Abstract
The size, shape, and number of chloroplasts in the palisade and spongy parenchyma layers of Haberlea rhodopensis leaves changed significantly during desiccation and following rehydration. The chloroplasts became smaller and more rounded during desiccation, and aggregated in the middle of the cell. The size and number of chloroplasts in the palisade parenchyma cells were higher than in spongy parenchyma. The good correlation observed between the size or number of chloroplasts and the cross-sectional area of mesophyll cells, the cross-sectional width of the leaf and its water content suggested that the palisade cells were more responsive to water availability than the spongy cells. Changes in chloroplast number during desiccation and rehydration process are characteristic features for desiccation-tolerant plants (especially in homoiochlorophyllous strategy).
Similar content being viewed by others
Abbreviations
- Ac:
-
cross-sectional area of chloroplasts
- Am:
-
cross-sectional area of mesophyll cells
- DT:
-
desiccation tolerant
- HDT:
-
homoiochlorophyllous DT
- Lc:
-
length of chloroplasts
- Nc:
-
chloroplast number per cell
- PCE:
-
piece
- PDT:
-
poikilochlorophyllous DT
- PP:
-
palisade parenchyma
- SP:
-
spongy parenchyma
- W:
-
cross-sectional width of the leaf
- Wc:
-
width of chloroplasts
- WC:
-
water content
References
Abdelkader, A.F., Aronsson, H., Solymosi, K., Boddi, B., Sundqvist, C.: High salt stress induces swollen prothylakoids in dark-grown wheat and alters both prolamellar body transformation and reformation after irradiation. — J. Exp. Bot. 58: 2553–2564, 2007.
Barhoumi, Z., Djebali, W., Chaibi, W., Abdelly, C., Smaoui, A.: Salt impact on photosynthesis and leaf ultrastructure of Aeluropus littoralis. — J. Plant Res. 120: 529–537, 2007.
Bartoskova, H., Naus, J., Vykruta, M.: The arrangement of chloroplasts in cells influences the reabsorption of chlorophyll fluorescence emission. The effect of desiccation on the chlorophyll fluorescence spectra of Rhizomnium punctatum leaves. — Photosynth. Res. 62: 251–260, 1999.
Black, C.C., Jr, Mollenhauer, H.H.: Structure and distribution of chloroplasts and other organelles in leaves with various rates of photosynthesis. — Plant Physiol. 47: 15–23, 1971.
Bray, E.A.: Plant responses to water deficit. — Trends Plant Sci. 2: 48–54, 1997.
Brighigna, L., Bennici, A., Tani, C., Tani, G.: Structural and ultrastructural characterization of Selaginella lepidophylla, a desiccation-tolerant plant, during the rehydration process. — Flora 197: 81–91, 2002.
Eckardt, N.: Controlling organelle positioning: A novel chloroplast movement protein. — Plant Cell 15: 2755–2757, 2003.
Farrant, J.M., Vander Willigen, C., Loffell, D.A., Bartsch, S., Whittaker, A.: An investigation into the role of light during desiccation of three angiosperm resurrection plants. — Plant Cell Environ. 26: 1275–1286, 2003.
Farrant, J.M., Lehner, A., Cooper, C., Wiswedel, S.: Desiccation tolerance in the vegetative tissues of the fern Mohria caffrorum is seasonally regulated. — Plant J. 57: 65–79, 2009.
Gaff, D.F.: Responses of desiccation-tolerant ‘resurrection’ plants to water stress. — In: Kreeb, K.H., Richter, H., Hinckley, T.M. (ed.): Structural and Functional Responses to Environmental Stresses: Water Shortage. Pp. 255–268. SPB Academic Publishing, The Hague 1989.
Georgieva, K., Maslenkova, L., Peeva, V., Markovska, Y., Stefanov, D., Tuba, Z.: Comparative study on the changes in photosynthetic activity of the homoiochlorophyllous desiccation- tolerant Haberlea rhodopensis and desiccationsensitive spinach leaves during desiccation and rehydration. — Photosynth Res. 85: 191–203, 2005.
Georgieva, K., Szigeti, Z., Sarvari, E., Gaspar, L., Maslenkova, L., Peeva, V., Péli, E., Tuba, Z.: Photosynthetic activity of homoiochlorophyllous desiccation tolerant plant Haberlea rhodopensis during dehydration and rehydration. — Planta 225: 955–964, 2007.
Georgieva, K., Röding, A., Büchel, C.: Changes in some thylakoid membrane proteins and pigments upon desiccation of the resurrection plant Haberlea rhodopensis. — J. Plant. Physiol. 166: 1520–1528, 2009.
Georgieva, K., Sárvári, É., Keresztes, Á.: Protection of thylakoids against combined light and drought by luminal substance in the resurrection plant Haberlea rhodopensis. — Ann. Bot. 105: 117–126, 2010.
