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Review

Growth, Nutrient Accumulation, and Drought Tolerance in Crop Plants with Silicon Application: A Review

by
Rafea Sultana Rea
1,*,
Mohammad Rafiqul Islam
2,*,
Mohammad Mahmudur Rahman
3,
Bibhash Nath
4 and
Ken Mix
1
1
Department of Agricultural Sciences, Texas State University, San Marcos, TX 78666, USA
2
Department of Soil Science, Bangladesh Agricultural University, Mymensingh 2202, Bangladesh
3
Global Centre for Environmental Remediation, College of Engineering Science and Environment, The University of Newcastle, Callaghan, Newcastle, NSW 2308, Australia
4
Department of Geography and Environmental Science, Hunter College, The City University of New York, New York, NY 10021, USA
*
Authors to whom correspondence should be addressed.
Sustainability 2022, 14(8), 4525; https://doi.org/10.3390/su14084525
Submission received: 4 March 2022 / Revised: 30 March 2022 / Accepted: 8 April 2022 / Published: 11 April 2022

Abstract

:
Plants take up silicon (Si) from the soil which impacts their growth and nutrient accumulation. It increases plant resistance to abiotic and biotic stresses such as drought, salinity, and heavy metal, diseases, and pest infestation. However, until recently, research of Si application on the crop is limited. This article reviews the recent progress of research on Si application on crop growth and yield, nutrient availability in soil and accumulation, and drought tolerance of crop plants. The review’s findings show that Si improves crop development and output under stressful environmental conditions. Silicon increases the availability and accumulation of both macronutrients (nitrogen, potassium, calcium, and sulphur) and micronutrients (iron and manganese). It improves drought resistance by increasing plant water usage efficiency and reducing water loss during transportation. Silicon application is a crucial aspect of crop productivity because of all of these favorable attributes. The gaps in current understandings are identified. Based on the outcome of the present research, future scopes of research on this field are proposed.

1. Introduction

Most of the major crops accumulate a significant amount of Si though it is considered non-essential for plant growth and development [1]. While Si does not directly contribute to plant metabolism [2,3], there is evidence that Si improves: crop productivity [4,5,6,7], nutrient accumulation in plants [8,9,10,11], heavy metal resistance in grain crops [12,13,14], and increases drought tolerance of plants [15,16,17]. Since these benefits for crop production have been recognized, the global use of Si as a soil amendment is increasing.
The Earth’s pedosphere of Si is estimated to be 28.2% by weight [3]. Si, along with oxygen and metals, forms silicon dioxide (Si2O) and water-soluble silicates. Si minerals go through various physical and chemical weathering and release Si in solution under suitable pH condition. The source of silica and silicates in soil and clays is from the weathered Si minerals such as quartz and feldspar present in the pedosphere [18,19]. Si is present in soil mainly in three different phases such as solid, liquid, and adsorbed. Solid phases can be either amorphous or crystalline. Amorphous silica contributes significantly more to dissolve Si in soil solution because of its higher solubility than the crystalline form [3]. However, the plant does not uptake any Si as amorphous silica; rather it is taken up by plants in the form of monosilicic acid (H4SiO4) [20].
The addition of Si as a soil amendment in the crop field is a recent phenomenon, and few reports have been published on the impact of Si on plants. The recent publications report that Si affects growth, yield [21,22,23], and disease resistance [24,25,26,27] among other plant conditions.
Figure 1 shows the number of publications vs. year for the time period 1950–2021. The research on the plant silicon relationship began after 1935. Until 1980, research on this field was minimal. However, between 1980–2000, the overall number of publications started to increase gradually. After 2010, a dramatic increase in publication indicates that this field is getting more research attention [28].
It is noteworthy, that among the ten major produced crops in the world, seven crops (rice, wheat, sugarcane, sugar beet, soybean, tomato, and barley) are Si accumulators and their biomasses consist of more than 1% Si in dry matter [29]. Though the ability of Si accumulation in these plants highly varies [30], production of these crops takes away large amounts of Si from the soil. For instance, rice and sugarcane individually can remove approximately 500 kg and 300 kg of Si per ha, respectively, while harvesting [20,31]. After several years of continuous cropping and harvesting of plants, available Si declines in the soil. This fact necessitates the application of Si from external sources. In different parts of the world, such as India, Vietnam, China, researchers used rice [32], wheat [17], and sugarcane [20] for experiments on Si applications related to crop production. It has been observed that Si has a beneficial effect, including increasing crop yield, limiting abiotic stresses from salinity, increasing drought tolerance [33], and reducing the toxic effects [34,35] of heavy metals. [36]. The presence of higher Si in the plants’ roots, shoots, and leaves makes the plants more resistant to pest attack and enhances drought tolerance as it forms a thick layer under the cuticle. This Si layer reduces leaf digestibility for pests as well as water transpiration loss from plants [37]. Silicate application sharply decreased transpirational flow in rice about 4.2% to 0.8% [38]. It was reported that applications of amorphous silica minimize the cadmium stress in the plants by inhibiting root to shoot transfer of cadmium along with other metals [39,40]. When amorphous silica was applied at a rate of 1000 kg/ha, it increased the availability and accumulation of mineral nutrients: P (10–40%), Ca (up to 33%), S (up to 51%), Mo (up to 54%), and Cu (10–40%) [41]. Si helps make the nutrients available to plant root systems by impeding soil particles from bonding with mineral nutrients. It is known that the content of Si in agricultural soils is declining, both due to natural weathering and continuous agricultural and activities [42]. This work reviews the contemporary research on the application of Si to soils to in-crease crop production. The scope of this review includes the impact of Si fertilization on growth and yield, soil nutrient availability in uptake form, and drought stress tolerance of crop plants, with a general summary of Si application in crop fields from different sources following different methods of use. The gap between current understandings and the experimental results is identified throughout.

