EsturgeonV1, PascalFrancis, Checkpoint, bibRecord, 000362

Genetic structure of Atlantic sturgeon populations based on mitochondrial DNA control region sequences

Identifieur interne : 000362 ( PascalFrancis/Checkpoint ); précédent : 000361; suivant : 000363

Genetic structure of Atlantic sturgeon populations based on mitochondrial DNA control region sequences

Auteurs : I. Wirgin [États-Unis] ; J. R. Waldman [États-Unis] ; J. Rosko [États-Unis] ; R. Gross [États-Unis] ; M. R. Collins [États-Unis] ; S. G. Rogers [États-Unis] ; J. Stabile [États-Unis]

Source :

Transactions of the American Fisheries Society : (1900) [ 0002-8487 ] ; 2000.

RBID : Pascal:00-0228353

Descripteurs français

Pascal (Inist)
- Comparaison intraspécifique, Variabilité génétique, Séquence nucléotide, DNA mitochondrial, Diversité génétique, Structure population, Ressource biologique naturelle, Répartition géographique, Cours eau, Est, Etats Unis, Acipenser oxyrinchus, Acipenseridae.
Wicri :
- topic : Répartition géographique.

English descriptors

KwdEn :
- East, Genetic diversity, Genetic variability, Geographic distribution, Intraspecific comparison, Mitochondrial DNA, Natural biological resources, Nucleotide sequence, Population structure, Stream, United States.

Abstract

The Atlantic sturgeon Acipenser oxyrinchus oxyrinchus has a latitudinally broad distribution along the east coast of North America, with extant populations occurring from the Saint Lawrence River to rivers in southern Georgia. This species once supported intensive caviar-based fisheries that resulted in overharvest and sharply reduced population abundances; presently, directed commercial fishing for Atlantic sturgeon is banned in U.S. waters. We sequenced a 203-base-pair section of the mitochondrial DNA (mtDNA) control region of 322 Atlantic sturgeon specimens from 11 river systems across their range to elucidate their stock structure. We found a pronounced latitudinal dine in the number of composite mtDNA haplotypes and in haplotypic diversity, which increased from north to south, from previously glaciated and subsequently recolonized systems to the portion of their range unglaciated during the Pleistocene. The observed number of haplotypes per population ranged from 1 haplotype in each of the two northernmost population samples to 17 in the sample from the Savannah River. Haplotypic diversity ranged from 0.0 to 0.90. The greater genetic diversity within and among southern populations is likely a product of the persistence of these populations through the Pleistocene and to the faster mutation rates associated with their shorter generation times. Of 39 composite mtDNA haplotypes found, 64% were unique to particular populations. Monomorphism of the two Canadian populations suggested a strong founder effect. Three haplotypes unique to northern populations were probably the result of base substitutions that occurred within the past 10,000 years. In contrast with an earlier study, we found stock structure among southern populations and evidence of at least seven genetic stocks across this subspecies' range.

Affiliations:

États-Unis

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Le document en format XML

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<front><div type="abstract" xml:lang="en">The Atlantic sturgeon Acipenser oxyrinchus oxyrinchus has a latitudinally broad distribution along the east coast of North America, with extant populations occurring from the Saint Lawrence River to rivers in southern Georgia. This species once supported intensive caviar-based fisheries that resulted in overharvest and sharply reduced population abundances; presently, directed commercial fishing for Atlantic sturgeon is banned in U.S. waters. We sequenced a 203-base-pair section of the mitochondrial DNA (mtDNA) control region of 322 Atlantic sturgeon specimens from 11 river systems across their range to elucidate their stock structure. We found a pronounced latitudinal dine in the number of composite mtDNA haplotypes and in haplotypic diversity, which increased from north to south, from previously glaciated and subsequently recolonized systems to the portion of their range unglaciated during the Pleistocene. The observed number of haplotypes per population ranged from 1 haplotype in each of the two northernmost population samples to 17 in the sample from the Savannah River. Haplotypic diversity ranged from 0.0 to 0.90. The greater genetic diversity within and among southern populations is likely a product of the persistence of these populations through the Pleistocene and to the faster mutation rates associated with their shorter generation times. Of 39 composite mtDNA haplotypes found, 64% were unique to particular populations. Monomorphism of the two Canadian populations suggested a strong founder effect. Three haplotypes unique to northern populations were probably the result of base substitutions that occurred within the past 10,000 years. In contrast with an earlier study, we found stock structure among southern populations and evidence of at least seven genetic stocks across this subspecies' range.</div>
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<s5>12</s5>
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<fC03 i1="11" i2="X" l="FRE"><s0>Etats Unis</s0>
<s2>NG</s2>
<s5>13</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>United States</s0>
<s2>NG</s2>
<s5>13</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA"><s0>Estados Unidos</s0>
<s2>NG</s2>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE"><s0>Acipenser oxyrinchus</s0>
<s2>NS</s2>
<s4>INC</s4>
<s5>64</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>Acipenseridae</s0>
<s2>NS</s2>
<s4>INC</s4>
<s5>70</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Nord</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>North America</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>America del norte</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>America</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>America</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Milieu eau douce</s0>
<s5>14</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Freshwater environment</s0>
<s5>14</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Medio agua dulce</s0>
<s5>14</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Génétique population</s0>
<s5>15</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Population genetics</s0>
<s5>15</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Genética población</s0>
<s5>15</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Pisces</s0>
<s2>NS</s2>
<s5>60</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Pisces</s0>
<s2>NS</s2>
<s5>60</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Pisces</s0>
<s2>NS</s2>
<s5>60</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fN21><s1>157</s1>
</fN21>
</pA>
</standard>
</inist>
<affiliations><list><country><li>États-Unis</li>
</country>
</list>
<tree><country name="États-Unis"><noRegion><name sortKey="Wirgin, I" sort="Wirgin, I" uniqKey="Wirgin I" first="I." last="Wirgin">I. Wirgin</name>
</noRegion>
<name sortKey="Collins, M R" sort="Collins, M R" uniqKey="Collins M" first="M. R." last="Collins">M. R. Collins</name>
<name sortKey="Gross, R" sort="Gross, R" uniqKey="Gross R" first="R." last="Gross">R. Gross</name>
<name sortKey="Rogers, S G" sort="Rogers, S G" uniqKey="Rogers S" first="S. G." last="Rogers">S. G. Rogers</name>
<name sortKey="Rosko, J" sort="Rosko, J" uniqKey="Rosko J" first="J." last="Rosko">J. Rosko</name>
<name sortKey="Stabile, J" sort="Stabile, J" uniqKey="Stabile J" first="J." last="Stabile">J. Stabile</name>
<name sortKey="Waldman, J R" sort="Waldman, J R" uniqKey="Waldman J" first="J. R." last="Waldman">J. R. Waldman</name>
</country>
</tree>
</affiliations>
</record>

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Genetic structure of Atlantic sturgeon populations based on mitochondrial DNA control region sequences

Genetic structure of Atlantic sturgeon populations based on mitochondrial DNA control region sequences

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