Inputs of polycyclic aromatic hydrocarbons (PAHs) of regulatory interest from diffuse atmospheric sources within urban areas frequently elevate local soil concentrations to levels requiring remediation despite the lack of in-situ contamination. This research sought to determine the distribution and potential health effects of aerially deposited PAHs in soil within the urban core of metropolitan Milwaukee, Wisconsin, U.S.A. as part of a soil regulatory standards reevaluation. Park areas (n = 27) identified as undisturbed for 80+ years, containing no fill material, and receiving only atmospheric deposition were selected for composite surface and 92 cm core soil sample collection (n = 295). Samples were analyzed for the 16 USEPA priority PAHs, 1- and 2- methylnapthalene and ancillary soil properties. Soil core and ancillary data confirm lack of site disturbance. PAH diagnostic ratios and homologue summations indicate that diffuse multiple point source emissions contribute equally to PAH deposition throughout the area. Benzo(a)pyrene (BaP) and dibenz(a,h)anthracene mean concentrations exceed health-based clean up levels. Risk assessment shows only a worst-case exposure scenario (BaP at the 95% upper confidence limit) increasing cancer risk (1.67 × 10⁻⁶) over current regulatory thresholds (1.0 × 10⁻⁶). Health quotients show potential health risks from fluoranthene and pyrene for daily park users and from BaP for all others. Mean soil PAH values are similar to New Orleans, but lower than Chicago, Boston, and London reflecting industrial history and site selection protocols. The soil PAH results presented here for sites selected for non-manipulated soils combined with an almost 100-year uninterrupted atmospheric exposure effectively show the maximum potential PAH values that can be found at any given undisturbed location within the Milwaukee urban core due solely to atmospheric deposition.

Water contamination caused by radionuclides is a major environmental issue. Uranium (U) belongs to the actinide group of elements. Hexavalent uranium (U(VI)) is radioactively and chemically harmful and highly mobile in the environment and wastewater stream. Therefore, developing highly efficient materials for minimizing the environmental impact of U(VI) is essential. To achieve this goal, we successfully synthesized a novel material, namely graphene oxide (GO)/hydroxyapatite (HAP), by directly assembling GO and HAP through a facile hydrothermal method, which exhibits effective U(VI) removal and immobilization. The GO/HAP composite has an outstanding sorption capacity for U(VI) (i.e., 373.00 mg/g) within 5 min at a pH of 3.0. The parameters from thermodynamic analysis indicated that the GO/HAP composite absorbed U(VI) through a process of spontaneous and exothermic adsorption. XPS, XRD, and FT-IR results revealed that the composite’s phosphate group was mainly responsible for U(VI) retention and incorporation. The GO/HAP composite’s enhanced U(VI) sorption capacity is most likely ascribed to the synergistic effect after functionalizing with nano HAP. The current findings may greatly facilitate the creation of rational design strategies to develop highly efficient materials that can treat radioactive wastewater.

Tropospheric (ground-level) ozone is a harmful phytotoxic pollutant, and can have a negative impact on crop yield and quality in sensitive species. Ozone can also induce visible symptoms on leaves, appearing as tiny spots (stipples) between the veins on the upper leaf surface. There is little measured data on ozone concentrations in Africa and it can be labour-intensive and expensive to determine the direct impact of ozone on crop yield in the field. The identification of visible ozone symptoms is an easier, low cost method of determining if a crop species is being negatively affected by ozone pollution, potentially resulting in yield loss. In this study, thirteen staple African food crops (including wheat (Triticum aestivum), common bean (Phaseolus vulgaris), sorghum (Sorghum bicolor), pearl millet (Pennisetum glaucum) and finger millet (Eleusine coracana)) were exposed to an episodic ozone regime in a solardome system to monitor visible ozone symptoms. A more detailed examination of the progression of ozone symptoms with time was carried out for cultivars of P. vulgaris and T. aestivum, which showed early leaf loss (P. vulgaris) and an increased rate of senescence (T. aestivum) in response to ozone exposure. All of the crops tested showed visible ozone symptoms on their leaves in at least one cultivar, and ozone sensitivity varied between cultivars of the same crop. A guide to assist with identification of visible ozone symptoms (including photographs and a description of symptoms for each species) is presented.