2. Role of Si on Plant Growth and Yield

Application of Si-based fertilizer has been reported to be effective for plant growth and yield. To determine the effect of Si fertilizer on growth, yield, and nutrient accumulation of the rice plant, four different dosages of SiO2 were applied with identical recommended dosages of N, P, and K fertilizers. It was observed that yield components (number of tillers, number of panicles per plant, and number of grains per panicle) and yield were significantly affected by Si fertilizer doses. About 3716 kg/ha maximum grain yield was obtained when they applied SiO2 at a rate of 329 kg/ha. There was about a 23% increase in grain yield compared to the control [8]. Whereas in a similar study with different Si fertilizer (Na2SiO3) dosages, up to 17.4% yield increase along with increased panicle numbers were recorded from a field trial in China. The increased growth and yield recorded from this experiment are given in Table 1.
In India, researchers used diatomaceous earth (DE) as a source of Si and compared its use in two different moisture regimes: saturated/submerged and field capacity. It was found that biomass yield was high with almost all of the DE treatments in acidic (300 and 600 kg/ha) and alkaline (150, 300 and 600 kg/ha) soil condition. Analysis of soil and rice yield, before and after the application of DE, provided evidence that applications of DE increase rice yield regardless of the soil condition. The increases were 150, 300, and 600 kg/ha in alkaline, acidic, and neutral soil, respectively. According to the report, DE works best in submerged condition compared to field capacity condition of the rice field [4]. Si is also responsible for grain quality in rice. Formation of the quality hull with milky sap is high when the concentration of Si in rice shoot is high [43].
Si fertilization has a positive impact on wheat production. It increases the plant height, no. of spikelets, and number of spikes per spikelet. In irrigated fields, grain yield increased by 13.4% compared to no Si application. It has been reported that the application of K2SiO3, at a rate of 12 kg/ha, increased plant height, the number of effective tillers per m2 up to 515.33, spike length up to 12.25 cm, and number of spikelets per spike on an average 16.70. A maximum grain yield of 4380 kg/ha was observed when K2SiO3 was applied with four irrigations [17]. Exogenous application of Si or a combination of Si and Se were reported to change the physio-biochemical activity in wheat which resulted in the successful growth of wheat in saline soil [44]. Foliar application of sodium silicate salt (Na2Si3O7), especially at the tillering stage and anthesis stage, increases the yield for various wheat cultivars [45]. In contrast to other materials, volcanic tuff (Chem comp) was applied in Idaho and showed no remarkable effect. There is also evidence that these improvements in yield are only related to stressed conditions and that no improvement in yield is observed during ideal growing conditions [46].
Notable improvements were observed when Si fertilizer was applied for maize production [47]. In Pakistan, two hybrid maize varieties, P-33H25 and FH-810, were grown under 100% and 60% field capacity of water levels. In a water deficit condition, application of Si significantly increased plant height, stem diameter, and cob length (13.96 cm and 12.83 cm, respectively) for both maize varieties. It also increases the number of grains per cob (235.05 and 215.35) and grain yield (0.46 kg and 0.39 kg) correspondingly. This increased yield was due to the increased number of cobs, grains per cob, and weight of 1000 grains [7]. A similar result in the drought stressed condition was published on the improvement of maize plant growth and yield from Turkey and Greenville, South Carolina [22,48].
Si is not only beneficial for cereal and grain crops; it also increases the production and fresh weight of vegetables. In India, studies were conducted from 2013 to 2017 on three different potato varieties. Application of additional Si (ferti-silica 50 mg/dm3) increased tuber yield by 15–50% [21]. In a pot cultivation system, Ca and Mg silicate were used for growing potato in the absence and presence of water. According to this report, Si application enhances Si availability in soil, which increases overall tuber dry weight irrespective of water condition. Though there was no significant improvement on an increase in the number of tubers/plants [49].
Likewise, in soilless cultivation systems, the addition of Si increases Si content in green bean pods without any loss of biomass production [50]. Significant increase in shoot and root length of cowpea were observed in India when the water-soluble Si was applied at a concentration of 100 mg Si per Kg of Si fertilizer dose. In cowpea, it increased shoot yield by 128% [9]. In a legume (soybean) crop study in Brazil, the effect of Si (sodium–potassium silicate) and salicylic acid were examined. As stated by, individual application of sodium–potassium silicate and salicylic acid does not have any significant impact on legume plant growth. However, combined foliar application of these two Si materials has an adverse effect on the yield of soybean [51].
In the same way, the spraying of silicic acid increases lettuce yield quality and postharvest firmness [52]. Application of Si at a dose of 250 mg/dm3 significantly increases the head weight and total dry matter content in lettuce. In comparison to control treatments, the yield of cucumber increased by 9.35–26.6% as the number of fruits increased [5]. In India, several studies conducted on tomato and onion using diatomaceous earth at a rate of 500–700 kg/ha provided the highest yield for both of these crops [53,54].

3. Role of Si on Nutrients Availability and Accumulation

There are sixteen minerals playing essential roles in the plant’s cell metabolism, energy transfer, osmosis, and reproduction. Among these sixteen elements, nitrogen (N) is a major constituent of the plant structure which works with a combination of H, C, and P. Si mostly affects the availability of N in soil and N accumulation in plants [55]. It forms the organic compounds such as protein and nucleotide in the plant. Similar to N, phosphorus (P) also forms some organophosphorus compound such as sugar phosphate, pyrophosphate bond (ATP), phytin, etc. On the other hand, potassium (K) maintains the ionic balance among the cells along with the activation of enzymes. It also provides mechanical strength against the lodging of plants in water deficit condition. Among the micronutrients, Fe and Mn work as a cofactor of enzymes and help in N metabolism. Availability of Fe in the soil increases the amount of Fe in plant parts, which is good if the plants are used as food. Zn and Cu are two redox active micronutrients which operate to maintain the structural integrity and permeability of the plasma membrane [56]. Si influences the availability and accumulation of these nutrients in various plants species. It also affects the presence of nutrients in the root and shoot. The discussion of nutrient availability and accumulation follows in the next three sections on macronutrients, micronutrients, and silicon accumulation.

3.1. Macronutrients

In the published literature, the results of Si application reveal a mixed trend regarding macronutrient accumulation. Needless to say, the environmental parameters, Si dosage, and soil type of the research sites were widely variable. Therefore, one cannot argue the results are contradictory.
Some reports claim the improvement of nutrient accumulation by using silicon. According to Cuong et al. [8] (Figure 2), the application of silica has a positive impact on almost all the aspects such as availability, assimilation, and uptake of N, P, and K in rice plants, especially in grains [57,58]. The increase in N, P, and K accumulation recorded up to 33%, 69%, and 36.8%, respectively, compared to the control [8]. Similar results were also found utilizing diatomaceous earth on the rice field [58]. It was concluded in another study that Si fertilization has a positive correlation with P uptake making P more available in soil [59]. Generally, P concentration increases in root areas but in potato a higher concentration of P was found in the leaves due to the application of Ca and Mg silicate fertilizers [60]. The plant’s available forms of phosphorus also increased in soil because Si binds with iron and manganese, thus preventing phosphorus opportunity to bond with those elements [49]. Whereas potassium concentration in the shoots and roots decreased in lettuce due to the addition of Si and increased for some other crops such as maize and rice from 10–40% [42]. Hence, the accumulation of potassium with the addition of Si appears to be dependent on plant species. In addition to increased N accumulation, S and Mg accumulation also increased in total plant biomass with a high concentration in roots when Si treatments continued for a longer duration (3 weeks). Though, a very high dose of Si decreases the availability of Mg [42,61].
There appears to be evidence that very high doses of Si decreased the net accumulation of N and P in the plant’s shoots and roots, though it is thought that the concentration of N decreased due to the increased growth rate and decreased Mg availability caused by Si treatment [42,62]. Silicon deposition in endodermal cells of plant roots, which may contribute to decreased P uptake, is one probable reason for the decrease in P accumulation. The generation of apoplastic barriers to P permeability across roots produced by Si deposition in roots, which reduces P uptake, is primarily responsible for this effect [63,64]. Another concept is that the creation of a cuticle-silica double layer in leaves as a result of Si deposition lowers the plant’s transpiration rate. Transpiration is negatively connected with the Si content of rice aerial parts, and when the SiO2 concentration of shoots surpasses 10% of the dry matter weight, the rice transpiration rate might be lowered by 20–30% [65]. In contrast, another study found Si application does not have any measurable effect on increasing extractable phosphorus from soil, in fact it may increase P fixation in soil because Si increases soil pH which influences soil P to be strongly adsorbed by soil particles and silicic acid is not strong enough to break that bond [66]. Therefore, the supplemental Si application slightly affects the availability of P.

3.2. Micronutrients

Very limited reports are available on Si applications associated with micronutrient accumulation; however, Si application appears to have an impact on crop accumulation of most of the micronutrients. The net accumulation of Fe and Mn has been improved by Si application as well as boron accumulation in plant leaves. Fe concentration increased in both the roots and shoots, respectively, 20–40% and 10% [43]. While Si did not influence the accumulation of Cl and Mo, it decreased the accumulation of Cu and Zn by 20%. [10]. In numerous studies, Si has been shown to limit Zn bioavailability in soil by redistributing the metal to more stable fractions such as organic materials and crystalline Fe oxides [67]. Silicon impacts the exudation of several organic acids (e.g., oxalic, acetic, tartaric, maleic, and fumaric acids) from rice roots, which may be involved in Zn toxicity mitigation via immobilization/co-precipitation in the soil solution [68]. In general, the immobilization of harmful Cu ions by increased cell wall binding capacity and the creation of Cu-binding molecules, both in roots and shoots, is attributed to Si-mediated reduction in Cu toxicity. Si lowered the expression of two Cu transporter genes in Arabidopsis roots, AtCOPT1 and AtHMA5. According to the authors, Si deposits generated in cell walls boosted Cu-binding sites, reducing the impact of elevated Cu levels in plant cells [69]. According to Flora et al. [70], the Si-mediated reduction in Cu toxicity in tobacco (Nicotiana tabacum) via decreasing root uptake of Cu also lowers the expression of NtCOPT1 and raises the expression of genes involved in ethylene production. Kim et al. [71] proposed that increased Si buildup in the roots of Cu-stressed rice plants inhibited Cu influx through down-regulating metal transporter genes OsHMA2 and OsHMA3.
In many cases, the combined application of Si with other minerals such as Zn increases the availability and accumulation of micronutrients. Zn concentration increased up to 10 µg/L in all organs of rice plants when additional Zn was applied in combination with Si fertilizers. On the other hand, in Zn deficient conditions, Si application increases the Ca concentration in rice and maize shoots and grains [10,22]. In boron (B)-deficient conditions, Si increases Zn, Mo, Mn, and Cu in sunflower shoots. However, it decreases Fe concentration in roots but increases Fe in fully developed leaves, increasing its mobility [72].

