Injuries and diseases among commercial fishermen in the Northeast Atlantic and Barents Sea. Data from the Royal Norwegian Coast Guard

2003 ◽  
Vol 76 (3) ◽  
pp. 241-245 ◽  
Author(s):  
J. Norum ◽  
E. Endresen
2006 ◽  
Vol 63 (5) ◽  
pp. 840-850 ◽  
Author(s):  
Iciar Martinez ◽  
Michaela Aschan ◽  
Taran Skjerdal ◽  
Salah M. Aljanabi

Abstract The genetic structure of shrimp (Pandalus borealis) in the Northeast Atlantic was examined by RAPD analysis on specimens caught at eight stations in the Barents Sea, three off Svalbard, two off Jan Mayen, and in two northern Norwegian fjords (19 < n > 31 per station). A total of 34 polymorphic markers generated by seven 10-mer arbitrary primers was used to assess the genetic population structure using analysis of molecular variance (AMOVA). There was considerable RAPD diversity (>90%) among shrimp at all stations. The two Norwegian fjords and the Jan Mayen stations were different from all the others, and the Jan Mayen stations also differed from each other. More than 98% of the genetic variation between Barents Sea and Svalbard was ascribed to individual diversity, and there was no significant difference between the two areas, although there seemed to be a subpopulation structure in the Barents Sea. Principal component analysis on the frequency of each RAPD marker on each sampled station confirmed the presence of three populations: Barents Sea and Svalbard, northern Norwegian fjords, and Jan Mayen. We postulate that the large genetic variability found at an individual level may provide the total population with a diverse genetic pool from which traits can be selected to respond to variations in local environmental conditions, and that this local selection may be the cause of the subpopulation structure observed.


2020 ◽  
Vol 11 ◽  
Author(s):  
Deanna Leonard ◽  
Nils Øien

A ship-based mosaic survey of Northeast Atlantic cetaceans was conducted over a 5-year period between 2014–2018. The area surveyed extends from the North Sea in the south (southern boundary at 53oN), to the ice edge of the Barents Sea and the Greenland Sea. Survey vessels were equipped with 2 independent observer platforms that detected whales in passing mode and applied tracking procedures for the target species, common minke whales (Balaenoptera acutorostrata acutorostrata). Here we present abundance estimates for all non-target species for which there were sufficient sightings. We estimate the abundance of fin whales (Balaenoptera physalus) to be 11,387 (CV=0.17, 95% CI: 8,072–16,063), of humpback whales (Megaptera novaeangliae) to be 10,708 (CV=0.38, 95% CI: 4,906–23,370), of sperm whales (Physeter macrocephalus) to be 5,704 (CV=0.26, 95% CI: 3,374–9,643), of killer whales (Orcinus orca) to be 15,056 (CV=0.29, 95% CI: 8,423–26,914), of harbour porpoises (Phocoena phocoena) to be 255,929 (CV=0.20, 95% CI: 172,742–379,175), dolphins of genus Lagenorhynchus to be 192,767 (CV=0.25, 95% CI: 114,033–325,863), and finally of northern bottlenose whales (Hyperoodon ampullatus) to be 7,800 (CV=0.28, 95% CI: 4,373–13,913). Additionally, our survey effort in the Norwegian Sea in 2015 contributed to the 6th North Atlantic Sightings Survey (NASS) and the survey was extended into the waters north and east of Iceland around Jan Mayen island. This NASS extension, along with our Norwegian Sea survey in 2015, was used to estimate the abundance of fin whales, humpback whales, and sperm whales. All estimates presented used mark-recapture distance sampling techniques and were thus corrected for perception bias. Our estimates do not account for additional variance due to distributional shifts between years or biases due to availability or responsive movement.


2000 ◽  
Vol 2 ◽  
pp. 65 ◽  
Author(s):  
Lars P Folkow ◽  
Tore Haug ◽  
Kjell T Nilssen ◽  
Erling S Nordøy

Data on energy requirements, diet composition, and stock size were combined to estimate the consumption of various prey species by minke whales (Balaenoptera acutorostrata) in Northeast Atlantic waters. In the period 1992-1995, the stock of 85,000 minke whales appeared to have consumed more than 1.8 million tonnes of prey per year in coastal waters off northern Norway, in the Barents Sea and around Spitsbergen during an assumed 6 month stay between mid-April and mid-October.Uncertainties in stock estimates suggest a 95% confidence range of 1.4 - 2.1 million tonnes. The point estimate was composed of 602,000 tonnes of krill Thysanoessa spp., 633,000 tonnes of herring Clupea harengus, 142,000 tonnes of capelin Mallotus villosus, 256,000 tonnes of cod Gadus morhua, 128,000 tonnes of haddock Melanogrammus aeglefinus and 54,500 tonnes of other fish species, including saithe Pollaehius virens and sand eel Ammodytes sp. Consumption of various prey items by minke whales may represent an important mortality factor for some of the species. For example, the estimated annual consumption of herring corresponds to about 70% of the herring fisheries in the Northeast Atlantic in 1995. Minke whale diets are subject to year-to-year variations due to changes in the resource base in different feeding areas. Thus, the regional distribution of consumption of different prey items is highly dynamic.


