Abstract
With the advancement in nanotechnology, nanoparticles are reported to have applications in various fields. Their positive role in the environment, especially in plant ecosystem, is extensively studied nowadays. Among the metal nanoparticles, the silver nanoparticles (AgNP) are receiving special attention because of their ability to increase the growth and yield in many crops. Although many studies are found containing toxic effects of AgNPs the perspective of the present review is to collect the information about their positive role in growth and yield enhancement of crops. During this brief overview, many important crop plants are found to have a positive response towards the application of AgNPs. The appropriate elucidation of physiological, biochemical and molecular mechanism of nanoparticles in plant leads to better plant growth and development. It is concluded from this review that cautious and sensible use of nanotechnology can warrant food security through boosting agricultural production.
Inspec keywords: crops, botany, reviews, silver, nanoparticles, nanobiotechnology, biochemistry
Other keywords: review, silver nanoparticles, crop plant growth, plant ecosystem, physiological mechanism, molecular mechanism, biochemical mechanism, plant development, food security, agricultural production, Ag
1 Introduction
Recently, research in nanotechnology has gotten a lot of attention because of its applications and beneficial uses. Nanoparticles, size ranges from 1 to 100 nm, have been widely used in various fields of bioscience and biomedicine with an increasing number of commercials [1]. In addition to these, nanotechnology is also making its influence in the field of agriculture. Nanotechnology is establishing as a growing field of science because of its potential to transform our agriculture and to advance the conditions of the poor. Nanotechnology is improving agricultural yields for mushrooming population in Asian countries. It has potential to provide food security by enhancing crop production through precision farming, efficient utilisation of water, protection against insects and diseases. It is continuing to provide new tools and materials for molecular biology and pathogen detection and is also playing a role in the protection of the environment. Nanoscience is proven as one of the important tools in the modern era of agriculture and agri‐food nanotechnology. It is predicted to become a driving force for economic revolution in the near future. The focus of the agri‐food technology is for sustainable utilisation and safety of agriculturally grown foods including the production of crops for human and animal feeding.
Nanoparticles have both growth promoting and harmful effects on crops. Uses of nanoparticles in crop sciences are consistently increasing. It is observed that foliar application of nanomaterial as fertiliser boosts the agriculture production [2]. Various types of nanoparticles, particularly metal and carbon nanoparticles, have been explored for their absorption, accumulation, translocation and especially, for their influence on the growth and development of a wide variety of agricultural plants [3, 4]. The positive morphological impacts of nanoparticles have been recorded in many crop cultivars such as wheat, soybean, radish, alfalfa, onion, corn, rape, lettuce, cucumber, watermelon, spinach and tomato in terms of enhancing the seed germination rate, germination percentage, root and soot lengths, and fresh and dry weight. Similarly, nanomaterials have also improved the chlorophyll contents, carotenoids and nitrogen metabolism in some crops including peanut, soybean and spinach [5, 6, 7, 8, 9].
Among all the nanoparticles, silver nanoparticles (AgNPs) have remarkable uses in crop production. The uptake and accumulation of nanoparticles were found in plants when grown in a nutrient medium containing nanosilver [10]. Application of nanoparticles improved agronomic traits of soybean [11]. It is observed that when the seeds of cotton were soaked in AgNPs prior to germination, AgNPs produced advantageous effects [12]. AgNPs also have strong antimicrobial effects [13]. They can control and avoid plant diseases. These particles in concentrations of 0.5–1000 ppm caused the faster growth of plants and controlled pathogens [14]. AgNPs are beneficial for seed growth and germination [15] and act as growth stimulators [16]. They can enable plants to inhibit senescence caused by reactive oxygen species (ROS) as a result of oxidative stress. Senescence induced by oxidative stress and ROS generation triggered by 2,4‐D in mungbean was repressed by application of 100 μl of AgNPs [17]. Thus keeping in view the importance of AgNPs, the data about their positive effect on crop plants is collected and presented in the brief overview form.
2 AgNPs and plant growth
The application of AgNPs in pharmaceuticals and medical is very focused and promoted area of research. However, application of AgNPs in agriculture is recent. Besides other remarkable applications of AgNPs such as antimicrobial and drug delivery, recent studies explored their role in the improvement of growth of many crop plants.
