Sequential oogenesis is controlled by an oviduct factor in the locusts Locusta migratoria and Schistocerca gregaria: Overcoming the doctrine that patency in follicle cells is induced by juvenile hormone.

In insects that lay eggs in large clutches, yolk accumulation in each of the many ovarioles is restricted to the basal (terminal) oocyte, the one closest to the lateral oviduct. All succeeding (subterminal) oocytes remain small until the terminal oocytes finished their development and were ovulated into the oviduct. The major step regulating yolk uptake by terminal oocytes is the formation of gaps between cells of the follicle layer, a process termed patency. In the migratory as well as in the desert locust, patency is induced by a Patency Inducing Factor (PIF) produced by the lateral oviducts. PIF is secreted in all regions of the lateral oviducts and interacts with the basal follicle cells via the pedicel, a fine duct that connects an ovariole with the oviduct. By this mechanism, patency is triggered in the follicle cells of the terminal oocyte only, restricting yolk accumulation to the oocytes next to ovulation. In contrast to the previous hypothesis, juvenile hormone (JH) is not necessary to induce patency, rather JH amplifies the effect of PIF.

Wings and legs are production sites for the desert locust courtship-inhibition pheromone, phenylacetonitrile.

Mature gregarious male desert locusts, Schistocerca gregaria, emit the courtship inhibition pheromone phenylacetonitrile. Wings and legs, in particular the fore wings, have been identified as the main releasing sites. Abdomen and head emit only trace amounts of this pheromone. In contrast veratrole, another typical component of male volatiles, is emitted by all body parts. Epidermal gland cells in the identified phenylacetonitrile releasing appendages are the putative sites of its biosynthesis. Incubation of these body parts in the presence of (14)C-phenylalanine results in the production of (14)C-phenylacetonitrile. Some of the phenylacetonitrile appears to be degraded to HCN and benzaldehyde presumably enhancing the repellent character of phenylacetonitrile. HCN is only detectable in volatiles of mature gregarious male desert locusts. Possible advantages of the observed distribution of the phenylacetonitrile release sites and of the cyanogenesis in relation to mating behaviour are discussed.