- Citado por SciELO
- Citado por Google
- Similares en SciELO
- Similares en Google
versión On-line ISSN 0718-5839
Chilean J. Agric. Res. vol.72 no.1 Chillán mar. 2012
Chilean Journal of Agricultural Research 72(1) January - March
Increased Growth and Changes in Wheat Mineral Composition through Calcium Silicate Fertilization under Normal and Saline Field Conditions
Aumento de Crecimiento y Cambios en la Composición Mineral de Trigo por Fertilización con Silicato de Calcio bajo Condiciones de Campo Normales y Afectadas por Sales
Anser Ali1*, Shahzad M.A. Basra2, Safdar Hussain1, and Javaid Iqbal1
1University of Agriculture, Sub-Campus D.G. Khan, Faisalabad, Pakistan-38040. "Corresponding author (email@example.com).
2University of Agriculture, Department of Crop Physiology, Faisalabad, Pakistan-38040.
Salinity stress is a major and ever-present threat to crop production, especially where irrigation is necessary for agriculture. Two independent field experiments were carried out in natural non-saline (site-I; electrical conductivity [EC] < 4 dS m-1) and saline (site-II; EC = 10-13.8 dS m-1) fields to test the efficacy of different doses of Si (0, 75, and 150 mg kg-1) on two wheat (Triticum aestivum L.) cultivars with different salt susceptibility, i.e., 'Auqab-2000' (salt-sensitive) and 'SARC-5' (salt-tolerant). The crop was harvested at maturity and various ionic and yield parameters were recorded. The concomitant increase in the number of tillers, number of grains per spike, grain yield, and biological yield were observed given that Si was applied under both optimal and salt-affected field conditions. It was concluded that 'SARC-5' is better than 'Auqab-2000' under salt stress. When Si was applied, similar effects were observed in both cultivars regardless of their salt sensitivity and whether the field was saline or non-saline, and it enhanced wheat growth by improving K+:Na+, which was adversely influenced by salt stress.
Key words: Triticum aestivum, salt stress, silicon, wheat growth, K+:Na+, water potential, stomatal conductance.
El estrés salino es un riesgo importante y siempre presente para la producción de cultivos, especialmente donde el riego es una inevitable ayuda a la agricultura. Se realizaron dos experimentos de campo independientes en campos no salino natural (sitio I; conductividad eléctrica [EC] < 4 dS m-1) y salino (sitio II; EC = 10-13.8 dS m-1) para probar la eficacia de diferentes dosis de Si (0, 75, y 150 mg kg-1) en dos cultivares de trigo (Triticum aestivum L.) difiriendo en susceptibilidad a sales: 'Auqab-2000' (sensible a sales) y 'SARC-5' (tolerante a sales). El cultivo se cosechó a la madurez y se registraron varios parámetros iónicos y de rendimiento. Se observó que el aumento concomitante en número de macollas, número de granos por espiga, rendimiento de grano, y rendimiento biológico se debió a aplicación de Si bajo condiciones de campo óptimas y afectadas por sales. Se concluyó que 'SARC-5' rinde mejor que 'Auqab-2000' bajo condiciones de estrés salino. Efectos casi similares por aplicación de Si se observaron para ambos cultivares independiente de la sensibilidad a sales y su inclusión en el campo ya sea salino o no salino aumentó el crecimiento del trigo mejorando la relación K+:Na+ adversamente influenciada por el estrés salino.
Palabras clave: Triticum aestivum, estrés salino, silicio, crecimiento de trigo, K+:Na+, potencial hídrico, conductancia estomática.
The global population of about 6.3 billion is increasing at an alarming rate. It is estimated that it will be 9.0 billion by 2050 (Lal, 2007). Efforts are underway to enhance the production of different crops to meet the food requirements of a rapidly increasing population. Salinity is one of the major factors responsible for soil degradation and low crop productivity. About one third of the world's land surface has arid or semiarid conditions (4.8 x 109 ha) of which half is estimated to be affected by salinity (Croughan and Rains, 1982) and accounts for about 7% of the world's total land area (Szaboles, 1989). Approximately 6.67 Mha of the total agricultural area in Pakistan is also affected by various degrees of salinity/ sodicity (Khan, 1998).
