Science to Understand Low-Level Exposures to Neonicotinoid Pesticides, their Metabolites, and Chlorinated Byproducts in Drinking Water
Scientists reported the discovery of three neonicotinoid pesticides in drinking water and their potential for transformation and removal during water treatment. The research provides new insights into the persistence of neonicotinoids and their potential for transformation during water treatment and distribution, while also identifying granulated activated carbon as a potentially effective management tool for decreasing neonicotinoid concentrations in finished drinking water.
Neonicotinoids are widely used insecticides for control of insects in urban and agricultural areas. These pesticides have gained popularity owing to their potency and their selective toxicity for insects, which limits acute toxicity for nontarget animals. However, because of their widespread use, neonicotinoids commonly are detected in surface waters and groundwaters and have been detected in tap water samples in Iowa and other areas of the United States.
Neonicotinoids break down to metabolites in the environment through microbial degradation and abiotic processes (for example, photolysis and hydrolysis). As a result, metabolites are present in surface waters, some of which are used as sources of drinking water. The U.S. Geological Survey (USGS) reported neonicotinoids in treated drinking water and demonstrated that metabolites can form from select neonicotinoids during disinfection processes where neonicotinoid metabolites and parent compounds react with chlorine, leading to potentially toxic next-generation disinfection byproducts.
University of Iowa and USGS scientists studied neonicotinoid metabolites in raw and treated drinking water samples collected from the University of Iowa and the Iowa City drinking water treatment plants after maize and soy planting. Both of these facilities use free chlorine disinfection. Tap water samples also were collected from two buildings on the University of Iowa campus and three residences in the Iowa City distribution system.
Clothianidin, imidacloprid, and thiamethoxam were detected in finished water samples at concentrations ranging from 0.24 to 57.3 nanograms per liter. Samples collected along the University of Iowa treatment train indicate no apparent removal of clothianidin or imidacloprid, with modest thiamethoxam removal (about 50 percent). In contrast, the concentrations of all neonicotinoids were substantially lower in the Iowa City treatment facility water after using granular activated carbon (GAC) filtration. GAC filtration rapidly and nearly completely removed all three neonicotinoids; however, follow-up studies determined GAC filtration is less effective at removing imidacloprid metabolites than the parent compound. The scientists also determined that clothianidin is susceptible to reaction with free chlorine and may undergo at least partial transformation during chlorination.
Understanding the identity, fate, and bioactivity of transformation products generated in natural and engineered systems is critical to understanding human and wildlife exposure. This work provides new insights into the persistence of neonicotinoids and their potential for transformation during water treatment and distribution.
This study was funded by University of Iowa Center for Health Effects of Environmental Contamination (Grant 18018213 BR05); a National Science Foundation Graduate Research Fellowship; and the USGS Environmental Health Program (Contaminant Biology and Toxic Substances Hydrology), which is part of the USGS Ecosystems Mission Area.
Related science listed below.
Clothianidin Exposure Associated with Changes in Tadpole Behavior
Environmental Health Program Drinking Water Science
Mixtures of Organic and Inorganic Chemicals Characterized in Water from the Taps of Residences in the Greater Chicago Area— Science to Understand Contaminant Exposures in Drinking Water
Effect of Chronic Neonicotinoid Insecticide Exposure upon Monarch Development
Scientists Examined Native Pollinator Exposure Risk to Neonicotinoids in Native Prairie Strips
Do Neonicotinoid Pesticide Seed Coatings Pose a Hazard to Seed-eating Birds?
Related publications listed below.
Chlorinated byproducts of neonicotinoids and their metabolites: An unrecognized human exposure potential?
Differences in neonicotinoid and metabolite sorption to activated carbon are driven by alterations to the insecticidal pharmacophore
Reconnaissance of mixed organic and inorganic chemicals in private and public supply tapwaters at selected residential and workplace sites in the United States
Safe drinking water at the point-of-use (tapwater, TW) is a United States public health priority. Multiple lines of evidence were used to evaluate potential human health concerns of 482 organics and 19 inorganics in TW from 13 (7 public supply, 6 private well self-supply) home and 12 (public supply) workplace locations in 11 states. Only uranium (61.9 μg L–1, private well) exceeded a National Prim
Occurrence of neonicotinoid insecticides in finished drinking water and fate during drinking water treatment
Scientists reported the discovery of three neonicotinoid pesticides in drinking water and their potential for transformation and removal during water treatment. The research provides new insights into the persistence of neonicotinoids and their potential for transformation during water treatment and distribution, while also identifying granulated activated carbon as a potentially effective management tool for decreasing neonicotinoid concentrations in finished drinking water.
