High salt concentration |
Pisum sativum (L.) |
10–5 M |
Osmoregulation, increased proline content |
Annual |
Dicot |
Fedina and Tsonev, 1997 |
|
Glycine max (L.) |
20 and 30 μM |
Increase in growth and proline content |
Annual |
Dicot |
Yoon et al., 2009 |
|
Arabidopsis thaliana (L.) |
5 and 10 μM |
Compliments lox3 mutant rescues salt stress |
Annual |
Dicot |
Ding H. et al., 2016 |
|
Triticum aestivum (L.) |
0.1 μM |
Increases cytokinin production and plant growth |
Annual |
Monocot |
Avalbaev et al., 2016 |
|
Solanum lycopersicum (L.) |
10, 20, 30, 40, 50, and 60 μM |
Increase in levels of osmo-protectants and enzymatic antioxidants |
Annual |
Dicot |
Manan et al., 2016 |
|
Brassica napus (L.) |
100 μM |
Increases relative water content, soluble sugar, photosynthesis |
Annual |
Dicot |
Ahmadi et al., 2018 |
|
|
|
JA |
|
|
|
|
|
|
Pisum sativum (L.) |
10–5 M |
Decreased activity of sodium and chloride ions, increased endogenous level of proline |
Annual |
Dicot |
Velitchkova and Fedina, 1998 |
|
Oryza sativa (L.) |
30 μM |
Increases ion uptake, growth, ABA levels |
Annual |
Monocot |
Kang et al., 2005 |
|
Hordeum vulgare (L.) |
12 μM |
Induction of genes having role in imparting salt tolerance |
Annual |
Monocot |
Walia et al., 2007 |
|
Brassica napus (L.) |
10–6, 10–9, and 10–12 M |
Sugar accumulation |
Annual |
Dicot |
Kaur et al., 2013 |
|
Triticum aestivum (L.) |
2 mM |
Increase in concentration of GSH, enhanced activity of SOD, CAT, APX |
Annual |
Monocot |
Qiu et al., 2014 |
|
|
|
GSH |
|
|
|
|
|
|
Oryza sativa (L.) |
2 mM |
Positive influence on yield contributing traits |
Annual |
Monocot |
Wang et al., 2014 |
|
Arabidopsis thaliana (L.) |
400 μM |
Abscisic acid, auxin and jasmonic acid biosynthesis |
Annual |
Dicot |
Cheng et al., 2015 |
|
Vigna radiata (L.) |
1 mM |
Activation of glyoxalase system and improved antioxidant system |
Annual |
Dicot |
Nahar et al., 2015b |
|
Solanum lycopersicum (L.) |
5 mM |
Increased GSH biosynthesis, improved activity of SOD, CAT, POD |
Annual |
Dicot |
Zhou et al., 2017 |
|
Glycine max (L.) |
2 mM |
Improved stress tolerance and yield attributes |
Annual |
Dicot |
Akram et al., 2017 |
|
|
|
Ca2+
|
|
|
|
|
|
|
Solanum lycopersicum (L.) |
5 and 10 mM |
Increased growth, physiology and fruit production |
Annual |
Dicot |
Parvin et al., 2015 |
|
Glycine max (L.) |
6 mM |
Positive effect on growth and metabolic activities. |
Annual |
Dicot |
Yin et al., 2015 |
|
Oryza sativa (L.) |
3 and 5 mM |
Elevated antioxidant enzyme levels |
Annual |
Monocot |
Tahjib-Ul-Arif et al., 2018 |
|
|
Lead |
|
JA |
|
|
|
|
|
Heavy metal stresses |
Wolffia arrhiza (L.) |
0.1 μM |
Preventing Pb accumulation by restoring plant growth and primary metabolite level |
Perennial |
Monocot |
Piotrowska et al., 2009 |
|
Solanum lycopersicum (L.) |
0.1, 1, and 100 μM |
Increase osmolytes concentration and ascorbate glutathione cycle |
Annual |
Dicot |
Bali et al., 2018 |
|
|
|
|
|
GSH |
|
|
|
|
|
Gossypium sp. (L.) |
50 μM |
Stabilized ultra-structure and increased antioxidant activity |
Perennial |
Dicot |
Khan M. et al., 2016 |
|
Triticum aestivum (L.) |
1 mM |
Enhancement of enzymatic and non-enzymatic antioxidant activities and improved seedling growth |
Annual |
Monocot |
Hasanuzzaman et al., 2018 |
|
|
Cadmium |
|
JA |
|
|
|
|
|
|
Glycine max (L.) |
20 μM |
Increased antioxidant response |
Annual |
Dicot |
Noriega et al., 2012 |
|
Vicia faba (L.) |
0.01 mM |
Restoration of growth and pigment system |
