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  • Temporal patterns in % abundance of Atlantic salmon, brown trout, and anadromous Arctic charr from catch statistics in Iceland rivers monitored from 1992 to 2016, showing results from (a) west, (b) south, (c) north, and (d) east Iceland. State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 81 - Figure 4-41

  • 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

  • Variation of average annual trawling activity (in hours) and macrobenthic biomass (g m-2), (a) and relationship of biomass with a four-year lag (mean value of time of the turnover in biomass value) to trawling activity, (b) along the Kola section of the Barents Sea during 1920-1997 (Denisenko 2001, 2013). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/benthos" target="_blank">Chapter 3</a> - Page 97 - Figure 3.3.5

  • Boundaries of the 22 ecoregions (grey lines) as defined in the CSMP (Irons et al. 2015) and the Arctic Marine Areas (colored polygons with names in legend). Filled circles show locations of seabird colony sites recommended for monitoring (‘key sites’). The current level of monitoring plan implementation are green = fully implemented, amber = partially implemented, red = not implemented. The CSMP provides implementation maps for each forage guild. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/seabirds" target="_blank">Chapter 3</a> - Page 132 - Figure 3.5.1 This graphic displays the status of seabird monitoring at key sites in CBMP areas across the Arctic.

  • Figure 4-5 Terrestrial ecoregions that are included within the circumpolar region within the CAFF boundary and/or the ABA boundaries. Source: Terrestrial Ecoregions of the World (TEOW; Olson et al. 2001). State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 28 - Figure 4-5

  • The number of key sites (monitored colonies) for seabirds (in 22 CSMP ecoregions) by country (a total of 125 sites). Sites are categorized as having fully, partially, or not met the CSMP criteria for parameters monitored (see 2.6.2). Data were from Appendix 3 of the CSMP (Irons et al. 2015); the degree of implementation may have changed at some sites since this summary was compiled. STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/seabirds" target="_blank">Chapter 3</a> - Page 134 - Figure 3.5.2

  • 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.

  • Trends and distribution of muskoxen populations based on Table 3-5. Modified from Cuyler et al. 2020. STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 79 - Figure 3.30

  • Box plot represents the homogeneity of assemblages in high Arctic (n=190), low Arctic (n=370) and sub-Arctic lakes (n=1151), i.e., the distance of individual lake phytoplankton assemblages to the group centroid in multivariate space. The mean distance to the centroid for each of the regions can be seen as an estimated of beta diversity, with increasing distance equating to greater differences among assemblages. State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 48 - Figure 4-18

  • 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.