Personal care product use and lifestyle affect phthalate and DINCH metabolite levels in teenagers and young adults

Humans are widely exposed to phthalates and their novel substitutes, and considering the negative health effects associated with some phthalates, it is crucial to understand population levels and exposure determinants. This study is focused on 300 urine samples from teenagers (aged 12-17) and 300 from young adults (aged 18-37) living in Czechia collected in 2019 and 2020 to assess 17 plasticizer metabolites as biomarkers of exposure. We identified widespread phthalate exposure in the study population. The diethyl phthalate metabolite monoethyl phthalate (MEP) and three di (2-ethylhexyl) phthalate metabolites were detected in the urine of >99% of study participants. The highest median concentrations were found for metabolites of low-molecular-weight (LMW) phthalates: mono-n-butyl phthalate (MnBP), monoisobutyl phthalate (MiBP) and MEP (60.7; 52.6 and 17.6 μg/L in young adults). 1,2-cyclohexanedicarboxylic acid diisononyl ester (DINCH) metabolites were present in 68.2% of the samples with a median of 1.24 μg/L for both cohorts. Concentrations of MnBP and MiBP were similar to other European populations, but 5-6 times higher than in populations in North America. We also observed large variability in phthalate exposures within the study population, with 2-3 orders of magnitude differences in urinary metabolites between high and low exposed individuals. The concentrations varied with season, gender, age, and lifestyle factors. A relationship was found between high levels of MEP and high overall use of personal care products (PCPs). Cluster analysis suggested that phthalate exposures depend on season and multiple lifestyle factors, like time spent indoors and use of PCPs, which combine to lead to the observed widespread presence of phthalate metabolites in both study populations. Participants who spent more time indoors, particularly noticeably during colder months, had higher levels of high-molecular weight phthalate metabolites, whereas participants with higher PCP use, particularly women, tended to have higher concentration of LMW phthalate metabolites.Authors thank the Research Infrastructure RECETOX RI (No. LM2018121) and CETOCOEN EXCELLENCE (CZ.02.1.01/0.0/0.0/17_043/0009632) for a supportive background. The work was supported by the Operational Programme Research, Development and Innovation – project Cetocoen Plus (CZ.02.1.01/0.0/0.0/15_003/0000469) and the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 857560. This study has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 733032. We thank all collaborating field workers, laboratory and administrative personnel, and especially the cohort participants who invested their time and provided samples and information for this study. This study reflects only the authors’ view and the European Commission is not responsible for any use that may be made of the information it contains.S

Widespread pesticide distribution in the European atmosphere questions their degradability in air

Risk assessment of pesticide impacts on remote ecosystems makes use of model-estimated degradation in air. Recent studies suggest these degradation rates to be overestimated, questioning current pesticide regulation. Here, we investigated the concentrations of 76 pesticides in Europe at 29 rural, coastal, mountain, and polar sites during the agricultural application season. Overall, 58 pesticides were observed in the European atmosphere. Low spatial variation of 7 pesticides suggests continental-scale atmospheric dispersal. Based on concentrations in free tropospheric air and at Arctic sites, 22 pesticides were identified to be prone to long-range atmospheric transport, which included 15 substances approved for agricultural use in Europe and 7 banned ones. Comparison between concentrations at remote sites and those found at pesticide source areas suggests long atmospheric lifetimes of atrazine, cyprodinil, spiroxamine, tebuconazole, terbuthylazine, and thiacloprid. In general, our findings suggest that atmospheric transport and persistence of pesticides have been underestimated and that their risk assessment needs to be improved

Changes in Flame Retardant and Legacy Contaminant Concentrations in Indoor Air during Building Construction, Furnishing, and Use

A newly constructed university building was selected for targeted assessment of changes in the levels of flame retardants and legacy contaminants during the installation of building equipment, furniture, electronics, and first year of building use. Indoor air samples were collected during several periods of intensive equipment installation to determine a relationship between newly introduced equipment and changes in the concentrations and profiles of contaminants in indoor air. Samples were analyzed for polybrominated diphenyl ethers (PBDEs), hexabromocyclododecanes (HBCDDs), and new types of flame retardants: brominated (BFRs) and organophosphate esters (OPEs). Additionally, typical outdoor contaminants such as polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were also analyzed for comparison. From the set of 90 compounds analyzed here, hexabromobenzene (HBB) and tris­(2-chloroisopropyl)­phosphate (TCIPP) showed a significant concentration increase in indoor air concentrations during computer installation and operation, suggesting emission by operating computers, while an order of magnitude concentration increase in tris­(1,3-dichloro-2-propyl)­phosphate (TDCIPP) and tri-m-cresyl phosphate (TMTP) was observed after the furniture and carpet was introduced to the computer room, suggesting furniture or carpet as a source. However, the majority of compounds had no systematic change in concentrations during equipment installation, indicating that no sources of target compounds were introduced or, that source introduction was not reflected in indoor air concentrations. Generally, low levels of legacy flame retardants compared to their novel alternatives were observed

Questioning the appropriateness of sieving for processing indoor settled dust samples

