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Petition to List Lynn Canal Pacific Herring under the Endangered ...

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<strong>Pacific</strong> herring populations would result in a high degree of gene flow, and thus<br />

little <strong>to</strong> no genetic differentiation among populations.<br />

(S<strong>to</strong>ut et al. 2001).<br />

In <strong>the</strong> Kensing<strong>to</strong>n Gold Project Biological Opinion, NMFS biologists concluded<br />

that <strong>Lynn</strong> <strong>Canal</strong> <strong>Herring</strong> population is probably distinct from o<strong>the</strong>r <strong>Pacific</strong> <strong>Herring</strong> in<br />

Sou<strong>the</strong>ast Alaska.<br />

<strong>Herring</strong> populations, or s<strong>to</strong>cks, are scattered across <strong>the</strong> region from <strong>Lynn</strong> <strong>Canal</strong> <strong>to</strong><br />

Prince of Wales Island, with <strong>the</strong> main spawning concentrations occurring in <strong>the</strong><br />

vicinities of Ketchikan, Craig, Frederick Sound, Sitka, and Auke/Berners Bays<br />

(Skud 1959). Population research conducted in sou<strong>the</strong>ast Alaska and Prince<br />

William Sound suggests that regional herring s<strong>to</strong>cks are comprised of multiple,<br />

distinct subpopulations, or races, which are part of a larger regional<br />

metapopulation, with potential recruitment occurring between subregions<br />

(Rounsefell and Dahlgren 1935, Skud 1959, Brown and Norcross 2001).<br />

Recent genetic analysis of satellite mi<strong>to</strong>chondrial DNA loci from 65 <strong>Pacific</strong><br />

herring sampling locations in British Columbia, sou<strong>the</strong>ast Alaska and Washing<strong>to</strong>n<br />

state found herring spawning in Sou<strong>the</strong>ast Alaska <strong>to</strong> be distinct from those<br />

spawning fur<strong>the</strong>r south in <strong>the</strong> Queen Charlotte Islands (Beacham et al. 2001).<br />

There was little evidence of genetic substructure among <strong>the</strong> herring s<strong>to</strong>cks<br />

examined, but for locations where genetically distinct populations were identified,<br />

differences in timing of spawning was <strong>the</strong> main isolating mechanism and<br />

geographic isolation of <strong>the</strong> spawning population was thought <strong>to</strong> have an effect in<br />

maintaining genetic distinctiveness of <strong>the</strong> spawning population.<br />

Applying <strong>the</strong> metapopulation model (Levins 1970) <strong>to</strong> sou<strong>the</strong>ast Alaska herring<br />

s<strong>to</strong>cks, it is probable that <strong>the</strong> viability of <strong>the</strong> <strong>Lynn</strong> <strong>Canal</strong> subpopulation that<br />

spawns in and around Berners Bay will indirectly impact <strong>the</strong> viability of o<strong>the</strong>r<br />

sou<strong>the</strong>ast regional herring populations through recruitment, genetic diversity, and<br />

sharing of predation pressures from marine mammal populations in nor<strong>the</strong>rn<br />

sou<strong>the</strong>ast Alaska waters.<br />

(NMFS 2005a: 58-59)(emphasis added).<br />

A. Comparison with <strong>Pacific</strong> <strong>Herring</strong> Populations in <strong>the</strong> Gulf<br />

of Alaska and Bering Sea; Grant and Utter (1984),<br />

O’Connell et al. (1998).<br />

Grant and Utter (1984) determined that <strong>Pacific</strong> <strong>Herring</strong> in <strong>the</strong> Bering Sea are a distinct<br />

“race” separated from all herring <strong>to</strong> south along North America’s west coast.<br />

III

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