We investigated changes in trophic level and feeding location over time in juvenile male northern fur seals Callorhinus ursinus from the Pribilof Islands, Alaska, using stable nitrogen ( 15 N) and carbon ( 13 C) isotope analyses of their fur, muscle, blubber, brain, liver, and kidney tissues. Mean 15 N values were non-uniform between tissues and ranged from 14.9 (fur) to 17.1 (lipid extracted blubber). Mean 13 C values also varied with tissue type and ranged from -24.7 (non-lipid extracted blubber) to -17.5 (fur). Mean isotope values of tissues clustered into groups coincident with their estimated protein and isotope turnover times, with fur representing the most remote incorporation of isotopic data, followed by muscle ( 15 N = 15.1 to 15.6 ; 13 C -18.1 ), brain ( 15 N 17.0 ; 13 C = -18.4 to -18.1 ), blubber ( 15 N = 17.1 ; 13 C = -19.7 to -18.1 ), kidney ( 15 N 16.4 ; 13 C = -18.5 to -18.2 ), and liver ( 15 N = 16.0 to 16.2 ; 13 C = -18.4 to -18.2 ). Mean kidney and liver 15 N values (~16.3 ) indicated that juvenile males from St. Paul and St. George Islands were feeding at the same trophic level during summer 1997. Mean kidney and liver 13 C values suggested that juvenile males from St. George Island ( 13 C = -18.2 ) were feeding at the Bering Sea shelf break, while juvenile males from St. Paul Island ( 13 C = -18.5 ) were feeding more on the continental shelf. Comparing 15 N ratios of fur with 15 N values from all other tissues allowed us to estimate that juvenile males were at their lowest trophic level when they were at the youngest age (~2 yr old) targeted in this study. Mean 15 N values from tissues collected opportunistically from 2 nulliparous females ( 15 N values ranged from 16.1 for muscle to 18.0 for blubber) and 2 postparturient females ( 15 N values ranged from 16.1 for muscle to 18.9 for blubber) suggested that, at all times, females were feeding at higher trophic levels than juvenile males. Lipid-extracted blubber samples from juvenile males had much higher 15 N values (17.1 ) and 13 C values (-19.7 to -18.1 ) than non-lipid extracted blubber (~16.0 and ~-24.7 , respectively), underscoring the importance of lipid removal when analyzing tissues for stable isotopes.
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Kurle et al. (2002) studied this question.
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