棉铃虫发育历期的地理变异

为探明棉铃虫Helicoverpa armigera Hübner不同地理种群发育历期及其地理变异,通过对棉铃虫不同地理种群在不同温度和光周期下幼虫和蛹发育历期的研究,本论文系统比较了来自中国的4个地理种群,广东广州(23.08°N,113.14°E)、江西永修(29.04°N,115.82°E)、山东泰安(36.15°N,116.59°E)、辽宁喀佐(41.34°N,120.27°E)在20℃、22℃、25℃和28℃恒温下的幼虫、非滞育蛹和滞育蛹发育历期及其与栖息地纬度的关系。结果表明,棉铃虫幼虫发育历期随栖息地纬度的升高而缩短,在25℃下,与地理纬度存在明显的负相关关系,其它温度下呈不显著的负相关关系,雌雄幼虫发育历期相似,差异不显著;在20℃下,蛹历期(包括滞育蛹和非滞育蛹)与栖息地纬度呈显著负相关,其它温度下的蛹历期与栖息地纬度呈正相关,雄蛹历期均要略长于雌蛹历期,但差异不显著。棉铃虫幼虫和蛹发育历期随着纬度的变化呈现一种渐变的趋势,存在地理变异;北方种群的幼虫发育历期较南方种群的短;适温(22℃-28℃)范围内,北方种群的非滞育蛹发育历期比南方种群的更长些;不同地理种群间滞育蛹的历期亦存在较大的差别。这些结果进一步揭示了即使在同一种类昆虫中,不同实验条件,其各个虫态发育历期的地理变异也可能不同。     

棉铃虫温度依赖的生长发育及雌性先熟现象

在昆虫中,雄虫先于雌虫羽化,称为雄虫先熟现象,而雌虫先于雄虫羽化,称为雌虫先熟现象。前者最为普遍,后者报道较少。本试验在20、22和25℃下对棉铃虫Helicoverpa armigera（Hilbner）的生长发育进行了详细的研究。结果显示发育历期随温度的升高而缩短,雌雄间发育历期有着显著的差异,各个温度下雌虫均比雄虫先羽化,表明棉铃虫属于雌性先熟种类,而这种差异主要是由于雌虫的蛹期较短所致。幼虫发育历期与蛹重呈显著的正相关性。     

Temperature-dependent development and protogyny in Helicoverpa armigera

在昆虫中,雄虫先于雌虫羽化,称为雄虫先熟现象,而雌虫先于雄虫羽化,称为雌虫先熟现象.前者最为普遍,后者报道较少.本试验在20、22和25℃下对棉铃虫Helicoverpa armigera(Hübner)的生长发育进行了详细的研究.结果显示发育历期随温度的升高而缩短,雌雄间发育历期有着显著的差异,各个温度下雌虫均比雄虫先羽化,表明棉铃虫属于雌性先熟种类,而这种差异主要是由于雌虫的蛹期较短所致.幼虫发育历期与蛹重呈显著的正相关性.     

竹缺爪螨生态学初步研究

本报道严重危害毛竹生长和害螨－－竹缺爪螨在不同温度下生长,发育历期以及在竹林间种群动态。结果表明：在20－35℃范围内随着温度升高其发育历期缩短,温度与发育历期呈直线回归关系：Y全代＝651573-1.6250X（=-0.98);光照是影响竹缺爪螨的卵,幼螨存活及成螨产卵量的重要因素。在竹林间,毛竹换叶,降雨量,天敌数量是影响竹缺爪螨种群消长的和重要因素,最后提出综合防治的措施。     

外源水杨酸甲酯(MeSA)处理茶树对茶园主要害虫及其天敌的影响

研究了4种豆科寄主植物及5个不同温度处理对西花蓟马生长发育的影响,并对各虫态的发育起点温度和有效积温进行了分析。结果表明:同一温度条件下,西花蓟马取食不同豆科寄主植物时,各虫态的发育历期差异显著,但不同温度下不同寄主处理间的差异性不同;西花蓟马的未成熟期取食四季豆叶片时发育最快,取食蚕豆叶片时发育最慢,两寄主间存在显著差异;取食同一寄主植物时,不同温度处理下,西花蓟马各虫态的发育历期差异显著,且随温度升高历期缩短,发育速率和温度之间为直线关系;西花蓟马各虫态在不同寄主植物上的发育起点温度和有效积温各不相同,未成熟期取食蚕豆叶片时发育起点温度最低为6.35℃,但需要的有效积温最高为331.36日度。     

寄主和温度对西花蓟马生长发育的影响

研究了4种豆科寄主植物及5个不同温度处理对西花蓟马生长发育的影响,并对各虫态的发育起点温度和有效积温进行了分析.结果表明:同一温度条件下,西花蓟马取 食不同豆科寄主植物时,各虫态的发育历期差异显著,但不同温度下不同寄主处理间的差异性不同;西花蓟马的未成熟期取食四季豆叶片时发育最快,取食蚕豆叶片时发育最慢,两寄主间存在显著差异;取食同一寄主植物时,不同温度处理下,西花蓟马各虫态的发育历期差异显著,且随温度升高历期缩短,发育速率和温度之间为直线关系;西花蓟马各虫态在不同寄主植物上的发育起点温度和有效积温各不相同,未成熟期取食蚕豆叶片时发育起点温度最低为6.35℃,但需要的有效积温最高为331.36日度.     

