Use of IR thermography in screening wheat (Triticum aestivum L.) cultivars for salt tolerance

Thermography is proposed to be an alternative non-destructive and rapid technique for the study and diagnosing of salt tolerance in plants. In a pot experiment, 30 cultivars of wheat (Triticum aestivum L.) were evaluated in terms of their leaf temperature and shoot growth and their ion distribution responses to NaCl salinity at two concentration levels: the control with electrical conductivity (EC) of 1 dS m^?1 and salinity treatment with EC of 16 dS m^?1 (150 mM). A completely randomized block design with factorial treatments was employed with three replications. The results indicated that thermography may accurately reflect the physiological status of salt-stressed wheat plants. The salt stress-based increase in leaf temperature of wheat cultivars grown at 150 mM NaCl reached 1.34°C compared to the control. According to the results obtained, it appears that thermography has the capability of discerning differences of salinity tolerance between the cultivars. Three salt-tolerant wheat cultivars, namely Roshan, Kharchia and Sholeh, had higher mean shoot dry matter (0.039 g plant^?1) and higher mean ratio of leaf K⁺/Na⁺ (14.06) and showed lower increase in the mean leaf temperature (0.37°C) by thermography compared to the control. This was while nine salt-sensitive cultivars, namely Kavir, Ghods, Atrak, Parsi, Bahar, Pishtaz, Falat, Gaspard and Tajan, had lower mean plant dry matter production (0.027 g plant^?1), lower mean ratio of K⁺/Na⁺ (9.49) and higher mean increases in leaf temperature (1.24°C).     

Effect of Enhanced Nickel Levels on Wheat Plant Growth and Physiology under Salt Stress

A pot experiment was conducted to study the response of wheat to concurrent stresses of salinity and nickel (Ni)-toxicity. Soil was spiked with Ni (0, 20 and 40 mg kg^?1) combined with two levels of salinity (control and 10 dS m^?1) using Ni(ii) nitrate hexahydrate (Ni(NO₃)₂.6H₂O) and sodium chloride (NaCl), respectively, in a completely randomized design with four replicates. Plants were harvested at the tailoring stage and the results showed that wheat growth was positively affected by Ni at 20 mg kg^?1, and negatively at 40 mg kg^?1 concentration both in control and at 10 dS m^?1. Ni (20 mg kg^?1) had a nonsignificant positive effect on tissue potassium (K⁺) and a significant negative effect on Na⁺ concentration. Moreover, Ni translocation from root to shoot and accumulation decreased by increasing the levels of Ni in both control and salinity treatments. It can be concluded that Ni at 20 mg kg^?1 increased wheat growth by alleviating salinity stress; however, at 40 mg kg^?1 it aggravated the plant stress and decreased the plant growth.     

Growth and ion accumulation responses of four grass species to salinity

Ion inclusion or ion exclusion are the two main strategies developed by plants to tolerate saline environments. Shoot sodium (Na⁺), potassium (K⁺), and calcium (Ca²⁺) in four perennial grass species (tall wheatgrass, Nuttall's alkaligrass, creeping foxtail, and switchgrass) treated with nutrient solution salinity levels ranging from 2 to 32 dS m^?1 were measured. As the nutrient solution salinity was increased from 2 to 10 dS m^?1, tall wheatgrass, creeping foxtail and Nuttall's alkali grass had increased shoot Na⁺ and decreased Ca²⁺ concentration while maintaining growth suggesting that these species tolerated these changes in shoot ion concentration. In contrast, switchgrass excluded Na⁺ from the shoot and maintained K⁺ and Ca²⁺ concentrations but suffered dramatic shoot dry weight reduction. Thus, the Na⁺ exclusion mechanisms present in switchgrass were less efficient in maintaining growth under the 10 dS m^?1 nutrient solution treatment than the Na⁺ inclusion mechanisms used by the other three species.     

