Larval morphology and searching efficiency in aphidophagous syrphid larvae

The effects of larval morphology and substrate quality on the searching efficiency of third stage larvae of Epistrophe eligans (Harris) and Metasyrphus luniger (Meigen) were examined. E. eligans has a smooth, flat undersurface and was able to grasp smooth, flat substrates where it achieved high casting rates and capture efficiencies. It is probably best suited to exploiting leaf-feeding, rather than stem-feeding aphids. However, M. luniger did best on stems and petiles where it used a special U-shaped grasping organ and lateral movements to hold on and move. On these substrates, as opposed to smooth, flat surfaces, it achieved high casting rates and capture efficiencies.

---

Résumé L'examen a proté sur les effets de la morphologie larvaire et de la nature du substrat sur les succès de la prospection des larves de troisième stade de E. elegans et de M. luniger. La surface ventrale de E. elegans est plate et molle, sans proéminences locomotrices. Sur les feuilles plutôt que sur les pétioles, il a mieux adhéré au substrat et a réalisé plus de captures avec une meilleure efficacité. E. elegans est probablement mieux adapté à l'exploitation des pucerons sur des surfaces molles et plates, comme les feuilles. M. luniger présente une disposition complexe de proéminences locomotrices, comprenant un organe de préhension en forme de U à l'extrémité du corps. Sur les tiges, les pétioles et les feuilles avec des nervures saillantes, il est capable de se fixer efficacement et de se déplacer sur des structures cylindriques en utilisant son organe de préhension, ses pièces buccales et des mouvements latéraux. Il a réalisé plus de captures avec une plus grande efficacité sur tiges et pétioles par comparaison avec des surfaces molles; il peut être mieux adapté à exploiter les pucerons associés aux surfaces cylindriques de ce type.

     

Host searching and oviposition behaviour of some parasitoids of aphidophagous Syrphidae

Abstract.

• 1 An analysis of host searching behaviour suggests that female parasitoids respond to aphid odours bringing them to the region of an aphid colony.
• 2 Syrphid hosts are located within the aphid colony by response to contact chemicals on the larval integument.
• 3 The behavioural mechanisms used by syrphid larvae to resist attacks and the subsequent responses made by parasitoids are described.
• 4 Oviposition behaviour and host size preferences of parasitoids are described.

     

The effect of egg load and host deprivation on oviposition behaviour in aphidophagous hoverflies

1. Two species of aphidophagous hoverfly, Episyrphus balteatus and Syrphus ribesii, were tested for the effects of egg load and host deprivation on oviposition choices. 2. Egg load affected the total number of eggs laid in E. balteatus but not in S. ribesii, however it did not affect the proportion laid on any one aphid in E. balteatus but did affect the proportion laid on any one aphid in S. ribesii. The rank order of preferences remained unchanged by age or host deprivation. 3. The dominant effects on host choices were aphid species (in both syrphids) and presentation order (in E. balteatus). 4. Being deprived of hosts increased egg load substantially in E. balteatus, and increasing time of deprivation also had an effect on discrimination; there was no effect of host deprivation in S. ribesii. 5. Reasons for these patterns are discussed.     

Synchrony between parasite development and host behaviour change

Teleost fish are commonly used as model species in laboratory studies of behaviour and ecology. In comparison to other groups of vertebrates used routinely in such studies, however, relatively little attention has been paid to their environmental requirements from a welfare perspective. Fish naturally inhabit a wide variety of aquatic habitats that differ enormously in the range of light environments they provide, and light regime has enormous potential to affect behaviour. Yet the level and quality of illumination (in terms of intensity and wavelength spectrum) provided in experimental studies of fish behaviour is generally designed to maximize ease of recording by the observer. In addition, display or home aquaria provide illumination that maximizes the 'viewing pleasure' of the observer, and specialist lighting tubes are available to stimulate rapid plant growth and to 'show off' the colours of fish, rather than to provide 'natural' light environments. Here we present the results of three studies designed to examine the effects of light intensity, wavelength spectrum and their interactions on the behaviour of a model species commonly used in behavioural studies, the three‐spined stickleback Gasterosteus aculeatus . Our aims are to determine whether unnatural light environments, generated by manipulating light intensity and wavelength spectrum, affect behaviour in ways that may lead to concern for the welfare of fish as research animals or pets.     