The available literature shows that a large number of studies have been carried out on the application of AgNPs as antimicrobial and cytotoxic, however, only a few number of studies were done on an application of AgNPs on plants [18, 19].
2.1 Studies where AgNPs showed a toxic effect
There are many studies where AgNPs showed toxicity to a great extent. They produced a negative impact on seedling growth by reducing plant biomass and root elongation. They also caused morphological modifications such as reduction in the stem and shoot size. They interrupt replication of DNA and effect gene expression by producing ROS. The toxic effect of AgNPs on plants is shown in Table 1.
Table 1.
Plants (cultivars) | Ag nanoparticles (shape, size, conc.) | Findings | Reference |
---|---|---|---|
Triticum aestivum | 10 nm, 0–5 mg/kg | root and shoot lengths reduced | [20] |
Arabidopsis thaliana | 5 and 10 nm, 1 ppm | inhibited the root growth | [21] |
Populus deltoides nigra | 25 nm, 100 ppm | decreased in biomass | [21] |
Cucurbita pepo | <100 nm, 500 ppm | reduction in transcription and biomass | [22] |
Lolium perenne, Linum usitatissimum, Hordeum vulgare | 0.6–2 nm (colloidal), 10 and 20 ppm | reduction in seed germination rate, percentage and shoot length | [23] |
Vicia faba | 60 nm, 12.5, 25, 50 and 100 ppm | chromosomal aberrations | [24] |
Lolium multiflorum | 6 nm, 1–40 ppm | declined in biomass and root length | [25] |
Allium cepa | 70 nm, 0–80 ppm | DNA damage, cell wall disruption | [26] |
Oryza sativa | 1000 ppm | cell wall breakage | [27] |
tomato | <100 nm | decrease in chlorophyll, Genotoxicity | [28] |
Lemna gibba | 50 nm, spherical, 0–10 ppm | frond number decreased | [29] |
Raphanus sativus | 1–10 nm, 0, 125, 250 and 500 ppm | reduction in seed germination, seedling growth and nutrient | [30] |
Triticum aestivum | 10 and 100 mg/l | Fresh and dry weight of roots and shoots decreased. Totally chlorophyll, carotenoids and protein content also decreased. | [31] |
Triticum aestivum | 10 mg/l | decreased seedling growth and modified root tip cells | [32] |
Nicotiana tabacum | 1–100 nm | chloroplast size changed | [33] |
2.2 Studies where AgNPs showed a positive effect
The positive effect of AgNPs on different plant species is shown in Table 2. Study of Krishnaraj et al. [19] reveals a significant effect of biosynthesised AgNPs on seed germination of Bacopa monnieri, induced the synthesis of important metabolites like carbohydrate and protein and reduced the amount of phenols, catalase and peroxidase activities. Application of biologically synthesised AgNPs on Boswellia ovaliofoliolata enhanced seed germination and seedling growth [34]. The studies of Salama [35] and Sharma et al. [36] show that application of AgNPs improved plant growth parameters including length of root and shoot and leaf area and biochemicals including chlorophyll, carbohydrate, protein and antioxidant enzymes in Brassica juncea, Phaseolus vulgaris and Zea mays. However, Gruyer et al. [37] suggested both positive and negative effects of AgNPs on the growth of roots, depending upon the type of plant species. They reported an increase in the length of root in barley plant but decrease in lettuce. In an another study, the effect of AgNPs on the rate of seed germination in 11 wetland plants including Carex lurida, C. scoparia, C. vulpinoidea, C. crinita, Lolium multiflorum, Panicum virgatum, Eupatorium fistulosum, Scirpus cyperinus, Phytolaca americana, Juncus effusus and Lobelia cardinalis was studied and increase in germination rate was found only in E. fistulosum [55]. The study of Rezvani et al. [38] shows that AgNPs enhanced root growth in Crocus sativus. They suggested that AgNPs improve growth by blocking the action of ethylene. Some studies suggested that the impact of AgNPs on morphological and physiological aspects of plants related to the morphology of nanoparticles used. Syu et al. [39] reported the effect of AgNPs with three different morphologies (triangular, spherical and decahedral) on molecular and physiological responses of Arabidopsis. Their findings suggested that the decahedral AgNPs have the highest degree of potential to promote the root growth. On the other hand, spherical AgNPs did not show any effect on root elongation but they were involved in the accumulation of the highest level of anthocyanin in seedlings. The life of Asparagus leaves extended from 2 to 21 days when they were applied with AgNPs with a higher amount of chlorophyll, ascorbate and fibres opposed to untreated leaves [40]. Jasim et al. [41] reported that fenugreek seedlings (Trigonella foenum‐graecum L.) after treated with AgNPs have shown significant enhancement in leaf number, root and shoot length and fresh weight. A 23% increase in diosgenin (chief phytochemical of fenugreek) was also reported with the application of AgNPs.