Sodicity Intensifies the Effect of Salinity on Grain Yield and Yield Components of Wheat

ABSTRACT

This study reports the relationship of the leaf ionic composition with the grain yield and yield components of wheat in response to salinity x sodicity and salinity alone. The study was conducted in soil culture in pots with three treatments including control (ECe 2.6 dS m^{? 1} and SAR 4.53), salinity (ECe 15 dS m^{? 1} and SAR 9.56), and salinity x sodicity (ECe 15 dS m^{? 1} and SAR 35). The soil was treated before being put in the pots and the pots were arranged in a completely randomized factorial arrangement with five replications. The seeds of three wheat genotypes were sown directly in the pots and the study was continued till the crop maturity. At booting stage, the leaf second to the flag leaf of each plant was collected and analyzed for sodium (Na⁺), potassium (K⁺), and chloride (Cl^?). At maturity, plants were harvested and data regarding grain yield and yield components were recorded. This study shows that salinity and sodicity in combination decreases the grain yield of wheat more than the salinity alone with a greater difference in the sensitive genotype. This study also shows that as for salinity, the maintenance of lower Na⁺ and higher K⁺ concentrations and higher K⁺: Na⁺ ratio in the leaves relates positively with the better development of different yield components and higher grain yield in saline sodic soil conditions. Although, the leaf Cl^? concentration was increased significantly by salinity as well as salinity x sodicity and would have affected the growth and yield, yet it does not seem to determine the genotypic tolerance or sensitivity to either salinity or salinity x sodicity.     

EFFECTS OF SALINITY STRESS ON PHYSIOLOGICAL PERFORMANCE OF VARIOUS WHEAT AND BARLEY CULTIVARS

An experiment with factorial arrangement of treatments on a randomized complete block (RCB) design basis with three replications was conducted in a greenhouse during Spring 2010 to investigate changes in sodium ion (Na⁺), potassium ion (K⁺), Na⁺/K⁺ and to determine proline, protein content, and superoxide dismutase (SOD) of four wheat and four barley cultivars. Three salt levels {1, control (no salt), 7, and 13 dS m^?1 [2.5 and 5 g salt [sodium chloride (NaCl) and sodium sulfate (Na₂SO₄) in 1:1 ratio] per kg of soil, respectively]} were used in this investigation. Salt stress treatments were applied 4 weeks after planting (at 2 leaf stage). Leaf samples were taken four weeks after imposition of salt treatment. The results showed that salinity caused an increased in proline and protein content, and SOD in all wheat and barley cultivars. The highest proline and protein content of barley and wheat cultivars at all salinity levels were observed in ‘Nimrooz’ and ‘Bam’ cultivars, respectively. At all salinity levels, wheat and barley cultivars ‘Kavir’ and ‘Nimrooz’, respectively, had the lowest Na⁺ content. Barley cultivar ‘Kavir’ and wheat cultivar ‘Bam’ had higher K⁺ and K⁺:Na⁺ ratios. This might be related to salt tolerance in these two cultivars. Wheat and barley cultivars showed differences with regard to proline, protein, and SOD content, Na⁺, K⁺, and K⁺:Na⁺ ratio, indicating existence of genetic diversity among the cultivars. These findings indicated that higher K⁺, K⁺:Na⁺ ratio, proline, protein, and SOD content could be the key factors, which offer advantage to barley over wheat for superior performance under saline conditions.     

