Silicon and Salinity: Crosstalk in Crop-Mediated Stress Tolerance Mechanisms

Salinity stress hinders the growth potential and productivity of crop plants by influencing photosynthesis, disturbing the osmotic and ionic concentrations, producing excessive oxidants and radicals, regulating endogenous phytohormonal functions, counteracting essential metabolic pathways, and manipulating the patterns of gene expression. In response, plants adopt counter mechanistic cascades of physio-biochemical and molecular signaling to overcome salinity stress; however, continued exposure can overwhelm the defense system, resulting in cell death and the collapse of essential apparatuses. Improving plant vigor and defense responses can thus increase plant stress tolerance and productivity. Alternatively, the quasi-essential element silicon (Si)—the second-most abundant element in the Earth’s crust—is utilized by plants and applied exogenously to combat salinity stress and improve plant growth by enhancing physiological, metabolomic, and molecular responses. In the present review, we elucidate the potential role of Si in ameliorating salinity stress in crops and the possible mechanisms underlying Si-associated stress tolerance in plants. This review also underlines the need for future research to evaluate the role of Si in salinity stress in plants and the identification of gaps in the understanding of this process as a whole at a broader field level.

Introduction

Soil salinity is one of the major abiotic stress that hinders crop growth and productivity worldwide (Ahmad et al., 2019b). It has been reported that approximately 20% of irrigated land is salt-affected, which represents one-third of food-producing land (Shrivastava and Kumar, 2015; Gregory et al., 2018). Further to this, half of all the fertile land will be affected by salinity by the middle of the 21^st century (Shahid et al., 2018). The salt-affected areas are increasing at a rate of 10% annually for various reasons, including low precipitation, the weathering of native rocks, high surface evaporation, poor cultural practices, and irrigation using saline water (Shrivastava and Kumar, 2015). This issue has been further aggravated by the continued trends in global warming and climatic changes. Thus, enhancing crop plant tolerance to abiotic stresses is an important challenge to overcome deteriorating food production system and to meet the demand of food supply for ever-increasing world population (Shah and Wu, 2019). To ensure sustainable food supply, a considerable 50% increase in the grain yields of major crop plants such as wheat, rice, and maize (Godfray et al., 2010; Shrivastava and Kumar, 2015) is required. However, soil, which represents a major ecosystem that often operates at a subsistence level in the growth of crops, is often compromised by salinity.

Salinity stress affects the morphological, physiological, and biochemical processes of plants (Singh and Chatrath, 2001; Ashraf, 2004). High salinity not only decreases plant growth, biomass, yield, photosynthesis, and water use efficiency, but also leads to physiological drought and ion toxicity in plants, thus reducing agricultural productivity and yields (Shahid et al., 2018). Salinity stress also causes ionic imbalances, the osmotic effect, water use insufficiency, and nutrient (e.g. N, Ca, K, P, Fe, and Zn) deficiency, which ultimately leads to oxidative stress in plants (Rehman et al., 2019). Reactive oxygen species (ROS) are produced in plant cells under normal physiological conditions, either in a radical or non-radical form (Winterbourn, 2019). However, excessive ROS production leads to oxidative damage to the proteins, lipids, nucleic acids, and plasma membrane of the cell. During normal cellular metabolism, the plant produces several antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), glutathione peroxidase (GPX), glutathione reductase (GR), and ascorbate peroxidase (APX) for the detoxification of ROS. In addition to high ROS production, salinity stress significantly reduces the uptake of phosphorus (P) and potassium (K), while increasing the uptake of toxic elements such as sodium (Na⁺) and chlorine (Cl^-), which have negative effects on plant growth and productivity. High concentrations of Na⁺ create osmotic stress, which consequently leads to cell death (Munns, 2002; Ahanger et al., 2017). Photosynthesis machinery is also affected by salinity stress, mainly due to the reduction in the leaf area, stomatal conductance, and chlorophyll levels, and to a lesser extent by the decrease in photosystem II efficiency (Netondo et al., 2004). Any mechanisms that maintain optimal K⁺/Na⁺ ratios, nutrient concentrations, and ROS production in plants are thus likely to provide effective resistance against salinity stress (Assaha et al., 2017).

Various mitigation and adaptation approaches have been used to overcome these negative impacts of high soil salinity (Wang et al., 2019). The use of different approaches to alleviate the negative effects of salinity is likely to ensure the sustainable production of food, but salinity stress management is very challenging due to its multigenic and quantitative nature (Ahmad and Rasool, 2014). Strategies have been reported for the amelioration of the negative effects of salinity on plants, such as developing salt-tolerant crops, transgenic varieties, plant growth-promoting bacteria, endophytes, the leaching of salt from the root zone, and micro-jet irrigation to optimize the use of water (Chanchal Malhotra et al., 2016; Ibrahim et al., 2016). However, very little knowledge still exist about the mineral status and dynamics of plants and their salinity tolerance (Manchanda and Garg, 2008).

The exogenous application of silicon (Si) has been a recent eco-friendly approach to enhance the salinity stress response in plants (Almeida et al., 2017). Silicon is the second-most abundant element on Earth, making up 27.7% of the Earth’s crust, second only to oxygen. It occurs naturally in the form of complex silicate minerals, either in crystalline, amorphous, or poorly crystalline phases (Sommer et al., 2006; Frew et al., 2018). Most soils contain an Si concentration ranging from 14 to 20 mg Si/L (Montpetit et al., 2012; Vivancos et al., 2015). Silicon is available in the form of silicic acid (Si(OH)₄) in soil solutions in a concentration range of 0.1–0.6 mM (Luyckx et al., 2017). Plant roots absorb Si in the form of monosilicic acid via aquaporin-type channels (NOD26-like intrinsic proteins, NIPs; Deshmukh et al., 2013). However, the translocation and movement of Si is a very slow process, thus amendment with exogenous soluble Si is needed in order to ameliorate stress conditions and improve the yields of crops. In the early 1900s, Si was recognized as one of the 15 most important elements needed for plant life (Debona et al., 2017). All plants grown in soil contain a certain level of Si in their tissues, as reported for more than 44 angiosperm clades that represent over 100 orders or families (Debona et al., 2017). Many terrestrial plants accumulate a noticeable concentration of Si (Etesami and Jeong, 2018) while, in most dicots, less than 0.1% Si is found based on dry weight. A large number of grass species have the capacity to accumulate up to 10% of Si (Vivancos et al., 2015), with rice the most effective Si accumulator (Kaur and Greger, 2019). Si is coming to the fore as a true “Cinderella” element (Artyszak, 2018), gaining interest among scientists from across the world because of its effective role in plant physiology, nutrition, and defense response. The valuable role of exogenous Si on plant growth and yield has been well-documented in the literature, but its true potential lies in the amelioration of abiotic and biotic stresses (Rodrigues and Datnoff, 2015; Khan et al., 2018; Wu et al., 2019).

The available literature has clearly described the role of Si in combating abiotic and biotic stresses in plants; however, it has still not been listed as an essential element for plants because no clear evidence has been presented, unlike other essential elements. Numerous studies have reported that Si increases plant resistance against biotic and biotic stresses (Epstein, 1999; Ma and Takahashi, 2002; Ma and Yamaji, 2006), such as salt and drought (Zhu and Gong, 2014; Rizwan et al., 2015), extreme temperature stress (Ma, 2004), nutrient deficiency (Marafon and Endres, 2013), aluminum toxicity (Galvez and Clark, 1991; Shen et al., 2014; Pontigo et al., 2015; Pontigo et al., 2017), disease resistance (Van Bockhaven et al., 2012; Marafon and Endres, 2013), and resistance to damage by wild rabbits (Cotterill et al., 2007). It also contributes to plant growth in different ways by enhancing multiple adaptive responses, such as antioxidant activity, mineral uptake, organic acid anion and phenolic compound exudation, the photosynthesis rate, the accumulation of compatible solutes, water status, and hormonal regulation (Barcelo et al., 1993; Cocker et al., 1998; Kidd et al., 2001; Al-Aghabary et al., 2005; Shahnaz et al., 2011; Shen et al., 2014; Sivanesan and Jeong, 2014; Kim et al., 2016; Kim et al., 2017; Tripathi et al., 2017; Ahanger et al., 2018; Ahmad et al., 2019a) and significantly reducing the adverse effects of salinity on chlorophyll levels and plant biomass (Seal et al., 2018). Despite this, most of these findings are scattered and need to come up with a comprehensive image of progress made on this topic. There have been some recent review articles published on Si, such as those by Etesami and Jeong (2018) and Malhotra and Kapoor (2019), but they do not address the crosstalk of physio-molecular functions in response to salinity stress. In this review, we focus on studies that have investigated plant metabolism and physiology under salinity stress and have elucidated the complex mechanisms and interactions involving Si in the amelioration of the detrimental effect of salinity on crops.

Plant Physiology Under Salinity Stress

High salinity can increase the uptake of Na⁺ and Cl^- from the soil, consequently suppressing the transport of other essential nutrients such as N, P, K, and Ca (Shrivastava and Kumar, 2015; Safdar et al., 2019). The resulting ionic and secondary stresses, such as nutritional imbalances, disturb the overall osmotic balance, resulting in physiological drought, i.e. the prevention of water uptake (Riaz et al., 2019). In the case of halophytic plants that are resistant to sodium toxicity, osmotic stress is a possible reason for the inhibition of their growth. Photosynthesis is also affected by salinity because of the reduction in chlorophyll content, stomatal conductance, and leaf area. Photosystem II is also primarily affected by salinity (Najar et al., 2019). Salinity affects reproductive development by inhibiting microsporogenesis, elongating stamen filaments, accelerating programmed cell death, and promoting the senescence of fertilized embryos and ovule abortion (Suo et al., 2017). Under saline conditions, the absorption of atmospheric carbon dioxide is reduced, leading to greater stomatal closure and the lower utilization of NADPH via the Calvin cycle (Suo et al., 2017). These conditions favor the electron acceptor behavior of molecular oxygen, leading to the accumulation of ROS. High ROS levels can damage essential macromolecules necessary for the normal growth of plants by altering their metabolism via oxidative lipids, nucleic acids, and protein damage (Figure 1). ROS are produced continuously during normal metabolic events in peroxisomes, mitochondria, and the cytoplasm (Saini et al., 2018). Other processes that are affected by salt stress include stem and root growth, ion transport, plant morphology, the enzymatic activity of solutes, cell structure maturation, and nutrient uptake. A significant reduction in stem height and root length has also been observed for cases of high osmotic stress (Shrivastava and Kumar, 2015). In response to higher concentrations of NaCl in the soil, sodium uptake by the roots is enhanced while phosphorus, nitrogen, magnesium, and potassium uptake is lowered significantly, leading to the disruption of the intracellular ionic balance (Jayakannan et al., 2013). Under these circumstances, plant roots cannot absorb enough water and significant energy is required to adjust the osmotic balance via compatible solute accumulation (Acosta-Motos et al., 2017).

FIGURE 1

Figure 1 Higher ROS levels in plants under salinity stress conditions. Toxic levels of ROS stunt plant growth by inhibiting the electron transport chain, and photosynthesis in plastids, and by causing mutations in DNA and damaging mitochondria.

Plant Cellular Mechanisms That Improve Tolerance to Salinity Stress

The salt tolerance level varies from species to species and even different cultivars, whereas the individual plants of the same cultivar would show a variation. Some species such as redbay, Anemopsis californica, and Quercus geminate are more resistant to high levels of salt (Roy et al., 2014), while others, such as Schoenus spp., Polypogon viridis, and Juncus spp. are sensitive or even hypersensitive to low salinity levels (Gibson et al., 1984). The biochemical and physiological mechanisms underlying plant salinity tolerance can be divided into those that minimize osmotic stress and ion imbalances and those that act on secondary effects caused by this stress, such as imbalances in plant nutrition and oxidative stress. The principle mechanisms are ion homeostasis, ion uptake and transport, the biosynthesis of compatible solutes and osmo-protectants, antioxidant enzyme activation, antioxidant and polyamine synthesis, nitric oxide (NO) generation, and hormonal alterations. Past research that has elucidated these mechanisms is briefly summarized below.

Significance of Ion Homeostasis in Plant Tolerance to Salinity

Under salinity stress, plants accumulate high levels of Na⁺ and Cl^- compared to other cations like K⁺ and Ca²⁺ (Tavakkoli et al., 2010), creating physiological problems and ion imbalances (James et al., 2011; Hasegawa, 2013; Ahmad et al., 2018). Neither halophytes nor glycophytes can tolerate high salt concentrations in the cytoplasm. H⁺ pumps (Na⁺/H⁺ antiporters) are responsible for the transport of Na⁺ ions from the cytoplasm to the vacuoles. The vacuolar membrane has two types of H⁺ pump, i.e. vacuolar-type H⁺-ATPase (V-ATPase) and vacuolar pyrophosphatase (V-PPase; Graus et al., 2018). V-ATPase pumps occur in high numbers in plant cells. H⁺ pumps are responsible not only for maintaining solute homeostasis under normal conditions but also for facilitating secondary transport and vesicle fusion. However, during stress, the survival of plants is determined by the action of V-ATPase pumps (Bozza et al., 2019). Otoch et al. (2001) reported that V-ATPase pump activity increased in Vigna unguiculata seedlings (a hypocotyl) when exposed to salinity, while V-PPase pump activity was inhibited under similar conditions. In Suaeda salsa (a halophyte), the activity of V-ATPase pumps was upregulated while that of V-PPase pumps were downregulated (Wang et al., 2001a). Hence, both H⁺ pumps are responsible for maintaining solute homeostasis at the cellular level (Graus et al., 2018).

Several studies have reported that salt plays a role in the Salt Overly Sensitive (SOS) pathway, which consists of the three proteins SOS1, SOS2, and SOS3. The cytoplasmic membrane Na⁺/H⁺ antiporter encodes SOS1, which plays an important role in the regulation of Na⁺ efflux at the cellular level (Numan et al., 2018). However, SOS1 is also essential for the regulation of the long-distance diffusion of Na⁺ between the roots and shoots (Abbas et al., 2017). In saline conditions, the overexpression of SOS1 increase salt tolerance levels (Fan et al., 2019). The salinity stress activates the Ca²⁺ signaling pathway, which consequently stimulates the production of threonine/serine kinase encoded by the SOS2 gene, which consists of a regulatory domain on the C-terminal and a catalytic domain on the N-terminal (Zhu, 2016). The third gene SOS3 encodes a myristoylated Ca²⁺ binding protein that contains a myristoylation site on the N-terminus. This site is very important for the conferral of salinity resistance on plants (Ishitani et al., 2000). The SOS2 protein consists of a FISL motif on the C-terminal, composed of 21 amino acids, and provides an interaction site for the binding of Ca²⁺ to the SOS3 protein (Köster et al., 2019). The interaction between the SOS2 and SOS3 proteins triggers protein kinase activation. This activated protein kinase is responsible for the phosphorylation of SOS1 protein and eventually leads to an increase in the efflux of Na⁺ and a decrease in Na⁺ ion toxicity (Figure 2).

FIGURE 2

Figure 2 SOS pathway under salinity stress. The transport of ions across the membrane is conducted by various carrier proteins, e.g. channel proteins, antiporters, and symporters. The ion hemostasis (Na⁺, K⁺, and Ca²⁺) in the cell is crucial for its survival under salt-stress conditions.

The role of SOS1 in controlling ion homeostasis has been demonstrated through a combination of biochemical, genetic, and physiological analyses. Using yeast mutant strains and isolated plasma-membrane vesicles, SOS1 was first shown to be able to specifically transport Na⁺ out of cells under salt stress (Qiu et al., 2002; Shi et al., 2002). These proteins not only regulate ion hemostasis but are also essential for the regulation of pH homeostasis, vacuole functions, and membrane vesicle trafficking (Oh et al., 2010). In addition to the SOS stress signaling pathway, another method of developing resistance to salinity stress has been reported for many plants that maintain a minimum ion concentration in the cytosol. During stress conditions, membranes and their linked components maintain the ion concentration in the cytoplasm by regulating ion transport across the membrane (Sairam and Tyagi, 2004).

