Calcium Sulfate Improves Salinity Tolerance in Rootstocks of Plum

ABSTRACT

Three vegetative rootstocks of plum (Prunus domestica), Marianna GF 8-1 (Prunus cerasifera × munsoniana), Myrobolan B (P. Cerasifera) and Pixy (P. Insititia) were grown in pots containing sand and irrigated with complete nutrient solution to investigate the effect of calcium sulfate supplied to the nutrient solution on plants grown under salt stress. Treatments were (1) control (C): nutrient solution alone; (2) S (salinity stress): 40 mM NaCl; (3) S+Ca1: 40 mM NaCl +2.5 mM calcium (Ca) and (4) S+Ca₂: 40 mM NaCl + 5 mM Ca. Calcium was supplied as CaSO₄. The plants grown under 40 mol L^?1 NaCl produced less dry matter and had lower chlorophyll content than those without NaCl. Supplementary CaSO₄ at both 2.5 and 5 mM concentrations ameliorated the negative effects of salinity on plant dry matter and chlorophyll content. Salt treatment impaired membrane permeability by increasing electrolyte leakage. The addition of calcium sulfate partially maintained membrane permeability. Sodium (Na) concentration in plant tissues increased in both leaves and roots of plants under the high NaCl treatment. Pixy had much lower Na. The CaSO₄ treatments lowered significantly the concentrations of Na in both leaves and roots. Pixy was more tolerant to salinity than the other two rootstocks. The accumulation of Na in leaves and roots indicates a possible mechanism whereby Pixy copes with salinity in the rooting medium, and/or may indicate the existence of an inhibition mechanism of Na transport to leaves. Concentrations of Ca and K were lower in the plants grown at high NaCl than in those under the control treatment, and these two element concentrations were increased by calcium sulfate treatments in both leaves and roots, but remained lower than control values in most cases.     

Gas exchange,water relations,and Ion concentrations of salt‐stressed tomato and melon plants

Abstract

Tomato and melon plants were grown in a greenhouse and irrigated with nutrient solution having an EC of 2 dS m^?1 (control treatment) and 4, 6, and 8 dS m^?1, produced by adding NaCl to the control nutrient solution. After 84 days, leaf water relations, gas exchange parameters, and ion concentrations, as well as plant growth, were measured. Melon plants showed a greater reduction in shoot weight and leaf area than tomato at the two highest salinity levels used (6 and 8 dS m^?1). Net photosynthesis (Pn) in melon plants tended to be lower than in tomato, for all saline treatments tested. Pn was reduced by 32% in melon plants grown in nutrient solution having an EC of 4 dS m^?1, relative to control plants, and no further decline occurred at higher EC levels. In tomato plants, the Pn decline occurred at EC of 6 dS m^?1, and no further reduction was detected at EC of 8 dS m^?1. The significant reductions in Pn corresponded to similar leaf Cl^? concentrations (around 409 mmol kg^?1 dry weight) in both plant species. Net Pn and stomatal conductance were linearly correlated in both tomato and melon plants, Pn being more sensitive to changes in stomatal conductance (g_s) in melon than in tomato leaves. The decline in the growth parameters caused by salinity in melon and tomato plants was influenced by other factors in addition to reduction in Pn rates. Melon leaves accumulated larger amounts of Cl^? than tomato, which caused a greater reduction in growth and a reduction in Pn at lower salinity levels than in tomato plants. These facts indicate that tomato is more salt‐tolerant than melon.     

