桔小实蝇抗性个体流动对抗性个体频率的影响

为了解害虫个体的迁移对害虫群体抗药性发展的影响, 本研究利用实验室内建立的桔小实蝇Bactrocera dorsalis对敌百虫和高效氯氰菊酯两种抗性品系以及相对敏感品系, 设计5%~25%个体的迁移比例, 研究桔小实蝇抗、 感个体流动对原始种群抗性个体频率的影响。结果表明: 桔小实蝇抗性个体迁入敏感种群, 使得敏感种群抗性个体频率增加, 在抗性个体迁移率为25%时, 影响敏感种群敌百虫和高效氯氰菊酯抗性个体频率的变化值分别为20.04%和41.75%; 同样随着敏感个体迁入比例的增加, 抗性种群中抗性个体频率降低程度越大, 在敏感个体迁移率为25%时, 抗性种群敌百虫和高效氯氰菊酯抗性个体频率的变化值分别为56.20%和25.88%。利用抗性个体频率变化值与相应迁移率的比值来表示迁移的相对效率, 在抗性个体迁移率为5%时, 影响敏感种群抗性个体频率变化的相对效率最高; 在敏感个体迁移率分别为5%和10%时, 影响敌百虫抗性种群和高效氯氰菊酯抗性种群抗性个体频率变化的相对效率最高。以抗、 感个体迁移引起的抗性个体频率变化值进行趋势拟合, 发现抗敌百虫与抗高效氯氰菊酯桔小实蝇品系不同迁移比例下的抗性个体频率变化趋势分别符合密度模型(density model)和房屋模型(housing model), 相关系数分别是0.9696和0.9647。研究结果表明通过合理地设计抗、 感迁移比例能有效地延缓桔小实蝇抗性水平的上升, 达到抗性治理的目的。     

抗马拉硫磷淡色库蚊不同基因型的自然内禀增长率及其对抗性演化的影响

本文涉及淡色库蚊(Culex pipiens pallens)抗马拉硫磷纯合子(RR)、杂合子(RS)和敏感纯合子(SS)的自然内禀增长率及其对马拉硫磷抗性演化的影响。RR、RS和SS的内禀增长率分别为0.1118、0.1171和0.1339。RR和RS基因型在无杀虫剂时呈现出繁殖不利性,RR和RS的相对适合度分别是SS的0.65和0.68。 影响淡色库蚊对马拉硫磷进化的某些因子在计算机上进行了模拟。模拟的因子包括R等位基因的起始频率(P_o)、所用马拉硫磷的剂量和迁入率(m)。模拟结果表明(I)不用药时R等位基因衰减是由于RR和RS基因型的繁殖不利性;(2)在起始种群N_o=200,P_o=0.1,使用杀死全部SS和RS的剂量(8ppm)处理,使R等位基因为有效隐性,并且m≥0.15时可阻止马拉硫磷抗性的发生。     

抗马拉硫磷淡色库蚊不同基因型的自然内禀增长率及其对抗性演化的影响

本文涉及淡色库蚊(Culex pipiens pallens)抗马拉硫磷纯合子(RR)、杂合子(RS)和敏感纯合子(SS)的自然内禀增长率及其对马拉硫磷抗性演化的影响.RR、RS和SS的内禀增长率分别为0.1118、0.1171和0.1339.RR和RS基因型在无杀虫剂时呈现出繁殖不利性,RR和RS的相对适合度分别是SS的0.65和0.68. 影响淡色库蚊对马拉硫磷进化的某些因子在计算机上进行了模拟.模拟的因子包括R等位基因的起始频率(P_o)、所用马拉硫磷的剂量和迁入率(m).模拟结果表明(I)不用药时R等位基因衰减是由于RR和RS基因型的繁殖不利性;(2)在起始种群N_o=200,P_o=0.1,使用杀死全部SS和RS的剂量(8ppm)处理,使R等位基因为有效隐性,并且m≥0.15时可阻止马拉硫磷抗性的发生.     

