The objective of this research was to measure the short term osmotic adjustment of Saticornia europaea L. ssp. rubra (A. Nels) Breitung when suddenly exposed to 100 millimolar NaCl. Plants were grown hydroponically, shocked with 100 millimolar NaCI added to the culture solution, and stem tips analyzed for free inorganic ions and small organic molecules at intervals up to 72 hours. In the first 2 hours, the calculated leaf osmoticum showed a net increase of 158.8 millimolar most (16,18,20,28,32). Compartmentation of extraneous ions in the vacuole would necessitate an equal amount of compatible solutes in the cytoplasm to balance the water potential. Small organic molecules that could act alone as osmotica in the cytoplasm without disruption of metabolic reactions have been reported (4,10,21,24,26,27 possible mechanism for cytoplasmic osmotic adjustment is a general increase in osmotica as suggested by Greenway and Sims (15) or an increase in two or more organic solutes together (10, 24).The experimental design used by most investigators of salt tolerance mechanisms in terrestrial halophytes has been to grow them in ranges of salinity, followed by analyses of potential osmotica. There is little experimental evidence for the changes that occur in the leaves of halophytes when subject to salinity shock, i.e. a sudden increase in exogenous salt concentration (13). The objective of this study was to investigate the short term osmotic adjustment by a succulent, C3, salt-accumulating halophyte when subjected to a saline shock, measuring the degree of osmotic adjustment achieved, and ascertaining which solutes might be responsible.
MATERIALS AND METHODSSeeds of Salicornia europaea L. ssp. rubra (A. Nels.) Breitung were collected locally and germinated in vermiculite wet with Hoagland solution. When about 2 cm high, the seedlings were transferred to large hydroponic tanks containing Hoagland solution plus 10 mM NaCl. The tanks were continuously aerated and the culture solution was changed at 2-week intervals. Sixty d after transplanting, the plants were still vegetative, profusely branched, and about 30 cm tall. At this time (time 0), 4 h after sunrise, 1-to 2-cm samples were taken from the terminal ends of the succulent stems. NaCl was then added to the culture solution to bring it to 100 mm NaCl, and samples were again taken at 2,4,6,8,12,16,20,24, 48, and 72 h after the addition of salt. Sampling was terminated at 72 h, because previous experiments indicated that 96% of the osmotic adjustment had occurred by this time, complete adjustment required 195 h. The samples were all taken from the terminal ends of the stems to insure similar ages and stages ofdevelopment ofthe tissues. They were rapidly rinsed in distilled H20, damp dried, sealed in bottles, and frozen in liquid N2.Extraction and Analysis. Osmotic potential of the terminal shoots was measured cryoscopically with an osmometer. Pressure extraction of the frozen and thawed shoots did not provide satisfactory reproducible results, so the following proce...