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  • PANGAEA  (3)
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Years
  • 1
    Publication Date: 2024-02-07
    Description: The data set was acquired during the PHYCOB cruise in the frame of the Eurofleets+ programme (https://www.eurofleets.eu/2021/10/22/phycob-an-international-oceanographic-expedition-into-the-western-black-sea-coordinated-by-the-alfred-wegner-institut-helmholtz-zentrum-fur-polar-und-meeresforschung-awi/) within the Regional call in the territorrial waters of Romania and Bulgaria in the Western Baltic Sea from 11th to 17th September 2021. The aim of the cruise was to assess the occurrence of potentially harmfal algae and their associated phycotoxins in the Black Sea and the accompanying environmental parameters. Sampling was performed by CTD casts and Rosette water sampling in addition to vertical phytoplankton net hauls from 30 m depth to surface. The determined parameters include the following: Quantitative phytoplankton cell counts in water samples, qulitative determination of toxigenic species next generation sequencing data in plankton net concentrates, monoclonanal cultures established from water sample isolates, phycotoxins in plankton net concentrates, inorganic nitruinets (nitrate/nitrite, phosphate, silicate) , vitamin B12, particulate organic carbon, particulate organic nitrogen, flowcytometry data, and CTD data (temperature, salinity, chlorophyll-a, oxygen, turbidity, radiance).
    Keywords: chlorophyll-a; CTD profile; HAB species; isolated strains; net tows; NOC; Nutrient data; phycotoxins; POC; vitamin B12
    Type: Dataset
    Format: application/zip, 8 datasets
    Location Call Number Limitation Availability
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  • 2
    Publication Date: 2024-02-07
    Description: At each station two vertical net tows were taken from the water column using a 20 μm plankton net (438-030, Hydro-Bios, Kiel, Germany) for analyses of plankton and phycotoxins. The depth of the hauls was fixed to 0 - 30 m. The collected net tow concentrates were adjusted to 1 L with filtered seawater. 50 mL aliquots were fixed with formaldehyde solution, buffered to pH 8-8.2 with disodiumtetraborate (4% final concentration) for microscopic analyses of phytoplankton. Taxonomic identification and cell counts of the net samples were done under inverted microscope (Nikon Eclipse TE2000-U) connected to a video-interactive image analysis system (L.U.C.I.A, Version 4.8, Laboratory Imaging Ltd, Prague, Czech Republic) at 400 × magnification in Sedgwick-Rafter counting chambers. Only dinoflagellates species and the diatom Pseudo-nitzschia genus were considered during the analyses. 400 cells were counted from each sample, while rare and large species were checked in the whole counting chamber (Moncheva and Parr 2010). Cell abundance was expressed in cells per net tow. Taxonomic nomenclature was according to the on-line data-base of World Register of Marine Species (WoRMS) http://www.marinespecies.org/. The QC/QA of the data was performed following the quality control Guidelines for phytoplankton (Moncheva 2010). IOC-UNESCO Taxonomic Reference List of Harmful Micro Algae was used as a reference database of toxic microalgal species selection.
    Keywords: chlorophyll-a; Class; Code; Comment; Country; Counts; CTD profile; Date; Depth, bottom/max; Depth, top/min; Event label; Family; Genus; HAB species; Investigator; isolated strains; Kingdom; LATITUDE; Location; LONGITUDE; MULT; Multiple investigations; net tows; NOC; Nutrient data; Order; PHYCOB; PHYCOB_1; PHYCOB_10; PHYCOB_11; PHYCOB_12; PHYCOB_13; PHYCOB_14; PHYCOB_15; PHYCOB_16; PHYCOB_17; PHYCOB_18; PHYCOB_19; PHYCOB_2; PHYCOB_20; PHYCOB_21; PHYCOB_22; PHYCOB_23; PHYCOB_3; PHYCOB_4; PHYCOB_5; PHYCOB_6; PHYCOB_7; PHYCOB_8; PHYCOB_9; phycotoxins; Phylum; POC; Provenance/source; Sample ID; Scientific name; Species; Species, unique identification (Semantic URI); Species, unique identification (URI); Tübitak Marmara; vitamin B12; Year of analysis
    Type: Dataset
    Format: text/tab-separated-values, 22397 data points
    Location Call Number Limitation Availability
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  • 3
    Publication Date: 2024-02-07
    Description: At each station two vertical net tows were taken from the water column using a 20 μm plankton net (438-030, Hydro-Bios, Kiel, Germany) for analyses of plankton and phycotoxins. The depth of the hauls was fixed to 0 – 30 m. The collected net tow concentrates were adjusted to 1 L with filtered seawater. 150 mL aliquots were filtered under gentle vacuum (〈 0.2 bar) through 1 μm pore-size polycarbonate filters (Whatman, USA) for DNA analysis. DNA from the filters was immediately extracted by using 5% Chelex buffer (Tanabe et al. 2016). For detection of eukaryotic species, universal primers for 18S rRNA gene V7-V9 variable region (18S-V7F: TGGAGYGATHTGTCTGGTTDATTCCG and 18S-V9R: TCACCTACGGAWACCTTGTTACG; modified from Tanabe et al. 2016) were used. The procedures and techniques, applicable to the treatment of the obtained sequences, selection and taxonomic identification of operational taxonomic units (OTUs), were administered according to the workflow described in Dzhembekova et al. (2017). Taxonomic assignment was performed using BLAST against a sequence database downloaded from GenBank.
    Keywords: According to Schoch et al. (2020); Basic Local Alignment Search Tool; BLAST; chlorophyll-a; Code; Country; CTD profile; Date/Time of event; Depth, bottom/max; Depth, top/min; Event label; Genetic lineage; HAB species; Identity; isolated strains; Latitude of event; Location; Longitude of event; MULT; Multiple investigations; net tows; NOC; Nutrient data; PHYCOB; PHYCOB_1; PHYCOB_10; PHYCOB_11; PHYCOB_12; PHYCOB_13; PHYCOB_14; PHYCOB_15; PHYCOB_16; PHYCOB_17; PHYCOB_18; PHYCOB_19; PHYCOB_2; PHYCOB_20; PHYCOB_21; PHYCOB_22; PHYCOB_23; PHYCOB_3; PHYCOB_4; PHYCOB_5; PHYCOB_6; PHYCOB_7; PHYCOB_8; PHYCOB_9; phycotoxins; POC; Provenance/source; Reads; Species; Tübitak Marmara; vitamin B12
    Type: Dataset
    Format: text/tab-separated-values, 8272 data points
    Location Call Number Limitation Availability
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