Abstract
Key message
Leaf relative water content, leaf area, leaf fresh weight, and SPAD chlorophyll meter readings along with Co - rbcL and Co - rbcS expression can be used for evaluating Camellia oleifera responses to combined drought and heat stress and subsequent recovery after rainfall events.
Abstract
Leaf characteristics, soluble protein and total soluble sugar contents as well as Rubisco-related gene expression in three cultivars of C. oleifera were measured during a combined drought and heat stress period and after subsequent rainfall events. Leaf relative water content (RWC) was significantly correlated with leaf area (LA), leaf fresh weight (FW), SPAD chlorophyll meter readings, and the levels of Co-rbcL and Co-rbcS expression. Results suggest that leaf RWC, LA, leaf FW, SPAD readings together with Co-rbcL and Co-rbcS expression can be used for evaluating responses of C. oleifera cultivars to combined drought and heat stress and subsequent recovery after rainfall events. Rubisco activase might be used for evaluating plant recovery after rainfall. This study identified cultivars differing in tolerance to the combined stress and recovery. Information derived from this study should be valuable for improving survivability and productivity of C. oleifera cultivars.
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Ashraf M (2010) Inducing drought tolerance in plants: recent advances. Biotechnol Adv 28:169–183
Bartholomew DM (1991) Abscisic acid control of rbcS and cab transcript in tomato leaves. Plant Physiol 96:291–296. doi:10.1104/pp.96.1.291
Basu PS, Ali M, Chaturvedi SK (2007) Osmotic adjustment increases water uptake, remobilization of assimilates and maintains photosynthesis in chickpea under drought. Indian J Exp Biol 45:261–267
Bradford MM (1976) Rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254. doi:10.1016/0003-2697(76)90527-3
Bray EA (1993) Molecular responses to water deficit. Plant Physiol 103:1035–1040. doi:10.1104/pp.103.4.1035
Carmo-Silva AE, Gore MA, Andrade-Sanchez P, French AN, Hunsaker DJ, Salvucci Mi E (2012) Decreased CO2 availability and inactivation of Rubisco limit photosynthesis in cotton plants under heat and drought stress in the field. Environ Exp Bot 83:1–11. doi:10.1016/j.envexpbot.2012.04.001
Chen Y, Wang B, Chen J, Wang X, Wang R, Peng S, Chen L, Ma L, Luo J (2015) Identification of Rubisco rbcL and rbcS in Camellia oleifera and their potential as molecular markers for selection of high tea oil cultivars. Front Plant Sci 6:189. doi:10.3389/fpls.2015.00189
Ciais P, Reichstein M, Viovy N, Granier A, Ogee J, Allard V, Aubinet M, Buchmann N, Bernhofer C, Carrara A, Chevallier F, De Noblet N, Friend AD, Friedlingstein P, Grunwald T, Heinesch B, Keroner P, Knohl A, Krinner G, Loustau D, Manca G, Matteucci G, Miglietta F, Ourcival JM, Papale D, Pilegaard K, Rambal S, Seufert G, Soussana JF, Sanz MJ, Schulze ED, Vesala T, Valentini R (2005) Europe-wide reduction in primary productivity caused by the heat and drought in 2003. Nature 437:529–533
Cottee NS, Bange MP, Wilson IW, Tan DKY (2012) Developing controlled environment screening for high temperature tolerance in cotton that accurately reflects performance in the field. Funct Plant Biol 39:670–678
Crafts-Brandner SJ, van de Loo FJ, Salvucci ME (1997) The two forms of ribulose-1,5-bisphosphate carboxylase/oxygenase activase differ in sensitivity to elevated temperature. Plant Physiol 114:439–444
Cramer G, Ergül A, Grimplet J, Tillett R, Tattersall E, Bohlman M, Vincent D, Sonderegger J, Evans J, Osborne C, Quilici D, Schlauch K, Schooley D, Cushman J (2007) Water and salinity stress in grapevines: early and late changes in transcript and metabolite profiles. Funct Integr Genomic 7:111–134. doi:10.1007/s10142-006-0039-y
