Abstract
Abiotic stresses are the most important limiting factors for crop productivity worldwide in the wake of climatic change. Among the various kinds of abiotic stresses, chilling is one of the important components that limit the growth and final productivity of field crops. Chilling-induced adversities in plant growth and yield mainly occur due to physical and biochemical damages, physiological alterations, and molecular disruptions. Several management approaches are being tested in reducing the detrimental impacts of chilling stress. Seed priming can be a good approach to overcome the negative effects of the chilling stress in different crops. Primed seeds show increased germination rates and better seedling establishment which result in high level of chilling stress tolerance and vigorous plant growth. This chapter provides an overview of physiological, morphological, and biochemical responses of crops to chilling stress and highlights the role of seed priming in augmenting chilling tolerance in crop plants.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- ABA:
-
Abscisic acid
- APX:
-
Ascorbate peroxidase
- AQP:
-
Aquaporin
- But:
-
Butenolide
- CAT:
-
Catalase
- Ct:
-
Chitosan
- GA3:
-
Gibberellic acid
- H2O2:
-
Hydrogen peroxide
- KNO3:
-
Potassium nitrate
- LEAs:
-
Late embryogenesis abundant proteins
- PAs:
-
Polyamines
- PB:
-
Plant biostimulants
- PEG:
-
Polyethylene glycol
- POD:
-
Peroxidase
- Put:
-
Putrescine
- ROS:
-
Reactive oxygen species
- SMP:
-
Solid matrix priming
- SOD:
-
Superoxide dismutase
References
Abebe AT, Modi AT (2009) Hydropriming in dry bean (Phaseolus vulgaris L.). Res J Seed Sci 2:23–31
Afzal I, Basra SM, Ahmad N, Cheema MA, Warraich EA, Khaliq A (2002) Effect of priming and growth regulator treatments on emergence and seedling growth of hybrid maize (Zea mays L.). Int J Agric Biol 4:303–306
Ajouri H, Asgedom H, Becker M (2004) Seed priming enhances germination and seedling growth of barley under conditions of P and Zn deficiency. J Plant Nutr Soil Sci 167:630–636
Alcazar R, Altabella T, Marco F, Bortolotti C, Reymond M, Koncz C, Carrasco P, Tiburcio A (2010) Polyamines: molecules with regulatory functions in plant abiotic stress tolerance. Planta 231:1237–1249
Allen DJ, Ort DR (2001) Impacts of chilling temperatures on photosynthesis in warm-climate plants. Trends Plant Sci 6:36–42
Al-Mudaris MA, Jutzi SC (1999) The influence of fertilizer-based seed priming treatment on emergence and seedling growth of Sorghum bicolor and Pennisetum glaucum in pot trials under greenhouse conditions. J Agron Crop Sci 182:135–141
Altman A (2006) Polyamines and wounded storage tissues–inhibition of RNase activity and solute leakage. Physiol Plant 54:194–198
Amooaghaie R, Nikzad K (2013) The role of nitric oxide in priming-induced low-temperature tolerance in two genotypes of tomato. Seed Sci Res 23:123–131
Andaya VC, Mackill DJ (2003) Mapping of QTLs associated with cold tolerance during the vegetative stage in rice. J Exp Bot 54:257–2585
Arif M, Waqas M, Nawab K, Shahid M (2007) Effect of seed priming in Zn solutions on chickpea and wheat. Afr Crop Sci Conf Proc 8:237–240
Arif M, Jan MT, Marwat KB, Khan MA (2008) Seed priming improves emergence and yield of soybean. Pak J Bot 40:1169–1177
Aroca R, Vernieri P, Irigoyen JJ, Sancher-Diaz M, Tognoni F, Pardossi A (2003) Involvement of abscisic acid in leaf and root of maize (Zea mays L.) in avoiding chilling-induced water stress. Plant Sci 165:671–679
Baker SS, Wilhelm KS, Thomashow MF (1994) The 5′-region of Arabidopsis thaliana Cor15a has cis-acting elements that confer cold-regulated, drought-regulated and ABA-regulated gene-expression. Plant Mol Biol 24:701–713
Barba-Espın G, Hernandez JA, Diaz-Vivancos P (2012) Role of H2O2 in pea seed germination. Plant Signal Behav 7:193–195
Barea JM, Salamanca CP, Herrera MA (1993) Inoculation of woody legumes with selected arbuscular mycorrhizal fungi and rhizobia to recover desertified mediterranean ecosystem. Appl Environ Microbiol 59:129–133
Beckers GJM, Jaskiewicz M, Liu YD (2009) Underwood WR, He SY, Zhang SQ, Conrath U. mitogen-activated protein kinases 3 and 6 are required for full priming of stress responses in Arabidopsis thaliana. Plant Cell 21:944–953
Ben-Haj-Salah H, Tardieu F (1995) Temperature affects expansion rate of maize leaves without change in spatial distribution of cell length. Plant Physiol 109:861–870
Bennett AJ, Whipps JM (2008) Dual application of beneficial microorganisms to seed during drum priming. Appl Soil Ecol 38:83–89
