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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 2006triangular in A. peruvianum andrectangular with a left extensi<strong>on</strong> inA. ostenfeldii, the presence of thesepeculiar toxins in both species couldbe an indicati<strong>on</strong> of a possiblesyn<strong>on</strong>ymy.PO.15-29Development of real-time PCRassays for the detecti<strong>on</strong> ofCylindrospermopsis raciborskiiSessi<strong>on</strong>: PO.15 - M<strong>on</strong>itoringM S Fuentes, J J Rick, J L Noel, J ABaezaUniversity of Louisiana at Lafayette,LAFAYETTE, United States of AmericaBlooms caused by toxic blue-greenalgae have repeatedly producedepisodes of wild and domesticanimal illness and death. Since2002 the toxin producingCylindrospermopsis raciborskii isfrequently abundant from summerto fall in the Caernarv<strong>on</strong>/Bret<strong>on</strong>Sound Estuary in Louisiana, posinga potential risk of a bloom of thisspecies in that area. Recently(10/04) the species was detected inabundant biomasses in the wholeAtchafalaya Basin. M<strong>on</strong>itoring theseareas for the presence ofCylindrospermopsis is essential inassessing the potential for bloomformati<strong>on</strong>. However, detecti<strong>on</strong> andquantificati<strong>on</strong> of Cylindrospermopsisis sometimes problematic,especially if individual chains lackthe characteristic terminalheterocyst.To circumvent this problem wedeveloped a real-time PCR assayfor rapid detecti<strong>on</strong> of the species. Inthis assay, detecti<strong>on</strong> of amplifiedtarget DNA requires annealing offluorescent-labelled probes,resulting in added level of specificitycompared with assays based <strong>on</strong>traditi<strong>on</strong>al PCR methodology. Thissensitive technique detects evenlow densities of this speciesinstantly, allowing the creati<strong>on</strong> ofreal-time species abundancedistributi<strong>on</strong> maps, enablingmanagers to resp<strong>on</strong>d immediatelyto increases in biomass of thisharmful species and for timelynotificati<strong>on</strong> of possible health risksto the publicPO.13-57Summer Alexandrium catenellabloom and the impact <strong>on</strong> fishfarming, in the XI regi<strong>on</strong>, ChileSessi<strong>on</strong>: PO.13 - Regi<strong>on</strong>al eventsClaudio G Fuentes Grünewald, AAAguilera Belm<strong>on</strong>te, A Clément DíazPlanct<strong>on</strong> Andino LTDA., CASTRO, ChileDuring the summer of 2005 and2006 a bloom of Alexandriumcatenella was observed in thenorthern inland sea of the XI regi<strong>on</strong>.This species is well known as aPSP producer. Unusual behaviourof caged salm<strong>on</strong> and high A.catenella abundance, more than356 cells/mL in surface waters atthe fish farm, indicated damage tothe fish gill and caused a serioussalm<strong>on</strong> kill at the site.The cells were distributed mainly inthe upper surface layer, numbersdiminishing with depth. At <strong>on</strong>e sitelocated in the GuaitecasArchipelago (ca. 44º lat. South) themaximum c<strong>on</strong>centrati<strong>on</strong> was 961cells/mL, representing 86 % of thetotal phytoplankt<strong>on</strong> community. Thebloom began in December 2005,and the maximum abundance of A.catenella was observed during the2nd and 3rd week of January. At allsites with positive presence of thedinoflagellate the sea temperaturewas higher than 12.0 ºC.175

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