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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

The figs (Ficus spp.) and fig wasps (Chalcidoidea) of Hong Kong.

Hill, Dennis S., January 1966 (has links)
Thesis (Ph. D.)--University of Hong Kong, 1967.
2

The figs (Ficus spp.) and fig wasps (Chalcidoidea) of Hong Kong

Hill, Dennis S. January 1966 (has links)
published_or_final_version / Zoology / Doctoral / Doctor of Philosophy
3

Polymorphism and fighting in male fig wasps

Vincent, Stephanie Louise January 1992 (has links)
Male fig wasps (Hymenoptera: Chalcidoidea) exhibit a fascinating range of morphology and behaviour. A cluster analysis, based on descriptions of the males of several hundred species, distinguished six major morphological groups. Behaviourial observations suggest that male morphology is related to the levels of inter-male aggression. Three behaviourial groupings were identified. Fighting species generally mated in the fig cavity, pacifist species mated in the females' galls or outside the figs. Mating sites are thus the primary determinants of male morphology and behaviour. In fighting species males were larger than their females, whereas pacifists and aggressors were equal in size or smaller than conspecific females. The large males in fighting fig wasps appear to be a consequence of sexual selection because larger males tended to win fights. Within a species there were no differences in the size of the galls that produced males and females, even in species where sexual size differences were present, suggesting that there is a heritable component to wasp size. No alternative advantages for smaller males were detected. Although fights were sometimes fatal, damage was not always a consequence of fighting behaviour and was recorded in both fighting and pacifist species. Sex ratios in several species were more female biased at higher population densities. Sex ratios of species with 'internally' ovipositing species were heavily female biased, but approached 1:1 in more outbred species with 'externally' ovipositing females. Levels of matedness, among females ranged from 73% to 99%. No evidence for sperm exhaustion was obtained. Species of Philotrypesis with both winged and flightless males were present only in southern African Ficus species from subsections Platyphyllae and Chlamydodorae. No species had only winged males. The flightless males of some Philotrypesis species were themselves polymorphic. In one polymorphic Philotrypesis species, winged males were found to be rare at high densities, but common at low densities. Digitata and religiosa males of Otitesella differed in coloration, size and behaviour. Digitata males were aggressors while religiosa males were fighters. Digitata males escaped from the figs whereas religiosa males remained inside the figs, perhaps because only digitata males were attracted to Light. Proportionally more digitata than religiosa males were present in low density populations and females were found to respond differently to the two morphs.
4

The systematics and phylogenetics of the Sycoecinae (Agaonidae, Chalcidoidea, Hymenoptera)

Noort, Simon van January 1993 (has links)
The Sycoecinae are a distinct and well-defined subfamily of old world fig wasps (Agaonidae, Chalcidoidea 1 Hymenoptera) , exclusively associated with the figs of Ficus species (Moraceae). The most likely sister group of the Sycoecinae was determined to be the Sycoryctini (Sycoryctinae) based largely on synapomorphies of the underside of the head. 67 sycoecine species and 3 subspecies were recognised and included in a phylogenetic analysis of the subfamily. This analysis clearly delimited six genera (four African and two extra-African), although the phylogenetic relationships between the genera were not strongly supported and remain flexible. Comparisons of the phylogeny of the Sycoecinae with the classifications of the Agaoninae and their host fig trees (Ficus, Moraceae) suggest a degree of cospeciation sensu lato. Numerous homoplasies were detected within the Sycoecinae, some of which were shared with another group of fig wasps that also enter the fig to oviposit, the Agaoninae. The anatomy of the figs apparently provides strong selection pressures that have resulted in both parallelisms and convergences within and between the two subfamilies. Among the 67 species and 3 subspecies that were recognised, 43 species and 2 subspecies are described as new. The males of three previously recognised species are also described for the first time. One generic and two specific synonyms are established together with five new combinations. Keys are provided to the genera and species, for both sexes.
5

Phylogenetics of Pteromalidae and Eulophidae (Hymenoptera: Chalcidoidea) with a study of cranial bridges in Chalcidoidea

Burks, Roger Allen. January 2009 (has links)
Thesis (Ph. D.)--University of California, Riverside, 2009. / Includes abstract. Available via ProQuest Digital Dissertations. Title from first page of PDF file (viewed March 16, 2010). Includes bibliographical references. Also issued in print.
6

Hymenopteran systematics an investigation of selected techniques for the cladistic analysis of molecular data /

Munro, James Burton. January 2009 (has links)
Thesis (Ph. D.)--University of California, Riverside, 2009. / Includes abstract. Includes bibliographical references. Issued in print and online. Available via ProQuest Digital Dissertations.
7

Aspects of the behavioral ecology of Edovum puttleri Grissell (Hymenoptera: Eulophidae), an egg parasitoid of Colorado potato beetle, Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae).

Idoine, Karen 01 January 1989 (has links) (PDF)
No description available.
8

Interactions between figs (Ficus spp., Moraceae) and fig wasps (Chalcidoidea, Agaonidae)

Ware, Anthony Brian January 1993 (has links)
Fig trees (Ficus spp., Moraceae) and fig wasps (Chalcidoidea, Agaonidae) are uniquely associated. In one fig wasp group, the pollinators (Agaoninae), each species is generally host species-specific. The relationship is one of obligate mutualism where the wasps provide pollination services and in return utilises some of the ovules for larval development. Non-pollinating fig wasps (generally belonging to subfamilies other than the Agaoninae) may be gallers or parasitoids, and can also be host species-specific. In the accompanying studies we examined the factors governing the interactions between fig wasps and their host trees. Surveys of fig trees and their associated pollinating fig wasps conducted in southern Africa, Madagascar and The Comores generally confirmed their specific relationships. An examination of F. sycomorlls in Madagascar resulted in the reclassification of F. sakalavarum as a distinct species with its own specific pollinator species. Biological and chemical evidence is presented demonstrating that the pollinators were able to distinguish their hosts through volatiles which emanated from the figs when they were ready to be pollinated. Environmental factors were found to influence wasp behaviour. Ambient temperature governed the timing of wasp emergence from their natal figs. When dispersing from their natal figs, the fig wasps flew upwards and then were blown downwind. Once nearing trees bearing figs ready to be pollinated, the wasps lost height and flew upwind towards the trees. E. baijnathi females apparently avoided figs which already contained a conspecific foundress. Scanning electron microscope studies of pollinating female fig wasp antennae showed that while all the species possessed multiporous plate sensilla, in only a few species were these sensilla elongated. Multiporous plate sensilla elongation is rare or absent among other female chalcids and may have evolved within the Agaoninae in order to facilitate their location on receptive host figs. Pollinator choice specificity appears to break down in a number of cases. In the first case examined, two pollinator species were recorded from the figs of African F. sycomorus. One. C. arabicus, pollinates the figs while the other, C. galili, acts as a 'cuckoo' by utilising some of ovules for oviposition without providing pollen. In the second case three pollinating fig wasp species were recorded from the rigs of F. lutea. Two were found to be incidental visitors and were not specifically attracted to the tree. The hybrid seeds from these crosses were successfully germinated but the seedlings did not grow passed the cotyledon stage of their development. In the concluding study the consequences of Ficus phenology and the structure of the fig's unusual inflorescence on the nonpollinating fig wasp community were examined. Various factors affecting the population levels and species richness were also examined. Future possible research directions were discussed.

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