[go: up one dir, main page]
More Web Proxy on the site http://driver.im/
Next Article in Journal
Appropriate Matching Locations of Rail Expansion Regulator and Fixed Bearing of Continuous Beam Considering the Temperature Change of Bridge
Next Article in Special Issue
A Coaxial Dielectric Barrier Discharge Reactor for Treatment of Winter Wheat Seeds
Previous Article in Journal
Terrain Estimation for Planetary Exploration Robots
Previous Article in Special Issue
Effects of Atmospheric-Pressure Cold Plasma Treatment on Deoxynivalenol Degradation, Quality Parameters, and Germination of Barley Grains
You seem to have javascript disabled. Please note that many of the page functionalities won't work as expected without javascript enabled.
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Applied Sciences
Volume 10
Issue 17
10.3390/app10176045
applsci-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Effects of Plasma on Plant Growth, Development, and Sustainability

by
Bhawana Adhikari
1,†,
Manish Adhikari
1,† and
Gyungsoon Park
2,*
1
Plasma Bioscience Research Center, Kwangwoon University, Seoul 01897, Korea
2
Department of Electrical and Biological Physics and Plasma Bioscience Research Center, Kwangwoon University, Seoul 01897, Korea
*
Author to whom correspondence should be addressed.
†
Equally contributed.
Appl. Sci. 2020, 10(17), 6045; https://doi.org/10.3390/app10176045
Submission received: 4 August 2020 / Revised: 26 August 2020 / Accepted: 28 August 2020 / Published: 31 August 2020
(This article belongs to the Special Issue Plasma Techniques in Agriculture, Biology and Food Production)
Browse Figures
Figure 1
<p>Plausible events of seed germination initiated by plasma seed priming. Plasma treatment causes mechanical damage and facilitates a redox environment for the seed. This redox environment induces different pathways of seed germination. EMW: Electromagnetic wave, GA: Gibberellic acid, MAPK: Mitogen activated protein kinase, OxPPP: Oxidative pentose phosphate pathway, PCB: Protein carbonylation, TRX: Thioredoxin.</p> "> Figure 2
<p>Effects of plasma-generated reactive oxygen and nitrogen species (RONS) in different plant organs at different growth stages. Direct and indirect exposure to plasma induces RONS in various plant organs (shoots, roots, leaves, and flowers) and activates different signaling cascades that crosstalk with other small signaling molecules and hormones to affect growth, development, and immunity. BR: Brassinosteroid, ABA: Abscisic acid, SA: Salicylic acid, JA: Jasmonic acid, MAPK: Mitogen activated protein kinase, WUS: WUSCHEL.</p> ">
Versions Notes

Abstract

:
Cold atmospheric or low pressure plasma has activation effects on seed germination, plant growth and development, and plant sustainability, and prior experimental studies showing these effects are summarized in this review. The accumulated data indicate that the reactive species generated by cold plasma at atmospheric or low pressure may be involved in changing and activating the physical and chemical properties, physiology, and biochemical and molecular processes in plants, which enhances germination, growth, and sustainability. Although laboratory and field experiments are still required, plasma may represent a tool for efficient adaptation to changes in the climate and agricultural environments.

1. Introduction

Agriculture faces many problems due to continuous global population growth, environmental pollution, lack of agricultural land, and climate change. Climate change, in particular, has caused significant reductions in crop yield, threatening global food security [1]. According to the Food and Agriculture Organization (FAO), 20–45%, 5–50%, and 20–30% yield reductions are expected for maize, wheat, and rice, respectively, by 2100 under the current rates of climate change [1]. The distribution of plant pathogens and pests has shifted, the virulence of pathogens has been altered, and new diseases have emerged as a consequence of climatic changes [2,3]. Climate change has also altered the optimal locations of crop culture and reduced the quality and quantity of crop products [4].
Various strategies and technologies have been developed to adapt to changing agricultural environments. Efficient land use and management, altered food demand patterns, and reduced food waste and loss are often suggested as adaptation strategies [5]. Technological crop improvements also provide reliable solutions to overcome environment-associated challenges. Genetic engineering and breeding-based technologies are frequently used to produce crop plants with higher yield and stress tolerance [5]. However, the genetic regulations for crop production and tolerance are complicated processes involving many genes, which complicates crop improvement via genetic manipulation. Safety issues are another barrier that limits the broad application of genetic approaches.
The multi-disciplinary approach has received great attention, and cold atmospheric or low pressure plasma developed by physicists has been actively explored for its agricultural applications [6]. Plasma is an ionized gas produced at room temperature under atmospheric pressure. It generates reactive species, so the activation of plant vitality and the inactivation of microorganisms are frequently observed in agricultural applications [6]. Cold atmospheric or low pressure plasma is a potential tool to increase crop plant vitality and production, and several studies have investigated plasma-induced improvements to seed germination, plant growth and reproduction, and plant sustainability. In this review, we summarize the agriculture-based studies of cold atmospheric or low pressure plasma. Due to space limitations, we are unable to review all the published work in this rapidly expanding field.

