Use Of Passive Samplers Research Articles

Lessons learnt from the use of passive samplers to measure ammonia emissions in multi-plot experiments

Lessons learnt from the use of passive samplers to measure ammonia emissions in multi-plot experiments

Use of passive samplers as sewage surveillance tool to monitor a hepatitis A outbreak at a school in Amsterdam, the Netherlands, Oct 2022 – March 2023

BackgroundEnteric hepatitis A virus (HAV) infections during childhood are often asymptomatic but may cause severe illness in adults. To improve public health surveillance we assessed the applicability of sewage monitoring during an HAV outbreak at a primary school.MethodsBetween October 19 and December 27, 2022, five symptomatic HAV cases were notified to the Public Health Service Amsterdam; all attended the same primary school. Passive samplers, small absorbent tools, were deployed in sewage near the school from November 14, 2022, to March 22, 2023. The absorbents were subjected to RNA extraction, HAV PCR testing, and, if positive, sequencing. PCR and sequencing were also performed on plasma and feces samples of HAV cases.ResultsIn 22 out of 88 (25%) of sewage samples, HAV RNA was detected. All HAV-RNA-positive sewage samples until 8 February 2023 were subgenotype IB, matching the strain detected in all cases. Another strain of HAV (subgenotype IA) was detected in sewage from 15 February 2023 onwards, without associated cases.ConclusionsPassive sampler-based sewage monitoring is an effective method to rapidly detect HAV shedding linked to diagnosed cases. It detects unnoticed viral infections and allows monitoring of outbreaks. This suggests that passive sampler-based monitoring is a promising tool supporting the public health response during HAV and other outbreaks.

Surface water monitoring of chemicals associated with animal husbandry in an agricultural region in the Netherlands using passive sampling

Compounds originating from animal husbandry can pollute surface water through the application of manure to soil. Typically, grab sampling is employed to detect these residues, which only provides information on the concentration at the time of sampling. To better understand the emission patterns of these compounds, we utilized passive samplers in surface water to collect data at eight locations in a Dutch agricultural region, during different time intervals. As a passive sampler, we chose the integrative-based Speedisk® hydrophilic DVB. In total, we targeted 46 compounds, among which 25 antibiotics, three hormones, nine antiparasitics, and nine disinfectants. From these 46 compounds, 22 compounds accumulated in passive samplers in amounts above the limit of quantification in at least one sampling location. Over the 12-week deployment period, a time integrative uptake pattern was identified in 53% of the examined cases, with the remaining 47% not displaying this behavior. The occurrences without this behavior were primarily associated with specific location, particularly the most upstream location, or specific compounds. Our findings suggest that the proposed use of passive samplers, when compared in this limited context to traditional grab sampling, may provide enhanced efficiency and potentially enable the detection of a wider array of compounds. In fact, a number of compounds originating from animal husbandry activities were quantified for the first time in Dutch surface waters, such as flubendazole, florfenicol, and tilmicosine. The set-up of the sampling campaign also allowed to distinguish between different pollution levels during sampling intervals on the same location. This aspect gains particular significance when considering the utilization of different compounds on various occasions, hence, it has the potential to strengthen ongoing monitoring and mitigation efforts.

Validation of cheap axial passive sampler and procedure suitable for atmospheric NO2 community-based monitoring

Nitrogen dioxide (NO2) is an air pollutant highly impacting on human health, and its measurement is crucial for air quality assessment. Use of passive samplers for long-term large-scale monitoring is a reasonably reliable and economic alternative to more sophisticated and expensive equipment employed in active air sampling by environmental control authorities. In recent years the Citizen Science approach, based on low-cost devices, is spreading more and more in environmental control. Passive samplers available on the market (like the consolidated “Palmes” tubes) are often used in community-based monitoring campaigns. We describe validation of a new cheap axial diffusion tube for NO2 monitoring, used in combination with a new user-friendly App for smartphone that represents an innovation to speed up recording of geo-localization and exposition period data. Affordability and availability of materials, simple construction protocol and easy App procedure, allow possible self-production by school students and non-expert users, making the proposed tube a potential tool to realize extended Citizen Science monitoring campaigns. Accuracy within 25% and precision within 20%, evidenced in validation, show comparability of the tube performance with Palmes-type tubes and agreement with the official monitoring station results. Two small-scale trial monitoring campaigns, involving high school students, were performed to test the efficacy of the proposed “tube-App” system in combining educational impact and community value of air quality monitoring.