To mark the host or the patch: Decisions of a parasitoid searching for concealed host larvae

We found evidence for patch marking in the parasitic wasp Halticoptera laevigata (Hymenoptera: Pteromalidae) foraging for concealed hosts. Wasps attack larvae of the fruit fly Myoleja lucida (Diptera: Tephritidae) in fruits of honeysuckle. A special feature of this host-parasitoid system is the limited food supply of a patch (i.e. a fruit of honeysuckle), which allows the successful development of only a single host fly larva. Females of the parasitoid H. laevigata were found to mark the host patch with a pheromone and to abandon the patch following oviposition into a single host larva. Field data revealed that eggs of the parasitoid were spread out evenly among infested patches, with several larvae of the host fly left unparasitized in those patches that contained more than one host. Since many parasitic insects mark the parasitized host after oviposition, we assumed host marking to be the ancestral character state and studied the patch-marking behaviour of H. laevigata as a derived character state as an alternative foraging strategy. We used stochastic dynamic modelling to investigate under what conditions mutant (patch) markers would be able to invade a population of normal (larval) markers. The models suggested that, under a variety of conditions, wasps marking the patch obtained higher fitness than wasps only marking the larva. Consequently, the results from our model predict the evolution of the patch-marking behaviour found in the empirical investigation. Finally, we discuss alternative pathways to the evolution of patch marking and point out under what circumstances the evolution of a patch-marking behaviour can generally be expected.     

The adaptiveness of searching and host selection behaviour in Pieris rapae (L.)

This study evaluates the adaptive significance of host preferences and searching behaviour in Vancouver and Canberra populations of the cabbage butterfly Pieris rapae (L.). As a result of a complex of responses to plant age, the butterflies concentrate their eggs on middle-aged plants. Young larvae develop faster and survive better on young plants than old ones, but larvae on smaller plants are more susceptible to crowding effects. Thus a preference for plants which are well-grown but not too old is selectively advantageous. By contrast, the butterflies’ host species preferences appear non-adaptive, and are unrelated to the quality of the host as larval food. Vancouver butterflies change their flight direction often and are very responsive to hosts, thereby generating a very aggregated distribution at a low cost in flight time. Canberra butterflies tend to fly in straight lines and are less responsive to hosts; their egg distribution is consequently more nearly random, but they fly further for each egg they lay. The relative costs of aggregation and increased flight time differ between the populations in a manner consistent with the observed behavioural differences.     

Immature stages of some aphidophagous syrphid flies of India (Insecta, Diptera, Syrphidae)

Immature stages, viz. egg, larva and puparium, of six species of the economically most important syrphid flies, Scaeva latimaculata (Brunetti), Ischiodon scutellaris (Fabricius), Episyrphus altemans (Macquart), Sphaerophoria Indiana Bigot, Metasyrphus confrater (Wiedemann), and M. latilunulatus (Collin), have been studied. These species are voracious feeders on three aphid species, Lipaphis erysimi (Kaltenbach), Myzus persicae (Sulzer) and Brevicoryne brassicae (L.), which are serious pests of mustard, Brassica campestris L.     

The biology and epidemiology of Eimeria exigua, a parasite of wild rabbits invading the host cell nucleus.

Prevalence and intensity of infection with Eimeria exigua were studied by monthly sampling of caecal faeces of 254 wild rabbits (Oryctolagus cuniculus) from 5 localities in France (Arjuzanx, Versailles, Donzere-Mondragon, Massereau, Gerstheim) and by a single sampling in autumn in a small island off the coast of Britany (Beniguet). Intensity was heavier in young than in adult rabbits but usually remained low. It decreased from north to south, was at a maximum during autumn and winter, and declined in spring. Prevalences were relatively high and their rank (4th or 5th out of 10) was constant in all localities. Prevalences decreased from north-west to south-east; they increased progressively during autumn and winter, were at a maximum during spring and declined in summer. E. exigua developed in the ileum, at the top of the villi and inside the host-cell nucleus. It is distinguished from congeneric species by a number of features: micro-localisation, multiplication in autumn and winter rather than in summer, low intensity and high prevalence. These characteristics may be the consequence of a short schizogony phase and of strong resistance of oocysts.     

