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

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net air-sea CO2 exchange, fishery yields, and dominant basin-scale biological<br />

regimes.<br />

(Behrenfeld 2006: 754)(internal citations omitted). Oceanic food-web changes have<br />

already been documented in <strong>the</strong> North <strong>Pacific</strong>. These changes are implicated in <strong>the</strong><br />

severe decline of many species of fish and marine mammals.<br />

The “ocean climate hypo<strong>the</strong>sis” is an alternative explanation for <strong>the</strong> rapid changes<br />

that were observed <strong>to</strong> cross all trophic levels of <strong>the</strong> North <strong>Pacific</strong> (National<br />

Research Council 1996, Trites et al. in press). This bot<strong>to</strong>m-up hypo<strong>the</strong>sis is<br />

supported by a large and growing body of evidence (e.g., Ware and Thomson<br />

2005, Trites et al. in press). For <strong>the</strong> past 100 yr, 10–30-yr periods of stable<br />

physical conditions have been punctuated by rapid shifts <strong>to</strong> alternative stable<br />

physical oceanographic conditions (Ebbesmeyer et al. 1991, Graham 1994,<br />

Beamish et al. 2000, McKinnell et al. 2001, King 2005). These sudden and welldocumented<br />

“regime shifts” significantly affect sea temperatures, currents, and<br />

ice coverage—and correspond in space and time with ecosystem changes noted in<br />

Alaska and in British Columbia (Hare and Mantua 2000, Benson and Trites 2002,<br />

King 2005).<br />

(Trites et al. 2006). An ecological risk assessment performed on Cherry Point <strong>Herring</strong> by<br />

Landis et al. (2004) concluded that ocean conditions significantly affect <strong>Pacific</strong> <strong>Herring</strong>.<br />

An analysis of <strong>the</strong> Cherry Point <strong>Pacific</strong> herring age structure and population<br />

dynamics indicates that <strong>the</strong> loss of reproductive potential of <strong>the</strong> older age class<br />

fish was <strong>the</strong> population characteristic that led <strong>to</strong> <strong>the</strong> decline of <strong>the</strong> run.<br />

Exploitation, habitat alteration and climate change are <strong>the</strong> risk fac<strong>to</strong>rs that<br />

contribute <strong>to</strong> <strong>the</strong> decline of <strong>the</strong> Cherry Point <strong>Pacific</strong> herring. The retrospective<br />

assessment identified <strong>the</strong> cyclic nature of climate change, as expressed by <strong>the</strong><br />

warmer sea surface temperatures associated with a warm <strong>Pacific</strong> Decadal<br />

Oscillation (PDO), as <strong>the</strong> primary fac<strong>to</strong>r altering <strong>the</strong> dynamics of <strong>the</strong> <strong>Pacific</strong><br />

herring.<br />

(Landis et al. 2004).<br />

Reduced phy<strong>to</strong>plank<strong>to</strong>n productivity in <strong>the</strong> <strong>Lynn</strong> <strong>Canal</strong> area would have dire<br />

consequences for <strong>Pacific</strong> <strong>Herring</strong>. In particular, juvenile herring during <strong>the</strong> first winter<br />

are susceptible <strong>to</strong> environmental changes with little room for error <strong>to</strong> ensure survival.<br />

Marine perturbations that decrease food availability would inevitably cause greater winter<br />

mortality of juvenile herring, <strong>the</strong>reby depressing <strong>the</strong> future spawning generations.<br />

Cooney et al. (2001) found that juvenile herring were subject <strong>to</strong> substantial starvation<br />

losses during a winter period of plank<strong>to</strong>n diminishment.<br />

[W]e determined that if a juvenile herring arrives at <strong>the</strong> beginning of<br />

oceanographic winter in late November or early December with an energy content<br />

of 5.0 kJ/g and burns energy without supplemental feeding at 23 J/g day–1, it will<br />

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