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  • Amphidoma languida; ARK-XXIX/1, TRANSSIZ; Azadinium; Azadinium poporum; Azadinium spinosum; AZAHAB; Azaspiracids; Baltic Sea; Cells, total; Celtic Sea; CT; CTD, towed system; CTD/Rosette; CTD-RO; CTD-twoyo; DATE/TIME; Dinoflagellates; DNA; English Channel; Event label; Field observation; HE516; HE516_10-2; HE516_1-1; HE516_11-1; HE516_12-1; HE516_13-1; HE516_14-1; HE516_15-1; HE516_16-1; HE516_17-1; HE516_18-1; HE516_19-1; HE516_20-1; HE516_21-1; HE516_2-2; HE516_22-1; HE516_23-1; HE516_24-1; HE516_25-1; HE516_26-1; HE516_27-1; HE516_28-1; HE516_29-1; HE516_30-1; HE516_3-1; HE516_31-1; HE516_32-1; HE516_33-1; HE516_34-1; HE516_35-1; HE516_36-1; HE516_37-1; HE516_38-1; HE516_39-1; HE516_40-1; HE516_4-1; HE516_41-1; HE516_42-1; HE516_43-1; HE516_44-1; HE516_45-1; HE516_46-1; HE516_47-1; HE516_48-1; HE516_49-1; HE516_50-2; HE516_5-1; HE516_51-1; HE516_52-1; HE516_53-1; HE516_54-1; HE516_55-1; HE516_56-1; HE516_57-1; HE516_58-1; HE516_59-1; HE516_60-1; HE516_6-1; HE516_61-1; HE516_62-1; HE516_63-1; HE516_64-1; HE516_65-1; HE516_66-1; HE516_67-1; HE516_68-1; HE516_69-2; HE516_70-1; HE516_7-1; HE516_71-1; HE516_72-1; HE516_73-1; HE516_74-2; HE516_75-2; HE516_8-1; HE516_9-2; HE517; HE517_10-1; HE517_11-3; HE517_1-2; HE517_12-1; HE517_13-2; HE517_14-1; HE517_15-1; HE517_16-1; HE517_17-1; HE517_19-1; HE517_21-1; HE517_22-1; HE517_23-1; HE517_25-1; HE517_26-1; HE517_27-1; HE517_28-1; HE517_30-1; HE517_35-2; HE517_36-2; HE517_37-1; HE517_8-1; HE517_9-1; HE534; HE534_11-3; HE534_1-4; HE534_22-3; HE534_28-4; HE534_30-2; HE534_33-4; HE534_36-4; HE534_38-5; HE534_42-5; HE534_4-3; HE534_43-1; HE534_47-2; HE534_8-4; HE541; HE541_105-1; HE541_36-1; HE541_57-1; HE541_75-1; Heincke; Kattegat; LATITUDE; LONGITUDE; North Atlantic; North Sea; Polarstern; PS92; PS92-track; qPCR; QPCR; Quantitative real-time PCR (qPCR); Reference/source; South Atlantic Ocean; The Great Belt; Underway cruise track measurements; UT1606; UT1606/01-1; UT1606/02-1; UT1606/03-1; UT1606/04-1; UT1606/05-1; UT1606/06-1; UT1606/07-1; UT1606/08-1; UT1606/09-1; UT1606/10-1; UT1606/11-1; UT1606/12-1; UT1606/13-1; UT1606/14-1; UT1606/15-1; UT1606/16-1; UT1606/17-1; UT1606/18-1; UT1606/19-1; UT1606/20-1; UT1606/21-1; UT1606/22-1; UT1606/23-1; UT1606/24-1; UT1606/25-1; UT1606/26-1; UT1606/27-1; UT1606/28-1; UT1606/29-1; UT1606/30-1; UT1606/31-1; UT1606/32-1; UT1606/33-1; UT1606/34-1; UT1606/35-1; UT1606/36-1; UT1606/37-1; UT1606/38-1; UT1606/39-1; UT1606/40-1; UT1606/41-1; UT1606/42-1; UT1606/43-1; UT1606/44-1; Uthörn  (1)
  • Arctic  (1)
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  • 1
    Publication Date: 2024-05-11
    Description: The data represent species counts (cells L-1) of the three AZA-producing dinoflagellate species Azadinium spinosum, Az. poporum and Amphidoma languida (all members of the taxonomic family Amphidomataceae) of water samples taken during in total six different field expeditions on several research vessels (RV Heincke, RV Uthörn, RV Polarstern) and on in total five stationary sampling stations (Scapa Flow/Scotland, Cuxhaven/Germany, Helgoland/Germany, Wilhelmshaven/Germany, Sylt/Germany) between 