The release of arsenic (As) from sediments poses a risk to human health especially at high pH levels. Despite this, the distribution and kinetic response of mobile As remains unclear under varying pH conditions. In this study, a microcosm incubation experiment was performed, using sediment cores in combination with dialysis (Peeper) and thin film diffusive gradients (DGT), to investigate the distributions of mobile As (soluble As in pore water and DGT-labile As) at high vertical resolutions (2–4 mm). Results show that the concentrations of soluble As present in the water column increased 1.5-fold with an increase in pH from 5.4 to 11.2. Both soluble As in pore water and DGT-labile As exhibited stable low-level distributions in the uppermost layer beneath the sediment-water interface, followed by increasing concentration distribution with decreasing layers to middle depths. The mean concentrations of mobile As species increased with increased water pH in both sediment profiles and with upward diffusion gradients, showing a 0.2-fold increase of soluble As in the top 20-mm layer and a 0.6-fold increase in deeper 20–52-mm layers, while DGT-labile As showed a 1.0- and 1.1-fold increase in these two layers, respectively. Modeling of DGT-induced flux in sediments (DIFS) showed that the desorption rate constant increased more rapidly than the absorption rate constant, resulting in the increased availability of solid As pools, therefore resupplying the soluble As in pore water from sediments.

The intensive use of pesticides has increased exponentially in Brazil and worldwide due to the need to meet the food demands of a growing population. If the management/monitoring of the use of pesticides is adequately performed, it would not compromise the expected benefits or have negative effects on the environment as a whole. In order to examine the information available on herbicide use in Brazil and worldwide, this paper presents a review of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) and its chemical properties, action on target organisms, environmental fate, and toxicity to non-target organisms. This herbicide is a synthetic auxin used to control broad-leaved weeds, and the action in target organisms is well known. Although 2,4-D has been widely used worldwide, many studies have shown that this herbicide induces alterations in non-target organisms. Therefore, ecotoxicology studies are important to assess the risk the herbicides can be to different ecosystems. Thus, it is advised to use this herbicide and other pesticides with caution.

Herein, we report the synthesis of carbon spheres (CS) using a relatively low-temperature hydrothermal technique using lactose as precursor pre-treated with HCl. The successful synthesis, spherical morphology, porous morphology, and monodispersed nature of CS were confirmed via scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Isoelectric point (IEP) was determined as 3.8, and at neutral conditions the prepared carbon particles are negatively charged at − 43 ± 2.50 mV. Owing to their spherical morphology, almost uniform distribution and negatively charged surface at neutral conditions, the prepared CS were used as adsorbent for the removal of methylene blue (MB) and Geimsa stain (GS) from aqueous environments at pH 7. It was shown that CS has 97% adsorption capability for GS, whereas for methylene MB, the maximum adsorption capacity was 67% for 0.1-g CS from 50-ppm dye solutions in DI water. The adsorption studies revealed that the Langmuir and modified Fruendlich (MFE) adsorption models resulted in considerably high linear correlation coefficient (r ²) values and the efficient adsorption of positively charged species on CS can be represented better with the MFE model. Graphical Abstract Carbon spheres from D-lactose for environmental application

To investigate the differential contribution of extracellular polymeric substances (EPS) to polycyclic aromatic hydrocarbon (PAH) degradation by fungi and bacteria, the PAH-degrading ability and characteristics of EPS from the bacterium Mycobacterium gilvum SN12 and the fungus Mucor mucedo were compared. The fungus degraded 11% more pyrene and 21% more benzo[a]pyrene (B[a]P) than the bacterium. The biodegradation of pyrene and B[a]P increased after EPS were introduced into the PAH degradation solution, and 5.0% more pyrene and 4.5% more B[a]P were achieved for the added EPS from the fungal compared with the bacterial isolate. The comparison of two EPS indicated that the amount of protein and carbohydrate in EPS from the fungus was greater than that from the bacterium and was especially enriched for tryptophan, which is positively related to the increase of PAH biodegradation by fungal EPS. Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) further revealed that higher molecular weight (HMW) of proteins over 200 kDa only existed in EPS from the fungus, and the polymorphism of proteins in EPS from the fungus was more abundant than that from the bacterium. The HMW proteins with stronger hydrophobicity in the fungal EPS also enabled the fungus to absorb more PAH than the bacterium. The results demonstrated that the pronounced differences in the characteristics of EPS from the fungal and the bacterial sources are responsible for the differential effects on PAH biodegradation.

