Interactive effects of excess boron and salinity on histological and ultrastructural leaves of Zea mays amylacea from the Lluta Valley (Arica-Chile)

  1. Elizabeth Bastías
  2. María B González-Moro
  3. Carmen González-Murua
Aldizkaria:
Ciencia e investigación agraria: revista latinoamericana de ciencias de la agricultura

ISSN: 0718-1620

Argitalpen urtea: 2013

Alea: 40

Zenbakia: 3

Orrialdeak: 581-595

Mota: Artikulua

DOI: 10.4067/S0718-16202013000300011 DIALNET GOOGLE SCHOLAR lock_openDialnet editor

Beste argitalpen batzuk: Ciencia e investigación agraria: revista latinoamericana de ciencias de la agricultura

Laburpena

E.I. Bastías, M.B. González-Moro, and C. González-Murua. 2013. Interactive effects of excess boron and salinity on histological and ultrastructural leaves of Zea mays amylacea from the Lluta Valley (Arica-Chile). Cien. Inv. Agr. 40(3): 581-595. Maize is widely cultivated throughout the world, and more maize is produced each year than any other grain. Studies on the response of maize to salinity have typically focused on physiological aspects, but few studies have addressed the effects of salinity on the anatomical and ultrastructural characteristics of different plant organs. We analyzed the cell structure and changes in tissue organization in young leaves of Zea mays L. amylacea as a consequence of high salt and boron (B) levels. Plants were treated in nutrient solutions for 20 days with concentrations of 100 mM NaCl (Low salinity, L) or 430 mM NaCl (High salinity, H) in the case of saline treatments or with an excess of B supplied as boric acid to obtain 20 mg (334 μM) or 40 mg (668 μM) B kg-1. The application of B under no salt and low salinity conditions did not result in ultrastructure changes in mesophyll cells (MC) or bundle sheath cells (BSC). The high salinity conditions the amylacea leaf cells showed some alterations in MC chloroplasts, which appeared swollen and rounded. The BSC chloroplasts lost their perpendicular disposition to the cell wall. Moreover, the absolute absence of plastoglobuli could indicate a greater resistance to oxidative damage.