3.3. Silicon

Increased Si availability in soil solution is the main reason for increased Si uptake in plants. Additional Si application stimulates Si uptake by plants as it improves the root system. Si uptake and accumulation are highest for Si accumulator plants, which consist of more than 1% of total biomass silicon [73]. In Table 2, a few major crops are listed with Si percentage in total biomass. Rice plants are the highest Si accumulators, followed by wheat, barley, tomato, and sugarcane. In rice cultivation systems, the application of SiO2 at a rate of 100–400 kg/ha increases Si uptake 26.8–58.5% in total plant biomass [8].
In potato, the soil and foliar application of sodium metasilicate have different effects on the leaf, stem, and tuber Si concentration, and accumulation. The concentration of Si was maximum in stems for soil-applied Si compared to foliar-applied Si and untreated control. No significant differences were found in tuber Si concentration. Whereas Si accumulation in the stem was maximum for foliar application of Si. Overall, soil application of Si provides maximum Si concentration and accumulation in different parts of the potato plant [38]. Figure 3 shows the comparison of Si concentration and accumulation in leaves, roots, stems, and tubers of potato for soil- and foliar-applied sodium metasilicate.
In the same way, maximum uptake and accumulation of Si in cowpea (Vigna unguiculata) roots and leaves were observed for 800 g/kg soil-applied Si. Application of sodium metasilicate increased leaf Si concentration up to 4259.7 µg/g and root Si concentration up to 3126 µg/g [9].

4. Silicon Application as Nano-Fertilizers and Nano-Pesticides

Nanotechnology is a potential interdisciplinary research subject that has applications in a variety of sectors, including medical, pharmacology, electronics, and agriculture [74]. Because of their small size, higher surface-area-to-weight ratio, and distinct forms, nanoparticles may have different properties than their bulk material [75]. Similar to their bulk material, Si nanoparticles (Si-NPs) have been shown to have various physical and chemical properties [76]. As a result, it is crucial to understand how Si-NPs interact with their surroundings. Si-NPs have a lot of potential in agriculture because of their unique features, and they might be superior to bulk material in alleviating various abiotic stresses [77,78,79,80]. Si-NPs can be employed as nano-pesticides, nano-herbicides, and nano-fertilizers in addition to their direct impact on plant growth and development. Silicon nanoparticles can easily infiltrate plant cells and alter plant growth and development by affecting their metabolism through a variety of interactions, triggering the capacity to battle stress circumstances. In the present decade, where the focus is to increase crop productivity or to eradicate weeds, Si-NPs may act as an agent for target-specific delivery of herbicides and fertilizers [81]. Herbicides (chloroacetanilide, anilide, and benzimidazole) embedded in a diatom fistula have been seen to be carried by silicon nanocarriers and delivered to the field in their active state [82]. In the instance of fertilizer distribution, research has shown that using nano-silicon dioxide in conjunction with organic fertilizer can promote plant production [83]. Mesoporous silica nanoparticles (MSNs) with a specific pore size (2–10 nm) were found to be an effective delivery vector for urea, boron, and nitrogenous fertilizers [81,84]. As a result, Si-NPs have the potential to be employed as a stand-alone fertilizer for specific crops, as well as a delivery system for herbicides and fertilizers in plants. Nanotechnology has aided in the development of disease-free agricultural crops in the last decade [85]. Nanosilica, a unique sort of nanomaterial, is used as a nano-pesticide under the broad umbrella of nanotechnology. Several research studies suggest that Si-NPs could be used as nano-pesticides [86,87,88,89,90]. Si-NPs have been reported to be used in two ways: either as pesticides in the field, killing insects and larvae, or as nanocarriers that release commercial pesticides to improve their efficiency. SiO2 NPs were found to have lethal properties for Callosobruchus maculatus [87]; it was discovered that the nanoparticles were more effective on adults than larvae, and it was speculated that the impact could be due to the dehydrating properties of silica, which could result in digestive tract impairment or integument surface enlargement. The deadly effect of Si-NPs on pests can also be attributed to the blockage of spiracles and tracheas, as well as sorption and abrasion damage to the protective wax layer on the cuticle. A modified hydrophobic nano-silica with a surface charge of 3 to 5 nm displayed the ability to eliminate a variety of crop insects, pests, and veterinary ectoparasites [86]. The process by which nano-silica kills pests is thought to be physisorption of nano-silica, which breaks the protective lipid water barrier, resulting in the death of the targeted organisms [86,91]. It is critical to release pesticides at the desired spot in order to improve their efficacy. However, mesoporous silica nanoparticles are required for the controlled release of bioformulations in order to deliver insecticides [92,93]. Several researchers have found that mesoporous nano-silica improved the durability and efficacy of commercial insecticides. The trials clearly showed that Si-NPs are effective pesticides that may be employed alone or to help other commercial pesticides get to where they need to go.

5. Effect of Si on Drought Tolerance in Plants

The prevalence of drought is increasing due to global warming worldwide, which is one of the greatest threats to crop production because one-third of the world land area is drought prone [16]. Drought has several harmful impacts on plant growth, metabolic activity, photosynthesis, and nutrient uptake [73]. Lack of water due to drought stress inhibits photosynthesis, damages the cell membranes, and limits cell division. About 5% to 10% of leaf transpiration occurs through the leaf cuticle, not the stomata [94]. When Si deposits under the leaf cuticle, it forms a double layer which creates an extra barrier to prevent water loss (Figure 4). Si deposition has been observed in stomata as well, and it has been reported that Si can reduce transpiration up to 30% in rice, which has a thin cuticle. It also increases structural reinforcements and changes the photosynthetic rate to increase water use efficiency [95]. Furthermore, Si application was reported to increase drought tolerance by elongating roots. These elongated roots are strong enough to extract water from soil at a drought-stressed condition [96].
Drought stress is a severe constraint to rice production [97,98]. Si has been verified to increase rice plant resistance against the drought stress condition. To prove the increased drought resistance of rice due to Si, one experiment was conducted using K2SiO3 at a concentration of 0. 0.5, 1.0, 1.5, and 2.0 mm Si. They imposed drought treatment for 15 days after 28 days of rice transplanting. The study showed that Si application decreases the leaf water potential up to −1.92 Mpa, which was −1.33 Mpa for the wet field with Si. It also increased water utilization efficiency from 0.16 g/cm2 to 0.39 g/cm2. Biomass accumulation, nutrient accumulation of K, Ca, and Mg, and root activity of rice plants were increased significantly under the drought-stressed condition after Si application [99]. Similarly, in an Egyptian study, 70, 80, 90 100, and 120% soil saturation were maintained to identify the effect of Si on drought tolerance of rice. Reduction in water saturation from 120% to 70% without Si application decreased the plant height by 32% and grain yield by 27%. Whereas with the application of Si 8.4 mg/10 increased the plant height by 38% and grain yield by 106% compared to no Si application [100]. In the same way, Ca and Mg silicate applications at a rate of 200–600 kg/ha in different soil water contents, 60, 70, and 80% of field capacity, also increased the rice yield [101].
Application of sodium silicate increased chlorophyll contents and maintained required leaf water potential by reducing leaf transpiration in the drought stress condition of wheat. Sodium silicate at a rate of 6 mM increased relative water content under the drought-stressed condition. Foliar application of sodium silicate at the active tillering and anthesis stage provided maximum positive influence both in a drought-stressed and non-stressed condition [102]. In the same way, under reduced moisture level, potassium metasilicate (K2SiO3) at a rate of 12 kg/ha also increased leaf water potential by increasing K contents in wheat [17]. Another experiment in China observed the regulatory activities of Si on water relations of wheat leaves in a drought condition. They maintained drought treatments in the field by withholding irrigation and used moveable rainwater shelter. They did not find any differences in soil moisture contents under drought condition, but Si-applied plants had better water potential and moisture content in the leaf area [38,103].
A study in Utah found that the additional application of Si also increased drought tolerance in corn. The effects of Si on corn were studied under three cultivation techniques: hydroponic and subjected to salt stress, gradual drought stress in low Si soilless medium, and acute drought stress in low Si soilless medium. They found inconsistent results in the case of drought tolerance but about an 18% increase in the corn dry mass. According to the study, Si increased water use efficiency in corn up to 36% [6]. It was also found that applications of Si increase corn growth and grains per cob in drought-stressed plants [7].
Recently, in a study in Pakistan, it was reported that application of plant growth-promoting rhizobacterium in combination with Si in a drought stress condition, increases the drought tolerance and mineral nutrient (K, Ca and Mg) accumulation in tomato. They followed two drought conditions: 45% field capacity and 35% field capacity with 50 mg/L Si as sodium silicate. Maximum fruit yields were reported to be 92.9 g/plant at 45% field capacity and 8.6 g/plant at 35% field capacity [104]. On the other hand, foliar application of Si reduces flower drop and young pod drop of soybean. An experiment was conducted on soybean following 25–70% water capacity of the soil. They used optysil and silvit stimulators at a concentration of 0.25%. It was observed that optysil and silvit stimulators decreased flower drop and increased the number of pods per plant compared to the control by 20% and 18%, respectively [5]. Antioxidant parameters and the photosynthetic rate of soybean were also influenced significantly by Si application [105]. It has also been reported that Si also increases drought tolerance in cucumber [106], sorghum [96], and sunflower [107] (Table 3).