Cyanotoxin Monitoring and Detection Using Passive Sampling Application

Cyanobacterial blooms in water have been extensively studied as they produce bioactive and toxic metabolites, commonly known as cyanotoxins. Additionally, the presence of cyanobacteria and, consequently, the production of cyanotoxins, have increased in extent and frequency worldwide. Therefore, the risk associated with the presence of these microorganisms and their toxins has become a matter of great concern. On the other hand, conventional processes for water treatment are inefficient for their elimination and/or degradation, so their presence in water persists at trace and ultra-trace concentrations. In this regard, it is important to develop alternatives to monitor cyanotoxins and allow their detection at low levels in water supply and purification systems, in order to ensure water of good quality for human consumption. In this work, different methodologies, implemented both at laboratory scale and in situ in aqueous bodies, are described. Among these methodologies, traditional and passive techniques are highlighted. Appropriate analytical and sample preparation methods used in the detection and quantification of cyanotoxins are also addressed. It was found that the use of passive samplers is a convenient and a cost-effective method of identifying the presence of these toxins in water at concentrations in the order of µg/L and ng/L. Moreover, studying the by-products generated from the degradation of natural toxins in aquatic environments and evaluating their possible adverse effects is crucial in terms of the management and control of cyanobacteria and cyanotoxin pollution in water.

Food and Environmental Virology: Use of Passive Sampling to Characterize the Presence of SARS-CoV-2 and Other Viruses in Wastewater.

Fecal shedding of SARS-CoV-2 leads to a renaissance of wastewater-based epidemiology (WBE) as additional tool to follow epidemiological trends in the catchment of treatment plants. As alternative to the most commonly used composite samples in surveillance programs, passive sampling is increasingly studied. However, the many sorbent materials in different reports hamper the comparison of results and a standardization of the approach is necessary. Here, we compared different cost-effective sorption materials (cheesecloths, gauze swabs, electronegative filters, glass wool, and tampons) in torpedo-style housings with composite samples. Despite a remarkable variability of the concentration of SARS-CoV-2-specific gene copies, analysis of parallel-deposited passive samplers in the sewer demonstrated highest rate of positive samples and highest number of copies by using cheesecloths. Using this sorption material, monitoring of wastewater of three small catchments in the City of Dresden resulted in a rate of positive samples of 50% in comparison with composite samples (98%). During the investigation period, incidence of reported cases of SARS-CoV-2 in the catchments ranged between 16 and 170 per 100,000 persons and showed no correlation with the measured concentrations of E gene in wastewater. In contrast, constantly higher numbers of gene copies in passive vs. composite samples were found for human adenovirus and crAssphage indicating strong differences of efficacy of methods concerning the species investigated. Influenza virus A and B were sporadically detected allowing no comparison of results. The study contributes to the further understanding of possibilities and limits of passive sampling approaches in WBE.

Use of passive sampling in environmental DNA metabarcoding technology: Monitoring of fish diversity in the Jiangmen coastal waters

Environmental DNA (eDNA) metabarcoding technology is proving to be the most up-to-date and promising method for monitoring marine fish diversity. Fish eDNA is usually collected on a filter membrane after the filtration of water. Not only does this require the use of specialized equipment, but the amount of filtered water needed is also difficult to meet. The recently proposed passive eDNA collection method can expand the sampling scale, providing new perspectives for monitoring marine biodiversity. The role of collection methods in eDNA surveys, however, remains unclear. In this study, a low-cost custom framework with two types of filter membrane materials was used to conduct passive submersion samplings at the north and south ends of Shangchuan Island, Jiangmen, China. After defined periods of submersion, the filter membranes were recovered and eDNA extracted. Metabarcoding techniques were applied to detect fish species information in the eDNA samples. A total of 106 marine fish species from 27 orders, 53 families, and 92 genera, including one cartilaginous fish, were identified in the samples. The majority of fish detected by active filtration were also found in the passively collected samples, within the same location. Both sampling methods, therefore, showed similar species richness. Passive sampling was effective in identifying fish species diversity and provided a higher spatial resolution owing to the sample replicates. Passive sampling was also more sensitive in detecting species that differ significantly in abundance (biomarkers) between different sampling depths. When active filtration is not possible, or when large-scale sampling is the purpose of the study, passive sampling methods certainly provide a promising alternative. The findings of our study provide guidance for fish surveys and continuous bio-stereoscopic monitoring in coastal waters.

