Time series of relative proportions of Arctic and Atlantic Calanus species in Kongsfjorden (top) and Rijpfjorden (bottom) (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 77 - Figure 3.2.8

In 2017 the SAMBR synthesized data about biodiversity in Arctic marine ecosystems around the circumpolar Arctic.. SAMBR highlighted observed changes and relevant monitoring gaps. This 2021 update provides information on the status of marine mammals in the Arctic from 2015–2020: More detail can be found in the Marine Mammals 2021 Technical report. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT

Distributions of all capelin species (light green) and Pacific capelin (Mallotus catervarius; dark green pattern) based on participation in research sampling, examination of museum voucher collections, the literature and molecular genetic analysis (Mecklenburg and Steinke 2015, Mecklenburg et al. 2016). 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 117 - Figure 3.4.5

Ice algal community similarity of central Russian Arctic drifting stations from the 1980s to 2010s based on unpublished data by I.A. Melnikov, Shirshov Institute of Oceanology.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."

Arthropods (e.g., shrimps, crabs, sea spiders, amphipods, isopods) dominate taxon numbers in all Arctic regions, followed by polychaetes (e.g., bristle worms) and mollusks (e.g., gastropods, bivalves). Other taxon groups are diverse in some regions, such as bryozoans in the Kara Sea, cnidarians in the Atlantic Arctic, and foraminiferans in the Arctic deep-sea basins. This pattern is biased, however, by the meiofauna inclusion for the Arctic Basin (macro- and meiofauna size ranges overlap substantially in deep-sea fauna, so nematodes and foraminiferans are included) and the influence of a lack of specialists for some difficult taxonomic groups. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/benthos" target="_blank">Chapter 3</a> - Page 89 - Box figure 3.3.1 Each region of the Pan Arctic has been sampled with a set of different sampling gears, including grab, sledge and trawl, while other areas has only been sampled with grab. Here is the complete species/taxa number and the % distribution of species/taxa in main phyla, per region of the Pan Arctic.

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

Figure 3.2.1a: Map of high throughput sequencing records from the Arctic Marine Areas. Figure 3.2.1b: Map of records of phytoplankton taxa using microscopy from the Arctic Marine Areas. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/plankton" target="_blank">Chapter 3</a> - Page 35 - Figure 3.2.1a and Figure 3.2.1b In terms of stations sampled, the greatest sampling effort of high-throughput sequencing in Arctic marine water columns, by far, has been in the Beaufort Sea/Amundsen Gulf region and around Svalbard. High through-put sequencing has also been used on samples from the Chukchi Sea, Canadian Arctic Archipelago, Baffin Bay, Hudson Bay, the Greenland Sea and Laptev Sea.

Cumulative scores of various environmental and anthropogenic drivers of change of the benthic ecosystem across the eight Arctic Marine Areas (AMA). A cumulative score is the median score of sub-regions per AMA (Table 3.3.1). Median score for the whole Arctic is given in the centre. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/benthos" target="_blank">Chapter 3</a> - Page 100 - Figure 3.3.7

Seasonal abundance (1000 individuals m- 2) of sea ice meiofauna at landfast sea ice (Barrow, 2005-2006, A and C) and pack ice (North of Svalbard, 2015, B and D). A and B show larval stages (polychaete juveniles and nauplii, respectively), while C and D show nematodes and harpacticoid copepods, respectively. Circles represent individual cores (n = 107 for A and C, and 39 for B and D), shading the extent of minimum as well as maximum values, and blue line indicates mean values. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/sea-ice-biota" target="_blank">Chapter 3</a> - Page 43 - Figure 3.1.5 From the report draft: "In addition to showing composition and peak abundance ranges, we illustrate the phenology of ice meiofauna over the ice-covered season in the entire combined data set. For this purpose, the data were normalized to the daylight hours at each location during the date of sampling using R package geosphere (Hijmans 2015) and a method described in Forsythe et al. (1995). This was necessary, because ‘spring’ arrives earlier at lower latitudes than at higher latitudes, so that using month or day of year would obscure the pan-Arctic integration of the data. Other influential factors such as snow depth, ice thickness and nutrient concentrations were not accounted for in this analysis."

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."