Acute toxicity of chlorpyrifos to some non-target freshwater organisms: which one is more toxic-technical grade or commercial formulation?

Ecotoxicology

Department of Zoology, Vivekananda Mahavidyalaya, Hooghly, 712405, W.B., India.

Published: December 2024

AI Article Synopsis

  • Chlorpyrifos is a common organophosphate pesticide used in agriculture, and this study tested its toxicity on four freshwater species: zooplankton, oligochaete worms, gastropods, and tadpole larvae.
  • The commercial formulation of chlorpyrifos was found to be significantly more toxic than the technical grade, with toxicity levels varying greatly among the tested organisms.
  • The sensitivity of these organisms to chlorpyrifos also depended on exposure time, highlighting differences in acute toxicity between the two formulations.

Article Abstract

Chlorpyrifos is among the most widely sold organophosphates in the agriculture sector worldwide. Static bioassays were performed in the laboratory to compare the acute toxicity between the technical grade (94% a.i.) and commercial formulation (20% EC) of chlorpyrifos to four freshwater organisms: the crustacean zooplankton Cyclops viridis, the oligochaete worm Branchiura sowerbyi, the gastropod Pila globosa, and tadpole larvae of Duttaphrynus melanostictus. The recovery of actual chlorpyrifos concentrations in water after 2 h of exposure to the nominal concentrations ranged from 82.98% to 88.56%. The commercial formulation (F) of chlorpyrifos was found to be 1.94 to 2.76 times more toxic than the technical grade (T). Based on 96 h LC values of T and F chlorpyrifos, C. viridis was found to be most sensitive (0.56 and 0.25 μg/L) and P. globosa as most tolerant (1482 and 536 μg/L) to chlorpyrifos. Changes in LC values of both T and F chlorpyrifos were noted in respect of exposure hours for the three aquatic invertebrates and the tadpole larvae of the toad. In conclusion, the acute toxicity of chlorpyrifos to some non-target freshwater organisms differs between technical grade and commercial formulations.

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Source
http://dx.doi.org/10.1007/s10646-024-02806-3DOI Listing

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