Analysis of drug of abuse compounds using passive sampling and ultrahigh-liquid chromatography coupled to mass spectrometry

The present study proposes the monitoring of compounds of drugs of abuse through the use of passive samplers in water systems. Initially, four positive ion compounds of interest were determined according to national surveys, and then composite sampling and passive sampling were implemented using continuous-flow passive samplers containing two types of sorbents, the Empore disk and Gerstel Twister. Two study sites were established at the beginning and at the end of the middle Bogotá River basin. After 4 days, the sorbents were removed so that they could be desorbed and analyzed using UHPLC–MS in the laboratory. For the composite samples, the results were below the first calibration curve point (FCCP) of the chromatographic method, and for passive sampling, peaks of benzoylecgonine (BE) (21427.3 pg mL−1), methamphetamine (MET) (67101.5 pg mL−1), MDMA (ecstasy) (225844.8 pg mL−1) and 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) (15908.4 pg mL−1) were found. Therefore, passive sampling could be suggested as an alternative to composite sampling for the monitoring of compounds.

Use of atmospheric concentrations and passive samplers to assess surface-atmosphere exchange of gaseous mercury in forests

Direct measurements of gaseous elemental mercury (GEM) exchanges over global ecosystems are challenging and require extensive and costly measurement systems. Here, we explore the use of atmospheric GEM concentration variability and passive samplers to assess underlying ecosystem GEM exchanges at two rural temperate forests in the northeastern United States. We find strong temporal alignments between atmospheric GEM concentration declines and ecosystem GEM deposition in spring at both forests, which followed patterns of CO2 and suggests that ambient air GEM concentration monitoring provides a proxy measurement to assess forest GEM sinks. In fall, we observe GEM concentration increases and reversal of GEM fluxes to emissions, but with poor temporal alignments. Diel GEM concentration variability did not correspond to diel patterns of ecosystem GEM fluxes, which is driven by boundary layer dynamics with different atmospheric mixing depths during day- and nighttime. Passive samplers (PASs) deployed to measure vertical GEM gradients across six heights throughout one of the forest canopies showed excellent agreements with active measurements in detecting seasonal concentration patterns at all deployment heights. We find frequent qualitative agreement between the direction of active and PAS derived concentration gradients, but small concentration differences over small (1.3 and 4.9 m) distances prevent a quantitative comparison of methods. Furthermore, time-averaged GEM concentration gradient measurements are always biased towards stable nighttime periods, while ecosystem GEM fluxes are dominated by daytime exchanges, which results in the inability of integrated measurements such as PAS to correctly quantify forest GEM exchanges. We conclude that concentration measurements both via active and passive sampling can serve as proxies to assess underlying ecosystem GEM sinks and sources, but that the use of passive samplers to quantify GEM exchange via gradient measurements is limited due their strong nighttime biases.

Evaluation of ceramic passive samplers using a mixed-mode strong cation-exchange sorbent to monitor polar contaminants in river water

Although most of the analytical methods developed for the monitoring of contaminants in environmental waters are based on discrete grab sampling, an alternative of increasing interest is the use of passive sampling. Methods based on passive sampling provide the sampling and pre-concentration of the analytes in-situ, which makes the sample treatment less time consuming and costly than using discrete grab sampling. In this study, ceramic passive samplers (CPSs) using mixed-mode strong cation-exchange sorbent (Oasis MCX) as retention phase were evaluated for the determination of a group of 21 therapeutic and illicit drugs and some of their metabolites in river water samples that were determined by liquid chromatography-tandem mass spectrometry. After assessing the stability of the analytes, the CPSs were calibrated for 9 days with bottled water and river water, obtaining, for the 19 stable compounds, sample rates (Rs) ranging between 0.180 and 1.767 mL/day and diffusion coefficients (De) between 2.02E-8 and 2.81E-7 cm2/s. Once calibrated, CPSs were deployed for the determination of contaminants in the Ebre River, with good reproducibility, and some of the analytes were determined, including amongst others, gabapentin at 76 ng/L, caffeine at 203 ng/L or diclofenac amine at 57 ng/L. The passive sampling method herein presented is simple and feasible and allows the time-integrated analysis of pharmaceuticals and drugs at trace levels in river water. This study opens the possibility of using other mixed-mode sorbents or other types of sorbents as retaining phase on CPSs for the determination of very polar contaminants in water.