Salinity is a major actual abiotic stress (Rueda-Puente et al., 2007), one of the most severe environmental problems affecting crop growth (Lopez et al., 2002), and along with drought, it seems to be one of the world's most serious agricultural problems. Excess of soluble salts in the root zone negatively affects plant growth and yield through osmotic effects, nutritional imbalances, and specific ion toxicities (Grattan and Grieve, 1999; Munns, 2005; Tahir et al., 2006) due to the excessive buildup of Na+ and Cl-(Cramer and Nowak, 1992; Lutts et al., 1996; Khan, 1998; Grattan and Grieve 1999). It is reported that Na+ disturbs K+ nutrition, which in turn inhibits enzyme activity (Jaleel et al., 2007). Wheat (Triticum aestivum L.), a glycophytic plant, is adversely affected by salinity stress (Zhu, 2003), and yield losses of up to 45% have been reported because of this (Qureshi and Barrett-Lennard, 1998).
Several chemical, physical (engineering), and biological approaches were used for better crop production in saline soils in the past. The integrated use of these approaches was crucial due to economic and environmental limitations. Genotypic variation is useful to screen and develop more salt-tolerant genotypes. Wheat genotypes also differ significantly in salinity tolerance (Munns, 2002; Flowers, 2004; Saqib et al., 2005) since salt-tolerant plants accumulate less Na+ than salt-sensitive plants, which maintain the ionic balance in plant tissues (Tahir et al., 2006). The exogenous application of nutrients was considered as a shotgun approach to alleviate salt stress (Raza et al., 2006), so the damaging effects of salts were lessened with exogenously applied K+ in wheat (Akram et al., 2007), N in Phaseolus vulgaris L. (Wagenet et al., 1983), and Ca in snap bean (Awada et al., 1995). Furthermore, some beneficial mineral nutrients have been studied that can counteract the adverse effects of salt stress such as silicon (Si), which provides significant benefits to plants at various growth stages.
Silicon is the second most abundant element on the earth's crust after oxygen. It is accumulated in plants at a rate comparable to those of macronutrient elements such as Ca, Mg, and P (Epstein, 1999) and is beneficial for the growth of many plants under various abiotic (e.g., salt, drought, and metal toxicity) and biotic (plant diseases and pests) stresses (Liang et al., 2003; Ma, 2004). Graminaceous plants accumulate more Si in their tissues than other species (Matichenkov and Kosobrukhov, 2004); wheat is a member of the Gramineae family and Si is designated as an accumulator so that adding Ca-silicate to salt-stressed plants can reduce their salinity stress, and it plays a multiple role in the existence of plants and crop performance. The responsible mechanism involved in salt tolerance is still not clear; however, it has been reported that Si reduces Na+ uptake by forming a complex with Na+ in the soil (Ahmad et al., 1992). Silicon is deposited in the leaves, which leads to decreased transpiration and diluted salts accumulated in the saline environment (Matoh et al., 1986).
The purpose of this study was to provide some additional experimental evidence about the role of Si on wheat crop biology under field conditions. To achieve this objective, the effect of Si was assessed for two cultivars with different salinity tolerances. The hypothesis was to corroborate whether Si can enhance the salt tolerance of this species under field conditions.