Uptake of Boron by Kiwifruit Plants Under Various Levels of Shading and Salinity

Abstract

Two experiments were conducted. In the first one, kiwifruit plants were grown in sand/perlite mixtures and irrigated with modified Hoagland's nutrient solutions containing two boron (B) concentrations (0.025 and 0.2 mM) combined with four levels of salinity (0.75, 2, 4, and 6 dS m^?1). Certain growth parameters and B concentration of the various plant parts were investigated. The highest level of salinity imposed was toxic for kiwifruit plants. Significant correlations (significance 0.000***) were found between B and salinity levels of the nutrient solutions and shoot height, mean shoot fresh weight, number of new leaves, mean leaf fresh weight, B concentration of upper leaves, basal leaves, 2-year old shoots and roots of kiwifruit plants. By increasing salinity level, the B concentration of leaves decreased when B concentration in solution was 0.2 mM. In another experiment, the nutrient solutions contained three B concentrations (0.025, 0.15, and 0.3 mM) and the plants were subjected to shading (100, 70, and 30% of full sunshine). Regression analysis indicated that significant correlations were found between B and shading (independent variables) and shoot height, mean shoot fresh weight, number of new leaves, B concentration of various plant organs (significance 0.000***) and mean leaf fresh weight (significance 0.018*).     

The role of antioxidative metabolism of tomato leaves in long‐term salt‐stress response

The antioxidative protection system as adaptation strategy to high soil salinity in the leaves of two tomato (Lycopersicon esculentum Mill.) hybrids (Buran F1 and Berberana F1) was investigated. Changes in the activity of superoxide‐dismutase (SOD, EC 1.15.1.1), peroxidase (POD, EC 1.11.1.7), ascorbate peroxidase (APX, EC 1.11.1.11), as well as total and oxidized ascorbate concentrations (AA and DHA) in the plant leaves subjected to three salinity levels (EC 3.80 dS m⁻¹, 6.95 dS m⁻¹, and 9.12 dS m⁻¹) relative to non‐saline control were analyzed during the fruiting phase. The obtained results clearly indicate a relation between SOD activity and AA concentration in the antioxidative protection without any peroxidase‐related H₂O₂ detoxification. Increased SOD activity accompanied by high AA concentration was noticed at all salinity levels, but the response of hybrids was specific for the particular salt concentration. The first salinity level (EC 3.80 dS m⁻¹) induced the highest level of AA in the Buran F1 (70%), while in Berberana F1 hybrid leaves the highest AA concentration (64%) was noticed at the third salinity level (9.12 dS m⁻¹). All salinity levels caused a decline in POD and APX activities in both hybrids. The possibility of a predominant role of ascorbate and SOD in the antioxidative protection of mature tomato leaves under long‐term salt stress is discussed.     

Effects of biofertilizers and cycocel on some physiological and biochemical traits of wheat (Triticum aestivum L.) under salinity stress

In order to study the effects of biofertilizers and cycocel on some physiological and biochemical characteristics of wheat (Triticum aestivum L.) under salinity condition, a factorial experiment was conducted based on randomized complete block design with three replications under greenhouse condition in 2015. Treatments were included salinity in four levels [no salt (control or S₀), salinity 30 (S₁), 60 (S₂) and 90 (S₃) mM NaCl equivalent of 2.76, 5.53 and 8.3 dS m^?1, respectively], four biofertilizers levels [no biofertilizer (F₀), seed inoculation by Azotobacter chrocoocum strain 5 (F₁), Pseudomonas putida strain 186 (F₂), both inoculation Azotobacter + Pseudomonas (F₃)] and three cycocel levels [without cycocel as control (C₀), application of 600 (C₁) and 1000 (C₂) mg L^?1]. Results showed that salinity severe stress (90 mM) decreased chlorophyll content, relative water content (RWC), total chlorophyll, photochemical efficiency of PSII and yield of wheat. Whereas, soluble sugars and proline content, electrical conductivity (EC), the activity of catalase (CAT), peroxidase (POD), polyphenol oxidase (PPO) enzymes were increased. Similar results were observed in CAT, POD and PPO activities due to inoculation by biofertilizers and cycocel. Salinity at 30 mM increased the photochemical efficiency of PSII and chlorophyll content in plants grown under biofertilizer and cycocel treatment but with increasing salinity up to 90 mM mentioned parameters were decreased. The highest proline and soluble carbohydrate at all salinity levels were observed in plants treated in the highest cycocel level and Azotobacter+ Pseudomonas application. Generally, it was concluded that biofertilizers and cycocel can be used as a proper tool for increasing wheat yield under salinity condition.     