Table 2.
Plants (cultivars) | Ag nanoparticles (shape, size, conc.) | Findings | Reference |
---|---|---|---|
Glycine max | — | increase in total chlorophyll, chl‐a, chl‐b and root FW | [15] |
Bacopa monnieri | — | significantly increased seed germination | [19] |
Boswellia ovalifoliolata | spherical, 30–40 nm, 10, 20 and 30 mg/ml | promotion in seed germination and seedling growth with an increase in AgNPs concentration | [34] |
phaseolus vulgaris L. and Zea mays L. | spherical, 10–30 nm, 20, 40, 60, 80 and 100 ppm | low concentration increased the growth (20–60 ppm) and higher concentration reduced it (80–100 ppm) | [35] |
Brassica juncea | spherical, 0, 25, 50, 100, 200 and 400 ppm | increase in growth and antioxidant status (50 ppm AgNPs were optimum) | [36] |
Radish, barley and lettuce | spherical, 10 nm, 1, 2.5, 5 and 10 mg/l | low concentration promote root length (1 mg/l) while higher concentration reduced it (10 mg/l) | [37] |
Crocus sativus | 0, 40, 80 or 120 ppm | 40 and 120 ppm AgNPs increased root length and dry weight, respectively, in flooding stress | [38] |
Arabidopsis | decahedral (45 ± 5 nm), triangular (47 ± 7 nm) and spherical (8 ± 2 nm) | decahedral AgNPs showed the highest degree of root growth promotion | [39] |
Asparagus | — | chlorophyll, ascorbat and fibre were found higher in treated leaves | [40] |
Trigonella foenum‐graecum | Spherical, 8–21 nm, 1 μg/ml | significant enhancement in leaf number, root and shoot lengths and fresh weight | [41] |
Vigna radiata | 50 ppm | increase plant height, fresh and dry weight, length of root and shoot of Vigna radiata | [42] |
Trigonella foenum‐graecum | 20 nm, 0, 10, 20, 30 and 40 μg/ml | low concentration of AgNPs promoted seed germination and early growth (10 μg/ml) | [43] |
Zea mays, Citrullus lanatus and Cucurbita pepo | 20 nm, 0.05, 0.1, 0.5, 1, 1.5, 2 and 2.5 mg/ml | positive effect was recorded in Cucurbita pepo and Citrullus lanatus and while negative in Zea mays | [44] |
Pisum sativum | spherical, 10–100 nm, 0, 30, 60 and 90 ppm | improvement in yield components (optimum 60 ppm) | [45] |
Triticum aestivum | 10–20 nm, 0, 25, 50, 75, 100, 125 and 150 ppm | Increase in seedling growth (chlorophyll contents, plant height, fresh and dry weight) and yield. Optimum concentration was 25 ppm | [46] |
Cucurbita pepo | 0, 1.0, 10, 50, 100, 500 and1000 mg/l | stimulate growth at low dose but retard growth at high dosage | [47] |
Triticum aestivum, Vigna sinensis and Brassica juncea | 50 and 75 ppm | Optimum improves in in cowpea at 50 ppm and in brassica at 75 ppm. Wheat was found unaffected | [48] |
Borage plant | 20–60 ppm | increase seed yield | [49] |
Zea mays | spherical | significantly increase root and shoot growth (optimum concentration 40 ppm) | [50] |
Mungbean, Pigeon pea, Chick pea | spherical, 12–20 nm | increase in root and shoot lengths | [51] |
Eruca sativa | — | increase root length | [32] |
Pisum sativum | spherical, 54 nm, 0, 30, 60 and 90 ppm | significant increase in protein and carbohydrate contents | [52] |
Triticum aestivum | 9–35 nm | significantly increase shoot length, fresh and dry weight, chlorophyll, carbohydrate and protein contents | [53] |
Phaseolus vulgaris L. | 16.7 nm, 0.0, 5, 10, 20 and 60 ppm | significantly increased growth parameters and physiological response | [54] |
In addition to the morphology, the concentration of applied AgNPs also plays an important role. It is found that 50 ppm AgNPs increased plant height, fresh and dry weight, length of root and shoot of Vigna radiata [42], fresh weight, root and shoot lengths, and vigor index and chlorophyll contents of seedlings of Brassica juncea [36], total chlorophyll, chl‐a, chl‐b, root FW in Glycine max plants [15]. Similarly, different concentrations of AgNPs (0, 10, 20, 30 and 40 μg/ml) were applied to examine their effect on growth parameters of fenugreek and it was observed that low concentration of AgNPs promoted seed germination and early growth opposed to control while higher concentration reduced the rate of seed germination and growth [43]. Dose depended effect of AgNPs was also observed on Zea mays (corn), Citrullus lanatus (watermelon) and Cucurbita pepo (zucchini) treated with different concentrations of AgNPs (0.05, 0.1, 0.5, 1, 1.5, 2 and 2.5 mg/ml). Increase growth rate and seed germination were observed for watermelon and zucchini depending on concentration of nanoparticles. 