Besford RT, Richardson CM, Campos JL, Tiburcio AF (1993) Effect of polyamines on stabilization of molecular complexes in thylakoid membranes of osmotically stressed oat leaves. Planta 189:201–206
Bies-Ethève N, Gaubier-Comella P, Debures A, Lasserre E, Jobet E, Raynal M, et al. (2008) Inventory, evolution and expression profiling diversity of the LEA (late embryogenesis abundant) protein gene family in Arabidopsis thaliana. Plant Mol Biol 67:107–124
Blomster T, Salojarvi J, Sipari N, Brosche M, Ahlfors R, Keinanen M, Overmyer K, Kangasjarvi J (2011) Apoplastic reactive oxygen species transiently decrease auxin signaling and cause stress-induced morphogenic response in Arabidopsis. Plant Physiol 157:1866–1883
Bolkhina O, Virolainen E, Fagerstedt K (2003) Antioxidants, oxidative damage and oxygen deprivation stress: a review. Ann Bot 91:179–194
Boucher V, Buitink J, Lin X, Boudet J, Hoekstra FA, Hundertmark M, Renard D, Leprince O (2010) MtPM25 is an atypical hydrophobic late embryogenesis-abundant protein that dissociates cold and desiccation-aggregated proteins. Plant Cell Environ 33:418–430
Bowler C, Van Montagu M, Inze D (1992) Superoxide dismutase and stress tolerance. Annu Rev Plant Physiol Plant Mol Biol 43:83–116
Bradford KJ (1986) Manipulation of seed water relations via osmotic priming to improve germination under stress conditions. Hortic Sci 21:1005–1112
Bulgari R, Cocetta G, Trivellini A, Vernieri P, Ferrante A (2014) Biostimulants and crop responses: a review. Biol Agric Hortic 31:1–17
Callan NW, Mathre DE, Miller JB (1990) Bio-priming seed treatment for biological control of Pythium ultimum pre emergence damping off in sh2 sweet corn. Plant Dis 74:368–372
Candat A, Paszkiewicz G, Neveu M, Gautier R, Logan DC, Avelange-Macherel MH, Macherel D (2014) The ubiquitous distribution of late embryogenesis abundant proteins across cell compartments in Arabidopsis offers tailored protection against abiotic stress. Plant Cell:114
Casenave EC, Toselli ME (2007) Hydropriming as a pre-treatment for cotton germination under thermal and water stress conditions. Seed Sci Technol 35:88–98
Chen K, Arora R (2011) Dynamics of the antioxidant system during seed osmopriming, post-priming germination, and seedling establishment in spinach (Spinacia oleracea). Plant Sci 180:212–220
Chen K, Arora R, Arora U (2010) Osmopriming of spinach (Spinacia oleracea L. cv. Bloomsdale) seeds and germination performance under temperature and water stress. Seed Sci Technol 38:45–57
Chen H, Chu P, Zhou Y, Li Y, Liu J, Ding Y et al (2012a) Overexpression of AtOGG1, a DNA glycosylase/AP lyase, enhances seed longevity and abiotic stress tolerance in Arabidopsis. J Exp Bot 63:4107–4121
Chen K, Fessehaie A, Arora R (2012b) Dehydrin metabolism is altered during seed osmopriming and subsequent germination under chilling and desiccation in Spinacia oleracea L. cv. Bloomsdale: possible role in stress tolerance. Plant Sci 183:27–36
Chen K, Fessehaie A, Arora R (2013) Aquaporin expression during seed osmopriming and post-priming germination in spinach. Biol Plant 57:193–198
Chen W, Guo C, Hussain S, Zhu B, Deng F, Xue Y, et al. (2015) Role of xylo-oligosaccharides in protection against salinity-induced adversities in Chinese cabbage. Environ Sci Pollut Res 23:1254–1264
Chen W, Guo C, Hussain S, Zhu B, Deng F, Xue Y, Geng M, Wu L (2016) Role of xylo-oligosaccharides in protection against salinity-induced adversities in Chinese cabbage. Environ Sci Pollut Res 23:1254–1264
Cheng C, Yun KY, Ressom HW, Mohanty B, Bajic VB, Jia Y et al (2007) An early response regulatory cluster induced by low temperature and hydrogen peroxide in seedlings of chilling-tolerant japonica rice. BMC Genomics 8:175
Chinnusamy V, Zhu J, Zhu JK (2007) Cold stress regulation of gene expression in plants. Trends Plant Sci 12:444. https://doi.org/10.1016/j.tplants.2007.07.00
Clarke HJ, Siddique KHM (2004) Response of chickpea genotypes to low temperature stress during reproductive development. Field Crop Res 90:323–334
Cruz R, Milach S (2004) Cold tolerance at the germination stage of rice: methods of evaluation and characterization of genotypes. Sci Agric 61:1–8
Cuevas JC, Lopez-Cobollo R, Alcazar R, Zarza X, Koncz C, Altabella T, Salinas J, Tiburcio AF, Ferrando A (2008) Putrescine is involved in Arabidopsis freezing tolerance and cold acclimation by regulating abscisic acid levels in response to low temperature. Plant Physiol 148:1094–1105