Two species of Pb-adapted shrubs, Alyssum montanum and Daphne jasminea, were evaluated in vitro for their tolerance to elevated concentrations of cadmium. Shoot cultures were treated with 0.5, 2.5, and 5.0 μM CdCl₂ for 16 weeks and analyzed for their organogenic response, biomass accretion, pigment content, and macronutrient status. Cadmium accumulation and its root-to-shoot translocation were also determined. In both species, rooted microplantlets, suitable for acclimatization, were obtained in the presence of Cd applied as selection agent. In A. montanum, low and moderate dose of Cd stimulated multiplication, rooting, and biomass production. Growth tolerance index (GTI) in Cd-treated shoots ranged from 120 to 215%, while in the roots 51–202%. In turn, in Cd-treated D. jasminea proliferation and rooting were inhibited, and GTI for shoots decreased with increasing doses of Cd. However, roots exposed to Cd had higher biomass accretion. Both species accumulated Cd in developed organs, and its content increased with increasing CdCl₂ dose. Interestingly, D. jasminea accumulated higher amounts of Cd in the roots than A. montanum and immobilized this metal in the root system. On the contrary, A. montanum translocated some part of accumulated Cd to the shoots, but with low efficiency. In the presence of Cd, A. montanum maintained macronutrient homeostasis and synthesized higher amounts of phytosynthetic pigments in the shoots. D. jasminea accumulated root biomass, immobilized Cd, and restricted its translocation at the expense of nutrient balance. Considering remediation potential, A. montanum could be exploited in phytoextraction, while D. jasminea in phytostabilization of polluted substrate.

Nanoscale zero valent iron (NZVI) was synthesized by the reduction of natural limonite under hydrogen conditions. The adsorption performance of the as-prepared NZVI on phosphate was evaluated through batch and column experiments. The removal of phosphate (PO₄³⁻) significantly decreased with an increase of pH from 2.0 to 11, whereas a remarkable increase of PO₄³⁻ removal was observed in the presence of SO₄²⁻ and S₂O₃²⁻. In addition, Cl⁻ and NO₃⁻ also improved phosphate removal at concentrations of more than 0.2 mmol/L. Kinetic studies indicated that the removal process of PO₄³⁻ on NZVI can be easily followed with the pseudo-second-order kinetic model. The removal of phosphate from the oxic system was significantly higher than that of the anoxic system, which was attributed to the formation of the secondary phase by the further oxidization of Fe²⁺. The adsorption capacity of the as-prepared NZVI of the oxic system was 16 mg/g, and the pH was 6.3. The column experiments further demonstrated that the as-prepared NZVI presented a high removal capacity for PO₄³⁻-P. These findings indicated that the as-prepared NZVI displayed an excellent ability to remove phosphate from aqueous solutions.

The aim of this work was to analyse the response of Rosa rubiginosa to salinity induced by different concentrations of sodium chloride and calcium chloride (0, 25, 50, 100, 150 and 200 mM). Besides salt accumulation and pH changes, other parameters were investigated including photosynthetic activity, leaf water content, the dynamics of necrosis and chlorosis appearance and leaf drying. The study was complemented with microscopic analysis of changes in leaf anatomy. R. rubiginosa was more sensitive to the salinity induced by calcium chloride than by sodium chloride. Plant response to salinity differed depending of the salt concentration. These differences were manifested by higher dynamics of necrosis and chlorosis appearance and leaf drying. CaCl₂ showed greater inhibition of the photosynthetic apparatus and photosynthetic activity. Treatment with CaCl₂ caused more visible deformation of palisade cells, reduction in their density and overall reduction in leaf thickness. The study demonstrated higher accumulation of CaCl₂ in the soil, and thus greater limitations in water availability resulting in reduced leaf water content and quicker drying of leaves as compared with NaCl-treated plants.