EFFECT OF MIXED-SALT SALINITY ON GROWTH AND ION RELATIONS OF A QUINOA AND A WHEAT VARIETY

ABSTRACT

Salinity is among the most widespread and prevalent problems in irrigated agriculture. Many members of the family Chenopodiaceae are classified as salt tolerant. One member of this family, which is of increasing interest, is quinoa (Chenopodium quinoa Willd.) which is able to grow on poorer soils. Salinity sensitivity studies of quinoa were conducted in the greenhouse on the cultivar, “Andean Hybrid” to determine if quinoa had useful mechanisms for salt tolerant studies. For salt treatment we used a salinity composition that would occur in a typical soil in the San Joaquin Valley of California using drainage waters for irrigation. Salinity treatments (EC_i ) ranging from 3, 7, 11, to 19?dS?m^?1 were achieved by adding MgSO₄, Na₂SO₄, NaCl, and CaCl₂ to the base nutrient solution. These salts were added incrementally over a four-day period to avoid osmotic shock to the seedlings. The base nutrient solution without added salt served as the non-saline control solution (3?dS?m^?1). Solution pH was uncontrolled and ranged from 7.7 to 8.0. For comparative purposes, we also examined Yecora Rojo, a semi-dwarf wheat, Triticum aestivum L. With respect to salinity effects on growth in quinoa, we found no significant reduction in plant height or fresh weight until the electrical conductivity exceeded 11?dS?m^?1. The growth was characteristic of a halophyte with a significant increase in leaf area at 11?dS?m^?1 as compared with 3?dS?m^?1 controls. As to wheat, plant fresh and dry weight, canopy height, and leaf area did not differ between controls (3?dS?m^?1) and plants grown at 7?dS?m^?1. Beyond this threshold, however, plant growth declined. While both quinoa and wheat exhibited increasing Na⁺ accumulation with increasing salinity levels, the percentage increase was greater in wheat. Examination of ion ratios indicated that K⁺:Na⁺ ratio decreased with increasing salinity in both species. The decrease was more dramatic in wheat. A similar observation was also made with respect to the Ca²⁺:Na⁺ ratios. However, a difference between the two species was found with respect to changes in the level of K⁺ in the plant. In quinoa, leaf K⁺ levels measured at 19?dS?m^?1 had decreased by only 7% compared with controls. Stem K⁺ levels were not significantly affected. In wheat, shoot K⁺ levels had decreased by almost 40% at 19?dS?m^?1. Correlated with these findings, we measured no change in the K⁺:Na⁺ selectivity with increasing salinity in quinoa leaves and only a small increase in stems. In wheat however, K⁺:Na⁺ selectivity at 3?dS?m^?1 was much higher than in quinoa and decreased significantly across the four salinity levels tested. A similar situation was also noted with Ca²⁺:Na⁺ selectivity. We concluded that the greater salt tolerance found in quinoa relative to wheat may be due to a variety of mechanisms.     

Adjustment of mineral ratio and composition in rice genotypes under varied salinity regimes

A study of the salinity effect on mineral content in rice genotypes differing in salt tolerance was conducted in a factorial Completely Randomized Design experiment. The results indicated that the genotypes developed differently by mutation conventional breeding. NS15 represented as salt-sensitive, Pokkali was included as an internationally salt-tolerant check and Iratom24 was moderately tolerant. The content of Na⁺, Ca²⁺, Mg²⁺ and Cl^? followed an increasing pattern in roots and shoots of all the rice genotypes due to increasing salinity levels except Ca²⁺ and Mg²⁺ in the root. However, the concentration of K⁺ showed more or less an increasing pattern in root and a decreasing pattern in shoot. The concentration of Na⁺ and Ca²⁺ sharply increased with increasing the salinity levels in both the roots and shoots of NS15. The concentration of K⁺ sharply decreased in shoot and increased in the root of susceptible genotype NS15 with increasing salinity over 6 dS m^?1 salinity levels, where the transformation of K⁺ from root to shoot was disrupted by Na⁺. The Cl^? content sharply increased with increasing salinity in the root of NS15 as compared to shoot. The effect of different salinity levels on Na⁺/K⁺ ratio in the shoots of the selected rice genotypes sharply increased in susceptible genotype NS15 as compared to the other genotypes.     