2015 and 2019. The water samples have been taken using Niskin bottles (on research vessels attached to a CTD). After DNA extraction, the species cell numbers have been calculated by quantitative PCR (qPCR) analysis using respective standard curves. These samples gained from different geographical areas in the eastern North Atlantic have been analyzed as part of the RIPAZA Project (funded by the German BMBF; in cooperation with the Third Institute of Oceanography, Xiamen/China) and the results are presented and discussed in the doctoral thesis of Stephan Wietkamp (Suppl.Tab.S6, Suppl.Tab.S7). Aim of the project and especially of this data set was to provide first reference data on the biogeography (geographical distribution and seasonality) of toxigenic Amphidomataceae in the eastern North Atlantic.
    Keywords: Amphidoma languida; ARK-XXIX/1, TRANSSIZ; Azadinium; Azadinium poporum; Azadinium spinosum; AZAHAB; Azaspiracids; Baltic Sea; Cells, total; Celtic Sea; CT; CTD, towed system; CTD/Rosette; CTD-RO; CTD-twoyo; DATE/TIME; Dinoflagellates; DNA; English Channel; Event label; Field observation; HE516; HE516_10-2; HE516_1-1; HE516_11-1; HE516_12-1; HE516_13-1; HE516_14-1; HE516_15-1; HE516_16-1; HE516_17-1; HE516_18-1; HE516_19-1; HE516_20-1; HE516_21-1; HE516_2-2; HE516_22-1; HE516_23-1; HE516_24-1; HE516_25-1; HE516_26-1; HE516_27-1; HE516_28-1; HE516_29-1; HE516_30-1; HE516_3-1; HE516_31-1; HE516_32-1; HE516_33-1; HE516_34-1; HE516_35-1; HE516_36-1; HE516_37-1; HE516_38-1; HE516_39-1; HE516_40-1; HE516_4-1; HE516_41-1; HE516_42-1; HE516_43-1; HE516_44-1; HE516_45-1; HE516_46-1; HE516_47-1; HE516_48-1; HE516_49-1; HE516_50-2; HE516_5-1; HE516_51-1; HE516_52-1; HE516_53-1; HE516_54-1; HE516_55-1; HE516_56-1; HE516_57-1; HE516_58-1; HE516_59-1; HE516_60-1; HE516_6-1; HE516_61-1; HE516_62-1; HE516_63-1; HE516_64-1; HE516_65-1; HE516_66-1; HE516_67-1; HE516_68-1; HE516_69-2; HE516_70-1; HE516_7-1; HE516_71-1; HE516_72-1; HE516_73-1; HE516_74-2; HE516_75-2; HE516_8-1; HE516_9-2; HE517; HE517_10-1; HE517_11-3; HE517_1-2; HE517_12-1; HE517_13-2; HE517_14-1; HE517_15-1; HE517_16-1; HE517_17-1; HE517_19-1; HE517_21-1; HE517_22-1; HE517_23-1; HE517_25-1; HE517_26-1; HE517_27-1; HE517_28-1; HE517_30-1; HE517_35-2; HE517_36-2; HE517_37-1; HE517_8-1; HE517_9-1; HE534; HE534_11-3; HE534_1-4; HE534_22-3; HE534_28-4; HE534_30-2; HE534_33-4; HE534_36-4; HE534_38-5; HE534_42-5; HE534_4-3; HE534_43-1; HE534_47-2; HE534_8-4; HE541; HE541_105-1; HE541_36-1; HE541_57-1; HE541_75-1; Heincke; Kattegat; LATITUDE; LONGITUDE; North Atlantic; North Sea; Polarstern; PS92; PS92-track; qPCR; QPCR; Quantitative real-time PCR (qPCR); Reference/source; South Atlantic Ocean; The Great Belt; Underway cruise track measurements; UT1606; UT1606/01-1; UT1606/02-1; UT1606/03-1; UT1606/04-1; UT1606/05-1; UT1606/06-1; UT1606/07-1; UT1606/08-1; UT1606/09-1; UT1606/10-1; UT1606/11-1; UT1606/12-1; UT1606/13-1; UT1606/14-1; UT1606/15-1; UT1606/16-1; UT1606/17-1; UT1606/18-1; UT1606/19-1; UT1606/20-1; UT1606/21-1; UT1606/22-1; UT1606/23-1; UT1606/24-1; UT1606/25-1; UT1606/26-1; UT1606/27-1; UT1606/28-1; UT1606/29-1; UT1606/30-1; UT1606/31-1; UT1606/32-1; UT1606/33-1; UT1606/34-1; UT1606/35-1; UT1606/36-1; UT1606/37-1; UT1606/38-1; UT1606/39-1; UT1606/40-1; UT1606/41-1; UT1606/42-1; UT1606/43-1; UT1606/44-1; Uthörn
