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12th International Conference on Harmful Algae

12th International Conference on Harmful Algae

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INTERNATIONAL SOCIETY FOR THE STUDY OF HARMFUL ALGAE12 th <str<strong>on</strong>g>Internati<strong>on</strong>al</str<strong>on</strong>g> <str<strong>on</strong>g>C<strong>on</strong>ference</str<strong>on</strong>g> <strong>on</strong> <strong>Harmful</strong> <strong>Algae</strong>, Copenhagen, Denmark, 4-8 September 2006to model, and further the number ofsampling stati<strong>on</strong>s. Our results showthat ANN models, with a lownumber of input variables, are ableto reproduce trends in D. acuminatapopulati<strong>on</strong> dynamics.O.05-03Temporal changes inmicrocystin-producing and n<strong>on</strong>microcystin-producingMicrocystis populati<strong>on</strong>s of aJapanese LakeSessi<strong>on</strong>: O.05 - Populati<strong>on</strong> dynamics 1Presentati<strong>on</strong> time: 09:50 - 10:10Mitsuhiro YoshidaFukui Prefectural University, OBAMA,JapanTemporal changes in hepatotoxinmicrocystin-producing and n<strong>on</strong>microcystin-producingMicrocystisaeruginosa populati<strong>on</strong>s wereexamined in Lake Mikata, Japan. Tom<strong>on</strong>itor densities of the total M.aeruginosa populati<strong>on</strong> andpotentially microcystin-producingcells, we used quantitative real-timePCR assays targeting thephycocyanin intergenic spacer (PC-IGS) and the microcystin synthetasegene (mcyA), respectively. Duringthe sampling period, the ratios ofcell numbers of mcyA genotypes tothe total M. aeruginosa variedc<strong>on</strong>siderably with the range from0.005 to 0.35. When surface nitratec<strong>on</strong>centrati<strong>on</strong>s increaseddramatically, there was an apparentrise in cell number ratios of mcyAgenotypes. As an alternativeapproach, the 16S-23S rDNAinternal transcribed spacer (16S-23S ITS) genotyping was employedfor the identificati<strong>on</strong> of potentiallymicrocystin-producing and n<strong>on</strong>microcystin-producinggenotypes innatural communities. Thephylogenetically closely related butdistinct microcystin genotypes werefound between different sampleswhen ratios of cell numbers of mcygenotypes were relatively high.Thus, our data suggest that multipleecotypes, which are adapted toecological parameters, mightcoexist within the M. aeruginosacommunity.O.05-04Vertical migrati<strong>on</strong>: an keystrategy for the ecologicalsuccess of the toxicdinoflagellate Gymnodiniumcatenatum in south eastTasmania, AustraliaSessi<strong>on</strong>: O.05 - Populati<strong>on</strong> dynamics 1Presentati<strong>on</strong> time: 10:10 - 10:30SIE Blackburn 1 , K Wild-Allen 1 , MADoblin 2 , PA Armstr<strong>on</strong>g 3 , CJ Bolch 4 , PAThomps<strong>on</strong> 1 , GM Hallegraeff 41 CSIRO, HOBART, Australia2 University of Technology, SYDNEY,Australia3 University of Tasmania, Aquafin CRC,LAUNCESTON, Australia4 University of Tasmania, LAUNCESTON,AustraliaThe toxic dinoflagellateGymnodinium catenatum hasformed recurrent blooms in theHu<strong>on</strong> Estuary, south east Tasmaniasince the mid 1980s. The estuary ischaracterised by humic-ladensurface river flow and micro-tidalsalt wedge estuarine circulati<strong>on</strong>. Adistinctive feature of the blooms isdiurnal vertical migrati<strong>on</strong> (DVM), upto 20 metres of the water column.Laboratory studies using verticallystratified columns dem<strong>on</strong>strate thatDVM facilitates nutrient retrieval atdepth. In additi<strong>on</strong>, G. catenatumgrows equally well <strong>on</strong> nitrate,amm<strong>on</strong>ium or urea and, in the field,G. catenatum utilises whichever ofthese nitrogen sources are availableduring DVM. This indicates an38

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