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Photosynthetic response of different pea cultivars to low and high temperature treatments

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Photosynthetica

Abstract

The thermo-sensitivity of two new pea (Pisum sativum L.) cultivars—Afila (mutant in the gene transforming leaves into mustaches) and Ranen (mutant for early ripening)—as compared to the control cultivar Pleven-4 to either low (4 °C, T4) or high temperature (38 °C, T38) was investigated by means of chlorophyll (Chl) fluorescence kinetics. The low temperature treatment decreased the photosynthetic activity, measured via a decline of the Chl fluorescence decrease ratios RFd690 and RFd735, and this was mainly due to a decline of the Chl fluorescence decrease parameter Fd and maximum Chl fluorescence Fm. In the new cv. Ranen the RFd ratios at first decreased and increased again after 24-h exposure to 4 °C, indicating its good acclimation ability to low temperature. The cold-induced changes in the photosynthetic performance of all cultivars were reversed after transferring plants back to 23 °C for 48 h. In the Chl and carotenoid (Car) contents no or little changes occurred during the T4 treatment, except for a slight but clear increase of the ratio Chl a/b and a decrease in the ratio Chl/Car. In contrast to this, the T38 treatment for 72 h decreased the RFd ratios more strongly than the T4 exposure did. In fact, an irreversible injury of the photosynthetic apparatus was caused in the control pea cv. Pleven-4 by a 48-h T38 exposure and for the new cv. Afila after a 72-h T38 exposure. In contrast, the cv. Ranen was less and little sensitive to the T38 exposure. In the heat-sensitive cvs. Pleven-4 and Afila, the decrease in RFd values at T38 was associated with a strong decline of the Chl a+b and total Car contents. The Chl a+b decline could also be followed via an increase of the Chl fluorescence ratio F690/F735. Parallel to this, a strong decline of Chl a/b from ca. 3.0 (range 2.85–3.15) to ca. 1.9 (range 1.85–1.95) occurred indicating a preferential decline of the Chl a-pigment proteins but not of the Chl a/b-pigment protein LHC2. In the relatively heat-tolerant cv. Ranen, however, the ratio Chl a/b declined only partially. After the T4 treatment the stress adaptation index Ap was higher in cv. Ranen than in controls and reached in heat-treated Ranen plants almost the starting value indicating a cold and heat stress hardening of the treated plants. The Chl fluorescence parameters and pigment contents were influenced by T38 and T4 treatments in various ways indicating that the mechanisms of low and high temperature injury of the photosynthetic apparatus are different. The new cv. Ranen exhibited a cross tolerance showing a fairly good acclimation ability to both T4 and T38, hence it is a very suitable plant for outdoor growth and for clarification of the acclimation mechanisms to unfavourable temperatures.

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Abbreviations

Ap:

stress adaptation index

Car:

carotenoid

Chl:

chlorophyll

cv.:

cultivar

Fm :

maximal Chl fluorescence

Fs :

steady state Chl fluorescence

F690 :

red Chl fluorescence band near 690 nm

F735 :

far-red Chl fluorescence band near 735 nm

F680/F735 :

ratio of red to far-red Chl fluorescence

PS:

photosystem

RFd :

Chl fluorescence decrease ratio, measured at red (RFd690) and far-red Chl fluorescence maximum (RFd735), respectively

T4 and T38 :

low and high temperature treatments at 4 and 38 °C, respectively

References

  • Babani, F., Lichtenthaler, H.K.: Light-induced and age-dependent development of chloroplasts in etiolated barley leaves as visualized by determination of photosynthetic pigments, CO2 assimilation rates and different kinds of chlorophyll fluorescence ratios.-J. Plant Physiol. 148: 555–566, 1996.

    CAS  Google Scholar 

  • Berry, J., Björkman, O.: Photosynthetic response and adaptation to temperature in higher plants.-Annu. Rev. Plant Physiol. 31: 491–543, 1980.

    Article  Google Scholar 

  • Buschmann, C., Schrey, H.: Fluorescence induction kinetics of green and etiolated leaves by recording the complete in-vivo emission spectra.-Photosynth. Res. 1: 233–241, 1980.

    Article  CAS  Google Scholar 

  • Enami, I., Kitamura, M., Tomo, T., Isokawa, Y., Ohta, H., Katoh, S.: Is the primary cause of thermal inactivation of oxygen evolution in spinach PS II membranes release of the 33 extrinsic kDa protein or of Mn?-Biochim. biophys. Acta 1186: 52–58, 1994.

    Article  CAS  Google Scholar 

  • Fork, D.C., Satoh, K.: The control by state transitions of the distribution of excitation energy in photosynthesis.-Annu. Rev. Plant Physiol. 37: 335–361, 1986.

    Article  CAS  Google Scholar 

  • Franck, F., Juneau, P., Popovic, R.: Resolution of the photosystem I and photosystem II contributions to chlorophyll fluorescence of intact leaves at room temperature.-Biochim. biophys. Acta 1556: 239–246, 2002.

