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Operational Plan for the Restoration of Diadromous Fishes to the ...

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4. American Shad<br />

Management S<strong>to</strong>ck Structure<br />

A peer review <strong>of</strong> <strong>the</strong> ASMFS s<strong>to</strong>ck assessment <strong>for</strong> shad (Limburg et al. 2007)<br />

confirmed <strong>the</strong> use <strong>of</strong> individual river s<strong>to</strong>cks as <strong>the</strong> management unit and also<br />

suggested <strong>the</strong> use <strong>of</strong> assessment approaches using regional models that reflect life<br />

his<strong>to</strong>ry differences in <strong>the</strong> s<strong>to</strong>cks (sou<strong>the</strong>rn, Mid-Atlantic and North Atlantic). The<br />

State <strong>of</strong> Maine currently manages shad s<strong>to</strong>cks based on <strong>the</strong> river <strong>of</strong> origin. No<br />

specific in<strong>for</strong>mation is known about <strong>the</strong> s<strong>to</strong>ck structure, size, or spawning locations<br />

<strong>of</strong> shad in <strong>the</strong> Penobscot River or tributaries except that a remnant population exists.<br />

Anecdotal in<strong>for</strong>mation suggest that <strong>the</strong> remnant population is small because <strong>of</strong> <strong>the</strong><br />

low frequency and number <strong>of</strong> shad documented in <strong>the</strong> Veazie Project fishway, <strong>the</strong><br />

low frequency collected during past surveys, and <strong>the</strong> estimated starting populations<br />

in o<strong>the</strong>r river systems.<br />

Meristic/Morphology or Genetic Investigations<br />

Earlier work on American shad included <strong>the</strong> analysis <strong>of</strong> o<strong>to</strong>liths (Williams 1985) and<br />

meristic and morphometric characteristic (Melvin 1984) <strong>to</strong> assign shad from a mixeds<strong>to</strong>ck<br />

summer fishery <strong>to</strong> one <strong>of</strong> three broad regions (Canadian Atlantic, mid-US<br />

Atlantic, and south-US Atlantic). Later work by Melvin et al. (1992) examined<br />

morphology and meristic characteristics <strong>for</strong> American shad from fourteen rivers<br />

between Florida and Quebec. They were able <strong>to</strong> discern a south <strong>to</strong> north separation<br />

within four broad regions (Florida <strong>to</strong> Cape Lookout; Cape Lookout <strong>to</strong> Cape Cod; Bay<br />

<strong>of</strong> Fundy; and Gulf <strong>of</strong> Saint Lawrence). The separation between adjacent regions<br />

was less apparent than between regions more geographically distant. They were<br />

able <strong>to</strong> correctly classify individuals from a mixed-s<strong>to</strong>ck <strong>to</strong> each region with a 79 and<br />

89 percent correct classification.<br />

Genetic investigations <strong>to</strong> discriminate populations <strong>of</strong> American shad based on<br />

morphology, protein electrophoresis, and analysis <strong>of</strong> mi<strong>to</strong>chondrial DNA (mtDNA)<br />

and nuclear DNA microsatellite variation have found shad populations <strong>to</strong> be only<br />

weakly <strong>to</strong> moderately differentiated and subject <strong>to</strong> substantial amounts <strong>of</strong> gene flow<br />

(Nolan et al. 2003).<br />

Four studies that used restriction endonuclease (RE) analysis <strong>of</strong> mi<strong>to</strong>chondrial DNA<br />

(mtDNA) found that differences among 23 east coast shad populations occurred<br />

primarily as variations in <strong>the</strong> frequencies <strong>of</strong> common and shared mtDNA haplotypes<br />

(Bentzen et al. 1989; Nolan et al. 1991; Epifanio et al. 1995), and haplotype<br />

frequencies generally were temporally stable (Brown et al. 1996). Because no<br />

single or group <strong>of</strong> haplotypes completely discriminated river s<strong>to</strong>cks or regional<br />

complexes, only 28 percent <strong>of</strong> individual fish could be correctly reallocated <strong>to</strong> <strong>the</strong>ir<br />

river <strong>of</strong> origin (Epifanio et al. 1995). Surprisingly, a major life his<strong>to</strong>ry variation<br />

(semelparity in populations south <strong>of</strong> Chesapeake Bay and iteroparity <strong>to</strong> <strong>the</strong> north)<br />

was not revealed by <strong>the</strong> mtDNA analysis. In a study <strong>of</strong> three anadromous fish<br />

PRFP Page 122

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