6. Conclusions

A careful review of the published article suggests that soil silicon has a positive impact on growth and development of most of the major crops, especially when they are under environmental stress. It increases crop yield significantly for the crops such as rice, wheat, maize, and sugarcane which are Si accumulators. Si has limited effects on vegetable crop growth and yield because of less absorption capability and availability of Si. In the case of nutrient accumulation, Si increases availability and accumulation of macronutrients N, K, Ca, and S except for P. Phosphorus availability in soil decreases due to high soil pH caused by Si application. On the other hand, Si application was noted to increase availability and accumulation of micronutrients, Fe and Mn, but decreased Cu and Zn. Though, it is worth mentioning that the Si effects on yield, nutrient availability, and accumulation varied between crops and different soil environmental conditions. However, in a drought-stressed condition, Si application resulted in a positive impact in almost every case. It increases drought tolerance as it increases plant water use efficiency and reduces water transpiration loss. All these positive attributes make Si application an important aspect of crop production. Numerous plant yield and growth studies were focused on Si-accumulating cereal crops such as rice and wheat. However, the vegetable cultivation did not attract enough research attention in this regard. Research efforts may need to be directed to highly cultivated vegetables to improve understanding and potential value in horticulture. As discussed earlier, contradictory outcomes were observed on nutrient uptake after silicon application. In some cases, the same nutrient uptake is reported to be increased and decreased by different research groups. Thus, further investigations are essential for understanding the exact mechanism and environmental conditions of nutrient uptake. In addition, the application method (soil and foliar) of Si fertilizer is known to have an impact on plant growth and nutrient uptake. Different application methods have relevant pros and cons on different varieties of crops. Comparative studies can be conducted to understand the models involved in different application methods to determine the optimum method. In summary, research on Si application for agricultural products is an emerging field. The systematic study of Si application in farmlands has commercial prospects to increase crop production as well as profit.

Author Contributions

Conceptualization, R.S.R. and K.M.; software, M.R.I. and M.M.R.; validation, M.R.I., M.M.R. and B.N.; data curation, R.S.R., M.R.I., M.M.R., B.N. and. K.M.; writing—original draft preparation, R.S.R.; writing—review and editing, M.R.I., M.M.R., B.N. and K.M.; visualization, M.R.I., M.M.R. and K.M.; supervision, K.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not Applicable.

Informed Consent Statement

Not Applicable.

Data Availability Statement

The data used to support the findings of this study are available from the corresponding authors upon request.

