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<br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br /> <br />12 <br /> <br />Percent survival was calculated for all three size <br />classes and feeding regimes on a daily basis throughout the <br />210-day winter period. Percent survival was calculated by <br />dividing the number of fish in a given size class and <br />feeding regime that were alive at the end of each day by the <br />original number of fish minus the number removed for lipid <br />analysis on days 70 and 140. <br />Due to their small size, several fish from each size <br />class and feeding regime had to be pooled to provide enough <br />material for lipid extraction. Approximately 11 small fish, <br />8 medium, or 4 large fish were pooled to provide sufficient <br />material for each extraction. Lipid analysis was performed <br />as follows. Frozen fish weighing 1-2 g (wet weight obtained <br />prior to freezing) were placed in an aluminum drying pan. <br />Fish were dried at 90-1000 C for 20-24 hours. After cooling <br />for 24 hours in a desiccator, dried fish were reweighed, and <br />percent water was calculated. Dried samples were finely <br />ground with mortar and pestle and placed in cellulose <br />extraction thimbles. Each thimble and its ground sample was <br />redried for 20-24 hours, cooled in a desiccator, and weighed <br />to 0.0001 g. Samples were extracted on a GoldfisctlID fat <br />extraction apparatus for 6-7 h with di-ethyl ether. The <br />precision of the lipid-extraction technique was tested by <br />running several analyses on large (3-4 g) homogenized <br />samples of non-experimental fish. In all cases, the <br />calculated lipid values were within 4% of each other. The <br />