Effects of three commercial rootstocks on mineral nutrition,fruit yield,and quality of salinized tomato

Tomato (Solanum lycopersicum Mill. cv. Belladona F₁) plants were either self‐rooted, self‐grafted, or grafted onto the commercial rootstocks “Beaufort”, “He‐Man”, and “Resistar” and grown in a recirculating hydroponic system. Three nutrient solutions differing in NaCl‐salinity level (2.5, 5.0, and 7.5 dS m^–1, corresponding to 0.3, 22, and 45 mM NaCl) were combined with the five grafting treatments in a two‐factorial (3 × 5) experimental design. At the control NaCl level (0.3 mM), fruit yield was not influenced by any of the grafting treatments. However, at low (22 mM NaCl) and moderate (45 mM NaCl) salinity levels, the nongrafted and the self‐grafted plants gave significantly lower yields than the plants grafted onto He‐Man. The plants grafted onto the other two rootstocks gave higher yields only in comparison with the nongrafted plants, and the differences were significant only at low (Beaufort) or moderate (Resistar) salinity. Yield differences between grafting treatments at low and moderate salinity arose from differences in fruit number per plant, while mean fruit weight was not influenced by grafting or the rootstock. NaCl salinity had no effect on the yield of plants grafted onto He‐Man but restricted the yield in all other grafting treatments due to reduction of the mean fruit weight. With respect to fruit quality, salinity enhanced the titratable acidity, the total soluble solids, and the ascorbic acid concentrations, while grafting and rootstocks had no effect on any quality characteristics. The leaf Na concentrations were significantly lower in plants grafted onto the three commercial rootstocks, while those of Cl were increased by grafting onto He‐Man but not altered by grafting onto Beaufort or Resistar in comparison with self‐grafted or nongrafted plants. Grafting onto the three tested commercial rootstocks significantly reduced the leaf Mg concentrations, resulting in clear Mg‐deficiency symptoms 19 weeks after planting.     

MITIGATION EFFECTS OF SILICON ON TOMATO PLANTS BEARING FRUIT GROWN AT HIGH BORON LEVELS

Interactive effects of silicon (Si) and high boron (B) on growth and yield of tomato (Lycopercison esculentum cv. ‘191 F1’) plants were studied. Treatments were: 1) control (B1), normal nutrient solution including 0.5 mg L^?1 B (boron), 2) B1 +Si treatment: 0.5 mg L^?1 boron plus 2 mM Si, 3) B2 treatment: 3.5 mg L^?1 B, 4) B2 +Si treatment: 3.5 mg L^?1 B plus 2 mM Si, 5) B3 treatment: 6.5 mg L^?1 B, and 6) B3 +Si: 6.5 mg L^?1 B plus 2 mM Si. High B reduced dry matter, fruit yield and chlorophyll (Chl) in tomato plants compared to the control treatment, but increased the proline accumulation. Supplementary Si overcame the deleterious effects of high B on plant dry matter, fruit yield and chlorophyll concentrations. High B treatments increased the activities of superoxide dismutase (SOD; EC 1.15.1.1), peroxidase (POD; EC. 1.11.1.7) and polyphenol oxidase (PPO; EC 1.10.3.1). However, supplementary Si in the nutrient solution containing high B reduced SOD and PPO activities in leaves, but POD activity remained unchanged. These data suggest that excess B-induced oxidative stress and alterations in the antioxidant enzymes. Boron (B) concentrations increased in leaves and roots in the elevated B treatment as compared to the control treatment. Concentrations of calcium (Ca) and potassium (K) were significantly lower in the leaves of plants grown at high B than those in the control plants. Supplementing the nutrient solution containing high B with 2 mM Si increased both nutrients in the leaves. These results indicate that supplementary Si can mitigate the adverse effects of high B on fruit yield and whole plant biomass in tomato plants.     