Acknowledgments

The graduate research assistantship to author one by the Department of Agricultural Sciences, Texas State University is gratefully acknowledged. The authors are thankful to Shihab Uddin of Bangladesh Agricultural University for his effort in editing the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Guntzer, F.; Keller, C.; Meunier, J.D. Benefits of plant silicon for crops: A review. Agron. Sustain. Dev. 2012, 32, 201–213. [Google Scholar] [CrossRef] [Green Version]
  2. Ma, J.F.; Takahashi, E. Soil, Fertilizer, and Plant Silicon Research in Japan; Elsevier: Amsterdam, The Netherlands, 2002. [Google Scholar]
  3. Tubana, B.S.; Babu, T.; Datnoff, L.E. A review of silicon in soils and plants and its role in us agriculture: History and future perspectives. Soil Sci. 2016, 181, 393–411. [Google Scholar] [CrossRef] [Green Version]
  4. Sandhya, K.; Prakash, N.B.; Meunier, J.D.; Sandhya, K.; Prakash, N.B.; Meunier, J.D. Diatomaceous earth as source of silicon on the growth and yield of rice in contrasted soils of Southern India. J. Soil Sci. Plant Nutr. 2018, 18, 344–360. [Google Scholar] [CrossRef] [Green Version]
  5. Artyszak, A. Effect of Silicon Fertilization on Crop Yield Quantity and Quality—A Literature Review in Europe. Plants 2018, 7, 54. [Google Scholar] [CrossRef] [Green Version]
  6. Janislampi, K.W. Effect of Silicon on Plant Growth and Droucht Stress Tolerance. All Graduate Theses and Dissertations, UtahState University, Logan, UT, USA, 2012. [Google Scholar] [CrossRef]
  7. Amin, M.; Ahmad, R.; Ali, A.; Hussain, I.; Mahmood, R.; Aslam, M.; Lee, D.J. Influence of Silicon Fertilization on Maize Performance Under Limited Water Supply. Silicon 2018, 10, 177–183. [Google Scholar] [CrossRef]
  8. Cuong, T.X.; Ullah, H.; Datta, A.; Hanh, T.C. Effects of Silicon-Based Fertilizer on Growth, Yield and Nutrient Uptake of Rice in Tropical Zone of Vietnam. Rice Sci. 2017, 24, 283–290. [Google Scholar] [CrossRef]
  9. Mali, M.; Aery, N.C. Effect of silicon on growth, biochemical constituents, and mineral nutrition of cowpea. Commun. Soil Sci. Plant Anal. 2009, 40, 1041–1052. [Google Scholar] [CrossRef]
  10. Mehrabanjoubani, P.; Abdolzadeh, A.; Sadeghipour, H.R.; Aghdasi, M. Impacts of silicon nutrition on growth and nutrient status of rice plants grown under varying zinc regimes. Theor. Exp. Plant Physiol. 2015, 27, 19–29. [Google Scholar] [CrossRef]
  11. Neu, S.; Schaller, J.; Dudel, E.G. Silicon availability modifies nutrient use efficiency and content, C:N:P stoichiometry, and productivity of winter wheat (Triticum aestivum L.). Sci. Rep. 2017, 7, 3–10. [Google Scholar] [CrossRef]
  12. Luo, W.; Ma, J.; Khan, M.A.; Liao, S.; Ruan, Z.; Liu, H.; Zhong, B.; Zhu, Y.; Duan, L.; Fu, L.; et al. Cadmium accumulation in rice and its bioavailability in paddy soil with application of silicon fertilizer under different water management regimes. Soil Use Manag. 2021, 37, 299–306. [Google Scholar] [CrossRef]
  13. Cai, Y.; Zhang, S.; Cai, K.; Huang, F.; Pan, B.; Wang, W. Cd accumulation, biomass and yield of rice are varied with silicon application at different growth phases under high concentration cadmium-contaminated soil. Chemosphere 2020, 242, 125128. [Google Scholar] [CrossRef] [PubMed]
  14. Wang, B.; Chu, C.; Wei, H.; Zhang, L.; Ahmad, Z.; Wu, S.; Xie, B. Ameliorative effects of silicon fertilizer on soil bacterial community and pakchoi (Brassica chinensis L.) grown on soil contaminated with multiple heavy metals. Environ. Pollut. 2020, 267, 115411. [Google Scholar] [CrossRef] [PubMed]
  15. Zhu, Y.; Gong, H. Beneficial effects of silicon on salt and drought tolerance in plants. Agron. Sustain. Dev. 2014, 34, 455–472. [Google Scholar] [CrossRef] [Green Version]
  16. Santi, L.P.; Nurhaimi-Haris; Mulyanto, D. Effect of bio-silicon on drought tolerance in plants. In Proceedings of the Earth and Environmental Science, IOP Conference Series: Earth and Environmental Science, Jakarta, Indonesia, 18–20 October 2017; IOP Publishing: Bristol, UK, 2018; 183, p. 12014. [Google Scholar]
  17. Ahmad, M.; El-Saeid, M.H.; Akram, M.A.; Ahmad, H.R.; Haroon, H.; Hussain, A. Silicon fertilization—A tool to boost up drought tolerance in wheat (Triticum aestivum L.) crop for better yield. J. Plant Nutr. 2016, 39, 1283–1291. [Google Scholar] [CrossRef]
  18. Shakoor, S.A.; Bhat, M.A.; Mir, S.H. Phytoliths in Plants: A Review. J. Bot. Sci. 2014, 3, 10–24. [Google Scholar]
  19. Green, S.W.; Piperno, D.R. Phytolith Analysis: An Archaeological and Geological Perspective. Am. J. Archaeol. 1991, 95, 741. [Google Scholar] [CrossRef]
  20. Keeping, M.G. Uptake of Silicon by Sugarcane from Applied Sources May Not Reflect Plant-Available Soil Silicon and Total Silicon Content of Sources. Front. Plant Sci. 2017, 8, 1–14. [Google Scholar] [CrossRef] [Green Version]
  21. Khan, M.A.; Goyal, V.; Jain, N. Impact of Ortho Silicic Acid Formulation on Yield and Disease incidence of Potatoes. In Proceedings of the 7th International Conference on Silicon in Agriculture, Bengaluru, India, 24–28 October 2017; p. 137. [Google Scholar]
  22. Kaya, C.; Tuna, L.; Higgs, D. Effect of silicon on plant growth and mineral nutrition of maize grown under water-stress conditions. J. Plant Nutr. 2006, 29, 1469–1480. [Google Scholar] [CrossRef]
  23. Korndörfer, G.H.; Lepsch, I. Effect of silicon on plant growth and crop yield. Stud. Plant Sci. 2001, 8, 133–147. [Google Scholar] [CrossRef]
  24. Ashtiani, F.A.; Kadir, J.; Nasehi, A.; Rahaghi, S.R.H.; Sajili, H. Effect of silicon on rice blast disease. Pertanika J. Trop. Agric. Sci. 2012, 35, 1–12. [Google Scholar]
  25. Ning, D.; Song, A.; Fan, F.; Li, Z.; Liang, Y. Effects of slag-based silicon fertilizer on rice growth and brown-spot resistance. PLoS ONE 2014, 9, e102681. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Rodrigues, F.A.; Datnoff, L.E. Silicon and Plant Diseases; Springer: Berlin/Heidelberg, Germany, 2015; ISBN 9783319229300. [Google Scholar]
  27. Ahammed, G.J.; Yang, Y. Mechanisms of silicon-induced fungal disease resistance in plants. Plant Physiol. Biochem. 2021, 165, 200–206. [Google Scholar] [CrossRef] [PubMed]
  28. Coskun, D.; Deshmukh, R.; Sonah, H.; Menzies, J.G.; Reynolds, O.; Ma, J.F.; Kronzucker, H.J.; Bélanger, R.R. The controversies of silicon’s role in plant biology. New Phytol. 2019, 221, 67–85. [Google Scholar] [CrossRef] [PubMed]
  29. Hodson, M.J.; White, P.J.; Mead, A.; Broadley, M.R. Phylogenetic Variation in the Silicon Composition of Plants. Ann. Bot. 2005, 96, 1027–1046. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  30. Mandlik, R.; Thakral, V.; Raturi, G.; Shinde, S.; Nikolić, M.; Tripathi, D.K.; Sonah, H.; Deshmukh, R. Significance of Silicon Uptake, Transport, and Deposition in plants. J. Exp. Bot. 2020, 71, 6703–6718. [Google Scholar] [CrossRef]
  31. Makabe, S.; Kakuda, K.; Sasaki, Y.; Ando, T.; Fujii, H.; Ando, H. Relationship between mineral composition or soil texture and available silicon in alluvial paddy soils on the Shounai Plain, Japan. Soil Sci. Plant Nutr. 2009, 55, 300–308. [Google Scholar] [CrossRef]
  32. Agostinho, F.; Tubana, B.; Martins, M.; Datnoff, L. Effect of Different Silicon Sources on Yield and Silicon Uptake of Rice Grown under Varying Phosphorus Rates. Plants 2017, 6, 35. [Google Scholar] [CrossRef]
