Single Locus Minisatellite DNA Variation in European Populations of Atlantic Salmon (Salmo Salar L.)

Hereditas ◽  
2004 ◽  
Vol 126 (3) ◽  
pp. 269-275 ◽  
Author(s):  
C. E. Stone ◽  
J. B. Taggarti ◽  
A. Ferguson
1995 ◽  
Vol 52 (11) ◽  
pp. 2305-2311 ◽  
Author(s):  
John B. Taggart ◽  
Eric Verspoor ◽  
Paul T. Galvin ◽  
Paloma Morán ◽  
Andrew Ferguson

A highly discriminatory and practical nuclear DNA genetic marker that can distinguish between Atlantic salmon (Salmo salar) of European and North American origin is described. Screening of 2847 European and 247 North American Atlantic salmon from much of its geographic range for variability at a minisatellite locus, Ssa-A45/2/2, revealed the continental stocks to be almost fixed for two different-sized, easily discernable alleles. Virtually all European Atlantic salmon were homozygous for a 3.00-kb allele (frequency > 0.999), while a smaller 2.77-kb allele (frequency = 0.946) predominated in all North American populations. Whereas the 2.77-kb allele was found exclusively in North American salmon, an allele indistinguishable in size from the 3.00-kb European diagnostic allele was also observed at low frequency (0.036) in North American fish. Eight other continent-specific rare alleles (highest frequency = 0.006) were also observed. The results suggest that little, if any, natural gene flow occurs between the two continental groups of Atlantic salmon.


1993 ◽  
Vol 42 (1) ◽  
pp. 25-33 ◽  
Author(s):  
D. P. F. King ◽  
S. J. Hovey ◽  
D. Thompson ◽  
A. Scott

1998 ◽  
Vol 55 (9) ◽  
pp. 2011-2018 ◽  
Author(s):  
C E Thompson ◽  
W R Poole ◽  
M A Matthews ◽  
A Ferguson

Secondary males, either subdominant adults or, more usually, parr which mature in freshwater, are known to successfully fertilise Atlantic salmon (Salmo salar) ova. This study has estimated the reproductive success of such secondary males in redds formed by pairs of wild and sea-ranched adults. Eight wild and 11 ranched redds were sampled from the Burrishoole system, western Ireland, in two consecutive years. Representative samples of fertilised ova were screened at three minisatellite loci to reconstruct the genotypes of putative anadromous parents and to estimate the proportion of eggs fertilised by secondary males. Multiple paternal genotypes were detected in 18 of the 19 samples, and of the 1484 progeny examined, 593 could not have been derived from the primary adult male genotype. The level of secondary male contribution detected among wild redds from Burrishoole (mean 28.9%) was similar to that found in previous published studies. The level among ranched redds was significantly higher (mean 48.2%) (P = 0.042). The difference was greater when data from 1995 were considered alone, with the average level of secondary male contribution in ranched redds being almost twice that in wild redds. Minimum numbers of secondary males were not significantly different between wild (mean 2.6) and ranched (mean 2.7) redds.


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