A long-term passive sampling approach for wastewater-based monitoring of SARS-CoV-2 in Leipzig, Germany

Wastewater-based monitoring of SARS-CoV-2 has become a promising and useful tool in tracking the potential spread or dynamics of the virus. Its recording can be used to predict how the potential number of infections in a population will develop. Recent studies have shown that the use of passive samplers is also suitable for the detection of SARS-CoV-2 genome copies (GC) in wastewater. They can be used at any site, provide timely data and may collect SARS-CoV-2 GC missed by traditional sampling methods. Therefore, the aim of this study was to evaluate the suitability of passive samplers for the detection of SARS-CoV-2 GC in wastewater in the long-term at two different scales. Polyethylene-based plastic passive samplers were deployed at the city-scale level of Leipzig at 13 different locations, with samples being taken from March 2021 to August 2022. At the smaller city district level, three types of passive samplers (cotton-cloth, unravelled polypropylene plastic rope and polyethylene-based plastic strips) were used and sampled on a weekly basis from March to August 2022. The results are discussed in relation to wastewater samples taken at the individual passive sampling point. Our results show that passive samplers can indicate at a city-scale level an accurate level of positive infections in the population (positive-rate: 86 %). On a small-scale level, the use of passive samplers was also feasible and effective to detect SARS-CoV-2 GC easily and cost-effectively, mirroring a similar trend to that at a city-scale level. Thus, this study demonstrated that passive samplers provide reproducible SARS-CoV-2 GC signals from wastewater and a time-integrated measurement of the sampled matrix with greater sensitivity compared to wastewater. We thus recommend the use of passive samplers as an alternative method for wastewater-based epidemiology. Passive samplers can in particular be considered for a better estimation of infections compared to incidence levels.

Field Evaluation of the Sentinel™ Integrative Passive Sampler for the Measurement of Perfluoroalkyl and Polyfluoroalkyl Substances in Water Using a Modified Organosilica Adsorbent

AbstractA passive sampler specifically designed to measure perfluoroalkyl and polyfluoroalkyl substances (PFAS) in water was tested in four study areas (Ellsworth and Peterson Air Force bases, CO and SD; the Ohio River, OH, WV, KY, IN; and the Santa Ana River, CA). Locations included both groundwater and surface water locations. Over the 2‐year study, 96 passive samplers were deployed at 33 sample locations and were compared with co‐collected grab samples, all of which were measured for 19 PFAS analytes by HPLC–MS/MS. Correlations were observed (typically within 2× difference) between aqueous PFAS concentrations measured by passive versus discrete grab samples across over 5 orders of magnitude in concentration (0.5 to 150,000 ng/L). Overall relative percent difference between grab and passive results displayed a median of 18% (interquartile range of −19 to 73%). Detection limits were around 1 ng/L for a 2‐week sampling time with sampling rates ranging from 12 to 70 mL/day in flowing systems. Duplicate samplers were deployed in all study areas which indicated a 14 to 42% (median 24%) relative standard deviation in the precision of passive sampling. Larger variances were seen with sites with higher and potentially more variable water flows. A sub‐set of duplicate samplers were measured by a commercial laboratory which returned equivalent data to research laboratory measurements (43 [±26 SD]% relative percent difference). Standardized protocols and calculation methods were developed to facilitate expanded testing and future broader use of passive sampling for PFAS by site investigators.

Determination of triacetone triperoxide (TATP) traces using passive samplers in combination with GC-MS and GC-PCI-MS/MS methods

The use of organic peroxides for the preparation of homemade explosives (HMEs) is common among terrorists due to inexpensive precursor chemicals and simple synthetic procedures. Triacetone triperoxide (TATP) is the most notable peroxide explosive, and has been deployed in several terrorist attacks as explosive filling of improvised explosive devices (IEDs). Forensic identification of TATP in pre-blast and post-blast residues, including on-site analysis, poses significant analytical challenges and induces demand for practicable and sensitive detection techniques. This work presents a concept suitable for laboratory and on-site identification of TATP residues in liquid samples (aqueous TATP synthetic waste) and in gas phase. It is based on TATP enrichment from the aqueous or gas phase using different types of passive samplers (polydimethylsiloxane (PDMS) sampling rods and activated carbon sampling tubes (ACST)) and subsequent identification of the explosive by gas chromatography-mass spectrometry (GC-MS) or GC with positive chemical ionization and tandem MS (GC-PCI-MS/MS) analytical techniques. Additionally, investigation of the stability of TATP in aqueous solutions and of the stability of enriched TATP in passive samplers under different storage conditions, as well as development of TATP re-extraction procedures from passive samplers have been performed in this study. The practical use of passive samplers was demonstrated during and after TATP production processes. Moreover, post-blast sampling of TATP under different conditions of controlled blasting events was investigated using the passive sampling concept.

