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Salinity is a widespread environmental stress that severely limits crop yield worldwide. Cerium oxide nanoparticles (nanoceria) have the unique capability of catalytically reducing levels of stress-induced reactive oxygen species (ROS) including hydroxyl radicals (˙OH) that lack enzymatic scavenging pathways. The underlying mechanisms of how nanoceria ROS scavenging augments plant tolerance to environmental stress are not well understood. Herein, we demonstrate that catalytic ˙OH scavenging by nanoceria in Arabidopsis thaliana leaves significantly improves mesophyll K + retention, a key trait associated with salinity stress tolerance. Leaves with mesophyll cells interfaced with 50 mg L −1 poly(acrylic acid) coated nanoceria (PNC) have significantly higher ( P < 0.05) carbon assimilation rates (85%), quantum efficiency of photosystem II (9%), and chlorophyll content (14%) compared to controls after being exposed to 100 mM NaCl for 3 days. PNC infiltrated leaves (PNC-leaves) under salinity stress exhibit lower ROS levels – including hydroxyl radical (41%) and its precursor hydrogen peroxide (44%) – and one fold higher ( P < 0.05) cytosolic K + dye intensity in leaf mesophyll cells relative to controls. Non-invasive microelectrode ion flux electrophysiological (MIFE) measurements indicated that PNC-leaves have about three-fold lower NaCl-induced K + efflux from leaf mesophyll cells compared to controls upon exposure to salinity stress. The ROS-activated nonselective cation channels (ROS-NSCC) in the plasma membrane of leaf mesophyll cells were identified as the main ˙OH-inducible K + efflux channels. Long term catalytic scavenging of ˙OH in leaves by PNC enhances plant photosynthetic performance under salinity stress by enabling plasma membrane channels/transporters to coordinately retain higher levels of K + in the leaf mesophyll cell cytosol. PNC augmented plant ROS scavenging provides a key tool for understanding and improving plant tolerance against abiotic stresses such as salinity. 

Active removal of Na⁺from the cytosol into the vacuole plays a critical role in salinity tissue tolerance, but another, often neglected component of this trait is Na⁺retention in vacuoles. This retention is based on an efficient control of Na⁺‐permeable slow‐ and fast‐vacuolar channels that mediate the back‐leak of Na⁺into cytosol and, if not regulated tightly, could result in a futile cycle. This Tansley insight summarizes our current knowledge of regulation of tonoplast Na⁺‐permeable channels and discusses the energy cost of vacuolar Na⁺sequestration, under different scenarios. We also report on a phylogenetic and bioinformatic analysis of the plant two‐pore channel family and the difference in its structure and regulation between halophytes and glycophytes, in the context of salinity tolerance.