昆虫血细胞功能、形态及细胞免疫反应研究前沿

细胞免疫反应是昆虫先天免疫系统的重要组成部分,与体液免疫反应共同作用以防御外源物。不同类群的昆虫其血细胞种类不同,空间形态及免疫应答功能也各具特征,但在细胞免疫中大都发挥着吞噬、结节与包囊作用。本文根据国内外的研究,对昆虫血细胞的类型、功能、形态、吞噬过程、细胞表面吞噬受体、以蚜虫为代表的不完全变态昆虫免疫学和影响蚜虫免疫系统的共生体等研究动态进行了综述,以期为害虫防治提供思路和防治策略。     

昆虫复眼的仿生学应用

昆虫复眼结构独特、功能优异,是重要的仿生对象。仿生学家模拟复眼特性研发了人造同位复眼照相机;模拟蜻蜓复眼结构研制了相控阵雷达;从蚂蚁、蜜蜂和其他昆虫的复眼结构中得到启示,研制了偏振光导航仪;根据甲虫的视动反应机制研制出空对地速度计。科学家还对昆虫复眼的信息加工原理进行研究,研制出寻的末制导装置;法国科学家研制出仿复眼视觉导航装置及昆虫化机器人。     

基于服务功能的昆虫生态调控理论

鉴于昆虫在植物传粉授精、害虫生物控制、土壤有机物分解中提供多种生态系统服务功能,本文在害虫生态调控、区域性害虫生态调控与生境管理的基础上,进一步提出基于多种生态服务功能的农田景观昆虫生态调控理论、方法与实践。认为:昆虫管理不仅仅是害虫的管理,还应包括有益昆虫(如传粉昆虫、天敌昆虫、分解昆虫)的管理,这种管理应从单一农田生态系统扩展到农田景观生态系统,充分考虑农田景观中昆虫的传粉功能、生物控害功能和分解功能,通过对功能植物、作物与非作物生境的空间布局以及时间序列上的生态设计,从空间上明确昆虫(包括害虫、天敌、传粉昆虫、分解昆虫)在不同生境中的转移扩散动态,从时间上掌握昆虫在不同寄主植物与非作物生境上的演替过程,从技术上着重发挥有利于昆虫的传粉功能、生物控害功能和分解功能的综合措施,在研究方法上突出使用稳定同位素、生态能量学、化学生态学等定量分析手段,研究景观区域内中"植物-昆虫"互作过程及其生态调控措施的作用,寻求不同时空条件下控害保益的关键措施,设计和组装出维持多功能的农田景观昆虫生态调控技术体系,创造有利于天敌控害、蜜蜂传粉、土壤分解的环境条件,以发挥昆虫类群在农田景观中最大的生态服务功能。     

昆虫天然免疫反应研究前沿

昆虫天然免疫反应分为体液免疫和细胞免疫两种,二者共同作用抵御细菌、真菌、病毒等外源病原物的侵染。体液免疫反应主要包括黑色素形成和抗菌肽产生两种机制,细胞免疫反应包括吞噬、集结和包囊等作用类型。在昆虫天然免疫反应中,昆虫模式识别蛋白负责识别并结合外源物表面特有的模式分子,丝氨酸蛋白酶、丝氨酸蛋白酶抑制剂、各种配体、受体等负责级联信号途径的激活和调控,抗菌肽、黑色素等效应分子则负责对入侵物的杀灭和清除。本文根据国外和作者自己的研究,综述了昆虫天然免疫反应的研究进展,并针对该领域最新的研究动态展望了昆虫肠道免疫、昆虫免疫致敏以及不完全变态昆虫免疫学等这些研究前沿。     

植物挥发物对蛾类昆虫性信息素的影响

在植物与昆虫的协同进化过程中,植物挥发物与昆虫性信息素的相互关系一直以来被认为是物种间的重要通信系统。这种相互关系表现为植物挥发物对昆虫生理和行为的影响上,影响昆虫性信息素的合成和昆虫对性信息素的行为反应。本文针对植物挥发物对蛾类昆虫性信息素的影响进行了综述。评述了寄主植物挥发物对蛾类昆虫性信息素或前体的合成及性信息素的产生与释放的影响,总结了寄主植物和非寄主植物挥发物对蛾类昆虫的求偶行为的调控作用及对蛾类昆虫性信息素的增效或抑制作用阐述了植物挥发物影响蛾类昆虫对性信息素行为反应的机理,并且讨论了目前存在的问题。     

