Organophosphate pesticides, especially chlorpyrifos, are one of the most widely used insecticides in agriculture, but their toxicity and potential sensitivity effects on Anura, especially Fejervarya limnocharis are still unknown. The purpose of this investigation is to study F. limnocharis (Anura: Dicroglossidae) tadpole sensitivity to lethal (survivability) and sublethal effects (morphological alterations and swimming activity) of chlorpyrifos in Dursban 200EC commercial formula under acute exposure. An acute toxicity test was carried out on ten tadpoles (Gosner 25) in each repetition. The sample was obtained from artificial reproduction by injecting the Trial Batch 2000 IU hCG by Kings Lab. The acute toxicity testing consisted of three replicates with a chlorpyrifos concentration of 0; 0.4; 0.8; 1; 2; 4; and 8 µg/L. Physico-chemical parameters, mortality, morphological, and swimming alterations of each concentration were observed at 24th, 48th, 72nd, and 96th hours. The LC50 of chlorpyrifos for F. limnocharis tadpoles was 2.86 µg/L. The percentage of survivability F. limnocharis tadpoles decreased after exposure to chlorpyrifos above 1µg/L, while morphological alterations were observed in 2 µg/L and 4 µg/L after 48th hours exposure, and the swimming alterations have occurred at 24th hours in 1; 2; 4 and 8 µg/L. Morphological alterations were observed including asymmetrical body shape, edema, and abnormal tail shape. Based on the LC50 value, commercial chlorpyrifos has high-level toxicity on F. limnocharis tadpoles.Keywords: Acute, Chlorpyrifos, Dursban 200 EC, Fejervarya limnocharis, Tadpoles

The potential for genotoxicity of pesticides is currently one of the world's concerns. Chlorpyrifos is the organophosphate active ingredient with the largest sales, but the potential for genotoxicity in amphibians is still not widely known. The purpose of this study was to assess the genotoxicity effect of a commercial chlorpyrifos formulation Dursban 200EC in F. limnocharis tadpole erythrocyte (Anura: Dicroglossidae) under acute and chronic exposure using by micronucleus assay. Acute and chronic toxicity tests consisted of negative control, positive control, and 0.4, 0.8, and 1 µg.L -1 of chlorpyrifos with three replications. A toxicity test was carried out on ten tadpoles (Gosner 25) from artificial reproductions in each treatment. The results showed that the formulation of Dursban 200EC in low concentrations (0.4 µg l -1 ) had the potential to induce DNA damage in erythrocytes of F. limnocharis tadpoles, and there was a positive correlation between chlorpyrifos concentrations and an increase in the frequency of MN. Erythrocytes exposed to chlorpyrifos in both acute and chronic treatment had significantly different MN frequencies between negative and positive controls, 0.4, 0.8, and 1 µg.L -1 (p<0.01). Meanwhile, positive controls were not significantly different from 1 µg.L -1 ( p>0.05). However, the increase in the frequency of MN in chronic treatment was almost twice as high.