Growth and mineral distribution of Sesuvium portulacastrum l., a salt marsh halophyte,under sodium chloride stress

Abstract

Response of Sesuvium portulacastrum L., to the elogenous addition of sodium chloride (NaCl), applied at different concentrations ranging from 100 to 900 mM was evaluated. Leaf area, shoot and root weight of the treated plants were increased significantly. Total nitrogen (N) content of leaves, stem and root was significantly increased up to 600 mM NaCl, and thereafter declined moderately. Accumulation of potassium (K), and calcium (Ca) were exponentially increased with NaCl treatment as also observed in the case of N. Sodium content of shoot and roots of S. portulacastrum increased significantly with increasing NaCl concentrations. Certain essential elements like copper (Cu), iron (Fe), manganese (Mn) and zinc (Zn) were also accumulated in all plant parts significantly, up to 600 mM. However, due to high salinization, growth and development of plants inhibited markedly. Furthermore, elemental concentration decreased beyond 600 mM level of NaCl. Due to aging and senescence, marked changes in leaf area, shoot, root volume and mineral content were observed between sampling time.     

Salt Stimulation and Tolerance in an Intertidal Stem-Succulent Halophyte

ABSTRACT

Salt tolerance of Arthrocnemum macrostachyum (Moric.) C. Koch (Chenopodiaceae), a stem-succulent halophyte most commonly found in the intertidal regions of the provinces of Sind and Balochistan, Pakistan, was investigated. Plants were grown for 125 d at six sodium chloride (NaCl) concentrations from 0 to 1000 mM to determine the effects of salinity on ion accumulation, plant water status, and biomass. Shoot biomass was greatest at 200 to 400 mM NaCl, but it was inhibited at salinities of 600 mM NaCl or higher. Tissue water content (g g^?1dry mass) of shoots under 200 to 600 mM NaCl treatments was higher than under the control nutrient solution, equal to the control at 800 mM NaCl, but significantly lower at 1000 mM NaCl than under all other treatments, indicating an increase in shoot succulence at salinity levels up to that of seawater. Ash content increased with added salt, but was about 60% of plant dry mass under all salinity treatments. The Na⁺ and Cl^? concentrations of shoots were significantly higher under 1000 mM NaCl than under the control treatment. These results indicate that A. macrostachyum is salt tolerant and capable of accumulating large quantities of Na⁺ and Cl^? when treated with from 200 to 1000mM NaCl.     

Soluble root exudates of maize: Influence of potassium supply and rhizosphere microorganisms

Maize was grown for 36 days in solution culture with roots either under axenic conditions or in the presence of rhizosphere organisms. In other experiments with sterile roots the plants were grown with different concentrations of potassium. At the end of the experiments sugars, organic acids and amino acids in the nutrient solutions were determined. Under axenic conditions the exudates consisted of up to 65% sugars, up to 33% organic acids and only up to 2% amino acids. The same substances were detected in non-sterile nutrient solutions. In the presence of microorganisms fructose, arabinose and the predominating glucose decreased to almost one half, while sucrose was not affected. The amounts of organic acids were not changed by microbial growth. The main amino acid, glutamic acid, was nearly doubled by the presence of microorganisms, whereas other amino acids remained unchanged. The lower O₂ content of the nutrient solutions of non-sterile roots suggested microbial decomposition of monosaccharides. In another experiment with roots grown under axenic conditions and with different K treatments low K supply significantly increased the total amounts of sugars, organic acids and amino acids exuded g^?1 root dry matter. As in the previous experiment glucose, fumaric and oxalacetic acid as well as glutamic and aspartic acid dominated in the respective fractions. Again sugars and organic acids represented the major quantity of exudates, while amino acids amounted to less than 2%. In an additional experiment with another cultivar, with nitrate as N source and a 5-day longer growth period, somewhat different results were obtained. In the exudates sugars were found in lower amounts, probably due to a higher growth rate. Under these conditions organic acids were the prevailing root exudates. Unlike sugars and amino acids, their total quantity was not affected by K nutrition, but the proportion of malic acid increased with increasing K supply, while oxalacetic acid dominated at low K nutrition. Similarly the total amount of organic acids within the root was independent of K nutrition. However malic acid content increased with increasing K application, while the likewise dominating citric and oxalacetic acid decreased.     

