Arsenic contamination poses a significant threat to agricultural productivity and food security, especially in Cicer arietinum L. (chickpea). This study evaluates the potential of silicon nanoparticles (SiNPs) to mitigate arsenic stress in C. arietinum (Noor 2022). The experiment was conducted at The Islamia University of Bahawalpur using a randomized complete block design (RCBD) with a factorial arrangement and three replications. A pot experiment was conducted using seven treatments comprising various concentrations of SiNPs applied alone or combined with arsenic [T0 (control, no SiNPs), T1 (3.5% SiNPs), T2 (7% SiNPs), T3 (10.5% SiNPs), T4 (3.5% SiNPs + 30 ppm Ar), T5 (7% SiNPs + 30 ppm Ar), and T6 (10.5% SiNPs + 30 ppm Ar)]. SiNPs were applied as foliar sprays in three splits from the second to fourth weeks after sowing. Morphological, physiological, and biochemical parameters were assessed, including chlorophyll content, total soluble proteins, proline, and antioxidant enzyme activities. The results demonstrated that SiNPs significantly enhanced stress tolerance in chickpea plants. At 10.5% SiNPs, chlorophyll content increased by 35%, carotenoids by 42%, and proline by 68% compared to arsenic-stressed plants without SiNPs, indicating improved photosynthetic efficiency and osmotic adjustment. Antioxidant enzyme activities, including peroxidase (POD), superoxide dismutase (SOD), and ascorbate peroxidase (APX), increased by 50%, 47%, and 53%, respectively, mitigating oxidative damage. Soluble sugars and phenolic content also rose by 28% and 32%, respectively, under 10.5% SiNPs. However, when combined with arsenic, some antagonistic effects were observed, with a slight decrease in chlorophyll and antioxidant activity compared to SiNPs alone. These findings suggest that SiNPs are a promising tool for improving crop resilience in arsenic-contaminated soils, offering insights into sustainable agricultural practices. Further research is warranted to explore long-term impacts and optimize application strategies.

Aluminum (Al) is the third, most abundant element in the Earth's crust. When soil pH drops below 5.5, Al is released from minerals, which threatens plant growth. The roots are particularly vulnerable to Al stress because Al ions can penetrate them, causing growth reduction by inhibiting the cell cycle and decreasing root cell elongation. Al has the ability to bind to cell structures, including cell walls, cytoskeleton, or DNA, which disturb their functions. Plants have developed various response strategies, such as the exclusion of organic acids into the rhizosphere or the detoxification of Al in the vacuole. STOP1 (Sensitive To Proton Rhizotoxicity 1) is the critical regulator of the expression of tolerance-related genes and is present in both mono- and dicots plants. The activity of STOP1 can be regulated on post-transcription and post-translation levels. This review paper presents an overview of the latest literature, aiming to accurately present the problem of Al toxicity and its effect on plant functioning. Moreover, the well-studied mechanisms of plant response and future prospects, like the use of polyamines, miRNAs, or DDR (DNA Damage Response) pathway, will be presented, which are opportunities to develop new plant varieties that are tolerant to Al stress.

In acidic soils, aluminum (Al) toxicity inhibits the growth and development of plant roots and affects nutrient and water absorption, leading to reduced yield and quality. Therefore, it is crucial to investigate and identify candidate genes for Al tolerance and elucidate their physiological and molecular mechanisms under Al stress. In this study, we identified a new gene OsAlR3 regulating Al tolerance, and analyzed its mechanism from physiological, transcriptional and metabolic levels. Compared with the WT, malondialdehyde (MDA) and hydrogen peroxide (H2O2) content were significantly increased, superoxide dismutase (SOD) activity and citric acid (CA) content were significantly decreased in the osalr3 mutant lines when exposed to Al stress. Under Al stress, the osalr3 exhibited decreased expression of antioxidant-related genes and lower organic acid content compared with WT. Integrated transcriptome and metabolome analysis showed the phenylpropanoid biosynthetic pathway plays an important role in OsAlR3-mediated Al tolerance. Exogenous CA and oxalic acid (OA) could increase total root length and enhance the antioxidant capacity in the mutant lines under Al stress. Conclusively, we found a new gene OsAlR3 that positively regulates Al tolerance by promoting the chelation of Al ions through the secretion of organic acids, and increasing the expression of antioxidant genes.