The combined application of organic and synthetic nitrogen (N) fertilizers is being widely recommended in China’s vegetable systems to reduce reliance on synthetic N fertilizer. However, the effect of substituting synthetic fertilizer with organic fertilizer on vegetable productivity (yield, N uptake and nitrogen use efficiency) and reactive nitrogen (Nr) losses (N₂O emission, N leaching and NH₃ volatilization) remains unclear. A meta-analysis was performed using peer-reviewed papers published from 2000 to 2019 to comprehensively assess the effects of combined application of organic and synthetic N fertilizers. The results indicate that overall, the vegetable yield, N₂O emission and NH₃ volatilization were not significantly changed, whereas N leaching was reduced by 44.6% and soil organic carbon (SOC) concentration increased by 12.5% compared to synthetic N fertilizer alone. Specifically, when synthetic N substitution rates (SRs) were ≤70%, vegetable yields and SOC concentration were increased by 5.5%–5.6% and 13.1–18.0%, and N leaching was reduced by 41.6%–48.1%. At the high substitution rate (SR>70%), vegetable yield was reduced by 13.6%, N₂O emission was reduced by 14.3%, and SOC concentration increased by 16.4%. Mixed animal-plant sources of organic N preferentially increased vegetable yield and SOC concentration, and reduced N₂O emission and N leaching compared with single sources of organic-N. Greenhouse gas (GHG) emission was decreased by 28.4%–34.9% by combined applications of organic and synthetic N sources, relative to synthetic N fertilizer alone. We conclude that appropriate rates (SR ≤ 70%) of combined applications of organic and synthetic N fertilizers could improve vegetable yields, decrease Nr and GHG emission, and facilitate sustainable development of coupled vegetable-livestock systems.

To understand the characteristics of particulate matter (PM) and other air pollutants in Xinjiang, a region with one of the largest sand-shifting deserts in the world and significant natural dust emissions, the concentrations of six air pollutants monitored in 16 cities were analyzed for the period January 2013–June 2019. The annual mean PM₂.₅, PM₁₀, SO₂, NO₂, CO, and O₃ concentrations ranged from 51.44 to 59.54 μg m⁻³, 128.43–155.28 μg m⁻³, 10.99–17.99 μg m⁻³, 26.27–31.71 μg m⁻³, 1.04–1.32 mg m⁻³, and 55.27–65.26 μg m⁻³, respectively. The highest PM concentrations were recorded in cities surrounding the Taklimakan Desert during the spring season and caused by higher amounts of wind-blown dust from the desert. Coarse PM (PM₁₀₋₂.₅) was predominant, particularly during the spring and summer seasons. The highest PM₂.₅/PM₁₀ ratio was recorded in most cities during the winter months, indicating the influence of anthropogenic emissions in winters. The annual mean PM₂.₅ (PM₁₀) concentrations in the study area exceeded the annual mean guidelines recommended by the World Health Organization (WHO) by a factor of ca. ∼5–6 (∼7–8). Very high ambient PM concentrations were recorded during March 19–22, 2019, that gradually influenced the air quality across four different cities, with daily mean PM₂.₅ (PM₁₀) concentrations ∼8–54 (∼26–115) times higher than the WHO guidelines for daily mean concentrations, and the daily mean coarse PM concentration reaching 4.4 mg m⁻³. Such high PM₂.₅ and PM₁₀ concentrations pose a significant risk to public health. These findings call for the formulation of various policies and action plans, including controlling the land degradation and desertification and reducing the concentrations of PM and other air pollutants in the region.

Quinolones are ranked as the second most commonly used class of antibiotics in China, despite their adverse clinical and environmental effects. However, information on their cardiac developmental toxicity to zebrafish is limited. This study investigates the relationships between different quinolone structures and toxicity in zebrafish embryos using in vivo and in silico methods. All of the experimentally tested quinolones show cardiac developmental toxicity potential and present mortality and teratogenic effects in a dose-dependent manner. Theoretically, the acute toxicity values predicted using quantitative structure−toxicity relationship (QSTR) modeling based on previously reported LC₅₀ values are in good agreement with the in vivo results. Further investigation demonstrates that the hormetic concentration response of some quinolones may be related to methylation on the piperazine ring at the C-7 position. The amino group at the C-5 position, the methylated or ethylated piperazine group at the C-7 position, halogens at the C-8 position and a cyclopropyl ring at N1 position may be responsible for cardiac developmental toxicity. In terms of survival (key ecological endpoint), the naridine ring is more toxic than the quinoline ring. This combined approach can predict the acute and cardiac developmental toxicity of other quinolones and impurities.

Thousands of abandoned mines throughout the western region of North America contain elevated total-mercury (THg) concentrations. Mercury is mobilized from these sites primarily due to erosion of particulate-bound Hg (THg-P). Organic matter-based soil amendments can promote vegetation growth on mine tailings, reducing erosion and subsequent loading of THg-P into downstream waterbodies. However, the introduction of a labile carbon source may stimulate microbial activity that can produce methylmercury (MeHg)—the more toxic and bioaccumulative form of Hg. Our objectives were to investigate how additions of different organic matter substrates impact Hg mobilization and methylation using a combination of field observations and controlled experiments. Field measurements of water, sediment, and porewater were collected downstream of the site and multi-year monitoring (and load calculations) were conducted at a downstream gaging station. MeHg production was assessed using stable isotope methylation assays and mesocosm experiments that were conducted using different types of organic carbon soil amendments mixed with materials from the mine site. The results showed that >80% of the THg mobilized from the mine was bound to particles and that >90% of the annual Hg loading occurred during the period of elevated discharge during spring snowmelt. Methylation rates varied between different types of soil amendments and were correlated with the components of excitation emission matrices (EEMs) associated with humic acid fractions of organic matter. The mesocosm experiments showed that under anoxic conditions carbon amendments to tailings could significantly increase porewater MeHg concentrations (up to 13 ± 3 ng/L). In addition, the carbon amendments significantly increased THg partitioning into porewater. Overall, these results indicate that soil amendment applications to reduce surface erosion at abandoned mine sites could be effective at reducing particulate Hg mobilization to downstream waterbodies; however, some types of carbon amendments can significantly increase Hg methylation as well as increase the mobilization of dissolved THg from the site.