Erreferentzia bibliografikoak

  • Barhoumi, Z, Djebali, W, Chaibi, W, Abdelly, C.H., Amaoui, A. (2007). Salt impact on photosynthesis and leaf ultrastructure of Aeluropus littoralis. Journal of Plant Research. 120. 529-537
  • Bastías, E, Fernandez-Garcia, N, Carvajal, M. (2004). Aquaporin functionality in roots of Zea mays in relation to the interactive effects of boron and salinity. Plant Biology. 6. 415-421
  • Bastías, E, González-Moro, M.B., González-Murua, C. (2004). Zea mays L. amylacea from the Lluta Valley (Arica-Chile) tolerates salinity stress when high levels of boron are available. Plant and Soil. 267. 73-84
  • Bastías, E, Alcaraz-López, C, Bonilla, I, Martínez-Ballesta, M.C., Bolaños, L, Carvajal, M. (2010). Interactions between salinity and boron toxicity in tomato plants involve apoplastic calcium. Journal of Plant Physiology. 167. 54-60
  • Beerling, D.J., Woodward, F.I.. (1995). Stomatal responses of variegated leaves to CO2 enrichment. Annals Botany. 75. 507-511
  • Bonilla, I, Abadía, J, Bolaños, L. (2010). Agricultural Sciences: Topics in Modern Agriculture. Studium Press. Houston. 145-171
  • Burssens, S, Himanen, K, Van de Cotte, B, Beeckman, T, Van Montagu, M, Inze, D, Verbrug-gen, N. (2000). Expression of cell cycle regulatory genes and morphology alterations in response to salt stress in Arabidopsis thaliana. Planta. 211. 632-640
  • Cramer, G.R., Alberico, G.J., Schmidt, C. (1994). Salt tolerance is not associated with the sodium accumulation of two maize hybrids. Australian Journal Plant Physiology. 21. 675-692
  • Dekov, I, Tsonev, T, Yordanov, I. (2000). Effects of water stress and high-temperature stress on the structure and activity of photosynthethic apparatus of Zea mays and Helianthus annus. Photosynthetica. 38. 361-366
  • Dengler, N, Dengler, R, Donnelly, P, Hattersley, P. (1994). Quantitative leaf Anatomy of C3 and C4 grasses (Poaceae): bundle sheath and mesophyll surface area relationships. Annals of Botany. 73. 241-255
  • Flowers, T.J., Yeo, A.R.. (1995). Breeding for salinity resistance in crop plants: Where next?. Australian Journal of Plant Physiology. 22. 875-884
  • González-Moro, B, Lacuesta, M, Becerril, J.M., González-Murua, C, Muñoz-Rueda, A. (1997). Glycolate accumulation causes a decrease of photosynthesis by inhibiting RUBISCO activity in maize. Journal of Plant Physiology. 150. 388-394
  • Hernández, J.A., Ferrer, M.A., Jiménez, A, Ros-Barceló, A, Sevilla, F. (2001). Antioxidant systems and O2-/H2O2 production in the apoplast of Pisum sativum L. leaves: its relation with NaCl-induced necrotic lesions in minor veins. Plant Physiology. 127. 817-834
  • Hsiao, T.C., Silk, W.K., Jing, J. (1985). Leaf growth and water deficits: biophysical effects. Cambridge Univ. Press. 239-266
  • Jiao, J, Chollet, R. (1988). Light/dark regulation on maize leaf phosphoenolpyruvate carboxylase by in vivo phosphorilation. Arch Biochemical and Biophysical. 261. 409-417
  • Kanai, R, Edwards, G.E.. (1973). Separation of mesophyll protoplasts and bundle sheath cells from maize leaves for photosynthetic studies. Plan Physiology. 51. 1133-1137
  • Kirch, H.H., Vera-Estrella, R, Golldack, D, Quigley, F, Michalowski, C.B., Barkla, B.J., Bohnert, H.J.. (2000). Expression of water channel proteins in Mesembryanthemumcrystallinum. Plant Physiology. 123. 111-124
  • Laemli, U. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophageT4. Nature. 227. 680-686
  • Lal, A, Edwards, G.E.. (1996). Analysis of inhibition of photosynthesis under water stress in the C4 species Amaranthus cruentus and Zea mays: electron transport, CO2 fixation and carboxylation capacity. Australian Journal of Plant Physiology. 23. 403-412
  • Leegood, R.C.. (1985). The intercellular compartmentation of metabolites in leaves of Zea mays. Planta. 164. 163-171
  • Martínez-Ballesta, M.C., Bastías, E, Zhu, C, Schaffner, A.R., González-Moro, B, González-Murua, C, Carvajal, M. (2008). Boric acid and salinity effects on maize roots: Response of aquaporins ZmPIP1 and ZmPIP2, and plasma membrana H+-ATPase, in relation to water and nutrient uptake. Physiology Plantarum. 132. 479-490
