Photosynthetica 2011, 49(4):593-602 | DOI: 10.1007/s11099-011-0075-2

Photosynthetic characteristics of ornamental passion flowers grown under different light intensities

M. V. Pires1, A. A. F. Almeida1,*, A. L. Figueiredo1, F. P. Gomes1, M. M. Souza1
1 Departamento de Ciências Biológicas, Universidade Estadual de Santa Cruz (DCB/UESC), Ilhéus, BA, Brazil

Responses of leaf gas exchange, fluorescence emission, chlorophyll concentration, and morpho-anatomical features to changes in photosynthetic photon flux density (PPFD) were studied in three wild ornamental species of Passiflora L. to select sun and shade species for landscaping projects. Artificial shade was obtained with different shading nylon nets, under field conditions, which allowed the reduction of 25, 50, and 75% of global radiation, along with a control treatment under full sunlight. For Passiflora morifolia the highest mean values of light-saturated net photosynthetic rate (P Nmax) and light compensation point (LCP) were observed at 50 and 25% shade, respectively, while the highest values of dark respiration rate (R D) and apparent quantum yield (α) were observed at 75% shade. For Passiflora suberosa litoralis the highest value of P max was observed at full sunlight. The highest mean values for P max, R D, and LCP for Passiflora palmeri var. sublanceolata were obtained at 25% shade. The highest values of net photosynthetic rate (P N) for P. morifolia, P. palmeri var. sublanceolata, and P. suberosa litoralis were 21.09, 16.15, and 12.36 μmol(CO2) m-2 s-1, observed at 50 and 75% shade and full sunlight, respectively. The values of the minimal chlorophyll fluorescence (F0) were significantly different in P. suberosa litoralis and P. palmeri var. sublanceolata, increasing with the increase of the irradiance. In contrast, the values of maximum photochemical efficiency of PSII (Fv/Fm) were significantly different only in P. suberosa litoralis, being higher at 75%, progressively reducing with the increase of PPFD levels. The total concentration of chlorophyll (Chl) was higher in shaded plants than in the ones cultivated in full sunlight. On the other hand, the values of Chl a/b ratio were reduced in shaded plants. A significant effect of shade levels on leaf area (LA) and specific leaf area (SLA) was found for the three species, whose highest mean values were observed at 75% shade. The thickness of foliar tissues was significantly higher for the three species at full sunlight and 25% shade. These results suggested that P. morifolia and P. palmeri var. sublanceolata appeared to be adapted to moderate shade conditions. P. suberosa litoralis presented higher plasticity to greater variation of the irradiance levels, while the photoinhibition was one of the limiting factors for this species at full sunlight.

Keywords: gas exchange; ornamental; Passifloraceae; photoinhibition; shade

Received: November 12, 2010; Accepted: September 4, 2011; Published: December 1, 2011Show citation

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Pires, M.V., Almeida, A.A.F., Figueiredo, A.L., Gomes, F.P., & Souza, M.M. (2011). Photosynthetic characteristics of ornamental passion flowers grown under different light intensities. Photosynthetica49(4), 593-602. doi: 10.1007/s11099-011-0075-2.
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References

