Abstract:The aim of this study was to determine the range of NaCl concentrations in the nutrient solution that allow Suaeda altissima (L.) Pall., a salt-accumulating halophyte, to maintain the upward gradient of water potential in the "medium-root-leaf" system. We evaluated the contribution of Na + ions in the formation of water potential gradient and demonstrated that Na + loading into the xylem is involved in this process. Plants were grown in water culture at NaCl concentrations ranging from zero to 1 M. The water p… Show more
“…When the salt concentration in the medium is further increased to 750 mM, organ mass decreases 4 -5-fold (Figures 1(a) and (c)). These results support the known data that NaCl concentration of 250 mM in the medium is optimal for seablite growth and development [9]. In the glycophyte, an increase in NaCl concentration in the medium up to 250 mM leads to a slight decrease in fresh biomass (Figure 1(b)), while dry mass does not change significantly (Figure 1(d)).…”
Section: Resultssupporting
confidence: 90%
“…Seablite is a salt-accumulating halophyte. It adapts to high salinity by accumulating high quantities of ions in vacuoles of shoot cells in order to create a gradient of water potential along the axis of the plant [9]. These data indicate the presence of an efficient mechanism of Na + loading into the xylem in the halophyte.…”
Section: Resultsmentioning
confidence: 84%
“…However, they do not explain the diversity of reactions in whole organisms from different ecological groups. Studies on the physiological functions in the whole plant conducted previously [9,10], as well as data presented in this work on the accumulation and distribution of Na …”
Section: Resultsmentioning
confidence: 93%
“…Plants were grown with solution culture, as described in [9,16], with the use of Robinson and Dounton mineral solution [17] On the forth week the sodium chloride was added to the growth medium every 2 -3 days so that NaCl concentration in a pot increased by no more than 50 mM. Finish sodium chloride concentration in the solution was 0.5, 150, 250 mM for spinach and 0.5, 250, 750 mM for seablite.…”
Section: Methodsmentioning
confidence: 99%
“…High salt tolerance in dicotyledonous halophytes, for example, from the Chenopodiaceae family, is due to their ability to accumulate up to 1 -1.5 M of sodium ions in shoot vacuoles in high salinity conditions, as well as their ability to use Na + to maintain turgor and act instead of K + [9,10]. In high salinity conditions, the halophytes show increase in growth rate, caused by the effect of sodium on cell extension growth and plant water balance.…”
We have done a comparative study of ion status, growth and biochemical parameters in shoots and roots of seablite (Suaeda altissima (L.) Pall.) and spinach (Spinacia oleracea L.) grown with different salinity levels in the medium (0.5 -750 mМ). A distinctive feature of the halophyte was a high Na + content in tissues at its low concentration in the medium (0.5 mM). In these conditions, Na + accumulation in seablite roots was four-fold higher than in spinach roots, and Na + content in seablite leaves was almost 20-fold higher than in spinach. Together with an increase in sodium concentration in the medium, K + content decreased six-fold in seablite leaves, while in spinach it did not decrease so drastically. We can suppose that in the halophyte, some processes occur only in the presence of sodium, and these functions of sodium cannot be fully fulfilled by potassium. Analysis of protein and total nitrogen content in tissues shows that at high salinity, the ability to synthesize non-protein nitrogen-containing compounds increases in the halophyte and decreases in the glycophyte. Data on proline content dynamics show that its increase in tissues of spinach (salinity levels 150 and 250 mМ) and seablite (salinity levels 0.5 and 750 mМ) is an indicator of plant injury. In seablite and spinach, proline is not a major osmoregulator. Its concentration both in roots and leaves was no more than 2.5 µmol/g fresh weight. The data presented in this work concern the accumulation and distribution of Na + , Cl − , K + and 3 NO ions, as well as growth and biochemical parameters. Our data show that the development of adaptation reactions in the whole plants in the conditions of high salinity is determined by morphofunctional systems and their interaction.
