No description available.

No description available.

Studies were carried out to evaluate the repellent properties of the seeds of alligator pepper, <i>Aframomum melegueta </i>and Black pepper, <i>Piper guineense, </i>and ginger, <i>Zingiber officinale </i>rhizomes against <i>S. zeamais</i>. In 4-way olfactometry bioassays, <i>S. zeamais</i> adults showed strong attraction to maize and wheat seed volatiles but were significantly repelled by odours emanating from the seeds of <i>A. melegueta</i>, <i>P. guineense</i> and <i>Z. officinale</i> rhizomes. In field trials crushed <i>A. melegueta </i>seeds and <i>Z. officinale </i>rhizomes, significantly repelled <i>S. zeamais</i> from traditional maize granaries with treated maize cobs giving higher germination than untreated cobs. Laboratory reproductive potential studies showed that <i>A. melegueta </i>and <i>Z. officinale </i>powders caused significant adult mortality and reproductive potential deterrence against <i>S. zeamais</i> resulting in a reduction in F₁ progeny emergence. Olfactometer bioassays also confirmed that vacuum distilled <i>A. melegueta</i> and <i>Z. officinale </i>extracts and oleoresins were repellent towards adult <i>S. zeamais</i> when tested alone, and in combination with maize grains. Bioassay-guided liquid chromatography of the distillates showed that fractions containing polar compounds accounted for the repellent activity. Coupled gas chromatography-mass spectrometry (GC-MS), followed by GC peak enhancement and enantioselective GC using authentic compounds, identified 3 major compounds in the behaviourally active <i><span style='text-transform:uppercase'>A. melegueta </i>fraction to be (<i>S)</i>-2-heptanol, (<i>S)</i>-2-heptyl acetate and (<i>R)</i>-linalool in the ratio 1:6:3. <i>Z. officinale</i> had 1,8-cineole, neral and geranial in the ratio of 5.48:1:2.13. The identification of these behaviourally active compounds provides a scientific basis for the observed repellent properties of <i><span style='text-transform:uppercase'>A. melegueta </i>and <i>Z. officinale </i>extracts, and demonstrates the potential for their development in stored-product protection at the small-scale level in Africa.

No description available.

Call number: LD2668 .T4 1950 S775 / Master of Science

A dissertation submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, in fulfilment of the requirements for the degree of Master of Science. Year: 2016. / Entomopathogenic nematodes in the genera Heterorhabditis and Steinernema have emerged excellent as non-chemical alternatives for control of insect pest population. They have a specific mutualistic symbioses with bacterial symbionts in the genera Photorhabdus and Xenorhabdus, respectively. Native EPN species that are able to tolerate environmental stress including desiccation are of great interest for application. The aim of this study was to isolate indigenous EPN species from soil samples collected from Brits, North West province in South Africa, and to investigate their ability to tolerate desiccation stress. The second aim was to isolate the bacterial symbiont and sequence, assemble and annotate its whole genomic DNA. Insect baiting technique and White trap method proved useful in the recovery of nematodes from collected soil samples and infected cadaver, respectively. Molecular identification based on the amplification of the 18S rDNA and phylogenetic relationships revealed high affinity of the unknown EPN isolate 10 to Steinernema species and due to variation in evolutionary divergence distance, the unknown isolate was identified as Steinernema spp. isolate 10 . Isolates 35 and 42 revealed high similarity to Heterorhabditis zealandica strain Bartow (accession number: GU174009.1), Heterorhabditis zealandica strain NZH3 (accession number: EF530041.1) and the South African isolate Heterorhabditis zealandica strain SF41 (EU699436.1). Both Steinernema spp. isolate 10 and Heterorhabditis species could tolerate desiccation. Steinernema spp. isolate 10 was tolerant up to 11 days of desiccation exposure in loamy sand and up to 9 days of exposure in river sand, causing 26, 6% and 13, 4% cumulative larval mortality after 96 hours, post resuscitation by rehydration, respectively. Heterorhabditis spp. could tolerate desiccation up to 13 days of exposure and induced 26.6% cumulative larval mortality on both loamy and river sand after 96 hours post resuscitation. Swarming, aggregation, coiling and clumping behavioural characteristics were observed when Steinernema spp. isolate 10 was exposed to desiccation and Heterorhabditis species displayed no similar behavioural characteristics associated with desiccation tolerance. Morphological characteristics of the unknown Steinernema spp. isolate 10 have been described, and the thick cuticle and sheath which are both associated with tolerance to desiccation stress have been noted. The bacterial symbiont was isolated from larval hosts infected with Steinernema spp. isolate 10 and molecular identification through NCBI Blastn based on the 16S rDNA revealed high affinity to Xenorhabdus bacterial species. Phylogenetic relationships and evolutionary divergence estimates 16 revealed genetic variation and the species was identified as Xenorhabdus bacterial isolate. The genome assembly of Xenorhabdus bacterial isolate using CLC Bio revealed a total length of 4, 183, 779 bp with 231 contigs (>=400bp), GC content of 44.7% and N50 of 57,901 bp. Annotation of the assembled genome through NCBI PGAAP annotation pipeline revealed 3,950 genes (3,601 protein coding sequences (CDS) and 266 pseudogenes), 12 rRNAs and 70 tRNAs. RAST annotation revealed 55 of virulence, disease and defense subsystem features which are involved in the pathogenicity of Xenorhabdus bacterial isolate. The ability of EPNs to tolerate environmental stress is highly crucial and one of the determining factors for biocontrol potential and successful application, thus the indigenous desiccation tolerant EPN isolate, Steinernema spp. isolate 10 holds great potential as a biological control agent. The genome sequencing and annotation reveals insight to behavioural and physiological attributes of bacterial symbionts and this study will contribute to the understanding of pathogenicity and evolution of the bacteria–nematode complex. / GR 2016

