Abstract
Drought (water stress) is one of the most important stresses that occurs widely in agricultural fields and can affect different aspects of crop growth, development, and metabolism. There are several reasons of drought stress in agriculture fields, including low rainfall or irrigation, high and low temperature, high intensity of light, high EC (electrical conductivity) due to salinity and fertilizer misapplication, etc. Plant water potential and turgor decline in dehydration condition; therefore, plant cells could not do normal functions and inducing all drought stress aspects in plants. In addition, it can negatively affect quantity and quality of growth and yield in crops. Plants are sessile organisms and must tolerate environmental stresses; hence, they have developed various mechanisms for resistance to stresses such as drought stress. Moreover, as plants are multicellular organisms, their responses to environmental stresses such as drought are complex. Generally, plant resistance to environmental stress is divided into two main strategies: stress avoidance and stress tolerance. Besides tolerance, avoidance is one of the common drought resistance mechanisms in annual plants. Escape from stress conditions is the strategy for plant growth under drought condition that is less important in agronomic plants. The alteration in resistance capacity of crops’ seeds and young seedlings by priming methods, production of tolerant crops by traditional breeding methods, and the generation of transgenic plants by gene manipulation are useful procedures to minimize the negative effects of drought on agronomic products. In addition, several strategies for drought management in agricultural fields on multiple levels can be effective.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- 5-HTP:
-
5-hydroxy-L-tryptophan
- ABA:
-
abscisic acid
- AFLP:
-
amplified fragment length polymorphism
- ALA:
-
5-aminolevulinic acid
- AM:
-
arbuscular mycorhizal fungi
- APX:
-
ascorbate peroxidase
- BABA:
-
β-aminobutyric acid
- BR:
-
brassinosteroid
- CAT:
-
catalase
- CPK:
-
Ca2+-dependent protein kinase
- EC:
-
electrical conductivity
- ERF:
-
ethylene response factors
- GABA:
-
γ- aminobutyric acid
- Gas:
-
Gibberellins
- GB:
-
glycine betaine
- GR:
-
glutathione reductase
- GSH:
-
glutathione
- H2O2:
-
hydrogen peroxide
- IAA:
-
indole-3- acetic acid
- JA:
-
jasmonic acid
- L-DOPA:
-
L-3,4-dihydroxyphenylalanine
- LEA:
-
late embryogenesis abundant
- LMW:
-
low molecular weight
- MGDG:
-
monogalactosyldiacylglycerol
- O2•−:
-
superoxide radical
- OH:
-
hydroxyl radical
- P5CR:
-
pyrroline-5-carboxylate reductase
- PEG:
-
polyethylene glycol
- PM-ATPase:
-
plasma membrane ATPase
- POD:
-
peroxidase
- PP2Cs:
-
protein phosphatase 2Cs
- QTL:
-
quantitative trait loci
- RAPDs:
-
random amplified polymorphic DNA
- RCS:
-
reactive carbonyl species
- RFLPs:
-
restriction fragment length polymorphisms
- RNS:
-
reactive nitrogen species
- RO:
-
alkoxy radicals
- ROS:
-
reactive oxygen species
- RSS:
-
reactive sulfur species
- RuBisCO:
-
ribulose bisphosphate carboxylase/oxygenase
- RWC:
-
relative water content
- SA:
-
salicylic acid
- SCARs:
-
sequence characteristic amplified regions
- SnRK2s:
-
SNF1-related protein kinase 2s
- SOD:
-
superoxide dismutase
- SSRs:
-
simple sequence repeats
- TF:
-
transcription factors
- VOCs:
-
volatile organic compounds
References
Abdelmoneim TS, Tarek AAM, Almaghrabi OA, Alzahrani HS, Abdelbagi I (2014) Increasing plant tolerance to drought stress by inoculation with arbuscular mycorrhizal fungi. Life Sci J 11:10–17
Acharya BR, Assmann SM (2009) Hormone interactions in stomatal function. Plant Mol Biol 69:451–462
Akhtar I, Nazir N (2013) Effect of water logging and drought stress in plants. Int J Water Res Environ Sci 2:34–40
Arbona V, Manzi M, de Ollas C, Gómez-Cadenas A (2013) Metabolomics as a tool to investigate abiotic stress tolerance in plants. Int J Mol Sci 14:4885–4911
