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Location and ultrastructure of sex pheromone glands in female Callosobruchus maculatus (Fabricius) (Coleoptera : Bruchidae)
Affiliation:1. State Key Laboratory of Biocontrol, Key Laboratory of Biodiversity Dynamics and Conservation of Guangdong Higher Education Institute, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, PR China;2. Australian National Insect Collection, CSIRO National Research Collections Australia, GPO Box 1700, Canberra, ACT 2601, Australia;3. College of Life Sciences, Capital Normal University, Xisanhuanbeilu 105, Haidian District, Beijing, 100048, PR China;1. School of Life Sciences, North Maharashtra University, Post Box 80, Jalgaon, 425001, Maharashtra, India;2. North Maharashtra Microbial Culture Collection Centre (NMCC), North Maharashtra University, Post Box 80, Jalgaon, 425001, Maharashtra, India;1. Institute of Vertebrate Paleontology, College of Life Science and Technology, Gansu Agricultural University, Lanzhou City, 730070, Gansu Province, China;2. College of Life Sciences and Academy for Multidisciplinary Studies, Capital Normal University, 105 Xisanhuanbeilu, Haidian District, Beijing 100048, China;3. Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC, 20013 USA;4. College of Life Science and Technology, Gansu Agricultural University, Lanzhou City, 730070, Gansu Province, China
Abstract:The ultrastructure of the female sex pheromone glands in Callosobruchus maculatus (Coleoptera : Bruchidae) were localized using a masking technique, combined with eiectro-antennography and by a comparison of the glandular cells of sexually active (flightless) females and non-sexually active (flight-form) females. Each unicellular gland is an invagination of the integumental membrane capped by a single secretory cell. These glands are situated on the fine intersegmental membrane, which joins the pygidium to the ovipositor. The secretory cells of the glands of active females are characterized by well-developed microvilli, with many elongated mitochondria among the latter. The high metabolic activity of these cells is revealed by the presence of heterogeneous secretion vesicles, some of which contain abundant crystallized material. Deep basal invaginations indicate the uptake of substances from the haemolymph. The receptor canal is a network of fine cuticular filaments which have the same structure regardless of the female's sexual status. Cells from the glands of non-sexually active females are underdeveloped and show no invaginations of the basal membrane and very few microvilli. The localization of these glands was made possible by the use of SEM, TEM and EAG as well as by masking the suspected zones and by comparing females in different physiological states: flightless females, which were sexually active and producing pheromones; and flight-form females, non-sexually active and producing no sex pheromones. Only by adopting such a stringent method was it possible to confirm the function of the glands whose ultrastructure was studied.
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