Response of Two Olive Cultivars to Salt Stress and Potassium Supplement

ABSTRACT

The effects of saline water containing 0, 50, 100, and 150 mM sodium chloride (NaCl), and 100 mM NaCl + 100 mM potassium (K) on photosynthesis, water relations, and ion and carbohydrate content of olive (Olea europaea L.) cultivars ‘Koroneiki’ and ‘Mastoidis’ were studied on five-year-old trees. Salinity increased sodium (Na⁺) and chloride (Cl^?) in tissues of both cultivars, but more so in ‘Koroneiki’ than in ‘Mastoidis.’ Salt-toxicity symptoms were observed at 100 and 150 mM, but not in plants receiving extra K. In salt-stressed plants, leaf water potential declined, whereas turgor potential remained positive due to a rapid decrease in osmotic potential. Salinity increased mannitol content up to 41.3% in ‘Mastoidis’ and 15.8% in ‘Koroneiki’, but reduced starch content in leaves. Photosynthetic rates fell significantly with increasing salinity in both cultivars, but more so in ‘Koroneiki’ than in ‘Mastoidis’. Potassium supplements reduced the concentration of Na⁺ and increased the concentrations of K⁺ in leaves, but decreased photosynthesis.     

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.     

Improving salt stress responses of the symbiosis in alfalfa using salt-tolerant cultivar and rhizobial strain

Salt stress can affect alfalfa growth directly by adversely affecting metabolism, or indirectly by its effect on Rhizobium capacity for symbiotic N₂ fixation. Growth and carbohydrate metabolism in leaves, roots and nodules of two alfalfa cultivars (Medicago sativa cv Apica and salt-tolerant cv Halo) in association with two rhizobial strains (A2 and salt-tolerant Rm1521) exposed to different levels of NaCl (0, 20, 40, 80 or 160 mM NaCl) were assessed under controlled conditions. For both cultivars, shoot and root biomasses and shoot to root ratio significantly declined with increasing NaCl concentrations. Under 80 mM NaCl, Halo plants yielded 20% more fresh shoot biomass than Apica while plants inoculated with Rm1521 allocated more biomass to the roots than to the shoots compared to A2. Halo plants maintained a steady shoot water content (about 80%) under the entire range of NaCl concentrations. Shoot water content was more variable in Apica. Apica in association with salt-tolerant strain Rm1521 maintained a better water status than with strain A2, as indicated by the higher shoot water content at 80 mM NaCl. Under salt stress, two major compatible sugars involved in plant osmoregulation, sucrose and pinitol, increased in leaves while a large accumulation of starch was observed in roots. In nodules, pinitol, sucrose and starch increased under salt stress and were much more abundant with strain Rm1521 than with A2. This suggests that there could be an active transport from the shoot to the nodules to help maintain nodule activity under NaCl stress and that strain Rm1521 increases the sink strength toward nodules. Our results show that combining cultivars and rhizobial strains with superior salt tolerance is an effective strategy to improve alfalfa productivity in salinity affected areas.     

Response of Digitalis purpurea plants to temporary salinity

Abstract

The effect of two different levels of salinity upon adult plants of Digitalis purpurea has been studied. Seeds of D. purpurea plants were sown in pots of equal size and moistened with deionized water during one year. Afterwards, different treatments with NaCl were initiated, the concentrations being 100 mM and 200 mM NaCl in irrigation water during 63 days. Growth, measured as dry and fresh weight, and soluble protein contents, were lower in stressed plants than in control plants. Monovalent cation analysis showed that in leaves K⁺ plus Na⁺ (Total M) values did not change with the different treatments, but that in roots these values increased with the increasing salinity stress. On the other hand, proline levels were higher in stressed plants although the accumulation of this amino acid was not significant In leaves, Cl^? levels increased linearly with salinity degree, and the accumulation of this ion was faster than that of Na⁺, whereas in roots, the Cl^? level remained relatively low.

