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Abstract For the application of biochar in restoring pesticide-contaminated soils and minimizing the risk associated with their uptake in plants, it is crucial to understand the biochar impact on soil biological activities and dissipation and accumulation of pesticides in plant and soil systems. In this study, the effect of Mentha-distilled waste-derived biochar was investigated on chlorpyrifos and atrazine contaminated sandy loam soil. The four application rates of atrazine (2, 4, 6, and 8 mg kg−1) and chlorpyrifos (2, 4, 6, and 12 mg kg−1) and a single application rate of biochar (4%) were used in this study. The degradation of pesticides, the diversity of the bacterial community, and enzymatic activities (alkaline phosphatase, dehydrogenase, arylsulfatase, phenol oxidase, urease activity and N-acetyl glucosaminidase) were examined in soil. The uptake of two pesticides and their effect on growth and stress parameters were also investigated in plants (A. paniculata). The dissipation of chlorpyrifos and atrazine followed simple first-order kinetics with a half-life of 6.6–74.6 and 21–145 days, respectively. The presence of deisopropyl atrazine desethyl atrazine (metabolites of atrazine) and 3,5,6-trichloro-2-pyridinol (a metabolite of chlorpyrifos) was observed in soil and plant tissues. Biochar application significantly (p = 0.001) enhanced the degradation rate of chlorpyrifos and atrazine leading to the lower half-life of chlorpyrifos and atrazine in soil. A significant reduction (p = 0.001) in the uptake of chlorpyrifos and atrazine and alteration in their binding affinity and uptake rate in plant tissues was observed in biochar treatments. The incorporation of biochar improved chlorpyrifos/atrazine degrader and plant growth-promoting bacterial genera such as Balneimonas, Kaistobacter, Rubrobacter, Ammoniphilus, and Bacillus. The upregulation of functional genes associated with nucleotide, energy, carbohydrate, amino acid metabolism, xenobiotic biodegradation, and metabolism: atrazine degradation was observed in biochar treatments. The biochar amendments significantly (p = 0.001) reduced the plant’s uptake velocity (Vmax) and affinity (Km) of chlorpyrifos and atrazine. These results delineated that Mentha-distilled waste-derived biochar can potentially remediate chlorpyrifos and atrazine contaminated soils and ensure the safety of plants for consumption. Graphical Abstract

For the application of biochar in restoring pesticide-contaminated soils and minimizing the risk associated with their uptake in plants, it is crucial to understand the biochar impact on soil biological activities and dissipation and accumulation of pesticides in plant and soil systems. In this study, the effect of Mentha-distilled waste-derived biochar was investigated on chlorpyrifos and atrazine contaminated sandy loam soil. The four application rates of atrazine (2, 4, 6, and 8 mg kg−1) and chlorpyrifos (2, 4, 6, and 12 mg kg−1) and a single application rate of biochar (4%) were used in this study. The degradation of pesticides, the diversity of the bacterial community, and enzymatic activities (alkaline phosphatase, dehydrogenase, arylsulfatase, phenol oxidase, urease activity and N-acetyl glucosaminidase) were examined in soil. The uptake of two pesticides and their effect on growth and stress parameters were also investigated in plants (A. paniculata). The dissipation of chlorpyrifos and atrazine followed simple first-order kinetics with a half-life of 6.6–74.6 and 21–145 days, respectively. The presence of deisopropyl atrazine desethyl atrazine (metabolites of atrazine) and 3,5,6-trichloro-2-pyridinol (a metabolite of chlorpyrifos) was observed in soil and plant tissues. Biochar application significantly (p = 0.001) enhanced the degradation rate of chlorpyrifos and atrazine leading to the lower half-life of chlorpyrifos and atrazine in soil. A significant reduction (p = 0.001) in the uptake of chlorpyrifos and atrazine and alteration in their binding affinity and uptake rate in plant tissues was observed in biochar treatments. The incorporation of biochar improved chlorpyrifos/atrazine degrader and plant growth-promoting bacterial genera such as Balneimonas, Kaistobacter, Rubrobacter, Ammoniphilus, and Bacillus. The upregulation of functional genes associated with nucleotide, energy, carbohydrate, amino acid metabolism, xenobiotic biodegradation, and metabolism: atrazine degradation was observed in biochar treatments. The biochar amendments significantly (p = 0.001) reduced the plant's uptake velocity (Vmax) and affinity (Km) of chlorpyrifos and atrazine. These results delineated that Mentha-distilled waste-derived biochar can potentially remediate chlorpyrifos and atrazine contaminated soils and ensure the safety of plants for consumption. Highlights: Biochar amendments reduced the half-life of chlorpyrifos and atrazine in soil. Biochar altered the binding affinity and uptake rate of chlorpyrifos and atrazine in plant tissues. Biochar up-regulated gene assigned to xenobiotic, energy, and carbohydrate metabolism in soil. Biochar enhanced Pseudomonas and Bacillus species in soil. [ABSTRACT FROM AUTHOR]

This study investigates the uptake and retention of stable fluorescent organosilica nanoparticles by macrophages, which play a vital role in scavenging environmental nanoparticles and nanomedicines within the body. We used rhodamine 6G-loaded fluorescent organosilica nanoparticles (SiNP-R6G) synthesized from a thiol-functionalized organosilane precursor. Our primary objective was to establish a quantitative relationship between fluorescent measurements and nanoparticle tracking analysis, enabling the precise "counting" of nanoparticles taken up by macrophages under kinetic measurement conditions. Our kinetic study demonstrated a concentration-dependent, saturable internalization of nanoparticles in a model macrophage (RAW 264.7 cells), with a maximum uptake rate (Vmax) of 7.9 × 104 nanoparticles per hour per cell. The estimated number concentration of nanoparticles for half-maximum uptake was approximately 0.8 trillion nanoparticles per milliliter, and a significant portion (∼80%) of internalized SiNP-R6G remained entrapped within the cells for 48 h, indicating the sustained particle retention capacity of macrophages. Our data further demonstrate that the internalized nanoparticles occupy more than 10% of the total cell volume, without inducing cytotoxic effects. This heightened capacity for nanoparticle uptake is attributed to intracellular vesicles capable of accommodating up to 50 densely packed, yet nonaggregated, nanoparticles within a single vesicle. In summary, our study underscores the effective development of a methodology for precise "counting" of cellular nanoparticle uptake in macrophages, providing valuable insights into the kinetics and retention capabilities of macrophages for nanoparticle-based drug delivery. [ABSTRACT FROM AUTHOR]

Arsenic (As) pollution in wetlands, mainly as As(III) and As(V), has threatened wetland plant growth. It has been well documented that arbuscular mycorrhizal (AM) fungi can alleviate As stress in terrestrial plants. However, whether AM fungi can protect natural wetland plants from As stress remains largely unknown. Therefore, three hydroponic experiments were conducted in which Iris tectorum Maxim. (I. tectorum) plants were exposed to As(III) or As(V) stresses, to investigate the effects of mycorrhizal inoculation on As uptake, efflux, and accumulation. The results suggested that short-term kinetics of As influx in I. tectorum followed the Michaelis–Menten function. Mycorrhizal inoculation decreased the maximum uptake rate (Vmax) and Michaelis constant (Km) of plants for As(III) influx, while yielding no significant difference in As(V) influx. Generally, mycorrhizal plants released more As into environments after 72 h efflux, especially under As(V) exposure. Moreover, mycorrhizal plants exhibited potential higher As accumulation capacity, probably due to more active As reduction, which was one of the mechanisms through which AM fungi mitigate As phytotoxicity. Our study has revealed the role of aerobic microorganism AM fungi in regulating As translocation in wetland plants and supports the involvement of AM fungi in alleviating plant As stress in anaerobic wetlands. [ABSTRACT FROM AUTHOR]