Neonicotinoids are widely used insecticides for control of insects in urban and agricultural areas. These pesticides have gained popularity owing to their potency and their selective toxicity for insects, which limits acute toxicity for nontarget animals. However, because of their widespread use, neonicotinoids commonly are detected in surface waters and groundwaters and have been detected in tap water samples in Iowa and other areas of the United States.
Neonicotinoids break down to metabolites in the environment through microbial degradation and abiotic processes (for example, photolysis and hydrolysis). As a result, metabolites are present in surface waters, some of which are used as sources of drinking water. The U.S. Geological Survey (USGS) reported neonicotinoids in treated drinking water and demonstrated that metabolites can form from select neonicotinoids during disinfection processes where neonicotinoid metabolites and parent compounds react with chlorine, leading to potentially toxic next-generation disinfection byproducts.
University of Iowa and USGS scientists studied neonicotinoid metabolites in raw and treated drinking water samples collected from the University of Iowa and the Iowa City drinking water treatment plants after maize and soy planting. Both of these facilities use free chlorine disinfection. Tap water samples also were collected from two buildings on the University of Iowa campus and three residences in the Iowa City distribution system.
Clothianidin, imidacloprid, and thiamethoxam were detected in finished water samples at concentrations ranging from 0.24 to 57.3 nanograms per liter. Samples collected along the University of Iowa treatment train indicate no apparent removal of clothianidin or imidacloprid, with modest thiamethoxam removal (about 50 percent). In contrast, the concentrations of all neonicotinoids were substantially lower in the Iowa City treatment facility water after using granular activated carbon (GAC) filtration. GAC filtration rapidly and nearly completely removed all three neonicotinoids; however, follow-up studies determined GAC filtration is less effective at removing imidacloprid metabolites than the parent compound. The scientists also determined that clothianidin is susceptible to reaction with free chlorine and may undergo at least partial transformation during chlorination.
Understanding the identity, fate, and bioactivity of transformation products generated in natural and engineered systems is critical to understanding human and wildlife exposure. This work provides new insights into the persistence of neonicotinoids and their potential for transformation during water treatment and distribution.
This study was funded by University of Iowa Center for Health Effects of Environmental Contamination (Grant 18018213 BR05); a National Science Foundation Graduate Research Fellowship; and the USGS Environmental Health Program (Contaminant Biology and Toxic Substances Hydrology), which is part of the USGS Ecosystems Mission Area.
Related science listed below.
Clothianidin Exposure Associated with Changes in Tadpole Behavior
Environmental Health Program Drinking Water Science
Mixtures of Organic and Inorganic Chemicals Characterized in Water from the Taps of Residences in the Greater Chicago Area— Science to Understand Contaminant Exposures in Drinking Water
Effect of Chronic Neonicotinoid Insecticide Exposure upon Monarch Development
Scientists Examined Native Pollinator Exposure Risk to Neonicotinoids in Native Prairie Strips
Do Neonicotinoid Pesticide Seed Coatings Pose a Hazard to Seed-eating Birds?
Related publications listed below.
Chlorinated byproducts of neonicotinoids and their metabolites: An unrecognized human exposure potential?
Differences in neonicotinoid and metabolite sorption to activated carbon are driven by alterations to the insecticidal pharmacophore
Reconnaissance of mixed organic and inorganic chemicals in private and public supply tapwaters at selected residential and workplace sites in the United States
Safe drinking water at the point-of-use (tapwater, TW) is a United States public health priority. Multiple lines of evidence were used to evaluate potential human health concerns of 482 organics and 19 inorganics in TW from 13 (7 public supply, 6 private well self-supply) home and 12 (public supply) workplace locations in 11 states. Only uranium (61.9 μg L–1, private well) exceeded a National Prim