Largemouth bass (Micropterus salmoides) exposed to a 1.0-yitg/mL solution of the lampricide 3-trifluoromethyl-4-nitro[14C]phenol (TFM) for up to 24 h accumulated radioactive residues in all tissues analyzed at each of five successive sampling periods. Maximum concentrations occurred after 8 h in brain and muscle and after 12 h in blood, liver, kidney, and head plus viscera. Concentrations of radioactivity in the bile increased throughout the experiment. In a second group of fish exposed to 1.0 Mg/mL of [14C]TFM for 12 h and then transferred to lampricide-free flowing water, the concentration of radioactive materials in tissues generally decreased with time throughout a 72-h elimination period. No TFM was detected in muscle tissue 12 h after the fish were transferred to lampricide-free water. The presence of conjugated TFM in the bile was confirmed. Hexane/ether extracts contained [14C]TFM and other unidentified 14C materials from muscle and head plus viscera, whereas methanol extracts taken after the hexane/ether extraction contained only a negligible amount of [14C]TFM but large quantities of unidentified, polar 14C compounds.
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A gas-liquid chromatographic (GLC) method is described for determining residues of Bayer 73 (2-aminoethanol salt of 2’,5-dichloro-4’-nitrosalicylanilide) in fish muscle, aquatic invertebrates, mud, and water by analyzing for 2-chloro-4-nitroaniline (CNA), a hydrolysis product of Bayer 73. Bayer 73 residues are extracted from fish muscle tissue, invertebrates, and mud with acetone-formic acid (98+2), and partitioned from water samples with chloroform. After sample cleanup by solvent and acid-base partitioning, the concentrated extract is hydrolyzed with 2N NaOH and H2O2 for 10 min at 95°C. The CNA is then partitioned into hexane-ethyl ether (7+3) and determined by electron capture GLC. Average recoveries were 88% for fish, 82% for invertebrates, 82% for mud, and 98% for water at 3 or more fortification levels.
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