昆虫化学感受蛋白研究进展

昆虫化学感受蛋白(chemosensory proteins)是在长期进化过程中形成的一类低分子量酸性可溶性蛋白,广泛分布于昆虫触角、跗节等各种化学感受器中,蛋白质序列具有较高的保守性,种内种间同源性一般为30%～90％。其主要功能是感受、识别、转运、传导环境化学因子刺激信息,参与调节生理节律和生长发育。该文从昆虫化学感受蛋白的生态进化意义、分布表达部位、生化特性、分子结构、生理功能和研究方法等角度,较详细地综述了近年来国内外昆虫化学感受蛋白的研究进展,指出昆虫化学感受蛋白的深入研究,对于阐明昆虫与环境化学信息联系规律、昆虫行为反应本质原因,探索害虫综合治理和益虫利用效率新途径,开辟创制昆虫行为控制剂新领域等具有重要的理论和实践意义。     

昆虫的生态服务功能

昆虫作为生物多样性最丰富的物种,在传粉、生物控制、物质分解与资源供给等方面发挥着重要作用。昆虫生态服务功能是指昆虫类群在生态系统过程中发挥的功能作用,以及为人类提供的各种收益,包括有形收益的产品和无形收益的服务。它主要包括昆虫的供给服务、调节服务、文化服务和支持服务4种服务类型,体现在直接使用价值、间接使用价值、条件价值和存在价值4个方面。基于昆虫类群在传粉、生物控制、物质分解与资源供给等维持生态系统功能、满足人类需求做出重大的贡献,本文阐述了昆虫生态服务功能概念、类型,讨论了昆虫生态服务功能价值的评估方法,提出了未来发展的方向。     

昆虫趋光行为的光胁迫假说

趋光性是昆虫的固有行为特征之一,被广泛的应用在害虫物理防治中。本文综述了几种主流的昆虫趋光性假说,着重介绍了昆虫在趋光过程中的行为反应、受光胁迫后生理应激和补偿效应,提出了昆虫趋光行为的光胁迫假说,以期为昆虫趋光性理论研究提供新的思路。     

昆虫天然免疫反应分子机制研究进展

昆虫体内缺乏高等脊椎动物所具有的获得性免疫系统, 只能依赖发达的天然免疫系统抵抗细菌、 真菌、 病毒等外源病原物的侵染。本文概括了昆虫天然免疫反应发生和作用的分子机制相关进展, 重点阐述了重要免疫相关因子在昆虫天然免疫反应中的功能和作用机制。昆虫天然免疫反应分为体液免疫和细胞免疫两种, 二者共同作用完成对病原物的吞噬 (phagocytosis)、 集结 (nodulation)、 包囊 (encapsulation)、 凝结 (coagulation)和黑化（melanization）等。当昆虫受到外界病原物的侵染时, 首先通过体内的模式识别蛋白（pattern recognition proteins/receptor, PRPs）识别并结合病原物表面特有的模式分子（pathogen-associated molecular pattern, PAMPs）, 继而一系列包括丝氨酸蛋白酶和丝氨酸蛋白酶抑制剂在内的级联激活反应被激活和调控, 产生抗菌肽、 黑色素等免疫效应分子, 清除或杀灭外源物。抗菌肽是一类小分子量的阳离子肽, 具有广谱抗菌活性, 针对不同类型的病原物, 抗菌肽的产生机制也不尽相同。昆虫体内存在着两种信号转导途径调节抗菌肽的产生： 一是由真菌和大部分革兰氏阳性菌激活的Toll途径; 二是由革兰氏阴性菌激活的Imd途径（immune deficiency pathway）。这两个途径通过激活不同转录因子调控不同抗菌肽基因的表达参与昆虫体内的天然免疫反应。     