Total cardenolide levels in leaves and roots of the 100 mM NaCl plants were higher than those in 200 mM NaCl and control plants. We infer that moderate salinity conditions lead to raised cardenolide levels, principally in leaves, but the reason for this is not clear.     

Effects of sodium chloride treatments on growth and ion accumulation of the halophyte Haloxylon recurvum

Abstract

Effects of increasing salt concentrations 0, 180, 360 mol im³ sodium chloride (NaCl), on growth, succulence, mineral composition, and glycinebetaine content in Haloxylon recurvum was investigated. Fresh and dry weight of plants increased with an increase in salinity. Succulence of shoots increased at low salinity and decreased at high salinity. Root and shoot Ca⁺, Mg⁺, and K⁺content decreased with increasing salinity while both Na⁺ and Cl^‐ content increased, reaching 4,900 and 5,300 mmol kg^‐1 dry weight, respectively. Glycinebetaine (mol m^‐3 tissue water) significantly increased in shoots at 360 mol m^‐3 NaCl, but did not differ significantly in roots treated with from 0 to 360 mol m^‐3 NaCl. Haloxylon recurvum is a highly salt tolerant stem succulent plant which accumulate a high quantity of salt, which makes it a good candidate to use for phytoremediation in highly saline areas of the sub‐tropics.     

Genotype-Dependent Differential Responses of Three Forage Species to Calcium Supplement in Saline Conditions

Salt toxicity comprises of osmotic and ionic components both of which can severely affect root and shoot growth. In many crop species, supplemental calcium (Ca) reduces the inhibition of growth typical of exposure to salt stress. The objective of this study was to compare whole plant growth and physiological responses to interactive effect of salinity and Ca level on three forage species [African millet (AM), tall wheat grass (TW), and perennial ryegrass (PR)] differing in tolerance to sodium chloride (NaCl) salinity. Plants were grown under glasshouse condition and supplied with nutrient solution containing 0, 100, and 250 mM NaCl supplemented with 0.5, 5, or 10 mM calcium chloride (CaCl₂). Plant growth, ionic concentration, water relations, and solute (proline and glycinebetaine) concentrations of the plants were determined two weeks after the salinity treatments. At 100 mM NaCl, there was a moderate reduction in dry matter (DM) production of all three species. A drastic decrease in DM occurred at 250 mM NaCl. Supplemental Ca reduced the adverse effects of salinity on all three species. The TW showed higher shoot and root growth in 100 and 250 mM NaCl than AM and PR. It also showed the highest DM at 5 and 10 mM Ca supplement. The shoot and root DM of TW increased by about 45 and 15%, respectively compared to the control. Chemical analysis indicated that in TW, Ca restricted both uptake and transport of sodium (Na) from root to shoot. It also increased Ca and potassium (K) concentrations in both organs. The transport of K and Ca from root to shoot of AM and PR were decreased by NaCl, but were restored with increasing Ca in the medium. The opposite occurred for Na. In PR, more K uptake was observed in shoot at 250 mM NaCl with 10 mM Ca supplement. The sap osmotic potential (Ψ_S) was the highest in TW at 10 mM Ca in the presence of 250 mM NaCl. Contribution of various solutes to the difference in Ψ_S among the species from the control and 250 mM salt treatment differed greatly. Supplemental Ca induced decline in the leaf Ψ_S of TW which was predominately due to K, glycinebetaine, Na and proline accumulation. Addition of 10 mM Ca to the growth medium maintained a low Na and a high K level. Accumulation of glycinebetaine and proline in leaf contributed the NaCl tolerance of TW. The presented results suggest that supplement Ca, not only improved ionic relations but also induced plant ability in production of compatible solutes (glycinebetaine and proline) and osmotic adjustment. Accordingly, genotype dependent capacity could be found using supplemental Ca.     

