Temporal trends of arthropod abundance for three habitat types at Zackenberg Research Station, Greenland, 1996–2016. Data are grouped as the FEC ‘arthropod prey for vertebrates’ and separated by habitat type. Solid lines indicate significant regression lines at the p<0.05. Modified from Gillespie et al. 2020a. STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 39 - Figure 3.9

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.

Three-quarters of Octocorallia species are found in deep waters. These cold- water octocoral colonies can form a major constituent of structurally complex habitats. The global distribution and the habitat requirements of deep-sea octocorals are poorly understood given the expense and difficulties of sampling at depth. Habitat suitability models are useful tools to extrapolate distributions and provide an understanding of ecological requirements. Here, we present global habitat suitability models and distribution maps for seven suborders of Octocorallia: Alcyoniina, Calcaxonia, Holaxonia, Scleraxonia, Sessiliflorae, Stolonifera and Subselliflorae. Reference: Yesson C, Taylor ML, Tittensor DP, Davies AJ, Guinotte J, Baco A, Black J, Hall-Spencer JM, Rogers AD (2012) Global habitat suitability of cold-water octocorals. Journal of Biogeography 39:1278–1292.

Trends in abundance of marine mammal Focal Ecosystem Components across each Arctic Marine Area. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - Chapter 4 - Page 182 - Figure 4.6

Results of circumpolar assessment of river benthic macroinvertebrates, indicating (a) the location of river benthic macroinvertebrate stations, underlain by circumpolar ecoregions; (b) ecoregions with many river benthic macroinvertebrate stations, colored on the basis of alpha diversity rarefied to 100 stations; (c) all ecoregions with river benthic macroinvertebrate stations, colored on the basis of alpha diversity rarefied to 10 stations; (d) ecoregions with at least two stations in a hydrobasin, colored on the basis of the dominant component of beta diversity (species turnover, nestedness, approximately equal contribution, or no diversity) when averaged across hydrobasins in each ecoregion. State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 67 - Figure 4-30

Assessment of monitoring implementation STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/marine-mammals" target="_blank">Chapter 3</a> - Page 168 - Table 3.6.2

Appendix 10.2. Data on diversity of lichens and lichenicolous fungi in the Arctic and separately for the sectors of the Arctic (Beringia, Canada, North Atlantic, European Russia, W and E Siberia) and the single floristic provinces: numbers of species, numbers of species in the low and high Arctic, percentage of species with respective growth form (crustose, squamulose, foliose, fruticose), the estimated number of missing crustose lichen species (explanations below), percentage of species on the respective substrate on which the lichen species grow, and rarity of species within and outside the Arctic.

Appendix 17.3. Phylogeographic and population genetics studies of selected Arctic species.

Trends in kittiwake colonies 2001-2010, based on linear regression with year as the explanatory variable. Slope of the regression is red = negative trend, blue = positive trend; shaded circle = significant trend (at p<0.05), open circle = non-significant trend. Non-significant deviation from zero could imply a stable population, but in some cases was due to low sample size and low power. Provided with permission from Descamps et al. (in prep). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/seabirds" target="_blank">Chapter 3</a> - Page 135 - Figure 3.5.3 This figure is compiled from data from researchers working throughout circumpolar regions, primarily members of the Circumpolar Seabird Group, an EN of CAFF/seabirds. Dr. Sebastien Decamps conducted the analysis and produced the original figure; the full results will be available in an article in prep titled: “Descamps et al. in prep. Circumpolar dynamics of black-legged kittiwakes track large-scale environmental shifts and oceans' warming rate.” [expected submission spring 2016]. Colony population trends were analyzed using a linear regression with the year as explanatory variable. Based on slope of the regression (which cannot be exactly 0) colonies are either Declining (Slope of the regression <0) or Increasing (Slope of the regression >0). (Colonies may have had a negative but not significant slope, and could be stable but for some others, the slope is not significant due to small sample size / low power; thus we cannot say that all colonies with a non- significant slope are stable. The threshold was put at 5% to assess the significance of the trend.

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.