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Review

Nanotechnological Interventions in Agriculture

1
Co-Innovation Centre for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China
2
Bamboo Research Institute, Nanjing Forestry University, Nanjing 210037, China
3
Plant Biotechnology Section, Department of Botany, Aligarh Muslim University, Aligarh 202002, India
*
Authors to whom correspondence should be addressed.
Nanomaterials 2022, 12(15), 2667; https://doi.org/10.3390/nano12152667
Submission received: 4 May 2022 / Revised: 28 July 2022 / Accepted: 29 July 2022 / Published: 3 August 2022

Abstract

:
Agriculture is an important sector that plays an important role in providing food to both humans and animals. In addition, this sector plays an important role in the world economy. Changes in climatic conditions and biotic and abiotic stresses cause significant damage to agricultural production around the world. Therefore, the development of sustainable agricultural techniques is becoming increasingly important keeping in view the growing population and its demands. Nanotechnology provides important tools to different industrial sectors, and nowadays, the use of nanotechnology is focused on achieving a sustainable agricultural system. Great attention has been given to the development and optimization of nanomaterials and their application in the agriculture sector to improve plant growth and development, plant health and protection and overall performance in terms of morphological and physiological activities. The present communication provides up-to-date information on nanotechnological interventions in the agriculture sector. The present review deals with nanoparticles, their types and the role of nanotechnology in plant growth, development, pathogen detection and crop protection, its role in the delivery of genetic material, plant growth regulators and agrochemicals and its role in genetic engineering. Moreover, the role of nanotechnology in stress management is also discussed. Our aim in this review is to aid researchers to learn quickly how to use plant nanotechnology for improving agricultural production.

1. Introduction

Agriculture is one of the most promising sectors to play in the world economy as it provides food for humans and animals and produces raw materials for various industries. For decades, the demographic data of the world population has been constantly changing, and the number of people is expected to exceed 9.7 billion by 2050 [1]. Moreover, according to the estimation of the Food and Agriculture Organization [2], the agriculture sector needs to produce twice as much food to meet the global demands by 2050. The increasing world population, decreasing cultivable land, high rate of deforestation and changing climatic conditions, especially increasing temperature and CO2 levels, stress the need to develop new technologies to enhance the yield and productivity of plants during challenging environmental conditions. The challenges of abiotic stress on plant development and growth are among the emerging ecological impacts of climatic change [3]. Plants are fixed and hence exposed to extreme environmental situations such as drought, heavy metals, light intensities, UV, flood, etc., and these stressors from the environment can cause various stress to a variety of species [4,5]. These stressful conditions induce reactive oxygen species (ROS) which in turn cause degradation of the membrane, increase cell toxicity and retard plant growth. Meanwhile, antioxidant systems through enzymatic and non-enzymatic methods remove ROS and relieve stress produced due to oxidation.
However, in field conditions, distinctive effects on plants frequently take place due to this combination of stresses leading to unanticipated physiological effects [6]. Nowadays, various methodologies have been explored focusing on stress tolerance in plants. An effort has been made to breed crops with stress-tolerant traits in the past few decades by considering two important approaches, viz., conventional and mutation breeding. However, the uncertainty of results and the time-consuming process were the drawbacks of these two processes [7]. Introduction of exogenous genes or changing the expression level to improve stress tolerance and obtaining a genetically modified plant is another method [7]. However, this practice is limited and unacceptable in many countries leading to the limitation of this technique. Priming is another approach to make the plants resistant to environmental stresses. Chemical priming is helpful in the establishment of resistance because it induces the existing defense mechanism of the plant without resorting to genetic changes. Pre-treating or priming plants with natural or synthetic compounds enhanced response under stresses such as heat, salinity, drought, etc., in comparison to unprimed plants [8]. The defense mechanism of plants is enhanced by priming due to its ability to activate and amplify those signals which can control the accretion of ROS, redox signaling and expressions of the genes involved in resisting stresses [9]. Most frequently utilized priming agents are amino acids, polyamines, melatonin fungicides, phytohormones, reactive nitrogen, sulfur and oxygen species, etc. [10,11,12].
Today, the application of nanotechnology and its tools in the chemical priming field improved the effectiveness of the chemicals used for priming and thus reduced the chemical release into the environment [13]. Nanotechnology is a novel and innovative approach to develop and design real-world applications of materials at the nanoscale [14,15]. In the agricultural sector, nanotechnology has a great role in dealing with various issues such as making crop plants more resistant to biotic and abiotic stresses and increasing the productivity of the plants. In addition to this, problems associated with the overuse of fertilizers and pesticides and their harmful impact in relation to the environment could also be tackled with a targeted and proper use of nanotechnology [16,17]. Gradually, the nanotechnological intervention in agricultural sectors is increasing and making this sector an income-generating business [18]. Overall, the use of nanotechnology will enhance food quality and global production in an environmentally friendly way by solving the problem associated with water and soil [19,20].
Furthermore, NPs participate in growth and development and also provide protection to the plants. During stress responses, NPs can also modify and change the expression of the genes that cause biosynthesis and organization of cells, electrons and transport of energy [21]. The diverse physicochemical characteristics of nanoparticles is due to their smaller size. They are known for higher reactivity, biochemical activity and solubility due to a higher surface-to-volume ratio [22]. The target-specific and low-quantity release of NPs make them different from various other elements used in plants [23] In addition, the behavior of NPs depends strongly on their chemical composition, particle size and function. Moreover, NPs play a significant role in protecting the plant against different stressors, accelerating the scavenging of ROS, protecting photosynthetic machinery and reducing osmotic and oxidative stress [24,25,26]. Different types of NPs with their unlimited potential to revolutionize the agricultural sector have been used these days along with their benefits and drawbacks [19,27]. From various studies, it was established that nanoparticles are crucial for crop improvement, but their actual working mechanism and mode of interaction are still at an initial stage [28,29].
Nanomaterials (NMs) have become an elemental part of NPs due to their distinctive characteristics in terms of physical, chemical, mechanical and thermal properties. The NMs can be natural or tailored by using physical, chemical or biological methods [30]. In terms of the recent progress, an emphasis has been placed on the use of nanomaterials (NMs) or engineered nanoparticles (ENPs) in agriculture sectors. Nowadays, engineered NPs are used as nanoherbicides and nanopesticides by considering two important factors: controlling the release of agrochemicals with minimized nutrient loss and enhancing plant morphogenesis by targeting particular cellular organs of plants. These days, nanomaterials are present in different aspects of day-to-day life, such as the environment, agriculture, food and cosmetic industry, waste water treatment, medicine, energy information and communication [31,32,33,34,35]. Various NMs such as single-walled carbon nanotubes (SWCNTs), multi-walled carbon nanotubes (MWCNTs), silver, silicon, zinc, iron and titanium dioxide (TiO2) have been observed to improve plant growth and development [19,27,36]. Therefore, NPs are involved in different aspects of agriculture such as making the plant resistant to disease and pests, improving nutrient absorption, acting as a carrier for various vital compounds and improving the effectiveness of fungicides, pesticides, herbicides and the delivery of fertilizers leading to a boosted growth of plants [27,37]. However, the use of NMs for the improvement of the crop and sustainable agriculture is still in its initial phase. Hence, to address the problems in agriculture, the knowledge of NPs and their application in agriculture is crucial for workers. It is also mandatory to build up a fundamental understanding of NPs in relation to agriculture. This section briefly describes the role of nanotechnology in different aspects. Considering the importance of nanotechnology, the aim of this review is to summarize the available information and developments on nanotechnological interventions in agriculture. Furthermore, the current communication relates to the use of tailored NMs for sustainable agriculture with a special emphasis on handling plant stress.

2. Nanoparticles: Scientific Aspects

The term “nano” is derived from a Greek word that means “dwarf”, and it signifies 10−9 parts of any unit [38]. It can be organic or inorganic molecules having dimensions of less than 100 nm and a wide surface area [39]. Plants react differently in the presence of different NPs depending on the size, shape and chemical and physical properties of the NPs [40]. Figure 1 describes the different types of NPs based on function, morphology, chemical structure and physiochemical properties. Applied NPs in agriculture are categorized into three groups, i.e., organic, inorganic (metal and metal oxide NPs) and combined NPs [27]. In most studies, inorganic NPs are used, i.e., metal 25% and metal oxides 54%, while carbon-based NPs are used in only 10% of studies; ZnO, TiO2, CuO and CeO2 are the most commonly utilized metal oxide NPs, whereas Ag NPs are most commonly used in the metallic NP group [41]. Various other distinctive forms of NPs are core-shell NPs, polymer-coated magnetite NPs, photochromic polymer NPs, Au NPs, Pd NPs and Ni NPs, while some other NPs are metal oxides, for example, MgO NPs, TiO2 NPs, CeO2 NPs, ZrO2 NPs and ZnO NPs. All these NPs have a specific set of properties and can be synthesized by conventional or unconventional approaches [42]. Generally, two processes (top down and bottom up) are employed for the synthesis of NPs [43,44] (Figure 2). Different lithographic techniques, for example, milling, grinding, etc., are employed to break down bulk material into substances at the nanoscale in top-down approaches. While in the case of bottom-up approaches, atoms self-assemble into new nuclei and eventually grow into particles with a nanoscale that also includes physical and chemical methods. Toxic starting materials, high running costs, toxic contamination and high temperature are required in these methods to obtain the final products [43,44]. Several attempts have also been performed to use biological catalysts, viz., plants, bacteria, fungi and yeast, in order to avoid obstacles found in physical and chemical methods [45].

3. Nanotechnological Interventions in Agriculture

3.1. Role of Nanotechnology in Germination and Growth of Crop

In the past few years, researchers’ interest has increased in nanomaterials and their impact on agriculture. It appears that NMs are involved in the germination of plants and seeds as well as plant growth [34]. Moreover, some researchers have acknowledged that the size of NPs might enhance the breakdown of organic materials and absorption of inorganic compounds, resulting in an improved photosynthetic rate and generation of oxygen-free radicals during photosynthesis [34]. Zheng et al. stated that spinach seeds that were treated with nano-TiO2 produced plants that in comparison to non-treated plants consisted of 73% more dry weight, a 45% percent increase in chlorophyll and a 3-fold increase in photosynthetic rate during the germination period of 30 days. In spinach seeds, the germination rate depends on the size of the nanomaterial; hence, the smaller the size, the higher the germination [46]. Ling and Xing investigated NP phytotoxicity and its effect on canola, radish, rapeseed, ryegrass, corn, cucumber and lettuce germination [47]. In ryegrass and maize, the germination was inhibited by a higher concentration of nano-Zn, which was 2000 mg/L, whereas inhibitory effects on root length were produced on 200 mg/L ZnO in the case of the other plants [47]. The effect of four NPs (CeO2, Lanthanum (III) oxide-La2O3, Gadolinium (III) oxide-Gd2O3, Ytterbium oxide-Yb2O3) on radish, rape, lettuce, wheat, tomato, cabbage and cucumber root growth was studied by [48]. They concluded that root growth depends on the type and concentration of NPs as supported by the study of Lin and Xing [47]. Moreover, nano-CeO2 did not produce any effect on elongation of the root, while, at the same concentration, the other three above-mentioned NPs affected the various stages of root growth, and most of them were inhibitory [48]. Munir et al. studied the effect of ZnO NPs on the seed priming of wheat [49]. They found that the priming of seeds enhanced the total biomass content, photosynthetic efficiency and various other growth criteria of wheat seedlings. Moreover, it was observed that wheat is capable of accumulating ZnO NPs at a higher concentration in its shoot, roots and grains [49]. Similarly, foliar application of ZnSO4 and ZnO NPs on the coffee plant resulted in a change in the fresh and dry weight of roots and leaves in comparison to the non-treated plant [50]. A total of 10 mg L−1 of Zn either in the form of ZnSO4H2O or ZnO NPs was used for foliar application on a one-year-old greenhouse-grown coffee plant. It was found that ZnO NPs positively affect the fresh weight of roots by 37% and leaves by 95% as compared to control, and similarly, a dry weight increase was reported as 28% in roots and 20% in leaves, whereas 85% was reported for the stem [50]. In tomatoes, salt stress can be reduced by applying 250 mg L−1 of Cu NPs. The decrease in stress might be due to an increase in the ratio of the Na+/K+ pump. Moreover, the fruit of treated plants contains more Cu, glutathione, vitamin C and phenols in comparison to non-treated plants [51]. Khan et al. evaluated the influence of Ag NPs on various growth parameters of Silybum marianum [52]. They observed that the Ag NPs at a lower concentration of 30 μg/mL were able to enhance germination and growth, while at higher concentrations, they showed an inhibitory effect [52]. Similarly, Mehta et al. studied the effect of Ag NPs on Brassica juncea, Triticum aestivum and Vigna sinensis at different concentrations of 0, 50 and 75 ppm [53]. Moreover, bacteria-synthesized (Bacillus cereus, Brevundimonas diminuta, Serratia marcescens) Ag NPs improve the germination of seeds, length of shoot and root, number of leaves and fresh weight in Triticum aestivum [54]. In the germination of rice seeds, the effect of fluorescein isothiocyanate (FTIC)-labeled silica and photostable cadmium-selenide (CdSe) quantum dots were investigated. It was observed that the FTIC-labeled Si NPs improve germination while quantum dots inhibit the rate of germination [55]. Another study on seed-priming-improved germination in Citrus lanatus showed that the seedling emergence rate at 14 days was higher in Ag NP treated seeds as compared to the other treatment [56]. They found that glucose and fructose content was enhanced during germination in Ag NP treated seeds at the interval of 96 h. In a recent study on Vigna radiata, it was found that TiO2 NPs from a seed extract of Trachyspermum ammi significantly improved the growth of V. radiata in both in vitro and in vivo conditions [57]. Application of carbon nanomaterials, viz., CNTs and CNPs, stimulated corn seed germination with Cu stress alleviation [58]. They found that both CNTs and CNPs have a positive effect, but the improvement made by CNPs on plant growth was found to be stronger than CNTs. Similarly, seed priming with MWCNTs modulates plant growth and seed germination in two maize varieties under cadmium stress [59]. The study found that MWCNT application increases the germination rate by 11.42% and 24.76% in both varieties, and along with this, an increase in shoot and root fresh weight and antioxidant enzyme activity was also reported. Overall, the studies reported above showed that seed priming with NPs could enhance seed germination growth and rate while maintaining the quality of the plant/fruit using sustainable nanotechnological approaches.

3.2. Role of Nanotechnology for Delivery of Plant Growth Regulators (PGRs)

PGRs are classified under a special family of pesticides, are synthesized artificially and play a very crucial role in plant growth and development at very low concentrations. They belong to the five major categories similar to phytohormones, viz., auxin, cytokinins, gibberellins, ethylene and abscisic acid (ABA). Both phytohormones and PGRs are similar in structure and physiological effects but different in their derivations [60]. The combination of NMs and PGRs is employed in agriculture in detecting the trace amount of plant hormones in the plant and its availability to obtain a better response. In addition, it is also found that NMs help in the absorption and transport of PGRs into the plant. One of the characteristic features of sustainable agriculture is the efficient delivery of agrochemicals and organic molecules. Usually, broadcasting or spraying is used to add agrochemicals to the crops. These methods are not appropriate because most of the pesticides, fertilizers and phytohormones are wasted and only a small amount, which is far below the actual required amount, reaches the crops. Hydrolysis, photolysis, chemical leaching and microbial decays are the major factors responsible for the losses. Therefore, in recent years, the use of NPs has increased for agrochemical delivery as they provide efficient transfer systems due to their wide surface area, ease of binding and quick mass transfer [34]. Similarly, encapsulation of GA-3 (gibberellic acid) was carried out using alginate–chitosan and chitosan–tripolyphosphate, and it was reported that leaf area and chlorophyll and carotenoid content increased in the latter case [61]. β-Cyclodextrin-modified magnetic graphene oxide materials were used to trace the five PGRs in a vegetable sample [62]. Similarly, a crystalline porous polymer material (Fe3O4@COF(TpDA)) was used for PGR detection in fruits and vegetables [63]. In another study on coriander and garlic growth, it was observed that graphene quantum dots were found suitable to enhance the PGR level [64]. They reported that graphene quantum dots promoted the growth rate in almost all plant parts such as roots, shoots, leaves, flowers and fruits. However, the main difficulties in the utilization of PGRs are their degradation when coming into contact with heat and light. Hence, to cope with these environmental problems, nanoscale materials are employed that promote more stability and less environmental risk [65].