  • Mitsuya, S, Takeoka, Y, Miyake, H. (2000). Effects of sodium chloride on foliar ultrastructure of sweet potato (Ipomoea batatas Lam.) plantlets grown under light and dark conditions in vitro. Journal of Plant Physiology. 157. 661-667
  • Navarro, A, Boñan, S, Olmos, E, Sánchez-Blanco, M.J.. (2007). Effects of sodium chloride on water potential components, hydraulic conductivity, gas exchange and leaf ultrastructure of Arbutus unedo plants. Plant Science. 172. 473-480
  • Niu, X, Damsz, B, Kononowicz, A.K., Bressan, R.A., Hasegawa, P.M.. (1996). NaCl-induced alterations in both cell structure and tissue-specific plasma membrane H+-ATPase gene expression. Plant Physiology. 111. 679-686
  • Novoa, R.S., Villaseca, P, Del Canto, P, Ravanet, J.L., Sierra, C, Del Pozo, A. (1989). Mapa Agroclimático de Chile. INIA. Santiago.
  • Omoto, E, Taniguchi, M, Miyake, H. (2012). Adaptation responses in C4 photosynthesis of maize under salinity. Journal of Plant Physiology. 169. 469-477
  • Papadakis, I.E., Dimassi, K.N., Bosabadilis, A.M., Therios, I.N., Patakas, A, Iannakoula, A. (2004). Boron toxicity in "Clementine" mandarin plants grafted on two rootstocks. Plant Science. 166. 539-547
  • Papadakis, I.E., Dimassi, K.N., Bosabadilis, A.M., Therios, I.N., Patakas, A, Innakoula, A. (2004). Effects of boron excess on some physiological and anatomical parameters of "Navelina" orange plants grafted on two rootstocks. Environmental and Experimental Botany. 51. 247-257
  • Pareek, A, Singla, S.L., Grover, A. (1997). Short-term salinity and high temperature stress-associated ultrastructure alterations in young leaf cells of Oryza sativa L.. Annals Botany. 80. 629-639
  • Pessarakli, M, Szabolics, I. (1999). Handbook of Plant and Crop Stress. 2. Marcel Dekker. New York. 1-16
  • Rahman, M.S., Matsumuro, T, Miyake, H, Takeoka, Y. (2000). Salinity induced ultrastructural alterations in leaf cells of rice (Oryza sativa L.). Plant Production Science. 3. 422-429
  • Ruiz, J.M., Lopez-Lefrere, L.R., Sánchez, E, Rivero, R.M., García, P.C., Romero, L. (2001). Preliminary studies on the influence of boron on the foliar biomass and quality of tobacco leaves subjected to NO-3 fertilization. Journal of the Science of Food and Agriculture. 81. 739-744
  • Sam, O, Ramírez, C, Coronado, M.J., Testillano, P.S., Risueño, C. (2003). Changes in tomato leaves induced by NaCl stress: leaf organization and cell ultrastructure. Biología Plantarum. 47. 361-366
  • Serraj, R, Fleurat-Lessard, P, Jaillard, B, Drevon, J.J.. (1995). Structural changes in the inner-cortex cells of soybean root-nodules are induced by short-term exposure to high salt or oxygen concentrations. Plant, Cell and Environment. 18. 455-462
  • Shi, H.Z., Ishitani, M, Kim, C, Zhu, J.K.. (2000). The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na/H antiporter. Proc. Natl. Acad. Sc. USA. 97. 6896-6901
  • Singh, N.K., Nelson, E, Kuhn, D, Hasegawa, P.M., Bressan, R.A.. (1989). Molecular cloning of osmotin and regulation of its expression by ABA and adaptation to low water potential. Plant Physiology. 90. 1096-1101
  • Sotiropoulos, T.E., Therios, I.N., Dimassi, K.N., Bosabalidis, A.M., Kofidis, G. (2002). Nutritional status, growth, CO2 assimilation, and leaf anatomical responses in two kiwifruit species under boron toxicity. Journal of Plant Nutrition. 25. 1249-1261
  • Suarez, N, Sobrado, M.A., Medina, E. (1998). Salinity effects on the leaf water relations component sand ion accumulation patterns in Avicennia germinans L. seedlings. Oecologia. 114. 299-304
  • Utrillas, M.J., Alegre, L. (1997). Impact of water stress on leaf anatomy and ultrastructure in Cynodon dactylon (L.) Pers. under natural conditions. International Journal of Plant Sciences. 158. 313-324
  • Vera Estrella, R, Barkla, B.J., Bohnert, H.J., Pantoja, O. (2004). Novel regulation of plant aqua-porins. Plant Physiology. 135. 2318-2329
  • Yamane, K, Mitsuya, S.H., Kawasaki, M, Taniguchi, M, Miyake, H. (2004). Salinity-induced chloroplast damages in rice leaves (Oryza sativa L.) are reduced by pretreatment with methyl viologen. 4 International Crop Science Congress. Brisbone.7