The effects of host distributional patterns on parasite transmission: Aedes aegypti larvae and Plagiorchis noblei Cercariae

The effects of distributional patterns of the host on the acquisition of Plagiorchis noblei cercariae by Aedes aegypti larvae were determined. Mosquito larvae that were allowed to disperse were more susceptible to infection than confined larvae. Because these mosquito larvae are known to aggregate in light and disperse in darkness, they are more likely to acquire P. noblei infections at night. The timing of cercarial emergence in relation to the distributional patterns of the mosquito host is discussed.     

The area of discovery and searching strategy of a primary parasite and two hyperparasites

• 1 Two hyperparasites, Cheiloneurus paralia (Walker) and Marietta exitiosa Compere, of Microterys flavus (Howard), a primary parasite of the brown soft scale Coccus hesperidum L. have been studied.
• 2 The area of discovery of the hyperparasites for secondary hosts (scale insects) is greater than that of the primary parasite, indicating higher searching efficiency of the secondary parasites.
• 3 Cheiloneurus has a higher searching efficiency measured as its area of discovery for discovering both the secondary (scale insect) and the primary (Microterys) hosts, as compared with Marietta.
• 4 The searching efficiency of Cheiloneurus increased in the presence of its own males.
• 5 In each species there is a non-linear relationship between the searching efficiency and female density.
• 6 Cheiloneurus and Marietta present two differing searching strategies. Cheiloneurus tends to exploit as many primary hosts as possible in each secondary host encountered, whereas Marietta, tends to disperse its progeny more regularly by avoiding, to a certain extent, the exploitation of more than one host in each scale insect encountered.

     

The parasite capacity of the host population

The estimation of parasitic pressure on the host populations is frequently required in parasitological investigations. The empirical values of prevalence of infection are used for this, however the latter one as an estimation of parasitic pressure on the host population is insufficient. For example, the same prevalence of infection can be insignificant for the population with high reproductive potential and excessive for the population with the low reproductive potential. Therefore the development of methods of an estimation of the parasitic pressure on the population, which take into account the features the host population, is necessary. Appropriate parameters are to be independent on view of the researcher, have a clear biological sense and be based on easily available characteristics. The methods of estimation of parasitic pressure on the host at the organism level are based on various individual viability parameters: longevity, resistance to difficult environment etc. The natural development of this approach for population level is the analysis of viability parameters of groups, namely, the changing of extinction probability of host population under the influence of parasites. Obviously, some critical values of prevalence of infection should exist; above theme the host population dies out. Therefore the heaviest prevalence of infection, at which the probability of host population size decreases during the some period is less than probability of that increases or preserves, can serve as an indicator of permissible parasitic pressure on the host population. For its designation the term "parasite capacity of the host population" is proposed. The real parasitic pressure on the host population should be estimated on the comparison with its parasite capacity. Parasite capacity of the host population is the heaviest possible prevalence of infection, at which, with the generation number T approaching infinity, there exists at least one initial population size ni(0) for which the probability of size decrease through T generations is less than the probability of its increase. [formula: see text] The estimation of the probabilities of host population size changes is necessary for the parasite capacity determination. The classical methods for the estimation of extinction probability of population are unsuitable in this case, as these methods require the knowledge of population growth rates and their variances for all possible population sizes. Thus, the development methods of estimate of extinction probability of population, based on the using of available parameters (sex ratio, fecundity, mortality, prevalence of infection PI) is necessary. The population size change can be considered as the Markov process. The probabilities of all changes of population size for a generation in this case are described by a matrix of transition probabilities of Markov process (pi) with dimensions Nmax x Nmax (maximum population size). The probabilities of all possible size changes for T generations can be calculated as pi T. Analyzing the behaviour matrix of transition at various prevalence of infection, it is possible to determine the parasite capacity of the host population. In constructing of the matrix of transition probabilities, should to be taken into account the features the host population and the influence of parasites on its reproductive potential. The set of the possible population size at a generation corresponds to each initial population size. The transition probabilities for the possible population sizes at a generation can be approximated to the binomial distribution. The possible population sizes at a generation nj(t + 1) can be calculated as sums of the number of survived parents N1 and posterities N2; their probabilities--as P(N1) x P(N2). The probabilities of equal sums N1 + N2 and nj(t + 1) > or = Nmax are added. The number of survived parents N1 may range from 0 to (1-PI) x ni(t). The survival probabilities can be estimated for each N1 as [formula: see text] The number of survived posterities N2 may range from 0 to N2max (the maximum number of posterities). N2max is [formula: see text] and the survival probabilities for each N2, is defined as [formula: see text] where [formula: see text], ni(t) is the initial population size (including of males and infected specimens of host), PI is the prevalence of infection, Q1 is the survival probabilities of parents, Pfemales is the frequency of females in the host population, K is the number of posterities per a female, and Q2 is the survival probabilities of posterities. When constructing matrix of transition probabilities of Markov process (pi), the procedure outlined above should be repeated for all possible initial population size. Matrix of transition probabilities for T generations is defined as pi T. This matrix (pi T) embodies all possible transition probabilities from the initial population sizes to the final population sizes and contains a wealth of information by itself. From the practical point of view, however, the plots of the probability of population size decrease are more suitable for analysis. They can be received by summing the probabilities within of lines of matrix from 0 to ni--1 (ni--the population size, which corresponds to the line of the matrix). Offered parameter has the number of advantages. Firstly, it is independent on a view of researcher. Secondly, it has a clear biological sense--this is a limit of prevalence, which is safe for host population. Thirdly, only available parameters are used in the calculation of parasite capacity: population size, sex ratio, fecundity, mortality. Lastly, with the availability of modern computers calculations do not make large labour. Drawbacks of this parameter: 1. The assumption that prevalence of infection, mortality, fecundity and sex ratio are constant in time (the situations are possible when the variability of this parameters can not be neglected); 2. The term "maximum population size" has no clear biological sense; 3. Objective restrictions exist for applications of this mathematical approach for populations with size, which exceeds 1000 specimens (huge quantity of computing operations--order Nmax 3*(T-1), work with very low probabilities). The further evolution of the proposed approach will allow to transfer from the probabilities of size changes of individual populations to be probabilities of size changes of population systems under the influence of parasites. This approach can be used at the epidemiology and in the conservation biology.     