昆虫的表皮腺体

<正> 一、昆虫的表皮腺体及其分类 昆虫的表皮腺体是由昆虫体壁表皮细胞层中的某些特化的具有外分泌功能的细胞组成。这些表皮腺体除口腔中的唾腺在昆虫的消化、造丝等方面的功能之外,主要具有分泌种信息素和防御性物质的功能。近年来,由于人们逐渐认识到昆虫表皮腺体的分泌物对昆虫行为和生理的重要性,特别是利用昆虫性信息素在控制害虫和研究害虫的成功,加上扫描和透射电子显微镜使用的普及,促进了对表皮腺体的研     

Functional response: rigorous estimation and sensitivity to genetic variation in prey

Holling's type II functional response is a cornerstone of community ecology and coevolutionary theory. The so‐called disc equation is the most widely used model of the type II response, yet thus far no robust experimental assessment has been achieved in any single system. Fundamental issues that remain to be assessed include whether the assumptions of the disc equation are fulfilled, whether the disc equation yields accurate estimates of predation‐related individual traits, and whether differences in disc equation parameters can capture genetic variation in prey behaviour. This paper provides a rigorous approach to all of these questions. The functional response of the predatory mite Pergamasus crassipes on three genetically distinct clones of the springtail Folsomia candida was measured at six levels of prey density in controlled conditions where prey number and arena size were concomitantly manipulated. A crucial assumption of Holling's disc equation was fulfilled by maintaining a constant prey density for the entire experimental period of predation. The timing of each attack and capture, as well as the duration of the handling time, were recorded by constant observation. We contrasted three different methods to calculate functional response curves: (1) indirect estimation of the disc equation's parameters from the number of prey killed by the end of each experimental run; (2) direct estimation of the parameters via a unique protocol of constant observation; and (3) independently deriving a function based on direct measurements of encounter rate and attack success. The basic assumptions of the disk equation were globally fulfilled. Estimations of the functional response's parameters (type II) were remarkably congruent across approach (1) and (2). A single genetic effect was detected – the relationship between the encounter rate and prey density differed significantly between clones – whereas a direct comparison of functional response across clones failed to reveal genetic variation.     

Permanence of a predator–prey discrete system with Holling-IV functional response and distributed delays

A predator–prey discrete-time model with Holling-IV functional response and distributed delays is investigated in this paper. By using the comparison theorem of the difference equation and some analysis technique, some sufficient conditions are obtained for the permanence of the discrete predator–prey system. Two examples are given to illustrate the feasibility of the obtained result.     

The effect of temperature on the functional response of Phytoseiulus persimilis (Acari: Phytoseiidae)

Environmental variables, such as temperature, are important in determining the efficiency of biological control in ornamental crops. This paper examines the effect of temperature on the functional response of adult female Phytoseiulus persimilis to eggs of the spider mite, Tetranychus urticae. The functional response was determined using a new functional response assay technique with plant stems as an arena, rather than leaf discs. The use of plant stems allows the influence that plant structure has on predation to be incorporated into the assay. Control assays were also used (without predators) to estimate natural losses of prey. The data were analysed using a binomial model, with the use of Abbot's formula to correct for the losses in the controls. A combined equation to describe the effect of temperature and prey density on the predation rate of Phytoseiulus persimilis was derived. The results showed that more prey are eaten as the temperature increases from 15 degrees C to 25 degrees C, but the number of prey eaten then declines at 30 degrees C, although not to the levels seen at 20 degrees C. The implication of these results for biological control in ornamental crops, where the temperature can often exceed 30 degrees C, is discussed.     