2 mg/ml AgNPs produced the highest seed germination rate (1.59 seeds/day) and percentage (73.33%) in watermelon while 0.5 and 2.5 mg/ml AgNPs triggered highest germination rate (1.68 and 1.66 seeds/day) and percentage (86.67 and 90%) in zucchini plants, respectively. However, in the corn, the toxic effect was noted in the sense of a reduction in root elongation as compared to control [44]. This study also showed the species dependent effect of AgNPs as positive in watermelon and zucchini and adverse in the corn. An improvement in the yield components of pea varieties was observed when AgNPs (0, 30, 60 and 90 ppm) were applied. The optimum concentration was 60 ppm [45].
Razzaq et al. [46] studied the effect of 0–150 ppm AgNPs on wheat and found that 25–50 ppm has the potential to significantly increase chlorophyll contents, plant height, fresh and dry weight over the control. Similar results were reported by Salama [35], where an increasing amount of AgNPs from 20 to 60 ppm resulted in an increase in the growth (length of root and shoot and leaf surface area) and biochemical attributes (chlorophyll, carbohydrate and protein contents) of Phaseolus vulgaris and Zea mays. Further increase in the level of AgNPs, 80–100 ppm decreased these parameters. This suggests that nanoparticles encourage growth at small dose but disappoint growth at large level of dosage [47]. It is further supported from the result of Seif et al. [48] that AgNPs from 20 to 60 ppm promote seed yield in treated borage plants opposed to control.
The impact of AgNPs is also species dependent. A study carried out by Pallavi Mehta and Srivastava [49] demonstrates the effect of AgNPs (0, 50 and 75 ppm) on Triticum aestivum (wheat), Vigna sinensis (cowpea) and Brassica juncea (Brassica). No effect was found on root and shoot parameters of wheat. However, optimum improvement in growth and root nodulation in cowpea was observed at 50 ppm and improved shoot parameters were found in Brassica at 75 ppm AgNPs. In Zea mays, a significant increase in growth of root and shoot was observed at 40 ppm AgNPs as compared to 20 and 60 ppm AgNPs [50]. An increase in root and shoot germination of mung bean, pigeon pea and chickpea was recorded when AgNPs treated seeds were germinated [51]. Similarly, the root length of Eruca sativa increased by 10 mg/l AgNPs [32]. In Pisum sativum, increase in seed protein and carbohydrate contents was found at 60 ppm AgNPs [52]. The effect of biosynthesised AgNPs studied on the growth and chemical attributes of Triticum aestivum and found that shoot length, fresh and dry weight, chlorophyll, carbohydrate and protein contents significantly increased at 20 and 40 ppm AgNPs [53]. A significant increase in growth characteristics and the physiological response was found in Phaseolus vulgaris under the application of AgNPs [54].
There are different suggestions and views exist about the mechanism of action of AgNPs to trigger the positive effect. It is thought that nanoparticles enter the seed coat and employ a useful effect on the seed germination processes. The possible reasons of increasing seed germination by nanoparticles, based on studies about the mechanism of effect of nanoparticles on seed germination, may include that they increase water absorption by seeds [5], increase the ability of seeds to absorb and utilise water and fertiliser, increase the level of nitrate reductase, promote the antioxidant system of seeds [15], drop H2 O2, superoxide radicals and malonyldialdehyde content to decrease antioxidant stress, and promote the activities of some important enzymes including guaiacol peroxidase, superoxide dismutase catalase and ascorbate peroxidase [48]. These changes help in the improvement of seed germination in plants.