    Type: Dataset
    Format: text/tab-separated-values, 995 data points
    Location Call Number Limitation Availability
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  • 2
    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2016. This is the author's version of the work. It is posted here by permission of Inter-Research for personal use, not for redistribution. The definitive version was published in Marine Ecology Progress Series 547 (2016): 33-46, doi:10.3354/meps11660.
    Description: The bloom-forming dinoflagellate Alexandrium fundyense has been extensively studied due its toxin-producing capabilities and consequent impacts to human health and economies. This study investigated the prevalence of resting cysts of A. fundyense in western Greenland and Iceland to assess the historical presence and magnitude of bloom populations in the region, and to characterize environmental conditions during summer, when bloom development may occur. Analysis of sediments collected from these locations showed that Alexandrium cysts were present at low to moderate densities in most areas surveyed, with highest densities observed in western Iceland. Additionally, laboratory experiments were conducted on clonal cultures established from isolated cysts or vegetative cells from Greenland, Iceland, and the Chukchi Sea (near Alaska) to examine the effects of photoperiod interval and irradiance levels on growth. Growth rates in response to the experimental treatments varied among isolates, but were generally highest under conditions that included both the shortest photoperiod interval (16h:8h light:dark) and higher irradiance levels (~146-366 µmol photons m-2 s-1), followed by growth under an extended photoperiod interval and low irradiance level (~37 µmol photons m-2 s-1). Based on field and laboratory data, we hypothesize that blooms in Greenland are primarily derived from advected Alexandrium populations, as low bottom temperatures and limited light availability would likely preclude in situ bloom development. In contrast, the bays and fjords in Iceland may provide more favorable habitat for germling cell survival and growth, and therefore may support indigenous, self-seeding blooms.
    Description: Funding for this study was provided by the James M. and Ruth P. Clark Arctic Research Initiative to Anderson and Richlen, and for the ARCHEMHAB expedition via the Helmholtz Institute initiative Earth and Environment under the PACES Program Topic 2 Coast (Workpackage 3) of the Alfred Wegener Institute. Additional support was provided by the Woods Hole Center for Oceans and Human Health through National Science Foundation (NSF) Grant OCE-1314642 and National Institute of Environmental Health Sciences (NIEHS) Grant 1-P01-ES021923-01.
    Description: 2017-04-07
    Keywords: Arctic ; Alexandrium ; Dinoflagellate ; Cysts ; Harmful algal bloom
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Location Call Number Limitation Availability
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