2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) was difficult to degrade in sediments. In this study, the environmental behavior of BDE-47 with/without the effect of benthos (Tubificidae Limnodrilus) and electron acceptors in sediments was investigated using C-14 tracer. Generally, extractable residues of BDE-47 were dominant in sediment and posed high environment risk. The amount of non-extractable residues (NERs) accounted for 39.0% of initial radioactivity in oxic sediments was significantly higher than those in anoxic sediments (17.6%). Most of NERs were localized in the humin fraction and presented as sequestrated forms. Under oxic conditions, the present of Limnodrilus significantly increased the proportion of NERs in sediment. Limnodrilus accumulated 34.2% of initial radioactivity. Under anoxic conditions, the addition of iron (Ⅲ) [Fe(III)], sulfate and nitrate reduced the environmental risk of BDE-47 with the increase of NERs formation, while manganese (IV) [Mn(IV)] addition had no effect on the formation of NERs. The present of Limnodrilus and electron acceptors promoted the production of metabolites. Meanwhile, BDE-47 changed the microbial community structure of sediments. These findings indicated that the environmental behavior and risk of BDE-47 was affected by benthos and electron acceptors, and the high proportion of sequestrated NERs posed high bioactivity and toxic threat to ecological environment.

Mapping soil contamination enables the delineation of areas where protection measures are needed. Traditional soil sampling on a grid pattern followed by chemical analysis and geostatistical interpolation methods (GIMs), such as Kriging interpolation, can be costly, slow and not well-suited to highly heterogeneous soil environments. Here we propose a novel method to map soil contamination by combining high-resolution aerial imaging (HRAI) with machine learning algorithms. To support model establishment and validation, 1068 soil samples were collected from an arsenic (As) contaminated area in Zhongxiang, Hubei province, China. The average arsenic concentration was 39.88 mg/kg (SD = 213.70 mg/kg), with individual sample points determined as low risk (66.9%), medium risk (29.4%), or high risk (3.7%), respectively. Then, identified features were extracted from a HRAI image of the study area. Four machine learning algorithms were developed to predict As risk levels, including (i) support vector machine (SVM), (ii) multi-layer perceptron (MLP), (iii) random forest (RF), and (iii) extreme random forest (ERF). Among these, we found that the ERF algorithm performed best overall and that its prediction performance was generally better than that of traditional Kriging interpolation. The accuracy of ERF in test area 1 reached 0.87, performing better than RF (0.81), MLP (0.78) and SVM (0.77). The F1-score of ERF for discerning high-risk points in test area 1 was as high as 0.8. The complexity of the distribution of points with different risk levels was a decisive factor in model prediction ability. Identified features in the study area associated with fertilizer factories had the most important contribution to the ERF model. This study demonstrates that HRAI combined with machine learning has good potential to predict As soil risk levels.

Nitrous acid (HONO) production from the heterogeneous photochemical reaction of NO₂ on several Chinese soils was performed in a cylindrical reactor at atmospheric pressure. The NO₂ uptake coefficient (γ) and HONO yield (YHONO) on different soils were (0.42–5.16) × 10⁻⁵ and 6.3%–69.6%, respectively. Although the photo-enhanced uptake of NO₂ on different soils was observed, light could either enhance or inhibit the conversion efficiency of NO₂ to HONO, depending on the properties of the soils. Soils with lower pH generally had larger γ and YHONO. Soil organics played a key role in HONO formation through the photochemical uptake of NO₂ on soil surfaces. The γ showed a positive correlation with irradiation and temperature, while it exhibited a negative relationship with relative humidity (RH). YHONO inversely depended on the soil mass (0.32–3.25 mg cm⁻²), and it positively relied on the irradiance and RH (7%–22%). There was a maximum value for YHONO at 298 K. Based on the experimental results, HONO source strengths from heterogeneous photochemical reaction of NO₂ on the soil surfaces were estimated to be 0.2–2.7 ppb h⁻¹ for a mixing layer height of 100 m, which could account for the missing daytime HONO sources in most areas.