Cseri A, Cserháti M, Von Korff M, Nagy B, Horváth GV, Palágyi A, Pauk J, Dudits D, Törjék O (2011) Allele mining and haplotype discovery in barley candidate genes for drought tolerance. Euphytica 181:341–356. doi:10.1007/s10681-011-0445-7
Feng B, Liu P, Li G, Dong ST, Wang FH, Kong LA, Zhang JW (2014) Effect of heat stress on the photosynthetic characteristics in flag leaves at the grain-filling stage of different heat-resistant winter wheat varieties. J Agro Crop Sci 200:143–155. doi:10.1111/jac.12045
Ge Y, He X, Wang J, Jiang B, Ye R, Lin X (2014) Physiological and biochemical responses of Phoebe bournei seedlings to water stress and recovery. Acta Physiol Plant 36:1241–1250. doi:10.1007/s11738-014-1502-3
Hsiao TC (1973) Plant responses to water stress. Annu Rev Plant Physiol 24:519–570. doi:10.1146/annurev.pp.24.060173.002511
IPCC (2007) Climate change 2007: the physical science basis, vol 1009. Cambridge University Press, Cambridge
Ji K, Wang Y, Sun W, Lou Q, Mei H, Shen S, Chen H (2011) Drought-responsive mechanisms in rice genotypes with contrasting drought tolerance during reproductive stage. J Plant Physiol 169:336–344. doi:10.1016/j.jplph.2011.10.010
Lawlor DW, Tezara W (2009) Causes of decreased photosynthetic rate and metabolic capacity in water-deficient leaf cells: a critical evaluation of mechanisms and integration of processes. Ann Bot 103:561–579
Mahajan S, Tuteja N (2005) Cold, salinity and drought stresses: an overview. Arch Biochem Biophys 444:139–158
Markwell J, Osterman JC, Mitchell JL (1995) Calibration of the Minolta SPAD-502 leaf chlorophyll meter. Photosynth Res 46:467–472. doi:10.1007/BF00032301
Marquard RD, Tipton JL (1987) Relationship between extractable chlorophyll and an in situ method to estimate leaf greenness. HortScience 22:1327
Morgan JM (1984) Osmoregulation and water stress in higher plants. Annu Rev Plant Physiol 35:299–319
Mullan D, Pietragalla J (2012) Leaf relative water content. In: Pask AJD, Pietragalla J, Mullan D, Reynolds M (eds) Physiological breeding II: A field guide to wheat phenotyping. CIMMYT, Mexico, pp 25–27
Osakabe Y, Osakabe K, Shinozaki K, Tran LP (2014) Response of plants to water stress. Front Plant Sci 5:86. doi:10.3389/fpls.2014.00086
Park SY, Noh KJ, Yoo JH, Yu JW, Lee BW, Kim JG, Seo HS, Paek NC (2006) Rapid upregulation of Dehyrin3 and Dehydrin4 in response to dehydration is a characteristic of drought-tolerant genotypes in barley. J Plant Biol 49:455–462
Parry MAJ, Andralolc J, Khan S, Lea PJ, Keys AJ (2002) Rubisco activity: effects of drought stress. Ann Bot 89:833–839. doi:10.1093/aob/mcf103
Pelloux J, Jolivet Y, Fontaine V, Banvoy J, Dizengremel P (2001) Changes in Rubisco and Rubisco activase gene expression and polypeptide content in Pinus halepensis M. subjected to ozone and drought. Plant Cell Environ 24:123–131
Pinheiro C, Chaves MM (2011) Photosynthesis and drought: can we make metabolic connections from available data? J Exp Bot 62:869–882. doi:10.1093/jxb/erq340
Pinheiro C, Chaves MM, Ricardo CP (2001) Alterations in carbon and nitrogen metabolism induced by water deficit in the stems and leaves of Lupinus albus L. J Exp Bot 52:1063–1070. doi:10.1093/jexbot/52.358.1063
Sareen S, Tyagi BS, Sarial AK, Tiwari V, Sharma I (2014) Trait analysis, diversity, and genotype x environment interaction in some wheat landraces evaluated under drought and heat stress conditions. Chil J Agric Res 74:135–142. doi:10.4067/S0718-58392014000200002
Shah NH, Paulsen GM (2003) Interaction of drought and high temperature on photosynthesis and grain-filling of wheat. Plant Soil 257(1):219–326