MATERIALS AND METHODS
Two experiments were conducted in normal and saline fields, respectively. To assess the role of Si in field level salinity tolerance, two contrasting wheat genotypes (salt-sensitive 'Auqab-2000' and salt-tolerant 'SARC-5') were grown at site-I (normal soil with EC < 4 dS m-1) and site-II (naturally saline with EC = 10-13.8 dS m-1). Both sites were located within a radius of less than 500 m in the Post Graduate Agricultural Research Station (PARS), University of Agriculture Faisalabad, Pakistan. The seed bed was prepared with 2-3 cultivations followed by planking. Soil samples from both sites were collected at a 0 to 15 cm depth to determine various physiochemical soil characteristics of the selected fields (Table 1). Seeds were sown at a dose of 100 kg ha-1 at distance of 22.5 cm between rows. Treatments mentioned below were triplicated according to a randomized complete block design with a factorial design in a 6 x 1.5 m2 net plot size. A uniform dose of basal fertilizer was applied to all plots with 75 kg N ha-1 as urea, 50 kg P ha-l as single super phosphate, and 30 kg K ha-l as sulfate of potash (SOP). After seedling emergence (23 d after sowing), Si was applied at both sites in the respective plots at 0 (control), 75, and 150 mg Si kg-1 soil with calcium silicate after dissolving it with KOH at 71 °C on a hotplate. All of the Si was applied to the plots of the Si+ treatment through the placement method employing a calcium silicate solution.
A CaCl2 solution was applied to the Si-deficient treatment plots to balance the same total Ca as in the Si+ treatment so as to identify only the effect of Si. Observations were recorded in both field experiments.
Determination of Na+, K+, and Si from wheat straw
The ground oven-dried leaf material (0.1 g) was digested with a mixture of 2 mL of sulfuric acid and hydrogen peroxide according to Wolf's (1980) method. Potassium and Na in the digested material were determined with a flame photometer (Jenway, PFP-7, Staffordshire, UK).
Silicon was determined in harvested leaves; these were oven-dried and ground into a fine powder in a Wiley mill with a built-in stainless steel chamber. The ground samples (0.5 g) were digested in 2 mL of 50% hydrogen peroxide (H2O2) and 4.5 g of 50% NaOH in open vessels (Teflon beakers) on a hotplate at 150 °C for 4 h. The Si concentration was measured by the calorimetric amino molybdate blue color method (Elliot and Snyder, 1991). In a 50 mL of polypropylene volumetric flask, 1 mL of supernatant filtrate liquid was added to 10 mL of ammonium molybdate (54 g L-1) solution and 25 mL of 20% acetic acid. After 5 min, 5 mL of 20% tartaric acid and 1 mL of reducing solution were added to a flask and the volume was made up of 20% citric acid. After 30 min, the absorbance was measured at the 650 nm wavelength with a UV visible spectrophotometer (Spectronic 100, Shimadzu, Kyoto, Japan). The reducing agent was prepared by dissolving 0.5 g 1-amino-2-naphthol-4-sulfonic acid, 1 g Na2SO3, and 30 g NaHSO3 in 200 mL water (Elliott and Snyder, 1991).
Yield and yield components
The number of tillers per m2 was counted, recorded, and converted into the total number of tillers per plot. Ten spikes were randomly selected from each subplot; the mean spike length, number of spikelets per spike, number of grains per spike, and 1000 grain weight were recorded. Central rows from each subplot were harvested, tied into bundles left to dry in the sun. The samples were then weighed with a spring balance and yield was converted into kg ha-1. Grain yield was measured at harvest from the central rows of each subplot and yield converted into kg ha-1. Finally, the harvest index (HI) for each plot was calculated with the following formula:
HI = (Grain yield/biological yield) x 100 Data collected during the study were statistically analyzed by Fisher's ANOVA Technique and significant means were separated by the Least Significant Difference (LSD) Test at P = 0.05 (Steel and Torrie, 1996).
Data regarding plant height, number of tillers, number of spikelets per spike, number of grains per spike influenced by salinity and Si are shown in Table 2. Salinity stress significantly (P < 0.05) reduced these parameters in the saline field (site-II) when compared with the normal field (site-I). Calcium silicate fertilization increased values significantly by 0 < 75 < 150 mg kg-1 in both saline and non-saline field conditions. Comparing the cultivars for plant height, 'Auqab-2000' (salt-sensitive) was higher than 'SARC-5' (salt-tolerant) at both site-I and site-II.
Si0, Si1, and Si2 represent 0, 75, and 150 mg Si kg-1, respectively. The values are means of three replicates. Means with the same letter do not differ at P = 0.05.
