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Application of Nanoparticles Alleviates Heavy Metals Stress and Promotes Plant Growth: An Overview

Pingfan Zhou, Muhammad Adeel, Noman Shakoor and 6 more

Nanomaterials · 2020 · Review · CC BY

doi:10.3390/nano11010026

Abstract

Nanotechnology is playing a significant role in addressing a vast range of environmental challenges by providing innovative and effective solutions. Heavy metal (HM) contamination has gained considerable attention in recent years due their rapidly increasing concentrations in agricultural soil. Due to their unique physiochemical properties, nanoparticles (NPs) can be effectively applied for stress alleviation. In this review, we explore the current status of the literature regarding nano-enabled agriculture retrieved from the Web of Science databases and published from January 2010 to November 2020, with most of our sources spanning the past five years. We briefly discuss uptake and transport mechanisms, application methods (soil, hydroponic and foliar), exposure concentrations, and their impact on plant growth and development. The current literature contained sufficient information about NPs behavior in plants in the presence of pollutants, highlighting the alleviation mechanism to overcome the HM stress. Furthermore, we present a broad overview of recent advances regarding HM stress and the possible mechanism of interaction between NPs and HM in the agricultural system. Additionally, this review article will be supportive for the understanding of phytoremediation and micro-remediation of contaminated soils and also highlights the future research needs for the combined application of NPs in the soil for sustainable agriculture.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 24, 2026. Paragraph numbers are ours, so an answer can point at one.

1. Introduction

Rapid urbanization and industrialization, constant application of agrochemicals and fertilizers, unreasonable mining and waste management have caused heavy metal (HM) contamination to become an increasingly prominent issue. There are over 10 million contaminated sites worldwide and more than 50 percent of them are contaminated with HM. According to the China Ministry of Environmental Protection, the percentage of exceedance in agricultural soils is even greater than 19.4%. Among them, the average contents of Cd, Hg, As, Cu, Pb, Cr, Zn and Ni in the soil exceed the standard by 7.0%, 1.6%, 2.7%, 2.1%, 1.5%, 1.1%, 0.9% and 4.8%, respectively. Due to the Chinese diet structure, the risk screening values for soil contamination of agricultural land are low. For example, the China agricultural land Cd limit is 0.3~0.6 mg/kg, while the screening value (ECOSSL) recommended by the United States Environmental Protection Agency (US-EPA) is 0.4~0.8 mg/kg. Only in China, the HM contaminated area of farmland soil is about 2 × 107 Hm2, the annual amount of polluted grains is 1.2 × 107 t and the economic loss is $3 × 109. Recently, several studies have shown that HM pollution in farmland soil is continuously increasing.

In recent years, HM contamination has attracted public attention due to the frequent detection in food and blood. HM stress affects the plants growth and indirectly affects human health via the food chain. Cereal, as a predominant food in China, are susceptible to HM pollution. Rice in particular accumulates more HM than other plants. The notorious “Itai-Itai disease” in Japan is caused by long-term consumption of Cd-contaminated rice. Besides, excessive accumulation of HM causes systemic bone softening, nervous system damage, reproductive dysfunction and even death. The Agency for Toxic Substances and Disease Registry (ATSDR) and the US-EPA have listed Cd, Pb, As and Hg among the top 20 hazardous substances. Furthermore, the current status of the rare earth elements (REEs) in the environment and potential effects on biota were described in our previous publication. The deleterious effects of REEs and HM pollution in the soil environment require serious attention to overcome.

HM pollution is one of the key factors restricting crop production and threatening food security. HM mainly affect the normal cell structure, the antioxidant system and plant growth to restrict crop production. More importantly, the global population is estimated to grow to 8.54 billion in 2030 and 9.73 billion in 2050, which means that current food production must increase by 70~100 percent to meet the needs of the world population. Therefore, it is necessary to improve and popularize HM removal/immobilization technology in polluted farmland.

In recent years, the applications of nanoparticles (NPs) have increased dramatically in industry, medicine, agriculture and cosmetics fields. NPs usually refer to materials with at least one dimension smaller than 100 nm. NPs with different particle sizes, geometries and functions can be synthesized according to the needs. Compared with ordinary materials, NPs have many advantages, such as high surface activity, more surface reaction sites, good catalytic efficiency, and unique optical and magnetic properties. The effects of NPs on environment have been discussed in our previous studies, such as Hao et al. demonstrated that fungal endophytes in rice were sensitive to carbon-based NMs even at 10 mg/L. Rui et al. reported that biomass and quality of peanut were negatively influenced by exposure to Ag NPs at 50 mg/kg. Additionally, Adeel et al. found that low doses (5 and 50 mg/kg) of NiO did not affect the survival, reproduction, and growth rate of adult earthworms, while high doses (200 and 500 mg/kg) significantly affected the physiological and biochemical endpoints.

NPs have been already successfully applied in agriculture and in environmental applications. Several studies have revealed that NPs could improve plant seed germination, plant photosynthesis, resistance to oxidative stress, rhizome growth and development, crop yield and quality. On the one hand, NPs are applied as nanofertilizers and nanopesticides, which have the advantages of being easily absorbed by plants and slowly released in the environment compared with traditional fertilizers, but the potential ecological risks still need further research. On the other hand, NPs (such as CeO2, TiO2, and Mn3O4 NPs) can enhance the activity of antioxidant enzymes, which can reduce the accumulation of reactive oxygen species (ROS) in plants, alleviating plant stress and improving the quality and yield.

The development of nanoscience provides a new direction for the advancement of soil remediation. Due to the unique properties, NPs not only have a better repair effect than traditional materials but also can add some new functions. Except through soil, foliar spraying is another way to improve plants resistance to HM. For example, selenium and silicon NPs alleviated Cd and Pb stress in rice through foliar application. Foliar spraying of TiO2 NPs is more effective than soil addition in reducing Cd toxicity to maize.

Considering the worldwide high levels of contamination of HM, especially in China, this article will focus on HM stress management. Based on the published literature (January 2010 to November 2020), this review will discuss applying different NPs to plants under HM stress and the possible mechanisms of interaction between NPs and HM.

2.1. Data Collection and Processing

Literature data was collected from the Web of Science (WoS) Core Collection database, regarded as the most comprehensive. The search terms for the data were set as Topic: (Heavy metal contaminated soil or heavy metal stress or soil with heavy metal pollution) and Topic: (Plant or botany or crop) and Topic: (Nano or nanomaterials or nanoparticles or NPs). After screening according to the title and abstract, a total of 124 articles were eventually retrieved. We found that according to our retrieved documents, the first relevant literature appeared in 2010.

2.2. Scientometrics Analysis Methods

CiteSpace is a bibliometric software developed by Chen et al. used to analyze documents. It can provide the functions of analyzing research status, finding research frontiers and hotspots, and promoting knowledge interaction between different fields. Time-zone chart of high frequency keywords, keywords clustering and top 10 keywords with the strongest citation bursts were conducted in CiteSpace 5.6. R5.

2.3. Results and Discussion

The number of relevant articles have increased exponentially in the past ten years (Figure 1). Through the analysis of keywords, we can reveal the characteristics and development trends of this field. As shown in (Figure 2A), each circle represents a keyword that first appeared in the data set being analyzed. We can judge the research interest (frequency) according to the node’s size and judge the publication year based on the time zone. Moreover, the clustering of keywords indicates some research topics, which can help us understand the structure of this field. Besides, top 10 keywords with the strongest citation bursts can be obtained according to the changes of citations over time (Figure 2B). All keywords with the strongest citation bursts indicate the most active area of research.

Based on the analysis of the data in Figure 2A,B, the literature regarding the NPs used to treat HM-contaminated soil emerged in 2010. In the early stage, the research mainly focused on the use of NPs for remediation of HM in the soil as an amendment and the adsorption kinetics of NPs. Literature regarding Cd first appeared in 2016, and the reason may be the high over-the-standard rate of Cd levels in China. In more recent literature, the focus has turned to HM bioavailability and HM accumulation in plants. In real environmental conditions, soil HM pollution is caused by a combination of several metals and not only Cd. Therefore, to get closer to the actual pollution situation, researchers began to study the composite pollution of HM in recent years. Later, interest in plant physiology and biochemistry have increased because some researchers found that the application of NPs may enhance plant antioxidant enzyme activity, thereby reducing plant oxidative stress damage caused by HM, promoting plant growth and reducing HM content in the edible parts of plants. Since 2017 CeO2 NPs have been extensively studied because CeO2 NPs can effectively reduce ROS levels and protect chloroplasts of the plant under stress due to Ce3+ and Ce4+ dangling bonds on the surface. In addition to the aforementioned topics, phytoremediation, biochar, and combined applications are emerging research areas, based on the findings that NPs may increase plant resistance to HM and significantly increase the plant’s ability to adsorb HM. Moreover, the research about the combined use of NPs with biochar, microorganisms or other materials is increasing rapidly in recent years, showing excellent application potential.

