Thesis (M.S.)--Worcester Polytechnic Institute. / Keywords: juvenile hormone; Limulus; horseshoe crab. Includes bibliographical references (p. 68-79).

No description available.

The role of juvenile hormone (JH) in alate-apterous polymorphism was investigated in the green peach aphid, Myzus persicae. At higher concentrations (65 ppm), the juvenile hormone analogue (JHA), kinoprene, was immediately toxic to apteriform nymphs. At lower concentrations (10 ppm), the compound was non-toxic and exhibited no apparent morphological activity in apteriform stages. In contrast, 65 ppm kinoprene administered to alatiform nymphs had juvenilizing and apterizing effects. The extent of these effects depended upon when the kinoprene was applied. Fourth instar alatiforms were the least sensitive as kinoprene-treated nymphs developed into normal adults with reduced sclerotization and pigmentation. Kinoprene-treated third instars underwent a supernumerary moult before metamorphosing into adults with malformed wings. Sclerotization and pigmentation were also lacking in these insects. When first and second instar alatiformsiwere treated with kinoprene, they also underwent a supernumerary moult. The adults which emerged exhibited both larval and apterous characteristics. Wing development was almost totally inhibited; the cauda and genital plate were poorly developed. In addition, sclerotization and pigmentation were reduced and ocell lacking. The secondary antennal sensoria were also malformed. These findings clearly (1) demonstrate that kinoprene can be employed as a JH mimic to alter the normal programming of the epidermal cells in alatiform nymphs and (2) indicate that JH plays an important role in aphid morphogenesis and polymorphism. The differential responses of the four alatiform nymphal instars suggest that elevated JH levels during the first and second instars are particularly important in inhibiting wing development. To determine the prenatal effects of JH on wing development and morphogenesis, kinoprene was also administered to newly ecdysed apterous adults. Even though conditions favoured alate production, 75% of the offspring produced by kinoprene-treated virginoparae developed into normal apterae. This suggests that elevated JH titers in maternal haemolymph inhibit wing development and promote development of apterae. Topical application of the anti-allatotropin, precocene-II, had variable effects on apteriform nymphs and adults. In all stages, precocene produced a significant decline in larvi-position. The effects were more pronounced in first and second instar apteriform nymphs and apterous adults than in third and fourth instar nymphs. When kinoprene was applied to these insects, larviposition increased significantly after 2 days. The findings demonstrate that JH stimulates reproduction in viviparous morphs of persicae. / Land and Food Systems, Faculty of / Graduate

No description available.

Thesis (Ph. D.)--University of Wisconsin--Madison, 1983. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

Thesis (Ph. D.)--University of Washington, 2000. / Vita. Includes bibliographical references (leaves 123-151).

"Lipid-based hormones known as the juvenile hormones (JH) are ubiquitous among the arthropods, but their presence, functions, and sites of production in the horseshoe crab, Limulus polyphemus, remain unknown. Large size and lack of secondary sex characteristics in adult female horseshoe crabs may indicate continuous growth and molting throughout life, which is the outcome of high JH levels in insects and crustaceans. Here a study was undertaken to detect and localize lipid-based hormones in horseshoe crab hemolymph and tissue. Capillary electrophoresis and RP-HPLC analyses indicate the presence of a JH-like compound in subadult horseshoe crab hemolymph. The compound is present only in much lower amounts in the hemolymph of adult male and adult female horseshoe crabs. Identification of this compound was based on its similar retention time to standard JH, co-migration with added JH, and cross-reactivity with a polyclonal antibody to JH III. In addition, immunohistochemistry was used to localize the production site of this compound. Analysis of neural tissue, the assumed site of production, yielded no reactivity with labeled anti-JH III antiserum. In larval animals, however, reactivity was noted in yolk contained within the digestive tract. Since the larvae are lecithotrophic and feeding only on their yolk reserves, JH in the gut may be maternal, deposited in the egg before laying. Based on these results, we conclude that horseshoe crabs produce a lipid-based, JH-like hormone, with functional similarity to JH III in insects (i.e., maintenance of the juvenile form during growth and molting.) This paper is the first substantiation of such a hormone in horseshoe crabs. Our findings suggest that JH will be found in other chelicerates as well."

A strategy for the discovery of new insect growth regulators from arid lands plants was developed. Plant genera with a history of toxicity, medicinal use, or incorporation in native american cultures were selected. Forty-five species from twenty-one families were collected, extracted, and tested for biological activity on the large milkweed bug, Oncopeltus fasciatus. Eight extracts were toxic and the extract of Nama hispidum (Hydrophyllaceae) caused nymphs to undergo precocious metamorphosis to an adult. The active component of N. hispidum was precocene II (6,7-dimethoxy-2,2-dimethyl chromene). Nine Nama species, representing four of the five sections in the genus were gathered from Hawaii, California, Nevada, Arizona, New Mexico, and the Dominican Republic. In addition to the insect anti-hormone, precocene II (PII), present in N. hispidum, N. rothrockii contained at least two different insect juvenile hormone mimics, and N. sandwicense contained insect anti-hormone and insect juvenile hormone mimics. Fifth instar larvae of Heliothis zea were used as model insects to distinguish between post-ingestive intoxication and feeding deterrency during exposure to PII. Larvae fed artificial diet with PII were deterred from eating, and had retarded weight gain, growth, and development. Insects grown on diet with PII consumed less food, could not digest the food, or convert ingested food to body mass. in vivo radiotracer studies with the nutrient, ¹⁴C linoleic acid, show a lower rate of transport and incorporation of radioactivity into fat body tissue. A change in the midgut epithelial cells from PII resulted in reduced transport efficiency and retarded larval growth and development. Scanning electron microscopy of the midgut epithelia indicated that cytotoxic damage is induced by PII. Observed changes in the midgut epithelial cells are consistent with a destructive alkylation of cell structures by PII.