The face fly, Musca autumnalis De Geer, is continuously present in the field at Guelph, Ont., from April to late October, with peak populations occurring near 1 August. The flies enter buildings only to hibernate, the females doing so in an unfertilized, nulliparous condition. The flies feed only during the daylight hours and primarily on cattle and horses. Infestations on these hosts arc subject to wide daily and hourly variation dependent on temperature, light, precipitation, wind, and behavior of the host.Mating normally occurs as a result of males waiting at particular stations in the pasture to apprehend females flying past. Experiments and observations on a laboratory colony of face flies has disclosed other facets of their sexual behavior.Provided with a suitable proteinaceous diet the face fly can produce an average of 26 eggs per ovarial cycle and a probable maximum of near 230 eggs in a lifetime. Oviposition and (or) successful development will apparently occur only in bovine feces having a certain consistency. Face flies are among the first of the coprophagous insects to reach a dropping; arriving normally within 5 to 10 minutes of its deposition. The dropping remains suitable for oviposition for up to about 3 hours, depending on the rate of drying of its surface.Under normal summer temperature conditions eggs hatched within about 24 hours. The young larvae were initially restricted to the surface layers of the dropping by their respiratory requirements but by the end of the normal 5 to 7 day development period the larvae occupied the entire dropping. Mature third stage larvae pupated in the soil surrounding the dropping.Two hymenopterous pupal parasites Aphaereta pallipes (Say) and Xylaphora sp. accounted for approximately 10% mortality. Face fly adults were preyed upon by the staphylinid beetle Ontholestes cingulatus Gravelle, and the common dung fly, Scatophaga stercoraria (L.).

An artificial diet for rearing the codling moth is described. It is a modification of a casein–wheat germ diet that was initially developed for the cabbage looper. Agar was replaced by a mixture of wood sawdust, wheat flour, and wood pulp. Growth of microorganisms was controlled by sorbic acid and aureomycin, and by lowering the pH of the diet to 3.5 with citric acid. Production cost for dietary ingredients was about $1/1000 moths. The moths were slightly smaller than those reared on apple. When confined in cages, the sterilized diet-reared moths were somewhat less competitive than the apple-reared insects. However, sterilized diet-reared male moths released in an apple orchard dispersed more rapidly than sterilized apple-reared males.

Orchex-796 oil and Volck Supreme oil at 2.5 gal per acre gave equal commercial control of adults and nymphs of the pear psylla, Psylla pyricola Foerster, on Anjou pears. Control was better at 5 gal per acre but at this rate, both oils caused sporting and marginal burn on leaves and russet spots on the fruit of Anjou pears. The 2.5-gal rate caused slight leaf spotting, but no fruit injury.This indicates that the recommended rate of 6 gal of oil per acre for Bartlett pears cannot be used on the Anjou variety, and raises the question whether this high rate is necessary for pear psylla control.

Some 35 species (mostly Neotropical, 22 new) of acalypterate flies representing 17 genera (3 new) in six families, as follows, are treated: Family Cypselosomatidae. One species from Nepal, Cypselosoma gephyrae Hendel (?), is discussed.Family Pseudopomyzidae. The classification of the family is reviewed, and a key to the world genera is provided. The genus Latheticomyia Wheeler is placed here for the first time, and two new species, L. longiterebra (Peru) and L. rotundicornis (Mexico), are described. Two new genera, Pseudopomyzella and Rhinopomyzella, are erected for three new species, P. flava (Peru), R. albimana (Brazil), and R. nigrimana (Brazil).Family Periscelidae. The genus Periscelis Loew is recorded from Mexico and Peru. Neoscutops peruvianus and Scutops striatus, both from Peru, are described as new.Family Aulacigastridae. The classification of the family is reviewed and a key to the world genera is provided. Schizochroa plesiomorphica (Peru), S. minuta (Ecuador), S. ecuadoriensis (Ecuador), Cyamops neotropicus (Peru), C. australicus (Queensland), and Planinasus venezuelensis (Venezuela) are described as new.Family Odiniidae. The classification of the family is reviewed and a key to the subfamilies and the world genera is provided. Two new species of Schildomyia Malloch, S. peruviana (Peru) and S. trinidadensis, are described. A new genus, Shewellia, is erected for the species S. agromyzina (Peru).Family Heleomyzidae. One new species of Cephodapedon Malloch, C. nigriventer (Chile), is described. The genera Mayomyia Malloch and Cinderella Steyskal are reviewed and placed in this family for the first time. Four species of Cinderella, C. macalpinei (Ecuador), C. pollinosa (Chile), C. hirsuta (Chile), and C. steyskali are described as new.The paper is accompanied by 72 illustrations.

The male of Xysticus rugosus Buckle and Redner, 1964, is described for the first time, the diagnostic parts of the palpus are drawn, and a key is provided for distinguishing the males of the Nearctic species of the Xysticus labradorensis group.

The "pars stridens–plectrum" terminology of stridulatory organs is discussed. A list of 77 species of Scolytidae known or presumed to bear stridulatory structures is presented. The three types of scolytid stridulatory organs, vertex–pronotal, gula–prosternal, and elytra–abdominal tergites, are described and discussed.All North American species in the genus Ips were examined for stridulatory organs. The gula–prosternal type was found on females, and possibly males, of I. concinnus (Mannerheim) and I. mexicanus (Hopkins). The vertex–pronotal type occurs on females of 14 other species. No stridulatory structures were found on either sex of the remaining 17 Ips species. Females of 15 of the 18 pine-infesting species have stridulatory organs, while 14 of the 15 spruce-infesting species apparently lack them. Female I. confusus (LeConte) stridulate when entering the male entrance tunnels. Removal of the stridulatory organ has two effects: males do not permit some of these non-stridulating females to enter, and they deny entry to others for an unusually long period of time.Possession of a stridulatory apparatus in the Scolytidae appears to be associated with the sex opposite to that which initiates the entrance tunnel.No significant differences were found between gallery systems constructed by female I. confusus with the stridulatory organ removed and those constructed by stridulating females except that more single stridulating females excavated two or more egg galleries from a nuptial chamber.