Dust is a widely-used matrix for estimating human exposure to chemicals or as a screening tool for the identification of indoor chemicals of concern. As dust sampling became more common in exposure assessment, techniques used in processing soil have been adapted to dust samples, and separation of dust particles by sieving is common practice. However, there are no defined pore sizes, which results in inconsistent or difficult data interpretation and exposure estimates. Moreover, dust consists of more particle types than soil, particularly fibers, which behave differently during the sieving process. In this study, composite samples from seven microenvironments (homes, apartments, kindergartens, schools, public spaces, offices, and cars) were used to investigate the impact of the separation of dust by sieving on the observed chemical distributions. Dust was sieved to four particle size fractions (1-2 mm, 0.5-1 mm, 0.25-0.5 mm, and < 0.25 mm) and each fraction was analyzed for organic carbon content and polycyclic aromatic hydrocarbons (PAHs), and images of dust samples were taken by optical microscope. We identified irregular distributions across size fractions for carbon and PAHs as well as for fibrous particles. Based on the combination of chemical analyses and microscopy, we recommend careful consideration of pre-processing of dust samples to limit bias in dust exposure assessments, and sieving should be used only when necessary

Screening for halogenated flame retardants in European consumer products, building materials and wastes

To fulfill national and international fire safety standards, flame retardants (FRs) are being added to a wide range of consumer products and building materials consisting of flammable materials like plastic, wood and textiles. While the FR composition of some products and materials has been identified in recent years, the limited global coverage of the data and the large diversity in consumer products necessitates more information for an overall picture of the FR composition in common products/materials. To address this issue, 137 individual samples of various consumer products, building materials and wastes were collected. To identify and characterize potential sources of FRs in indoor environment, all samples were analyzed for content of polybrominated diphenyl ethers (PBDEs), hexabromocyclododecanes (HBCDDs) and novel flame retardants (NFRs). The most frequently detected were HBCDDs (85%), with the highest median concentration of Σ4HBCDDs of 300 mg kg−1 in polystyrenes. The highest median concentration of Σ10PBDEs was found in recycled plastic materials, reaching 4 mg kg−1. The lowest concentrations were observed for NFRs, where the median of Σ12NFRs reached 0.4 mg kg−1 in the group of electrical & electronic equipment wastes. This suggests that for consumer products and building materials that are currently in-use, legacy compounds still contribute to the overall burden of FRs. Additionally, contrasting patterns of FR composition in recycled and virgin plastics, revealed using principle component analysis (PCA), suggest that legacy flame retardants are reentering the market through recycled products, perpetuating the potential for emissions to indoor environments and thus for human exposure

Application of Land Use Regression to Identify Sources and Assess Spatial Variation in Urban SVOC Concentrations

Land use regression (LUR), a geographic information system (GIS), and measured air concentrations were used to identify potential sources of semivolatile organic contaminants (SVOCs) within an urban/suburban region, using Toronto, Canada as a case study. Regression results suggested that air concentrations of polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), polycyclic aromatic hydrocarbons (PAHs), and polycyclic musks (PCMs) were correlated with sources at a scale of <5 km. LUR was able to explain 73–90% of the variability in PCBs and PCMs, and 36–89% of PBDE and PAH variability, suggesting that the latter have more spatially complex emission sources, particularly for the lowest and highest molecular weight compounds/congeners.LUR suggested that ∼75% of the PCB air concentration variability was related to the distribution of PCBs in use/storage/building sealants, ∼60% of PBDE variability was related to building volume, ∼55% of the PAH variability was related to the distribution of transportation infrastructure, and ∼65% of the PCM variability was related to population density. Parameters such as population density and household income were successfully used as surrogates to infer sources and air concentrations of SVOCs in Toronto. This is the first application of LUR methods to explain SVOC concentrations

Knowns and unknowns of novel entities

New synthetic chemicals and materials are rising rapidly and are already widespread as novel entities in our daily lives. Although knowledge of their disruptive and long-lasting effects on the Earth system is accumulating, unknowns remain. This Voices asks: what risks do novel entities pose, and what are the emerging concerns?Environmental Biolog

Perfluorinated alkyl substances (PFASs) in household dust in Central Europe and North America

Concentrations of 20 perfluorinated alkyl substances (PFASs) were measured in dust samples from 41 homes in Canada, the Czech Republic, and United States in the spring-summer of 2013. The most frequently detected compounds were perfluorohexanoic acid (PFHxA) and perfluorooctane sulfonate (PFOS). PFOS and perfluorooctanoic acid (PFOA) had the highest concentrations of PFASs in all countries. PFOS median concentrations for the three countries were between 9.1 and 14.1 ng/g, and PFOA medians ranged between 8.2 and 9.3 ng/g. In general, concentrations in North America were higher than in the Czech Republic, which is consistent with usage patterns. No differences were found for perfluorooctane sulfonamides/sulfonamidoethanols (FOSA/Es) levels due to the low number of detections. Homologue profiles suggest that the shift from longer to shorter chain PFASs is more advanced in North America than in Europe. Significant relationships were found among individual homologues and between PFAS concentrations in dust and type of floor, number of people living in the house, and building age