3.3. Role of Nanotechnology in Plant Genetic Engineering

Plant genetic engineering is found to be an important tool used to improve the quality of the crop plants in terms of their yield, enhancement in secondary metabolite contents in medicinal plants, etc. Agrobacterium-mediated and gene-gun transformation methods are widely employed techniques in plants. However, there are some limitations to these techniques; for example, Agrobacterium-mediated transformation is purely host specific, whereas tissue damage may be reported in the gene-gun method. A new method based on nanoparticle-mediated genetic transformation opens the door to shaping modern agriculture systems by removing these restrictions. The NP-mediated transformation boost is a completely new strategy in plant biotechnology in promoting a sustainable agriculture system. Gene transfer and protein delivery with the use of nanotechnology have their role in crop engineering, drug delivery and environmental monitoring. Conjugation of DNA with NPs decreases the chance of degradation of DNA through DNase enzymes and ultrasound. These benefits allow transferring genetic material in plant cells by the use of ultrasound-assisted nanotechnology. It is based on the introduction of part of the exogenous nucleic acid into the target leading to the interference in the normal transcription of the target gene. NPs have the ability to deliver DNA, RNA and proteins (Figure 3A–C), and in addition to this, chloroplast-targeted transgene delivery has also been widely employed by several scientists. Among these, RNA interference (RNAi) is a widely employed technique to protect and enhance the quality of the crop. RNAi delivers double-stranded RNA or small interfering (si) RNA in the nucleus affecting the normal gene coding process [66] (Figure 3B). It is found that NP-mediated RNA delivery is most widely employed due to its high specificity and low-cost development. The applied NMs in the RNAi delivery system protect siRNA and help them to reach the target site with high efficacy [67].
Layered double hydroxide (LDH) bioclay was used as a carrier for the delivery of dsRNA (double-stranded RNA) in cowpea and tobacco for crop protection [68]. The stability of dsRNA was maintained by LDH bioclay followed by the release of dsRNA by the formation of carbonic acid on the surface of the leaf from atmospheric CO2 and H2O. Kwak et al. and Demirer et al. found that single-walled carbon nanotubes have the ability to deliver genetic material into chloroplasts and nuclei separately [69,70]. Carbon nanotubes (CNTs) can enter the plant cells through the LEEP (lipid exchange envelope penetration) process [71]. Similarly, mesoporous silica nanoparticles (MSNPs) are able to deliver genes with controlled release aided by Au NPs. Meanwhile, the loading of a gene and its chemical inducer takes place on MSN and its capping is performed by Au NPs which reduce leaching and increase efficient gene expressions [72]. A successful transfer of a gene with the help of silicon dioxide NPs was achieved in maize and tobacco. Insect-tolerant novel crop varieties are also developed using the NP-assisted delivery process. For instance, DNA-coated NPs are used to bombard cells and tissues as bullets in gene-gun technology in order to transmit the requested genes to selected plants [34]. Moreover, in tobacco plants, a DNA nanostructure was used to transfer siRNA for silencing continuously expressing the GFP gene [73]. Similarly, in Arabidopsis plants, PEI-coated Au NPs were used to transfer siRNA and silenced the NPR1 (nonexpressor of pathogenesis-related gene 1) gene [74]. Ideally, positively charged low-cost NMs devoid of heavy metals are best suited for the delivery of negatively charged genetic material into plant cells. The above reports show the potential of biomolecules in plant cells and explore the possible ways for the development of NP-mediated genetic transformation.

3.4. Role of Nanotechnology in Plant Pathogen Detection and Crop Protection

Pathogen infection of the crops is one of the important factors accountable for the reduction in crop yield. Numerous emerging contagious diseases along with the old ones reduce the continuous supply of food [75]. As per the estimation, insect pests caused a 14% loss worldwide, whereas a 13% loss was caused by weeds and plant diseases separately, and the overall value of this crop loss is USD 2000 billion per year. Reduced plant growth, low yield and poor productivity are some of the consequences of chronic stress in plants due to pathogen attacks. Generally, the symptoms can be seen on leaves, stems and fruits, on the basis of which the diagnosis of diseases could be initiated [76]. However, early diagnosis is not possible because plant diseases are initially symptomless. Therefore, early detection of disease and pathogens along with the regular monitoring of plant health should be a prerequisite process in agriculture. This approach will also help to prevent the development of other diseases. Various methods have been employed for the detection of the disease such as polymerase chain reaction (PCR)-assisted techniques of DNA hybridization [77], ELISA-based tissue print or direct dot-blot immunoassay (DTBIA) DNA-based methods and immunoassays [75]. However, the above methods have some limitations such as that they show low sensitivity, are time consuming and require a large amount of target tissue. Nanotechnology, NPs and QDs (quantum dots) have emerged as important tools for the rapid detection of pathogens with high accuracy. NPs are able to detect pathogens directly or be utilized for the detection of the compounds specific to the disease. Similarly, biosensor-based antibodies and DNA, nanoimaging and nanopore DNA sequencing have the potential to play an important role in the early recognition of pathogens with a high rate of specificity and rapid detection [78]. Moreover, nanodiagnostic kits have the potential to detect the plant pathogen and help farmers in the control and prevention of epidemic diseases. In addition to this, various nanosystems and nanodevices are being employed for the sequencing of DNA, and the use of these techniques is rapidly growing due to their flexibility and high sensitivity as compared to conventional techniques. Therefore, for rapid detection using these advanced techniques, phytopathologists and nanopathologists need to work constantly, so as to benefit the farmers. Figure 4a depicts the role of nanotechnology in plant disease control.
Nanophytopathology is a new era in plant pathogen detection and crop protection that uses nanotechnology to detect and diagnose plant pathogens at an early stage which may open doors to preventing epidemic diseases. Nowadays, plant pathologists apply the combination technique of nanophytopathology to explore plant pathogen detection and measurements. Nanophytopathology is applied to monitor the pathogen population, the interaction between the plant and microbes and the transfer of genetic material between the pathogen and the host. Figure 4b summarizes the potential role of nanophtopathology. Similarly, nanochips are a kind of microarrays that comprises fluorescent oligo capture probes through which hybridization can be detected [79]. These nanochips are well known for their ability to sense single nucleotide variations of the virus and bacterial genome [79]. To detect Xanthomonas axonopodis pv. Vesicatoria, the causal organism of bacterial spots in solanaceous crops, Yao et al. used fluorescence Si NPs along with antibodies [79]. Similarly, Singh et al. utilized nano-Au immunosensors to sense Tilletia indica which causes Karnal bunt in wheat [80]. The physiological condition of plants changes in response to stress conditions. Many of these defense responses are controlled by plant hormones, mainly methyl jasmonate and salicylic and jasmonic acid. Furthermore, carbon nanotubes are also used to detect pathogens in plants and the environment. To detect Botrytis cinerea in healthy-looking apple plants before the appearance of symptoms of the disease, carbon-nanotube-based nanosensors were utilized that helped to give information about the pathogen before the spread of the infection to the field. Hence the information derived through these sensors is also useful to design pesticides against the specific pathogen [81,82]. Another study on strawberry crop wherein ZnO NPs were applied in the visible light resulted in remarkable strawberry crops [83,84]. They found that ZnO NPs inhibited the growth of the plant pathogen (B. cinerea) by 12% as compared to the control plant. Similarly, the antifungal activity of Cu NPs and Ag NPs against Alternaria brassicicola and Bipolaris sorokiniana was examined, and it was found that mycelium growth was moderate on Cu NPs, whereas strong inhibition was reported in the case of Ag NPs [83]. Peptide-encapsulated SWCNTs were used for bacterial detection and classification, where 16 different peptides were used [85]. Gold NPs were applied for the detection of Begomovirus in chilli and tomato, and the results show that the assay was able to detect 500 ag/µL of begomoviral DNA [85]. The above report helps in broadening our understanding of early pathogen detection and monitoring plant health which will be beneficial for better crop yield and productivity.

4. Tailored Nanomaterials for Sustainable Agriculture

The agricultural control process can be monitored by nanotechnology, especially through its nanosize size. The potential interests such as improvement in the quantity and quality of food, reduced participation in agriculture and increased absorption of nanoscale nutrients from the soil are the main reasons for the rapidly increasing constraint. Natural resources, agriculture and food are part of competitions such as susceptibility, sustainability and human health. The purpose of nanomaterials in agriculture is to reduce the amount of dispersed chemicals, loss of nutrients in fertilization and management of the nutrients and pests to increase the yield. Nanomaterials are being tailored in a special way for agricultural use, viz., nanofertilizers, nanopesticides, nanofungicides, nanobioremediation and nanobased biosensors and absorbent materials. Figure 5 summarizes the positive effect of different nanomaterials in sustainable agriculture.
Sustainable development and food security are the major rising problems in agriculture which can be controlled by recently developed important technological advancements. These continuous agricultural advancements and the use of natural and synthetic materials play a vital role in overcoming the world’s booming population’s rising food demand. In particular, nanotechnology has the capacity to propose useful alternatives to different types of issues related to agriculture. Nanoparticles are scientifically important because the distance between bulk materials and molecular or atomic structures is negligible in this case. To save many species from extinction and conserve the environment, sustainable farming includes the possible use of fewer agrochemicals. For instance, sustainable agriculture and environmental systems are influenced by scrutiny and quality control, soil and plant health, and protection. Critical aspects of sustainable agriculture are agrochemical and organic molecule delivery systems, as well as the transfer of DNA molecules or oligonucleotides into plant cells. Recently, the slow and controlled release of fertilizers, herbicides and pesticides synthesized by nanotechnology has gained great interest in agriculture in order to assure environmentally sustainable agricultural activities [34]. In this section, we discuss the customized nanomaterials and their use in sustainable agriculture.

4.1. Nanofertilizers

The use of nanotechnology in agriculture could be a potential solution to the ever-increasing human hunger problem. The integration of nanotechnology with fertilizer may serve as a promising advance to combat food scarcity and environmental degradation. Nanoparticles containing nutrients, which are protected by a thin nanoscale polymeric layer, can enhance plant growth and improve the efficiency of conventional fertilizers as one or more nutrients can be delivered to the target as a nanoemulsion or nanoparticle. Furthermore, the increased surface tension by nanocoating on fertilizers allows plants to adhere to material more efficiently. The beneficial effect of nanofertilizers led to an increase in plant potential and a reduction in the negative consequences of conventional fertilizers [86]. Some approved nanofertilizers that are being used in the world today are Katra nano magnesium sulphate, prime aavirat growth booster, Iffco nano 12 manure, agro kill, carbon nano powder, nano calcium, nano capsule, nano micro nutrient, PPC nano, nano max NPK, TAG nano, Nano green, nano agro care and Biozar nanofertilizer [87]. It is known that conventional fertilizers are usually applied by foliar spray and soil dispersal. The final concentration of fertilizer that needs to reach the plant is the determining factor of the mode of application. Usually, a very small amount of conventional fertilizers affect the target site [88]. In applied conventional fertilizers, about 40–70% of nitrogen, 80–90% of phosphorous and 50–90% of potassium content is lost to the environment, causing unsustainability and economic losses [89]. These complications increase the constant use of fertilizers which adversely affect the balance of nutrients in the soil and the native flora and fauna and increase environmental pollution [88]. In recent years, the requirement for conventional fertilizers has been reduced by using nanofertilizers which increase the fertility of the soil and the quantity and quality of crops. Nanofertilizers are less harmful and non-toxic to humans, increase crop resistance to disease and drought, decrease crop involvement and increase earnings [90]. NFs are tailored nutrient fertilizers made up of a nanostructured articulation that delivers nutrients to plants either completely or partially for the assimilation or slow release of active constituents. Nanofertilizers provide the nutrients to the plant either by encapsulating inside nanomaterials and nanoporous materials or by coating with a thin polymer film. It is proved that nanofertilizers show better results compared to conventional fertilizers in fulfilling the requirements of plant roots, promoting disease resistance, enhancing plant growth, improving the stability of plants and encouraging deeper rooting of the crops [91].

4.2. Nanofungicides

In the field of agriculture, pathogenic fungi are the major barriers to and problems of agricultural growth, which cause more than 70% of diseases in plants and reduce the yields by up to 100% [92]. Conventionally, fungal diseases are treated by chemical fungicides which have harmful impacts on plants’ health and the surrounding environment. The use of nanofungicides is a valuable solution to overcome these problems depending on the size and shape of the NPs. The danger induced by fungicides is significant as their effects are both harmful and beneficial. NPs are predicted to be a valuable alternative to fungicides that come with phytocompounds and biocontrol agents. Some commercially available nanomaterial-based fungicides are Subdue MAXX and Cruiser MaXX [87]. Initial studies on nanofungicides were directed in early 1997 to unravel the incorporation of fungicides in solid wood [93,94]. Subsequently, conventional biocides and broad NPs with anti-fungal properties have been studied. Chitosan, polymer mixes and silica are the most commonly used nanoparticle transporters. A wide range of fungi was studied which are used as nanocarriers for nanofungicides and insecticides. Silver, TiO2, carbon, silica and alumino-silicates have been considered as effective antifungal agents [95]. Among them, Ag has the highest potential which increased the percent of seed germination and seedling weight [95]. Silver and TiO2 nanoparticles were reported to inhibit various plant pathogens. Kannan et al. reported that nanosilica treatment enhanced plant resistance by increasing phenolic compounds [96]. Besides these, Ag NPs are widely studied nanoparticles for their innumerable applications and due to their fast response delivery in bacteria and fungi [97]. Gajbhiye et al. found that AgNPs and fluconazoles have antifungal activity toward different fungi such as Fusarium semitectum, Phoma herbarum and Phoma glomerata [98]. Similarly, Ag2S NPs and Ag NPs have also been used against Aspergillus niger, Fusarium oxysporum, Magnaporthe grisea, Bipolaris sorokiniana, Fusarium culmorum and Colletotrichum [99,100,101,102]. Similarly, MgO and ZnO were used against Fusarium oxysporum, Alternaria alternata, Rhizopus stolonifer and Mucor plumbeus [103]. Park et al. showed the antifungal activity of Ag-silica NPs (nanocomposites) against powdery mildew infection by spraying them over pumpkin leaves for 3 days [104]. Copper also shows efficient antifungal activity in a nanocomposite with a polymer [105]. Nanofungicides are also synthesized by using algae [106]. In tomato, pepper, potato and eggplant, Sargassum longifolium with silver nanoparticles was used as a nanofungicide against Fusarium wilt which is caused by Fusarium oxysporum [107].

4.3. Nanopesticides

In commercial agriculture, the use of pesticides is a regular process, and for this purpose, new, efficient and target-specific pesticides are continuously developed. Approximately, 2 million tonnes of pesticides are utilized annually worldwide [108], and this is the reason why every year, a large number of pesticides are screened. It is also observed that a very small amount (0.1%) of pesticides used reaches the target pests while the rest (99.9%) remain in the environment which adversely affects the environment and human health [109]. Regarding their effect on non-targeted species, pesticides resulted in resistance in insects, pathogens and weeds [110]. However, it is noteworthy that if pesticides were not available in the world, they would cause a loss of life by a factor of 1000 compared to each life lost due to pesticides [111]. Biopesticides have been shown to have the potential to reduce the destructive effects of synthetic insecticides, but their sluggish and environment-dependent efficacy against pests creates a limitation in their use. To overcome these limitations, nanopesticides are the best viable alternative to conventional pesticides. The main advantage of using nanopesticides is that they have minimal effect on non-targeted insects and are eco-friendly. Moreover, nanopesticides are water-soluble components, unlike conventional hydrophobic pesticides, possess high bioactivity, are applied in small quantities and are quickly taken up by cells [112,113,114]. Some commercially available nanopesticides include nano green, nano-pole insecticides, encapsulated plant protection agent (PRIMO Maxx and Karate® ZEON), insecticides such as cruiser MaXX, nano-pole insecticides, etc. In addition to these nanomaterials, copper oxide (CuO NPs), zinc oxide (ZnO NPs), magnesium hydroxide (MgOH NPs), magnesium oxide (MgO NPs) and silica dioxide (SiO2 NPs) are also effective against harmful pests [112,113,114].
In the presence of suitable nanomaterials, the active ingredients are gradually degraded and released in a controlled manner which can lead to effective pest control in the long run [115]. Therefore, it can be said that the use of nanopesticides is very important for the sustainable and effective management of various pests and has the potential to reduce the use of synthetic chemicals. The mode of action of nanopesticides is different from that of conventional pesticides [116], and they are transported in colloidal and dissolved states [117]. In the case of nanopesticides, mobility and degradation of active ingredients by soil-inhabiting microorganisms could be increased by the solubility of active ingredients. In other words, nanopesticides are quite efficient, revolutionary and target-specific pesticides. Recent developments in the field of nanotechnology have resulted in the creation of a new generation of pesticides. While chemical pesticides have deteriorating consequences on biodiversity and human beings by killing the non-targeted organisms, nanopesticides are transported to their targets in the form of nanospheres, nanocapsules, nanopolymers, etc. Besides the benefits of nanopesticides, there are some matters of concern such as biosafety issues in the agricultural field and their long-term effect on humans, the surrounding environment and frequently exposed workers. The nanometric size of the permitted pesticide formulations should be carefully analyzed before exposing them to the environment. For example, Europe has approved synthetic amorphous silicon dioxide as a nanomaterial in the form of stable aggregated particles of particle size > 1 μm, with primary particles of nanosize [118]. The protection of plants and the production of food by using nanomaterials is an under-explored area, and it is very helpful for the environment and humans to develop non-toxic and encouraging pesticide transport systems to increase global food production by reducing harmful environmental effects on the ecosystem [119].

