Effects of drought stress on growth, photosynthesis and alkaloid accumulation of Lycoris aurea

2020 ◽  
Vol 52 (4) ◽  
Author(s):  
Juan Liang ◽  
Miaohua Quan ◽  
Chaowen She ◽  
Anna He ◽  
Xiaoliang Xiang ◽  
...  
Keyword(s):  
Drought Stress ◽  
Lycoris Aurea ◽  
Effects Of Drought

Effects of Drought Stress on Physiological Characteristics and Dry Matter Production in Maize Silking Stage

2013 ◽  
Vol 38 (10) ◽  
pp. 1884-1890 ◽  
Author(s):  
Ren-He ZHANG ◽  
Dong-Wei GUO ◽  
Xing-Hua ZHANG ◽  
Hai-Dong LU ◽  
Jian-Chao LIU ◽  
...  
Keyword(s):  
Drought Stress ◽  
Dry Matter ◽  
Physiological Characteristics ◽  
Dry Matter Production ◽  
Matter Production ◽  
Effects Of Drought

Effects of Drought Stress on Photosynthetic Characteristics of Maize Hybrids at Seedling Stage

2015 ◽  
Vol 41 (1) ◽  
pp. 154 ◽  
Author(s):  
Xing-Hua ZHANG ◽  
Jie GAO ◽  
Wei-Li DU ◽  
Ren-He ZHANG ◽  
Ji-Quan XUE
Keyword(s):  
Drought Stress ◽  
Photosynthetic Characteristics ◽  
Seedling Stage ◽  
Maize Hybrids ◽  
Effects Of Drought

The Effects of Drought on Leaf Gas Exchange and Growth of Three Species of Herbaceous Perennials

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 540a-540
Author(s):  
K.J. Prevete ◽  
R.T. Fernandez
Keyword(s):  
Drought Stress ◽  
Stomatal Conductance ◽  
Gas Exchange ◽  
Drought Tolerance ◽  
Transpiration Rate ◽  
Leaf Gas Exchange ◽  
Gas Analysis ◽  
Herbaceous Perennials ◽  
Effects Of Drought ◽  
Analysis System

Three species of herbaceous perennials were tested on their ability to withstand and recover from drought stress periods of 2, 4, and 6 days. Eupatorium rugosum and Boltonia asteroides `Snowbank' were chosen because of their reported drought intolerance, while Rudbeckia triloba was chosen based on its reported drought tolerance. Drought stress began on 19 Sept. 1997. Plants were transplanted into the field the day following the end of each stress period. The effects of drought on transpiration rate, stomatal conductance, and net photosynthetic rate were measured during the stress and throughout recovery using an infrared gas analysis system. Leaf gas exchange measurements were taken through recovery until there were no differences between the stressed plants and the control plants. Transpiration, stomatal conductance, and photosynthesis of Rudbeckia and Boltonia were not affected until 4 days after the start of stress. Transpiration of Eupatorium decreased after 3 days of stress. After rewatering, leaf gas exchange of Boltonia and Rudbeckia returned to non-stressed levels quicker than Eupatorium. Growth measurements were taken every other day during stress, and then weekly following transplanting. Measurements were taken until a killing frost that occurred on 3 Nov. There were no differences in the growth between the stressed and non-stressed plants in any of the species. Plants will be monitored throughout the winter, spring, and summer to determine the effects of drought on overwintering capability and regrowth.

Involvement of dehydrin proteins in mitigating the negative effects of drought stress in plants

2021 ◽  
Author(s):  
Riyazuddin Riyazuddin ◽  
Nisha Nisha ◽  
Kalpita Singh ◽  
Radhika Verma ◽  
Ravi Gupta
Keyword(s):  
Drought Stress ◽  
Negative Effects ◽  
Effects Of Drought

Penconazole and calcium ameliorate drought stress in canola by upregulating the antioxidative enzymes

2020 ◽  
Vol 47 (9) ◽  
pp. 825 ◽  
Author(s):  
Maryam Rezayian ◽  
Vahid Niknam ◽  
Hassan Ebrahimzadeh
Keyword(s):  
Oxidative Stress ◽  
Lipid Peroxidation ◽  
Drought Stress ◽  
Drought Tolerance ◽  
Antioxidative Enzymes ◽  
Proline Content ◽  
Fresh Weight ◽  
Negative Effects ◽  
Mda Content ◽  
Effects Of Drought

The aim of this research was to gauge the alternations in the lipid peroxidation and antioxidative enzyme activity in two cultivars (cv. RGS003 and cv. Sarigol) of canola under drought stress and drought tolerance amelioration by penconazole (PEN) and calcium (Ca). Plants were treated with different polyethylene glycol (PEG) concentrations (0, 5, 10 and 15%) without or with PEN (15 mg L–1) and Ca (15 mM). The Ca treatment prevented the negative effects of drought on fresh weight (FW) in RGS003 and Sarigol at 5 and 15% PEG respectively. Ca and PEN/Ca treatments caused significant induction in the proline content in Sarigol at 15% PEG; the latter treatment was accompanied by higher glycine betaine (GB), lower malondialdehyde (MDA) and growth recovery. Hydrogen peroxide (HO2) content in Sarigol was proportional to the severity of drought stress and all PEN, Ca and PEN/Ca treatments significantly reduced the H2O2 content. PEN and PEN/Ca caused alleviation of the drought-induced oxidative stress in RGS003. RGS003 cultivar exhibited significantly higher antioxidative enzymes activity at most levels of drought, which could lead to its drought tolerance and lower MDA content. In contrast to that of Sarigol, the activity of catalase and superoxide dismutase (SOD) increased with Ca and PEN/Ca treatments in RGS003 under low stress. The application of PEN and Ca induced significantly P5CS and SOD expression in RGS003 under drought stress after 24 h. Overall, these data demonstrated that PEN and Ca have the ability to enhance the tolerance against the drought stress in canola plants.

scholarly journals Spermine: Its Emerging Role in Regulating Drought Stress Responses in Plants

Cells ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 261
Author(s):  
Md. Mahadi Hasan ◽  
Milan Skalicky ◽  
Mohammad Shah Jahan ◽  
Md. Nazmul Hossain ◽  
Zunaira Anwar ◽  
...  
Keyword(s):  
Drought Stress ◽  
Drought Tolerance ◽  
Stress Responses ◽  
Abiotic Stresses ◽  
Defense Mechanisms ◽  
Antioxidant Defense ◽  
Severe Drought ◽  
New Information ◽  
Effects Of Drought

In recent years, research on spermine (Spm) has turned up a lot of new information about this essential polyamine, especially as it is able to counteract damage from abiotic stresses. Spm has been shown to protect plants from a variety of environmental insults, but whether it can prevent the adverse effects of drought has not yet been reported. Drought stress increases endogenous Spm in plants and exogenous application of Spm improves the plants’ ability to tolerate drought stress. Spm’s role in enhancing antioxidant defense mechanisms, glyoxalase systems, methylglyoxal (MG) detoxification, and creating tolerance for drought-induced oxidative stress is well documented in plants. However, the influences of enzyme activity and osmoregulation on Spm biosynthesis and metabolism are variable. Spm interacts with other molecules like nitric oxide (NO) and phytohormones such as abscisic acid, salicylic acid, brassinosteroids, and ethylene, to coordinate the reactions necessary for developing drought tolerance. This review focuses on the role of Spm in plants under severe drought stress. We have proposed models to explain how Spm interacts with existing defense mechanisms in plants to improve drought tolerance.

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