Selection and characterization of wheat genotypes for saline soils prone to water‐logging

Wheat (Tritcum aestivum L.) genotypes were screened and characterized for performance under salt stress and/or water‐logging. In a solution‐culture study, ten wheat genotypes were tested under control, 200 mM–NaCl salt stress and 4‐week water‐logging (nonaerated solution stagnated with 0.1% agar), alone or in combination. Shoot and root growth of the wheat genotypes was reduced by salinity and salinity × water‐logging, which was associated with increased leaf Na⁺ and Cl^– concentrations as well as decreased leaf K⁺ concentration and K⁺ : Na⁺ ratio. The genotypes differed significantly for their growth and leaf ionic composition. The genotypes Aqaab and MH‐97 were selected as salinity×water‐logging‐resistant and sensitive wheat genotypes, respectively, on the basis of their shoot fresh weights in the salinity × water‐logging treatment relative to control. In a soil experiment, the effect of water‐logging was tested for these two genotypes under nonsaline (EC = 2.6 dS m^–1) and saline (EC = 15 dS m^–1) soil conditions. The water‐logging was imposed for a period of 21 d at various growth stages, i.e., tillering, stem elongation, booting, and grain filling alone or in combinations. The maximum reduction in grain yield was observed after water‐logging at stem‐elongation + grain‐filling stages followed by water‐logging at grain‐filling stage, booting stage, and stem‐elongation stage, respectively. Salinity intensified the effect of water‐logging at all the growth stages. It is concluded that the existing genetic variation in wheat for salinity × water‐logging resistance can be successfully explored using relative shoot fresh weight as a selection criterion in nonaerated 0.1% agar–containing nutrient solution and that irrigation in the field should be scheduled to avoid temporary water‐logging at the sensitive stages of wheat growth.     

Barley growth,yield, antioxidant enzymes,and ion accumulation affected by PGRs under salinity stress conditions

Application of plant growth regulator (PGR) may alleviate some negative effects of environmental stresses such as salinity. A controlled environment experiment was conducted to study barley (Hordeum vulgare L. cv. Reyhane) growth, yield, antioxidant enzymes and ions accumulation affected by PGRs under salinity stress conditions at Shiraz University during 2012. The treatments were PGRs at four levels—water (as control), cycocel (CCC, 19 mM), salicylic acid (SA, 1 mM), and jasmonic acid (JA, 0.5 mM)—and four salinity levels—no stress (0.67 dS m^?1, as control), 5, 10, and 15 dS m^?1, which were arranged in a factorial experiment based on completely randomized design with four replicates. The results showed that salinity stress significantly decreased plant height, peduncle length, leaf area, ear length, grain number, dry weight, grain yield, harvest index, potassium (K⁺) accumulation, and potassium/sodium (K⁺/Na⁺) concentration ratio, which were closely associated with stress severity. However, PGRs compensated some of these negative effects, so that SA foliar application had the most ameliorative effect. Salt stress also increased Na⁺ accumulation as well as the activity of peroxidase, catalase, and superoxide dismutase (SOD). Since ion discrimination and enhanced antioxidant enzymes are associated with salt tolerance, in this experiment PGRs application might have enhanced K⁺ accumulation and antioxidant enzyme activity. The activity of SOD and K⁺/Na⁺ ratio were found to be useful in salt tolerance manipulation in barley plants.     

Germination,growth and ions uptake of moringa (Moringa oleifera L.) grown under saline condition

Salinity is the major environmental stress that affects the growth and productivity of plants. The present study was conducted to determine the effect of salinity on growth and ions uptake by moringa (Moringa oleifera L.) plant. The experiment was carried out in two phases. Initially, a germination test was conducted in the laboratory under the different salinity levels (control, 5, 10, 15, and 20 dS m^?1) and found that moringa seeds were germinated only at 5 and 10 dS m^?1 salinity levels, and no germination occurred at higher salinity levels (15 and 20 dS m^?1). The experiment was laid out in a completely randomized design (CRD) with five replications. In the second phase, three-week old nursery grown plants of moringa were shifted in pots under the five salinity levels (control, 5, 10, 15, and 20 dS m^?1). The experiment was laid out in CRD and replicated four times. In pot experiment, the root, shoot length, and dry weights were significantly affected by increasing the salinity levels. The uptake of K⁺ and Ca²⁺ was highly affected at different salinity levels as compared to control and Na⁺ ions accumulation was higher in roots rather than shoot. The results reveal that moringa plant can germinate, survive, and can be cultivated in areas with moderate saline condition.     

