<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJSS</journal-id><journal-title-group><journal-title>Open Journal of Soil Science</journal-title></journal-title-group><issn pub-type="epub">2162-5360</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojss.2019.911013</article-id><article-id pub-id-type="publisher-id">OJSS-96151</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Earth&amp;Environmental Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Review on Plant Responses to Soil Salinity and Amelioration Strategies
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohammad</surname><given-names>Golam Kibria</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Md.</surname><given-names>Anamul Hoque</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Soil Science, Bangladesh Agricultural University, Mymensingh, Bangladesh</addr-line></aff><pub-date pub-type="epub"><day>01</day><month>11</month><year>2019</year></pub-date><volume>09</volume><issue>11</issue><fpage>219</fpage><lpage>231</lpage><history><date date-type="received"><day>7,</day>	<month>October</month>	<year>2019</year></date><date date-type="rev-recd"><day>29,</day>	<month>October</month>	<year>2019</year>	</date><date date-type="accepted"><day>1,</day>	<month>November</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Soil salinity is a major abiotic stress, limiting plant growth and development worldwide. Plants grown under saline soil condition experiences a significant amount of high osmotic stress, ion toxicities and nutritional disorder, and these are responsible for poor soil physical condition as well as lead to reduced plant productivity. Plants exhibit a number of responses under salt stress by affecting morphological, physiological and biochemical process. A complete understanding of how plants respond to soil salinity and comprehensive management approaches of combining physiological and biochemical attributes with molecular tools are essential for mitigating the adverse effects of salinity on plant growth and productivity. Recent reports on the plant responses due to soil salinity highlighted the importance of integration of different advanced strategies to address the problem of soil salinity. This review will focus on morphological and physiological changes of plants under saline soil and an overview of suitable strategies to regulate plant adaptation and tolerance to salinity stress.
 
</p></abstract><kwd-group><kwd>Salinity</kwd><kwd> Antioxidant Enzymes</kwd><kwd> Adaptation To Salinity</kwd><kwd> Proline</kwd><kwd> Plant Physiology</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Saline soil is one of the major environmental threats that limit plant growth due to high salt concentration and the process of increasing salt content is known as salinization [<xref ref-type="bibr" rid="scirp.96151-ref1">1</xref>]. Soil salinization is a global land degradation issue [<xref ref-type="bibr" rid="scirp.96151-ref2">2</xref>] and mostly affects the coastal areas by developing soil salinity. Approximately 7% of the total world’s land, 20% of the world’s cultivated land and nearly half of the irrigated land are affected by soil salinity [<xref ref-type="bibr" rid="scirp.96151-ref1">1</xref>]. Furthermore, the salt-affected areas are increasing annually by 10% each year and if the problem is not addressed now, more than 50% of the arable land would be salinized by the year 2050 [<xref ref-type="bibr" rid="scirp.96151-ref3">3</xref>].</p><p>Soil salinity imposes a significant number of negative impacts on plants growth and productivity. Reduced plant growth and productivity may result from an unbalanced supply of photosynthetic assimilates or hormones to the growing tissues [<xref ref-type="bibr" rid="scirp.96151-ref4">4</xref>]. In addition, ionic toxicity in saline soil can also contribute to limiting plant growth due to the replacement of K<sup>+</sup> by Na<sup>+</sup> in biochemical reactions, and Na<sup>+</sup> and Cl<sup>−</sup> induced conformational changes in proteins [<xref ref-type="bibr" rid="scirp.96151-ref5">5</xref>]. Ionic toxicities may also cause metabolic imbalance and protein synthesis [<xref ref-type="bibr" rid="scirp.96151-ref6">6</xref>]. The adverse effects of salinity on plant development are more profound during the reproductive phase and lead to cell cycle imbalance and differentiation. Hence, the adverse effects of salinity may be attributed to the salt-stress effect on the cell cycle and differentiation. Salt tress restricts cell cycle transiently by interfering with cyclins and kinase activities within the plant system, and thereby results in fewer cells in the meristem, thus limiting growth [<xref ref-type="bibr" rid="scirp.96151-ref1">1</xref>]. Salt stress may also affect plant growth by interfering in seed germination, enzymatic activity and unbalancing mitosis [<xref ref-type="bibr" rid="scirp.96151-ref7">7</xref>].