Honeybees (Apis mellifera) frequently live in complex environments where exposure to mixtures of pesticides is possible. Although several studies have expressed concern regarding the combined effects of pesticide mixtures, other studies did not find increased toxicity. Thus, the primary objective of this study was to identify peer-reviewed literature measuring the toxicity of pesticide mixtures to honeybees and determine how frequently synergistic interactions occur. Many experiments (258) were identified that met the criteria for inclusion. When considering all experiments, 34% of experiments had model deviation ratios (MDR; expected toxicity/observed toxicity) greater than 2, suggesting greater-than-additive toxicity. Twelve percent of experiments had MDR values greater than 5, with several studies exceeding 100. However, most experiments that had higher MDRs included azole fungicides or acaricides as a component of the mixture. After removal of these groups, only 8% of experiments exceeded an MDR of 2, and no experiments exceeded 5. Moreover, the influence of the azole fungicides was dose dependent. If only experiments that used azole exposure at environmentally relevant concentrations were considered, azole fungicides had limited impact on neonicotinoid insecticides. However, pyrethroid insecticides still had greater than expected toxicity with 80% of experiments having MDR values greater than 2. Acaricides also had greater than expected incidence of synergy with approximately 30% of studies reporting MDR values greater than 2. It should be noted that even the azole studies considered environmentally relevant frequently used maximum exposure rates and worst-case exposure scenarios. The primary finding is that synergy is uncommon except for a few cases where known synergists (azole fungicides) and pesticides with variable metabolism potential, such as some pyrethroids, are in combination. Future work is still needed to refine the relevance of azole fungicides at commonly occurring environmental concentrations. Integr Environ Assess Manag 2022;18:1694-1704. © 2022 SETAC.
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http://dx.doi.org/10.1002/ieam.4595 | DOI Listing |
Bull Environ Contam Toxicol
January 2025
Centro de Investigaciones en Bioquímica Clínica e Inmunología-CIBICI, Facultad de Ciencias Químicas, CONICET, Universidad Nacional de Córdoba, Haya de La Torre Esq., Medina Allende, 5000, Córdoba, Argentina.
The co-occurrence of pesticides in aquatic ecosystems highlights the need for studies investigating their potential toxicity as mixtures to the aquatic biota. Well-designed studies are essential to assess the presence and toxicity of relevant pesticide mixtures, particularly those such as the chloroacetamide herbicide metolachlor (MET), the triazole fungicide epoxiconazole (EP) and the diamide anthranilic insecticide chlorantraniliprole (CAP), which have not been previously tested, and whose co-occurrence is possible in waters close to cultivated areas. A solid phase extraction ultra-performance liquid chromatography-tandem quadrupole mass spectrometry method was developed to quantify equivalent toxicity concentrations for CAP, EP, and MET in artificial freshwater during acute toxicity tests.
View Article and Find Full Text PDFJ Agric Food Chem
January 2025
Fujian Engineering Research Center for Green Pest Management/Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests/East China Branch of the National Center for Agricultural Biosafety Sciences, Institute of Plant Protection, Fujian Academy of Agricultural Sciences, Fuzhou 350013, China.
Azole and benzimidazole fungicides are widely used agrochemicals to prevent and treat fungal growth and are frequently detected in aquatic environments. Here, we aimed to assess the aquatic ecological risks of ten currently used azole and benzimidazole fungicides, which with the aryl hydrocarbon receptor (AhR) agonistic activity, and their transformation products (TPs). We obtained over 400 types of aerobic TPs for ten fungicides.
View Article and Find Full Text PDFHeliyon
January 2025
Division of Biochemistry, Department of Physiology and Biochemistry, University of Veterinary Medicine Budapest, István Street 2, H-1078, Budapest, Hungary.
The widespread and excessive agricultural use of azole fungicide tebuconazole poses a major threat to pollinator species including honey bee colonies as highlighted by recent studies. This issue is of growing importance, due to the intensification of modern agriculture and the increasing amount of the applied chemicals, serving as a major and recent problem from both an ecotoxicological and an agricultural point of view. The present study aims to detect the effects of acute sublethal tebuconazole exposure focusing on the redox homeostasis of honey bee flight muscles.
View Article and Find Full Text PDFPathogens
December 2024
M.M. Shemyakin and Yu.A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia.
Today, is still the most common cause of both local and life-threatening systemic candidiasis. The spread of resistant fungal strains has resulted in an urgent need to search for new promising antimycotics. Here, we investigated the antifungal action of the tobacco defensin NaD1 against susceptible and resistant to azoles and echinocandins strains of .
View Article and Find Full Text PDFAntibiotics (Basel)
December 2024
Centro de Ciências da Saúde, Universidade Federal do Maranhão, São Luís 65080-805, MA, Brazil.
: Antifungal resistance to azoles, coupled with the increasing prevalence of infections, represents a significant public health challenge and has driven the search for new natural compounds that can act as alternatives or adjuvants to the current antifungals. Ellagic acid (EA) has demonstrated antifungal activity; however, its effects are not fully understood. In this study, we investigated the in vitro anti- activity of EA and its ability to potentiate the effects of fluconazole (FLZ) on : The Minimum Inhibitory Concentration (MIC) of EA was determined by broth microdilution and its interaction with FLZ was assessed using a checkerboard assay.
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