3.1. Mechanisms of Nanoparticles to Alleviate the HM Stress

The morphology, physiology and biochemistry of the plant have been shown to be influenced by HM stress. There are several strategies applied to overcome the HM stress in plants (Figure 3). For example, (1) reducing the concentration of bioavailable HM in the soil, (2) regulating the expression of HM transport genes in plants, (3) enhancing the ability of plant antioxidant systems and improving the physiological functions and (4) promoting the production of protective agents (such as root exudates, phytochelatin and organic acids).

The HMs in the soil can be absorbed and transformed by the NPs, reducing the mobility and bioavailability of HM. For example, Fe3O4 NPs decreased the mobility of Cd and other HMs in the soil. Wang et al. reported that mercapto Si NPs transformed Cd into a more stable constituent under field conditions after three years. Besides, some NPs can improve soil properties, such as hydroxyapatite NPs can release phosphate and increase soil pH, reducing the harmful effects of HM in the soil.

Apoplastic barriers in the plant root have the physiological function of protecting the plant and controlling the flow of water, ions and oxygen. The formation of apoplastic barriers can be influenced by NPs, which may decrease the amount of HM in the root. However, the apoplastic barriers alone may not be an effective strategy to reduce the damage caused by HM stress because plant roots contain various ion and protein transporters in the root cell plasma membrane, which can transport HM simultaneously. Moreover, plant metal transport genes can be regulated by specific NPs, thereby enhancing the plant’s extracellular barrier to intercept HM.

Most NPs accumulate in the cell walls, bind with HM and make them unavailable by forming complexes. These complexes become adsorbed on the cell surface, thereby hindering the migration of HM in plants and reducing their biological activity. Besides, organic acids accumulated in the cell walls of plant roots and leaves can be chelated with HM to reduce the damage of HM stress to plants. The production of structural protective agents has been shown to be enhanced by NPs, such as applying exogenous Si NPs which promoted the synthesis of organic acids and reduced the damage of Cd to the plant.

Another strategy to alleviate HM stress is to activate the oxidation defense system of the plant. Plants usually produce ROS due to specific biochemical reactions. For example, during the metabolic processes such as respiration and photosynthesis, plants continuously produce ROS in chloroplasts and other parts of cells. At low levels, ROS act as signal molecules involved in growth, development, and defense. However, under stress conditions, excessive ROS accumulation is harmful to cell membranes, proteins, and other cellular components. ROS in plants is mainly scavenged by antioxidant enzymes, such as superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), glutathione reductase (GR), glutathione peroxidase (GPX) and peroxidase (POD). In addition, non-enzymatic low-molecular weight metabolites also can scavenge ROS, such as vitamin C, vitamin E and polyphenols. Metabolic pathways related to ROS clearance will be triggered under stress. For example, shikimate-phenylpropanoid biosynthesis and galactose, alanine, aspartic acid and ascorbate metabolism can alleviate the oxidative stress of the plant. Therefore, application of NPs with antioxidant enzyme activity (such as CeO2 NPs, Fe3O4 NPs, Mn3O4 NPs and C60) can enhance the ability of plants to reduce ROS, ultimately minimize the effects on crop growth and yield losses.

3.2.1. Cerium Dioxide

CeO2 NPs are light rare earth elements (LREEs), recommended by the Organization for Economic Co-operation and Development (OECD) for safety evaluation compared to other ENPs due to their widespread applications and beneficial effects in agriculture systems. CeO2 NPs to alleviate the stress is mainly due to the Ce3+ and Ce4+ dangling bonds on the surface that can scavenge ROS and minimize oxidative stress caused by HM. For example, negatively charged CeO2 NPs effectively accumulated in chloroplasts and eliminated ROS in Arabidopsis leaf mesophyll cells compared with positively charged NPs, while the process was affected by the ratio of Ce3+/Ce4+. Several studies have indicated that the low concentration of CeO2 NPs is beneficial to the plant growth. For example, Cao et al. found that CeO2 NPs (100 mg/kg), both uncoated and polyvinylpyrrolidone (PVP) coated, can increase the photosynthesis rate of soybeans and stimulate plant growth, whereas 500 mg/kg CeO2-NPs reduced the net photosynthesis rate by 36%. CeO2 NPs (100 and 200 mg/kg) also improved the physiological parameters of Brassica napus L. under salt stress (100 mM NaCl). Ma et al. determined that bulk CeO2 (10 and 100 mg/L) increased biomass of Brassica rapa, while at the same concentration, CeO2 NPs exerted no significant effect. This might happen due to the formation of aggregates and the selected concentration of CeO2 NPs. These studies indicate that there are still many unknowns regarding the effect of NPs surface modifications, which strongly affect the stability and mobility of NPs, on the plant health.

Foliar application of CeO2 NPs (200 mg/L) effectively stimulated the antioxidant defense system in rice grown in hydroponic conditions (CdCl2 50 μM) and inhibited the accumulation of Cd. Furthermore, CeO2 NPs (500 mg/kg) did not affect the accumulation of Cd in soybeans in Cd-contaminated soil (0.2542 and 1.0 mg/kg) while significantly increased the accumulation of Ce in plant tissues. This was partly caused by the co-exposure of Cd and CeO2 NPs that influenced root apoplastic barriers. Wang et al. reported that CeO2 NPs (100 mg/L) did not affect the accumulation of As (III) (1.0 mg/L) and As (V) (1.0 mg/L) in rice in hydroponic conditions. As mentioned above, several contradictory studies are reported, and more in-depth investigations are needed to understand the alleviation mechanisms.

3.2.2. Titanium Dioxide Nanoparticles

Titanium dioxide NPs (TiO2 NPs), widely used in coatings, cosmetics and pigments, are among the most produced engineered NPs in the world due to the low toxicity, favorable optical properties, strong adhesive properties and high stability. It is estimated that the global annual production of TiO2 NPs was 1,175,176 tons in 2012. The primary mechanisms of TiO2 NPs in alleviating HM stress include adsorption of HM and activation of the oxidation defense system. Several studies have found that application of TiO2 NPs can reduce the oxidative stress of plants. For example, Wang et al. found that adding TiO2 NPs to the nutrient solution increased antioxidant enzymes’ activity in corn tissues. Singh et al. reported that the physiological parameters and photosynthetic rate of soybean increased after applying TiO2 NPs to soil, effectively limiting the toxicity of Cd to soybean plants. Therefore, TiO2 NPs have great application potential in alleviating plant oxidative stress caused by HM.

Cai et al. documented that accumulation of Pb in rice co-exposed to Pb(NO3)2 (1.0 mg/L) and four types of TiO2 NPs (10 and 1000 mg/L). They found that none of the TiO2 NPs affected rice growth, but three types of NPs (anatase, pristine rutile and rutile with hydrophilic) effectively decreased the Pb accumulation in roots by >80% and in shoots by 77~97%. The same results were obtained by Ji et al., who showed that TiO2 NPs had little effect on rice seedling biomass in hydroponic cultivation. However, the root length, plant height, hormone level, antioxidant enzyme activity and other physiological parameters were improved after exposure of TiO2 NPs, indicating that the addition of TiO2 NPs reduced the damage of Cd stress to rice seedlings.

Maize was grown in Cd-contaminated soil then TiO2 NPs (100 and 250 mg/L) were applied by mixing in soil and by foliar application. The results showed that foliar application of TiO2 NPs inhibited Cd absorption by maize and increased biomass, while soil application promoted the absorption of Cd by maize and substantially decreased the biomass. They also found that foliar spraying of TiO2 NPs increased SOD and GST activities and up-regulated galactose, alanine, aspartame acid and other metabolic pathways to alleviate Cd stress damage to maize. The results indicated that the application method had a significant influence on the alleviation effect.

Dai et al. studied the effect of uncoated TiO2 NPs and TiO2 NPs coated with sodium dodecylbenzene sulfonate (SDBS) on wheat seedlings under Cd stress. After SDBS coating, the hydrodynamic diameter of TiO2 NPs was reduced, and the dispersion stability of TiO2 NPs was improved through spatial and electrostatic repulsion, thereby exposing more available adsorption sites and increasing the adsorption capacity of Cd2+. They also found that the effect of SDBS coated TiO2 NPs on relieving Cd toxicity were significantly better than these of bare TiO2 NPs. This suggests that NPs coated with surfactants or other materials affect the bioavailability and toxicity of HM.

Singh et al. reported that the accumulation of 133Cs in soybean effectively increased after the application of TiO2 NPs in 133Cs contaminated soil. It suggests that NPs may be applied for phytoremediation, but long-term field-based studies are needed.