</p><p>Soil salinity is a prevalent abiotic stress that alters geographical distribution of plants. The impact of salinity is most serious in countries where all or most of agricultural production is based on irrigation [<xref ref-type="bibr" rid="scirp.96151-ref8">8</xref>]. As irrigated agriculture expands, more salinity problems will develop because there are millions of hectares of potentially irrigable land that could become saline. A lot of research has been conducted on this issue and it is found that it has many detrimental effects on plant growth and development [<xref ref-type="bibr" rid="scirp.96151-ref9">9</xref>]. There are many factors that influence plant responses to salinity by affecting plant growth and production. The effects of osmotic stress can also be observed in different physiological and biochemical parameters of plants. Researchers have identified a number of plant responses due to soil salinity and also recommended different approaches to address the problem. But there is a lack of coordination between the plants physiological as well as biochemical responses with a possible selection of management strategies. Therefore, the objective of this review is to explore the effects of salinity on plant growth and how management practices can prevent soil and water salinization and mitigate the adverse effects of salinity. The design of framework has been presented in <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p></sec><sec id="s2"><title>2. How Plants Respond to Soil Salinity?</title><p>Plants show differential responses to salinity which is efficiently expressed into physiological attributes adopting or alleviating the shock from salt stress [<xref ref-type="bibr" rid="scirp.96151-ref10">10</xref>]. <xref ref-type="fig" rid="fig2">Figure 2</xref> represents the whole plant responses under salt stress.</p><p>The earliest response of plants exposed to elevated soil salinity level is the slow growth rate of leaves. Under low soil salinity level, root growth is almost always less affected than shoot growth, so the root: shoot ratio increases [<xref ref-type="bibr" rid="scirp.96151-ref11">11</xref>], but root growth also decreases when they are exposed to higher soil salinity level [<xref ref-type="bibr" rid="scirp.96151-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.96151-ref13">13</xref>]. Plant experiences a significant decrease in dry biomass accumulation due to decrease in shoot and root growth under elevated salt-stressed condition [<xref ref-type="bibr" rid="scirp.96151-ref14">14</xref>].</p><p>Decreasing rates of new cell production may cause the inhibition of growth as reported by Shabala, Babourina and Newman [<xref ref-type="bibr" rid="scirp.96151-ref15">15</xref>]. The reduction in dry weight accumulation could be attributed to increasing stiffness of the cell wall due to altered cell wall structure induced by salinity. Salt stress in the root zone causes the development of osmotic stress, which disrupts cell ion homeostasis by inducing both the inhibition in uptake of essential nutrients such as K<sup>+</sup> and increased accumulation of Na<sup>+</sup> and Cl<sup>−</sup> [<xref ref-type="bibr" rid="scirp.96151-ref16">16</xref>]. Higher uptake of Na<sup>+</sup> competes with the uptake of other nutrient ions, especially K<sup>+</sup>, and causes K<sup>+</sup> deficiency which leads to lower K<sup>+</sup>/Na<sup>+</sup> ratio in plants under salt stress [<xref ref-type="bibr" rid="scirp.96151-ref10">10</xref>]. Salt-stressed plants also show significant changes in physiological and biochemical parameters of plants such as lower level of leaf chlorophyll content, decrease in protein synthesis, increased ROS accumulation, enhanced accumulation of compatible solutes such as proline, changes in antioxidant enzymatic activities. Thus all the morphological, physiological and biochemical changes of plants exposed to salt stress are combinedly responsible for overall changes in plant growth and productivity.