节消长的基本原因之一。尤其在不良的低温环境中,昆虫耐寒力的高低是其种群存在与发展的种要前提,昆虫对低温的适应能力及其机理也因而成为昆虫生态学和生物进化研究中的一个深受重视的问题,本文论述了与耐寒性直接相关的过冷却点昆虫的抗寒对策,明确了昆虫耐寒性的一些基本概念,一方面从环境影响昆虫的角度对耐寒性的一般规律,如季节性变化,地理变异快速冷驯化的作用等做了简要的概念括,另一方面阐述了昆虫适应环境的生理生化机制,包括低分子量的抗冻物质的产生,冰核剂的作用及抗冻蛋白的功能等做了简要的概括,另一方面简单述了昆虫适应环境的生理生化机制,包括低分子量的抗冻物质的产生,冰核剂的作用及抗冻蛋白的功能等。强调昆虫与环境相互作用过程中的生态生理适应,并指出昆虫耐寒性应当与生活史中别的因素联系起来,这样才能对耐寒性有一个更加全面的理解。     

昆虫病原线虫研究概况

昆虫病原线虫 (ｅｎｔｏｍｏｐａｔｈｏｇｅｎｉｃｎｅｍａｔｏｄｅｓ)是本世纪发展起来的一种有潜能的生物防治因子[1] 。它具有寄主范围广、能主动寻找寄主、对人畜及环境安全无毒 ,并能人工大量培养等优点。因此 ,在农药污染日益严重、害虫抗药性发展迅速的今天 ,昆虫病原线虫已成为可持续发展农业的迫切需要 ,受到国际生防领域的重视。特别是斯氏科线虫和小杆科线虫 ,已成为当前国际生防领域研究热点之一。本文简要概述了线虫的生物学特性、分类及致病机理等方面的研究 ,并结合目前存在的问题探讨了昆虫病原线虫的研究方向和发展前景。1…     

我国关于昆虫病原线虫分类的研究进展

我国关于昆虫病原线虫分类的研究进展图立红（首都师范大学生物学系１０００３７）昆虫病原线虫是目前国内外发展较快的一类生物杀虫剂,随着昆虫病原线虫学科的发展,对其资源的调查、开发和利用越来越受到重视。昆虫病原线虫,寄主范围广,寄生杀虫效果好,致死速度快,...     

昆虫病原线虫的共生细菌

昆虫病原线虫与其共生细菌二者互惠共生 :共生细菌需要昆虫病原线虫作为载体以寄生寄主昆虫并做为自己的营养来源 ,而昆虫病原线则需要依靠共生细菌来杀死昆虫。综述了共生细菌的病原作用、抗菌作用与杀虫作用 ,评述了共生细菌的基因工程进展 ,讨论了昆虫共生细菌在昆虫病原线虫致病性的作用。     

一种昆虫病原斯氏线虫杂交的新方法

将大蜡螟幼虫或蛹剪成2—3段,挑入配对种的感染期幼虫各一条,24—26℃保湿条件下,一周左右可获杂交结果。较常规的注射法和昆虫血液悬滴法操作方便,培养条件也要求不严,试用效果良好。做过的1594对线虫的交配试验,成功率在95％以上。     

昆虫病原线虫液体培养研究概况

综述昆虫病原线虫液体培养的研究概况。包括液体培养的研究历史,不同培养基组分对昆虫病原线虫产量的影响,营养源的选择,培养参数在昆虫病原线虫液体培养过程中的作用,感染期昆虫病原线虫脂肪酸含量,以及昆虫病原线虫应用前景等。     

昆虫病原线虫与粘合剂混用的增效试验

应用一定浓度的水溶性粘合剂POA与病原线虫混合,可提高线虫的存活率、毒力及对寄主的致死速度.LRT50为0.74,共毒系数大于100,混剂增效显著.田间防治龟背天牛、桑天牛的效果比单用病原线虫提高10-25%.POA是一种有利用价值的增效剂.     