3.2.3. Iron

Iron (Fe) is an essential element for humans, animals and plants’ growth and development. It plays a vital role in physiological and biochemical reactions, such as cell metabolism, photosynthesis, and respiration. For example, the synthesis of specific chlorophyll-protein complexes in chloroplasts requires Fe, and Fe deficiency causes yellowing leaves and reduced photosynthetic capacity. Iron is also a cofactor for certain enzymes, closely related to enzyme activity. Iron NPs (Fe NPs) are particularly powerful adsorbents due to the unique structure and electronic properties. Magnetic NPs (γ-Fe2O3 and Fe3O4) can be easily separated from the adsorbing medium by a magnetic field. The alleviation mechanisms of nano Fe mainly include adsorption of HM, acting as an essential element, promotion of the formation of root surface iron film, activation of the oxidation defense system, and scavenging the ROS. Several studies have demonstrated that nano Fe has high application potential in the field of fertilizers. For example, Fe2O3 NPs have been proposed as Fe-containing fertilizers in the cultivation of peanuts, but the potential risks still need to be fully elucidated. In addition, it has been shown that legume root growthwas enhanced by 88~366% after using low dose Fe2O3 NPs pre-soaking.

Nanoscale zero-valent iron (nZVI) has been shown to reduce the accumulation of HM in sunflowers, increase SOD and POD in plant leaves, and promote plant growth. Guha reported that after applying nZVI (100 mg/L) to rice seedlings, gene expressions of Fe transporters (IRT1, IRT2, YSL2, YSL15) responsible for both Fe and Cd uptake were significantly down-regulated. In contrast, OsVIT1 and OsCAX4 genes were overexpressed, which lead to sequestration of Cd in vacuoles.

Hussain et al. found that soil and foliar application of Fe2O3 NPs (5, 10, 15, and 20 ppm) to wheat under Cd stress (available Cd 0.93 mg/kg) both reduced the leaf electrolyte leakage rate, the Cd content in grains and increased the antioxidant enzyme activity and the dry weight of the wheat. They also found that the foliar spraying of Fe NPs is preferred to the soil application because the absorption of Fe in the soil may be affected by many factors, such as pH, and the combination with other minerals during the absorption process. In the case of combined application, the alleviating effects of Fe NPs (foliar) application on Cd stress in rice were further enhanced when the soil was applied with biochar. However, the biochar-Fe3O4 nanocomposites facilitated Cd transport in water-saturated natural soil, indicating that the risks are still not fully understood. In composite stress conditions, drought stress increased the Cd concentration in grains, and the soil application of Fe2O3 NPs to wheat under drought and Cd stress improved the photosynthesis, yield and decreased the Cd content in grains.

3.2.4. Zinc Oxide Nanoparticles

Zinc (Zn) is an essential trace element for plants and humans. Zinc oxide NPs (ZnO NPs) are common metal oxide NPs (MNPs), widely used in personal care products, paints and coatings. Its alleviation mechanisms include providing nutritional value, activation of oxidative stress system, and enhancement of plant’s physiological and biochemical functions. For example, seed soaking with ZnO NPs (50 mg/L) promoted glycolytic metabolism and cell wall biosynthesis, promoting the germination of corn seeds and the growth of roots and embryos. The combined application of ZnO NPs (500 mg/kg) and arbuscular mycorrhiza (AM) significantly promoted soybean growth. Applying ZnO NPs to wheat reduced the leaves’ electrolyte leakage (EL) rate and increased the antioxidant enzyme activity in the leaves. ZnO NPs can relieve the drought stress to sorghum by increasing the absorption of nitrogen and potassium.

Ali et al. reported that combined application of ZnO NPs (foliar spraying) and biochar (soil application) effectively relieved the Cd stress, which was more efficient than the treatment of adding ZnO NPs or biochar separately. It suggests that the combined application of NPs with other materials may be a promising approach in plant HM reduction.

Arsenic content in roots and shoots of rice was significantly reduced by both ZnO NPs and Zn2+. In contrast, Cd accumulation in rice shoots was only reduced by ZnO NPs, while Zn2+ increased the Cd accumulation in shoots. Khan et al. found that wheat biomass, yield and photosynthesis decreased under normal water conditions and Cd stress, while drought stress further enhanced the negative impact of Cd stress on wheat, while the addition of ZnO NPs alleviated both Cd and drought stress. Hussain et al. applied different concentrations of ZnO NPs (25, 50 and 100 mg/L) to Cd-stressed wheat by foliar spray and soil application, and they found that both applications of ZnO NPs promoted wheat growth, photosynthesis and grain yield under Cd stress. However, the foliar application was more efficient than soil application in increasing grain yield and reducing Cd content in grains.

Rizwan et al. soaked wheat seeds in ZnO NPs (25, 50, 75 and 100 mg/L) containing medium in the dark at 25 °C for 20 h, then selected seeds with similar germination to be sown in cadmium-contaminated soil. Compared with the control group, the grain yield of wheat increased, the content of Cd in the grain decreased, the content of chlorophyll a and b, and SOD and POD activity of wheat increased significantly, and the electrolyte leakage rate decreased. The results showed that using an appropriate concentration of ZnO NPs to germinate wheat seeds can enhance wheat resistance to Cd.

3.3.1. Selenium

Selenium (Se) is an essential trace element for humans, which has many important biological functions, such as immune regulation, antioxidant, antiviral and anti-cancer properties. Se is mainly supplemented by eating cereal crops, but in most rice-producing countries in Asia, the content is low. A recent survey shows that about 72% of areas in China are Se-deficient areas. According to WHO, approximately 15% of the world’s population is deficient in Se, and China is one of the world’s 40 Se-deficient countries. Therefore, Se containing fertilizer application to increase the Se content in cereal crops is essential for human health.

As an important active component of glutathione peroxidase, Se can regulate the activity of antioxidant enzymes, remove the ROS accumulated in plants, and thus effectively enhance the stress resistance of plants. For example, it has been found that the application of Se may reduce Cd uptake and toxicity in rice. Recently, Huang et al. found that the inhibition effect of Se on Cd absorption of rice may be related to the formation of root surface iron film. With the addition of Fe2+, Se promoted the formation of root surface iron film of rice and greatly reduced Cd accumulation in rice.

Zhang reported that Chinese cabbage’s biomass, height, leaf chlorophyll content, SOD, and GSH-Px increased and the Cd content and MDA of leaves decreased after foliar spraying of Se NPs (1.25 and 12.5 mg/L) to Chinese cabbage under Cd stress (10 and 20 mg/kg). Both in-soil (0.5 and 2.5 mg/kg) and foliar (0.5 and 1.0 mmol/L) application of Se NPs improved the physiological indices of rice in Cd-contaminated soil (total Cd 1.62 mg/kg), among which the foliar spraying had better effects on increasing the yield, relative content of chlorophyll in rice and reducing the content of Cd in rice than soil application. In Cd and Pb co-contaminated soil, foliar spraying of Se NPs on rice effectively increased rice yield, biomass, protein content and Se content and reduced phytic acid production in brown rice. It was also demonstrated that Se content and phytic acid are negatively correlated with Cd and Pb concentrations. Considering the safety factor, foliar spraying of Se NPs can significantly reduce the content of Cd in grains, making it more practical in actual production.

3.3.2. Silicon

Silicon (Si) is the second most abundant element in the Earth’s crust after oxygen. Although it is not an essential element for higher plants, it is inextricably linked to plant growth, especially for Gramineae species (such as rice). Several studies have found that the application of Si can enhance plant resistance to abiotic stress. At present, the widely recognized alleviation of HM stress by Si is through the following four mechanisms: 1) activation of the physiological and biochemical defense systems to enhance ROS scavenging, 2) immobilization and complexation of HM to reduce HM biological activity, 3) acting as a nutrient source and stimulating the production of structural protective agents chelated with HM, 4) regulation of the expression of HM transport genes, such as overexpression of vacuolar H+-pyrophosphatase1 (OVP1).

Most of the early research has been carried out in the hydroponic conditions. For example, rice growing in the nutrient solution (20 μM CdCl2, foliar application of 2.5 mM nano Si) was shown to have smaller MDA and Cd content in the shoot, indicating that nano Si reduced the Cd stress. In a rice cell culture experiment, the proportions of live cells in Cd solution (40 μM) were increased by 95.4%, 78.6% and 66.2% after addition of different size Si NPs (19, 48 and 202 nm: 1.0 mM), respectively. This may be explained by the down-regulation of Cd uptake and transport (OsLCT1 and OsNramp5) genes and up-regulation of Cd transport (OsHMA3) and Si uptake (OsLsi1) genes. In composite stress conditions, Si NPs treatments improved wheat growth and alleviated Cd (bioavailable Cd 1.21 mg/kg) and drought (35% of soil water holding capacity) stress. Hussain et al. reported that foliar application of Si NPs (10 and 20 mg/L) effectively decreased the accumulation of Cd in grains and increased the yield. Besides, they demonstrated that combined application of Se NPs (20 mg/L) and Si NPs (10 mg/L) highly reduced Cd (62%) and Pb (52%) in rice grains.

