Received 21 January 2009, revised 11 February 2009, accepted 16 February 2009.

Similar documents
The Raphidophytes the enigmatic class!

Introduction to raphidophytes

Ingvild Riisberg. Dissertation for the degree of philosophiae doctor

Ochrophyta -2. Class: Raphidophyceae = Nålflagellater Chrysophyceae = Gullalger Synurophyceae = Eustigmatophyceae = Flekkalger

HELCOM Red List Category: Previous HELCOM Red List threat assessments BSEP 75 (HELCOM 1998): BSEP 113 (HELCOM 2007): Greater concern stated by:

Characteristics of 3 classes OCHROPHYTA. single celled. Most marine, planktonic. Some may form harmful blooms. +/- flagella

Phytoplankton. Zooplankton. Nutrients

North Sea Ballast Water Exchange Area

The role of phytoplankton in the transport and distribution of polynuclear aromatic hydrocarbons(pahs) in the southern Baltic environment

Leibniz Institute for Baltic Sea Research Warnemünde

Seasonal cycle of phytoplankton community composition off Newport, Oregon, in 2009

Cytotoxic Effects of Vicicitus globosus (Class Dictyochophyceae) and Chattonella marina (Class Raphidophyceae) on Rotifers and Other Microalgae

Life cycle strategies and occurrences of red tides of Heterosigma akashiwo and Chattonella spp. in temperate coastal sea

American Harris mud crab Rhithropanopeus harrisii

INTERNATIONAL CONVENTION FOR THE CONTROL AND MANAGEMENT OF SHIPS' BALLAST WATER AND SEDIMENTS, 2004

ECOSTAT nutrient meeting ( ) Session 1: Comparison of European freshwater and saline water nutrient boundaries

National Polish services using regional products

2SEA. Requirements Report SOILS2SEA DELIVERABLE NO. 1.2

Memo of the on-line meeting of the HELCOM EN-Marine Litter (30 May 2017)

FLOW: Amigos de Bolsa Chica Citizen Science Program. Plankton Collection and Identification Report

Technical Reports Nos. 142, 143, 144, 145, 146, 147, 148, and 149. and

Azaspiracids producing dinoflagellates

Marine Primary Producers. Primary production

Phytoplankton biomass and species succession in the Gulf of Finland, Northern Baltic Proper and Southern Baltic Sea in 2010

FLOW: Amigos de Bolsa Chica Citizen Science Program. Plankton Collection and Identification Report

Annual algae communities on Baltic infralittoral coarse sediment

Influence of microphytobenthos photosynthesis on the spectral characteristics of the signal reflected from Baltic sandy sediments

Marine Primary Producers

HELSINKI COMMISSION HELCOM MONAS 4/2002 Monitoring and Assessment Group Fourth Meeting Warnemünde, Germany, October 2002

f r o m a H i g h - R e s o l u t i o n I c e - O c e a n M o d e l

David W. Seaborn 1, A. Michelle Seaborn 2, William M. Dunstan 2, and Harold G. Marshall 1

Culture of green Noctiluca under laboratory conditions: I. Feeding behavior and sexual reproduction

Light scattering in Baltic crude oil seawater emulsion

Effects of environmental variables on midsummer dinoflagellate community in the Neva Estuary. Mikhail Golubkov, Vera Nikulina, Sergey Golubkov

Recent Harmful Algal blooms (HABs) Events in Indonesia

A new fauna intercalibration typology

OCEANOGRAPHY. 13. Biological Productivity and Energy Transfer. Alessandro Grippo, Ph.D. part 2: Photosynthetic Marine Organisms

The Microbial World. Microorganisms of the Sea

Identification of maritime spatial planning best practices in the Baltic Sea Region and other EU maritime regions

Cyanobacterial blooms in the Baltic Sea

Amoeba hunts and kills paramecia and stentor. Eukaryotic photosynthetic cells

Baltic Sea Research Institute Warnemünde. Cruise report No. 40/04/11. r/v Professor Albrecht Penck. Monitoring cruise. 30 April 10 May 2004

HELCOM-VASAB Maritime Spatial Planning Working Group Twelfth Meeting Gdansk, Poland, February 2016

Fluorometry Project Chlorophyll Temperature Time Series

Parting the Red Seas: The Optics of Red Tides

Unvegetated epifaunal communities on Baltic infralittoral coarse sediment

Primary Producers. Key Ideas

The North Atlantic Bloom: Species composition and vertical fluxes

Prokaryotes Vs. Eukaryotes

Phytoplankton biomass and species succession in the Gulf of Finland, Northern Baltic Proper and Southern Baltic Sea in 2009