Annual |
Dicot |
Ahmad et al., 2017 |
|
Brassica napus (L.) |
25 μM |
Osmolytes and antioxidant activity increased |
Annual |
Dicot |
Ali et al., 2018 |
|
|
|
|
MeJA |
|
|
|
|
|
|
Oryza sativa (L.) |
5 μM |
GSH homeostasis, JA biosynthesis |
Annual |
Monocot |
Singh and Shah, 2014 |
|
Arabidopsis thaliana (L.) |
0.01 μM |
Suppression of genes involved in Cd uptake |
Annual |
Dicot |
Lei et al., 2020 |
|
|
|
GSH |
|
|
|
|
|
Hordeum vulgare (L.) |
20 mg/L |
Improved photosynthesis |
Annual |
Monocot |
Chen et al., 2010 |
|
Oryza sativa (L.) |
50 μM |
Enhanced photosynthetic performance |
Annual |
Monocot |
Cai et al., 2011a |
|
Gossypium sp. (L.) |
50 μM |
Reverses stressful effects, leaf ultra-morphology revived |
Perennial |
Monocot |
Daud et al., 2016 |
|
Populus sp. (L.) |
100 μM |
Increased Cd detoxifying gene transcript |
Perennial |
Monocot |
Ding et al., 2017 |
|
|
|
|
Ca2+
|
|
|
|
|
|
|
Vicia faba (L.) |
2% |
Antioxidant enzyme up regulation |
Annual |
Dicot |
Siddiqui et al., 2012 |
|
Brassica juncea (L.) |
50 mM |
Improved photosynthesis |
Annual |
Dicot |
Ahmad et al., 2015 |
|
Arabidopsis thaliana (L.) |
3 mM |
Alleviated the inhibition of Cd on the root growth |
Annual |
Dicot |
Li P. et al., 2016 |
|
Sesamum indicum (L.) |
50 mM |
Improved growth and proline levels |
Annual |
Dicot |
Abd-Allah et al., 2017 |
|
|
Copper |
|
JA |
|
|
|
|
|
|
Oryza sativa (L.) |
0.5 mM |
Phytoalexin production |
Annual |
Monocot |
Rakwal et al., 1996 |
|
Cajanus cajan (L.) |
1 μM, 1 nM, |
Osmolytes and antioxidant enzyme increased |
Perennial |
Dicot |
Poonam et al., 2013 |
|
Triticum Aestivum (L.) |
5 mM |
Increased transcript of glutathione–s- transferase |
Annual |
Monocot |
Li et al., 2013 |
|
|
|
|
MeJA |
|
|
|
|
|
|
Phaseolus coccineus (L.) |
10–5 M |
Promoted plant growth and development |
Perennial |
Dicot |
Hanaka et al., 2015 |
|
|
|
|
GSH |
|
|
|
|
|
|
Triticum aestivum (L.) |
2.5 mM/L |
Accumulation of nitrogen, sulfur, and phosphorous |
Annual |
Monocot |
Peng et al., 2012 |
|
Glycine Max (L.) |
0.16 and 0.32 Mm/L |
Enhances amylase activity |
Annual |
Dicot |
Chen, 2012 |
|
Oryza Sativa (L.) |
100 mg/L |
Increased germination rate and vigor index |
Annual |
Monocot |
Mostofa et al., 2015 |
|
|
|
|
Ca2+
|
|
|
|
|
|
|
Drought |
JA |
|
Water stress |
Glycine Max (L.) |
4.5 and 9 mM/L |
Maintenance of membrane integrity |
Annual |
Dicot |
Chen et al., 2008 |
|
Vigna radiata (L.) |
5 mM |
Solution improved the growth of Cu-treated seedling and lowering the concentration of Polyamines putrescine and increased concentrations of spermine and spermidine in epicotyl of plants |
Annual |
Dicot |
Shen et al., 1998 |
|
Brassica sp. (L.) |
0.5 mM |
Increase in physiological, antioxidant and glyoxalase system activities |
Annual |
Dicot |
Alam et al., 2014 |
|
Allium cepa (L.) |
25, 50, and 100 μM |
Pigment and compatible solute enhancement |
Annual |
Monocot |
Ahmad and Murali, 2015 |
|
Beta vulgaris (L.) |
5 and 10 μM |
Increased germination rate |
Annual |
Dicot |
Ghafari and Tadayon, 2019 |
|
|
|
|
MeJA |
|
|
|
|
|
|
Brassica oleracea (L.) |
10 μM |
Increased Net photosynthetic rate and antioxidant machinery activation |
Annual |
Dicot |
Wu et al., 2012 |
|
Triticum aestivum (L.) |
0.25 μM |
Water status and antioxidant capacity increased |
Annual |
Monocot |
Ma et al., 2014 |
|
Satureja hortensis (L.) |
75, 150, and 225 μM |
Improved many characteristics of plant like growth, water content, proline level, antioxidant activity |