Growth and micronutrient acquisition of some apple varieties in response to gradual in vitro induced salinity

Growth and micronutrient acquisition of some apple (Malus dometsica Borkh) varieties (Galla, MM 111, MM I06, M 26, and M6 York) were studied under gradually in vitro induced NaCl (from 0, 50 to 100 mM) salinity. Microshoot dry weight tended to increase with increasing salinity level in all varieties except in M 26 and M6 York as some decline was obtained at 100 mM NaCl. Shoot proliferation was decreased significantly in Galla at 100 mM NaCl and at both salinity levels in M 26 compared to the control (0 mM). A significant decrease in shoot zinc (Zn) acquisition with increasing salinity level was obtained in all varieties except MM 111. M6 York and MM 111 decreased their copper (Cu) acquisition significantly at 50 mM NaCl and then increased at 100 mM salinity level. Meanwhile, a significant decrease in Cu acquisition with increasing NaCl concentration was obtained in Galla and M 26. Galla, MM 106, and M 26 showed a significant increase in manganese (Mn) acquisition at 50 mM NaCl followed by a decrease at 100 mM salinity level. On the other hand, Mn acquisition continued to decrease significantly in MM 111 while M6 York increased its Mn acquisition with increasing salinity. M 111 and M6 York showed a significant decrease in iron (Fe) acquisition at 50 mMNaCl followed by an increase at 100mM NaCl. Galla and M 26 continued to decrease Fe acquisition with elevated salinity level, whereas Fe in MM 106 increased with salinity.     

Salt Stress Induces Accumulation of γ–Aminobutyric Acid in Germinated Foxtail Millet (Setaria italica L.)

Effects of NaCl treatments on sprout length, the contents of soluble protein, free amino acids, and γ‐aminobutyric acid (GABA) and on glutamate decarboxylase (GAD) activity in germinated foxtail millet were investigated, and the regulating effects of exogenous Ca²⁺, along with lanthanum chloride (LaCl₃, a specific inhibitor of the Ca²⁺ pathway) and ethylene glycol tetraacetic acid (EGTA, a chelator of Ca²⁺) under salt stress, on GABA accumulation in germinated millet were examined in this paper. The results showed that NaCl treatments caused a decrease in sprout length of millet. Low concentration of NaCl treatments increased soluble protein content, but high concentration decreased soluble protein content. The level of free amino acids, GAD activity, and GABA content increased significantly under NaCl stress. Exogenous Ca²⁺ application under NaCl stress further increased GAD activity and GABA content; the optimal concentration of Ca²⁺ for GAD activity and GABA accumulation was 5.0mM under 100mM NaCl for 48 hr, at which GABA content was 31.92 mg/100 g, a 1.41‐fold increase as compared with that in seeds under NaCl stress (22.64 mg/100 g). GAD activity and GABA accumulation in germinated millet decreased when treated with LaCl₃ or EGTA under NaCl stress. Our results suggest that salt stress combined with Ca²⁺ treatment may be used for preparation of millet with higher GABA content, which can be used as a natural resource for functional foods.     

Effect of Sodium Chloride on Growth,Nutrient Accumulation,and Nitrogen Fixation of Common Bean Plants in Symbiosis with Isogenic Strains

The effect of sodium chloride (NaCl)-salinity on growth responses and tissues organic solutes and mineral content was investigated in common bean plants inoculated with salt-tolerant Rhizobium tropici wild-type strain CIAT899 and four mutant derivatives having decreased salt-tolerance (DST). Under non-saline conditions two mutants formed partially effective (HB10, HB12) and another two almost ineffective (HB8, HB13) nodules. A great variation of NaCl tolerance in the different symbiosis tested was observed at harvest, 32 day after planting. Common bean plant responded to salinity by decreasing the content of dry plant biomass, nodule number and the nitrogen fixation, and increasing the root to shoot ratio. The salt dose of 25 mM produced an increase of total soluble sugar and free amino acids content. This result suggest that these metabolites might be related with a nodule osmotic adjustment response under saline conditions, however cannot be excluded that the increase of amino acids content could be a consequence of protein degradation. In the other hand, sodium, calcium and phosphorus contents in shoot increased under the saline treatments. Potassium (K) and calcium (Ca) contents, unlike phosphorus (P) content, in shoot were not related with the symbiotic efficiency of mutant, however the decrease of P content suggest that these symbioses have limited their P absorption process independently of the saline treatment. NaCl tolerance associated with a retention of sodium and maintenance of potassium selectivity seem to be a strategy used for the salt stressed common bean plants in symbiosis assayed here.     