杀虫剂轮用和混用对害虫种群抗性演化的影响

杀虫剂轮用和混用是当前害虫抗药性治理中最常采用的两种用药策略。该文用抗性模型和室内试验对轮用和混用延缓害虫抗性演化的效果及轮用最佳间隔期问题作了研究。模型模拟结果表明,在延缓害虫抗性演化方面轮用和混用对抗性演化的影响主要取决于杀虫剂作用强度、抗性基因型个体的适合度大小和杀虫剂混用后的毒理效应类型。两种杀虫剂轮用时,轮用间隔期以1(即两种杀虫剂隔次施用)为佳。以模型昆虫小菜蛾Plutella xylostella在室内试验结果表明,氰戊菊酯单用(I)及与杀虫单轮用(II)和混用(1∶1)(III)连续处理8代后,抗性个体频率为0.01的小菜蛾种群其3龄幼虫对氰戊菊酯的抗性分别上升了75.87(I)、28.67(II)和58.72(III)倍,与模型模拟结果表现出较好的一致性。据此,作者认为抗性模型可用于预测害虫抗性演化和评价抗性治理策略。     

生境破碎化对生物多样性的影响

生境破碎化对生物多样性和生态系统功能的影响是当前国内外生态学家研究的热点问题之一。生境破碎化导致原生境的总面积减小,产生隔离的异质种群,从而影响个体行为特性、种群间基因交换、物种间相互作用及生态过程。生境破碎化的过程引起栖息地内部食物、繁殖场所、局部小气候、边缘效应等生物和非生物条件的变化,从而影响植物种群的大小和灭绝速率、扩散和迁入、遗传和变异以及存活力等,影响动物种群的异质种群动态、适宜生境比例、灭绝阈值、种间关系等。随着景观生态学与农业科学的融合,探索利用景观布局控制害虫发生将是人类利用生境破碎化为人类服务的一条新途径。     

截形叶螨对阿维·哒螨灵的抗性遗传方式研究

【目的】明确截形叶螨Tetranychus truncatus Ehara对阿维·哒螨灵药剂的抗性遗传方式,为今后合理使用药剂,有效地制定害螨抗性治理策略提供一定的理论指导。【方法】通过杂交和回交试验,确定截形叶螨抗阿维·哒螨灵种群的显性度(D)、细胞质影响因子和遗传基因。【结果】所测得的截形叶螨抗性种群的杂交F1代(SS♀?RR♂和RR♀SS♂)的显性度D值分别为0.625和0.802,均在0 D 1范围内,表明抗性都由不完全显性基因控制;两个D值(DSR和DRS)95%置信限有重叠,并且经t-检验,两个D值不存在显著差异(P0.05),证明截形叶螨对阿维·哒螨灵的抗性遗传受母体或核外效应的影响不大,其抗性基因在常染色体上;回交F2代两个种群的(BC1SR和BC1RS)的实际死亡率和期望值经χ2检验,均差异显著,证实由多基因控制。【结论】不完全显性多基因控制的遗传方式产生的抗谱很宽,抗性一旦产生则很难延缓其抗性的迅速发展,因此田间应用该药剂时应交替轮换不同作用机制的药剂,重点采用预防性抗性治理策略。     

靶标害虫对Bt玉米的抗性发展和治理策略

全生育期有效表达Bt杀虫蛋白的转基因抗虫玉米为靶标害虫的防治提供了新途径。但是,靶标害虫抗性种群的发展严重威胁了转基因抗虫玉米的可持续应用。截止到2018年,已经有13例报道表明靶标害虫对转基因抗虫玉米产生了田间抗性;5例监测结果表明靶标种群没有降低对Bt玉米的敏感性,其中包括转vip3Aa玉米。抗性治理策略成功的关键主要包括:Bt杀虫蛋白的高剂量表达、靶标害虫的隐性遗传、初始抗性等位基因频率较低、不完全抗性、适合度代价等。当抗性为非隐性遗传时,可以通过增加庇护所的种植面积达到延缓抗性发展的目的。     