</p></sec><sec id="s3"><title>3. Effects of Salinity on Physiological and Biochemical Attributes of Plants</title><p>Salinity stress involves changes in various biochemical and metabolic processes, depending on severity and duration of the stress, and ultimately inhibits crop growth and productivity. Excessive soluble salt concentrations affect biochemical attributes of plants by increasing the osmotic potential of the soil solution as well as specific ion toxicities in soil. Different biochemical attributes like chlorophyll content and intercellular proline accumulation are greatly influenced under salt stress.</p><sec id="s3_1"><title>3.1. Leaf Chlorophyll Contents under Salt Stress</title><p>Chlorophyll is the most important component in the photosynthesis process and the rate of photosynthesis depends on the level of chlorophyll content in plant leaves. The decline in productivity has been observed in many plant species subjected to salt stress is often associated with a reduction in leaf photosynthetic capacity [<xref ref-type="bibr" rid="scirp.96151-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.96151-ref17">17</xref>]. Decrease in leaf chlorophyll content is the first visible symptom of plants subjected to salt stress [<xref ref-type="bibr" rid="scirp.96151-ref14">14</xref>]. Changes in leaf chlorophyll content vary depending on the level of salt tolerance of plants and salt-tolerant genotypes showed less loss of chlorophyll than relatively sensitive genotypes [<xref ref-type="bibr" rid="scirp.96151-ref8">8</xref>]. Plant experiences lower chlorophyll content in plant leaves probably due to inhibition of chlorophyll pigment formation through the accumulation of Na<sup>+</sup> under salt stress [<xref ref-type="bibr" rid="scirp.96151-ref18">18</xref>] or cell membrane deterioration [<xref ref-type="bibr" rid="scirp.96151-ref19">19</xref>]. Usually there is dominance of chlorophyll-a over chlorophyll-b in plants but their values become closer with the increasing salinity level [<xref ref-type="bibr" rid="scirp.96151-ref20">20</xref>]. The decrease in leaf chlorophyll contents (a &amp; b) of salt-stressed plants is a result of either slow synthesis or fast breakdown, indicated that there was a photoprotection mechanism through reducing light absorbance by decreasing chlorophyll contents [<xref ref-type="bibr" rid="scirp.96151-ref21">21</xref>].</p></sec><sec id="s3_2"><title>3.2. Compatible Solute Accumulation and Osmotic Protection</title><p>Compatible solutes are the group of chemically diverse organic compounds generated in plants and they do not interfere with the cellular metabolism even at high concentration [<xref ref-type="bibr" rid="scirp.96151-ref2">2</xref>]. These compatible solutes include amino acid proline [<xref ref-type="bibr" rid="scirp.96151-ref22">22</xref>], glycinebetaine [<xref ref-type="bibr" rid="scirp.96151-ref23">23</xref>], sugar [<xref ref-type="bibr" rid="scirp.96151-ref24">24</xref>], etc. As the accumulation of these compounds is proportional to the external osmolarity, they protect cellular structures by maintaining osmotic balance within the cell via continuous water influx [<xref ref-type="bibr" rid="scirp.96151-ref25">25</xref>]. Accumulation of compatible solutes is one of the adaptive mechanisms of plants to withstand salt stress [<xref ref-type="bibr" rid="scirp.96151-ref26">26</xref>]. Enhanced salt stress causes a significant decrease in number of amino acids such as cysteine, arginine, and methionine (around 55% of total free amino acids in plant), but proline, proteinogenic amino acid concentration increases [<xref ref-type="bibr" rid="scirp.96151-ref27">27</xref>]. Proline accumulation under abiotic stress occurs in taxonomically diverse sets of plants [<xref ref-type="bibr" rid="scirp.96151-ref28">28</xref>], and increased proline accumulation in plants is correlated with enhanced salt tolerance [<xref ref-type="bibr" rid="scirp.96151-ref29">29</xref>]. Increased proline accumulation in plants under salt stress showed higher salt tolerance in a number of plant species such as rice [<xref ref-type="bibr" rid="scirp.96151-ref10">10</xref>], barley [<xref ref-type="bibr" rid="scirp.96151-ref30">30</xref>], pea [<xref ref-type="bibr" rid="scirp.96151-ref17">17</xref>] and soybean [<xref ref-type="bibr" rid="scirp.96151-ref31">31</xref>]. Therefore, it is evident that leaf proline index shows a strong positive relationship with plant yield potential [<xref ref-type="bibr" rid="scirp.96151-ref32">32</xref>] and is thus a promising index for deploying in breeding programs for evolving salt tolerant cultivars [<xref ref-type="bibr" rid="scirp.96151-ref33">33</xref>].