Subtle population structuring within a highly vagile marine invertebrate, the veined squid Loligo forbesi , demonstrated with microsatellite DNA markers

Subtle population structuring within a highly vagile marine invertebrate, the veined squid Loligo... Microsatellite DNA markers were applied for the first time in a population genetic study of a cephalopod and compared with previous estimates of genetic differentiation obtained using allozyme and mitochondrial DNA (mtDNA) markers. Levels of genetic variation detected with microsatellites were much higher than found with previous markers (mean number of alleles per locus=10.6, mean expected heterozygosity (HE)=0.79; allozyme HE=0.08; mtDNA restriction fragment length polymorphism (RFLP) HE=0.16). In agreement with previous studies, microsatellites demonstrated genetic uniformity across the population occupying the European shelf seas of the North East Atlantic, and extreme genetic differentiation of the Azores population (RST/FST=0.252/0.245; allozyme FST=0.536; mtDNA FST=0.789). In contrast to other markers, microsatellites detected more subtle, and significant, levels of differentiation between the populations of the North East Atlantic offshore banks (Rockall and Faroes) and the shelf population (RST=0.048 and 0.057). Breakdown of extensive gene flow among these populations is indicated, with hydrographic (water depth) and hydrodynamic (isolating current regimes) factors suggested as possible barriers to migration. The demonstration of genetic subdivision in an abundant, highly mobile marine invertebrate has implications for the interpretation of dispersal and population dynamics, and consequent management, of such a commercially exploited species. Relative levels of differentiation indicated by the three different marker systems, and the use of measures of differentiation (assuming different mutation models), are discussed. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Molecular Ecology Wiley

Subtle population structuring within a highly vagile marine invertebrate, the veined squid Loligo forbesi , demonstrated with microsatellite DNA markers

Molecular Ecology, Volume 8 (3) – Mar 1, 1999

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Publisher
Wiley
Copyright
1999 Blackwell Science Ltd
ISSN
0962-1083
eISSN
1365-294X
DOI
10.1046/j.1365-294X.1999.00588.x
Publisher site
See Article on Publisher Site

Abstract

Microsatellite DNA markers were applied for the first time in a population genetic study of a cephalopod and compared with previous estimates of genetic differentiation obtained using allozyme and mitochondrial DNA (mtDNA) markers. Levels of genetic variation detected with microsatellites were much higher than found with previous markers (mean number of alleles per locus=10.6, mean expected heterozygosity (HE)=0.79; allozyme HE=0.08; mtDNA restriction fragment length polymorphism (RFLP) HE=0.16). In agreement with previous studies, microsatellites demonstrated genetic uniformity across the population occupying the European shelf seas of the North East Atlantic, and extreme genetic differentiation of the Azores population (RST/FST=0.252/0.245; allozyme FST=0.536; mtDNA FST=0.789). In contrast to other markers, microsatellites detected more subtle, and significant, levels of differentiation between the populations of the North East Atlantic offshore banks (Rockall and Faroes) and the shelf population (RST=0.048 and 0.057). Breakdown of extensive gene flow among these populations is indicated, with hydrographic (water depth) and hydrodynamic (isolating current regimes) factors suggested as possible barriers to migration. The demonstration of genetic subdivision in an abundant, highly mobile marine invertebrate has implications for the interpretation of dispersal and population dynamics, and consequent management, of such a commercially exploited species. Relative levels of differentiation indicated by the three different marker systems, and the use of measures of differentiation (assuming different mutation models), are discussed.

Journal

Molecular EcologyWiley

Published: Mar 1, 1999

References

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