It is known that electron leakage during the cellular electron exchange produces ROS that cause a reduction in plant production. It is suggested that AgNPs improve the efficiency of electron transport pathway and prevent the formation of ROS leading to a higher yield of plants [36]. Another suggestion is that silver prevents the action of ethylene and improves the growth and yield of plants. As it is already established that ethylene reduces the plant height. It was found that mutants of tobacco and Arabidopsis have shown lesser height opposed to their wild because mutants produced ethylene in high concentration [56]. Due to small size, AgNPs have a large surface area in contact with plants and thus they attach to the cell surface to a great extent leading to their higher efficiency [57].
3 Conclusions
Nanotechnology has offered numerous inventive applications in different fields of science like medicines, energy, electronics and biology, which make this branch as a revolutionary science. AgNPs, because of their unique physical and chemical properties, are now intensively introducing in the field of agriculture for the betterment of human life. However, only a few number of studies were found to have a beneficial effect of AgNPs on the growth and development of crop plants. This compiled information evident that effect of AgNPs depends on the size, concentration and modes of application and varies from species to species. Yet, studies are unable to fix any convincing outcomes on the effective, lethal or optimum concentrations of AgNPs as a whole and species wise on which some controlling outlines can be made. This brief overview also suggests that sensible usage of AgNPs can promote the yield of our agricultural crops. However, further trials are needed to specify a particular concentration, suitable mode and time of application to appreciate the growth and yield enhancing ability of AgNPs for crops in eco‐friendly manners.
4 References
- 1. Salata O.: ‘Applications of nanoparticles in biology and medicine’, J. Nanobiotechnol., 2004, 2, p. 3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. Raliya R. Tarafdar J.C.: ‘ZnO nanoparticle biosynthesis and its effect on phosphorous‐mobilizing enzyme secretion and gum contents in cluster bean (Cyamopsis tetragonoloba L.)’, Agric. Res., 2013, 2, pp. 48 –57 [Google Scholar]
- 3. Rico C.M. Majumdar S. Duarte‐Gardea M. et al.: ‘Interaction of nanoparticles with edible plants and their possible implications in the food chain’, J. Agric. Food Chem., 2011, 59, pp. 3485 –3498 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Nair R. Varghese S.H. Nair B.G. et al.: ‘Nanoparticulate material delivery to plants’, Plant Sci., 2013, 179, pp. 154 –163 [Google Scholar]
- 5. Zheng L. Hong F. Lu S. et al.: ‘Effect of nano‐TiO(2) on strength of naturally aged seeds and growth of spinach’, Biol. Trace Elem. Res., 2005, 104, (1), pp. 83 –92 [DOI] [PubMed] [Google Scholar]
- 6. Gao F. Hong F. Liu C. et al.: ‘Mechanism of nano‐anatase TiO2 on promoting photosynthetic carbon reaction of spinach’, Biol. Trace Elem. Res., 2006, 111, pp. 239 –253 [DOI] [PubMed] [Google Scholar]
- 7. Yang F. Liu C. Gao F. et al.: ‘The improvement of spinach growth by nano‐anatase TiO2 treatment is related to nitrogen photoreduction’, Biol. Trace Elem. Res., 2007, 119, (1), pp. 77 –88 [DOI] [PubMed] [Google Scholar]
- 8. Giraldo J.P. Landry M.P. Faltermeier S.M. et al.: ‘Plant nanobionics approach to augment photosynthesis and biochemical sensing’, Nat. Mater., 2014, 13, (4), pp. 400 –408 [DOI] [PubMed] [Google Scholar]