4.4. Nanobased Biosensors

Identification of contaminants, heavy metals and toxic compounds from domestic and industrial waste sources, soil monitoring and other dynamic formations is comprehensive and exhaustive work which requires fast, consistent and low-cost systems for detection [120,121]. For a quantitative analysis of environmental samples, traditional precise and sensitive analytical systems such as chromatographic and spectroscopic techniques are used which require advanced equipment, expert staff and complex multistep sample preparation. To eliminate the issues related to these technologies, a variety of new biosensors are being developed. Biosensors are analytical tools, and some of these biosensors rely on nanotechnological tools called nanobiosensors. Nanobiosensors are a revolution in this field with great potential to solve these problems by increasing robustness, sensitivity, point of use and flexibility [122,123]. A nanobiosensor has the ability to find any biochemical and biophysical signal connected to a particular analyte [124] and to estimate its existence and concentration in water, soil and wastewater [125]. In the field of agriculture, nanobiosensors are used for the detection of pesticides, herbicides, fertilizers, toxins, heavy metals and pathogens, soil monitoring for quality and fertility and as indicators for seed viability and precision agriculture (Figure 6a) [126,127]. Heavy metals can be detected by biosensors with aptamer- and DNA-based properties which are appropriate for screening and monitoring food safety. In the case of nanofertilizer nanobiosensors, nanosensors may also be used to observe plant growth by evaluating the cross-talk between the rhizosphere and roots which leads to the development of an energetic, accurate and intellectual nanofertilizer delivery platform. Nanobiosensors are transportable, small, specific, extra sensitive, reliable and also used for real-time monitoring. On the basis of these properties, nanobiosensors have priority over current conventional sensors.
Different types of nanosensors have been explored in plants such as plasmonic nanosensors, carbon-based electrochemical nanosensors, fluorescence resonance energy transfer (FRET)-based nanosensors, nanowire nanosesnsors and antibody nanosensors. In addition to the above, different molecular methods, for example, polymerase chain reaction (PCR), real-time PCR, Raman and fluorescence spectroscopy, infrared spectroscopy, etc., exist [128]. Research has been focused on genetically encoded nanosensors or FRET-based nanosensors for improving the resource allocation efficiency for pathogens or early recognition and amplification of resource deficiency and their regulation for pathogens. Some examples of nanosensors in plant pathogen detection, plant disease monitoring and management are discussed here, such as: (1) Fluorescent silica nanoparticles (FSNPs) detect pathogens related to bacterial spot disease in tomato [79]. (2) Gold nanoparticles detect Tilletia indica responsible for Karnal bunt disease in wheat [80]. (3) Luminescent semiconductor nanocrystals (QD) detect beet necrotic yellow vein virus (BNYVV) responsible for rhizomania disease in beet [129]. (4) Gold nanoparticles detect tristeza virus responsible for tristeza disease in citrus [130,131].

4.5. Nanobioremediation

Due to rapid urbanization and colonization, there has been a significant increase in the rich industrial release of various types of wastewater which is an anthropogenetic activity that destroys soil health and air and water quality. To control the waste materials released from various sources, a large number of technologies have been developed including physical remediation, chemical remediation, phytoremediation and microbial remediation. Bacterial and fungal metabolisms also destroy various toxic substances trapped in the waste materials. For the bioremediation process of waste materials, some important bacterial communities are Bacillus, Streptomyces, Pseudomonas, Thiobacillus, Achromobacter, Acinetobacter, Nitrobacter, Alcaligenes, Flavobacterium and Micrococcus; among the fungi are Fusarium, Penicillium, Mucor, Pleurotus, Aspergillus, Trichoderma and white rot mushrooms, and AMF are known to be efficient organisms. In other words, bioremediation for sustainable development is an innovative method of developing waste management, and the use of microbes for this process is considered economically and environmentally safe [132]. In addition to the use of soil microbes, earthworms also play a dynamic role in bioremediation waste management [133]. Nanotechnology is also involved in bioremediation (nanobioremediation) and plays an important role (Figure 6b). In other words, nanobioremediation is a progressive and fast-developing advanced technology in which biologically synthesized nanoparticles are used to eradicate contaminants from the environment. Nanobioremediation significantly enhances the efficiency of the disinfection process. Different types of nanomaterials are used instantaneously or successively with microbes and plants, or they can be utilized as nanocarriers for microbial bioabsorbents to expedite heavy metal removal [134]. Rizwan et al. showed the main nanomaterials that are involved in nanobioremediation, for example, nanosized dendrimers, nanoiron and its derivatives, single enzyme nanoparticles, carbon nanotubes, engineered nanoparticles, etc. [135], whereas in the case of nanobioremediation, engineered polymeric nanoparticles, bioremediated soil and hydrophobic contaminants [136].

5. Role of NPs in Biotic and Abiotic Stress

Agriculture is the economic pillar of developing countries for the better life of human beings on a global scale [137]. In ecosystems, biotic and abiotic stresses drive climate change that damages the particular balance between the environment and food production, is related to crop productivity and crop failure and can lead to significant issues [138]. Abiotic stress (salinity, drought, heat, high light and heavy metals) causes morphological, physiological, biochemical and molecular changes, production of ROS (reactive oxygen species) and damage of membrane and alters other metabolic activities [139]. Meanwhile, biotic stress (viruses, bacteria, fungi, nematodes, parasitic plants, weeds and insects) [140] leads to changes in plant metabolism and physiological damage, leading to decreased crop production. In order to reduce the harmful effects of biotic and abiotic stresses, several approaches to plant metabolism have been applied, including the use of nanomaterials. Table 1 and Table 2 and Figure 7 depict the role of nanomaterials in improving plant growth under biotic and abiotic stress. Nanomaterials are gaining global attention nowadays for protecting plants from biotic and abiotic stresses. For example, to enhance stress tolerance, plants employ key strategies such as upregulation of functional and structural protectants including compatible solutes (osmolytes) and antioxidants [141]. It is known that a low concentration of ROS acts as a signal that promotes the growth, development and defense mechanisms of the plant, but over-accumulation of ROS under stress conditions causes damage to cell membranes, DNA, proteins and other cell components which results in the inhibition of plant growth. Nanomaterials containing antioxidant enzyme activities enhance the ability of plants to scavenge ROS which improves the resistance of the plant to abiotic stress and therefore increases the yield. On the other hand, plants developed an advanced immune system to cope with biotic stresses. In plants, the first line of defense is passive. To prevent the entry of insects or pathogens into the plants, physical barriers such as cuticles, trichrome and waxes are found. Chemical compounds are also produced by plants in response to herbivory and pathogen infection [142]. Moreover, plants also have two levels of pathogen recognition that activate the defense system. Nanomaterials are also used to nullify the effect of biotic stresses. For example, Ag NPs biosynthesized by Pseudomonas poae strain CO showed antifungal activity against Fusarium graminearum, and it reduced the mycelia growth, spore germination and germ tube length, as well as severely damaged the cell wall at a remarkable level, and therefore, the production of fungal mycotoxins could be diminished by exposure to Ag NPs [143].

5.1. Mode of Action of NPs in Combating the Stress

The growing threat of climate change, rapid urbanization, growing population and shrinking agricultural land have increased concern about food security. Nanotechnology offers an opportunity to address various challenges faced by the agriculture sector today. However, the central focus of nanotechnology has been on increasing crop production with minimal impact on ecological sustainability. A proposed mechanism of action of NPs is given in Figure 8. The small size of the nanomaterial is essential for crossing biological membranes and transporting the drug to the targeted site in plants. The size and concentration of a particular nanoparticle are vital for the tolerance against abiotic stresses. Zinc oxide (ZnO) NPs have been applied at various concentrations to overcome Zn deficiency in plants and alleviate the toxic effect of superoxide radicals [183]. The application of ZnO NPs to Gossypium hirsutum increases the activity of POX and SOD while subsequently decreasing the lipid peroxidation rate. Similarly, ZnO NPs come in various shapes and sizes such as spherical (38 nm), floral (59 nm) and rod-like (>500 nm); however, the most effective were observed to be spherical ZnO NPs of a size less than 40 nm which reportedly enhances the antioxidant response against oxidative stress in the case of soybean. The pretreatment of TiO2 and ZnO nanoparticles results in a significant enhancement in SOD and GPX activity against extreme temperature stress and stabilization of the membrane by reducing H2O in wheat plants [184]. Similarly, a significant increase in APX, GPX, CAT and GR was reported in Brassica juncea when exposed to gold nanoparticles (GNPs), besides increasing the content of proline to a greater amount [185].

5.1.1. Salt Stress

In the age of climate change, salinity stress is posing a serious threat to agriculture, significantly reducing overall crop production with both primary and secondary effects. Primary effects include osmotic and ionic disturbances while secondary effects include disturbances in hormonal balances, oxidative stress and nutrient imbalance [186]. Various evidence suggests that the supplementation of different types of nanomaterials substantially attenuates various types of injuries caused by salt stress and, therefore, holds promise for an adaptive adjustment. Nanotechnology is an emerging field of science and has attracted attention over the years because of its potential to promote sustainability in agriculture. Furthermore, an excess intake of sodium ions causes disturbances in various intracellular processes, particularly the generation of reactive oxygen species (ROS) that damage membrane structure and disturb metabolic pathways, which in turn deplete the cell’s energy pool [187]. Various plant growth parameters have often shown negative effects on exposure to salt stress such as decreased leaf area, chlorophyll content, gas exchange characteristics and photosynthetic pigments [188]. Ag NPs are emerging as a very important nanomaterial as it has wide applicability in various fields of science which is attributed to its small size with physicochemical properties [189]. It has been reported that Ag NPs have antibacterial and antifungal properties and can potentially be used for wastewater treatment. Khan et al. reported that treatment of seeds with silver nanoparticles before sowing reduced the ratio of Na+/K+ while increasing the activity of antioxidants [189]. Wahid et al. reported that the combination of Ag NPs and NaCl reduced hydrogen peroxide (H2O2) and electrolyte leakages [190]. It has been reported that nanoparticles efficiently transport nutrients to various locations of the plant [191]. Rizwan et al. reported that Ag NPs may be acting as agents in mediating the interaction of various nutrients with key metabolic processes, therefore promoting the growth of a plant [192]. Chlorophyll as a vital component of photosynthesis has been reported to reduce the overall photosynthetic activity under salt stress; however, silver nanoparticles have been reported to enhance photosynthetic activity at lower concentrations [193]. Similarly, in the case of pearl millet, the application of Ag NPs significantly increases the antioxidant activities of superoxide dismutase (SOD), CAT (catalase) and POD (peroxidase) [194]. Pre-treatment of seeds with Ag NPs at 100–150 nm concentration significantly improved the activity of SOD, CAT and POD under salt stress conditions in the roots and shoots of the pearl millet [194]. Oxygen radicals are reported to be scavenged by SOD and converted further into H2O2; thereafter, the enzymes such as CAT and POD break down the H2O2 into water and oxygen molecules. CAT might have a direct link to the developmental phenomenon of a plant under salinity stress due to its significant ability to scavenge ROS [195]. Moreover, the oxygen radical outburst may be a consequence of salt stress; however, increasing the activity of antioxidants could be related to the nanoparticles to reduce the stress caused by ROS [192]. Similarly, smaller-size Ag NPs have shown lower CAT activity, and larger-size Ag NPs have shown increased activity of CAT, and this behavior could be attributed to the size, nature and type of the plant species exposed to nanoparticles [196]. More importantly, one study has revealed that a lower Na+ and Cl- concentration has been reported in various organs of the plant when subjected to Ag NP exposure. It can be assumed that Ag NPs promote the absorbance of nutrients in different locations of a plant [197]. Due to the natural ability of silicon to alleviate various kinds of abiotic stresses in plants, research has been conducted to study the effect of SiO2 NPs on the “Valencia” sweet orange under salt stress conditions. NaCl exposure to the “Valencia” sweet orange at 60 and 120 mM treatment significantly reduced the relative water capacity of a leaf and membrane damage which is believed to be caused by the leakage of electrolytes [191]. The exogenous application of SiO2 NPs has significantly increased the chlorophyll content and root length of Valencia plants suggesting a decrease in osmotic stress [198].
The SOS pathway plays an important role in the regulation of Na+ transportation from roots to the other parts of the plant [48]. Subsequently, it also aids in maintaining the ionic balance of the cell and thus endows the plant with salt tolerance [199]. It has been reported that the expression of CsSOS1, CsSOS2 and CsSOS3 genes was upregulated upon the exposure of plants to Si NPs, and therefore, a decrease in Na+ was reported in leaf and root tissues. Moreover, aquaporin (AQP) isoforms have a vital role in regulating the uptake of water by the roots in various plant species, and under salt stress conditions, aquaporin proteins decrease the water potential of the cell and therefore facilitate water uptake in order to mitigate the impact of salt stress [200]. The plasma membrane intrinsic protein (PIP) family plays an important role in mediating the intercellular transport of soluble solutes. The transcription regulation of CsPIP1 and CsPIP2 is upregulated by Si [201].

5.1.2. Drought Stress

As stated above, abiotic stresses are limiting crop productivity worldwide and therefore pose a major challenge to global food security [202]. Drought stress has significantly affected agricultural yields in many arid regions. It has been reported that silica NP treatments of hawthorns (Crataegus sp.) have significantly increased their resistance level against various abiotic stresses. In addition, changes have been observed in various physiological and biochemical parameters such as malondialdehyde content (MDA), relative water content (RWC) and chlorophyll, carotenoid, proline and carbohydrate content upon the treatment of hawthorn seedlings with a series of silica nanoparticles. Chitosan nanoparticles (CSNPs) have been reported to increase stomatal conductance in both stressed and non-stressed plants. Stomatal closure through ABA signaling caused by CSNPs has also been reported in some species, whereas in some species, higher stomatal conductance was reported. This fact has been compared with the sensitivity of a plant to water stress. Furthermore, the stress activates ROS which causes lipid oxidative damage and membrane injury. Disruption in membrane integrity is often observed in plants subjected to drought stress indicated by MDA content and free radicals [203]. Drought stress has been reported to cause membrane deterioration in a large number of species [204]. The application of CSNPs has been reported to increase drought tolerance by considerably reducing the H2O2 and MDA content under drought stress in C. roseus leaves. Therefore, CSNPs are reported to maintain the membrane integrity and functions of the cell under drought stress. Chitosan positively regulates osmotic pressure and therefore significantly reduces the ROS-led adverse effect on the cell. Similarly, HANP (hydroxylapatite nanoparticle)-treated seeds of jute have shown significant tolerance to drought stress by activating the proline biosynthesis pathway [205]. Drought stress severely impacts the growth of corn seedlings; however, the treatment of yttrium-doped Fe2O3 NPs was reported to significantly improve the photosynthetic activity and chlorophyll content of the plant [144]. ZnO is reported to improve the seed germination rate by increasing the activity of gibberellin hormones. Similarly, Fe2O3 has been reported to cause an increase in drought stress tolerance in plants by modifying their carbohydrate metabolism and stomatal movement. The ZnO NP treatment of maize plants has been reported to downregulate the degradation of photosynthetic pigments and enhance photosynthesis. Therefore, ZnO NPs act as a potential agent for improving the drought tolerance in a number of plant species. Similarly, CuO NP treatment in maize has significantly reduced the ROS content and positively regulates the pigment system under drought stress conditions [206].

5.1.3. Extreme Temperature

Temperature above a threshold level is called heat stress and below a threshold level is known as cold stress. The heat and cold stress is believed to cause significant ion imbalance in the cell and create a serious hindrance in the growth and development of the plant. The extreme temperature becomes a source of ROS which causes severe damage to the physiological and biochemical activity of a cell, besides damaging the most vital proteins—heat shock proteins (HSPs) [207]. Selenium nanoparticles were reported to combat high temperature stress. Djanaguiraman et al. reported that treatment of sorghum with selenium NPs activates the antioxidant machinery to scavenge the ROS produced by high temperature stress, therefore mitigating the heat stress effect [208]. Similarly, selenium NPs were reported to improve both cold and high temperature tolerance in Lycopersicum esculentum [209]. Similarly, photosynthetic machinery in wheat plants was reported to be affected by heat stress; however, the application of AgNPs imparts tolerance against heat stress and significantly improves various growth parameters such as root length, shoot length and fresh and dry weight [210].

5.1.4. Metal Stress

Since industrialization, metal toxicity has percolated in agricultural fields and has severely reduced the overall yield and production of the crop. The metal stress is reported to cause a decrease in enzyme activities, and ion imbalance leads to the deficiency of some key nutrient elements. Furthermore, it was reported that metal accumulation in plants generates excess ROS which cause damage to the structure of the cell membrane and destroy some important enzymes [211]. However, plants possess a wide range of defense systems to tackle abiotic stresses. Moreover, the accumulation of metal ions by plants causes the formation of metal chelates which significantly restricts the efflux of metal ions, sequestration of metals and activation of the antioxidant defense system. Nanoparticles have been reported to cause alleviation of metal-induced toxicity [212]. Being small in size, nanoparticles easily penetrate into various parts of the plant and contain a strong affinity toward metal ions. Similarly, quantum dots have been reported to reduce the availability of lead (Pb) and act as an additional barrier to the cell wall. It has been further reported that if a metal ion manages to enter the plant cell, the plants counteract it by accumulating various biomolecules and nutrients in order to establish a defense system to mitigate the stress effect. Nano-TiO2 is believed to mitigate various harmful impacts of abiotic stress; it also significantly restricts cadmium toxicity and enhances photosynthesis in plants [213].