Determination of groundwater origins and vulnerability based on multi-tracer investigations: New contributions from passive sampling and suspect screening approach

Knowledge about groundwater origins and their interactions with surface water is fundamental to assess their vulnerability. In this context, hydrochemical and isotopic tracers are useful tools to investigate water origins and mixing. More recent studies examined the relevance of contaminants of emerging concern (CECs) as co-tracers to distinguish sources contributing to groundwater bodies. However, these studies focused on known and targeted CECs a priori selected regarding their origin and/or concentrations. This study aimed to improve these multi-tracer approaches using passive sampling and qualitative suspect screening by exploring a larger variety of historical and emerging concern contaminants in combination with hydrochemistry and water molecule isotopes. With this objective, an in-situ study was conducted in a drinking water catchment area located in an alluvial aquifer recharged by several water sources (both surface and groundwater sources). CECs determined by passive sampling and suspect screening allowed to provide in-depth chemical fingerprints of groundwater bodies by enabling the investigation of >2500 compounds with an increased analytical sensitivity. Obtained cocktails of CECs were discriminating enough to be used as chemical tracer in combination with hydrochemical and isotopic tracers. In addition, the occurrence and type of CECs contributed to a better understanding of groundwater-surface water interactions and highlighted short-time hydrological processes. Furthermore, the use of passive sampling with suspect screening analysis of CECs lead to a more realistic assessment and mapping of groundwater vulnerability.

Catchment sourcing urban pesticide pollution using constructed wetlands in Melbourne, Australia

A survey of 111 urban constructed stormwater wetlands (median watershed area = 86.8 ha) was conducted to identify the major pesticides present and to determine their major catchment sources (residential, industrial, commercial, sporting ovals) and associations with catchment imperviousness. Melbourne, Australia, has separate stormwater and sewerage systems and these wetlands are designed to treat urban stormwater. To maximise the pesticides that could be detected, three types of passive samplers (POCIS, Chemcatcher® SDB-XC and Chemcatcher® C18) were deployed, along with collection of fine sediments. A total of 231 pesticides were screened using these methods. Pesticides that were detected in >5 % of wetlands were checked to determine their registered use in urban areas using an Australian government database (PubCris). Twenty-five pesticides were detected in >5 % of wetlands: 4 pesticides were associated with non-urban land uses (agriculture and forests), another 4 pesticides had no known registered use in urban areas and 17 were associated with urban areas. The pesticides associated with urban areas were the herbicides simazine, diuron, metolachlor, bromacil, propyzamide and paclobutrazol, the fungicides tebuconazole, propiconazole, metalaxyl, trifloxystrobin, iprodione and carbendazim and the insecticides fipronil, bifenthrin, chlorantraniliprole, thiamethoxam and permethrin. Atrazine was also detected in 59 % of wetlands but has not been registered for urban uses in Australia since 2010. It's presence in Melbourne may be due to legacy issues or aerial transportation from rural areas where it's still widely used in crop cultivation. Generally, the major urban catchment source of pesticides is from residential areas (particularly fipronil and simazine), most likely in wood preservatives, paints and from weed or insect control. Many of these widely used pesticides were correlated with increased catchment imperviousness. Some pesticides (bromacil and imidacloprid) were correlated with commercial premises and chlorantraniliprole was correlated with the presence of sporting ovals in the catchment. No pesticides were specifically correlated with industrial areas. The use of passive samplers and fine sediments, in conjunction with detailed land use mapping of stormwater wetland catchments is very effective and efficient in monitoring and sourcing pesticide contamination in urban environments.

