Stimulation of genital eversion in the land snailHelix aspersa by extracts of the glands of the dart apparatus
β Scribed by Chung, Daniel J. D.
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 963 KB
- Volume
- 238
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
β¦ Synopsis
The dart apparatus, used during courtship in some groups of hermaphroditic land snails, has long been assumed to have a "stimulatory" effect on the mating partner, though how stimulation occurs and exactly what function it serves has never been determined. In this study, extracts of the mucous glands of the dart apparatus of the land snail Helix aspersa were injected into conspecifics and into a related snail, Cepaea nemoralis, in order to test the hypothesis that the dart is used to achieve inflow of bioactive mucous gland secretions into the darted snail. Helix aspersa injected with the extract responded by everting their terminal genitals; eversion normally takes place during courtship and mating. Boiling the extract increased the bioactivity. Pronase-treated extract lost bioactivity, and gel filtration of the boiled extract indicated that the active substance has a molecular weight of about 5,000. The active substance may be a polypeptide. Cepaea nemoralis also everted their genitals when injected with the boiled Helix extract. The active substance appears to be a contact sex pheromone, the second such pheromone in a pulmonate land snail for which experimental evidence has been obtained.
π SIMILAR VOLUMES
## Abstract Pheromone biosynthesis in the redbanded leafroller moth, __Argyrotaenia velutinana__, was stimulated by homogenates of the bursa copulatrix. Although pheromonotropic activity was also extractable from the ovary, the activity of pheromone biosynthesis activating neuropeptide (PBAN) or bu
Glutamine may serve as an activator and/or regulator of the N6-hydroxylase (E.C. 1.14.99) of Aerobacter aerogenes 62-1. Activation and stabilization of N6-hydroxylase activity was observed both in vivo and in vitro. Growth in a glutamine-supplemented medium resulted in (1) maximum N6-hydroxylase act