2. Effect of Plasma on Seed Germination

Seeds are the reproductive products of plants which have totipotency, i.e., the capacity to develop into whole plants. Seeds are necessary for plant survival, dispersal, and the maintenance of progeny. At the time of dispersal, seeds undergo a period of dormancy to avoid unfavorable environmental conditions. Many dormant seeds fail to germinate, even if favorable conditions exist. Therefore, it is necessary to break the dormancy stage to increase germination. Other than the environmental factors, the dormant phase and seed germination are influenced by the hard seed coat, the presence of inhibitors, the seed maturation period, the immature embryo, seed coat impermeability to oxygen and water, and hormone imbalances. The phytohormone abscisic acid (ABA) is responsible for maintaining dormancy, whereas gibberellic acid (GA) is responsible for breaking the dormancy phase. These phytohormones are synthesized in the seeds in response to physical factors, and they activate the signaling cascades and enzymes that promote the degradation of seed reserves and initiate germination. Germination occurs in different phases and involves various physiological, biochemical, and molecular events (Figure 1).
Various seed treatment procedures have been applied to overcome dormancy. Popular seed treatment or priming methods, such as scarification, stratification, and chemical treatments, are used to induce germination in dormant seeds [7]. Cold (non-thermal) atmospheric or low pressure plasma is a new technology to enhance seed germination (Table 1 and Table 2), and seed treatment involves (1) direct exposure to plasma (Table 1) or (2) indirect exposure via plasma-treated water and solutions (Table 2).
The first reported case of plasma application to seeds was in a US patent by Krapivina et al. [67], where cold atmospheric pressure plasma generated from a mixture of inorganic gases (atmospheric air, oxygen, and nitrogen) was applied to soybean seeds for 5 to 300 s and the germination and growth were enhanced [67]. In the past 20 years, various plasma sources (dielectric barrier discharge (DBD) jet plasma, microwave discharge, radio-frequency (RF) discharge, gliding discharge) have been developed and used for treating vegetables (tomato, radish, coriander, green peas, and sunflower) and crops (rapeseed, cotton, maize, oat, wheat, mustard, soybean, legumes, and honey clover) (Table 1). Plasma treatment (direct or indirect) has enhanced seed germination in most studies, although no changes in the germination percentage were observed in several studies [15,19,41,44,56,59,64]. Plasma promoted the germination speed, overall germination percentage, or both.
Studies have also demonstrated variable effects on seed germination depending on the plasma sources, plant species, treatment time, feeding gases, and moisture content. Šerá et al. [17] compared different plasma sources for buckwheat seed germination and found that a GlidArc plasma source with an air feeder gas induced improved germination compared to downstream microwave plasma, planar rotating electrode plasma, and surface dielectric barrier discharge plasma. Other studies have reported variations in seed germination efficiency among plant species when treated with the same plasma source (Table 1 and Table 2) [9,13,14,16,46,50,56,57,65]. Most studies identified an optimal treatment time for the best germination efficiency for each plant species and plasma source. Effects of the feeding gases on the plasma-mediated seed germination have also been reported. Zhou et al. [32] found that mung bean seed germination was most efficient with microplasma generated in an aqueous solution using oxygen as the feeding gas, as opposed to helium, nitrogen, and air. Meng et al. [35] reported germination increases of 24, 28, and 35.5% for DBD plasma-treated wheat seeds with air, nitrogen, and argon feeding gases, respectively. Most studies have been under laboratory conditions, but field-based investigations have also been reported [14,44]. Filatova et al. [14] observed a 10–20% increase in the field germination capacity of soy, honey clover, and catgut seeds with microwave plasma treatment, whereas Ahn et al. [44] did not observe any changes in the germination percentage.
The mechanisms of enhanced seed germination by plasma have been thoroughly investigated. The most frequently reported factors are changes in the physical and chemical properties of the seed coat or surface. Physical and chemical changes to the seed surface can result in elevated hydrophilicity and water permeability that enhances water imbibition, which is required for seed germination. Increased hydrophilicity and water permeability of the seed surface after plasma treatment has been frequently observed [16,68,69]. Chemical changes and leaching of the seed surface membrane have also been analyzed in many studies [14,18,34,42,68]. Cold atmospheric pressure plasma decreases the water contact angle from 115° to 0° and modulates the hydrophilicity of the seed surface, which increases the uptake of water and initiates subsequent biochemical processes [16]. Similarly, Ling et al. [18] reported that cold plasma treatment decreases the contact angle of soybean seeds from 70.14° to 20.94°. There is abundant data to support the plasma-induced changes in the physicochemical properties of the seed surface and the increases in water absorption. However, enhanced seed germination was also observed without increased hydrophilicity of the seed surface [34]. The surface of quinoa seeds treated with RF plasma was chemically modified, but the hydrophilicity of the seed surface did not change. Nitrogen oxide (NOx−) and potassium (K+) ions accumulated on the seed surface via chemical alterations from the plasma treatment and penetrated the seeds after water addition, providing nutrients for seed germination. Another possible mechanism for plasma-induced enhanced seed germination is that the biochemical and molecular processes inside the seed are activated by plasma generated reactive oxygen and nitrogen species (RONS). Plasma generates a diverse range of RONS, depending on the feeder gas. These RONS can act as signaling molecules and initiate a germination cascade [70]. Reactive oxygen species (ROS) facilitate the oxidation of the aleurone layer and the mobilization food reserves during seed germination. Mildažienė et al. [71] showed that RF cold plasma (at low pressure) treatment (7 min) increased the GA (gibberellic acid) content of sunflower seeds and increased the germination rate by 10–24%. Increased GA promotes the activity of α-amylase, which degrades complex starches to metabolize sugar to initiate the germination process [71]. Accumulation of the GA3 germination hormone and amylolytic mRNA in spinach seeds treated with DBD plasma has also been reported [28]. Rahman et al. [43] detected high concentrations of hydrogen peroxide (H2O2) in cold plasma (Ar/Air, at low pressure) treated seeds and concluded that H2O2 is a signaling molecule that stimulates seed germination. Hydrogen peroxide serves to maintain a low ABA/GA ratio, which promotes the activation of amylase, the mobilization of food reserves, and the low production of antioxidant enzymes. Nitric oxide (NO) is another reactive species that plays a regulatory role in seed germination. NO regulates the production of ABA, a vital phytohormone that initiates germination and breaks dormancy. In plants, NO is produced from the reduction of nitrate (NO3−) to nitrite (NO2−) by nitrate reductase. Hence, NO3− in plasma-activated water is primarily responsible for enhanced seed germination [57]. A model of the plasma effects on seed germination and the possible molecular and biochemical events is presented in Figure 1.

