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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 2006O.19-01Field applicati<strong>on</strong>s for remotedetecti<strong>on</strong> of harmful algae usingthe Envir<strong>on</strong>mental SampleProcessor: Spring-Summer 2006Sessi<strong>on</strong>: O.19 - M<strong>on</strong>itoring 2Presentati<strong>on</strong> time: 11:00 - 11:20Dianne I Greenfield 1 , CA Scholin 1 , SJensen 1 , R III Marin 1 , B Roman 1 , BMassi<strong>on</strong> 1 , GJ Doucette 21 M<strong>on</strong>terey Bay Aquarium ResearchInstitute, MOSS LANDING, United Statesof America2 NOAA/Nati<strong>on</strong>al Ocean Service,CHARLESTON, SC 29412, United Statesof AmericaMolecular approaches for identifyingharmful algal bloom (HAB) speciesand affiliated toxins are central toresearch and m<strong>on</strong>itoring, but suchmethods require the return ofdiscrete samples for laboratoryanalysis. This impediment isovercome with the Envir<strong>on</strong>mentalSample Processor (ESP), aninstrument that detects remotely,subsurface, and in near real-time, awide range of microorganisms andsubstances they produce(http://www.mbari.org/microbial/ESP). The first-generati<strong>on</strong> ESP verifiedbasic c<strong>on</strong>cepts, such as samplearchive and DNA array processing.The sec<strong>on</strong>d-generati<strong>on</strong> (2G ESP), acomparatively smaller, faster, andmore robust versi<strong>on</strong>, was beendeployed for the first time inM<strong>on</strong>terey Bay, CA (USA) duringspring-summer of 2006 for ~20d perdeployment. During this fieldseas<strong>on</strong>, the 2G ESP successfullyautomated detecti<strong>on</strong> of a number ofharmful species, including diatomsof the genus Pseudo-nitzschia,some of which produce the toxindomoic acid. In additi<strong>on</strong> to in situdetecti<strong>on</strong>, we attempted to groundtruth instrument data by periodwater sampling and analyses usinglaboratory versi<strong>on</strong>s of molecularassays that are emulated within theESP. Here we present our fieldfindings to date, including speciesdetected remotely during 2006,domoic acid (Doucette et al.),envir<strong>on</strong>mental data, and ourcapability to ground-truth instrumentdata.O.19-02M<strong>on</strong>itoring of lipophilic shellfishtoxins using SPATT (Solid PhaseAdsorpti<strong>on</strong> Toxin Tracking) inNova Scotia, CanadaSessi<strong>on</strong>: O.19 - M<strong>on</strong>itoring 2Presentati<strong>on</strong> time: 11:20 - 11:40CM Garnett 1 , CM Rafuse 1 , NI Lewis 1 , SKirchhoff 2 , J Cullen 2 , MA Quilliam 11 Nati<strong>on</strong>al Research Council of Canada,HALIFAX, Canada2 Dalhousie University, HALIFAX, CanadaField studies were undertaken inShip Harbour and Lunenburg Bay,Nova Scotia, Canada, from May toNovember, 2005. Solid PhaseAdsorpti<strong>on</strong> Toxin Tracking (SPATT)bags were deployed weekly inc<strong>on</strong>juncti<strong>on</strong> with a variety ofphysico-chemical measurementsincluding temperature, c<strong>on</strong>ductivityand light attenuati<strong>on</strong>. Sampling ofphytoplankt<strong>on</strong> was c<strong>on</strong>ducted atboth sites and blue mussels (Mytilisedulis) were collected at the ShipHarbour site. SPATT extracts wereanalysed by LC-MS/MS using amulti-toxin analysis for lipophilictoxins. The following toxins weredetected: spirolides,dinophysistoxin-1, pectenotoxin-2,pectenotoxin-2 seco acid,yessotoxin and azaspiracids. Thec<strong>on</strong>centrati<strong>on</strong> effect of toxins fromthe water column by the SPATTbags was supported by evidence oftoxins in the SPATT extracts whenno toxins were detected inplankt<strong>on</strong>ic net tow samples. Inadditi<strong>on</strong>, changes in the toxin72

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