[Display omitted] Today, macromolecular compounds such as microRNAs (miRNAs) are becoming more and more widespread as leading therapeutics. However, their application is limited mostly due to their poor stability, limited cellular uptake, and poor target specificity. Cell-penetrating peptides (CPPs), a group of positively charged peptides, represent a breakthrough as delivery systems for macromolecules. In the present study, we used two types of nanoparticles which differ in the type of CPP used for their manufacturing. The first type is composed of protamine, an arginine rich CPP, which is highly positively charged. The arginine residues are able to form electrostatic interactions with miRNAs, stabilize them, and deliver them to cells. The second type is composed of the N-Ter peptide (also known as MPG), an amphipathic peptide rich in lysine. The positively charged parts of the N-Ter peptide electrostatically stabilize miRNAs, whereas its amphipathic character allows it to successfully traverse cell membranes. We used miRNA-27a, a negative regulator of adipogenesis, to form nanoparticles with the peptides and traced their uptake in 3T3-L1 preadipocytes. Motivated by the lengthy discourse regarding the uptake mechanism of CPPs, the focus of our study was to analyse and understand the internalization of proticles (protamine nanoparticles) and N-Ter complexes. The nanoparticles were characterized regarding size, size distribution, and zeta potential, and their cytotoxicity was tested in 3T3-L1 cells. The uptake studies were performed by varying the experimental conditions such as time, concentration, and temperature, as well as by applying different inhibitors of endocytosis. Furthermore, we assessed the biological effect of miRNA-27a on the pro-adipogenic machinery. The obtained data have shown that protamine and the N-Ter peptide form positively charged nanoparticles through non-covalent complexation. The uptake of proticles and N-Ter complexes was found to be dependent on time, concentration, and temperature, and different uptake pathways were discovered to be involved in the internalization of the different nanoparticles. Furthermore, both types of nanoparticles induced the anti-adipogenic effect of miRNA-27a, demonstrating that this approach can be used as a novel miRNA replacement therapy in the treatment of obesity and obesity-related disorders. [ABSTRACT FROM AUTHOR]

Copyright of Asian Journals of Ecotoxicology is the property of Gai Kan Bian Wei Hui and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Removing hazardous metals and recovering valuable strategic metals from wastewater has become an important challenge for the industry. Herein, brown algal biomass residue (AR, after bio‐stimulant extraction, currently poorly valorized) is tested for the removal of Ni(II), Cd(II), and La(III) from aqueous solutions. This valorization of industrial waste makes profit of residual amounts of alginate‐based materials, which have a strong affinity for metal cations. Fourier transform infrared (FTIR) and X‐ray photoelectron spectroscopy (XPS) techniques are used for characterizing metal/biosorbent interactions. Uptake kinetics are relatively fast (equilibrium being reached in 180–240 min). The Sips equation fits the sorption isotherms; the maximum sorption capacities at pH ≈5 reach up to 0.84 mmol La g−1, 0.92 mmol Cd g−1, and 0.78 mmol Ni g−1. In binary solutions, AR shows marked preference for La(III) over divalent cations. This selectivity may be increased by complexing base metals with EDTA, opening the route for the selective recovery of rare earth elements. HCl solution reveals more efficient (>90% for La(III), ≈82% for Cd(II) and Ni(II)) than CaCl2 solution at pH 2 for metal desorption. This waste residue from biostimulant extraction (in brown algal biomass) can be valorized for the recovery of hazardous and strategic metal ions. [ABSTRACT FROM AUTHOR]

Phosphonic acid functionalization of gellan gum and chitosan biopolymers was successfully performed. In the first step, the sorption was investigated using La(III) ions before testing for the recovery of rare earth elements (REEs) from pretreated industrial acidic leachate. The sorbent was characterized by Fourier-transform infrared (FTIR), scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDX), thermogravimetric analysis (TGA), Brunauer–Emmett–Teller (BET), and pH of zero charge (pHPZC) determination. FTIR and EDX results show efficient grafting of phosphoryl groups. The sorption was determined for the crude materials before functionalization (PGEG) and after phosphorylation (TBP-PGEG). More efficient sorption was seen for phosphorylated sorbent than for the crude composite. The sorption capacity is 0.226 mmol La g−1 for the PGEG while the value is 0.78 mmol La g−1 for the TBP-PGEG. We infer that phosphonate groups participate in the sorption. The most effective sorption is at pH = 4. The kinetic behavior was described using pseudo first-order equations (PFORE), pseudo second-order equations (PSORE), and resistance to intraparticle diffusion (RIDE). The sorption isotherms can be better represented by Langmuir and Sips equations than by the Freundlich equation. The sorbent shows high stability performance during reuse cycles with a limit on the decrease in the sorption performances and stability in the desorption performances. We have thus developed a good tool for the recovery of REEs with a selectivity higher than that of the non-functionalized components. [ABSTRACT FROM AUTHOR]

Although Cs(I) and Sr(II) are not strategic and hazardous metal ions, their recovery from aqueous solutions is of great concern for the nuclear industry. The objective of this work consists of designing a new sorbent for the simultaneous recovery of these metals with selectivity against other metals. The strategy is based on the functionalization of algal/polyethyleneimine hydrogel beads by phosphonation. The materials are characterized by textural, thermo-degradation, FTIR, elemental, titration, and SEM-EDX analyses to confirm the chemical modification. To evaluate the validity of this modification, the sorption of Cs(I) and Sr(II) is compared with pristine support under different operating conditions: the pH effect, kinetics, and isotherms are investigated in mono-component and binary solutions, before investigating the selectivity (against competitor metals) and the possibility to reuse the sorbent. The functionalized sorbent shows a preference for Sr(II), enhanced sorption capacities, a higher stability at recycling, and greater selectivity against alkali, alkaline-earth, and heavy metal ions. Finally, the sorption properties are compared for Cs(I) and Sr(II) removal in a complex solution (seawater sample). The combination of these results confirms the superiority of phosphonated sorbent over pristine support with promising performances to be further evaluated with effluents containing radionuclides. [ABSTRACT FROM AUTHOR]

This study investigated the effects of nitrogen form on root activity and nitrogen uptake kinetics of Camellia oleifera Abel. seedlings, providing a scientific basis for improving nitrogen use efficiency and scientific fertilization in C. oleifera production. Taking one-year-old C. oleifera cultivar 'Xianglin 27' seedlings as subjects, 8 mmol·L−1 of nitrogen in varied forms ( NO 3 − : NH 4 + = 0:0, 10:0, 7:3, 5:5, 3:7, 0:10) was applied in this study as the treatment conditions to investigate the effects of different nitrogen forms on root activity and nitrogen uptake kinetics in C. oleifera seedlings. Comparing the performance of nutrient solutions with different NO 3 − : NH 4 + ratios, the results showed that a mixed nitrogen source improved the root activity of C. oleifera seedlings based on total absorption area, active absorption area, active absorption area ratio, specific surface area, and active specific surface area. When NO 3 − : NH 4 + = 5:5, the total absorption area and active absorption area of the seedling roots reached the maximum. The results of uptake kinetic parameters showed that Vmax NH 4 + > Vmax NO 3 − and Km NO 3 − > Km NH 4 + , indicating that the uptake potential of ammonium–nitrogen by C. oleifera seedlings is greater than that of nitrate–nitrogen. The conclusion was that compared to either ammonium– or nitrate–nitrogen, the mixed nitrogen source was better for promoting the root activity of C. oleifera seedlings, and the best nitrate/ammonium ratio was 5:5. [ABSTRACT FROM AUTHOR]

Arsenic (As) pollution in wetlands, mainly as As(III) and As(V), has threatened wetland plant growth. It has been well documented that arbuscular mycorrhizal (AM) fungi can alleviate As stress in terrestrial plants. However, whether AM fungi can protect natural wetland plants from As stress remains largely unknown. Therefore, three hydroponic experiments were conducted in which Iris tectorum Maxim. (I. tectorum) plants were exposed to As(III) or As(V) stresses, to investigate the effects of mycorrhizal inoculation on As uptake, efflux, and accumulation. The results suggested that short-term kinetics of As influx in I. tectorum followed the Michaelis–Menten function. Mycorrhizal inoculation decreased the maximum uptake rate (Vmax) and Michaelis constant (Km) of plants for As(III) influx, while yielding no significant difference in As(V) influx. Generally, mycorrhizal plants released more As into environments after 72 h efflux, especially under As(V) exposure. Moreover, mycorrhizal plants exhibited potential higher As accumulation capacity, probably due to more active As reduction, which was one of the mechanisms through which AM fungi mitigate As phytotoxicity. Our study has revealed the role of aerobic microorganism AM fungi in regulating As translocation in wetland plants and supports the involvement of AM fungi in alleviating plant As stress in anaerobic wetlands.

Increasing amounts of nanoplastics (NPs) in the environment are a great threat to human health, causing intestinal inflammation when consumed through seafood and water. There is, however, still a lack of understanding of the immunomodulatory role of NPs in immune cells, especially the early signal events behind inflammation resulting from NPs ingestion. In this study, we explored the dynamic internalization of polystyrene NPs and their carboxy and amino-functionalized products (PS, PS-COOH and PS-NH2) followed by activation of ROS-MAPK/NF-κB signaling pathways in macrophage RAW 264.7. The inflammatory and cytotoxic potentials of NPs were evaluated by ELISA and apoptosis assays. Results showed that PS-COOH accumulated most in cells and induced more pronounced ROS and apoptosis than PS, PS-NH2 and PS-μm. PS-COOH and PS-NH2 showed stronger MAPK/NF-κB activation potential to at a low concentration of 10 μg/mL than unmodified PS, followed by production of IL-6 and TNF-α cytokines. Furthermore, PS-COOH induced MAPK/NF-κB activation and cytokine secretion could be inhibited by NAC, indicating that ROS was responsible for signal dysregulation and immunogenicity of PS-COOH, but not for PS-NH2. The results suggested that the MAPK and NF-κB pathways were involved in NPs-induced macrophage inflammation, which was influenced by surface functionalization of NPs, with carboxylated PS NPs exhibiting a greater pro-inflammatory and cytotoxic potential.