3. Effects of Plasma on Plant Vegetative Growth and Reproduction

The life cycle of plants is divided into three distinct phases: vegetative, reproductive, and seed formation, followed by senescence. Vegetative growth is an important phase in which plants perform photosynthesis, increase their biomass, synthesize the reserve food, and prepare for reproduction. It is also a very sensitive stage because growth is influenced by environmental factors (i.e., heat, drought, pathogen, alkalinity, UV rays) and biological stimuli. Overall crop productivity depends on the vegetative growth phase, and, therefore, the regulation of vegetative growth is critical for plant development and survival [72].
Plasma can regulate the vegetative growth phase of plants, and plasma seed treatment has long-term effects on the early vegetative growth, as reported in several studies (Table 1). Plasma treatment promotes seed germination and subsequent seedling growth, increasing the length and biomass of seedlings (Table 1). As mentioned earlier, enhanced seedling growth without changes to the germination efficiency has been also observed after plasma treatment [15,19,41,44,56,59,64]. Plasma treatment at the seedling stage has also reported, which promoted seedling growth [10,48,55,61,63]. As for seed germination, the effects of plasma on seedling growth varies with the plasma dose, treatment time, feeding gases, and moisture. Extended plasma exposure or high power or atmospheric pressure reduced seedling growth; wheat seeds treated for 3 min had higher sprout biomass than seeds treated for 10, 20, or 40 min [13]. Milder plasma treatments (2.7 W) accelerates early growth and increases the root to shoot ratio [22]. Sarinont et al. [31] investigated the effects of feeding gases and moisture on plasma-mediated seedling growth and found that DBD plasma-treated radish seeds had better seedling growth when air, oxygen (O2), nitric oxide (NO) (10%), and nitrogen (N2) were used as the feeding gases (rather than N2, helium (He), and argon (Ar)). Additional moisture during plasma treatment also accelerated the growth enhancement effects.
Compared to vegetative growth, the effects of plasma on flowering and fruit production have rarely been reported. Studies have shown that plasma seed treatment has positive effects on the reproductive stage and harvesting product of tomatoes, soybeans, and peanuts [10,49]. A field study of okra (Abelmoschus esculentus) in India, found that cold low pressure plasma seed treatment improved different agronomic attributes, including the harvesting time, 50% flowering time, flower number, fruit number and weight, and okra yield [73]. Recently, Li et al. [74] reported increase in pod numbers (13.8%) and grain weight (8.2%) after priming oilseed rape plants with cold low pressure plasma at the reproduction stage. In another report, cold atmospheric pressure plasma seed priming increased the flower number (41.5%) and fresh weight (24%) in Cichorium intybus [51]. Cold atmospheric pressure plasma treatment alone or as a co-treatment with multi-walled carbon nanotubes increased the flower number and diameter of melons, which resulted in more melon fruits [75].
When investigating the mechanism of plasma action on seedling growth, many reports have focused on the increased nitrogen nutrient levels, changes in the amount growth hormones and other physiological processes, and the activation of growth-related gene expression. These mechanisms are likely related to the plasma-generated reactive species. Plasma-generated reactive species can produce nitrogen species, such as NO2− and NO3−, after interacting with water. Plasma-treated water acts as a nitrogen fertilizer and is responsible for growth induction in seedlings [57]. Other reactive species, such as H2O2 and NO, can act as growth stimulators. These reactive species may disturb redox homeostasis and trigger mild oxidative stress in plants at the vegetative and reproductive stages. Elevated in situ H2O2 and NOx concentrations in tomato seedlings in response to plasma-activated water (PAW) was detected by Adhikari et al. [61]. Similar observations the accumulation of RONS in response to plasma treatment in plants have also been reported in other studies [43,54]. The impact of RONS on plant development is well known [76,77], so plasma-generated RONS may similarly influence plant growth and development. Redox reactions play an important role in the cell cycle and cytokinesis. Many small antioxidants (i.e., ascorbate and glutathione) are essential for the cell cycle and act as redox buffers [78,79]. A study of wheat (Triticum sp.) and Arabidopsis roots suggests that the chemical impediment of ROS disturbs microtubule assembly and promotes microtubule formation in the root tip cells. This disturbance to tubulin organization leads to a distorted cytokinesis process [80]. ROS, such as H2O2, hydroxyl radical (OH•), and superoxide (O2−•, affect cell expansion via their control of the cell wall rigidity. Peroxidase in the apoplasts maintains the H2O2 level, regulates the crosslinking of phenolics and extensins, and maintains the cell wall rigidity. In contrast, OH• oxidizes polysaccharides (e.g., xyloglucans and pectins) and facilitates cell wall loosening [76]. Another study showed that the O2−• gradient in the meristem of the roots can play a role in cell division—high O2−• levels are present in root tips, the highest cell division zone, and the peripheral elongation zone has high H2O2 levels [81]. In Arabidopsis, the ROS content varies during floral bud formation and maturation, indicating the crucial role of ROS during flower development. In rice, the MADS3 gene, which is responsible for stamen formation during early floral bud development, regulates the O2−• concentration. Abnormal MADS3 expression causes pollen sterility by accumulating O2−• [82]. ROS can crosstalk with phytohormones and influence plant growth and development. In the roots, meristem cell growth is influenced by the interplay of H2O2 and brassinosteroids (BRs); intracellular H2O2 induces the binding of BR to its receptor kinase BRI. H2O2 can oxidize BZR1 (Brassinazole-Resistant 1) and BES1 (Brassinosteroid insensitive 1-Emssuppressor 1), the key transcription factors of BR signaling, and modify their activities. BZR1 interacts with PIF4 (Phytochrome Interacting Factor 4) and ARF6 (Auxin Response Factor 6), which are responsible for promoting meristem growth and development [83]. The redox reaction and ROS also regulate the post-translational modification of histones, transcription factors, and the chemical modifications of the nitrogenous DNA bases. Therefore, ROS epigenetically regulates plant growth. Under oxidative stress, ROS downregulates the histone demethylase gene, interacts with DME1 (DNA methylase), and epigenetically modifies the stress response of plants [77].
Seed reserve food utilization and the contents of soluble sugar and protein in seedlings are elevated after plasma treatments [84]. Cold atmospheric pressure plasma treatment of seeds affects the growth hormone concentration in the vegetative stage. Stolárik et al. [27] observed that the concentration of auxin (IAA) was upregulated in 14- and 21-day-old seedlings exposed to LTP (low-thermal plasma) for 120 s and 600 s at the seed stage. Interestingly, the cytokinin content was also significantly increased in 14 days old seedlings exposed to LTP for 120 s (compared to non-exposed seedlings) [27]. Other reports suggest that the redox homeostasis of plants is modified by cold atmospheric or low pressure plasma treatment. The modulation of superoxide dismutase (SOD), ascorbate peroxidase (APX), and chloramphenicol acetyltransferase (CAT) enzyme activities was observed in wheat plants after low pressure DBD plasma exposure [43]. Likewise, changes in the antioxidant (proline, ascorbic, guaiacol peroxidase, phenylalanine ammonia-lyase, phenolic, and flavonoid) status were also observed in plants at the vegetative stage after cold atmospheric pressure plasma treatment [40,61,85,86]. The expression patterns of different growth-regulating genes in response to cold atmospheric pressure plasma treatment have been investigated—argon plasma downregulates the expression of the methylation-related genes in soybeans and epigenetically regulates the expression of the metabolism-related genes [40].
The underlying mechanisms of RONS in plant growth and development are well known, and enormous amounts of information are available. As indicated by several studies, cold plasma and plasma-activated solutions can act as oxidative stimulants and disturb redox equilibrium. Redox non-equilibrium promotes the interaction of RONS with biomolecules, leading to oxidative modification or damage. Elevated RONS can also crosstalk with other metabolic reactions, phytohormones, and growth and development signaling cascades that change the plant across different physiological, biochemical, and molecular levels (Figure 2).

