Drought is one of the major constraints for sustainable crop production worldwide, especially in arid and semiarid regions. The global warming and climate change scenario has worsened the dilemma of water scarcity, creating an immediate threat to food security. Conserving water resources and exploiting various strategies that enable plants to withstand water deficits need to be urgently addressed. Drought adversely affects plant growth by modulating a range of physio-chemical, metabolic, and molecular processes inside the plant body, which ultimately reduces crop productivity. Besides developing drought-tolerant cultivars, better nutrient management could be a promising strategy to enhance drought tolerance in crop plants. Silicon, a quasi-essential element, is known to play a vital role in improving crop performance under a range of biotic and abiotic stresses. This review discusses the potential of Si application in attenuating the adverse effects of water-deficit stress. Silicon enhances plant growth by improving seed germination, cell membrane stability, carbon assimilation, plant–water relations and osmotic adjustment (by accumulating soluble sugars, proline and glycine betaine). It triggers the activity of antioxidants, promotes the biosynthesis of phytohormones, enhances nutrient acquisition and regulates the activity of vital enzymes in plants under drought stress. Silicon also induces anatomical changes in the plant cell wall through the deposition of polymerized amorphous silica (SiO₂-nH₂O), thereby improving stem and leaf erectness and reducing lodging. Further, Si-mediated physiological, biochemical and molecular mechanisms associated with drought tolerance in plants and future research prospects have been elucidated.

Low use efficiency of nitrogen (N) and phosphorus (P) is major challenge of modern agriculture. Coating of conventional fertilizers with nanomaterials is a promising technique for improved nutrient use efficiency. In current study, nanoparticles (NPs) of potassium ferrite (KFeO2 NPs) were coated on di-ammonium phosphate (DAP) fertilizer with three rates (2, 5, 10%) of KFeO2 NPs and were evaluated for release of N, P, K and Fe supplementation in clay loam and loam soil up to 60 days. The NPs were characterized for crystal assemblage, bond formation, morphology and configuration using the x-ray diffraction (XRD), scanning electron microscope (SEM) and Fourier transform-infra red spectroscopy (FT-IR). The results showed that size of NPs ranged between 7 and 18 nm. The controlled release of P in 10% KFeO2 nano-coated DAP was observed throughout the incubation period. The P release kept on increasing from day-1 (14.5 µg g-1) to day-60 (178.6 µg g-1) in coated DAP (10%) in loam soil. The maximum release of 50.4 µg g-1 NH4+1-N in coated DAP (10%) was observed after 30 days of incubation. The release of NO3-1-N was consistent up to 45 and 60 days in clay loam and loam soil, respectively. The average release of potassium and iron in 60 days was 19.7 µg g-1 and 7.3 µg g-1 higher in 10% coated DAP than traditional DAP in clay loam soil. It was concluded that KFeO2 nano-coated DAP supplied P and mineral N for longer period of time in both soils, and some higher coating levels should be tested in future.

Cadmium (Cd) is a readily available metal in the soil matrix, which obnoxiously affects plants and microbiota; thus, its removal has become a global concern. For this purpose, a multifunctional nanoscale zerovalent—iron enriched biochar (nZVI/BC) was used to alleviate the Cd—toxicity in maize. Results revealed that the nZVI/BC application significantly enhanced the plant growth (57%), chlorophyll contents (65%), intracellular permeability (61%), and biomass production index (76%) by restraining Cd uptake relative to Cd control. A Cd stabilization mechanism was proposed, suggesting that high dispersion of organic functional groups (C–O, C–N, Fe–O) over the surface of nZVI/BC might induce complex formations with cadmium by the ion exchange process. Besides this, the regular distribution and deep insertion of Fe particles in nZVI/BC prevent self-oxidation and over-accumulation of free radicals, which regulate the redox transformation by alleviating Cd/Fe⁺ translations in the plant. Current findings have exposed the diverse functions of nanoscale zerovalent-iron-enriched biochar on plant health and suggest that nZVI/BC is a competent material, feasible to control Cd hazards and improve crop growth and productivity in Cd-contaminated soil.

Nitrogen (N) is an essential element for plant growth and development. The application of a balanced and optimal amount of N is required for sustainable plant yield. For this, different N sources and forms are used, that including ammonium (NH₄⁺) and nitrate (NO₃⁻). These are the main sources for N uptake by plants where NH₄⁺/NO₃⁻ ratios have a significant effect on the biomass, quality and metabolites composition of lettuce grown in soil, substrate and hydroponic cultivation systems. A limited supply of N resulted in the reduction in the biomass, quality and overall yield of lettuce. Additionally, different types of metabolites were produced with varying concentrations of N sources and can be used as metabolic markers to improve the N use efficiency. To investigate the differential metabolic activity, we planted lettuce with different NH₄⁺/NO₃⁻ ratios (100:0, 75:25, 50:50, 25:75 and 0:100%) and a control (no additional N applied) in soil, substrate and hydroponic cultivation systems. The results revealed that the 25% NH₄^+/75% NO₃⁻ ratio increased the relative chlorophyll contents as well as the biomass of lettuce in all cultivation systems. However, lettuce grown in the hydroponic cultivation system showed the best results. The concentration of essential amino acids including alanine, valine, leucine, lysine, proline and serine increased in soil and hydroponically grown lettuce treated with the 25% NH₄^+/75% NO₃⁻ ratio. The taste and quality-related compounds in lettuce showed maximum relative abundance with the 25% NH₄^+/75% NO₃⁻ ratio, except ascorbate (grown in soil) and lactupicrin (grown in substrate), which showed maximum relative abundance in the 50% NH₄^+/50% NO₃⁻ ratio and control treatments, respectively. Moreover, 1-O-caffeoylglucose, 1,3-dicaffeoylquinic acid, aesculetin and quercetin-3-galactoside were increased by the application of the 100% NH₄^+/0% NO₃⁻ ratio in soil-grown lettuce. The 25% NH₄^+/75% NO₃⁻ ratio was more suitable in the hydroponic cultivation system to obtain increased lettuce biomass. The metabolic profiling of lettuce showed different behaviors when applying different NH₄⁺/NO₃⁻ ratios. Therefore, the majority of the parameters were largely influenced by the 25% NH₄^+/75% NO₃⁻ ratio, which resulted in the hyper-accumulation of health-promoting compounds in lettuce. In conclusion, the optimal N applications improve the quality of lettuce grown in soil, substrate and hydroponic cultivation systems which ultimately boost the nutritional value of lettuce.

Grain phosphorus (P) and phytate contents are important for early growth and quality of wheat, respectively. We studied seed P and phytate contents of 57 wheat genotypes released during last 6 decades. The grain total P and phytate P concentrations ranged from 2.0 to 8.9 mg g⁻¹ and 1.6 to 4.7 mg g⁻¹, respectively. Grain P was higher in genotypes released in current or last decade than pre-green revolution period and it correlated well with grain phytate contents. Indicating that breeders worked only for increased grain P and did not consider the phytate contents. Twenty-five genotypes were selected based on differences in grain P and phytate contents to observe the P use efficiency under field conditions. Genotypes differed significantly for grain P and yield at both 0 and 60 kg ha⁻¹ P levels. In conclusion, phytate fraction in grains of recent wheat genotypes was more as compared to old genotypes and genotype Inqlab-91 and Chakwal-86 had maximum grain total P. Moreover, number of productive tillers, spikelet per spike, grain weight, harvest index and grain P concentration and uptake were found responsible for P tolerance under P deficiency.