Table 2 indicates that spike length and grain weight were lower at site-II (saline field) than at site-I. Applying Ca-silicate did not influence spike length and grain weight of wheat plants at site-I resulting in non-significant differences among all Si levels; nonetheless, applying Si at site-II improved the unpleasant effect of salinity and caused a significant increase in spike length and grain weight values in both genotypes. The 'Auqab-2000' cultivar had higher spike length than 'SARC-5' at site-I and the contrary was true for site-II.
Biological and grain yield data at site-I and site-II influenced by Si and salinity are shown in Table 2. Dry matter and wheat grain production of in both cultivars was negatively affected at site-II by salinity stress when compared with site-I. Calcium silicate fertilization remarkably improved and enhanced yield at site-I and site-II in both cultivars with the increasing rate of Si, i.e., 0, 75, and 150 mg kg-1. At site-I, 'Auqab-2000' performed
better and had a higher yield than 'SARC-5' and the contrary was true for site-II. It is evident that as the harvest index value increases, the plant's physiological efficiency to convert dry matter into grain yield is higher (Table 2). Fertilization of saline and non-saline fields with Ca-silicate improved the harvest index in both cultivars. 'SARC-5'shad a higher harvest index than 'Auqab-2000' in the saline field. Table 3 shows a higher concentration of Na+ in wheat straw grown in a saline field than in a non-saline field. Applying Si significantly lowered Na+ concentration in wheat straw at both sites. The reduction in Na+ content in the flag leaf occurred by 0 > 75 > 150 mg kg-1 at both sites. Site-I had a higher Na+ content reduction than site-II. 'SARC-5' contained less Na+ than 'Auqab-2000' at both sites. Table 3 shows that on the average lower values of K+ and Si concentrations were observed at site-II than site-I in both cultivars. Substantial increases in K+ and Si concentrations in wheat straw were noted when Si was applied in both cultivars grown at site-I and site-II. At both sites, the highest K+ and Si contents were observed in the wheat plot fertilized with Si at 150 mg kg-1 and the lowest where it was not applied. 'SARC-5' contained a significantly lower K content than 'Auqab-2000' at site-I and the contrary is true for site-II, while Si concentration was higher in 'SARC-5' at both sites. Figure 1 shows that higher values of K+:Na+ were observed at site-II than site-I in both cultivars. At site-II, 'Auqab-2000' had a lower value than 'Sarc-5'. A considerable increase of K+:Na+ in wheat straw was noted when Si was applied in both cultivars grown at site-I and site-II. 'SARC-5' contained a significantly higher K+:Na+ content than 'Auqab-2000' at both sites.
Si0, Si1, and Si2 represent 0, 75, and 150 mg Si kg-1, respectively The values are means of three replicates. Means with the same letter do not differ at P = 0.05.
Salinity stress limits crop yield mostly in arid and semiarid regions of the world (Munns, 2005). Wheat is a frequent crop in these regions; therefore, its growth and yield is severely affected by salt stress. In the present field study, a lower yield and yield components of both cultivars were observed in a saline field as compared to a non-saline field. The reduced crop growth and yield was attributed to excessive accumulation of soluble salts in the root zone (Grattan and Grieve, 1999; Munns, 2005; Tahir et al., 2006).
It is reported that Si is beneficial for the growth of many plants under various abiotic (e.g., salt, drought, and metal toxicity) and biotic (plant diseases and pests) stresses (Liang et al., 2003; Ma, 2004). Silicon is known to improve the growth of plants subjected to salinity stress (Liang et al., 1996). A similar positive effect of Si was observed in the current study, thus indicating that when fields were fertilized with Ca-silicate, both biological and grain yield increased in both saline and non-saline fields (Table 2).
