Usage of atrazine, a widely used herbicide, is now banned in many countries. Although forbidden to use, significant concentration of this herbicide is still present in the environment. The study focused not only on the toxicity of atrazine itself but also on products of homogeneous photocatalytic degradation. Such degradation was very fast in given conditions (sufficient amount of Fe(III) in the reaction system)—more than 95% of the initial amount of atrazine was eliminated after 30 min of irradiation. The toxicity of atrazine and its photodegradation products were examined on the aquatic plant Lemna minor and microcrustacean Daphnia magna in both acute and chronic tests. While the growth inhibition assay of atrazine for Lemna minor revealed EC₅₀ value of 128.4 μg dm⁻³, the herbicide did not affect Daphnia in the acute toxicity assay. A degradation product, desethyl-atrazine, has been demonstrated to have a pronounced negative effect on the plant growth. Both atrazine and desethyl-atrazine affect negatively the number of juveniles and number of clutches of Daphnia magna in the chronic toxicity assay. Photocatalytic degradation lowers the negative effect of atrazine in Daphnia magna while photodegradation products still negatively affect Lemna growth.

The endophytic bacteria live in close nuptial relationship with the host plant. The stress experienced by the plant is expected to be transferred to the endophytes. Thus, plants thriving at polluted sites are likely to harbor pollutant-degrading endophytes. The present study reports the isolation of phenylurea herbicides assimilating Bacillus sps. from Parthenium weed growing at diuron-contaminated site. The isolated endophytes exhibited plant growth–promoting (PGP) activities. Among five isolated diuron-degrading endophytes, the most efficient isolate Bacillus licheniformis strain SDS12 degraded 85.60 ± 1.36% of 50 ppm diuron to benign form via formation of degradation intermediate 3, 4-dichloroaniline (3,4-DCA). Cell-free supernatant (CFS) obtained after diuron degradation by strain SDS12 supported algal growth comparable with the pond water. The chlorophyll content and photosynthetic efficiency of green algae decreased significantly in the presence of diuron-contaminated water; however, no such change was observed in CFS of strain SDS12, thus, suggesting that strain SDS12 can be applied in aquatic bodies for degrading diuron and reducing diuron toxicity for primary producers. Further, the use of PGP and diuron-degrading bacteria in agriculture fields will not only help in remediating the soil but also support plant growth.

Improving digestibility, fermentation characteristics, and reducing greenhouse biogases to protect the environment without the use of synthetic materials is an important goal of modern-day farming and nutritionist. Plant extracts are capable of solving these. This is due to the digestive enzymes and the bioactive components capable of performing antimicrobial functions inherent in these plants. This study was aimed to investigate the effect of standard maize substrate treated with selected herbs and spices extracts on ruminal environmental biogas production and pressure during fermentation via biogas production technique. Herbs (Azadirachta indica leaves (T1), Moringa oleifera leaves (T2), Ocimum gratissimum leaves (T3) and spices (Allium sativum bulb (T4), Zingiber officinale rhizome (T5)) were harvested, air dried, and milled using standard procedures. Methanolic extracts of the herbs and spices were prepared and used as additives at different concentrations (50, 100, and 150 μL) to the maize substrate for in vitro biogas production. Data were analyzed using regression analysis. There were significant (P < 0.05) differences across all the treatments on the volume and pressure of biogas. The pressure and volume of biogas when compared with the levels tested showed differences (P < 0.05) across all the treatments for the prediction of volume from pressure of biogas. The pressure and volume of gas produced in vitro increased (P < 0.05) and biogases decreased (P < 0.05) by the substrate treated with herbs and spices but for the drum stick leaves which was similar for the levels of concentration tested. This means that the level tested had a pronounced mitigation effect on pressure of biogas and volume of biogas produced. It was concluded that the herb and spice extracts have the potential to improve rumen fermentation and reduce the production of biogases in ruminant diet.

