n-Type doping of BiVO4 with different F-doped concentrations for improving the electronic character of BiVO4 as a photoanode nanomaterial for solar water splitting: a first-principles study.

Atom doping has been realized as an effective way to improve the photocatalytic performance of the most promising photoanode material, BiVO4, but the effects of doping mass concentration still need to be explored. In this work, the effects of F-doping with different doping mass concentrations (1%, 2%, 5%, 10%, 15%, and 20%) on the electronic character of BiVO4 were examined theoretically using density functional theory (DFT) calculations. The thermal stability of BiVO4 with different F-doped mass concentrations was confirmed using formation energy (Ef) calculations though F-doped BiVO4 becomes harder as the mass concentration of induced dopants increases. n-Type doping effects on the electronic character of BiVO4 were observed upon F-doping, leading to the energy level of CBM shifting far away from the Fermi level and giving F-doped BiVO4 metallic character. Moreover, a linear relationship between the frontier energy level shifts and the total charge transfer amounts from doped F atoms to other atoms involved in F-doped BiVO4 was observed, which means the oxidizing capacity of the VBM is increased and the reducing capacity of the CBM is decreased upon increased F-doped mass concentration. Moreover, the recombination of photogenerated electron-hole pairs is suppressed by F-doping strategies, which will not change a lot with the increased F-doped mass concentration. This means atom doping is an effective strategy to improve the photocatalytic efficiency of the BiVO4, but the number of atoms introduced into BiVO4 should be appropriate.

Molecular modification effects on the electrochromic and photochromic properties of diarylethene with intramolecular isomerization behavior.

Diarylethene (DAE) is one of the most widely used functional units for electrochromic or photochromic materials. To better understand the molecular modification effects on the electrochromic and photochromic properties of DAE, two modification strategies, substitution with functional groups or heteroatoms, were investigated theoretically by density functional theory calculations. It is found that red-shifted absorption spectra caused by a decreased highest occupied molecular orbital-lowest unoccupied molecular orbital energy gap and S0 → S1 transition energy during the ring-closing reaction become more significant by adding different functional substituents. In addition, for two isomers, the energy gap and S0 → S1 transition energy decreased by heteroatom substitution of S atoms with O or NH, while they increased by replacing two S atoms with CH2. For intramolecular isomerization, one-electron excitation is the most effective way to trigger the closed-ring (O → C) reaction, while the open-ring (C → O) reaction occurs most readily in the presence of one-electron reduction. Moreover, it is confirmed that substitution with strong electron donating groups (-OCH3/-NH2) or with one O/two CH2 heteroatoms leads to a more favorable closed-ring (O → C) reaction. Functionalized with strong electron-withdrawing groups (-NO2 and -COOH) or one/two NH heteroatom substitutions, the open-ring (C → O) reaction is easier. Our results confirmed that the photochromic and electrochromic properties of DAE can be tuned effectively by molecular modifications, which provides theoretical guidance for the design of new DAE-based photochromic/electrochromic materials.

Application of ferromanganese functionalized biochar simultaneously reduces Cd and Pb uptake of wheat in contaminated alkaline soils.

The reduction of Cd and Pb accumulation in wheat grains grown on Cd and Pb contaminated alkaline soils is a pressing issue that needs to be solved. In this study, ferromanganese functionalized biochar (FM-BC) was used to remediate Cd and Pb contaminated alkaline soils and mitigate Cd and Pb accumulation in wheat grains. The immobilization capacity and mechanism of FM-BC were investigated by Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) characterization and chemical analysis. Fe and Mn loaded on FM-BC improved the removal efficiencies of DTPA-Cd and DTPA-Pb in soil with DTPA-Cd removal of 22.99%- 52.04% (JM22) and 25.54%- 53.32 (AK58) and DTPA-Pb removal of 11.39%- 22.36% (JM22) and 5.38%- 13.00% (AK58). The FT-IR and XRD results indicated that the complexation and precipitation of Cd and Pb with the Fe-Mn oxides and the oxygen-containing functional groups on biochar surface stabilized the Cd and Pb in soil for the observation of Cd2Mn3O8, PbHPO4, CdCO3, and PbO2 on FM-BC isolated from contaminated soils. FM-BC with excellent adsorption capacity reduced the available Cd and Pb in the soil, therefore, thereby inhibiting the Cd and Pb accumulation in wheat. In the 3% FM-BC treatment, Cd and Pb contents in wheat grains were lower than 0.10 mg/kg and 0.20 mg/kg, respectively, reaching the national safety standards. And FM-BC increased the Fe, Mn, Na and Zn contents in wheat grains, and improved the growth and yield of wheat. These findings suggest that FM-BC can be considered a prospective and effective material for remediation of alkaline soils contaminated with Cd and Pb.

