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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 20061 Nati<strong>on</strong>al Ocean Service, NOAA, SILVERSPRING, MD, United States of America2 NOAA/GLERL, MUSKEGON, MI, UnitedStates of America3 NOAA/NCCOS, BEAUFORT, NC, UnitedStates of AmericaThe toxic cyanobacterium,Microcystis aeruginosa, hasbecome a dominant comp<strong>on</strong>ent ofthe summer phytoplankt<strong>on</strong>populati<strong>on</strong> in Saginaw Bay andwestern Lake Erie, USA. Expansiveblooms of Microcystis have causedc<strong>on</strong>siderable c<strong>on</strong>cern to the GreatLakes regi<strong>on</strong> due to the use ofthese waters for recreati<strong>on</strong>. Thetoxin, microcystin, has beenobserved in both regi<strong>on</strong>s above therecommended limit of 1 µg L -1 andposes a threat to human health.Microcystis blooms have uniquescattering and absorpti<strong>on</strong>properties, due to the producti<strong>on</strong> ofsurface scum and the dominantaccessory pigment, phycocyanin.In an effort to better detect andm<strong>on</strong>itor these blooms, satellitederived products from SeaWiFSand MODIS which highlight theseoptical properties will be comparedwith in situ measurements ofMicrocystis and its toxin, from 2004and 2005. Phycocyanin has anabsorpti<strong>on</strong> peak centered at 620nm. Therefore, changes in theabsorpti<strong>on</strong> spectra centered at thiswavelength will be investigatedusing spectral curvature methods.In additi<strong>on</strong>, the use of a particulatebackscatter ratio method will betested for its ability to detect theseblooms. The ability to detectsurface scum using the MODISnear-infrared band (865 nm) may becompromised by shallow waterdepth but looks promising in deeperwater.PO.09-10Fatty acid esters of pectenotoxinseco acids in Norwegian andIrish musselsSessi<strong>on</strong>: PO.09 - Toxin synthesis andchemical structure of toxinsT. Torgersen 1 , AL Wilkins 2 , NRehman 3 , T Rundberget 1 , D Petersen 4 ,P Hess 3 , F Rise 4 , CO Miles 11 Nati<strong>on</strong>al Veterinary Institute, OSLO,Norway2 The University of Waikato, HAMILTON,New Zealand3 Marine Institute, GALWAY, Ireland4 University of Oslo, OSLO, NorwayPectenotoxin-2 (PTX-2) from marinedinoflagellates of the genusDinophysis is rapidly hydrolyzed inmany shellfish to pectenotoxin-2seco acid (PTX-2 SA), whichisomerises to 7- 7-epi-PTX-2 SA.Pectenotoxin-12 (PTX-12) from thesame dinoflagellates is alsobelieved to be hydrolyzed inshellfish to PTX-12 SAs, which arein equilibrium with isomerspresumed to be 7-epi-PTX-12 SAs.Three series of fatty acid esters ofPTX-2 SA and 7-epi-PTX-2 SAwere detected by LC-MS analysis ofan extract from Irish blue mussels(Mytilus edulis). Fatty acids werec<strong>on</strong>jugated <strong>on</strong> C-11, C-33 and C-37of the PTX-skelet<strong>on</strong>. In methanolicextracts from two samples of bluemussels from Norway, three seriesof fatty acid esters of PTX-2 SA,with <strong>on</strong>ly minor accompanyingamounts of the 7-epi-analogues,and a series of fatty acid esters ofPTX-12 SAs and its presumed 7-epi-analogues, were detected.The locati<strong>on</strong> of the fatty acid esterlinkages were identified by LC-MSnin positive- and negative-i<strong>on</strong>izati<strong>on</strong>modes, LC-MS analysis of theproducts of the reacti<strong>on</strong> with sodiumperiodate, and NMR analysis ofpurified samples of the mostabundant derivatives. For PTX-2293

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