Cry1Ie毒素胁迫下亚洲玉米螟的抗性发展及汰选种群对其他Bt毒素的交互抗性

亚洲玉米螟Ostrinia furnacalis (Guenée) 是危害玉米的重要害虫之一, 转Bt基因抗虫玉米为其防治提供了新的途径。然而, 靶标害虫产生抗性将严重阻碍Bt制剂及转Bt基因抗虫玉米的持续应用。明确害虫对转Bt基因玉米表达的毒素蛋白的抗性演化, 对于制定科学有效的抗性治理策略具有重要的理论和实际意义。本实验通过人工饲料汰选法研究了Bt Cry1Ie毒素胁迫下亚洲玉米螟的抗性发展及汰选14代的种群对其他Bt毒素（Cry1Ab, Cry1Ac和Cry1Fa）的交互抗性, 并观察了Cry1Ie蛋白胁迫对亚洲玉米螟生物学的影响。结果表明： 随着汰选压不断提高, 亚洲玉米螟种群对Cry1Ie毒素的敏感性逐渐下降。汰选14代后, 种群对Cry1Ie毒素的抗性水平提高了23倍。然而, Cry1Ab, Cry1Ac和Cry1Fa对所获Cry1Ie汰选种群的毒力与对敏感种群的毒力相比没有显著差异, 说明Cry1Ie汰选没有引起亚洲玉米螟对Cry1Ab, Cry1Ac和Cry1Fa毒素产生交互抗性。同时, 与敏感种群相比, Cry1Ie汰选14代的种群幼虫平均发育历期延长5.7 d, 蛹重减轻13.7%, 单雌产卵量下降40.0%。本研究结果说明, 大面积单一种植转cry1Ie基因抗虫玉米, 可能引起亚洲玉米螟产生抗性; 亚洲玉米螟Cry1Ie抗性种群对Cry1Ab, Cry1Ac和Cry1Fa没有交互抗性, 含有cry1Ie和cry1Ab, cry1Ac或cry1F双/多基因抗虫玉米, 可作为靶标害虫抗性治理的重要策略。     

家蝇的抗药性及其对策

据Georghiou, G. P. (1985年)报道,仅1980—1984年全世界害虫对杀虫剂产生抗性的种类由428种增加到447种。其中,重要的卫生害虫占全部害虫抗性种类的38％。多年来由于新杀虫剂的大量开发和应用,害虫抗性种群的地理分布,抗性基因频率的比例不断地增加,而导致害虫对杀虫剂产生多种抗性,家蝇     

杀虫剂混用方法——抗性治理的一种策略

本文根据种群遗传学的基本原理,采用计算机数值模拟的方法定量比较了合理混用、轮用、棋盘式使用等用药策略对害虫抗性增长的影响.结果表明,对半显性遗传,两性繁殖的害虫来说,在较有利的条件下合理混用与轮用效果基本一致,而优于棋盘式用药;在条件不利(抗性基因初始频率高,稀释作用小等)时,合理混用的方法明显优于其他两种方法.因此合理混用是一种有希望的抗性治理方法.     

Analytical methods for detecting pesticide switches with evolution of pesticide resistance

After a pest develops resistance to a pesticide, switching between different unrelated pesticides is a common management option, but this raises the following questions: (1) What is the optimal frequency of pesticide use? (2) How do the frequencies of pesticide applications affect the evolution of pesticide resistance? (3) How can the time when the pest population reaches the economic injury level (EIL) be estimated and (4) how can the most efficient frequency of pesticide applications be determined? To address these questions, we have developed a novel pest population growth model incorporating the evolution of pesticide resistance and pulse spraying of pesticides. Moreover, three pesticide switching methods, threshold condition-guided, density-guided and EIL-guided, are modelled, to determine the best choice under different conditions with the overall aim of eradicating the pest or maintaining its population density below the EIL. Furthermore, the pest control outcomes based on those three pesticide switching methods are discussed. Our results suggest that either the density-guided or EIL-guided method is the optimal pesticide switching strategy, depending on the frequency (or period) of pesticide applications.     

