Filter-based toxicology studies are conducted to establish the biological plausibility of the well-established health impacts associated with fine particulate matter (PM₂.₅) exposure. Ambient PM₂.₅ collected on filters is extracted into solution for toxicology applications, but frequently, characterization is nonexistent or only performed on filter-based PM₂.₅, without consideration of compositional differences that occur during the extraction processes. To date, the impact of making associations to measured components in ambient instead of extracted PM₂.₅ has not been investigated. Filter-based PM₂.₅ was collected at locations (n = 5) and detailed characterization of both ambient and extracted PM₂.₅ was performed. Alveolar macrophages (AMJ2-C11) were exposed (3, 24, and 48 h) to PM₂.₅ and the pro-inflammatory cytokine interleukin (IL)-6 was measured. IL-6 release differed significantly between PM₂.₅ collected from different locations; surprisingly, IL-6 release was highest following treatment with PM₂.₅ from the lowest ambient concentration location. IL-6 was negatively correlated with the sum of ambient metals analyzed, as well as with concentrations of specific constituents which have been previously associated with respiratory health effects. However, positive correlations of IL-6 with extracted concentrations indicated that the negative associations between IL-6 and ambient concentrations do not accurately represent the relationship between inflammation and PM₂.₅ exposure. Additionally, seven organic compounds had significant associations with IL-6 release when considering ambient concentrations, but they were not detected in the extracted solution. Basing inflammatory associations on ambient concentrations that are not necessarily representative of in vitro exposures creates misleading results; this study highlights the importance of characterizing extraction solutions to conduct accurate health impact research.

Chicken feather, which is consisted of keratin, has always been abandoned as solid waste. The utilization technologies of waste keratin have been developed in electric zones and materials fields so far. Recently, numerous new types of adsorbents have been used for antibiotic removal. The chicken feather carbon is supposed to be a potential one. In this study, an activated feather carbon (AFC) was developed as the absorbent of amoxicillin (AMOX) in simulated wastewater. The micropore structures of AFC were detected by the scanning electron microscope (SEM). X-ray photoelectron spectrum (XPS) was recorded and analyzed. A BET surface area, as high as 1838.86 m²/g, was measured in this study. At the meantime, a rapid adsorption (5∼7 min) and high removal efficiency (99.63%) could be observed. The kinetics, isotherms, and thermodynamic studies indicated that the adsorption of AMOX by AFC was an exothermic physic-adsorption. The interaction between AMOX and AFC surface was supposed to be a multiple-layer adsorption process for it is well fitted with the Freundlich model. The adsorption behavior could be described by pseudo-second-order model almost perfectly in kinetic studies. In addition, effect of pH, ionic strength, and reusability properties were also discussed in this paper. The AFC was proved to be the most rapid, efficient, and economically absorbent for AMOX removal, which was effective enough under various temperatures and saline circumstances. It was also proved useful, convenient, and renewable in dealing with the tough antibiotic pollutant problems and rebuilding of antibiotic sewage treatment facilities.

Acute (24 h) and sublethal (35 days) effects of cadmium chloride (CdCl₂) were examined in Cirrhinus mrigala using various endpoints (accumulation pattern, thyroid hormones (THs), and antioxidants). The mean concentrations of CdCl₂ for 24 and 96 h were found to be 35.974 and 22.387 mg L⁻ˡ, respectively. LC50 concentration of CdCl₂ for 24 h (35.97 mg L⁻ˡ) was used for the acute study. For the sublethal studies, fish were exposed to 3.59 mg L⁻¹ (Treatment I) and 7.19 mg L⁻¹ (Treatment II) corresponding to 1/10th and 1/5th of 24 h LC50 of the CdCl₂. During acute exposure, higher accumulation of CdCl₂ was noticed in the gill, liver, and kidney of C. mrigala, which is found in the order gill > liver > kidney tissues. Similarly, in sublethal treatments (Treatment I and II), a concentration and time-dependent increase of CdCl₂ accumulation was noticed in the order of gill > liver > kidney. GSH, GST, and GPx activities were found to be relatively lower from the treated groups in both acute and sublethal treatments. However, LPO activity was significantly increased in CdCl₂-treated fish C. mrigala. Further, plasma T₃ reduction was more pronounced than T₄ in acute study. During sublethal treatments, both T₄ and T₃ levels showed a continuous decrease as the exposure period extended. All the values in this study were statically significant (P < 0.01 and P < 0.05).