Growth,nutrient acquisition,and physiological responses of three olive cultivars to induced salt stress

Three olive (Olea europaea L.) cultivars Nabali Baladi (NB), Nabali Muhassan (NM), and Grossi Di'Espagna (GE) were evaluated under salt stress. Seedlings were treated with salinity induced by a 3:1 ratio of calcium chloride and sodium chloride to four concentration levels measured as electrical conductivity (EC) [1.2, 4.1, 7.0, and 14.0 dS/m] for 122 days. Olive seedlings varied in their response to salinity. In all treatments, NB had the highest root; stem and leaf dry weights had among the highest total plant dry weights, specific stem length (SSL) and relative water content (RWC). NB seedlings maintained the highest stomatal conductance at 7.0 dS/m and highest chlorophyll index at 14.0 dS/m. Olive seedlings that tolerated salt tolerance developed mechanisms of nutrient acquisition and distribution in the organs, by storing minimal amounts of sodium (Na⁺) and chloride (Cl^?) in the stems and loading the most in the leaves and roots.     

Interactive Influences of Salinity Stress and Leaf Thinning on the Growth,Yield, Water use Efficiency,and Fruit Quality of Cherry Tomatoes

This research has experimentally investigated the interactive influences of salinity stress and leaf thinning on the growth, yield, water use efficiency, and fruit quality of cherry tomatoes cultivated under soilless conditions. The experiment was conducted in a plastic house (width of 5 m and length of 11 m) located in Gifu University. The seedlings were transplanted in a randomized complete block design with six plants per treatment, and a total of 36 plants in 18 pots (two plants per pot). The experiment received salinity treatment (no-salinity and salinity with electrical conductivity (EC) of 0.8 dS m^?1 and 3.0 dS m^?1, respectively) and leaf thinning treatment (no leaf thinning, basal leaf thinning and intersegment leaf thinning except the closest two). The experimental results showed that salinity stress negatively affected the growth, yield, marketable yield and water use efficiency of cherry tomatoes, but positively affected the fruit quality. Basal leaf removal significantly decreased the biomass, chlorophyll, and yield but significantly improved the fruit quality; that basal leaf removal coupled with salinity stress showed no influence on plant growth, but reduced the yield and greatly improved the fruit quality. Besides, tender leaves around truss removal significantly decreased the biomass, chlorophyll, yield, and water consumption, but improved the fruit quality; that tender leaves around truss removal coupled with salinity stress greatly decreased the biomass, chlorophyll, yield, and water consumption, but significantly improved the fruit quality.     

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.     

RESPONSES OF SOME ENZYMES AND KEY GROWTH PARAMETERS OF SALT-STRESSED MAIZE PLANTS TO FOLIAR AND SEED APPLICATIONS OF KINETIN AND INDOLE ACETIC ACID

The study examined the effects of kinetin (KIN) and indoleacetic acid (IAA) applied as seed treatment or sprayed on leaves of salinity stressed plants. Five -week old maize (Zea mays L. cv. ‘DK 647 F1’) plants were grown in pots containing peat and perlite in 1:1 (v/v) mixture. Different treatments used were: 1) control (nutrient solution alone), 2) salt stress [100 mM sodium chloride (NaCl)], 3) 100 mM NaCl and 1 mM kinetin (KIN), 4) 100 mM NaCl and 2 mM KIN, 5) 100 mM NaCl and 1 mM indole acetic acid (IAA), 6) 100 mM NaCl and 2 mM IAA, 7) 100 mM NaCl and 25 mg L^?1 KIN and 8) 100 mM NaCl and 25 mg L^?1 IAA. In treatments 7 and 8 application was to the seeds, for treatments 3-6 it was applied to foliage. The seeds were soaked in KIN or IAA solution for 12 h. Salt stress reduced the total dry matter, chlorophyll content, and relative water content (RWC), but increased proline accumulation, activities of superoxide dismutase (SOD; EC 1.15.1.1), peroxidase (POD; EC. 1.11.1.7), catalase (CAT; EC. 1.11.1.6) and polyphenol oxidase (PPO; 1.10.3.1) and electrolyte leakage. Both foliar applications of KIN and IAA treatments overcame to variable extents the adverse effects of NaCl stress on the above mentioned physiological parameters. However, seed treatments with KIN or IAA did not improve salinity tolerance in maize plants. Furthermore, foliar application or seed treatments with KIN and IAA reduced the activities of antioxidant enzymes in the salt stressed-plants. Salt stress lowered some macronutrient concentrations [calcium (Ca) and potassium (K) in leaves and roots, phosphorus (P) in roots] but foliar application of both KIN and IAA increased Ca in both leaves and roots and P in leaves. Foliar application of IAA increased K concentrations in leaves of the salt-stressed plants. Foliar application of KIN and IAA, especially at 2 mM concentration, counteracted some of the adverse effects of NaCl salinity by causing the accumulation of proline and essential inorganic nutrients as well as by maintaining membrane permeability.     