GROWTH,YIELD, AND ION RELATIONS OF STRAWBERRY IN RESPONSE TO IRRIGATION WITH CHLORIDE-DOMINATED WATERS

Strawberry is listed as the most salt sensitive fruit crop in comprehensive salt tolerance data bases. Recently, concerns have arisen regarding declining quality of irrigation waters available to coastal strawberry growers in southern and central California. Over time, the waters have become more saline, with increasing sodium (Na⁺) and chloride (Cl^?). Due to the apparent extreme Cl^? sensitivity of strawberry, the rising Cl^? levels in the irrigation waters are of particular importance. In order to establish the specific ion causing yield reduction in strawberry, cultivars ‘Ventana’ and ‘Camarosa’ were grown in twenty-four outdoor sand tanks at the ARS-USDA U. S. Salinity Laboratory in Riverside, CA and irrigated with waters containing a complete nutrient solution plus Cl^? salts of calcium (Ca²⁺), magnesium (Mg²⁺), Na⁺, and potassium (K⁺). Six salinity treatments were imposed with electric conductivities (EC) = 0.835, 1.05, 1.28, 1.48, 1.71, and 2.24 dS m^?1, and were replicated four times. Fresh and dry weights of ‘Camarosa’ shoots and roots were significantly higher than those of ‘Ventana’ at all salinity levels. Marketable yield of ‘Camarosa’ fruit decreased from 770 to 360 g/plant as salinity increased and was lower at all salinity levels than the yield from the less vigorous ‘Ventana’ plants. ‘Ventana’ berry yield decreased from 925 to 705 g/plant as salinity increased from 0.835 to 2.24 dS m^?1. Relative yield of ‘Camarosa’ decreased 43% for each unit increase in salinity once irrigation water salinity exceeded 0.80 dS m^?1. Relative ‘Ventana’ yield was unaffected by irrigation water salinity up to 1.71 dS m^?1, and thereafter, for each additional unit increase in salinity, yield was reduced 61%. Both cultivars appeared to possess an exclusion mechanism whereby Na⁺ was sequestered in the roots, and Na⁺ transport to blade, petiole and fruit tissues was limited. Chloride content of the plant organs increased as salinity increased to 2.24 dS m^?1 and substrate Cl increased from 0.1 to13 mmol_cL^?1. Chloride was highest in the roots, followed by the leaves, petioles and fruit. Based on plant ion relations and relative fruit yield, we determined that, over the range of salinity levels studied, specific ion toxicity exists with respect to Cl^?, rather than to Na⁺ ions, and, further, that the salt tolerance threshold is lower for ‘Camarosa’ than for ‘Ventana’.     

Sodium exclusion is a reliable trait for the improvement of salinity tolerance in bread wheat

Identification of novel wheat (Triticum aestivum L.) germplasm is imperative to develop salt tolerant varieties. In the first phase, 400 accessions were screened against high salt stress (200 mM NaCl) on the basis of Na⁺ accumulation in leaf blade, and 40 genotypes with contrast reaction to salinity were selected. Salt tolerant group (25 genotypes) had higher leaf K⁺/Na⁺ ratio, maximum root and shoot lengths, leaf fresh/dry weights and chlorophyll content as compared to the salt sensitive group (15 genotypes). In second phase, physiologically based screening was performed on selected genotypes against varying salinity levels (0, 100 and 200 mM NaCl). GGE biplot analysis indicates that genotypes TURACO, V-03094, V0005, V-04178, Kharchia 65 and V-05121 were the most salt-tolerant and declared winners as depicted by more gaseous exchange relations and growth potential which was strongly correlated with proper Na⁺, K⁺ discrimination in leaf and root tissues. Genotypes PBW343*2, NING MAI 50, PGO, PFAU, V-04181, PUNJAB 85, KIRITATI, TAM200/TUI and TAM200 were poor performer due to more Na⁺ accumulation in leaf ultimately retarded growth. In conclusion, low Na⁺ accumulation in leaf can be used as the best screening criteria, employing a large set of genotypes in a breeding program.     