  33. Wang, M.; Wang, R.; Mur, L.A.J.; Ruan, J.; Shen, Q.; Guo, S. Functions of silicon in plant drought stress responses. Hortic. Res. 2021, 8, 1–13. [Google Scholar] [CrossRef]
  34. Liu, X.; Yin, L.; Deng, X.; Gong, D.; Du, S.; Wang, S.; Zhang, Z. Combined application of silicon and nitric oxide jointly alleviated cadmium accumulation and toxicity in maize. J. Hazard. Mater. 2020, 395, 122679. [Google Scholar] [CrossRef]
  35. Zajaczkowska, A.; Korzeniowska, J.; Sienkiewicz-Cholewa, U. Effect of soil and foliar silicon application on the reduction of zinc toxicity in wheat. Agriculture 2020, 10, 522. [Google Scholar] [CrossRef]
  36. Ranjan, A.; Sinha, R.; Bala, M.; Pareek, A.; Singla-Pareek, S.L.; KumarSingh, A. Silicon-mediated abiotic and biotic stress mitigation in plants: Underlying mechanisms and potential for stress resilient agriculture. Plant Physiol. Biochem. 2021, 163, 15–25. [Google Scholar] [CrossRef] [PubMed]
  37. Debona, D.; Rodrigues, F.A.; Datnoff, L.E. Silicon’s Role in Abiotic and Biotic Plant Stresses. Annu. Rev. Phytopathol. 2017, 55, 85–107. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Gong, H.; Chen, K. The regulatory role of silicon on water relations, photosynthetic gas exchange, and carboxylation activities of wheat leaves in field drought conditions. Acta Physiol. Plant. 2012, 34, 1589–1594. [Google Scholar] [CrossRef]
  39. Pilon, C.; Soratto, R.P.; Moreno, L.A. Effects of soil and foliar application of soluble silicon on mineral nutrition, gas exchange, and growth of potato plants. Crop Sci. 2013, 53, 1605–1614. [Google Scholar] [CrossRef]
  40. Zaheer, M.M.; Yasin, N.A.; Ahmad, S.R.; Khan, W.U.; Ahmad, A.; Ali, A.; Rehman, S.U. Amelioration of cadmium stress in gladiolus (Gladiolus grandiflora L.) by application of potassium and silicon. J. Plant Nutr. 2018, 41, 461–476. [Google Scholar] [CrossRef]
  41. Bocharnikova, E.A.; Khomiakov, D.M.; Zhang, P.; Matichenkov, V.V.; Liu, Y.; Pakhnenko, E.P. Effect of Amorphous Silicon Dioxide on Cadmium Behavior in the Soil–Rice Plant System. Moscow Univ. Soil Sci. Bull. 2018, 73, 34–38. [Google Scholar] [CrossRef]
  42. Greger, M.; Landberg, T.; Vaculík, M. Silicon Influences Soil Availability and Accumulation of Mineral Nutrients in Various Plant Species. Plants 2018, 7, 41. [Google Scholar] [CrossRef] [Green Version]
  43. Savant, N.K.; Datnoff, L.E.; Snyder, G.H. Depletion of plant-available silicon in soils: A possible cause of declining rice yields. Commun. Soil Sci. Plant Anal. 1997, 28, 1245–1252. [Google Scholar] [CrossRef]
  44. Taha, R.S.; Seleiman, M.F.; Shami, A.; Alhammad, B.A.; Mahdi, A.H.A. Integrated Application of Selenium and Silicon Enhances Growth and Anatomical Structure, Antioxidant Defense System and Yield of Wheat Grown in Salt-Stressed Soil. Plants 2021, 10, 1040. [Google Scholar] [CrossRef]
  45. Savant, N.K.; Snyder, G.H.; Datnoff, L.E. Silicon Management and Sustainable Rice Production. Adv. Agron. 1997, 58, 151–199. [Google Scholar]
  46. Maghsoudi, K.; Emam, Y.; Ashraf, M. Foliar Application of Silicon at Different Growth Stages Alters Growth and Yield of Selected Wheat. J. Plant Nutr. 2016, 39, 1194–1203. [Google Scholar] [CrossRef]
  47. Sirisuntornlak, N.; Ullah, H.; Sonjaroon, W.; Anusontpornperm, S.; Arirob, W.; Datta, A. Interactive Effects of Silicon and Soil pH on Growth, Yield and Nutrient Uptake of Maize. Silicon 2021, 13, 289–299. [Google Scholar] [CrossRef]
  48. Walsh, O.S.; Shafian, S.; Mcclintick-chess, J.R.; Belmont, K.M.; Blanscet, S.M. Potential of Silicon Amendment for Improved Wheat Production. Plants 2018, 7, 26. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Owino-Gerroh, C.; Gascho, G.J. Effect of Silicon on Low pH Soil Phosphorus Sorption and on Uptake and Growth of Maize. Commun. Soil Sci. Plant Anal. 2005, 35, 2369–2378. [Google Scholar] [CrossRef]
  50. Crusciol, C.A.C.; Pulz, A.L.; Lemos, L.B.; Soratto, R.P.; Lima, G.P.P. Eff ects of Silicon and Drought Stress on Tuber Yield and Leaf Biochemical Characteristics in Potato. Crop Sci. 2009, 49, 949–954. [Google Scholar] [CrossRef] [Green Version]
  51. Montesano, F.F.; D’Imperio, M.; Parente, A.; Cardinali, A.; Renna, M.; Serio, F. Green bean biofortification for Si through soilless cultivation: Plant response and Si bioaccessibility in pods. Sci. Rep. 2016, 6, 31662. [Google Scholar] [CrossRef] [Green Version]
  52. Barros, T.C.; De Mello Prado, R.; Garcia Roque, C.; Ribeiro Barzotto, G.; Roberto Wassolowski, C. Silicon and salicylic acid promote different responses in legume plants. J. Plant Nutr. 2018, 41, 2116–2125. [Google Scholar] [CrossRef]
  53. Olle, M. the Effect of Silicon on the Organically Grown Iceberg Lettuce Growth and Quality. Agraarteadus 2017, 28, 82–86. [Google Scholar] [CrossRef]
  54. Ashok, L.B.; Swamy, G.S.K.; Prakash, N.B. Diatomaceous earth as source of silicon in tomato crop. In Proceedings of the 7th International Conference on Silicon in Agriculture, Bengaluru, India, 24–28 October 2017; p. 128. [Google Scholar]
  55. Pavlovic, J.; Kostic, L.; Bosnic, P.; Kirkby, E.A.; Nikolic, M. Interactions of Silicon with Essential and Beneficial Elements in Plants. Front. Plant Sci. 2021, 12, 697592. [Google Scholar] [CrossRef]
  56. Nazirkar, R.B.; Narale, B.; Durgude, A.G. Effect of sources and levels of silicon on soil properties, uptake, yield and quality of Kharif Onion. In Proceedings of the 7th International Conference on Silicon in Agriculture, Bengaluru, India, 24–28 October 2017; p. 141. [Google Scholar]
  57. Gou, T.; Yang, L.; Hu, W.; Chen, X.; Zhu, Y.; Guo, J.; Gong, H. Silicon improves the growth of cucumber under excess nitrate stress by enhancing nitrogen assimilation and chlorophyll synthesis. Plant Physiol. Biochem. 2020, 152, 5361. [Google Scholar] [CrossRef]
  58. Hasanuzzaman, M.; Fujita, M.; Oku, H.; Nahar, K.; Hawrylak-Nowak, B. Nutrients and Abiotic Stress Tolerance; Springer: Singapore, 2018; ISBN 9789811090431. [Google Scholar]
  59. Pati, S.; Pal, B.; Badole, S.; Hazra, G.C. Effect of Silicon Fertilization on Growth, Yield, and Nutrient Uptake of Rice. Commun. Soil Sci. Plant Anal. 2016, 3624, 1532–2416. [Google Scholar] [CrossRef]
  60. Eneji, A.E.; Inanaga, S.; Muranaka, S.; Li, J.; Hattori, T.; An, P.; Tsuji, W.; Eneji, A.E.; Inanaga, S.; Muranaka, S.; et al. Growth and Nutrient Use in Four Grasses Under Drought Stress as Mediated by Silicon Fertilizers. J. Plant Nutr. 2008, 31, 355–365. [Google Scholar] [CrossRef]
  61. Pulz, A.L.; Crusciol, C.A.C.; Lemos, L.B.; Soratto, R.P. Silicate and Limestone Effects on Potato Nutrition, Yield and Quality under Drought Stress. Rev. Bras. Ciência do Solo 2008, 32, 1651–1659. [Google Scholar] [CrossRef] [Green Version]
  62. Reboredo, F.; Lidon, F.C.; Pessoa, F.; Duarte, M.P.; Silva, M.J. The uptake of macronutrients by an active silicon accumulator plant growing in two different substrata. Emirates J. Food Agric. 2013, 25, 986–993. [Google Scholar] [CrossRef] [Green Version]
  63. Ma, J.F. Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses. Soil Sci. Plant Nutr. 2004, 50, 11–18. [Google Scholar] [CrossRef]
  64. Gouharrizi, Z.Z.; Khorassani, R.; Halajnia, A. The effect of silicon on phosphorus uptake and wheat growth under drought stress in a calcareous soil. Environ. Stresses Crop Sci. 2021, 14(3), 665–673. [Google Scholar]
  65. Ma, J.F.; Takahashi, E. Function of silicon in plant growth. In Soil, Fertilizer and Plant Silicon Research in Japan, 1st ed.; Elsevier: Amsterdam, The Netherlands, 2002; pp. 151–154. [Google Scholar]
