Anatomy and ultrastructure of the female and male reproductive system in Acarus siro L. were investigated by light and electron microscopy. The female system consists of paired ovaries of nutrimentary type in which oogonia and oocytes are connected by bridges with a large central cell. The oviducts empty into the uterus, which passes into preoviporal duct lined by cuticle, and opening as a longitudinal slit (oviporus). An elongated accessory gland composed of one type of secretory cell is located along each oviduct. The copulatory opening occurs at the posterior margin of the body and leads, via the inseminatory canal, to the receptaculum seminis, consisting of the basal and saccular part. Both inseminatory canal and basal part of receptaculum seminis are lined by cuticle, whereas the wall of the sac is formed by cells covered only by long, numerous microvilli. The basal part of the receptaculum seminis joins the ovaries via two lumenless transitory cones. The male reproductive system contains paired testes, in which spermatogonia tightly surround the central cell. The proximal part of the paired vasa deferentia serves as a sperm reservoir, while the distal one has a glandular character. An unpaired, cuticle-lined ejaculatory duct opens into the apex of the aedeagus. The single accessory gland is located asymmetrically at the level of, or slightly posterior to, coxae IV. The structure of the genital papillae, which are topographically related to the genital opening in both sexes, is also briefly described.

The central nervous system of Ixodes scapularis is fused into a single compact synganglion. The esophagus runs through the synganglion and divides it into supraesophageal and subesophageal parts. The supraesophageal portion contains a single protocerebrum with four pairs of glomeruli, paired optic lobes and cheliceral ganglia, and a single stomodeal bridge. The subesophageal portion contains a centrally located network of commissures and connectives, a pair of palpal ganglia, paired olfactory lobes of the first pedal ganglia, four pairs of pedal ganglia, and a single opisthosomal ganglion. A retrocerebral organ complex (ROC) in close vicinity of the digestive tract, as described in some other tick species, apparently is lacking. Perhaps the function of the ROC is performed by the paired, large, ganglion-like bodies that lie anterolaterad to the cheliceral ganglia. The rind, which is formed from the neuronal somata and glial cells, surrounds the central fibrous core or neuropile. Neurosecretory cells (NSC) are distinct among rind cells due to their large size and concentration of cytoplasmic neurosecretions. NSC are present throughout the synganglion, although the subesophageal portion contains larger groups of these cells. Histological serial sections, stained with Meola's (Trans Am Microsc Soc 89:66-71, '70) paraldehyde fuchsin (PAF) procedure revealed 24 PAF-stained, putative neurosecretory regions in the synganglion of virgin, unfed females. All of these regions appear to be connected and associated with the nearest ganglion and are correspondingly named. Eighteen PAF-positive regions occur in the synganglion. In addition, PAF-negative (green-stained) cells occupy 6 distinct regions in the synganglion of unfed, unmated females.

Development and reproduction of the predatory mite Parasitus consanguineus Oudemans et Voigts (Acari: Parasitidae) reared on a diet of first and second instars of Megaselia halterata (Diptera: Phoridae) or Lycoriella ingenua (Diptera: Sciaridae) were studied. Mites were allowed to feed on these diets until death. The developmental time of immature stages of P. consanguineus was significantly longer when reared on L. ingenua than on M. halterata larvae (8.3 vs. 7.9 days, respectively). Survival to adulthood of P. consanguineus reared on L. ingenua or M. halterata larvae was 63 and 49%, and mite fecundity was 17.8 and 12.3 eggs/female, respectively. Adult females reared on L. ingenua lived on average 6.9 days, whereas those reared on M. halterata lived for 5.7 days. Mite survival, female longevity and fecundity were significantly different among the two diet types.

The response to pirimiphos-methyl, in one strain of Acarus farris and two strains of Acarus siro, was assessed using an impregnated filter paper bioassay and by the selection of adults following exposure to pirimiphos-methyl. It was concluded that one of the strains of A. siro was resistant to pirimiphos-methyl and that a major resistance mechanism was involved. The second strain of A. siro gave a response similar to that of a laboratory strain unexposed to organophosphates and was considered to be susceptible. The A. farris strain responded to selection at the ED50 but not at the ED99, and it was concluded that a minor resistance mechanism is present in this strain. Assays of esterase activity were used to attempt to identify the biochemical mechanisms involved in the resistance detected by the bioassays. The A. farris and susceptible A. siro strains showed similar levels of esterase activity but the esterase activity of the resistant A. siro strain was significantly greater. An increase in esterase activity followed selection of both the A. farris strain and the resistant A. siro strain. An acetylcholinesterase assay showed no significant difference between the susceptible and pirimiphos-methyl selected strains of A. siro. The results suggest that esterases are involved in the resistance to pirimiphos-methyl found in A. siro and A. farris but that in A. siro, at least, other mechanisms may also be present.

Immature individuals of Acarus siro L. ingest a total of 0.1408 J of food energy, 58.5% of which is consumed by the deutonymph, 27.1% by the protonymph and only 14.1% by the larva. The total ingestion is much greater (2.8169 J +/- 0.0981 SE). Much energy, 0.7031 J +/- 0.0231 SE, is used for egg production, which is concentrated in the first 20 days of adult life. Assimilation efficiency during this period varies from 63 to 71%. Most energy ingested between the 20th and 40th days of adult life is used in biomass production, and biomass increases significantly up to the 30th day. Afterwards, old individuals expend a large amount of assimilated energy on respiration due to the increased cost of maintenance.

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