Effects on antioxidant enzyme activities and osmolytes in Halocnemum strobilaceum under salt stress

The seedlings of Halocnermum strobilaceum were cultivated in 0.5% hoagland nutrient solution containing 0.0%, 0.9%, 2.7% and 5.4% of NaC1 as well as composite salt （Na^＋, Ca^2＋, K^＋, Si^4＋） for 20 days; all the contents are in weight ratio. Succulent level, inorganic ions （Na^＋, K^＋）, organics such as betaine, proline, malondialdehyde, and antioxidant enzyme activities including superoxide dismutase （SOD）, catalase （CAT）, peroxidase （POD）, betaine aldehyde dehydrogenase （BADH） were measured to reveal its salt tolerance mechanism. When the composite salt concentration reaches 5.4%, SOD activity level, and MDA content is five times the control group; when it reaches 2.7%, the succulent level of seedlings, and the content ofK＋ in roots is nearly two times the NaCl treatment; the dry weight is more than three times the control group; with the NaCl treatment, MDA is three times the contrast; when the salt concentration is 2.7%, POD reaches the maximum. Results indicate that Si^4＋, K^＋, and Ca^20 from composite salt in the roots of H. strobilaceum improved the water-holding capacity. The activities of antioxidant enzyme were raised by the accumulation ofproline and betaine, which increased the salt tolerance. The absorption of K^＋ promoted the high ratio of K^＋/Na^＋ and alleviated the damage of cell membranes of H. strobilaceum, which is associated with osmotic contents such as betaine and proline.

Eco-physiological mechanisms of Caragana korshinskii Kom. adaptation to extreme drought stress: Leaf abscission and maintaining stem chloroplast integrity

In order to study the eco-physiological mechanisms of C. korshinskii adaptation to extreme drought stress, we investigated the variations of water content in soil, leaves, and stems, the chlorophyll a and b and the carotenoid content in leaves and stems, as well as changes of chloroplast ultrastructure in 2-year-old C. korshinskii specimens during a progressive soil drought process （by ceasing watering until all leaves were shed） and a subsequent rehydmtion process. During the dehydration process, the chlorophyll a and b and carotenoid contents in the leaves decreased, as did the carotenoid content in the stems. During the 4-day rehydration process, the chlorophyll a and b and carotenoid contents in the leaves and stems increased and gradually returned to normal levels. During ongoing drought stress, chloroplasts in the leaves broke away from cell walls and appeared in the center of cells. Under severe drought stress, the mesophyll ultrastmcture and chloroplast configuration in leaves were irreversibly disturbed, as mani- fested by the inner and outer membranes being destroyed; the thylakoid system disintegrated, the starch grain disappeared, and parts of cell tissue were dismantled into debris. However, the mesophyll ultrasWacture and chloroplast configuration in the stems remained complete. This indicates that C. korshinskii utilizes leaf abscission to reduce the surface area to avoid damage from ex- treme drought stress, and maintains chloroplast integrity and a considerable amount of chlorophyll to enable a rapid recovery of photosynthesis under the rehydration process.