A study was undertaken to test the hypothesis that the presence of fly ash and other artifactual materials (AMs) significantly increases the toxicity of urban soil and street dust. AMs were distinguished as artifacts (artificial particles > 2 mm in size), and particulate artifacts (≤2 mm in size); street dust was the <63 μm fraction of street sediments. Reference artifacts, street dusts, and topsoils representing different land use types in Detroit, Michigan were analyzed for miscellaneous radionuclides, trace elements, magnetic susceptibility (MS), and acetic acid-extractable (leachable) Pb. Background levels were established using native glacial sediments. Street sediments were found to have a roadside provenance, hence street dusts inherited their contamination primarily from local soils. All soils and dusts had radionuclide concentrations similar to background levels, and radiological hazard indices within the safe range. Artifacts, fly ash-impacted soils and street dusts contained elevated concentrations of toxic trace elements, which varied with land use type, but none produced a significant amount of leachable Pb. It is inferred that toxic elements in AMs are not bioavailable because they are occluded within highly insoluble materials. Hence, these results do not support our hypothesis. Rather, AMs contribute to artificially-elevated total concentrations leading to an overestimation of toxicity. MS increased with increasing total concentration, hence proximal sensing can be used to map contamination level, but the weak correlation between total and leachable Pb suggests that such maps do not necessarily indicate the associated biohazard. Home site soils with total Pb concentrations >500 mg kg−1 were sporadically toxic. Thus, these results argue against street dust as the local cause of seasonally elevated blood-Pb levels in children. Lead-bearing home site soil tracked directly indoors to form house dust is an alternative exposure pathway.

While the distribution and effects of microplastics (MPs) have been extensively studied in aquatic systems, there exits little information on their occurrence in the terrestrial environment and their potential impacts on human health. In the present study, street dust and suspended dust were collected from the city and county of Asaluyeh, Iran. Samples were characterized by various microscopic techniques (fluorescence, polarized light, SEM) in order to quantify and classify MPs and microrubbers (MRs) in the urban and industrial environments that are potentially ingestible or inhalable by humans. In < 5-mm street dust retrieved from 15 sites, there were an average of 900 MPs and 250 MRs per 15 g of sample, with MPs exhibiting a range of colours and sizes (<100 to >1000 μm). Most street dust samples were dominated by spherical and film-like particles and MRs largely made up of different sizes of black fragments and fibrous particulates. Airborne dust collected daily over an eight-day period at two locations revealed the ubiquity of fibrous MPs of sizes ranging from about 2 μm to 100 μm and an abundance of about 1 per m⁻³. These samples contained small MR fragments whose precise characteristics were more difficult to define. Based on the median concentrations in street dust, estimates of acute exposure through ingestion are about 5 and 15 MP d⁻¹ and 2 and 7 MR d⁻¹ for construction workers and young children, respectively. Quantities of inhalable particulates were more difficult to define but the potential toxicity of MPs and MRs taken in by this route was evaluated from assays performed using particulates isolated from street dusts in the presence of an artificial lung fluid. Both types of particle exhibited oxidative potential, with MPs displaying consumptions of different antioxidants that were comparable with corresponding values for a reference urban particulate dust but lower than those for London ambient particulate matter. Thus, MPs and MRs contribute towards the health impacts of urban and industrial dusts but their precise roles remain unclear and warrant further study.

The Athabasca Oil Sands Region (AOSR) in Alberta, Canada, is an important source of atmospheric pollutants, such as aerosols, that have repercussions on both the climate and human health. We show that the mean freezing temperature of snow-borne particles from AOSR was elevated (−7.1 ± 1.8 °C), higher than mineral dust which freezes at ∼ −15 °C and is recognized as one of the most relevant ice nuclei globally. Ice nucleation of nanosized snow samples indicated an elevated freezing ability (−11.6 ± 2.0 °C), which was statistically much higher than snow-borne particles from downtown Montreal. AOSR snow had a higher concentration (∼2 orders of magnitude) of >100 nm particles than Montreal. Triple quadrupole ICP-(QQQ)-MS/MS analysis of AOSR and Montreal snow demonstrated that most concentrations of metals, including those identified as emerging nanoparticulate contaminants, were much more elevated in AOSR in contrast to Montreal: 34.1, 34.1, 16.6, 5.8, 0.3, 0.1, and 9.4 mg/m³ for Cr, Ni, Cu, As, Se, Cd, and Pb respectively, in AOSR and 1.3, 0.3, 2.0, <0.03, 0.1, 0.03, and 1.2 mg/m³ in Montreal snow. High-resolution Scanning Transmission Electron Microscopy/Energy-dispersive X-ray Spectroscopy (STEM-EDS) imaging provided evidence for various anthropogenic nano-materials, including carbon nanotubes resembling structures, in AOSR snow up to 7–25 km away from major oil sands upgrading facilities. In summary, particles characterized as coming from oil sands are more efficient at ice nucleation. We discuss the potential impacts of AOSR emissions on atmospheric and microphysical processes (ice nucleation and precipitation) both locally and regionally.

