Abstract:Polymorphisms at five microsatellite DNA loci provide evidence that Atlantic cod Gadus morhua inhabiting Gilbert Bay, Labrador are genetically distinguishable from offshore cod on the north-east Newfoundland shelf and from inshore cod in Trinity Bay, Newfoundland. Antifreeze activity in the blood suggests that Gilbert Bay cod overwinter within the Bay. Gilbert Bay cod are also smaller (weight and length) for their age and consequently less fecund for their age, than cod elsewhere within the northern cod comple… Show more
“…This phenomenon has also been reported recently for cod in Canadian waters (Robichaud & Rose 2001). Genetically distinct sub-populations in bays, inlets and fjords have been identified in Canada (Ruzzante et al 1996a(Ruzzante et al , 1997(Ruzzante et al , 2000 and Iceland (Jonsdottir et al 2002), and among local spawning populations in the North Sea (Hutchinson et al 2001). Tag-release-recapture experiments have shown that the juvenile and adult coastal cod in Norwegian waters tend to remain in their local areas (Salvanes & Ulltang 1992, Jakobsen 1987, Nordeide & Pettersen 1998, Svåsand et al 2000.…”
Section: Local Retention Of Early Life Stagessupporting
This study provides evidence of countergradient variations in life-history traits among coastal cod Gadus morhua off the Norwegian coast, suggesting the existence of sub-populations. One-yr-old wild-caught individuals from 70°N were smaller, grew slower, weighed less, and had a lower condition factor (CF) than southern cod from 60°N during the sampling period from June to February. In contrast, both a higher growth potential and an increase in CF were found in northern cod when offspring of northern and southern cod from the same area and of the same age as the wild cod were housed together in a 'common-garden' experiment. The rapid growth in northern cod was achieved by higher success in food competition when given a restricted amount of food. Active feeding behaviour and larger energy allocation to storage tissues, as suggested by the higher increase in condition, represents adaptations to the high-latitude environment for northern cod and countergradient variation. These differences suggest the existence of genetically distinct sub-populations along the Norwegian coast. Development of sub-populations that differ in behaviour and life-history strategies are discussed in relation to mechanisms for local retention of early life stages and local adaptation of older stages. Sub-populations with different life histories may respond differently to fisheries, and attention to this could be beneficial for improving fisheries management.
“…This phenomenon has also been reported recently for cod in Canadian waters (Robichaud & Rose 2001). Genetically distinct sub-populations in bays, inlets and fjords have been identified in Canada (Ruzzante et al 1996a(Ruzzante et al , 1997(Ruzzante et al , 2000 and Iceland (Jonsdottir et al 2002), and among local spawning populations in the North Sea (Hutchinson et al 2001). Tag-release-recapture experiments have shown that the juvenile and adult coastal cod in Norwegian waters tend to remain in their local areas (Salvanes & Ulltang 1992, Jakobsen 1987, Nordeide & Pettersen 1998, Svåsand et al 2000.…”
Section: Local Retention Of Early Life Stagessupporting
This study provides evidence of countergradient variations in life-history traits among coastal cod Gadus morhua off the Norwegian coast, suggesting the existence of sub-populations. One-yr-old wild-caught individuals from 70°N were smaller, grew slower, weighed less, and had a lower condition factor (CF) than southern cod from 60°N during the sampling period from June to February. In contrast, both a higher growth potential and an increase in CF were found in northern cod when offspring of northern and southern cod from the same area and of the same age as the wild cod were housed together in a 'common-garden' experiment. The rapid growth in northern cod was achieved by higher success in food competition when given a restricted amount of food. Active feeding behaviour and larger energy allocation to storage tissues, as suggested by the higher increase in condition, represents adaptations to the high-latitude environment for northern cod and countergradient variation. These differences suggest the existence of genetically distinct sub-populations along the Norwegian coast. Development of sub-populations that differ in behaviour and life-history strategies are discussed in relation to mechanisms for local retention of early life stages and local adaptation of older stages. Sub-populations with different life histories may respond differently to fisheries, and attention to this could be beneficial for improving fisheries management.
“…The year-round residency of the Gadus morhua population in Gilbert Bay is well documented (Ruzzante et al, 2000;Green & Wroblewski, 2000;Morris & Green, 2002). We collected both juvenile and adult G. morhua, as would be expected for a self-sustaining, local population (Wroblewski et al, 2005).…”
Section: Gilbert Bay Resident Speciesmentioning
confidence: 99%
“…These cod have a reddish or golden-brown colour due to their carotenoid-rich diet of invertebrates (Gosse & Wroblewski, 2004;Wroblewski et al, 2005). The Gilbert Bay cod population is genetically distinguishable from coastal cod of eastern Newfoundland and from offshore cod of the Grand Banks (Ruzzante et al, 2000;Beachem et al, 2002). Gilbert Bay cod are a subpopulation of the northern cod metapopulation (Smedbol & Wroblewski, 2002).…”
The fish fauna of Gilbert Bay, Labrador: a marine protected area in the Canadian subarctic coastal zoneThe Marine Protected Area in Gilbert Bay, Labrador is the first established in the subarctic coastal zone of eastern Canada. A standardized survey of the fish fauna of Gilbert Bay was initiated during the ice-free season of 2004 to provide baseline information on the fish present in water less than 15 m deep. Beach seines and gill-nets sampled three management zones within the bay which are afforded different levels of protection from human activity. The 25 species in 15 families recorded belong to five ecological guilds: (1) estuarine and marine fish resident in the bay; (2) anadromous species transiting the bay; (3) marine species which migrate into the bay to spawn; (4) offshore-spawning marine fish for which the bay is a nursery area; and (5) marine species which occasionally migrate into the bay to feed. Gilbert Bay lies in a transition zone between Arctic and coldtemperate biogeographical provinces, and its fish fauna is dissimilar from a cold-temperate fish assemblage described for Trinity Bay in eastern Newfoundland.
“…Part of the difficulty is that different signals seem to emanate from the various genetic systems used. There is an apparent disagreement among workers about the utility of the various molecular markers for population studies (eg, Frydenberg et al, 1965;Jamieson and Jones, 1967;Mork et al, 1985;Carr et al, 1995;Á rnason et al, 2000;Ruzzante et al, 2000;Jó nsdó ttir et al, 2002).…”
Variation in a 250 base pair (bp) fragment of the mitochondrial cytochrome b (cyt b) has been used extensively for population studies in Atlantic cod Gadus morhua. To study the shape of the gene genealogy and the nature of the polymorphism, sequences of another region of the cyt b gene and the TP intergenic spacer were added, making a total of 566 bp from 74 cod from the Faroe Islands. A total of 44 segregating sites defined 41 haplotypes, many at frequencies greater than 5%. Haplotype diversity was 0.97 and nucleotide diversity 0.73% per base. A topology referred to as a constellation gene genealogy was observed with four major haplotypes at high frequencies, from each of which a number of rare variants were derived. A young relative age of the haplotypes was gauged from the structure of the genealogy. The variation was mostly at synonymous sites within the coding region and thus likely to be neutral or under weak purifying selection. By comparative analysis this also applies to the TP spacer. Applying the locus to study population variation in the Faroe Islands by AMOVA revealed that the overall areas and localities within areas accounted for none of the variation, and all the variation was due to differences among individuals.
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