Role of Antioxidants Under Salinity Stress

Plant salt stress can negatively affect the electron transport chain (ETC) in mitochondria and chloroplasts by unbalancing or completely distorting the regulation process (Numan et al., 2018). Molecular oxygen acts as an electron acceptor, which can lead to the overproduction of ROS, including hydroxyl radicals, singlet oxygen, superoxide radicals, and H₂O₂. ROS are powerful oxidizing compounds that can damage the plasma membrane and endomembrane systems (Ahanger and Agarwal, 2017; Foyer, 2018). However, they also act as signals of stress, thus activating the antioxidant enzymes SOD, GPX, APX, CAT, and GR and non-enzymatic compounds (e.g. glutathione, non-protein amino acids, ascorbic acid, and phenolic compounds) to sustain a balanced level of ROS in cells under both normal and stress conditions (Caverzan et al., 2016; Ahanger et al., 2018). These enzymes are responsible for removing ROS that have accumulated in plants due to salinity stress. Tuteja et al. (2013) reported that the proteins DESD-box helicase and OsSUV3 dual helicase increase the tolerance to salinity by maintaining or improving photosynthesis and antioxidant enzyme machinery. Thus, understanding the mechanisms that regulate ROS signaling at the cellular level during stress can provide a more powerful approach for developing resistance to high salt levels.

Role of Nitric Oxide (NO) in Salt Tolerance in Plants

Nitric oxide (NO) is small volatile gaseous molecule that is essential for the maintenance of various physiological and biochemical mechanisms at the cellular level in plants, e.g. root growth, stomata closure, respiration, stress signaling, flowering, cell death, seed germination, and stress responses (Besson-Bard et al., 2008; Zhao et al., 2009). Under stress conditions, NO either directly or indirectly regulates many genes involved in developing tolerance to salinity stress, including various redox-related and antioxidant enzyme genes (e.g. GPX, GR, SOD, CAT, and APX), and suppresses lipid peroxidation or malondialdehyde (MDA), consequently restoring normal plant growth (Bajguz, 2014). NO increases plasma membrane expression and/or tonoplast H⁺-ATPase and H⁺-PPase to maintain a high K⁺/Na⁺ ratio in the cytoplasm in response to salinity (Sung and Hong, 2010; Zhang et al., 2017). NO also assists the cell in accumulating various compatible solutes, such as proline, organic osmolytes, and soluble sugars, to facilitate cell turgor and balanced water acquisition (Guo et al., 2005).

Improved Salinity Tolerance via the Accumulation of Compatible Solutes

Salinity stress promotes the accumulation of compatible solutes or osmolytes, a set of chemically altered organic compounds that are polar or uncharged in nature that do not affect the biochemical processes of the cell at high concentrations (Ashraf et al., 2011; Vyrides and Stuckey, 2017). They generally include mannitol, proline (Hoque et al., 2007; Nounjan et al., 2012; Tahir et al., 2012), glycine betaine (Khan et al., 2000), sugar (Ford, 1984; Wang and Nii, 2000), raffinose oligosaccharides, and N-containing compounds such as amino acids, polyamines, and polyols (Saxena et al., 2013). Organic osmolytes are produced in variable amounts between different plant species. For example, the quaternary ammonium compound beta-alanine is found only in a few species belonging to the Plumbaginaceae family (Hanson et al., 1994), whereas proline accumulation occurs in a diverse range of plants (Saxena et al., 2013). The concentration of compatible solutes is regulated either by irrevocable synthesis or by a process of degradation and synthesis. The rate at which compatible solutes accumulate in the cell is determined by the external osmolarity, and the current understanding of the mode of action of these solutes includes providing osmotic adjustment via continuous water influx, stabilizing proteins and the cell structure, and scavenging ROS when under salt stress (Turkan, 2011).

Of the nitrogen-containing compounds, some amino acids accumulate to higher levels under salt stress. The concentration of arginine, cysteine, and methionine decrease under salt stress, whilst that of proline increases (El-Shintinawy and El-Shourbagy, 2001). These amino acids play a vital role in the salt stress response by instigating K⁺ homeostasis, leading to a plant’s adaptation to salinity by reducing NaCl-induced K⁺ efflux (Cuin and Shabala, 2007). Of these, proline has a substantial role, and its concentration rises significantly in many plants. Additionally, glycine betaine is another primary osmoprotectant, synthesized in response to salinity stress by many plants. It maintains the osmotic cell status to improve the response to abiotic stress (Kumar et al., 2018). For example, Rahman et al. (2002) reported the positive effect of glycine betaine on the ultrastructure of Oryza sativa seedlings when exposed to salt stress.

Phytohormone Regulation Under Salinity Stress

Phytohormones play an important role in plant growth and development under both normal and stressful conditions. In the literature, they are often regarded as plant growth regulators (compounds that derive from plant biosynthetic pathways; Peleg and Blumwald, 2011). Several hormones such as abscisic acid (ABA), indole acetic acid (IAA), salicylic acid (SA), brassinosteroids (BR), cytokinins (CKs), ethylene (ETHY), gibberellic acid (GA), and jasmonic acid (JA; Iqbal et al., 2014) have been reported to regulate plant growth and development in a coordinated fashion by either acting locally or being transported to another site within the plant (Fahad et al., 2015). Harsh conditions disrupt the production and distribution of hormones that may promote specific protective mechanisms in plants (Eyidogan et al., 2012; Fahad et al., 2015). Thus, plant stress-related hormones have an important role in mediating plant responses to abiotic stress, by which plants attempt to avoid or survive stressful conditions and in doing so exhibit reduced growth so that the plant can focus its resources on withstanding the stress.

ABA acts as a cellular signaling or stress hormone, and exogenous application has been suggested for increasing salt tolerance (Sah et al., 2016). Endogenous ABA accumulates in various plants, especially in osmotic and salt stress conditions (Sah et al., 2016). ABA improves tolerance, partly due to the accumulation of ions and compatible solutes (such as proline and sugar) in the vacuoles of the root, neutralizing the uptake of Na⁺ and Cl^- (Chen et al., 2001; Gurmani et al., 2011; Cho et al., 2018). Similarly, the increased production of ABA can ameliorate the negative effect of stress on photosynthesis. Fricke et al. (2004) reported that the increase in the ability of xylem to uptake water under saline conditions is hindered by ABA homeostasis. However, the role of ABA in the regulation of important cellular signals has been clearly demonstrated, controlling the expression of many important water and salt deficit responsive genes such as cinnamyl alcohol dehydrogenase, 9-cisepoxycarotenoid dioxygenase, zeaxanthin oxidase, molybdenum cofactor sulfurase, and ABA-aldehyde oxidase through a calcium-dependent phosphorylation pathway (Dubos and Plomion, 2003; Ryu and Cho, 2015).

Another important hormone is GA; GA₃ regulates ion uptake and the homeostasis of hormones under saline conditions in Lycopersicon esculentum and T. aestivum (Maggio et al., 2010). Similarly, Maggio et al. (2010) reported that GA₃ applied to tomato plants reduced stomatal resistance and enhanced the water status. Iqbal and Ashraf (2013) reported that GA₃ treatment under saline conditions modulated ion uptake and partitioning and hormone homeostasis in wheat. It has also been reported that plant phytohormones such as indole IAA respond to salinity stress in crop plants (Fahad et al., 2015). Additionally, IAA levels in the root system fall significantly after NaCl treatment in Triticum aestivum (Sakhabutdinova et al., 2003), Oryzasativa (Dunlap and Binzel, 1996), and Esculentum L. (Smirnoff, 1997). It has been observed that the activity of JA increased under salinity stress (Farhangi-Abriz and Ghassemi-Golezani, 2018). For example, JA treatment recovered the negative effect of salt on seedling development and photosynthetic activity in several cultivar crops (Yoon et al., 2009; Javid et al., 2011). These results are strongly indicative of the positive role of JA in salt stress responses in plants.

Other phytohormones, such as BR and SA, also play an important role in plant abiotic stress responses (Wani et al., 2016). SA controls different features of plant responses to stress via widespread signaling with other growth hormones (Horváth et al., 2007; Jayakannan et al., 2013). Undesirable salinity effects may be alleviated by BR (Ashraf et al., 2010b; El-Mashad and Mohamed, 2012). The application of BR enhances the antioxidant activity of SOD, POX, APX, and GPX and the accumulation of non-enzymatic antioxidant compounds (tocopherol, ascorbate, and reduced glutathione; El-Mashad and Mohamed, 2012; Iqbal et al., 2014; Simura et al., 2018) (El-Mashad and Mohamed, 2012). Indeed, a stress signal triggers signal transduction cascades in plants, with phytohormones acting as baseline transducers (Fahad et al., 2015).

Silicon Uptake, Transport, and Assimilation in Plants

The concentration of Si in soil is similar to that of macronutrients assimilated by plants (Sommer et al., 2006), but it cannot be directly absorbed (Mitani et al., 2005). Furthermore, Si absorption, accumulation, and transport capacity differ significantly between species (Ma and Takahashi, 2002). Generally, the concentration of monosilicic acid ranges from 0.1 to 0.6 mM in soil solutions in which Si is present as an uncharged monomeric molecule at pH 9. Many factors, such as temperature, pH, the presence of cations, water conditions, and the organic compounds present in solution directly influence solvable silicic acid formation in the soil and indirectly affect the accumulation rate in plants (Liu et al., 2003). The lower availability of Si in the soil was reported to be the probable reason for decreasing rice yields (Meena et al., 2014). Tropical and subtropical soils have low Si levels due to de-silication caused by weathering and leaching processes (Epstein, 1999), while an estimated 210–224 million tons of Si are taken out annually from the world’s arable soils (Meena et al., 2014).

All plants contain Si in considerable amounts in all parts such as the roots, shoots, and leaves but various levels are found in different species (Takahashi et al., 1990). The roots take up Si in silicic acid form and it is transported to the rest of the plant using active, passive, and rejective transport. Based on the take-up capacity of Si, plants are categorized as high, intermediate, or non-Si accumulators (Marafon and Endres, 2013; Table 1). Previously, the active uptake of Si has been demonstrated in different plants such as rice (Klotzbucher et al., 2018), wheat (Rains et al., 2006), maize (Mitani et al., 2009), and barley (Chiba et al., 2009), while tomato limits the transport of Si from the roots to shoots (Wang et al., 2015a). Liang et al. (2005a) and Mitani and Ma (2005) reported different results for cucumber plants. Liang et al. (2006) also reported both active and passive transport in rice, maize, sunflower, and wax gourd. These findings suggest that both the passive diffusion of silicic acid and transporter-mediated uptake are involved in the radial root transport of Si, with transporter-mediated Si uptake an energy-dependent process because metabolic inhibitors and low temperatures inhibit Si transport (Liang et al., 2006; Feng et al., 2011). Furthermore, these results suggest that the occurrence of both types of transporters is somehow dependent on the species and concentration of Si in the soil. Hence, the differences in Si uptake reported for cucumber plants might be due to the coexistence of both active and passive uptake in various cultivars or due to the concentration of Si in the soil.

TABLE 1

Table 1 Plant categories based on Si uptake capacity (Bakhat et al., 2018).

After absorption by the roots, Si is transported to other parts of the plant via the xylem of the roots (Ma and Yamaji, 2008). With the loss of water from a plant, inorganic amorphous oxides of silicic acid crystalize and precipitate, forming solid silica bodies called opal phytoliths that accumulate in the extracellular or intracellular spaces of plants, e.g. in the cell wall and trichomes (Ma et al., 2006; Cooke and Leishman, 2011). However, the mechanisms that prevent silicic acid polymerizing in the cell wall are not clear. Recently, it has been reported that the low silicon (Lsi1, Lsi2, and Lsi6) genes are responsible for Si uptake in the roots and its distribution to other organs in barley, rice, cucumber, and maize (Wang et al., 2015b). The Lsi2 gene is expressed in the root endodermis and is considered a putative anion transporter (Ma et al., 2007; Mitani et al., 2011). On the other hand, the Lsi1 and Lsi6 transporters belong to the aquaporin family and have a major role in Si distribution in shoot and root tissue (Mitani et al., 2011). Furthermore, proton-driven transport activity has been reported in the Lsi2 transporter (Ma et al., 2007), and it works as an Si/H⁺ antiport. The leaf epidermis and cell walls accumulate 90% of the total absorbed Si, which accounts for 10% of the dry weight of grass shoots (Yoshida, 1965; Ma and Takahashi, 2002; Raven, 2003). Silica that has accumulated intracellularly in the cytoplasm and vacuoles is stable even after plant decomposition and is abundant in soils (Lins et al., 2002). A schematic model of the Si transport system in rice is presented in Figure 3.

FIGURE 3

Figure 3 A schematic representation of Si uptake, transport, and accumulation in rice. Silicic acid from the soil solution is absorbed by the roots and transported to the root exodermis by the influx transporter (Lsi1) and subsequently released to the apoplast by the efflux transporter (Lsi2). Subsequently, it enters the root endodermis via Lsi1 and is released to the stele portion of the root via Lsi2. Finally, silicic acid is translocated by an unknown transporter into the xylem and transported to the shoots via the transpiration stream. In the leaves, silicic acid is unloaded by another influx transporter (Lsi6) and localized in the xylem parenchyma cells of leaf sheaths and leaf blades. In the shoots and leaves, Si is transformed from an aqueous form (silicic acid) to solid amorphous silica (SiO2–nH2O) and primarily deposited in the cell walls of different tissues, such as leaf epidermal cells. Modified from Yan et al. (2018).

Silicon-Mediated Mechanisms Involved in Increasing Salinity Tolerance in Crops

Previous studies have reported the significant regulatory role of Si in numerous plant physiological processes under salinity stress (Rios et al., 2017). In fact, the many different complex biological functions reported by different studies suggests that the mechanisms by which Si improves the salt tolerance of plants have not been well studied. However, an improvement in the salt tolerance of different plant species following the exogenous application of Si has been reported, including in wheat (T. riaestivum L.; Tuna et al., 2008), barley (Hordeum vulgare L.; Liang et al., 2005a), maize (Zea mays L.), rice (Oryza sativa L.; Yeo et al., 1999), soybean (Glycine max; Lee et al., 2010), canola (Brassica napus L.; Haddad et al., 2018), spinach (Spinacia oleracea L.), cucumber (Cucumis sativus L.; Khoshgoftarmanesh et al., 2014), and tomato (Lycopersicon esculentum L.; Romero-Aranda et al., 2006), as summarized in Table 2. The exogenous application of Si improves plant growth either directly, i.e. by blocking the transport of Na⁺ ions into the plant, or indirectly, i.e. by activating different physiological processes to ameliorate the effect of salinity stress. The current understanding of the mechanisms underlying the Si-based mitigation of salinity-induced stress and its interaction with crops is shown in Figure 4.

TABLE 2

Table 2 Effect of exogenous Si on plant stress tolerance mechanisms in various plant species under salinity stress.

FIGURE 4

Figure 4 Schematic representation of silicon crosstalk with plants tolerance mechanisms during salinity stress.

Exogenous Si Regulation of the Antioxidant Machinery to Increase Salinity Stress Tolerance in Crops

The overproduction of ROS under salinity stress poses a threat to cells due to lipid peroxidation, protein oxidation, nucleic acid damage, enzyme inhibition, and the activation of programmed cell death pathways (Gill and Tuteja, 2010; Liang et al., 2018). To scavenge ROS, antioxidant enzymes such as CAT, SOD, and GPX, enzymes in ascorbate glutathione (AsA-GSH) cycles such as GR, MDHAR, APX, and DHAR, and non-enzymatic antioxidant molecules (ascorbate, alkaloids, flavonoids, phenolic compounds, proline, glutathione, α-tocopherol, and carotenoids) are activated (Kim et al., 2011; Wang et al., 2015b; Ahmad et al., 2019a). Several researchers have reported enhanced activity of the antioxidant machinery in plants to counteract oxidative stress induced by salinity (Zaefyzadeh et al., 2009; Chen et al., 2011). In a similar context, Si has been reported to alleviate the adverse effect of salinity by strengthening the antioxidant defense ability of crops.

