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Aquatic Environment and Biodiversity Annual Review 2012

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AEBAR <strong>2012</strong>: Protected species: Sea lions<br />

essential amino acids <strong>and</strong> were of low to medium energy levels (Meynier 2010). This may indicate<br />

that the nutritional content of prey species is not limiting the metabolic activity of NZ sea lions,<br />

although vitamin <strong>and</strong> mineral content were not considered. Meynier (2010) also developed a bioenergetic<br />

model <strong>and</strong> used it to estimate the amount of prey consumed by NZ sea lions at 17 871<br />

tonnes (95% CI 17 738–18 000 t) per year. This is equivalent to ~30% of the tonnage of arrow squid,<br />

<strong>and</strong> ~15% of the hoki harvested annually by the fisheries in the Sub-Antarctic between 2000 <strong>and</strong> 2006<br />

(Meynier 2010). Comparison of the temporal <strong>and</strong> spatial distributions of sea lion prey, sea lion<br />

foraging <strong>and</strong> of historical fishing extractions may help to identify the mechanisms whereby resource<br />

competition might occur (Bowen <strong>2012</strong>). The effects of fishing on sea lion prey species are likely to be<br />

complicated by food web interactions <strong>and</strong> multispecies models may help to assess the extent to which<br />

resource competition can impact on sea lion populations, such as those currently being developed by<br />

NIWA (Project SA123098). In addition, multispecies models may provide a means for simultaneously<br />

assessing multiple drivers of sea lion population change (a review of potential causes is given in<br />

Robertson & Chilvers 2011) which may be a more effective approach than focussing on single factor<br />

explanations for the recent observed decline in NZ sea lions (Bowen <strong>2012</strong>).<br />

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