Robust and simple composite films for the removal of methyl orange (MO) and Cr(VI) have been prepared by combining chitosan, saponin, and bentonite at a specific ratio. There are several composite films (chitosan-saponin-bentonite (CSB)) prepared; among them, the composite films CSB₂:₃ and CSB₁:₁ have the highest removal efficiency toward MO and Cr(VI) where the maximum removal is 70.4% (pH 4.80) and 92.3% (pH 5.30), respectively. It was found that different types of adsorbate have different thermodynamic properties of the adsorption process; the adsorption of MO onto CSB₂:₃, chitosan, and acid-activated bentonite (AAB) proceeded endothermically, while the adsorption of Cr(VI) onto CSB₁:₁, chitosan, and AAB proceeded exothermically. The parameters of the adsorption were modeled by using isotherm and kinetic equations. The models of Langmuir, Freundlich, Redlich-Peterson, Sips, and Toth were used for fitting the adsorption isotherm data at a temperature of 30, 45, and 60 °C; all of the isotherm models could represent the data well. The result indicates that CSB₂:₃ has the highest adsorption capacity toward MO with qₘ of 360.90 mg g⁻¹ at 60 °C; meanwhile, CSB₁:₁ has the highest adsorption capacity toward Cr(VI) with qₘ 641.99 mg g⁻¹ at 30 °C. The pseudo-second-order model could represent the adsorption kinetics data better than the pseudo-first-order equation. The adsorption mechanism was proposed, and the thermodynamic properties of the adsorption were also studied.

Global trade plays an imperative role in the world economy that yields environmental degradation. Therefore, the current paper’s ambitions are to explore the trade–air pollution nexuses by introducing the value-added trade (VT) concept from a global value chain stance. The value-added trade (VT) indicator is constructed by the World Input-Output (WIOD) classifications database. Owing to scanty data accessibility, the sample set is reduced to 39 countries covering the period from 1995 to 2009. Furthermore, this paper is also contributing by including the eight different pathways of per capita air pollution in terms of ammonia (NH3), carbon monoxide (CO), carbon dioxide (CO₂), methane (CH₄), nitrogen oxides (NOₓ), nitrous oxide (N₂O), sulphur oxides (SOₓ) and non-methane volatile organic compounds (NMVOC) respectively. The valuable outcomes from empirical analysis have been found; Firstly, it explores that the preliminary stage of the development of value-added trade (VT) has a positive impact on air-bonds pollution. However, in the later stage of the economic development, trade improves the environmental quality as the square of value-added trade (VT²) has a negative impact on air pollution. Moreover, it also elaborates that the magnitude impact of trade on carbon monoxide (CO) air pollution is more than the other seven air pollutants. Thirdly, the inverted U-shape in the trade–air pollution Environmental Kuznets Curve (EKC) hypothesis, the non-linear relationship between trade and pollution is also validated in all eight air pollutants indicators. Policy proposals for green economy that underlines the global value chain stance and environmental factors in the growing economy are proposed.

Since the ban of tributyltin in antifouling paints, many alternative biocides have been introduced to prevent settlement and growth of marine organisms on ship hulls. Zinc pyrithione (ZnPT) is one of the most frequently used alternative biocides in antifouling paints. This paper reviewed the overall chemical properties, toxicological characteristics, and environmental fates of ZnPT, as well as the analytical challenges of studying pertinent processes. ZnPT is generally toxic to a wide range of marine organisms, including algae, bivalves, sea urchins, polychaetes, crustaceans, and fish, typically at μg/L levels. ZnPT can be transchelated into other compounds in the presence of metal ions, and photodegrades when exposed to UV light. ZnPT is also reported to be biodegraded or hydrolyzed forming several metabolites of their own toxicity and stability. However, ZnPT accumulates in the water column or sediment, if it does not degrade at certain environmental conditions. To determine potential risks caused by ZnPT in the marine environment, studies have evaluated the environmental distribution of ZnPT with various chromatographic or voltammetry methods. Unfortunately, rapid transchelation and degradation of ZnPT in both the marine environment and laboratory interfered with most of the methods employed, making it difficult to evaluate its environmental distribution. More robust and sensitive analytical methods need to be developed to reliably describe the environmental release and distribution of ZnPT. To comprehensively understand the risk posed by the input of ZnPT into the marine environment, total degradation processes and its potential products also need to be adequately addressed.

