Several smaller populations of caribou inhabit sub-Arctic portions of Alaska, including five populations along the Aleutian Archipelago and west coast. These populations are considered part of the migratory tundra ecotype based on genetics, although in some instances their ecology and habitat are similar to the mountain caribou ecotype found in western Canada. Population dynamics and trends for these populations are variable (Figure 3-29). They are managed by the Alaska Department of Fish and Game through hunting quotas. STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 72 - Figure 3.29

Workflow of the Circumpolar Biodiversity Monitoring Program (CBMP). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/marine" target="_blank">Chapter 1</a> - Page 13 - Figure 1.1

Trends in Arctic terrestrial bird population abundance for four taxonomic groupings in four global flyways. Data are presented as total number of taxa (species, subspecies). Modified from Smith et al. 2020. These broad patterns were generally consistent across flyways, with some exceptions. Fewer waterfowl populations increased in the Central Asian and East Asian–Australasian Flyways. The largest proportion of declining species was among the waders in all but the Central Asian Flyway where the trends of a large majority of waders are unknown. Although declines were more prevalent among waders than other taxonomic groups in both the African–Eurasian and Americas Flyways, the former had a substantially larger number of stable and increasing species than the latter (Figure 3-23). STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 55 - Figure 3.23

Figure 4 23 Species richness of aquatic macrophytes excluding mosses and algae in five geographic regions of the Arctic. Ame = North America, Fen = Fennoscandia, Far = Faroes, Ice = Iceland, Gre = Greenland. State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 55 - Figure 4-22

Regional differences are more pronounced in the insectivore guild (Figure 3-24). Although diversity of waders was moderate in the East Asian–Australasian Flyway, 88% (15 of 17) of taxa with known trends were declining—the largest proportion of any group. Both short-term (the last 15 years) and long-term (more than 30 years) trends were available for 157 taxa. Trends were unchanged over the two time periods for 80% of taxa, improved for 11% and worsened for 9%.. STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 56 - Figure 3.24

The Arctic marine food web includes the exchange of energy and nutrition, and also provides cultural, social and spiritual meaning for human communities. Adapted from Darnis et al. (2012) and Inuit Circumpolar Council-Alaska (2015). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/marine" target="_blank">Chapter 2</a> - Page 23 - Figure 2.2a

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.

Map of Arctic Marine Areas as defined by the Circumpolar Biodiversity Monitoring Program (CBMP), with one sample finding from each area.

Megafauna distribution of biomass (g/15 min trawling) in the Barents Sea in 2007, 2011 and 2015. The green circles show the distribution of the snow crab as it spreads from east to west, and the blue triangles show the invasion of king crab along the coast of the southern Barents Sea. Data from Institute of Marine Research, Norway and the 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 95 - Figure 3.3.2 The annual joint Norwegian–Russian Ecosystem Survey provides from more than 400 stations and during extensive cruise tracks covering more or less the whole Barents Sea in August– September. The sampling is based on a regular grid spanning about 1.5 millionkm2 with fixed positions of stations which make it possible to measure changes in spatial distribution over time. The trawl is a Campelen 1800 bottom trawl rigged with rock-hopper groundgear and towed on double Warps. The mesh size is 80 mm (stretched) in the front and 16–22 mmin the cod end, allowing the capture and retention of smaller fish and the largest benthos from the seabed (benthic megafauna). The horizontal opening was 11.7 m, and the vertical opening 4–5 m (Teigsmark and Øynes, 1982). The trawl configuration and bottom contact was monitored remotely by SCANMAR trawl sensors. The standard distance between trawl stations was 35 nautical miles (65 km), except north and west of Svalbard where a stratified sampling was adapted to the steep continental shelve. The standard procedure was to tow 15 min after the trawl had made contact with the bottom, but the actual tow duration ranged between 5 min and 1 h and data were subsequently standardized to 15 min trawl time. Towing speed was 3 knots, equivalent to a towing distance of 0.75 nautical miles (1.4 km) during a 15 min tow. The trawl catches were recorded using the same procedures on the Russian and the Norwegian Research vessels to ensure comparability across Barents Sea regions. The benthic megafauna was separated from the fish and shrimp catch, washed, and sorted to lowest possible taxonomic level, in most cases to species, on-Board the vessel. Species identification was standardized between the researcher teams by annually exchanging the benthic expert’s among the vessels and taxon names were fixed each year according toWORMSwhen possible.This resulted in an Electronic identification manual and photo-compendium as a tool to standardize taxon identifications, in addition to various sources of identification literature. Difficult taxa were photographed and, in some cases, brought back as preserved voucher specimens for further identification. Wet-weight biomass was recorded with electronic scales in the ship laboratories for each taxon.The biomass determination included all fragments.

Temporal patterns in % abundance of Atlantic salmon, brown trout, and anadromous Arctic charr from catch statistics in northern Norway rivers monitored from 1993 to 2016, including basins dominated by (a) rivers and (b) lakes. State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 81- Figure 4-42