Protists: Algae Lecture 5 Spring 2014

Emerging physical and biological properties in a new Arctic ice regime

Ireland: Predictions. NMP Current closures ASP AZP DSP PSP

Protists: Algae Lecture 5 Spring Protist Phylogeny. Meet the algae. Primary & Secondary Endosymbiosis. Endosymbiosis. Secondary Endosymbiosis

The 2 nd war winter Arctic Skagerrak

Protists. Protists. Protist Feeding Strategies. Protist Body Plans. Endosymbiosis. Protist Reproduction 3/3/2011. Eukaryotes Not a monophyletic group

Figure 14 p.385 5/11/2016. Plankton Production and Food Webs. Plankton Production and Food Webs

Activities of HAB group in Acore-CMS program

AMBER Annual Meeting. Identification and Quantification of Submarine Groundwater Discharge (SGD) in the Puck Bay/ Poland (WP B.4 and B.

2001 State of the Ocean: Chemical and Biological Oceanographic Conditions in the Newfoundland Region

Supplementary Figure 1 Surface distribution and concentration of the dinoflagellate N. scintillans

Taxonomic recognition of plankton using optics

The Domain Eukarya is a large, diverse and complex group or organisms that consist of one or more Eukaryotic Cells

Eukaryotic photosynthetic cells

Lesson: Primary Production

Finnish Maritime Administration BULLETIN 5/

Lecture #9-2/8 Dr. Kopeny

Marine Ecology I: Phytoplankton and Primary production

Dab (Limanda limanda) in Subarea 4 and Division 3.a (North Sea, Skagerrak and Kattegat)

Papers. Sea salt emission from the coastal zone. 1. Introduction

MERIS Reprocessing Neural Net Algorithm. Roland Doerffer, Carsten Brockmann,

Baltic Sea Region cooperation in Maritime Spatial Planning - HELCOM/VASAB

Ireland: Predictions. NMP Current closures ASP AZP DSP PSP

Look For the Following Key Ideas

Ireland: Predictions. NMP Current closures ASP AZP DSP PSP DSP event: Low. AZP event: Moderate. PSP event: Very low. Why do we think this?

The Microbial World. Chapter 5

Ireland: Current Conditions

DSP: This is currently a low risk period for early DSP events. All sites are currently below regulatory limits.

International Conference and Summer School-Seminar Dynamics Of The Coastal Zone Of Non-Tidal Seas

Microbial Grazers Lab

Acoustical recognition of the bottom sediments in the southern Baltic Sea

Microbial Grazers Lab

Eutrophication (H01.05), Contaminant pollution (H01.05), Contaminant pollution (H03),

Understanding the role of the YS Bottom Cold Water ( 10 C) on the survival strategy of Euphausia pacifica throughout the hot summer

The observed global warming of the lower atmosphere

KINGDOM SYSTEM OF CLASSIFICATION OF LIVING ORGANISM. Dr. Urvashi Sinha, Asst. Prof., Department of Botany Patna Women s College, Patna

Predicting phytoplankton blooms

DSP: This is currently a low risk period for early DSP events. All sites are currently below regulatory limits.

NATIONAL REPORT OF POLAND

Ecology 3/15/2017. Today. Autotrophs. Writing Assignment: What does it mean. Last readings on Chlamydomonas populations

Leibniz Institute for Baltic Sea Research Warnemünde

Fig. 16. Majority rule consensus tree depicting phylogenetic relationships inferred among 74 species of heterokont algae. Note that A.

Ireland: Current Conditions

Spreading and reproduction limitations of the American comb jelly Mnemiopsis leidyi in the Baltic Sea

The Water Planet Ch. 22

The only contamination levels for microbial contaminants in recreational and source waters are coliforms and the fecal bacteria E.

METHODS OF CLASSIFYING INTO A CERTAIN KINGDOM: 1. prokaryote OR eukaryote 2. single OR multi celled 3. autotroph OR heterotroph

Cruise Report R/V Oceania, AREX 2007

Cruise Report R.V. Oceania, AREX2004

Plankton. -Plankton are almost always at the bottom of the food chain in any marine environment, making them possibly the most important group.