Arnao MB, Hernandez-Ruiz J (2015) Functions of melatonin in plants: a review. J Pineal Res 59:133–150
Ashraf M, Foolad MR (2007) Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environ Exp Bot 59:206–216
Ashraf M, Ozturk M, Athar HR (2009) Salinity and water stress, improving crop efficiency. Springer, Dordrecht
Barriopedro D, Gouveia C, Trigo RM, Wang L (2012) The 2009/10 drought in China: possible causes and impacts on vegetation. Amer Meteor Soc 13:1251–1267
Baxter A, Mittler R, Suzuki N (2014) ROS as key players in plant stress signaling. J Exp Bot 65:1229–1240
Bej S, Basak J (2014) MicroRNAs: the potential biomarkers in plant stress response. Amer J Plant Sci 5:748–759
Bernacchia G, Furini A (2004) Biochemical and molecular responses to water stress in resurrection plants. Physiol Plant 121:175–181
Bhargava S, Sawant K (2013) Drought stress adaptation: metabolic adjustment and regulation of gene expression. Plant Breed 132:21–32
Bray EA (2001) Plant response to water-deficit stress. Encyclopedia of Life Sciences. Wiley, Chichester
Chaves MM, Maroco JP, Pereira JS (2003) Understanding plant responses to drought-from genes to the whole plant. Func Plant Biol 30:239–264
Chepsergon J, Mwamburi L, KipkemboiKassim M (2012) Mechanism of drought tolerance in plants using Trichoderma spp. Int J Sci Res 3:1592–1595
Chernyad’ev II (2005) Effect of water stress on the photosynthetic apparatus of plants and the protective role of cytokinins: a review. Appl Biochem Microbiol 41:115–128
Choi WG, Toyota M, Kim SH, Hilleary R, Gilroy S (2014) Salt stress-induced Ca2+ waves are associated with rapid, long-distance root-to-shoot signaling in plants. Proc Natl Acad Sci U S A 111:6497–6502
Cutler SR, Rodriguez PL, Finkelstein RR, Abrams SR (2010) Abscisic acid: emergence of a core signaling network. Annu Rev Plant Biol 61:651–679
Dai A (2012) Drought under global warming: a review. Wires Clim Change 2:45–65
Ding Y, Tao Y, Zhu C (2013) Emerging roles of MicroRNAs in the mediation of drought stress response in plants. J Exp Bot 64:3077–3086
Dodd AN, Kudla J, Sanders D (2010) The language of calcium signaling. Annu Rev Plant Biol 61:593–620
Du W, Yu D, Fu S (2009) Detection of quantitative trait loci for yield and drought tolerance traits in soybean using a recombinant inbred line population. J Integr Plant Biol 51:868–878
Einset J, Nielsen E, Connolly EL, Bones A, Sparstad T, Winge P, Zhu JK (2007) Membrane-trafficking RabA4c involved in the effect of glycinebetaine on recovery from chilling stress in Arabidopsis. Physiol Plant 130:511–518
Farooq M, Wahid A, Kobayashi N, Fujita D, Basra SMA (2009) Plant drought stress: effects, mechanisms and management. Agron Sustain Dev 29:185–212
Franco JA (2011) Root development under drought stress. Technol Knowl Transf e-Bull 2:1–3
Gill SS, Tuteja N (2010) Polyamines and abiotic stress tolerance in plants. Plant Signal Behav 51:26–33
Gilroy S, Suzuki N, Miller G, Choi WG, Toyota M, Devireddy AR, Mittler R (2014) A tidal wave of signals: calcium and ROS at the forefront of rapid systemic signaling. Trends Plant Sci 19:623–630
Hayat S, Hasan SA, Fariduddin Q, Ahmad A (2008) Growth of tomato (Lycopersicon esculentum) in response to salicylic acid under water stress. J Plant Interact 3:297–304
Hayat Q, Hayat S, Irfan M, Ahmad A (2010) Effect of exogenous salicylic acid under changing environment: a review. Environ Exp Bot 68:14–25
Hirt H, Shinozaki K (eds) (2004) Plant responses to abiotic stress. Springer, Berlin
Huang GT, Ma SL, Bai LP, Zhang L, Ma H, Jia P, Liu J, Zhong M, Guo ZF (2012) Signal transduction during cold, salt, and drought stresses in plants. Mol Biol Rep 39:969–987
Hubbard KE, Nishimura N, Hitomi K, Getzoff ED, Schroeder JI (2010) Early abscisic acid signal trans-duction mechanisms: newly discovered components and newly emerging questions. Genes Dev 24:1695–1708
Hussain SS, Ali M, Ahmad M, Siddique KHM (2011) Polyamines: natural and engineered abiotic and biotic stress tolerance in plants. Biotechnol Adv 29:300–311