The application of Si restores normal metabolism by reducing lipid peroxidation in maize, barley, and grapevine rootstocks (Liang et al., 2003; Moussa, 2006; Soylemezoglu et al., 2009; Kim et al., 2017). The reduction in lipid peroxidation under stress is thought to be the result of the maintenance of antioxidant enzyme production in plants. Hasanuzzaman et al. (2018) reported that the exogenous application of Si (1 mM) enhanced the activity of APX, MDHAR, GR, GST, DHAR, GPX, and CAT and raised AsA and GSH levels in Brassica napus. Similarly, higher production of SOD, CAT, and POD has been reported in Abelmoschus esculentus under salinity stress (Abbas et al., 2015). Recently, Ahmad et al. (2019a) described higher activity levels of SOD, CAT, APX, and GR in Si-treated Vigna radiata L. exposed to salinity stress. Gong et al. (2005) reported that Si application strengthens the antioxidant defense system and maintains normal physiological processes. Saqib et al. (2008) explained that Si enhanced the activity of antioxidative enzymes and reduced plasma membrane permeability.

To date, various studies have described enhanced antioxidant machinery in Si-treated plants under salinity stress. In Glycyrrhiza uralensis, the addition of Si increased POD and SOD activity and condensed MDA concentration (Li et al., 2016). However, the effect of Si on the antioxidant system is dependent on time, the concentration of Si, the severity of stress, and plant species. This can be illustrated by the results reported for two cultivars (‘Jinlu 4’ and ‘Jinyan 4’) of cucumber (Cucumis sativus L.). It was found that GPX and SOD activity decreased significantly in both cultivars under salt stress. In both varieties, Si did not affect GPX activity on the fifth day; however, activity increased significantly on the tenth day of treatment. Zhu et al. (2004) thus demonstrated that the activity of SOD, GPX, APX, DHAR, and GR increased with the application of Si under salt stress, but an increase in CAT activity was not observed. Liang et al. (2003) observed that CAT enzymatic activity increased in barley on day 2 under salt stress compared with the control regardless of whether Si was applied or not. On the day 4 and 6 of salt treatment, CAT activity reduced, but the addition of Si significantly rescued CAT activity. For grapevine plants under salt stress, the addition of Si did not affect SOD activity and reduced CAT activity, whereas APX activity was unchanged or increased depending on the cultivar (Soylemezoglu et al., 2009).

The studies suggest that Si supplementation can reduce the adverse effects of salinity by regulating the antioxidant defense system, which consequently decreases lipid peroxidation and ultimately maintains membrane integrity and decreases plasma membrane permeability. The literature suggests that Si-treated and non-Si treated plants exhibit different responses under salinity stress and that Si improves antioxidant activity, thus playing a protective role against salinity stress. Although important advances have been achieved in recent years, gaps still remain in the understanding of the interaction between exogenous Si and the plant antioxidant machinery. It should be noted that most of these results are from hydroponics experiments and require field trials. In addition to this, the effect of supplemented Si is known to be dependent on plant species, time, and organ, but the effect of Si on different isoforms is still not clear. Furthermore, most studies describe the effect of exogenous Si on antioxidant enzymes at a protein level. Hence, there is a need for comprehensive research to clearly demonstrate the interaction of exogenous Si with different isoforms of antioxidant enzymes at the protein and mRNA levels. If Si plays an active role in regulating ROS scavenging, it should be further specified when, where, and how this occurs (e.g. by regulating stress acclimation proteins and enzymes or by regulating the expression of the genes involved in managing ROS levels). Plants are affected not by a single stress factor but rather by a combination of harsh conditions. Elucidating the combination of salinity-induced changes in soil chemistry or in environmental contamination such as heavy metals is pivotal to understanding the interaction of exogenous Si with the antioxidant system. In the future, advanced imaging and ecophysiolomics techniques can lead to a better understanding of this interaction. Advanced approaches such as functional genomics, live-cell imaging, proteomics, and metabolomics will offer detailed insight into Si interactions with the antioxidant machinery.

Silicon-Induced Reduction in Salinity Toxicity by Hindering the Uptake of Na⁺ From the Roots

Prolonged exposure to a high-salinity environment results in higher levels of Na⁺ and Cl^- and lower levels of other cations such as K⁺ and Ca⁺², leading to a shift in the ion balance (Halperin and Lynch, 2003; Ahmad et al., 2019a). This ultimately results in changes to the K⁺/Na⁺ ratio in plants (Khan et al., 2000; Wang and Han, 2007). High concentrations of Na⁺ adversely affect plant metabolism and growth and lead to the overproduction of ROS (Mahajan and Tuteja, 2005). Recently, it has been reported that Si can ameliorate ion toxicity arising from salinity stress by enhancing K⁺ and reducing Na⁺ uptake (Tuna et al., 2008). It has been shown in several crops that the application of Si significantly reduces the accumulation of Na⁺ in the roots and hinders its translocation to sensitive plant tissues, consequently raising the K⁺/Na⁺ ratio.

The regulation of the K⁺/Na⁺ ratio is a well-reported mechanism by which Si alleviates Na⁺ ion toxicity (Tuna et al., 2008). Silicon accumulates in the form of phytoliths or discrete silica bodies in different parts of the plant, e.g. the roots, leaves, and stem (Figure 5). This deposition takes place beneath the cell walls of the roots, where discrete Si bodies bind with Na⁺, resulting in the increased uptake of K⁺ and the reduced transport of Na⁺ to the upper regions of the plant. A study by Tahir et al. (2006) on the two wheat genotypes Auqab 2000 and SARC-5 found an increase in K⁺ ion concentrations and a decrease in Na⁺ ion concentrations following Si application under salt stress. Silicon has also been shown to play a role in Na⁺ ion detoxification by increasing the binding of Na⁺ to cell walls in both the salt-resistant wheat genotype SARC-1 and the salt-sensitive 7-Cerros (Saqib et al., 2008). Similarly, the exogenous application of Si decreases Na⁺ ion levels in alfalfa (Medicago sativa L.) roots but not in the shoots, though K⁺ levels notably increased in the shoots (Wang and Han, 2007). In rice, Gong et al. (2006) reported a dramatic reduction in Na⁺ concentrations in the shoots of salt-stressed plants following the application of Si. Gunes et al. (2007b) reported lower Na⁺ and Cl^- translocation from the roots to shoots in tomato plants following the application of Si. This mechanism has been reported by several studies, as shown in Table 2. Many nutrients have exhibited synergistic effects in wheat (Khan et al., 2015b) and facilitated its uptake within the plant body. Similarly, Si has demonstrated a synergistic effect with K⁺ by increasing its concentration within plant cells, such as in maize (Khan et al., 2015a) and wheat (Tahir et al., 2012).

FIGURE 5

Figure 5 Accumulation of Si in different parts of plants. Silicon accumulates in the form of phytoliths or discrete silica bodies in different parts of a plant, e.g. the roots, leaves, and stems. This deposition takes place beneath the cell wall of the roots, where the discrete bodies of Si bind with the Na⁺, resulting in the increased uptake of K⁺ and the reduced transport of Na⁺ to the upper regions of the plants.

The Na⁺/H⁺ antiporter is also known to play a vital role in maintaining low Na⁺ concentrations. This occurs with the removal of Na⁺ from the cytosol or its compartmentalization in vacuoles (Yue et al., 2012). Gene SOS1 encodes plasma membrane Na⁺/H⁺ antiporters and has been cloned from Arabidopsis (Shi et al., 2000). The plasma membrane uses energy from ATP hydrolysis to pump H⁺ out of the cell, thereby generating an electrochemical H⁺ gradient, which is the main force driving Na⁺/H⁺ antiporter function. Tonoplast Na⁺/H⁺ antiporters play a role in Na⁺ compartmentation and are driven by H⁺-ATPase and H⁺-PPase in tonoplasts (Shi et al., 2000; Yamaguchi et al., 2013). Liang (1999) observed lower plasma membrane H⁺-ATPase activity in salt-stressed barley roots, but higher activity was observed following the application of Si to plants. Increased H⁺-ATPase levels facilitate Na⁺ export from the cell. Na⁺ compartmentation also plays an important role in preventing Na⁺ toxicity (Yamaguchi et al., 2013). Liang et al. (2005b) reported that the activity of H⁺-ATPase and H⁺-PPase in the tonoplast cells of barley roots was stimulated by the addition of Si under salt stress. This facilitates Na⁺ compartmentalization in vacuoles by tonoplast Na⁺/H⁺ antiporters. Mali and Aery (2008) reported that Si increases K⁺ uptake by increasing H⁺-ATPase activity in both hydroponics and soil. Recently, Soleimannejad et al. (2019) reported that Si improves plasma membrane activity by lowering electrolyte leakage, possibly via greater H⁺-ATPase activity, which could assist in Na+ secretion and exclusion from sensitive tissues. Therefore, under salt stress, the application of Si may lead to an increase in K⁺ levels and a decrease in Na⁺ levels in the cytoplasm due to H⁺-ATPase activity in the plasma membrane and tonoplasts and H⁺-PPase activity in tonoplasts. However, whether Si directly regulates the transport activity or expression of the Na⁺/H⁺ antiporter under salt stress remains unclear. In tomato, the addition of Si had no significant effect on Na⁺ and Cl^- concentrations in leaves, though it improved the storage of water in plants (Romero-Aranda et al., 2006). Tuna et al. (2008) reported that Si increased water content in wheat plants under saline conditions, whereas there was no effect on unstressed plants. The hydrophilic nature of Si to some extent may contribute to water restoration in salt-stressed plants.

These studies suggest that Si might alleviate the adverse effects of salinity by preventing Na⁺ uptake by the roots and subsequent movement to the shoots. The current literature suggests that the application of Si can provide protection against salinity stress and thus increase the yield and productivity of various crops. Silicon hinders Na⁺ translocation to aerial parts of a plant either by depositing Na⁺ in epidermal cells, creating a barrier to ion movement, or forming a complex between freely available Na⁺ and Si ions. However, some studies have linked the Si-mediated increase in tolerance to salinity with the activity of tonoplast H⁺-ATPase and H⁺-PPase in roots and plasma membrane H⁺-ATPase. The regulation of the K⁺/Na⁺ ratio by exogenous Si is thought to be a key mechanism in the Si-mediated increase in salt tolerance in crops. However, the effect of Si on Na⁺ dynamics across membranes and through extracellular spaces in plants needs to explored further. Many determinants have not been studied in sufficient detail in salt-stressed plants with or without the addition of Si, such as the Na⁺ signal perception process. Moreover, it is unclear whether the reduction in Na⁺ levels with the addition of Si is due to changes in the root structure and/or a reduction in the transpiration stream in the xylem, so this needs to be studied in more species. Moreover, the current literature lacks mRNA-level evidence for the role of Si in the regulation of the K⁺/Na⁺ ratio. More experiments are required to investigate the mechanisms involved in the regulation of this ratio in plants following the exogenous application of Si under saline conditions.

Salinity Tolerance, Compatible Osmolytes, and the Role of Silicon

Of the widely accepted mechanisms for tolerance that have evolved to enable a plant to avoid the deleterious effects of stress, compatible solute accumulation marks a key position. Researchers have long sought to understand the role of compatible solutes that accumulate upon exposure of a plant to salinity stress, including proline (Kaur and Asthir, 2015), polyamines (PAs; Liu et al., 2015), carbohydrates (Negrao et al., 2017), glycine betaine (Hussain et al., 2018), and polyols (Parida and Das, 2005). These solutes are chemically diverse, uncharged in neutral pH, water-soluble, and accumulate in high concentrations during stress without inhibiting normal biochemical reactions (Zhang et al., 2004). They interact with membrane proteins or other protein complexes due to their hydrophilic nature. However, this interaction occurs without disturbing the normal structure and role of the protein (Bohnert and Shen, 1998). Compatible osmolytes are known to stabilize functional proteins, enzymes, protein complexes, and the membrane under salinity stress (Rajasheker et al., 2019). Osmotic adjustment has been shown to be an important component of stress tolerance, and the accumulation of osmoprotectants such as proline, glycine betaine, gamma-aminobutyric acid (GABA), and sugars has been regularly observed in different plant systems (Ashraf and Foolad, 2007; Chen and Jiang, 2010). The genetic engineering of metabolic conduits for a number of compatible solutes such as proline, glycine betaine, sorbitol, mannitol, and trehalose has led to the successful development of transgenic plants that exhibit increased resistance to drought stress, high salinity, and the cold (Bhatnagar-Mathur et al., 2008; Reguera et al., 2012). Interestingly, various studies have suggested that the application of exogenous Si can enhance the salinity stress tolerance of various crops by regulating the synthesis of compatible osmolytes (Seckin et al., 2009). Al-Huqail et al. (2017) reported that the application of Si protects Talh trees (Acacia gerrardii Benth) from the negative effects of high concentrations of salt by increasing the production of proline and glycine betanin, which help the plants to maintain their metabolic activity by conserving water levels in their tissues. However, several studies have shown that the levels of proline are lowered by the addition of Si in various species under salt stress, such as grapevine (Soylemezoglu et al., 2009), soybean (Lee et al., 2010), wheat (Tuna et al., 2008), barley (Gunes et al., 2007a), and sorghum (Yin et al., 2013). Lower levels of proline in salt-stressed plants following the addition of Si indicates the alleviation of stress damage. Yin et al. (2013) reported that the short-term application of Si significantly enhanced the levels of sucrose and fructose in sorghum plants under salt stress. Similarly, Si reversed the lower concentrations of the PAs putrescine and spermine in the roots of salt-stressed cucumbers (Wang et al., 2015b). Higher glycine accumulation following the application of Si illustrates its effect in modifying osmotic capacity and antioxidant levels in okra under saline conditions (Abbas et al., 2015). Recently, Yin et al. (2019) reported that the application of Si increases the accumulation of polyamines such as spermidine and spermine in cucumber plants. Their study suggested that enhanced polyamine accumulation might play a role in modulating the antioxidant defense system and reducing oxidative stress, thus increasing the salt tolerance of cucumber plants.

Silicon-mediated osmotic adjustment under salinity stress to protect subcellular structures has been considered a major mechanism underlying Si-based salinity stress tolerance; however, it is still debated whether higher osmolyte accumulation benefits crop yield (Seeraj and Sinclair, 2002). A variety of studies have reported conflicting results for the interaction between Si and compatible osmolytes such as proline. Some studies have concluded that the application of Si reduces the accumulation of compatible osmolytes such proline in different plants in the presence of salt, claiming that the lower synthesis of proline following the addition of Si reflects the alleviation of stress damage. On the other hand, other studies have found a higher accumulation of proline due to Si. Hence, more research is needed to clarify the relationship between the exogenous application of Si and the metabolism of compatible solutes and water transport.

Silicon-Induced Improvement in Salinity Tolerance in Crops by Restoring the Rate of Photosynthesis

Photosynthesis is a fundamental process that takes place in the chloroplasts, resulting in the transformation of sunlight into energy to fuel a plant’s biochemical activities (Gong et al., 2010). The growth and productivity of plants largely depend on photosynthesis. From the large volume of data available on Si-induced improvement in shoot growth and net photosynthetic rate, it is reasonable to speculate that Si may maintain a high photosynthetic rate in salt-stressed plants. Previous reports have confirmed that salinity stress adversely disturbs the ultrastructure of chloroplasts, e.g. the dilation of thylakoid membranes and grana (Parida and Das, 2005), consequently disrupting the growth rate and productivity of plants.

Positive effects of Si on chlorophyll biosynthesis and photosynthetic machinery under abiotic stress have been widely reported. For example, under salinity stress, the exogenous application of Si has been found to improve photosynthesis in many species. Detmann et al. (2012) described the mechanisms behind the positive effect of Si on rice plants by analyzing photosynthetic gas exchange parameters alongside transcriptomic and metabolomic profiling. It was concluded that the rate of photosynthesis and the primary metabolism of a plant is enhanced by the application of Si. Silicon mitigates saline stress by maintaining stomatal conductance, transpiration, net photosynthesis, membrane permeability, and chlorophyll levels, which is partly due to the higher K⁺ ion concentrations and lower Na⁺ ion levels induced by the presence of Si in salt-stressed environments (Coskun et al., 2016). Tuna et al. (2008) reported that the application of Si to salt-stressed wheat restored chlorophyll levels. In barley, the application of Si increased chlorophyll levels and photosynthetic lead cell activity with or without salt stress (Nikolic et al., 2019). Advantageous effects of Si on the photosynthetic apparatus and pigments have also been observed in Spartina densiflora (Al-Aghabary et al., 2005; Mateos-Naranjo et al., 2013). Parveen and Ashraf (2010) studied various photosynthetic parameters, such as the net CO₂ assimilation rate, stomatal conductance, the internal CO₂ concentration in leaves, and the rate of transpiration in maize cultivars and reported that the exogenous application of Si improved all parameters under non-saline and saline regimes. Research on barley (Hordeum vulgare L.), rice (Oryza sativa L.), sugarcane (Saccharum officinarum L.), and wheat (Triticum aestivum L.) crops has shown that Si deposited in leaves is able to improve the potential and efficiency of photosynthesis by opening the angle of the leaves, decreasing self-shading, and keeping the leaf erect, thus it plays an important role in increasing the growth and yield of crops (Soratto et al., 2012).