    Article  PubMed  CAS  Google Scholar 

  • Georgieva, K., Lichtenthaler, H.K.: Photosynthetic activity and acclimation ability of pea plants to low and high temperature treatment as studied by means of chlorophyll fluorescence.-J. Plant Physiol. 155: 416–423, 1999.

    CAS  Google Scholar 

  • Georgieva, K., Yordanov, I.: Temperature dependence of chlorophyll fluorescence parameters of pea seedlings.-J. Plant Physiol. 142: 151–155, 1993.

    CAS  Google Scholar 

  • Georgieva, K., Yordanov, I., Tsonev, T.: Influence of low temperature treatment on the functional activity and acclimation ability of the photosynthetic apparatus of pea plants.-Compt. rend. bulg. Acad. Sci. 52: 71–74, 1992.

    Google Scholar 

  • Gitelson, A.A., Buschmann, C., Lichtenthaler, H.K.: Leaf chlorophyll fluorescence corrected for re-absorption by means of absorption and reflectance measurements.-J. Plant Physiol. 152: 283–296, 1998.

    CAS  Google Scholar 

  • Govindjee: Chlorophyll a fluorescence: a bit of basics and history.-In: Papageorgiu, G.C., Govindjee (ed.): Chlorophyll a Fluorescence. A Signature of Photosynthesis. Pp. 1–42. Springer, Dordrecht 2004.

    Google Scholar 

  • Havaux, M.: Rapid photosynthetic adaptation to heat stress triggered in potato leaves by moderately elevated temperatures.-Plant Cell Environ. 16: 461–467, 1993.

    Article  Google Scholar 

  • Havaux, M.: Temperature-dependent modulation of the photoinhibition-sensitivity of photosystem II in Solanum tuberosum leaves.-Plant Cell Physiol. 35: 757–766, 1994.

    CAS  Google Scholar 

  • Havaux, M., Strasser, R.J.: Antagonistic effects of red and farred lights on the stability of photosystem II in pea leaves exposed to heat.-Photochem. Photobiol. 55: 621–624, 1992.

    CAS  Google Scholar 

  • Janssen, L.H.J., Wams, H.E., van Hasselt, P.R.: Temperature dependence of chlorophyll fluorescence induction and photosynthesis in tomato as affected by temperature and light conditions during growth.-J. Plant Physiol. 139: 549–554, 1992.

    CAS  Google Scholar 

  • Kocsányi, L., Haitz, M., Lichtenthaler, H.K.: Measurement of the laser-induced chlorophyll fluorescence kinetics using a fast acousto optic device.-In: Lichtenthaler, H.K. (ed.): Applications of Chlorophyll Fluorescence. Pp. 99–107. Kluwer Academic Publishers, Dordrecht-Boston-London 1988.

    Google Scholar 

  • Krause, G.H., Weis, E.: Chlorophyll fluorescence and photosynthesis: The basics.-Annu. Rev. Plant Physiol. Plant mol. Biol. 42: 313–349, 1991.

    Article  CAS  Google Scholar 

  • Lichtenthaler, H.K.: Chlorophyll fluorescence signatures of leaves during the autumnal chlorophyll breakdown.-J. Plant Physiol. 131: 101–110, 1987a.

    CAS  Google Scholar 

  • Lichtenthaler, H.K.: Chlorophylls and carotenoids-pigments of photosynthetic biomembranes.-In: Colowick, S.P., Kaplan, N.O. (ed.): Methods in Enzymology. Vol. 148. Pp. 350–382. Academic Press, San Diego-New York-Berkeley-Boston-London-Sydney-Tokyo-Toronto 1987b.

    Google Scholar 

  • Lichtenthaler, H.K.: Vegetation stress: an introduction to the stress concept in plants.-J. Plant Physiol. 148: 4–14, 1996.

    CAS  Google Scholar 

  • Lichtenthaler, H.K., Babani, F.: Light adaptation and senescence of the photosynthetic apparatus: changes in pigment composition, chlorophyll fluorescence parameters and photosynthetic activity.-In: Papageorgiou, G.C., Govindjee (ed.): Chlorophyll a Fluorescence. A Signature of Photosynthesis. Pp. 713–736. Springer, Dordrecht 2004.

    Google Scholar 

  • Lichtenthaler, H.K., Burkart, S., Schindler, C., Stober, F.: Changes in photosynthetic pigments and in vivo chlorophyll fluorescence parameters under photoinhibitory growth conditions.-Photosynthetica 27: 343–353, 1992.

    CAS  Google Scholar 

  • Lichtenthaler, H.K., Buschmann, C.: Chlorophylls and carotenoids-Measurement and characterisation by UV-VIS.-Current Protocols in Food Analytical Chemistry (CPFA), (Supplement 1), F4.3.1-F 4.3.8. John Wiley, New York 2001.

    Google Scholar 

  • Lichtenthaler, H.K., Buschmann, C., Knapp, M.: How to correctly determine the different chlorophyll fluorescence parameters and the chlorophyll fluorescence decrease ratio RFd of leaves with the PAM fluorometer.-Photosynthetica 43: 379–393, 2005a.

