crenatus Corbett 1966 (Gr, Ap, Sb), P. curvitatus Van der Linde 1938 (Gr, Ap, Pe, Bc), P. hamatus Thorne & Allen 1950 (Gr, Ap, Pe, Bc, Rb), P. microdorus Andrássy 1959 (Gr, Sb), P. nanus Cobb 1923 (Gr, Ap, Pe), P. tenuicaudatus Wu 1961 (Ap), P. veruculatus Wu 1962 (Ap); family Neotylenchidae: Deladenus durus (Cobb 1922) (Sb); family Psilenchidae: Psilenchus aestuarius Andrássy 1962 (Gr, Sb), P. aberrans Thorne 1949 (Ap), P. hilarulus de Man 1921 (Ap); family Telotylenchidae: Amplimerlinius macrurus (Goodey 1932) (Gr), Bitylenchus dubius (Bütschlii 1873) (Gr, Ap, Pe, Sb), B. parvus (Allen 1955) (Bc), Merlinius brevidens (Allen 1955) (Gr, Ap, Sb), Tylenchorhynchus cylindricus Cobb 1913 (Gr, Ap, Pe, Bc, Rb), T. elegans Siddiqi 1961 (Sb); family Hoplolaimidae: Helicotylenchus digonicus Perry 1959 (Gr), H. dihystera (Cobb 1893) (Gr, Ap, Pe, Gb, Sb), H. crenatus Das, 1960 (Gr, Pe, Bc, Rb), H. erythrinae (Zimmermann 1904) (Gr, Bc, Gb, Sb), H. multicinctus (Cobb 1893) (Gr, Ap, Pe, Bc, Rb, Gb, Sb), H. varicaudatus Yuen 1964 (Gr), H. vulgaris Yuen 1964 (Gr, Ap, Pe, Bc, Rb, Gb, Sb), Rotylenchus agnetis Szczygiel 1968 (Gr, Ap, Pe, Bc, Rb, Gb, Sb), R. incultus Sher 1965 (Gr, Ap, Pe, Bc), R. robustus (de Man 1876) (Gr); family Pratylenchidae: Pratylenchoides crenicauda Winslow 1958 (Gr, Pe, Sb), P. leiocauda Sher 1970 (Ap, Pe), Pratylenchus brachyuris (Godfrey 1929) (Gr, Ap), P. neglectus (Rensch 1924) (Gr, Gb, Sb), P. penetrans (Cobb 1917) (Gr, Ap, Pe, Bc, Rb), P. pratensis (de Man 1880) (Gr, Ap, Pe, Bc, Rb, Gb, Sb), P. subpenetrans Taylor & Jenkins 1957 (Gr, Sb); Pratylenchus sp.1 (Gb), Pratylenchus sp. 2 (Gb, Sb); family Ecphyadophoridae: Lelenchus leptosoma (de Man 1880) (Gr, Ap, Pe, Sb); family Anguinidae: Ditylenchus brevicauda (Micoletzky 1925) (Sb), D. dipsaci (Kühn 1857) (Gr, Ap, Pe, Bc, Rb, Gb, Sb), D. intermedius (de Man 1880) (Gr, Sb), D. minutus Husian et Khan, 1967 (Gr, Ap), D. triformis Hirschmann & Sasser 1955 (Gr, Pe), Nothotylenchus acris Thorne 1941 (Gr, Ap, Bc, Rb, Gb), N. acutus Khan 1965 (Gr, Ap); family Tylenchidae: Aglenchus agricola (de Man 1884) (Gr, Ap, Pe, Bc, Rb, Gb, Sb), Basiria aberrans (Thorne 1949) (Ap), Boleodorus impar Khan & Basir 1964 (Ap, Sb), B. thylactus Thorne 1941 (Ap, Pe, Bc, Rb, Gb, Sb), Coslenchus costatus (de Man 1921) (Gr, Ap, Rb), Filenchus liformis (Bütschli 1873) (Gr, Ap, Pe, Bc, Rb, Gb, Sb), F. misellus (Andrássy 1958) (Gr, Bc, Rb, Gb, Sb), F. orbus (Andrássy 1954) (Ap, Bc), F. sandneri (Wasilevska 1965) (Ap), F. thornei (Andrássy 1954) (Ap, Sb), Malenchus exiguus (Massey 1969) (Bc, Rb, Sb), M. fusiformis (Thorne & Malek 1968) (Sb), Tylenchus davainei Bastian 1865 (Gr, Ap, Pe, Bc, Rb, Gb, Sb), T. elegans de Man 1876 (Gr), T. minutus Cobb 1893 (Gr, Ap, Pe, Gb, Sb), T. striatus (Das, 1960) Meyl, 1960 (Pe, Bc, Rb). The trophic structure of plant parasitic nematode communities were studied for the different types of plantations according the feeding groups by Yeates et al. [9]. The ectoparasite species (28,6 – 48,6 % from total number of species) were predominated in all studied communities (Table 1). Abundance of nematodes including the free-living and plant parasitic nematodes at the soil pro les 0 – 20 cm were 503 – 2640 individs/100 g soil in the vineyards, 327 – 2461 individs/100g soil in the orchards of apple, 264 - 1144 individs/100 g soil in the orchards of peach, 570 – 1380 individs/100g soil in the plantations of strawberry, 787 – 1120 individs/100g soil in the plantations of black currant, 720 - 1140 individs/100g soil in the plantations of raspberry and 680 - 1200 individs/100g soil in the plantations 89
of goosberry [6]. The structure of plant parasitic nematode communities of perennial plants are formed for a long time and have a stable character. That is why in their communities the ectoparasites with the long-term life cycles such as Longidorus and Xiphinema prevailed. Some species of these genera are known as the virus-vectors: Longidorus macrosoma, Xiphinema diversicaudatum, X. index, X. italiae and X. rivesi. 90 Table 1. The trophic structure of plant parasitic communities from the different types of agricultural plantations in R.Moldova Trophic groups Grape Apple Peach migratory endoparasites semiendoparasites Black currant Raspberry Gooseberry Strawberry 7 / 12* 5 / 9,8 5 / 13,6 4 / 14,3 4 / 15,4 4 / 19,0 7 / 18,0 10 /17,2 5 / 9,8 6 / 16,2 5 / 17,8 4 / 15,4 5 / 23,8 5 / 12,8 ectoparasites 26 / 44,8 24 / 47 18 / 48,6 10 / 35,7 10/ 38,4 6 / 28,6 13 / 33,4 ectoparasites of epiderrmal cells feeders of algal, lichen 6 / 10,4 12 / 23,6 4 / 10,8 6 / 21,6 5 / 19,2 3 / 14,3 10 / 25,6 9 / 15,6 5 / 9,8 4 / 10,8 3 / 10,6 3 / 11,6 3 / 14,3 4 / 10,2 *- number of species/percent from total number of species The large populations of migratory endoparasites from genera Pratylenchus (especially P. pratensis and P. penetrans) and Ditylenchus (especially D. dipsaci) have been registered in the roots of some varieties of strawberry, gooseberry and raspberry. In one of the studied plantation of strawberry where it has been revealed numerous individs of species D. dipsaci most of plants grew badly, were dwarfed, colorless and some of them died. Conclusions In total 85 species of plant parasitic nematodes belonging to 29 genera, 