Cutforth HW, Shaykewich CF, Cho CM (1986) Effect of soil water and temperature on corn (Zea mays L.) root growth during emergence. Can J Soil Sci 66:51–58
Demir I, Ozuaydın I, Yasar F, Staden JV (2012) Effect of smoke derived butenolide priming treatment on pepper and salvia seeds in relation to transplant quality and catalase activity. S Afr J Bot 78:83–87
Deng B, Du W, Liu C, Sun W, Tian S, Dong H (2012) Antioxidant response to drought, cold and nutrient stress in two ploidy levels of tobacco plants: low resource requirement confers polytolerance in polyploids? Plant Growth Regul 66:37–47
Devinar G, Llanes A, Masciarelli O, Luna V (2013) Different relative humidity conditions combined with chloride and sulfate salinity treatments modify abscisic acid and salicylic acid levels in the halophyte Prosopis strombulifera. Plant Growth Regul 70:247–256
Draganić I, Lekić S (2012) Seed priming with antioxidants improves sunflower seed germination and seedling growth under unfavorable germination conditions. Turk J Agric For 36:421–428
Dure L, Crouch M, Harada JJ, Ho T, Mundy J, Quatrano RS, Thomas TL, Sung ZR (1989) Common amino acid sequence domains among the LEA proteins of higher plants. Plant Mol Biol 12:475–486
Elkoca E, Haliloglu K, Esitken A, Ercisli S (2007) Hydro- and osmopriming improve chickpea germination. Acta Agric Scand Sect B Soil Plant Sci 57:193–200
Fahad S, Nie L, Chen Y, Wu C, Xiong D, Saud S, Hongyan L, Cui K, Huang L (2015) Crop plant hormones and environmental stress. Sustain Agric Rev 15:371–400
Farooq M, Aziz T, Wahid A, Lee DJ, Siddique KHM (2009) Chilling tolerance in maize: agronomic and physiological approaches. Crop Pasture Sci 60:501–516
Finch-Savage WE, Dent KC, Clark LJ (2004) Soak conditions and temperature following sowing influence the response of maize (Zea mays L.) seeds to on-farm priming (pre-sowing seed soak). Field Crop Res 90:361–374
Foti R, Aburenia K, Tigerea A, Gotosab J, Gerec J (2008) The efficacy of different seed priming osmotica on the establishment of maize (Zea mays L.) caryopses. J Arid Environ 72:1127–1130
Gadjev I, Vanderauwera S, Gechev TS, Laloi C, Minkov IN, Shulaev V, Apel K, Inze D, Mittler R, Van Breusegem F (2006) Transcriptomic footprints disclose specificity of reactive oxygen species signaling in Arabidopsis. Plant Physiol 141:436–445
Gallardo K, Job C, Groot SPC, Puype M, Demol H, Vandekerckhove J, Job D (2001) Proteomic analysis of Arabidopsis seed germination and priming. Plant Physiol 126:835–848
Gao YP, Bonham-Smith PC, Gusta LV (2002) The role of peroxiredoxin antioxidant and calmodulin in ABA-primed seeds of Brassica napus exposed to abiotic stresses during germination. J Plant Physiol 159:951–958
Gao CH, Hu J, Zhang S (2009) Association of polyamines in governing the chilling sensitivity of maize genotypes. Plant Growth Regul 57:31–38
Ghana SG, Schillinger WF (2003) Seed priming winter wheat for germination, emergence, and yield. Crop Sci 43:2135–2141
Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930
Goswami A, Banerjee R, Raha S (2013) Drought resistance in rice seedlings conferred by seed priming: role of the anti-oxidant defense mechanisms. Protoplasma 250:1115–1129
Guan YJ, Hu J, Wang XJ, Shao CX (2009) Seed priming with chitosan improves maize germination and seedling growth in relation to physiological changes under low temperature stress. J Zhejiang Univ Sci B 10:427–433
Hamza B, Suggars A (2001) Biostimulants: myths and realities. TurfGrass Trends 8:6–10
Hancock JT, Neill SJ, Wilson ID (2011) Nitric oxide and ABA in the control of plant function. Plant Sci 181:555–559
Harris D, Joshi A, Khan PA, Gothkar P et al (1999) On-farm seed priming in semiarid agriculture: development and evaluation in maize, rice and chickpea in India using participatory methods. Exp Agric 35:15–29
Harris D, Rashid A, Miraj G, Arif M, Shah H (2007) ‘On-farm’ seed priming with zinc sulphate solution – a cost-effective way to increase the maize yields of resource-poor farmers. Field Crop Res 102:119–127
Hasanuzzaman M, Anwar HM, Fujita M (2010) Selenium in higher plants: physiological role, antioxidant metabolism and abiotic stress tolerance. J Plant Sci 5:354–375
Hasanuzzaman M, Hossain MA, Fujita M (2012) Exogenous selenium pretreatment protects rapeseed seedlings from cadmium-induced oxidative stress by upregulating antioxidant defense and methylglyoxal detoxification systems. Biol Trace Elem Res 149:248–261
He L, Nada K, Tachibana S (2002) Effects of spermidine pretreatment through the roots on growth and photosynthesis of chilled cucumber plants (Cucumis sativus L.). J Jpn Soc Hort Sci 71:490–498