温度对以截形叶螨为猎物的斯氏钝绥螨生长发育的影响

测定了斯氏钝绥螨Amblyseius swirskii（Athias—Henriot）在14、17、20、23、26、29、32、35℃和RH=85％的条件下,以截形叶螨为猎物各螨态的发育历期,分析发育速率与温度的关系。结果表明,14℃不适宜斯氏钝绥螨的生长发育,存活率仅17．5％;在17～35℃之间其生长发育正常,存活率均100％,各螨态的发育历期与温度均呈负相关关系,发育历期随着温度的升高明显缩短,未成熟期总发育历期从21．36d缩至3．97d。采用线性日度模型拟合温度与发育速率的关系表明,该模型能较好地描述其发育速率在适宜温度范围内随温度升高而加快的现象。斯氏钝绥螨不同发育阶段的发育起点温度和有效积温不同,未成熟期的发育起点温度和有效积温分别为11．92℃和94．69日·度。     

环境因子对烟粉虱子代发育历期的影响

温度、湿度、光周期和寄主植物是影响烟粉虱Bemisia tabaci(Gennadius)生长发育的重要环境因子,本研究采用正交试验设计,分析了各因子对烟粉虱子代发育历期的影响作用。结果表明:(1)温度、寄主对烟粉虱的子代发育历期有极显著的影响(P0.01),而湿度、光周期的影响显著(P0.05)。各因子影响作用大小顺序为温度(F=427.1,P=0.000)寄主(F=265.8,P=0.000)湿度(F=28.8,P=0.010)光周期(F=17.8,P=0.020)。(2)各因子配对分析结果表明:23℃条件下的子代历期要长于25℃、27℃、29℃,4个温度处理间差异均极显著(P0.01)。甘蓝寄主上烟粉虱子代发育历期最短;与番茄和一品红处理间差异极显著(P0.01)。低湿利于缩短烟粉虱子代发育历期,RH 50%条件下的子代历期要短于其它3个湿度,与RH70%处理间差异极显著(P0.01),与RH 60%、RH 80%处理间差异显著(P0.05)。光周期12∶12时,发育历期短于其它3个光周期,与14∶10处理间差异极显著(P0.01);12∶12与10∶14、16∶8处理间差异显著(P0.05)。(3)当寄主为甘蓝、温度29℃、湿度50%、光周期12∶12时,发育历期最短,此环境因子组合可用于指导室内饲养烟粉虱。     

光周期和温度对棉铃虫发育历期及蛹重的影响

以山东泰安棉铃虫Helicoverpa armigera Hübner为例,在人工饲养条件下、人工气候箱中,研究了不同光周期和温度条件对棉铃虫幼虫生长发育历期、蛹重及蛹历期的影响.结果表明,光周期对棉铃虫幼虫发育历期、非滞育蛹历期均存在一定的影响,短光照(滞育诱导的光周期)下的发育历期要长于长光照(诱导发育的光周期)的发育历期;温度对棉铃虫幼虫发育历期、非滞育蛹历期的影响十分明显,随着温度上升,发育历期明显缩短;棉铃虫蛹的重量形成受到幼虫期的光周期和温度的联合作用,在较高温度(28℃)下,光照时数与蛹重呈现极显著的负相关关系(R2=0.9257),在短光照(如11h光)下,蛹重与温度呈现正相关性(R2＝0.8564),而在长光照下如15h,蛹重与温度呈现一定的负相关性(R2=0.523);此外,同一光温下,雌雄蛹重量差异不显著,而滞育蛹要重于非滞育蛹,幼虫发育历期越长形成的蛹一般越重.     

白纹伊蚊幼虫龄期的发育历期

在实验室内20±1℃, 23±1℃, 25±1℃, 28±1℃和30±1℃恒温条件下, 观察了白纹伊蚊(Aedes albopictus)幼虫(广州株)的发育历期.幼虫的总发育历期和各龄幼虫的发育历期随温度的上升而缩短, 各龄幼虫历期在总发育历期中占有恒定的百分比, 据此计算出其捕获机率.各龄幼虫的发育历期与温度呈直线回归关系.通过积温公式, 求出各龄幼虫的积温常数.此外还探索了营养对幼虫发育历期的影响, 从而影响各龄幼虫捕获机率的计算.     

