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Physiology and Molecular Biology of Stress ... - KHAM PHA MOI

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52<br />

Z Dajic<br />

5. SALT ACCUMULATION<br />

High accumulation <strong>of</strong> salts in the shoot has been well established for salt- tolerant<br />

species (e.g. Waisel, 1972; Flowers et al., 1977; Ungar, 1991). In halophytes <strong>of</strong> the plant<br />

community Puccinellietum limosae in Serbia, which is spread on highly salinized soil<br />

(annual values <strong>of</strong> EC e<br />

ranged between 20.8 dS m -1 <strong>and</strong> 54.2 dS m -1 ), the level <strong>of</strong> total salt<br />

accumulation in the shoot during the vegetative season (June-October), <strong>and</strong> the relations<br />

among accumulated ions (Table 2) were strictly species specific, depending on<br />

different adaptive strategies (Dajic, 1996), such as salt accumulation in the halophytes<br />

Suaeda maritima <strong>and</strong> Salsola soda, <strong>and</strong> salt exclusion in the halophytic grass Puccinellia<br />

limosa.<br />

Table 2. Average seasonal ion concentrations <strong>of</strong> the shoot (ìmol g -1 dry weight) in halophytes<br />

grown in natural habitat conditions<br />

Species Na + K + Mg 2+ Cl -<br />

1 660.9 ± 317.88 438.5.1± 162.96 155.2 ± 30.32 478.9 ± 180.71<br />

2 843.5 ± 375.38 467.3 ± 182.67 168.7 ± 32.20 615.5 ± 263.23<br />

2 2686.9 ± 982.06 341.5 ± 86.87 391.7 ± 132.81 1877.7 ± 614.2<br />

4 791.3 ± 234.78 365.6 ± 95.41 158.3 ± 49.31 555.5 ± 244.18<br />

5 1345.7 ± 608.58 363.5 ± 142.98 87.5 ± 22.05 504.9 ± 188.21<br />

6 1834.8 ± 664.11 375.2 ± 99.21 125.2 ± 56.3 901.4 ± 538.31<br />

7 127.5 ± 64.06 157.3 ± 54.82 61.1 ± 17.33 177.5 ± 65.2<br />

1- Atriplex tatarica, 2- Atriplex litoralis, 3- Suaeda maritima, 4- Aster tripolium var. pannonicus,<br />

5- Camphorosma annua, 6- Salsola soda, 7- Puccinellia limosa<br />

(after Dajic, 1996)<br />

5.1. Vacuolar Compartmentation<br />

The high content <strong>of</strong> salts in aboveground parts <strong>of</strong> the halophytic plants is feature<br />

associated with efficiency <strong>of</strong> such plants to deliver ions into the vacuoles. The ability<br />

<strong>of</strong> plants to transfer ions into the vacuole is dependent on the proportion <strong>of</strong> highly<br />

vacuolated cells <strong>and</strong> tissues, as well as the activity <strong>of</strong> transport systems located at the<br />

tonoplast, which prevent excessive concentration <strong>of</strong> ions in the cytoplasm. Sequestration<br />

<strong>of</strong> salts into the leaf <strong>and</strong>/or shoot vacuoles is typical attribute <strong>of</strong> dicotyledonous<br />

halophytes, coupled with other physiological adaptations, such as regulation <strong>of</strong> transpiration<br />

(<strong>and</strong> water regime in general) <strong>and</strong> performing <strong>of</strong> cell metabolism with low<br />

potassium concentrations (Flowers <strong>and</strong> Dalmond, 1992).

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