Responses of Batis maritima plants challenged with up to two‐fold seawater NaCl salinity

Batis maritima is a promising halophyte for sand‐dune stabilization and saline‐soil reclamation. This species has also applications in herbal medicine and as an oilseed crop. Here, we address the plant response to salinity reaching up to two‐fold seawater concentration (0–1000 mM NaCl), with a particular emphasis on growth, water status, mineral nutrition, proline content, and photosystem II integrity. Plant biomass production was maximal at 200 mM NaCl, and the plants survived even when challenged with 1000 mM NaCl. Plant water status was not impaired by the high accumulation of sodium in shoots, suggesting that Na⁺ compartmentalization efficiently took place in vacuoles. Concentrations of Mg²⁺ and K⁺ in shoots were markedly lower in salt‐treated plants, while that of Ca²⁺ was less affected. Soluble‐sugar and chlorophyll concentrations were hardly affected by salinity, whereas proline concentration increased significantly in shoots of salt‐treated plants. Maximum quantum efficiency (F_v/F_m), quantum yield of PSII (Φ_PSII), and electron‐transport rate (ETR) were maximal at 200–300 mM NaCl. Both nonphotochemical quenching (NPQ) and photochemical quenching (qP) were salt‐independent. Interestingly, transferring the plants previously challenged with supraoptimal salinities (400–1000 mM NaCl) to the optimal salinity (200 mM NaCl) substantially restored their growth activity. Altogether, our results indicate that B. maritima is an obligate halophyte, requiring high salt concentrations for optimal growth, and surviving long‐term extreme salinity. Such a performance could be ascribed to the plant capability to use sodium for osmotic adjustment, selective absorption of K⁺ over Na⁺ in concomitance with the stability of PSII functioning, and the absence of photosynthetic pigment degradation.     

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.     

RESPONSE OF LIME THYME TO SALINITY AND IONIC CONCENTRATION IN NUTRIENT SOLUTION

□ Plants from 60-day-old Lime Thyme (Thymus citriodorus) cuttings were potted in a medium of coconut fiber and peat moss and were treated with three different nutrient solutions: T1, T2, and T3. T1 was a standard nutrient solution; T2 was incremented with macronutrients up to an electrical conductivity (EC) of 2.8 dS m^?1; and T3 was the same as T1 but incremented up to an EC of 2.8 dS m^?1 with sodium chloride. The plants were then grown for 90 days in a greenhouse with natural daylight in Almería, Spain. Root growth was not affected by the treatments. The dry weight of the leaves and the total dry weight of the plants benefited from the salinity. The specific salinity of the sodium chloride negatively affected growth compared to the same salinity in the complete nutrient solution.     