Hodges DM, Andrews CJ, Johnson DA, Hamilton RI (1997) Antioxidant enzyme responses to chilling stress in differentially sensitive inbred maize lines. J Exp Bot 48:1105–1113
Huang M, Guo Z (2005) Responses of antioxidative system to chilling stress in two rice cultivars differing in sensitivity. Biol Plant 9:81–84
Hundertmark M, Hincha DK (2008) LEA (late embryogenesis abundant) proteins and their encoding genes in Arabidopsis thaliana. BMC Genomics 9:118. https://doi.org/10.1186/1471-2164-9-118
Hussain A, Maqsood MA (2011) Root zone temperature influences nutrient accumulation and use in maize. Pak J Bot 43:1551–1556
Hussain S, Zheng M, Khan F, Khaliq A, Fahad S, Peng S et al (2015) Benefits of rice seed priming are offset permanently by prolonged storage and the storage conditions. Sci Rep 5:8101. https://doi.org/10.1038/srep08101
Hussain S, Khan F, Hussain HA, Nie L (2016a) Physiological and biochemical mechanisms of seed priming-induced chilling tolerance in rice cultivars. Front Plant Sci 7:116. https://doi.org/10.3389/fpls.2016.00116
Hussain S, Khan F, Cao W, Wu L, Geng M (2016b) Seed priming alters the production and detoxification of reactive oxygen intermediates in rice seedlings grown under sub-optimal temperature and nutrient supply. Front Plant Sci 7:439
Hussain HA, Hussain S, Khaliq A, Ashraf U, Anjum SA, Men S, Wang L (2018a) Chilling and drought stresses in crop plants: implications, cross talk, and potential management opportunities. Front Plant Sci 9:393. https://doi.org/10.3389/fpls.2018.00393
Hussain S, Khaliq A, Tanveer M, Matloob A, Hussain HA (2018b) Aspirin priming circumvents the salinity-induced effects on wheat emergence and seedling growth by regulating starch metabolism and antioxidant enzyme activities. Acta Physiol Plant 40(4):68
Imran M, Mahmood A, Römheld V, Neumann G (2013) Nutrient seed priming improves seedling development of maize exposed to low root zone temperatures during early growth. Eur J Agron 49:141–148
Iqbal M, Ashraf M (2007) Seed preconditioning modulates growth, ionic relations, and photosynthetic capacity in adult plants of hexaploid wheat under salt stress. J Plant Nutr 30:381–396
Jain N, Kulkarni MG, Van Staden J (2006) Abutenolide isolated from smoke can overcome the detrimental effect of extreme temperatures during tomato seed germination. Plant Growth Regul 49:263–267
Janowiak F, Markowski A (1994) Changes in leaf water relations and injuries in maize seedlings induced by different chilling conditions. J Agron Crop Sci 172:19–28
Janowiak F, Maas B, Dörffling K (2002) Importance of abscisic acid for chilling tolerance of maize seedlings. J Plant Physiol 159:635–643
Jett LW, Welbaum GE, Morse RD (1996) Effect of matric and osmotic priming treatments on broccoli seed germination. J Am Soc Hortic Sci 121:423–429
Jisha KC, Vijayakumari K, Puthur JT (2013) Seed priming for abiotic stress tolerance: an overview. Acta Physiol Plant 35:1381–1396
Kaspar TC, Bland WL (1992) Soil temperature and root growth. Soil Sci 154:290–299
Kang HM, Saltveit ME (2002a) Chilling tolerance of maize, cucumber and rice seedling leaves and roots are differentially affected by salicylic acid. Physiol Plant 115(4):571–576
Kang HM, Saltveit ME (2002b) Reduced chilling tolerance in elongating cucumber seedling radicles is related to their reduced antioxidant enzyme and DPPH-radical scavenging activity. Physiol Plant 115(2):244–250
Kaur S, Gupta AK, Kaur N (2002) Effect of osmo- and hydropriming of chickpea on seedling growth and carbohydrate metabolism under water deficit stress. Plant Growth Regul 37:17–22
Kaya MD, Okcu G, Atak M, Cikili Y, Kolsarici O (2006) Seed treatments to overcome salt and drought stress during germination in sunflower (Helianthus annuus L.). Eur J Agron 24:291–295
Khaliq A, Aslam F, Matloob A, Hussain S, Geng M, Wahid A et al (2015) Seed priming with selenium: consequences for emergence, seedling growth, and biochemical attributes of rice. Biol Trace Elem Res 166:236–244
Khan MB, Gurchani MA, Hussain M, Freed S, Mahmood K (2011) Wheat seed enhancement by vitamin and hormonal priming. Pak J Bot 43:1495–1499
Khan TA, Fariduddin Q, Yusuf M (2017) Low-temperature stress: is phytohormones application a remedy? Environ Sci Pollut Res 24:21574–21590
Khan F, Hussain S, Tanveer M, Khan S, Hussain HA, Iqbal B, Geng M (2018) Coordinated effects of lead toxicity and nutrient deprivation on growth, oxidative status, and elemental composition of primed and non-primed rice seedlings. Environ Sci Pollut Res 25:21185. https://doi.org/10.1007/s11356-018-2262-1