</p><p>Glycinebetaine, a nontoxic cellular osmolyte, raises the osmolarity of plant cell during stress period [<xref ref-type="bibr" rid="scirp.96151-ref2">2</xref>] and protects cells by osmotic adjustment, protein stabilization [<xref ref-type="bibr" rid="scirp.96151-ref34">34</xref>] and scavenging reactive oxygen species (ROS) in plants [<xref ref-type="bibr" rid="scirp.96151-ref26">26</xref>]. When rice plants are exposed to enhanced salt stress, accumulated glycinebetaine positively protects the ultrastructure of seedlings [<xref ref-type="bibr" rid="scirp.96151-ref35">35</xref>]. Even foliar application of this amino acid showed a positive correlation with plant growth under salt stress by stabilizing photosynthetic pigments and scavenging ROS [<xref ref-type="bibr" rid="scirp.96151-ref36">36</xref>]. Other than amino acids, accumulation of carbohydrates such as sugar and starch is a common feature of salt-stressed plants [<xref ref-type="bibr" rid="scirp.96151-ref37">37</xref>]. The accumulated carbohydrates in plants under salt stress play important roles in stress mitigation involves osmoprotection, carbon storage, and scavenging of reactive oxygen species [<xref ref-type="bibr" rid="scirp.96151-ref2">2</xref>]. Salt stress increases the level of reducing sugars (sucrose and fructans) in plants and protects plants from osmotic damages by abiotic stresses such as soil salinity.</p></sec><sec id="s3_3"><title>3.3. Increased ROS Accumulation in Plants under Salt Stress</title><p>One of the biochemical changes occurring when plants are subjected to biotic or abiotic stresses is the production of reactive oxygen species [<xref ref-type="bibr" rid="scirp.96151-ref38">38</xref>]. Reactive oxygen species (ROS) are highly reactive and in the absence of any protective mechanism they can seriously disrupt normal metabolism through oxidative damage to lipids, protein and nucleic acids [<xref ref-type="bibr" rid="scirp.96151-ref39">39</xref>]. In salt-stressed plants, molecular oxygen (O<sub>2</sub>) acts as an electron acceptor, giving rise to the accumulation of ROS [<xref ref-type="bibr" rid="scirp.96151-ref2">2</xref>]. Reactive oxygen species include singlet oxygen, hydroxyl radical (OH<sup>−</sup>), superoxide radical, and hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) are all strongly oxidizing compounds and therefore potentially harmful for cell integrity [<xref ref-type="bibr" rid="scirp.96151-ref40">40</xref>].</p><p>As cell membranes are the first targets of many plant stresses, reactive oxygen species (ROS) may destroy normal metabolism through peroxidation of membrane lipids [<xref ref-type="bibr" rid="scirp.96151-ref39">39</xref>]. Lipid peroxidation of biological membranes might lead to structural alterations such as denaturalization of proteins and nucleic acids in salt-stressed plants. Experimental evidences suggest that lipid peroxidation reaction of cellular membranes may play an important role in radical mediated cell injury [<xref ref-type="bibr" rid="scirp.96151-ref41">41</xref>]. Therefore, activity of antioxidant enzymes may act as efficient determinant criteria in the toxicity degree to salt stressed plants. Crucial changes in soil salinity can lead to osmotic stress, which are primary effects of salt stress. Such free radicals and other active derivatives of oxygen may produce inevitably as by-products of physiological redox reactions. It has been reported that when ROS exceeded the capacity of scavenging system of plants [<xref ref-type="bibr" rid="scirp.96151-ref42">42</xref>], it results in oxidative damage [<xref ref-type="bibr" rid="scirp.96151-ref17">17</xref>]. The increased levels of ROS can inactivate enzymes, damage important cellular components, which induced plant growth arrest, and even death finally [<xref ref-type="bibr" rid="scirp.96151-ref39">39</xref>].