Hidrológiai Közlöny, 2014 (94. évfolyam)

2014 / 5-6. különszám - LV. Hidrobiológus Napok előadásai

34 HIDROLÓGIAI KÖZLÖNY 2014. 94. ÉVF. 5-6. SZ. Bhagavathy, S. and Sumathi, P. 2012. Purification and characterization of carote­noids from green algae Chlorococcum humicola by HPLC-NMR and LC- MS-APCI. Biomedicine and Preventive Nutrition, 2 (4): 276-282. Banker R., Carmeli S., Hadas O., Teltsch B., Porát R., Sukenik A., 1997. Identifi­cation of cylindrospermopsin in Aphanizomenon ovalisporum (Cyanophyce- ae) isolated from Lake Kinneret, Israel. J. Phycol. 33: 613-616. Bar-Yosef Y., Sukenik A., Hadas O., Viner-Mozzini Y., Kaplan A., 2010. Ensla­vements the water body by toxic Aphanizomenon ovalisporum, inducing al- kalinephosphatase in phytoplanktons. Curr. Biol. 20: 1-5. B-Béres V., Grigorszky I., Vasas G., Borics G., Várbíró G., Nagy S.A., Borbély G., Bácsi I., 2012. The effects of Microcystis aeruginosa (cyanobacterium) on Cryptomonas ovata (Cryptophyta) in laboratory cultures: why these orga­nisms do not coexist in steady-state assemblages? Hydrobiologia 691: 97- 107. Bernard C., Harvey M., Briand J.F., Bire R., Krys S., Fontaine J.J., 2003. Toxico­logical comparison of diverse Cylindrospermopsis raciborskii strains, eviden­ce of liver damage caused by a French C. raciborskii strain. Environ. Toxicol. 18: 176-186. Cloem, J.E., 1976. Recent limnological changes in southern Kootenay Lake, Bri­tish Columbia. Canadian Journal of Zoology 54: 1571-1578. Cloem, J.E., 1978. Simulation model of Cryptomonas ovata population dynamics in southern Kootenay Lake, British Columbia. Ecological Modelling 4: 133- 149. Fastner J., Heinze R., Humpage A.R., Mischke U., Eaglesham G.K., Chorus I., 2003. Cylindrospermopsin occurrence in two German lakes and preliminary assessment of toxicity and toxin production of Cylindrospermopsis racibor­skii (Cyanobacteria) isolates. Toxicon 42: 313-321. Felfoldy L., 1987. A biológiai vízminősítés. 4. kiad. In: Vízügyi Hidrobiológia 16.-VGI, Budapest, 258.7 Froscio S.M., Humpage A.R., Burcham P.C., Falconer I.R., 2003. Cylindrosper- mopsin-induced protein synthesis inhibition and its dissociation from acute toxicity in mouse hepatocytes. Environ. Toxicol. 18: 243-251. Gantar M., Berry J.P., Thomas S., Wang M., Perez R., Rein K.S., 2007. Allelopa- thic activity among Cyanobacteria and microalgae isolated from Florida fre­shwater habitats. FEMS Microbiol. Ecol. 64: 55-64. Hammer O., Harper D.A.T., Ryan P.D., 2001. PAST: paleontological statistics software package for education and data analysis. Palaeontologia Electronica, 4(1): Unpaginated. Harwati T.U., Willke T., Vorlop K.D. 2012. Characterization of the lipid accu­mulation in a tropical freshwater microalgae Chlorococcum sp. Bioresour. Technoi. 121:54-60. Hedger R.D., Olsen N.R.B., George D.B., Malthus T.J., Atkinson P.M., 2004. Modelling spatial distribution of Ceratium hirundnella and Microcystis spp. in a small productive British lake. Hydrobiologia 528: 217-227. Humpage A.R., Fenech M., Thomas P., Falconer I.R., 2000. Micronucleus induc­tion and chromosome loss in transformed human white cells indicate clasto- genic and aneugenic action of the cyanobacterial toxin, cylindrospermopsin. Mutat. Res. 472: 155-161 Keating, K.I., 1978. Blue-green algal inhibition of diatom growth: transition from mesotrophic to eutrophic community structure. Science 199: 971-973. Klochkova T.A., Kang S-H, Cho G.Y., Pueschel C.M., West J.A., Kim G.H. 2006. Biology of a terrestrial green alga, Chlorococcum sp. hlorococcales, Chlorophyta), collected from the Miruksazi stupa in Korea. Phycologia 45 (3): 349-358. Kroes H.W. 1971. Growth interactions between Chlamydomonas globosa Snow and Chlorococcum ellipsoideum Deason and Bold under different experimen­tal conditions, with special attention to the role of pI-L Limnol. Oceanogr. 