With the frequent use of chemical pesticides, the current-use pesticides (CUPs) emerge and concentrate in the sea. The partition between the sediment and seawater is essential for understanding the environmental fate of CUPs. However, there is little research on this topic. In the present study, seventeen CUPs were screened in seawater and sediment samples collected from the Yellow Sea and East China Sea. Total concentration of 17 CUPs in surface seawater samples ranged from 9.5 to 267.3 ng/L, with 6 CUPs presenting 100% detection frequency. Carbendazim, tricyclazole, tebuconazole, atrazine and imidacloprid accounted for >80% of all CUPs, which was due to their large application in the local agriculture and fishing activities. Higher concentration sites were located near the shore and Yangtze river estuary, indicating intense human activities and riverine input that elevated the level of CUPs in marginal sea. The pesticides in seawater were mainly found in the surface followed by the bottom layer, which indicated that atmospheric deposition and re-suspension played key roles for their vertical distribution characteristics. The high fugacity fraction ratios (ff > 0.5) indicated the non-equilibrium state of pesticides that might have been transferred from sediment to seawater at most sites. These 17 detectable pesticides in seawater were at low levels, presenting ignorable or low toxic effects to aquatic organisms.
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http://dx.doi.org/10.1016/j.envres.2021.112673 | DOI Listing |
J Hazard Mater
December 2024
College of Oceanography and Ecological Science, Shanghai Ocean University, Shanghai 201306, China.
With the phase-out of legacy persistent organic pollutants (POPs), the ocean's role is evolving, potentially acting as both a reservoir and a source. This study investigates the air-sea fluxes of the first banned POPs, such as organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs), using literature from Web of Science up to 2023. OCP and PCB concentrations in air and seawater show significant spatiotemporal variability.
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December 2024
School of Environmental Science and Safety Engineering, Tianjin University of Technology, 391 Binshui West Rode, Xiqing District, Tianjin, 300384, China.
The chronic ecological risks posed by residual PAEs in China remain unclear. In this study, we analyzed the spatial distribution of five typical PAEs in the surface waters of China, dibutyl phthalate (DBP), diethylhexyl phthalate (DEHP), butylbenzyl phthalate (BBP), diethyl phthalate (DEP), and dimethyl phthalate (DMP). The highest concentration of PAEs were detected in the Liao River, ranging from 5 to 79.
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January 2025
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Italy; Department of Eco-sustainable Marine Biotechnology, Stazione Zoologica Anton Dohrn, Naples, Italy. Electronic address:
Neonicotinoid insecticides (NNIs) are the fastest-growing class in agricultural protection. They target nicotinic acetylcholine receptors (nAChR) in pests, stimulating the nervous system at low doses and causing paralysis and death at higher concentrations. NNIs are used in crop protection, seed treatment, forestry, agriculture, and flea control in domestic cattle.
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December 2024
Catalan Institute for Water Research (ICRA- CERCA), Carrer Emili Grahit 101, Parc Científic I Tecnològic de la Universitat de Girona, 17003, Girona, Spain; Institut d'Ecologia Aquàtica (IEA), Universitat de Girona, Campus de Montilivi, 17003, Girona, Spain. Electronic address:
Urban runoff effluents transport multiple pollutants collected from urban surfaces. which ultimately reach freshwater ecosystems. We here collect the existing scientific evidence on the urban runoff impacts on aquatic organisms and ecosystem functions, assessed the potential toxicity of the most common pollutants present in urban runoff, and characterized the ecotoxicological risk for freshwaters.
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January 2025
Marine College, Shandong University, Weihai 264209, PR China. Electronic address:
A novel imprinted composite nanoprobe for fluorescence turn-on recognition of acetamiprid was fabricated and applied to rapidly and sensitively detect trace-level acetamiprid in seawater. The fluorescent probe was prepared using modified fluorescein isothiocyanate as a response unit to improve the sensitivity of signal transmission. The quantitative analysis of acetamiprid was obtained by measuring fluorescence enhancement efficiency of the probe.
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