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Estimating photosynthetic electron transport via chlorophyll fluorometry without Photosystem II light saturation

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Abstract

Estimates of thylakoid electron transport rates (Je) from chlorophyll fluorometry are often used in combination with leaf gas exchange measurements to provide detailed information about photosynthetic activity of leaves in situ. Estimating Je requires accurate determination of the quantum efficiency of Photosystem II (ΦP), which in turn requires momentary light saturation of the Photosystem II light harvesting complex to induce the maximum fluorescence signal (FM′). In practice, full saturation is often difficult to achieve, especially when incident photosynthetic photon flux density (Q) is high and energy is effectively dissipated by non-photochemical quenching. In the present work, a method for estimating the true FM′ under high Q was developed, using multiple light pulses of varying intensity (Q′). The form of the expected relationship between the apparent FM′ and Q′ was derived from theoretical considerations. This allowed the true FM′ at infinite Q′ to be estimated from linear regression. Using a commercially available leaf gas exchange/ chlorophyll fluorescence measurement system, Je was compared to gross photosynthetic CO2 assimilation (AG) under conditions where the relationship between Je and AG was expected to be linear. Both in C4 leaves (Zea mays) in ambient air and also in C3 leaves (Gossypium hirsutum) under non-photorespiratory conditions the apparent ratio between Je and AG declined at high Q when ΦP was calculated from FM′ measured simply using the highest available saturating pulse intensity. When FM′ was determined using the multiple pulse / linear regression technique, the expected relationship between Je and AG at high Q was restored, indicating that the ΦP estimate was improved. This method of determining FM′ should prove useful for verifying when saturating pulse intensities are sufficient, and for accurately determining ΦP when they are not.

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References

  • Demmig-Adams B and Adams III WW (1996) Xanthophyll cycle and light stress in nature: uniform response to excess direct sunlight among higher plant species. Planta 183: 460-470

    Article  Google Scholar 

  • Earl HJ and Tollenaar M (1997) Maize leaf absorptance of photosynthetically active radiation and its estimation using a chlorophyll meter. Crop Sci 37: 436-440

    Article  Google Scholar 

  • Earl HJ and Tollenaar M (1998) Relationship between thylakoid electron transport and photosynthetic CO2 uptake in leaves of three maize (Zea mays L.) hybrids. Photosynth Res 58: 245-257

    Article  CAS  Google Scholar 

  • Edwards GE and Baker NR (1993) Can CO2 assimilation in maize leaves be predicted accurately from chlorophyll fluorescence analysis? Photosynth Res 37: 89-102

    Article  CAS  Google Scholar 

  • Flexas J, Bota J, Escalona JM, Sampol B and Medrano H (2002) Effects of drought on photosynthesis in grapevines under field conditions: an evaluation of stomatal and mesophyll limitations. Funct Plant Biol 29: 461-471

    Article  Google Scholar 

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

    CAS  Google Scholar 

  • Harley PC, Loreto F, Di Marco G and 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 

  • Harbinson J, Genty B and Baker NR (1990) The relationship between CO2 assimilation and electron transport in leaves. Photosynth Res 25: 213-224

    Article  CAS  Google Scholar 

  • Kitajima M and Butler WL (1975) Quenching of chlorophyll fluorescence and primary photochemistry in chloroplasts by dibromothymoquinone. Biochim Biophys Acta 376: 105-115

    Article  PubMed  CAS  Google Scholar 

  • Krause H and Weis E (1991) Chlorophyll fluorescence and photosynthesis: the basics. Annu Rev Plant Physiol Plant Mol Biol 42: 313-349

    Article  CAS  Google Scholar 

  • Laisk A and Loreto F (1996) Determining photosynthetic parameters from leaf CO2 exchange and chlorophyll fluorescence. Ribulose-1,5-bisphosphate carboxylase. oxygenase specificity factor, dark respiration in the light, excitation distribution between photosystems, alternative electron transport rate, and mesophyll diffusion resistance. Plant Physiol 110: 903-912

    PubMed  CAS  Google Scholar 

  • Laisk A, Oja V, Rasulov B, Eichelmann H and Sumberg A (1997) Quantum yields and rate constants of photochemical and nonphotochemical excitation quenching. Experiment and model. Plant Physiol 115: 803-815

    CAS  Google Scholar 

  • Lal A, Ku MSB and Edwards GE (1996) Analysis of inhibition of photosynthesis due to water stress in the C3 species Hordeum vulgare and Vicia faba: electron transport, CO2 fixation and carboxylation capacity. Photosynth Res 49: 57-69

    Google Scholar 

  • Long SP and Bernacchi CJ (2003) Gas exchange measurements, what can they tell us about the underlying limitations to photosynthesis? Procedures and sources of error. J Exp Bot 54: 2393-2401

    Article  PubMed  CAS  Google Scholar 

  • Loreto F, Harley PC, Di Marco G and Sharkey TD (1992) Estimation of mesophyll conductance to CO2 flux by three different methods. Plant Physiol 98: 1437-1443

    PubMed  CAS  Google Scholar 

  • Loreto F, Di Marco G, Tricoli D and Sharkey TD (1994) Measurements of mesophyll conductance, photosynthetic electron transport and alternative electron sinks of field grown wheat leaves. Photosynth Res 41: 397-403

    Article  CAS  Google Scholar 

  • Markgraf T and Berry J (1990) Measurement of photochemical and non-photochemical quenching: correction for turnover of PS2 during steady-state photosynthesis. In: Baltscheffsky M (ed) Current Research in Photosynthesis Vol IV, pp 279-282. Kluwer Academic Publishers, Dordrecht, the Netherlands

    Google Scholar 

  • Oberhuber W, Dai Z-Y and Edwards GE (1993) Light dependence of quantum yields of Photosystem II and CO2 fixation in C3 and C4 plants. Photosynth Res 35: 265-274

    Article  CAS  Google Scholar 

  • Rohácek R and Barták M (1999) Technique of the modulated chlorophyll fluorescence: basic concepts, useful parameters, and some applications. Photosynthetica 37: 339-363

    Article  Google Scholar 

  • SAS Institute (1985) SAS User's Guide: Statistics, 5th ed. SAS Institute, Cary, North Carolina

    Google Scholar 

  • Schreiber U, Schliwa U and Bilger W (1986) Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. Photosynth Res 10: 51-62

    Article  CAS  Google Scholar 

  • Valentini R, Epron D, De Angelis P, Matteucci G and Dreyer E (1995) In situ estimation of net CO2 assimilation, photosynthetic electron flow and photorespiration in Turkey oak (Q. cerris L.) leaves: diurnal cycles under different levels of water supply. Plant Cell Environ 18: 631-640

    Article  CAS  Google Scholar 

  • Walker D (1992) Tansley review no. 36. Excited leaves. New Phytol 121: 325-345

    Article  CAS  Google Scholar 

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Earl, H.J., Ennahli, S. Estimating photosynthetic electron transport via chlorophyll fluorometry without Photosystem II light saturation. Photosynthesis Research 82, 177–186 (2004). https://doi.org/10.1007/s11120-004-1454-3

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  • DOI: https://doi.org/10.1007/s11120-004-1454-3

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