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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 2006mussel samples (Mytiluscalifornianus) for 16 m<strong>on</strong>ths at theSanta Cruz Wharf in M<strong>on</strong>terey Bay,we measured Dinophysisabundance in our lab and sentmussels to the regulatory FoodInspecti<strong>on</strong> Agency in Canada fortoxin analyses. Results indicatedthat Dinophysis average abundancewas higher (2,000 cells per Liter) insummer than in other m<strong>on</strong>ths (90cells per Liter) and DSP toxins inmussels were higher in summer(OA+DTX-1= 0.11 µg per gram)than in other m<strong>on</strong>ths (OA+DTX-1=0.04 µg per gram), though at least<strong>on</strong>e of the DSP toxins wasdetectable nearly year round. Asignificant correlati<strong>on</strong> betweenDinophysis fortii cell biomass, thedominant biomass c<strong>on</strong>tributor, andOA c<strong>on</strong>centrati<strong>on</strong>s in musselssuggests this species is the OAsource, whereas the correlati<strong>on</strong>coefficient became weaker whenthe biomass of other Dinophysisspecies was included. Thus DSPtoxins, not previously m<strong>on</strong>itored <strong>on</strong>the US west coast, mayoccasi<strong>on</strong>ally represent a potentialhealth threat to human c<strong>on</strong>sumersof mussels, and possibly other filterfeeding organisms.PO.05-13Preparati<strong>on</strong> and simultaneousLC-MS analysis of fourteenshellfish toxinsSessi<strong>on</strong>: PO.05 - Toxin analysisM Suzuki, R Sekiguchi, M Watai, TYasumotoJapan Food Research Laboratories, TAMA,JapanFor use as calibrants in LC-MSanalysis, we prepared fourteenshellfish toxin standards: okadaicacid (OA), dinophysistoxin-1(DTX1), pectenotoxin (PTX) -1, -2, -3, -6, azaspiracid (AZA) -1, -2, -3,yessotoxin (YTX), 45-OHYTX,brevetoxin-B2 (BTXB2), 7-OpalmitoylOAand 7-OpalmitoylDTX1.The former eleventoxins were purified fromc<strong>on</strong>taminated shellfish, except forYTX which was obtained fromcultures of Protoceratiumreticulatum. 7-O-PalmitoylOA and 7-O-palmitoylDTX1 were chemicallyprepared from OA and DTX1,respectively. The purity of thestandard toxins was checked by 1H-NMR, LC-DAD, and LC-MS. Alltoxins were quantifiable in 30 min ina single run by m<strong>on</strong>itoring negativei<strong>on</strong>s, except for AZAs that weredetected <strong>on</strong> positive i<strong>on</strong>s. Weproved the practicality of the methodby carrying out recovery tests using90% methanol extracts preparedfrom scallop and musselhepatopancreas spiked with thestandard toxins or extracts fromnaturally c<strong>on</strong>taminated shellfish.PO.13-30Species dominance andpermanence of Gymnodiniumcatenatum Graham blooms <strong>on</strong>the estern Mediterranean coast ofMorocco (1994-2004)Sessi<strong>on</strong>: PO.13 - Regi<strong>on</strong>al eventsLTJ Tahri JouteiInstitut Nati<strong>on</strong>al de Recherche Halieutiq,CASABLANCA, MoroccoThe chain-forming dinoflagellateGymnodinium catenatum is themain species associated withparalytic shellfish pois<strong>on</strong>ing (PSP)outbreaks in Moroccan coastalwaters, since 1994. The seas<strong>on</strong>aldistributi<strong>on</strong> of G. catenatum in theMediterranean coast of Morocco(35°05’N) during the period 1994-2004 is described. Gymnodiniumcatenatum is present throughout the287

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