昆虫抗药性的治理策略:一个数学模型的提出

本文用计算机模型分析及评价了昆虫抗药性的三种治理策略:顺序轮用,“高杀死”策略及棋盘式用药.假设昆虫具有一定的生物学特性:如抗性为单基因,单抗性,抗性基因为半显性,两性生殖,昆虫有扩散习性,感性系在不施药情况下有微弱的适应优势等.分析了用不同剂量造成的不同的死亡率,不同的反选择作用,不同的基因稀释作用等情况对三个策略的影响.结果显示出,在这些情况下,用3—5种杀虫剂隔代顺序轮用加上微弱的反选择作用是最为有效的.“高杀死”策略加上一定的稀释作用也极为有效.棋盘式用药在特殊情况下才有用.     

Ecology and genetics of insecticide resistance inHelicoverpa armigera: Interactions between selection and gene flow

Pyrethroid resistance inHelicoverpa armigera provides a model system in which to study evolution in natural populations. Resistance is seen to evolve as a consequence of selection pressure that varies within and between life-stages and gene flow. Although three different mechanisms are involved, present day fluctuations in phenotype frequency can be explained by variation in only one of these, metabolic resistance, that is inherited as a single, incompletely dominant gene,mfo. Selective mortality of phenotypes occurs in both larvae and adults in the presence of the pyrethroid insecticides. Although most individuals of all three genotypes are killed in young larvae, selection in this age-class contributes significantly to evolution of resistance. While there is some evidence of reduced fitness of resistant pupae during winter diapause, most of the decline in resistance frequencies each spring occurs as a result of immigration of susceptible individuals into insecticide-treated populations.     

Effects of temperature on fitness costs in chlorpyrifos‐resistant brown planthopper,Nilaparvata lugens (Hemiptera: Delphacidae)

Insecticide resistance is inevitable if an insecticide is widely used to control insect pests. Fortunately, the resistance‐associated fitness costs often give chances to manage resistances. In most cases, the fitness cost in resistant insects is often evaluated under laboratory conditions for insect development, which limits its practical application in pest control in the field. In a laboratory population R9 with 253‐fold resistance to chlorpyrifos after nine‐generation selection with chlorpyrifos, the relative fitness was only 0.206 under laboratory conditions (25°C, humidity 70%–80% and 16 h light/8 h dark photoperiod), when compared to S9, a susceptible counterpart (resistance ratio = 2.25‐fold) from the same origin as R9 but without any selection with insecticides. Temperatures varied the resistance‐associated fitness costs, with enhanced costs at high temperatures and reduced costs at low temperatures, such as 0.174 at 32°C and 0.527 at 18°C. The copulation rate and fecundity were two key factors for the reduced costs at low temperatures. Another finding was that R9 individuals needed much more time to recover from heat shock than that of S9, but R9 and S9 individuals were similarly sensitive to cold shock. The low fitness cost at low temperatures would increase the overwintering population, which might further increase risks of rapid development and widespread distribution of chlorpyrifos resistance in Nilaparvata lugens.     

Plant population dynamics, pollinator foraging, and the selection of self-fertilization

Many flowering plants rely on pollinators, self-fertilization, or both for reproduction. We model the consequences of these features for plant population dynamics and mating system evolution. Our mating systems-based population dynamics model includes an Allee effect. This often leads to an extinction threshold, defined as a density below which population densities decrease. Reliance on generalist pollinators who primarily visit higher density plant species increases the extinction threshold, whereas autonomous modes of selfing decrease and can eliminate the threshold. Generalist pollinators visiting higher density plant species coupled with autonomous selfing may introduce an effect where populations decreasing in density below the extinction threshold may nonetheless persist through selfing. The extinction threshold and selfing at low density result in populations where individuals adopting a single reproductive strategy exhibit mating systems that depend on population density. The ecological and evolutionary analyses provide a mechanism where prior selfing evolves even though inbreeding depression is greater than one-half. Simultaneous consideration of ecological and evolutionary dynamics confirms unusual features (e.g., evolution into extinction or abrupt increases in population density) implicit in our separate consideration of ecological and evolutionary scenarios. Our analysis has consequences for understanding pollen limitation, reproductive assurance, and the evolution of mating systems.     

