“…Following removal of contaminating lipids with chloroform, the T 3 concentration from subsequent alcohol extracts can be measured by immunoassay with allowance for T 3 recovery (Tagawa and Hirano, 1990). Alternatively, fish may be brought to isotopic equilibrium through constant *T a infusion, tissues homogenized, lipid removed, alcohol extracts prepared, *T 3 identified chromatographically, and absolute T 3 levels calculated from the specific activity of the *T3 based on plasma measurements (Fok et al, 1990). Such approaches have been employed to assess tissue T 3 levels of adult trout (Fok et al, 1990) or immature coho salmon during parr-smolt transformation (Specker et al, 1992), and in the whole eggs, yolk, larvae and fry of salmonids (Greenblatt et al, 1989;Leatherland et al, 1989;Tagawa and Hirano, 1990;deJesus and Hirano, 1992), flounder (Tagawa et al, …”