Mercapto-palygorskite efficiently immobilizes cadmium in alkaline soil and reduces its accumulation in wheat plants: A field study.

Cadmium (Cd) contamination in wheat fields has become a major environmental issue in many regions of the world. Mercapto-palygorskite (MPAL) is a high-performance amendment that can effectively immobilize Cd in alkaline wheat soil. However, MAPL as an in-situ Cd immobilization strategy for alkaline wheat soil remains to be evaluated on a field-scale and the underlying mechanisms requires further evaluation. Here, MPAL were used as soil amendment to evaluate their immobilization efficiency on Cd-contaminated alkaline soil in the field experiments. The field experiments showed that MPAL application significantly reduced wheat grain Cd concentration from 0.183 mg/kg to 0.056 mg/kg, with Cd concentration in wheat grain treated with MPAL all falling below the limit value of 0.1 mg/kg as defined in China's food safety standard (GB 2762-2022). The maximal immobilization efficiency of MPAL on soil Cd figured out by diethylenetriaminepentaacetic acid (DTPA) extraction was 61.5%. The mechanisms involved in Cd immobilization by MPAL were mainly related to the enhanced sorption of Cd onto Fe oxides, and the removal of amorphous or free Fe oxides from soil had a substantial impact on Cd immobilization efficiency by MPAL. Furthermore, the antagonistic effect between Mn and Cd uptake may also contribute to the reduction of wheat Cd accumulation after MPAL application. The current research can provide theoretical and technical support for the large-scale application of MPAL in Cd-contaminated wheat fields.

Electronic structure evolution induced by the charge redistribution during the construction of two-dimensional polymer networks from monomers to crystal frameworks.

Two-dimensional covalent organic frameworks (COFs) are a new type of porous crystalline material constructed by the linkage of organic building units through covalent bonds to produce predetermined structures. Here, the electronic structure evolution induced by the charge redistribution during the construction of two-dimensional polymer networks (sp2c-COF-2 and COF-66) from building units to crystal frameworks is examined theoretically. The calculated results demonstrate that the electronic structure of the framework is controlled by the relative energy level between the frontier orbitals of organic building core and linker units as well as the charge transfer amount between them during the construction of the framework. Moreover, it is observed that a noncoplanar framework becomes more conjugated because the charge transfer amount between core and linker units becomes larger during the construction of 2D frameworks, which leads to a larger charge carrier mobility within the 2D structure of COFs. The charge carrier mobility along the z-direction of the COF crystal is dominated by the interface interaction between COF layers. Thereby, we believed reasonable design or selection of organic building units plays a key role in improving the electronic and optoelectronic properties of such 2D organic frameworks.

Removal mechanisms of Cd from water and soil using Fe-Mn oxides modified biochar.

The development of remediation materials simultaneously suitable for Cd-contaminated water and soil is of great significance. In this study, the functional biochar (FM-RBC and FM-DBC) was prepared using branch and durian shell biochar (RBC and DBC, respectively) with iron-manganese oxide (Fe-Mn oxide) modification. The behaviors and mechanisms of Cd adsorption and stabilization in water and alkaline soil treated with FM-RBC and FM-DBC were explored. The results showed that the adsorption capacities of RBC and DBC for Cd had increased by 40-80 mg/g after the Fe-Mn oxide modification. The Cd adsorption was conformed to pseudo-second-order kinetic and the Langmuir isothermal models. After 35 days of soil cultivation, the maximum reduction rate of DTPA-Cd occurred in 3% FM-DBC treatments (37.73%), followed by in 3% FM-RBC (30.08%), all of which were significantly higher than that observed in 3% BC treatments (12.55-18.91%). Notably, the FM-RBC and FM-DBC treatments promoted the conversion of the exchangeable to the carbonate-bound and Fe/Mn oxyhydroxide fractions of Cd. The XRD, FTIR, and XPS analyses demonstrated that the loading amount of Fe-Mn oxide was positively correlated with the oxygen-containing functional group of biochar. CdO, Cd2Mn3O8 and CdCO3 were loaded on the FM-BC, indicating the existence of two main adsorption mechanisms: (1) the complexation with M-O (M: Fe, Mn) and acid oxygen-containing functional groups, (2) the precipitation with carbonate of Cd. In this work, we prepared two functional biochar that rapidly removes Cd from water and effectively fixes Cd in alkaline soil, thus, debasing the risk of Cd entry into the food chain.