Time‐to‐kill: measuring attack rates in a heterogenous landscape with multiple prey types

Although spatial heterogeneity of prey and landscapes are known to contribute to variation around predator‐prey functional response models, few studies have quantified these effects. We illustrate a new approach using data from winter movement paths of GPS‐collared wolves in the Rocky Mountains of Canada and time‐to‐event models with competing risks for measuring the effect of prey and landscape characteristics on the time‐to‐kill, which is the reciprocal of attack rate (aN) in a Holling's functional response. We evaluated 13 a priori models representing hypothesized mechanisms influencing attack rates in a heterogeneous landscape with two prey types. Models ranged from variants on Holling's disc equation, including search rate and prey density, to a full model including prey density and patchiness, search rates, satiation, and landscape features, which were measured along the wolf's movement path. Movement rates of wolves while searching explained more of the variation in time‐to‐kill than prey densities. Wolves did not compensate for low prey density by increasing movement rates and there was little evidence that spatial aggregation of prey influenced attack rates in this multi‐prey system. The top model for predicting time‐to‐kill included only search rate and landscape features. Wolves killed prey more quickly in flat terrain, likely due to increased vulnerability from accumulated snow, whereas attack rates were lower when wolves hunted near human‐made features presumably due to human disturbance. Understanding the sources of variation in attack rates provides refinements to functional response models that can lead to more effective predator–prey management in human‐dominated landscapes.     

Intake rates and the functional response in shorebirds (Charadriiformes) eating macro-invertebrates

As field determinations take much effort, it would be useful to be able to predict easily the coefficients describing the functional response of free-living predators, the function relating food intake rate to the abundance of food organisms in the environment. As a means easily to parameterise an individual-based model of shorebird Charadriiformes populations, we attempted this for shorebirds eating macro-invertebrates. Intake rate is measured as the ash-free dry mass (AFDM) per second of active foraging; i.e. excluding time spent on digestive pauses and other activities, such as preening. The present and previous studies show that the general shape of the functional response in shorebirds eating approximately the same size of prey across the full range of prey density is a decelerating rise to a plateau, thus approximating the Holling type II ('disc equation') formulation. But field studies confirmed that the asymptote was not set by handling time, as assumed by the disc equation, because only about half the foraging time was spent in successfully or unsuccessfully attacking and handling prey, the rest being devoted to searching.A review of 30 functional responses showed that intake rate in free-living shorebirds varied independently of prey density over a wide range, with the asymptote being reached at very low prey densities (<150/m-2). Accordingly, most of the many studies of shorebird intake rate have probably been conducted at or near the asymptote of the functional response, suggesting that equations that predict intake rate should also predict the asymptote.A multivariate analysis of 468 'spot' estimates of intake rates from 26 shorebirds identified ten variables, representing prey and shorebird characteristics, that accounted for 81% of the variance in logarithm-transformed intake rate. But four-variables accounted for almost as much (77.3%), these being bird size, prey size, whether the bird was an oystercatcher Haematopus ostralegus eating mussels Mytilus edulis, or breeding. The four variable equation under-predicted, on average, the observed 30 estimates of the asymptote by 11.6%, but this discrepancy was reduced to 0.2% when two suspect estimates from one early study in the 1960s were removed. The equation therefore predicted the observed asymptote very successfully in 93% of cases. We conclude that the asymptote can be reliably predicted from just four easily measured variables. Indeed, if the birds are not breeding and are not oystercatchers eating mussels, reliable predictions can be obtained using just two variables, bird and prey sizes. A multivariate analysis of 23 estimates of the half-asymptote constant suggested they were smaller when prey were small but greater when the birds were large, especially in oystercatchers. The resulting equation could be used to predict the half-asymptote constant, but its predictive power has yet to be tested. As well as predicting the asymptote of the functional response, the equations will enable research workers engaged in many areas of shorebird ecology and behaviour to estimate intake rate without the need for conventional time-consuming field studies, including species for which it has not yet proved possible to measure intake rate in the field.     

Functional response of the ladybird, Cydonia vicina nilotica to cowpea aphid, Aphis craccivora in the laboratory

The functional response of Cydonia vicina nilotica Muls. （Coleoptera： Coccinellidae） to six densities of Aphis craccivora Koch （Homoptera： Aphididae） nymphs on broad bean （Viciafaba Linn.） was investigated in the laboratory. A linear relationship between the rate of consumption and prey density was observed with r^2 values between 0.58 and 0.97. Plotting prey density against prey killed by four larval instars, and adult males and females of C. vicina nilotica fit well with the type Ⅱ model of Holling＇ s disc equation. Adult females consumed the highest number of prey, followed by fourth instars and adult males. Based on the functional response data, the model predicts a maximum of 144.9, 116.3, 86.2, 80.0, 72.5 and 20.0 nymphs to be consumed per day by an individual adult female, fourth instar, adult male, third, second and first instars, respectively. The differences in the responses of the predator to aphid densities are discussed.     