16: 869-879. Kroes, H.W. 1972. Extracellular Products from Chlorococcum ellipsoidoum and Chlamydomonas globosa. Archive Mikrobiologie, 84: 270-274. Mohamed Z.A., 2007. First report of toxic Cylindrospermopsis raciborskii and Raphidiopsis mediterranea (Cyanoprokaryota) in Egyptian fresh waters. FE­MS Microbiol. Ecol. 59: 749-761. Ohta S., Chang T., Ikegami N., Kondo M., Miyata H. 1993. Antibiotic Substance Produced by a Newly Isolated Marine Microalga, Chlorococcum HS-101. Bull Environ Contam Toxicol 50: 171-178. Pearson L., Mihali T., Moffitt M., Keilmann R., Neilan B., 2010. On the chemist­ry,toxicology and genetics of the cyanobacterial toxins, microcystin, nodula- rin, saxitoxin and cylindrospermopsin. Mar. Drugs 8 (5): 1650-1680. Pinheiro C., Azevedo J., Campos A., Loureiro S., Vasconcelos V., 2013. Absence of negative allelopathic effects of cylindrospermopsin and microcystin-LR on selected marine and freshwater phytoplankton species. Hydrobiologia, 705 (1): 27-42. Rücker J., Stuken A., Nixdorf B., Fastner J., Chorus I., Wiedner C., 2008. Con­centrations of particulate and dissolved cylindrospermopsin in 21 Aphanizo- menon-dominated temperate lakes. Toxicon 50: 800-809. Saker M.L., Nogueira I.C.G., Vasconcelos V.M., Neilan B.A., Eaglesham G.H., Pereira P., 2003. First report and toxicological assessment of the cyanobacte­rium Cylindrospermopsis raciborskii from Portuguese freshwaters. Ecotoxi- col. Environ. Saf. 55: 243-250. Shaw G.R., Sukenik A., Livne A., Chiswell R.K., Smith M.J., Seawright A.A., Norris R.L., Eaglesham G.K., Moore, M.R. (1999). Blooms of the hepatotox- ic cyanobacterium, Aphanizomenon ovalisporum (Forti) in newly constructed lakes, Queensland, Australia. Environ. Toxicol. 14: 167-177. Shen, X., Lam, P.K.S., Shaw, G.R., Wickramasinghe, W., 2002. Genotoxicity in­vestigation of a cyanobacterial toxin, cylindrospermopsin. Toxicon 40, 1499- 1501. Suikkanen S., Fistarol G.O., Granéli E., 2004. Allelopathic effects of the Baltic cyanobacteria Nodularia spumigena, Aphanizomenon jlos-aquae and Anaba- ena lemmermannii on algal monocultures. J. Exp. Mar. Biol. Ecol. 308: 85- 101. Sukenik A., Eshkol R., Livne A., Hadas O., Rom M., Tchemo, D., Vardi A., Ka­plan A., 2002. Inhibition of growth and photosynthesis of the dinoflagellate Peridinium gatunense by Microcystis sp. (cyanobacteria): a novel allelopath­ic mechanism. Limnol. Oceanogr. 47 (6): 1656-1663. Vasas G., Gáspár A., Surányi G., Batta Gy., Gyémánt Gy., Hamvas M., Máthé C., Grigorszky I., Molnár E., Borbély Gy., 2002. Capillary electrophoretic as­say and purification of cylindrospermopsin, a cyanobacterial toxin from Aph­anizomenon ovalisporum, by plant test (Blue-Green Sinapis Test) Anal. Bio- chem. 302: 95 - 103. Volk R.B., 2005. Screening of microalgal culture media for the presence of algic- idal compounds and isolation and identification of two bioactive metabolites, excreted by the Cyanobacteria Nostoc insulare and Nodularia harveyana. J. Appl. Phycol. 17: 339-347. Zar J. H., 1996. Biostatistical Analysis, 3rd ed. Prentice-Hall International, NJ, USA. Zhang D.H., Lee Y.K., Ng M.L. and Phang S.M. 1997. Composition and accu­mulation of secondary carotenoids in Chlorococcum sp. Jumal of Applied Phycology, 9 (2): 147-155. Investigation of the possible role of cylindrospermopsin in cyanobacterium - eukaryotic alga interaction Dobronoki, D., B-Béres, V, Vasas,. Rektor, A., Nagy, S.A., Bácsi, I. Abstract: Relations between phytoplankton and phytobentos taxa could be significant in lakes and ponds with extended litoral region. Phytoplank­ton could affect the individual number and species composition of benthic assemblages in many ways. In this work the interactions bet­ween the planktic, cylindrospermopsin producer Aphanizomenon ovalisporum (Cyanobacteria) and a benthic Chlorococcum species (Chlorophyta) were investigated in mixed cultures. The effect of A. ovalisporum crude extract on Chlorococcum cultures were also stu­died. Cell numbers of both species were lower in mixed cultures compared to control cultures. Cell number of Chlorococcum decreased by 77 % in the presence of 4-fold amount of Aphanizomenon, nevertheless extracellular cylindrospermopsin was not detectable. Crude extract of A. ovalisporum caused growth inhibition of Chlorococcum already to the 7th day of the experiment, but in lower extent (max. 50 %), than in mixed cultures. Nutrient levels changed in a cell number dependent manner in mixed cultures, while it seems that the cya­nobacterial extract has no significant effect to the nutrient uptake of the eukaryotic green alga. Keywords '.Aphanizomenon ovalisporum, Chlorococcum sp., interaction.

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