- 9. Agrawal S. Rathore P.: ‘Nanotechnology pros and cons to agriculture: a review’, Int. J. Curr. Microbiol. Appl. Sci., 2014, 3, (3), pp. 43 –55 [Google Scholar]
- 10. Lee W.M. Kwak J.I. An Y.J.: ‘Effect of silver nanoparticles in crop plants Phaseolus radiates and Sorghum bicolor; media effect on phytotoxicity’, Chemosphere, 2012, 86, pp. 492 –499 [DOI] [PubMed] [Google Scholar]
- 11. Sheykhbaglou R. Sedghi M. Shishevan M.T. et al.: ‘Effect of nano‐iron oxide particles on agronomic traits of soybean’, Notulae Sci. Biol., 2010, 2, pp. 112 –113 [Google Scholar]
- 12. Vakhrouchev A.V. Golubchikov V.B.: ‘Numerical investigation of the dynamics of nanoparticle systems in biological processes of plant nutrition’, J. Phys., 2007, 61, pp. 31 –35 [Google Scholar]
- 13. Shah V. Belozerova I.: ‘Influence of metal nanoparticles on the soil microbial community and germination of lettuce seeds’, Water Air Soil Pollut., 2009, 197, pp. 143 –148 [Google Scholar]
- 14. Ashrafi S.J. Rastegar M.F. Jafarpour B. et al.: ‘Possibility use of silver nanoparticles for controlling fussarium wilting in plant pathology’. Symp. of Int. Conf. on Food and Agriculture Application of Nanotechnologies, Sao Pedro, SP, Brazil, 2010. [Google Scholar]
- 15. Lu C.M. Zhang C.Y. Wen J.Q. et al.: ‘Research of the effect of nanometer materials on germination and growth enhancement of Glycine max and its mechanism’, Soybean Sci., 2002, 21, pp. 168 –172 [Google Scholar]
- 16. Sharon M. Choudhry A. Kumar R.: ‘Nanotechnology in agricultural disease and food safety’, J. Phytol., 2010, 2, pp. 83 –92 [Google Scholar]
- 17. Karuppanapandian T. Wang H.W. Prabakaran N. et al.: ‘2,4‐dichlorophenoxyacetic acid‐induced leaf senescence in mung bean (Vigna radiata L. Wilczek) and senescence inhibition by co‐treatment with silver nanoparticles’, Plant Physiol. Biochem., 2011, 49, pp. 168 –177 [DOI] [PubMed] [Google Scholar]
- 18. Monica R.C. Cremonini R.: ‘Nanoparticles and higher plants’, Caryologia, 2009, 62, pp. 161 –165 [Google Scholar]
- 19. Krishnaraj C. Jagan E.G. Ramachandran R. et al.: ‘Effect of biologically synthesized silver nanoparticles on Bacopa monnieri (Linn.) Wettst. plant growth metabolism’, Proc. Biochem., 2012, 47, pp. 51 –658 [Google Scholar]
- 20. Dimkpa C.O. McLean E. Martineau N. et al.: ‘Silver nanoparticles disrupt wheat (Triticum aestivum L.) growth in as and matrix’, Environ. Sci. Technol., 2013, 47, pp. 1082 –1090 [DOI] [PubMed] [Google Scholar]
- 21. Wang J. Koo Y. Alexander A. et al.: ‘Phytostimulation of poplars and Arabidopsis exposed to silver nanoparticles and AgC at sub lethal concentrations’, Environ. Sci. Technol., 2013, 47, pp. 5442 –5449 [DOI] [PubMed] [Google Scholar]
- 22. Musante C. White J.C.: ‘Toxicity of silver and copper to Cucurbita pepo: differential effects of nano and bulk‐size particles’, Environ. Toxicol., 2012, 27, pp. 510 –517 [DOI] [PubMed] [Google Scholar]
- 23. El‐Temsah Y.S. Joner E.J.: ‘Impact of Fe and Ag nanoparticles on seed germination and differences in bioavailability during exposure in aqueous suspension and soil’, Environ. Toxicol., 2012, 27, pp. 42 –49 [DOI] [PubMed] [Google Scholar]
- 24. Patlolla A.K. Berry A. May L. et al.: ‘Genotoxicity of silver nanoparticles in Vicia faba: a pilot study on the environmental monitoring of nanoparticles’, Int. J. Environ. Res. Public Health, 2012, 9, pp. 1649 –1662 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Yin L. Cheng Y. Espinasse B. et al.: ‘More than the ions: the effects of silver nanoparticles on Lolium multiflorum ’, Environ. Sci. Technol., 2011, 45, pp. 2360 –2367 [DOI] [PubMed] [Google Scholar]