RESPONSE OF SALT STRESSED STRAWBERRY PLANTS TO FOLIAR SALICYLIC ACID PRE-TREATMENTS

Salinity has deleterious effects on plant growth and development through membrane stability, photosynthetic activity, protein content, and ionic composition; however, salicylic acid (SA) could restore these properties in plants. The objective of this study was to determine the ameliorative effects of SA as foliar pre-treatments on membrane permeability, proline and protein contents, chlorophyll a, b and total chlorophyll and ionic composition of strawberry cv. ‘Camarosa’ under saline conditions. Membrane permeability and proline content significantly increased and protein and chlorophyll contents significantly decreased by 6 mS cm^?1 application without SA treatment compared with the control (2 mS cm^?1) treatment. Membrane permeability decreased from 6.9 in 0 mM SA treatment to 5.2 by application of 1.0 mM SA under saline conditions and same to the control (5.2). Compared with 0 mM SA treatment, the average increases of proline and protein contents were 66.7% in 0.25 mM SA treatment and 62.2% in 0.1 mM SA treatment in 6 mS cm^?1 level, respectively. Chlorophyll b and total chlorophyll significantly increased by 0.25 mM SA treatments under saline conditions. The lowest and the highest chlorophyll b and total chlorophyll were obtained from 0 mM SA treatment (19.6 and 44.5 mg L^?1) and 0.25 mM SA treatment (28.6 and 52.9 mg L^?1) in 6 mS cm^?1 salinity level. Ionic compositions of leaves were significantly affected by salinity and SA treatments. Nitrogen in 1.0 mM SA treatment and P contents of leaves in 0.1 mM SA treatment significantly increased but Na and Cl contents of leaves significantly decreased by SA treatments in 6 mS cm^?1 salinity level. The results of this study were clearly indicated that the SA application on strawberry plants could ameliorate the deleterious effect of salt stress on membrane permeability, proline, protein, and chlorophyll contents. Therefore, SA treatment could offer an economic and simple application to salinity stress.     

TREATED EFFLUENT AND SALINE WATER IRRIGATION INFLUENCES SOIL PROPERTIES,YIELD, WATER PRODUCTIVITY AND SODIUM CONTENT OF SNOW PEAS AND CELERY

To determine the effects of irrigation water quality, plants were irrigated with normal potable water [0.25 dS m^?1 electrical conductivity (EC), 25 mg L^?1 sodium (Na), 55 mg L^?1 chloride (Cl)], treated effluent (0.94 dS m^?1 EC, 122 mg L^?1 Na, 143 mg L^?1 Cl) and saline water with low salinity (1.24 dS m^?1 EC, 144 mg L^?1 Na and 358 mg L^?1 Cl) and high salinity (2.19 dS m^?1 EC, 264 mg L ^?1Na and 662 mg L^?1 Cl) for snow peas, and high salinity (3.07 dS m^?1 EC, 383 mg L^?1 Na and 965 mg L^?1 Cl) and very high salinity (5.83 dS m^?1 EC, 741 mg L^?1 Na and 1876 mg L^?1 Cl) for celery. The greater salts build up in the soil and ion toxicity (Cl and Na) with saline water irrigation contributed to significantly greater reduction in root and shoot biomass, water use, yield and water productivity (yield kg kL^?1 of water used) of snow peas and celery compared with treated effluent and potable water irrigation. There was 8%, 56% and 74% reduction in celery yield respectively with treated effluent, high salinity and very high salinity saline water irrigation compared with potable water irrigation. The Na concentration in snow peas shoots increased by 54%, 234% and 501% with treated effluent, low and high salinity saline water irrigation. Similarly, the increases in Na concentration in celery shoots were 19%, 35% and 82%. The treated effluent irrigation also resulted in a significant increase in soil EC, nitrogen (N) and phosphorus (P) content compared with potable water irrigation. The heavy metals besides salts build up appears to have contributed to yield reductions with treated effluent irrigation. The study reveals strong implications for the use of saline water and treated effluent for irrigation of snow peas and celery. The salt build up within the root zone and soil environment would be critical in the long-run with the use of saline water and treated effluent for irrigation of crops. To minimize the salinity level in rhizosphere, an alternate irrigation of potable water with treated effluent or low salinity level water may be better option.     