Biological yield is the mutual contribution of yield components such as the number of tillers per unit area, plant height, number of grains per spike, and grain weight. Any factor causing change in these components will reflect change in biological yield. Moreover, the efficiency and effectiveness of any technology package is ultimately reflected by the level of grain yield, which can also be described as a function of the cumulative behavior of yield components. Applying Ca-silicate resulted in a significant increase in yield and yield-contributing factors in both saline and non-saline fields (Table 2). The current findings were also supported by Ando et al. (1999), who indicated an increase in dry matter yield with an increasing rate of Si nutrition in a rice field. The increased rice yield was attributed to the increased number of grains per unit area and the percentage of mature grains through Si supplementation. Daren et al. (1994) also studied 10 rice cultivars grown at two different sites in Florida on Si-deficient organic Histosol and indicated a higher yield as a result of an increase in the number of grains per panicle due to applying Si, whereas 100 seed weight and panicles per m2 exhibited less change. In this study, the increase in wheat yield might be due to increased water status and a higher photosynthetic rate as suggested by Hattori et al.
(2005) for Sorghum bicolor. Comparing the cultivars on the basis of yield and its components, it was observed that 'Auqab-2000' (salt-sensitive) performed better in a non-saline field and had a higher biological yield, grain yield, harvest index, number of tillers, spike length, number of grains, 1000 grain weight, and number of spikelets per spike when compared to 'SARC-5' at all Si levels and the contrary was true in a saline field (Table 2).
Silicon deposited in plants helped to maintain a balanced and efficient absorption and translocation of mineral elements required for better growth (Islam and Saha, 1969; Marschner et al., 1990). Silicon also helps in competing with saline conditions by reducing Na+ toxicity while maintaining higher rates of K+ uptake, which is one of the major reasons for salt tolerance in wheat suggested by Ahmad et al. (1992) and Tahir et al. (2006) .
The current research (Table 3) showed that Si content in the plant body of both cultivars increased as Si increased under both saline and non-saline conditions. It is evident that Si deposition improved the toxic effects of salinity by enhancing K+ uptake as compared to the Na+ ion in saline and non-saline fields (Table 3). This might be due to the immobilization of toxic Na+ that occurred because Si was deposited in the root exodermis and endodermis (Gong et al., 2006). Liang et al. (2005) suggested a significant increase in K+ uptake and a decrease in Na+ uptake in barley (Hordeum vulgare L.) under salt stress due to the increased activity of the plasma membrane H+-ATPase. For wheat crops, Ahmad et al. (1992) reported the binding of soluble Si with Na+ in the roots, thus retarding its movement to the plant's aerial parts, which significantly decreased Na+ contents in flag leaves and roots of salt-stressed wheat plants.
It can be suggested that growth enhancement is associated with improved K+:Na+ as an indicator of salt tolerance (Figure 1) and shown by a positive relationship between grain yield and K+ and a negative relationship with Na+. Similarly, straw yield was positively correlated with K+ and negatively correlated with Na+. On the basis of ionic status change, it was observed that in the saline field, 'SARC-5' absorbed less Na+ than 'Auqab-2000' at all applied Si levels; therefore, 'SARC-5' is a higher accumulator of Si and K+ than salt-sensitive cultivars when fertilized with Si under both saline and non-saline conditions.
It was concluded from the current field study that using Si is beneficial to mitigate salinity stress under a wide range of field conditions. The improvement in crop growth was associated with reduced Na+ uptake and increased K+ uptake resulting in an improved K+:Na+ ratio; 'SARC-5' performed better than 'Auqab-2000' under salt stress.
We are very grateful to the Department of Crop Physiology, University of Agriculture, Faisalabad, for arranging saline and normal fields at PARS and the successful completion of this research by providing equipment and technical assistance in the laboratories. We express our gratitude to Dr. Rashid Ahmed, Dr. Irfan Ahmed, and Dr. Muhammad Shahid from the University of Agriculture, Faisalabad, Pakistan, for their support and encouragement during the execution of this project.