The application of Si also improves plant photosynthetic machinery under salinity stress either by lowering ion toxicity and ROS accumulation to maintain the structure and function of the organelles that are responsible for photosynthesis or by increasing stomatal conductance, the transpiration rate, and the number and size of the stomata. In addition, Zhu et al. reported that the application of Si reduces starch and soluble sugar levels in cucumber leaves while increasing starch levels in the roots. This is because salinity stress increases the accumulation of photosynthetic products such as sucrose and starch in the leaves by affecting their transport and allocation, causing feedback inhibition of the photosynthesis process. However, the available literature lacks strong evidence for the role of Si in the synthesis, translocation, and allocation of photosynthetic products. Thus, advance molecular biology, proteomics, and advanced imaging techniques should be employed to further explore the mechanisms by which Si affects carbohydrate metabolism.

In conclusion, Si modifies the gas exchange process, decreases Na⁺ accumulation, enhances chlorophyll levels, scavenges ROS, and regulates carbohydrate metabolism, all of which ultimately enhances the photosynthesis of salt-stressed plants. However, this improvement depends on the plant species, salt-stress levels, and the application levels of the Si. Further studies are required to understand the role of exogenous Si in carbohydrate metabolism and its positive effect on photosynthesis under salinity stress. In addition, in-depth research is required to collect strong evidence for the involvement of Si in the improvement of the photosynthetic machinery under both salinity stress and combined stress, such as salinity in conjunction with heavy metals, drought, or heat.

Silicon and the Regulation of Endogenous Phytohormones Under Salinity Stress

The impact of silicon on endogenous phytohormones in response to stress conditions has been widely reported. The effect of Si on endogenous phytohormones such as GA, ABA, JA, ET, SA, BR, and IAA has commonly been studied in the context of the response to stress situations (Fahad et al., 2015). Although the protective role of these hormones has been studied extensively for a variety of stress types, the crosstalk between Si and phytohormones under salinity stress is poorly understood. However, studies have reported that the application of Si might enhance stress resistance by modifying phytohormone homeostasis (Van Bockhaven et al., 2012).

ABA is a stress hormone that affects gene expression (Parida and Das, 2005) in response to salt stress (Wang et al., 2001b; Dodd and Davies, 2010). The short-term application of Si downregulated JA and upregulated ABA after 6 and 12 h in rice plants under stress. The application of Si in combination with salt stress transiently increased the expression of the ABA biosynthesis-related genes zeaxanthin epoxidase and 9-cis-epoxicarotenoid oxygenase 1 and 4 (ZEP, NCED1, and NCED4) compared to salt stress alone in rice (Kim et al., 2014b). The findings of the study conducted by Kim et al. (2011) on Oryza sativa suggest that the exogenous application of Si can modulate salinity-induced stress by regulating the phytohormonal response of plants, e.g. the upregulation of ABA (Maillard et al., 2018), with the effects dependent on time. However, the link between salt tolerance and Si-mediated changes in plant hormones has yet to be investigated. Lee et al. (2010) reported that ABA levels increase in soybean plants under salt stress but decrease when Si is applied. Furthermore, it was concluded that GA levels decrease under salt stress but increase with the application of Si. In soybean plants, Si alleviates the negative effects of NaCl on the growth of plants by enhancing endogenous GA₃ and lowering ABA levels (Lee et al., 2010). Adverse NaCl effects are reduced significantly with the application of Si by increasing bioactive gibberellin (GA₁ and GA₄) levels, but the levels of JA, which increase under salinity stress, decline sharply when plants are supplemented with Si (Zhang et al., 2018). Another report demonstrated that JA and SA concentrations decrease and increase, respectively, in Si-treated soybean plants under salt stress (Kim et al., 2014a). Thus, the regulatory effect of Si on salt tolerance levels in crop plants via the regulation of endogenous phytohormone signaling has been proposed. However, further research is required to clarify the relationship between Si, stress tolerance, and phytohormonal signaling, particularly with SA, JA, ETHY, BR, and melatonin.

Conclusion and Future Prospects

Saline environments have adverse effects on plant growth and yields worldwide. Plants respond to high-salinity stress using various mechanisms, including the regulation of Na⁺ uptake and translocation, the activation of their antioxidant defense system, compatible solute accumulation, osmotic regulation, the regulation of phytohormone synthesis, and the induction of various stress-signaling cascades. All of these responses play an important role in plant adaptation to salt stress. Silicon has been proven to increase tolerance to salinity stress by regulating various biochemical and physiological processes, such as the Na⁺ balance, water status, reactive oxygen species, photosynthesis, phytohormone levels, and compatible solutes in plants.

Various studies have shown that Si supplementation benefits the development of different plant species, specifically when they are exposed to ecological stresses. Of the various Si-mediated salinity stress tolerance mechanisms, the available literature suggests that the application of exogenous Si (i.e. foliar and root application) improves salinity tolerance in plants either by enhancing the activity of antioxidant enzymes or blocking Na⁺ uptake and translocation. Furthermore, we conclude that the positive effect of exogenous Si depends on a plant’s stress tolerance levels, which vary between species. This might be due to the differences in Si uptake capabilities among different species. Despite this, the effect of Si on plant stress tolerance generally depends on Si concentration, stress intensity and duration, Si application methods, and the cultivation methods used for experimental materials (e.g. soil culture or hydroponics).

It is known that approximately 20% of irrigated land is salt-affected which is one-third of all food-producing land. It has been estimated that about half of all fertile land will be affected by salinity by the middle of the 21^st century. To overcome salinity stress in the future, Si-mediated salt tolerance mechanisms will help to enhance salt stress tolerance in various crop plants. However, many determinants and regulatory mechanisms have not been studied in detail and thus need further elucidation. This paper suggests the following future research recommendations and prospects for Si-mediated salt tolerance in plants:

1. With the development of advanced omics technologies, more detailed research is required to explore Si-mediated salt tolerance at the transcriptome, proteome, and metabolome levels. 

2. SOS pathways have a vital role in salinity stress tolerance. However, the interaction of exogenous Si with plant SOS signaling pathways and other salt stress sensors remains obscure.

3. Most previous research has studied the role of Si in salt stress on its own and in the short-term. However, in nature, plants are exposed to multiple stresses simultaneously. Establishing stress tolerance over a longer period of time would be ideal for predicting and reacting to changing global climatic conditions, especially where one form of stress leads to another. Thus, the role of Si in long-term plant responses under multiple stresses requires in-depth research.

4. More work is needed to analyze the regulatory mechanisms of Si in salt-induced osmotic stress. Efforts should be made to clearly demonstrate how Si regulates osmotic adjustment under salinity stress. The genetic engineering of metabolic conduits for a number of compatible solutes, such as proline, glycine betaine, and sorbitol, could also be used to produce salt-tolerant plants.

In addition, Si-associated molecular and transcriptional changes at the plant level are yet to be elucidated, including the various metabolomic and proteomic changes in different plant organs. Currently, the mechanisms underlying the Si-mediated alleviation of salt stress in plants is poorly understood at the molecular and genetic levels. In addition, more focus is needed on the effects of Si under field conditions rather than greenhouse or laboratory studies.

Author Contributions

AK and ALK wrote the manuscript. SM and AA-H edited the manuscript. Y-HK organized graphical presentation. AA-R arranged funding.

Funding

The author(s) acknowledge the financial support of the Research Council Oman for research grant to corresponding authors.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors wish to acknowledge the efforts to all scientists and their work that has helped to understand role of Si in crop physiology and those whose work has not been cited here.

References

Abbas, T., Balal, R. M., Shahid, M. A., Pervez, M. A., Ayyub, C. M., Aqueel, M. A., et al. (2015). Silicon-induced alleviation of NaCl toxicity in okra (Abelmoschus esculentus) is associated with enhanced photosynthesis, osmoprotectants and antioxidant metabolism. Acta Physiol. Plant. 37, 6. doi: 10.1007/s11738-014-1768-5

CrossRef Full Text | Google Scholar

Abbas, T., Sattar, A., Ijaz, M., Aatif, M., Khalid, S., Sher, A. (2017). Exogenous silicon application alleviates salt stress in okra. Horticult. Environ. Biotechnol. 58, 342–349. doi: 10.1007/s13580-017-0247-5

CrossRef Full Text | Google Scholar

Acosta-Motos, J., Ortuño, M., Bernal-Vicente, A., Diaz-Vivancos, P., Sanchez-Blanco, M., Hernandez, J. (2017). Plant responses to salt stress: adaptive mechanisms. Agronomy 7, 18. doi: 10.3390/agronomy7010018

CrossRef Full Text | Google Scholar

Ahanger, M. A., Alyemeni, M. N., Wijaya, L., Alamri, S. A., Alam, P., Ashraf, M., et al. (2018). Potential of exogenously sourced kinetin in protecting Solanum lycopersicum from NaCl-induced oxidative stress through up-regulation of the antioxidant system, ascorbate-glutathione cycle and glyoxalase system. PloS One 13, e0202175. doi: 10.1371/journal.pone.0202175

PubMed Abstract | CrossRef Full Text | Google Scholar

Ahanger, M. A., Agarwal, R. (2017). Salinity stress induced alterations in antioxidant metabolism and nitrogen assimilation in wheat (Triticum aestivum L) as influenced by potassium supplementation. Plant Physiol. Biochem. 115, 449–460. doi: 10.1016/j.plaphy.2017.04.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Ahanger, M. A., Tomar, N. S., Tittal, M., Argal, S., Agarwal, R. (2017). Plant growth under water/salt stress: ROS production; antioxidants and significance of added potassium under such conditions. Physiol. Mol. Biol. Plants 23, 731–744. doi: 10.1007/s12298-017-0462-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Ahmad, P., Abass Ahanger, M., Nasser Alyemeni, M., Wijaya, L., Alam, P., Ashraf, M. (2018). Mitigation of sodium chloride toxicity in Solanum lycopersicum L. by supplementation of jasmonic acid and nitric oxide. J. Plant Interact. 13, 64–72. doi: 10.1080/17429145.2017.1420830

CrossRef Full Text | Google Scholar

Ahmad, P., Ahanger, M. A., Alam, P., Alyemeni, M. N., Wijaya, L., Ali, S., et al. (2019a). Silicon (Si) supplementation alleviates NaCl toxicity in mung bean [Vigna radiata (L.) Wilczek] through the modifications of physio-biochemical attributes and key antioxidant enzymes. J. Plant Growth Regul. 38, 70–82. doi: 10.1007/s00344-018-9810-2

CrossRef Full Text | Google Scholar

Ahmad, P., Rasool, S. (Eds.). (2014). Emerging technologies and management of crop stress tolerance: Volume 1-Biological Techniques (Vol. 1). Academic Press.

Google Scholar

Ahmad, R., Hussain, S., Anjum, M.A., Khalid, M.F., Saqib, M., Zakir, I., Hassan, A., Fahad, S., Ahmad, S. (2019b). "Oxidative Stress and Antioxidant Defense Mechanisms in Plants Under Salt Stress," in Plant Abiotic Stress Tolerance. Springer), 191–205. doi: 10.1007/978-3-030-06118-0_8

CrossRef Full Text | Google Scholar

Al-Aghabary, K., Zhu, Z., Shi, Q. (2005). Influence of silicon supply on chlorophyll content, chlorophyll fluorescence, and antioxidative enzyme activities in tomato plants under salt stress. J. Plant Nutr. 27, 2101–2115. doi: 10.1081/PLN-200034641

CrossRef Full Text | Google Scholar

Al-Huqail, A. A., Alqarawi, A. A., Hashem, A., Malik, J. A., Abd-Allah, E. F. (2017). Silicon supplementation modulates antioxidant system and osmolyte accumulation to balance salt stress in Acacia gerrardii Benth. Saudi J. Biol. Sci. doi: 10.1016/j.sjbs.2017.11.049

CrossRef Full Text | Google Scholar

Ali, A., Basra, S., Ahmad, R., Wahid, A. (2009). Optimizing silicon application to improve salinity tolerance in wheat. Soil Environ. 28, 136–144.

Google Scholar

Almeida, D. M., Oliveira, M. M., Saibo, N. J. (2017). Regulation of Na+ and K+ homeostasis in plants: towards improved salt stress tolerance in crop plants. Genet. Mol. Biol. 40, 326–345. doi: 10.1590/1678-4685-gmb-2016-0106

PubMed Abstract | CrossRef Full Text | Google Scholar

Artyszak, A. (2018). Effect of silicon fertilization on crop yield quantity and quality-a literature review in Europe. Plants 7, 54. doi: 10.3390/plants7030054

CrossRef Full Text | Google Scholar

Ashraf, M. (2004). Some important physiological selection criteria for salt tolerance in plants. Flora-Morphol. Distrib. Funct. Ecol. Plants 199, 361–376. doi: 10.1078/0367-2530-00165

CrossRef Full Text | Google Scholar

Ashraf, M. F. M. R., Foolad, M. (2007). Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environ. Exp. Bot. 59(2), 206–216.

Google Scholar

Ashraf, M., Afzal, M., Ahmed, R., Mujeeb, F., Sarwar, A., Ali, L. (2010a). Alleviation of detrimental effects of NaCl by silicon nutrition in salt-sensitive and salt-tolerant genotypes of sugarcane (Saccharum officinarum L.). Plant Soil 326, 381–391. doi: 10.1007/s11104-009-0019-9

CrossRef Full Text | Google Scholar

Ashraf, M., Akram, N. A., Al-Qurainy, F., Foolad, M. R. (2011). Drought tolerance: roles of organic osmolytes, growth regulators, and mineral nutrients. In Advances in Agronomy (Vol. 111, pp. 249–296). Academic Press. doi: 10.1016/B978-0-12-387689-8.00002-3

CrossRef Full Text | Google Scholar

Ashraf, M., Akram, N., Arteca, R., Foolad, M. (2010b). The physiological, biochemical and molecular roles of brassinosteroids and salicylic acid in plant processes and salt tolerance. Crit. Rev. Plant Sci. 29, 162–190. doi: 10.1080/07352689.2010.483580

CrossRef Full Text | Google Scholar

Assaha, D. V., Ueda, A., Saneoka, H., Al-Yahyai, R., Yaish, M. W. (2017). The role of Na+ and K+ transporters in salt stress adaptation in glycophytes. Front. Physiol. 8, 509. doi: 10.3389/fphys.2017.00509

PubMed Abstract | CrossRef Full Text | Google Scholar

Bae, E. J., Lee, K. S., Huh, M. R., Lim, C. S. (2012). Silicon significantly alleviates the growth inhibitory effects of NaCl in salt-sensitive 'Perfection'and 'Midnight'Kentucky bluegrass (Poa pratensis L.). Horticult. Environ. Biotechnol. 53, 477–483. doi: 10.1007/s13580-012-0094-3

CrossRef Full Text | Google Scholar

Bajguz, A. (2014). Nitric oxide: role in plants under abiotic stress. In Physiological mechanisms and adaptation strategies in plants under changing environment (pp. 137-159). (New York, NY: Springer) doi: 10.1007/978-1-4614-8600-8_5

CrossRef Full Text | Google Scholar

Bakhat, H. F., Bibi, N., Zia, Z., Abbas, S., Hammad, H. M., Fahad, S., et al. (2018). Silicon mitigates biotic stresses in crop plants: a review. Crop Prot. 104, 21–34. doi: 10.1016/j.cropro.2017.10.008

CrossRef Full Text | Google Scholar

Barcelo, J., Guevara, P., Poschenrieder, C. (1993). Silicon amelioration of aluminium toxicity in teosinte (Zea mays L. ssp. mexicana). Plant Soil 154, 249–255. doi: 10.1007/BF00012530

CrossRef Full Text | Google Scholar

Besson-Bard, A., Pugin, A., Wendehenne, D. (2008). New insights into nitric oxide signaling in plants. Annu. Rev. Plant Biol. 59, 21–39. doi: 10.1146/annurev.arplant.59.032607.092830

PubMed Abstract | CrossRef Full Text | Google Scholar

Bohnert, H. J., Shen, B. (1998). Transformation and compatible solutes. Scientia Hortic. 78, 237–260. doi: 10.1016/S0304-4238(98)00195-2

CrossRef Full Text | Google Scholar

Bozza, D. C., Freire, C. A., Prodocimo, V. (2019). Osmo-ionic regulation and carbonic anhydrase, Na+/K+-ATPase and V-H+-ATPase activities in gills of the ancient freshwater crustacean Aegla schmitti (Anomura) exposed to high salinities. Comp. Biochem. Physiol. Part A: Mol. Integr. Physiol. 231, 201–208. doi: 10.1016/j.cbpa.2019.02.024

CrossRef Full Text | Google Scholar

Bhatnagar-Mathur, P., Vadez, V., Sharma, K. K. (2008). Transgenic approaches for abiotic stress tolerance in plants: retrospect and prospects. Plant Cell Rep. 27(3), 411–424.