  1. Abreu, P.P., Souza, M.M., Santos, E.A., Pires, M.V., Pires, M.M., Almeida, A.-A.F.: Passion flower hybrids and their use in the ornamental plant market: perspectives for sustainable development with emphasis on Brazil. - Euphytica 166: 307-315, 2009. Go to original source...
  2. Akunda, E.M., Imbamba, S.K., Kumar, D.: High density planting of coffee. II. Adaptive changes in some plant characteristics. - East Afr. Agr. For. J. 45: 133-136, 1979. Go to original source...
  3. Aleric, K.M., Kirkman, K.: Growth and photosynthetic responses of the federally endangered shrub, Lindera melissifolia (Lauraceae), to varied light environments. - Amer. J. Bot. 92: 682-689, 2005. Go to original source...
  4. Arnon, D.I.: Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. - Plant Physiol. 24: 1-15, 1949. Go to original source...
  5. Baker, N.R.: Chlorophyll fluorescence: a probe of photosynthesis in vivo. - Annu. Rev. Plant Biol. 59: 89-113, 2008. Go to original source...
  6. Barth, C., Krause, G.H., Winter K.: Responses of photosystem I compared with photosystem II to high-light stress in tropical shade and sun leaves. - Plant Cell Environ. 24: 163-176, 2001. Go to original source...
  7. Björkman, O.: Responses to different quantum flux densities. - In: Lange, O.L., Nobel, P.S., Osmond, C.B., Ziegler, H. (ed.): Encyclopedia of Plant Physiology. Pp. 57-107. Springer-Verlag, Berlin 1981. Go to original source...
  8. Boardman, N.K.: Comparative photosynthesis of sun and shade plants. - Annu. Rev. Plant Physiol. 28: 355-377, 1977. Go to original source...
  9. Campos, M.A., Uchida, T.: [Influence of shade on the growth of seedlings of three Amazon species.] - Pesq. Agropec. Bras. 37: 281-288, 2002. [In Portuguese.] Go to original source...
  10. Chaves, A.R.M., Ten-Caten, A., Pinheiro, H.A., Ribeiro, A., DaMatta, F.M.: Seasonal changes in photoprotective mechanisms of leaves from shaded and unshaded field-grown coffee (Coffea arabica L.) trees. - Trees 22: 351-361, 2008. Go to original source...
  11. Chen, H.Y., Klinka, K.: Light availability and photosynthesis of Pseudotsuga menziesii seedlings grown in the open and in the forest understory. - Tree Physiol. 17: 23-29, 1997. Go to original source...
  12. Costa, L.C.B., Almeida, A-A.F., Valle, R.R.: [Growth, chlorophyll content and anatomical structure in seedlings of Theobroma cacao under different irradiances and nitrogen levels.] - Agrotrópica 10: 21-30, 1998. [In Port.]
  13. DaMatta, F.M.: Ecophysiological constraints on the production of shaded and unshaded coffee: a review. - Field Crops Res. 86: 99-114, 2004. Go to original source...
  14. DaMatta, F.M., Maestri, M.: Photoinhibition and recovery of photosynthesis in Coffea arabica and C. canephora. - Photosynthetica 34: 439-446, 1997. Go to original source...
  15. Engel, V.L., Poggiani, F.: [Study of foliar chlorophyll concentration and its light absorption spectrum as related to shading at the juvenile phase of four native forest tree species.] - Rev. Bras. Fisiol. Veg. 3: 39-45, 1991. [In Portuguese.]
  16. Farquhar, G.D.: Feedforward responses of stomata to humidity. - Aust. J. Plant Physiol. 5: 787-800, 1978. Go to original source...
  17. Farquhar, G.D., Sharkey, T.D.: Stomatal conductance and photosynthesis. - Annu. Rev. Plant Physiol. 33: 317-345, 1982. Go to original source...
  18. Gabrielsen, E.K.: Effects of different chlorophyll concentrations on photosynthesis in foliage leaves. - Physiol. Plant. 1: 5-37, 1948. Go to original source...
  19. Givnish, T.J., Montgomery, R.A., Goldstein, G.: Adaptive radiation of photosynthetic physiology in the Hawaiian lobeliads: light regimes, static light responses and whole-plant compensation points. - Amer. J. Bot. 91: 228-246, 2004. Go to original source...