Kovacs Z, Simon-Sarkadi L, Szucs A, Kocsy G (2010) Differential effects of cold, osmotic stress and abscisic acid on polyamine accumulation in wheat. Amino Acids 38:623–631
Kubala S, Garnczarska M, Wojtyla Ł, Clippe A, Kosmala A, Zmienko A et al (2015) Deciphering priming-induced improvement of rapeseed (Brassica napus L.) germination through an integrated transcriptomic and proteomic approach. Plant Sci 231:94–113
Kubik KK, Eastin JA, Eskridge KM (1988) Solid matrix priming of tomato and pepper. In: Proceedings of the international conference on stand establishment for horticultural crops. Lancaster, Pennsylvania, pp 86–96
Kumar RR, Goswami S, Singh K, Rai GK, Rai RD (2013) Modulation of redox signal transduction in plant system through induction of free radical/ROS scavenging redox-sensitive enzymes and metabolites. Aus J Crop Sci 7:1744–1751
Lee SS, Kim JH, Hong SB, Yuu SH, Park EH (1998) Priming effect of rice seeds on seedling establishment under adverse soil conditions. Korean J Crop Sci 43:194–198
Leyva A, Jarillo JA, Salinas J, Martinezzapater JM (1995) Low-temperature induces the accumulation of phenylalanine ammonia-lyase and chalcone synthase messenger-RNAs of Arabidopsis thaliana in a light-dependent manner. Plant Physiol 108:39–46
Li X, Jiang H, Liu F, Cai J, Dai T, Cao W, Jiang D (2013) Induction of chilling tolerance in wheat during germination by pre-soaking seed with nitric oxide and gibberellin. Plant Growth Regul 71:31–40
Li Z, Peng Y, Zhang XQ, Ma X, Huang LK, Yan YH (2014) Exogenous spermidine improves seed germination of white clover under water stress via involvement in starch metabolism, antioxidant defenses and relevant gene expression. Molecules 19:18003–18024
Li XN, Pu HC, Liu FL, Zhou Q, Cai J, Dai TB et al (2015) Winter wheat photosynthesis and grain yield responses to spring freeze. Agron J 107:1002–1010
Li Z, Xu J, Gao Y, Wang C, Guo G, Luo Y, Huang Y, Hu W, Sheteiwy MS, Guan Y, Hu J (2017) The synergistic priming effect of exogenous salicylic acid and H2O2 on chilling tolerance enhancement during maize (Zea mays L.) seed germination. Front Plant Sci 8:1153. https://doi.org/10.3389/fpls.2017.01153
Liu X, Wang L, Liu L, Guo Y, Ren H (2011) Alleviating effect of exogenous nitric oxide in cucumber seedling against chilling stress. Afr J Biotechnol 10:4380–4386
Lorenzo MCB (1991) Seed invigoration of soybean and corn through solid matrix priming. BS, Philippines
Lukatkin AS, Brazaitytė A, Bobinas Č, Duchovskis P (2012) Chilling injury in chilling-sensitive plants: a review. Zemdirbyste-Agriculture 99:111–124
Macovei A, Tuteja N (2013) Different expression of miRNAs targeting helicases in rice in response to low and high dose rate γ-ray treatments. Plant Signal Behav 8:25128
Manish K, Geetika S, Renu B, Sandeep K, Gaganodeep J (2010) Effect of exogenous H2O2 on antioxidant enzymes of Brassica juncea L. seedlings in relation to 24-epibrassinolide under chilling stress. Indian J Biochem Biophys 47:378–382
Manjunatha G, Raj SN, Shetty NP, Shetty HS (2008) Nitric oxide donor seed priming enhances defense responses and induces resistance against pearl millet downy mildew disease. Pestic Biochem Physiol 91:1–11
Marschner H (1995) Mineral nutrition of higher plants, 2nd edn. Academic, San Diego
Martínez-Tellez MA, Ramos-Clamont MG, Gardea AA, Vargas-Arispuro I (2002) Effect of infiltrated polyamines on polygalacturonase activity and injury response in zucchini squash (Cucurbita pepo L.). Biochem Biophys Res Commun 295:98–101
Maughan S, Foyer CH (2006) Engineering and genetic approaches to modulating the glutathione network in plants. Physiol Plant 126:382–397
McDonald MB (1999) Seed deterioration: physiology, repair and assessment. Seed Sci Technol 27:177–237
McDonald MB (2000) Seed priming. In: Black M, Bewley JD (eds) Seed technology and its biological basis. Sheffield Academic Press, Sheffield, pp 287–325
Mercado MFO, Fernandez PG (2002) Solid matrix priming of soybean seeds. Philipp J Crop Sci 27:27–35
Miao Y, LvD WP, Wang XC, Chen J, Miao C, Song CP (2006) An Arabidopsis glutathione peroxidase functions as both a redox transducer and a scavenger in abscisic acid and drought stress responses. Plant Cell 18:2749–2766
Miller G, Suzuki N, Ciftci-Yilmaz S, Mittler R (2009) Reactive oxygen species homeostasis and signaling during drought and salinity stresses. Plant Cell Environ 33:453–467