6. Plant–Nanoparticle Interactions

The interaction of NPs or ENMs with plants or biological systems may be chemical or mechanical, and the interaction depends upon various factors such as the nature and size of NPs, the physiological status of the plant and NP interaction with the environment [214,215]. The smaller size of NPs with a large surface area including catalytic reactivity is the main reason for interaction [214]. It is now well established that the size of the NPs is the main barrier to the entry of NPs into the plant cell as per the report that the maximum dimension of NPs that plants allow to accumulate in cells is typically 40–50 nm [216,217]. In addition to this, the chemical composition and type of NPs, morphology, coating of the NP surface, etc., greatly impact the absorption and accumulation by the plant [218,219,220]. Moreover, NPs also interact with other environmental components, for example, humic acids, organic matters, salt ions and biological organisms (bacteria, fungi, etc.) that affect NP uptake by plants [183,221].
Exploring the nature of interactions between NPs and plants is critical, and information is limited. The US Environment Protection Agency [222] has first suggested evaluating the effect of NPs on plant metabolism based on phenotypic characteristics, for example, germination of the seed and elongation of the root. Later, it was found that these standards were very specific to plant type and NP properties, lacking sensitivity during the evaluation of NP toxicity to terrestrial plant species. The action mechanism of NPs in the cell system is a complex and less explored area. However, various biochemical markers (e.g., metabolite composition, membrane integrity and enzyme activity) are being utilized from time to time to understand the plant–NP interaction. There are two ways (apoplastic and symplastic) that can be taken by NPs when penetrating into the plant tissue. Apoplastic movement takes place via extracellular space (outside the plasma membrane) and symplastic via plasmodesmata [223,224]. The apoplastic pathways lead to the entry of NPs inside the root central cylinder followed by movement through the xylem to the aerial part of the plant [225,226]. Certainly, the Casparian strip acts as a barrier that allows symplastic movement of the NPs via endodermal cells; moreover, restricted movement and accumulation of some NPs at the Casparian strips also take place [226,227,228]. Symplastic movement also allows NPs to move through sieve tube elements in the phloem that lead the distribution toward non-photosynthetic tissue [219,225]. In the case of symplastic movement, NPs must be internalized by the plant cell and cross the plasma membrane. There are various ways available for NPs to achieve this, such as endocytosis (Etxeberria et al. 2006), via carrier proteins [229], pore formation [71], plasmodesmata [224] and ion channels [218,230]. In another method, for example, the foliar application of NPs, they need to cross the barrier of the cuticle, and thereafter, two pathways (lipophilic and hydrophilic) mediate the mode of transport of NPs [231]. Lipophilic pathways mediate the transport through cuticular waxes following diffusion, while the case of hydrophilic pathways involves movement through polar aqueous pores present in cuticles or stomata [232]. Due to the size exclusion limit above 10 nm, the stomatal pathway appears as the most likely route for NP penetration. The movement of NPs within the plant is an important indicator that can reveal its location or accumulation in the plant. NPs transported mainly through the xylem are likely to move in an upward direction, for example, from the root to the aerial part. While in the case of phloem, NPs accumulate in plant organs (such as fruits, grains, flowers and young leaves) acting as sinks and must be applied through foliar application. However, lateral movement of NPs between the xylem and phloem is also possible [233]. In addition, the types of NPs and the plant species also play a role in influencing the transfer and accumulation of NPs [234,235]. Overall, the above information provides an idea in deciding the role of NMs we want to test.

7. Toxicological Concerns of Nanomaterials

It is evident from the above reports that many nanomaterial-based products are being used commercially. Day by day, many of these products are being engineered for better use. In addition, the use of these ENMs at the industrial level is increasing, and consequently, an increasing concentration of these materials is reaching the environment. Most of these ENMs are finally disposed of in the soil in uncontrolled quantities [236]. The tailored nanomaterials, for example, nanofertilizers, nanopesticides and nanobiosensors, are being utilized in agriculture systems leading to their accumulation in the soil. The accumulation of these affects soil health, soil microbiome and, most importantly, plant health [30]. Moreover, nitrogen fixation, mineralization and activities responsible for plant growth and development are also affected [30]. Some ENMs such as silver, SiO2, titania, iron oxides, zinc oxides, alumina, etc., are being discarded into the soil in large quantities without evaluating the risk [30]. As per the reports, ENMs are released into the environment at several stages such as the synthesis, manufacturing, usage and disposal of the products [237]. Figure 9 explains the possible ways of ENM accumulation in the soil. ENMs in the soil are accumulated directly or indirectly, via different routes, making it essential to examine the impact of this ENM accumulation in the soil, changes in their concentration and the life span of ENMs in the soil. So far, many studies have been published dealing with the impact of ENMs on soil, soil microbiome and plants, and almost no effect was observed when ENMs were used in lower doses. In one study, a positive effect of low doses of ENMs on plant growth was reported, and hence, exact doses should be taken into consideration for a real evaluation of ENM toxicity or growth-promoting activity. Overall, the regulation of the release of ENMs at various stages as shown in Figure 9 is mandatory [30]. Therefore, a careful evaluation of ENM accumulation in the environment and its risk to the plant microbiome is extremely desirable. It will enhance the wise and sustainable use of nanotechnology in agriculture systems.

8. Conclusions

Nanotechnology has great potential to improve the agricultural system by protecting plants from various environmental stresses, improving plant health and increasing agricultural yields. The above can be achieved by the application of nanoparticles and/or tailored nanomaterials in plants as a sustainable approach to make this field a multi-billion dollar industry. Currently, various nanobased products such as nanofertilizers (nano ultrafertilizer, nano capsule, nano max NPK, TAG NANO, etc.), fungicides and insecticides (Subdue MAXX, Cruiser MaXX, nano-pole insecticides, etc.), nanopesticides (nano green, encapsulated plant protection agent such as PRIMO Maxx, Karate® Zeon, etc.) and different types of nanosensors are being utilized in the market. The industry is facing difficulties in market access, and this may be due to high production costs and the need for high volumes of nanotechnology products in the agriculture sector. However, there are many reports available supporting these green sustainable products. Nevertheless, there are still some unanswered questions that need to be clarified. Further research is therefore needed to elucidate the interactions of nanomaterials with biological macromolecules and their effects on nanomaterial toxicity, the ecosystem and health outcomes.

Author Contributions

Concept, Z.A., A.S., A.E. and Y.D.; MS writing, Z.A., S.T., A.W., I.B.G., A.S., A.E., M.R. and Y.D.; supervision and funding acquisition, Y.D. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by The National Natural Science Foundation for Scholars of China (31870595) and the Priority Academic Program Development of Jiangsu Higher Education Institutions.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