</p></sec><sec id="s3_4"><title>3.4. Changes in Antioxidant Enzymatic Activities (CAT, POX, APX) of Plants</title><p>To mitigate the deleterious effects of salinity on regular metabolism, plants have evolved various strategies to contend with this problem [<xref ref-type="bibr" rid="scirp.96151-ref38">38</xref>]. Plants possess an array of enzymatic and non-enzymatic antioxidant defense systems to protect their cells against the damaging effects of ROS [<xref ref-type="bibr" rid="scirp.96151-ref43">43</xref>]. Superoxide dismutase (SOD) is a major scavenger of superoxide and its enzymatic action results in the formation of H<sub>2</sub>O<sub>2</sub> and O<sub>2</sub> [<xref ref-type="bibr" rid="scirp.96151-ref44">44</xref>]. The hydrogen peroxide produced is then scavenged by different antioxidant enzymes including catalase (CAT), a variety of peroxidase such as guaiacol peroxidase (POX) and ascorbate peroxidase (APX). Catalase converts H<sub>2</sub>O<sub>2</sub> into water and molecular oxygen [<xref ref-type="bibr" rid="scirp.96151-ref45">45</xref>], whereas peroxidase decomposes H<sub>2</sub>O<sub>2</sub> by oxidation of co-substrates such as phenolic compounds or antioxidants [<xref ref-type="bibr" rid="scirp.96151-ref46">46</xref>]. These antioxidant enzymes show differential responses varying in the level of salt tolerance.</p><p>Generally, plants exhibit an increase in CAT activity with the increasing magnitude of NaCl concentration in soil [<xref ref-type="bibr" rid="scirp.96151-ref47">47</xref>], but this increased accumulation is not similar for all the plant genotypes. Plants show differential responses on CAT activity under salt stress depending on their levels of salt tolerance. For example, in salt-sensitive soybean genotypes, CAT activity decreases with increasing salt stress [<xref ref-type="bibr" rid="scirp.96151-ref48">48</xref>]. But increased CAT activity was observed in salt-tolerant soybean genotypes [<xref ref-type="bibr" rid="scirp.96151-ref31">31</xref>]. A linear and significant increase in CAT activity is observed in response to increased salt concentration after exposure to salt stress in barley [<xref ref-type="bibr" rid="scirp.96151-ref30">30</xref>] and green bean [<xref ref-type="bibr" rid="scirp.96151-ref49">49</xref>]. Among the root crops, potato is comparatively more salt-tolerant and also exhibits a significant increase in CAT activity with the increasing salinity level [<xref ref-type="bibr" rid="scirp.96151-ref50">50</xref>]. Pea plants are normally sensitive to salt stress and CAT activity shows a declining trend with increasing the magnitude of NaCl stress accordingly [<xref ref-type="bibr" rid="scirp.96151-ref17">17</xref>]. From the research findings on different crops, it can be assumed that CAT activities were higher in the salt-tolerant one than the salt-sensitive cultivar and this increase in CAT activity helps plant to mitigate osmotic stress due to soil salinity [<xref ref-type="bibr" rid="scirp.96151-ref10">10</xref>].</p><p>Among the peroxidase enzymes, guaiacol peroxidase (POX) is considered as one of the most important enzymes for protecting plants from the oxidative damage of ROS [<xref ref-type="bibr" rid="scirp.96151-ref51">51</xref>]. Salt stress significantly increases the activity of antioxidant enzyme i.e. peroxidase (POX) in case of salt-sensitive rice varieties but tolerant varieties exhibit the declining trends of activity of POX enzyme activity with the increasing salt concentration [<xref ref-type="bibr" rid="scirp.96151-ref22">22</xref>]. In case of soybean, POX activity increases as a result of increasing salt concentration [<xref ref-type="bibr" rid="scirp.96151-ref31">31</xref>]. Salt stress significantly increases the POX activities in potato [<xref ref-type="bibr" rid="scirp.96151-ref50">50</xref>] and pea [<xref ref-type="bibr" rid="scirp.96151-ref17">17</xref>], which may help plants to mitigate osmotic damages by ROS. Other than POX, ascorbate peroxidase (APX) enzyme helps to protect plants from osmotic stress by neutralizing the ROS, evident in rice [<xref ref-type="bibr" rid="scirp.96151-ref22">22</xref>] and soybean [<xref ref-type="bibr" rid="scirp.96151-ref31">31</xref>]. Over expression of the APX gene in plants has been reported to improve protection against oxidative stress. APX activities increased with increasing salt stress in both salt-sensitive and salt-tolerant varieties and the activities were higher in the salt-tolerant one than the salt-sensitive cultivar [<xref ref-type="bibr" rid="scirp.96151-ref49">49</xref>]. These enzymes (CAT, POX and APX) were also reported to be important in salt tolerance mechanisms in some other crops such as mulberry [<xref ref-type="bibr" rid="scirp.96151-ref52">52</xref>], cotton [<xref ref-type="bibr" rid="scirp.96151-ref53">53</xref>] and maize [<xref ref-type="bibr" rid="scirp.96151-ref51">51</xref>].