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Naalakkersuisoq Karl-Kristian Kruses Tale Nordatlantisk
Naalakkersuisoq Karl-Kristian Kruses tale Nordatlantisk Fiskeriministerkonference i Shediac 29. august 2017 Dear friends and colleagues I would like to thank our hosts for this chance to visit beautiful New Brunswick and appreciate the hospitality we have been greeted with here. For Greenland, Canada is our closest neighbour and especially with Nunavut, we share a strong sense of culture. We experience similar challenges. We have strong partnerships on many issues as we share a like-minded approach to a safe and sustainable Arctic development with respect for local culture and traditional ways of life. Together Greenland and Nunavut communicate the cultural and social values of the indigenous peoples of the Arctic. Through cooperation we are able to promote greater understanding of the issues that are important to the people of the Arctic. Therefore, it is indeed a pleasure for us to meet with our friends and colleagues here in New Brunswick to talk about measures to protect our Arctic and North Atlantic Oceans. Intro The protection of the marine environment in Greenland falls under the remit of different ministries. The Ministry of Nature and Environment is responsible for the international agreements and conventions regarding biodiversity and overall nature conservation in Greenland, including protection of the marine environment. The Ministry of Fisheries and Hunting is responsible for the management of all living resources. It is therefore essential, when we talk about ocean governance, that we have close cooperation across sectors. It is also essential that we work across borders as we share marine ecosystems and resources among us. What we have done to protect the marine environment We have in Greenland almost 5 % marine protected areas according to IUCN standards. -
Marine Mammals of Hudson Strait the Following Marine Mammals Are Common to Hudson Strait, However, Other Species May Also Be Seen
Marine Mammals of Hudson Strait The following marine mammals are common to Hudson Strait, however, other species may also be seen. It’s possible for marine mammals to venture outside of their common habitats and may be seen elsewhere. Bowhead Whale Length: 13-19 m Appearance: Stocky, with large head. Blue-black body with white markings on the chin, belly and just forward of the tail. No dorsal fin or ridge. Two blow holes, no teeth, has baleen. Behaviour: Blow is V-shaped and bushy, reaching 6 m in height. Often alone but sometimes in groups of 2-10. Habitat: Leads and cracks in pack ice during winter and in open water during summer. Status: Special concern Beluga Whale Length: 4-5 m Appearance: Adults are almost entirely white with a tough dorsal ridge and no dorsal fin. Young are grey. Behaviour: Blow is low and hardly visible. Not much of the body is visible out of the water. Found in small groups, but sometimes hundreds to thousands during annual migrations. Habitat: Found in open water year-round. Prefer shallow coastal water during summer and water near pack ice in winter. Killer Whale Status: Endangered Length: 8-9 m Appearance: Black body with white throat, belly and underside and white spot behind eye. Triangular dorsal fin in the middle of the back. Male dorsal fin can be up to 2 m in high. Behaviour: Blow is tall and column shaped; approximately 4 m in height. Narwhal Typically form groups of 2-25. Length: 4-5 m Habitat: Coastal water and open seas, often in water less than 200 m depth. -
Sustained Disruption of Narwhal Habitat Use and Behavior in The
Sustained disruption of narwhal habitat use and behavior in the presence of Arctic killer whales Greg A. Breeda,1, Cory J. D. Matthewsb, Marianne Marcouxb, Jeff W. Higdonc, Bernard LeBlancd, Stephen D. Petersene, Jack Orrb, Natalie R. Reinhartf, and Steven H. Fergusonb aInstitute of Arctic Biology, University of Alaska, Fairbanks, AK 99775; bArctic Aquatic Research Division, Fisheries and Oceans Canada, Winnipeg, MB, Canada R3T 2N6; cHigdon Wildlife Consulting, Winnipeg, MB, Canada R3G 3C9; dFisheries Management, Fisheries and Oceans Canada, Quebec, QC, Canada G1K 7Y7; eAssiniboine Park Zoo, Winnipeg, MB, Canada R3R 0B8; and fDepartment of Biological Sciences, University of Manitoba, Winnipeg, MB, Canada