Sousa et al. found that Si NPs (4 mg/kg) alleviated the toxicity of Al to maize by activating the antioxidant defense systems; at the same time, Si NPs did not influence the accumulation of Al in maize. These results are contradictory with the above findings, and the reason may be related to different concentrations or types of HM used in these studies. In the field of combined application of NPs and microorganisms, Fatemi reported that Si NPs and Pb-resistant strains of the microbes more effectively alleviated the Pb toxicity to coriander than the single treatments of Si NPs or microbes.

3.3.3. Hydroxyapatite

Phosphorus-containing amendments have been proven effective in the in-situ remediation of HM contaminated soils because they can release phosphates to form precipitates and complexes with HM in the soil. Previous studies have shown that after adding hydroxyapatite (HAP) to the soil, it can release phosphate to form complexes with HM. Also, the Ca ions on the surface of HAP could exchange with the HM ions in the soil to reduce the harm of HMto plants. HAP with different particle sizes was proved to repair HM contaminated soil, for example, normal, micro, and nano HAP increased soil pH and decreased the amount of CaCl2-extractable, exchangeable Cu and Cd.

Furthermore, effects of HAP NPs (5, 10, 20 and 30g/kg) on Brassica chinensis L. under Cd stress (10 mg/kg) were studied in a pot experiment. Compared with the control, the biomass, chlorophyll, vitamin C, and the activities of SOD, CAT, and POD in plant shoots were enhanced; Cd and MDA contents in the shoots were decreased. Sun et al. reported that the content of Cu and Zn in ryegrass significantly decreased by adding HAP NPs. Xing investigated the soil properties and Cd, Cu, Zn and Pb content in soil and rice after addition of HAP NPs for one and three years. They concluded that HAP NPs significantly decreased the Cd content in roots and grains both after one and three years. Compared with one year, the immobilization ability of HAP NPs for Pb was slightly increased after three years, while significantly decreased for Zn, Cd and Cu after three years.

The pH of the Cd-contaminated soil (10 mg/kg) increased after application of HAP NPs (0.2%, 0.5%, and 1%) and significantly increased the catalase and urease activities in the soil. Besides, the plant height and biomass increased, and the Cd concentration in the edible part was reduced significantly, which shows that HAP NPs effectively alleviated the Cd stress. In Cd (37 mg/kg) and Pb (615 mg/kg) compound stress condition, the application of HAP significantly increased the soil pH, whereas the application of HAP NPs slightly reduced the soil pH, both of which significantly reduced the content of Diethylenetriaminepentaacetic acid (DTPA)-extracted Pb and Cd in soil. Although HAP application reduced Cd absorption by the shoots and roots, the addition of HAP and HAP NPs both significantly increased the Cd content in tobacco leaves. It indicates that although NPs can reduce the content of HM in some parts, they may also increase it. Therefore, potential ecological risks and mechanisms still need further research.

4. Summary and Future Prospective

This review summarized the research progress in applying various NPs through seed priming, soil application, foliar spraying, and solution application to improve plant HM stress resistance. The morphology, physiology and biochemistry of plants are significantly affected by HM stress. Crucial strategies to improve plant HM resistance include reducing the concentration of bioavailable HM in the soil, regulating the expression of HM transport genes in plants, improving the ability of the apoplastic barrier to intercept HM, providing more nutrition to plant, enhancing the ability of plant antioxidant systems, improving the function of organs and enhancing the production of structural protective agents (such as root exudates, phytochelatin and organic acids). In addition, we summarized the effect of different NPs on the plants under Cd stress (Table 1) and a schematic diagram of possible mechanisms of NPs to alleviate the HM stress in roots and cells (Figure 4).

With the continuous advancement of science and technology, several types of NPs become available in the market including surface coated or blended with other materials (such as surfactants), which can enhance or enrich their existing functions. Moreover, physicochemical properties of NPs (size and charge) that determine their interaction with HM in soil in the presence of agricultural plants still need to be further studied. Because the porosity of plant cell walls is 15 nm, some NPs may penetrate the cell wall. Besides, negatively charged NPs can penetrate the membrane more effectively than positive and neutral. Although several studies have reported on the toxicity of NPs to animals and plants, most of them are in the presence of single NPs, and more in-depth studies on the toxicity of more complex environments are still needed.

In the research on alleviating HM stress, the exposure level of NPs and the different application methods affect plants differently. It is an urgent problem that low dosage has a non-significant control effect, and excessive dosage will increase unnecessary costs or harmful effects on plants. Besides, there are still ambiguities regarding NPs application methods in the soil environment. Therefore, it is necessary to study further the mechanisms and treatment effects of different application methods. Furthermore, the combined application of different kinds of NPs with other materials is undoubtedly a new research direction. For example, NPs application with other alleviators like hydrogen peroxide, nitric oxide, auxin, biochar, and HM-resistant strains of the microbes need to be investigated.

Big data and artificial intelligence (AI) technology are already being integrated into environmental science alone with other disciplines. For example, Rossi et al. used AI to predict the accumulation of CeO2 NPs and Cd in Brassica napus according to the physiological parameters of B. napus. With experimental data accumulation and the development of technology, it is believed that various physiological parameters of plants and the content of HM in plants can be predicted based on the property of the soil, the variety of plants, and the property of NPs. It is possible to select appropriate types and concentrations of NPs for application, which would reduce unnecessary costs and maximize the beneficial effect.

Finally, the cost of NPs is one of the essential factors restricting their wider application in the agriculture sector. Therefore, synthesizing NPs efficiently, using green methods, and economically is an important part of nanotechnology’s future development. Researchers still need to conduct more in-depth research to understand how NPs can improve plant resistance, and it is necessary to study further the impact of NPs on terrestrial environment. Besides, the combination with computers and other disciplines will provide us with a more precise application of NPs and environmental impact to better promote the technology of NPs to control HM stress.

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    Khalid S., Shahid M., Niazi N.K., Murtaza B., Bibi I., Dumat C. A comparison of technologies for remediation of heavy metal contaminated soils. J. Geochem. Explor. 2017;182:247-268.

    Not in our library10.1016/j.gexplo.2016.11.021

  5. 5.

    The Ministry of Environmental Protection. The Ministry of Land and Resources Report on the National Soil Contamination Survey.

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  6. 6.

    Reimann C., de Caritat P. New soil composition data for Europe and Australia: Demonstrating comparability, identifying continental-scale processes and learning lessons for global geochemical mapping. Sci. Total Environ. 2012;416:239-252.

    Not in our library10.1016/j.scitotenv.2011.11.019

  7. 7.

    Cave M., Rawlins B., Mcgrath S., Scheib A., Breward N., Lister T., Ingham M., Gowing C., Carter S. The Advanced Soil Geochemical Atlas of England and Wales. 2012;277.

    Not in our library

  8. 8.

    QG Z., YM L. The macro strategy of soil protection in China. Bull. Chin. 2015;4:452-458.

    Not in our library

  9. 9.

    Teng Y., Wu J., Lu S., Wang Y., Jiao X., Song L. Soil and soil environmental quality monitoring in China: A review. Environ. Int. 2014;69:177-199.

    Not in our library10.1016/j.envint.2014.04.014

  10. 10.

    Li M., Xi X., Xiao G., Cheng H., Yang Z., Zhou G., Ye J., Li Z. National multi-purpose regional geochemical survey in China. J. Geochem. Explor. 2014;139:21-30.

    Not in our library10.1016/j.gexplo.2013.06.002

  11. 11.

    Arif N., Sharma N.C., Yadav V., Ramawat N., Dubey N.K., Tripathi D.K., Chauhan D.K., Sahi S. Understanding Heavy Metal Stress in a Rice Crop: Toxicity, Tolerance Mechanisms, and Amelioration Strategies. J. Plant. Biol. 2019;62:239-253.

    Not in our library10.1007/s12374-019-0112-4

  12. 12.

    Xue T., Liao X., Wang L., Gong X., Zhao F., Ai J., Zhang Y. Effects of adding selenium on different remediation measures of paddy fields with slight-moderate cadmium contamination. Environ. Geochem. Health. 2020;42:377-388.

    Not in our library10.1007/s10653-019-00365-9

  13. 13.

    Allevato E., Stazi S.R., Marabottini R., D’Annibale A. Mechanisms of arsenic assimilation by plants and countermeasures to attenuate its accumulation in crops other than rice. Ecotoxicol. Environ. Saf. 2019;185:109701.

    Not in our library10.1016/j.ecoenv.2019.109701

  14. 14.