Comparative growth and physiological responses of two wheat (Triticum aestivum L.) cultivars differing in salt tolerance to salinity and cyclic drought stress

Two cultivars of wheat (Triticum aestivum L.) with differential salinity tolerance were compared by evaluating the growth attributes, pigment composition and accumulation of Na⁺, K⁺, Zn²⁺, Fe ²⁺, Mn ²⁺ and proline. Wheat cultivars Al-Moiaya (AM) (salt tolerant) and Habbe-Druma (HD) (salt sensitive) were subjected to four levels of salinity (1.21 dS m^?1, 4.4 dS m^?1, 8.8 dS m^?1 and 13.2 dS m^?1) in factorial combinations with three drought stress (FC 30%, FC 60% and FC 90%) treatments in a randomized complete block design. Plant dry weight, leaf area ratio (LAR), soluble protein and total chlorophyll (Chl) content were higher in AM than HD. Salt-tolerant AM maintains a higher K⁺/ Na⁺ ratio and thereby is able to grow better than the salt-sensitive HD under both the stresses. The lower foliar Na⁺ in AM resulted in retention of higher Chl content, reflected in the strong positive correlations between plant ion status and Chl contents (Na⁺-Chl r² = 0.83; Chl- Fe²⁺ r² = 0.76; Zn²⁺ r² = 0.93 and Mn²⁺ r² = 0.88). In conclusion, our results suggested that the K⁺/Na⁺ ratio, exclusion of Na⁺ and ion homeostasis play much more important roles in the tolerance to salinity and drought stress than the compatible osmolyte, proline.     

Evaluation of Salt Tolerance and Its Relationship with Carbon Isotope Discrimination and Physiological Parameters of Barley Genotypes

Soil management through the cultivation of salt-tolerant plants is a practical approach to combat soil salinization. In this study, salt tolerance of 35 barley (Hordeum vulgare L.) genotypes was tested at four salinity levels (0, 100, 200, and 300 mM NaCl in Hoagland nutrient solution) at two growth stages (germination and vegetative). The relationship between salinity tolerance and carbon isotope discrimination (CID) was also accessed. Results of the study carried out under laboratory conditions showed that a negative linear relationship was observed between salt concentration and germination as well as other growth parameters. Some genotypes showed good salt tolerance at germination but failed to survive at seedling stage. However, five genotypes, namely, Jau-83, Pk-30109, Pk-30118, 57/2D, and Akermanns Bavaria showed better tolerance to salinity (200 mM) both at germination and at vegetative growth stage. The salt tolerance of these barley genotypes was significantly correlated with minimum decrease in K⁺:Na⁺ ratio in plant tissue with increase in the root zone salinity. However, the case was reversed in sensitive genotypes. CID was decreased linearly with increase in root zone salinity. However, salt-tolerant genotypes maintained their turgor by osmotic adjustment and by minimum increase in diffusive resistance and showed minimum reduction in CID (Δ) with gradual increase in rooting medium salt concentration. Results suggested that the tolerant genotypes make osmotic adjustments by selective uptake of K⁺ and by maintaining a higher K⁺:Na⁺ ratio in leaves. Moreover, CID technique can also be good criteria for screening of salt-tolerant germplasm.     