  66. Hawk, C.; Hyland, J.; Rupert, R.; Colonvega, M.; Hall, S. Assessment of balance and risk for falls in a sample of community-dwelling adults aged 65 and older. Chiropr. Osteopat. 2006, 14, 3. [Google Scholar] [CrossRef] [Green Version]
  67. Vieira da Cunha, K.P.; Williams Araújo do Nascimento, C.; José da Silva, A. Silicon alleviates the toxicity of cadmium and zinc for maize (Zea mays L.) grown on a contaminated soil. J. Plant Nutr. Soil Sci. 2008, 171, 849–853. [Google Scholar] [CrossRef]
  68. Fan, X.; Wen, X.; Huang, F.; Cai, Y.; Cai, K. Effects of silicon on morphology, ultrastructure and exudates of rice root under heavy metal stress. Acta Physiol. Plant. 2016, 38, 197. [Google Scholar] [CrossRef]
  69. Li, J.; Leisner, M.; Frantz, J. Alleviation of copper toxicity in Arabidopsis thaliana by silicon addition to hydroponic solutions. J. Am. Soc. Hortic. Sci. 2008, 133, 70–77. [Google Scholar] [CrossRef] [Green Version]
  70. Flora, C.; Khandekar, S.; Boldt, J.; Leisner, S. Silicon alleviates long-term copper toxicity and influences gene expression in Nicotiana tabacum. J. Plant Nutr. 2019, 42, 864–878. [Google Scholar] [CrossRef]
  71. Kim, Y.H.; Khan, A.L.; Kim, D.H.; Lee, S.Y.; Kim, K.M.; Waqas, M.; Jung, H.Y.; Shin, J.H.; Kim, J.G.; Lee, I.J. Silicon mitigates heavy metal stress by regulating P-type heavy metal ATPases, Oryza sativa low silicon genes, and endogenous phytohormones. BMC Plant. Boil. 2014, 14, 13. [Google Scholar] [CrossRef] [Green Version]
  72. Savić, J.; Marjanović-Jeromela, A. Effect of silicon on sunflower growth and nutrient accumulation under low boron supply. Helia 2013, 36, 61–68. [Google Scholar] [CrossRef] [Green Version]
  73. Elsokkary, I.H. Silicon as a Beneficial Element and as an Essential Plant Nutrient: An Outlook (Review). Alexandria Sci. Exch. J. 2018, 39, 534–550. [Google Scholar] [CrossRef]
  74. Rastogi, A.; Tripathi, D.K.; Yadav, S.; Chauhan, D.K.; Živčák, M.; Ghorbanpour, M.; El-Sheery, N.I.; Brestic, M. Application of silicon nanoparticles in agriculture. 3 Biotech. 2019, 9, 90. [Google Scholar] [CrossRef] [Green Version]
  75. Roduner, E. Size matters: Why nanomaterials are different. Chem. Soc. Rev. 2006, 35, 583–592. [Google Scholar] [CrossRef]
  76. O’Farrell, N.; Houlton, A.; Horrocks, B.R. Silicon nanoparticles: Applications in cell biology and medicine. Int. J. Nanomed. 2006, 1, 451–472. [Google Scholar] [CrossRef]
  77. Tripathi, D.K.; Singh, V.P.; Prasad, S.M.; Chauhan, D.K.; Dubey, N.K. Silicon nanoparticles (SiNp) alleviate chromium (VI) phytotoxicity in Pisum sativum (L.) seedlings. Plant Physiol. Biochem. 2015, 96, 189–198. [Google Scholar] [CrossRef]
  78. Tripathi, D.K.; Singh, S.; Singh, V.P.; Prasad, S.M.; Dubey, N.K.; Chauhan, D.K. Silicon nanoparticles more effectively alleviated UV-B stress than silicon in wheat (Triticum aestivum) seedlings. Plant Physiol. Biochem. 2017, 110, 70–81. [Google Scholar] [CrossRef]
  79. Cui, J.; Liu, T.; Li, F.; Yi, J.; Liu, C.; Yu, H. Silica nanoparticles alleviate cadmium toxicity in rice cells: Mechanisms and size effects. Environ. Pollut. 2017, 228, 363–369. [Google Scholar] [CrossRef]
  80. Abdel-Haliem, M.E.F.; Hegazy, H.S.; Hassan, N.S.; Naguib, D.M. Effect of silica ions and nano silica on rice plants under salinity stress. Ecol. Eng. 2017, 99, 282–289. [Google Scholar] [CrossRef]
  81. Wanyika, H.; Gatebe, E.; Kioni, P.; Tang, Z.; Gao, Y. Mesoporous silica nanoparticles carrier for urea: Potential applications in agrochemical delivery systems. J. Nanosci. Nanotechnol. 2012, 12, 2221–2228. [Google Scholar] [CrossRef] [PubMed]
  82. Lodriche, S.S.; Soltani, S.; Mirzazadeh, R. Silicon Nanocarrier for Delivery of Drug, Pesticides and Herbicides, and for Waste Water Treatment. U.S. Patent Application No. 13/406, 28 February 2012. [Google Scholar]
  83. Janmohammadi, M.; Amanzadeh, T.; Sabaghnia, N.; Ion, V. Effect of nano-silicon foliar application on safflower growth under organic and inorganic fertilizer regimes. Bot. Lithuan. 2016, 22, 53–64. [Google Scholar] [CrossRef] [Green Version]
  84. Torney, F.; Trewyn, B.G.; Lin, V.S.Y.; Wang, K. Mesoporous silica nanoparticles deliver DNA and chemicals into plants. Nat. Nanotechnol. 2007, 2, 295–330. [Google Scholar] [CrossRef] [PubMed]
  85. Gogos, A.; Knauer, K.; Bucheli, T.D. Nanomaterials in plant protection and fertilization: Current state, foreseen applications, and research priorities. J. Agric. Food Chem. 2012, 60, 9781–9792. [Google Scholar] [CrossRef] [PubMed]
  86. Ulrichs, C.; Mewis, I.; Goswami, A. Crop Diversification Aiming Nutritional Security in West Bengal: Biotechnology of Stinging Capsules in Nature’s Water-Blooms. Nanotechnol. Sci. Appl. 2014, 31–53. [Google Scholar]
  87. Rouhani, M.; Samih, M.A.; Kalamtari, S. Insecticidal effect of silica and silver nanoparticles on the cowpea seed beetle, Callosobruchus maculatus F. (Col.: Bruchidae). J. Entomol. Res. 2012, 4, 297. [Google Scholar]
  88. El-Bendary, H.M.; El-Helaly, A.A. First record nanotechnology in agricultural: Silica nano-particles a potential new insecticide for pest control. App. Sci. Rep. 2013, 4, 241–246. [Google Scholar]
  89. Magda, S.; Hussein, M.M. Determinations of the effect of using silica gel and nano-silica gel against Tutaabsoluta (Lepidoptera: Gelechiidae) in tomato fields. J. Chem. Pharm. Res. 2016, 8, 506–512. [Google Scholar]
  90. Ziaee, M.; Ganji, Z. Insecticidal efficacy of silica nanoparticles against Rhyzopertha dominica F. and Tribolium confusum Jacquelin du Val. J. Plant Protect. Res. 2016, 56, 250–256. [Google Scholar] [CrossRef]
  91. Rai, M.; Ingle, A. Role of nanotechnology in agriculture with special reference to management of insect pests. Appl. Microbiol. Biotechnol. 2012, 94, 287–293. [Google Scholar] [CrossRef]
  92. Li, Z.Z.; Chen, J.F.; Liu, F.; Liu, A.Q.; Wang, Q.; Sun, H.Y.; Wen, L.X. Study of UV-shielding properties of novel porous hollow silica nanoparticle carriers for avermectin. Pest Manag. Sci. 2007, 63, 241–246. [Google Scholar] [CrossRef] [PubMed]
  93. Chen, J.; Wang, W.; Xu, Y.; Zhang, X. Slow-release formulation of a new biological pesticide, pyoluteorin, with mesoporous silica. J. Agric. Food Chem. 2011, 59, 307–311. [Google Scholar] [CrossRef] [PubMed]
  94. Xiong, J.; Zhang, L.; Fu, G.; Yang, Y.; Zhu, C.; Tao, L. Drought-induced proline accumulation is uninvolved with increased nitric oxide, which alleviates drought stress by decreasing transpiration in rice. J. Plant Res. 2012, 125, 155–164. [Google Scholar] [CrossRef] [PubMed]
  95. Taiz, L.; Zeiger, E. Plant Physiology, 4th ed.; Sinauer Associates: Sunderland, MA, USA, 2006. [Google Scholar]
  96. Perez, C.E.A.; Rodrigues, F.Á.; Moreira, W.R.; Damatta, F.M. Leaf Gas Exchange and Chlorophyll a Fluorescence in Wheat Plants Supplied with Silicon and Infected with Pyricularia oryzae. Biochem. Cell Biol. 2014, 104, 143–149. [Google Scholar] [CrossRef] [Green Version]
  97. Hattori, T.; Inanaga, S.; Araki, H.; An, P.; Morita, S.; Luxová, M.; Lux, A. Application of silicon enhanced drought tolerance in Sorghum bicolor. Physiol. Plant. 2005, 123, 459–466. [Google Scholar] [CrossRef]
  98. Chen, W.; Yao, X.; Cai, K.; Chen, J. Silicon Alleviates Drought Stress of Rice Plants by Improving Plant Water Status, Photosynthesis and Mineral Nutrient Absorption. Biol. Trace Res. 2011, 142, 67–76. [Google Scholar] [CrossRef]
