No description available.

No description available.

No description available.

Differences in plant structure and host abundance, distribution and density within and between plants may affect host finding success of searching parasitoids. The main objective of this research consisted in developing and validating a model that can predict parasitism by Trichogramma evanescens on various plant structures. Also, we evaluated the effect of both artificial and natural plant structures on host encountering success and on searching behavior of two species of Trichogramma. / Size (S), heterogeneity (H) and connectivity (C) define plant structure. The development of the model of parasitism was based on laboratory experiments using three dimensional artificial plants of different combinations of S, H and C. The model was then validated with experiments, within greenhouse, using natural cruciferous plants of different structures. Significant regressions of observed values of parasitism as a function of those predicted by the model were obtained. / The effect of plant structure on two species of Trichogramma was studied by using three species of Lepidoptera and three structurally different but closely related crucifers. Also the distribution pattern of parasitized eggs according to leaf side and plant height was characterized. A repeated measure ANOVA in time where plant ages defined the repeated measures showed that all three main effects (plant, host, parasitoid) had significant effect on parasitism and only the parasitoid x plant structure interaction was significant. Mean percent of parasitism was higher on cabbage, intermediate on broccoli and lower on Brussels sprouts whereas cabbage appeared to be intermediate in plant structure, broccoli appeared to be the most simple and Brussels sprouts the most complex plant structure. On simple plant structure, both wasp species performed well on the three varieties of plant but T. evanescens outperformed T. pretiosum more often on the various plant structures. A doubly repeated measures ANOVA in space revealed significant effects of leaf side and plant height on parasitism, being greatest under leaf surface and at the base of the plant. The interaction between those two variables was not significant. / The effect of plant structure on searching behavior of T. evanescens was determined by direct observation of individual females searching on simple and complex plant structures during 1 hour. Time, frequence and sequence associated to activities and plant parts explored were obtained and analyzed. Plant structure had significant effect on time budget associated to activities (walking, resting, flying) and plant parts explored. / This study demonstrates that plant structure mediates ecological interactions by affecting host finding success and this may have important implications in population dynamics, evolution of hosts and parasitoids but also in biological control programs.

During a two years study (1993-1994) in southwestern Quebec, Artogeia rapae and Plutella xylostella were found to be the most important lepidopterous pests of cruciferous crops, followed by Trichoplusia ni and four minor species. The relationship between plant sampling and the use of degree-days, pheromone traps (P. xylostella) or butterflies counts (A. rapae) was assessed for A. rapae and P. xylostella. Three generations of A. rapae were observed annually, with a duration of 319.7 degree-days above $ rm 10 sp circ C (DD sb{10}),$ while P. xylostella had three to four generations with a duration of 277.7 $ rm DD sb{10}.$ Captures of P. xylostella were not linked to the level of infestations. By the end of summer, A. rapae was the most abundant species, especially on broccoli, while P. xylostella was often abundant early in the season. The complex of lepidopterous pests' natural enemies was identified, and the data were analyzed using an illustrated parasitoid web. Fourteen parasitoid and three hyperparasitoid species (12 Hymenoptera, 2 Diptera) were identified. The most important parasitoid, Cotesia rubecula, is a larval parasitoid of A. rapae that is newly established in Quebec. Overall, parasitism of lepidopterous eggs is almost not existent, whereas parasitism and infection of larvae and pupae by pathogens are important, but not significant to reduce butterfly populations. In order to evaluate the potential of oophagous parasitoids, the parasitism of up to 42 species/strains of Trichogramma was studied with different development stages of P. xylostella, A. rapae and T. ni eggs. Generally, Trichogramma females attacked preferably young eggs of a given host species. Females modified the number of offspring according to host size and host age, as fewer offspring emerged from the smallest or the oldest hosts. Host age had no impact on sex allocation. (Abstract shortened by UMI.)

No description available.

The diamondback moth, Plutella xylostella (L.) (Lepidoptera: Plutellidae), is an important pest of cruciferous crops worldwide. The prolonged use of synthetic chemical insecticides as a primary means of control has resulted in the development of resistance in pest populations. In addition, the pest has also evolved resistance to the bacterial insecticidal protein of Bacillus thuringiensis which is also widely used as a method of control. Baculoviruses are considered as effective alternatives to conventional methods of control when incorporated into integrated pest management (IPM) programmes. These viruses target the larval stages of insects, are generally host-specific and are safe for use in the environment. This study aimed to isolate a baculovirus from a laboratory-reared P. xylostella colony, characterise it genetically and then evaluate its virulence against neonate and fourth instar larvae. A laboratory colony of P. xylostella was established using pupae and asymptomatic larvae collected from a cabbage plantation outside Grahamstown in the Eastern Cape province of South Africa. The colony flourished in the laboratory due to prime conditions and availability of food. The duration of development from egg to adult was determined by observation and imaging of the various life stages. The mean developmental time from egg to adult was observed to be 14.59 ± 0.21 days. The population of the insects increased rapidly in number leading to overcrowding of the insect colony, and hence appearance of larvae with viral symptoms. Occlusion bodies (OBs) were extracted from symptomatic larval cadavers and purified by glycerol gradient centrifugation. Analysis of the purified OBs by transmission electron microscopy revealed the presence of a granulovirus which was named PlxyGV-SA. The virus isolate was genetically characterised by restriction endonuclease analysis of the genomic DNA, and PCR amplification and sequencing of selected viral genes. The complete genome sequence of a Japanese P. xylostella granulovirus isolate, PlxyGV-Japan, has been deposited on the GenBank database providing a reference strain for comparison with DNA profiles and selected gene sequences of PlxyGV-SA. BLAST analysis of the granulin gene confirmed the isolation of a novel South African PlxyGV isolate. Comparison of the restriction profiles of PlxyGV-SA with profiles of PlxyGV-Japan and other documented PlxyGV profiles obtained by agarose gel electrophoresis revealed that PlxyGV-SA is a genetically distinct isolate. The data obtained from the sequencing and alignment of ecdysteroid UDP-glucosyltransferase (egt), late expression factor 8 (lef-8) and late expression factor 9 (lef-9) genes with those of PlxyGV-Japan also showed that PlxyGV-SA is a genetically different isolate. In order to determine the biological activity of PlxyGV-SA against neonate and fourth instar P. xylostella larvae, surface dose bioassays were conducted. The median lethal concentration of the virus required to kill 50% (LC₅₀) and 90% (LC₉₀) of the larvae was estimated by feeding insects with a range of doses. In addition, the time to kill 50% of the larvae (LT₅₀) was determined by feeding insects with the LC₉₀ concentration. Larval mortality was monitored daily until pupation. The data obtained from the dose response assays were subjected to probit analysis using Proban statistical software. The time response was determined using GraphPad Prism software (version 6.0). The LC₅₀ and LC₉₀ values for the neonate larvae were 3.56 × 10⁵ and 1.14 × 10⁷ OBs/ml respectively. The LT₅₀ was determined to be 104 hours. The neonate larvae were found to be more susceptible to infection than the fourth instar larvae with the same virus concentration. The concentrations used for the neonate larvae assay did not have a significant effect on the fourth instar as no mortality was recorded. This is the first study to describe a novel South African PlxyGV isolate and the results suggest that PlxyGV-SA has significant potential for development as an effective biopesticide for the control of P. xylostella in the field.