Abstract

Since their discovery in the late 1980s, neonicotinoid pesticides have become the most widely used class of insecticides worldwide, with large-scale applications ranging from plant protection (crops, vegetables, fruits), veterinary products, and biocides to invertebrate pest control in fish farming. In this review, we address the phenyl-pyrazole fipronil together with neonicotinoids because of similarities in their toxicity, physicochemical profiles, and presence in the environment. Neonicotinoids and fipronil currently account for approximately one third of the world insecticide market; the annual world production of the archetype neonicotinoid, imidacloprid, was estimated to be ca. 20,000 tonnes active substance in 2010. There were several reasons for the initial success of neonicotinoids and fipronil: (1) there was no known pesticide resistance in target pests, mainly because of their recent development, (2) their physicochemical properties included many advantages over previous generations of insecticides (i.e., organophosphates, carbamates, pyrethroids, etc.), and (3) they shared an assumed reduced operator and consumer risk. Due to their systemic nature, they are taken up by the roots or leaves and translocated to all parts of the plant, which, in turn, makes them effectively toxic to herbivorous insects. The toxicity persists for a variable period of time—depending on the plant, its growth stage, and the amount of pesticide applied. A wide variety of applications are available, including the most common prophylactic non-Good Agricultural Practices (GAP) application by seed coating. As a result of their extensive use and physicochemical properties, these substances can be found in all environmental compartments including soil, water, and air. Neonicotinoids and fipronil operate by disrupting neural transmission in the central nervous system of invertebrates. Neonicotinoids mimic the action of neurotransmitters, while fipronil inhibits neuronal receptors. In doing so, they continuously stimulate neurons leading ultimately to death of target invertebrates. Like virtually all insecticides, they can also have lethal and sublethal impacts on non-target organisms, including insect predators and vertebrates. Furthermore, a range of synergistic effects with other stressors have been documented. Here, we review extensively their metabolic pathways, showing how they form both compound-specific and common metabolites which can themselves be toxic. These may result in prolonged toxicity. Considering their wide commercial expansion, mode of action, the systemic properties in plants, persistence and environmental fate, coupled with limited information about the toxicity profiles of these compounds and their metabolites, neonicotinoids and fipronil may entail significant risks to the environment. A global evaluation of the potential collateral effects of their use is therefore timely. The present paper and subsequent chapters in this review of the global literature explore these risks and show a growing body of evidence that persistent, low concentrations of these insecticides pose serious risks of undesirable environmental impacts.

Highlights

  • Neonicotinoids and the phenyl-pyrazole fipronil are insecticides with systemic properties

  • Maize is the largest single use, seed treatments in other large acreage crops, including soybeans (31.4 million ha), wheat (23 million ha), and cotton (4.2 million ha) combine to make this class of insecticides the most widely used in the USA in history, when measured by area of application (USDA-NASS 2013)

  • The use of D. melanogaster strains presenting mutations at Dα1 and Dβ2 nicotinic acetylcholine receptors (nAChRs) subunits, or resistant silverleaf whitefly (B. tabaci) strains revealed no cross-resistance between sulfoxaflor and imidacloprid or spinosyns, despite the fact that sulfoxaflor shares nAChR as a common target with other neonicotinoids

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Summary

Introduction

Neonicotinoids and the phenyl-pyrazole fipronil are insecticides with systemic properties. The binding sites of neonicotinoids to nicotinic acetylcholine receptors (nAChRs) and fipronil to γ-aminobutiric acid (GABA) receptors in the nervous systems of vertebrates are different from those in insects. Shi et al (2011) noted no crossresistance between imidacloprid and two other neonicotinoids (thiamethoxam and clothianidin), but did find a 3.68–5.79fold cross-resistance for acetamiprid, nitenpyram, and thiacloprid.

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