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

Interannual differences in taxonomic composition of phytoplankton during summer in a) Kongsfjorden and b) Rijpfjorden (Source: MOSJ, Norwegian Polar Institute). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/plankton" target="_blank">Chapter 3</a> - Page 74 - Figure 3.2.5

Circumpolar map of known polynyas. Note that polynyas are dynamic systems and some may no longer exist in the form known from their recent history. Adapted from Meltofte (2013) and based on Barber and Massom (2007). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/marine" target="_blank">Chapter 2</a> - Page 28 - Figure 2.5

Average September sea ice extent in 1979 (blue) compared with 2016 (white) and the median sea ice extent (yellow line) from 1981 to 2010 (Data: NSDIC 2016). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/marine" target="_blank">Chapter 2</a> - Page 27 - Figure 2.4

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.

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

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

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

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