The sulfate pollution in water environment gains more and more concerns in recent years. The discharge of domestic, municipal, and industrial wastewaters increases the riverine sulfate concentrations, which may cause local health and ecological problems. To better understand the sources of sulfate, this study collected water samples in a typical agricultural watershed in East Thailand. The source apportionment of sulfide was conducted by using stable isotopes and receptor models. The δ³⁴SSO₄ value of river water varied from 1.2‰ to 16.4‰, with a median value of 8.9‰. The hydrochemical data indicated that the chemical compositions of Mun river water were affected by the anthropogenic inputs and natural processes such as halite dissolution, carbonate, and silicate weathering. The positive matrix factorization (PMF) model was not suitable to trace source of riverine sulfate, because the meaning of the extracted factors seems to be vague. Based on the elemental ratio and isotopic composition, the inverse model yielded the relative contribution of sulfide oxidation (approximately 46.5%), anthropogenic input (approximately 41.5%), and gypsum dissolution (approximately 12%) to sulfate in Mun river water. This study indicates that the selection of models for source apportionment should be careful. The large contribution of anthropogenic inputs calls an urgent concern of the Thai government to establish effective management strategies in the Mun River basin.

Marine atmospheric aerosols play important roles in the global radiation balance and climate change. Hence, measuring physiochemical aerosol properties is essential to better understand their formation, aging processes, and source origins. However, high temporal resolution measurements of submicron particles are currently scarce in the northern South China Sea (SCS). In this study, we conducted a ship-based cruise campaign with a scanning mobility particle sizer and an online time of flight aerosol chemical speciation monitor to measure the particle number size distribution (PNSD) and the chemical composition of submicron particles over the northern SCS during summer 2018. The mean concentration of non-refractory submicron particulate matter (NR-PM₁) was generally 9.11 ± 4.86 μg m⁻³; sulfate was the most abundant component, followed by organics, ammonium, nitrate, and chloride. Positive matrix factorization (PMF) analysis was applied to the PNSD (size PMF) and organic aerosols (OA PMF) and further investigated the source apportionment of the submicron particles. The size PMF identified four factors, including ship exhaust, ship influencing marine primary, continent affected marine secondary, and mixed accumulation aerosols. The most abundant particles in the number concentration were associated with ship emissions, which accounted for approximately 44 %. The submicron organic aerosols were highly oxidized and composed of low-volatility oxygenated OA (LV-OOA, 68 %), semi-volatile OOA (SV-OOA, 21 %), and hydrocarbon-like OA (HOA, 11 %). The backward trajectory of air masses showed that the northern SCS was most frequently (64.7 %) influenced by air masses from the Indo-Chinese Peninsula (ICP) during the campaign, implying that pollutants from ICP have a significant impact on the atmosphere of the northern SCS during summer. Thus, in situ ship-based cruise measurements can provide valuable data on the physiochemical characteristics of marine atmospheric aerosols to better understand their source origins.

Toxicokinetic (TK) model provides a new approach to mechanistically elucidate the natural variation of metal handling strategy by adaptive and sensitive earthworm populations. Here, TK model was applied to explore the metal handling and resistance strategy of wild Metaphire californica with different historical exposure history through a 12-day re-exposure and another 12-day elimination incubation. M. californica populations showed different kinetic strategies for non-essential metals (Cd and Pb) and essential metals (Zn and Cu), which were closely related to their exposure history. M. californica from the most serious Cd-contaminated soil showed the fastest kinetic rates of both Cd uptake (K₁ = 0.78 gₛₒᵢₗ/gwₒᵣₘ/day) and elimination (K₂ = 0.23 day⁻¹), and also had the lowest Cd half-life (t₁/₂ = 3.01 day), which demonstrated the potential Cd-resistance of wild M. californica from Cd-contaminated soils. Besides, the comparative experiment showed totally different metal kinetics of laboratory Eisenia fetida from field M. californica, suggesting the impacts of distinct exposure history and species-specifical sensitivities. These findings provide a novel approach to identify and quantify resistance using TK model and also imply the risk of overlooking existing exposure background and interspecies extrapolation in eco-toxicological studies and risk assessments.

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.

The aggregation kinetics of fragmental polyethylene glycol terephthalate (PET) nanoplastics under various chemistry conditions in aqueous environment were firstly investigated in this work. The aggregation of PET nanoplastics increased with increasing electrolyte concentrations and decreasing solution pH, which became stronger with the presence of divalent cations (e.g. Ca²⁺ and Mg²⁺) than that of monovalent cations (e.g. Na⁺ and K⁺). The effect of cations with the same valence on the aggregation of PET nanoplastics was similar. The measured critical coagulation concentrations (CCC) for PET nanoplastics at pH 6 were 55.0 mM KCl, 54.2 mM NaCl, 2.1 mM CaCl₂ and 2.0 mM MgCl₂, which increased to 110.4 mM NaCl and 5.6 mM CaCl₂ at pH 10. In addition, the aggregation of PET nanoplastics was significantly inhibited with the presence of humic acid (HA), and the CCC values increased to 558.8 mM NaCl and 12.3 mM CaCl₂ (1 mg L⁻¹ HA). Results from this study showed that the fragmental PET nanoplastics had the quite higher CCC values and stability in aqueous environment. In addition, the aggregation behaviors of PET nanoplastics can be successfully predicted by the Derjguin Landau Verwey Overbeek (DLVO) theory.