R3T 2N2 Edited by James A. Estes, University of California, Santa Cruz, CA, and approved January 10, 2017 (received for review July 17, 2016) Although predators influence behavior of prey, analyses of elec- Electronic tracking tags are also frequently used to track verte- tronic tracking data in marine environments rarely consider how brates in marine systems. Although there is evidence that marine predators affect the behavior of tracked animals. We collected animals adjust their behavior under predation threat (21, 22, 12), an unprecedented dataset by synchronously tracking predator few data or analyses exist showing how predators affect the (killer whales, N = 1; representing a family group) and prey movement of tracked marine animals. These data are lacking (narwhal, N = 7) via satellite telemetry in Admiralty Inlet, a because marine environments are more difficult to observe and large fjord in the Eastern Canadian Arctic. Analyzing the move- tracked animals often move over scales much larger than their ment data with a switching-state space model and a series of terrestrial counterparts, making it difficult to measure predator mixed effects models, we show that the presence of killer whales density in situations where tracking tags are deployed on prey. -
Variation of Bowhead Whale Progesterone Concentrations Across Demographic Groups and Sample Matrices
Vol. 22: 61–72, 2013 ENDANGERED SPECIES RESEARCH Published online November 7 doi: 10.3354/esr00537 Endang Species Res FREEREE ACCESSCCESS Variation of bowhead whale progesterone concentrations across demographic groups and sample matrices Nicholas M. Kellar1,*, Jennifer Keliher1, Marisa L. Trego1,2, Krista N. Catelani1,2, Cyd Hanns3, J. C. ‘Craig’ George3, Cheryl Rosa3 1Protected Resources Division, Southwest Fisheries Science Center, National Marine Fisheries Services, National Oceanic and Atmospheric Administration, 8901 La Jolla Shores Dr., La Jolla, California 92037, USA 2Ocean Associates, 4007 N. Abingdon St., Arlington, Virginia 22207, USA 3North Slope Borough, Department of Wildlife Management, PO Box 69, Barrow, Alaska 99723, USA ABSTRACT: Bowhead whale Balaena mysticetus progesterone concentrations were measured in different sample matrices (serum, blubber, and urine) to investigate (1) concordance among sam- ple type and (2) variation among life-history class. Samples were collected from subsistence- hunted whales (n = 86) taken from 1999 to 2009. In general, irrespective of sample matrix, preg- nant females had the highest concentrations by orders of magnitude, followed by mature animals of both sexes, and subadults had the lowest concentrations. Subadult males and females had sim- ilar progesterone concentrations in all sample matrices measured. When pregnant animals were included in our analyses, permuted regression models indicated a strong positive relationship between serum and blubber progesterone levels (r2 = 0.894, p = 0.0002). When pregnant animals were not included, we found no significant relationship between serum and blubber levels (r2 = 0.025, p = 0.224). These results suggest that progesterone concentrations are mirrored in these sample types over longer periods (i.e. -
Balaenoptera Bonaerensis – Antarctic Minke Whale
Balaenoptera bonaerensis – Antarctic Minke Whale compared to B. bonaerensis. This smaller form, termed the “Dwarf” Minke Whale, may be genetically different from B. bonaerensis, and more closely related to the North Pacific Minke Whales, and thus has been classified B. acutorostrata (Wada et al. 1991; IWC 2001). This taxonomic position, although somewhat controversial, has been accepted by the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), and the Convention on Migratory Species (CMS). Assessment Rationale The current IWC global estimate of abundance of Antarctic Dr. Meike Scheidat Minke Whales is about 500,000 individuals. The abundance estimates declined from about 700,000 for the second circumpolar set of abundance survey cruises Regional Red List status (2016) Least Concern* (1985/86 to 1990/91) to about 500,000 for the third National Red List status (2004) Least Concern (1991/92 to 2003/04). Although this decline was not statistically significant, the IWC Scientific Committee does Reasons for change No change consider these results to reflect a change. However, Global Red List status (2008) Data Deficient whether this change is genuine or attributed to greater proportions of pack ice limiting the survey extent, has not TOPS listing (NEMBA) (2007) None yet been determined. More detailed results from an CITES listing (1986) Appendix I assessment model are available for the mid-Indian to the mid-Pacific region, and suggest that the population Endemic No increased to a peak in 1970 and then declined, with it *Watch-list Data being unclear whether this decline has levelled off or is still continuing past 2000. -