Mittler R, Kim Y, Song LH, Coutu J, Coutu A, Ciftci-Yilmaz S, Lee H, Stevenson B, Zhu JK (2006) Gain- and loss-of-function mutations in Zat10 enhance the tolerance of plants to abiotic stress. FEBS Lett 580:6537–6542
Moeinzadeh A, Sharif-Zadeh F, Ahmadzadeh M, Heidari Tajabadi F (2010) Biopriming of sunflower (Helianthus annuus L.) seeds with Pseudomonas fluorescens for improvement of seed invigoration and seedling growth. Aust J Crop Sci 4:564–570
Moradi A, Younesi O (2009) Effects of osmo- and hydropriming on seed parameters of grain sorghum (Sorghum bicolor L.). Aust J Basic Appl Sci 3:1696–1700
Munekage YN, Inoue S, Yoneda Y, Yokota A (2015) Distinct palisade tissue development processes promoted by leaf autonomous signalling and long‐distance signalling in A rabidopsis thaliana. Plant, Cell Environ 38(6):1116–116
Nakayama K, Okawa K, Kakizaki T, Inaba T (2008) Evaluation of the protective activities of a late embryogenesis abundant (LEA) related protein, Cor15am, during various stresses in vitro. Biosci Biotechnol Biochem 72:1642–1645
Nascimento WM, West SH (1998) Priming and seed orientation affect emergence and seed coat adherence and seedling development of muskmelon transplants. Hortic Sci 33:847–848
Nayyar H (2005) Putrescine increases floral retention, pod set and seed yield in cold stressed chickpea. J Agron Crop Sci 191:340–345
Nayyar H, Bains T, Kumar S (2005) Low temperature induced floral abortion in chickpea: relationship to abscisic acid and cryoprotectants in reproductive organs. Environ Exp Bot 53:39–48
Neill SJ, Desikan R, Hancock JT (2003) Nitric oxide signalling in plants. New Phytol 159:11–35
Oliver SN, Dennis ES, Dolferus R (2007) ABA regulates apoplastic sugar transport and is a potential signal for cold-induced pollen sterility in rice. Plant Cell Physiol 48:1319–1330
Pandita VK, Anand A, Nagarajan S, Seth R, Sinha SN (2010) Solid matrix priming improves seed emergence and crop performance in okra. Seed Sci Technol 38:665–674
Paparella S, Araújo SS, Rossi G, Wijayasinghe M, Carbonera D, Balestrazzi A (2015) Seed priming: state of the art and new perspectives. Plant Cell Rep 34:1281–1293
Patade VY, Khatri D, Manoj K, Kumari M, Ahmed Z (2012) Cold tolerance in thiourea primed capsicum seedlings is associated with transcript regulation of stress responsive genes. Mol Biol Rep 39:10603–10613
Posmyk MM, Janas KM (2007) Effects of seed hydropriming in presence of exogenous proline on chilling injury limitation in Vigna radiata L. seedlings. Acta Physiol Plant 29:509–517
Posmyk MM, Corbineau F, Vinel D, Bailly C, Côme D (2001) Osmoconditioning reduces physiological and biochemical damage induced by chilling in soybean seeds. Physiol Plant 111:473–482
Pozo MJ, Azcón-Aguilar C (2007) Unraveling mycorrhiza-induced resistance. Curr Opin Plant Biol 10:393–398
Prasad TK (1997) Role of catalase in inducing chilling tolerance in pre emergence maize seedlings. Plant Physiol 114:1369–1376
Rakesh P, Prasad RD, Devi GU, Bhat BN (2017) Effect of biopolymers and synthetic seed coating polymers on castor and groundnut seed. Int J Pure Appl Biosci 5(4):2043–2048
Rehman A, Farooq M, Naveed M, Nawaz A, Shahzad B (2018) Seed priming of Zn with endophytic bacteria improves the productivity and grain biofortification of bread wheat. Eur J Agron 94:98–107
Richner W, Soldati A, Stamp P (1996) Shoot-to-root relations in field-grown maize seedlings. Agron J J88:56–61
Ros CR, Belland W, White PF (2000) Phosphorous seed coating and soaking for improving seedling growth of Oryza sativa (rice) cv IR66. Seed Sci Technol 28:391–401
Rossel JB, Wilson PB, Hussain D, Woo NS, Gordon MJ, Mewett OP, Howell KA, Whelan J, Kazan K, Pogson BJ (2007) Systemic and intracellular responses to photooxidative stress in Arabidopsis. Plant Cell 19:4091–4110
Ruelland E, Vaultier MN, Zachowski A, Hurry V (2009) Cold signalling and cold acclimation in plants. Adv Bot Res 49:35–150
Sahu MP, Kumawat SM, D’Souza SF, Ramaswamy NK, Singh G (2005) Sulphydryl bioregulator technology for increasing mustard production. Res Bull RAUBARC:1–52
Sakhabutdinova AR, Fatkhutdinova DR, Beazrukova MV, Shakirova FM (2003) Salicylic acid prevents the damaging action of stress factor of wheat plants. Bulg J Plant Physiol Spec Issue:314–319
Sarhan F, Oullet F, Vazquez-Tello A (1997) The wheat wcs 120 gene family. A useful model to understand the molecular genetics of freezing tolerance in cereals. Physiol Plant 101:439–445
Savvides A, Ali S, Tester M, Fotopoulos V (2016) Chemical priming of plants against multiple abiotic stresses: mission possible? Trends Plant Sci 21:329–340
