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Species Diversity of Carp, Cyprinus Carpio (Cypriniformes, Cyprinidae), Parasites in Some Cultivation Regions

Zoogeographical comparison for species diversity of carp parasites in different cultivation regions including aquatic ecosystems of Ukraine, Uzbekistan, Russia, and Vietnam was carried out. Totally, 160 parasitic species were recorded in carp within these regions. Parasitic species with direct and complex life cycles important in epizootic, veterinary, and health areas were registered.


The aim of this study was to describe the proportion of floristic geoelements and plant biodiversity in the macroregions of Transdanubia. The core data source used for the analysis was the database of the Hungarian Flora Mapping Programme. The analysed data were summarized in tables and distribution maps. The percentage of continental elements was higher in dry areas, whereas the proportion of circumboreal elements was higher in humid and rainy parts of Transdanubia. According to the climatic zones, the highest value of continental geoelement group occurred in the forest-steppe zone. The plant species diversity and geoelements were analysed also on a lower scale, with Transdanubia specified into five macroregions. The highest diversity values were found in the Transdanubian Mountain and West-Transdanubian regions because of the climatic, topographic, and habitat diversity.


Wild bees (Apiformes) were studied in 4 crop fields and 8 refuge habitats for 2 - 5 years in agricultural landscapes in the Pleven and Plovdiv regions of Bulgaria. In total, 233 bee species were recorded. Bee forage plants visited by the honey bee and wild Apiformes are listed for each refuge habitat. Species composition is given for individual habitats, including fields of alfalfa (Medicago sativa), oilseed rape (Brassica napus), sunflower (Helianthus annuus), and radish (Raphanus sativus). Species richness and dominance structure of bee communities in the 2 regions are compared, and species responsible for significant differences are identified.

livestock grazing and human uses on herbaceous species diversity in oriental beech (Fagus orientalis Lipsky) forests, Guilan, Masal, northern Iran. Journal of Forestry Research , 25 (2): 455−462. E shaghi R ad , J., V aladi , G., Z argaran , M.R., 2017. Effects of man-made disturbances on understory plant richness of oak forests in Iran. Folia Oecologica , 44: 61–68. E temad , S., Z obeiry , M., N amiranian , M., G hahramany , L., 2014. Determine the most appropriate surface sampling method for estimating spiral tree diversity in the forests of northern Zagros. In

–529. Cousins, S. A. O., Kaligarič, M., Bakan, B., Lindborg, R., 2014: Political systems affect mobile and sessile species diversity – a legacy from the post-WWII period. Plos One 9/8, e103367. Dahlstrom, A., Cousins, S. A. O., Eriksson, O., 2006: The history (1620–2003) of land use, people and livestock, and the relationship to present plant species diversity in a rural landscape in Sweden. Environment and History 12, 191–212. Denslow, J. S., 1980: Patterns of plant species diversity during succession under different disturbance regimes. Oecologia 46, 18–21. Devillers, P

–316. Braun-Blanquet, J. 1964: Pflanzensoziologie, Grundzüge der Vegetationskunde, 3rd edn. Springer-Verlag, Wien, 865 pp. Burton, M. L., Samuelson, L. J. & Pan, S. 2005: Riparian woody plant diversity and forest structure along an urban-rural gradient. Urban Ecosystems 8: 93–106. Case, T. J. 1990: Invasion resistance arises in strongly interacting species-rich model competition communities. Proceedings of the National Academy of Sciences of USA 87(24): 9610–9614. Chen, X., Wang, W., Liang, H., Liu, X. & Da, L. 2014: Dynamics of ruderal species diversity under the rapid