温度对产虫茶昆虫紫斑谷螟生长发育的影响

为探明温度对贵州主要产虫茶昆虫紫斑谷螟Pyralis farinalis (Linnaeus)生长发育的影响, 本研究以白茶Litsea coreana为寄主植物, 分别设置5个恒温（19, 22, 25, 28和31℃）条件, 研究温度对紫斑谷螟卵、 幼虫、 蛹和未成熟期平均发育历期、 发育速率和存活率的影响, 计算各虫态发育起点温度和有效积温。 结果表明： 温度对紫斑谷螟各虫态发育历期、 发育速率和存活率影响显著。 在19 ~ 31℃范围内, 各虫态的平均发育历期均随温度的升高而缩短, 卵期、 幼虫期、 蛹期及未成熟期均在31℃达到最小值, 分别为4.56±0.24, 43.33±1.50, 7.89±0.20和55.78±1.69 d。 紫斑谷螟各虫态发育速率与温度呈二次回归关系, 且极显著相关。 此外, 温度显著影响各虫态存活率, 卵的存活率在28℃时最高, 为93%; 幼虫和蛹的存活率则在25℃最高, 分别为88%和93%; 温度过高或过低均不利于其生长发育。 由直接最优法计算得到紫斑谷螟卵期、 幼虫期、 蛹期及未成熟期的发育起点温度分别为13.30, 15.48, 13.19和14.82℃, 有效积温依次为88.36, 679.51, 159.73和952.04日·度。 这些结果为紫斑谷螟的繁殖提供了基础参考数据, 对指导虫茶生产有实用参考价值。     

How to compare the lower developmental thresholds

According to the hypothesis of isomorphy rate, all the lower developmental thresholds of different developmental stages of an insect are equal. However, there is lack of a formal statistical method for testing whether there is a significant difference among the lower developmental thresholds on the basis of the traditional linear model describing developmental rate as a linear function of temperature. For comparing the lower developmental thresholds of different developmental stages, a new method based on the Chow test is proposed in the current study. Another feasible way based on the linear model proposed by Ikemoto and Takai is also proposed. The lower developmental thresholds can be compared by the analysis of covariance on this linear model. The current study can be used to test the hypothesis of isomorphy rate. When comparing the lower developmental thresholds of different geographical populations for one insect species, the two methods proposed here are also applicable.     

On the canopy structure manipulation to buffer climate change effects on insect herbivore development

Insect pest development is often linearly related to air temperature, without taking into account the multiple interactions between the particular host plant and pest, the microclimatic conditions actually experienced by the insect, and the non-linear response of insect development rate to temperature. In this study, using an integrative biophysical model, we have investigated effects of both climatic and tree structure changes on the development of a phytophagous leaf mining moth (Phyllonorycter blancardella), taking into account the heterogeneous microclimatic conditions provided by its host plant, the domestic apple (Malus domestica), the larval body temperature rather than the ambient air temperature, and a non-linear development rate model. Hourly body temperature dynamics of larvae homogeneously dispersed in tree canopies were simulated from hourly meteorological conditions (medium IPCC climate change scenario) within the canopy of apple trees. To analyse the effect of tree architecture on leaf miner development, both pruned and unpruned trees, and one, two and three scaffold branched trees were used. Body temperature dynamics was used to compute larval development time and mortality following the non-linear developmental model for this insect. The results showed that tree pruning influences significantly larval development time and mortality. Nevertheless, the effects of manipulating tree structure on larval development and survival were relatively weak compared with the impact of chosen climate variations. This survey also showed that the variability in insect development time within a year and insect mortality change markedly with climatic variations, and highlights the importance of using non-linear rate curves and insect body temperatures instead of air temperature in forecasting models of climate-related insect pest outbreaks.     

Developmental rate isomorphy in insects and mites

When the proportion of total developmental time spent in a particular developmental stage does not change with temperature, an organism shows "rate isomorphy." This is the case only if the lower developmental threshold is the same for all developmental stages. In this study, the incidence of rate isomorphy in seven species of mites and 342 species from 11 insect orders (some represented by several populations) was determined. Whether a species shows rate isomorphy or not was determined over a range of temperatures where the relationship between the rate of development and temperature is linear. Proportion of total developmental time spent in a particular stage was plotted against temperature and the existence of rate isomorphy inferred from a zero change in proportion. Rate isomorphy was detected in 243 (57%) of 426 populations. In the rest of the cases, rate isomorphy was violated by deviations in the proportion of time spent in a stage by an average of 0.2% (range 4.5E-06% to 2.8%) at the mean of the range of temperatures of all the data sets (11 degrees C). The violations occurred most frequently at the extremes of the linear phase, which is attributed to methodical biases, mortality at low temperatures, or too coarse an estimate of developmental time at high temperatures. Similarly, a meta-analysis also revealed an overall prevalence of rate isomorphy. Consequently, in insect and mite species, all the developmental stages appear to have the same population-specific lower developmental threshold. The existence of rate isomorphy could be of great practical importance, for example, in the timing of life-history events and in determining preadult thermal requirements. There are also indications that it may act as a phylogenetic constraint.     