PubMed Abstract | Google Scholar

Caverzan, A., Casassola, A., Brammer, S. P. (2016). Reactive oxygen species and antioxidant enzymes involved in plant tolerance to stress. Embrapa Trigo-Capítulo Em Livro Científico (ALICE). 463–480. doi: 10.5772/61368

CrossRef Full Text | Google Scholar

Chanchal Malhotra, C., Kapoor, R., Ganjewala, D. (2016). Alleviation of abiotic and biotic stresses in plants by silicon supplementation. Scientia 13, 59–73. doi: 10.15192/PSCP.SA.2016.13.2.5973

CrossRef Full Text | Google Scholar

Chen, H., Jiang, J. G. (2010). Osmotic adjustment and plant adaptation to environmental changes related to drought and salinity. Environ. Rev. 18, 309–319.

Google Scholar

Chen, Q., Zhang, M., Shen, S. (2011). Effect of salt on malondialdehyde and antioxidant enzymes in seedling roots of Jerusalem artichoke (Helianthus tuberosus L.). Acta Physiol. Plantarum 33, 273–278. doi: 10.1007/s11738-010-0543-5

CrossRef Full Text | Google Scholar

Chen, S., Li, J., Wang, S., Hüttermann, A., Altman, A. (2001). Salt, nutrient uptake and transport, and ABA of Populus euphratica; a hybrid in response to increasing soil NaCl. Trees 15, 186–194. doi: 10.1007/s004680100091

CrossRef Full Text | Google Scholar

Chiba, Y., Mitani, N., Yamaji, N., Ma, J. F. (2009). HvLsi1 is a silicon influx transporter in barley. Plant J. 57, 810–818. doi: 10.1111/j.1365-313X.2008.03728.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Cho, S. H., Von Schwartzenberg, K., Quatrano, R. (2018). The role of abscisic acid in stress tolerance. Annu. Plant Rev. Online, 15, 282–297. doi: 10.1002/9781119312994.apr0394

CrossRef Full Text | Google Scholar

Cocker, K. M., Evans, D. E., Hodson, M. J. (1998). The amelioration of aluminium toxicity by silicon in wheat (Triticum aestivum L.): malate exudation as evidence for an in planta mechanism. Planta 204, 318–323. doi: 10.1007/s004250050262

CrossRef Full Text | Google Scholar

Conceição, S. S., Oliveira Neto, C. F. D., Marques, E. C., Barbosa, A. V. C., Galvão, J. R., Oliveira, T. B. D., et al. (2019). Silicon modulates the activity of antioxidant enzymes and nitrogen compounds in sunflower plants under salt stress. Arch. Agron. Soil Sci. 65, 1237–1247. doi: 10.1080/03650340.2018.1562272

CrossRef Full Text | Google Scholar

Cooke, J., Leishman, M. R. (2011). Silicon concentration and leaf longevity: is silicon a player in the leaf dry mass spectrum? Funct. Ecol. 25, 1181–1188. doi: 10.1111/j.1365-2435.2011.01880.x

CrossRef Full Text | Google Scholar

Coskun, D., Britto, D. T., Huynh, W. Q., Kronzucker, H. J. (2016). The role of silicon in higher plants under salinity and drought stress. Front. Plant Sci. 7, 1072. doi: 10.3389/fpls.2016.01072

PubMed Abstract | CrossRef Full Text | Google Scholar

Cotterill, J. V., Watkins, R. W., Brennon, C. B., Cowan, D. P. (2007). Boosting silica levels in wheat leaves reduces grazing by rabbits. Pest Manage. Sci.: Formerly Pesticide Sci. 63, 247–253. doi: 10.1002/ps.1302

CrossRef Full Text | Google Scholar

Cuin, T. A., Shabala, S. (2007). Amino acids regulate salinity-induced potassium efflux in barley root epidermis. Planta 225, 753. doi: 10.1007/s00425-006-0386-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Debona, D., Rodrigues, F. A., Datnoff, L. E. (2017). Silicon's role in abiotic and biotic plant stresses. Annu. Rev. Phytopathol. 55, 85–107. doi: 10.1146/annurev-phyto-080516-035312

PubMed Abstract | CrossRef Full Text | Google Scholar

Deshmukh, R. K., Vivancos, J., Guérin, V., Sonah, H., Labbé, C., Belzile, F., et al. (2013). Identification and functional characterization of silicon transporters in soybean using comparative genomics of major intrinsic proteins in Arabidopsis and rice. Plant Mol. Biol. 83, 303–315. doi: 10.1007/s11103-013-0087-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Detmann, K. C., Araújo, W. L., Martins, S. C., Sanglard, L. M., Reis, J. V., Detmann, E., et al. (2012). Silicon nutrition increases grain yield, which, in turn, exerts a feed-forward stimulation of photosynthetic rates via enhanced mesophyll conductance and alters primary metabolism in rice. New Phytol. 196, 752–762. doi: 10.1111/j.1469-8137.2012.04299.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Dodd, I. C., Davies, W. J. (2010). Hormones and the regulation of water balance. In Plant Hormones (Dordrecht: Springer). pp. 519–548. doi: 10.1007/978-1-4020-2686-7_23

CrossRef Full Text | Google Scholar

Dubos, C., Plomion, C. (2003). Identification of water-deficit responsive genes in maritime pine (Pinus pinaster Ait.) roots. Plant Mol. Biol. 51, 249–262. doi: 10.1023/1021168811590

PubMed Abstract | CrossRef Full Text | Google Scholar

Dunlap, J. R., Binzel, M. L. (1996). NaCI reduces indole-3-acetic acid levels in the roots of tomato plants independent of stress-induced abscisic acid. Plant Physiol. 112, 379–384. doi: 10.1104/pp.112.1.379

PubMed Abstract | CrossRef Full Text | Google Scholar

El-Mashad, A.a.A., Mohamed, H. I. (2012). Brassinolide alleviates salt stress and increases antioxidant activity of cowpea plants (Vigna sinensis). Protoplasma 249, 625–635. doi: 10.1007/s00709-011-0300-7

PubMed Abstract | CrossRef Full Text | Google Scholar

El-Shintinawy, F., El-Shourbagy, M. (2001). Alleviation of changes in protein metabolism in NaCl-stressed wheat seedlings by thiamine. Biol. Plant. 44, 541–545. doi: 10.1023/A:1013738603020

CrossRef Full Text | Google Scholar

Epstein, E. (1999). Silicon. Annu. Rev. Plant Biol. 50, 641–664. doi: 10.1146/annurev.arplant.50.1.641

CrossRef Full Text | Google Scholar

Etesami, H., Jeong, B. R. (2018). Silicon (Si): review and future prospects on the action mechanisms in alleviating biotic and abiotic stresses in plants. Ecotoxicol. Environ. Saf. 147, 881–896. doi: 10.1016/j.ecoenv.2017.09.063

PubMed Abstract | CrossRef Full Text | Google Scholar

Eyidogan, F., Oz, M. T., Yucel, M., Oktem, H. A. (2012). Signal transduction of phytohormones under abiotic stresses. In Phytohormones and Abiotic Stress Tolerance in Plants. (Berlin, Heidelberg: Springer) pp. 1-48. doi: 10.1007/978-3-642-25829-9_1

CrossRef Full Text | Google Scholar

Fahad, S., Hussain, S., Matloob, A., Khan, F. A., Khaliq, A., Saud, S., et al. (2015). Phytohormones and plant responses to salinity stress: a review. Plant Growth Regul. 75, 391–404. doi: 10.1007/s10725-014-0013-y

CrossRef Full Text | Google Scholar

Fan, Y., Yin, X., Xie, Q., Xia, Y., Wang, Z., Song, J., et al. (2019). Co-expression of SpSOS1 and SpAHA1 in transgenic Arabidopsis plants improves salinity tolerance. BMC Plant Biol. 19, 74. doi: 10.1186/s12870-019-1680-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Farhangi-Abriz, S., Ghassemi-Golezani, K. (2018). How can salicylic acid and jasmonic acid mitigate salt toxicity in soybean plants? Ecotoxicol. Environ. Saf. 147, 1010–1016. doi: 10.1016/j.ecoenv.2017.09.070

PubMed Abstract | CrossRef Full Text | Google Scholar

Feng, J., Yamaji, N., Mitani-Ueno, N. (2011). Transport of silicon from roots to panicles in plants. Proc. Japan Acad. Ser. B 87, 377–385. doi: 10.2183/pjab.87.377

CrossRef Full Text | Google Scholar

Ford, C. W. (1984). Accumulation of low molecular weight solutes in water-stressed tropical legumes. Phytochemistry 23, 1007–1015. doi: 10.1016/S0031-9422(00)82601-1

CrossRef Full Text | Google Scholar

Foyer, C. H. (2018). Reactive oxygen species, oxidative signaling and the regulation of photosynthesis. Environ. Exp. Bot. 154, 134–142. doi: 10.1016/j.envexpbot.2018.05.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Frew, A., Weston, L. A., Reynolds, O. L., Gurr, G. M. (2018). The role of silicon in plant biology: a paradigm shift in research approach. Ann. Bot. 121, 1265–1273. doi: 10.1093/aob/mcy009

PubMed Abstract | CrossRef Full Text | Google Scholar

Fricke, W., Akhiyarova, G., Veselov, D., Kudoyarova, G. (2004). Rapid and tissue-specific changes in ABA and in growth rate in response to salinity in barley leaves. J. Exp. Bot. 55, 1115–1123. doi: 10.1093/jxb/erh117

PubMed Abstract | CrossRef Full Text | Google Scholar

Galvez, L., Clark, R. (1991). “Effects of silicon on growth and mineral composition of sorghum (Sorghum bicolor) grown with toxic levels of aluminium,” in Plant-Soil Interactions at Low pH (Springer), 815–823. doi: 10.1007/978-94-011-3438-5_92

CrossRef Full Text | Google Scholar

Garg, N., Bhandari, P. (2016). Silicon nutrition and mycorrhizal inoculations improve growth, nutrient status, K+/Na+ ratio and yield of Cicer arietinum L. genotypes under salinity stress. Plant Growth Regul. 78, 371–387. doi: 10.1007/s10725-015-0099-x

CrossRef Full Text | Google Scholar

Gibson, T., Speirs, J., Brady, C. (1984). Salt-tolerance in plants. II. In vitro translation of m-RNAs from salt-tolerant and salt-sensitive plants on wheat germ ribosomes. Responses to ions and compatible organic solutes. Plant Cell Environ. 7, 579–587. doi: 10.1111/j.1365-3040.1984.tb01858.x

CrossRef Full Text | Google Scholar

Gill, S. S., Tuteja, N. (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 48, 909–930. doi: 10.1016/j.plaphy.2010.08.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Godfray, H. C. J., Beddington, J. R., Crute, I. R., Haddad, L., Lawrence, D., Muir, J. F., et al. (2010). Food security: the challenge of feeding 9 billion people. science 327, 812–818. doi: 10.1126/science.1185383

PubMed Abstract | CrossRef Full Text | Google Scholar

Gong, H., Blackmore, D., Clingeleffer, P., Sykes, S., Jha, D., Tester, M., et al. (2010). Contrast in chloride exclusion between two grapevine genotypes and its variation in their hybrid progeny. J. Exp. Bot. 62, 989–999. doi: 10.1093/jxb/erq326

PubMed Abstract | CrossRef Full Text | Google Scholar

Gong, H., Randall, D., Flowers, T. (2006). Silicon deposition in the root reduces sodium uptake in rice (Oryza sativa L.) seedlings by reducing bypass flow. Plant Cell Environ. 29, 1970–1979. doi: 10.1111/j.1365-3040.2006.01572.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Gong, H., Zhu, X., Chen, K., Wang, S., Zhang, C. (2005). Silicon alleviates oxidative damage of wheat plants in pots under drought. Plant Sci. 169, 313–321. doi: 10.1016/j.plantsci.2005.02.023

CrossRef Full Text | Google Scholar

Graus, D., Konrad, K. R., Bemm, F., Patir Nebioglu, M. G., Lorey, C., Duscha, K., et al. (2018). High V-PPase activity is beneficial under high salt loads, but detrimental without salinity. New Phytol. 219, 1421–1432. doi: 10.1111/nph.15280

PubMed Abstract | CrossRef Full Text | Google Scholar

Gregory, P. J., Ismail, S., Razaq, I. B., Wahbi, A. (2018). Soil salinity: current status and in depth analyses for sustainable use. Chapter 2 (No. IAEA-TECDOC--1841).

Google Scholar

Gunes, A., Inal, A., Bagci, E. G., Coban, S. (2007a). Silicon-mediated changes on some physiological and enzymatic parameters symptomatic of oxidative stress in barley grown in sodic-B toxic soil. J. Plant Physiol. 164, 807–811. doi: 10.1016/j.jplph.2006.07.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Gunes, A., Inal, A., Bagci, E. G., Pilbeam, D. J. (2007b). Silicon-mediated changes of some physiological and enzymatic parameters symptomatic for oxidative stress in spinach and tomato grown in sodic-B toxic soil. Plant Soil 290, 103–114. doi: 10.1007/s11104-006-9137-9

CrossRef Full Text | Google Scholar

Guo, Y., Tian, Z., Yan, D., Zhang, J., Qin, P. (2005). Effects of nitric oxide on salt stress tolerance in Kosteletzkya virginica. LifeSci. J. 6.

Google Scholar

Gupta, B., Huang, B. (2014). Mechanism of salinity tolerance in plants: physiological, biochemical, and molecular characterization. Int. J. Genomics 2014 (18). doi: 10.1155/2014/701596

CrossRef Full Text | Google Scholar

Gurmani, A., Bano, A., Khan, S., Din, J., Zhang, J. (2011). Alleviation of salt stress by seed treatment with abscisic acid (ABA), 6-benzylaminopurine (BA) and chlormequat chloride (CCC) optimizes ion and organic matter accumulation and increases yield of rice ('Oryza sativa'L.). Aust. J. Crop Sci. 5, 1278.

Google Scholar

Haddad, C., Arkoun, M., Jamois, F., Schawarzbenberg, A., Yvin, J.-C., Etienne, P., et al. (2018). Silicon Promotes Growth of Brassica napus L. and Delays Leaf Senescence Induced by Nitrogen Starvation. Front. Plant Sci. 9, 516. doi: 10.3389/fpls.2018.00516

PubMed Abstract | CrossRef Full Text | Google Scholar

Halperin, S. J., Lynch, J. P. (2003). Effects of salinity on cytosolic Na+ and K+ in root hairs of Arabidopsis thaliana: in vivo measurements using the fluorescent dyes SBFI and PBFI. J. Exp. Bot. 54, 2035–2043. doi: 10.1093/jxb/erg219

PubMed Abstract | CrossRef Full Text | Google Scholar

Hamayun, M., Sohn, E.-Y., Khan, S. A., Shinwari, Z. K., Khan, A. L., Lee, I.-J. (2010). Silicon alleviates the adverse effects of salinity and drought stress on growth and endogenous plant growth hormones of soybean (Glycine max L.). Pak. J. Bot. 42, 1713–1722.

