Time-depth-speed recorders and stomach-temperature sensors were deployed on 11 harbor seals (Phoca vitulina) in the St. Lawrence estuary to examine their diving and foraging behavior. Fifty-four percent of dives were to depths of <4 m. Dives that were [Formula: see text] 4 m deep were classified into five distinct types, using a combination of principal components analysis and hierarchical and nonhierarchical clustering analyses. Feeding, indicated by a sharp decline in stomach temperature, occurred during dives of all five types, four of which were U-shaped, while one was V-shaped. Seals swam at speeds near the minimum cost of transport (MCT) during descents and ascents. V-shaped dives had mean depths of 5.8 m, lasted an average of 40 s, and often preceded or followed periods of shallow-water (<4 m) activity. Seals invariably dove to the bottom when performing U-shaped dives. These dives were to an average depth of 20 m during daylight and occurred in shallower waters (~8 m) at twilight and during the night. Once on the bottom, seals (i) swam at MCT speeds with occasional bursts of speed, (ii) swam at speeds near MCT but not exceeding it, or (iii) remained stationary or swam slowly at about 0.15 m/s, occasionally swimming faster. It is unlikely that all dives to depths [Formula: see text] 4 m are dedicated to foraging. However, the temporal segregation of dive types suggests that all types are used during foraging, although they may represent different strategies.
The trophic relationships of both the benthic and pelagic communities in the Estuary and Gulf of St Lawrence regions were examined, with a special focus on the trophic position (TP) and relationship(s) among harbour, grey, hooded and harp seals and beluga whales. A multiple stable isotope and multiple tissue approach, used in conjunction with conventional dietary information, suggested that marine mammals occupied the highest trophic positions in the food webs of both communities and that they overlapped with one another to some extent trophically. Harbour seals Phoca vitulina and hooded seals Cystophora cristata occupied the highest TP, grey seals Halichoerus grypus, Gulf harp seals Phoca groenlandica, and male beluga whales Delphinapterus leucas were intermediate, and Estuary harp seals and female beluga whales were at the lowest TP. A general pattern of increasing enrichment of 13 C or 15 N with age was observed in marine mammals (as well as fishes), although yearlings showed a decreased enrichment compared to both younger and older age classes. Sex also influenced δ 15 N values. Males were more 15 N-enriched than females, with the difference between the sexes increasing with age, and being most pronounced in species that are sexually dimorphic with respect to body size. Geographical location also influenced isotope abundance. Estuary organisms were generally 13 C-enriched relative to Gulf animals. δ 13 C values were on average lower in short-term diet integrators (blood serum) than in longer-term diet integrators (red blood cells) of harbour seals captured in April to June in the Estuary, which suggests that they probably did not move outside the Lower Estuary during the winter. Grey seals captured in the Lower Estuary did, however, show evidence of having been in the Gulf region some weeks or months before capture.
Pinnipeds rely primarily on oxygen stores in blood and muscles to support aerobic diving; therefore rapid development of body oxygen stores (TBO(2)) is crucial for pups to transition from nursing to independent foraging. Here, we investigate TBO(2) development in 45 harp (Pagophilus groenlandicus) and 46 hooded (Cystophora cristata) seals ranging in age from neonates to adult females. We found that hooded seal adults have the largest TBO(2) stores yet reported (89.5 ml kg(-1)), while harp seal adults have values more similar to other phocids (71.6 ml kg(-1)). In adults, large TBO(2) stores resulted from large blood volume (harp169, hood 194 ml kg(-1)) and high muscle Mb content (harp 86.0, hood 94.8 mg g(-1)). In contrast, pups of both species had significantly lower mass-specific TBO(2 )stores than adults, and stores declined rather than increased during the nursing period. This decline was due to a reduction in mass-specific blood volume and the absence of an increase in the low Mb levels (harp 21.0, hood 31.5 mg g(-1)). Comparisons with other phocid species suggests that the pattern of blood and muscle development in the pre- and post-natal periods varies with terrestrial period, and that muscle maturation rates may influence the length of the postweaning fast. However, final maturation of TBO(2) stores does not take place until after foraging begins.
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