Hepatic and renal cytopathological alterations in fingerl~ng rainbow trout Oncorhynchus mykiss following 5 \vk exposure to 30, 120, and 240 pg I -' linuron [3(3,4-dichloropheny1)-l-methoxy-lmethylurea] were studied by electron microscopy. Ultrastructural alterations were detected in liver and kidney at 230 pg l.', 2 orders of magnitude below conventional LCo. The response suggested a doseresponse relationship with a change from adaptive to degenerative features at 120 pg I-' Hepatocyte changes included: stimulation of mitosis; segmentation of nuclei; partial reorganization of heterochromatin; multiplication of nucleoli; fractionation, vesiculation and transformation of rough endoplasmic reticulum (RER) into myelinated bodies; induction of smooth endoplasmic reticulum; moderate steatosis; apparent proliferation of mitochondria, peroxlsomes, Golgi fields and lysosomal elements; depletion of glycogen; perisinusoidal lipid accumulat~on; elevated rate of hepatocytes in various stages of necrosis; infiltration and increased phagocytic activity of macrophages. Reactions of renal tubular cells were differentiated in different nephron segments. Major alterations by site in kidney were (1) renal corpuscle: lobulation of podocyte nuclei; (2) proximal segment I: elevated heterogeneity of all cell components, increased heterochromatin and nuclear size, rearrangement of RER, proliferation of Golgi fields, novel lysosomal elements, decreased mitochondria and lysosomes at 240 1-19 I-'; (3) proximal segment 11: nuclear lobulation, binucleated cells, proliferation of lysosomes and peroxisomes (lower concentrations), decreased peroxisomes and mitochondria (240 pg I-'), crystalline inclusions in lysosomal matrix, fragmentation, degranulation and circular arrangement of RER; (4) distal segment: induction of giant mitochondria with longitudinal crystalline inclusions, atypical lysosomes with long crystalline matrix inclusions, and augmentation of various lysosomal elements. Comparison of linuroninduced cellular alterations with cytopathological effects by potential linuron breakdown products, namely 4-chloroaniline and 3,4-dichloroaniline, revealed a high degree of s~milarity of cytopathological phenomena, indicating that part of the changes observed after linuron exposure might well be due to the action of linuron metabolites.