Google Scholar

Hanson, A. D., Rathinasabapathi, B., Rivoal, J., Burnet, M., Dillon, M. O., Gage, D. A. (1994). Osmoprotective compounds in the Plumbaginaceae: a natural experiment in metabolic engineering of stress tolerance. Proc. Natl. Acad. Sci. 91, 306–310. doi: 10.1073/pnas.91.1.306

CrossRef Full Text | Google Scholar

Hasanuzzaman, M., Nahar, K., Rohman, M., Anee, T., Huang, Y., Fujita, M. (2018). Exogenous silicon protects brassica napus plants from salinity-induced oxidative stress through the modulation of AsA-GSH pathway, thiol-dependent antioxidant enzymes and glyoxalase systems. Gesunde Pflanzen 70, 185–194. doi: 10.1007/s10343-018-0430-3

CrossRef Full Text | Google Scholar

Hasegawa, P. M. (2013). Sodium (Na+) homeostasis and salt tolerance of plants. Environ. Exp. Bot. 92, 19–31. doi: 10.1016/j.envexpbot.2013.03.001

CrossRef Full Text | Google Scholar

Hoque, M. A., Banu, M. N. A., Okuma, E., Amako, K., Nakamura, Y., Shimoishi, Y., et al. (2007). Exogenous proline and glycinebetaine increase NaCl-induced ascorbate-glutathione cycle enzyme activities, and proline improves salt tolerance more than glycinebetaine in tobacco Bright Yellow-2 suspension-cultured cells. J. Plant Physiol. 164, 1457–1468. doi: 10.1016/j.jplph.2006.10.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Horváth, E., Szalai, G., Janda, T. (2007). Induction of abiotic stress tolerance by salicylic acid signaling. J. Plant Growth Regul. 26, 290–300. doi: 10.1007/s00344-007-9017-4

CrossRef Full Text | Google Scholar

Hussain, M., Fatima, H., Khan, A., Ghani, A., Nadeem, M., Aziz, A., et al. (2018). Improving salinity tolerance in brassica (Brassica napus var. Bsa and Brassica campestris var. Toria) by exogenous application of proline and glycine betaine. Biol. Sci.-PJSIR 61, 1–8.

Google Scholar

Ibrahim, M., Merwad, A., Elnaka, E., Burras, C., Follett, L. (2016). Application of silicon ameliorated salinity stress and improved wheat yield. J. Soil Sci. Environ. Manage. 7, 81. doi: 10.5897/JSSEM2016.0571

CrossRef Full Text | Google Scholar

Iqbal, M., Ashraf, M. (2013). Gibberellic acid mediated induction of salt tolerance in wheat plants: Growth, ionic partitioning, photosynthesis, yield and hormonal homeostasis. Environ. Exp. Bot. 86, 76–85. doi: 10.1016/j.envexpbot.2010.06.002

CrossRef Full Text | Google Scholar

Iqbal, N., Umar, S., Khan, N. A., Khan, M. I. R. (2014). A new perspective of phytohormones in salinity tolerance: regulation of proline metabolism. Environ. Exp. Bot. 100, 34–42. doi: 10.1016/j.envexpbot.2013.12.006

CrossRef Full Text | Google Scholar

Ishitani, M., Liu, J., Halfter, U., Kim, C.-S., Shi, W., Zhu, J.-K. (2000). SOS3 function in plant salt tolerance requires N-myristoylation and calcium binding. Plant Cell 12, 1667–1677. doi: 10.1105/tpc.12.9.1667

PubMed Abstract | CrossRef Full Text | Google Scholar

James, R. A., Blake, C., Byrt, C. S., Munns, R. (2011). Major genes for Na+ exclusion, Nax1 and Nax2 (wheat HKT1; 4 and HKT1; 5), decrease Na+ accumulation in bread wheat leaves under saline and waterlogged conditions. J. Exp. Bot. 62, 2939–2947. doi: 10.1093/jxb/err003

PubMed Abstract | CrossRef Full Text | Google Scholar

Javid, M. G., Sorooshzadeh, A., Moradi, F., Modarres Sanavy, S.a.M., Allahdadi, I. (2011). The role of phytohormones in alleviating salt stress in crop plants. Aust. J. Crop Sci. 5, 726.

Google Scholar

Jayakannan, M., Bose, J., Babourina, O., Rengel, Z., Shabala, S. (2013). Salicylic acid improves salinity tolerance in Arabidopsis by restoring membrane potential and preventing salt-induced K+ loss via a GORK channel. J. Exp. Bot. 64, 2255–2268. doi: 10.1093/jxb/ert085

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaur, G., Asthir, B. (2015). Proline: a key player in plant abiotic stress tolerance. Biol. Plant. 59, 609–619. doi: 10.1007/s10535-015-0549-3

CrossRef Full Text | Google Scholar

Kaur, H., Greger, M. (2019). A review on si uptake and transport system. Plants 8, 81. doi: 10.3390/plants8040081

CrossRef Full Text | Google Scholar

Khan, M. A., Ungar, I. A., Showalter, A. M. (2000). Effects of sodium chloride treatments on growth and ion accumulation of the halophyte Haloxylon recurvum. Commun. Soil Sci. Plant Anal. 31, 2763–2774. doi: 10.1080/00103620009370625

CrossRef Full Text | Google Scholar

Khan, W., Aziz, T., Maqsood, M., Farooq, M., Abdullah, Y., Ramzani, P., et al. (2018). Silicon nutrition mitigates salinity stress in maize by modulating ion accumulation, photosynthesis, and antioxidants. Photosynthetica 56, 1047–1057. doi: 10.1007/s11099-018-0812-x

CrossRef Full Text | Google Scholar

Khan, W.-U.-D., Aziz, T., Waraich, E. A., Khalid, M. (2015a). Silicon application improves germination and vegetative growth in maize grown under salt stress. Pakistan J. Agric. Sci. 52.

Google Scholar

Khan, W. U. D., Faheem, M., Khan, M. Y., Hussain, S., Maqsood, M. A., Aziz, T. (2015b). Zinc requirement for optimum grain yield and zinc biofortification depends on phosphorus application to wheat cultivars. Roman. Agric. Res. 32, 1–9.

Google Scholar

Khoshgoftarmanesh, A. H., Khodarahmi, S., Haghighi, M. (2014). Effect of silicon nutrition on lipid peroxidation and antioxidant response of cucumber plants exposed to salinity stress. Arch. Agron. Soil Sci. 60, 639–653. doi: 10.1080/03650340.2013.822487

CrossRef Full Text | Google Scholar

Kidd, P., Llugany, M., Poschenrieder, C., Gunse, B., Barcelo, J. (2001). The role of root exudates in aluminium resistance and silicon-induced amelioration of aluminium toxicity in three varieties of maize (Zea mays L.). J. Exp. Bot. 52, 1339–1352. doi: 10.1093/jexbot/52.359.1339

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, Y.-H., Khan, A. L., Lee, I.-J. (2016). Silicon: a duo synergy for regulating crop growth and hormonal signaling under abiotic stress conditions. Crit. Rev. Biotechnol. 36, 1099–1109. doi: 10.3109/07388551.2015.1084265

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, Y.-H., Khan, A. L., Hamayun, M., Kang, S. M., Beom, Y. J., Lee, I.-J. (2011). Influence of short-term silicon application on endogenous physiohormonal levels of Oryza sativa L. under wounding stress. Biol. Trace Element Res. 144, 1175–1185. doi: 10.1007/s12011-011-9047-4

CrossRef Full Text | Google Scholar

Kim, Y.-H., Khan, A. L., Kim, D.-H., Lee, S.-Y., Kim, K.-M., Waqas, M., et al. (2014a). Silicon mitigates heavy metal stress by regulating P-type heavy metal ATPases, Oryza sativa low silicon genes, and endogenous phytohormones. BMC Plant Biol. 14, 13. doi: 10.1186/1471-2229-14-13

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, Y.-H., Khan, A. L., Waqas, M., Lee, I.-J. (2017). Silicon regulates antioxidant activities of crop plants under abiotic-induced oxidative stress: a review. Front. Plant Sci. 8, 510. doi: 10.3389/fpls.2017.00510

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, Y. H., Khan, A. L., Waqas, M., Shim, J. K., Kim, D. H., Lee, K. Y., et al. (2014b). Silicon application to rice root zone influenced the phytohormonal and antioxidant responses under salinity stress. J. Plant Growth Regul. 33, 137–149. doi: 10.1007/s00344-013-9356-2

CrossRef Full Text | Google Scholar

Klotzbucher, A., Klotzbücher, T., Jahn, R., Van Chien, H., Hinrichs, M., Sann, C., et al. (2018). Effects of Si fertilization on Si in soil solution, Si uptake by rice, and resistance of rice to biotic stresses in Southern Vietnam. Paddy Water Environ., 16(2), 243–252. doi: 10.1007/s10333-017-0610-2

CrossRef Full Text | Google Scholar

Köster, P., Wallrad, L., Edel, K., Faisal, M., Alatar, A., Kudla, J. (2019). The battle of two ions: Ca2+ signalling against Na+ stress. Plant Biol. 21, 39–48. doi: 10.1111/plb.12704

CrossRef Full Text | Google Scholar

Kumar, V., Khare, T., Shaikh, S., Wani, S. H. (2018). Compatible solutes and abiotic stress tolerance in plants. In Metabolic adaptations in plants during abiotic stress (CRC Press.) pp. 213–220. doi: 10.1201/b22206-18

CrossRef Full Text | Google Scholar

Lee, S., Sohn, E., Hamayun, M., Yoon, J., Lee, I. (2010). Effect of silicon on growth and salinity stress of soybean plant grown under hydroponic system. Agroforestry Syst. 80, 333–340. doi: 10.1007/s10457-010-9299-6

CrossRef Full Text | Google Scholar

Li, H., Zhu, Y., Hu, Y., Han, W., Gong, H. (2015). Beneficial effects of silicon in alleviating salinity stress of tomato seedlings grown under sand culture. Acta Physiol. Plantarum 37, 71. doi: 10.1007/s11738-015-1818-7

CrossRef Full Text | Google Scholar

Li, Y.-T., Zhang, W.-J., Cui, J.-J., Lang, D.-Y., Li, M., Zhao, Q.-P., et al. (2016). Silicon nutrition alleviates the lipid peroxidation and ion imbalance of Glycyrrhiza uralensis seedlings under salt stress. Acta Physiol. Plant. 38, 96. doi: 10.1007/s11738-016-2108-8

CrossRef Full Text | Google Scholar

Liang, W., Ma, X., Wan, P., Liu, L. (2018). Plant salt-tolerance mechanism: a review. Biochem. Biophys. Res. Commun. 495, 286–291. doi: 10.1016/j.bbrc.2017.11.043

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, Y. (1999). Effects of silicon on enzyme activity and sodium, potassium and calcium concentration in barley under salt stress. Plant Soil 209, 217. doi: 10.1023/A:1004526604913

CrossRef Full Text | Google Scholar

Liang, Y., Chen, Q., Liu, Q., Zhang, W., Ding, R. (2003). Exogenous silicon (Si) increases antioxidant enzyme activity and reduces lipid peroxidation in roots of salt-stressed barley (Hordeum vulgareL.). J. Plant Physiol. 160, 1157–1164. doi: 10.1078/0176-1617-01065

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, Y., Hua, H., Zhu, Y. G., Zhang, J., Cheng, C., Römheld, V. (2006). Importance of plant species and external silicon concentration to active silicon uptake and transport. New Phytol. 172, 63–72. doi: 10.1111/j.1469-8137.2006.01797.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, Y., Si, J., Römheld, V. (2005a). Silicon uptake and transport is an active process in Cucumis sativus. New Phytol. 167, 797–804. doi: 10.1111/j.1469-8137.2005.01463.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, Y., Zhang, W., Chen, Q., Ding, R. (2005b). Effects of silicon on H+-ATPase and H+-PPase activity, fatty acid composition and fluidity of tonoplast vesicles from roots of salt-stressed barley (Hordeum vulgare L.). Environ. Exp. Bot. 53, 29–37. doi: 10.1016/j.envexpbot.2004.02.010

CrossRef Full Text | Google Scholar

Lins, U., Barros, C., Da Cunha, M., Miguens, F. C. (2002). Structure, morphology, and composition of silicon biocomposites in the palm tree Syagrus coronata (Mart.) Becc. Protoplasma 220, 0089–0096. doi: 10.1007/s00709-002-0036-5

CrossRef Full Text | Google Scholar

Liu, J.-H., Wang, W., Wu, H., Gong, X., Moriguchi, T. (2015). Polyamines function in stress tolerance: from synthesis to regulation. Front. Plant Sci. 6, 827. doi: 10.3389/fpls.2015.00827

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, W., Wang, L., Bai, Y. (2003). Research progress in the beneficial elements-silicon for plants. Acta Botanica Boreali-Occidentalia Sin. 23, 2248–2253.

Google Scholar

Luyckx, M., Hausman, J.-F., Lutts, S., Guerriero, G. (2017). Silicon and plants: current knowledge and technological perspectives. Front. Plant Sci. 8, 411. doi: 10.3389/fpls.2017.00411

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, J., Yamaji, N. (2008). Functions and transport of silicon in plants. Cell. Mol. Life Sci. 65, 3049–3057. doi: 10.1007/s00018-008-7580-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, J. F. (2004). Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses. Soil Sci. Plant Nutr. 50, 11–18. doi: 10.1080/00380768.2004.10408447

CrossRef Full Text | Google Scholar

Ma, J. F., Takahashi, E., (2002). Soil, fertilizer, and plant silicon research in Japan. Elsevier. doi: 10.1016/B978-044451166-9/50009-9

CrossRef Full Text | Google Scholar

Ma, J. F., Yamaji, N. (2006). Silicon uptake and accumulation in higher plants. Trends Plant Sci. 11, 392–397. doi: 10.1016/j.tplants.2006.06.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, J. F., Tamai, K., Yamaji, N., Mitani, N., Konishi, S., Katsuhara, M., et al. (2006). A silicon transporter in rice. Nature 440, 688. doi: 10.1038/nature04590

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, J. F., Yamaji, N., Mitani, N., Tamai, K., Konishi, S., Fujiwara, T., et al. (2007). An efflux transporter of silicon in rice. Nature 448, 209. doi: 10.1038/nature05964

PubMed Abstract | CrossRef Full Text | Google Scholar

Maggio, A., Barbieri, G., Raimondi, G., De Pascale, S. (2010). Contrasting effects of GA 3 treatments on tomato plants exposed to increasing salinity. J. Plant Growth Regul. 29, 63–72. doi: 10.1007/s00344-009-9114-7

CrossRef Full Text | Google Scholar

Mahajan, S., Tuteja, N. (2005). Cold, salinity and drought stresses: an overview. Arch. Biochem. Biophys. 444, 139–158. doi: 10.1016/j.abb.2005.10.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Maillard, A., Ali, N., Schwarzenberg, A., Jamois, F., Yvin, J.-C., Hosseini, S. A. (2018). Silicon transcriptionally regulates sulfur and ABA metabolism and delays leaf senescence in barley under combined sulfur deficiency and osmotic stress. Environ. Exp. Bot. 155, 394–410. doi: 10.1016/j.envexpbot.2018.07.026

CrossRef Full Text | Google Scholar

Malhotra, C., Kapoor, R. T. (2019). “Silicon: a sustainable tool in abiotic stress tolerance in plants,” in Plant Abiotic Stress Tolerance (Springer). doi: 10.1007/978-3-030-06118-0_14

CrossRef Full Text | Google Scholar

Mali, M., Aery, N. (2008). Influence of silicon on growth, relative water contents and uptake of silicon, calcium and potassium in wheat grown in nutrient solution. J. Plant Nutr. 31, 1867–1876. doi: 10.1080/01904160802402666

CrossRef Full Text | Google Scholar

Manchanda, G., Garg, N. (2008). Salinity and its effects on the functional biology of legumes. Acta Physiol. Plantarum 30, 595–618. doi: 10.1007/s11738-008-0173-3

CrossRef Full Text | Google Scholar

Marafon, A. C., Endres, L. (2013). Silicon: fertilization and nutrition in higher plants. Embrapa Tabuleiros Costeiros-Artigo Em Periódico Indexado (ALICE. Rev. Cienc. Agrar. 6, 80–88. doi: 10.4322/rca.2013.057

CrossRef Full Text | Google Scholar

Mateos-Naranjo, E., Andrades-Moreno, L., Davy, A. J. (2013). Silicon alleviates deleterious effects of high salinity on the halophytic grass Spartina densiflora. Plant Physiol. Biochem. 63, 115–121. doi: 10.1016/j.plaphy.2012.11.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Meena, V., Dotaniya, M., Coumar, V., Rajendiran, S., Kundu, S., Rao, A. S. (2014). A case for silicon fertilization to improve crop yields in tropical soils. Proc. Natl. Acad. Sci. India Sec. B: Biol. Sci. 84, 505–518. doi: 10.1007/s40011-013-0270-y

CrossRef Full Text | Google Scholar

Mitani, N., Ma, J. F. (2005). Uptake system of silicon in different plant species. J. Exp. Bot. 56, 1255–1261. doi: 10.1093/jxb/eri121

PubMed Abstract | CrossRef Full Text | Google Scholar

Mitani, N., Chiba, Y., Yamaji, N., Ma, J. F. (2009). Identification and characterization of maize and barley Lsi2-like silicon efflux transporters reveals a distinct silicon uptake system from that in rice. Plant Cell 21, 2133–2142. doi: 10.1105/tpc.109.067884

PubMed Abstract | CrossRef Full Text | Google Scholar

Mitani, N., Ma, J. F., Iwashita, T. (2005). Identification of the silicon form in xylem sap of rice (Oryza sativa L.). Plant Cell Physiol. 46, 279–283. doi: 10.1093/pcp/pci018

PubMed Abstract | CrossRef Full Text | Google Scholar

Mitani, N., Yamaji, N., Ago, Y., Iwasaki, K., Ma, J. F. (2011). Isolation and functional characterization of an influx silicon transporter in two pumpkin cultivars contrasting in silicon accumulation. Plant J. 66, 231–240. doi: 10.1111/j.1365-313X.2011.04483.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Montpetit, J., Vivancos, J., Mitani-Ueno, N., Yamaji, N., Rémus-Borel, W., Belzile, F., et al. (2012). Cloning, functional characterization and heterologous expression of TaLsi1, a wheat silicon transporter gene. Plant Mol. Biol. 79, 35–46. doi: 10.1007/s11103-012-9892-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Moussa, H. R. (2006). Influence of exogenous application of silicon on physiological response of salt-stressed maize (Zea mays L.). Int. J. Agric. Biol. 8, 293–297.

