Interactive effects of excess boron and salinity on response curves of gas exchange to increase in the intensity of light of Zea mays amylacea from the Lluta Valley (Arica-Chile)

  1. Elizabeth Bastías
  2. María B González-Moro
  3. Carmen González-Murua
Journal:
Idesia

ISSN: 0073-4675 0718-3429

Year of publication: 2015

Volume: 33

Issue: 1

Pages: 33-38

Type: Article

DOI: 10.4067/S0718-34292015000100004 DIALNET GOOGLE SCHOLAR lock_openDialnet editor

More publications in: Idesia

Sustainable development goals

Abstract

High levels of B (boron) are accompanied by conditions of excessive salinity, as occurs in the Lluta Valley in northern Chile; the consequences can be drastic for crops. In the present study, seeds of Zea mays L. amylacea were grown in order to study the response curves of gas exchange to increase in the intensity of light at high levels of NaCl and B. Concentrations of 100 mM NaCl (low salinity) or 430 mM NaCl (high salinity), or an excess of B supplied as boric acid to obtain 20 and 40 mg kg-1 B were applied in the nutrient solution for 20 days. Our results complement other studies with the amylacea ecotype and confirm the high degree of tolerance to salinity and excess boron. Higher light intensified the gas exchange parameters photosynthetic rate, transpiration rate and CO2 stomatal conductance, which gradually increased. Intercellular CO2 concentration and water-use efficiency (WUE) showed no differences between treatments, except for high leaf CO2 at high salinity. The plants grown under high salt, independent of the presence of B, showed a high quantum requirement at higher light intensities.

Bibliographic References

  • Ahuja, I. (2010). Plant molecular stress responses face climate change. Trends in Plant Science. 15. 64-674
  • Araus, J.L, Slafer, G.A, Royo, C, Serret, M.D. (2008). Breeding for yield potential and stress adaptation in cereals. Critical Reviews in Plant Science. 27. 377-412
  • Bastías, E, Fernández-García, N, Carvajal, M. (2004). Aquaporin functionality in rotos 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, González-Moro, M.B, González-Murua, C. (2013). Interactive effects of excess boron and salinity on histological and ultrastructure leaves of Zea mays amylacea from Lluta Valley (Arica-Chile). Ciencia e Investigación Agraria. 40. 589-603
  • Bastías, E, González-Moro, M.B, González-Murua, C. (2013). Leaf micromorphology in Zea mays amylacea from Lluta Valley (Arica-Chile) with excess boron and salinity. Idesia. 31. 75-80
  • Borlaug, N.E. (2000). The green revolution revisited and the road ahead. Norwegian Nobel Institute. Oslo.
  • Calatayud, A, Deltoro, V. I, Barreno, E, Valle-Tascon, S.D. (1997). Changes in in vivo chlorophyll fluorescence quenching in lichen thalli as a function of water content and suggestion of zeaxanthin-associated photoprotection. Physiologia Plantarum. 101. 93-102
  • Edgerton, M.D. (2009). Increasing crop productivity to meet global needs for feed, food, and fuel. Plant physiology. 149. 7-13
  • Edwards, G.E, Nakamoto, H, Burnell, J.N, Hatch, M.D. (1985). Pyruvate, Pi dikinase and NADP-malate dehydrogenase in C4 photosynthesis: properties and mechanism of light/ dark regulation. Annual review of plant physiology. 36. 255-286
  • (2008). Land and Plant Nutrition Management Service.
  • 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
  • Hsiao, T. C. (1993). Interacting stresses on plants in a changing climate. Springer Berlin Heidelberg.
  • Lichtenthaler, H. K, Babani, F. (2000). Detection of photosynthetic activity and water stressby imaging the red chlorophyll fluorescence. Plant Physiology and Biochemistry. 38. 889-895
  • Martínez-Ballesta, M.C, Bastías, E, Zhu, C, Scháffner, 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.
  • Mittler, R. (2006). Abiotic stress, the field environment and stress combination. Trends in Plant Science. 11. 1-19
  • Nable, R.O, Bañuelos, G.S, Paull, J.G. (1997). Boron Toxicity. Plant and Soil. 193. 181-198
  • Omoto, E, Taniguchi, M, Miyake, H. (2012). Adaptation responses in C sub 4/sub photosynthesis of maize under salinity. Journal of plant physiology. 169. 469-477
  • Rivelli, A. R, Lovelli, S, Perniola, M. (2002). Effects of salinity on gas exchange, water relations and growth of sunflower (Helianthus annuus). Functional Plant Biology. 29. 1405-1415
  • Tilman, D, Cassman, K.G, Matson, P.A, Naylor, R, Polasky, S. (2002). Agricultural sustainability and intensive production practices.
  • Wang, W, Vinocur, B, Altman, A. (2003). Plant response to drought, salinity and extreme temperature: towards genetic engineering for salt stress tolerance. Planta. 218. 1-140
  • Zhang, K, Guo, Lian L., Wang, J. Lv, Zhang, . J. (2011). Improved salt tolerance and seed cotton yield in cotton (Gossypium hirsutum L.) by transformation with betA gene for glycinebetaine synthesis. Euphytica. 181. 1-16