EFFECTS OF WATER SALINITY ON GROWTH INDICES AND PHYSIOLOGICAL PARAMETERS IN SOME PISTACHIO ROOTSTOCKS

Pistachio is one of the most important horticultural crops in Iran. The majority of the pistachio producing regions is located in arid and semi-arid areas with saline conditions. Therefore, selection of suitable rootstocks is important for increasing yield efficiency of this important nut crop. In this study, the effect of four water salinity levels (0.75, 5, 10 and 15 ds m^?1) on growth indices and physiological parameters of four Pistacia vera L. rootstocks (Badami-e-Zarand A, Badami-e-Zarand B, Qazvini, and Sarakhs) were investigated under greenhouse conditions. After treatment for three months, leaf dry weight was reduced by about 30-50% at an irrigation water electrical conductivity (EC_w) of 10 ds m^?1. Badami-e-Zarand B was the most vigorous rootstock at the highest EC. Decreases in root and stem dry weight (average of all rootstocks combined) occurred at water salinity of 10 ds m^?1. Chemical analysis of shoot and root indicated that the salinity affected the concentration and distribution of sodium (Na⁺), potassium (K⁺), and calcium (Ca²⁺) in pistachio rootstocks. The concentrations of Na⁺ and K⁺ increased with a rise in water salinity levels. Comparison between Na⁺ concentration of shoot and root showed that all examined rootstocks limited the Na⁺ transportation to shoot tissue up-to 15 ds m^-1, and retained it in the roots. However, this ability was less in the Sarakhs rootstock. Based on measured parameters, Badami-e-Zarand B and Sarakhs could be considered as tolerant and sensitive pistachio rootstocks to water salinity, respectively.     

RESPONSE OF LISIANTHUS TO IRRIGATION WITH SALINE WATER: ION RELATIONS

Eustoma grandiflorum (Raf.) Shinn. (lisianthus) is a moderately salt tolerant species that can be produced commercially under irrigation with saline wastewaters prevalent in two salt-affected areas of California. The objective of the present studies was to determine the effect of irrigation with saline waters of two different compositions on the ion accumulation and ion relations of lisianthus ‘Pure White’ and ‘Echo Blue’. The ionic composition of irrigation waters simulated the compositions typical of i) seawater dilutions (SWD) and ii) concentrations of Colorado River water (CCRW). Electrical conductivities (EC) of SWD and CCRW were between 2 and 12 dS · m^?1. Plants irrigated with CCRW were higher in Ca²⁺ compared to plants irrigated with SWD water. Calcium was also higher in ‘Pure White’ than in ‘Echo Blue’. Increasing EC of irrigation water caused a significant decrease in shoot and leaf Ca²⁺ concentration in ‘Echo Blue’, but had no effect on Ca²⁺ content of ‘Pure White’ shoots and leaves. Magnesium concentration in ‘Echo Blue’ was higher than in ‘Pure White’. Electrical conductivity did not significantly affect Mg²⁺ concentration of either cultivar, despite the increasingly higher external concentration. Potassium concentration of young and mature leaves of ‘Echo Blue’ increased as EC increased from 2 to 8 dS · m^?1, then decreased significantly once EC exceeded 8 dS · m^?1. Potassium concentration of ‘Pure White’ leaves decreased over the range of salinity treatments tested, suggesting that the reduced potassium ion (K⁺) activity at EC levels of 8 dS · m^?1, or less, that resulted in lower leaf?K⁺ in ‘Pure White’ did not cause a decrease in K⁺ uptake in ‘Echo Blue’. Increases in external Na⁺ caused a significant increase in Na⁺ in ‘Pure White’ leaves and these plants exhibited the best growth even when levels of Na⁺ were high enough to be considered detrimental for growth.     

Growth and acquisition of Na,K and Ca in some elite sweetpotato [Ipomoea batatas (Lam.) L.] genotypes under salinity stress

Soil salinity is a concern in the wake of climate change challenges due to rising sea levels and coastal salinity in Papua New Guinea. A greenhouse experiment was conducted in Split Plot design, with five elite sweet potato genotypes (main-plot factors) and three levels of sodium chlroide (NaCl) concentrations (sub-plot factors) replicated six times. The vine cuttings of genotype RAB 45 showed very low mortality percentage (33%) at 600 mM NaCl concentration. At salinity level of 200 mM NaCl, aerial dry biomass of the genotypes was inversely but significantly (r = –0.40; p < 0.05) related to the accumulation of sodium (Na⁺) in the tissues. The Na⁺ accumulation in the tissues was antagonistic to the potassium (K⁺) and calcium (Ca²⁺) ions. Among the sweetpotato genotypes, Na⁺/K⁺ ratio decreased in the following order: RAB 45> KAV 11 > Northern Star > DOY 2 > L 46, which was more or less corroborated with the trend in the aerial dry matter.     