Jain M, Tiwary S, Gadre R (2010) Sorbitol-induced changes in various growth and biochemical Param-eters in maize. Plant Soil Environ 6:263–267
Jaleel CA, Manivannan P, Wahid A, Farooq M, Somasundaram R, Panneerselvam R (2009) Drought stress in plants: a review on morphological characteristics and pigments composition. Int J Agric Biol 11:100–105
Jones XIM, Turner NC, Osmond CB (1981) Mechanisms of drought resistance. In: Paleg LPG, Aspmall D (eds) The physiology and biochemistry of drought resistance in plants. Academic, Brisbane, pp 15–37
Kang GZ, Li GZ, Liu GQ, Xu W, Peng XQ, Wang CY, Zhu YJ, Guo TC (2013) Exogenous salicylic acid enhances wheat drought tolerance by influence on the expression of genes related to ascorbate-glutathione cycle. Biologia Planta 57:718–724
Keyvan S (2010) The effects of drought stress on yield, relative water content, proline, soluble carbohydrates and chlorophyll of bread wheat cultivars. J Anim Plant Sci 8:1051–1060
Khan MA, Iqbal M, Jameel M, Nazeer W, Shakir S, Aslam MT, Iqbal B (2011) Potentials of molecular based breeding to enhance drought tolerance in wheat (Triticum aestivum L.). Afr J Biotechnol 10:11340–11344
Khan MA, Iqbal M, Akram M, Ahmad M, Hassan MW, Jameel M (2013) Recent advances in molecular tool development for drought tolerance breeding in cereal crops: a review. Zemdirbyste 100:325–334
Kheradmand MA, Shahmoradzadeh Fahraji S, Fatahi E, Raoofi MM (2014) Effect of water stress on oil yield and some characteristics of Brassica napus. Int Res J Appl Basic Sci 8:1447–1453
Kudla J, Batistic O, Hashimoto K (2010) Calcium signals: the lead currency of plant information processing. Plant Cell 22:541–563
Kuznetsov V, Shorina M, Aronova E, Stetsenko L, Rakitin V, Shevyakova N (2007) NaCl and ethylene-dependent cadaverine accumulation and its possible protective role in the adaptation of the common ice plant to salt stress. Plant Sci 172:363–370
Labudda M, SafiulAzam FM (2014) Glutathione-dependent responses of plants to drought: a review. Acta Soc Bot Pol 83:3–12
Lee HY, Byeon Y, Tan D-X, Reiter RJ, Back K (2015) Arabidopsis serotonin N-acetyltransferase knockout mutant plants exhibit decreased melatonin and salicylic acid levels resulting in susceptibility to an avirulent pathogen. J Pineal Res 58:291–299
Li F, Lei HJ, Zhao XJ, Tian RR, Li TH (2011) Characterization of three sorbitol transporter genes in micro-propagated apple plants grown under drought stress. Plant Mol Biol Rep 30:123–130
Li C, Tan DX, Liang D, Chang C, Jia D, Ma F (2015) Melatonin mediates the regulation of ABA metabolism, free-radical scavenging, and stomatal behaviour in two Malus species under drought stress. J Exp Bot 66:669–680
Madhava Rao KV, Raghavendra AS, Janardhan Reddy K (eds) (2006) Physiology and molecular biology of stress tolerance in plants. Springer, Dordrecht
Mafakheri A, Siosemardeh A, Bahramnejad B, Struik PC, Sohrabi E (2010) Effect of drought stress on yield, proline and chlorophyll contents in three chickpea cultivars. Amer J Chin Stud 4:580–585
Merewitz EB, Gianfagna T, Huang B (2011) Protein accumulation in leaves and roots associated with improved drought tolerance in creeping bentgrass expressing an ipt gene for cytokinin synthesis. J Exp Bot 62:5311
Minguet EG, Vera-Sirera F, Marina A, Carbonell J, Blazquez MA (2008) Evolutionary diversification in polyamine biosynthesis. Mol Biol Evol 25:2119–2128
Mishra AK, Singh VP (2011) Drought modeling—a review. J Hydrol 403:157–175
Mondal S, Bose B (2014) An impact of seed priming on disease resistance: a review. In: Kharwar (ed) Microbial diversity biotechnology food seconds. Springer, New York, pp 193–203
Muller B, Pantin F, Génard M, Turc O, Freixes S, Piques M, Gibon Y (2011) Water deficits uncouple growth from photosynthesis, increase C content, and modify the relationships between C and growth in sink organs. J Exp Bot 62:1715–1729