Transcription:

Communications The first recorded bloom of Pseudochattonella farcimen (Dictyochophyceae, Heterokonta),(Riisberg I.,2008)intheGulfof Gdańsk* OCEANOLOGIA, 51(1), 2009. pp. 139 143. C 2009,byInstituteof Oceanology PAS. KEYWORDS Pseudochattonella farcimen Bloom Gulf of Gdańsk Maria Łotocka Institute of Oceanology, Polish Academy of Sciences, Powstańców Warszawy 55, PL 81 712 Sopot, Poland; e-mail: lotocka@iopan.gda.pl Received 21 January 2009, revised 11 February 2009, accepted 16 February 2009. Abstract In April 2001 a local bloom of the heterokont phytoflagellate Pseudochattonella farcimen(riisberg I., 2008)(initially named Chattonella aff. verruculosa) was observedforthefirsttimeinthesouthernpartofthegulfofgdańsk.thespecies occurredinhighcelldensities:thecountwas11.5 10 6 cellsdm 3 andthebiomass 927.5 µgcdm 3. 1. Introduction The first large bloom of Pseudochattonella along the European coast (the Netherlands, Germany, Denmark, Norway and Sweden) was observed in1998. DuringMay2000,asecondbloomofthisspecieswasreported from the German Bight and western Denmark with a maximum density of11.0 10 6 cellsdm 3 (Bourdelaisetal.2002,Naustvolletal.2002). In spring 2001, Pseudochattonella farcimen formed a similar large-scale bloom in the Skagerrak, Kattegat, along the west coast of Sweden and off southern Norway. During that episode an extensive fish kill took place: * The investigation were carried out within the framework of research programme II.3. of the Institute of Oceanology PAS. The complete text of the paper is available at http://www.iopan.gda.pl/oceanologia/

140 M. Łotocka innorway, forexample, asmanyas1100 tonsofrearedsalmonwere killed(edvardsen et al. 2007). In 2004, two smaller blooms were recorded, oneoffthedanishnorthseacoastandtheotherofftheswedishwest coast. P. farcimen produces fish-killing neurotoxins such as the brevetoxins (Bourdelais et al. 2002). Thenameofthespeciesandthetaxonomicgroupthisshouldbeassigned to are matters of debate. Some experts believe that this organism should be classified as a raphidophyte(khan et al. 1996). Earlier, this species from European waters had been identified as Chattonella cf. verruculosa, described from Japan (Bourdelais et al. 2002). A detailed study by Edvardsen et al.(2007) has shown, however, that this organism differs both morphologically and genetically from its Japanese counterpart. These authors propose transferring Ch. cf. verruculosa from the class Raphidophyceae to the Dictyochophyceae and suggest giving it the new name of Verrucophora farcimen. Another study, based on combined molecular data and morphological characteristics, places this species among the Dictyochophyceae; its authors have put forward the name Pseudochattonella verruculosa gen. nov., comb. nov. (Hosoi-Tanabe et al. 2007). Finally, on the basis of nuclear, mitochondrial and plastid DNA sequence data ofv.farcimen,riisberghasproposedthenewnamep.farcimenforthe identified heterokont flagellate blooming in the Skagerrak Basin(Riisberg 2008, Riisberg& Edvardsen 2008). 2. Methods GulfofGdańsksurfacewaterwassamplednearSopotpierinspring 2001. The organisms were studied live and with Lugol s solution under an inverted microscope(axiovert 35; Carl Zeiss, Germany) fitted with phase contrast and differential interference contrast. Cells were photographed with a Contax 167MT (Japan) camera. The individual phytoplankters were counted in accordance with the COMBINE programme of HELCOM (HELCOM 1997). The volume of each cell was calculated from the relevant morphometriccharacteristics,thenconvertedtobiomass,assuming1µm 3 tobeequivalent to1pg(edlered.1979). Thecarboncontent ofthe phytoplankton samples was calculated with a formula given in Menden- Deuer& Lessard(2000). 3. Results and discussion Pseudochattonella farcimen formed a local bloom in the southern part of thegulfofgdańskinspring2001.cellsofthisorganismwereidentifiedfor

The first recorded bloom of Pseudochattonella farcimen... 141 the first time in phytoplankton samples collected in this basin on 20 April 2001.Anintensebloomofthisorganismoccurredbetween25and30April (Figure1). Maximumcellconcentrationswere11.5 10 6 cellsdm 3,and thebiomasswas18.1mgdm 3 /927 µgcdm 3.Thisheterokontflagellate remainedinthegulfofgdańskuntil5may. 6-3 10 dm 14 12 10 8 6 4 2 0 20.04.2001 25.04.2001 27.04.2001 30.04.2001 2.05.2001 5.05.2001 date Figure 1. Densities of Pseudochattonella farcimen off Sopot pier during the spring 2001 bloom The hydrological parameters of the surface water layer were recorded duringthebloomperiod:watertemperature7.2 9.8 C,salinity7.3 7.5PSU and ph 8.01 8.27. P. farcimen is a cold-water species, with optimal growth attemperaturesbetween2and10 C(Edvardsenetal.2007),andhasbeen recorded in waters of different salinities between 12 and 35 PSU. These figures are corroborated by the results of laboratory studies. All the available dataindicatethatp.farcimenisunabletosurviveinwaterofsalinity <10PSU,athresholdlikelytopreventitsspreadintotheBalticProper (Naustvoll L.-J. 2006, Edvardsen et al. 2007). This may be the reason why thisspecieswasnotrecordedinthegulfofgdańskinthefollowingyears. The examined organisms displayed morphological variations: cells varied in shape from the typical pyriform to spherical (Figure 2) and were 10 39 µminlength(meanlength21 µm,n=200)(figure3).p.farcimen has two flagella of unequal length, but microscopic examination revealed only the longer one, along with numerous, golden-brown chloroplasts and many mucocyst-like bodies. Studiesofthealga smorphologyandgenetics,aswellasofitssteroland fatty acid composition, have shown that the European P. farcimen differs from the Japanese Chattonella(Edvardsen et al. 2007, Giner et al. 2008). The present report almost certainly rules out the possibility that the