Should "handled" prey be considered? Some consequences for functional response, predator-prey dynamics and optimal foraging theory

Predator-prey models consider those prey that are free. They assume that once a prey is captured by a predator it leaves the system. A question arises whether in predator-prey population models the variable describing prey population shall consider only those prey which are free, or both free and handled prey together. In the latter case prey leave the system after they have been handled. The classical Holling type II functional response was derived with respect to free prey. In this article we derive a functional response with respect to prey density which considers also handled prey. This functional response depends on predator density, i.e., it accounts naturally for interference. We study consequences of this functional response for stability of a simple predator-prey model and for optimal foraging theory. We show that, qualitatively, the population dynamics are similar regardless of whether we consider only free or free and handled prey. However, the latter case may change predictions in some other cases. We document this for optimal foraging theory where the functional response which considers both free and handled prey leads to partial preferences which are not observed when only free prey are considered.     

The functional response of a predatory mite and the nature of the attack rate

The assumptions of the Random Predator equation are discussed and the problems associated with parameter estimation and prediction are pointed out. Experiments are described in which the functional response characteristics of a mesostigmatid mite Pergamasus crassipes, preying upon a collembolan, Onycbiurus armatus, were observed over four successive time intervals. In a series of separate experiments the handling-time, T_h, was estimated directly. A modification of the random predator equation is proposed in which a searching time sub-model is incorporated. Predictions from this model suggest that the attack rate is not a constant but is a function of prey density. An attack rate sub model is formulated and the resultant functional response model is shown to be more accurate and more readily usable for prediction than the random predator equation.     

斜纹猫蛛对茶尺蠖幼虫捕食作用的初步研究

在室温条件下测定了斜纹猫蛛亚成蛛及成蛛对茶尺蠖1～2龄幼虫的日捕食量及功能反应、捕食者自身密度效应和温度对功能反应的影响。斜纹猫蛛亚成蛛及成蛛对茶尺蠖幼虫的功能反应均呈Holling Ⅱ型反应,模拟模型分别为Na=0.9195Nt/(1 0.004703Nt)和Na=0.92268Nt/(1 0.005081Nt),自身密度反应模型分别为E=0.5419P~(-0.6052)和E=0.5139P~(-0.5812)。经X~2检验,以上模型模拟效果较好。     

A functional response model of a predator population foraging in a patchy habitat

1. Functional response models (e.g. Holling's disc equation) that do not take the spatial distributions of prey and predators into account are likely to produce biased estimates of predation rates. 2. To investigate the consequences of ignoring prey distribution and predator aggregation, a general analytical model of a predator population occupying a patchy environment with a single species of prey is developed. 3. The model includes the density and the spatial distribution of the prey population, the aggregative response of the predators and their mutual interference. 4. The model provides explicit solutions to a number of scenarios that can be independently combined: the prey has an even, random or clumped distribution, and the predators show a convex, sigmoid, linear or no aggregative response. 5. The model is parameterized with data from an acarine predator-prey system consisting of Phytoseiulus persimis and Tetranychus urticae inhabiting greenhouse cucumbers. 6. The model fits empirical data quite well and much better than if prey and predators were assumed to be evenly distributed among patches, or if the predators were distributed independently of the prey. 7. The analyses show that if the predators do not show an aggregative response it will always be an advantage to the prey to adopt a patchy distribution. On the other hand, if the predators are capable of responding to the distribution of prey, then it will be an advantage to the prey to be evenly distributed when its density is low and switch to a more patchy distribution when its density increases. The effect of mutual interference is negligible unless predator density is very high. 8. The model shows that prey patchiness and predator aggregation in combination can change the functional response at the population level from type II to type III, indicating that these factors may contribute to stabilization of predator-prey dynamics.