    Huang Y., Wang L., Wang W., Li T., He Z., Yang X. Current status of agricultural soil pollution by heavy metals in China: A meta-analysis. Sci. Total Environ. 2019;651:3034-3042.

    Not in our library10.1016/j.scitotenv.2018.10.185

  15. 15.

    Adeel M., Lee J.Y., Zain M., Rizwan M., Nawab A., Ahmad M.A., Shafiq M., Yi H., Jilani G., Javed R., et al. Cryptic footprints of rare earth elements on natural resources and living organisms. Environ. Int. 2019;127:785-800.

    Not in our library10.1016/j.envint.2019.03.022

  16. 16.

    Javaid S. Heavy metals stress, mechanism and remediation techniques in rice (Oryza sativa L.): A review. Pure Appl. Biol. 2020;9.

    Not in our library10.19045/bspab.2020.90045

  17. 17.

    Irshad H.M.K., Noman A., Alhaithloul H., Adeel M., Yukui R., Shah T., Zhu S., Shang J. Goethite-modified biochar ameliorates the growth of rice (Oryza sativa L.) plants by suppressing Cd and As-induced oxidative stress in Cd and As co-contaminated paddy soil. Sci. Total Environ. 2020;137086.

    Not in our library10.1016/j.scitotenv.2020.137086

  18. 18.

    United Nations. World Population Prospects: The 2019 Revision, Key Findings and Advance Tables.

    Not in our library

  19. 19.

    Mueller N.D., Gerber J.S., Johnston M., Ray D.K., Ramankutty N., Foley J.A. Closing yield gaps through nutrient and water management. Nature. 2012;490:254-257.

    Not in our library10.1038/nature11420

  20. 20.

    Adeel M., Ma C., Ullah S., Rizwan M., Hao Y., Chen C., Jilani G., Shakoor N., Li M., Wang L., et al. Exposure to nickel oxide nanoparticles insinuates physiological, ultrastructural and oxidative damage: A life cycle study on Eisenia fetida. Environ. Pollut. 2019;254.

    Not in our library10.1016/j.envpol.2019.113032

  21. 21.

    Adeel M., Tingting J., Hussain T., He X., Muhammad Ahmad M., Irshad H.M.K., Shakoor N., Xie C., Hao Y., Zhang P., et al. Bioaccumulation of ytterbium oxide nanoparticles insinuate oxidative stress, inflammatory, and pathological lesions in ICR mice. Environ. Sci. Pollut. Res. 2020;27.

    Not in our library10.1007/s11356-020-09565-8

  22. 22.

    Wang Y., Jiang F., Ma C., Rui Y., Tsang D.C.W., Xing B. Effect of metal oxide nanoparticles on amino acids in wheat grains (Triticum aestivum) in a life cycle study. J. Environ. Manag. 2019;241:319-327.

    Not in our library10.1016/j.jenvman.2019.04.041

  23. 23.

    Yang J., Cao W., Rui Y. Interactions between nanoparticles and plants: Phytotoxicity and defense mechanisms. J. Plant Interact. 2017;12:158-169.

    Not in our library10.1080/17429145.2017.1310944

  24. 24.

    Yang J., Jiang F., Ma C., Rui Y., Rui M., Adeel M., Cao W., Xing B. Alteration of Crop Yield and Quality of Wheat upon Exposure to Silver Nanoparticles in a Life Cycle Study. J. Agric. Food Chem. 2018;66:2589-2597.

    Not in our library10.1021/acs.jafc.7b04904

  25. 25.

    Hao Y., Ma C., White J.C., Adeel M., Jiang R., Zhao Z., Rao Y., Chen G., Rui Y., Xing B. Carbon-based nanomaterials alter the composition of the fungal endophyte community in rice (Oryza sativa L.). Environ. Sci. Nano. 2020;7:2047-2060.

    Not in our library10.1039/c9en01400d

  26. 26.

    Rui M., Ma C., Tang X., Yang J., Jiang F., Pan Y., Xiang Z., Hao Y., Rui Y., Cao W., et al. Phytotoxicity of Silver Nanoparticles to Peanut (Arachis hypogaea L.): Physiological Responses and Food Safety. ACS Sustain. Chem. Eng. 2017;5:6557-6567.

    Not in our library10.1021/acssuschemeng.7b00736

  27. 27.

    Kah M., Tufenkji N., White J.C. Nano-enabled strategies to enhance crop nutrition and protection. Nat. Nanotechnol. 2019;14:532-540.

    Not in our library10.1038/s41565-019-0439-5

  28. 28.

    Li J., Hu J., Ma C., Wang Y., Wu C., Huang J., Xing B. Uptake, translocation and physiological effects of magnetic iron oxide (γ-Fe2O3) nanoparticles in corn (Zea mays L.). Chemosphere. 2016;159:326-334.

    Not in our library10.1016/j.chemosphere.2016.05.083

  29. 29.

    Palchoudhury S., Jungjohann K.L., Weerasena L., Arabshahi A., Gharge U., Albattah A., Miller J., Patel K., Holler R.A. Enhanced legume root growth with pre-soaking in α-Fe2O3 nanoparticle fertilizer. RSC Adv. 2018;8:24075-24083.

    Not in our library10.1039/c8ra04680h

  30. 30.

    Ghafariyan M.H., Malakouti M.J., Dadpour M.R., Stroeve P., Mahmoudi M. Effects of Magnetite Nanoparticles on Soybean Chlorophyll. Environ. Sci. Technol. 2013;47:10645-10652.

    Not in our library10.1021/es402249b

  31. 31.
  32. 32.

    Rui M., Ma C., White J.C., Hao Y., Wang Y., Tang X., Yang J., Jiang F., Ali A., Rui Y., et al. Metal oxide nanoparticles alter peanut (Arachis hypogaea L.) physiological response and reduce nutritional quality: A life cycle study. Environ. Sci.-Nano. 2018;5:2088-2102.

    Not in our library10.1039/c8en00436f

  33. 33.

    Li M., Adeel M., Peng Z., Yukui R. Physiological impacts of zero valent iron, Fe3O4 and Fe2O3 nanoparticles in rice plants and their potential as Fe fertilizers. Environ. Pollut. 2020.

    Not in our library10.1016/j.envpol.2020.116134

  34. 34.

    Adeel M., Farooq T., White J., Hao Y., He Z., Rui Y. Carbon-based nanomaterials suppress Tobacco Mosaic Virus (TMV) infection and induce resistance in Nicotiana benthamian. J. Hazard. Mater. 2020.

    Not in our library10.1016/j.jhazmat.2020.124167

  35. 35.

    Hao Y., Fang P., Ma C., White J.C., Xiang Z., Wang H., Zhang Z., Rui Y., Xing B. Engineered nanomaterials inhibit Podosphaera pannosa infection on rose leaves by regulating phytohormones. Environ. Res. 2019;170:1-6.

    Not in our library10.1016/j.envres.2018.12.008

  36. 36.

    Hao Y., Yuan W., Ma C., White J.C., Zhang Z., Adeel M., Zhou T., Rui Y., Xing B. Engineered nanomaterials suppress Turnip mosaic virus infection in tobacco (Nicotiana benthamiana). Environ. Sci.-Nano. 2018;5:1685-1693.

    Not in our library10.1039/c8en00014j

  37. 37.

    Zhao X., Jia Y., Li J., Dong R., Zhang J., Ma C., Wang H., Rui Y., Jiang X. Indole Derivative-Capped Gold Nanoparticles as an Effective Bactericide in Vivo. ACS Appl. Mater. Interfaces. 2018;10:29398-29406.

    Not in our library10.1021/acsami.8b11980

  38. 38.

    Lowry G.V., Avellan A., Gilbertson L.M. Opportunities and challenges for nanotechnology in the agri-tech revolution. Nat. Nanotechnol. 2019;14:517-522.

    Not in our library10.1038/s41565-019-0461-7

  39. 39.

    Lombi E., Donner E., Dusinska M., Wickson F. A One Health approach to managing the applications and implications of nanotechnologies in agriculture. Nat. Nanotechnol. 2019;14:523-531.

    Not in our library10.1038/s41565-019-0460-8

  40. 40.

    Usman M., Farooq M., Wakeel A., Nawaz A., Cheema S.A., Rehman H.U., Ashraf I., Sanaullah M. Nanotechnology in agriculture: Current status, challenges and future opportunities. Sci. Total Environ. 2020;721:137778.

    Not in our library10.1016/j.scitotenv.2020.137778

  41. 41.

    Wang Z., Yue L., Dhankher O.P., Xing B. Nano-enabled improvements of growth and nutritional quality in food plants driven by rhizosphere processes. Environ. Int. 2020;142:105831.

    Not in our library10.1016/j.envint.2020.105831

  42. 42.

    Liu Y., Wu T., White J.C., Lin D. A new strategy using nanoscale zero-valent iron to simultaneously promote remediation and safe crop production in contaminated soil. Nat. Nanotechnol. 2020.