Figures 3, 8 and 9 were created with https://biorender.com/ (accessed on 1 August 2022) and the authors sincerely thank BioRender.com. The authors A.W. and S.T. want to acknowledge the Council of Scientific and Industrial Research (CSIR), India (Award No. 09/112(0677)/2020-EMR-I), and the Department of Science and Technology (DST), India (Award No. IF; 190296), respectively, for providing financial assistance in the form of junior research fellowship (JRF).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. United Nations, Department of Economic and Social Affairs, Population Division. World Population Prospects 2019: Highlights (ST/ESA/SER.A/423); Department of Economic and Social Affairs, Population Division: New York, NY, USA, 2019. [Google Scholar]
  2. Food and Agricultural Organization (FAO). The State of Food and Agriculture: Moving Forward on Food and Waste Reduction; License: CC BY-NC-SA 3.0 IGO; Food and Agricultural Organization (FAO): Rome, Italy, 2019. [Google Scholar]
  3. Bellard, C.; Bertelsmeier, C.; Leadley, P.; Thuiller, W.; Courchamp, F. Impacts of climate change on the future of biodiversity. Ecol. Lett. 2012, 15, 365–377. [Google Scholar] [CrossRef] [Green Version]
  4. He, M.; He, C.Q.; Ding, N.Z. Abiotic stresses: General defenses of land plants and chances for engineering multistress tolerance. Front. Plant Sci. 2018, 9, 1771. [Google Scholar] [CrossRef] [Green Version]
  5. Faraji, J.; Sepehri, A. Exogenous nitric oxide improves the protective effects of TiO2 nanoparticles on growth, antioxidant system, and photosynthetic performance of wheat seedlings under drought stress. J. Soil. Sci. Plant Nutr. 2020, 20, 703–714. [Google Scholar] [CrossRef]
  6. Suzuki, N.; Rivero, R.M.; Shulaev, V.; Blumwald, E.; Mittler, R. Abiotic and biotic stress combinations. New Phytol. 2014, 203, 32–43. [Google Scholar] [CrossRef]
  7. Hu, H.; Xiong, L. Genetic engineering and breeding of drought–resistant crops. Annu. Rev. Plant Biol. 2014, 65, 715–741. [Google Scholar] [CrossRef] [PubMed]
  8. Savvides, A.; Ali, S.; Tester, M.; Fotopoulos, V. Chemical priming of plants against multiple abiotic stresses: Mission possible? Trends Plant Sci. 2016, 21, 329–340. [Google Scholar] [CrossRef] [Green Version]
  9. Balmer, A.; Pastor, V.; Gamir, J.; Flors, V.; Mauch-Mani, B. The ‘prime-ome’: Towards a holistic approach to priming. Trends Plant Sci. 2015, 20, 443–452. [Google Scholar] [CrossRef] [PubMed]
  10. Jisha, K.C.; Puthur, J.T. Seed priming with beta-amino butyric acid improves abiotic stress tolerance in rice seedlings. Rice Sci. 2016, 23, 242–254. [Google Scholar] [CrossRef] [Green Version]
  11. Horváth, E.; Csiszár, J.; Gallé, Á.; Poór, P.; Szepesi, Á.; Tari, I. Hardening with salicylic acid induces concentration-dependent changes in abscisic acid biosynthesis of tomato under salt stress. J. Plant Physiol. 2015, 183, 54–63. [Google Scholar] [CrossRef] [PubMed]
  12. Antoniou, C.; Savvides, A.; Christou, A.; Fotopoulos, V. Unravelling chemical priming machinery in plants: The role of reactive oxygen-nitrogen–sulfur species in abiotic stress tolerance enhancement. Curr. Opin. Plant Biol. 2016, 33, 101–107. [Google Scholar] [CrossRef]
  13. Khan, I.; Saeed, K.; Khan, I. Nanoparticles: Properties, applications and toxicities. Arab. J. Chem. 2019, 12, 908–931. [Google Scholar] [CrossRef]
  14. Ali, M.A.; Rehman, I.; Iqbal, A.; Din, S.; Rao, A.Q.; Latif, A.; Samiullah, T.R.; Azam, S.; Husnain, T. Nanotechnology, a new frontier in agriculture. Adv. Life Sci. 2014, 1, 129–138. [Google Scholar]
  15. Singh, A.; Singh, N.B.; Hussain, I.; Singh, H.; Singh, S.C. Plant-nanoparticle interaction: An approach to improve agricultural practices and plant productivity. Int. J. Pharm. Sci. Invent. 2015, 4, 25–40. [Google Scholar]
  16. Chen, H.; Yada, R. Nanotechnologies in agriculture: New tools for sustainable development. Trends Food Sci. Technol. 2011, 22, 585–594. [Google Scholar] [CrossRef]
  17. Parisi, C.; Vigani, M.; Rodríguez-Cerezo, E. Agricultural nanotechnologies: What are the current possibilities? Nano Today 2015, 10, 124–127. [Google Scholar] [CrossRef]
  18. Fraceto, L.F.; Grillo, R.; de Medeiros, G.A.; Scognamiglio, V.; Rea, G.; Bartolucci, C. Nanotechnology in agriculture: Which innovation potential does it have? Front. Environ. Sci. 2016, 4, 20. [Google Scholar] [CrossRef]
  19. Khot, L.R.; Sankaran, S.; Maja, J.M.; Ehsani, R.; Schuster, E.W. Applications of nanomaterials in agricultural production and crop protection: A review. Crop Prot. 2012, 35, 64–70. [Google Scholar] [CrossRef]
  20. Sekhon, B.S. Nanotechnology in agri-food production: An overview. Nanotechnol. Sci. Appl. 2014, 7, 31. [Google Scholar] [CrossRef] [Green Version]
  21. Mittal, D.; Kaur, G.; Singh, P.; Yadav, K.; Ali, S.A. Nanoparticle-based sustainable agriculture and food science: Recent advances and future outlook. Front. Nanotechnol. 2020, 2, 10. [Google Scholar] [CrossRef]
  22. Dubchak, S.; Ogar, A.; Mietelski, J.W.; Turnau, K. Influence of silver and titanium nanoparticles on arbuscular mycorrhiza colonization and accumulation of radio caesium in Helianthus annuus. Span. J. Agric. Res. 2010, 1, 103–108. [Google Scholar] [CrossRef]
  23. Sukhanova, A.; Bozrova, S.; Sokolov, P.; Berestovoy, M.; Karaulov, A.; Nabiev, I. Dependence of nanoparticle toxicity on their physical and chemical properties. Nanoscale Res. Lett. 2018, 13, 1–21. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Rico, C.M.; Hong, J.; Morales, M.I.; Zhao, L.; Barrios, A.C.; Zhang, J.Y.; Peralta-Videa, J.R.; Gardea-Torresdey, J.L. Effect of cerium oxide nanoparticles on rice: A study involving the antioxidant defense system and in vivo fluorescence imaging. Environ. Sci. Technol. 2013, 47, e5635–e5642. [Google Scholar] [CrossRef] [PubMed]
  25. Qi, M.; Liu, Y.; Li, T. Nano-TiO2 improve the photosynthesis of tomato leaves under mild heat stress. Biol. Trace Elem. Res. 2013, 156, 323–328. [Google Scholar] [CrossRef]
  26. Gohari, G.; Safai, F.; Panahirad, S.; Akbari, A.; Rasouli, F.; Dadpour, M.R.; Fotopoulos, V. Modified multiwall carbon nanotubes display either phytotoxic or growth promoting and stress protecting activity in Ocimum basilicum L. In a concentration dependent manner. Chemosphere 2020, 13, 126171. [Google Scholar] [CrossRef] [PubMed]
  27. He, X.; Deng, H.; Hwang, H.M. The current application of nanotechnology in food and agriculture. J. Food Drug Anal. 2019, 27, 1–21. [Google Scholar] [CrossRef] [Green Version]
  28. Elemike, E.E.; Uzoh, I.M.; Onwudiwe, D.C.; Babalola, O.O. The role of nanotechnology in the fortification of plant nutrients and improvement of crop production. Appl. Sci. 2019, 9, 499. [Google Scholar] [CrossRef] [Green Version]
  29. Singh, S.; Vishwakarma, K.; Singh, S.; Sharma, S.; Dubey, N.K.; Singh, V.K.; Liu, S.; Tripathi, D.K.; Chauhan, D.K. Understanding the plant and nanoparticle interface at transcriptomic and proteomic level: A concentric overview. Plant Gene 2017, 11, 265–272. [Google Scholar] [CrossRef]
  30. Khan, S.T.; Adil, S.F.; Shaik, M.R.; Alkhathlan, H.Z.; Khan, M.; Khan, M. Engineered Nanomaterials in Soil: Their Impact on Soil Microbiome and Plant Health. Plants 2022, 11, 109. [Google Scholar] [CrossRef] [PubMed]
  31. Hillie, T.; Hlophe, M. Nanotechnology and the challenge of clean water. Nat. Nanotechnol. 2007, 2, 663–664. [Google Scholar] [CrossRef]
  32. Göde, C.; Yola, M.L.; Yılmaz, A.; Atar, N.; Wang, S. A novel electrochemical sensor based on calixarene functionalized reduced graphene oxide: Application to simultaneous determination of Fe (III), Cd (II) and Pb (II) ions. J. Coll. Interface Sci. 2017, 508, 525–531. [Google Scholar] [CrossRef]
  33. Yola, M.L.; Eren, T.; Atar, N. Molecularly imprinted electrochemical biosensor based on Fe and Au nanoparticles involved in 2-aminoethanethiol functionalized multi-walled carbon nanotubes for sensitive determination of cefexime in human plasma. Biosens. Bioelectron. 2014, 60, 277–285. [Google Scholar] [CrossRef] [PubMed]
  34. Archana, S. The Application of Nanomaterials in Agricultural Field. Int. J. Mod. Agric. 2021, 10, 3038–3045. [Google Scholar]
  35. Hema, S.; Thambiraj, S.; Shankaran, D.R. Nanoformulations for targeted drug delivery to prostate cancer: An overview. J. Nanosci. Nanotechnol. 2018, 18, 5171–5519. [Google Scholar] [CrossRef] [PubMed]
  36. Khodakovskaya, M.; Dervishi, E.; Mahmood, M.; Xu, Y.; Li, Z.; Watanabe, F.; Biris, A.S. Carbon nanotubes are able to penetrate plant seed coat and dramatically affect seed germination and plant growth. ACS Nano 2009, 3, 3221–3227. [Google Scholar] [CrossRef]
  37. Kashyap, P.L.; Xiang, X.; Heiden, P. Chitosan nanoparticle based delivery systems for sustainable agriculture. Int. J. Biol. Macromol. 2015, 77, 36–51. [Google Scholar] [CrossRef]
  38. Abobatta, W.F. Nanotechnology application in agriculture. Acta Scient. Agric. 2018, 2, 99–102. [Google Scholar]
  39. Ioannou, A.; Gohari, G.; Papaphilippou, P.; Panahirad, S.; Akbari, A.; Dadpour, M.R.; Fotopoulos, V. Advanced nanomaterials in agriculture under a changing climate: The way to the future? Environ. Exp. Bot. 2020, 176, 104048. [Google Scholar] [CrossRef]
  40. Dazon, C.; Fierro, V.; Celzard, A.; Witschger, O. Identification of nanomaterials by the volume specific surface area (VSSA) criterion: Application to powder mixes. Nanoscale Adv. 2020, 2, 4908–4917. [Google Scholar] [CrossRef]
  41. Rastogi, A.; Zivcak, M.; Sytar, O.; Kalaji, H.M.; He, X.; Mbarki, S.; Brestic, M. Impact of metal and metal oxide nanoparticles on plant: A critical review. Front. Chem. 2017, 5, 78. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Rodrigues, E.S.; Gomes, M.H.F.; Corrêa, C.G.; Pereira, A.E.S.; de Almeida, E.; Ghoshal, S.; de Carvalho, H.W.P. Are nanomaterials making agriculture more productive? Outputs from a metadata analysis of 2009–2020 research. agriRxiv 2021. [Google Scholar] [CrossRef]
  43. Kulkarni, S.K. Synthesis of nanomaterials–I (physical methods). In Nanotechnology: Principles and Practices; Kulkarni, S.K., Ed.; Springer Nature: Berlin, Germany, 2014; pp. 55–76. [Google Scholar]
  44. Kulkarni, S.K. Synthesis of nanomaterials–I (chemical methods). In Nanotechnology: Principles and Practices; Kulkarni, S.K., Ed.; Springer Nature: Berlin, Germany, 2014; pp. 77–109. [Google Scholar]
  45. Singh, P.; Kim, Y.J.; Zhang, D.; Yang, D.C. Biological synthesis of nanoparticles from plants and microorganisms. Trends Biotechnol. 2016, 34, 588–599. [Google Scholar] [CrossRef] [PubMed]
  46. Samuel, J.P.; Samboju, N.C.; Yau, K.Y.; Webb, S.R.; Burroughs, F. Use of Dendrimer Nanotechnology for Delivery of Biomolecules into Plant Cells. U.S. Patent US8686222B2, 1 April 2014. [Google Scholar]
  47. Ling, D.H.; Xing, B.S. Phytotoxicity of nanoparticles: Inhibition of seed germination and root elongation. Environ. Pollut. 2007, 50, 243–250. [Google Scholar]
  48. Ma, X.; Geiser-Lee, J.; Deng, Y.; Kolmakov, A. Interactions between engineered nanoparticles (ENPs) and plants: Phytotoxicity, uptake and accumulation. Sci. Total Environ. 2010, 408, 3053–3061. [Google Scholar] [CrossRef] [PubMed]
  49. Munir, T.; Rizwan, M.; Kashif, M.; Shahzad, A.; Ali, S.; Amin, N.; Zahid, R.; Alam, M.; Imran, M. Effect of zinc oxide nanoparticles on the growth and Zn uptake in wheat (Triticum aestivum L.) by seed priming method. Dig. J. Nanomater. Biostruct. 2018, 13, 315–323. [Google Scholar]
  50. Rossi, L.; Fedenia, L.N.; Sharifan, H.; Ma, X.; Lombardini, L. Effects of foliar application of zinc sulfate and zinc nanoparticles in coffee (Coffea arabica L.) plants. Plant Physiol. Biochem. 2019, 135, 160–166. [Google Scholar] [CrossRef]
  51. Pérez-Labrada, F.; López-Vargas, E.R.; Ortega-Ortiz, H.; Cadenas-Pliego, G.; Benavides-Mendoza, A.; Juárez-Maldonado, A. Responses of tomato plants under saline stress to foliar application of copper nanoparticles. Plants 2019, 8, 151. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Khan, M.S.; Zaka, M.; Abbasi, B.H.; Rahman, L.; Shah, A. Seed germination and biochemical profile of Silybum marianum exposed to monometallic and bimetallic alloy nanoparticles. IET Nanobiotechnol. 2016, 10, 359–366. [Google Scholar] [CrossRef] [PubMed]
  53. Mehta, C.M.; Srivastava, R.; Arora, S.; Sharma, A.K. Impact assessment of silver nanoparticles on plant growth and soil bacterial diversity. 3 Biotech. 2016, 6, 1–10. [Google Scholar]
  54. Wagi, S.; Ahmed, A. Green production of AgNPs and their phyto stimulatory impact. Green Process Synth. 2019, 8, 885–894. [Google Scholar] [CrossRef]
  55. Nair, R.; Poulose, A.C.; Nagaoka, Y.; Yoshida, Y.; Maekawa, T.; Sakthi Kumar, D. Uptake of FITC labelled silica nanoparticles and quantum dots by rice seedlings: Effects on seed germination and their potential as biolabels for plants. J. Fluoresc. 2011, 21, 2057–2068. [Google Scholar] [CrossRef] [PubMed]
  56. Acharya, P.; Jayaprakasha, G.K.; Crosby, K.M.; Jifon, J.L.; Patil, B.S. Nanoparticle-Mediated Seed Priming Improves Germination, Growth, Yield, and Quality of Watermelons (Citrullus lanatus) at multi-locations in Texas. Sci. Rep. 2020, 10, 5037. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Sunny, N.S.; Mathew, S.S.; Kumar, S.V.; Saravanan, P.; Rajeshkannan, R.; Rajasimman, M.; Vasseghian, Y. Effect of green synthesized nano-titanium synthesized from Trachyspermum ammi extract on seed germination of Vigna radiate. Chemosphere 2022, 300, 134600. [Google Scholar] [CrossRef] [PubMed]
  58. Chen, J.; Zeng, X.; Yang, W.; Xie, H.; Ashraf, U.; Mo, Z.; Liu, J.; Li, G.; Li, W. Seed Priming with Multiwall Carbon Nanotubes (MWCNTs) Modulates Seed Germination and Early Growth of Maize Under Cadmium (Cd) Toxicity. J. Soil Sci. Plant Nutr. 2021, 21, 1793–1805. [Google Scholar] [CrossRef]
  59. Oliveira, H.C.; Gomes, B.C.R.; Pelegrino, M.T.; Seabra, A.B. Nitric oxide-releasing chitosan nanoparticles alleviate the effects of salt stress in maize plants. Nitric Oxide 2016, 61, 10–19. [Google Scholar] [CrossRef]
  60. Santo-Pereira, A.E.; Silva, P.M.; Oliveira, J.L.; Oliveira, H.C.; Fraceto, L.F. Chitosan nanoparticles as carrier systems for the plant growth hormone gibberellic acid. Colloid Surf. B 2017, 150, 141–152. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  61. Quiñones, J.P.; García, Y.C.; Curiel, H.; Covas, C.P. Microspheres of chitosan for controlled delivery of brassinosteroids with biological activity as agrochemicals. Carbohydr. Polym. 2010, 80, 915–921. [Google Scholar] [CrossRef]
  62. Chen, J.; Cao, S.; Xi, C.; Chen, Y.; Li, X.; Zhang, L.; Wang, G.; Chen, Y.; Chen, Z. A novel magnetic β-cyclodextrin modifed graphene oxide adsorbent with high recognition capability for 5 plant growth regulators. Food Chem. 2018, 239, 911–919. [Google Scholar] [CrossRef]
  63. Li, N.; Wu, D.; Li, X.; Zhou, X.; Fan, G.; Li, G.; Wu, Y. Effective enrichment and detection of plant growth regulators in fruits and vegetables using a novel magnetic covalent organic framework material as the adsorbents. Food Chem. 2020, 306, 125455. [Google Scholar] [CrossRef]
  64. Chakravarty, D.; Erande, M.B.; Late, D.J. Graphene quantum dots as enhanced plant growth regulators: Effects on coriander and garlic plants. J. Sci. Food Agric. 2015, 95, 2772–2778. [Google Scholar] [CrossRef]
  65. Grillo, R.; Abhilash, P.C.; Fraceto, L.F. Nanotechnology applied to bio-encapsulation of pesticides. J. Nanosci. Nanotechnol. 2016, 16, 1231–1234. [Google Scholar] [CrossRef] [PubMed]
  66. Zhang, J.; Khan, S.A.; Heckel, D.G.; Bock, R. Next-generation insectresistant plants: RNAi-mediated crop protection. Trends Biotechnol. 2017, 35, 871–882. [Google Scholar] [CrossRef]
  67. Yan, S.; Ren, B.Y.; Shen, J. Nanoparticle-mediated double-stranded RNA delivery system: A promising approach for sustainable pest management. Insect Sci. 2021, 28, 21–34. [Google Scholar] [CrossRef] [PubMed]
  68. Mitter, N.; Worrall, E.A.; Robinson, K.E.; Li, P.; Jain, R.G.; Taochy, C.; Fletcher, S.J.; Carroll, B.J.; Lu, G.Q.; Xu, Z.P. Clay nanosheets for topical delivery of mai for sustained protection against plant viruses. Nat. Plants 2017, 3, 16207. [Google Scholar] [CrossRef]
  69. Kwak, S.Y.; Lew, T.T.S.; Sweeney, C.J.; Koman, V.B.; Wong, M.H.; Bohmert-Tatarev, K.; Snell, K.D.; Seo, J.S.; Chua, N.H.; Strano, M.S. Chloroplast-selective gene delivery and expression in planta using chitosan-complexed single-walled carbon nanotube carriers. Nat. Nanotechnol. 2019, 14, 447–455. [Google Scholar] [CrossRef] [PubMed]
  70. Demirer, G.S.; Zhang, H.; Matos, J.L.; Goh, N.S.; Cunningham, F.J.; Sung, Y.; Chang, R.; Aditham, A.J.; Chio, L.; Cho, M.J.; et al. High aspect ratio nanomaterials enable delivery of functional genetic material without DNA integration in mature plants. Nat. Nanotechnol. 2019, 14, 456–464. [Google Scholar] [CrossRef] [PubMed]
