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Toxicity evaluation of the active ingredient acetamiprid and a commercial formulation (Assail® 70) on the non-target gastropod Biomphalaria straminea (Mollusca: Planorbidae)

Ecotoxicology and Environmental Safety 2020 63 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 50 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Analía F. Pérez, Paula Fanny Cossi, Paula Fanny Cossi, Paula Fanny Cossi, Lucila Thomsett Herbert Analía F. Pérez, Analía F. Pérez, María Soledad Yusseppone, Analía F. Pérez, Analía F. Pérez, Gisela Kristoff, Analía F. Pérez, Analía F. Pérez, Analía F. Pérez, Lucila Thomsett Herbert

Summary

Researchers conducted 14-day exposures of the freshwater snail Biomphalaria straminea to the neonicotinoid acetamiprid and a commercial formulation, finding that both induced detoxification and oxidative stress responses while the commercial formulation showed greater toxicity, though neither affected cholinesterase activity, reproduction, or offspring survival.

Neonicotinoids emerged as an environmentally safe alternative to previous generations of insecticides becoming one of the most widely applied in modern agriculture. Nevertheless, they have been reported to affect several non-target organisms. Most toxicity studies focus on the effects on pollinators or terrestrial invertebrates and evaluate either the active ingredient or the commercial formulation. In the present study, we aimed to assess the long-term effects of the active ingredient acetamiprid and a broadly used commercial formulation (Assail® 70) on the non-target freshwater gastropod Biomphalaria straminea using a battery of biomarkers. A 14 day-exposure of adult organisms to both active ingredient and commercial formulation increased carboxylesterase activity and glutathione content, inhibited superoxide dismutase activity and decreased reactive oxygen species levels. The commercial formulation additionally increased glutathione S-transferase activity and inhibited catalase activity. The results indicate a greater toxicity of the commercial formulation than that of the active ingredient alone. Cholinesterase activity, development and offspring survival of B. straminea were not impaired. We conclude that the toxicity of acetamiprid on this gastropod species is mainly related to effects on detoxification and oxidative metabolism responses. This study provides novel information about the adverse effects of the active ingredient and a commercial formulation of a widely used neonicotinoid on a non-target aquatic species.

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