The Bowhead Vs. the Gray Whale in Chukotkan Aboriginal Whaling IGOR I
ARCTIC VOL. 40, NO. 1 (MARCH 1987) P. 16-32 The Bowhead vs. the Gray Whale in Chukotkan Aboriginal Whaling IGOR I. KRUPNIK’ (Received 5 September 1984; accepted in revised form 22 July 1986) ABSTRACT. Active whaling for large baleen whales -mostly for bowhead (Balaena mysricetus) and gray whales (Eschrichrius robustus)-has been practiced by aborigines on the Chukotka Peninsula since at least the early centuries of the Christian era. Thehistory of native whaling off Chukotka may be divided into four periods according to the hunting methods used and the primary species pursued: ancient or aboriginal (from earliest times up to the second half of the 19th century); rraditional (second half of the 19th century to the1930s); transitional (late 1930s toearly 1960s); and modern (from the early 1960s). The data on bowhead/gray whale bone distribution in theruins of aboriginal coastal sites, available catch data from native settlements from the late 19th century and local oral tradition prove to be valuable sources for identifying specific areas of aboriginal whaling off Chukotka. Until the 1930s, bowhead whales generally predominated in the native catch; gray whales were hunted periodically or locally along restricted parts of the coast. Some 8-10 bowheads and 3-5 gray whales were killed on the average in a “good year”by Chukotka natives during the early 20th century. Around the mid-20th century, however, bowheads were completely replaced by gray whales. On the basis of this experience, the author believes that the substitution of gray whales for bowheads, proposed recently by conservationists for modemAlaska Eskimos, would be unsuccessful. -
Order CETACEA Suborder MYSTICETI BALAENIDAE Eubalaena Glacialis (Müller, 1776) EUG En - Northern Right Whale; Fr - Baleine De Biscaye; Sp - Ballena Franca
click for previous page Cetacea 2041 Order CETACEA Suborder MYSTICETI BALAENIDAE Eubalaena glacialis (Müller, 1776) EUG En - Northern right whale; Fr - Baleine de Biscaye; Sp - Ballena franca. Adults common to 17 m, maximum to 18 m long.Body rotund with head to 1/3 of total length;no pleats in throat; dorsal fin absent. Mostly black or dark brown, may have white splotches on chin and belly.Commonly travel in groups of less than 12 in shallow water regions. IUCN Status: Endangered. BALAENOPTERIDAE Balaenoptera acutorostrata Lacepède, 1804 MIW En - Minke whale; Fr - Petit rorqual; Sp - Rorcual enano. Adult males maximum to slightly over 9 m long, females to 10.7 m.Head extremely pointed with prominent me- dian ridge. Body dark grey to black dorsally and white ventrally with streaks and lobes of intermediate shades along sides.Commonly travel singly or in groups of 2 or 3 in coastal and shore areas;may be found in groups of several hundred on feeding grounds. IUCN Status: Lower risk, near threatened. Balaenoptera borealis Lesson, 1828 SIW En - Sei whale; Fr - Rorqual de Rudolphi; Sp - Rorcual del norte. Adults to 18 m long. Typical rorqual body shape; dorsal fin tall and strongly curved, rises at a steep angle from back.Colour of body is mostly dark grey or blue-grey with a whitish area on belly and ventral pleats.Commonly travel in groups of 2 to 5 in open ocean waters. IUCN Status: Endangered. 2042 Marine Mammals Balaenoptera edeni Anderson, 1878 BRW En - Bryde’s whale; Fr - Rorqual de Bryde; Sp - Rorcual tropical. -
Geology of Greenland Bulletin 185, 67-93