Shrimp shells are an abundant natural resource for chitosan generation as bio sorbent. In this work, imine was prepared through the modified free amino group –NH2 of chitosan using 4-fluorobenzaldehyde. The ion-imprinted method was used to prepare a new bulk polymer as a selective, fast, high-performance approach to remove copper ions. Adsorbents were characterized using Fourier-transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray, X-ray powder diffraction, transmission electron microscopy, and nuclear magnetic resonance techniques. Operational parameters including pH, contact time, adsorbent quantity, metal concentration, and temperature were evaluated. Results illustrated Cu(II) adsorption by Cu(II) ion-imprinted polymers (Cu(II)-IIP) is independent pH. The kinetic and isotherms dada fitted well to secondorder reaction and Langmuir model with the maximum adsorption capacities of 20.8 mg/g for imine and 22 mg/g for Cu(II)-IIP at pH 8.0. Thermodynamic parameters (ΔG° < 0 and ΔH° > 0) suggested a spontaneous and endothermic adsorption process. The recycling and reuse showed that imine retained its adsorption capacity for Cu(II) ions after four consecutive cycles, while Cu(II)-IIP showed high efficiency and no significant decrease for copper removal after ten cycles. [ABSTRACT FROM AUTHOR]

The recovery of strategic metals such as rare earth elements (REEs) requires the development of new sorbents with high sorption capacities and selectivity. The bi-functionality of sorbents showed a remarkable capacity for the enhancement of binding properties. This work compares the sorption properties of magnetic chitosan (MC, prepared by dispersion of hydrothermally precipitated magnetite microparticles (synthesized through Fe(II)/Fe(III) precursors) into chitosan solution and crosslinking with glutaraldehyde) with those of the urea derivative (MC-UR) and its sulfonated derivative (MC-UR/S) for cerium (as an example of REEs). The sorbents were characterized by FTIR, TGA, elemental analysis, SEM-EDX, TEM, VSM, and titration. In a second step, the effect of pH (optimum at pH 5), the uptake kinetics (fitted by the pseudo-first-order rate equation), the sorption isotherms (modeled by the Langmuir equation) are investigated. The successive modifications of magnetic chitosan increases the maximum sorption capacity from 0.28 to 0.845 and 1.25 mmol Ce g−1 (MC, MC-UR, and MC-UR/S, respectively). The bi-functionalization strongly increases the selectivity of the sorbent for Ce(III) through multi-component equimolar solutions (especially at pH 4). The functionalization notably increases the stability at recycling (for at least 5 cycles), using 0.2 M HCl for the complete desorption of cerium from the loaded sorbent. The bi-functionalized sorbent was successfully tested for the recovery of cerium from pre-treated acidic leachates, recovered from low-grade cerium-bearing Egyptian ore. [ABSTRACT FROM AUTHOR]

The development of new materials based on biopolymers (as renewable resources) is substantial for environmental challenges in the heavy metal and radionuclide ions removal contaminations. Functionalization of chitosan with sulfonic groups was achieved for improving the uranium sorption, not only from slightly acidic leachate, but also for the underground water. The prepared hydrogel based on chitosan was characterized by series of analysis tools for structure elucidation as FTIR spectroscopy, textural properties using nitrogen adsorption method, pHPZC (by pH-drift method), thermogravimetric analysis (TGA), SEM, and SEM-EDX analyses. The sorption was performed toward uranium (VI) ions for adjustment of sorption performances. The optimum sorption was performed at pH 4 (prior to the precipitation pH). The total sorption was achieved within 25 min (relatively fast kinetics) and was fitted by pseudo-first order rate equation (PFORE) and resistance to intraparticle diffusion equation (RIDE). The maximum sorption capacity was around 1.5 mmol U g−1. The sorption isotherms were fitted by Langmuir and Sips equations. Desorption was achieved using 0.3 M HCl solution and the complete desorption was performed in around 15 min of contact. The sorption desorption cycles are relatively stable during 5 cycles with limit decreasing in sorption and desorption properties (around 3 ± 0.2% and 99.8 ± 0.1%, respectively). The sorbent was used for removal of U from acid leachate solution in mining area. The sorbent showed a highly performance for U(VI) removal, which was considered as a tool material for radionuclides removing from aquatic medium. [ABSTRACT FROM AUTHOR]

Selenium (Se) is an essential trace element for human and animal health, and toward an understanding of the uptake and translocation of Se in plants is important from the perspective of Se biofortification. In this study, we conducted hydroponic experiments to investigate the mechanisms of organic Se [selenomethionine (SeMet) and selenomethionine-oxide (SeOMet)] uptake, translocation, and the interactions between SeMet and SeOMet in rice. We also investigated differences in the dynamics of organic and inorganic Se uptake by rice roots. Concentration-dependent kinetic results revealed that SeMet uptake during a 1 h exposure was 3.19-16.0 times higher than that of three other Se chemical forms, with uptake capacity (Vmax) values ordered as follows: SeMet>SeOMet>selenite>selenate. Furthermore, time-dependent kinetic analysis revealed that SeMet uptake by roots and content in shoots were initially clearly higher than those of SeOMet, although the differences gradually diminished with prolonged exposure time; while no significant difference was found in the transfer factor of Se from rice roots to shoots between SeMet and SeOMet. Root uptake of SeOMet was significantly inhibited by carbonyl cyanide 3-chlorophenylhydrazone (CCCP) (30.4%), AgNO3 (41.8%), and tetraethylammonium chloride (TEACl) (45.6%), indicating that SeOMet uptake is a metabolically active process, and that it could be mediated via aquaporins and KC channels. Contrarily, SeMet uptake was insensitive to CCCP, although markedly inhibited by AgNO3 (93.1%), indicating that rice absorbs SeMet primarily via aquaporins. Furthermore, Se uptake and translocation in rice treated simultaneously with both SeMet and SeOMet were considerably lower than those in rice treated with SeMet treatment alone and notably lower than the theoretical quantity, indicating interactions between SeMet and SeOMet. Our findings provide important insights into the mechanisms underlying the uptake and translocation of organic Se within plants. [ABSTRACT FROM AUTHOR]

Inorganic nitrogen (N) is an important element for eutrophication and harmful algal bloom (HAB) formation. However, the roles of inorganic N in HAB outbreaks are still unclear. Here, we compared the affinities and abilities for inorganic N uptake and assimilation among three typical bloom-forming algae in the East China Sea (ECS), Skeletonema costatum, Prorocentrum donghaiense and Alexandrium pacificum by investigating the uptake and enzymatic (nitrate reductase (NR) and glutamine synthetase (GS) kinetics for nitrate and ammonia. The Ks of nitrate and ammonium in S. costatum was lower than those in P. donghaiense and A. pacificum. The NR activity of S. costatum and P. donghaiense exhibited a positive relationship with the nitrate concentration, and NR activity of S. costatum was nearly 4-fold higher than that of P. donghaiense at high nitrate concentration. However, the NR activity of A. pacificum could not be detected. The GS activity of three species decreased with the increase of ammonium concentrations, and the highest GS activity was detected in A. pacificum. S. costatum presented the highest affinity for nitrate and ammonium, followed by P. donghaiense and A. pacificum. Moreover, P. donghaiense exhibited the highest affinity for intracellular ammonium. Our results characterized the differences in inorganic nitrogen uptake among the three typical bloom-forming algae, which may contribute to the formation of blooms in the coastal waters of the ECS. [ABSTRACT FROM AUTHOR]