- 26. Panda K.K. Achary V.M.M. Krishnaveni R. et al.: ‘In vitro biosynthesis and genotoxicity bioassay of silver nanoparticles using plants’, Toxicol. InVitro, 2011, 25, pp. 1097 –1105 [DOI] [PubMed] [Google Scholar]
- 27. Mazumdar H. Ahmed G.U.: ‘Phytotoxicity effect of silver nanoparticles on Oryza sativa ’, Int. J. Chem. TechRes., 2011, 3, pp. 1494 –1500 [Google Scholar]
- 28. Cekic F.O. Ekinci S. Inal M.S. et al.: ‘Silver nanoparticles induced genotoxicity and oxidative stress in tomato plants’, Turk. J. Biol., 2017, 41, pp. 700 –707 [Google Scholar]
- 29. Oukarroum A. Barhoumi L. Pirastru L. et al.: ‘Silver nanoparticle toxicity effect on growth and cellular viability of the aquatic plant Lemna gibba ’, Environ. Toxicol. Chem., 2013, 32, pp. 902 –907 [DOI] [PubMed] [Google Scholar]
- 30. Zuverza‐Mena N. Armendariz R. Peralta‐Videa J.R. et al.: ‘Effects of silver nanoparticles on radish sprouts: root growth reduction and modifications in the nutritional value’, Front. Plant Sci., 2016, 7, pp. 90 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Karimi J. Mohsenzadeh S.: ‘Physiological effects of silver nanoparticles and silver nitrate toxicity in Triticum aestivum ’, Iran. J. Sci. Technol. Trans. A, Sci., 2017, 41, pp. 111 –120 [Google Scholar]
- 32. Vannini C. Domingo G. Onelli E. et al.: ‘Phytotoxic and genotoxic effects of silver nanoparticles exposure on germinating wheat seedlings’, J. Plant Physiol., 2014, 171, pp. 1142 –1148 [DOI] [PubMed] [Google Scholar]
- 33. Cvjetko P. Zovko M. Štefanic P.P. et al.: ‘Phytotoxic effects of silver nanoparticles in tobacco plants’, Environ. Sci. Pollut. Res. Int., 2017, 25, (6), doi: 10.1007/s11356‐017‐0928‐8 [DOI] [PubMed] [Google Scholar]
- 34. Savithramma N. Ankanna S. Bhumi G.: ‘Effect of nanoparticles on seed germination and seedling growth of Boswellia ovalifoliolata an endemic and endangered medicinal tree taxon’, Nano Vision, 2012, 2, pp. 61 –68 [Google Scholar]
- 35. Salama H.M.H.: ‘Effects of silver nanoparticles in some crop plants, common bean (Phaseolus vulgaris L.) and corn (Zea mays L.)’, Int. Res. J. Biotechnol., 2012, 3, (10), pp. 190 –197 [Google Scholar]
- 36. Sharma P. Bhatt D. Zaidi M.G.H. et al.: ‘Silver nanoparticle‐mediated enhancement in growth and antioxidant status of Brassica juncea ’, Appl. Biochem. Biotechnol., 2012, 167, pp. 2225 –2233 [DOI] [PubMed] [Google Scholar]
- 37. Gruyer N. Dorais M. Bastien C. et al.: ‘Interaction between sliver nanoparticles and plant growth’. Int. Symp. on New Technologies for Environment Control, Energy‐Saving and Crop Production in Greenhouse and Plant Factory–greensys, Jeju, Korea, 2013, pp. 6 –11 [Google Scholar]
- 38. Rezvani N. Sorooshzadeh A. Farhadi N.: ‘Effect of nano‐silver on growth of saffron in flooding stress’, World Acad. Sci. Eng. Technol., 2012, 1, pp. 517 –522 [Google Scholar]
- 39. Syu Y.Y. Hung J.H. Chen J.C. et al.: ‘Impacts of size and shape of silver nanoparticles on Arabidopsis plant growth and gene expression’, Plant Physiol. Biochem., 2014, 83, pp. 57 –64 [DOI] [PubMed] [Google Scholar]
- 40. An J. Zhang M. Wang S. et al.: ‘Physical, chemical and microbiological changes in stored green Asparagus spears as affected by coating of silver nanoparticles‐PVP’, LWT‐Food Sci. Technol., 2008, 41, pp. 1100 –1107 [Google Scholar]
