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Appendix 9.3 Borderline vascular plant species (“b”) with indication of PAF code number, reaching the southernmost part of the Arctic subzone E. Arctic floristic provinces, subzones (A-E), neighbouring boreal or boreo-alpine zone (N) derived from Elven (2007).
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Boundaries of the 22 ecoregions (grey lines) as defined in the CSMP (Irons et al. 2015) and the Arctic Marine Areas (colored polygons with names in legend). Filled circles show locations of seabird colony sites recommended for monitoring (‘key sites’). The current level of monitoring plan implementation are green = fully implemented, amber = partially implemented, red = not implemented. The CSMP provides implementation maps for each forage guild. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/seabirds" target="_blank">Chapter 3</a> - Page 132 - Figure 3.5.1 This graphic displays the status of seabird monitoring at key sites in CBMP areas across the Arctic.
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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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Maximum LTA (long-term average) August air temperatures for the circumpolar region, with ecoregions used in the analysis of the SAFBR outlined in black. Source for temperature layer: Fick and Hijmans (2017). State of the Arctic Freshwater Biodiversity Report - Chapter 5 - Page 89 - Figure 5-5
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In 2012 and 2013, Fisheries and Oceans Canada conducted benthic imagery surveys in the Davis Strait and Baffin Basin in two areas then closed to bottom fishing, the Hatton Basin Voluntary Closure (now the Hatton Basin Conservation Area) and the Narwhal Closure (now partially in the Disko Fan Conservation Area). The photo transects were established as long-term biodiversity monitoring sites to monitor the impact of human activity, including climate change, on the region’s benthic marine biota in accordance with the protocols of the Circumpolar Biodiversity Monitoring Program established by the Council of Arctic Flora and Fauna. These images were analyzed in a techncial report that summarises the epibenthic megafauna found in seven image transects from the Disko Fan Conservation Area. A total of 480 taxa were found, 280 of which were identified as belonging to one of the following phyla: Annelida, Arthropoda, Brachiopoda, Bryozoa, Chordata, Cnidaria, Echinodermata, Mollusca, Nemertea, and Porifera. The remaining 200 taxa could not be assigned to a phylum and were categorised as Unidentified. Each taxon was identified to the lowest possible taxonomic level, typically class, order, or family. The summaries for each of the taxa include their identification numbers in the World Register of Marine Species and Integrated Taxonomic Information System’s databases, taxonomic hierarchies, images, and written descriptions. The report is intended to provide baseline documentation of the epibenthic megafauna in the Disko Fan Conservation Area, and serve as a taxonomic resource for future image analyses in the Arctic. Baker, E., Beazley, L., McMillan, A., Rowsell, J. and Kenchington, E. 2018. Epibenthic Megafauna of the Disko Fan Conservation Area in the Davis Strait (Eastern Arctic) Identified from In Situ Benthic Image Transects. Can. Tech. Rep. Fish. Aquat. Sci. 3272: vi + 388 p.
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Bacteria and Archaea across five Arctic Marine Areas based on number of operational taxonomic units (OTUs), or molecular species. Composition of microbial groups, with respective numbers of OTUs (pie charts) and number of OTUs at sampling locations (red dots). Data aggregated by the CBMP Sea Ice Biota Expert Network. Data source: National Center for Biotechnology Information’s (NCBI 2017) Nucleotide and PubMed databases. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/sea-ice-biota" target="_blank">Chapter 3</a> - Page 38 - Figure 3.1.2 From the report draft: "Synthesis of available data was performed by using searches conducted in the National Center for Biotechnology Information’s “Nucleotide” (http://www.ncbi.nlm.nih.gov/guide/data-software/) and “PubMed” (http://www.ncbi.nlm.nih.gov/pubmed) databases. Aligned DNA sequences were downloaded and clustered into OTUs by maximum likelihood phylogenetic placement."
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Arctic Marine Areas (AMAs) as defined in the CBMP Marine Plan. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/marine" target="_blank">Chapter 1</a> - Page 15 - Figure 1.2
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The two species of murres, thick-billed Uria lomvia and common U. aalge, both have circumpolar distributions, breeding in Arctic, sub-Arctic and temperate seas from alifornia and N Spain to N Greenland, high Arctic Canada, Svalbard, Franz Josef Land and Novaya Zemlya (Box 4.3 Fig. 1). Conservation of Arctic Flora and Fauna, CAFF 2013 - Akureyri . Arctic Biodiversity Assessment. Status and Trends in Arctic biodiversity. - Birds(Chapter 4) page 163
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Numbers and taxonomic composition of five single-celled eukaryote groups for the regional divisions of the Arctic Marine Areas (pie charts), as well as the number of data sources reviewed across the Arctic (red circles). Total number of taxa is given in parenthesis after each region. Flagellates include: chlorophytes, chrysophytes, cryptophytes, dictyochophytes, euglenids, prasinophytes, prymnesiophytes, raphidophytes, synurales, and xanthophytes, and- for practical purposes though not flagellates - cyanophytes. Heterotrophs include: choanoflagellates, kinetoplastea, incertae sedis. Updated from Poulin et al. (2011). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/sea-ice-biota" target="_blank">Chapter 3</a> - Page 39- Figure 3.1.3 From the report draft: "For a pan-Arctic assessment of diversity (here defined as species richness), the first comprehensive assessments of this FEC from a few years ago (Poulin et al. 2011, Daniëls et al. 2013) have been updated for regions, with taxonomic names standardized according to the World Register of Marine Species (www.marinespecies.org). 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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We present the first digital seafloor geomorphic features map (GSFM) of the global ocean. The GSFM includes 131,192 separate polygons in 29 geomorphic feature categories, used here to assess differences between passive and active continental margins as well as between 8 major ocean regions (the Arctic, Indian, North Atlantic, North Pacific, South Atlantic, South Pacific and the Southern Oceans and the Mediterranean and Black Seas). The GSFM provides quantitative assessments of differences between passive and active margins: continental shelf width of passive margins (88 km) is nearly three times that of active margins (31 km); the average width of active slopes (36 km) is less than the average width of passive margin slopes (46 km); active margin slopes contain an area of 3.4 million km2 where the gradient exceeds 5°, compared with 1.3 million km2 on passive margin slopes; the continental rise covers 27 million km2 adjacent to passive margins and less than 2.3 million km2 adjacent to active margins. Examples of specific applications of the GSFM are presented to show that: 1) larger rift valley segments are generally associated with slow-spreading rates and smaller rift valley segments are associated with fast spreading; 2) polar submarine canyons are twice the average size of non-polar canyons and abyssal polar regions exhibit lower seafloor roughness than non-polar regions, expressed as spatially extensive fan, rise and abyssal plain sediment deposits – all of which are attributed here to the effects of continental glaciations; and 3) recognition of seamounts as a separate category of feature from ridges results in a lower estimate of seamount number compared with estimates of previous workers. Reference: Harris PT, Macmillan-Lawler M, Rupp J, Baker EK Geomorphology of the oceans. Marine Geology.