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Limitation factors for photosynthesis in ‘Bluecrop’ highbush blueberry (Vaccinium corymbosum) leaves in response to moderate water stress

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Abstract

The levels of stomatal, mesophyll and biochemical limitations in CO2 assimilation of ‘Bluecrop’ highbush blueberry leaves were compared at two different levels of leaf water potential. The leaf water potentials were −1.49 and −1.94 MPa in daily-irrigated (DI) and non-irrigated (NI) shrubs, respectively. The NI shrubs represented plants under moderate water stress. Mesophyll conductance (g m) and chloroplastic CO2 concentration (C c) were estimated by combined measurements of gas exchange and chlorophyll fluorescence under various intercellular CO2 concentrations (C i). Net CO2 assimilation rates (A n) as a function of C c were used for calculating maximum carboxylation efficiency (α cmax) at the real sites of CO2 assimilation. Maximum A n (A nmax) from the light response curves at 400 μmol mol−1 air of ambient CO2 concentration (C a) were lower in the leaves of NI shrubs than in those of DI ones. However, electron transport rates were higher in the leaves of NI shrubs than in those of DI ones. The decrease in CO2 assimilation following water stress may be caused by a decrease in g m rather than a decrease in stomatal conductance (g s) according to limitation analysis. Limitation rates by g s, calculated at 400 μmol mol−1 air of C a in A n-C i curves, were not significantly different between the leaves of DI and NI shrubs. However, limitation rates by g m from A n-C c curves were significantly higher in the leaves of NI shrubs than in those of DI ones. Maximum carboxylation efficiency (α cmax) values calculated from the A n-C c curve, contrary to those calculated from the A n-C i curve, were higher in the leaves of NI shrubs than in those of DI ones. Consequently, mesophyll limitation than stomatal and biochemical limitations mainly down-regulated the photosynthesis in the leaves of ‘Bluecrop’ blueberry shrubs during moderate water stress.

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References

  • Bernacchi CJ, Portis AR, Nakano H, von Caemmerer S, Long SP (2002) Temperature response of mesophyll conductance: implications for the determination of RuBisCO enzyme kinetics and for limitations to photosynthesis in vivo. Plant Physiol 130:1992–1998

    Article  PubMed  CAS  Google Scholar 

  • Björkman O, Demmig B (1987) Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77K among vascular plants of diverse origins. Planta 170:489–504

    Article  Google Scholar 

  • Brooks A, Farquhar GD (1985) Effect of temperature on the CO2/O2 specificity of ribulose-1,5-bisphosphate carboxylase/oxygenase and the rate of respiration in the light. Planta 165:397–406

    Article  CAS  Google Scholar 

  • Demmig-Adams B, Adams III WW (1992) Photoprotection and other responses of plants to high light stress. Annu Rev Plant Physiol Plant Mol Biol 43:599–626

    Article  CAS  Google Scholar 

  • Escalona JM, Flexas J, Medrano H (1999) Stomatal and non-stomatal limitations of photosynthesis under water stress in field-grown grapevines. Austral J Plant Physiol 26:421–433

    Article  Google Scholar 

  • Evans JR, Kaldenhoff R, Genty B, Terashima I (2009) Resistances along the CO2 diffusion pathway inside leaves. J Exp Bot 60:2235–2248

    Article  PubMed  CAS  Google Scholar 

  • Farquhar GD, Sharkey TD (1982) Stomatal conductance and photosynthesis. Annu Rev Plant Physiol 33:317–345

    Article  CAS  Google Scholar 

  • Farquhar GD, von Caemmerer S, Berry JA (1980) A biochemical model of photosynthetic assimilation in leaves of C3 species. Planta 149:78–90

    Article  CAS  Google Scholar 

  • Flexas J, Baron M, Bota J, Ducruet JM, Galle A, Galmés J, Jimenez M, Pou A, Ribas-Carbó M, Sajnani C, Tomas M, Medrano H (2009) Photosynthesis limitations during water stress acclimation and recovery in the drought-adapted Vitis hybrid Richter-110 (V. berlandieri × V. rupestris). J Exp Bot 60:2361–2377

    Article  PubMed  CAS  Google Scholar 

  • Flexas J, Díaz-Espejo A, Berry JA, Cifre J, Galmés J, Kaldenhoff R, Medrano H, Ribas-Carbó M (2007a) Analysis of leakage in IRGA’s leaf chambers of open gas exchange systems: quantification and its effects in photosynthesis parameterization. J Exp Bot 58:1533–1543

    Article  PubMed  CAS  Google Scholar 

  • Flexas J, Díaz-Espejo A, Galmés J, Kaldenhoff R, Medrano H, Ribas-Carbó M (2007b) Rapid variations of mesophyll conductance in response to changes in CO2 concentration around leaves. Plant Cell Environ 30:1284–1298

    Article  PubMed  CAS  Google Scholar 

  • Flexas J, Escalona JM, Medrano H (1999) Water stress induces different levels of photosynthesis and electron transport rate regulation in grapevines. Plant Cell Environ 22:39–48