    Not in our library10.1038/s41565-020-00803-1

  43. 43.

    Moharem M., Elkhatib E., Mesalem M. Remediation of chromium and mercury polluted calcareous soils using nanoparticles: Sorption-desorption kinetics, speciation and fractionation. Environ. Res. 2019;170:366-373.

    Not in our library10.1016/j.envres.2018.12.054

  44. 44.

    Toumey C. Notes on environmental nanoscience. Nat. Nanotechnol. 2020;15:250-251.

    Not in our library10.1038/s41565-020-0677-6

  45. 45.

    Hussain B., Lin Q., Hamid Y., Sanaullah M., Di L., Hashmi M.L.U.R., Khan M.B., He Z., Yang X. Foliage application of selenium and silicon nanoparticles alleviates Cd and Pb toxicity in rice (Oryza sativa L.). The Sci. Total Environ. 2020;712:136497.

    Not in our library10.1016/j.scitotenv.2020.136497

  46. 46.

    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.

    Not in our library10.1016/j.chemosphere.2019.124794

  47. 47.

    Olawumi T.O., Chan D.W.M. A scientometric review of global research on sustainability and sustainable development. J. Clean. Prod. 2018;183:231-250.

    Not in our library10.1016/j.jclepro.2018.02.162

  48. 48.
  49. 49.

    Chen C., Ibekwe-SanJuan F., Hou J. The structure and dynamics of cocitation clusters: A multiple-perspective cocitation analysis. J. Am. Soc. Inf. Sci. Technol. 2010;61:1386-1409.

    Not in our library10.1002/asi.21309

  50. 50.

    Chen C. CiteSpace II: Detecting and visualizing emerging trends and transient patterns in scientific literature. J. Am. Soc. Inf. Sci. Technol. 2006;57:359-377.

    Not in our library10.1002/asi.20317

  51. 51.

    Chen C. Science Mapping: A Systematic Review of the Literature. J. Data Inf. Sci. 2017;2:1-40.

    Not in our library10.1515/jdis-2017-0006

  52. 52.

    Cao F., Dai H., Hao P.F., Wu F. Silicon regulates the expression of vacuolar H(+)-pyrophosphatase 1 and decreases cadmium accumulation in rice (Oryza sativa L.). Chemosphere. 2020;240:124907.

    Not in our library10.1016/j.chemosphere.2019.124907

  53. 53.

    Mengmeng S., Jie X., Lingling Z., Dejian S., Xitong Z. Research Progress on Effects of Silicon on Plant Growth under Cadmium Stress. Guangzhou Chem. Ind. 2019;47:41-43.

    Not in our library

  54. 54.

    Sebastian A., Nangia A., Prasad M.N.V. Cadmium and sodium adsorption properties of magnetite nanoparticles synthesized from Hevea brasiliensis Muell. Arg. bark: Relevance in amelioration of metal stress in rice. J. Hazard. Mater. 2019;371:261-272.

    Not in our library10.1016/j.jhazmat.2019.03.021

  55. 55.

    Wang Y., Liu Y., Zhan W., Zheng K., Lian M., Zhang C., Ruan X., Li T. Long-term stabilization of Cd in agricultural soil using mercapto-functionalized nano-silica (MPTS/nano-silica): A three-year field study. Ecotoxicol. Environ. Saf. 2020;197:110600.

    Not in our library10.1016/j.ecoenv.2020.110600

  56. 56.

    Cui H., Shi Y., Zhou J., Chu H., Cang L., Zhou D. Effect of different grain sizes of hydroxyapatite on soil heavy metal bioavailability and microbial community composition. Agric. Ecosyst. Environ. 2018;267:165-173.

    Not in our library10.1016/j.agee.2018.08.017

  57. 57.

    Chao-Dong Y., Xia Z., Guo-Feng L., Jun-Wei Z., Man-Zhu B., Zhi-Xiang Z. Progress on the Structure and Physiological Functions of Apoplastic Barriers in Root. Bull. Bot. Res. 2013;33:114-119.

    Not in our library

  58. 58.

    Rossi L., Zhang W., Schwab A.P., Ma X. Uptake, Uptake, Accumulation, and in Planta Distribution of Coexisting Cerium Oxide Nanoparticles and Cadmium in Glycine max (L.) Merr. Environ. Sci. Technol. 2017;51:12815-12824.

    Not in our library10.1021/acs.est.7b03363

  59. 59.

    Wang K., Wang Y., Wan Y., Mi Z., Wang Q., Wang Q., Li H. The fate of arsenic in rice plants (Oryza sativa L.): Influence of different forms of selenium. Chemosphere. 2021;264:128417.

    Not in our library10.1016/j.chemosphere.2020.128417

  60. 60.

    Cui J., Liu T., Li F., Yi J., Liu C., Yu H. Silica nanoparticles alleviate cadmium toxicity in rice cells: Mechanisms and size effects. Environ. Pollut. 2017;228:363-369.

    Not in our library10.1016/j.envpol.2017.05.014

  61. 61.

    Wu H., Tito N., Giraldo J.P. Anionic Cerium Oxide Nanoparticles Protect Plant Photosynthesis from Abiotic Stress by Scavenging Reactive Oxygen Species. ACS Nano. 2017;11:11283-11297.

    Not in our library10.1021/acsnano.7b05723

  62. 62.

    Zhao L., Lu L., Wang A., Zhang H., Huang M., Wu H., Xing B., Wang Z., Ji R. Nano-Biotechnology in Agriculture: Use of Nanomaterials to Promote Plant Growth and Stress Tolerance. J. Agric. Food Chem. 2020;68:1935-1947.

    Not in our library10.1021/acs.jafc.9b06615

  63. 63.

    Ullah S., Adeel M., Zain M., Rizwan M., Irshad M.K., Jilani G., Hameed A., Khan A., Arshad M., Raza A., et al. Physiological and biochemical response of wheat (Triticum aestivum) to TiO2 nanoparticles in phosphorous amended soil: A full life cycle study. J. Environ. Manag. 2020;263.

    Not in our library10.1016/j.jenvman.2020.110365

  64. 64.

    Zhang P., Ma Y., Liu S., Wang G., Zhang J., He X., Zhang J., Rui Y., Zhang Z. Phytotoxicity, uptake and transformation of nano-CeO2 in sand cultured romaine lettuce. Environ. Pollut. 2017;220:1400-1408.

    Not in our library10.1016/j.envpol.2016.10.094

  65. 65.

    Zhang H., Du W., Peralta-videa J., Gardea-Torresdey J., White J., Keller A., Guo H., Ji R., Zhao L. Metabolomics Reveals How Cucumber (Cucumis sativus) Reprograms Metabolites To Cope with Silver Ions and Silver Nanoparticle-Induced Oxidative Stress. Environ. Sci. Technol. 2018;52.

    Not in our library10.1021/acs.est.8b02440

  66. 66.

    Konate A., He X., Zhang Z., Ma Y., Zhang P., Alugongo G.M., Rui Y. Magnetic (Fe3O4) Nanoparticles Reduce Heavy Metals Uptake and Mitigate Their Toxicity in Wheat Seedling. Sustainability. 2017;9:790.

    Not in our library10.3390/su9050790

  67. 67.

    Guo K., Hu A., Wang K., Wang L., Fu D., Hao Y., Wang Y., Ali A., Adeel M., Rui Y., et al. Effects of spraying nano-materials on the absorption of metal(loid)s in cucumber. IET Nanobiotechnol. 2019;13:712-719.

    Not in our library10.1049/iet-nbt.2019.0060

  68. 68.
  69. 69.

    Wang Y., Wang L., Ma C., Wang K., Hao Y., Chen Q., Mo Y., Rui Y. Effects of cerium oxide on rice seedlings as affected by co-exposure of cadmium and salt. Environ. Pollut. 2019;252:1087-1096.

    Not in our library10.1016/j.envpol.2019.06.007

  70. 70.

    Dutta P., Pal S., Seehra M.S., Shi Y., Eyring E.M., Ernst R.D. Concentration of Ce3+ and Oxygen Vacancies in Cerium Oxide Nanoparticles. Chem. Mater. 2006;18:5144-5146.

    Not in our library10.1021/cm061580n

  71. 71.

    Cao Z., Stowers C., Rossi L., Zhang W., Lombardini L., Ma X. Physiological effects of cerium oxide nanoparticles on the photosynthesis and water use efficiency of soybean (Glycine max (L.) Merr.). Environ Sci.-Nano. 2017;4:1086-1094.

    Not in our library10.1039/c7en00015d

  72. 72.

    Rossi L., Zhang W., Lombardini L., Ma X. The impact of cerium oxide nanoparticles on the salt stress responses of Brassica napus L. Environ. Pollut. 2016;219:28-36.