昆虫病原线虫感染寄主行为研究进展

昆虫病原线虫斯氏属Steinernema和异小杆属Heterorhabditids线虫是新型的生物杀虫剂。其感染期幼虫是惟一能够侵染寄主昆虫的虫态。这类线虫感染寄主的行为分为寻找寄主、识别寄主和侵染寄主。文章综述昆虫病原线虫感染寄主昆虫的行为以及在感染寄主过程中的影响因素。     

昆虫病原线虫共生细菌胞内晶体蛋白的研究进展

初生型发光杆菌属(Photorhabdus)及嗜线虫致病杆菌属(Xenorhabdus)细菌分别与异小杆线虫属(Heterorhabditis)和斯氏线虫属(Steinernema)昆虫病原线虫互惠共生.这类昆虫病原细菌在稳定生长期分别产生两种形态各异的胞内晶体蛋白.本文回顾了这类蛋白的研究历史和最新的研究进展,特别是胞内晶体蛋白的理化性质和生物学功能,同时讨论这种晶体蛋白的研究方法与技术.     

Cold tolerance in nematodes

Summary The nematodesTrichostrongylus colubriformis (J3),Ditylenchus dipsaci (J4) andPanagrellus silusae (adults) are freezing-susceptible but can avoid freezing by supercooling. Their mean supercooling points were –30.0±0.7°C forT. colubriformis, –21.7±0.7°C forD. dipsaci and –20.7±0.84°C forP. silusae. T. colubriformis andD. dipsaci could prevent seeding by external ice butP. silusae could not. The glycerol concentrations of these nematodes are considered to be too low to have a significant antifreeze effect.Abbreviations J3 3rd-stage juvenile - J4 4th stage juvenile - SEM standard error of the mean - T ₅₀ 50% survival temperature     

Cold tolerance of steinernematid and heterorhabditid nematodes

• 1.1. Nematodes survive subzero temperatures using either a freeze-avoiding or freezing-tolerant strategy. Steinernema anomali, S. feltiae, and Heterorhabditis bacteriophora were all found to be freezing tolerant.
• 2.2. The lower lethal temperatures were −22, −19 and −14°C for S. feltiae, H. bacteriophora and S. anomali, respectively.
• 3.3. Survival after prolonged freezing at −4°C was 6, 5 and 3 days for S. feltiae, H. bacteriophora and S. anomali, respectively.
• 4.4. Acclimation to lower temperatures increased freezing tolerance. The freezing tolerance of Heterorhabditis bacteriophora increased under a stepwise acclimation regime; S. feltiae acclimated better under a direct acclimation regime.

     

Storage temperature influences desiccation and ultra violet radiation tolerance of entomopathogenic nematodes

1. The effect of cold (5 °C) and warm (35 °C) storage on desiccation tolerance of cold-adapted Steinernema feltiae, intermediate S. carpocapsae and warm-adapted S. riobrave was evaluated at 5 and 35 °C.     

Antagonism between entomopathogenic fungi and bacterial symbionts of entomopathogenic nematodes

Mutual effects between the symbiotic bacteria of entomopathogenic nematodes, Photorhabdus luminescens and Xenorhabdus poinarii, and entomopathogenic fungi were investigated in vitro. A dual culture assay on nutrient agar supplemented with bromothymol blue and triphenyltetrazolium chloride (NBTA) medium revealed that P. luminescens is antagonistic to Metarhizium anisopliae, Beauveria bassiana, B. brongniartii and Paecilomyces fumosoroseus by inhibiting their growth and conidial production; the fungal growth was not inhibited by X. poinarii. In a second laboratory experiment, crude extract produced by M. anisopliae was tested for its activity against P. luminescens and X. poinarii. Crude extract from M. anisopliae was antibacterial to P. luminescens and X. poinarii at 1000 g/ml and inhibited their growth on NBTA, but had no effect at 100 or 10 g/ml. The influence of the crude extract of M. anisopliae on the dispersal of infective juveniles (IJs) of Heterorhabditis megidis and Steinernema glaseri was assayed on Sabouraud Dextrose Agar (SDA) plates. Results showed that the crude extract of M. anisopliae had no toxic effects even at highest concentration (1000 g/ml).     