Plants of the urban environment are exposed to a wide range of pollutants, including heavy metals. This research studies in situ the eco-physiological and antioxidant responses of holm oak (Q. ilex) leaves to Pb and Cd to assess the mechanisms of metal tolerance in this species, widely used as biomonitor. Leaves of plants grown at parks and roadsides were analyzed for photosynthetic activity, Pb and Cd concentration in tissues and cell-free extracts, thiol groups, D1 and Rubisco protein content, ascorbic acid (AsA) amount, and catalase (CAT) activity. The main results evidenced that Cd concentration was higher in leaves collected at the park out from the downtown; whereas Pb was most abundant in leaves sampled at the roadside nearby the highway. Pb in cell-free extracts was higher in park than in roadside leaves. Although Cd in the leaf tissues was twofold lower than Pb, it was more abundant than Pb in cellular extracts deprived of all particulate matter. Leaves responded to different concentration of Cd and Pb modulating some eco-physiological and biochemical traits, roadside leaves showed reduced leaf lamina, higher content of photosynthetic pigments, hydrogen peroxide, and AsA, as well as higher CAT activity compared to park leaves. In the roadside leaves, a stress condition for photosynthetic apparatus can be hypothesized on the basis of the decline of photochemical activity, the increase of NPQ, and the reduction of Rubisco and D1 protein content. The elevated presence of thiol groups in these leaves suggests a possible role of Pb and Cd in activation of antioxidant responses.

Forest fire is a natural disturbance that occurs in many terrestrial ecosystems specifically in the semi-arid environments and is considered to be an important cause of environmental change. Though many causes of fire are identified, including lightning, volcanic eruption, power line sparks, etc., human involvement is the most significant factor. Fire events are able to alter the physical, chemical and biogeochemical properties of the soil and surface materials and are able to release major and trace metals into the environment. This may be more significant in mining-affected and industrial landscapes, where elevated concentrations of metals present in the soil. After the fire event, metals become more mobile due to the increase in soil surface exposure and the mobility associated with ash dispersal. This mobility may increase the bioavailability of the metals, which may generate water quality issues and may contribute to human and environmental health concerns. Even though, the influences of fire on many soil properties are well established, the behaviour of metals with respect to fire is not well investigated. However, a few studies report that major and trace metals include Cd, Cr, Co, Cu, Hg, Mn, Ni, Pb, Zn and As are mobilized after fire with increased concentrations in soil and water resources and this might pose a risk to human health and ecosystems. Climate change may increase the intensity, frequency and areal extend of fire events and hence increase the metal concentrations and their potential health impacts. This paper reviews post-fire (wild fire) mobility of metals in soil common in contaminated forest ecosystems. The human and ecological health risks of these metals are also considered.

In this work, we examined the effect of two different organic wastes, composted sheep manure and coir, on the sorption, persistence, and mobility of three pesticides (alachlor, chlorfenvinphos, and chlorpyrifos) included as priority substances in European Directive 2013/39/EU. With this aim, leaching studies were conducted using disturbed soil columns filled with a typical agricultural soil (hipercalcic calcisol) from a semiarid area (southeastern Spain) to determine their potential for groundwater pollution. The three compounds were found in leachates of unamended soil although in different proportions: 53% (alachlor), 9% (chlorfenvinphos), and 6% (chlorpiryfos). The addition of organic wastes significantly increased the sorption of the studied pesticides. As a consequence, the half-lives of the studied pesticides were higher in amended than in unamended soils. A marked reduction of the amount recovered in leachates was observed in the amended soils, except for chlorpiryfos, whose recoveries barely changed. According to their potential groundwater pollution calculated as the groundwater ubiquity score (GUS) index, alachlor and chlorfenvinphos show medium leachability while chlorpiryfos is unlikely to leach.

