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EPA's Vessel General Permit and Small Vessel General

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in leatherbacks <strong>and</strong> can block gastrointestinal tracts leading to death (Mrosovsky et al. 2009).<br />

Although global climate change may exp<strong>and</strong> foraging habitats into higher latitude waters,<br />

increasing temperatures may increase feminization of nests (Mrosovsky et al. 1984, James et al.<br />

2006, McMahon <strong>and</strong> Hays 2006, Hawkes et al. 2007b). It may also result in rising sea levels,<br />

which may inundate nests on some beaches. Natural threats include: predation on adults by<br />

sharks <strong>and</strong> killer whales (Pitman <strong>and</strong> Dutton 2004); predation on hatchlings by seabirds, l<strong>and</strong><br />

predators, <strong>and</strong> sharks; <strong>and</strong> tidal inundation of nests (Caut et al. 2009).<br />

Life history<br />

Both males <strong>and</strong> females exhibit some degree of philopatry, returning to their natal beaches for<br />

breeding <strong>and</strong> nesting (James et al. 2005b). Age to maturity remains elusive, with estimates<br />

ranging from 5 to 29 years (Spotila et al. 1996, Avens et al. 2009). Females lay up to seven<br />

clutches per season, with more than 65 eggs per clutch <strong>and</strong> eggs weighing >80 g (Reina et al.<br />

2002, Wallace et al. 2007). Females remigrate every 1-7 years, with most turtles returning every<br />

two years to nest in French Guiana (Rivalan et al. 2005) <strong>and</strong> every three years in Las Baulas,<br />

Costa Rica (Reina et al. 2002). The remigration interval for western Pacific leatherbacks is<br />

unknown but estimated as “several years” (Benson et al. 2011). According to Wallace (2007),<br />

high seasonal <strong>and</strong> lifetime fecundity likely reflect compensation for high <strong>and</strong> unpredictable<br />

mortality during early life history stages.<br />

Migration <strong>and</strong> movement<br />

Leatherback sea turtles migrate long distances between tropical nesting beaches temperate forage<br />

areas (i.e., remigration). Leatherbacks weigh ~33 percent more on their foraging grounds than at<br />

nesting, indicating that they probably catabolize fat reserves to fuel migration <strong>and</strong> subsequent<br />

reproduction (James et al. 2005a, Wallace et al. 2006). Sea turtles must meet an energy<br />

threshold before returning to nesting beaches (Rivalan et al. 2005, Sherrill-Mix <strong>and</strong> James 2008,<br />

Casey et al. 2010). Therefore, their remigration intervals (the time between breeding seasons)<br />

are dependent upon foraging success <strong>and</strong> duration (Hays 2000, Price et al. 2004). Eastern Pacific<br />

leatherbacks use a consistent migration corridor to forage in the South Pacific Gyre, a lowproductivity<br />

region (Shillinger et al. 2008). Western Pacific turtles that nest during the boreal<br />

summer migrate to forage in temperate waters of the North Pacific or tropical waters of the South<br />

China Sea; those that nest during the boreal winter forage in temperate <strong>and</strong> tropical waters of the<br />

southern hemisphere (Benson et al. 2011). Post-nesting, western Atlantic leatherbacks migrate<br />

to foraging areas in the North Atlantic or the equatorial eastern Atlantic (Ferraroli et al. 2004,<br />

Hays et al. 2004, Eckert et al. 2006, Eckert 2006). Eastern Atlantic leatherbacks migrate to<br />

foraging areas in the equatorial Atlantic, temperate waters off South America, or temperate<br />

waters off southern Africa (Witt et al. 2011).<br />

Diet<br />

Leatherbacks feed primarily on jellyfish, such as Stomolophus, Chryaora, <strong>and</strong> Aurelia (Rebel<br />

1974), <strong>and</strong> tunicates (salps, pyrosomas). These gelatinous zooplankton are relatively nutrientpoor<br />

(Doyle et al. 2007), such that leatherbacks must consume large quantities to support their<br />

body weight.<br />

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