Lichen transplants as indicators of gaseous elemental mercury concentrations

Lichens play an important role in the biogeochemical cycling of mercury (Hg) and are commonly used as indicators of Hg enrichment in remote and anthropogenically impacted environments. To assess their capacity for Hg uptake and accumulation, we determined the concentration of gaseous elemental mercury (GEM) in air and the concentration of total Hg (THg) in transplanted thalli of two lichen species. Lichen transplants and passive air samplers (PASs) were concurrently deployed, side by side, at 10 sites within an abandoned mining area, characterized by large gradients in atmospheric Hg contamination. Highly variable time-weighted GEM concentrations determined by the PASs, ranging from 17 to 4,200 ng/m3, were mirrored by generally high Hg concentrations in transplanted thalli of both Xanthoria parietina (174–8,800 ng/g) and Evernia prunastri (143–5,500 ng/g). Hg concentrations in the two species co-varied linearly indicating about 60% greater Hg accumulation in X. parietina than in E. prunastri. Whereas Hg uptake in the fruticose E. prunastri increased linearly with GEM, a power law equation with a fractional exponent described the uptake in the foliose X. parietina. Extrapolating the relationships observed here to higher GEM levels yielded concentrations in lichen that agree very well with those measured in an earlier fumigation experiment performed under laboratory-controlled conditions. The uptake model of X. parietina was further verified by correctly estimating GEM concentrations from the THg measured in autochthonous thalli collected from the urban area adjacent to the mine site. Passive sampling can effectively provide time-weighted data of suitable spatial resolution to quantitatively describe GEM assimilation by lichens. Therefore, the combined use of passive sampling and lichen transplants can contribute to a more comprehensive understanding of the role of lichens, and potentially also of other cryptogams, in the deposition of atmospheric Hg to terrestrial ecosystems.

Field Validation of a Novel Passive Sampler for Dissolved PFAS in Surface Waters.

Numerous per- and polyfluoroalkyl substances (PFAS) are of growing concern worldwide due to their ubiquitous presence, bioaccumulation and adverse effects. Surface waters in the United States have displayed elevated concentrations of PFAS, but so far discrete water sampling has been the commonly applied sampling approach. In the present study we field-tested a novel integrative passive sampler, a microporous polyethylene tube, and derived sampling rates (Rs ) for nine PFAS in surface waters. Three sampling campaigns were conducted, deploying polyethylene tube passive samplers in the effluent of two wastewater treatment plant (WWTP) effluents and across Narragansett Bay (Rhode Island, USA) for 1 month each in 2017 and 2018. Passive samplers exhibited linear uptake of PFAS in the WWTP effluents over 16-29 days, with in situ Rs for nine PFAS ranging from 10 ml day-1 (perfluoropentanoic acid) to 29 ml day-1 (perfluorooctanesulfonic acid). Similar sampling rates of 19 ± 4.8 ml day-1 were observed in estuarine field deployments. Applying these Rs values in a different WWTP effluent predicted dissolved PFAS concentrations mostly within 50% of their observations in daily composite water samples, except for perfluorobutanoic acid (where predictions from passive samplers were 3 times greater than measured values), perfluorononanoic acid (1.9 times), perfluorodecanoic acid (1.7 times), and perfluoropentanesulfonic acid (0.1 times). These results highlight the potential use of passive samplers as measurement and assessment tools of PFAS in dynamic aquatic environments. Environ Toxicol Chem 2022;41:2375-2385. © 2022 SETAC.

Health Risk Assessment of Ambient Nitrogen Dioxide Concentrations in Urban and Industrial Area in Rayong Province, Thailand

Nitrogen dioxide (NO2) is a hazardous gas and an air pollutant that is released from a variety of sources, including fossil fuel mining and burning, automobile emissions and other sources. The inhalation of NO2 has been linked to the exact causes of a variety of health issues, including respiratory disorders and a variety of other maladies. The largest source of NO2 exposure is through traffic density emissions. The concentrations of ambient NO2 in Rayong province’s urban, industrial and background areas were measured during rainy, winter and summer seasons. Samples of NO2 were collected with the use of passive samplers during September 2017 to April 2018. The result of the analysis revealed that NO2 concentration of urban area, industrial area and background area were 13.9 - 43.0, 10.4 - 34.0 and 5.8 - 35.2 µg/m3, respectively. It is to be noted that NO2 concentrations in urban and industrial areas were significantly higher than those in background areas (p < 0.05). The dominant source is located nearby high traffic density and industrial establishments. However, the NO2 values obtained from seasonal variations were not significantly different (p > 0.05). A weak correlation was observed between NO2 concentrations and total precipitation (r = −0.237). The low wind speed has no effect on NO2 dispersion. As a result of the geographical and seasonal variation of NO2 concentrations, it was determined that local activities such as traffic density had a much greater impact on NO2 levels than meteorological factors. The hazard quotient (HQ) values from NO2 exposure in Rayong province were less than 1, indicating that the risk was negligible. The inhalation of NO2 by residents who live near the roadside and highway, on the other hand, may endanger their health.
 HIGHLIGHTS
 