  20. Guiselini, C., Sentelhas, P.C., Oliveira, R.C., Prela, A.: [Use of plastic screens on greenhouse III: effect on growth and commercial production of Gerbera jamesonii.] - Rev. Bras. Agrometeorol. 12: 27-34, 2004. [In Portuguese.]
  21. Hikosaka, K., Terashima, I.: A model of the acclimation of photosynthesis in the leaves of C3 plants to sun and shade with respect to nitrogen use. - Plant Cell Environ. 18: 605-618, 1995. Go to original source...
  22. Iqbal, R.M., Rao, Aur-R., Rasul, E., Wahid, A.: Mathematical models and response functions in photosynthesis: an exponential model. - In: Pessarakli, M. (ed.). Handbook of Photosynthesis. Pp. 803-810. Marcel Dekker Inc., New York 1997.
  23. Laing, W.A., Greer, D.H., Schnell, T.: Photoinhibition of photosynthesis causes a reduction in vegetative growth rates of dwarf bean (Phaseolus vulgaris) plants. - Aust. J. Plant Physiol. 22: 511-520, 1995. Go to original source...
  24. Leverenz, J.W.: Shade shoot structure of conifers and the photosynthetic response to light at two CO2 partial pressures. - Funct. Ecol. 9: 413-421, 1995. Go to original source...
  25. Lloyd, J., Farquhar, G.D.: 13C discrimination during CO2 assimilation by the terrestrial biosphere. - Oecologia 99: 201-215, 1994. Go to original source...
  26. Lusk, C., Reich, P.B., Montgomery, R.A., Ackerly, D.D., Cavender-Bares, J.: Why are evergreen leaves so contrary about shade? - Trends Ecol. Evol. 23: 299-303, 2008. Go to original source...
  27. Matos, F.S., Wolfgramm, R., Cavatte, P.C., Villela, F.G., Ventrella, M.C., DaMatta, F.M. Phenotypic plasticity in response to light in the coffee tree. - Environ. Exp. Bot. 67: 421-427, 2009. Go to original source...
  28. Milward-de-Azevedo, M.A., Baumgratz, J.F.A.: [Passiflora L. subgenus Decaloba (DC.) Rchb. (Passifloraceae) in southeastern Brazil.] - Rodriguésia 55: 17-54, 2004. [In Portuguese.]
  29. Montanari, R.M., Sousa, L.A., Leite, M.N., Coelho, A.D., Viccini, L.F., Stefanini, M.B.: [Phenotypical plasticity of the external morphology in Lippia alba (Mill.) N.E.BR. ex Britt. & Wilson in response to level of luminosity and fertilization.] - Rev. Bras. Plant. Med. 6: 96-101, 2004. [In Portuguese.]
  30. Morais, H., Medri, M.E., Marur, C.J., Caramori, P.H., Ribeiro, A.M., Gomes, J.C.: Modifications on leaf anatomy of Coffea arabica caused by shade of Pigeonpea (Cajanus cajan). - Braz. Arch. Biol. Techn. 47: 863-871, 2004. Go to original source...
  31. Oguchi, R., Hikosaka, K., Hirose, T.: Does the photosynthetic light-acclimation need change in leaf anatomy. - Plant Cell Environ. 26: 505-512, 2003. Go to original source...
  32. Ramalho, J.D., Campos, P.S., Quartin, V.L., Silva, M.J., Nunes, M.A.: High irradiance impairments on photosynthetic electron transport, ribulose-1,5-bisphosphate carboxylase/oxygenase and N assimilation as a function of N availability in Coffea arabica L. plants. - J. Plant Physiol. 154: 319-326, 1999. Go to original source...
  33. Roháček, K.: Chlorophyll fluorescence parameters: the definitions, photosynthetic meaning and mutual relationships. - Photosynthetica 40: 13-29, 2002. Go to original source...
  34. Smith, W.K., Vogelmann, T.C., Delucia, E.H., Bell, D.T., Shepherd, K.A.: Leaf form and photosynthesis: Do leaf structure and orientation interact to regulate internal light and carbon dioxide? - Bioscience 47: 785-793, 1997. Go to original source...
  35. Ulmer, T., MacDougal, J.M.: Passiflora - Passion Flowers of the World. - Timber Press, Portland 2004.
  36. Vanderplank, J.: Passion flowers. - The MIT Press, Cambridge 2000.
  37. Zhang, S., Ma, K., Chen, L.: Response of photosynthetic plasticity of Paeonia suffruticosa to changed light environments. - Environ. Exp. Bot. 49: 121-133, 2003. Go to original source...