“…When the salt concentration in the medium is further increased to 750 mM, organ mass decreases 4 -5-fold (Figures 1(a) and (c)). These results support the known data that NaCl concentration of 250 mM in the medium is optimal for seablite growth and development [9]. In the glycophyte, an increase in NaCl concentration in the medium up to 250 mM leads to a slight decrease in fresh biomass (Figure 1(b)), while dry mass does not change significantly (Figure 1(d)).…”
Section: Resultssupporting
confidence: 90%
“…Seablite is a salt-accumulating halophyte. It adapts to high salinity by accumulating high quantities of ions in vacuoles of shoot cells in order to create a gradient of water potential along the axis of the plant [9]. These data indicate the presence of an efficient mechanism of Na + loading into the xylem in the halophyte.…”
Section: Resultsmentioning
confidence: 84%
“…However, they do not explain the diversity of reactions in whole organisms from different ecological groups. Studies on the physiological functions in the whole plant conducted previously [9,10], as well as data presented in this work on the accumulation and distribution of Na …”
Section: Resultsmentioning
confidence: 93%
“…Plants were grown with solution culture, as described in [9,16], with the use of Robinson and Dounton mineral solution [17] On the forth week the sodium chloride was added to the growth medium every 2 -3 days so that NaCl concentration in a pot increased by no more than 50 mM. Finish sodium chloride concentration in the solution was 0.5, 150, 250 mM for spinach and 0.5, 250, 750 mM for seablite.…”
Section: Methodsmentioning
confidence: 99%
“…High salt tolerance in dicotyledonous halophytes, for example, from the Chenopodiaceae family, is due to their ability to accumulate up to 1 -1.5 M of sodium ions in shoot vacuoles in high salinity conditions, as well as their ability to use Na + to maintain turgor and act instead of K + [9,10]. In high salinity conditions, the halophytes show increase in growth rate, caused by the effect of sodium on cell extension growth and plant water balance.…”
We have done a comparative study of ion status, growth and biochemical parameters in shoots and roots of seablite (Suaeda altissima (L.) Pall.) and spinach (Spinacia oleracea L.) grown with different salinity levels in the medium (0.5 -750 mМ). A distinctive feature of the halophyte was a high Na + content in tissues at its low concentration in the medium (0.5 mM). In these conditions, Na + accumulation in seablite roots was four-fold higher than in spinach roots, and Na + content in seablite leaves was almost 20-fold higher than in spinach. Together with an increase in sodium concentration in the medium, K + content decreased six-fold in seablite leaves, while in spinach it did not decrease so drastically. We can suppose that in the halophyte, some processes occur only in the presence of sodium, and these functions of sodium cannot be fully fulfilled by potassium. Analysis of protein and total nitrogen content in tissues shows that at high salinity, the ability to synthesize non-protein nitrogen-containing compounds increases in the halophyte and decreases in the glycophyte. Data on proline content dynamics show that its increase in tissues of spinach (salinity levels 150 and 250 mМ) and seablite (salinity levels 0.5 and 750 mМ) is an indicator of plant injury. In seablite and spinach, proline is not a major osmoregulator. Its concentration both in roots and leaves was no more than 2.5 µmol/g fresh weight. The data presented in this work concern the accumulation and distribution of Na + , Cl − , K + and 3 NO ions, as well as growth and biochemical parameters. Our data show that the development of adaptation reactions in the whole plants in the conditions of high salinity is determined by morphofunctional systems and their interaction.
Abiotic stresses affect adversely the growth and productivity of crops. Among abiotic stresses, salinity is one of the major factors leading to crop losses. According to the UN Food and Agriculture Organization, more than 800 Mha of land is salt-affected worldwide. The problem of soil salinization is becoming more serious due to scanty rainfall, repetitive sea water invasion, heavy utilization of ground water for agricultural and industrial purposes, and degradation of saline parent rock. The area under cultivation is fast getting depleted and becoming unsuitable for agricultural crops. Soil salinity adversely affects plant growth and development, and disturbs intracellular ion homeostasis, resulting in cellular toxicity. Plant adaptation to salinity stress involves a plethora of genes involved in ion transport and compartmentalization (ion homeostasis), compatible solutes/osmolytes, reactive oxygen species, and antioxidant defense mechanism. Transporters are an important group of genes that play a pivotal role in ion homeostasis in plants (Na þ /H þ antiporters like SOS1 and NHX1, and proton pump HKT1). Over the last two decades the major studies on the molecular mechanisms of salt tolerance have concentrated on glycophytes; however, only limited studies have been performed on halophytes. Halophytes have a unique genetic makeup that provides an advantage for the study of salt-tolerance mechanisms. Halophytes maintain a low salt concentration inside the cytosol by sequestration in vacuoles or extrusion of Na þ outside the plasma membrane or secretion of salt outside the plant (bladders, salt glands). Since halophytes are very important for the study of salt-tolerance mechanisms, this chapter is focused on the work carried out on transporter genes from halophytes present at the plasma membrane and tonoplast controlling Na þ homeostasis under salinity.
IntroductionPlants face different major abiotic stresses such as high salinity, drought, and temperature extremes on a day-to-day basis. These abiotic stresses cause adverse 685
The above image represents a depiction of activation of different signaling pathways by diverse stimuli that converge to activate intricate signaling and interaction networks to counter stress (top panel). Since environmental stresses infl uence most signifi cantly to the reduction in potential crop yield, progress is now largely anticipated through functional genomics studies in plants through the use of techniques such as large-scale analysis of gene expression pattern in response to stress and construction, analysis and use of plant protein interactome networks maps for effective engineering strategies to generate stress tolerant crops (top panel). The molecular aspects of these signaling pathways are extensively studied in model plant Arabidopsis thaliana and crop plant rice ( Oryza sativa ) (below).
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