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Salt stress response in tomato beyond the salinity tolerance threshold
Institution:1. Department of Plant Physiology, Faculty of Sciences, University of Granada, E-18071 Granada, Spain;2. Department of Plant Nutrition, CEBAS-CSIC, Campus de Espinardo, E-30100, Espinardo, Murcia, Spain;1. College of Agriculture and Biotechnology, China Agricultural University, Beijing 100193, PR China;2. College of Horticulture and Forestry Science, Huazhong Agricultural University, Wuhan 430070, PR China;3. School of Agriculture, Virginia State University, PO Box 9061, Petersburg, VA 23806, USA;1. School of Agricultural Science, University of Tasmania, Private Bag 54, Hobart, Tas 7001, Australia;2. Faculty of Science, University of Copenhagen, Højbakkegård Allé 13, 2630 Tåstrup, Denmark;3. Department of Physics, Faculty of Mathematics and Natural Sciences, University of Jember, Jember 68121, East Java, Indonesia;1. College of Life Science, State Key Laboratory of Crop Biology, Shandong Key Laboratory of Crop Biology, Shandong Agricultural University, Taian 271018, China;2. Department of Horticulture, ALS 4017, Oregon State University, Corvallis, OR 97331, USA
Abstract:Crop salt tolerance is generally assessed as the relative yield response to increasing root zone salinity, expressed as soil (ECe) or irrigation water (ECw) electrical conductivity. Alternatively, the dynamic process of salt accumulation into the shoot relative to the shoot biomass has also been considered as a tolerance index. These relationships are graphically represented by two intersecting linear regions, which identify (1) a specific threshold tolerance, at which yield begins to decrease, and (2) a declining region, which defines the yield reduction rate. Although the salinity threshold is intuitively a critical parameter for establishing plant salt tolerance, we focused our interest on physiological modifications that may occur in the plant at salinity higher than the so-called tolerance threshold. For this purpose, we exposed hydroponically grown tomato plants to eight different salinity levels (EC = 2.5 (non-salinized control); 4.2; 6.0; 7.8; 9.6; 11.4; 13.2; 15.0 dS m−1). Based on biomass production, water relations, leaf ions accumulation, leaf and root abscisic acid and stomatal conductance measurements, we were able to identify a specific EC value (approximately 9.6 dS m−1) at which a sharp increase of the shoot and root ABA levels coincided with (1) a decreased sensitivity of stomatal response to ABA; (2) a different partitioning of Na+ ions between young and mature leaves; (3) a remarkable increase of the root-to-shoot ratio. The specificity and functional significance of this response in salt stress adaptation is discussed.
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