Silva MA, Jifon JL, Da Silva JAG, Vivek S (2007) Use of physiological parameters as fast tools to screen for drought tolerance in sugarcane. Braz J Plant Physiol 19:193–201. doi:10.1590/S1677-04202007000300003
Silva MA, Jifon JL, Vivek S, Da Silva JAG, Caputo MM, Damaj MB, Guimarães ER, Ferro MIT (2011) Use of physiological parameters in screening drought tolerance in sugarcane genotypes. Sugar Tech 13:191–197. doi:10.1007/s12355-011-0087-z
Smart RE, Bingham GE (1974) Rapid estimates of relative water content. Plant Physiol 53:258–260
Taylor JA, Bates TR (2013) A discussion on the significance associated with Pearson’s correlation in precision agriculture studies. Precis Agric 14:558–564. doi:10.1007/s11119-013-9314-9
Voloudakis AE, Kosmas SA, Tsakas S, Eliopoulos E, Loukas M, Kosmidou K (2002) Expression of selected drought-related genes and physiological response of Greek cotton varieties. Funct Plant Biol 29:1237–1245. doi:10.1071/PP01253
Wang Q, Chen J, Li Y (2004) Nondestructive and rapid estimation of leaf chlorophyll and nitrogen status of peace lily using a chlorophyll meter. J Plant Nutr 27:557–569
Watkinson JI, Hendricks L, Sioson AA, Vasquez-Robinet C, Stromberg V, Heath LS, Schuler M, Bohnert HJ, Bonierbale M, Ruth Grene (2006) Accessions of Solanum tuberosum ssp. andigena show differences in photosynthetic recovery after drought stress as reflected in gene expression profiles. Plant Sci 171:745–758. doi:10.1016/j.plantsci.2006.07.010
Williams J, Bulaman MP, Neill SJ (1994) Wilt-induced ABA biosynthesis, gene-expression and down regulation of rbcS messenger-RNA levels in Arabidopsis thaliana. Physiol Plant 91:177–182. doi:10.1111/j.1399-3054.1994.tb00416.x
Wu S, Liang D, Ma F (2014) Leaf micromorphology and sugar may contribute to differences in drought tolerance for two apple cultivars. Plant Physiol Biochem 80:249–258
Xu ZZ, Zhou GS (2006) Combined effects of water stress and high temperature on photosynthesis, nitrogen metabolism and lipid peroxidation of a perennial grass Leymus chinensis. Planta 224:1080–1090
Xu Z, Zhou G, Shimizu H (2010) Plant responses to drought and rewatering. Plant Signal Behav 5:649–654
Xu LX, Yu JJ, Han LB, Huang BR (2013) Photosynthetic enzyme activities and gene expression associated with drought tolerance and post-drought recovery in Kentucky bluegrass. Environ Exp Bot 89:28–35. doi:10.1093/aob/mcn244
Author contribution statement
B. Wang designed and performed the research and analyzed data. Y. Chen designed and supervised the whole project and analyzed data. B. Wang and J. Chen wrote and revised the manuscript. X. Wang conducted the research. R. Wang and L. Chen participated in the experimental design, evaluation, and data analysis. S. Peng, L. Ma, and J. Luo participated in analysis of the data. All authors approved the final version of this manuscript.
Acknowledgments
This work was supported by National Natural Science Foundation of China (Grant No. 31370677) and Climate Change Special Program of China Meteorological Administration (Grant No. CCSF201525). The authors thank Mrs. Barbara Henny for critical reading of this manuscript.
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The authors declare that they have no conflict of interest.
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Communicated by J. Carlson.
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Wang, B., Chen, J., Chen, L. et al. Combined drought and heat stress in Camellia oleifera cultivars: leaf characteristics, soluble sugar and protein contents, and Rubisco gene expression. Trees 29, 1483–1492 (2015). https://doi.org/10.1007/s00468-015-1229-9
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DOI: https://doi.org/10.1007/s00468-015-1229-9