Thesis (Ph. D.)--University of Wisconsin--Madison, 1954. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 103-111).

Thesis (doctoral)--Tierärtzliche Hochschule zu Berlin, 1925. / Vita. Includes bibliographical references (p. 26-27).

Thesis (M. Sc.(Zoology and Entomology))--University of Pretoria, 2005. / Includes bibliographical references. Available on the Internet via the World Wide Web.

Thesis (Ph. D.)--University of Hawaii at Manoa, 2001. / Heading on electronic reproduction: Roberts, Guinnevere Ellen. Includes bibliographical references (leaves 104-131). Also available on microfiche.

Wax secretion in worker honeybees is significantly related to the age of the worker and, while the secretion pattern remains the same, the absolute amount of wax secreted varies seasonally. Comb building festoons, previously thought to be the site of wax secretion, contain only a fraction of the newly-secreted wax in the nest. Festooning behaviour was also found to be seasonal. The amount of wax secreted by workers was significantly affected by hive. Although age-related changes in behaviour and physiology of worker honeybees appears to be modulated by juvenile hormone (JH), wax secretion is not dependent on JH. Manipulating JH III titres by injecting the hormone and manipulating the only source of the hormone (the corpora allata: CA) did not affect wax secretion. Increasing haemolymph JH titre shortly after ec1osion did not affect the amount of wax produced by workers aged 3 to 21 days, nor could a critical period be found during which elevated hormone titres would affect the rate of wax secretion. Allatectomy of newly eclosed workers did not affect wax production. Removing the putative neural feedback inhibition on the CA did not result in a change in wax production. Implanting CA from older workers into younger workers had no significant effect. Methoprene, a widely-used JH analog, caused reduced wax secretion in workers. It is suggested that methoprene poisons worker honeybees. The results obtained are consistent with an alternative model for wax secretion proposed by Butler (1954). The methodological problems found in this work are present in many other studies. When viewed in this light, the role of JH in polyethism appears dubious and there are alternative models of polyethism that do not have these shortcomings.

The ultrastructure of the corpus allatum of the Cape worker honey bee has been examined in a systematic way during the first thirty days of adult life. Corpus allatum size in the Cape worker honey bee shows the age-dependent increase typical of the European worker honey bee, and in the Cape worker bee, the duration of increase is protracted. Analysis of ultrastructural development provides three indicators of metabolic status: mean mitochondrial size, "light and dark" cells, and extracted vacuoles. Significant fluctuations in mean mitochondrial size indicate a cyclical nature of cellular activity. New thought on the nature of "light and dark" cells proves that "dark" cells are almost certainly active in the process of JH biosynthesis, whilst "light" cells are definitely not active in JH biosynthesis. Extracted vacuoles found in corpus allatum cells during this study are thought to be remnants of lipid vacuoles, and the build up in number of these vacuoles is regarded as an indicator of reduced biosynthetic activity. Since the two indicators of decreased JH production ("light" cells and extracted vacuoles) co-exist with smaller mean mitochondrial size, larger mean mitochondrial size is taken as indicating increased levels of JH biosynthesis. Hence, fluctuations in mean mitochondrial size suggest cycles in the levels of JH production in individual corpora allata of the adult worker honey bee.

The ideal climatic conditions and diversity of floral resources allow Ethiopia to sustain millions of honeybee colonies. Beekeeping is widely practiced and plays a significant role in the livelihood of the farming community of the country. Despite this, information on the types of geographical races of honeybees, their behavioural characters and the related ecological factors are not established. In this work an attempt was made to characterise the honeybee populations of the northern parts of Ethiopia based on the analyses of morphological, behavioural and ecological characteristics. For morphological analysis, 155 honeybee colony samples from 31 localities were collected. 20 worker honeybees per colony sample totalled 3100 individual worker honeybees and thirteen morphological characters per bee, a total of 40 300 measurements were recorded following Ruttner's (1988) protocols. The behavioural characters such as reproductive swarming, migration, temperament and colony seasonal cycles were assessed based on survey work of a pre-structured questionnaire. Various univariate and multivariate statistical methods were employed to analyse the data. The principal components and step-wise linear discriminant analyses revealed the existence of four discrete morphoclusters or geographical races: A. m. jemenitica from eastern, northwestern and northern arid and semi-arid lowlands, A. m. scutellata from the western humid midlands, A. m. bandasii from sub-moist central highlands and A. m. monticola from the northern mountainous parts of the study areas. These different geographical races were found to be distinctively distributed in the different ecological parts of the study area. High intercolonial and intracolonial variances were observed in all localities, however particularly high values were obtained in areas of transitions between ecological zones indicating a region of gene flow or zones of hybridisation among the statistically defined populations. Such high variances were observed mostly in areas where A. m. jemenitica borders the other geographical races. Moreover. distinct behavioural variations were also noted among these geographical races. Generally. the highland and mountainous honeybees A. m. bandasii and A. m. monticola are relatively larger in body size. have less tendency to swarm. less inclination to migrate and are relatively gentle while the converse traits were noted for the lowlands and midlands honeybees A. m. jemenitica and A. m. scutellata. Both morphological and behavioural variations were highly correlated with environmental factors and the variations seem to be the result of long adaptation to the interrelated ecological factors in their respective areas. Variations in reproductive swarming periods were also noted among these honeybee populations as a result of variations in rainfall pattern. altitude and temperature in their respective ecological areas which are believed to alter the honeybee colonies' seasonal cycles and leads to partial temporal reproductive isolation among these different honeybee populations.

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