Biomarkers such as oxidase enzyme activity from flora exposed to chemicals in the water column and sediments have been widely used by ecotoxicologists to assess the quality of an environment. Biomarkers such as oxidase enzymes are especially useful indicators because they represent a direct biological response to environmental toxicity. A luminometer was used to quantify oxidase enzyme production in watercress (Nasturtium officinale) due to toxic chemical exposure of E85 (85% ethanol and 15% gasoline blend), gasoline, and 99% pure ethanol over a 72-h period in aquatic root exposure and volatile leaf exposure experiments. Aquatic exposure to E85 caused an increase in oxidative enzyme production while gasoline and ethanol caused no significant changes in oxidase concentrations. Aquatic root exposure results were compared to volatile leaf exposures where effects of E85, gasoline, and ethanol caused increases in oxidase production. Morphometric measurements were also conducted as plant stress comparisons to oxidative enzyme analyses. Measurements of root length showed increases in root growth at some concentrations of fuels with only the highest concentration of E85 resulting in a decrease in root growth when compared to the control.

Fe₃O₄ decorated multi-walled carbon nanotube (Fe₃O₄/MWCNT) nanocomposites were synthesized by co-precipitation process and used as heterogeneous Fenton catalyst for degradation of phenol and p-nitrophenol (p-NP). The Fe₃O₄ nanoparticles with size less than 20 nm were well-dispersedly coated on the surface of MWCNTs at relatively low loading. Some aggregations appear at high Fe₃O₄ content in composite. The Fe₃O₄/MWCNT with about 25 wt.% of Fe₃O₄ is the most cost-effective catalyst compared with others, whose phenol conversion and COD removal rates could, respectively, reach to 99.20 and 58.09%. And a high H₂O₂ utilization efficiency was achieved (about 132.41%) for this catalyst. For the p-NP degradation, the optimal reaction condition was that: 2.0 mg/L of catalyst dosage, 3 mmol/L of initial H₂O₂ concentration, 3 of pH value, and 40 °C of reaction temperature. At this condition, the removal rates of p-NP and COD in 120 min achieved 97.16 and 67.71%, respectively. And the Fe₃O₄/MWCNT nanocomposite also exhibits an acceptable stability and reusability.

A detailed investigation was conducted to study the effect of highway on the accumulation of heavy metals in soils of turfy swamps. The concentrations of Cr, Zn, Cu, and Cd showed a decreasing trend with increasing distance from the road, while such trend was not identified in Pb, Ni, Co, and As. The results of factor analysis and cluster analysis indicated that Cr, Zn, Cu, and Cd were in a closer relationship than other metals and might be derived from common sources. The soil samples from JY and LQ sites with the highest traffic volume had the highest heavy metal concentrations of the three highways, while the concentrations of Cr and Cu were significantly positively correlated with traffic volumes (p < 0.05). Contamination levels of traffic-related metals were evaluated using the geo-accumulation index (I gₑₒ) and enrichment factor (EF) in turfy soil. The I gₑₒ index for Cr, Zn, Cu, and Cd varied from unpolluted to the heavily polluted, and the enrichment factor (EF) ranged from 0.44 (no enrichment) to 8.38 (significant enrichment) at JY and LQ site. For HSD site, the I gₑₒ index and EFs of Cr, Zn, and Cd in turfy soils were lower than that in JY and LQ, ranged from uncontaminated to moderate contamination and no enrichment to moderate enrichment, respectively. The I gₑₒ index and EFs of Cd were higher than 1 among all three sites. Therefore, Cd should be paid more attention to avoid potential risk to the flora and fauna in turfy swamps. The affected area of traffic-related metals was <30 m from the highway; this may be due to the abundant precipitation and long cold winter in Changbai Mountain area. The heavy metals could move with rainfall runoff and snowmelt in both particulate and dissolved forms.

Stopped-flow technology and HPLC analysis were used to study the degradation mechanism and reaction kinetics of 4-chlorophenol (4-CP) in Fenton oxidation process. The results indicated that benzoquinone and hydroquinone were simultaneously produced in process of Fenton oxidizing 4-CP by stopped-flow technology analysis. The data obtained by HPLC showed that hydroquinone was generated in great quantities following the decrease of benzoquinone. It could be inferred by batch experiments that benzoquinone would be transformed into hydroquinone in Fenton process and hydroperoxyl radical (HO₂·) would take the main part in this process. In our study, there would exist two catalytic systems in Fenton process, and one was Fe²⁺and Fe³⁺, the other was hydroquinone and benzoquinone. Moreover, the rate constants of hydroquinone, benzoquinone, and 4-chlorocatechol were 2.78 × 10⁶ L s⁻¹ mol⁻¹, 9.38 × 10⁸ L s⁻¹ mol⁻¹, and 6.47 × 10⁶ L s⁻¹ mol⁻¹, respectively. Graphical Abstract