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Chapter One: General Introduction<br />

Many <strong>of</strong> the observed patterns are likely due to a complex interaction between<br />

historical changes in marine environments (e.g., the impact <strong>of</strong> ice ages), resource<br />

requirements and specialisations, and aspects <strong>of</strong> life history and demographics<br />

(Hoelzel et al. 2002a). In this context, the use <strong>of</strong> molecular markers has played an<br />

increasingly important role in the study <strong>of</strong> cetacean population structure and thus, in<br />

the management and conservation <strong>of</strong> these species (e.g., Rosel et al. 1994, Baker &<br />

Palumbi 1995, García-Martínez et al. 1999). Genetic data contain information on the<br />

present and past structure <strong>of</strong> the populations that can not be obtained by any other<br />

method (Avise 2004). As such, most examples <strong>of</strong> dolphin population structure<br />

mentioned in this thesis have been revealed by molecular studies. Note, however,<br />

that it is not the only tool, as photo-identification or telemetry data can provide<br />

valuable and complementary information on the patterns <strong>of</strong> individuals’ movements<br />

(Whitehead 2001).<br />

1.3.2. Factors driving dolphin population structure<br />

Different factors such as sea-surface temperature, behavioural specialisation,<br />

isolation-by-distance, social system and historical processes are thought to shape the<br />

structure <strong>of</strong> dolphin populations (Hoelzel et al. 2002a). This section presents a few<br />

examples which illustrate these factors.<br />

In the North Atlantic, the patterns <strong>of</strong> genetic differentiation in long-finned pilot whales<br />

(Globicephala melas) suggest that population isolation occurs between areas that<br />

differ in sea-surface temperature (Fullard et al. 2000). On the other hand, population<br />

differentiation shows no correlation with geographical distance (Fullard et al. 2000).<br />

Temperature also seems to be the primary factor determining the relative distribution<br />

<strong>of</strong> two populations <strong>of</strong> short-finned pilot whales <strong>of</strong>f the coast <strong>of</strong> Japan (Kasuya et al.<br />

1988). However, these correlations might not illustrate a particular sensitivity <strong>of</strong> these<br />

two species for sea-surface temperature, but instead may be the result <strong>of</strong> other<br />

ecological factors such as prey behaviour (Sergeant 1962). Such a pattern has been<br />

suggested for several other species <strong>of</strong> dolphins such as the dusky dolphin<br />

(Lagenorhynchus obscurus) in Argentina (Würsig & Würsig 1980). In temperate<br />

waters, water temperature could affect prey distribution and in turn affect the<br />

distribution <strong>of</strong> dolphin species (Norris 1967, Kasuya et al. 1988). For pilot whales, it is<br />

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