Advection of the Red King Crab larvae on the coast of North Norway—A Lagrangian model study

2006 ◽  
Vol 79 (3) ◽  
pp. 325-336 ◽  
Author(s):  
O.P. Pedersen ◽  
E.M. Nilssen ◽  
L.L. Jørgensen ◽  
D. Slagstad
Keyword(s):  
Lagrangian Model ◽  
Red King Crab ◽  
King Crab ◽  
Crab Larvae ◽  
Model Study ◽  
North Norway

Behavior of red king crab larvae: Phototaxis, geotaxis and rheotaxis

1988 ◽  
Vol 13 (4) ◽  
pp. 369-388 ◽  
Author(s):  
Susan M. Shirley ◽  
Thomas C. Shirley
Keyword(s):  
Red King Crab ◽  
King Crab ◽  
Crab Larvae

Temperature and salinity tolerances and preferences of red king crab larvae

1989 ◽  
Vol 16 (1) ◽  
pp. 19-30 ◽  
Author(s):  
Thomas C. Shirley ◽  
Susan M. Shirley
Keyword(s):  
Red King Crab ◽  
King Crab ◽  
Crab Larvae

Selecting species specific vitality metrics to predict red king crab (Paralithodes camtschaticus) discard survival

2021 ◽  
Vol 240 ◽  
pp. 105964
Author(s):  
Cory Lescher ◽  
Noëlle Yochum ◽  
Brad Harris ◽  
Nathan Wolf ◽  
John Gauvin
Keyword(s):  
Red King Crab ◽  
Paralithodes Camtschaticus ◽  
King Crab ◽  
Species Specific

scholarly journals Low allozyme heterozygosity in North Pacific and Bering Sea populations of red king crab (Paralithodes camtschaticus): adaptive specialization, population bottleneck, or metapopulation structure?

2011 ◽  
Vol 68 (3) ◽  
pp. 499-506 ◽  
Author(s):  
W. Stewart Grant ◽  
Susan E. Merkouris ◽  
Gordon H. Kruse ◽  
Lisa W. Seeb
Keyword(s):  
Bering Sea ◽  
North Pacific ◽  
Population Bottleneck ◽  
Ice Age ◽  
Red King Crab ◽  
Paralithodes Camtschaticus ◽  
Allozyme Diversity ◽  
King Crab ◽  
Metapopulation Structure ◽  
Adaptive Specialization

AbstractGrant, W. S., Merkouris, S. E., Kruse, G. H., and Seeb, L. W. 2011. Low allozyme heterozygosity in North Pacific and Bering Sea populations of red king crab (Paralithodes camtschaticus): adaptive specialization, population bottleneck, or metapopulation structure? – ICES Journal of Marine Science, 68: . Populations of red king crab in the North Pacific and Bering Sea have declined in response to ocean-climate shifts and to harvesting. An understanding of how populations are geographically structured is important to the management of these depressed resources. Here, the Mendelian variability at 38 enzyme-encoding loci was surveyed in 27 samples (n = 2427) from 18 general locations. Sample heterozygosities were low, averaging HE = 0.015 among samples. Weak genetic structure was detected among three groups of populations, the Bering Sea, central Gulf of Alaska, and Southeast Alaska, but without significant isolation by distance among populations. A sample from Adak Island in the western Aleutians was genetically different from the remaining samples. The lack of differentiation among populations within regions may, in part, be due to post-glacial expansions and a lack of migration-drift equilibrium and to limited statistical power imposed by low levels of polymorphism. Departures from neutrality may reflect the effects of both selective and historical factors. The low allozyme diversity in red king crab may, in part, be attributable to adaptive specialization, background selection, ice-age population bottlenecks, or metapopulation dynamics in a climatically unstable North Pacific.

scholarly journals Fishery-induced changes in Norwegian red king crab (Paralithodes camtschaticus) reproductive potential

2013 ◽  
Vol 71 (2) ◽  
pp. 365-373 ◽  
Author(s):  
Ann Merete Hjelset
Keyword(s):  
Egg Production ◽  
Barents Sea ◽  
Reproductive Potential ◽  
Size Composition ◽  
Red King Crab ◽  
Paralithodes Camtschaticus ◽  
King Crab ◽  
Males And Females ◽  
Induced Changes ◽  
Individual Fecundity

Abstract Hjelset, A. M. 2014. Fishery-induced changes in Norwegian red king crab (Paralithodes camtschaticus) reproductive potential. – ICES Journal of Marine Science, 71: 365–373. The introduced red king crab (Paralithodes camtschaticus) in the Barents Sea supports a valuable fishery in northern Norway. In this paper, I examine the effect of the increased harvest rate and the recently added female quota on the potential egg production of the stock. The size ranges of males and females in the period 1995–2011 were recorded, and estimated stock abundance of ovigerous females and established individual fecundity parameters from 2000–2007 were used to assess the reproductive potential of the stock from 1995–2011. The upper size ranges of males and females decreased throughout the period studied, presumably mainly due to fishing. The change in size composition among ovigerous females and functional mature males, and the reduced mean individual fecundity in the stock seem to have had a negative effect on the potential egg production of the stock.

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