biologia plantarum

International journal on Plant Life established by Bohumil Němec in 1959

Biologia plantarum 54:415-422, 2010 | DOI: 10.1007/s10535-010-0076-1

Chlorophyll fluorescence in micropropagated Rhododendron ponticum subsp. baeticum plants in response to different irradiances

M. L. Osório1,*, J. Osório2, A. Romano1
1 IBB/CGB, Faculty of Sciences and Technology, University of Algarve, Faro, Portugal
2 ICAAM, Faculty of Sciences and Technology, University of Algarve, Faro, Portugal

The aim of this study was to investigate acclimation of micropropagated plants of Rhododendron ponticum subsp. baeticum to different irradiances and recovery after exposure to high irradiance. Plants grown under high (HL) or intermediate (IL) irradiances displayed higher values of maximum electron transport rate (ETRmax) and light saturation coefficient (Ek) than plants grown under low irradiance (LL). The capacity of tolerance to photoinhibition (as assessed by the response of photochemical quenching, qp) varied as follows: HL > IL > LL. Thermal energy dissipation (qN) was also affected by growth irradiance, with higher saturating values being observed in HL plants. Light-response curves suggested a gradual replacement of qp by qN with increasing irradiance. Following exposure to irradiance higher than 1500 μmol m-2 s-1, a prolonged reduction of the maximal photochemical efficiency of PS 2 (Fv/Fm) was observed in LL plants, indicating the occurrence of chronic photoinhibition. In contrary, the decrease in Fv/Fm was quickly reverted in HL plants, pointing to a reversible photoinhibition.

Keywords: electron transport; photochemical quenching; photoinhibition; thermal energy dissipation
Subjects: chlorophyll fluorescence; electron transfer rate; ex vitro transfer; photoinhibition; photon flux density; photosynthetic rate; photosystems (PS 1, PS 2); Rhododendron pontium; thermal energy dissipation

Received: October 21, 2008; Accepted: April 11, 2009; Published: September 1, 2010  Show citation

ACS AIP APA ASA Harvard Chicago IEEE ISO690 MLA NLM Turabian Vancouver
Osório, M.L., Osório, J., & Romano, A. (2010). Chlorophyll fluorescence in micropropagated Rhododendron ponticum subsp. baeticum plants in response to different irradiances. Biologia plantarum54(3), 415-422. doi: 10.1007/s10535-010-0076-1
Download citation