GROWTH,NUTRIENT ACQUISITION,AND PHYSIOLOGICAL RESPONSES OF HYDROPONIC GROWN TOMATO TO SODIUM CHLORIDE SALT INDUCED STRESS

□ Growth and nutrient acquisition of tomato (Lycopersicon esculentum L.) cv ‘Amani’ were studied under induced salt stress in Hoagland's solution. The plants were treated for 37 days with salinity induced by incorporating different concentrations [0.0 (control), 50, 100, 150, or 200 mM] of sodium chloride (NaCl) to the nutrient solution. Slight reduction was obtained in growth represented by (shoot length and number, leaf number, and dry weight) when seedlings were directly exposed to NaCl stress from 0.0 to 100 mM. At higher concentrations (150 or 200 mM), growth parameters were adversely affected and seedlings died thereafter. Elevated salinity significantly reduced crude protein and fiber in shoots and roots. Tomato shoot and root contents of potassium (K), iron (Fe), and ash were reduced significantly in response to increased levels of salinity. Tissue contents of sodium (Na) and chloride (Cl) increased with elevated salinity treatments.     

Salicylic Acid–Induced Growth and Biochemical Changes in Salt‐Stressed Wheat

The interactive effect of salicylic acid and sodium chloride (NaCl) salinity on wheat (Triticum aestivum L.) cv. ‘Inqlab’ (salt‐sensitive) and cv. ‘S‐24’ (salt‐tolerant) was studied in a sand‐culture pot experiment in a net house. Wheat seeds soaked in water and 100 ppm salicylic acid solution for 6 h were sown in sand salinized with 0, 50, and 100 mM NaCl. Pots were irrigated with quarter‐strength Hoagland's nutrient solution. Fourteen‐day‐old seedlings were harvested, and growth parameters (leaf and root length, leaf and root dry weight) were recorded. Chlorophyll a and b content; soluble sugar (reducing, nonreducing, and total sugars) content; nitrate (NR) and nitrite reductase activity (NiR); soluble proteins, and total soluble amino acid content of fresh leaves were determined. Sodium chloride salinity significantly reduced growth parameters. Salicylic acid treatment alleviated the adverse salinity effect on growth. Salinity decreased the chlorophyll a and b content and chlorophyll a/b ratio in both varieties, but a decrease in the chlorophyll a/b ratio was less in salt‐tolerant wheat variety (‘S‐24’), which could be a useful marker for selecting a salt‐tolerant variety. Salinity (NaCl) stress considerably increased the accumulation of reducing sugars, nonreducing sugars, and total soluble sugars in leaves of 14‐day‐old wheat seedlings of both varieties. The salt‐tolerant variety (‘S‐24’) accumulated a higher sugar content, which also could be a useful marker for selecting a salt‐tolerant variety for slat‐affected areas. Salinity caused a reduction in nitrate reductase and nitrite reductase activity. The salt‐tolerant variety (‘S‐24’) showed resistance to a decrease of nitrate reductase activity under salinity. This could be a useful criterion for selecting salt‐tolerant varieties. In response to salinity, wheat seedlings accumulated soluble proteins and amino acids, which might reflect a salt‐protective mechanism.     

Growth Responses and Nitrogen-15 Absorption of Desert Saltgrass Under Salt Stress

