The data has been collected during Nansen Legacy Seasonal Study Q1, 2nd March - 25th March 2021, on research vessel RV Kronprins Haakon (toktnummer 2021703), along a transect from 76N to 82N east of Svalbard. The dataset contains mesozooplankton abundance (ind/m3). It has been sampled using a MultiNet Midi at 5 distinct depths. Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All specimens are identified to the lowest taxonomical level and the abundance is given for a specific species and stage or size group.
The data in this sampling event resource has been published as a Darwin Core Archive (DwC-A), which is a standardized format for sharing biodiversity data as a set of one or more data tables. The core data table contains 66 records.
2 extension data tables also exist. An extension record supplies extra information about a core record. The number of records in each extension data table is illustrated below.
This IPT archives the data and thus serves as the data repository. The data and resource metadata are available for download in the downloads section. The versions table lists other versions of the resource that have been made publicly available and allows tracking changes made to the resource over time.
The table below shows only published versions of the resource that are publicly accessible.
Researchers should respect the following rights statement:
The publisher and rights holder of this work is The Nansen Legacy Project. This work is licensed under a Creative Commons Attribution (CC-BY) 4.0 License.
This resource has been registered with GBIF, and assigned the following GBIF UUID: 0ce9fc33-d200-43da-8340-697b09610f74. The Nansen Legacy Project publishes this resource, and is itself registered in GBIF as a data publisher endorsed by GBIF Norway.
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The Northern Barents Sea
|Bounding Coordinates||South West [76, 28], North East [82, 35]|
|Start Date / End Date||2021-04-27 / 2021-05-20|
The dataset contains mesozooplankton abundance (ind/m3). It has been sampled at 5 distinct depths using a Multinet Midi (HydroBios, opening: 0.25m2, net length: 250 cm). Small mesozooplankton were collected with a mesh-size 64 µm and large mesozooplankton were collected with a mesh-size 180 µm. All samples were preserved in 4 % formaldehyde free from acid. PLEASE NOTE: THIS DATASET CONTAINS TWO COMPLETE DATASETS OF ZOOPLANKTON: ONE FOR SMALL MESOZOOPLANKTON (APPROX BODY SIZE BELOW 2 MM) COLLECTED WITH MULTINET 64 µM AND ONE FOR LARGE MESOZOOPLANKTON (APPROX BODY SIZE ABOVE 2 MM) COLLECTED WITH MULTINET 180 µM MESH SIZE. THE INFO ABOUT WHICH NET IS USED CAN BE FOUND IN gearType in extendedMeasurment andFacts USE EITHER 64 UM OR 180 UM DEPENDING ON WHETHER THE FOCUS IS SMALL OR LARGE MESOZOOPLANKTON
|Study Extent||The sampling covers a transect from the central Barents Sea (76N) to the Arctic Ocean (82N) east of Svalbard, including 7 stations (P1 to P7). Each sampling event includes 5 distinct depth layers The depth intervals were from the bottom-200, 200-100, 100-50, 50-20 and 20-0 m. At the deep stations, the sampling depths were from 1000-600, 600-200, 200-50, 50-20 and 20-0 m|
|Quality Control||The analysis of organisms has been done according to standard procedures used in multiple other studies. The results have been reviewed by several of the researchers listed under resource creators.|
Method step description:
- (IOPAN). The organisms were identified and counted under a stereomicroscope equipped with an ocular micrometer, according to standard procedures (Harris et al. 2000). Small-sized zooplankters (most of Copepoda, juvenile stages of Pteropoda, Euphausiacea, Ostracoda, Amphipoda and Chaetognatha) were identified and counted in sub-samples obtained from the fixed sample volume by automatic pipette (approximately 500 individuals). Large zooplankters (big Copepoda, Pteropoda, Euphausiacea, Ostracoda, Amphipoda, Decapoda, Appendicularia, Chaetognatha, and Pisces larvae) were sorted out and identified from the whole sample. Representatives of Calanus spp. were identified at the species level based on morphology and prosome lengths of individual copepodid stages (Kwasniewski et al. 2003).