Google Scholar

Munns, R. (2002). Comparative physiology of salt and water stress. Plant Cell Environ. 25, 239–250. doi: 10.1046/j.0016-8025.2001.00808.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Najar, R., Aydi, S., Sassi-Aydi, S., Zarai, A., Abdelly, C. (2019). Effect of salt stress on photosynthesis and chlorophyll fluorescence in Medicago truncatula. Plant Biosys.-An Int. J. Dealing All Aspects Plant Biol. 153, 88–97. doi: 10.1080/11263504.2018.1461701

CrossRef Full Text | Google Scholar

Negrao, S., Schmöckel, S., Tester, M. (2017). Evaluating physiological responses of plants to salinity stress. Ann. Bot. 119, 1–11. doi: 10.1093/aob/mcw191

PubMed Abstract | CrossRef Full Text | Google Scholar

Netondo, G. W., Onyango, J. C., Beck, E. (2004). Sorghum and salinity: II. Gas exchange and chlorophyll fluorescence of sorghum under salt stress. Crop Sci. 44, 806. doi: 10.2135/cropsci2004.0806

CrossRef Full Text | Google Scholar

Nilsen, E. T., Orcutt, D. M. (1996). Physiology of plants under stress. Abiotic factors. Physiology of plants under stress. Abiotic factors.

Google Scholar

Nikolic, D. B., Nesic, S., Bosnic, D., Kostic, L., Nikolic, M., Samardzic, J. T. (2019). Silicon alleviates iron deficiency in barley by enhancing expression of Strategy II genes and metal redistribution. Front. Plant Sci. 10, 416. doi: 10.3389/fpls.2019.00416

PubMed Abstract | CrossRef Full Text | Google Scholar

Nounjan, N., Nghia, P. T., Theerakulpisut, P. (2012). Exogenous proline and trehalose promote recovery of rice seedlings from salt-stress and differentially modulate antioxidant enzymes and expression of related genes. J. Plant Physiol. 169, 596–604. doi: 10.1016/j.jplph.2012.01.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Numan, M., Bashir, S., Khan, Y., Mumtaz, R., Shinwari, Z. K., Khan, A. L., et al. (2018). Plant growth promoting bacteria as an alternative strategy for salt tolerance in plants: a review. Microbiol. Res. 209, 21–32. doi: 10.1016/j.micres.2018.02.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Oh, D.-H., Lee, S. Y., Bressan, R. A., Yun, D.-J., Bohnert, H. J. (2010). Intracellular consequences of SOS1 deficiency during salt stress. J. Exp. Bot. 61, 1205–1213. doi: 10.1093/jxb/erp391

PubMed Abstract | CrossRef Full Text | Google Scholar

Otoch, M. D. L. O., Sobreira, A. C. M., De Aragão, M. E. F., Orellano, E. G., Lima, M. D. G. S., De Melo, D. F. (2001). Salt modulation of vacuolar H+-ATPase and H+-Pyrophosphatase activities in Vigna unguiculata. J. Plant Physiol. 158, 545–551. doi: 10.1078/0176-1617-00310

CrossRef Full Text | Google Scholar

Parida, A. K., Das, A. B. (2005). Salt tolerance and salinity effects on plants: a review. Ecotoxicol. Environ. Saf. 60, 324–349. doi: 10.1016/j.ecoenv.2004.06.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Parveen, N., Ashraf, M. (2010). Role of silicon in mitigating the adverse effects of salt stress on growth and photosynthetic attributes of two maize (Zea mays L.) cultivars grown hydroponically. Pak J. Bot. 42, 1675–1684.

Google Scholar

Peleg, Z., Blumwald, E. (2011). Hormone balance and abiotic stress tolerance in crop plants. Curr. Opin. Plant Biol. 14, 290–295. doi: 10.1016/j.pbi.2011.02.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Pontigo, S., Godoy, K., Jiménez, H., Gutiérrez-Moraga, A., Mora, M. D. L. L., Cartes, P. (2017). Silicon-Mediated Alleviation of Aluminum Toxicity by Modulation of Al/Si Uptake and Antioxidant Performance in Ryegrass Plants. Front. Plant Sci. 8, 642. doi: 10.3389/fpls.2017.00642

PubMed Abstract | CrossRef Full Text | Google Scholar

Pontigo, S., Ribera, A., Gianfreda, L., La Luz Mora, M., Nikolic, M., Cartes, P. (2015). Silicon in vascular plants: uptake, transport and its influence on mineral stress under acidic conditions. Planta 242, 23–37. doi: 10.1007/s00425-015-2333-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Qiu, Q.-S., Guo, Y., Dietrich, M. A., Schumaker, K. S., Zhu, J.-K. (2002). Regulation of SOS1, a plasma membrane Na+/H+ exchanger in Arabidopsis thaliana, by SOS2 and SOS3. Proc. Natl. Acad. Sci. 99, 8436–8441. doi: 10.1073/pnas.122224699

CrossRef Full Text | Google Scholar

Rahimi, R., Mohammakhani, A., Roohi, V., Armand, N. (2012). Effects of salt stress and silicon nutrition on cholorophyll content, yield and yield components in fennel (Foeniculum vulgar Mill.). Int. J. Agric. Crop Sci. 4, 1591–1595.

Google Scholar

Rahman, M. S., Miyake, H., Takeoka, Y. (2002). Effects of exogenous glycinebetaine on growth and ultrastructure of salt-stressed rice seedlings (Oryza sativa L.). Plant Prod. Sci. 5, 33–44. doi: 10.1626/pps.5.33

CrossRef Full Text | Google Scholar

Rains, D., Epstein, E., Zasoski, R., Aslam, M. (2006). Active silicon uptake by wheat. Plant Soil 280, 223–228. doi: 10.1007/s11104-005-3082-x

CrossRef Full Text | Google Scholar

Rajasheker, G., Jawahar, G., Jalaja, N., Kumar, S. A., Kumari, P. H., Punita, D. L., Kishor, P. B. K. (2019). Role and regulation of osmolytes and ABA interaction in salt and drought stress tolerance. In Plant Signaling Molecules. Woodhead Publishing. p. 417–436 doi: 10.1016/B978-0-12-816451-8.00026-5

CrossRef Full Text | Google Scholar

Raven, J. A. (2003). Cycling silicon-the role of accumulation in plants. New Phytol. 158, 419–421. doi: 10.1046/j.1469-8137.2003.00778.x

CrossRef Full Text | Google Scholar

Reguera, M., Peleg, Z., Blumwald, E. (2012). Targeting metabolic pathways for genetic engineering abiotic stress-tolerance in crops. Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms, 1819(2), 186-194.

Google Scholar

Rehman, S., Abbas, G., Shahid, M., Saqib, M., Farooq, A. B. U., Hussain, M., et al. (2019). Effect of salinity on cadmium tolerance, ionic homeostasis and oxidative stress responses in conocarpus exposed to cadmium stress: Implications for phytoremediation. Ecotoxicol. Environ. Saf. 171, 146–153. doi: 10.1016/j.ecoenv.2018.12.077

PubMed Abstract | CrossRef Full Text | Google Scholar

Rezende, R.a.L.S., Rodrigues, F. A., Soares, J. D. R., Silveira, H. R. D. O., Pasqual, M., Dias, G. D. M. G. (2018). Salt stress and exogenous silicon influence physiological and anatomical features of in vitro-grown cape gooseberry. Ciec. Rural 48(1). doi: 10.1590/0103-8478cr20170176

CrossRef Full Text | Google Scholar

Riaz, M., Arif, M. S., Ashraf, M. A., Mahmood, R., Yasmeen, T., Shakoor, M. B., et al., (2019). “A comprehensive review on rice responses and tolerance to salt stress,” in Advances in Rice Research for Abiotic Stress Tolerance (Elsevier), 133–158. doi: 10.1016/B978-0-12-814332-2.00007-1

CrossRef Full Text | Google Scholar

Rios, J. J., Martínez-Ballesta, M. C., Ruiz, J. M., Blasco, B., Carvajal, M. (2017). Silicon-mediated improvement in plant salinity tolerance: the role of aquaporins. Front. Plant Sci. 8, 948. doi: 10.3389/fpls.2017.00948

PubMed Abstract | CrossRef Full Text | Google Scholar

Rizwan, M., Ali, S., Ibrahim, M., Farid, M., Adrees, M., Bharwana, S. A., et al. (2015). Mechanisms of silicon-mediated alleviation of drought and salt stress in plants: a review. Environ. Sci. Pollut. Res. 22, 15416–15431. doi: 10.1007/s11356-015-5305-x

CrossRef Full Text | Google Scholar

Rodrigues, F. A., Datnoff, L. E. (Eds.) (2015). Silicon and plant diseases. (Cham, Switz: Springer). doi: 10.1007/978-3-319-22930-0

CrossRef Full Text | Google Scholar

Romero-Aranda, M. R., Jurado, O., Cuartero, J. (2006). Silicon alleviates the deleterious salt effect on tomato plant growth by improving plant water status. J. Plant Physiol. 163, 847–855. doi: 10.1016/j.jplph.2005.05.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Roy, S. J., Negrão, S., Tester, M. (2014). Salt resistant crop plants. Curr. Opin. Biotechnol. 26, 115–124. doi: 10.1016/j.copbio.2013.12.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Ryu, H., Cho, Y.-G. (2015). Plant hormones in salt stress tolerance. J. Plant Biol. 58, 147–155. doi: 10.1007/s12374-015-0103-z

CrossRef Full Text | Google Scholar

Safdar, H., Amin, A., Shafiq, Y., Ali, A., Yasin, R., Shoukat, A., et al. (2019). A review: impact of salinity on plant growth. Nat. Sci. 17, 34–40.

Google Scholar

Sah, S. K., Reddy, K. R., Li, J. (2016). Abscisic acid and abiotic stress tolerance in crop plants. Front. Plant Sci. 7, 571. doi: 10.3389/fpls.2016.00571

PubMed Abstract | CrossRef Full Text | Google Scholar

Saini, P., Gani, M., Kaur, J. J., Godara, L. C., Singh, C., Chauhan, S., et al. (2018). “Reactive oxygen species (ROS): a way to stress survival in plants,” in Abiotic Stress-Mediated Sensing and Signaling in Plants: An Omics Perspective (Singapore: Springer), 127–153. doi: 10.1007/978-981-10-7479-0_4

CrossRef Full Text | Google Scholar

Sairam, R., Tyagi, A. (2004). Physiological and molecular biology of salinity stress tolerance in deficient and cultivated genotypes of chickpea. Plant Growth Regul. 57(10), 109–114.

Google Scholar

Sakhabutdinova, A., Fatkhutdinova, D., Bezrukova, M., Shakirova, F. (2003). Salicylic acid prevents the damaging action of stress factors on wheat plants. Bulg. J. Plant Physiol. 21, 314–319.

Google Scholar

Saleh, J., Najafi, N., Oustan, S. (2017). Effects of silicon application on wheat growth and some physiological characteristics under different levels and sources of salinity. Commun. Soil Sci. Plant Anal. 48, 1114–1122. doi: 10.1080/00103624.2017.1323090

CrossRef Full Text | Google Scholar

Saqib, M., Zörb, C., Schubert, S. (2008). Silicon-mediated improvement in the salt resistance of wheat (Triticum aestivum) results from increased sodium exclusion and resistance to oxidative stress. Funct. Plant Biol. 35, 633–639. doi: 10.1071/FP08100

CrossRef Full Text | Google Scholar

Savvas, D., Giotis, D., Chatzieustratiou, E., Bakea, M., Patakioutas, G. (2009). Silicon supply in soilless cultivations of zucchini alleviates stress induced by salinity and powdery mildew infections. Environ. Exp. Bot. 65, 11–17. doi: 10.1016/j.envexpbot.2008.07.004

CrossRef Full Text | Google Scholar

Saxena, S. C., Kaur, H., Verma, P., Petla, B. P., Andugula, V. R., Majee, M. (2013). “Osmoprotectants: potential for crop improvement under adverse conditions,” in Plant Acclimation to Environmental Stress (New York, NY: Springer), 197–232. doi: 10.1007/978-1-4614-5001-6_9

CrossRef Full Text | Google Scholar

Seal, P., Das, P., Biswas, A. K. (2018). Versatile potentiality of silicon in mitigation of biotic and abiotic stresses in plants: a review. Am. J. Plant Sci. 9, 1433. doi: 10.4236/ajps.2018.97105

CrossRef Full Text | Google Scholar

Seckin, B., Sekmen, A. H., Türkan, I. (2009). An enhancing effect of exogenous mannitol on the antioxidant enzyme activities in roots of wheat under salt stress. J. Plant Growth Regul. 28, 12. doi: 10.1007/s00344-008-9068-1

CrossRef Full Text | Google Scholar

Serraj, R., Sinclair, T. R. (2002). Osmolyte accumulation: can it really help increase crop yield under drought conditions?. Plant Cell Environ. 25(2), 333-341.

PubMed Abstract | Google Scholar

Shah, F., Wu, W. (2019). Soil and crop management strategies to ensure higher crop productivity within sustainable environments. Sustainability 11, 1485. doi: 10.3390/su11051485

CrossRef Full Text | Google Scholar

Shahid, S. A., Zaman, M., Heng, L., (2018). “Soil salinity: historical perspectives and a world overview of the problem,” in Guideline for Salinity Assessment, Mitigation and Adaptation Using Nuclear and Related Techniques (Springer, Cham), 43–53. doi: 10.1007/978-3-319-96190-3_2

CrossRef Full Text | Google Scholar

Shahnaz, G., Shekoofeh, E., Kourosh, D., Moohamadbagher, B. (2011). Interactive effects of silicon and aluminum on the malondialdehyde (MDA), proline, protein and phenolic compounds in Borago officinalis L. J. Med. Plants Res. 5, 5818–5827.

