Marine Resources Assessment for the Marianas Operating ... - SPREP
Marine Resources Assessment for the Marianas Operating ... - SPREP
Marine Resources Assessment for the Marianas Operating ... - SPREP
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AUGUST 2005 FINAL REPORT<br />
3.1.1.2 <strong>Marine</strong> Mammal Distribution—Habitat and Environmental Associations<br />
<strong>Marine</strong> mammals inhabit most marine environments, from deep ocean canyons to shallow estuarine<br />
waters. They are not randomly distributed. <strong>Marine</strong> mammal distribution is affected by demographic,<br />
evolutionary, ecological, habitat-related, and anthropogenic factors (Bowen et al. 2002; Bjørge 2002;<br />
Forcada 2002; Stevick et al. 2002).<br />
Movements are often related to feeding or breeding activity (Stevick et al. 2002). A migration is <strong>the</strong><br />
periodic movement of all, or significant components of an animal population from one habitat to one or<br />
more o<strong>the</strong>r habitats and back again. Migration is an adaptation that allows an animal to monopolize areas<br />
where favorable environmental conditions exist <strong>for</strong> feeding, breeding, and/or o<strong>the</strong>r phases of <strong>the</strong> animal’s<br />
life history. Some baleen whale species, such as humpback whales, make extensive annual migrations to<br />
low-latitude mating and calving grounds in <strong>the</strong> winter and to high-latitude feeding grounds in <strong>the</strong> summer<br />
(Corkeron and Connor 1999). These migrations undoubtedly occur during <strong>the</strong>se seasons due to <strong>the</strong><br />
presence of highly productive waters and associated cetacean prey species at high latitudes and of warm<br />
water temperatures at low latitudes (Corkeron and Connor 1999; Stern 2002). The timing of migration is<br />
often a function of age, sex, and reproductive class. Females tend to migrate earlier than males and<br />
adults earlier than immature animals (Stevick et al. 2002; Craig et al. 2003). Not all baleen whales,<br />
however, migrate. Some individual fin, Bryde’s, minke, and blue whales may stay year-round in a specific<br />
area.<br />
Cetacean movements can also reflect <strong>the</strong> distribution and abundance of prey (Gaskin 1982; Payne et al.<br />
1986; Kenney et al. 1996). Cetacean movements have also been linked to indirect indicators of prey,<br />
such as temperature variations, sea-surface chlorophyll a concentrations, and features such as bottom<br />
depth (Fiedler 2002). Oceanographic conditions such as upwelling zones, eddies, and turbulent mixing<br />
can create regionalized zones of enhanced productivity that are translated into zooplankton<br />
concentrations, and/or entrain prey.<br />
As noted by MacLeod and Zuur (2005), however, even in <strong>the</strong> best studied marine mammal species,<br />
determining <strong>the</strong> fundamental reasons behind <strong>the</strong> linkage between habitat variables and distribution can<br />
be problematic, and often requires extensive datasets. For example, though topography might increase<br />
primary productivity, and as a result, provide a local increased availability of prey, not every marine<br />
mammal species is necessarily concentrated in that area. Additional factors may be involved, such as<br />
habitat segregation between o<strong>the</strong>r species that share <strong>the</strong> same ecological niche (MacLeod and Zuur<br />
2005). The degree of similarity in diet between two or more predators that occur in <strong>the</strong> same habitat will<br />
affect <strong>the</strong> level of competition between <strong>the</strong>se predators. Competition between predators can result in <strong>the</strong><br />
exclusion of one or more of <strong>the</strong>m from a specific habitat. For example, MacLeod et al. (2003) suggested<br />
that an example of niche segregation might be that Mesoplodon occupy a separate dietary niche from<br />
bottlenose whales (Hyperoodon) and Cuvier’s beaked whales (Ziphius), though <strong>the</strong>y share <strong>the</strong> same<br />
distribution. In contrast, Hyperoodon and Ziphius appear to occupy very similar dietary niches but have<br />
geographically segregated distributions, with Hyperoodon occupying cold-temperate to polar waters and<br />
Ziphius occupying warm-temperate to tropical waters.<br />
Since most too<strong>the</strong>d whales do not have <strong>the</strong> fasting capabilities of <strong>the</strong> baleen whales, too<strong>the</strong>d whales<br />
probably follow seasonal shifts in preferred prey or are opportunistic feeders, taking advantage of<br />
whatever prey happens to be in <strong>the</strong> area. Small-scale hydrographic fronts may act as convergence<br />
zones. Bottlenose dolphins have demonstrated a spatial association with <strong>the</strong> area near <strong>the</strong> surface<br />
features of tidal intrusion fronts, which could be related to increased <strong>for</strong>aging efficiency resulting from <strong>the</strong><br />
accumulation of prey in <strong>the</strong> frontal region (Mendes et al. 2002).<br />
Occurrence of cetaceans outside <strong>the</strong> area with which <strong>the</strong>y are usually associated may reflect fluctuations<br />
in food availability. Some studies have correlated shifts in <strong>the</strong> distribution of some baleen whale and<br />
too<strong>the</strong>d whale populations with ecological shifts in prey patterns after intense fishing ef<strong>for</strong>ts by<br />
commercial fisheries in <strong>the</strong> western North Atlantic (Payne et al. 1986, 1990; Kenney et al. 1996).<br />
DeMaster et al. (2001) predicted, based upon current data on human population growth and marine<br />
mammal fisheries interactions, that in <strong>the</strong> future, <strong>the</strong> most common type of competitive interaction would<br />
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