</p></sec><sec id="s3_5"><title>3.5. Changes in Potassium (K) and Sodium (Na) Ratio of Plants</title><p>Salinity imposes both ionic toxicity and osmotic stress to plants [<xref ref-type="bibr" rid="scirp.96151-ref25">25</xref>], leading to nutritional disorder [<xref ref-type="bibr" rid="scirp.96151-ref54">54</xref>]. In saline soil, the concentration and availability of Na<sup>+</sup> are comparatively higher than the concentration of K<sup>+</sup> in soil solution [<xref ref-type="bibr" rid="scirp.96151-ref55">55</xref>]. Salt stress disturbs cytoplasmic K<sup>+</sup>/Na<sup>+</sup> homeostasis, causing an increase in Na<sup>+</sup> to K<sup>+</sup> ratio in the cytosol [<xref ref-type="bibr" rid="scirp.96151-ref56">56</xref>]. Salt tolerance is directly associated with K<sup>+</sup> contents because of its involvement in osmotic regulation and competition with Na<sup>+</sup>. Salt tolerance mechanism of plants requires not only the adaptation to Na<sup>+</sup> toxicity but also the acquisition of abundant K<sup>+</sup> whose uptake by the plant cell is affected by high external Na<sup>+</sup> concentrations [<xref ref-type="bibr" rid="scirp.96151-ref57">57</xref>].</p><p>The salt-sensitive and salt-tolerant plants show differential responses in the aspect of K<sup>+</sup>/Na<sup>+</sup> ratio in both root and shoot under salt stress [<xref ref-type="bibr" rid="scirp.96151-ref58">58</xref>]. The tolerant genotypes can control the uptake of Na<sup>+</sup>, resulting in a higher K<sup>+</sup>/Na<sup>+</sup> ratio with greater dry biomass accumulation, which helps to dilute the absorbed Na<sup>+</sup> within plant system. Whereas, the sensitive genotypes had higher Na<sup>+</sup> and lower K<sup>+</sup> contents, resulting in lower K<sup>+</sup>/Na<sup>+</sup> ratio in plants [<xref ref-type="bibr" rid="scirp.96151-ref59">59</xref>]. There is a significant negative correlation between leaf Na<sup>+</sup> and K<sup>+</sup>/Na<sup>+</sup> ratio in different rice varieties differing in salt tolerance under salt stress [<xref ref-type="bibr" rid="scirp.96151-ref60">60</xref>]. Other than rice, soybean also experiences decrease in K<sup>+</sup>/Na<sup>+</sup> ratio with the increasing salinity level [<xref ref-type="bibr" rid="scirp.96151-ref48">48</xref>]. Root crops like potato also show the decrease in K<sup>+</sup>/Na<sup>+</sup> ratio under salt stress [<xref ref-type="bibr" rid="scirp.96151-ref50">50</xref>]. This decrease in K<sup>+</sup>/Na<sup>+</sup> ratio under salt stress causes Na<sup>+</sup> toxicity in plants and leads to cellular damage and deficiency in potassium in plant, which ultimately decreases crop growth and productivity.</p></sec></sec><sec id="s4"><title>4. Approaches to Mitigate the Adverse Effects of Soil Salinity on Crop Production</title><p>Worldwide, extensive research is being carried out, to develop strategies to cope with abiotic stresses, through development of salt-tolerant cultivars, shifting the crop calendars, resource management practices, etc. Possible soil salinity amelioration strategies are summarized in <xref ref-type="table" rid="table1">Table 1</xref> with few references.</p><p>Among the soil salinity management strategies, use of salt-tolerant plant genotypes showed better performance compared to others. Advanced plant breeding and molecular biology techniques suggest to use salt-tolerant genotypes with effective management strategies to mitigate the adverse effects of soil salinity. In alignment with this, exogenous application of compatible solutes shows significant increase in growth and productivity. Regulation of gene expression in salinity stress includes a wide array of mechanisms that are used by plants to up-regulate or down-regulate the production of specific gene to mitigate the adverse effect of</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Strategies to mitigate soil salinity problem</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Serial no.