    Not in our library10.1016/j.envpol.2016.09.060

  73. 73.

    Ma Y., Zhang P., Zhang Z., He X., Li Y., Zhang J., Zheng L., Chu S., Yang K., Zhao Y., et al. Origin of the different phytotoxicity and biotransformation of cerium and lanthanum oxide nanoparticles in cucumber. Nanotoxicology. 2014;9:262-270.

    Not in our library10.3109/17435390.2014.921344

  74. 74.

    Wang X., Sun W., Zhang S., Sharifan H., Ma X. Elucidating the Effects of Cerium Oxide Nanoparticles and Zinc Oxide Nanoparticles on Arsenic Uptake and Speciation in Rice (Oryza sativa) in a Hydroponic System. Environ. Sci. Technol. 2018;52:10040-10047.

    Not in our library10.1021/acs.est.8b01664

  75. 75.

    Mueller N.C., Nowack B. Exposure Modeling of Engineered Nanoparticles in the Environment. Environ. Sci. Technol. 2008;42:4447-4453.

    Not in our library10.1021/es7029637

  76. 76.

    Servin A.D., Morales M.I., Castillo-Michel H., Hernandez-Viezcas J.A., Munoz B., Zhao L., Nunez J.E., Peralta-Videa J.R., Gardea-Torresdey J.L. Synchrotron Verification of TiO2 Accumulation in Cucumber Fruit: A Possible Pathway of TiO2 Nanoparticle Transfer from Soil into the Food Chain. Environ. Sci. Technol. 2013;47:11592-11598.

    Not in our library10.1021/es403368j

  77. 77.

    Piccinno F., Gottschalk F., Seeger S., Nowack B. Industrial production quantities and uses of ten engineered nanomaterials in Europe and the world. J. Nanopart. Res. 2012;14.

    Not in our library10.1007/s11051-012-1109-9

  78. 78.

    Wang Z.Y., Yu X.L., Gao D.M., Feng W.Q., Xing B.S., Li F.M. Effect of Nano-rutile TiO2 and Multiwalled Carbon Nanotubes on the Growth of Maize (Zea mays L.) Seedlings and the Relevant Antioxidant Response. Environ. Sci. 2010;31:480-487.

    Not in our library10.13227/j.hjkx.2010.02.026

  79. 79.

    Singh J., Lee B. 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.

    Not in our library10.1016/j.jenvman.2016.01.015

  80. 80.

    Cai F., Wu X., Zhang H., Shen X., Zhang M., Chen W., Gao Q., White J.C., Tao S., Wang X. Impact of TiO2 nanoparticles on lead uptake and bioaccumulation in rice (Oryza sativa L.). Nanoimpact. 2017;5:101-108.

    Not in our library10.1016/j.impact.2017.01.006

  81. 81.

    Ji Y., Zhou Y., Ma C., Feng Y., Hao Y., Rui Y., Wu W., Gui X., Le V.N., Han Y., et al. Jointed toxicity of TiO2 NPs and Cd to rice seedlings: NPs alleviated Cd toxicity and Cd promoted NPs uptake. Plant Physiol. Biochem. 2017;110:82.

    Not in our library10.1016/j.plaphy.2016.05.010

  82. 82.

    Dai C., Shen H., Duan Y., Liu S., Zhou F., Wu D., Zhong G., Javadi A., Tu Y. TiO2 and SiO2 Nanoparticles Combined with Surfactants Mitigate the Toxicity of Cd2+ to Wheat Seedlings. Water Air Soil Pollut. 2019;230.

    Not in our library10.1007/s11270-019-4297-4

  83. 83.

    Singh J., Lee B. Effects of Nano-TiO2 particles on bioaccumulation of Cs-133 from the contaminated soil by Soybean (Glycine max). Process. Saf. Environ. 2018;116:301-311.

    Not in our library10.1016/j.psep.2018.02.016

  84. 84.

    Lin J., He F., Su B., Sun M., Owens G., Chen Z. The stabilizing mechanism of cadmium in contaminated soil using green synthesized iron oxide nanoparticles under long-term incubation. J. Hazard. Mater. 2019;379:120832.

    Not in our library10.1016/j.jhazmat.2019.120832

  85. 85.

    Konate A., Wang Y., He X., Adeel M., Zhang P., Ma Y., Ding Y., Zhang J., Yang J., Kizito S., et al. Comparative effects of nano and bulk-Fe3O4 on the growth of cucumber (Cucumis sativus). Ecotoxicol. Environ. Saf. 2018;165:547-554.

    Not in our library10.1016/j.ecoenv.2018.09.053

  86. 86.

    Briat J., Curie C., de Ric Gaymard F. Iron utilization and metabolism in plants Jean-Franc¸ois Briat, Catherine Curie and Fre’ de’ ric Gaymard. Curr. Opin. Plant Biol. 2007;10:276-282.

    Not in our library10.1016/j.pbi.2007.04.003

  87. 87.

    Michálková Z., Fernández D.M., Komárek M. Interactions of two novel stabilizing amendments with sunflower plants grown in a contaminated soil. Chemosphere. 2017.

    Not in our library10.1016/j.chemosphere.2017.08.009

  88. 88.

    Guha T., Barman S., Mukherjee A., Kundu R. Nano-scale zero valent iron modulates Fe/Cd transporters and immobilizes soil Cd for production of Cd free rice. Chemosphere. 2020;260:127533.

    Not in our library10.1016/j.chemosphere.2020.127533

  89. 89.

    Hussain A., Ali S., Rizwan M., Rehman M.Z.U., Qayyum M.F., Wang H., Rinklebe J. Responses of wheat (Triticum aestivum) plants grown in a Cd contaminated soil to the application of iron oxide nanoparticles. Ecotoxicol. Environ. Saf. 2019;173:156-164.

    Not in our library10.1016/j.ecoenv.2019.01.118

  90. 90.

    Rizwan M., Noureen S., Ali S., Anwar S., Rehman M.Z.U., Qayyum M.F., Hussain A. Influence of biochar amendment and foliar application of iron oxide nanoparticles on growth, photosynthesis, and cadmium accumulation in rice biomass. J. Soils Sediments. 2019;19:3749-3759.

    Not in our library10.1007/s11368-019-02327-1

  91. 91.

    Chen M., Tao X., Wang D., Xu Z., Xu X., Hu X., Xu N., Cao X. Facilitated transport of cadmium by biochar-Fe3O4 nanocomposites in water-saturated natural soils. Sci. Total Environ. 2019;684:265-275.

    Not in our library10.1016/j.scitotenv.2019.05.326

  92. 92.

    Adrees M., Khan Z.S., Ali S., Hafeez M., Khalid S., Ur Rehman M.Z., Hussain A., Hussain K., Shahid Chatha S.A., Rizwan M. Simultaneous mitigation of cadmium and drought stress in wheat by soil application of iron nanoparticles. Chemosphere. 2020;238:124681.

    Not in our library10.1016/j.chemosphere.2019.124681

  93. 93.

    Luying S., Fengbin S., Xiangnan L., Xiancan Z., Shengqun L., Yang W., Xiaoning Q. Effects of ZnO nanoparticles on seed germination and root carbon metabolism in maize (Zea mays L.). Soils Crop. 2020;9:40-49.

    Not in our library

  94. 94.

    Lihua W., Fayuan W., Xinxin J., Shuai L., Xueqin L. Effect of ZnO nanoparticles and inoculation with arbuscular mycorrhizal fungus on growth and nutrient uptake of soybean. Acta Ecol. Sin. 2015;35:5254-5261.

    Not in our library

  95. 95.

    Bashir A., Rizwan M., Ali S., Adrees M., Rehman M.Z., UrQayyum M.F. Effect of composted organic amendments and zinc oxide nanoparticles on growth and cadmium accumulation by wheat; a life cycle study. Environ. Sci. Pollut. Res. 2020;27:23926-23936.

    Not in our library10.1007/s11356-020-08739-8

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    Dimkpa C.O., Singh U., Bindraban P.S., Elmer W.H., Gardea-Torresdey J.L., White J.C. Zinc oxide nanoparticles alleviate drought-induced alterations in sorghum performance, nutrient acquisition, and grain fortification. Sci. Total Environ. 2019;688:926-934.

    Not in our library10.1016/j.scitotenv.2019.06.392

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    Ali S., Rizwan M., Noureen S., Anwar S., Ali B., Naveed M., Abd Allah E.F., Alqarawi A.A., Ahmad P. Combined use of biochar and zinc oxide nanoparticle foliar spray improved the plant growth and decreased the cadmium accumulation in rice (Oryza sativa L.) plant. Environ. Sci. Pollut. Res. 2019;26:11288-11299.

    Not in our library10.1007/s11356-019-04554-y

  98. 98.