  71. Wong, M.H.; Misra, R.P.; Giraldo, J.P.; Kwak, S.Y.; Son, Y.; Landry, M.P.; Swan, J.W.; Blankschtein, D.; Strano, M.S. Lipid exchange envelope penetration (LEEP) of nanoparticles for plant engineering: A universal localization mechanism. Nano Lett. 2016, 16, 1161–1172. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  72. Zhang, H.; Demirer, G.S.; Zhang, H.; Ye, T.; Goh, N.S.; Aditham, A.J.; Landry, M.P. DNA nanostructures coordinate gene silencing in mature plants. Proc. Natl. Acad. Sci. USA 2019, 116, 7543–7548. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  73. Lei, W.X.; An, Z.S.; Zhang, B.H.; Wu, Q.; Gong, W.J.; Li, J.M.; Chen, W.L. Construction of gold-sirnanpr1nanoparticles for effective and quick silencing ofnpr1 in Arabidopsis thaliana. RSC Adv. 2020, 10, 19300–19308. [Google Scholar] [CrossRef] [PubMed]
  74. Savary, S.; Ficke, A.; Aubertot, J.N.; Hollier, C. Crop losses due to diseases and their implications for global food production losses and food security. Food Secur. 2012, 4, 519–537. [Google Scholar] [CrossRef]
  75. López, M.M.; Bertolini, E.; Olmos, A.; Caruso, P.; Gorris, M.T.; Llop, P.; Penyalver, R.; Cambra, M. Innovative tools for detection of plant pathogenic viruses and bacteria. Int. Microbiol. 2003, 6, 233–243. [Google Scholar] [CrossRef] [PubMed]
  76. Yvon, M.; Thébaud, G.; Alary, R.; Labonne, G. Specific detection and quantification of the phytopathogenic agent ‘Candidatus Phytoplasma prunorum’. Mol. Cell Probe. 2009, 23, 227–234. [Google Scholar] [CrossRef] [PubMed]
  77. Singh, A.; Poshtiban, S.; Evoy, S. Recent advances in bacteriophage based biosensors for food-borne pathogen detection. Sensors 2013, 13, 1763–1786. [Google Scholar] [CrossRef] [Green Version]
  78. López, M.M.; Llop, P.; Olmos, A.; Marco-Noales, E.; Cambra, M.; Bertolini, E. Are molecular tools solving the challenges posed by detection of plant pathogenic bacteria and viruses? Curr. Issues Mol. Biol. 2009, 11, 13–46. [Google Scholar]
  79. Yao, K.S.; Li, S.J.; Tzeng, K.C.; Cheng, T.C.; Chang, C.Y.; Chiu, C.Y.; Liao, C.Y.; Hsu, J.J.; Lin, Z.P. Fluorescence silica nanoprobe as a biomarker for rapid detection of plant pathogens. Adv. Mater. Res. 2009, 79, 513–516. [Google Scholar] [CrossRef]
  80. Singh, S.; Singh, M.; Agrawal, V.V.; Kumar, A. An attempt to develop surface plasmon resonance based immunosensor for Karnal bunt (Tilletia indica) diagnosis based on the experience of nano-gold based lateral flow immunodipstick test. Thin Solid Films. 2010, 519, 1156–1159. [Google Scholar] [CrossRef] [Green Version]
  81. Ferna’ndez, A.; Picouet, P.; Lloret, E. Cellulose-silver nanoparticle hybrid materials to control spoilage-related microflora in absorbent pads located in trays of fresh-cut melon. Int. J. Food Microbiol. 2010, 142, 222–228. [Google Scholar] [CrossRef] [PubMed]
  82. Luksiene, N.; Rasiukeviciute, N.; Zudyte, B.; Uselis, N. Innovative approach to sunlight activated biofungicides for strawberry crop protection: ZnO nanoparticles. J. Photochem. Photobiol. B Biol. 2020, 203, 111656, ISSN 1011–1344. [Google Scholar] [CrossRef]
  83. Kumar, A.; Ghatak, A.; Nazreen, H.; Emmadi, V.; Kishore, B.; Hasan, W.U. Testing inhibitory efficacy of copper and silver nanoparticles against Alternaria brassicicola and Bipolaris sorokiniana. Pharma Innov. J. 2022, 11, 2690–2693. [Google Scholar]
  84. Shumeiko, V.; Zaken, Y.; Hidas, G.; Paltiel, Y.; Bisker, G.; Shoseyov, O. Peptide-Encapsulated Single-Wall Carbon Nanotube-Based Near-Infrared Optical Nose for Bacteria Detection and Classification. IEEE Sens. J. 2022, 22, 6277–6287. [Google Scholar] [CrossRef]
  85. Lavanya, R.; Arun, V. Detection of Begomovirus in chilli and tomato plants using functionalized gold nanoparticles. Sci. Rep. 2021, 11, 14203. [Google Scholar] [CrossRef] [PubMed]
  86. Iavicoli, I.; Leso, V.; Beezhold, D.H.; Shvedova, A.A. Nanotechnology in agriculture: Opportunities, toxicological implications, and occupational risks. Toxicol. Appl. Pharmacol. 2017, 329, 96–111. [Google Scholar] [CrossRef] [PubMed]
  87. Prasad, R.; Bhattacharyya, A.; Nguyen, Q.D. Nanotechnology in Sustainable Agriculture: Recent Developments, Challenges, and Perspectives. Front. Microbiol. 2017, 8, 1014. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  88. Manjunatha, R.L.; Naik, D.; Usharani, K.V. Nanotechnology application in agriculture: A review. J. Pharmacogn. Phytochem. 2019, 8, 1073–1083. [Google Scholar]
  89. Duhan, J.S.; Kumar, R.; Kumar, N.; Kaur, P.; Nehra, K.; Duhan, S. Nanotechnology: The new perspective in precision agriculture. Biotechnol. Rep. 2017, 15, 11–23. [Google Scholar] [CrossRef]
  90. Shang, Y.; Hasn, M.K.; Ahammed, G.J.; Li, M.; Yin, H.; Zhou, J. Applications of nanotechnology in plant growth and crop protection: A review. Molecules 2019, 24, 2558. [Google Scholar] [CrossRef] [Green Version]
  91. Singh, A.; Singh, N.B.; Hussain, I.; Singh, H. Effect of biologically synthesized copper oxide nanoparticles on metabolism and antioxidant activity to the crop plants Solanum lycopersicum and Brassica oleracea var. botrytis. J. Biotechnol. 2017, 262, 11–27. [Google Scholar] [CrossRef]
  92. Baker, S.; Volova, T.; Prudnikova, S.V.; Satish, S.; Prasad, N. Nano agroparticles emerging trends and future prospect in modern agriculture system. Environ. Toxicol. Phar. 2017, 53, 10–17. [Google Scholar] [CrossRef] [Green Version]
  93. Liu, Y.; Laks, P.; Heiden, P. Controlled release of biocides in solid wood. III. Preparation and characterization of surfactant-free nanoparticles. J. Appl. Polym. Sci. 2002, 86, 615–621. [Google Scholar] [CrossRef]
  94. Liu, Y.; Yan, L.; Heiden, P.; Laks, P. Use of nanoparticles for controlled release of biocides in solid wood. J. Appl. Polym. Sci. 2001, 79, 458–465. [Google Scholar] [CrossRef]
  95. Nikunj, P.; Purvi, D.; Niti, P.; Anamika, J.; Gautam, H.K. Agronanotechnology for plant fungal disease management: A review. Int. J. Curr. Microbiol. App. Sci. 2014, 3, 71–84. [Google Scholar]
  96. Kannan, N.; Rajendran, V.; Yuvakkumar, R.; Karunakaran, G.; Kavitha, K.; Suriyaprabha, R. Application of silica nanoparticles in maize to enhance fungal resistance. IET Nanobiotechnol. 2014, 8, 133–137. [Google Scholar]
  97. Thomas, R.; Mathew, S.; Nayana, A.R.; Mathews, J.; Radhakrishnan, E.K. Microbially and phytofabricated AgNPs with different mode of bactericidal action were identified to have comparable potential for surface fabrication of central venous catheters to combat Staphylococcus aureus biofilm. J. Photochem. Photobiol. B 2017, 171, 96–103. [Google Scholar] [CrossRef]
  98. Gajbhiye, M.; Kesharwani, J.; Ingle, A.; Gade, A.; Rai, M. Fungus-mediated synthesis of silver nanoparticles and their activity against pathogenic fungi in combination with fluconazole. Nanomed. Nanotechnol. Biol. Med. 2009, 5, 382–386. [Google Scholar] [CrossRef] [PubMed]
  99. Jo, Y.K.; Kim, B.H.; Jung, G. Antifungal activity of silver ions and nanoparticles on phytopathogenic fungi. Plant Dis. 2009, 93, 1037–1043. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  100. Min, J.S.; Kim, K.S.; Kim, S.W.; Jung, J.H.; Lamsal, K.; Kim, S.B.; Jung, M.Y.; Lee, Y.S. Effects of colloidal silver nanoparticles on sclerotium-forming phytopathogenic fungi. Plant Pathol. J. 2009, 25, 376–380. [Google Scholar] [CrossRef]
  101. Kasprowicz, M.J.; Kozioł, M.; Gorczyca, A. The effect of silver nanoparticles on phytopathogenic spores of Fusarium culmorum. Can. J. Microbiol. 2010, 56, 247–253. [Google Scholar] [CrossRef] [PubMed]
  102. Musarrat, J.; Dwivedi, S.; Singh, B.R.; Al-Khedhairy, A.A.; Azam, A.; Naqvi, A. Production of antimicrobial silver nanoparticles in water extracts of the fungus Amylomyces rouxii strain KSU-09. Bioresour. Technol. 2010, 101, 8772–8776. [Google Scholar] [CrossRef]
  103. Wani, A.H.; Shah, M.A. A unique and profound effect of MgO and ZnO nanoparticles on some plant pathogenic fungi. J. Appl. Pharma. Sci. 2012, 2, 4. [Google Scholar]
  104. Park, H.J.; Kim, S.H.; Kim, H.J.; Choi, S.H. A new composition of nanosized silica-silver for control of various plant diseases. Plant Pathol. J. 2006, 22, 295–302. [Google Scholar] [CrossRef]
  105. Cioffi, N.; Ditaranto, N.; Torsi, L.; Picca, R.A.; Sabbatini, L.; Valentini, A.; Novello, G.; Tantillo, T.; Bleve-Zacheo, T.; Zambonin, P.G. Analytical characterization of bioactive fluoropolymer ultra-thin coatings modified by copper nanoparticles. Anal. Bioanal. Chem. 2005, 381, 607–616. [Google Scholar] [CrossRef]
  106. Singh, S.; Singh, B.K.; Yadav, S.M.; Gupta, A.K. Applications of nanotechnology in agricultural and their role in disease management. Res. J. Nanosci. Nanotechnol. 2015, 5, 1–5. [Google Scholar] [CrossRef]
  107. Shofia, S.I.; Jayakumar, K.; Mukherjee, A.; Chandrasekaran, N. Efficiency of brown seaweed (Sargassum longifolium) polysaccharides encapsulated in nanoemulsion and nanostructured lipid carrier against colon cancer cell lines HCT 116. RSC Adv. 2018, 8, 15973–15984. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  108. De, A.; Bose, R.; Kumar, A.; Mozumdar, S. Worldwide pesticide use. In Targeted Delivery of Pesticides Using Biodegradable Polymeric Nanoparticles; Springer: Berlin, Germany, 2016; pp. 5–6. [Google Scholar]
  109. Carriger, J.F.; Rand, G.M.; Gardinali, P.R.; Perry, W.B.; Tompkins, M.S.; Fernandez, A.M. Pesticides of Potential Ecological Concern in Sediment from South Florida Canals: An Ecological Risk Prioritization for Aquatic Arthropods. Soil Sediment Contam. 2006, 15, 21–45. [Google Scholar] [CrossRef]
  110. 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] [PubMed]
  111. Lomborg, B. The Skeptical Environmentalist; Cambridge University Press: Cambridge, UK, 2001; p. 515. [Google Scholar]
  112. Rankic, I.; Zelinka, R.; Ridoskova, A.; Gagic, M.; Pelcova, P.; Huska, D. Nano/micro particle in conjunction with microalgae extract as novel insecticides against Mealworm beetles, Tenebrio molitor. Sci. Rep. 2021, 11, 17125. [Google Scholar] [CrossRef] [PubMed]
  113. Thabet, A.F.; Boraei, H.A.; Galal, O.A.; El-Samahy, M.F.M.; Mousa, K.M.; Zhang, Y.Z.; Tuda, M.; Helmy, E.A.; Wen, J.; Nozaki, T. Silica nanoparticles as pesticide against insects of different feeding types and their non-target attraction of predators. Sci. Rep. 2021, 11, 14484. [Google Scholar] [CrossRef]
  114. Kah, M. Nanopesticides and Nanofertilizers: Emerging Contaminants or Opportunities for Risk Mitigation? Front. Chem. 2015, 3, 64. [Google Scholar] [CrossRef] [Green Version]
  115. Chhipa, H. Nanofertilizers and nanopesticides for agriculture. Environ. Chem. Lett. 2017, 15, 15–22. [Google Scholar] [CrossRef]
  116. Kah, M.; Tufenkji, N.; White, J.C. Nano–enabled strategies to enhance crop nutrition and protection. Nat. Nanotechnol. 2019, 14, 532–540. [Google Scholar] [CrossRef]
  117. Kumpiene, J.; Lagerkvist, A.; Maurice, C. Stabilization of As, Cr, Cu, Pb and Zn in soil using amendments—A review. Waste Manag. 2008, 28, 215–225. [Google Scholar] [CrossRef] [PubMed]
  118. ECHA. Synthetic Amorphous Silicon Dioxide (PT18)—Assessment Report Finalized in the Standing Committee on Biocidal Products at Its Meeting on 13 March 2014 in France. Available online: http://dissemination.echa.europa.eu/Biocides/ActiveSubstances/1378–18/1378–8_Assessment_Report.pdf (accessed on 7 October 2016).
  119. Oliveira, J.L.; Campos, E.V.; Bakshi, M.; Abhilash, P.C.; Fraceto, L.F. Application of nanotechnology for the encapsulation of botanical insecticides for sustainable agriculture: Prospects and promises. Biotechnol. Adv. 2014, 32, 1550–1561. [Google Scholar] [CrossRef] [PubMed]
  120. Shahbazi, R.; Salouti, M.; Amini, B.; Jalilvand, A.; Naderlou, E.; Amini, A.; Shams, A. Highly selective and sensitive detection of Staphylococcus aureus with gold nanoparticle-based core-shell nano biosensor. Mol. Cell Probes. 2018, 41, 8–13. [Google Scholar] [CrossRef] [PubMed]
  121. Bellan, L.M.; Wu, D.; Langer, R.S. Current trends in nanobiosensor technology. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2011, 3, 229–246. [Google Scholar] [CrossRef] [Green Version]
  122. Amini, B.; Kamali, M.; Salouti, M.; Yaghmaei, P. Fluorescence bio-barcode DNA assay based on gold and magnetic nanoparticles for detection of Exotoxin A gene sequence. Biosens. Bioelectron. 2017, 92, 679–686. [Google Scholar] [CrossRef]
  123. Tripathi, D.; Ahmad, P.; Sharma, S.; Chauhan, D.; Dubey, N.K. Nanomaterials in Plants, Algae, and Microorganisms; Academic Press, Elsevier Inc.: Amsterdam, The Netherlands, 2017; pp. 1–534. [Google Scholar]
  124. Kabariya, J.H.; Ramani, V.M. Nanobiosensors, as a next-generation diagnostic device for quality & safety of food and dairy product. In Nanotechnology: Food and Environmental Paradigm; Prasad, R., Kumar, V., Kumar, M., Eds.; Springer: Singapore, 2017; pp. 115–129. [Google Scholar]
  125. Srivastava, A.K.; Dev, A.; Karmakar, S. Nanosensors and nanobiosensors in food and agriculture. Environ. Chem. Lett. 2018, 16, 161–182. [Google Scholar] [CrossRef]
  126. Farber, C.; Kurouski, D. Detection and identification of plant pathogens on maize kernels with a hand-held Raman spectrometer. Anal Chem. 2018, 90, 3009–3012. [Google Scholar] [CrossRef] [Green Version]
  127. Lin, H.Y.; Huang, C.-H.; Lu, S.H.; Kuo, I.T.; Chau, L.K. Direct detection of orchid viruses using nanorod-based fiber optic particle plasmon resonance immunosensor. Biosens. Bioelectron. 2014, 51, 371–378. [Google Scholar] [CrossRef] [PubMed]
  128. Wang, F.; Gu, X.; Zheng, C.; Dong, F.; Zhang, L.; Cai, Y.; You, Z.; Du, S.; Zhang, Z. Ehrlich reaction evoked multiple spectral resonances and gold nanoparticle hotspots for raman detection of plant hormone. Anal. Chem. 2017, 89, 8836–8843. [Google Scholar] [CrossRef] [PubMed]
  129. Safarpour, H.; Safarnejad, M.R.; Tabatabaei, M.; Mohsenifar, A.; Rad, F.; Basirat, M.; Basirat, M.; Hasanzadeh, F. Development of a quantum dots FRET-based biosensor for efficient detection of Polymyxa betae. Can. J. Plant Pathol. 2012, 34, 507–515. [Google Scholar] [CrossRef]
  130. Shojaei, T.R.; Salleh, M.A.; Sijam, K.; Rahim, R.A.; Mohsenifar, A.; Safarnejad, R.; Tabatabaei, M. Detection of Citrus tristeza virus by using fluorescence resonance energy transfer-based biosensor. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2016, 169, 216–222. [Google Scholar] [CrossRef] [PubMed]
  131. Kaushal, M.; Wani, S. Nanosensors: Frontiers in precision agriculture. In Nanotechnolgy; Springer: Singapore, 2017; pp. 279–291. [Google Scholar]
  132. Gupta, C.; Prakash, D. Novel bioremediation methods in waste management: Novel bioremediation methods. In Waste Management: Concepts, Methodologies, Tools, and Applications; Khosrow-Pour, M., Ed.; IGI Global: Hershey, PA, USA, 2020; pp. 1627–1643. [Google Scholar]
  133. Sun, L.; Song, F.; Guo, J.; Zhu, X.; Liu, S.; Liu, F.; Li, X. Nano-ZnO-Induced Drought Tolerance is Associated with Melatonin Synthesis and Metabolism in Maize. Int. J. Mol. Sci. 2020, 21, 782. [Google Scholar] [CrossRef] [Green Version]
  134. Abdia, O.; Kazemi, M. A review study of biosorption of heavy metals and comparison between different biosorbents. J. Mater. Environ. Sci. 2015, 6, 1386–1399. [Google Scholar]
  135. Rizwan, M.; Singh, M.; Mitra, C.K.; Morve, R.K. Ecofriendly Application of Nanomaterials: Nanobioremediation. J. Nanopart. 2014, 2014, 431787. [Google Scholar] [CrossRef] [Green Version]
  136. Tungittiplakorn, W.; Lion, L.W.; Cohen, C.; Kim, J.Y. Engineered polymeric nanoparticles for soil remediation. Environ. Sci. Technol. 2004, 38, 1605–1610. [Google Scholar] [CrossRef]
  137. Pouratashi, M.; Iravani, H. Farmers’ knowledge of integrated pest management and learning style preferences: Implications for information delivery. Int. J. Pest Manag. 2012, 58, 347–353. [Google Scholar] [CrossRef]
  138. Robroek, B.J.M.; Jassey, V.E.J.; Beltman, B.; Hefting, M. Diverse fen plant communities enhance carbon-related multifunctionality, but do not mitigate negative effects of drought. R. Soc. Open Sci. 2017, 4, 170449. [Google Scholar] [CrossRef] [Green Version]
  139. Atkinson, N.J.; Urwin, P.E. The interaction of plant biotic and abiotic stresses: From genes to the field. J. Exp. Bot. 2012, 63, 3523–3543. [Google Scholar] [CrossRef] [Green Version]
  140. Roghani, A. The infuence of COVID-19 vaccine on daily cases, hospitalization, and death rate in Tennessee: A case study in the United States. medRxiv 2021. [Google Scholar] [CrossRef]
  141. Wang, W.; Vinocur, B.; Altman, A. Plant responses to drought, salinity and extreme temperatures: Towards genetic engineering for stress tolerance. Planta 2003, 218, 1–14. [Google Scholar] [CrossRef]