Igboanugo, A.B.I.: Adaptations to changes in illumination of chloroplast structure, chlorophyll content and light transmission of mature leaves of some deciduous tree seedlings. — Bot. Bull. Acad. Sin. 30: 133–142, 1989.
Ingle, R.A., Schmidt, U.G., Farrant, J.M., Thomson, J.A., Mundree, S.G.: Proteomic analysis of leaf proteins during dehydration of the resurrection plant Xerophyta viscosa. — Plant Cell Environ. 30: 435–446, 2007.
Jeong, W.J., Park, Y.I., Suh, K., Raven, J.A., Yoo, O.J., Liu, J.R.: A large population of small chloroplasts in tobacco leaf cells allows more effective chloroplast movement than a few enlarged chloroplasts. — Plant Physiol. 129: 112–121, 2002.
Kappen, L., Valladares, F.: Opportunistic growth and desiccation tolerance: The ecological success of poikilohydrous autotrophs. — In: Pugnaire, F., Valladares, F. (ed.): Functional Plant Ecology. Pp. 8–65. Taylor and Francis, New York 2007.
Königer, M., Delamaide, J.A., Marlow, E.D., Harris, G.C.: Arabidopsis thaliana leaves with altered chloroplast numbers and chloroplast movement exhibit impaired adjustments to both low and high light. — J. Exp. Bot. 59: 2285–2297, 2008.
McCain, D.C.: Combined effects of light and water stress on chloroplast volume regulation. — Biophys. J. 69: 1105–1110, 1995.
Papadakis, I.E., Giannakoula, A., Therios, I.N., Bosabalidis, A.M., Moustakas, M., Nastou, A.: Mn-induced changes in leaf structure and chloroplast ultrastructure of Citrus volkameriana (L.) plants. — J. Plant Physiol. 164: 100–103, 2007.
Radwan, D.E.M., Lu, G.Q., Fayez, K.A., Mahmoud, S.Y.: Protective action of salicylic acid against bean yellow mosaic virus infection in Vicia faba leaves. — J. Plant Physiol. 165: 845–857, 2008.
Sárkány, S., Szalai, I.: [Dehydration and embedding of the fixed samples to paraffin. — In: Sárkány, S., Szalai, I. (ed.): Practicum for Plant Anatomy. I. Plant Anatomical Exercises.] Pp. 550–551. Tankönyvkiadó, Budapest 1957. [In Hungarian.]
Sherwin, H.W., Farrant, J.M.: Differences in rehydration of three desiccation-tolerant angiosperm species. — Ann. Bot. 78: 703–710, 1996.
Tuba, Z.: Light, temperature and desiccation responses of CO2- exchange in desiccation tolerant moss, Tortula ruralis. — In: Pócs, T., Simon, T., Tuba, Z., Podani, J. (ed.): Proceedings of the IAB Conference of Bryoecology, Symp. Biol. Hung. 35., Part A. Pp. 137–150. Akadémiai Kiadó, Budapest 1987.
Tuba, Z., Proctor, M.C.F., Csintalan, Z.: Ecophysiological responses of homoiochlorophyllous and poikilochlorophyllous desiccation tolerant plants: a comparison and an ecological perspective. — Plant Growth Regul. 24: 211–217, 1998.
Vicré, M., Lerouxel, O., Farrant, J., Lerouge, P., Driouich, A.: Composition and desiccation-induced alternations of the cell wall in the resurrection plant Craterostigma wilmsii. — Physiol. Plant. 120: 229–239, 2004.
Wada, M., Kagawa, T., Sato, Y.: Chloroplast movement. — Annu. Rev. Plant Biol. 54: 455–468, 2003.
Wang, S., Zhang, F.: Effect of different water treatments on photosynthesis characteristics and leaf ultrastructure of cucumber growing in solar greenhouse. — Acta Hort. 633: 397–401, 2004.
Wang, X.Q., Yang, P.F., Liu, Z., Liu, W.Z., Hu, Y., Chen, H., Kuang, T.Y., Pei, Z.M., Shen, S.H., He, Y.K.: Exploring the mechanism of Physcomitrella patens desiccation tolerance through a proteomic strategy. — Plant Physiol. 149: 1739–1750, 2009.
Williams, W.E., Gorton, H.L., Witiak, S.M.: Chloroplast movements in the field. — Plant Cell Environ. 26: 2005–2014, 2003.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Nagy-Déri, H., Péli, E.R., Georgieva, K. et al. Changes in chloroplast morphology of different parenchyma cells in leaves of Haberlea rhodopensis Friv. during desiccation and following rehydration. Photosynthetica 49, 119–126 (2011). https://doi.org/10.1007/s11099-011-0020-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11099-011-0020-4