Sedimentary basins concealed by Acknowledgements volcanic rocks The map sheet was compiled by J.C. Escher (onshore) In two areas, one off East Greenland between latitudes and T.C.R. Pulvertaft (offshore), with final compilation 72° and 75°N and the other between 68° and 73°N off and legend design by J.C. Escher (see also map sheet West Greenland, there are extensive Tertiary volcanic legend). In addition to the authors’ contributions to the rocks which are known in places to overlie thick sedi- text (see Preface), drafts for parts of various sections mentary successions. It is difficult on the basis of exist- were provided by: L. Melchior Larsen (Gardar in South ing seismic data to learn much about these underlying Greenland, Tertiary volcanism of East and West Green- sediments, but extrapolation from neighbouring onshore land); G. Dam (Cretaceous–Tertiary sediments of cen- areas suggests that oil source rocks are present. tral West Greenland); M. Larsen (Cretaceous–Tertiary Seismic data acquired west of Disko in 1995 have sediments in southern East Greenland); J.C. Escher (map revealed an extensive direct hydrocarbon indicator in of dykes); S. Funder (Quaternary geology); N. Reeh the form of a ‘bright spot’ with a strong AVO (Amplitute (glaciology); B. Thomassen (mineral deposits); F.G. Versus Offset) anomaly, which occurs in the sediments Christiansen (petroleum potential). Valuable comments above the basalts in this area. If hydrocarbons are indeed and suggestions from other colleagues at the Survey are present here, they could either have been generated gratefully acknowledged. below the basalts and have migrated through the frac- Finally, the bulletin benefitted from thorough reviews tured lavas into their present position (Skaarup & by John Korstgård and Hans P. -
Greenland Turbot Assessment
6HFWLRQ STOCK ASSESSMENT OF GREENLAND TURBOT James N. Ianelli, Thomas K. Wilderbuer, and Terrance M. Sample 6XPPDU\ Changes to this year’s assessment in the past year include: 1. new summary estimates of retained and discarded Greenland turbot by different target fisheries, 2. update the estimated catch levels by gear type in recent years, and 3. new length frequency and biomass data from the 1998 NMFS eastern Bering Sea shelf survey. Conditions do not appear to have changed substantively over the past several years. For example, the abundance of Greenland turbot from the eastern Bering Sea (EBS) shelf-trawl survey has found only spotty quantities with very few small fish that were common in the late 1970s and early 1980s. The majority of the catch has shifted to longline gear in recent years. The assessment model analysis was similar to last year but with a slightly higher estimated overall abundance. We attribute this to a slightly improved fit to the longline survey data trend. The target stock size (B40%, female spawning biomass) is estimated at about 139,000 tons while the projected 1999 spawning biomass is about 110,000 tons. The adjusted yield projection from F40% computations is estimated at 20,000 tons for 1999, and increase of 5,000 from last year’s ABC. Given the continued downward abundance trend and no sign of recruitment to the EBS shelf, extra caution is warranted. We therefore recommend that the ABC be set to 15,000 tons (same value as last year). As additional survey information become available and signs of recruitment (perhaps from areas other than the shelf) are apparent, then we believe that the full ABC or increases in harvest may be appropriate for this species. -
Fin Whale Balaenoptera Physalus
Natural Heritage Fin Whale & Endangered Species Balaenoptera physalus Program State Status: Endangered www.mass.gov/nhesp Federal Status: Endangered Massachusetts Division of Fisheries & Wildlife DESCRIPTION: Fin Whales can weigh between 40 and 80 tons and measure 22 to 26 meters long, second in size only to the Blue Whale. Females tend to be slightly larger than males by 5-10%. Fin Whales have a sleek, streamlined body with a V-shaped head and are dark grey to brown on top, with white underneath. They have a tall, hooked, dorsal fin located two-thirds of the way down their body. Fin Whales are commonly called Razorbacks for the ridges on the middle of the back behind the dorsal fin. The unique asymmetrical coloration on the head easily separates this species from all of the other baleen whales. On the right side, the lower jaw is white, and the baleen plates in the front half of the mouth are also white, but abruptly change to dark Photo courtesy of NOAA in the back half of the mouth. By contrast, the lower left jaw is gray and all of the baleen plates on the left side are dark. This coloration may aid in herding fish during east of Boston and Cape Ann. Although there are feeding, although its primary purpose is unknown. seasonal fluctuations, the Fin Whale is most common in New England from April to November. Massachusetts RANGE: Fin Whales prefer deep, offshore waters of all waters are a major feeding ground for Fin Whales on the the major oceans, primarily in temperate and polar east coast of the U.S. -