Compatibility of entomopathogenic nematodes with fipronil

The survival and infectivity of infective juveniles (IJs) of three species of entomopathogenic nematodes, Steinernema carpocapsae Weiser, S. arenarium (Artyukhovsky) (Rhabditida: Steinernematidae) and Heterorhabditis bacteriophora Poinar (Rhabditida: Heterorhabditidae), were determined after exposure to different concentrations (250, 500, 1000 and 2000 ppm) of fipronil, an insecticide acting on the GABA receptors to block the chloride channel. Heterorhabditis bacteriophora was very tolerant to all concentrations of fipronil, with the highest mortality of 17% being observed at 2000 ppm of fipronil after 72 h exposure. Steinernema carpocapsae showed a similar response, with the highest mortality of 11.25% of IJs being observed after 72 h exposure to 2000 ppm of fipronil. Steinernema arenarium was, however, more sensitive to fipronil, and at 2000 ppm mortality rates of 94.6% and 100% were observed after 24 and 72 h, respectively. Fipronil had negligible effects on the infectivity of the three nematode species tested. The IJs which survive exposure to all concentrations of fipronil tested can infect and reproduce in Galleria larvae. The moderate effects on entomopathogenic nematodes of a lower fipronil concentration (250 ppm) and the field rates (12-60 ppm) of fipronil used as insecticide, suggest that direct mixing of entomopathogenic nematodes and fipronil at field rates is a viable integrated pest management option.     

Distribution of entomopathogenic nematodes in Southern Cameroon

A first survey of entomopathogenic nematodes (EPN) was conducted in three agro-ecological zones of Southern Cameroon in 2007 and 2008. Entomopathogenic nematodes were recovered from 26 of 251 soil samples (10.4%). Three species, Heterorhabditis baujardi, Steinernema sp. A and Steinernema sp. B were found. The two steinernematids were considered unidentified species. Among the positive samples, 23 samples contained only H. baujardi (88.5%), two contained Steinernema sp. A co-occurring with H. baujardi (7.7%), and one sample contained Steinernema sp. B (3.9%). H. baujardi was frequent in forest and fruit crop (cocoa and oil palm plantations). Steinernema sp. A was found in a tree plantation of teak, Steinernema sp. B in a forest habitat. Nematodes were mostly present in acidic soils with pH ranging from 3.7 to 7.0. The highest EPN presence was recorded in sandy loam, sandy clay loam, sandy clay and clay soils. EPNs were not recovered in sand, loamy sand and clay loam soils. Using principal component analysis for elucidating the major variation patterns among sampling sites, four factors explaining for 73.64% of the overall variance were extracted. Factors were a combination of geographical (latitude, longitude, altitude), soil (pH, contents of sand, silt and clay, organic carbon, texture), and moisture (wilting point, field capacity) parameters as well as climatic parameters (mean annual rainfall, mean air temperature). Logistic regression and redundancy analyses (RDA) revealed that soil pH, longitude, available water and altitude were associated with presence and absence of EPN. Both logistic regression and RDA indicated that, increasing soil pH and longitude, associated with decreasing altitude, led to higher percentages of samples containing entomopathogenic nematodes.     

Factors limiting short-term persistence of entomopathogenic nematodes

Abstract:  Entomopathogenic nematodes are commonly applied to soil and crops for biocontrol of insects. Typically, when nematodes are applied, recoverable numbers decline quickly. Because ultra-violet light is known to kill entomopathogenic nematodes in the laboratory, many researchers blame poor field persistence on the action of ultra-violet light. We conducted a field experiment to test this hypothesis, using Heterorhabditis bacteriophora applied to turf as a model system. We compared persistence of surface-applied nematodes with subsurface-applied nematodes and found no difference in persistence. Numbers of potential nematode antagonists (mites and collembola) were also monitored. Poor persistence was positively correlated with numbers of mites and collembola in plots where nematodes were surface-applied, but not in plots where they were subsurface-applied.