Nan Zhang

Rice, a staple food for over half of the global population, faces significant threats from environmental stressors such as heavy metal (HMs) contamination, notably cadmium (Cd) and arsenic (As), and increasing drought severity, exacerbated by climate change. These challenges not only compromise rice yield and quality but also pose serious food safety risks due to HM accumulation in grains, endangering human health. Modified biochar (MBC), a carbon-rich material derived from the pyrolysis of organic matter with post-treatment enhancements, has emerged as a strategy to address these dual stressors. MBC application (typically 5–20 t ha⁻¹) reduces Cd and As bioavailability in paddy soils by 40–60% and decreases metal accumulation in rice grains by 20–85% compared to the control. Under drought conditions, MBC improves soil water-holding capacity by 11–45% and enhances crop water use efficiency by 15–24%, leading to yield improvements of 20–50% under moderate water deficit. Furthermore, MBC supports nutrient availability, fosters robust root systems, and enhances soil aeration, collectively improving rice growth under adverse conditions. Beyond its agronomic benefits, MBC provides a framework for addressing multiple challenges by integrating scientific innovation, policy alignment, and community participation. This approach not only reduces heavy metal toxicity and strengthens plant resilience but also enhances food security and advances Sustainable Development Goals (SDGs 2, 3, 4, 12, 13, 15, 17). By promoting environmentally sustainable agriculture and contributing to climate change mitigation, MBC represents a transformative tool for ensuring sustainable rice production in the face of global challenges.

Summary: Arsenic contamination threatens rice ( Oryza sativa ) production, yet the synergistic use of iron plaque (IP) and root‐associated biofilms as a rhizosphere barrier to limit arsenic uptake remains unexplored. To address this, we engineered an arsenic‐resistant (AR) plant growth‐promoting rhizobacterium (AR‐PGPR), Bacillus subtilis p43‐ Taglo1 , expressing the speciation‐inert arsenic‐binding protein TaGlo1. In a contaminated paddy, this strain increased grain yield by 10.7–11.6% and reduced grain arsenic by 28.2–37.4% compared to the wild‐type. The engineered strain robustly colonized roots and enhanced the formation of a functional IP‐biofilm composite, which sequestered more arsenic. This was driven by a 2.87‐fold increase in Fe(II) oxidation and elevated production of extracellular polymeric substances (EPS) (1.4‐fold) and siderophores (1.5‐fold). Transcriptomic analysis revealed that inoculation upregulated bacterial genes for Fe(II) oxidation, siderophore, and EPS biosynthesis, while in rice roots, it activated phytohormone pathways and downregulated arsenite transporters (OsLsi1 and OsLsi2). We conclude that AR‐PGPR can restore beneficial root–microbe interactions under arsenic stress. The IP‐biofilm composite acts as an inducible barrier essential for the dual benefits of arsenic exclusion and growth promotion. Our study shows that AR rhizobacteria fortify the IP‐biofilm composite to reduce arsenic uptake and promote rice growth, providing a route toward safer rice production in arsenic‐affected regions.

The contamination of paddy soils with arsenic (As) and cadmium (Cd), coupled with the depletion of soil organic carbon (SOC), poses significant threats to rice yields and quality. There is an urgent need to identify a suitable soil additive capable of achieving simultaneous heavy metal remediation and promotion of organic matter enrichment. The current study introduced two novel iron (Fe)/magnesium (Mg)-based bimetal-oxide-modified rice straw biochar (RSB), namely RSB-Fe/Mn and RSB-Fe/Mg. It evaluated their effectiveness in As/Cd immobilization and SOC preservation. An 8-week cultivation experiment was carried out in sequential drying–flooding moisture fluctuation conditions, with the soil pore water As/Cd (PWAs/Cd) and SOC fractions monitored. The mechanisms of As/Cd immobilization were investigated using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), and X-ray Photoelectron Spectroscopy (XPS) characterizations. Results revealed that PWAs and PWCd were reduced by up to 67.1% and 80.2% during the drying period and by 27.0% and 76.5% during the flooding period, respectively. Additionally, SOC content increased by 16.3% and 33.9% with RSB-Fe/Mn addition during the drying and flooding period, respectively, with an increase in the mineral-associated organic carbon (MAOC) fraction. The study proves that RSB-Fe/Mn and RSB-Fe/Mg are effective for soil As/Cd passivation and SOC stabilization, offering a promising solution to mitigate As and Cd pollution in paddy soils while maintaining soil quality.

