The activity concentrations of naturally occurring and anthropogenic radionuclides in agriculture soils as well as in several food products at four locations within the phosphate area of South Tunisia were investigated. Soil-to-plant transfer factors as well as feed-to-animal products transfer coefficients were determined for the first time for the region. Activity concentrations of ⁴⁰K, ²¹⁰Pb, ²²⁶Ra, ²²⁸Ra and ¹³⁷Cs in soils of agriculture fields were lower than worldwide average values. The soil-to-plant transfer factors (TFs) for ⁴⁰K in leafy vegetables were higher than those in fruit vegetables. Soil-to-grass transfer factor (Fᵥ) values were in the following order: ⁴⁰K > ²¹⁰Pb > ²²⁶Ra. The grass-to-milk transfer coefficient (Fₘ) values for ⁴⁰K and ²¹⁰Pb ranged between 2 × 10⁻³ and 4 × 10⁻³(day L⁻¹). The concentration ratios for the animal products (CRₘᵢₗₖ₋fₑₑd, CRₘₑₐₜ₋fₑₑd and CRₑgg₋fₑₑd) varied in the ranges of 2 × 10⁻²–4 × 10⁻² L kg⁻¹, 1 × 10⁻²–2 × 10⁻¹ (L kg⁻¹) and 5 × 10⁻²–1 (L kg⁻¹)for ⁴⁰K, ²¹⁰Pb and ²²⁶Ra, respectively. Transfer parameters determined in the present study were compared with those reported in International Atomic Energy Agency reports and other published values. The absorbed gamma dose rate in air and the external hazard index associated with these natural radionuclides were computed to assess the radiation hazard of radioactivity in this region, and the results indicated that these areas are within set safety limits.

Among air pollutants, particulate matter (PM) has been identified as a major cause of environmental pollutants due to the advancement of industrial development and the generation of smaller particles. Particulate matter, in particular, is defined only by the size of particles and thus is not enough to study its composition yet. However, edible crops grown in contaminated atmospheres can be contaminated with heavy metals contained in particulate matter in the atmosphere, which can seriously damage food safety. In this study, we investigated the influence of the accumulation of particulate matter on leafy vegetables cultivated at areas with different levels of PM in atmosphere. Four districts of Gyeongsangnam-do were chosen to conduct this experiment: outdoor spaces of three respectively located in industrial, near-highway, and rural areas were considered, and research plant growth chambers at Gyeongsang National University were used as the control. After 3 weeks of cultivation in those conditions, the results showed that Pb in milligrams per kilogram of fresh weight (FW) was 0.383 in Chrysanthemum coronarium and 0.427 in Spinacia oleracea that were grown near the highway, which exceeded the 0.3 mg kg⁻¹ FW standard set by the Republic of Korea, EU, and CODEX. However, when those vegetables were sufficiently washed with tap water, it was confirmed that the heavy metal content fell into the safety standard range.

In this work, a novel biochar was prepared from the Artemisia argyi stem at 300 °C (AS300), 450 °C (AS450), and 600 °C (AS600). The structural properties of these biochars were characterized with various tools. The sorption kinetic processes of Cr(VI) and Cu(II) onto these biochars were better described by the pseudo-second order. The sorption isotherm processes of Cr(VI) onto these biochars were better described by the Freundlich model while the adsorption processes of Cu(II) were consistent with the Langmuir model. Batch sorption experiments showed that AS600 had the maximum adsorption capacity to Cr(VI) and Cu(II) with 161.92 and 155.96 mg/g, respectively. AS600 was selected for the follow-up batch and dynamic adsorption experiments. Results showed that AS600 had larger adsorption capacity for Cr(VI) at lower pH while the larger adsorption capacity for Cu(II) was found at higher pH. The effect of ionic strength on the adsorption of Cu(II) by AS600 was greater than that on the adsorption of Cr(VI). Dynamic adsorption experiments showed that Cu(II) had a higher affinity for the adsorption sites on the AS600 compared with Cr(VI). The adsorption mechanisms mainly involved electrostatic attraction, ion exchange, pore filling, and chemical bonding effect. Graphical abstract