    Article  CAS  Google Scholar 

  • Lichtenthaler, H.K., Kuhn, G., Prenzel, U., Buschmann, C., Meier, D.: Adaptation of chloroplast-ultrastructure and of chlorophyll-protein levels to high-light and low-light growth conditions.-Z. Naturforsch. 37c: 464–475, 1982a.

    CAS  Google Scholar 

  • Lichtenthaler H.K., Langsdorf, G., Lenk, S., Buschmann, C.: Chlorophyll fluorescence imaging of photosynthetic activity with the flash-lamp fluorescence imaging system.-Photosynthetica 43: 355–369, 2005b.

    Article  CAS  Google Scholar 

  • Lichtenthaler, H.K., Miehé, J.A.: Fluorescence imaging as a diagnostic tool for plant stress.-Trends Plant Sci. 2: 316–320, 1997.

    Article  Google Scholar 

  • Lichtenthaler, H.K., Prenzel, U., Kuhn, G.: Carotenoid composition of chlorophyll-carotenoid-proteins from radish chloroplasts.-Z. Naturforsch. 37c: 10–12, 1982b.

    CAS  Google Scholar 

  • Lichtenthaler, H.K., Rinderle, U.: The role of chlorophyll fluorescence in the detection of stress conditions in plants.-CRC crit. Rev. anal. Chem. 19: S29–S85, 1988.

    Google Scholar 

  • Maciejewska, U., Bauer, H.: Effects of cold acclimation on chlorophyll fluorescence in winter rape leaves.-Photosynthetica 28: 559–562, 1993.

    CAS  Google Scholar 

  • Mamedov, M., Hayashi, H., Murata, N.: Effects of glycinebetaine and unsaturation of membrane lipids on heat stability of photosynthetic electron transport and phosphorylation reactions in Synechocystis PCC6803.-Biochim. biophys. Acta 1142: 1–5, 1993.

    Article  CAS  Google Scholar 

  • Nishiyama, Y., Kovacs, E., Lee, C.B., Hayashi, H., Watanabe, T., Murata, N.: Photosynthetic adaptation to high temperature associated with thylakoid membranes of Synechococcus PCC7002.-Plant Cell Physiol. 34: 337–343, 1993.

    CAS  Google Scholar 

  • Öquist, G., Hurry, V.M., Huner, N.P.A.: The temperature dependence of the redox state of QA and susceptibility of photosynthesis to photoinhibition.-Plant Physiol. Biochem. 31: 683–691, 1993.

    Google Scholar 

  • Papageorgiou, G.: Chlorophyll fluorescence: an intrinsic probe of photosynthesis.-In: Govindjee (ed.): Bioenergetics of Photosynthesis. Pp. 319–371. Academic Press, New York-San Francisco-London 1975.

    Google Scholar 

  • Pfündel, E.: Estimating the contribution of Photosystem I to total leaf chlorophyll fluorescence.-Photosynth. Res. 56: 185–195, 1998.

    Article  Google Scholar 

  • Roháček, K.: Chlorophyll fluorescence parameters: the definitions, photosynthetic meaning, and mutual ralationships.-Photosynthetica 40: 13–29, 2002.

    Article  Google Scholar 

  • Sayed, O.H., Earnshaw, M.J., Emes, M.J.: Characterization of the heat-induced stimulation of photosystem-I-mediated electron transport.-Acta bot. neerl. 43: 137–143, 1994.

    CAS  Google Scholar 

  • Schindler, C., Reith, P., Lichtenthaler, H.K.: Differential levels of carotenoids and decrease of zeaxanthin cycle performance during leaf development in a green and an aurea variety of tobacco.-J. Plant Physiol. 143: 500–507, 1994.

    CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Strasser, R.J., Schwarz, B., Bucher, J.: Simultane Messung der Chlorophyll Fluoreszenz-Kinetik bei verschiedenen Wellenlängen als rasches Verfahren zur Frühdiagnose von Immissionsbelastungen an Waldbäumen. Ozoneinwirkungen auf Buchen und Pappeln.-Eur. J. Forest Pathol. 17: 149–157, 1987.

    CAS  Google Scholar 

  • Subhash, N., Mohanan, C.N., Mallia, R.J., Murlidharan, V.: Quantification of stress adaptation by laser-induced fluorescence spectroscopy of plants exposed to engine exhaust emission and drought.-Funct. Plant Biol. 31: 709–713, 2004.

    Article  CAS  Google Scholar 

  • Zhang, F., Zhang, L., Li, S.Y.: Effect of high temperature stress on leaf photosynthesis of citrus during blossom and young fruit stage.-Acta Horticult. sin. 22: 11–15, 1995.

    Google Scholar 

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Correspondence to H. K. Lichtenthaler.

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Georgieva, K., Lichtenthaler, H.K. Photosynthetic response of different pea cultivars to low and high temperature treatments. Photosynthetica 44, 569–578 (2006). https://doi.org/10.1007/s11099-006-0073-y

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  • DOI: https://doi.org/10.1007/s11099-006-0073-y

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