    Article  Google Scholar 

  • Flexas J, Medrano H (2002) Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited. Ann Bot 89:183–189

    Article  PubMed  CAS  Google Scholar 

  • Flexas J, Ribas-Carbó M, Díaz-Espejo A, Galmés J, Medrano H (2008) Mesophyll conductance to CO2: current knowledge and future prospects. Plant Cell Environ 31:602–621

    Article  PubMed  CAS  Google Scholar 

  • Galle A, Florez-Sarasa I, Tomas M, Pou A, Medrano H, Ribas-Carbó M, Flexas J (2009) The role of mesophyll conductance during water stress and recovery in tobacco (Nicotiana sylvestris): acclimation or limitation? J Exp Bot 60:2379–2390

    Article  PubMed  CAS  Google Scholar 

  • Genty B, Briantais JM, Baker NR (1989) The relationship between the quantum yield of the photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990:87–92

    Article  CAS  Google Scholar 

  • Grassi G, Magnani F (2005) Stomatal, mesophyll conductance and biochemical limitations to photosynthesis as affected by drought and leaf ontogeny in ash and oak trees. Plant Cell Environ 28:834–849

    Article  CAS  Google Scholar 

  • Harley PC, Loreto F, Marco GD, Sharkey TD (1992) Theoretical considerations when estimating the mesophyll conductance to CO2 flux by analysis of the response of photosynthesis to CO2. Plant Physiol 98:1429–1436

    Article  PubMed  CAS  Google Scholar 

  • Iqbal RM, Rao AR, Rasul E, Wahid A (1996) Mathematical models and response functions in photosynthesis: an exponential model, In M Pessarakli, ed, Handbook of photosynthesis, Marcel Dekker Inc., New York, pp 803–810

    Google Scholar 

  • Kaldenhoff R (2012) Mechanisms underlying CO2 diffusion in leaves. Curr Opin Plant Biol 15:276–281

    Article  PubMed  CAS  Google Scholar 

  • Keenan T, Sabate S, Gracia C (2010) The importance of mesophyll conductance in regulating forest ecosystem productivity during drought periods. Global Change Biol 16:1019–1034

    Article  Google Scholar 

  • Laisk AK (1977) Kinetics of photosynthesis and photorespiration in C3-plants. Nauka, Moscow, Russia

    Google Scholar 

  • Lawlor DW, Cornic G (2002) Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ 25:275–294

    Article  PubMed  CAS  Google Scholar 

  • 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

    Article  PubMed  CAS  Google Scholar 

  • Li-Cor (2008) Using the LI-6400/LI-6400XT portable photosynthesis system, Ver. 6. Li-Cor Biosciences Inc., Lincoln, NE, USA

    Google Scholar 

  • Niinemets Ü, Díaz-Espejo A, Flexas J, Galmés J, Warren CR (2009) Importance of mesophyll diffusion conductance in estimation of plant photosynthesis in the field. J Exp Bot 60:2271–2282

    Article  PubMed  CAS  Google Scholar 

  • Niyogi KK (1999) Photoprotection revisited: genetic and molecular approaches. Annu Rev Plant Physiol Plant Mol Biol 50:333–359

    Article  PubMed  CAS  Google Scholar 

  • Rho H, Yu DJ, Kim SJ, Chun C, Lee HJ (2011) Estimation of carboxylation efficiency from net CO2 assimilation rate as a function of chloroplastic CO2 concentration in strawberry (Fragaria × ananassa cv. Maehyang) leaves. Hort Environ Biotechnol 52:547–552

    Article  CAS  Google Scholar 

  • Sharkey TD, Bernacchi CJ, Faquhar GD, Singsaas EL (2007) Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant Cell Environ 30:1035–1040

    Article  PubMed  CAS  Google Scholar 

  • Tezara W, Mitchell VJ, Driscoll SD, Lawlor DW (1999) Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP. Nature 401:914–917

    Article  CAS  Google Scholar 

  • Warren CR (2008) Stand aside stomata, another actor deserves center stage: the forgotten role of the internal conductance to CO2 transfer. J Exp Bot 59:1475–1487

    Article  PubMed  CAS  Google Scholar 

  • Yin X, Struik PC (2009) Theoretical reconsiderations when estimating the mesophyll conductance to CO2 diffusion in leaves of C3 plants by analysis of combined gas exchange and chlorophyll fluorescence measurements. Plant Cell Environ 32:1513–1524

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Hee Jae Lee.

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Rho, H., Yu, D.J., Kim, S.J. et al. Limitation factors for photosynthesis in ‘Bluecrop’ highbush blueberry (Vaccinium corymbosum) leaves in response to moderate water stress. J. Plant Biol. 55, 450–457 (2012). https://doi.org/10.1007/s12374-012-0261-1

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  • DOI: https://doi.org/10.1007/s12374-012-0261-1

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