Annual |
Dicot |
Miranshahi and Sayyari, 2016 |
|
|
|
|
GSH |
|
|
|
|
|
|
Arabidopsis thaliana (L.) |
400 μM |
Changes at translational level of numerous hormones |
Annual |
Dicot |
Cheng et al., 2015 |
|
Vigna radiata (L.) |
1 mM |
Improved their antioxidant components under drought stress |
Annual |
Dicot |
Nahar et al., 2015a |
|
|
|
|
Ca2+
|
|
|
|
|
|
|
Zoysia japonica (L.) |
5 and 10 mM |
Improved photosynthesis, growth and antioxidant response |
Perennial |
Monocot |
Xu et al., 2013 |
|
Zea mays (L.) |
5 mg/L |
Improved photosynthesis, growth and soluble sugar content |
Annual |
Monocot |
Naeem et al., 2018 |
|
Nicotiana tabacum (L.) |
10 mM/L |
Stabilization of gaseous exchange and photosynthetic organelles |
Annual |
Dicot |
Hu et al., 2018 |
|
|
Flooding |
|
JA |
|
|
|
|
|
|
Citrus spp. (L.) |
1 mM |
Increase in abscisic acid levels |
Perennial |
Dicot |
de Ollas et al., 2013 |
|
|
|
|
Ca2+
|
|
|
|
|
|
|
Zea mays (L.) |
0.75% (W/V) |
Regulates the cell wall integrity and mitigates effect of oxidative stress during flood stress conditions |
Annual |
Monocot |
Porto et al., 2013 |
|
Glycine max (L.) |
50 mM |
Increase the root elongation and inhibited the cell death of root tip of under flood stress |
Annual |
Dicot |
Oh et al., 2014 |
|
|
|
JA |
|
|
|
|
|
Ozone stress |
Capsicum annuum (L.) |
10 mM |
Regulates osmotic and antioxidant metabolism |
Annual |
Dicot |
Yang et al., 2016 |
|
Arabidopsis thaliana (L.) |
1.4 μM |
Inhibited cell death and lesion containment |
Annual |
Dicot |
Overmyer et al., 2000 |
|
Arabidopsis thaliana (L.) (JA insensitive mutants) |
10 μM |
Extremely susceptible to ozone |
Annual |
Dicot |
Kanna et al., 2004 |
|
|
|
GSH |
|
|
|
|
|
|
Transgenic Nicotiana tabacum (L.) |
Overexpression of glutathione synthetase in plastid |
Ozone tolerance developed |
Annual |
Dicot |
Wellburn et al., 1998 |
|
Populus sp. (L.) |
Overexpression of Glutathione reductase |
Ozone tolerance developed |
Perennial |
Monocot |
Foyer et al., 1995 |
|
|
Heat |
|
JA |
|
|
|
|
|
Temperature stress |
Vitis sp (L.) seedling |
50 μM/L |
Thermotolerance |
Perennial |
Dicot |
Chen et al., 2006 |
|
|
|
|
Ca2+
|
|
|
|
|
|
|
Solanum lycopersicum (L.) |
1 Mm |
Operating efficiency of photosystem II increased |
Annual |
Dicot |
Sakhonwasee and Phingkasan, 2017 |
|
Nicotiana tabacum (L.) |
20 Mm |
Improved stomatal conductance and thermostablity |
Annual |
Dicot |
Tan et al., 2011 |
|
|
Cold |
|
JA |
|
|
|
|
|
|
Prunus persica (L.) |
0.1 Mm/L |
Maintenance of fruit quality |
Perennial |
Dicot |
Meng et al., 2009 |
|
|
|
|
MeJA |
|
|
|
|
|
|
Cucumis sativus (L.) |
100 μM |
Enhances chilling tolerance by regulating antioxidant enzymes |
Annual |
Dicot |
Li et al., 2012 |
|
Arabidopsis thaliana (L.) |
30 μM |
Induced freezing tolerance |
Annual |
Dicot |
Hu et al., 2013 |
|
Eriobotrya japonica (L.) |
10 μM |
Alleviates the chilling injury in the fruits of plants |
Perennial |
Dicot |
Cai et al., 2011b |
|
|
|
|
Ca2+
|
|
|
|
|
|
|
Solanum lycopersicum (L.) |
27 mM |
Improvement carbon fixation, electron transport, etc. |
Annual |
Dicot |
Zhang G. et al., 2014 |
|
Cynodon dactylon (L.) |
1, 5, 10, and 20 mM |
Antioxidant activation and metabolic homeostasis |
Perennial |
Monocot |
Shi et al., 2014 |
|
|
|
|
GSH |
|
|
|
|
|
|
Eriobotrya japonica (L.) |
50, 100, and 300 mg/L |
Increase in membrane fluidity and decrease in lipid peroxidation |
Perennial |
Dicot |
Wu et al., 2010 |