Short Depuration of Oysters Intended for Human Consumption Is Effective at Reducing Exposure to Nanoplastics.

Nanoplastics (NPs; <1 µm) have greater availability to marine organisms than microplastics (1-5000 µm). Understanding NP uptake and depuration in marine organisms intended for human consumption is imperative for food safety, but until now it has been limited due to analytical constraints. Oysters (Crassostrea gigas) were exposed to polystyrene NPs doped with palladium (Pd), allowing the measurements of their uptake into tissues by inductively coupled plasma mass spectrometry (ICP-MS) combined with electron microscopy. Oysters were exposed for 6 days (d) to "Smooth" or "Raspberry" NPs, followed by 30 d of depuration with the aim of assessing the NP concentration in C. gigas following exposure, inferring the accumulation and elimination rates, and understanding the clearance of Pd NPs during the depuration period. After 6 d, the most significant accumulation was found in the digestive gland (106.6 and 135.3 µg g-1 dw, for Smooth and Raspberry NPs, respectively) and showed the most evident depuration (elimination rate constant KSmooth = 2 d-1 and KRaspberry = 0.2 d-1). Almost complete depuration of the Raspberry NPs occurred after 30 d. While a post-harvesting depuration period of 24-48 h for oysters could potentially reduce the NP content by 75%, more research to validate these findings, including depuration studies of oysters from the field, is required to inform practices to reduce human exposure through consumption.

Screening of pesticides and veterinary drugs in small streams in the European Union by liquid chromatography high resolution mass spectrometry.

Water samples from 29 small waterways located in 10 different countries in the European Union were screened for the presence of a large number of pesticides (275) and veterinary drugs (101). Solid phase extraction was combined with liquid chromatography coupled to Orbitrap high resolution tandem mass spectrometry to quantify the levels of pesticides in the samples and to detect the presence of veterinary drugs. All the sampled European rivers and canals included in this investigation were contaminated with mixtures of pesticides and, in most of the cases, with several veterinary drugs at the time of sampling, without a clear national or regional pattern. In total, 103 different pesticides, 24 of them banned in the EU, and 21 veterinary drugs were found in the analysed samples. Herbicides were the main contributor to the total amount of pesticides found in the samples, with terbuthylazine present in all the samples. The maximum individual concentration recorded was of dimethenamid at 59.85 µg L-1. The maximum combined pesticide concentration was found in a sample from the Wulfdambeek canal, Belgium, with 94.02 µg L-1 comprised of a mixture of 70 different pesticides. European regulatory standards defining acceptable concentration levels were exceeded for at least one pesticide in 13 of the 29 samples analysed, with the neonicotinoid insecticides imidacloprid and clothianidin most frequently present above such limits. The majority of the veterinary drugs detected were antimicrobials, most being antibiotics. The ß-lactam antibiotic dicloxacillin was present in two thirds of the analysed samples. The application of this consistent research approach across Europe allowed the identification of a significant threat to the aquatic environment associated with pesticide contamination, and in some cases veterinary drugs, at the time of sampling in the water bodies tested.

Levels and distribution of polybrominated diphenyl ethers in soil, sediment and dust samples collected from various electronic waste recycling sites within Guiyu town, southern China.

Electronic waste recycling operations in some parts of Asia are conducted using rudimentary techniques which result in workplace and environmental contamination with toxic metals and persistent organic pollutants. This study reports concentrations of 14 polybrominated diphenyl ethers (PBDEs), from tri- to deca-brominated, in 31 samples of soil, sediment, dust or ash collected in the vicinity of e-waste recycling sites in Guiyu (southeast China) which were engaged in common activities such as dismantling, shredding, solder recovery, acid processing and open burning. The concentrations detected in this study far exceed those reported previously in urban soil and sediment and are consistent with or exceed those reported in previous studies around e-waste processing facilities. Some of the highest PBDE concentrations reported to date (e.g. 390 000 ng g (-1) dw (∑ 14 PBDEs)) were found in a sample collected from a site used for open-burning of e-waste, while an average concentration of 220 000 ng g (-1) dw (∑ 14 PBDEs) occurred in sediments impacted by circuit board shredding. A decrease in PBDE concentrations observed with increasing distance from workshops in samples associated with acid processing of wastes provides evidence that such operations are a significant source of PBDEs to the environment. Principal components analysis reveals a complex PBDE congener distribution, suggesting contamination by two or even three commercial formulations consistent with the diverse range of wastes processed.