Bird and distance transect biodiversity GRID data from Barrow, Alaska-

Number of marine mammal species in Arctic marine regions classified by resident species (n = 11 total) or all species (including seasonal visitors, n = 35 total). CAFF 2013. Arctic Biodiversity Assessment. Status and Trends in Arctic biodiversity. Conservation of Arctic Flora and Fauna, Akureyri - Mammal (Chapter 3) page 84

<img src="http://geo.abds.is/geonetwork/srv/eng//resources.get?uuid=59d822e4-56ce-453c-b98d-40207a2e9eec&fname=cbmp_small.png" alt="logo" height="67px" align="left" hspace="10px"> The Arctic marine data set contains a total of 111 species and 310 population time series from 170 locations. Species coverage is about 34% of Arctic marine vertebrate species (100% of mammals, 53% of birds, and 27% of fishes) (Bluhm et al. 2011). At the species level, even though the representation of Arctic fish species is lower than that of mammals and birds, the data are dominated by fishes, primarily from the Pacific Ocean (especially the Bering Sea and Aleutian Islands). However, there are more population time series in total for bird species, which is reflective of this group being both better studied historically and also monitored at many small study sites compared to fish and marine mammal species, which are regularly monitored at a much larger scale through stock management. Note that the time span selected for marine analyses is 1970 to 2005 (compared with 1970 to 2007 for the ASTI for all species). CAFF Assessment Series No. 7 April 2012 - <a href=http://caff.is/asti/asti-publications/28-arctic-species-trend-index-tracking-trends-in-arctic-marine-populations" target="_blank"> The Arctic Species Trend Index - Tracking trends in Arctic marine populations </a>

A national Canadian Science Advisory Secretariat (CSAS) science advisory process was held in Winnipeg, Manitoba from June 14-17, 2011 to provide science advice on the identification of Ecologically and Biologically Significant Areas (EBSAs) in the Canadian Arctic based on guidance developed by Fisheries and Oceans Canada. This science advisory process focused on the identification of EBSAs within the following marine biogeographic units: the Hudson Bay Complex, the Arctic Basin, the Western Arctic, the Canadian Arctic Archipelago and the Eastern Arctic. Source: <a href="http://www.dfo-mpo.gc.ca/Library/344747.pdf" target="_blank">Fisheries and Oceans Canada</a> Reference: DFO. 2011. Identification of Ecologically and Biologically Significant Areas (EBSA) in the Canadian Arctic. DFO Can. Sci. Advis. Sec. Sci. Advis. Rep. 2011/055. DFO. 2011. Identification of Ecologically and Biologically Significant Areas (EBSAs) in the Canadian Arctic; June 14-17, 2011. DFO Can. Sci. Advis. Sec. Proceed. Ser. 2011/047.

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.

Boundaries of the geographic area covered by the Arctic Biodiversity Assessment. Includes sub, low and high Arctic bounbaries

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."

Locations and associated attributes of circumpolar Muskox studies. Attributes include animal count, population estimate, estimate error and associated report citation.

Commercial fishery impact on zoobenthos of the Barents Sea. Figure A) Intensity and duration of fishery efforts in standard commercial fishery areas in the Barents Sea. The darker the area the longer the fishery has been in operation. Figure B) Level of decline in macrobenthic biomass between 1926-1932 and 1968-1970 calculated as 1-b1968/b1930. The largest biomass decreases correspond to the darker colour, whereas lighter colour refers to no change (Denisenko 2013). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/benthos" target="_blank">Chapter 3</a> - Page 97 - Figure 3.3.4

Abiotic drivers in North America, including (a) long-term average maximum August air temperature, (b) spatial distribution of ice sheets in the last glaciation of the North American Arctic region, and (c) geological setting of bedrock geology underlying North America. Panel (a) source Fick and Hijmans (2017). Panel (b) adapted from: Physical Geology by Steve Earle, freely available at http://open.bccampus.ca. Panel (c) source: Geogratis. State of the Arctic Freshwater Biodiversity Report - Chapter 5 - Page 86 - Figure 5-3