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.

The Wiśniówka rock strip mining area (south-central Poland) with quartzite quarries, acid water bodies and tailings piles is one of the most unique acid mine drainage (AMD) sites throughout the world. This is due to the occurrence of enormous amounts of pyrite unknown in sedimentary formations worldwide. Of the two mineralization zones, one that is the most abundant in arsenical pyrite occurs in the lowermost Upper Cambrian formation of the Podwiśniówka quarry. The As-rich pyritiferous clastic rocks are exposed as a result of deep quartzite extraction during 2013–2014. In addition, the clayey-silty shale interbeds are enriched in rare earth element (REE) minerals. The mining operation left an acidic lake with a pH of about 2.4–2.6 and increased contents of sulfates, metal(loid)s and REE. The Podwiśniówka pyrite-rich waste material was stacked up in many places of the mining area giving rise to strongly acidic spills that jeopardized the neighboring environment. One of these unexplored tailings piles was a source of extremely sulfate- and metal(loid)-rich pools with unusual enrichments in As (up to 1548 mg L⁻¹) and REE (up to 24.84 mg L⁻¹). These distinctly exceeded those previously reported in the Wiśniówka area. A broad scope of geochemical, mineralogical and petrographic methods was used to document these specific textural and mineralogical properties of pyrite facilitating its rapid oxidation. The pyrite oxidation products reacted with REE-bearing minerals releasing these elements into acid water bodies. Statistical methods were employed to connect the obtained tailings pool hydrogeochemical data with those derived from this and the previous studies of the Podwiśniówka and Wiśniówka Duża acid pit lakes. In contrast to metal(loid) profiles, the characteristic shale-normalized REE concentration patterns turned out to be more suitable for solving different AMD issues including provenance of mine waste material in the tailings pile examined.

PAHs were analyzed in the liver of 5 species of pelagic seabirds (Procellariiformes) from the northeast Atlantic and the Mediterranean. The main objective was to assess the trophic and geographic trends of PAHs in seabirds to evaluate their suitability as bioindicators of chronic marine pollution by these compounds. Although higher levels of PAHs have been described in the Mediterranean compared to other oceanic regions, we did not find significant spatial patterns and observed only minor effects of the geographic origin on seabird PAHs. However, we found significant higher PAH levels in petrel compared to shearwater species, which could be related to differences in their exploitation of mesopelagic and epipelagic resources, respectively, and the vertical dynamic of PAHs in the water column. Overall, although this study enhances the need of multi-species approaches to show a more comprehensive evaluation of marine pollution, seabirds emerged as poor indicators of pelagic chronic PAH levels.

The beneficial uptake of nutrients by wetland plants is countered to some extent by nutrient release back into the aquatic environment due to vegetative die-back. This current study examined whether Leersia oryzoides, a common wetland plant, exhibits luxury uptake of nutrients from simulated farm runoff. The study also tested whether with subsequent decomposition, these nutrients are released back into the water column. When exposed to elevated (>2 mg/L N and P) runoff, L. oryzoides assimilated significantly higher concentrations of nitrogen (p < 0.001) and phosphorus (p < 0.001) in above-ground biomass as compared to non-enriched treatments (<0.05 mg/L N and P). Subsequently, senescence of enriched above-ground biomass yielded significantly higher concentrations of phosphorus (2.19 ± 0.84 mg P/L). Using L. oryzoides as our model, this study demonstrates nitrogen and phosphorus sequestration during the growing season and release of phosphorus in the winter. Release of sequestered nutrients during plant senescence.

Globally, arsenic (As) contamination is widespread in hydrological systems and the link between As enrichment and regional tectonic and climatic factors is still not well understood in orogenic environments. This work provides new insights on the relationship between As, tectonics, and climate by assessing the hydrochemistry of Chile, an active subduction zone with highly diverse natural settings. Selected study sites include fluvial courses along four regional transects connecting the Chilean coast to the Andes Cordillera in the northern, central, and southern areas of the country. The results indicate that As concentrations in surface water and fluvial sediments show a general positive correlation to crustal thickness and they tend to decrease progressively from northern to southern Chile. In contrast, As concentrations are negatively correlated to average annual precipitation which shows a significant increase toward southern Chile. From a regional tectonic perspective, northern Chile presents greater Andes shortening and higher crustal thicknesses, which induces increased crustal contamination and As content at the surface. Extremely low precipitation rates are also tied to local As enrichment and a sediment-starved trench that might favor higher plate coupling and shortening. On the contrary, decreased shortening of the Andes in southern Chile and related lower crustal thickness induces lower crustal contamination, thus acting as an As-poor provenance for surficial sediments and surface water. High precipitation rates further induce dilution of surface water, potential mobilization from the solid phase, and a significant amount of trench sediments that could induce lower plate coupling and lower shortening. At the local scale, a low potential for As mobilization was found in northern Chile where a greater distribution of As-bearing minerals was observed in sediments, mostly as finer particles (<63 μm). The abundance of Fe-oxides potentially acts as a secondary surficial sink of As under the encountered physicochemical conditions.

The exposure of benzo [a]pyrene (BaP) in recent times is rather unavoidable than ever before. BaP emissions are sourced majorly from anthropogenic rather than natural provenance from wildfires and volcanic eruptions. A major under-looked source is via the consumption of foods that are deep-fried, grilled, and charcoal smoked foods (meats in particular). BaP being a component of poly aromatic hydrocarbons has been classified as a Group I carcinogenic agent, which has been shown to cause both systemic and localized effects in animal models as well as in humans; has been known to cause various forms of cancer, accelerate neurological disorders, invoke DNA and cellular damage due to the generation of reactive oxygen species and involve in multi-generational phenotypic and genotypic defects. BaP's short and accumulated exposure has been shown in disrupting the fertility of gamete cells. In this review, we have discussed an in-depth and capacious run-through of the various origins of BaP, its economic distribution and its impact as well as toxicological effects on the environment and human health. It also deals with a mechanism as a single compound and its ability to synergize with other chemicals/materials, novel sensitive detection methods, and remediation approaches held in the environment.