Phosphate fertilizers facilitated the Cd contaminated soil remediation by sepiolite: Cd mobilization, plant toxicity, and soil microbial community.

In-situ immobilization does not remove Cd from the contaminated soil. It is vital to investigate the effects of fertilizers on soil Cd mobility during remediation with amendments. In the current study, a pot experiment was conducted to investigate the effects of calcium magnesium phosphate (CMP) and calcium superphosphate (SSP) on the remediation of Cd-contaminated soil by sepiolite. We mainly focused on changes in soil Cd immobilization, plant toxicity, and soil microbial communities after applying two phosphates during Cd-contaminated soil remediation by sepiolite. The results demonstrated that sepiolite decreased Cd concentration in brown rice, straw, and roots by 32.66%, 38.89%, and 30.94%, respectively. During soil remediation by sepiolite, the Cd concentrations of brown rice and straw were not affected by CMP or SSP, except for the treatment with sepiolite plus high-dose CMP. Sepiolite significantly decreased HCl-extractable Cd and DTPA-extractable Cd by 32.21% and 10.50%, respectively. During soil remediation by sepiolite, the HCl-extractable and DTPA-extractable Cd further decreased with CMP or SSP. The decreasing amplitude with CMP was 40.57-72.60% and 7.05-14.53%, and that of SSP was 37.68-59.66% and 20.71-25.07%, respectively. The superoxide dismutase, peroxidase, catalase activities, and malondialdehyde concentration in rice roots decreased inordinately with the addition of sepiolite, CMP, and SSP, indicating that the application of sepiolite, CMP, or SSP alleviated Cd-induced rice root stress and protected rice roots from Cd toxicity. Alpha diversity estimators (including the Chao, ACE, and Shannon indices) indicated that sepiolite, CMP, or SSP applications had no adverse effects on soil bacterial richness and diversity. Hierarchical clustering analysis revealed that the two phosphate fertilizers and sepiolite were the main factors affecting changes in the bacterial communities structure. Redundancy analysis revealed that soil pH, Eh, and soil-extractable Cd were critical factors affecting the structure of the bacterial communities.

Adsorption performance and mechanism of Ca-Al-LDHs prepared by oyster shell and pop can for phosphate from aqueous solutions.

The anion exchange properties of layered composite metal hydroxide (LDHs) make it a significant anion purification material in aquatic environment. Ca-Al-LDHs as a calcium-based adsorbent can significantly improve the removal rate of phosphate. In this manuscript, waste oyster shell was used as the source of calcium and waste cans as the source of aluminum, and compared with the LDHs prepared by chemical reagents. The optimal molar ratio of for both the types of materials prepared from waste material as well as reagents was found to be 4:1 for best adsorption performance, with the waste group and reagent group materials showing similar adsorption capacities of 127.50 mg g-1 and 126.67 mg g-1, respectively. The effects of adsorbent dosage, initial solution pH and presence of coexisting ions on the adsorption capacity were investigated. Langmuir adsorption isotherm, quasi-second-order kinetic equation and mass transfer kinetics was found to describe the phosphorus adsorption process of CAs-4 and CA-4 in better way. The maximum adsorption capacities of Langmuir equation for CAs-4 and CA-4 adsorption process were 126.41 mg g-1 and 127.43 mg g-1, respectively, for CAs-4 and CA-4. The characterization results of FTIR, XRD and ICP showed that the main adsorption mechanisms were intercalation anion exchange, electrostatic attraction and dissolution precipitation. This work not only provides a method to prepare Ca-Al-LDHs for efficient utilization of solid waste, but also provides theoretical significance for controlling water eutrophication and realize waste recycling.

In-situ stabilization of Cd by sepiolite co-applied with organic amendments in contaminated soils.