Mineral Uptake of Mycorrhizal Wheat (Triticum aestivum L.) under Salinity Stress

The hypothesis was that arbuscular mycorrhizal (AM) fungi are able to alleviate salt stress on plant growth by enhancing and adjusting mineral uptake. The objectives were to determine (1) the effects of soil salinity on mineral uptake by different wheat genotypes and (2) the effectiveness of different mycorrhizal treatments on the mineral uptake of different wheat (Triticum aestivum L.) genotypes under salinity. Wheat seeds of Chamran and Line 9 genotypes were inoculated with different species of AM fungi including Glomus mosseae, G. intraradices, and G. etunicatum and their mixture at planting using 100 g inoculum. Pots were treated with the salinity levels of 4, 8, and 12 dS/m before stemming. Different arbuscular mycorrhizal treatments, especially the mixture treatment, increased wheat mineral uptake for both genotypes. Although Line 9 genotype resulted in greater nutrient uptake under salinity stress, Chamran was more effective on adjusting sodium (Na⁺) and chloride (Cl^?) uptake under salt stress.     

SOYBEAN RESPONSE AND ION ACCUMULATION UNDER SPRINKLER IRRIGATION WITH SODIUM-RICH SALINE WATER

The magnitude of crop growth and yield depends on the salinity level, the toxic ions present, and the irrigation system used. In order to study the effect of saline sprinkler irrigation on soybean growth and ionic accumulation in plant tissues a pot experiment was set up. There were three irrigation water quality treatments [electrical conductivity (EC) 0, 2, and 4 dS m^?1]. Soybean aerial biomass was 25% lower than the Control when irrigation salinity was 4 dS m^?1. Clearly salinity entering via leaves affected the grain filling stage and severely reduced soybean grain production (80% reduction) when salinity in irrigation water surpassed 2 dS m^?1. Sprinkler irrigation aggravates soybean's low salinity tolerance and restricts its cropping in such conditions. For early stages two linear relationships between leaf chloride (Cl^?) concentration (Y = 14.2–2x) or potassium (K⁺)/ sodium (Na⁺) ratio (Y = 5.3x?3.4) and soybean grain yield were found. Both relationships may be used as diagnostic tools for soybean growing under saline sprinkler irrigation.     

Use of Potassium Fertilization to Ameliorate the Adverse Effects of Saline-sodic Stress Condition (ECw: SARw Levels) in Rice (Oryza Sativa L.)

ABSTRACT

Salt-affected soils expand around the world and become a critical handicap for high crop yield. Saline-sodic soil contributed a major portion in salt-affected soils. Such types of soils have a sizable amount of Na⁺ in nutrient medium and that reduce the K⁺ uptake in plants. A hydroponic experiment was performed to investigate the ameliorative effect of different doses of potassium fertilizer (K₁ = 0.3, K₂ = 0.6 and K₃ = 1.2 mM L^?1) on rice (Oryza sativa L.) under different EC_w (6 dS m^?1) and SAR_w [12 and 24 (mmol L^?1)^1/2] levels. Application of K⁺ at elevated levels under saline-sodic conditions improved the concentration of anti-oxidant enzymes, plant physiological, and biochemical attributes by improving the K⁺: Na⁺ ratio in plant tissues. Total phenolic content, total soluble protein, and soluble sugar content of rice plant were increased with an increase in potassium dose and saline-sodicity. Maximum K⁺: Na⁺ ratios, 4.13 and 2.0 were observed in shoot and root, respectively upon application of K⁺ at 1.2 mM L^?1 in a solution having EC_w: SAR_w level of 6: 12. This study suggested that application of potassium at elevated levels (1.2 mM L^?1) has enhanced the rice growth by reducing the harmful effect of Na⁺ salts on plant physiology, biochemical attributes, and anti-oxidant enzymes under specific saline-sodic conditions.