Phytostabilisation can benefit from phytostimulatory rhizobacteria. Forty-three bacterial strains were isolated from the roots of the metallicolous legume Anthyllis vulneraria ssp. carpatica grown in a highly contaminated mine tailing (total Cd, Pb and Zn were up to 1200; 34,000; and 170,000 mg kg⁻¹, respectively). We aimed at evaluating their phytostimulatory effects on the development of leguminous metallophytes. Strains were screened for fluorescent siderophores and auxin synthesis, inorganic P solubilisation and 1-amino-cyclopropane-1-carboxylate deaminase (ACCd) activity to define a subset of 11 strains that were inoculated on the leguminous metallophytes A. vulneraria and Lotus corniculatus grown in diluted mine spoil (Zn 34,653; Pb 6842; and Cd 242, all in mg kg⁻¹). All strains were affiliated to Pseudomonas spp. (except two), synthetised auxins and siderophores and solubilised P (except three), and seven of them were ACCd positive. The inoculation effects (shoot-root-nodule biomass, chlorophyll content) depended on legume species and bacterial strain genotype. Phytostimulation scores were unrelated to siderophore/auxin synthesis and P solubilisation rates. Inoculations of the strain nos. 17–43 triggered a 1.2-fold significant increase in the chlorophyll content of A. vulneraria. Chlorophyll content and root biomass of L. corniculatus were significantly increased following the inoculations of the strain nos. 17–22 (1.5–1.4-fold, respectively). The strongest positive effects were related to increases in the nodule biomass of L. corniculatus in the presence of three ACCd-positive strains (1.8-fold), one of which was the highest auxin producer. These data suggest to focus on interactions between ACCd activity and auxin synthesis to enhance nodulation of metallicolous legumes.

Although every year, thousands of people die from asbestos-related diseases, many people disregard things that are past. Meanwhile, a lot of people, in particular, in many Asia countries that have no guideline values for waterborne asbestos are currently in a fever of anxiety about the possibility of its health hazards. This study focused on a grasping the actual situation of asbestos in household tap water. An intensive collection of the tract drinking-water was conducted in Iksan, Korea (at six homes), and Fukuoka, Japan (at nine homes). After pretreatment, both morphological observation and elemental analysis were simultaneously carried out using a scanning electron microscopy (SEM) with an energy dispersive X-ray spectrometer (EDX). The concentrations of waterborne asbestos fiber varied from place to place in both local cities. Their average concentrations at all sites in Iksan and Fukuoka were 213.3 and 181.1 f/L, respectively. Although the measured values in this study were the sum of chrysotile, amosite, and crocidolite fibers with a high risk of cancer, they were found to be consistently below the MCL (the Maximum Contaminant Level recommended by the U.S. toxicological profile for Asbestos). A significant link was found between open water supply channels and waterborne asbestos. The backward wind trajectory projections indicated that the present water sampling sites might be affected by the airborne asbestos fiber in the upwind atmosphere.

Water contamination has reached an alarming state due to industrialization and urbanization and has become a worldwide issue. Dyes contaminate water and are addressed extensively by researchers. Various technologies and materials have been developed for the treatment of contaminated water. Among them, adsorption has attracted great attention due to its ease and cost-effective nature. In recent years, graphene-based composites have shown great potential for the removal of contaminants from water. The literature reveals the usefulness of composites of graphene with metal oxides, carbon derivatives, metal hybrids and polymers for the removal of organic dyes from contaminated water. In this review, efforts have been made to compile the studies on the removal of cationic and anionic dyes from water using graphene-based composites.