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Population trends for springtails in Empetrum nigrum plant community in Kobbefjord, Greenland, 2007–2017. (a) mean population abundance of total Collembola in individuals per square metre, (b) mean number of species per sample, and (c) Shannon-Wiener diversity index per sample. Vertical error bars are standard errors of the mean. Solid lines indicate significant regression lines. Modified from Gillespie et al. 2020a. STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 40 - Figure 3.13
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Study sites across the Arctic where phenological mismatches between timing of reproduction and peak abundance in food have been studied for terrestrial bird species. Grey symbols show study sites where this phenomenon has been studied for <10 years, light red symbols show sites with >10 years of data but no strong evidence of an increasing mismatch, and dark red symbols indicate sites with >10 years of data and strong evidence of an increasing mismatch. Circles indicate studies of shorebirds, squares for waterfowl and diamonds(triancle) for both shorebirds and passerines. Graphic: Thomas Lameris, adapted from Zhemchuzhnikov (submitted). STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 65 - Figure Box 3.3
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Global catches of Greenland halibut (FAO 2015). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/marine-fishes" target="_blank">Chapter 3</a> - Page 121 - Figure 3.4.8
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Abundance of the copepod Calanus glacialis in the Chukchi Sea, 1945-2012 (after Ershova et al. 2015b). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/plankton" target="_blank">Chapter 3</a> - Page 75 - Figure 3.2.6
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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
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Average relative abundance of the main zooplankton groups (calanoid copepods, cyclopoid copepods, cladocerans) for the sub-Arctic (n=150), low- Arctic (n=154), and high-Arctic (n=55) regions. Samples with a single taxon have been excluded. State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 61 - Figure 4-28
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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
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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
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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."
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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.
CAFF - Arctic Biodiversity Data Service (ABDS)