Leaf tissue damaging to seedlings can limit their subsequent growth, and the effects may be more extensive. Compensatory photosynthesis responses of the remnant cotyledon and primary leaf of Pharbitis purpurea to clipping and the effect of clipping on seedling growth were evaluated in a pot-cultivated experiment. Three treatments were conducted in the experiment, which were clipped cotyledon (CC), clipped second leaf (CL), and control group (CG). The area, thickness, mass, and longevity of the remaining cotyledon of CC exhibited over-compensatory growth. In contrast, seedlings of CC had under-compensatory growth in seedling height, root length, seedling mass, and root to shoot ratio. However, the traits of remnant cotyledon and seedling in CL treatment exhibited equal-compensatory growth. Net photosynthetic rate of the cotyledon of CC was significantly higher than those of CL and CG treatments, and the diurnal changes in photosynthetic rates showed significantly different patterns which were unimodal curve (CC) and bimodal curve (CL and CG), respectively. There was no significant difference between CL and CG treatment. Net photosynthetic rate of the primary leaf of CL was significantly higher than that of CG treatment. However, the photosynthetic rates of primary leaves of CL and CG treatments showed similar photosynthetic patterns characterized by a bimodal curve. P. purpurea seedlings used a compensatory growth strategy in the remaining cotyledon or the primary leaf to resist leaf loss and minimize any adverse effects. and W. Zheng ... [et al.].
Soil salinization and alkalinization frequently co-occur in naturally saline and alkaline soils. To understand the characteristics of mixed salt-alkali stress and adaptive response of Medicago ruthenica seedlings to salt-alkali stress, water content of shoots, growth and photosynthetic characteristics of seedlings under 30 salt-alkaline combinations (salinity 24-120 mM and pH 7.03-10.32) with mixed salts (NaCl, Na2SO4, NaHCO3, and Na2CO3) were examined. The indices were significantly affected by both salinity and pH. The interactive effects between salt and alkali stresses were significant, except for photosynthetic pigments. Water content of shoots, relative growth rates of shoots and roots and pigment concentrations showed decreasing trends with increasing salinity and alkalinity. The root activity under high alkalinity and salinity treatments gradually decreased, but was stimulated by the combined effects of low alkalinity and salinity. The survival rate decreased with increased salinity, except at pH 7.03-7.26 when all plants survived. Net photosynthetic rate, stomatal conductance and intercellular CO2 concentration decreased with increased salinity and pH. M. ruthenica tolerated the stress of high salt concentration when alkali concentration was low, and the synergistic effects of high alkali and high salt concentrations lead to the death of some or all seedlings. M. ruthenica appeared to be salt-alkali tolerant. Reducing the salt concentration or pH based on the salt components in the soil may be helpful to abate damage from mixed salt-alkaline stress. and J. Y. Yang ... [et al.].