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  • 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.

  • Estimated consumption of polar cod by Atlantic cod in the Barents Sea (yellow line) and biomass of the Atlantic cod stock in the Barents Sea (red line) (ICES 2016). The blue line is the biomass of the Barents Sea polar cod (Prozorkevich 2016). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/marine-fishes" target="_blank">Chapter 3</a> - Page 116 - Box figure 3.4.1

  • 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.

  • Multi-decadal time series of A) abundance (individuals m-2) and B) biomass (g wet weight m-2) of ice amphipods from 1977 to 2012 across the Arctic. Bars and error bars indicate median and median absolute deviation (MAD) values for each year, respectively. Numbers above bars represent number of sampling efforts (n). Modified from Hop et al. (2013). STATE OF THE ARCTIC MARINE BIODIVERSITY REPORT - <a href="https://arcticbiodiversity.is/findings/sea-ice-biota" target="_blank">Chapter 3</a> - Page 45 - Figure 3.1.7 From the report draft: "The only available time-series of sympagic biota is based on composite data of ice-amphipod abundance and biomass estimates from the 1980s to present across the Arctic, with most observations from the Svalbard and Fram Strait region (Hop et al. 2013). Samples were obtained by SCUBA divers who collected amphipods quantitatively with electrical suction pumps under the sea ice (Lønne & Gulliksen 1991a, b, Hop & Pavlova 2008)."

  • Arctic foxes are currently monitored at 34 sites throughout the North, with most monitoring efforts concentrated in Fennoscandia (Figure 3-32). The duration of monitoring across all sites is variable at between 2 and 56 years and was ongoing at 27 of the 34 sites (79%) as of 2015. Monitoring projects cover almost equally the four climate zones of the species’ distribution—high Arctic, low Arctic, sub-Arctic, and montane/alpine. STATE OF THE ARCTIC TERRESTRIAL BIODIVERSITY REPORT - Chapter 3 - Page 82 - Figure 3.32

  • Colored Dissolved Organic Matter (CDOM) is a measurement of the absorption of light in the UV and visible spectrum by the colored components of dissolved organic carbon. It is essentially the yellow substance in water as a result of decaying detritus. It is important to measure because it limits the amount of sunlight penetration, and thus restricts the growth of plankton populations. It is measured in a unit-less CDOM index. Data generated as part of CAFFs Circumpolar Biodiversity Monitoring Program (CAFF) and its Land Cover Change Initiative (LCC) Trends visible in the MODIS dataset show an overall decrease in the mean CDOM from 2003 to 2012, with a percent change of -31.7%. This trend can be seen in Figure 40. This decrease corresponds to the increase in total yearly primary productivity (Figure 30), as a decrease in the CDOM allows for sunlight to penetrate deeper into the water, boosting chlorophyll concentrations and thus primary productivity.

  • The U.S. National Ice Center (NIC) is an inter-agency sea ice analysis and forecasting center comprised of the Department of Commerce/NOAA, the Department of Defense/U.S. Navy, and the Department of Homeland Security/U.S. Coast Guard components. Since 1972, NIC has produced Arctic and Antarctic sea ice charts. This data set is comprised of Arctic sea ice concentration climatology derived from the NIC weekly or biweekly operational ice-chart time series. The charts used in the climatology are from 1972 through 2007; and the monthly climatology products are median, maximum, minimum, first quartile, and third quartile concentrations, as well as frequency of occurrence of ice at any concentration for the entire period of record as well as for 10-year and 5-year periods. NIC charts are produced through the analyses of available in situ, remote sensing, and model data sources. They are generated primarily for mission planning and safety of navigation. NIC charts generally show more ice than do passive microwave derived sea ice concentrations, particularly in the summer when passive microwave algorithms tend to underestimate ice concentration. The record of sea ice concentration from the NIC series is believed to be more accurate than that from passive microwave sensors, especially from the mid-1990s on (see references at the end of this documentation), but it lacks the consistency of some passive microwave time series. Source: <a href="http://nsidc.org/data/G02172" target="_blank">NSIDC</a> Reference: National Ice Center. 2006, updated 2009. National Ice Center Arctic sea ice charts and climatologies in gridded format. Edited and compiled by F. Fetterer and C. Fowler. Boulder, Colorado USA: National Snow and Ice Data Center. Source: <a href="http://nsidc.org/data/G02172" target="_blank">NSIDC</a>

  • Estimation of diatom assemblage changes over a period of about 200 years (top versus bottom sediment cores). State of the Arctic Freshwater Biodiversity Report - Chapter 4 - Page 41 - Figure 4-14

  • 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.

  • In 2012 and 2013, Fisheries and Oceans Canada conducted benthic imagery surveys in the Davis Strait and Baffin Basin in two areas then closed to bottom fishing, the Hatton Basin Voluntary Closure (now the Hatton Basin Conservation Area) and the Narwhal Closure (now partially in the Disko Fan Conservation Area). The photo transects were established as long-term biodiversity monitoring sites to monitor the impact of human activity, including climate change, on the region’s benthic marine biota in accordance with the protocols of the Circumpolar Biodiversity Monitoring Program established by the Council of Arctic Flora and Fauna. These images were analyzed in a techncial report that summarises the epibenthic megafauna found in seven image transects from the Disko Fan Conservation Area. A total of 480 taxa were found, 280 of which were identified as belonging to one of the following phyla: Annelida, Arthropoda, Brachiopoda, Bryozoa, Chordata, Cnidaria, Echinodermata, Mollusca, Nemertea, and Porifera. The remaining 200 taxa could not be assigned to a phylum and were categorised as Unidentified. Each taxon was identified to the lowest possible taxonomic level, typically class, order, or family. The summaries for each of the taxa include their identification numbers in the World Register of Marine Species and Integrated Taxonomic Information System’s databases, taxonomic hierarchies, images, and written descriptions. The report is intended to provide baseline documentation of the epibenthic megafauna in the Disko Fan Conservation Area, and serve as a taxonomic resource for future image analyses in the Arctic. Baker, E., Beazley, L., McMillan, A., Rowsell, J. and Kenchington, E. 2018. Epibenthic Megafauna of the Disko Fan Conservation Area in the Davis Strait (Eastern Arctic) Identified from In Situ Benthic Image Transects. Can. Tech. Rep. Fish. Aquat. Sci. 3272: vi + 388 p.