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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 2006results imply that the filamentouschains might play the role of oocyteand the single cells may bespermatocytes. In spite of identicalculture c<strong>on</strong>diti<strong>on</strong>s of T. cf stellarisand T. stellaris, sexual reproducti<strong>on</strong>was observed <strong>on</strong>ly in T. cf stellaris.PO.10-41Examinati<strong>on</strong> of the cell cycle,growth rate, and meiosis ofKarlodinium spp. by flowcytometrySessi<strong>on</strong>: PO.10 - Ecophysiology &AutecologyMW Parrow 1 , JM Burkholder 2 , EGarcés 31 University of North Carolina Charlotte,CHARLOTTE, United States of America2 Center for Applied Aquatic Ecology,RALEIGH, United States of America3 IRTA, Inst. de Recerca i Tecnol. Agroal.,SANT CARLES DE LA RÀPITA, SpainThe DNA c<strong>on</strong>tent, DNA synthesiscycles, and growth rates of differentstrains of Karlodinium veneficumand K. armiger were studied inculture by flow cytometry. A 3-folddifference in DNA c<strong>on</strong>tent wasfound between K. veneficum and K.armiger, indicating a significantdifference in genome size. K.veneficum strains had a dielperiodicity of DNA synthesis (S) andcell divisi<strong>on</strong> (G2M) that was phasedwith the photocycle. Cells with 1CDNA (G1) began DNA synthesis (S)during the latter half of the lightperiod, then entered G2M anddivided during the dark period.Variati<strong>on</strong> am<strong>on</strong>g K. veneficumstrains was found in the durati<strong>on</strong> ofthe S phase (3.2-8.4 h) and G2Mphase (2.0-12.7 h). Potential growthrates derived from cell cycle dataranged from 0.55 to 1.03 divisi<strong>on</strong>sday -1 , and were higher than netgrowth rates calculated from cellnumbers. In most strains, a distinctsubpopulati<strong>on</strong> of cells with a singlenucleus c<strong>on</strong>taining 4C DNA alsooccurred during the dark period.Based <strong>on</strong> observati<strong>on</strong>s of thesexual life cycle of K. veneficum, itis proposed that these 4C DNA cellswere zygotes undergoing meiosis.This potentially co-occurring meioticcycle could impact determinati<strong>on</strong>sof the mitotic cell cycle ofKarlodinium.PO.08-20Impacts of the toxicdinoflagellate Alexandriumm<strong>on</strong>ilatum <strong>on</strong> three ecologicallyimportant shellfish speciesSessi<strong>on</strong>: PO.08 - ToxicologySE Pate 1 , JM Burkholder 1 , SEShumway 21 North Carolina State University, RALEIGH,United States of America2 University of C<strong>on</strong>necticut, GROTON,United States of AmericaAlexandrium m<strong>on</strong>ilatum is a toxicdinoflagellate that forms bloomsmostly in the Gulf of Mexico. ToxicA. m<strong>on</strong>ilatum has been linked to fishand invertebrate kills, and producesendotoxins with hemolytic andneurotoxic properties. Weexperimentally assessed resp<strong>on</strong>sesof ecologically important shellfish totoxic A. m<strong>on</strong>ilatum (AMO3 isolate).Grazing studies were c<strong>on</strong>ductedwith eastern oysters (Crassostreavirginica), northern quahogs(Mercenaria mercenaria) and greenmussels (Perna viridis), all of whichinhabit areas where A. m<strong>on</strong>ilatumblooms occur. Clearance rates ofeach shellfish species weredepressed when exposed to toxic A.m<strong>on</strong>ilatum al<strong>on</strong>e or with n<strong>on</strong>toxicInstant <strong>Algae</strong>® Pavlova, incomparis<strong>on</strong> to c<strong>on</strong>trol animals thatwere fed benign algal prey.Exposure to A. m<strong>on</strong>ilatum alsosignificantly decreased shellfish258

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