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Water deficit stress can reduce the postproduction shelf life and marketability of floriculture crops. To alleviate the damage by water deficiency, plants need to limit transpirational water loss by inducing stomatal closure. Osmotic stress induces stomatal closure like the response to water deficit stress. It could be used as a convenient tool to enhance water deficit stress tolerance by reducing water loss. The objective of this research was to investigate whether osmotic treatment with a high concentration of chemical solutions could trigger a response to osmotic stress so that stomatal closure can be induced, resulting in enhanced water deficit stress tolerance in viola (Viola cornuta ‘Sorbet XP Yellow’). Osmotic treatments with CaCl₂, Ca(NO₃)₂, NaCl, NaNO₃, BaCl₂, Ba(NO₃)₂, and mannitol were applied at the osmotic potentials (ψ_S) of −1.3 and −2.0 MPa. Chemical treatments [except Ca(NO₃)₂, NaCl, and mannitol] helped to delay wilting and gave a longer shelf life, up to 5.2 days over that of the control, 2.5 days. However, leaf necrosis was observed on the violas treated with NaCl, NaNO₃, BaCl₂, Ba(NO₃)₂, and mannitol. CaCl₂ was the most effective agent in delaying wilting under water deficit stress in viola without leaf necrosis. Compared with the control, violas treated with CaCl₂ at 200 and 300 mm showed an increase in shelf life by 2.6 and 1.2 days, respectively. Stomatal conductance (g _S) was reduced within 4 hours after treatment with CaCl₂ compared with that of control violas. Leaf relative water content (RWC) of control violas was dramatically reduced 3 days after treatment and fell below 50% on day 4, while CaCl₂-treated violas maintained higher leaf RWC (70% to 81%) during the water deficit period. These results indicated that osmotic treatment with the high concentration of CaCl₂ caused stomatal closure, resulting in a reduction of water loss and an extension of shelf life under water deficit stress in viola.

Kale (Brassica oleracea L. and other species) is considered a rich source of important minerals. Kale at the early stage of leaf development is assumed to contain higher levels of minerals than at maturity. However, literature supporting this assumption is scarce. In this study, the concentrations of macronutrients [potassium (K), calcium (Ca), magnesium (Mg), and phosphorus (P)] and micronutrients [sodium (Na), iron (Fe), manganese (Mn), zinc (Zn), and copper (Cu)] either essential to plant growth and development, or important to human health, were determined. Three kale cultivars (green leaf ‘Dwarf Blue Curled’ and red leaf ‘Scarlet’ in B. oleracea, and green leaf with purple midvein ‘Red Russian’ in Brassica napus) were evaluated at five different leaf developmental stages; cotyledon [microgreen 1 (MG1)], two true leaf [microgreen 2 (MG2)], four true leaf [baby leaf 1 (BL1)], six true leaf [baby leaf 2 (BL2)], and adult. As kale matured, total mineral (ash) decreased from 14.6–19.1% at the microgreen stages to 3.9–6.4% at the adult stage, on a dry weight (DW) basis. Microgreen kale contained higher concentrations of most minerals than adult kale, on a DW basis, in all cultivars. On a fresh weight (FW) (as consumed) basis, the highest level of total mineral concentration was detected at baby leaf stage 1 (1.3–1.7%) and there was no difference between microgreen and adult stages. Fresh microgreens generally contained lower K, Ca, Mg, Fe, and Zn than fresh baby leaves, and lower concentrations of Ca and Mg and higher Na compared with fresh adult kale. Overall, water content deceased from 95.1% at MG1 stage to 80.0% at adult stage. The variation in water content and mineral accumulation during leaf development might contribute to the discrepancy. In addition, fresh leaves of ‘Scarlet’ contained higher concentration of total minerals than that of ‘Dwarf Blue Curled’ or ‘Red Russian’. Although ‘Dwarf Blue Curled’ and ‘Red Russian’ are different species, their mineral content profile during leaf development was similar. Together, cultivar and leaf developmental stage influenced mineral content in kale.