This study evaluated the NOₓ adsorption and desorption performance as well as the casual relationship underlying a Mn-incorporated catalyst (Pt/Ba/Ce/xMn/γ-Al₂O₃). NOₓ adsorption and desorption are regarded as a prominent index for the NOₓ removal performance of NOₓ storage and reduction; we utilized NOₓ storage experiments with various inlet NO and O₂ concentrations and cycling adsorption/desorption experiments with a couple of adsorption time protocols for performance evaluation. In-suit DRIFT and NOₓ-TPD tests were implemented to reveal the instant stored species and their thermal stability. Eight percent of Mn catalyst at 350 °C was adopted in the described experiments for its desirable NOₓ adsorption characteristics. The optimal NOₓ storage performance was found under 10% O₂, deteriorating when the concentration was further increased. Furthermore, elevating NO concentration impaired the NOₓ adsorption due to the low NO₂/NOₓ ratio. It was also found that shorter adsorption time facilitated NOₓ removal via maintaining an unsaturated state for active storage components in terms of a fixed desorption time. The stored species existed as nitrites and nitrates with a good low-temperature thermal stability which however decayed at higher temperatures as exhibited in the DRIFT and NOₓ-TPD tests. These findings provided invaluable information for the application of Mn-incorporated catalyst for NOₓ removal in diesel exhaust purification to relieve the aerial pollution.

Fishmeal is a fundamental ingredient of feedstuffs and is used globally in aquaculture. However, there are few data on the antibiotic resistance genes (ARGs) and human pathogenic bacteria in fishmeal and little understanding of the potential risks of fishmeal application in mariculture systems. Here, we investigated the high-throughput profiles of ARGs and human potential pathogenic bacteria (HPPB) in representative fishmeals (n = 5) and the potential impact of fishmeal on mariculture sediments. ARGs were quantified with microbial DNA quantitative PCR arrays and HPPB were analyzed with Illumina sequencing of 16S rRNA genes. The impact of the fishmeal on the aquaculture sediments was assessed in a microcosm study. Twenty-four unique ARGs (3–14 per sample) and 25 HPPB species were detected in the fishmeal samples. The most prevalent ARGs were fluoroquinolone resistance genes. The overall abundance of HPPB was 5.0–25.5%, and the HPPB species were dominated by Vibrio parahaemolyticus, Clostridium novyi, and Escherichia coli. In the mariculture microcosm sediment, fishmeal significantly increased the normalized abundance of the class I integrase gene (25.4-fold), which plays an important role in the dissemination of ARGs. Dosing with fishmeal also contributed to increases in a resident sulfanilamide resistance gene (sulI gene) and the emergence of a macrolide resistance gene (ermB gene) in the sediment. These findings demonstrated that fishmeal itself is an underestimated reservoir and source of ARGs and HPPBs, and that the application of fishmeal facilitates the dissemination of ARGs in aquaculture sediments. Our results extend our knowledge of the ARGs and HPPB within fishmeal and may provide a feasible and effective approach to the detection of ARGs and HPPB in fishmeal during food safety inspection. Graphical abstract ᅟ

The photochemical role of Fe(III)-citrate complex is significant in natural waters due to its ubiquitous existence and excellent photoreactivity at near neutral pH. Although there are many reports on the photoinduced degradation of pollutants in the Fe(III)-citrate system, the optimum pH for its photoreactivity is yet not clearly understood. Here, for the first time, we demonstrated that the optimum pH was 5.5 for the photoproduction of •OH in the Fe(III)-citrate system via kinetics modeling based on the steady-state approximation. According to the experimental results, the •OH photoproduction increased with increasing pH until 5.5 and then decreased in Fe(III)-citrate solution, which agreed well with the prediction trend of kinetic modeling. The effect of the common ligand oxalate on the photoreactivity of Fe(III)-citrate system was also investigated. The addition of oxalate promoted the photoproduction of •OH in Fe(III)-citrate solutions, and the measured [•OH]ₛₛ increased with oxalate concentration under a fixed Fe(III)-to-citrate ratio. Little synergistic effect exists in Fe(III)-citrate-oxalate system at pH 4.0–5.5. In contrast, an appreciable synergistic effect was observed at near neutral pH (6.0–8.0). Higher oxalate-to-citrate ratio facilitated the synergistic effect. Furthermore, antifungal drug fluconazole could be removed efficiently in the Fe(III)-citrate-oxalate system. The photodegradation kinetics also verified the optimum pH of Fe(III)-citrate system and synergistic effect of oxalate. By LC-ESI-MS/MS analyses, the photoproducts of fluconazole in the Fe(III)-citrate-oxalate system were identified and the reaction mechanism involving hydroxylation substitution and subsequent cleavage of heterocyclic amine was proposed. These findings suggest that Fe(III)-citrate exhibits best photoreactivity at pH 5.5, and the coexistence of reactive ligands will enhance its photoreactivity at circumneutral pH, indicating potential application in wastewater treatment via addition of appropriate citrate and co-ligands.