Modified chitosan has been widely used for heavy metals removal during the last few decades. In this research, the study was focused on the effect of modified chitosan particles after grafting with heterocyclic constituent for enhancing the sorption of Cr(VI) ions. Chitosan was functionalized by 2-thioxodihydropyrimidine-4,6(1H,5H)-dione, in which the synthesized composite considered as a nanoscale size with average 5–7 nm. This explains the fast kinetics of sorption with large surface area. The prepared sorbent was characterized by Fourier-transform infrared (FTIR), elemental analysis (EA), Brunauer–Emmett–Teller (BET surface area) theory, thermogravimetric analysis (TGA), mass spectroscopy, and scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDX) analyses. The experimental part of this work involved the application of the synthesized sorbent for the removal of Cr(VI) ions from highly contaminated tannery effluents that are characterized by a high concentration toward chromate ions with other associated toxic elements, i.e., Pb(II) and Cd (II) ions, which underscore the importance of this treatment. Under the selected conditions (K2Cr2O7 salt, Co: 100 mg L−1 and pH: 4), the sorption diagram shows high Cr(VI) sorption and fast uptake kinetics. The sorption was enhanced by functionalization to 5.7 mmol Cr g−1 as well as fast uptake kinetics; 30 min is sufficient for total sorption compared with 1.97 mmol Cr g−1 and 60 min for the non-grafted sorbent. The Langmuir and Sips equations were fitted for the sorption isotherms, while the pseudo-first order rate equation (PFORE) was fitted for the uptake kinetics. [ABSTRACT FROM AUTHOR]

This study aims to evaluate the functionalization of chitosan biopolymer with heterocyclic moieties of 2-thioxodihydropyrimidine-4,6(1H,5H)-dione used for enhancing the sorption of Cr ions from aqueous solution. A synthesized sorbent is a nanoscale particle (around 5–7 nm), which explains the fast kinetics of sorption. The sorbent is specified using elemental analysis (EA), FTIR, BET (nitrogen sorption desorption isotherms), TGA, and SEM-EDX analyses. Sorption properties are investigated using ultraviolet emission (UV) but also using visible light (L). In the sorption diagram, the high sorption uptake and fast kinetics observed using ultraviolet conditions are shown. This work is conducted by removing Cr ions from highly contaminated tannery effluents, which have a high concentration of Cr associated with other poisonous elements such as Cd(II) and Pb(II). Under the selected conditions, complete sorption is performed during the first 60 and 45 min with a capacity of 2.05 and 2.5 mmol Cr g−1 for the crosslinked chitosan (without functionalization) in L and UV, respectively. This sorption is enhanced by functionalizing to 5.7 and 6.8 mmol Cr g−1 at the L and UV, respectively, as well as improving the sorption kinetics to 35 and 30 min for both techniques, respectively. The PFORE, and (Langmuir and Sips equations) fit the kinetics and isotherms, respectively. [ABSTRACT FROM AUTHOR]

Short-chained perfluoroalkyl acids (PFAAs, C n F 2n+1 –R, n ≤ 6) have merged as global concerns due to their extensive application and considerable toxicity. However, long-chained PFAAs (n ≥ 7) featured with high persistence are still ubiquitously observed in aquatic environment. To understand the uptake behavior of short-chained PFAAs in aquatic macrophytes, the uptake kinetics, bioconcentration, and translocation of short-chained PFAAs (3 ≤n ≤ 6) in two typical free-floating macrophytes (Eichhornia crassipes and Ceratophyllum demersum) were investigated in the treatments with and without long-chained PFAAs (7 ≤n ≤ 11). Results showed that short-chained PFAAs can be readily accumulated in both E. crassipes and C. demersum , and the uptake of short-chained PFAAs fit the two-compartment kinetic model well (p < 0.05). In the treatments with long-chained PFAAs, significant concentration decreases of all concerned short-chained PFAAs in E. crassipes and PFAAs with n ≤ 5 in C. demersum were observed. Long-chained PFAAs could hinder the uptake rates, bioconcentration factors, and translocation factors of most short-chained PFAAs in free-floating macrophytes (p < 0.01). Significant correlations between bioconcentration factors and perfluoroalkyl chain length were only observed when long-chained PFAAs were considered (p < 0.01). Our results underlined that the effects of long-chained PFAAs should be taken into consideration in understanding the uptake and bioaccumulation behaviors of short-chained PFAAs. [Display omitted] • Uptake of short-chained PFAAs in two free-floating plants fit a two-compartments model well. • Long-chained PFAAs hindered the bioconcentration and translocation of short-chained PFAAs. • C. demersum showed higher accumulation potential than E. crassipes in all treatments. • Competitions with adsorption and translocators/organelles binding may be the key mechanisms. [ABSTRACT FROM AUTHOR]

The synthesis and developments of magnetic chitosan nanoparticles for high efficiency removal of the cadmium ions from aquatic medium are one of the most challenging techniques. Highly adsorptive composite (MCH-ATA) was produced by the reaction of chitosan with formaldehyde and amino thiazole derivative. The sorbent was characterized by FTIR, elemental analyses (EA), SEM-EDX, TEM analysis, TGA and titration (volumetric). The modified material includes high nitrogen and sulfur contents (i.e., 4.64 and 1.35 mmol g−1, respectively), compared to the pristine material (3.5 and 0 mmol g−1, respectively). The sorption was investigated for the removal of Cd(II) ions from synthetic (prepared) solution before being tested towards naturally contaminated groundwater in an industrial area. The functionalized sorbent shows a high loading capacity (1.78 mmol Cd g−1; 200 mg Cd g−1) compared to the pristine material (0.61 mmol Cd g−1; 68.57 mg Cd g−1), while removal of about 98% of Cd with capacity (6.4 mg Cd g−1) from polymetallic contaminated groundwater. The sorbent displays fast sorption kinetics compared to the non-modified composite (MCH); 30 min is sufficient for complete sorption for MCH-ATA, while 60–90 min for the MCH. PFORE fits sorption kinetics for both sorbents, whereas the Langmuir equation fits for MCH and Langmuir and Sips for MCH-ATA for sorption isotherms. The TEM analysis confirms the nano scale size, which limits the diffusion to intraparticle sorption properties. The 0.2 M HCl solution is a successful desorbing agent for the metal ions. The sorbent was applied for the removal of cadmium ions from the contaminated underground water and appears to be a promising process for metal decontamination and water treatment. [ABSTRACT FROM AUTHOR]

Pistachio is an economically valuable crop, and Iran is among the biggest producers, exporters, and consumers of this product in the world. During the growing season, pistachios are subjected to multiple sprayings with various pesticides, which result in the accumulation of their residues in nuts. These residues have raised concerns regarding consumers' health. In this research, uptake and dissipation kinetics of insecticides imidacloprid (IMI), thiacloprid (THI), thiamethoxam (THX), and abamectin (ABA) were investigated in pistachio nuts. Field experiments were conducted in a pistachio orchard. Pistachio trees were sprayed with the recommended dose of each insecticide formulation and water as the control. Samplings were performed for up to 49 days. Based on the results, pesticides uptake and dissipation kinetics were best fitted to first-order exponential growth (FOEG) and single first-order kinetic (SFOK) models, respectively. Variations in pesticides uptake/dissipation rates were mostly related to their water solubility, pKa, and log Kow. THX showed a higher uptake rate (0.16 ± 0.04) compared to IMI (0.10 ± 0.01) and THI (0.06 ± 0.01). The fastest dissipation rates were observed for IMI (0.04 ± 0.002 day−1) and THX (0.03 ± 0.001 day−1), while the slowest belonged to THI (0.02 ± 0.003 day−1). ABA residues were below the quantification limit (LOQ) throughout the experiment. Based on FOEG and SFOK model predictions, multiple sprayings with THI and THX resulted in final concentrations exceeding the maximum residue limit (MRL). Hazard quotients for all pesticides were <1, indicating no risk to humans via consumption of the pistachio nut. [ABSTRACT FROM AUTHOR]

Nanoparticles hold great preclinical promise in cancer therapy but continue to suffer attrition through clinical trials. Advanced, three dimensional (3D) cellular models such as tumor spheroids can recapitulate elements of the tumor environment and are considered the superior model to evaluate nanoparticle designs. However, there is an important need to better understand nanoparticle penetration kinetics and determine how different cell characteristics may influence this nanoparticle uptake. A key challenge with current approaches for measuring nanoparticle accumulation in spheroids is that they are often static, losing spatial and temporal information which may be necessary for effective nanoparticle evaluation in 3D cell models. To overcome this challenge, we developed an analysis platform, termed the Determination of Nanoparticle Uptake in Tumor Spheroids (DONUTS), which retains spatial and temporal information during quantification, enabling evaluation of nanoparticle uptake in 3D tumor spheroids. Outperforming linear profiling methods, DONUTS was able to measure silica nanoparticle uptake to 10 μm accuracy in both isotropic and irregularly shaped cancer cell spheroids. This was then extended to determine penetration kinetics, first by a forward-in-time, center-in-space model, and then by mathematical modelling, which enabled the direct evaluation of nanoparticle penetration kinetics in different spheroid models. Nanoparticle uptake was shown to inversely relate to particle size and varied depending on the cell type, cell stiffness and density of the spheroid model. The automated analysis method we have developed can be applied to live spheroids in situ , for the advanced evaluation of nanoparticles as delivery agents in cancer therapy. [Display omitted] • Analysis platform designed to measure nanoparticle uptake in 3D tumor models • Nanoparticles investigated in live cell models of brain, lung and childhood cancer • Particle penetration over time influenced by tumor cell stiffness and density • Nanoparticle uptake studied in biological models with mathematical modelling data • Accessible quantitative method with analysis platform and user guide available [ABSTRACT FROM AUTHOR]

