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Distribution of polar cod (Boreogadus saida) based on participation in research sampling, examination of museum voucher collections and the literature (Mecklenburg et al. 2011, 2014, 2016; Mecklenburg and Steinke 2015). Map shows the maximum distribution observed from point data and includes both common and rare locations. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/marine-fishes" target="_blank">Chapter 3</a> - Page 114 - Figure 3.4.2
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Number of megafauna species/taxa in the Arctic (7,322 stations in total), based on recent trawl investigations. Stations with highest species/taxon number are sorted to the top, meaning that dense concentrations of stations (e.g. Eastern Canada, Barents Sea), with low species numbers are hidden behind stations with higher species numbers. Also note that species numbers are somewhat biased by differing taxonomic resolution between studies. Data from: Icelandic Institute of Natural History, Iceland; Marine Research Institute, Iceland; University of Alaska, Fairbanks, U.S.; Greenland Institute of Natural Resources, Greenland; Zoological Institute of the Russian Academy of Sciences, St. Petersburg, Russia; Université du Québec à Rimouski, Canada; Fisheries and Oceans Canada; Institute of Marine Research, Norway; and Polar Research Institute of Marine Fisheries and Oceanography, Murmansk, Russia. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/benthos" target="_blank">Chapter 3</a> - Page 91 - Box figure 3.3.2 Several regions of the Pan Arctic have been sampled with trawl. Even though the trawl configurations and the taxonomic level are different from area to area, we choose to consider the taxonomic richness as relatively comparative.
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In 2017, the SAMBR synthesized data about biodiversity in Arctic marine ecosystems around the circumpolar Arctic. SAMBR highlighted observed changes and relevant monitoring gaps using data compiled through 2015. In 2021 an update was provided on the status of seabirds in circumpolar Arctic using data from 2016–2019. Most changes reflect access to improved population estimates, orimproved data for monitoring trends,independent of recognized trends in population size.
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Sea ice meiofauna composition (pie charts) and total abundance (red circles) across the Arctic, compiled by the CBMP Sea Ice Biota Expert Network from 27 studies between 1979 and 2015. Scaled circles show total abundance per individual ice core while pie charts show average relative contribution by taxon per Arctic Marine Area (AMA). Number of ice cores for each AMA is given in parenthesis after region name. Note that studies were conducted at different times of the year, with the majority between March and August (see 3.1 Appendix). The category ‘other’ includes young stages of bristle worms (Polychaeta), mussel shrimps (Ostracoda), forams (Foraminifera), hydroid polyps (Cnidaria), comb jellies (Ctenophora), sea butterflies (Pteropoda), marine mites (Acari) and unidentified organisms. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/sea-ice-biota" target="_blank">Chapter 3</a> - Page 40 - Figure 3.1.4 From the report draft: "Here, we synthesized 19 studies across the Arctic conducted between 1979 and 2015, including unpublished sources (B. Bluhm, R. Gradinger, UiT – The Arctic University of Norway; H. Hop, Norwegian Polar Institute; K. Iken, University of Alaska Fairbanks). These studies sampled landfast sea ice and offshore pack ice, both first- and multiyear ice (Appendix 3.1). Meiofauna abundances reported in individual data sources were converted to individuals m-2 of sea ice assuming that ice density was 95% of that in melted ice. Due to the low taxonomic resolution in the reviewed studies, ice meiofauna were grouped into: Copepoda, nauplii (for copepods as well as other taxa with naupliar stages), Nematoda, Polychaeta (mostly juveniles, but also trochophores), flatworms (Acoelomorpha and Platyhelminthes; these phyla have mostly been reported as one category), Rotifera, and others (which include meroplanktonic larvae other than Polychaeta, Ostracoda, Foraminifera, Cnidaria, Ctenophora, Pteropoda, Acari, and unidentified organisms). Percentage of total abundance for each group was calculated for each ice core, and these percentages were used for regional averages. Maximum available ice core length was used in data analysis, but 50% of these ice cores included only the bottom 10 cm of the ice, 12% the bottom 5 cm, 10% the bottom 2 cm, and 11% the entire ice-thickness. Data from 617 cores were used."
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Trends in biomass of marine fish Focal Ecosystem Components across each Arctic Marine Area STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - Chapter 4 - Page 180 - Figure 4.4
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Ice algal community similarity of central Russian Arctic drifting stations from the 1980s to 2010s based on unpublished data by I.A. Melnikov, Shirshov Institute of Oceanology. The closer two samples (symbols) are to each other in this multi-dimensional scaling plot, the more similar their algal communities were, based on presence/absence of algal species. Samples from the same year tend to be similar and group together on the plot, with some exceptions. Dispersion across the plot suggests that community structure has changed over the decades, although sampling locations in the central Arctic have also shifted, thus introducing bias. An analysis of similarity (PRIMER version 6) with a high Global R=0.80 indicates strong community difference among decades (global R=0 indicates no difference, R=1 indicates complete dissimilarity). Regional differences were low (global R=0.26) and difference by ice type moderate (global R=0.38). Grey arrows point to the very different and only two samples from 2013. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/sea-ice-biota" target="_blank">Chapter 3</a> - Page 47 - Figure 3.1.8 "For the analysis of possible interannual trends in the ice algal community, we used a data set from the Central Arctic, the area most consistently and frequently sampled (Melnikov 2002, I. Melnikov, Shirshov Institute, unpubl. data). Multivariate community structure was analysed based on a presence-absence matrix of cores from 1980 to 2013. The analysis is biased by the varying numbers of analysed cores taken per year ranging widely from 1 to 24, ice thickness between 0.6 and 4.2 m, and including both first-year as well as multiyear sea ice. Locations included were in a bounding box within 74.9 to 90.0 °N and 179.9°W to 176.6°E and varied among years."
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Global catches of all capelin species from 1950 to 2011 (FAO 2015). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/marine-fishes" target="_blank">Chapter 3</a> - Page 119 - Figure 3.4.6
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Harvest marine mammal Focal Ecosystem Component stocks in Arctic Marine Areas. Harvested without quotas, with quotas or not harvested. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/marine-mammals" target="_blank">Chapter 3</a> - Page 158 - Figure 3.6.4
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Relative abundance of major eukaryote taxonomic groups found by high throughput sequencing of the small-subunit (18S) rRNA gene. Time series collected by sampling every 2-6 weeks in Amundsen Gulf of the Beaufort Sea over the winter-spring transition in 2007–2008. Sampling DNA gives information about presence/absence, while sampling RNA gives information about the state of activity of different taxa. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/plankton" target="_blank">Chapter 3</a> - Page 72 - Figures 3.2.3
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Trends in abundance of plankton Focal Ecosystem Components across each Arctic Marine Area. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - Chapter 4 - Page 178 - Figure 4.2