The ultrastructure of a pheromone-secreting gland in the male scorpion-fly Harpobittacus Australis (Bittacidae: Mecoptera)

The eversible vesicles of the sex pheromone glands consist of three cell types, secreting the cuticle, the duct and the pheromone, respectively. Each pheromone-secreting cell has an end apparatus, bounded by microvilli and lined by a granular mass, that is penetrated by remarkable elongate filaments extending far up into the secretory duct. Vesicles containing secretion or secretion precursors abound. The possible role is discussed of the various organelles in the elaboration and transport of the pheromone.     

THE IDENTITY OF THE SWEDE MIDGE, WITH NOTES ON ITS BIOLOGY

A brief historical summary is given of the literature concerning Contarinia nasturtii Kieffer, C. torquens de Meijere and C. geisenheyneri Riibsaamen, three gall midges (Cecidomyidae) which have been associated respectively with leaf damage on Brassica spp. in England, identical malformation on the Continent and swollen and closed flowers of Brassica spp. in Europe.
Following the discovery in England of the true Contarinia nasturtii causing swollen and closed flowers oiRorippa amphibia, preliminary experiments have shown that midges from this source will also cause similar damage to swede flowers and that they are the same species as those attacking R. amphibia blossom in the Netherlands.
Further preliminary experiments have shown that swede midge derived from rape leaf axils will also cause identical damage to radish flowers in addition to breeding successfully on the leaves of turnip, swede, cabbage and radish.
Male midges derived from Rorippa blossom have been mated with females from rape leaf axils, and their offspring have been reared on Rorippa flowers and on turnip leaves.
This biological evidence confirms the previous supposition based on morphological grounds that the swede midge is Contarinia nasturtii Kieffer and will cause either flower or leaf damage. Consequently, C. torquens de Meijere and C. geisenheyneri Riibsaamen must remain synonyms.
The shortest time for a generation (from parent to first offspring midge) to develop was 24–39 days in an unheated open glasshouse during June-July in 1949 at Harpenden. Under the same conditions, the shortest time for the next generation from late July to August was 29–32 days. C. nasturtii is the first Contarinia species in which unisexual families have been discovered.     

The Epidemiology of Dental Diseases in the Elderly1

This paper summarizes and evaluates epidemiologic evidence on adult dental conditions with a focus on older adults. Information is presented on coronal caries; root caries; loss of teeth, attrition, abrasion, and erosion; periodontal diseases; and oral cancer. The author concludes that the oral health status of the elderly in the United States is essentially unknown. There are no recent, representative population base studies of oral conditions in the elderly. Studies of prevalence or incidence of oral diseases typically include few elderly persons or describe a select group of elderly who are at high risk. Furthermore, it is not really known whether the incidence and prevalence of coronal caries or root caries is actually increasing or is part of a cohort effect. While oral cancers have been shown to increase with age, there is no information as to whether their incidence rates are increasing. While, clinically, there are indications that attrition, abrasion and erosion are characteristics that are more likely to be seen in older adults, there is no information about their distribution in the population. There is evidence that loss of teeth is decreasing but nothing is known about the patterning of that loss. As for periodontal diseases, much work is needed to identify various syndromes that may be distinguished by their distribution in the population as well as determining whether periodontitis is a condition responsible for a majority of tooth loss or just the majority of tooth loss in a small high risk group. In addition, some suggestions are presented for future directions of research in this area.     

THE SUSCEPTIBILITY OF THE PLANT CELL TO VIRUS DISEASE

A number of spraying experiments showed that the virus cannot enter a plant unless some of the cells are injured. It is not essential that such injury should be brought about in the presence of the virus. The chances of infection fall off rapidly in the first few minutes after injury, but infection occurs occasionally as long as half an hour after the cell is damaged.
Inoculations by micropipette into single cells of the host plant yielded only about one-tenth of the expected number of infections. This suggests differences in the susceptibility of the cells to virus attack.