Munns R, Weir R (1981) Contribution of sugars to osmotic adjustment in elongating and expanded zones of wheat leaves during moderate water deficits at two light levels. Aust J Plant Physiol 8:93–105
Nakashima K, Yamaguchi-Shinozaki K, Shinozaki K (2014) The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat. Front Plant Sci 5:1–8
Nezhadahmadi A, Hossain Prodhan Z, Faruq G (2013) Drought tolerance in wheat. Sci World J 2013:1–12
Nounjana N, Nghiab PT, Theerakulpisuta P (2012) Exogenous proline and trehalose promote recovery of rice seedlings from salt-stress and differentially modulate antioxidant enzymes and expression of related genes. J Plant Physiol 169:596–604
Osakabe Y, Osakabe K, Shinozaki K, Tran LSP (2014) Response of plants to water stress. Front Plant Sci 5:1–7
Paparella S, Araujo SS, Rossi G et al (2015) Seed priming: state of the art and new perspectives. Plant Cell Rep 34:1281–1293
Peng Z, Lu Q, Verma DPS (1996) Reciprocal regulation of D1-pyrroline-5-carboxylate synthetase and proline dehydrogenase genes control levels during and after osmotic stress in plants. Mol Gen Genet 253:334–341
Peng LX, Gu LK, Zheng CC, Li DQ, Shu HR (2006) Expression of MaMAPK gene in seedlings of Malus L. under water stress. Acta Biochim Biophys Sin Shanghai 38:281–286
Rahdari P, Hoseini SM (2012) Drought stress: a review. Int J Agron Plant Prod 3:443–446
Rana RM, Rehman SU, Ahmed J, Bilal M (2013) A comprehensive overview of recent advances in drought stress tolerance research in wheat (Triticum aestivumL.). Asian J Agric Biol 1:29–37
Rangan P, Subramani R, Kumar R, Singh AK, Singh R (2014) Recent advances in polyamine metabolism and abiotic stress tolerance. Biomed Res Int 2014:1–9
Rauf M, Shahzad K, Ali R, Ahmad M, Habib I, Mansoor S, Berkowitz GA, Saeed NA (2014) Cloning and characterization of Na+/H+ antiporter (LfNHX1) gene from a halophyte grass Leptochloa fusca for drought and salt tolerance. Mol Biol Rep 41:1669–1682
Rossato L, Laine P, Ourry A (2001) Nitrogen storage and remobilization in Brassica napus L. during the growth cycle: nitrogen fluxes within the plant and changes in soluble protein patterns. J Exp Bot 52:1655–1663
Sagi M, Fluhr R (2006) Production of reactive oxygen species by plant NADPH oxidases. Plant Physiol 141:336–340
Sakamoto A, Murata N (2000) Genetic engineering of glycinebetaine synthesis in plants: current status and implications for enhancement of stress tolerance. J Exp Bot 51:81–88
Salehi-lisar SY, Bakhshayeshan-Agdam H (2016) In: Hossain MA, Wani SH, Bhattacharjee S, Burritt DJ, Tran L-SP (eds) Drought stress in plants: causes, consequences, and tolerance, drought stress tolerance in plants, vol 1. Springer, New York
Salehi-lisar SY, Motafakkerazad R, Hossain MM, Rahman IMM (2012) Water stress in plants: causes, effects and responses, water stress. In: Ismail Md. Mofizur Rahman (ed). InTech
Sapeta H, Costa M, Lourenc T, Marocod J, Van der Linde P, Oliveiraa MM (2013) Drought stress response in Jatropha curcas: growth and physiology. Environ Exp Bot 85:76–84
Schenk PM, Kazan K, Wilson I, Anderson JP, Richmond T, Somerville SC, Manners JM (2000) Coordinated plant defense responses in Arabidopsis revealed by microarray analysis. Proc Natl Acad Sci U S A 97:11655–11660
Shao HB, Chu LY, Jaleel CA, Zhao CX (2008a) Water-deficit stress-induced anatomical changes in higher plants. C R Biol 331:215–225
Shao HB, Chu LY, Lu ZH, Kang CM (2008b) Primary antioxidant free radical scavenging and redox signaling pathways in higher plant cells. Int J Biol Sci 4:8–14
Singh M, Kumar J, Singh S, Singh VP, Prasad SM (2015) Roles of osmoprotectants in improving salinity and drought tolerance in plants: a review. Rev Environ Sci Bio Technol 14:407–426
Song XG, She XP, He JM, Huang C, Song TS (2006) Cytokinin-and auxin-induced stomatal opening involves a decrease in levels of hydrogen peroxide in guard cells of Vicia faba. Funct Plant Biol 33:573–583
Steinhorst L, Kudla J (2013) Calcium and reactive oxygen species rule the waves of signaling. Plant Physiol 163:471–485