Abstract

Saltgrass [Distichlis spicata (L.) Greene var. stricta (Gray) Beetle], accession WA-12, collected from a salt playa in Wilcox, AZ, was studied in a greenhouse to evaluate its growth responses in terms of shoot and root lengths, shoot dry-matter yield, and nitrogen (N) (regular and ¹⁵N) absorption rates under control and salt (sodium chloride, NaCl) stress conditions. Plants were grown under a control (no salt) and three levels of salt stress (100, 200, and 400 mM NaCl, equivalent to 5850, 11700, and 23400 mg L^{? 1} sodium chloride, respectively), using Hoagland solution in a hydroponics system. Ammonium sulfate [(¹⁵NH₄)₂SO₄], 53% ¹⁵N (atom percent ¹⁵N) was used to enrich the plants. Plant shoots were harvested weekly, oven-dried at 60°C, and the dry weights measured. At each harvest, both shoot and root lengths were also measured. During the last harvest, plant roots were also harvested and oven-dried, and dry weights were determined and recorded. All harvested plant materials were analyzed for total N and ¹⁵N. The results showed that shoot and root lengths decreased under increasing salinity levels. However, both shoot fresh and dry weights significantly increased at 200 mM NaCl salinity relative to the control or to the 400 mM NaCl level. Shoot succulence (fresh weight/dry weight) also increased from the control (no salt) to 200 mM NaCl, then declined. The root dry weights at both 200 mM and 400 mM NaCl salinity levels were significantly higher than under the control. Concentrations of both total-N and ¹⁵N in the shoots were higher in NaCl-treated plants relative to those under the control. Shoot total-N and ¹⁵N contents were highest in 200 mM NaCl-treated plants relative to those under the control and 400 mM salinity.     

Influence of soluble carbohydrates,free amino acids,and protein content on the decomposition of Lolium multiflorum shoots

The aim of the present investigation was to determine how the chemical composition of L. multiflorum (var. Imperial) shoots influences the initial dynamic decomposition phase. Decomposition in soil was monitored by taking semicontinuous respiration measurements with a resolution of 1 h. Shoots with six different total N contents(2.0–5.2%) were compared. The carbohydrate content of the shoots decreased with increasing total N content, whereas the free amino acid and protein contents increased. Two respiration peaks were observed during the 1-week-long incubation. Comparisons of C mineralisation curves for water-extracted and whole shoots showed that the first peak was derived from water-soluble plant components. Lengths of lag phases and values of specific microbial growth rates obtained from respiration curves of sugars and amino acids implied that these substances were mineralised during the time of the first respiration peak. Amounts of CO₂-C evolved from the shoots during the first peak increased linearly as a function of the sum of the content of glucose, fructose, sucrose, fructans, and free amino acids in the shoots. The shoots with two highest N contents showed net N mineralisation during the first respiration peak, whereas at a lower N content there was net immobilisation. It was concluded that soluble carbohydrates and free amino acids were important C and energy sources for the decomposers during the time encompassed by the first respiration peak. The second peak was derived from both water-soluble and water-insoluble plant components, and the amount of C respired increased with an increasing protein content.     

Effects of NaCl salinity on miniature dwarf tomato ‘Micro‐Tom’: I. Growth analyses and nutrient composition 1

The growth and nutrient composition of miniature dwarf tomato selection Lycopersicon esculentum ’Micro‐Tom’ plants grown from seedling to harvest in solution batch culture at four different NaCl salinity levels (2.4 [control, no NaCl], 7.6, 12.8, or 18 dS‐m^‐1 solution conductivities) was studied. Specific leaf area and relative growth rate generally decreased with increased NaCl. Shoot‐root, root mass, and leaf area ratios initially increased but later resumed control values. Although reduction in leaf area in response to higher NaCl was noted at 4 weeks, leaf and root dry mass was not significantly reduced until 12 weeks. At 12 weeks, enhanced carbohydrate partitioning toward shoot vegetative growth was observed in the highest NaCl level as reduced harvest index and increased leaf and stem mass ratios. An immediate proportional increase in leaf Na and decrease in Ca occurred with solution NaCl concentration. Although leaf K declined significantly between 4 and 8 weeks, there were no differences between treatments. Cu and Zn content escalated with increasing NaCl, with Zn increasing three fold between the lowest and highest NaCl levels.     