  99. Ibrahim, M.A.; Merwad, A.M.; Elnaka, E.A. Rice (Oryza Sativa L.) Tolerance to Drought Can Be Improved by Silicon Application. Commun. Soil Sci. Plant Anal. 2018, 49, 945–957. [Google Scholar] [CrossRef]
  100. Nolla, A.; Faria, R.J.; Korndorfer, G.H.; Silva, T.R.B. Effect of Silicon on Drought Tolerance of Upland Rice. J. Food Agric. Environ. 2012, 10, 269–272. [Google Scholar]
  101. Gong, H.J.; Chen, K.M.; Zhao, Z.G.; Chen, G.C.; Zhou, W.J. Effects of silicon on defense of wheat against oxidative stress under drought at different developmental stages. Biol. Plant. 2008, 52, 592–596. [Google Scholar] [CrossRef]
  102. Ullah, U.; Ashraf, M.; Shahzad, S.M.; Siddiqui, A.R.; Piracha, M.A.; Suleman, M. Growth behavior of tomato (Solanum lycopersicum L.) under drought stress in the presence of silicon and plant growth promoting rhizobacteria Characterization bacterial strain. Soil Environ. 2016, 35, 65–75. [Google Scholar]
  103. Kaushik, P.; Saini, D.K. Silicon as a Vegetable Crops Modulator—A Review. Plants 2019, 8, 148. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  104. Hattori, T.; Sonobe, K.; Inanaga, S.; An, P.; Morita, S. Effects of silicon on photosynthesis of young cucumber seedlings under osmotic stress. J. Plant Nutr. 2008, 31, 1046–1058. [Google Scholar] [CrossRef]
  105. Gunes, A.; Pilbeam, D.J.; Inal, A.; Coban, S. Influence of silicon on sunflower cultivars under drought stress, I: Growth, antioxidant mechanisms, and lipid peroxidation. Commun. Soil Sci. Plant Anal. 2008, 39, 1885–1903. [Google Scholar] [CrossRef]
  106. Dupree, P.; Babu, T.; White, B.; Tubana, B.; Datnoff, L. Survey of the plant-available silicon status of agricultural soils in Louisiana. J. Plant Nutr. 2017, 41, 273–287. [Google Scholar] [CrossRef]
  107. Pedreira, N.G.; de Souza Junior, J.P.; dos Santos, A.C.A.; Flores, R.A.; Aragão, A.S.; de Mello Prado, R.; Arruda, E.M.; da Costa, C.F. Nutrition and production of Helianthus annuus in a function of application of leaf silicon. J. Plant Nutr. 2018, 42, 137–144. [Google Scholar] [CrossRef]
Figure 1. Number of Si-related publications in the plant sciences from 1950 to 2021 [28].
Figure 1. Number of Si-related publications in the plant sciences from 1950 to 2021 [28].
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Figure 2. Linear regression between Si uptake and nitrogen (N), phosphorus (P), and potassium (K) uptakes in above-ground biomass of rice variety BC15 [8].
Figure 2. Linear regression between Si uptake and nitrogen (N), phosphorus (P), and potassium (K) uptakes in above-ground biomass of rice variety BC15 [8].
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Figure 3. Comparison of soil- and foliar-applied sodium metasilicate on Si concentration and accumulation in potato leaves, roots, stems, and tubers [39]. Bars having common letters do not differ significantly at 5% level of significance.
Figure 3. Comparison of soil- and foliar-applied sodium metasilicate on Si concentration and accumulation in potato leaves, roots, stems, and tubers [39]. Bars having common letters do not differ significantly at 5% level of significance.
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Figure 4. Diagram of Si deposits between cuticle and epidermal cells in plant leaf.
Figure 4. Diagram of Si deposits between cuticle and epidermal cells in plant leaf.
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Table 1. Effect of Si fertilization on rice growth and yield in China [4].
Table 1. Effect of Si fertilization on rice growth and yield in China [4].
Application Rate
(kg/ha)
Number of Panicles
(×104/ha)
Number of Spikelets/PanicleYield
(kg/ha)
04.8474.77010
754.9473.97870
1055.0374.88160
1355.0376.88230
Table 2. Si% in above-ground parts of major crop plants [74].
Table 2. Si% in above-ground parts of major crop plants [74].
Plant SpeciesSi% in Plant Biomass
Rice (O. sativa)4.17
Wheat (Triticum aestivum)2.45
Barley (Hordeum vulgare)1.82
Tomato (Lycopersicon esculentum)1.54
Sugarcane (Saccharum officianum)1.51
Soybean (Glycine max)1.39
Lettuce (Lactuca serriola)0.97
Corn (Zea mays)0.82
Potato (Solanum tuberosum)0.4
Table 3. Si used as a fertilizer for major crops in different parts of the world with time of research, materials used as a source of Si, and the outcomes (SA: Soil Application, FA: Foliar Application).
Table 3. Si used as a fertilizer for major crops in different parts of the world with time of research, materials used as a source of Si, and the outcomes (SA: Soil Application, FA: Foliar Application).
Crop SpeciesPlace & TimeMaterials Used DosageApplication MethodFindingsReferences
Rice (O. sativa)
 a.
India (2018)
 b.
Vietnam (2017)
 c.
Florida (1997)
 a.
Diatomaceous earth,
 bc.
SiO2
 a.
0, 150, 300, 600 kg/ha (DE)
 bc.
100, 200, 300,400 kg/ha (SiO2)
 a.
SA (pot)
 bc.
Broadcast in 3 split doses
 ab.
Significant increase in biomass and grain yield (up to 600 kg/ha)
 c.
Compete with arsenic ions in root entry point
 bc.
Disease management and yield of rice
 a.
Sandhya et al. [4],
 b.
Cuong et al. [8],
 c.
Savant et al. [45]
Wheat (Triticum aestivum)
 a.
India (2016)
 b.
Florida, b Louisiana (2017),
 c.
Iran (2015)
K2SiO3
 a.
0 and 12 kg/ha (Iran)
 b.
Survey on different dose (LA)
SA
 ac.
Si application causes increased grain yield, no. of spikelets, number of grains per spike
 b.
Increased K concentration up to 28.65 mg/g shoot and 3.5 mg/g grain
 abc.
Increased drought tolerance
 a.
Ahmad et al. [17]
 b.
Dupree et al. [106]
 c.
Savant et al. [45]
Potato (Solanum tuberosum)
 c.
Israel (2012)
 a.
Brazil (2013)
 b.
India (2017), c Poland (2018)
 bc.
Silicic acid (H4SiO4),
 a.
Ferti-silica, aSilamol
 a.
250 L/ha (Silamol)
 a.
50 mg/dm3 Si (Ferti-silica)
 c.
SA
 ab.
FA
 a.
Delayed skin maturation
 abc.
Average tuber weight increase
 b.
Yield increase approximately 15%
 a.
Gong and Chen [38]
 b.
Khan et al. [21]
 c.
Artyszak [5]
Lettuce (Lactuca sativa), Pea (Pisum sativum), Carrot (Daucus carota)Sweden (2018)K2SiO380 and 1000 kg Si/ha Soil
100, 500, 1000 and 5000 µM Si in nutrient medium
SAIncreases mineral nutrient (Ca, P, S, Mn, Zn, Cu) accumulationBocharnikova et al. [41], Greger et al. [42]
Chard (Beta vulgaris),
Kale (B. oleracea var. sabellica)
Brazil (2019)NaKSiO3,
K2SiO3
0.00; 0.84; 1.68 and 2.52 g/LFAIncreased accumulated Si in both sources and vegetables
Increased fresh matter content
Pedreira et al. [107]
Corn (Zea mays)Turkey (2017)Exogenous Si0, 300, 750 kg Si/haSA (broadcasting)Formation of less soluble zinc silicates in the cytoplasmKeeping et al. [20]
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Rea, R.S.; Islam, M.R.; Rahman, M.M.; Nath, B.; Mix, K. Growth, Nutrient Accumulation, and Drought Tolerance in Crop Plants with Silicon Application: A Review. Sustainability 2022, 14, 4525. https://doi.org/10.3390/su14084525

AMA Style

Rea RS, Islam MR, Rahman MM, Nath B, Mix K. Growth, Nutrient Accumulation, and Drought Tolerance in Crop Plants with Silicon Application: A Review. Sustainability. 2022; 14(8):4525. https://doi.org/10.3390/su14084525

Chicago/Turabian Style

Rea, Rafea Sultana, Mohammad Rafiqul Islam, Mohammad Mahmudur Rahman, Bibhash Nath, and Ken Mix. 2022. "Growth, Nutrient Accumulation, and Drought Tolerance in Crop Plants with Silicon Application: A Review" Sustainability 14, no. 8: 4525. https://doi.org/10.3390/su14084525

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