Flame retardants (FRs), such as brominated flame retardants (BFRs) and organophosphorus flame retardants (OPFRs), are diverse groups of compounds used in various products related to the indoor environment. In this study concentrations of eight polybrominated diphenyl ethers (PBDEs), two alternative BFRs and ten OPFRs were determined in indoor dust (n = 20) and pet cat hair (n = 11) from South Africa. The OPFRs were the major FRs, contributing to more than 97% of the total FR concentration. The median Ʃ₁₀OPFRs concentrations were 44,800 ng/g in freshly collected dust (F-dust), 19,800 ng/g in the dust collected from vacuum cleaner bags (V-dust), and 865 ng/g in cat hair (C-hair). Tris(1-chloro-2-propyl) phosphate (TCIPP) was the dominant OPFR in the dust samples with median concentrations of 7,010 ng/g in F-dust and 3,590 ng/g in V-dust. Tris(2-butoxyethyl) phosphate (TBOEP) was the dominant OPFR in C-hair, with a median concentration of 387 ng/g. The concentrations of Ʃ₈PBDEs were higher in F-dust than in V-dust. BDE209 was the dominant BFR in all three matrices. Bis(2-ethylhexyl)-3,4,5,6-tetrabromo-phthalate (BEH-TEBP) and 2-ethylhexyl-2,3,4,5- tetrabromobenzoate (EH-TBB) showed notable contributions to the BFR profile in cat hair. A worst-case dust exposure estimation was performed for all analytes. The estimated TCIPP daily intake through dust ingestion was up to 1,240 ng/kg bw for toddlers. The results indicate that OPFRs are ubiquitous in South African indoor environment. Indoor dust is a major source of human exposure to environmental contaminants. This can for example occur through hand-to-mouth contact of toddlers, and is an important route of exposure to currently used FRs accumulated on dust particles. The presence of FRs, in particular high concentrations of OPFRs, suggests that children and indoor pet cats may have greater exposure to FRs than adults.

We have previously reported on the ubiquitous presence of perchlorate in the deposited and airborne fine dusts of Malta and shown that the source of the chemical in the dusts of this small central Mediterranean island is fireworks. There are no local geologic or anthropogenic sources of perchlorate other than firework manufacture and display. The hypothesis was tested that ground-deposited perchlorate will be mobilized in runoff and would partly migrate to the water table and eventually also affect tap water, one third of which being derived from groundwater. Forty four percent of 36 groundwater samples contained perchlorate above detection limit with mean and median values of 1.09 and 1.1 μg L−1. Sixty-two percent of 16 runoff samples collected during storms contained perchlorate above detection limit with mean and maximum concentrations, respectively, of 50.8 and 129 μg L−1, values which are far too high to be explained by atmospheric inputs given that rainwater perchlorate levels are typically <3 μg L−1. Between 42 and 89% of the tap waters analyzed in three sampling campaigns contained perchlorate above detection limit and had mean concentrations ranging from 0.4 to 1.6 μg L−1 suggesting contamination levels similar to those reported from China but lower than levels reported from the USA. The phenomenon of contamination of the water resources of Malta by perchlorate is probably unique in that it results not from geologic or industrial inputs but from an intense and prolonged pyrotechnic activity that is deeply rooted in the popular culture of the islanders.

While infants are developing, they are easily affected by toxic chemicals existing in their environments, such as semi-volatile organic compounds (SVOCs): phthalates, polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), and organophosphate esters (OPEs). However, the specific living environment of infants, including increased plastic products and foam floor mats, may increase the presence of these chemicals. In this study, 68 air, dust, and window film samples were collected from homes, with 3- to 6-month-old infant occupants, to analyze phthalates, PAHs, PBDEs, and OPEs. High detection rates and concentrations suggest that these SVOCs are widespread in infant environments and are associated with cooking methods, smoking habits, the period of time after decoration, and room floors. The partitioning behavior of SVOCs indicates that the logarithms of the dust/gas-phase air partition coefficient (logKD) and the window film/gas-phase air partition coefficient (logKF) in homes are not at an equilibrium state when the logarithm of the octanol/air partition coefficient (logKOA) is less than 8 or greater than 11. Considering the 3 exposure routes, ingestion and dermal absorption have become the main routes of infant exposure to phthalates and OPEs, and ingestion and inhalation have become the dominant routes of exposure to PAHs and PBDEs. The total carcinogenic risk of SVOCs, which have carcinogenic toxicities, via ingestion and dermal absorption for infants in homes exceeds the acceptable value, suggesting that the current levels of these SVOCs in homes might pose a risk to infant health.