In its introduced southern hemisphere range, Sirex noctilio causes considerable mortality in non-native pine forests. In its native Eurasian range however, S. noctilio is of little concern perhaps due to interactions with a well-developed community of pine-inhabiting insects and their associated microorganisms. If such interactions occur, they may limit the woodwasp’s impact in its newly introduced range in North America. My research addresses two broad questions: 1) Does S. noctilio share its habitat with other insects and if so, with whom? 2) Is there evidence that co-habitants affect S. noctilio, and if so how might such interactions occur? Field studies undertaken to describe the woodwasp’s host-attack ecology in Pinus sylvestris showed S. noctilio activity occurred between mid-July and late August, and other phloem- and woodborers sometimes entered the tree after the woodwasp. Tree mortality occurred from two weeks to several months after initial woodwasp symptoms. Suppressed or intermediate trees, those with ≤ 25% residual foliage, or those with stem injury or previous woodwasp symptoms were most likely to have symptoms of woodwasp attack. A second field study conducted to identify associated insect species in S. noctilio-infested Pinus sp. showed the wasp was sometimes found alone, but usually shared the tree with other phloem- or woodboring insects, most commonly the curculionids Tomicus piniperda, Pissodes nemorensis and Ips grandicollis and the cerambycid Monochamus carolinensis. I found no indication that wasps were absent when beetles were present, but there was evidence that woodwasps were less abundant, but larger, when beetles were present. Experiments showed that indirect interactions can occur between the two insect groups via fungal associates of one or both. In the laboratory, the woodwasp symbiont was outcompeted by two beetle-associated fungi, Leptographium wingfieldii and Ophiostoma minus, over a range of temperatures. Under field conditions the woodwasp was able to detect and avoid ovipositing in P. sylvestris inoculated with L. wingfieldii, but its oviposition was unaffected by O. minus. My results show that insects co-habiting pine with S. noctilio have potential to exert a measure of biological control on the woodwasp and may help to limit its impact in North America.

In its introduced southern hemisphere range, Sirex noctilio causes considerable mortality in non-native pine forests. In its native Eurasian range however, S. noctilio is of little concern perhaps due to interactions with a well-developed community of pine-inhabiting insects and their associated microorganisms. If such interactions occur, they may limit the woodwasp’s impact in its newly introduced range in North America. My research addresses two broad questions: 1) Does S. noctilio share its habitat with other insects and if so, with whom? 2) Is there evidence that co-habitants affect S. noctilio, and if so how might such interactions occur? Field studies undertaken to describe the woodwasp’s host-attack ecology in Pinus sylvestris showed S. noctilio activity occurred between mid-July and late August, and other phloem- and woodborers sometimes entered the tree after the woodwasp. Tree mortality occurred from two weeks to several months after initial woodwasp symptoms. Suppressed or intermediate trees, those with ≤ 25% residual foliage, or those with stem injury or previous woodwasp symptoms were most likely to have symptoms of woodwasp attack. A second field study conducted to identify associated insect species in S. noctilio-infested Pinus sp. showed the wasp was sometimes found alone, but usually shared the tree with other phloem- or woodboring insects, most commonly the curculionids Tomicus piniperda, Pissodes nemorensis and Ips grandicollis and the cerambycid Monochamus carolinensis. I found no indication that wasps were absent when beetles were present, but there was evidence that woodwasps were less abundant, but larger, when beetles were present. Experiments showed that indirect interactions can occur between the two insect groups via fungal associates of one or both. In the laboratory, the woodwasp symbiont was outcompeted by two beetle-associated fungi, Leptographium wingfieldii and Ophiostoma minus, over a range of temperatures. Under field conditions the woodwasp was able to detect and avoid ovipositing in P. sylvestris inoculated with L. wingfieldii, but its oviposition was unaffected by O. minus. My results show that insects co-habiting pine with S. noctilio have potential to exert a measure of biological control on the woodwasp and may help to limit its impact in North America.

Thesis (Ph. D.)--Washington State University, May 2009. / Title from PDF title page (viewed on Feb. 12, 2010). "Department of Entomology." Includes bibliographical references.

Thesis (Ph. D.)--Swedish University of Agricultural Sciences, 2001. / Includes bibliographical references.