The immunostimulating and therapeutic properties of Ginkgo biloba (GB) have always been the focus of traditional medicine over thousands of years. During last decade, special attentions were paid to use of GB in aquaculture to enhance fish health and survival. In the present study, we investigated for the first time the immunogenic effects of dietary GB against oxidative and toxicity induced by organophosphate pesticide, diazinon. In non-diazinon-exposed fish, the plasma total immunoglobulin, lysozyme activity, and peroxidase activity significantly elevated after 60-day experiment in fish supplemented with 1 and 2 g GB/kg diet (p < 0.05). The respiratory burst activity and complement activity significantly increased only in groups supplemented with 0.5 g GB/kg diet (p < 0.05). Furthermore, the peroxidase activity, total immunoglobulin, and lysozyme activity significantly declined in groups supplemented with 4 g GB/kg diet during feeding trial (p < 0.05). There were no significant differences in expression of interleukin 1 beta (IL-1β) and transforming growth factor beta 1 (TGF-β1) genes in kidney between control group (non-GB-supplemented fish) and GB-supplemented fish (p > 0.05). In diazinon-exposed fish, all immunity components significantly decreased during exposure in control and those fed 0.5 and 4 g GB/kg diet (p < 0.05). In fish fed 1 and 2 g GB/kg diet, no alternations were found in immunity components during exposure period (p > 0.05). In addition, diazinon induced the expression of IL-1β and TGF-β1 genes in control and fish fed 0.5 and 4 g GB/kg diet (p < 0.05). No significant changes were observed in expression of IL-1β and TGF-β1 genes in fish supplemented with 1 and 2 g GB/kg (p > 0.05). In conclusion, the results of the present study suggest an immunogenic role for dietary GB at optimum dietary levels (1–2 g GB/kg diet) against toxicity induced by diazinon. Nevertheless, GB at high dietary levels (4 g GB/kg diet) showed immunosuppressive effects, which makes it necessary to optimize its levels in diet.

Water level and wind speed have important influences on radon release in particle-packing emanation media. Based on radon migration theory in porous media under three water level conditions, an experimental setup was designed to measure the surface radon exhalation rate of uranium tailings from heap leaching uranium mine at different water levels and wind speeds. When the water level was at 0.3 m (overlying depth 0.05 m), radon transfer velocities at the gas–liquid interface were also measured at different wind speeds. Results show that when the water level was equal to or lower than the surface of the sample, the radon exhalation rate increased with increasing wind speed and decreased with increasing water level. When the water level was higher than the surface of the sample, radon exhalation rate of the water surface increased with increasing surface wind speed. The wind speed, however, was less influential on the radon exhalation rate as the depth of the overlying water increased, with a dramatic decrease in radon release. That said, at different wind speeds, radon transfer velocities at the gas–liquid interface were consistent with literature. On the other hand, changes in wind speed had significant influences on the radon transfer velocity at the gas–liquid interface, with the effect less pronounced at higher wind speeds.

This study aims to investigate the validity of pollution haven hypothesis for the period from 1982 to 2013 in ten newly industrialized countries. For this purpose, we examine the relationship between real income, foreign direct investment, energy consumption, and ecological footprint using second-generation panel data methodology to take into account the cross-sectional dependence among newly industrialized countries. In doing so, the possible nonlinear relationship between foreign direct investment and environmental degradation is also searched. The results show that increased energy consumption and economic growth lead to increase in ecological footprint. Moreover, the U-shaped relationship between foreign direct investment and ecological footprint is confirmed in newly industrialized countries.

In this study, we focused on the rate of adsorption of phosphate on to the surface of magnetite in the presence of coexisting anions, organic matters and heavy metals. Magnetite particles were prepared using a co-precipitation method. Iron (II) sulfate heptahydrate and iron (III) chloride hexahydrate were mixed and then a sodium hydroxide solution was added drop-wise in the mixed iron solution. Coexisting anions were found to have no effect on the decrease in phosphate adsorption. However, phosphate adsorbed on to magnetite surface decreased with increasing total organic carbon (TOC) concentration of natural organic matter (NOM) such as citric, oxalic, and humic acid. The amount of phosphate adsorbed rapidly decreased with the increase of NOM concentration; therefore, it can be noted that NOM concentration considerably affects the adsorption of phosphate due to the negative charge exiting on the surface of NOMs. Glucose and ethanol, meanwhile, were found to have no effect on the phosphate adsorption. The amount of phosphate adsorbed did not change in the presence of heavy metals, namely, Pb and Cd, under acidic conditions. However, under alkaline conditions, the amount of phosphate adsorbed decreased with increasing concentrations of Pb and Cd. In the case of coexisting As(III), the amount of phosphate adsorbed decreased at all pH levels with increasing As(III) concentrations.