Genetics and evolution of resistance to insecticides

The evolution of resistance to insecticides has become a serious problem world-wide. It is important to identify patterns of insecticide use whereby insecticides can be used in integrated pest management programmes to help control insect numbers, but in such a manner that the evolution of resistance to insecticides will be retarded. The principal mechanisms of insecticide action and of resistance to these are reviewed. Some generalizations that can be made about the evolution of resistance are examined. In general, to control resistance it appears better to use an intense dose of non-persistent pesticides over a circumscribed area. Some features of the problem where population genetics and evolutionary theory might contribute to controlling resistance are discussed.     

Growth and development of Bacillus thuringiensis Cry1Ab-susceptible and Cry1Ab-resistant sugarcane borer on diet and conventional maize plants

The sugarcane borer, Diatraea saccharalis (F.) (Lepidoptera: Crambidae), is a dominant maize borer pest and a major target of Bacillus thuringiensis (Bt)‐maize in Louisiana and the Gulf Coast area of Texas (USA). Growth and development of D. saccharalis on non‐toxic diet, diet treated with three low concentrations (0.01, 0.05, and 0.1 μg g^?1) of Cry1Ab toxin, and on non‐Bt maize plants were compared for five insect genotypes: a Bt‐susceptible strain (BT‐SS), a Cry1Ab‐resistant strain (BT‐RR), a back‐crossed and re‐selected resistant strain (BT‐R’R’), and two F₁ progeny of the BT‐SS and BT‐R’R’ strains. Fitness of the five genotypes was examined by infesting neonates on diet with/without Cry1Ab toxin in the laboratory and on intact non‐Bt maize plants in the greenhouse. Biological parameters measured were neonate‐to‐pupa development time and pupation rate, larval survival, larval and pupal weight, and sex ratio. Larvae of BT‐SS and BT‐R’R’ on non‐toxic diet and non‐Bt maize plants grew normally and there were no significant differences between the two strains in all measured parameters, suggesting a lack‐of‐fitness cost of the Cry1Ab resistance in D. saccharalis. Except for the development time on non‐Bt diet, all other parameters on both non‐Bt diet and non‐Bt maize plants were similar among the five genotypes. Larval development of BT‐SS was significantly affected on diet treated with Cry1Ab toxin at 0.05 and 0.1 μg g^?1, whereas the effect to BT‐RR and BT‐R’R’ was not significant. Pupal weight and sex ratio reared on Cry1Ab‐diet were similar and there were no significant differences among the five genotypes. Neonate‐to‐pupation rate decreased as Cry1Ab concentrations increased but the decrease was more significant for BT‐SS than for the other four genotypes. The lack‐of‐fitness costs of Bt resistance in D. saccharalis imply a greater challenge in managing Bt resistance for this maize borer species.     

Population dynamics of obligate cooperators

Obligate cooperative breeding species demonstrate a high rate of group extinction, which may be due to the existence of a critical number of helpers below which the group cannot subsist. Through a simple model, we study the population dynamics of obligate cooperative breeding species, taking into account the existence of a lower threshold below which the instantaneous growth rate becomes negative. The model successively incorporates (i) a distinction between species that need helpers for reproduction, survival or both, (ii) the existence of a migration rate accounting for dispersal, and (iii) stochastic mortality to simulate the effects of random catastrophic events. Our results suggest that the need for a minimum number of helpers increases the risk of extinction for obligate cooperative breeding species. The constraint imposed by this threshold is higher when helpers are needed for reproduction only or for both reproduction and survival. By driving them below this lower threshold, stochastic mortality of lower amplitude and/or lower frequency than for non-cooperative breeders may be sufficient to cause the extinction of obligate cooperative breeding groups. Migration may have a buffering effect only for groups where immigration is higher than emigration; otherwise (when immigrants from nearby groups are not available) it lowers the difference between actual group size and critical threshold, thereby constituting a higher constraint.