Google Scholar

Shahzad, M., Zörb, C., Geilfus, C. M., Mühling, K. (2013). Apoplastic Na+ in Vicia faba leaves rises after short-term salt stress and is remedied by silicon. J. Agron. Crop Sci. 199, 161–170. doi: 10.1111/jac.12003

CrossRef Full Text | Google Scholar

Shen, X., Xiao, X., Dong, Z., Chen, Y. (2014). Silicon effects on antioxidative enzymes and lipid peroxidation in leaves and roots of peanut under aluminum stress. Acta Physiol. Plantarum 36, 3063–3069. doi: 10.1007/s11738-014-1676-8

CrossRef Full Text | Google Scholar

Shi, H., Ishitani, M., Kim, C., Zhu, J.-K. (2000). The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter. Proc. Natl. Acad. Sci. 97, 6896–6901. doi: 10.1073/pnas.120170197

CrossRef Full Text | Google Scholar

Shi, H., Quintero, F. J., Pardo, J. M., Zhu, J.-K. (2002). The putative plasma membrane Na+/H+ antiporter SOS1 controls long-distance Na+ transport in plants. Plant Cell 14, 465–477. doi: 10.1105/tpc.010371

PubMed Abstract | CrossRef Full Text | Google Scholar

Shrivastava, P., Kumar, R. (2015). Soil salinity: a serious environmental issue and plant growth promoting bacteria as one of the tools for its alleviation. Saudi J. Biol. Sci. 22, 123–131. doi: 10.1016/j.sjbs.2014.12.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Simura, J., Antoniadi, I., Siroka, J., Tarkowska, D., Strnad, M., Ljung, K., et al. (2018). Plant hormonomics: multiple phytohormone profiling by targeted metabolomics. Plant Physiol. 177, 476–489. doi: 10.1104/pp.18.00293

PubMed Abstract | CrossRef Full Text | Google Scholar

Singh, K., Chatrath, R. (2001). “Application of physiology in wheat breeding. international maiz,” in Wheat Improvement Center (CIMMYT). Eds. Reynolds, M. P., Monasterio, J. I. O., Mc Nab, A., 101–110.

Google Scholar

Sivanesan, I., Jeong, B. R. (2014). Silicon promotes adventitious shoot regeneration and enhances salinity tolerance of ajuga multiflora bunge by altering activity of antioxidant enzyme. Sci. World J. 2014, 10. doi: 10.1155/2014/521703

CrossRef Full Text | Google Scholar

Smirnoff, N. (1997). “The physiology of plants under stress,” in Abiotic factors (JSTOR).

Google Scholar

Soleimannejad, Z., Abdolzadeh, A., Sadeghipour, H. R. (2019). Beneficial effects of silicon application in alleviating salinity stress in halophytic puccinellia distans plants. Silicon 11, 1001–1010. doi: 10.1007/s12633-018-9960-7

CrossRef Full Text | Google Scholar

Sommer, M., Kaczorek, D., Kuzyakov, Y., Breuer, J. (2006). Silicon pools and fluxes in soils and landscapes-a review. J. Plant Nutr. Soil Sci. 169, 310–329. doi: 10.1002/jpln.200521981

CrossRef Full Text | Google Scholar

Soratto, R. P., Crusciol, C.a.C., Castro, G. S. A., Costa, C. H. M. D., Ferrari Neto, J. (2012). Leaf application of silicic acid to white oat and wheat. Rev. Bras. Ciec. Do Solo 36, 1538–1544. doi: 10.1590/S0100-06832012000500018

CrossRef Full Text | Google Scholar

Soundararajan, P., Manivannan, A., Ko, C. H., Jeong, B. R. (2018). Silicon enhanced redox homeostasis and protein expression to mitigate the salinity stress in Rosa hybrida 'Rock Fire'. J. Plant Growth Regul. 37, 16–34. doi: 10.1007/s00344-017-9705-7

CrossRef Full Text | Google Scholar

Soylemezoglu, G., Demir, K., Inal, A., Gunes, A. (2009). Effect of silicon on antioxidant and stomatal response of two grapevine (Vitis vinifera L.) rootstocks grown in boron toxic, saline and boron toxic-saline soil. Scientia Hortic. 123, 240–246. doi: 10.1016/j.scienta.2009.09.005

CrossRef Full Text | Google Scholar

Sung, C. H., Hong, J. K. (2010). Sodium nitroprusside mediates seedling development and attenuation of oxidative stresses in Chinese cabbage. Plant Biotechnol. Rep. 4, 243–251. doi: 10.1007/s11816-010-0138-z

CrossRef Full Text | Google Scholar

Suo, J., Zhao, Q., David, L., Chen, S., Dai, S. (2017). Salinity response in chloroplasts: insights from gene characterization. Int. J. Mol. Sci. 18, 1011. doi: 10.3390/ijms18051011

CrossRef Full Text | Google Scholar

Tahir, M. A., Aziz, T., Rahmatullah, (2011). Silicon-induced growth and yield enhancement in two wheat genotypes differing in salinity tolerance. Commun. Soil Sci. Plant Anal. 42, 395–407. doi: 10.1080/00103624.2011.542219

CrossRef Full Text | Google Scholar

Tahir, M. A., Aziz, T., Farooq, M., Sarwar, G. (2012). Silicon-induced changes in growth, ionic composition, water relations, chlorophyll contents and membrane permeability in two salt-stressed wheat genotypes. Arch. Agron. Soil Sci. 58, 247–256. doi: 10.1080/03650340.2010.518959

CrossRef Full Text | Google Scholar

Tahir, M. A., Rahmatullah, T., Aziz, M., Ashraf, S., Kanwal, S., Maqsood, M. A. (2006). Beneficial effects of silicon in wheat (Triticum aestivum L.) under salinity stress. Pakistan J. Bot. 38, 1715–1722.

Google Scholar

Takahashi, E., Ma, J., Miyake, Y. (1990). The possibility of silicon as an essential element for higher plants. Comments Agric. Food Chem. 2, 99–102.

Google Scholar

Tavakkoli, E., Rengasamy, P., Mcdonald, G. K. (2010). High concentrations of Na+ and Cl-ions in soil solution have simultaneous detrimental effects on growth of faba bean under salinity stress. J. Exp. Bot. 61, 4449–4459. doi: 10.1093/jxb/erq251

PubMed Abstract | CrossRef Full Text | Google Scholar

Torabi, F., Majd, A., Enteshari, S. (2015). The effect of silicon on alleviation of salt stress in borage (Borago officinalis L.). Soil Sci. Plant Nutr. 61, 788–798. doi: 10.1080/00380768.2015.1005540

CrossRef Full Text | Google Scholar

Tripathi, D., Bashri, G., Shweta, S., Ahmad, P., Singh, V. (2017). Efficacy of silicon against aluminum toxicity in plants: an overview. Silicon Plants: Adv. Future Prospects 1, 355–366. doi: 10.1201/9781315369310-20

CrossRef Full Text | Google Scholar

Tuna, A. L., Kaya, C., Higgs, D., Murillo-Amador, B., Aydemir, S., Girgin, A. R. (2008). Silicon improves salinity tolerance in wheat plants. Environ. Exp. Bot. 62, 10–16. doi: 10.1016/j.envexpbot.2007.06.006

CrossRef Full Text | Google Scholar

Turkan, I. (2011). Plant responses to drought and salinity stress: developments in a post-genomic era. Academic Press.

Google Scholar

Tuteja, N., Sahoo, R. K., Garg, B., Tuteja, R. (2013). O s SUV 3 dual helicase functions in salinity stress tolerance by maintaining photosynthesis and antioxidant machinery in rice (O ryza sativa L. cv. IR 64). Plant J. 76, 115–127. doi: 10.1111/tpj.12277

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Bockhaven, J., De Vleesschauwer, D., Höfte, M. (2012). Towards establishing broad-spectrum disease resistance in plants: silicon leads the way. J. Exp. Bot. 64, 1281–1293. doi: 10.1093/jxb/ers329

PubMed Abstract | CrossRef Full Text | Google Scholar

Vivancos, J., Labbé, C., Menzies, J. G., Bélanger, R. R. (2015). Silicon-mediated resistance of A rabidopsis against powdery mildew involves mechanisms other than the salicylic acid (SA)-dependent defence pathway. Mol. Plant Pathol. 16, 572–582. doi: 10.1111/mpp.12213

PubMed Abstract | CrossRef Full Text | Google Scholar

Vyrides, I., Stuckey, D. C. (2017). Compatible solute addition to biological systems treating waste/wastewater to counteract osmotic and other environmental stresses: a review. Crit. Rev. Biotechnol. 37, 865–879. doi: 10.1080/07388551.2016.1266460

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, B., Lüttge, U., Ratajczak, R. (2001a). Effects of salt treatment and osmotic stress on V-ATPase and V-PPase in leaves of the halophyte Suaeda salsa. J. Exp. Bot. 52, 2355–2365. doi: 10.1093/jexbot/52.365.2355

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, H.-S., Yu, C., Fan, P.-P., Bao, B.-F., Li, T., Zhu, Z.-J. (2015a). Identification of two cucumber putative silicon transporter genes in Cucumis sativus. J. Plant Growth Regul. 34, 332–338. doi: 10.1007/s00344-014-9466-5

CrossRef Full Text | Google Scholar

Wang, S., Liu, P., Chen, D., Yin, L., Li, H., Deng, X. (2015b). Silicon enhanced salt tolerance by improving the root water uptake and decreasing the ion toxicity in cucumber. Front. Plant Sci. 6, 759. doi: 10.3389/fpls.2015.00759

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, W., Xu, Y., Chen, T., Xing, L., Xu, K., Ji, D., et al. (2019). Regulatory mechanisms underlying the maintenance of homeostasis in Pyropia haitanensis under hypersaline stress conditions. Sci. Total Environ. 662, 168–179. doi: 10.1016/j.scitotenv.2019.01.214

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X. S., Han, J. G. (2007). Effects of NaCl and silicon on ion distribution in the roots, shoots and leaves of two alfalfa cultivars with different salt tolerance. Soil Sci. Plant Nutr. 53, 278–285. doi: 10.1111/j.1747-0765.2007.00135.x

CrossRef Full Text | Google Scholar

Wang, Y., Nii, N. (2000). Changes in chlorophyll, ribulose bisphosphate carboxylase-oxygenase, glycine betaine content, photosynthesis and transpiration in Amaranthus tricolor leaves during salt stress. J. Hortic. Sci. Biotechnol. 75, 623–627. doi: 10.1080/14620316.2000.11511297

CrossRef Full Text | Google Scholar

Wang, Y., Mopper, S., Hasenstein, K. H. (2001b). Effects of salinity on endogenous ABA, IAA, JA, and SA in Iris hexagona. J. Chem. Ecol. 27, 327–342. doi: 10.1023/A:1005632506230

PubMed Abstract | CrossRef Full Text | Google Scholar

Wani, S. H., Kumar, V., Shriram, V., Sah, S. K. (2016). Phytohormones and their metabolic engineering for abiotic stress tolerance in crop plants. Crop J. 4, 162–176. doi: 10.1016/j.cj.2016.01.010

CrossRef Full Text | Google Scholar

Winterbourn, C. C. (2019). “Reactive oxygen species in biological systems,” in Vitamin E, 98–117. doi: 10.1039/9781788016216-00098

CrossRef Full Text | Google Scholar

Wu, J., Mock, H.-P., Giehl, R. F., Pitann, B., Mühling, K. H. (2019). Silicon decreases cadmium concentrations by modulating root endodermal suberin development in wheat plants. J. Hazard. Materials 364, 581–590. doi: 10.1016/j.jhazmat.2018.10.052

CrossRef Full Text | Google Scholar

Yamaguchi, T., Hamamoto, S., Uozumi, N. (2013). Sodium transport system in plant cells. Front. Plant Sci. 4, 410. doi: 10.3389/fpls.2013.00410

PubMed Abstract | CrossRef Full Text | Google Scholar

Yan, G.-C., Nikolic, M., Ye, M.-J., Xiao, Z.-X., Liang, Y.-C. (2018). Silicon acquisition and accumulation in plant and its significance for agriculture. J. Integr. Agric. 17, 2138–2150. doi: 10.1016/S2095-3119(18)62037-4

CrossRef Full Text | Google Scholar

Yeo, A., Flowers, S., Rao, G., Welfare, K., Senanayake, N., Flowers, T. (1999). Silicon reduces sodium uptake in rice (Oryza sativa L.) in saline conditions and this is accounted for by a reduction in the transpirational bypass flow. Plant Cell Environ. 22, 559–565. doi: 10.1046/j.1365-3040.1999.00418.x

CrossRef Full Text | Google Scholar

Yin, J., Jia, J., Lian, Z., Hu, Y., Guo, J., Huo, H., et al. (2019). Silicon enhances the salt tolerance of cucumber through increasing polyamine accumulation and decreasing oxidative damage. Ecotoxicol. Environ. Saf. 169, 8–17. doi: 10.1016/j.ecoenv.2018.10.105

PubMed Abstract | CrossRef Full Text | Google Scholar

Yin, L., Wang, S., Li, J., Tanaka, K., Oka, M. (2013). Application of silicon improves salt tolerance through ameliorating osmotic and ionic stresses in the seedling of Sorghum bicolor. Acta Physiol. Plant. 35, 3099–3107. doi: 10.1007/s11738-013-1343-5

CrossRef Full Text | Google Scholar

Yoon, J. Y., Hamayun, M., Lee, S.-K., Lee, I.-J. (2009). Methyl jasmonate alleviated salinity stress in soybean. J. Crop Sci. Biotechnol. 12, 63–68. doi: 10.1007/s12892-009-0060-5

CrossRef Full Text | Google Scholar

Yoshida, S. (1965). Chemical aspects of the role of silicon in physiology of the rice plant. Bull. Nat. Inst. Agr. Sci. 15, 18–58.

Google Scholar

Yue, Y., Zhang, M., Zhang, J., Duan, L., Li, Z. (2012). SOS1 gene overexpression increased salt tolerance in transgenic tobacco by maintaining a higher K+/Na+ ratio. J. Plant Physiol. 169, 255–261. doi: 10.1016/j.jplph.2011.10.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Zaefyzadeh, M., Quliyev, R. A., Babayeva, S. M., Abbasov, M. A. (2009). The effect of the interaction between genotypes and drought stress on the superoxide dismutase and chlorophyll content in durum wheat landraces. Turkish J. Biol. 33, 1–7.

Google Scholar

Zhang, F., Yang, Y., He, W., Zhao, X., Zhang, L. (2004). Effects of salinity on growth and compatible solutes of callus induced from Populus euphratica. In Vitro Cell. Dev. Biol.-Plant 40, 491–494. doi: 10.1079/IVP2004546

CrossRef Full Text | Google Scholar

Zhang, J., Wei, J., Li, D., Kong, X., Rengel, Z., Chen, L., et al. (2017). The role of the plasma membrane H+-ATPase in plant responses to aluminum toxicity. Front. Plant Sci. 8, 1757. doi: 10.3389/fpls.2017.01757

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, X., Zhang, W., Lang, D., Cui, J., Li, Y. (2018). Silicon improves salt tolerance of Glycyrrhiza uralensis Fisch. by ameliorating osmotic and oxidative stresses and improving phytohormonal balance. Environ. Sci. Pollut. Res. 25, 25916–25932. doi: 10.1007/s11356-018-2595-9

CrossRef Full Text | Google Scholar

Zhao, M.-G., Chen, L., Zhang, L.-L., Zhang, W.-H. (2009). Nitric reductase-dependent nitric oxide production is involved in cold acclimation and freezing tolerance in Arabidopsis. Plant Physiol. 151, 755–767. doi: 10.1104/pp.109.140996

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, Y., Guo, J., Feng, R., Jia, J., Han, W., Gong, H. (2016). The regulatory role of silicon on carbohydrate metabolism in Cucumis sativus L. under salt stress. Plant Soil, 406(1-2), 231–249.

Google Scholar

Zhu, Y., Gong, H. (2014). Beneficial effects of silicon on salt and drought tolerance in plants. Agron. Sustain. Dev. 34, 455–472. doi: 10.1007/s13593-013-0194-1

CrossRef Full Text | Google Scholar

Zhu, Z., Wei, G., Li, J., Qian, Q., Yu, J. (2004). Silicon alleviates salt stress and increases antioxidant enzymes activity in leaves of salt-stressed cucumber (Cucumis sativus L.). Plant Sci. 167, 527–533. doi: 10.1016/j.plantsci.2004.04.020

CrossRef Full Text | Google Scholar