    Rizwan M., Ali S., Rehman M.Z.U., Adrees M., Arshad M., Qayyum M.F., Hussain A., Chatha S.A.S., Imran M. Alleviation of cadmium accumulation in maize (Zea mays L.) by foliar spray of zinc oxide nanoparticles and biochar to contaminated soil. Environ. Pollut. 2019;358-367.

    Not in our library10.1016/j.envpol.2019.02.031

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    Ma X., Sharifan H., Dou F., Sun W. Simultaneous reduction of arsenic (As) and cadmium (Cd) accumulation in rice by zinc oxide nanoparticles. Chem. Eng. J. 2020;384.

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    Khan Z.S., Rizwan M., Hafeez M., Ali S., Javed M.R., Adrees M. The accumulation of cadmium in wheat (Triticum aestivum) as influenced by zinc oxide nanoparticles and soil moisture conditions. Environ. Sci. Pollut. Res. Int. 2019;26:19859-19870.

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    Hussain A., Ali S., Rizwan M., Rehman M.Z.U., Javed M.R., Imran M., Chatha S.A.S., Nazir R. Zinc oxide nanoparticles alter the wheat physiological response and reduce the cadmium uptake by plants. Environ. Pollut. 2018.

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    Rizwan M., Ali S., Ali B., Adrees M., Arshad M., Hussain A., Rehman M.Z.U., Waris A.A. Zinc and iron oxide nanoparticles improved the plant growth and reduced the oxidative stress and cadmium concentration in wheat. Chemosphere. 2018;214:269-277.

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    Fairweather-Tait S.J., Bao Y., Broadley M.R., Collings R., Ford D., Hesketh J.E., Hurst R. Selenium in Human Health and Disease. Antioxid. Redox Signal. 2011;14:1337-1383.

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    Lv Y., Yu T., Yang Z., Zhao W., Zhang M., Wang Q. Constraint on selenium bioavailability caused by its geochemical behavior in typical Kaschin-Beck disease areas in Aba, Sichuan Province of China. Sci. Total Environ. 2014;493:737-749.

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    Rayman M.P. Selenium and human health. Lancet. 2012;379:1256-1268.

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    Dinh Q.T., Cui Z., Huang J., Tran T.A.T., Wang D., Yang W., Zhou F., Wang M., Yu D., Liang D. Selenium distribution in the Chinese environment and its relationship with human health: A review. Environ. Int. 2018;112:294-309.

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    Tan L.C., Nancharaiah Y.V., van Hullebusch E.D., Lens P.N.L. Selenium: Environmental significance, pollution, and biological treatment technologies. Biotechnol. Adv. 2016;34:886-907.

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    Chang H., Zhou X., Wang W., Zhou Y., Dai W., Zhang C., Yu S., Bu J., Kim Y.H. Effects of Selenium Application in Soil on Formation of Iron Plaque outside Roots and Cadmium Uptake by Rice Plants. Advanced Materials Research. 2013;Volume 750–752:1573-1576.

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    Hu Y., Norton G.J., Duan G., Huang Y., Liu Y. Effect of selenium fertilization on the accumulation of cadmium and lead in rice plants. Plant Soil. 2014;384:131-140.

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    Lin L., Zhou W., Dai H., Cao F., Zhang G., Wu F. Selenium reduces cadmium uptake and mitigates cadmium toxicity in rice. J. Hazard. Mater. 2012;235–236:343-351.

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    Huang G., Ding C., Li Y., Zhang T., Wang X. Selenium enhances iron plaque formation by elevating the radial oxygen loss of roots to reduce cadmium accumulation in rice (Oryza sativa L.). J. Hazard. Mater. 2020;398:122860.

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    Shengrong Z. Mechanism of Migration and Transformation of Nano Selenium and Mitigates Cadmium Stress in Plants. Master’s Thesis. 2019.

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    Mengting L. Effect of Selenium application on Cadmium accumulation and in Rice (Oryza sativa). Master’s Thesis. 2018.

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    Gaur S., Kumar J., Kumar D., Chauhan D.K., Prasad S.M., Srivastava P.K. Fascinating impact of silicon and silicon transporters in plants: A review. Ecotoxicol. Environ. Saf. 2020;202:110885.

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    Mateos-Naranjo E., Gallé A., Florez-Sarasa I., Perdomo J.A., Galmés J., Ribas-Carbó M., Flexas J. Assessment of the role of silicon in the Cu-tolerance of the C4 grass Spartina densiflora. J. Plant Physiol. 2015;178:74-83.

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    Emamverdian A., Ding Y., Xie Y., Sangari S. Silicon Mechanisms to Ameliorate Heavy Metal Stress in Plants. BioMed Res. Int. 2018;2018:1-10.

    Not in our library10.1155/2018/8492898

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    Liang Y., Sun W., Zhu Y., Christie P. Mechanisms of silicon-mediated alleviation of abiotic stresses in higher plants: A review. Environ. Pollut. 2007;147:422-428.

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    Savvas D., Ntatsi G. Biostimulant activity of silicon in horticulture. Sci. Hortic.-Amst. 2015;196:66-81.

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    Wang S., Wang F., Gao S. Foliar application with nano-silicon alleviates Cd toxicity in rice seedlings. Environ. Sci. Pollut. Res. 2015;22:2837-2845.

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    Khan Z.S., Rizwan M., Hafeez M., Ali S., Adrees M., Qayyum M.F., Khalid S., Ur Rehman M.Z., Sarwar M.A. Effects of silicon nanoparticles on growth and physiology of wheat in cadmium contaminated soil under different soil moisture levels. Environ. Sci. Pollut. Res. 2020;27:4958-4968.

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    de Sousa A., Saleh A.M., Habeeb T.H., Hassan Y.M., Zrieq R., Wadaan M.A.M., Hozzein W.N., Selim S., Matos M., AbdElgawad H. Silicon dioxide nanoparticles ameliorate the phytotoxic hazards of aluminum in maize grown on acidic soil. Sci. Total Environ. 2019;693.

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    Fatemi H., Pour B.E., Rizwan M. Isolation and characterization of lead (Pb) resistant microbes and their combined use with silicon nanoparticles improved the growth, photosynthesis and antioxidant capacity of coriander (Coriandrum sativum L.) under Pb stress. Environ. Pollut. 2020;266.

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    Oliva Moncunill J., Pablo Ribas J.D., Cortina Pallás J.L., Cama J., Ayora Ibáñez C. Removal of cadmium, copper, nickel, cobalt and mercury from water by Apatite IITM: Column experiments. J. Hazard. Mater. 2011;194:312-323.

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    Mignardi S., Corami A., Ferrini V. Evaluation of the effectiveness of phosphate treatment for the remediation of mine waste soils contaminated with Cd, Cu, Pb, and Zn. Chemosphere. 2012;86:354-360.

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    Xu L., Cui H., Zheng X., Zhu Z., Liang J., Zhou J. Immobilization of copper and cadmium by hydroxyapatite combined with phytoextraction and changes in microbial community structure in a smelter-impacted soil. RSC Adv. 2016;6:103955-103964.

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    Mingxin W., Caicai W., Jinyong Z., Yang X., Shize W. Joint remediation of heavy metal contaminated soil by EDTA and nano-hydroxyapatite. Chin. J. Environ. Eng. 2019;13:396-405.

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    Li Z., Huang J. Effects of Nanoparticle Hydroxyapatite on Growth and Antioxidant System in Pakchoi (Brassica chinensis L.) from Cadmium-Contaminated Soil. J. Nanomater. 2014.

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    Sun R., Chen J., Fan T., Zhou D., Wang Y. Effect of nanoparticle hydroxyapatite on the immobilization of Cu and Zn in polluted soil. Environ. Sci. Pollut. Res. 2018;25:73-80.

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    Jin-feng X., Long C., Li-qiang G., Dong-mei Z. Long-term stability of immobilizing remediation of a heavy metal contaminated soil with nano-hydroxyapatite. J. Agro-Environ. Sci. 2016;35:1271-1277.

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    Qingqing Z., Shuokang W., Chenchen Z., Qing W., Ying Z., Lin N., Shu Xuan L., Wei L. Adsorption and Desorptlon of Cd on nHAP and Remediation test on Cd Contaminated Soil. Environ. Eng. 2017;35:179-184.

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    Fayuan W., Ling W., Xugang W., Zhaoyong S. Role of immobilization amendments in phytoremediation of Pb-Cd-contaminated soil using tobacco plants. Chin. J. Environ. Eng. 2014;8:789-794.

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    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.

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    Rossi L., Bagheri M., Zhang W., Chen Z., Burken J.G., Ma X. Using artificial neural network to investigate physiological changes and cerium oxide nanoparticles and cadmium uptake by Brassica napus plants. Environ. Pollut. 2019;381-389.

    Not in our library10.1016/j.envpol.2018.12.029

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