Field experiments was conducted to evaluate the effectiveness of sepiolite (S), sepiolite + fungi residues (SFR) and sepiolite + vermicompost (SVC) on in situ immobilization remediation of Cd contaminated soils. The results showed that treatments of S, SFR and SVC decreased soil Cd availability by 15.2-47.8%, 17.5-44.9% and 13.2-44.9%, respectively, when compared with the control groups. Moreover, the content of Cd in edible parts of Lactuca sativa L., Cichorium endivia L. and Brassica campestris L. was experienced a decrease of 15.9-41.9%, 1.6-38.0% and 29.0-37.4% reduction, respectively, under the amended soil. The improvement of soil fertility was obtained under addition of SVC and SFR, while the amounts of available P, K, organic matter, microbial carbon, microbial nitrogen and dehydrogenase activity were increased by 9.6-68.2%, 1.2-28.3%, 37.5-70.5%, 4.1-121.0%, 220-640% and 6.8-56.8%, respectively, in contrast to CK. Moreover, high-throughput sequencing analysis showed that the combined treated soils got higher values of alpha diversity indices, Chao1, ACE and Shannon. The number of dominant phyla (Proteobacteria, Acidobacteria, Gemmatimonadetes, Crenarchaeota) and genera (Aquicella, Lysobacter, Candidatus Nitrososphaera, Sphingopyxis, Mesorhizobium) were enhanced. Therefore, the use of sepiolite and organic amendments could be an adequate strategy to immobilization remediation of Cd-contaminated soils.

Comparative effects of Tagetes patula L. extraction, mercapto-palygorskite immobilisation, and the combination thereof on Cd accumulation by wheat in Cd-contaminated soil.

Phytoextraction and in situ immobilisation are two of the most commonly used remediation techniques for Cd-contaminated farmland. In theory, phytoextraction followed by immobilisation can reduce the total Cd and available Cd contents of the soil, making it suitable for the remediation of heavily Cd-contaminated alkaline soil. However, the real remediation efficiency is uncertain, and it is also unknown whether phytoextraction affects subsequent wheat Cd accumulation. In this study, two seasonal pot experiments were conducted to determine the effects of S,S-ethylenediamine disuccinic acid (EDDS)-assisted Tagetes patula L. (T. patula) extraction, mercapto-palygorskite (MPAL) immobilisation, and the combination thereof on subsequent Cd accumulation in wheat. EDDS application significantly increased the Cd content in the subsequent-soil solution, but the EDDS-activated Cd could not be absorbed by wheat roots. T. patula extraction decreased the subsequent soil pH value by 0.1-0.2 pH units, increased the available Cd content by 0.19 mg/kg, but had no effect on subsequent wheat Cd accumulation. The Cd absorption capacity of wheat roots and the Cd translocation capacity of wheat stems to grains of high-Cd wheat were higher than that of low-Cd wheat cultivar. The application of MPAL had no effect on soil pH value, but significantly decreased soil available Cd and exchangeable Cd contents by 17.78-36.76% and 21.13-52.63%; it also increased the Fe/Mn oxide-bound Cd fraction by 14.02-64.00%. MPAL application decreased the wheat grain Cd concentrations from 0.51 to 0.13 mg/kg (high-Cd wheat) and 0.35 to 0.05 mg/kg (low-Cd wheat), but had no negative effect on Fe, Mn, Cu, and Zn elements. Compared with the single MPAL application treatments, the combination treatments had no inhibition effect on Cd accumulation in wheat. MPAL is an efficient amendment, and considering the remediation efficiency, stability, and time of these methods, the combination of MPAL application with a low-Cd accumulation wheat cultivar represents a suitable proposal to ensure the safe production of wheat in Cd-contaminated alkaline soil.

Pivotal role for root cell wall polysaccharides in cultivar-dependent cadmium accumulation in Brassica chinensis L.