Ahmad, R., S.H. Zaheer, and S. Ismail. 1992. Role of Si in salt tolerance of wheat (Triticum aestivum L.). Plant Science 85:43-50. [ Links ]
Akram, M.S., H.R. Athar, and M. Ashraf. 2007. Improving growth and yield of sunflower (Helianthus annuus L.) by foliar application of potassium hydroxide (KOH) under salt stress. Pakistan Journal of Botany 39:2223-2230. [ Links ]
Ando, H., H. Fujii, T. Hayasaka, K. Yokoyama, and H. Mayum. 1999. New silicon source for rice cultivation. 3. Growth and yield of wetland rice with reference to silica gel application. p. 32. In Conference "Silicon in Agriculture". 26-30 September 1999. University of Florida, Fort Lauderdale, Florida, USA. [ Links ]
Awada, S., W.F. Campbell, L.M. Dudley, J.J. Jurinak, and M.A. Khan. 1995. Interactive effects of sodium chloride, sodium sulfate, calcium sulfate, and calcium chloride on snapbean growth, photosynthesis, and ion uptake. Journal of Plant Nutrition 18:889-900. [ Links ]
Cramer, G.R., and R.S. Nowak. 1992. Supplemental manganese improves the relative growth, net assimilation and photosynthetic rates of salt-stressed barley. Physiology Plantarum 84:600-605. [ Links ]
Croughan, T.P., and D.W. Rains. 1982. Biosolar resources. p. 245255. In Mitsui, A., and C.C. Black (eds.) CRC Handbook of biosolar resources. CRC Press, Boca Raton, Florida, USA.
Daren, C.W., L.E. Datnoff, G.H. Snyder, and F.G. Martin. 1994. Silicon concentration, disease response and yield components of rice genotypes grown on flooded organic Histosol. Crop Science 34:733-737. [ Links ]
Elliot, C.L., and G.H. Snyder. 1991. Autoclave-induced digestion for the calorimetric determination of silicon in rice straw. Journal of Agricultural and Food Chemistry 39:1118-1119. [ Links ]
Epstein, E. 1999. Silicon. Annual Review of Plant Physiology and Plant Molecular Biology 50:641-664. [ Links ]
Flowers, T.J. 2004. Improving crop salt tolerance. Journal of Experimental Botany 55:307-319. [ Links ]
Gong, H.J., D.P. Randall, and T.J. Flowers. 2006. Silicon deposition in the root reduces sodium uptake in rice seedlings by reducing bypass flow. Plant Cell Environment 111:1-9. [ Links ]
Grattan, S.R., and C.M. Grieve. 1999. Salinity-mineral nutrient relations in horticultural crops. Scientia Horticulturae 78:127-157. [ Links ]
Hattori, T., S. Inanaga, H. Araki, P. An, S. Morita, M. Luxova, and A. Lux. 2005. Application of silicon enhanced drought tolerance in Sorghum bicolor. Physiologia Plantarum 123:459-466. [ Links ]
Islam, A., and R.C. Saha. 1969. Effect of silicon on chemical composition of rice plants. Plant and Soil 30:446-458. [ Links ]
Jaleel, C.A., G. Manivannan, and R. Panneerselvam. 2007. Responses of antioxidant defense system of Catharanthus roseus (L.) G. Don. to paclobutrazol treatment under salinity. Acta Physiologiae Plantarum 29:205-209. [ Links ]
Khan, G.S. 1998. Soil salinity/sodicity status in Pakistan. 59 p. Soil Survey of Pakistan, Lahore, Pakistan. [ Links ] Lal, R. 2007. Soils and sustainable agriculture. A review. Agronomy for Sustainable Development 28:57-64. [ Links ]
Liang, Y.C., Q. Chen, Q. Liu, W. Zhang, and R. Ding. 2003. Effects of silicon on salinity tolerance of two barley cultivars. Journal of Plant Physiology 160:1157-1164. [ Links ]
Liang, Y.C., W.Q. Zhang, J. Chen, and R. Ding. 2005. Effect of silicon on H+-ATPase and H+-PPase activity, fatty acid composition and fluidity of tonoplast vesicles from roots of salt-stressed barley (Hordeum vulgare L.). Environmental and Experimental Botany 53:29-37. [ Links ]