A comparative study of the searching efficiencies of a parasite and a hyperparasite

The searching efficiencies of a primary parasite (Diaeretiella rapae (McIntosh )) and a hyperparasite (Alloxysta brassicae (Ash. )) were investigated and compared. In both species, at all parasite densities, there was a curvilinear relationship (P<0.001) between the number of hosts parasitised and the host density. A linear regression (log a=log Q−m log P) was fitted for log area of discovery against log parasite density (P<0.001). The area of discovery for its immediate (i.e. primary) host (viz. Diaeretiella for the hyperparasite and aphid for Diaeretiella) is lower in the hyperparasite than in the primary parasite. In Diaeretialla both the searching efficiency and the mutual interference constant increased (but not significantly, P>0.05) in the presence of its males.     

The effect of host heterogeneity and parasite intragenomic interactions on parasite population structure

Understanding the processes that shape the genetic structure of parasite populations and the functional consequences of different parasite genotypes is critical for our ability to predict how an infection can spread through a host population and for the design of effective vaccines to combat infection and disease. Here, we examine how the genetic structure of parasite populations responds to host genetic heterogeneity. We consider the well-characterized molecular specificity of major histocompatibility complex binding of antigenic peptides to derive deterministic and stochastic models. We use these models to ask, firstly, what conditions favour the evolution of generalist parasite genotypes versus specialist parasite genotypes? Secondly, can parasite genotypes coexist in a population? We find that intragenomic interactions between parasite loci encoding antigenic peptides are pivotal in determining the outcome of evolution. Where parasite loci interact synergistically (i.e. the recognition of additional antigenic peptides has a disproportionately large effect on parasite fitness), generalist parasite genotypes are favoured. Where parasite loci act multiplicatively (have independent effects on fitness) or antagonistically (have diminishing effects on parasite fitness), specialist parasite genotypes are favoured. A key finding is that polymorphism is not stable and that, with respect to functionally important antigenic peptides, parasite populations are dominated by a single genotype.     