Salinity-Induced Changes in Ion Concentrations of ‘Hass’ Avocado Trees on Three Rootstocks

ABSTRACT

The effect of salinity (1.5, 3.0, 4.5, or 6.0 dS m^{? 1}) on ion concentrations [magnesium (Mg), calcium (Ca), potassium (K), sodium (Na), and chloride (Cl)] of one-year-old ‘Hass’ avocado (Persea americana Mill.) trees on one of three rootstocks [‘Duke 7’ (D7), ‘Toro Canyon’ (TC), or ‘Thomas’ (TH)] was investigated. Concentrations of Mg decreased in roots, stems, and older leaves with increasing substrate salinity. Salinity had no effect on Ca concentration of the trees. Potassium concentrations decreased in roots of all trees and stems of trees on TH. Potassium concentrations either remained unchanged or increased at salinity levels of 3.0 dS m^{? 1} and above in leaves and buds of all trees. Sodium increased in roots and woody organs in trees on all rootstocks. Leaf Na concentrations increased with salinity in trees on D7 and TH, but not TC. Chloride increased in all organs of all trees with increasing salinity, but to the greatest extent in trees on TH and to the least extent in trees on TC. At high substrate salinity concentrations, leaves of trees on TH rootstock had the highest leaf concentrations of Na and Cl, and the highest Na:K ratios. Sodium and chloride concentrations were correlated with necrosis in older leaves of TH, but less so in leaves of trees on TC or D7. Based on percent necrosis in older leaves with increased salinity, trees on TH performed poorest, whereas trees on TC exhibited the greatest salt tolerance. Leaf necrosis was consistently observed at Cl concentrations of 4 mg g^{? 1} or more, and at Na:K ratios of 0.01 or more in older leaves. Chloride concentration and Na:K ratio in older leaves appears to be a useful marker for salinity tolerance screening in avocado rootstocks. The relative tolerance of the various rootstocks appeared to be due primarily to their ability to exclude Na and Cl from the leaves.     

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 salt stress on growth and biochemical parameters of Pisum sativum L.

Abstract

The effect of salinity on some physio-biochemical parameters in plants of pea (Pisum sativum L. cv. EC 33866) has been investigated. Plants were subjected to four salt treatments, 50, 100, 150 and 200 mM NaCl, for 30 days in sand culture and the physiological responses were measured. Salinity affected all of the considered parameters. Thus, high NaCl concentrations caused a great reduction in growth parameters such as fresh and dry weight of leaves and roots, but the leaf number was less affected. These changes were associated with a decrease in the relative water content and the K⁺ concentrations. The proline and sugar content was increased, but nitrate reductase activity and chlorophyll was found to decrease in leaves. The significance of organic solute accumulation in relation to osmotic adjustment has been discussed.     

Alleviation of salt stress by arbuscular mycorrhizal in zucchini plants grown at low and high phosphorus concentration

With the aim of determining whether the arbuscular mycorrhizal (AM) inoculation would give an advantage to overcome salinity problems and if the phosphorus (P) concentration can profoundly influence zucchini (Cucurbita pepo L.) plant responses to AM, a greenhouse experiment was carried out with AM (+AM) and non-AM (−AM). Plants were grown in sand culture with two levels of salinity (1 and 35 mM NaCl, giving electrical conductivity values of 1.8 and 5.0 dS m⁻¹) and P (0.3 and 1 mM P) concentrations. The percentages of marketable yield and shoot biomass reduction caused by salinity were significantly lower in the plants grown at 0.3 mM P, compared to those grown at 1 mM P. However, even at high P concentration, the absolute value of yield and shoot biomass of +AM zucchini plants grown under saline conditions was higher than those grown at low P concentration. The +AM plants under saline conditions had higher leaf chlorophyll content and relative water content than −AM. Mycorrhizal zucchini plants grown under saline conditions had a higher concentration of K and lower Na concentration in leaf tissue compared to −AM plants. The P content of zucchini leaf tissue was similar for +AM and −AM treatments at both low and high P concentrations in the saline nutrient solution. The beneficial effects of AM on zucchini plants could be due to an improvement in water and nutritional status (high K and low Na accumulation).