Stepanova AN, Alonso JM (2009) Ethylene signaling and response: where different regulatory modules meet. Curr Opin Plant Biol 12:548–555
Suarez Rodriguez MC, Petersen M, Mundy J (2010) Mitogen-activated protein kinase signaling in plants. Annu Rev Plant Biol 61:621–649
Taiz L, Zeiger E (2010) Plant physiology, 5th edn. Sinauer Associates, Sunderland
Tari I, Kiss G, Deér AK, Csiszár J, Erdei L, Gallé Á, Gémes K, Horváth F, Poór P, Szepesi Á, Simon LM (2010) Salicylic acid increased aldose reductase activity and sorbitol accumulation in tomato plants under salt stress. Biol Plant 54:677–683
Trenberth KE, Dai A, van der Schrier G, Jones PD, Barichivich J, Briffa KR, Sheffield J (2014) Global warming and changes in drought. Nat Clim Change 4:17–22
Trujillo LE, Sotolongo M, Menendez C, Ochogavia ME, Coll Y, Hernandez I, Borras-Hidalgo O, Thomma BPHJ, Vera P, Hernandez L (2008) SodERF3, a novel sugarcane ethylene responsive factor (ERF), enhances salt and drought tolerance when overexpressed in tobacco plants. Plant Cell Physiol 49:512–525
Verbruggen N, Hermans C (2008) Proline accumulation in plants: a review. Amino Acids 35:753–759
Vinocur B, Altman A (2005) Recent advances in engineering plant tolerance to abiotic stress: achievements and limitations. Curr Opin Biotechnol 16:123–132
Wang J, Ding H, Zhang A, Ma F, Cao J, Jiang M (2010) A novel mitogen-activated protein kinase gene in maize (Zea mays), ZmMPK3, is involved in response to diverse environmental cues. J Integr Plant Biol 52:442–452
Wang P, Sun X, Li C, Wei Z, Liang D, Ma F (2013) Long-term exogenous application of melatonin delays drought-induced leaf senescence in apple. J Pineal Res 54:292–302
Wu H, Wu X, Li Z, Duan L, Zhang M (2012) Physiological evaluation of drought stress tolerance and recovery in cauliflower (Brassica oleracea L.) seedlings treated with methyl jasmonate and coronatine. J Plant Growth Regul 31:113–123
Xia XJ, Zhou YH, Shi K, Zhou J, Foyer CH, Yu JQ (2015) Interplay between reactive oxygen species and hormones in the control of plant development and stress tolerance. J Exp Bot 66:2839–2856
Xiong L, Schumaker KS, Zhu JK (2002) Cell signaling during cold, drought, and salt stress. Plant Cell 14:165–183
Xoconostle-Cazares B, Ramirez-Ortega FA, Flores-Elenes L, Ruiz-Medrano R (2010) Drought tolerance in crop plants. Am J Plant Physiol 5:241–256
Xu Q, Burgess P, Huang B (2016) Stress-inhibition and gibberellin-mitigation of leaf elongation associated with up-regulation of genes controlling cell expansion. Physiologia Planta 131:101
Yu K, Wei J, Ma Q, Yu D, Li J (2009) Senescence of aerial parts is impeded by exogenous gibberellic acid in herbaceous perennial Paris polyphylla. J Plant Physiol 166:819–830
Zare M, Azizi MH, Bazrafshan F (2011) Effect of drought stress on some agronomic traits in ten barley (Hordeum vulgare) cultivars. Tech J Eng Appl Sci 1:57–62
Zhang S, Liu Y (2001) Activation of salicylic acid–induced protein kinase, a mitogen activated protein kinase, induces multiple defense responses in tobacco. Plant Cell 13:1877–1889
Zlatev Z, Lidon FC (2012) An overview on drought induced changes in plant growth, water relations and photosynthesis. Emir J Food Agric 24:57–72
Zuo B, Zheng X, He P, Wang L, Lei Q, Feng C, Zhou J, Li Q, Han Z, Kong J (2014) Over expression of MzASMT improves melatonin production and enhances drought tolerance in transgenic Arabidopsis thaliana plants. J Pineal Res 57:408–417
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Salehi-Lisar, S.Y., Bakhshayeshan-Agdam, H. (2020). Agronomic Crop Responses and Tolerance to Drought Stress. In: Hasanuzzaman, M. (eds) Agronomic Crops. Springer, Singapore. https://doi.org/10.1007/978-981-15-0025-1_5
Download citation
DOI: https://doi.org/10.1007/978-981-15-0025-1_5
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-15-0024-4
Online ISBN: 978-981-15-0025-1
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)