  142. Taiz, L.; Zeiger, E. Secondary Metabolites and Plant Defense. In Plant Physiology; Taiz, L., Zeiger, E., Eds.; Sinauer Associates: Sunderland, UK, 2006; Volume 4, pp. 315–344. ISBN 9780878935659. [Google Scholar]
  143. Ibrahim, E.; Zhang, M.; Zhang, Y.; Hossain, A.; Qiu, W.; Chen, Y.; Wang, Y.; Wu, W.; Sun, G.; Li, B. Green-synthesization of silver nanoparticles using endophytic bacteria isolated from garlic and its antifungal activity against wheat Fusarium head blight pathogen Fusarium graminearum. Nanomaterials 2020, 10, 219. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  144. Van Nguyen, D.; Nguyen, H.M.; Le, N.T.; Nguyen, K.H.; Nguyen, H.T.; Le, H.M.; Nguyen, A.T.; Dinh, N.T.T.; Hoang, S.A.; van Ha, C. Copper nanoparticle application enhances plant growth and grain yield in maize under drought stress conditions. J. Plant Growth Regul. 2021, 40, 1–12. [Google Scholar] [CrossRef]
  145. Song, Y.; Jiang, M.; Zhang, H.; Li, R. Zinc oxide nanoparticles alleviate chilling stress in rice (Oryza Sativa L.) by regulating antioxidative system and chilling response transcription factors. Molecules 2021, 26, 2196. [Google Scholar] [CrossRef]
  146. Semida, W.M.; Abdelkhalik, A.; Mohamed, G.F.; Abd El-Mageed, T.A.; Abd El-Mageed, S.A.; Rady, M.M.; Ali, E.F. Foliar application of zinc oxide nanoparticles promotes drought stress tolerance in eggplant (Solanum melongena L.). Plants 2021, 10, 421. [Google Scholar] [CrossRef]
  147. Shah, T.; Latif, S.; Saeed, F.; Ali, I.; Ullah, S.; Abdullah Alsahli, A.; Jan, S.; Ahmad, P. Seed priming with titanium dioxide nanoparticles enhances seed vigor, leaf water status, and antioxidant enzyme activities in maize (Zea mays L.) under salinity stress. J. King Saud. Univ. Sci. 2021, 33, 101207. [Google Scholar] [CrossRef]
  148. Adrees, M.; Khan, Z.S.; Hafeez, M.; Rizwan, M.; Hussain, K.; Asrar, M.; Alyemeni, M.N.; Wijaya, L.; Ali, S. Foliar exposure of zinc oxide nanoparticles improved the growth of wheat (Triticum aestivum L.) and decreased cadmium concentration in grains under simultaneous cd and water deficient stress. Ecotoxicol. Environ. Saf. 2021, 208, 111627. [Google Scholar] [CrossRef]
  149. Noohpisheh, Z.; Amiri, H.; Mohammadi, A.; Farhadi, S. Effect of the foliar application of zinc oxide nanoparticles on some biochemical and physiological parameters of Trigonella foenum-graecum under salinity stress. Plant Biosyst. Int. J. Deal. Asp. Plant Biol. 2021, 155, 267–280. [Google Scholar] [CrossRef]
  150. Gohari, G.; Mohammadi, A.; Akbari, A.; Panahirad, S.; Dadpour, M.R.; Fotopoulos, V.; Kimura, S. Titanium dioxide nanoparticles (TiO2 NPs) promote growth and ameliorate salinity stress effects on essential oil profile and biochemical attributes of Dracocephalum moldavica. Sci. Rep. 2020, 10, 912. [Google Scholar] [CrossRef] [PubMed]
  151. Ye, Y.; Cota-Ruiz, K.; Hernández-Viezcas, J.A.; Valdés, C.; Medina-Velo, I.A.; Turley, R.S.; Peralta-Videa, J.R.; Gardea-Torresdey, J.L. Manganese nanoparticles control salinity-modulated molecular responses in Capsicum annuum L. through priming: A sustainable approach for agriculture. ACS Sustain. Chem. Eng. 2020, 8, 1427–1436. [Google Scholar] [CrossRef]
  152. Emamverdian, A.; Ding, Y.; Mokhberdoran, F.; Ahmad, Z.; Xie, Y. Determination of heavy metal tolerance threshold in a bamboo species (Arundinaria pygmaea) as treated with silicon dioxide nanoparticles. Glob. Ecol. Cons. 2020, 24, e01306. [Google Scholar] [CrossRef]
  153. Hashimoto, T.; Mustafa, G.; Nishiuchi, T.; Komatsu, S. Comparative analysis of the effect of inorganic and organic chemicals with silver nanoparticles on soybean under flooding stress. Int. J. Mol. Sci. 2020, 21, 1300. [Google Scholar] [CrossRef] [Green Version]
  154. Alabdallah, N.M.; Alzahrani, H.S. The potential mitigation effect of ZnO nanoparticles on [Abelmoschus esculentus L. Moench] metabolism under salt stress conditions. Saudi J. Biol. Sci. 2020, 27, 3132–3137. [Google Scholar] [CrossRef] [PubMed]
  155. Elsheery, N.I.; Helaly, M.N.; El-Hoseiny, H.M.; Alam-Eldein, S.M. Zinc oxide and silicone nanoparticles to improve the resistance mechanism and annual productivity of salt-stressed mango trees. Agronomy 2020, 10, 558. [Google Scholar] [CrossRef]
  156. Mahmoud, L.M.; Dutt, M.; Shalan, A.M.; El-Kady, M.E.; El-Boray, M.S.; Shabana, Y.; Grosser, J.W. Silicon nanoparticles mitigate oxidative stress of in vitro-derived banana (Musa acuminata ‘Grand Nain’) under simulated water deficit or salinity stress. S. Afr. J. Bot. 2020, 132, 155–163. [Google Scholar] [CrossRef]
  157. Ghorbanpour, M.; Mohammadi, H.; Kariman, K. Nanosilicon-based recovery of barley (Hordeum vulgare) plants subjected to drought stress. Environ. Sci. Nano 2020, 7, 443–461. [Google Scholar] [CrossRef]
  158. Lian, J.; Zhao, L.; Wu, J.; Xiong, H.; Bao, Y.; Zeb, A.; Tang, J.; Liu, W. Foliar spray of TiO2 nanoparticles prevails over root application in reducing Cd accumulation and mitigating Cd-induced phytotoxicity in maize (Zea mays L.). Chemosphere 2020, 239, 124794. [Google Scholar] [CrossRef] [PubMed]
  159. Wenli, S.; Shahrajabian, M.H.; Huang, Q. Soybean seeds treated with single walled carbon nanotubes (SwCNTs) showed enhanced drought tolerance during germination. Int. J. Adv. Biol. Biomed. Res. 2020, 8, 9–16. [Google Scholar]
  160. Younis, A.; Khattab, H.; Emam, M. Impacts of silicon and silicon nanoparticles on leaf ultrastructure and TaPIP1 and TaNIP2 gene expressions in heat stressed wheat seedlings. Biol. Plant. 2020, 64, 343–352. [Google Scholar] [CrossRef]
  161. Hussain, A.; Rizwan, M.; Ali, Q.; Ali, S. Seed priming with silicon nanoparticles improved the biomass and yield while reduced the oxidative stress and cadmium concentration in wheat grains. Environ. Sci. Pollut. Res. 2019, 26, 7579–7588. [Google Scholar] [CrossRef] [PubMed]
  162. Kiapour, H.; Moaveni, P.; Habibi, D.; Sani, B. Evaluation of the application of gibbrellic acid and titanium dioxide nanoparticles under drought stress on some traits of basil (Ocimum basilicum L.). Int. J. Agron. Agric. Res. 2015, 6, 138–150. [Google Scholar]
  163. Haghighi, M.; Afifipour, Z.; Mozafarian, M. The effect of N-Si on tomato seed germination under salinity levels. J. Biol. Environ. Sci. 2012, 6, 87–90. [Google Scholar]
  164. Maisa’a, W.; Awwad, A.M. A novel route for the synthesis of copper oxide nanoparticles using Bougainvillea plant flowers extract and antifungal activity evaluation. Chem. Int. 2021, 7, 71–78. [Google Scholar]
  165. Ahmad, H.; Venugopal, K.; Bhat, A.; Kavitha, K.; Ramanan, A.; Rajagopal, K.; Srinivasan, R.; Manikandan, E. Enhanced biosynthesis synthesis of copper oxide nanoparticles (CuO-NPs) for their antifungal activity toxicity against major phyto-pathogens of apple orchards. Pharm. Res. 2020, 37, 1–12. [Google Scholar] [CrossRef] [PubMed]
  166. Ahmad, H.; Venugopal, K.; Rajagopal, K.; de Britto, S.; Nandini, B.; Pushpalatha, H.G.; Konappa, N.; Udayashankar, A.C.; Geetha, N.; Jogaiah, S. Green synthesis and characterization of zinc oxide nanoparticles using Eucalyptus globules and their fungicidal ability against pathogenic fungi of apple orchards. Biomolecules 2020, 10, 425. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  167. Cai, L.; Cai, L.; Jia, H.; Liu, C.; Wang, D.; Sun, X. Foliar exposure of Fe3O4 nanoparticles on Nicotiana benthamiana: Evidence for nanoparticles uptake, plant growth promoter and defence response elicitor against plant virus. J. Hazard. Mater. 2020, 393, 122415. [Google Scholar] [CrossRef] [PubMed]
  168. Irshad, M.A.; Nawaz Rur Rehman, M.Z.; Imran, M.; Ahmad, J.; Ahmad, S.; Inam, A.; Razzaq, A.; Rizwan, M.; Ali, S. Synthesis and characterization of titanium dioxide nanoparticles by chemical and green methods and their antifungal activities against wheat rust. Chemosphere 2020, 258, 127352. [Google Scholar] [CrossRef] [PubMed]
  169. Lipșa, F.D.; Ursu, E.L.; Ursu, C.; Ulea, E.; Cazacu, A. Evaluation of the antifungal activity of gold-chitosan and carbon nanoparticles on Fusarium oxysporum. Agronomy 2020, 10, 1143. [Google Scholar] [CrossRef]
  170. Shukla, G.; Gaurav, S.S.; Singh, A. Synthesis of mycogenic zinc oxide nanoparticles and preliminary determination of its efficacy as a larvicide against white grubs (Holotrichia sp.). Int. Nano. Lett. 2020, 10, 131–139. [Google Scholar] [CrossRef]
  171. Manikandaselvi, S.; Sathya, V.; Vadivel, V.; Sampath, N.; Brindha, P. Evaluation of bio control potential of AgNPs synthesized from Trichoderma viride. Adv. Nat. Sci. Nanosci. Nanotechnol. 2020, 11, 035004. [Google Scholar] [CrossRef]
  172. Al Shater, H.; Moustafa, H.Z.; Yousef, H. Synthesis, phytochemical screening and toxicity measuring against Earias insulana (Boisd.) (Lepidoptera: Noctuidae) of silver nano particles from Origanum marjorana extract in the field. Egypt. Acad. J. Biol. Sci. F Toxicol. Pest Control 2020, 12, 175–184. [Google Scholar] [CrossRef]
  173. Osonga, F.J.; Akgul, A.; Yazgan, I.; Akgul, A.; Eshun, G.B.; Sakhaee, L.; Sadik, O.A. Size and shape-dependent antimicrobial activities of silver and gold nanoparticles: A model study as potential fungicides. Molecules 2020, 25, 2682. [Google Scholar] [CrossRef]
  174. Khatua, A.; Priyadarshini, E.; Rajamani, P.; Patel, A.; Kumar, J.; Naik, A.; Saravanan, M.; Barabadi, H.; Prasad, A.; Paul, B. Phytosynthesis, characterization and fungicidal potential of emerging gold nanoparticles using Pongamia pinnata leave extract: A novel approach in nanoparticle synthesis. J. Cluster. Sci. 2020, 31, 125–131. [Google Scholar] [CrossRef]
  175. Masum, M.; Islam, M.; Siddiqa, M.; Ali, K.A.; Zhang, Y.; Abdallah, Y.; Ibrahim, E.; Qiu, W.; Yan, C.; Li, B. Biogenic synthesis of silver nanoparticles using Phyllanthus emblica fruit extract and its inhibitory action against the pathogen Acidovorax oryzae strain RS-2 of rice bacterial brown stripe. Front. Microbiol. 2019, 10, 820. [Google Scholar] [CrossRef]
  176. Saqib, S.; Zaman, W.; Ullah, F.; Majeed, I.; Ayaz, A.; Hussain Munis, M.F. Organometallic assembling of chitosan-Iron oxide nanoparticles with their antifungal evaluation against Rhizopus oryzae. Appl. Organomet Chem. 2019, 33, e5190. [Google Scholar] [CrossRef]
  177. Ogunyemi, S.O.; Abdallah, Y.; Zhang, M.; Fouad, H.; Hong, X.; Ibrahim, E.; Masum, M.M.I.; Hossain, A.; Mo, J.; Li, B. Green synthesis of zinc oxide nanoparticles using diferent plant extracts and their antibacterial activity against Xanthomonas oryzae pv. oryzae. Artif. Cells Nanomed. Biotechnol. 2019, 47, 341–352. [Google Scholar] [CrossRef] [Green Version]
  178. Zarnab, F.; Rimsha, T.; Mirza, A.Q.; Hafza, T.G.; Hafz, N.F. Evaluation of toxicity of nanoparticles against Bactrocera zonata as bio-control agent. Agric. Sci. J. 2019, 1, 25–33. [Google Scholar]
  179. Shaker, A.; Zaki, A.; Abdel-Rahim, E.; Khedr, M. TiO2 nanoparticles as an effective nanopesticide for cotton leaf worm. Agric. Eng. Int. CIGR. J. Special 2017, 61–68. [Google Scholar]
  180. Wang, X.; Zhou, Z.; Chen, F. Surface modifcation of carbon nanotubes with an enhanced antifungal activity for the control of plant fungal pathogen. Materials 2017, 10, 1375. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  181. Sahayaraj, K.; Madasamy, M.; Radhika, S.A. Insecticidal activity of bio-silver and gold nanoparticles against Pericallia ricini Fab. (Lepidaptera: Archidae). J. Biopestic. 2016, 9, 63. [Google Scholar]
  182. Boxi, S.S.; Mukherjee, K.; Paria, S. Ag doped hollow TiO2 nanoparticles as an effective green fungicide against Fusarium solani and Venturia inaequalis phytopathogens. Nanotechnology 2016, 27, 085103. [Google Scholar] [CrossRef]
  183. Wang, F.; Liu, X.; Shi, Z.; Tong, R.; Adams, C.A.; Shi, X. Arbuscular mycorrhizae alleviate negative effects of zinc oxide nanoparticle and zinc accumulation in maize plants—A soil microcosm experiment. Chemosphere 2016, 147, 88–97. [Google Scholar] [CrossRef] [PubMed]
  184. Thakur, S.; Asthir, B.; Kaur, G.; Kalia, A.; Sharma, A. Zinc oxide and titanium dioxide nanoparticles influence heat stress tolerance mediated by antioxidant defense system in wheat. Cereal Res. Commun. 2021, 49, 1–2. [Google Scholar] [CrossRef]
  185. Gunjan, B.; Zaidi, M.G.H.; Sandeep, A. Impact of gold nanoparticles on physiological and biochemical characteristics of Brassica juncea. J. Plant Biochem. Physiol. 2014, 2, 133. [Google Scholar]
  186. Evelin, H.; Devi, T.S.; Gupta, S.; Kapoor, R. Mitigation of Salinity Stress in Plants by Arbuscular Mycorrhizal Symbiosis: Current Understanding and New Challenges. Front. Plant Sci. 2019, 10, 470. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  187. Abdoli, S.; Ghassemi-Golezani, K.; Alizadeh-Salteh, S. Responses of ajowan (Trachyspermum ammi L.) to exogenous salicylic acid and iron oxide nanoparticles under salt stress. Environ. Sci. Pollut. Res. 2020, 27, 36939–36953. [Google Scholar] [CrossRef] [PubMed]
  188. Zhang, T.; Shi, Z.; Zhang, X.; Zheng, S.; Wang, J.; Mo, J. Alleviating effects of exogenous melatonin on salt stress in cucumber. Sci. Hortic. 2020, 262, 109070. [Google Scholar] [CrossRef]
  189. Khan, I.; Raza, M.A.; Awan, S.A.; Shah, G.A.; Rizwan, M.; Ali, B.; Tariq, R.; Hassan, M.J.; Alyemeni, M.N.; Brestic, M.; et al. Amelioration of salt induced toxicity in pearl millet by seed priming with silver nanoparticles (AgNPs): The oxidative damage, antioxidant enzymes and ions uptake are major determinants of salt tolerant capacity. Plant Physiol. Biochem. 2020, 156, 221–232. [Google Scholar] [CrossRef]
  190. Wahid, I.; Kumari, S.; Ahmad, R.; Hussain, S.J.; Alamri, S.; Siddiqui, M.H.; Khan, M.I.R. Silver Nanoparticle Regulates Salt Tolerance in Wheat through Changes in ABA Concentration, Ion Homeostasis, and Defense Systems. Biomolecules 2020, 10, 1506. [Google Scholar] [CrossRef] [PubMed]
  191. Liu, B.; Soundararajan, P.; Manivannan, A. Mechanisms of silicon-mediated amelioration of salt stress in plants. Plants 2019, 8, 307. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  192. Rizwan, M.; Ali, S.; Ali, B.; Adrees, M.; Arshad, M.; Hussain, A.; Rehman, M.Z.; Waris, A.A. Zinc and iron oxide nanoparticles improved the plant growth and reduced the oxidative stress and cadmium concentration in wheat. Chemosphere 2019, 214, 269–277. [Google Scholar] [CrossRef] [PubMed]
  193. Diao, M.; Ma, L.; Wang, J.; Cui, J.; Fu, A.; Liu, H.-y. Selenium promotes the growth and photosynthesis of tomato seedlings under salt stress by enhancing chloroplast antioxidant defense system. J. Plant Growth Regul. 2014, 33, 671–682. [Google Scholar] [CrossRef]
  194. Thuesombat, P.; Hannongbua, S.; Ekgasit, S.; Chadchawan, S. Effects of silver nanoparticles on hydrogen peroxide generation and antioxidant enzyme responses in rice. J. Nanosci. Nanotechnol. 2016, 16, 8030–8043. [Google Scholar] [CrossRef]
  195. Faisal, M.; Saquib, Q.; Alatar, A.A.; Al-Khedhairy, A.A.; Hegazy, A.K.; Musarrat, J. Phytotoxic hazards of NiO-nanoparticles in tomato: A study on mechanism of cell death. J. Hazard. Mater. 2013, 250, 318–332. [Google Scholar] [CrossRef] [PubMed]
  196. Misra, S.K.; Dybowska, A.; Berhanu, D.; Luoma, S.N.; Valsami-Jones, E. The complexity of nanoparticle dissolution and its importance in nanotoxicological studies. Sci. Total Environ. 2012, 438, 225–232. [Google Scholar] [CrossRef] [PubMed]
  197. Mahakham, W.; Theerakulpisut, P.; Maensiri, S.; Phumying, S.; Sarmah, A.K. Environmentally benign synthesis of phytochemicals-capped gold nanoparticles as nanopriming agent for promoting maize seed germination. Sci. Total Environ. 2016, 573, 1089–1102. [Google Scholar] [CrossRef] [PubMed]
  198. Pinheiro, C.; Chaves, M.M. Photosynthesis and drought: Can we make metabolic connections from available data. J. Exp. Bot. 2011, 62, 869–882. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  199. Ji, H.; Pardo, J.M.; Batelli, G.; van Oosten, M.J.; Bressan, R.A.; Li, X. The salt overly sensitive (SOS) pathway: Established and emerging roles. Mol. Plant 2013, 6, 275–286. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  200. Gao, Z.; He, X.; Zhao, B.; Zhou, C.; Liang, Y.; Ge, R.; Shen, Y.; Huang, Z. Overexpressing a putative aquaporin gene from wheat, TaNIP, enhances salt tolerance in transgenic Arabidopsis. Plant Cell Physiol. 2010, 51, 767–775. [Google Scholar] [CrossRef] [Green Version]
  201. Rios, J.J.; Martínez-Ballesta, M.C.; Ruiz, J.M.; Blasco, B.; Carvajal, M. Silicon mediated improvement in plant salinity tolerance: The role of aquaporins. Front. Plant Sci. 2017, 8, 948. [Google Scholar] [CrossRef] [Green Version]
  202. Martinez-Vilalta, J.; Pinol, J. Drought induced mortality and hydraulic architecture in pine populations of the NE Iberian Peninsula. For. Ecol. Manag. 2002, 161, 247–256. [Google Scholar] [CrossRef]