References

  1. Almeida, R., Gonçalves, S., Romano, A.: In vitro micropropagation of endangered Rhododendron ponticum L. subsp. baeticum (Boissier & Reuter) Handel-Mazzetti. - Biodiv. Conserv. 14: 1059-1069, 2005. Go to original source...
  2. Baker, N.R.: Possible role of photosystem II in environmental perturbations of photosynthesis. - Physiol. Plant. 81: 563-570, 1991. Go to original source...
  3. Bailey, S., Walters, R.G., Jansson, S., Hort, P.: Acclimation of Arabidopsis thaliana to the light environment: the existence of separate low light and high light responses. - Planta 213: 794-801, 2001. Go to original source...
  4. Bilger, W., Schreiber, U.: Energy-dependent quenching of dark level chlorophyll fluorescence in intact leaves. - Photosynth. Res. 10: 303-308, 1986. Go to original source...
  5. Bilger, W., Schreiber, U., Brock, M.: Determination of the quantum efficiency of photosystem II and nonphotochemical of chlorophyll quenching in the field. - Oecologia 102: 425-432, 1995. Go to original source...
  6. Björkman, O., Demmig, B.: Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77K among vascular plants of diverse origins. - Planta 170: 489-504, 1987. Go to original source...
  7. Čaňová, I., Ďurkovič, J., Hladká, D.: Stomatal and chlorophyll fluorescence characteristics in European beech cultivars during leaf development. - Biol. Plant. 52: 577-581, 2008. Go to original source...
  8. Carvalho, C.L., Osório, M.L., Chaves, M.M., Amâncio, S.: Chlorophyll fluorescence as an indicator of photosynthetic functioning of in vitro grapevine and chestnut plantlets under ex vitro acclimatization. - Plant Cell Tissue Organ Cult.- 67: 271-280, 2001. Go to original source...
  9. Demmig-Adams, B., Adams III, W.W., Logan, B.A, Verhoeven, A.S.: Xanthophyll cycle-dependent energy dissipation and flexible photosystem II efficiency in plants acclimated to light stress. - Aust. J. Plant. Physiol. 22: 249-260, 1995. Go to original source...
  10. Einhorn, K.S., Rosenqvist, E., Leverenz, J.W.: Photoinhibition in seedlings of Fraxinus and Fagus under natural light conditions: implications for forest regeneration? - Oecologia 140: 241-251, 2004. Go to original source...
  11. Ensminger, I., Foerster, J., Hagen, C., Braune, W.: Plasticity and acclimation to light reflected in temporal and spatial changes of small scale macroalgal distribution in a stream. - J. exp. Bot. 56: 2047-2058, 2005. Go to original source...
  12. Fay, M.: Conservation of rare and endangered plants using in vitro methods. - In Vitro cell. dev. Biol. Plant 28: 1-4, 1992. Go to original source...
  13. Fuentes, G., Talavera, C., Desjardins, Y., Santamaría, J.M.: High irradiance can minimize the negative effect of exogenous sucrose on the photosynthetic capacity of in vitro grown coconut plantlets. - Biol. Plant. 49: 7-15. 2005. Go to original source...
  14. Genty, B., Briantais, J.M., Baker, N.R.: The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. - Biochim. biophys. Acta 99: 87-92, 1989. Go to original source...
  15. Golding, A.J., Johnson, G.N.: Down-regulation of linear and activation of cyclic electron transport during drought. - Planta 218: 107-114, 2003. Go to original source...
  16. Guo, X.R., Cao, K.F., Xu, Z.F.: Acclimation to irradiance in seedlings of three tropical rain forest Garcinia species after simulated gap formation. - Photosynthetica 44: 193-201, 2006. Go to original source...
  17. Harbinson, J., Genty, B., Baker, N.R.: The relationship between CO2 assimilation and electron transport in leaves. - Photosynth. Res. 25: 213-224, 1990. Go to original source...
  18. Hu, Y.-A., Sun, G.-Y., Wang, X.-C.: Induction characteristics and response of photosynthetic quantum conversion to changes in irradiance in mulberry plants. - J. Plant Physiol. 164: 959-968, 2007. Go to original source...
  19. Kitao, M., Lei, T.T., Koike, T., Tobita, H., Maruyhama, Y.: Susceptibility to photoinhibition of three deciduous broadleaf tree species with different successional traits raised under various light regimes. - Plant Cell Environ. 23: 81-89, 2000. Go to original source...
  20. Kitao, M., Utsugi, H., Kuramoto, S., Tabuchi, R., Fujimoto, K., Lihpai, S.: Light-dependent photosynthetic characteristics species native to Pohnpei Island, Micronesia. - Physiol. Plant. 117: 376-382, 2003. Go to original source...
  21. Kosová, K., Haisel, D., Tichá, I.: Photosynthetic performance of two maize genotypes as affected by chilling stress. - Plant Soil Environ. 51: 206-212; 2005. Go to original source...
  22. Krall, J.P., Edwards, G.E.: Relationship between photosystem II activity and CO2 fixation in leaves. - Physiol. Plant. 86: 180-187, 1992. Go to original source...
  23. MacIntyre, H.L., Kana, T.M., Anning, T., Geider, R.J.: Photoacclimation of photosynthesis irradiance response curves and photosynthetic pigments in microalgae and cyanobacteria. - J. Phycol. 38: 17-38, 2002. Go to original source...
  24. Osmond, C.B.: What is photoinhibition? Some insights for comparisons of shade and sun plants. - In: Baker, N.B., Bowyer, J.R. (ed.): Photoinhibition of Photosynthesis - from Molecular Mechanisms to the Field. Pp. 1-24. Bios Scientific Publishers, Oxford 1994.
  25. Osório, M.L., Breia, E., Rodrigues, A., Osório, J., Le Roux, X., Daudet, F.A., Ferreira, I., Chaves, M.M.: Limitations to carbon assimilation by mild drought in nectarine trees growing under field conditions. - Environ. exp. Bot. 55: 235-247, 2006. Go to original source...
  26. Pearcy, R.W.: Acclimation to sun, shade. - In: Raghavendra, A.S. (ed.): Photosynthesis: a Comprehensive Treatise. Pp. 250-263. Cambridge University Press, Cambridge 1998.
  27. Platt, T., Gallegos, C.L., Harrison, W.G.: Photoinhibition of photosynthesis in natural assemblages of marine phytoplankton. - J. mar. Res. 38: 687-701, 1980.
  28. Pospíąilová, J., Synková, H., Haisel, D., Ba»ková, P.: Effect of abscisic acid on photosynthetic parameters during ex vitro transfer of micropropagated tobacco plantlets. - Biol. Plant. 53: 11-20, 2009. Go to original source...
  29. Pospíąilová, J., Tichá, I., Kadleček, P., Haisel, D., Plzáková, ©.: Acclimatization of micropropagated plants to ex-vitro conditions. - Biol. Plant. 42: 481-497, 1999. Go to original source...
  30. Ralph, P.J., Gademann, R.: Rapid light curves: a powerful tool to assess photosynthetic activity. - Aquat. Bot. 82: 222-237, 2005. Go to original source...
  31. Rascher, U., Liebig, M., Lüttge, U.: Evaluation of instant lightresponses curves of chlorophyll fluorescence parameters obtained with a portable chlorophyll fluorometer on site in the field. - Plant Cell Environ. 23: 1397-1405, 2000. Go to original source...
  32. Walters, R.G.: Towards an understanding of photosynthetic acclimation. - J. exp. Bot. 56: 435-447, 2005. Go to original source...
  33. Zhang, L.L., Wen, D.Z., Fu, S.L.: Responses of photosynthetic parameters of Mikania micrantha and Chromolaena odorata to contrasting irradiance and soil moisture. - Biol. Plant. 53: 517-522, 2009. Go to original source...