Although Cs(I) and Sr(II) are not strategic and hazardous metal ions, their recovery from aqueous solutions is of great concern for the nuclear industry. The objective of this work consists of designing a new sorbent for the simultaneous recovery of these metals with selectivity against other metals. The strategy is based on the functionalization of algal/polyethyleneimine hydrogel beads by phosphonation. The materials are characterized by textural, thermo-degradation, FTIR, elemental, titration, and SEM-EDX analyses to confirm the chemical modification. To evaluate the validity of this modification, the sorption of Cs(I) and Sr(II) is compared with pristine support under different operating conditions: the pH effect, kinetics, and isotherms are investigated in mono-component and binary solutions, before investigating the selectivity (against competitor metals) and the possibility to reuse the sorbent. The functionalized sorbent shows a preference for Sr(II), enhanced sorption capacities, a higher stability at recycling, and greater selectivity against alkali, alkaline-earth, and heavy metal ions. Finally, the sorption properties are compared for Cs(I) and Sr(II) removal in a complex solution (seawater sample). The combination of these results confirms the superiority of phosphonated sorbent over pristine support with promising performances to be further evaluated with effluents containing radionuclides.

This study investigated the effects of nitrogen form on root activity and nitrogen uptake kinetics of Camellia oleifera Abel. seedlings, providing a scientific basis for improving nitrogen use efficiency and scientific fertilization in C. oleifera production. Taking one-year-old C. oleifera cultivar ‘Xianglin 27’ seedlings as subjects, 8 mmol·L−1 of nitrogen in varied forms (NO3−:NH4+ = 0:0, 10:0, 7:3, 5:5, 3:7, 0:10) was applied in this study as the treatment conditions to investigate the effects of different nitrogen forms on root activity and nitrogen uptake kinetics in C. oleifera seedlings. Comparing the performance of nutrient solutions with different NO3−:NH4+ ratios, the results showed that a mixed nitrogen source improved the root activity of C. oleifera seedlings based on total absorption area, active absorption area, active absorption area ratio, specific surface area, and active specific surface area. When NO3−:NH4+ = 5:5, the total absorption area and active absorption area of the seedling roots reached the maximum. The results of uptake kinetic parameters showed that Vmax NH4+ > Vmax NO3− and Km NO3− > Km NH4+, indicating that the uptake potential of ammonium–nitrogen by C. oleifera seedlings is greater than that of nitrate–nitrogen. The conclusion was that compared to either ammonium– or nitrate–nitrogen, the mixed nitrogen source was better for promoting the root activity of C. oleifera seedlings, and the best nitrate/ammonium ratio was 5:5.

Heterogeneous reactions on mineral dust play pivotal roles in the removal/production of gaseous pollutants and the formation of secondary particles. However, the uptake coefficient (γ), a key kinetic parameter for a heterogeneous reaction, could vary by several orders of magnitude in different laboratory analyses and give rise to great uncertainties in modeling studies. Thus, a detailed understanding of heterogeneous uptake kinetics is vital to accurately evaluate the impacts of heterogeneous reactions on atmospheric chemistry. In order to reveal the key factors affecting uptake kinetics, heterogeneous reaction of NO2 on surfaces of typical mineral component alumina (α‐Al2O3, γ‐Al2O3, δ‐Al2O3, and AlOOH) was comprehensively studied using two widely used methods, including diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and flow tube reactor. The discrepancy between the true uptake coefficients (γBET) obtained via two techniques was within 1–2 orders of magnitude for alumina samples. The γBET depended positively on NO2 concentration in the DRIFTS measurements but negatively on NO2 concentration in the flow tube experiments, and the discrepancy might be attributed to different calculation methods of γBET, which was calculated based on nitrate formation kinetics in DRIFTS experiments while based on NO2 consumption kinetics in flow tube experiments. The results implied that an accurate selection of the uptake coefficient for modeling studies should base on the consideration of factors such as the measurement method, the concentration range of the reaction gas, and the characteristics of the sample such as crystal structure and effective surface area. Key Points: The discrepancy between the uptake coefficients obtained via diffuse reflectance infrared Fourier transform spectroscopy and flow tube is within 1–2 orders of magnitude for alumina samplesDependence of uptake coefficient on measurement method, concentration range of reaction gas, characteristics of particle was provedAn accurate selection of the uptake coefficient for modeling studies should base on the consideration of above factors [ABSTRACT FROM AUTHOR]

Lead (Pb) is a major toxicological concern of the present day that demands immediate attention. The use of aquatic macrophytes with high Pb tolerance and accumulation may be a very convenient and economically viable solution for remediating Pb. We examined the ability of Salvinia cucullata, Alternanthera sessilis, Lemna minor, and Pistia stratiotes to remove 0.12 mM, 0.24 mM, 0.36 mM, and 0.48 mM Pb for 96-h under hydroponic cultivation system. The plants accumulated variable amounts of Pb: S. cucullata > A. sessilis > P. stratiotes > L. minor, with low mobility of Pb from root to shoot. Lead uptake kinetics were monitored up to 96-h. After 96-h, the uptake efficiency for S. cucullata (98–99%), A. sessilis (79–96%), L. minor (45–79%), and P. stratiotes (40–76%) was noted. For S. cucullata and A. sessilis, an extremely high uptake rate was seen within the initial 24-h of trials, followed by slower uptake till 96-h. P. stratiotes and L. minor worked best at 0.12 mM Pb. Pb-Phytotoxicity became prominent at 0.48 mM exposure with biomass loss and morphological changes. The plants had a quick growth rate, extensive root system, high biomass yield, and the ability to tolerate and accumulate Pb that made them suitable for phytoremediation purposes. NOVELTY STATEMENT: Lead phytoremediation potential of four aquatic macrophytes found in Indian waters was evaluated. These macrophytes, often considered as weeds, could be used for phytoremediation purposes that would turn out to be a sustainable means of the utilization of natural resources in developing countries like India. In this study, not only metal accumulation by plants but also the lead uptake kinetics at several time intervals and valuable growth attributes were estimated to establish the suitability of these plants as probable lead phytoremediators. Two of the plant species, Salvinia cucullata, and Alternanthera sessilis, showed excellent Pb accumulation capacities that had not been reported earlier, to the best of our knowledge. The work is all the more significant as there have been needs for identifying Pb-phytoremediators well suited to native climate and growth conditions that could take up large amounts of metal from the substratum. [ABSTRACT FROM AUTHOR]

The recovery of strategic metals such as rare earth elements (REEs) requires the development of new sorbents with high sorption capacities and selectivity. The bi-functionality of sorbents showed a remarkable capacity for the enhancement of binding properties. This work compares the sorption properties of magnetic chitosan (MC, prepared by dispersion of hydrothermally precipitated magnetite microparticles (synthesized through Fe(II)/Fe(III) precursors) into chitosan solution and crosslinking with glutaraldehyde) with those of the urea derivative (MC-UR) and its sulfonated derivative (MC-UR/S) for cerium (as an example of REEs). The sorbents were characterized by FTIR, TGA, elemental analysis, SEM-EDX, TEM, VSM, and titration. In a second step, the effect of pH (optimum at pH 5), the uptake kinetics (fitted by the pseudo-first-order rate equation), the sorption isotherms (modeled by the Langmuir equation) are investigated. The successive modifications of magnetic chitosan increases the maximum sorption capacity from 0.28 to 0.845 and 1.25 mmol Ce g−1 (MC, MC-UR, and MC-UR/S, respectively). The bi-functionalization strongly increases the selectivity of the sorbent for Ce(III) through multi-component equimolar solutions (especially at pH 4). The functionalization notably increases the stability at recycling (for at least 5 cycles), using 0.2 M HCl for the complete desorption of cerium from the loaded sorbent. The bi-functionalized sorbent was successfully tested for the recovery of cerium from pre-treated acidic leachates, recovered from low-grade cerium-bearing Egyptian ore.