The paper presents the results of an investigation of physical-chemical features of water as well as rotifer and crustacean abundance and diversity measures, relating to the taxonomic richness and species diversity index, in three lobelia lakes differing in trophic status and morphometric features. The main purpose of this study was to establish the diversity of zooplankton communities in the open water area of lobelia lakes, including extracting species common for each lake and also to find environmental predictors which are responsible for the development of zooplankton communities. Despite the fact that the three studied lakes are of the same origin, located in the same vicinity and have generally similar environmental factors, zooplankton community structure revealed a great variation in reference to species diversity (only ca. 20% of the species were common for all lakes) and particularly in inhabiting species. Obrowo Lake had the most diverse assemblages of both rotifers and crustaceans compared to Modre and Pomysko lakes. In the taxonomic structure species that are rare for the Polish fauna, such as e.g. Holopedium gibberum and Heterocope appendiculata, occurred. Even though the examined lobelia lakes are ecosystems that undergo varying human-induced impacts, they still remain taxonomically very variable aquatic ecosystems, containing rare species of very high ecological status. The observed symptoms of deterioration of water quality, reflected in the zooplankton biocoenotic features, showed that the best conditions were attributed to Obrowo Lake in comparison with the two remaining lakes – Modre and Pomysko. Total nitrogen and chlorophyll a concentration were decisive for the distribution of zooplankton species in Pomysko and Obrowo lakes, while in case of Modre lake water reactivity and conductivity were of higher impact.

Gleboznawczego Oddział w Rzeszowie , 11: 96-101. Kędziora A., Karg J. 2010. Zagrożenia i ochrona różnorodności biologicznej. Nauka , 4: 107-114. Kempton R. A., Taylor L. R. 1976. Models and statistics for species diversity. Nature , 262: 818-820. Kim K. C., Byrne L. B. 2006. Biodiversity loss and the taxonomic bottleneck: emerging biodiversity science. Ecological Research , 21: 794-810. Klenner W., Arsenault A., Brockerhoff E. G., Vyse A. 2009. Biodiversity in forest ecosystems and landscapes: A conference to discuss future directions in biodiversity management for


Mites, and among them especially the Oribatida, are very abundant in bogs, being good bioindicators of various changes, but little is known about their reaction to heavy industrial exploitation of bogs. This study aimed to compare the acarofauna of the edges of small pools located in 2 bogs of Orawa-Nowy-Targ Basin (Kotlina Orawsko-Nowotarska), namely Łysa Puścizna (LP) and Bór Podczerwony (BP), degraded to different degrees by peat exploitation. The area of bog LP has decreased since the end of the 19th century by 34%, while that of BP has decreased during this time drastically (by 68%). Water in both studied pools differed from that in natural bogs, reported in the literature, especially in pH, colour, and oxygen conditions (COD and BOD5), and these differences were more pronounced at BP. The abundance of mites was similar to that observed in natural bogs, and the Oribatida dominated among mites, constituting over 99% of them. The species diversity of Oribatida was low in both pools, but especially in pool BP. In both bogs the aquatic species were the most abundant due to the wet study season. The species structure of Oribatida differed, however, from that reported from natural bogs as well as from each other. At the less degraded bog LP the most abundant was Hydrozetes lacustris (D = 69%), while at bog BP, with worse water parameters, Trimalaconothrus maior highly dominated (D = 93%). This suggests that the latter species is very tolerant to water parameters, being a successful coloniser of degraded bogs.

infection of Fraxinus angustifolia by Hymenoscyphus fraxineus in Slovakia. Baltic Forestry, 23:52–55. Keesing, F., Holt, R. D., Ostfeld, R. S., 2006: Effects of species diversity on disease risk. Ecology Letters, 9:485–498. Kiffer, E., Morelet, M., 2000: The Deuteromycetes – mitosporic fungi: classification and generic keys. Enfield, Science Publishers, 273 p. Kirisits, T., Schwanda, K., 2015: First definite report of natural infection of Fraxinus ornus by Hymenoscyphus fraxineus . Forest Pathology, 45:430–432. Kowalski, T., Czekaj, A., 2010: Symptomy chorobowe i