13 families, 4 suborders and 3 orders: Tylenchida, Dorylaimida and Triplonchida were revealed in the studied vineyards, orchards and berry plantations. The largest number of species were noted from families Tylenchidae (16 species) and Longidoridae (13). In the studied agricultural plantations such as grapes there have been revealed 58 species of plant parasitic nematodes, apple (51), peach (37), black currant (28), raspberry (26), gooseberry (21) and strawberry (39). The ectoparasite species (28,6 – 48,6 % from total number of species) were predominated in all studied plantations especially species from genera Xiphinema, including virus-vector species, also Mesocriconema and Paratylenchus. The large populations of Ditylenchus dipsaci caused the destruction of a plantation of strawberry. Bibliography 1. Boag B., Brown, D.J.F. and A.S.G. Banck. Optimizing sampling strategies for nematode-transmitted viruses and their vectors. //OEPP/EPPO Bull., <strong>198</strong>9, 19: 491-499. 2. Coomans, Huys, Heyns and Luc. Character analysis, phylogeny and biogeography of the genus
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198 CUPRINS Articole de fond Ф.И
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200 CONTENTS Basic articles T.Furdu
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4 ARTICOLE DE FOND СОВРЕМЕН
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биофизических, био
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В США и Великобрита
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социальные нормы р
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организма». Cannon W.B.
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разных лет. Кн. 1. - Т
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Регуляция количест
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переходят в VI-III, а ч
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оболочка (собствен
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лет у леща Верхне-В
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промысловых ценных
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строгого мониторин
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физические нагрузк
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санокреатология. К
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Materiale şi metode Caracteristica
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(după 31 zile) la hibridul Xenia,
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Tabelul 2. Variaţia numărului de
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of sun ower to the infection by Oro
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e cient raport lichid cultural : so
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142 Figura 3. Dependenţa randament
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144 Activitatea pectolitică a prep
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ECOLOGIA ŞI GEOGRAFIA ИСПОЛЬ
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водопользования и
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Табл. 2. Перечень пе
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Созданная пилотная
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of management tasks // Proceedings
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hidrogenului sulfurat. De asemenea,
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Fig. 1. Evoluţia cantităţii luna
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Concluzii: 1. Precipitaţiile căzu
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5,9) intermediar, se sedimentează
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9,4%. Variaţia coe cientului de do
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de acumulare a MG în plante la pol
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166 ANIVERSĂRI SAVANT ŞI CHIRURG
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altor indici hemodinamici la bolnav
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a veni în ajutorul celor mai nevoi
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altor componente ale mediului ambia
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174 PERSONALITĂŢI NOTORII A TRIBU
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176 ПРОФECCOP П. И. НЕСТ
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почвенные, энтомоп
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alte obiecte acvatice. În loc de
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1.3 şi 1.4 - „Râurile din bazin
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182 CRONICĂ ŞTIINŢIFICĂ FIZIOLO
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184 ABSTRACTS UDC 612.821 + 616.89
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UDC: 635.64:575. EVALUATION OF THE
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Moldovei. Ştiinţele Vieţii. 2008
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precipitations, which are trained f
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низких температура
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УДК:575.852 ПЕРЕЛЕТНЫЕ
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Aspergillus avus, Aspergillus alli