Sethi V, Raghuram B, Sinha AK, Chattopadhyay S (2014) A mitogen-activated protein kinase cascade module, MKK3-MPK6 and MYC2, is involved in blue light-mediated seedling development in Arabidopsis. Plant Cell 26:3343–3357
Shao CX, Hu J, Song WJ, Hu WM (2005) Effects of seed priming with chitosan solutions of different acidity on seed germination and physiological characteristics of maize seedling. J Zhejiang Univ Agric Life Sci 31:705–708
Sharma HSS, Fleming C, Selby C, Rao JR, Martin T (2014) Plant biostimulants: a review on the processing of macroalgae and use of extracts for crop management to reduce abiotic and biotic stresses. J Appl Phycol 26:465–490
Sharmila P, Puthur JT, Pardha Saradhi P (2000) Vesicular arbuscular mycorrhizal fungi improves establishment of micropropagated plants. In: Mukerji KG, Chamola BP, Singh J (eds) Mycorrhizal biology. Kluwer Academic/Plenum, New York, pp 236–250
Singh B, Usha K (2003) Salicylic acid induced physiological and biochemical changes in wheat seedlings under water stress. Plant Growth Regul 39:137–141
Soeda Y, Konings MC, Vorst O, van Houwelingen AM, Stoopen GM, Maliepaard CA et al (2005) Gene expression programs during Brassica oleracea seed maturation, osmopriming, and germination are indicators of progression of the germination process and the stress tolerance level. Plant Physiol 137:354–368
Srivastava AK, Lokhande VH, Patade VY, Suprasanna P, Sjahril R, D’Souza SF (2010) Comparative evaluation of hydro-, chemo-, and hormonal priming methods for imparting salt and PEG stress tolerance in Indian mustard (Brassica juncea L.). Acta Physiol Plant 32:1135–1144
Starck Z, Niemyska B, Bogdan J, Tawalbeh RNA (2000) RNA response of tomato plants to chilling stress in association with nutrient or phosphorus starvation. Plant Soil 226:99–106
Steponkus PL, Uemura M, Joseph RA, Gilmour SJ, Thomashow MF (1998) Mode of action of the COR15a gene on the freezing tolerance of Arabidopsis thaliana. Proc Natl Acad Sci U S A 95:14570–14575
Stewart CR, Martin BA, Reding L, Cerwick S (1990) Seedling growth, mitochondrial characteristics, and alternative respiratory capacity of corn genotypes differing in cold tolerance. Plant Physiol 92:761–766
Suzuki K, Nagasuga K, Okada M (2008) The chilling injury induced by high root temperature in the leaves of rice seedlings. Plant Cell Physiol 49:433–442
Suzuki N, Koussevitzky SHAI, Mittler RON, Miller GAD (2012) ROS and redox signalling in the response of plants to abiotic stress. Plant Cell Environ 35(2):259–270
Svensson J, Ismail A, Palva ET, Close TJ (2002) Dehydrins. In: Storey KB, Storey JM (eds) Sensing, signalling and cell adaptation. Elsevier Science, Amsterdam, pp 155–171
Taka T (2004) The relationship of antioxidant enzymes and some physiological parameters in maize during chilling. Plant Soil Environ 50:27–32
Taylor AG, Allen PS, Bennett MA, Bradford KJ, Burris JS, Misra MK (1998) Seed enhancements. Seed Sci Res 8(2):245–256
Taylor NL, Day DA, Millar AH (2002) Environmental stress causes oxidative damage to plant mitochondria leading to inhibition of glycine decarboxylase. J Biol Chem 277:42663–42668
Thakur P, Kumar S, Malik JA, Berger JD, Nayyar H (2010) An overview: cold stress effects on reproductive development in grain crops. Environ Exp Bot 67:429–443
Thomas UC, Varughese K, Thomas A, Sadanandan S (2000) Seed priming–for increased vigour, viability and productivity of upland rice. Leisa India 4:14
Timmusk S, Abd El-Daim IA, Copolovici L, Tanilas T, Kännaste A, Behers L et al (2014) Drought-tolerance of wheat improved by rhizosphere bacteria from harsh environments: enhanced biomass production and reduced emissions of stress volatiles. PLoS One 9:96086
Turk H, Erdal S, Genisel M, Atici O, Demir Y, Yanmis D (2014) The regulatory effect of melatonin on physiological, biochemical and molecular parameters in cold-stressed wheat seedlings. Plant Growth Regul 74:139–152
van Buer J, Cvetkovic J, Baier M (2016) Cold regulation of plastid ascorbate peroxidases serves as a priming hub controlling ROS signaling in Arabidopsis thaliana. BMC Plant Biol 16(1):163
Verslues PE, Agarwal M, Katiyar-Agarwal S, Zhu J, Zhu JK (2006) Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status. Plant J 45:523–539
Wang B, Vinocur O, Altman AS (2004) Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci 9:244–252