 NO2 concentrations in Rayong province related to traffic density and industrial establishments
 The ambient NO2 levels in urban and industrial areas were approximately 1.4 times higher than those in background areas (p < 0.05)
 Residents of Rayong province who live near the roadside and highway road may put their health at risk due to NO2 inhalation
 
 GRAPHICAL ABSTRACT

A look down the drain: Identification of dissolved and particle bound organic pollutants in urban runoff waters and sediments

Urban runoff contains a range of organic micropollutants which, if not removed during wastewater treatment, pose a risk to aquatic environments. These mixtures are complex and often site-specific. Street drains provide an ideal sampling point given they collect the runoff from local and defined catchments. In this study, runoff was collected and sampled in five street drains located in a medium sized town in Germany. A specially constructed trap was used to collect the particulate and total water fractions of the runoff. In addition, passive samplers were deployed to determine the freely dissolved concentrations of selected compounds in the runoff. In sum, 187 polar organic micropollutants could be quantified using LC-HRMS. Thirty of these could only be detected by the use of passive samplers. Traffic derived pollutants such as corrosion inhibitors, rubber- and plastic additives, but also pollutants of industrial origin were strongly represented with sum median concentrations of 100 μg/kg dry weight (DW) in the sediment and 400 ng/L in the water fraction. Several of these substances are of concern due to their environmental persistence and mobility. Perfluorinated compounds and pesticides occurred at lower levels of several μg/kg DW sediment or ng/L water. A number of substances including pharmaceuticals, sweeteners and stimulants indicated domestic wastewater influences. Furthermore, a total of 62 parent and alkylated PAHs were quantified by GC-MS and contributed 30–70% to the sum concentrations of the micropollutants. Non-EPA PAHs dominated the carcinogenic PAH toxicity. The increased PAH alkylation indices (0.7–0.9) showed these primarily came from combustion sources. The runoff particles were additionally microscopically characterized, and correlations were found between the rubber particle counts and the PAH alkylation-index as well as the levels of 2-(methylthio)benzothiazole, a marker compound for tire leaching.

Occupational Exposure of Canadian Nail Salon Workers to Plasticizers Including Phthalates and Organophosphate Esters.

Personal exposure of nail salon workers to 10 phthalates and 19 organophosphate esters (OPEs) was assessed in 18 nail salons in Toronto, Canada. Active air samplers (n = 60) and silicone passive samplers, including brooches (n = 58) and wristbands (n = 60), were worn by 45 nail salon workers for ∼8 working hours. Diethyl phthalate (median = 471 ng m-3) and diisobutyl phthalate (337 ng m-3) were highest in active air samplers. Most abundant OPEs in active air samplers were tris(2-chloroisopropyl)phosphate or TCIPP (303 ng m-3) and tris(2-chloroethyl)phosphate or TCEP (139 ng m-3), which are used as flame retardants but have not been reported for use in personal care products or nail salon accessories. Air concentrations of phthalates and OPEs were not associated with the number of services performed during each worker's shift. Within a single work shift, a combined total of 16 (55%) phthalates and OPEs were detected on passive silicone brooches; 19 (66%) were detected on wristbands. Levels of tris(2-chloroisopropyl)phosphate, tris(1,3-dichloro-2-propyl)phosphate or TDCIPP, and triphenyl phosphate or TPhP wristbands were significantly higher than those worn by e-waste workers. Significant correlations (p < 0.05) were found between the levels of some phthalates and OPEs in silicone brooches and wristbands versus those in active air samplers. Stronger correlations were observed between active air samplers versus brooches than wristbands. Sampler characteristics, personal characteristics, and chemical emission sources are the three main factors proposed to influence the use of passive samplers for measuring semi-volatile organic compound exposure.