</th><th align="center" valign="middle" >Strategies or management practices</th><th align="center" valign="middle" >References</th></tr></thead><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >Development and use of salt-tolerant genotypes</td><td align="center" valign="middle" >Kumar, Beena, Awana and Singh [<xref ref-type="bibr" rid="scirp.96151-ref9">9</xref>] Kibria, Hossain, Murata and Hoque [<xref ref-type="bibr" rid="scirp.96151-ref10">10</xref>]</td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >Exogenous application of compatible solutes such as proline, glycine-betaine</td><td align="center" valign="middle" >Sabagh, Sorour, Ragab, Saneoka and Islam [<xref ref-type="bibr" rid="scirp.96151-ref61">61</xref>] Okuma, Murakami, Shimoishi, Tada and Murata [<xref ref-type="bibr" rid="scirp.96151-ref29">29</xref>]</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >Use of fresh water as a safe source of irrigation for agricultural purposes in coastal belt</td><td align="center" valign="middle" >Panagea, Daliakopoulos, Tsanis and Schwilch [<xref ref-type="bibr" rid="scirp.96151-ref62">62</xref>]</td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >Organic amendment with proper K and Zn fertilization</td><td align="center" valign="middle" >Kibria, Farhad and Hoque [<xref ref-type="bibr" rid="scirp.96151-ref63">63</xref>] Rady [<xref ref-type="bibr" rid="scirp.96151-ref64">64</xref>]</td></tr><tr><td align="center" valign="middle" >5</td><td align="center" valign="middle" >Hormone regulation to improve the antioxidant defense mechanism of plants</td><td align="center" valign="middle" >Caverzan, Casassola and Brammer [<xref ref-type="bibr" rid="scirp.96151-ref65">65</xref>] Kim, Mun, Khan, Waqas, Kim, Shahzad, Imran, Yun and Lee [<xref ref-type="bibr" rid="scirp.96151-ref66">66</xref>]</td></tr><tr><td align="center" valign="middle" >6</td><td align="center" valign="middle" >Use of plant growth-promoting bacteria (PGPB)</td><td align="center" valign="middle" >Shrivastava and Kumar [<xref ref-type="bibr" rid="scirp.96151-ref1">1</xref>] Numan, Bashir, Khan, Mumtaz, Shinwari, Khan, Khan and Al-Harrasi [<xref ref-type="bibr" rid="scirp.96151-ref67">67</xref>]</td></tr><tr><td align="center" valign="middle" >7</td><td align="center" valign="middle" >Remote sensing and GIS in salinity mapping</td><td align="center" valign="middle" >Asfaw, Suryabhagavan and Argaw [<xref ref-type="bibr" rid="scirp.96151-ref68">68</xref>]</td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >Genetic engineering, modifying gene expression and transcriptional regulation</td><td align="center" valign="middle" >Gupta and Huang [<xref ref-type="bibr" rid="scirp.96151-ref2">2</xref>]</td></tr></tbody></table></table-wrap><p>soil salinity. Transcriptomic analysis provides detailed knowledge to screen candidate genes involved in stress responses. This is the baseline to start with molecular approaches to develop salt-tolerant genotypes from indigenous species. Recently, use of plant growth-promoting bacteria (e.g. Pseudomonas) and rhizospheric bacteria showed a positive relationship with plant growth and productivity under salt stress. Furthermore, saline soil survey through advanced technologies such as GIS may help to plan accordingly based on salinity level in a specific area. Soil salinity management includes a complex interaction between all the management strategies and no parameter can ameliorate this problem solely. Therefore, it is essential to interact with all the management strategies to mitigate the adverse effects of soil salinity on crop production.</p></sec><sec id="s5"><title>5. Conclusion and Recommendation</title><p>Soil salinity is prevalent abiotic stress that limits plant growth and productivity. Salinity tolerance mechanism of plants requires a complex interaction of genetic, cellular, metabolic and physiological responses. However, a lack of coordination of plant physiological and molecular responses is essential for sustainable and effective plant salinity tolerance. This review has highlighted that no single parameter could be suggested as sole possible way for salinity stress tolerance plants. A combination of all suitable management strategies can contribute to salt tolerance of plants. The future focus should be on the study of intercellular and intracellular molecular interaction involved in salinity stress responses.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Kibria, M.G. and Hoque, Md.A. (2019) A Review on Plant Responses to Soil Salinity and Amelioration Strategies. 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