Rainwater chemistry plays an important role in the earth-surficial ecosystem, but studies on rainwater chemical composition of karst agro-ecosystem are rare. To explore the rainwater alkalization and the provenance of components responsible for neutralization, two-years chemical monitoring of rainwater was carried out in a karst agricultural catchment in Southwest China. The main findings suggest that SO₄²⁻, NO₃⁻, Ca²⁺, and NH₄⁺ are the principal ions. All the ionic contents show distinctly seasonal variation (highest in winter) in response to variations in seasonal precipitation because the rain-scour process can efficiently remove atmospheric materials. Source identification indicates that Cl⁻ and Na⁺ are mainly derived from marine input whereas SO₄²⁻ and NO₃⁻ are controlled by anthropogenic emission, in particular, fixed emission sources. The source of NH₄⁺ is attributed to intense agricultural production, while Ca²⁺ and Mg²⁺ are mainly derived from calcite dissolution. The rainwater alkalization caused by the seasonal acid neutralization (via basic components, Ca²⁺ and NH₄⁺) is beneficial to crop growth but also reflect agricultural overfertilization. Sulfur controlled the total wet acid deposition (68%–94%) and could be a potential agent of weathering.

Rare earth elements (REEs) are widely used in optoelectronic industries, and they can be emitted into the environment and may induce biological effects. In this study, we investigated the provenance and bioaccessibility of REEs in atmospheric particles (APs) collected from areas impacted by the optoelectronic industry. The geoaccumulation index (Igₑₒ) values showed that Y, Eu, and Tb were much more enriched in the APs from the optoelectronic recycling sites than in those from the optoelectronic producing sites and were not enriched in the APs from the optoelectronic administrative sites and background sites. The characteristic parameters and the distribution patterns of REEs demonstrated that the AP samples from the recycling sites and producing sites showed remarkably positive Eu and Tb anomalies. According to the positive matrix factorization (PMF) model, the optoelectronic industry was quantitatively determined to contribute 82.8% of Y, 86.5% of Eu, and 83.4% of Tb. Furthermore, an in vitro physiologically based extraction test (PBET) was performed to assess the bioaccessibility of REEs in the APs. The results showed that the bioaccessibility of all the REEs in the APs was below 50.0% in the human gastrointestinal tract, with higher values in the gastric phases than in the intestinal phases. In particular, extremely low gastric bioaccessibilities of Tb and Ce and relatively high gastric bioaccessibilities of Y and Eu were observed in the APs from the recycling sites and producing sites, which may due to the chemical composition of the compounds containing REEs that are used in the optoelectronic industry. In conclusion, our results provide additional information about the contribution and influence of the optoelectronic industry on the provenance and bioaccessibility of REEs in APs.

To differentiate the source of aeolian dust between the desert sources from Pan-third pole and high mountain glaciers, therefore, we investigated the spatial variability of aeolian dust sources in the Pan-third polar region. The question of whether such changes reflect variable transport pathways from a unique source in the western China area was addressed. That is, the SrNd radiogenic isotope composition of modern desert samples do not support the hypothesis of a single dust provenance at higher elevation mountain glaciers by long-distance transport; regional sources also play a significant role. Based on previous studies and the data from this study, the five isotopic regions were divided, which are controlled by the geological characteristics in western China. The results suggest that mineral dust deposited into the high-mountain glaciers originated from the free ice region because of glacier melting and the physical and chemical erosion of rocks from the surrounding mountains by local wind systems. The Pb isotopic data further demonstrated that natural dust is the source of Pb for the high-mountain glaciers of Pan-third pole. These results provide an exhaustive documentation of the isotopic signature of the regional dust reaching the glacier regions.

Plastic litter in the marine environment is a major global issue. Discarded plastic shotgun ammunition shells and discharged wads are an unwelcome addition and feature among the top ten litter items found on reference beaches in Denmark.To understand this problem, its scale and origins, collections were made by volunteers along Danish coastal shorelines. In all 3669 plastic ammunition items were collected at 68 sites along 44.6 km of shoreline. The collected items were scored for characteristic variables such as gauge and length, shot type, and the legibility of text, the erosion, and the presence of metallic components. Scores for characteristics were related to the site, area, and season and possible influences discussed.The prevalence of collected plastic shotgun litter ranges from zero to 41 items per 100 m with an average of 3.7 items per 100 m. Most ammunition litter on Danish coasts originates from hunting on Danish coastal waterbodies, but a small amount may come from further afield. North Sea coasts are the most distinctive suggesting the possible contribution of long distance drift as well as the likelihood that such litter can persist in marine habitats for decades.The pathway from initial discard to eventual wash-up and collection depends on the physical properties of plastic components, marine tides and currents, coastal topography and shoreline vegetation.Judging from the disintegration of the cartridge and the wear and decomposition of components, we conclude that there is a substantial supply of polluting plastic ammunition materials that has and will accumulate. These plastic items pose a hazard to marine ecosystems and wash up on coasts for many years to come. We recommend that responsible managers, hunters and ammunition manufacturers will take action now to reduce the problem and, thereby, protect ecosystems, wildlife and the sustainability of hunting.