The uptake and elimination kinetics of pesticides from soil to earthworms are important in characterising the risk of pesticides to soil organisms and the risk from secondary poisoning. However, the understanding of the relative importance of chemical, soil, and species differences in determining pesticide bioconcentration into earthworms is limited. Furthermore, there is insufficient independent data in the literature to fully evaluate existing predictive bioconcentration models. We conducted kinetic uptake and elimination experiments for three contrasting earthworm species (Lumbricus terrestris , Aporrectodea caliginosa , Eisenia fetida) in five soils using a mixture of five pesticides (log K ow 1.69 – 6.63). Bioconcentration increased with pesticide hydrophobicity and decreased with soil organic matter. Bioconcentration factors were comparable between earthworm species for hydrophilic pesticides due to the similar water content of earthworm species. Inter-species variations in bioconcentration of hydrophobic pesticides were primarily accounted for by earthworm lipid content and specific surface area (SSA). Existing bioconcentration models either failed to perform well across earthworm species and for more hydrophilic compounds (log K ow < 2) or were not parameterised for a wide range of compounds and earthworm species. Refined models should incorporate earthworm properties (lipid content and SSA) to account for inter-species differences in pesticide uptake from soil. [Display omitted] ● Earthworm bioconcentration of pesticides increased with compound hydrophobicity. ● Earthworm bioconcentration of pesticides decreased with soil organic matter. ● Hydrophobic compound uptake varied with species lipid content and surface area. ● Existing bioconcentration models performed less well for larger earthworm species. ● Existing models performed less well for hydrophilic (log K ow < 2) compounds. [ABSTRACT FROM AUTHOR]

The development of new materials based on biopolymers (as renewable resources) is substantial for environmental challenges in the heavy metal and radionuclide ions removal contaminations. Functionalization of chitosan with sulfonic groups was achieved for improving the uranium sorption, not only from slightly acidic leachate, but also for the underground water. The prepared hydrogel based on chitosan was characterized by series of analysis tools for structure elucidation as FTIR spectroscopy, textural properties using nitrogen adsorption method, pHPZC (by pH-drift method), thermogravimetric analysis (TGA), SEM, and SEM-EDX analyses. The sorption was performed toward uranium (VI) ions for adjustment of sorption performances. The optimum sorption was performed at pH 4 (prior to the precipitation pH). The total sorption was achieved within 25 min (relatively fast kinetics) and was fitted by pseudo-first order rate equation (PFORE) and resistance to intraparticle diffusion equation (RIDE). The maximum sorption capacity was around 1.5 mmol U g−1. The sorption isotherms were fitted by Langmuir and Sips equations. Desorption was achieved using 0.3 M HCl solution and the complete desorption was performed in around 15 min of contact. The sorption desorption cycles are relatively stable during 5 cycles with limit decreasing in sorption and desorption properties (around 3 ± 0.2% and 99.8 ± 0.1%, respectively). The sorbent was used for removal of U from acid leachate solution in mining area. The sorbent showed a highly performance for U(VI) removal, which was considered as a tool material for radionuclides removing from aquatic medium.

Inorganic nitrogen (N) is an important element for eutrophication and harmful algal bloom (HAB) formation. However, the roles of inorganic N in HAB outbreaks are still unclear. Here, we compared the affinities and abilities for inorganic N uptake and assimilation among three typical bloom-forming algae in the East China Sea (ECS), Skeletonema costatum, Prorocentrum donghaiense and Alexandrium pacificum by investigating the uptake and enzymatic (nitrate reductase (NR) and glutamine synthetase (GS) kinetics for nitrate and ammonia. The Ks of nitrate and ammonium in S. costatum was lower than those in P. donghaiense and A. pacificum. The NR activity of S. costatum and P. donghaiense exhibited a positive relationship with the nitrate concentration, and NR activity of S. costatum was nearly 4-fold higher than that of P. donghaiense at high nitrate concentration. However, the NR activity of A. pacificum could not be detected. The GS activity of three species decreased with the increase of ammonium concentrations, and the highest GS activity was detected in A. pacificum. S. costatum presented the highest affinity for nitrate and ammonium, followed by P. donghaiense and A. pacificum. Moreover, P. donghaiense exhibited the highest affinity for intracellular ammonium. Our results characterized the differences in inorganic nitrogen uptake among the three typical bloom-forming algae, which may contribute to the formation of blooms in the coastal waters of the ECS.

Modified chitosan has been widely used for heavy metals removal during the last few decades. In this research, the study was focused on the effect of modified chitosan particles after grafting with heterocyclic constituent for enhancing the sorption of Cr(VI) ions. Chitosan was functionalized by 2-thioxodihydropyrimidine-4,6(1H,5H)-dione, in which the synthesized composite considered as a nanoscale size with average 5–7 nm. This explains the fast kinetics of sorption with large surface area. The prepared sorbent was characterized by Fourier-transform infrared (FTIR), elemental analysis (EA), Brunauer–Emmett–Teller (BET surface area) theory, thermogravimetric analysis (TGA), mass spectroscopy, and scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDX) analyses. The experimental part of this work involved the application of the synthesized sorbent for the removal of Cr(VI) ions from highly contaminated tannery effluents that are characterized by a high concentration toward chromate ions with other associated toxic elements, i.e., Pb(II) and Cd (II) ions, which underscore the importance of this treatment. Under the selected conditions (K2Cr2O7 salt, Co: 100 mg L−1 and pH: 4), the sorption diagram shows high Cr(VI) sorption and fast uptake kinetics. The sorption was enhanced by functionalization to 5.7 mmol Cr g−1 as well as fast uptake kinetics; 30 min is sufficient for total sorption compared with 1.97 mmol Cr g−1 and 60 min for the non-grafted sorbent. The Langmuir and Sips equations were fitted for the sorption isotherms, while the pseudo-first order rate equation (PFORE) was fitted for the uptake kinetics.

This study aims to evaluate the functionalization of chitosan biopolymer with heterocyclic moieties of 2-thioxodihydropyrimidine-4,6(1H,5H)-dione used for enhancing the sorption of Cr ions from aqueous solution. A synthesized sorbent is a nanoscale particle (around 5–7 nm), which explains the fast kinetics of sorption. The sorbent is specified using elemental analysis (EA), FTIR, BET (nitrogen sorption desorption isotherms), TGA, and SEM-EDX analyses. Sorption properties are investigated using ultraviolet emission (UV) but also using visible light (L). In the sorption diagram, the high sorption uptake and fast kinetics observed using ultraviolet conditions are shown. This work is conducted by removing Cr ions from highly contaminated tannery effluents, which have a high concentration of Cr associated with other poisonous elements such as Cd(II) and Pb(II). Under the selected conditions, complete sorption is performed during the first 60 and 45 min with a capacity of 2.05 and 2.5 mmol Cr g−1 for the crosslinked chitosan (without functionalization) in L and UV, respectively. This sorption is enhanced by functionalizing to 5.7 and 6.8 mmol Cr g−1 at the L and UV, respectively, as well as improving the sorption kinetics to 35 and 30 min for both techniques, respectively. The PFORE, and (Langmuir and Sips equations) fit the kinetics and isotherms, respectively.

Yeasts are the most predominant petroleum hydrocarbon-degrading fungi isolated from petroleum-contaminated soil. However, information of the transmembrane transport of petroleum hydrocarbon into yeast cells is limited. The present study was designed to explore the transmembrane transport mechanisms of the typical petroleum hydrocarbon n-hexadecane in Candida tropicalis cells with petroleum hydrocarbon biodegradation potential. Yeast cells were treated with n-hexadecane in different scenarios, and the percentage of intracellular n-hexadecane and transport dynamics were investigated accordingly. The intracellular concentration of n-hexadecane increased within 15 min, and transportation was inhibited by NaN3, an ATPase inhibitor. The uptake kinetics of n-hexadecane were well fitted by the Michaelis-Menten model, and Kt values ranged from 152.49 to 194.93 mg/L. All these findings indicated that n-hexadecane might cross the yeast cells in an energy-dependent manner and exhibit an affinity with the cell transport system. Moreover, the differentially expressed membrane proteins induced by n-hexadecane were identified and quantified by tandem mass tag labeling coupled with liquid chromatography tandem mass spectrometry analysis. The proteome analysis results demonstrated that energy production and conversion accounted for a large proportion of the functional classifications of the differentially expressed proteins, providing further evidence that sufficient energy supply is essential for transmembrane transport. Protein functional analysis also suggested that differentially expressed proteins associated with transmembrane transport processes are clearly enriched in endocytosis and phagosome pathways (p