  203. Hidangmayum, A.; Dwivedi, P.; Katiyar, D.; Hemantaranjan, A. Application of chitosan on plant responses with special reference to abiotic stress. Physiol. Mol. Biol. Plants 2019, 25, 313–326. [Google Scholar] [CrossRef]
  204. Hassan, F.A.S.; Ali, E.F.; Alamer, K.H. Exogenous application of polyamines alleviates water stress-induced oxidative stress of Rosa damascena Miller var. trigintipetala Dieck. S. Afr. J. Botany 2018, 116, 96–102. [Google Scholar] [CrossRef]
  205. Das, A.; Ray, R.; Mandal, N.; Chakrabarti, K. An analysis of transcripts and enzyme profiles in drought stressed jute (Corchorus capsularis) and rice (Oryza sativa) seedlings treated with CaCl2, hydroxyapatite nano-particle and β-amino butyric acid. Plant Growth Regul. 2016, 79, 401–412. [Google Scholar] [CrossRef]
  206. Palmqvist, N.G.M.; Seisenbaeva, G.A.; Svedlindh, P.; Kessler, V.G. Maghemite nanoparticles acts as nanozymes, improving growth and abiotic stress tolerance in Brassica napus. Nanoscale Res. Lett. 2017, 12, 631. [Google Scholar] [CrossRef]
  207. Hasanuzzaman, M.; Nahar, K.; Alam, M.M.; Roychowdhury, R.; Fujita, M. Physiological, biochemical, and molecular mechanisms of heat stress tolerance in plants. Int. J. Mol. Sci. 2013, 14, 9643–9684. [Google Scholar] [CrossRef] [PubMed]
  208. Djanaguiraman, M.; Nair, R.; Giraldo, J.P.; Prasad, P.V.V. Cerium oxide nanoparticles decrease drought-induced oxidative damage in sorghum leading to higher photosynthesis and grain yield. ACS Omega 2018, 3, 14406–14416. [Google Scholar] [CrossRef] [PubMed]
  209. Haghighi, M.; Abolghasemi, R.; Silva, J.A.T. Low and high temperature stress affect the growth characteristics of tomato in hydroponic culture with Se and nano-Se amendment. Sci. Hortic. 2014, 178, 231–240. [Google Scholar] [CrossRef]
  210. Iqbal, M.; Raja, N.I.; Hussain, M.; Ejaz, M.; Yasmeen, F. Effect of silver nanoparticles on growth of wheat under heat stress. Iran. J. Sci. Technol. Transac. A Sci. 2019, 43, 387–395. [Google Scholar] [CrossRef]
  211. Sharma, R.K.; Patel, S.; Pargaien, K.C. Synthesis, characterization and properties of Mndoped ZnO nanocrystals. Adv. Nat. Sci. Nanosci. Nanotechnol. 2012, 3, 035005. [Google Scholar] [CrossRef] [Green Version]
  212. 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 2015. Plant Physiol. Biochem. 2015, 96, 189–198. [Google Scholar] [CrossRef]
  213. Singh, J.; Lee, B.K. Influence of nano-TiO2 particles on the bioaccumulation of Cd in soybean plants (Glycine max): A possible mechanism for the removal of Cd from the contaminated soil. J. Environ. Manag. 2016, 170, 88–96. [Google Scholar] [CrossRef] [PubMed]
  214. Dietz, K.J.; Herth, S. Plant nanotoxicology. Trends Plant Sci. 2011, 16, 582–589. [Google Scholar] [CrossRef] [PubMed]
  215. Pérez-de-Luque, A. Interaction of Nanomaterials with Plants: What Do We Need for Real Applications in Agriculture? Front. Environ. Sci. 2017, 5, 12. [Google Scholar] [CrossRef] [Green Version]
  216. Sabo-Attwood, T.; Unrine, J.M.; Stone, J.W.; Murphy, C.J.; Ghoshroy, S.; Blom, D.; Bertsch, P.M.; Newman, L.A. Uptake, distribution and toxicity of gold nanoparticles in tobacco (Nicotiana xanthi) seedlings. Nanotoxicology 2012, 6, 353–360. [Google Scholar] [CrossRef]
  217. Taylor, A.F.; Rylott, E.L.; Anderson, C.W.; Bruce, N.C. Investigating the toxicity, uptake, nanoparticle formation and genetic response of plants to gold. PLoS ONE 2014, 9, e93793. [Google Scholar] [CrossRef] [Green Version]
  218. Rico, C.M.; Majumdar, S.; Duarte-Gardea, M.; Peralta-Videa, J.R.; Gardea-Torresdey, J.L. Interaction of nanoparticles with edible plants and their possible implications in the food chain. J. Agric. Food Chem. 2011, 59, 3485–3498. [Google Scholar] [CrossRef] [Green Version]
  219. Raliya, R.; Franke, C.; Chavalmane, S.; Nair, R.; Reed, N.; Biswas, P. Quantitative understanding of nanoparticle uptake in watermelon plants. Front. Plant Sci. 2016, 7, 1288. [Google Scholar] [CrossRef] [Green Version]
  220. Judy, J.D.; Unrine, J.M.; Rao, W.; Wirick, S.; Bertsch, P.M. Bioavailability of gold nanomaterials to plants: Importance of particle size and surface coating. Environ. Sci. Technol. 2012, 46, 8467–8474. [Google Scholar] [CrossRef] [PubMed]
  221. Navarro, E.; Baun, A.; Behra, R.; Hartmann, N.B.; Filser, J.; Miao, A.J.; Quigg, A.; Santschi, P.H.; Sigg, L. Environmental behavior and ecotoxicity of engineered nanoparticles to algae, plants, and fungi. Ecotoxicology 2008, 17, 372–386. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  222. United States Environmental Protection Agency. Ecological Test Guidelines (OPPTS 850, 4200): Seed Germination/Root Elongation Toxicity Test; US EPA: Washington, DC, USA, 1996. [Google Scholar]
  223. Sattelmacher, B. The apoplast and its significance for plant mineral nutrition. New Phytol. 2001, 149, 167–192. [Google Scholar] [CrossRef] [PubMed]
  224. Roberts, A.G.; Oparka, K.J. Plasmodesmata and the control of symplastic transport. Plant Cell Environ. 2003, 26, 103–124. [Google Scholar] [CrossRef] [Green Version]
  225. Wang, Z.; Xie, X.; Zhao, J.; Liu, X.; Feng, W.; White, J.C.; Xing, B. Xylem—And phloem-based transport of CuO nanoparticles in maize (Zea mays L.). Environ. Sci. Technol. 2012, 46, 4434–4441. [Google Scholar] [CrossRef]
  226. Sun, D.; Hussain, H.I.; Yi, Z.; Siegele, R.; Cresswell, T.; Kong, L.; Cahill, D.M. Uptake and cellular distribution, in four plant species, of fluorescently labeled mesoporous silica nanoparticles. Plant Cell Rep. 2014, 33, 1389–1402. [Google Scholar] [CrossRef]
  227. Robards, A.W.; Robb, M.E. Uptake and binding of uranyl ions by barley roots. Science 1972, 178, 980–982. [Google Scholar] [CrossRef]
  228. Lv, J.; Zhang, S.; Luo, L.; Zhang, J.; Yangc, K.; Christie, P. Accumulation, speciation and uptake pathway of ZnO nanoparticles in maize. Environ. Sci. Nano 2015, 2, 68–77. [Google Scholar] [CrossRef]
  229. Nel, A.E.; Mädler, L.; Velegol, D.; Xia, T.; Hoek, E.M.V.; Somasundaran, P.; Klaessig, F.; Castranova, V.; Thompson, M. Understanding biophysicochemical interactions at the nano-bio interface. Nat. Mater. 2009, 8, 543–557. [Google Scholar] [CrossRef] [PubMed]
  230. Schwab, F.; Zhai, G.; Kern, M.; Turner, A.; Schnoor, J.L.; Wiesner, M.R. Barriers, pathways and processes for uptake, translocation and accumulation of nanomaterials in plants—Critical review. Nanotoxicology 2015, 10, 257–278. [Google Scholar] [CrossRef] [PubMed]
  231. Schönherr, J. A mechanistic analysis of penetration of glyphosate salts across astomatous cuticular membranes. Pest Manag. Sci. 2002, 58, 343–351. [Google Scholar] [CrossRef] [PubMed]
  232. Eichert, T.; Goldbach, H.E. Equivalent pore radii of hydrophilic foliar uptake routes in stomatous and astomatous leaf surfaces—Further evidence for a stomatal pathway. Physiol. Plant 2008, 132, 491–502. [Google Scholar] [CrossRef] [PubMed]
  233. Pate, J.S. Exchange of solutes between phloem and xylem and circulation in the whole plant. In Transport in Plants I; Zimmermann, M.H., Milburn, J.A., Eds.; Springer: Berlin/Heidelberg, Germany, 1975; pp. 451–473. [Google Scholar]
  234. Cifuentes, Z.; Custardoy, L.; de la Fuente, J.M.; Marquina, C.; Ibarra, M.R.; Rubiales, D.; Pérez-de-Luque, A. Absorption and translocation to the aerial part of magnetic carbon-coated nanoparticles through the root of different crop plants. J. Nanobiotechnol. 2010, 8, 26. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  235. Zhu, Z.J.; Wang, H.; Yan, B.; Zheng, H.; Jiang, Y.; Miranda, O.R.; Rotello, V.M.; Xing, B.; Vachet, R.W. Effect of surface charge on the uptake and distribution of gold nanoparticles in four plant species. Environ. Sci. Technol. 2012, 46, 12391–12398. [Google Scholar] [CrossRef] [PubMed]
  236. Keller, A.A.; McFerran, S.; Lazareva, A.; Suh, S. Global life cycle releases of engineered nanomaterials. J. Nanopart. Res. 2013, 15, 1692. [Google Scholar] [CrossRef]
  237. Loureiro, S.; Tourinho, P.S.; Cornelis, G.; van den Brink, N.W.; Díez-Ortiz, M.; Vázquez-Campos, S.; Pomar-Portillo, V.; Svendsen, C.; van Gestel, C.A.M. Chapter 7—Nanomaterials as Soil Pollutants. In Soil Pollution; Duarte, A.C., Cachada, A., Rocha-Santos, T., Eds.; Academic Press: Cambridge, MA, USA, 2018; pp. 161–190. [Google Scholar]
Figure 1. Types of nanoparticles.
Figure 1. Types of nanoparticles.
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Figure 2. Synthesis of nanomaterials.
Figure 2. Synthesis of nanomaterials.
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Figure 3. (A) DNA, RNA (B) and protein (C) delivery using nanoparticles.
Figure 3. (A) DNA, RNA (B) and protein (C) delivery using nanoparticles.
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Figure 4. Application of nanotechnology in plant pathology: (a) plant disease control, (b) detection of plant pathogens.
Figure 4. Application of nanotechnology in plant pathology: (a) plant disease control, (b) detection of plant pathogens.
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Figure 5. Positive effect of different nanomaterials in sustainable agriculture.
Figure 5. Positive effect of different nanomaterials in sustainable agriculture.
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Figure 6. Application of nanotechnology: (a) role of nanobiosensors, (b) role in bioremediation.
Figure 6. Application of nanotechnology: (a) role of nanobiosensors, (b) role in bioremediation.
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Figure 7. Role of nanomaterials in improving plant growth under biotic and abiotic stress.
Figure 7. Role of nanomaterials in improving plant growth under biotic and abiotic stress.
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Figure 8. A proposed mechanism for nanoparticle-mediated abiotic stress management.
Figure 8. A proposed mechanism for nanoparticle-mediated abiotic stress management.
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Figure 9. Possible ways of ENM accumulation in environment [30].
Figure 9. Possible ways of ENM accumulation in environment [30].
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Table 1. Effect of different nanoparticle applications on some plant species growing under abiotic stress conditions.
Table 1. Effect of different nanoparticle applications on some plant species growing under abiotic stress conditions.
Name of Plant SpeciesNanoparticlesSizeConcentrationStress TypeResponseReferences
Zea mays L.Cu30–40 nm3.33, 4.44 and
5.55 mg L−1
Drought Higher biomass grain yield[144]
Oryza sativa L.ZnO30 nm50 mg L−1Chilling Regulated the antioxidative system and chilling response transcription factors[145]
Solanum melongena L.ZnO-50 and 100 ppmDrought stressImproved growth characteristics and increased fruit yield[146]
Zea mays L.TiO210–25 nm 60 ppmSalinity
stress
Enhancement of seed vigor, leaf water status and antioxidant enzyme activities[147]
Triticum aestivum L.ZnO20–30 nm25, 50 and 100 mgL−1Drought and
cadmium
Enhancement of growth, chlorophyll content,
SOD and POX activities
[148]
Trigonella foenum-graecumZnO10–30 nm0, 1000, and 3000 ppmSalinityUpregulation of protein and proline levels, enhancement of the antioxidants activities, reduction in H2O2 and MDA levels[149]
Dracocephalum
moldavica
TiO2 NPs20–30
Nm
0, 50, 100 and
200 mg L−1
Salinity stressImproved agronomic traits and increased antioxidant enzyme activity, increased essential oil content under 100 mg L−1 TiO2[150]
Triticum
aestivum L.
TiO2_500, 1000, and 2000 mg kg−1Drought stressImproved growth, antioxidant system and photosynthetic performance[5]
Zea mays L.ZnO37.7 ± 15.5 nm100 mg L−1Drought Enhanced melatonin synthesis and metabolism[133]
Capsicum annuum L.Manganese_0.1, 0.5, 1 mgL−1SalinityControlled salinity-modulated molecular responses[151]
Arundinaria pygmaeaSilicon dioxide20 nm100 μMHeavy metalIncreased protective enzymes, chlorophyll content and fluorescence, as well as plant biomass and shoot length[152]
Glycine maxAg NP15 nm5 ppmFlooding stressEnhancement of root length/weight and hypocotyl length/weight of soybean[153]
Abelmoschus esculentus L.ZnO16–35 nm10 mgL−1Salt stressEnhancement of the contents of the photosynthetic pigments, activity of both SOD and CAT, lowered accumulation of proline and total soluble sugar[154]
Mangifera indicaZinc oxide and siliconenZnO < 100 nm
Si = 5–15 nm
ZnO (50, 100, and 150 mgL−1)
Si (150 and 300 mgL−1)
Salt stressImproved resistance mechanism and annual productivity[155]
Musa acuminataSilicon nanoparticles_0, 200, 400 and 600 mgL−1Salinity stressMitigated oxidative stress of in vitro derived plant[156]
Dracocephalum
moldavica
TiO2 NPs70 –90 nm0, 50, 100 and 200 mg L−1Salinity stressPromoted growth and ameliorated salinity stress effects on essential oil profile and biochemical attributes[150]
Hordeum vulgareSilicon_125, 250 mgL−1Drought stressModified the plant morpho-physiological and antioxidative attributes and synthesis of specific metabolites[157]
Zea mays L.TiO2 NP_0, 100, 250 mgL−1Cd stressIncreased superoxide dismutase (SOD) and glutathione S-transferase (GST) activities[158]
Glycine maxSwCNTs_100 mLDrought stressEnhanced drought tolerance during germination[159]
Triticum aestivumSi NP20–30 nm1.66 mMHeat stressRestoration of the heat-stress-provoked ultrastructure-l distortions of chloroplast and nucleus, enhanced photochemical efficiency of the photosystem II[160]
Zea mays L.Si NPs_0, 300, 600, 900, 1200 mg L−1Cadmium stressEarly growth and enhanced physio-biochemical and metabolic profiles of fragrant[161]
Ocimum basilicum L.TiO2__Drought stressModulated toxic effects, improved biomass
accumulation and RWC
[162]
Lycopersicum esculentumSiO2_1–2 mMSalinity stressIncreased root growth, weight,
seed germination
[163]
Table 2. Effect of different nanoparticle applications on some plant species growing under biotic stress conditions.
Table 2. Effect of different nanoparticle applications on some plant species growing under biotic stress conditions.
Name of Plant SpeciesNanoparticlesSizeConcentrationStress TypesResponseReferences
BougainvilleaCuO NPs5–20 nm80 and 100 ppmA. nigerAntifungal[164]
Malus speciesCuO NPs80 nm0.05–1 mg mL−1Alternaria mali, Diplodia seriata, Botryosphaeria dothideaAntifungal[165]
Malus speciesZnO NPs52–70 nm0.05–1 mg mL−1A. mali, Botryosphaeria dothidea, D. seriatabyAntifungal[166]
Nicotiana benthamianaFe3O4 NPs20 nm100 μg mL−1Tobacco mosaic virus (TMV)Antiviral[167]
Triticum aestivum L.Ag NP19.8–44.9 nm5–20 μg mL−1F. graminearumAntifungal[143]
Triticum aestivum L.TiO2 NP<15 nm25, 50, 75 μL
from 0.1 mg mL−1
Puccinia triticinaAntifungal [168]
Lycopersicum esculentumAu NPs–chitosan, C-NP80 nm25–75 μg mL−1F. oxysporumAntifungal[169]
Saccharum officinarumZnO NPs
Zn NPs
72–183 nm3–20 ppmHolotrichia spInsecticidal [170]
Oryza sativaAg NPs100–250 nm_R. solani, F. moniliformeAntifungal[171]
Gossypium sp.Ag NPs63–85 nm1 mMEarias insulanaInsecticide[172]
Unidentified plantAg NPs,
Au NPs
8–510 nm4.5 mM AgNO3
5 mM gold
S. nidulans, Trichaptum biforme, P. italicum, F. oxysporum, Colletotrichum gloeosporioides, Pseudomonas aeruginosa, Aeromonas hydrophila, Escherichia coli, Citrobacter freundii, Listeria monocytogenes, Staphylococcus epidermidisAntifungal/Antibacterial[173]
Pongamia pinnataAg NPs10–25 nm0.0062–1.6 mg mL−1P. ultimumAntifungal [174]
Phyllanthus emblicaAg NPs19.8–92.8 nm5–30 μg mL−1A. oryzaeAntibacterial[175]
Oryza sativaChitosan–Fe2O3 NPs50–70 nm0.25–1%R. oryzaeAntifungal[176]
Oryza sativaZnO NPs40.5–124 nm4–16 μg mL−1X. oryzae pv.
oryzae
Antibacterial[177]
Mangifera indicaSNPs were synthesized by lemon plant leaves_20–160 ppmBactrocera zonataInsecticide [178]
Gossypium sp.TiO2 NPs95 nm31.25–1000 ppmSpodoptera littoralisInsecticide[179]
Triticum aestivumMWCNTs_62.5–500 μg mL−1F. graminearumAntifungal[180]
Ricinus communis (Linn)Ag NPs_103 MPericallia RiciniInsecticide[181]
Solanum tuberosum
Lycopersicon esculentum
Malus
Domestic
TiO2 NPs_0.8 mg plate−1F. solani
Venturia inaequalis
Antifungal[182]
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Ahmad, Z.; Tahseen, S.; Wasi, A.; Ganie, I.B.; Shahzad, A.; Emamverdian, A.; Ramakrishnan, M.; Ding, Y. Nanotechnological Interventions in Agriculture. Nanomaterials 2022, 12, 2667. https://doi.org/10.3390/nano12152667

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Ahmad Z, Tahseen S, Wasi A, Ganie IB, Shahzad A, Emamverdian A, Ramakrishnan M, Ding Y. Nanotechnological Interventions in Agriculture. Nanomaterials. 2022; 12(15):2667. https://doi.org/10.3390/nano12152667

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Ahmad, Zishan, Sabaha Tahseen, Adla Wasi, Irfan Bashir Ganie, Anwar Shahzad, Abolghassem Emamverdian, Muthusamy Ramakrishnan, and Yulong Ding. 2022. "Nanotechnological Interventions in Agriculture" Nanomaterials 12, no. 15: 2667. https://doi.org/10.3390/nano12152667

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