Movements of a Deep-Water Fish: Establishing Marine Fisheries Management Boundaries in Coastal Arctic Waters
University of Windsor Scholarship at UWindsor Biological Sciences Publications Department of Biological Sciences 2017 Movements of a deep-water fish: Establishing marine fisheries management boundaries in coastal Arctic waters Nigel E. Hussey University of Windsor K. J. Hedges A. N. Barkley M. A. Treble I. Peklova See next page for additional authors Follow this and additional works at: https://scholar.uwindsor.ca/biologypub Part of the Biology Commons Recommended Citation Hussey, Nigel E.; Hedges, K. J.; Barkley, A. N.; Treble, M. A.; Peklova, I.; Webber, D. M.; Ferguson, S. H.; Yurkowski, D. J.; Kessel, S. T.; Bedard, J. M.; and Fisk, A. T., "Movements of a deep-water fish: Establishing marine fisheries management boundaries in coastal Arctic waters" (2017). Ecological Applications, 27, 3, 687-704. https://scholar.uwindsor.ca/biologypub/813 This Article is brought to you for free and open access by the Department of Biological Sciences at Scholarship at UWindsor. It has been accepted for inclusion in Biological Sciences Publications by an authorized administrator of Scholarship at UWindsor. For more information, please contact [email protected]. Authors Nigel E. Hussey, K. J. Hedges, A. N. Barkley, M. A. Treble, I. Peklova, D. M. Webber, S. H. Ferguson, D. J. Yurkowski, S. T. Kessel, J. M. Bedard, and A. T. Fisk This article is available at Scholarship at UWindsor: https://scholar.uwindsor.ca/biologypub/813 INVITED FEATURE Ecological Applications, 27(3), 2017, pp. 687–704 © 2016 by the Ecological Society of America Movements of a deep- water fish: establishing marine fisheries management boundaries in coastal Arctic waters NIGEL E. -
Taxonomic Status of the Genus Sotalia: Species Level Ranking for “Tucuxi” (Sotalia Fluviatilis) and “Costero” (Sotalia Guianensis) Dolphins
MARINE MAMMAL SCIENCE, **(*): ***–*** (*** 2007) C 2007 by the Society for Marine Mammalogy DOI: 10.1111/j.1748-7692.2007.00110.x TAXONOMIC STATUS OF THE GENUS SOTALIA: SPECIES LEVEL RANKING FOR “TUCUXI” (SOTALIA FLUVIATILIS) AND “COSTERO” (SOTALIA GUIANENSIS) DOLPHINS S. CABALLERO Laboratory of Molecular Ecology and Evolution, School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand and Fundacion´ Omacha, Diagonal 86A #30–38, Bogota,´ Colombia F. TRUJILLO Fundacion´ Omacha, Diagonal 86A #30–38, Bogota,´ Colombia J. A. VIANNA Sala L3–244, Departamento de Biologia Geral, ICB, Universidad Federal de Minas Gerais, Avenida Antonio Carlos, 6627 C. P. 486, 31270–010 Belo Horizonte, Brazil and Escuela de Medicina Veterinaria, Facultad de Ecologia y Recursos Naturales, Universidad Andres Bello Republica 252, Santigo, Chile H. BARRIOS-GARRIDO Laboratorio de Sistematica´ de Invertebrados Acuaticos´ (LASIA), Postgrado en Ciencias Biologicas,´ Facultad Experimental de Ciencias,Universidad del Zulia, Avenida Universidad con prolongacion´ Avenida 5 de Julio, Sector Grano de Oro, Maracaibo, Venezuela M. G. MONTIEL Laboratorio de Ecologıa´ y Genetica´ de Poblaciones, Centro de Ecologıa,´ Instituto Venezolano de Investigaciones Cientıficas´ (IVIC), San Antonio de los Altos, Carretera Panamericana km 11, Altos de Pipe, Estado Miranda, Venezuela S. BELTRAN´ -PEDREROS Laboratorio de Zoologia,´ Colec¸ao˜ Zoologica´ Paulo Burheim, Centro Universitario´ Luterano de Manaus, Manaus, Brazil 1 2 MARINE MAMMAL SCIENCE, VOL. **, NO. **, 2007 M. MARMONTEL Sociedade Civil Mamiraua,´ Rua Augusto Correa No.1 Campus do Guama,´ Setor Professional, Guama,´ C. P. 8600, 66075–110 Belem,´ Brazil M. C. SANTOS Projeto Atlantis/Instituto de Biologia da Conservac¸ao,˜ Laboratorio´ de Biologia da Conservac¸ao˜ de Cetaceos,´ Departamento de Zoologia, Universidade Estadual Paulista (UNESP), Campus Rio Claro, Sao˜ Paulo, Brazil M.