- 41. Jasim B. Thomas R. Mathew J. et al.: ‘Plant growth and diosgenin enhancement effect of silver nanoparticles in Fenugreek (Trigonella foenum‐graecum L.)’, Saudi Pharm. J., 2017, 25, (3), pp. 443 –447 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42. Najafi S. Jamei R.: ‘Effect of silver nanoparticles and Pb(NO3)2 on the yield and chemical composition of mung bean (Vigna radiata)’, J. Stress Physiol. Biochem., 2014, 10, pp. 316 –325 [Google Scholar]
- 43. Hojjat S.S.: ‘Impact of silver nanoparticles on germinated fenugreek seed’, Int. J. Agric. Crop Sci., 2015, 8, (4), pp. 627 –630 [Google Scholar]
- 44. Almutairi Z.M. Alharbi A.: ‘Effect of silver nanoparticles on seed germination of crop plants’, Int. J. Biol. Biomol. Agric. Food Biotechnol. Eng., 2015, 9, (6), pp. 594 –598 [Google Scholar]
- 45. Mehmood A. Murtaza G.: ‘Application of SNPs to improve the yield of Pisum sativum L. (pea)’, IET Nanobiotechnol., 2017, 11, (4), pp. 390 –394 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46. Razzaq A. Ammara R. Jhanzab H.M. et al.: ‘A novel nanomaterial to enhance growth and yield of wheat’, J. Nanosci. Technol., 2016, 2, pp. 55 –58 [Google Scholar]
- 47. Stampoulis D. Sinha S.K. White J.C.: ‘Assay‐dependent phytotoxicity of nanoparticles to plants’, Environ. Sci. Technol., 2009, 43, pp. 9473 –9479 [DOI] [PubMed] [Google Scholar]
- 48. Seif S.M. Sorooshzadeh A. Rezazadeh H.S. et al.: ‘Effect of nano silver and silver nitrate on seed yield of borage’, J. Med. Plants Res., 2011, 5, (5), pp. 171 –175 [Google Scholar]
- 49. Pallavi Mehta C.M. Srivastava R. et al.: ‘Impact assessment of silver nanoparticles on plant growth and soil bacterial diversity’, 3 Biotech, 2016, 6, (2), p. 254 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50. Sriram T. Pandidurai V.: ‘In vitro growth analysis of Zea mays L. using silver nanoparticles’, Int. J. Pharma Bio. Sci., 2017, 8, (3), pp. 30 –37 [Google Scholar]
- 51. Singh A.K. Rathod V. Singh D. et al.: ‘Effect of silver nanoparticles (AgNPs) produced by an endophytic fungus Fusarium semitectum isolated from a medicinal plant Withania somnifera (Ashwagandha) on seed germination’, Int. J. Res. Studies Agric. Sci., 2016, 2, (5), pp. 6 –12 [Google Scholar]
- 52. Mehmood A. Murtaza G.: ‘Impact of biosynthesized silver nanoparticles on protein and carbohydrate contents in seeds of Pisum sativum L.’, Crop Breed. Appl. Biotech., 2017, 17, (4), pp. 334 –340 [Google Scholar]
- 53. Latif H.H. Ghareib M. Tahon M.A.: ‘Phytosynthesis of silver nanoparticles using leaf extracts from Ocimum basilicum and Mangifira indica and their effect on some biochemical attributes of Triticum aestivum ’, Gesunde Pflanz., 2017, 69, (1), pp. 39 –46 [Google Scholar]
- 54. El‐Batal A.I. Gharib F.A.E. Ghazi S.M. et al.: ‘Physiological responses of two varieties of common bean (Phaseolus vulgaris L.) to foliar application of silver nanoparticles’, Nanomater. Nanotechnol., 2016, 6, p. 13 [Google Scholar]
- 55. Yin L. Colman B.P. McGill B.M. et al.: ‘Effects of silver nanoparticle exposure on germination and early growth of eleven wetland plants’, PLoS ONE, 2012, 7, pp. 1 –7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56. Pessarakli M.: ‘Handbook of plant and crop physiology’ (CRC Press, USA, 2014) [Google Scholar]
- 57. Shah V. Belozerova I.: ‘Influence of metal nanoparticles on the soil microbial community and germination of lettuce seeds’, Water Air Soil Pollut., 2009, 197, pp. 143 –148 [Google Scholar]