The synthesis and developments of magnetic chitosan nanoparticles for high efficiency removal of the cadmium ions from aquatic medium are one of the most challenging techniques. Highly adsorptive composite (MCH-ATA) was produced by the reaction of chitosan with formaldehyde and amino thiazole derivative. The sorbent was characterized by FTIR, elemental analyses (EA), SEM-EDX, TEM analysis, TGA and titration (volumetric). The modified material includes high nitrogen and sulfur contents (i.e., 4.64 and 1.35 mmol g−1, respectively), compared to the pristine material (3.5 and 0 mmol g−1, respectively). The sorption was investigated for the removal of Cd(II) ions from synthetic (prepared) solution before being tested towards naturally contaminated groundwater in an industrial area. The functionalized sorbent shows a high loading capacity (1.78 mmol Cd g−1; 200 mg Cd g−1) compared to the pristine material (0.61 mmol Cd g−1; 68.57 mg Cd g−1), while removal of about 98% of Cd with capacity (6.4 mg Cd g−1) from polymetallic contaminated groundwater. The sorbent displays fast sorption kinetics compared to the non-modified composite (MCH); 30 min is sufficient for complete sorption for MCH-ATA, while 60–90 min for the MCH. PFORE fits sorption kinetics for both sorbents, whereas the Langmuir equation fits for MCH and Langmuir and Sips for MCH-ATA for sorption isotherms. The TEM analysis confirms the nano scale size, which limits the diffusion to intraparticle sorption properties. The 0.2 M HCl solution is a successful desorbing agent for the metal ions. The sorbent was applied for the removal of cadmium ions from the contaminated underground water and appears to be a promising process for metal decontamination and water treatment.

Background: The artificial mussel (AM) is a passive sampling device that was originally developed for monitoring metal concentrations in the marine environment, but is also increasingly used in freshwater environments. The AM consists of a non-permeable Perspex tube, which is closed on both sides with a semi-permeable membrane. The space in between contains Chelex-100 beads, which bind metals. The AM allows the determination of the dissolved, bioaccessible metal fraction in water bodies without killing organisms, as well as environments with unfavorable conditions for living bioindicators. In the present study, the use of the AM was adapted for the monitoring of platinum (Pt) in a freshwater ecosystem. Results: The elution of Pt from the Chelex-100 beads was optimized. Two modifications to the original method for the use of AMs are recommended, i.e., washing and separation of the beads through centrifugation and elution with a mixture of 4.5 mL HNO3 and 0.5 mL HCl for approximately 2–3 h to ensure the release of all Pt bound to the beads. Additionally, the uptake kinetics of the AM were determined under laboratory conditions over a wide exposure concentration range (0.1–1000 µg/L) showing highly correlated Pt accumulation in the AMs with the aqueous exposure concentration. For the tested Pt exposure concentrations of 0.1, 1, 10, and 100 µg/L, the Pt concentrations in the AMs increased during the exposure period of 6 weeks. At the highest exposure concentration of 1000 µg/L, the increase stagnated after 3 weeks. To validate the AM in the field, the Pt accumulation of the AM was assessed together with that of freshwater clams (Corbicula fluminalis africana), muscle and liver tissue of the three fish species sharptooth catfish (Clarias gariepinus), common carp (Cyprinus carpio) and Mozambique tilapia (Oreochromis mossambicus), as well as water hyacinths (Eichhornia crassipes) at two sampling sites in the Pt mining area of South Africa. Conclusion: Results from the present study showed that the AM is a promising tool to monitor Pt concentrations in the freshwater environment at contaminated sites. [ABSTRACT FROM AUTHOR]

Abstract Plant sucrose transporters are required for phloem loading, and therefore are essential for plant growth and development. In common beans (Phaseolus vulgaris) there are only two sucrose transporters functionally characterized. Through a previous RNA‐seq study, we identified a putative sucrose transporter in common bean, which we hypothesize to function in import of sucrose into plant cells. In silico analysis revealed that PvSUT1.1 is a putative sucrose‐proton co‐transporter distinct from other characterized sucrose transporters in common bean indicating that this is a previously undescribed transporter protein in beans. Further analysis revealed that PvSUT1.1 shares high protein sequence homology to the phloem loader Arabidopsis SUC2; both have 12 transmembrane domains, a typical characteristic of plant sucrose transporters. Heterologous expression in yeast further showed PvSUT1.1 to be functional and it imported sucrose into yeast cells with a Km of 0.7 mM sucrose. Import of sucrose through PvSUT1.1 is also pH‐dependent with highest uptake at pH 4.0, and activity is lost in the presence of the uncoupler carbonyl cyanide 3‐chlorophenylhydrazone. Consistent with identification of PvSUT1.1 as a Type I transporter, PvSUT1.1 also transports esculin. Finally, PvSUT1.1 showed expression in multiple tissues and the protein was localized to the plasma membrane. The results show that PvSUT1.1 is a sucrose transporter that is probably involved in the uptake of sucrose into source and sink cells. The potential role of PvSUT1.1 in leaf phloem loading of sucrose in common beans and its importance in heat tolerance of reproductive tissues are further discussed.

Three commercial resins bearing sulfonic, amino phosphonic, or phosphonic/sulfonic reactive groups have been tested for the removal of iron and cadmium from phosphoric acid solutions. The sorption properties are compared for different experimental conditions such as sorbent dosage (0.5–2.5 g L−1), phosphoric acid concentration (from bi-component solutions, 0.25–2 M), and metal concentrations (i.e., in the range 0.27–2.7 mmol Cd L−1 and 0.54 mmol Fe L−1) with a special attention paid to the impact of the type of reactive groups held on the resins. The sulfonic-based resin (MTC1600H) is more selective for Cd (against Fe), especially at high phosphoric acid concentration and low sorbent dosage, while MTS9500 (aminophosphonic resin) is more selective for Fe removal (regardless of acid concentration and sorbent dosage). Equilibrium is reached within 2–4 h. The resins can be ranked in terms of cumulative sorption capacities according the series: MTC1600H > MTS9570 > MTS 9500. Sulfuric acid (0.5–1 M) can be efficiently used for the desorption of both iron and cadmium for MTC1600H, while for MTS9570 (phosphonic/sulfonic resin) sulfuric acid correctly desorbs Cd (above 96% at 1 M concentration), contrary to Fe (less than 30%). The aminophosphonic resin shows much poorer efficiency in terms of desorption. The sulfonic resin (i.e., MTC1600H) shows much higher sorption capacity, better selectivity, comparable uptake kinetics (about 2 h equilibrium time), and better metal desorption ability (higher than 98% with 1 M acid concentration, regardless of the type of acid). This conclusion is confirmed by the comparison of removal properties in the treatment of different types of industrial phosphoric acid solutions (crude, and pre-treated H3PO4 solutions). The three resins are inefficient for the treatment of crude phosphoric acid, and activated charcoal pre-treatment (MTC1600H reduced cadmium content by 77%). However, MTC1600H allows removing over 93% of Fe and Cd for H3PO4 pre-treated by TBP solvent extraction, while the others show much lower efficiencies (< 53%). [ABSTRACT FROM AUTHOR]

Plant sucrose transporters are required for phloem loading, and therefore are essential for plant growth and development. In common beans (Phaseolus vulgaris) there are only two sucrose transporters functionally characterized. Through a previous RNA‐seq study, we identified a putative sucrose transporter in common bean, which we hypothesize to function in import of sucrose into plant cells. In silico analysis revealed that PvSUT1.1 is a putative sucrose‐proton co‐transporter distinct from other characterized sucrose transporters in common bean indicating that this is a previously undescribed transporter protein in beans. Further analysis revealed that PvSUT1.1 shares high protein sequence homology to the phloem loader Arabidopsis SUC2; both have 12 transmembrane domains, a typical characteristic of plant sucrose transporters. Heterologous expression in yeast further showed PvSUT1.1 to be functional and it imported sucrose into yeast cells with a Km of 0.7 mM sucrose. Import of sucrose through PvSUT1.1 is also pH‐dependent with highest uptake at pH 4.0, and activity is lost in the presence of the uncoupler carbonyl cyanide 3‐chlorophenylhydrazone. Consistent with identification of PvSUT1.1 as a Type I transporter, PvSUT1.1 also transports esculin. Finally, PvSUT1.1 showed expression in multiple tissues and the protein was localized to the plasma membrane. The results show that PvSUT1.1 is a sucrose transporter that is probably involved in the uptake of sucrose into source and sink cells. The potential role of PvSUT1.1 in leaf phloem loading of sucrose in common beans and its importance in heat tolerance of reproductive tissues are further discussed. [ABSTRACT FROM AUTHOR]