Wang W, Chen Q, Hussain S, Mei J, Dong H, Peng S, Huang L, Cui K, Nie L (2016) Pre-sowing seed treatments in direct-seeded early rice: consequences for emergence, seedling growth and associated metabolic events under chilling stress. Sci Rep 6. https://doi.org/10.1038/srep19637
Warrington IJ, Kanemasu ET (1983) Corn growth response to temperature and photoperiod I. seedling emergence, tassel initiation, and anthesis. Agron J 75:749–754
Wechsberg GE, Probert RJ, Bray CM (1994) The relationship between ‘dehydrinlike’ protein sand seed longevity in Ranunculus sceleratus L. J Exp Bot 45:1027–1030
Wilhelm KS, Thomashow MF (1993) Arabidopsis thaliana Cor15b, an apparent homolog of Cor15a, is strongly responsive to cold and ABA, but not drought. Plant Mol Biol 23:1073–1077
Wise RR (1995) Chilling-enhanced photo oxidation: the production, action and study of re active oxygen species produced during chilling in the light. Photosynth Res 45:7997
Wojtyla Ł, Lechowska K, Kubala S, Garnczarska M (2016) Molecular processes induced in primed seeds—increasing the potential to stabilize crop yields under drought conditions. J Plant Physiol 203:116–126
Xu S, Hu J, Li Y, Ma W, Zheng Y, Zhu S (2011) Chilling tolerance in Nicotiana tabacum induced by seed priming with putrescine. Plant Growth Regul 63:279–290
Yadav SK (2010) Cold stress tolerance mechanisms in plants. Agron Sustain Dev 30:515–527
Yadav PV, Kumari M, Ahmed Z (2011) Seed priming mediated germination improvement and tolerance to subsequent exposure to cold and salt stress in capsicum. Res J Seed Sci 4:125–136
Yagmur M, Kaydan D (2008) Alleviation of osmotic strength of water and salt in germination and seedling growth of triticale with seed priming treatments. Afr J Biotechnol 7:2156–2162
Yan Q, Duan Z, Jingdong M, Xun L, Fei D (2012) Effects of root-zone temperature and N, P, and K supplies on nutrient uptake of cucumber (Cucumis sativus L.) seedlings in hydroponics. Soil Sci Plant Nutr 58:707–717
Yilmaz AH, Ekiz I, Gültekin B, Torun H, Barut K, Cakmak I (1998) Effect of seed zinc content on grain yield and zinc concentration of wheat grown in zinc-deficient calcareous soils. J Plant Nutr 21:2257–2264
Yordanova R, Popova L (2007) Effect of exogenous treatment with salicylic acid on photosynthetic activity and antioxidant capacity of chilled wheat plants. Gen Appl Plant Physiol 33:155–170
Zarka DG, Vogel JT, Cook D, Thomashow MF (2003) Cold induction of Arabidopsis CBF genes involves multiple ICE (inducer of CBF expression) promoter elements and a cold-regulatory circuit that is desensitized by low temperature. Plant Physiol 133(2):910–918
Zhang J, Cui S, Li J, Wei J, Kirkham MB (1995) Protoplasmic factors, antioxidant responses, and chilling resistance in maize. Plant Physiol Biochem 33:567–575
Zhang S, Hu J, Liu N, Zhu Z (2006) Presowing seed hydration treatment enhances the cold tolerance of direct-sown rice. Seed Sci Technol 34(3):593–601
Zhang H, Tan ZQ, HuLY WSH, Luo JP, Jones RL (2010) Hydrogen sulfide alleviates aluminum toxicity in germinating wheat seedlings. J Integr Plant Biol 52(6):556–567
Zhao J, Li S, Jiang T, Liu Z, Zhang W (2012) Chilling stress- the key predisposing factor for causing Alternaria alternata infection and leading to cotton (Gossypium hirsutum L.) leaf senescence. PLoS One 7:36126
Zheng C, Jiang D, Liu F, Dai T, Liu W, Jing Q, Cao W (2009) Exogenous nitric oxide improves seed germination in wheat against mitochondrial oxidative damage induced by high salinity. Environ Exp Bot 67:222–227
Zheng M, Tao Y, Hussain S, Jiang Q, Peng S, Huang J et al (2016) Seed priming in dry direct-seeded rice: consequences for emergence, seedling growth and associated metabolic events under drought stress. Plant Growth Regul 78:167–178
Zhou YG, Yang YD, Qi YG, Zhang ZM, Wang XJ, Hu XJ (2002) Effects of chitosan on some physiological activity in germinating seed of peanut. J Peanut Sci 31:22–25
Zhu JJ, Li YR, Liao JX (2013) Involvement of anthocyanins in the resistance to chilling-induced oxidative stress in Saccharum officinarum L. leaves. Plant Physiol Biochem 73:427–433
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Hussain, H.A., Hussain, S., Anjum, S.A., Hussain, S. (2019). Seed Priming Toward Enhanced Chilling Tolerance in Field Crops: An Overview. In: Hasanuzzaman, M., Fotopoulos, V. (eds) Priming and Pretreatment of Seeds and Seedlings. Springer, Singapore. https://doi.org/10.1007/978-981-13-8625-1_13
Download citation
DOI: https://doi.org/10.1007/978-981-13-8625-1_13
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-13-8624-4
Online ISBN: 978-981-13-8625-1
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)