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Mosquito sampling was carried out in Volgograd city and its vicinity in August 2001 and 2002. In total 16 000 individuals belonging to 6 genera and 12 species were collected. Nine species were anthropophilic. Culex modestus and Aedes vexans dominated in all outdoor samples collected in Volgograd city. In addition to these species, Coquillettidia richiardii and Ae. caspius were abundant in the vicinity of Volgograd. Autogenous Cx. pipiens dominated among six species sampled indoors in Volgograd city. The possible role of different mosquito species in West Nile virus circulation in Volgograd city is discussed.

The midgut epithelim of feeding nymph is represented by the digestive cells of larval phase. Digestion of the main part of feed is performed by the one generation of digestive cells of nymphal phase after detachment, during moult. This period precedes the apolysis. The generation of secretory cells is absent on the nymphal phase. Secretory vacuoles are formed in the digestive cells of larval phase. All functioning cells form a peritrophic matrix on their apical surface. The replacement of the digestive cells of larval phase by the digestive cells of nymphal phase proceeds gradually, during the first 5—10 days after detachment. The beginning of the accumulation of digestive inclusions in the young digestive cells of nymphal phase takes place in the 10—15 days after detachment.

Several morphological forms (morphotypes) of Urospora chiridotae gamontes are found in White Sea holothuroid Chiridota laevis. All these morphotypes are differed by localization in the body of host, form and cytological features. The gregarines are situated in several host biotopes, such as blood vessels, intestine and mesenteries. In the blood vessels elongate skittle-like cells supplied with long thin cytopillia are observed. On the external surface of the intestine spherical gregarines are found. These parasites commonly covered with one layer of coelomic epithelium's cells. In some holothuria intratissue spherical cells of parasites located in intestinal epithelium are presented. Both of these types of parasites lack cytopillia, and folds or ridges on its surface. On different mesenteries, connections between intestine and body wall, and also on intestine elongate ounce-shaped cells and gamontocysts are observed. These cells are situated on the apices of finger-like processes of the intestine and mesenteries surface. Ounce-shaped gregarines have cytopillia shorter than in skittle-like gregarines. The differences between morphotypes of Urospora chiridotae are probably caused by different environmental conditions. In the narrow rift of blood vessel elongate cells are developed. The cytopillia may serve for making more or less wide space around gregarines, which is necessary for food uptake. Spherical cells surrounded by host's cells and have the form typical for tissue parasites. In the wide coelomic cavity where convection of liquid proceeds better than in blood vessel, ounce-shaped gregarines with short cytopillia are developed. We found only typical for Urospora chiridotae ovoid oocysts with dissimilar ends, anterior collar and spine-like posterior end. Thus, the all above-mentioned morphotypes undoubtedly belong to the same species. The relationships between defense host cells and the different morphotypes of trophozoites are variable.

An experimental microsporidiosis of the wax moth caterpillars from laboratory population had been caused by oral infecting of early stages larvae and by intracavity injections of the spores of the microsporidian species Vairimorpha ephestiae. Peculiarities of microsporidiosis proceeding, manifestations of host defence reactions, and also an effect of the temperature of caterpillars cultivation and conditions of spores keeping on liability of the insects to the infection were studied. The effect of the microsporidia on the host organism was the early death or the delay of larvae development, but in several cases external manifestations of the effect of the parasite on the host were absent. The development of the parasites from the moment of infecting to the appearing of the mature spores congestions in the host organism proceeded 6 days. Microsporidia invaded insect fat body and caused its hypertrophy and disappearance of lipid granules. In the intestine and salivary glands microsporidia were not observed in the period from 6 to 16 day of the development. On the final stage of microsporidiosis the all contents of fatty tissue cells were replaced by spores of microsporidia. Under microscope only diplocaryotic spores of the Nozema type had been found in infected and died specimens, but not octospores. The spores threw out polar tubes under the change of pH in incubating solution from neutral to alkaline. The effects of microsporidiosis on the wax moth haemolymph were the increased rate of prohaemocytes, appearing of multinuclear free-circulating cells at 6 day after infection, and suppression of the reaction of haemolymph melanization with the mass sporogenesis of the parasite. The characteristic symptom of the wax moth microsporidiosis had been revealed, accumulation of black points and small spots of irregular form under cuticle ("reaction of attretization"). Increase of the temperature of insect cultivation up to 32°C during 3 days after infection contributed to the full deliverance of the insects from the infection in first and second generations. It can be considered as a method of treatment of wax moth laboratory colonies from microsporidiosis. Oral infection of III and IV stage caterpillars by the spores being kept during 3—6 months under 4°C in form of water suspension caused the death of 63.0—61.5 and 91% of caterpillars being cultivated under 25 and 21°C respectively. Under the temperature of cultivation equal 30°C the mortality did not differed from the control sample (8—10%). The spores extracted from dried bodies of caterpillars lost their vitality. It was demonstrated by the test on infectious ability in vivo and by acridine orange staining. This host-parasite system appears to be perspective in investigations of resistance mechanisms in insects and immunosuppressive features of entomopathogen microsporidia.

Ecological analysis of parasite fauna associated with Perccottus glehni from water basins of the Primorye has been carried out. The 31 species of parasites have been found: protozoan — 10, monogeneans — 3, trematodes — 6, cestodes — 2, proboscis worms — 3, nematodes — 2, crustaceans — 3, hirudinis — 1, and molluscs — 1 species.

The author maintains Moravec's (1994) point of view about attachment of valid taxon status to the genus Ichthyobronema Gnedina et Savina, 1930 with type and single species I. hamulatum (Moulton, 1931) Moravec, 1994.

Experimental infecting of the fleas Coptopsylla lamellifer rostrata by plague was carried out. The fleas were infected by feeding through biomembrane (skin of a white mouse) with a mixture of defibrinated blood of guinea-pig and plague microbes. Under concentration 2—3 milliard of the microbes in 1 millilitre, from 60 to 100% of the fleas were infected. Forming of the block of proventriculus was observed in 9—13 day. Mean percent of blocking for all experiments was lesser than 1%. Maximal rate of blocking (2.8%) was observed in the experiment under everyday 3-hours feeding. After planting of the fleas with blocks on great gerbil (2 fleas on one gerbil) 20% of the gerbils were infected. The conclusion had been made that C. lamellifer rostrata has only insignificant effectiveness as a vector of plague agent in Kyzylkum. Probably it is caused by some specific features of this subspecies.

The acanthocephal Corynosoma shackletoni Zdzitowiecki, 1978 is recorded for the first time as the parasite of sea leopard Hydrurga leptonix (Blainville, 1820) from the Pacific sector of Antarctica. A description and drawings of examined specimens are given.