Effect of peduncle‐perfused nitrogen,sucrose, and growth regulators on barley and wheat amino acid composition

Abstract

Nitrogen (N) or growth regulator application to small grain cereals near anthesis has been demonstrated to alter grain fill and grain yield, the protein yield and nutritional quality may also be modified by these management factors. The objective of this study was to determine whether delivery of N, growth regulator, or sucrose solutions into greenhouse‐grown barley (Hordeurn vulgare L. cv. Leger) or wheat (Triticum aestivum L. cv. Katepwa), plants through peduncle perfusion altered the amino acid composition of the grain. The following treatments were tested: N (25 and 50 mM), chlormequat (30 μM), ethephon (15 μM), N + chlormequat, N + ethephon, detillering + N, sucrose (250 mM), distilled water check, and non‐perfused check. Perfusion lasted 30 d beginning 5 to 8 d after spike emergence. Addition of N via peduncle perfusion increased protein concentrations and concentrations of all amino acids in both barley and wheat when expressed in terms of grain dry matter. Protein yield and lysine content were also increased. However, the increase in essential amino acids such as lysine, methionine, threonine, isoleucine, arginine, and leucine was relatively small, and the proportions of these amino acids in the grain protein were actually reduced. The sucrose treatment only affected wheat, increasing lysine concentration and decreasing the total protein concentration. Growth regulators used in this study did not alter protein yield or amino acid composition in either crop.     

Influence of Salinity on Chlorophyll,Leaf Water Potential,Total Soluble Sugars,and Mineral Nutrients in Two Young Olive Cultivars

The effect of salinity (NaCl) on chlorophyll, leaf water potential, total soluble sugars, and mineral nutrients in two young Iranian commercial olive cultivars (‘Zard’ and ‘Roghani’) was studied. One-year-old trees of these cultivars were planted in 10-L plastic pots containing equal ratio of sand-perlite mixture (1:1). Sodium chloride at concentrations of 0, 40, 80, 120, or 160 mM plus Hoagland's solution were applied to these pots for 150 days. The results showed that chlorophylls (a), (b), and (a+b) reduced with increasing of salinity up to 40 mM. There was no difference between cultivars for chlorophylls (b) and (a+b) while ‘Roghani’ showed more decreased in content of chlorophyll (a) than did ‘Zard’. Total soluble sugars in leaves increased with an increase in salinity up to 80 mM but decreased with additional increase in salinity. Salinity stress reduced water potential equally in both cultivars. The concentrations of sodium (Na) and chloride (Cl) and Na/potassium (K) ratio were increased and K decreased with increasing of salinity up to 80 mM in leaves and roots. Concentrations of K, magnesium (Mg), calcium (Ca), phosphorus (P), and nitrogen (N) reduced significantly in leaves, shoots and roots with increasing salinity.     

The Rhizofiltration of Sodium from Hydroponic Fluid using Scented Geraniums

The ability of two scented geraniums, Pelargonium sp. `Frensham' and Pelargonium sp. `Citrosa' to tolerate and accumulate salt was assessed in a hydroponic system under greenhouse conditions. Rooted cuttings were exposed to a range of salt concentrations (0 to 200 mM NaCl) over a two-week period. No visible signs of phytotoxicity were observed on scented geranium plants grown in solutions up to 100 mM sodium chloride. Tolerance to salt exposure was assessed with chlorophyll a fluorescence parameters. A significant decline in the efficiency of the photosystem (Fv/Fm) was observedin Frensham plants exposed to 200 mM NaCl for 14 days. The numberand size of active reaction centers (Fv/Fo) declined with increasing NaCl treatments in both species. Total chlorophyll content of both species decreased with increasing salt treatmentas a result of significant reductions in the chlorophyll acontent. At higher levels of sodium chloride treatment, salt extrusion was observed on the petioles and the leaf lamina. An accumulation in excess of 3.7 and 2.6% of the dry weight of Frensham plants as sodium was observed in shoots and roots, respectively. The effect of the accumulated sodium on the physiology of scented geraniums was assessed through biochemicalanalysis. The determination of amino nitrogen and stress-relatedmarkers revealed an initial increase in 4-aminobutyrate, proline,asparagine, glutamine, and alanine in the root tissues. Shoot analysis showed gradual increases in asparagine, aspartate, andalanine. These data provide the first evidence for the salt tolerating and accumulating potential of Pelargonium sp. and demonstrate the efficacy of this plant species for the remediation of salt contaminated hydroponic solutions.