Phytoplankton, National Monitoring Study 2019, EMBLAS Plus Project

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此資源sampling event的資料已發佈為達爾文核心集檔案（DwC-A），其以一或多組資料表構成分享生物多樣性資料的標準格式。 核心資料表包含 36 筆紀錄。

亦存在 2 筆延伸集的資料表。延伸集中的紀錄補充核心集中紀錄的額外資訊。 每個延伸集資料表中資料筆數顯示如下。

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如何引用

研究者應依照以下指示引用此資源。:

Grandova M., Terenko G. Ukrainian Scientific Centre of Ecology of the Sea (UkrSCES)

權利

研究者應尊重以下權利聲明。:

此資料的發布者及權利單位為 Ukrainian Scientific Centre of Ecology of the Sea (UkrSCES)。 To the extent possible under law, the publisher has waived all rights to these data and has dedicated them to the Public Domain (CC0 1.0). Users may copy, modify, distribute and use the work, including for commercial purposes, without restriction.

GBIF 註冊

此資源已向GBIF註冊，並指定以下之GBIF UUID: 9c576dc5-7b09-4033-b2fb-718daae7727b。  Ukrainian Scientific Centre of Ecology of the Sea (UkrSCES) 發佈此資源，並經由Ocean Biodiversity Information System同意向GBIF註冊成為資料發佈者。

關鍵字

Samplingevent

聯絡資訊

地理涵蓋範圍

"Data collected within the EMBLAS-Plus “EU-UNDP Project 'Improving Environmental Monitoring in the Black Sea' (EMBLAS-Plus)” (http://emblasproject.org/). Quantitative phytoplankton samples (35 samples at 20 stations) were collected by vertical series consisting from several sampling depths, so that the material could be collected from main hydrophysical layers. Layers at each station were identified according to CTD-sounding, conducted prior the phytoplankton sampling. Special attention was paid to fluorescence profile obtained simultaneously with the CTD-sounding. Depending on the features of the station, the samples in NMS were collected from upper mixed (0-1m) layer, upper thermocline layer, lower thermocline layer, near-bottom layer. Were used 5L Niskis bottles, attached to CTD rosette system for sampling at each depth; 1-2 L water samples were taken during NMS. Samples of the phytoplankton were fixed with 4% buffered formaldehyde up to the final concentration of 2% in a sample and delivered to the laboratory. After sedimentation of the phytoplankton cells during 2 weeks, samples were slowly decanted to 30-40 ml. These concentrated samples were kept at temperature of 5-7 oC during a month before further processing. Before counting, the concentrated samples were concentrated one more time, down to 10-20 cm3 by slow decantation. Identification of species and cells counting were carried out under a light microscope with magnifications of 600 in the drop with the volume of 0.05 ml (Naguotte chamber). The wet biomass was calculated by the method of geometric similarity equating shapes of cells to corresponding geometrical shapes and assuming that the cell density is equal to 1. Species were identified mainly using Schiller (1937), Kisselew (1950), Carmelo (1997), Steidinger and Tangen (1997), Cronberg and Annadotter (2006) and the taxonomic nomenclature according to the on-line data-base of World Register of Marine Species (WoRMS) and the Black Sea check-list http://phyto.bss.ibss.org.ua."

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