Effects of temperature on development, survival and reproduction of insects: experimental design, data analysis and modeling

The developmental response of insects to temperature is important in understanding the ecology of insect life histories. Temperature-dependent phenology models permit examination of the impacts of temperature on the geographical distributions, population dynamics and management of insects. The measurement of insect developmental, survival and reproductive responses to temperature poses practical challenges because of their modality, variability among individuals and high mortality near the lower and upper threshold temperatures. We address this challenge with an integrated approach to the design of experiments and analysis of data based on maximum likelihood. This approach expands, simplifies and unifies the analysis of laboratory data parameterizing the thermal responses of insects in particular and poikilotherms in general. This approach allows the use of censored observations (records of surviving individuals that have not completed development after a certain time) and accommodates observations from temperature transfer treatments in which individuals pass only a portion of their development at an extreme (near-threshold) temperature and are then placed in optimal conditions to complete their development with a higher rate of survival. Results obtained from this approach are directly applicable to individual-based modeling of insect development, survival and reproduction with respect to temperature. This approach makes possible the development of process-based phenology models that are based on optimal use of available information, and will aid in the development of powerful tools for analyzing eruptive insect population behavior and response to changing climatic conditions.     

不同温度条件对利用黄粉甲繁育管氏肿腿蜂的影响

在恒温 2 0 ,2 2 ,2 4,2 6,2 8和 3 0℃的实验条件下 ,利用黄粉甲TenebriomolitorL .做中间寄主繁育管氏肿腿蜂SclerodermaguaniXiaoetWu ,测定了其发育历期和寄生率等生物学参数。结果显示 ,在被测温度范围内 ,管氏肿腿蜂的发育速率与温度呈正比关系 ,即随着温度的升高 ,发育历期逐渐缩短。卵至羽化的发育起点温度为 1 3 60℃ ,有效积温为 3 2 0 0 7日·度。温度对管氏肿腿蜂的寄生率、寄生成功率、产卵量、子代蜂的数量和性比都有较显著影响。结合发育历期的结果 ,认为适于人工大量繁蜂的温度范围为 2 4～ 2 8℃ ,2 6℃为最适温度。     

用非线性模型估测恒温和变温下棉铃虫蛹的发育率

为了深入分析和探讨昆虫发育与环境温度的关系, 在恒温（15~37℃）和交替变温（12/18~34/40℃）下测定了棉铃虫Helicoverpa armigera蛹的发育历期(d),分别用线性模型和非线性模型（Logan模型﹑Lactin模型和王氏模型）拟合其发育率(1/d)数据。结果表明,这3个非线性模型能更准确地描述发育率与温度之间的曲线关系,判定系数（R2）在0.9878～0.9991之间。对全部观测数据的进一步研究表明,只要有6个分布合适的观测数据,就可以用这些非线性模型获得相当满意的估测效果。如果缺乏高温下的测定数据,用非线性模型预测的昆虫发育率可能失真。分析了蛹在恒温和变温下发育率差异的可能原因,讨论了应用这3个非线性模型预测蛹期发育的优点和缺点,指出用非线性模型取代线性日·度模型进行害虫发生预测和益虫饲养管理的合理性和必要性。     

Testing the rate isomorphy hypothesis using five statistical methods

Abstract Organisms are said to be in developmental rate isomorphy when the proportions of developmental stage durations are unaffected by temperature. Comprehensive stage‐specific developmental data were generated on the cabbage beetle, Colaphellus bowringi Baly (Coleoptera: Chrysomelidae), at eight temperatures ranging from 16°C to 30°C (in 2°C increments) and five analytical methods were used to test the rate isomorphy hypothesis, including: (i) direct comparison of lower developmental thresholds with standard errors based on the traditional linear equation describing developmental rate as the linear function of temperature; (ii) analysis of covariance to compare the lower developmental thresholds of different stages based on the Ikemoto‐Takai linear equation; (iii) testing the significance of the slope item in the regression line of versus temperature, where p is the ratio of the developmental duration of a particular developmental stage to the entire pre‐imaginal developmental duration for one insect or mite species; (iv) analysis of variance to test for significant differences between the ratios of developmental stage durations to that of pre‐imaginal development; and (v) checking whether there is an element less than a given level of significance in the p‐value matrix of rotating regression line. The results revealed no significant difference among the lower developmental thresholds or among the aforementioned ratios, and thus convincingly confirmed the rate isomorphy hypothesis.