A better understanding of the P dynamic resupply roles of fertilization from soil solids to solution is urgently required to optimize sustainable P fertilizer management practices for efficient supply. A five–year fertilization experiment was used to investigate the effects on soil P fractions and availability, the kinetic P resupply based on a novel simulation technique (Diffusive gradients in thin films (DGT) and DGT–induced fluxes in sediments and soils (DIFS) ) and to identify dominant factors during the maize season under five treatments (no fertilizer (CK), chemical fertilizer (NPK), chemical fertilizer combined with bone meal fertilizer (NPKC), crop straw (NPKS) and bioorganic fertilizer (NPKM)). The results showed that the NPKC and NPKM treatments had higher enhancement effects on Olsen–P and organic P and inorganic Ca₂–P, Ca₈–P, Al–P and Fe–P at maize growth stages, and they buffered pH decrease to delay the substantial Fe–P and Al–P release until a late stage. Inorganic Ca₂–P, Ca₈–P, Al–P and Fe–P heavily effected the Olsen–P levels. The NPKS, NPKC and NPKM treatments yielded higher C_DGT–P levels and a stronger resupply capacity, reflected by higher R and C_E/C_soln and smaller T_c values. The simulation and path model results revealed that the maize plant P uptake was determined by soil P resupply and an inorganic P supply pool. They were positively dominated by soil organic matter (SOM). Our results suggested that organic fertilization, especially NPKC and NPKM treatments, provided greater enhancement effects on the P supply pool and P resupply for higher plant P uptake, identifying them as highly effective P management practices for developing sustainable agriculture.

In this study, a newly synthesized sepiolite-supported nanoscale zero-valent iron (S-nZVI) adsorbent was tested for the efficient removal of As(III) and As(V) in aqueous solution. Compared with ZVI nanoparticles, the As(III) and As(V) adsorption abilities of S-nZVI were substantially enhanced to 165.86 mg/g and 95.76 mg/g, respectively, owing to the good dispersion of nZVI on sepiolite. The results showed that the adsorption kinetics were well fitted with the pseudo-second-order model, and the adsorption isotherms were fitted with the Freundlich model, denoting a multilayer chemical adsorption process. The increase in the initial solution pH of the solution inhibited As(III) and As(V) adsorption, but a weaker influence on As(III) than As(V) adsorption was observed with increasing pH. Additionally, the presence of SO₄²⁻ and NO₃⁻ ions had no pronounced effect on As(III) and As(V) removal, while PO₄³⁻ and humic acid (HA) significantly restrained the As(III) and As(V) adsorption ability, and Mg²⁺/Ca²⁺ promoted the As(V) adsorption efficiency. Spectral analysis showed that As(III) and As(V) formed inner-sphere complexes on S-nZVI. As(III) oxidation and As(V) reduction occurred with the adsorption process on S-nZVI. Overall, the study demonstrated a potential adsorbent, S-nZVI, for the efficient removal of As(III) and As(V) from contaminated water.

Cobalt Hexacyanoferrate (CoHCF) was tested for the selective uptake of K from seawater and the electrochemical method was adopted for the desorption and regeneration of the material. Powder form CoHCF could adsorb about 6.5 mmol/g of K from the seawater. For the ease of the electrochemical desorption and regeneration, CoHCF thin film was coated onto the Indium Tin Oxide (ITO) glass to obtain a CoHCF electrode. K adsorption kinetics on CoHCF thin film was found to be well fitted with the intraparticle diffusion model, which was a two-step process. Five consecutive adsorption-desorption-regeneration cycles were carried out to know the gradual decrease in the adsorption capacity owing to changes in the redox states of two metals, Co and Fe, in the material. Fourier Transform Infrared Spectroscopy (FT-IR) and Ultraviolet-Visible (UV-Vis) measurement results corresponded to the color change of CoHCF thin film, indicating the valence change of transition metals and the exchange of alkali metal cations happened on the CoHCF at different operation stages. In order to elucidate the reaction mechanism, composition of the material was analysis in the following steps: adsorption, desorption, and regeneration. It was proved that the system based on CoHCF thin film modified electrode had the potential of recovering potassium from seawater.