2015 ◽  
Vol 35 ◽  
pp. 9 ◽  
Author(s):  
Andrey Sikorski ◽  
Lyudmila Pavlova

<p>The species <em>Scolelepis finmarchicus</em> sp. nov. is described from the Norwegian and Barents Seas along the northern Norwegian coast and Kola peninsula. The occurrence of this species in the Kola Bay could be seen as a sign of climate warming in the area. Taxonomic issues existing in the genus <em>Scolelepis</em> within the area along the Norwegian coast and in the Barents Sea are briefly touched upon. Seven species belonging to <em>Scolelepis</em> have recently been recorded from the Atlantic sector of the Arctic. <em>Scolelepis</em> (<em>S</em>.) <em>matsugae</em> Sikorski, 1994 is newly synonymized with <em>S</em>. (<em>S</em>.) <em>laonicola</em> (Tzetlin, 1985). This article provides a brief review of <em>Scolelepis</em> together with an identification key for the genus from the Atlantic sector of the Arctic</p>


2009 ◽  
Vol 6 (2) ◽  
pp. 261-264 ◽  
Author(s):  
Anders Frugård Opdal

Prior to the 1920s, the northeast Arctic (NA) cod were caught at spawning grounds ranging from the southernmost to the northernmost parts of the Norwegian coast, but have for the last 50 yr mainly been caught around the Lofoten archipelago and northwards. The NA cod have their feeding and nursery grounds in the Barents Sea, and migrate south towards the Norwegian coast in the winter to spawn. This study uses commercial fisheries' data from landing ports along the entire Norwegian coast during the period 1866–1969 as evidence of long-term truncation and northerly shift of spawning grounds. Nearly all spawning grounds south of Lofoten have been abandoned, while an increasing proportion of the spawning stock only uses the northernmost areas of the Norwegian coast, Troms and Finnmark. The truncation can hardly be attributed to long-term climatic variations, but may result from an intensive size-selective trawl fishery in the Barents Sea causing a sudden increase in fishing mortality, probably altering the size structure and migratory capacity of the stock.


2009 ◽  
Vol 97 (3) ◽  
pp. 234-242 ◽  
Author(s):  
O.P. Pedersen ◽  
K.S. Tande ◽  
T. Pedersen ◽  
D. Slagstad

2016 ◽  
Vol 73 (2) ◽  
pp. 177-188 ◽  
Author(s):  
Geir Huse

Johan Hjort’s so-called second recruitment hypothesis addressed the fate of offspring that drift out of areas suitable for their survival. This hypothesis has forged the concept of a population as a closed life cycle, making countercurrent adult spawning migration a necessary mechanism in balancing larval drift. The Norwegian spring-spawning (NSS) herring stock (Clupea harengus), the object of much of Hjort’s work, is spread over large areas in the Northeast Atlantic, with spawning along the Norwegian coast, nursery areas in the Barents Sea, feeding areas in the Norwegian Sea, and overwintering areas outside northern Norway. Understanding the spatial dynamics of highly migratory fish stocks such as the NSS herring, therefore, is critical to understanding their population dynamics. Here I review hypotheses on the spatial dynamics of fish focusing on NSS herring and discuss consequences for population dynamics and interactions with other ecosystem components. The results illustrate the key role that strong herring cohorts play both as predators in the Barents and Norwegian seas and as prey on the overwintering and spawning grounds along the Norwegian coast. It is advocated that spatial full life cycle models should be developed for key fish stocks as a meeting place for model assumptions and observations and as a test bed for a multiple hypothesis testing approach.


2015 ◽  
Vol 72 (9) ◽  
pp. 2732-2741 ◽  
Author(s):  
Atal Saha ◽  
Lorenz Hauser ◽  
Matthew Kent ◽  
Benjamin Planque ◽  
Francis Neat ◽  
...  

Abstract The identification of isolated populations in widely distributed marine species is often impeded by low levels of genetic differentiation. However, modern genetic approaches now allow for the efficient detection of potentially large numbers of novel genetic variations, thereby improving the power to identify biologically meaningful management units. To investigate the genetic structuring of saithe (Pollachius virens L.), we applied seascape genetic approaches to 131 single nucleotide polymorphism loci genotyped in 584 fish collected from 11 locations across the North Atlantic. Wombling analysis and the Monmonier algorithm revealed four genetic clusters (Barents Sea, Central Northeast Atlantic, Rockall, and Canada) across the species distribution range. These results imply that genetic structuring in saithe may be influenced by abiotic factors such as geographical distance, and bathymetry as well as biotic factors such as sex-biased migration, and natal homing. The results suggest a potential mismatch between management and biological units across the Northeast Atlantic, which may have implications for sustainable exploitation of the species.


2005 ◽  
Vol 62 (5) ◽  
pp. 948-955 ◽  
Author(s):  
Anthony W. Ryan ◽  
Valeria Mattiangeli ◽  
Jarle Mork

Abstract The blue whiting, Micromesistius poutassou (Teleostei, Gadidae) is found between latitudes 26° and 82°N along the continental margin of the Northeast Atlantic, with smaller populations in the Northwest Atlantic and the Mediterranean. There is an annual spawning aggregation on the Porcupine Bank and Hebridean Shelf (west of Ireland and Scotland, respectively), where most of the blue whiting population of the Northeast Atlantic spawns. Analysis of samples from the Barents Sea, the Northeast Atlantic, and the Mediterranean (n = 850, 11 samples) using one minisatellite and five microsatellite loci revealed significant geographic heterogeneity and isolated populations at the extremes of the species range in the Barents Sea and the Mediterranean. Furthermore, there was evidence of genetic heterogeneity among samples taken during the spawning season on the Porcupine Bank and Hebridean Shelf, with highly significant differentiation between the samples taken in the Hebrides in 1992 and 1998.


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