A particulate matter (PM) source apportionment study was carried out in one of the most polluted districts of Tuscany (Italy), close to an old waste incinerator plant. Due to the high PM10 levels, an extensive field campaign was supported by the Regional Government to identify the main PM sources and quantify their contributions. PM10 daily samples were collected for one year and analysed by different techniques to obtain a complete chemical characterisation (elements, ions and carbon fractions). Hourly fine (<2.5 μm) and coarse (2.5–10 μm) aerosol samples were collected by a Streaker sampler for a shorter period and hourly elemental concentrations were obtained by PIXE.Positive Matrix Factorization (PMF) analysis of daily and hourly data allowed the identification of 10 main sources: six anthropogenic (Biomass Burning, Traffic, Secondary Nitrates, Secondary Sulphates, Incinerator, Heavy Oil combustion), two natural (Saharan Dust and Fresh Sea Salt) and two mixed sources (Local Dust and Aged Sea Salt). Biomass burning turned out to be the main source of PM, accounting for 30% of the PM10 mass as annual average, followed by Traffic (18%) and Secondary Nitrates (14%). Emissions from the Incinerator turned out to be only 2% of PM10 mass on average.PM10 composition and source apportionment have been assessed in a polluted area near a waste incinerator, by PMF analysis on daily and hourly compositional data sets.

This work explores the use of Raman micro-spectroscopy to determine sources of airborne particulate matter collected on PM₂.₅ air filters in Imperial Valley, California. The goal is to examine if nearby soil is a potential source of particles sampled on air filters deployed in an urbanized desert area during events of unusually high PM₂.₅ excursions. Particle specific composition information can be an indicator of potential origin. This can provide insights into the source of unexpectedly high proportion of large particles sampled on PM₂.₅ filters in the vicinity of Imperial Valley. The measured spectral correspondence between the filter and soil particles, in the size range of 2.5–10 μm, is consistent with windblown dust being a likely source of the larger (>2.5 μm) particles collected on the PM₂.₅ filters. Additionally, these particles were identified as components of commonly occurring crustal minerals in the vicinity of the sampling site, such as iron oxides, hydroxides, sulfides, titanium dioxides and aluminosilicates. A substantial portion of the analyzed filter particles displayed a strong broadband fluorescence signal, which is consistent with the presence of organic matter and has been recognized as a marker for soil related origin of the filter particles. Elemental carbon (soot) was found to be prevalent among the particles as well, suggesting the existence of combustion related sources. Comparison between a heavily loaded filter sample and a filter with a more typical, lower loading did not show any obvious difference in chemical compositions. In both cases the particles appeared to be of crustal origin with the prevalence of elemental carbon. The primary difference between these two filter samples appear to be their particle size distribution - the heavily loaded filter sample contained greater proportion of large particles (>2.5 μm), and was more consistent with spectral signature of soils analyzed from the region.

Magnetic properties of urban street dust can be used as a proxy of urban pollution. In this study, magnetic measurements on 160 street dust samples, collected from five different functional areas (industrial, traffic, commercial, residential and clean areas) in sixteen administrative districts in Shanghai, China, were systematically conducted. It is showed that magnetic carriers were predominately coarse-grain ferrimagnetic particles. Meantime, concentration-related magnetic parameters showed significant variations among the functional areas and administrative units. Magnetic susceptibility (χ) decreased in the following order: industrial area (IA) > traffic area (TA) > commercial area (CoA) > residential area (RA) > clean area (ClA). Moreover, combined with the analyses conducted using a scanning electron microscope and an energy dispersive X-ray spectrometer (SEM-EDX), it is found that spherical magnetic particles originating mainly from anthropogenic sources were abundant in industrial areas. Baoshan district, which is heavily impacted by industrial activities, showed the highest χ value among the administrative units. Additionally, the correlations of street dust χ value with population, value of industrial output and the gross domestic product (GDP) in Shanghai and other cities indicated that χ is positively correlated with the city GDP as well as the population size (PS) to some extent. This study demonstrates that magnetic parameters of street dust can be used as an effective tool for monitoring environmental pollution and industrial activities in urban environments.

As the second largest economy in the world, China experiences severe particulate matter (PM) pollution in many of its cities. Meteorological factors are critical in determining both areal and temporal variations in PM pollution levels; understanding these factors and their interactions is critical for accurate forecasting, comprehensive analysis, and effective reduction of this pollution. This study analyzed areal and temporal variations in concentrations of PM₂.₅, PM₁₀, and PMcₒₐᵣₛₑ (PM₁₀ - PM₂.₅) and PM₂.₅ to PM₁₀ ratios (PM₂.₅/PM₁₀) and their relationships with meteorological conditions in 366 Chinese cities from January 1, 2015 to December 31, 2017. On the national scale, PM₂.₅ and PM₁₀ decreased from 48 to 42 μg m⁻³ and from 88 to 84 μg m⁻³, respectively, and the annual mean concentrations were 45 μg m⁻³ (PM₂.₅) and 84 μg m⁻³ (PM₁₀) during the time period (2015–2017). In most regions, largest PM concentrations occurred in winter. However, in northern China, in spring PMcₒₐᵣₛₑ concentrations were highest due to dust. The PM₂.₅/PM₁₀ ratio was higher in southern than in northern China. There were large regional disparities in PM diurnal variations. Generally, PM concentrations were negatively correlated with precipitation, relative humidity, air temperature, and wind speed, but were positively correlated with surface pressure. The sunshine duration showed negative and positive impacts on PM in northern and southern cities, respectively. Meteorological factors impacted particulates of different size differently in different regions and over different periods of time.