Liang, Y.C., S.Q. Zhenguo, and M. Tongsheng. 1996. Effect of silicon on salinity tolerance of two barley genotypes. Journal of Plant Nutrition 19:173-183. [ Links ]
Lopez, C.M.L., H. Takahashi, and S. Yamazaki. 2002. Plant-water relations of kidney bean plants treated with NaCl and foliarly applied glycinebetaine. Journal of Crop Science 188:73-80. [ Links ]
Lutts, S., J.M. Kinet, and J. Bouharmont. 1996. NaCl-induced senescence in leaves of rice (Oryza sativa L.) cultivars differing in salinity resistance. Annals of Botany 78:389-398. [ Links ]
Ma, J.F. 2004. Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses. Journal of Soil Science and Plant Nutrition 50:11-18. [ Links ]
Marschner, H., H. Cabrie, I. Cakmak, and B. Romeheld. 1990. Silicon deficiency and its effect on availability of P and Zn. Plant and Soil 124:211-219. [ Links ]
Matichenkov, V.V., and A.A. Kosobrukhov. 2004. Silicon effect on the plant resistance to salt toxicity. 13th International Soil Conservation Organization Conference. Conserving soil and water for society, Brisbane. 4-8 July 2004. Australian Society of Soil Inc. (ASSSI) and International Erosion Control Association, Denver, Colorado, USA. [ Links ]
Matoh, T., P. Kairusmee, and E. Takahashi. 1986. Salt-induced damage to rice plants and alleviation effect of silicate. Journal of Plant Nutrition 32:295-311. [ Links ]
Munns, R. 2002. Comparative physiology of salt and water stress. Plant Cell and Environment 25:239-250. [ Links ]
Munns, R. 2005. Genes and salt tolerance: Bringing them together. New Phytologist 167:645-663. [ Links ]
Qureshi, R.H., and E.G. Barrett-Lennard. 1998. Saline agriculture for irrigated land in Pakistan: A handbook. 146 p. Australian Centre for International Agricultural Research, Canberra, Australia. [ Links ]
Raza, S.H., H.R. Athar, and M. Ashraf. 2006. Influence of exogenously applied glycinebetaine on the photosynthetic capacity of two differently adapted wheat cultivars under salt stress. Pakistan Journal of Botany 38:341-351. [ Links ]
Rueda-Puente, E.O., J.L. García-Hernández, P. Preciado-Rangel, B. Murillo-Amador, M.A. Tarazón-Herrera, A. Flores-Hernández, et al. 2007. Germination of Salicornia bigelovii ecotypes under stressing conditions of temperature and salinity and ameliorative effects of plant growth-promoting bacteria. Journal of Crop Science 193:167-176. [ Links ]
Saqib, M., C. Zorb, Z. Rengel, and S. Schubert. 2005. The expression of the endogenous vacuolar Na+/H+ antiporters in roots and shoots correlates positively with the salt resistance of wheat (Triticum aestivum L.) Plant Science 169:959-965. [ Links ]
Steel, R., and J. Torrie. 1996. Principles and procedures of statistics. A biometrical approach. 3rd ed. McGraw Hill Book, New York, USA. [ Links ]
Szaboles, I. 1989. Salt-affected soils. CRC Press, Boca Raton, Florida, USA. [ Links ]
Tahir, M., A. Rahmatullah, T. Aziz, M. Ashraf, S. Kanwal, and A. Muhammad. 2006. Beneficial effects of silicon in wheat under salinity stress-pot culture. Pakistan Journal of Botany 38:1715-1722. [ Links ]
Wagenet, R.J., R.R. Rodriguez, W.F. Campbell, and D.L. Turner. 1983. Fertilizer and salty water effects on Phaseolus. Agronomy Journal 75:161-166. [ Links ]
Wolf, B.A. 1980. Comprehensive system of leaf analysis and its use for diagnosing crop nutrient status. Communications in Soil Science and Plant Analysis 13:1035-1059. [ Links ]
Zhu, J.K. 2003. Regulation of ion homeostasis under salt stress. Current Opinion in Plant Biology 6:441-445. [ Links ]
Received: 4 April 2011.
Accepted: 20 December 2011.