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The amended diagnosis of the genus Pratylenchoides and list of its valid species with synonyms are given. All the efficient diagnostic characters are listed. Modern taxonomic standard for the description of Pratylenchoides species is proposed; it may be used also in taxonomic databases. Tabular and text keys for all species of the genus are given. Five folowing groups are considered within the genus Pratylenchoides. The group arenicola differs from other groups in the primitive adanal bursa type; the groups magnicauda, crenicauda, ritteri, and megalobatus differ from each other in the position of cardium along the body axis in relation to the pharyngeal gland nuclei, pharynx types are named according to the stages of its evolution from the primitive tylenchoid pharynx (cardium situated posteriorly) to the advanced hoplolaimoid one (cardium situated anteriorly). Diagnoses and species compositions of the groups are given. Basing on the matrix of species characters, the dendrogram has been generated for all species of Pratylenchoides and for all characters (UPGMA, distance, mean character dif-ference, random, characters ordered). Taking in view that the PAUP software gives equal weights to all characters, including the most important ones which define the prognostic species groups, the separate dendrograms for each prognostic species group were generated using the same above mentioned tree parameters. On the base of the records of Pratylenchoides species the matrices of plant host ranges, geographic distribution, and preferred soil-climatic conditions were developed. The dendrograms of the faunal similarities were generated using these matrices, with conclusions on a possible origin and evolution of the genus. The genus evolved from the flood lands with swampy soils and prevalence of dicotyledons (herbaceous Lamiaceae and woody Salicaceae families) to the forest mainland communities with balanced humidity and predominance of herbaceous Роасеае and Fabaceae with woody Fagaceae, Betulaceae, and Oleaceae. The leading factor of the evolutional adaptation to soil-climatic conditions was the factor of humidity, but its significance gradually decreased with the host change to more advanced plant taxa adapted to the communities with more dry balanced humidity. The genus took its origin on the south shores of Laurasia in the Cainozoe. Later, when Hindistant and Arabian Peninsula joined with Laurasia creating the Himalayas barrier, the Pratylenchoides spp. distributed by two branches: the northern one moved into Central Asia, East Europe and North America, and the south branch came into Indo-Malaya, West Asia and the north of Africa. The remnants of the ancient species groups remain in West Europe and East Asia. In the North America the genus gave an origin to its sister genus Apratylenchoides, which spread to the south up to Antarctica; another advanced branch spread in the North America reaching Alaska.

Estimation of the invasion character and distribution of the Diplostomum huronense metacercariae depending on the fish host age has been carried out in roach of Lake Ladoga. Distribution of D. huronense in the young roach (up to age 5+) is negative binomial. Aggregation of the parasite is caused not only by individual differences in the fish host resistance to the metacercariae invasion, but by a high mortality of hyperinfected fishes as well. In older individual hosts the host-parasite system is destroyed, and the parasite distribution approximates to normal. The parasite system of the diplostomids in roach is characterized by the spatial asymmetry, when most part of parasites inhabit few individual hosts, and probability of the case when a parasite get into previously infected host is higher than that of the invasion of parasite-free host. Thus, the Diplostomum huronense metacercaria is an important factor regulating the fish fry number both in direct (death of infected fry) and indirect (elimination of hyperinfected fishes by ichthyophagous birds) way.

Helminth fauna of Insectivora was investigated in canal banks situated in meliorated territories of Belorussian Polesie during 1996—1999. Thirty-three helminth species were found in the animals examined. Most of the parasites are usual in common shrew Sorex araneus L., which is a predominate insectivore species in canal banks.

Gradual dispersion of an abundant flea species Ctenophyllus hirticrus specific to the Pallas's pika (the main plague carrier), is revealed in the Gorno-Altai natural plague focus on the territory, occupied by two populations of this lagomorph. Spreading of Yersinia pestis in these areas took place a short time later the rise of this ectoparasite's abundance. It is supposed that the colonization of these areas by C. hirticrus was one of the factors determined epizooties spreading within the focus and formation of new sites of stable Y. pestis preservation.

Palptarsus of the chicken mite bears 5 single-wall upper-pore (SW-UP) chemo-mechanoreceptor sensilla (type A); 4 double-wall upper-pore (DW-UP) chemosensitive sensilla (type B), and 6 no-pore (NP) mechanoreceptor sensilla (type M). The author assumes that sensilla of the type A participate in perception of the aggregation pheromone; of the type B, in perception of trophic stimuli; and of the type M, in determination of mechanical properties of the substrate.

Eleven mosquito species of the communis species group (genus Ochlerotatus, family Culicidae) were found in the Novgorod Province as a result of nine-year investigations (1996—2004). Ochlerotatus impiger, O. nigrinus, and O. sticticus are recorded in the Novgorod Province for the first time.

Histopathology in the sites of localization and parasiting of the mites Psorergates apodemi Fain et al., 1966 and P. dissimilis Fain et al., 1966 on the Ural field mouse Apodemus uralensis (Pallas) and the bank vole Clethrionomys glareolus (Schreber) is described. The mites affected all epidermis cell layers down to the cambium layer and caused hyperkeratosis.