Polysaccharides are the main components of plant cell walls in which they make an important contribution to cadmium (Cd) fixation. However, knowledge regarding the role of root cell wall polysaccharides in Cd accumulation in low-Cd cultivars is limited. Here, we compared the differences in root cell wall polysaccharides between two cultivars of Brassica chinensis L. (pakchoi) with different Cd accumulation abilities. A hydroponic experiment was conducted using low- (Huajun 2) and high-Cd (Hanlv) pakchoi cultivars. We investigated Cd subcellular distribution and Cd accumulation in cell wall polysaccharides and examined polysaccharide modifications in root cell walls by Fourier transform infrared spectroscopy. A Cd adsorption kinetics experiment was conducted to examine the connection between Cd-induced polysaccharide modifications and Cd fixation by cell walls. Amounts of Cd were significantly higher and more Cd was bound to cell walls in the roots of Huajun 2 than in those of Hanlv. These results indicated that the greater Cd retention capacity of the root cell wall in Huajun 2 accounted for the low Cd accumulation in the shoot. Up to 79.4% and 32.1% of cell-wall-bound Cd was found in the pectin and hemicellulose 1, respectively, and higher amounts of Cd were found in these cell wall components of Huajun 2 than in those of Hanlv. Exposure to Cd significantly increased amounts of pectin and hemicellulose 1 in both pakchoi cultivars, but the pectin levels were significantly higher in Huajun 2 than in Hanlv. Huajun 2 had higher pectin methylesterase (PME) activity and a lower degree of pectin methyl-esterification (DM) than Hanlv, although Cd treatments resulted in increased PME activity and decreased DM in both cultivars. The higher Cd treatment (44.5 µM) resulted in enhanced Cd-binding capacity in root cell walls of the two cultivars with higher Cd adsorption levels in the root cell wall of Huajun 2. These results indicate that differences in the amount of cell wall polysaccharide and DM play key roles in establishing the genotypic differences underlying Cd accumulation in pakchoi. These findings conduce to a better understanding of the physiological mechanisms underlying low Cd accumulation in pakchoi and the breeding of new, low-Cd pakchoi cultivars.

Diastereoselective Total Synthesis of (±)-Basiliolide B and (±)-epi-8-Basiliolide B.

The C8 and C9 stereogenic centers of the basiliolide/transtaganolide family have been established stereoselectively using a cyclopropane ring-opening strategy, which has been studied by DFT calculations of a variety of lithium-chelating models. The highly functionalized intermediates obtained in this strategy were successfully employed for the diastereoselective total synthesis of (±)-basiliolide B and (±)-epi-8-basiliolide B. The decalin core with a lactone bridge was constructed via a 2-pyrone Diels-Alder (DA) cycloaddition, and the unprecedented seven-membered acyl ketene acetal was established by a biomimetic intramolecular O-acylation cyclization.

Joint Prior Learning for Visual Sensor Network Noisy Image Super-Resolution.

The visual sensor network (VSN), a new type of wireless sensor network composed of low-cost wireless camera nodes, is being applied for numerous complex visual analyses in wild environments, such as visual surveillance, object recognition, etc. However, the captured images/videos are often low resolution with noise. Such visual data cannot be directly delivered to the advanced visual analysis. In this paper, we propose a joint-prior image super-resolution (JPISR) method using expectation maximization (EM) algorithm to improve VSN image quality. Unlike conventional methods that only focus on upscaling images, JPISR alternatively solves upscaling mapping and denoising in the E-step and M-step. To meet the requirement of the M-step, we introduce a novel non-local group-sparsity image filtering method to learn the explicit prior and induce the geometric duality between images to learn the implicit prior. The EM algorithm inherently combines the explicit prior and implicit prior by joint learning. Moreover, JPISR does not rely on large external datasets for training, which is much more practical in a VSN. Extensive experiments show that JPISR outperforms five state-of-the-art methods in terms of both PSNR, SSIM and visual perception.

Evaluation of the effectiveness of sepiolite, bentonite, and phosphate amendments on the stabilization remediation of cadmium-contaminated soils.