寄生虫与宿主的关系

对寄生虫与宿主的关系进行论述,探求寄生关系的实质,明确这二者之间的关系是认识寄生虫病发生发展规律,更好地防治寄生虫病的基础.     

The migratory behaviour and survival pattern of Ancylostoma caninum larvae in an adoptively immunised host

The migratory behaviour and survival pattern of a challenge dose of Ancylostoma caninum larvae was found to be affected by the immunological damage caused and the degree of immunity acquired by the adoptively immunised isogenic female Swiss albino mice. In experimental recipients, larval entry into the lungs during migration was prevented by the liver which acts as an immunological barrier; instead they proceeded into the muscles within 4 h after challenge, where they met allergic death in experimental animals only.     

The parasitic nematodes Hysterothylacium sp. type MB larvae as bioindicators of lead and cadmium: a comparative study of parasite and host tissues

Cadmium and lead concentrations were compared in tissues of cutlassfish, Trichiurus lepturus L., its intestinal nematode Hysterothylacium sp. type MB larvae, and in water from the same location in the Sea of Oman. Metal accumulation in hosts, parasites and sea water was measured by ICP-OES. Hysterothylacium larvae from the intestinal lumen and visceral cavity showed much higher metal concentrations than in host tissues or sea water. Statistical analyses revealed no significant differences in metal accumulation between infected and uninfected hosts. Cadmium concentration in the host muscle was lower than in intestine, liver and gonad tissues. The mean concentrations of lead and cadmium in nematodes were 289·03 and 81·5 times higher than in host intestine, 188·4 and 225 times higher than in host muscle, 108·6 and 65·3 times higher than in host gonads, 70·5 and 19·5 times higher than in host liver and 3351 and 148 times higher than in sea water. The results show the value of this and possibly related nematodes as bioindicators of heavy metals and their potential use in environmental studies.     

Effect of host density on searching behaviour of Nemeritis canescens (Hymenoptera: Ichneumonidae)

Observations were made over one hour of individual parasites, N. canescens, searching for their hosts, larvae of the moth Plodia interpunctella, at five different host densities. Records were made of the total number of hosts encountered at each density, the total number of eggs laid and the handling time per host.Holling's disc equation was found to fit the data well and gave estimates for rate of parasite search (a) and handling time (b) close to values actually observed. Despite the good fit, rate of search and handling time both declined as host density increased. The time spent handling already parasitised hosts, avoidance time was found to be about half the value of handling time.

---

Resume Les observations ont été faites durant une heure sur des parasites isolés, N. canescens, prospectant des lots de chenilles de Plodia interpunctella — leurs hôtes — à cinq densités différentes. Pour chaque densité, ont été notés: le nombre total d'hôtes rencontrés, le nombre total d'ufs pondus et le temps d'examen par hôte.L'équation de Holling s'est bien adaptée aux données et a fourni des estimations pour le taux de prospection des parasites (a) et le temps d'examen (b) proches des valuers réellement observées. Malgré une bonne adaptation, le taux de prospection et le temps d'examen diminuent tous deux quand la densité de l'hôte augmente. Le temps dépensé à l'examen des hôtes déjà parasités, temps de rejet correspond à environ la moitié du temps d'examen.

     

The biology and behaviour ofIphiaulax varipalpis [Hymenoptera: Braconidae] as a parasite ofDirphya nigricornis [Coleoptera: Cerambycidae]

The ability of the braconid parasite,Iphiaulax varipalpis Cary to control the beetleDyrphya nigricornis Olivier was evaluated. Field collected samples and specimens reared in polyethylene paper tubes under laboratory conditions (23.0°C±1.0 at 70% r.h) were used. Field parasitism was low (10.72%) while laboratory parasitism was high (57.66%). The parasite detected the hosts very easily in the laboratory. This ability is minimised in thick canopies ofCoffea arabica L. Host colonization was brisk (90 seconds) and confined to a near absolute area of discovery, measuring 4.18±0.41 cm. The parasite reproduces gregariously with female lifespan being approximately double the male period. The parasites are very active at the age of 10 days. As they age their potential fecundity (232 oocytes) reduces drastically with oviposition.