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.

Forchlorfenuron (CPPU) has been used worldwide, to boost size and improve quality of various agricultural products. CPPU and its metabolites are persistent and have been detected frequently in fruits, water, sediments, and organisms in aquatic systems. Although the public became aware of CPPU through the exploding watermelon scandal of 2011 in Zhenjiang, China, little was known of its potential effects on the environment and wildlife. In this study, adverse effects of CPPU on developmental angiogenesis and vasculature, which is vulnerable to insults of persistent toxicants, were studied in vivo in zebrafish embryos (Danio rerio). Exposure to 10 mg CPPU/L impaired survival and hatching, while development was hindered by exposure to 2.5 mg CPPU/L. Developing vascular structure, including common cardinal veins (CCVs), intersegmental vessels (ISVs) and sub-intestinal vessels (SIVs), were significantly restrained by exposure to CPPU, in a dose-dependent manner. Also, CPPU caused disorganization of the cytoskeleton. In human umbilical vein endothelial cells (HUVECs), CPPU inhibited proliferation, migration and formation of tubular-like structures in vitro. Results of Western blot analyses revealed that exposure to CPPU increased phosphorylation of FLT-1, but inhibited phosphorylation of FAK and its downstream MAPK pathway in HUVECs. In summary, CPPU elicited developmental toxicity to the developing endothelial system of zebrafish and HUVECs. This was do, at least in part due to inhibition of the FAK/MAPK signaling pathway rather than direct interaction with the VEGF receptor (VEGFR).

Passive biomonitoring was applied in four Atlantic forest plots in southeast Brazil, affected by different levels of trace metal pollution (OP site located in Minas Gerais State and PEFI, PP and STG located in São Paulo State). Native tree species were selected as biomonitors according to their abundance in each plot and successional classification. Current trace metal concentrations in total suspended particles, leaves of non-pioneer (NPi) and pioneer (Pi) species, topsoil (0–20 cm) and litter and concentration ratios at the plant/soil interface were analyzed to verify the atmosphere-plant-soil interactions, basal concentrations, spatial variations and metal accumulation at the ecosystem level. Redundant analysis helped to identify similar characteristics of metal concentrations in PP and PEFI, which can be influenced by the high concentrations of elements related to anthropogenic inputs. Analysis of variance and multivariate statistics indicated that the trees of OP presented higher concentrations of Cr, Fe, Mn and Ni than those in the other sites. High enrichment of Cd, Fe, Ni in non-pioneer plants indicated that the PP forest (initially considered as the least polluted) has still been affected by metal pollution. Soil collected in STG was enriched by all elements, however these elements were low available for plant uptake. Metal deposited in leaves and litter was an important sink for soil cycling, nevertheless, these metals are not bioavailable in most cases. Non-pioneer tree species revealed to be more appropriate than pioneer species to indicate the current panorama of the contamination and bioavailability levels of trace metals in the tree community-litter-soil interface of the Atlantic forest remnants included in this study.

The fate of many chemicals in the environment, particularly contaminants of emerging concern (CEC), have been characterised to a limited extent with a major focus on occurrence in water. This study presents the characterisation, distribution and fate of multiple chemicals including pharmaceuticals, recreational drugs and pesticides in surface water, sediment and fauna representing different food web endpoints in a typical UK estuary (River Colne, Essex, UK). A comparison of contaminant occurrence across different benthic macroinvertebrates was made at three sites and included two amphipods (Gammarus pulex &Crangon crangon), a polychaete worm (Hediste diversicolor) and a gastropod (Peringia ulvae). Overall, multiple contaminants were determined in all compartments and ranged from; <LOQ – 386 ng L⁻¹ in surface water (n = 59 compounds), <LOQ – 146 ng g⁻¹ in sediment (n = 39 compounds) and <LOQ – 91 ng g⁻¹ biota (n = 33 compounds). H. diversicolor and P. ulvae (sediment dwellers) showed greater chemical body burden compared with the two swimming amphipod species sampled (up to 2.5 - 4-fold). The most frequently determined compounds in biota (100%, n = 36 samples) included; cocaine, benzyoylecgonine, carbamazepine, sertraline and diuron. Whilst some of the highest concentrations found were in species H. diverscolor and P. ulvae for psychoactive pharmaceuticals including citalopram (91 ng g⁻¹), sertraline (69 ng g⁻¹), haloperidol (66 ng g⁻¹) and the neonicotinoid, imidacloprid (33 ng g⁻¹) Sediment was noted as an important exposure route for these benthic dwelling organisms and will be critical to monitor in future studies. Overall, the analysis of multiple species and compartments demonstrates the importance of including a range of exposure pathways in order to appropriately assess chemical fates and associated risks in the aquatic environment.