A pot trial was conducted to assess the effectiveness of sepiolite, bentonite, and phosphate on the immobilization remediation of cadmium (Cd)-contaminated soils using a set of variables, namely, physiological traits, sequential extraction procedure, plant growth and Cd concentration, and soil enzymatic activities and microbial population. Results showed that superoxide dismutase and peroxidase activities in the leaves of Oryza sativa L. and catalase activities in soils were stimulated after applying the amendments. However, soluble protein contents in leaves and urease and invertase activities in soils were reduced from 7.1% to 31.7%, 1.0%-23.3%, and 21.1%-62.5%, respectively, compared with the control. Results of the sequence extraction procedures revealed that the exchangeable fraction of Cd in soils was mostly converted into carbonated-associated forms. The water soluble plus exchangeable fraction (SE) of Cd in soil decreased when treated with single and compound materials of sepiolite, bentonite and phosphate, which resulted in 13.2%-69.2% reduction compared with that of CK (control test). The amendments led to decreased Cd concentrations in roots, stems, leaves, brown rice, and rice hull by 16.2%-54.5%, 16.6%-42.8%, 19.6%-59.6%, 5.0%-68.2%, and 6.2%-20.4%, respectively. Higher bacterial and actinomycete amount indicated that remediation measures improved soil environmental quality. Composite amendments could be more efficiently used for the stabilization remediation of Cd contaminated soils with low Cd uptake and translocation in the plants and available contents of Cd in soil.

Generic Learning-Based Ensemble Framework for Small Sample Size Face Recognition in Multi-Camera Networks.

Multi-camera networks have gained great interest in video-based surveillance systems for security monitoring, access control, etc. Person re-identification is an essential and challenging task in multi-camera networks, which aims to determine if a given individual has already appeared over the camera network. Individual recognition often uses faces as a trial and requires a large number of samples during the training phrase. This is difficult to fulfill due to the limitation of the camera hardware system and the unconstrained image capturing conditions. Conventional face recognition algorithms often encounter the "small sample size" (SSS) problem arising from the small number of training samples compared to the high dimensionality of the sample space. To overcome this problem, interest in the combination of multiple base classifiers has sparked research efforts in ensemble methods. However, existing ensemble methods still open two questions: (1) how to define diverse base classifiers from the small data; (2) how to avoid the diversity/accuracy dilemma occurring during ensemble. To address these problems, this paper proposes a novel generic learning-based ensemble framework, which augments the small data by generating new samples based on a generic distribution and introduces a tailored 0-1 knapsack algorithm to alleviate the diversity/accuracy dilemma. More diverse base classifiers can be generated from the expanded face space, and more appropriate base classifiers are selected for ensemble. Extensive experimental results on four benchmarks demonstrate the higher ability of our system to cope with the SSS problem compared to the state-of-the-art system.

A biomimetic synthesis of (±)-basiliolide B.

A highly diastereoselective and practical biomimetic total synthesis of (±)-basiliolide B has been achieved through the study of the two proposed biosynthetic pathways (O-methylation and O-acylation) for the unprecedented 7-methoxy-4,5-dihydro-3H-oxepin-2-one (C ring). The synthesis featured a cyclopropanation/ring opening strategy for establishing the stereogenic centers at C8 and C9, a biomimetic 2-pyrone Diels-Alder cycloaddition for the synthesis of the ABD ring system, and finally a highly efficient biomimetic intramolecular O-acylation for the C ring formation. This result provides an important perspective on the biosynthetic origin of the unprecedented 7-membered acyl ketene acetal moiety of the C ring.

Influence of Foliar Zinc Application on Cadmium and Zinc Bioaccessibility in Brassica chinensis L.: In Vitro Digestion and Chemical Sequential Extraction.

Foliar zinc (Zn) application can affect the accumulation and bioaccessibility of cadmium (Cd) and Zn in crops. However, the mechanisms by which foliar Zn application influences Cd and Zn bioaccessibility remain elusive. This study examined the effects of spraying ZnSO4 and ZnNa2EDTA on bioaccessibility and chemical forms of Cd and Zn in pakchoi (Brassica chinensis L.) shoots and evaluated human health risks via pakchoi consumption. Spraying ZnSO4 reduced the concentrations of ethanol-extractable (Fethanol) and deionized water-extractable (Fd-H2O) Cd, as well as the corresponding bioaccessible Cd concentrations (20.3-66.4%) and attendant health risks of Cd, whereas spraying high-dose ZnNa2EDTA significantly increased the concentrations of both Cd forms and bioaccessible Cd. Spraying ZnSO4 and high-dose ZnNa2EDTA significantly increased the concentrations of Zn in Fethanol and Fd-H2O and the corresponding bioaccessible Zn concentrations (0.8-8.3-fold). Fethanol and Fd-H2O were the primary sources of bioaccessible Cd and Zn, contributing more than 59% of the bioaccessible Cd and Zn. These results indicate that foliar Zn application can affect Cd and Zn bioaccessibility in pakchoi mainly by modulating Cd and Zn in Fethanol and Fd-H2O. These findings provide scientific support for the development of more efficient measures to produce safe and high-quality leafy vegetables from Cd-polluted soils.