An electrokinetic batch treatment scheme was investigated combining sequential electrocoagulation (EC) and chemical coagulation treatment (CC) processes. Synthetic and microbrewery wastewaters were tested in this investigation. The generated results demonstrated the capacity for the integration of EC-CC to effectively remove phosphorus contamination from wastewater under varying operating conditions. The effect of several operational parameters such as current density, conductivity, nutrient loading, and electrolysis time were investigated. The results showed that increased salinity can significantly accelerate the removal of phosphorous during EC treatment with 84.2% and 92.4% removal found for the applied power of 5 and 10 W, respectively. The addition of a sequential chemical coagulant stage following treatment by EC demonstrated the potential for an integrated EC-CC system to lower energy consumption while maintaining effective nutrient removal capabilities. Removal of phosphorous at 95% and 98% was achieved in just 10 min of EC treatment coupled with the addition of 15 mg/L aluminum sulfate. The estimated power consumption over a 10-min period was found to be 0.28 Kwh/m³ with a dissolution rate of 0.28 g/cm² min held at a constant current density. The experimental anode dissolution rate for the synthetic wastewater ranged between 0.13 and 0.24 g/cm² min encompassing all salinity levels. The anode dissolution rate increased during treatment of microbrewery wastewater with 0.67 g/cm² min for 10 W EC treatment. This was attributed to the increase in current density and nutrient loading resulting in increased energy consumption and electrode passivation.

The use of aqueous film-forming foams (AFFFs) have been related to environmental contamination due to handling, storage, and use in the firefighting against class B fire. Studies have associated the use of AFFFs with toxic effects from its perfluorinated compounds (PFCs) to the aquatic ecosystem, which led the Stockholm Convention to restrict their use. In Brazil, despite the large-scale use, there is no data on employment or annual commercialization of these products. This study evaluated the toxicity of seven brands of AFFFs used in the firefighting of the petrochemical’s terminal of fuel storage in Port of Santos (Santos, São Paulo, Brazil) which occurred in 2015, in which more than 61,000 L of AFFFs drained into the adjacent aquatic ecosystems. The toxicity evaluation was performed by means of the acute bioassay using the freshwater microcrustacean Daphnia similis. The AFFF brands tested were considered toxic to D. similis, including at much lower dilutions than those recommended by the manufacturers. The brand that showed the lowest toxicity was Kidde Sintex® 3% × 6%, followed by Kidde Sintex® 1% × 3%, Argus Prime®, Cold Fire®, Ageofoam®, and Liovac®, and the one with the highest toxicity was F-500 fire®. These results provide valuable information for the development of public policies aimed at managing the AFFF discharge in freshwater ecosystems.

Water encountering biomass can affect the change in its chemical composition and properties through the leaching process. In the leaching process, leachates are formed, and their composition depends on the type of biomass and the time of exposure to the solvent (water). The aim of the study was to analyze the influence of time of contact of water with biomass on changing the chemical composition of the leachates formed during long-term (counted in days) leaching of pine bark (Pinus sylvestris). Long-term leaching contributes to a loss of organic and inorganic compounds, and in this study, an intensive extraction of biomass components was noted from the first day of leaching. Along with the extension of the leaching time, values for electrical conductivity, concentration of mineral fraction (ashes), concentration of volatile matter, and concentration of total organic carbon significantly increased in the leachates. However, no linear relationship between the extension of the leaching time and the increase in the concentration of chlorides, sulfates, nitrogen, phosphorus, and other elements in the leachates was observed. This study will allow to better understand the impact of vegetation communities on the aquatic and terrestrial ecosystems, as well as help to provide adequate conditions of storage of biomass for technological purposes. Graphical Abstract

In the original publication, the given name of the fourth author was mispelled as Adolp instead of Adolph. The correct name of the fourth author is Adolph Anga Muleja.