142 M. Łotocka 20 µm Figure 2. Pseudochattonella farcimen bloom in the Gulf of Gdańsk in spring 2001 70 60 50 40 30 20 10 0 < 10 10-15 16-20 21-25 26-30 31-35 36-40 range of cell length [µm] Figure 3. Length of Pseudochattonella farcimen cells sampled from the Gulf of Gdańsk during the spring 2001 bloom species was introduced from Japanese waters. Nevertheless, the pathway bywhichp.farcimenreachedthecoastalwatersofthegulfofgdańsk from the western Baltic remains unclear. Routine programmes to monitor this species, run at different localities on the Baltic coast, will be needed if theharmfuleffectsoftoxicbloomsaretobepreventedinthefuture.

References The first recorded bloom of Pseudochattonella farcimen... 143 BourdelaisA.J.,TomasC.R.,NaarJ.,KubanekJ.,BadenD.G.,2002,Newfishkilling alga in Coastal Delaware produces neurotoxins, Environ. Health Persp., 110(5), 465 470. Edler L.(ed.), 1979, Recommendations on methods for marine biological studies in the Baltic Sea. Phytoplankton and chlorophyll, Balt. Mar. Biol. Publ. No. 5, 1 38. Edvardsen B., Eikrem W., Shalchian-Tabrizi K., Riisberg I., Johnsen G., Naustvoll L., Throndsen J., 2007, Verrucophora farcimen gen. et sp. nov. (Dictyochophyceae, Heterokonta) a bloom-forming ichthyotoxic flagellate from the Skagerrak, Norway, J. Phycol., 43(5), 1054 1070. GinerJ.-L.,ZhaoH.,TomasC.R.,2008,Sterolsandfattyacidsofthreeharmful algae previously assigned as Chattonella, Phytochemistry, 69(11), 2167 2171. HELCOM, 1997, Manual for marine monitoring in the COMBINE programme of HELCOM, Part C. Programme for monitoring of eutrophication and its effects, Annex C-6: Phytoplankton species composition, abundance and biomass, Balt. Mar. Environ. Prot. Commiss., Helsinki, C6-1 C6-8, 22 pp. Hosoi-Tanabe S., Hond D., Fukaya S., Otake I., Inagaki Y., Sako Y., 2007, Proposal of Pseudochattonella verruculosa gen. nov., comb. nov. (Dictyochophyceae) for a former raphidophycean alga Chattonella verruculosa, based on 18S rdna phylogeny and ultrastructural characteristics, Phycol. Res., 55(3), 185 192. Khan S., Arakawa O., Onoue Y., 1996, A toxicological study of the marine phytoflagellate Chattonella antiqua (Raphidophyceae), Phycologia, 35(3), 239 244. Menden-Deuer S., Lessard E. J., 2000, Carbon to volume relationships for dinoflagellates, diatoms, and other protist plankton, Limnol. Oceanogr., 45(3), 569 579. Naustvoll L.-J., 2006, NOBANIS invasive alien species fact sheet, Chattonella aff. verruculosa, Database of the North European and Baltic Network on Invasive Alien Species, NOBANIS, http://www.nobanis.org/files/factsheets/ Chattonella verruculosa.pdf. NaustvollL.-J.,DahlE.,DanielssenD.,2002,AnewbloomofChattonellain Norwegian waters, Harmful Algae News, 23, 3 5. Riisberg I., 2008, Genetic characterization of the marine ichthyotoxic flagellate Pseudochattonella farcimen (Heterokonta) and phylogenetic relationships among heterokonts, Ph. D. thesis, Univ. Oslo, Oslo, 1 33. Riisberg I., Edvardsen B., 2008, Genetic variation in bloom-forming ichthyotoxic Pseudochattonella species (Dictyochophyceae, Heterokonta) using nuclear, mitochondrial and plastid DNA sequence data, Eur. J. Phycol., 43(4), 413 422.