Transcriptome and ultrastructural analysis revealed the mechanism of Mercapto-palygorskite on reducing Cd content in wheat.

Large areas of crop yields in northern China have faced with cadmium (Cd) contamination problems. Mercapto-modified palygorskite (MP), as a highly efficient immobilization material, could reduce Cd absorption in wheat and alleviate its biotoxicity. However, the molecular mechanism underlying MP-mediated Cd reduction and detoxification processes in wheat is not well understood. This aim of this study was to investigate the biochemical and molecular mechanisms underlying the reduction in Cd accumulation in wheat (Triticum aestivum L.). The results showed that MP application decreased the Cd concentration by 68.91-74.32% (root) and 70.68-77.2% (shoot), and significantly increased the glutathione (GSH) and phytochelatins (PCs) contents in root and shoot. In addition, with the application of MP, the percentage of Cd in the cell walls and organelles of wheat decreased, while that of Cd in soluble components was increased. The content of Cd in all components was significantly reduced. Ultrastructural analysis revealed that MP thickened the cell wall, promoted vesicle formation in the membrane and protected the integrity of intracellular organelles in wheat. Transcriptome analysis further confirmed the above results. MP upregulated the expression of several genes (CCR, CAD COMT and SUS) involved in cell wall component biosynthesis and promoted vesicle formation on cell membranes by upregulating the expression of PLC and IPMK genes. In addition, genes related to antioxidant synthesis (PGD, glnA and GSS) and photosynthesis (Lhca, Lhcb) were altered by MP to alleviate Cd toxicity in wheat. This present work will help to more thoroughly elucidate the molecular mechanism by which wheat defends against Cd contamination under MP application and provide and important research basis for the application of this material in the future.

Variations in Cadmium and Lead Bioaccessibility in Wheat Cultivars and Their Correlations with Nutrient Components.

To reduce the health risks of exposure to Cd and Pb in wheat, a field experiment was conducted to investigate the differences in Cd and Pb bioaccessibility among the grains of 11 wheat cultivars and their relationships with the nutrient compositions of grains. The grain concentrations (Cd: 0.14-0.56 mg kg-1, Pb: 0.08-0.39 mg kg-1) and bioaccessibility (5.28-57.43% and 0.72-7.72% for Cd and Pb in the intestinal phase, respectively) of Cd and Pb differed significantly among the 11 cultivars. A safe wheat cultivar (Shannong16) with a relatively low health risk and the lowest grain Cd and Pb concentrations was selected. Ca, Mg, phytate, and methionine played key roles in affecting Cd and Pb bioaccessibility in wheat, with Ca and phytate significantly negatively correlated with Cd and Pb bioaccessibility. These findings can be used to optimize the selection strategy for safe wheat cultivars for healthy grain production in Cd-polluted farmland.

The role and transcriptomic mechanism of cell wall in the mutual antagonized effects between selenium nanoparticles and cadmium in wheat.

Selenium nanoparticles (SeNPs) has been reported as a beneficial role in alleviating cadmium (Cd) toxicity in plant. However, underlying molecular mechanisms about SeNPs reducing Cd accumulation and alleviating Cd toxicity in wheat are not well understood. A hydroponic culture was performed to evaluate Cd and Se accumulation, cell wall components, oxidative stress and antioxidative system, and transcriptomic response of wheat seedlings after SeNPs addition under Cd stress. Results showed that SeNPs application notably reduced Cd concentration in root and in shoot by 56.9% and 37.3%, respectively. Additionally, SeNPs prompted Cd distribution in root cell wall by 54.7%, and increased lignin, pectin and hemicellulose contents by regulating cell wall biosynthesis and metabolism-related genes. Further, SeNPs alleviated oxidative stress caused by Cd in wheat through signal transduction pathways. We also observed that Cd addition reduced Se accumulation by downregulating the expression level of aquaporin 7. These results indicated that SeNPs alleviated Cd toxicity and reduced Cd accumulation in wheat, which were associated with the synergetic regulation of cell wall biosynthesis pathway, uptake transporters, and antioxidative system via signaling pathways.