1,298 research outputs found

    Comparative analysis of pesticide effects on natural enemies in western orchards: A synthesis of laboratory bioassay data

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    Pesticides are commonly used for pest management in apple, pear and walnut orchards in the western U.S. and may disrupt biological control of secondary pests in these crops. A comparative analysis was made of results obtained from a series of laboratory bioassays of acute mortality and life table response experiments to estimate lethal and sublethal effects of eight pesticides on seven natural enemy species through use of stage-structured population models. Even though a number of the pesticides tested were reduced-risk products, all of them with the exception of copper plus mancozeb and chlorantraniliprole, caused more than 80% acute mortality of at least one life stage of at least one of the natural enemy species at a full field-rate concentration and could thus be considered moderately harmful according to the International Organization for Biological Control classification for laboratory bioassays. Important sublethal effects included reductions in daily fecundity and egg fertility. From integration of the lethal and sublethal effects in matrix models, the mean of the estimated intrinsic rates of increase for natural enemy species was negative for exposure to cyantraniliprole, lambda-cyhalothrin and spinetoram, but positive and not significantly different from the control for exposure to chlorantraniliprole, copper plus mancozeb, novaluron, and sulfur. For comparisons among pesticides, there appears to be considerable variation in response among natural enemy species that can only be represented effectively from a full life table response experiment and a population-level endpoint, whereas among natural enemy species, their population-level response to the range of pesticides tested could frequently be represented by acute adult mortality alone

    Evaluation of the joint effect of glyphosate and dimethoate using a small-scale terrestrial ecosystem

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    In the present work a small-scale terrestrial ecosystem (STEM) containing a soil collected from an agricultural field in Central Portugal was used to evaluate the effects of the combination of the herbicide glyphosate and the insecticide dimethoate. Earthworms (Eisenia andrei), isopods (Porcellionides pruinosus), turnip seeds (Brassica rapa), and bait-lamina strips were placed in the STEM. The results showed that the application of the recommended field dose of both pesticides did not cause any effect on the weight variation of earthworms and growth of the plants. The application of the herbicide, even at 5 and 10 times the field dose, increased feeding activity in soil (bait-lamina test), although the application of dimethoate led to a decrease in feeding activity in all concentrations tested. The binary mixtures performed showed that according to the Independent Action model, synergism (higher effect than expected from the single exposures) was observed in both the shoot length and fresh weight of B. rapa at 5 times the field dose, but antagonism was observed at 10 times the field dose. Regarding the germination success, synergism was observed at the field dose, but antagonism was detected at 5 times and 10 times the field dose. There was a decrease on the earthworm's weight in all concentrations tested, although no statistical differences were observed in any of the treatments made. Regarding depth distribution of E. andrei, worms were found in the upper layer more than it was predicted for all concentrations. In the mixtures with the field and 5 times the field dose there was a decrease in the feeding activity (bait-lamina consumption) by the soil fauna. From the four biomarkers assessed on the isopods (Catalase, Acetylcholinesterase, Glutathione-S-transferase, and Lipid peroxidation), only a significant decrease in the Acetylcholinesterase activity upon dimethoate and the binary mixtures exposures performed with the field dose was observed and on Lipid peroxidation at the field doses of single and binary exposures. (C) 2011 Elsevier Inc. All rights reserved
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