The research work focuses on the application of Cr(VI)-resistant plant growth–promoting bacteria Pannonibacter phragmetitus for enhancing Cr(VI) uptake by Sorghum bicolor. Significant increase in plant shoot and root characters was found when assisted by P. phragmetitus. The obtained strain showed 700 mg/L of chromium reduction at 24-h incubation. Indole-3 acetic acid (IAA) production by the bacterial strain was found to be 86.45 μg/mL. Pannonibacter phragmetitus solubilized tricalcium phosphate showing maximum solubilizing activity of PSI = 3.31. The qmax of P. phragmetitus was high in the wavelength of 600 nm. Langmuir isotherm best described the Cr(VI) ion uptake by the plant. The RL values reliably reduced with expanding Cr(VI) ion concentration from 25 to 150 mg/L. The outcomes of kinetic studies showed that compared with pseudo first-order, pseudo second-order kinetics better describes the plant Cr(VI) uptake rate. Elovich model describes the increased rates for attaining equilibrium. The equilibrium parameter values for different Cr(VI) ion concentrations range between 0 and 1 which describes the favorable condition for plant metal uptake at different concentrations. [ABSTRACT FROM AUTHOR]

Quantifying the relative bioavailability of particles versus ions is a key step toward understanding the mechanisms of bioaccumulation and toxicity of silver nanoparticles (AgNPs). Here we investigated AgNP uptake kinetics by wheat Triticum aestivum L. at different ages (i.e. 15- and 30-day after germination) in hydroponics. The concentration-dependent accumulation of AgNPs under the experimental conditions, in which AgNP dissolution in bulk suspension and at the biological interface was ruled out, confirmed the direct uptake of particles. This was further validated by the detection of Ag-containing particles within plants by single particle inductively coupled plasma mass spectrometry. Plants differentiated particles and dissolved ions, with uptake rate constants of particles and dissolved ions 4.3 ± 0.6 to 5.2 ± 0.6 and 288.6 ± 13.4 to 450.6 ± 63.4 L kg−1 h−1, respectively. Plant age appeared to have a negligible influence on uptake rate constant ratio of particles to ions. As a result, the relative contribution of particulate uptake to overall AgNP accumulation varied as a function of AgNP dissolution in nature. Particulate uptake was dominant when the dissolution was less than 1.2%. These findings help clearing up the inconsistency of uptake mechanisms of AgNPs in literature and could be used to predict their environmental impact and significance. [ABSTRACT FROM AUTHOR]

BACKGROUND: The recovery of metal ions from aqueous solutions for environmental preservation or resource saving requires the development of new sorbents with enhanced separation properties. A new process has been designed for the functionalization of magnetic chitosan microparticles with grafting of either amidoxime (AO‐AHC) or hydrazinyl amine (HZ‐AHC). Their sorption properties have been tested for the recovery of uranium(VI) and zirconium(IV) from aqueous solutions. RESULTS: A wide range of analytical tools is used for characterizing not only the chemical modifications but also the interaction mode between the sorbent and target metal ions; including elemental analysis and titration, Fourier‐transform infrared (FTIR) spectroscopy and X‐ray photoelectron spectroscopy (XPS) characterizations, transmission electron microscopy (TEM) and scanning electron microscopy (SEM) observations, energy‐dispersive X‐ray spectroscopy (EDX) analysis and textural characterization. The optimum pH values were found in the range 4–5. The maximum sorption capacities depend on the metal and the kind of functionalization: up to 1.38 mmol U g−1 for AO‐AHC and up to 1.96 mmol Zr g−1 for HZ‐AHC. The small size of magnetic particles limits the contribution of diffusion mechanisms in the overall control of uptake kinetics and the equilibrium is reached within 40–60 min. Metal desorption is highly effective (almost quantitative over five successive cycles of sorption and desorption) using 0.3 M hydrochloric acid solutions. CONCLUSION: AO‐AHC sorbent is more selective than HZ‐AHC in terms of separation of uranium(VI) from zirconium(IV), especially at pH close to 4. The results obtained in the treatment of acidic ore leachates confirm these trends. © 2019 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

Grafting of quaternary ammonium group is the main goal of this research for uranium recovery. The sorbent was investigated by FTIR, SEM–EDX, elemental analysis, thermogravemetric and XPS analyses, it shows high and fast loading performance (176.49 mg U g−1), the total equilibrium reached within 25 min, fitted by first order rate equation and Sips model for sorption kinetics and isotherms respectively. Complete desorption achieved after 30 min by 1.0 M NaCl in 0.1 M H2SO4. Sorption/desorption was measured after 10 cycles without significant loss in the capacity. Finally, the sorbent applied for uranium recovery of leaching solution from sulfuric acid on gibbsite bearing shale ore materials. [ABSTRACT FROM AUTHOR]

The fate and the accumulation kinetics of mercurychloride (HgCl2) were investigated in the invasive copepod species Pseudodiaptomus marinus, which originates from the North-Western Pacific Ocean and was recently recorded from the Atlantic and Mediterranean coasts. The main objective of this study was to determine lethal concentrations (LC50 %) of HgCl2 in P. marinus and to study its bioaccumulation kinetics in the laboratory. Lethality experiments were performed for 24, 48, 72, and 96 h. Experiments in presence and absence of food source using one sub-lethal concentration of HgCl2 (14.15 μg/L) were carried out to study the uptake, the accumulation and the influence of exposure pathways of HgCl2 in P. marinus. LC50 for 96 h was calculated as 42.4 μg/L in response to HgCl2. The uptake and bioaccumulation kinetics of HgCl2 in P. marinus are not depending on the exposure pathways, where no significant differences were depicted between the uptake/accumulation of HgCl2 from the micro-algal diet and from the seawater medium. Those results could be helpful in the understanding of mercury uptake, bioaccumulation and bio-amplification processes especially concerning invasive copepod species. Article Highlights: LC50 for 96h was calculated as 42.4 μg/L HgCl2. I. galbana uptaked and accumulated Hg more than starved and fed P. marinus. The uptake and the bioaccumulation kinetics of Hg was slow during the 1st and 4th days in starved and fed P. marinus. The uptake and bioaccumulation kinetics of HgCl2 in P. marinus were not depending on the exposure pathway. [ABSTRACT FROM AUTHOR]

• Grafted anion exchangers were synthesized by "grafting from" method with DMAPAA. • Protein binding capacity reached over 360 mg/mL at an ionic capacity of 458 mmol/L. • Very high uptake rate was maintained below 100 mmol/L NaCl. • Dynamic binding capacity kept over 180 mg/mL at flow velocity up to 1350 cm/h. • Dynamic binding capacity kept over 120 mg/mL below 100 mmol/L NaCl. Ion exchangers of high binding capacity and uptake rate are desired for high performance purification of proteins by ion exchange chromatography. For this purpose, we have herein developed a new anion exchanger by grafting N,N - Dimethylaminopropyl acrylamide (DMAPAA) onto Sepharose FF by atom transfer radical polymerization. Six DMAPAA-grafted Sepharose FF resins of the same grafting density but different chain lengths (ionic capacities, ICs) were prepared, and named as FF-pDMAPAA n (n denotes IC value, 65–831 mmol/L). Bovine serum albumin (BSA) adsorption and its chromatography were studied to evaluate the anion exchange resins. It was found that the equilibrium protein adsorption capacity (q m) increased rapidly from 91 mg/mL at IC = 65 mmol/L till reaching a peak value (368 mg/mL) at IC = 458 mmol/L and then decreased slightly with further increasing IC (chain length) to 831 mmol/L. The uptake rate, D e / D 0 , defined as the ratio of effective diffusion coefficient (D e) to free diffusivity of the protein (D 0), also presented similar changes as a function of IC. Namely, D e / D 0 increased from 0.25 to 2.45 in the IC range of 65 to 458 mmol/L, kept almost unchanged from 458 to 573 mmol/L and then decreased slightly with further increase of IC to 831 mmol/L. Therefore, FF-pDMAPAA458 presented the best performance of the six resins for BSA adsorption, possessing very high q m and D e / D 0 values (368 mg/mL and 2.45, respectively). The resin was thus extensively characterized in the effect of ionic strength and column chromatography. The q m and D e / D 0 of FF-pDMAPAA458 were much higher than other anion exchangers reported in literatures and kept over 230 mg/mL and 2.3, respectively, at salt concentrations up to 100 mmol/L. Therefore, the dynamic binding capacity of the FF-pDMAPAA458 column was remarkably higher than Q Sepharose FF and other two typical polymer-grafted anion exchangers reported in literatures in the salt concentration range, and kept as high as 180–220 mg/mL in the superficial flow velocity rang of 150–1350 cm/h. Taken together, the results demonstrated that FF-pDMAPAA resins of appropriate ionic capacities are promising for high-performance protein chromatography. [ABSTRACT FROM AUTHOR]