4. Plasma Technology for Crop Sustainability and Food Processing

Sustainable crop production and food security are important issues for modern society. Therefore, the development of technologies to address these issues is urgently needed. Sustainable agriculture technologies can not only increase crop production and tolerance but also help to preserve natural resources and ecosystems. Cold atmospheric or low pressure plasma is a modern-age technique that may alleviate the risks associated with agriculture and food processing systems. Cold atmospheric or low pressure plasma is an eco-friendly approach that positively affects crop production under adverse conditions. Various biotic and abiotic factors affect crop production, and several old agrochemical and biotechnological approaches have been used to address these issues. However, they often have negative impacts on the ecosystem. Plasma represents a risk-free approach because it requires low energy, is waste-free, and has no negative effects on the environment.
The effects of cold atmospheric or low pressure plasma treatment on seed germination and seedling growth under drought, salt, and chemical toxicity have been currently more studied (Table 3).
Several studies have shown improved tolerance to abiotic stress after plasma treatment. Ling et al. [84] treated the seeds of two Brassica napus cultivars (Zhongshuang 7, a drought-sensitive cultivar, and Zhongshuang 11, a drought-resistant cultivar) with helium plasma and found that plasma treatment enhanced seed germination under 15% (w/v) PEG 6000-mediated drought conditions. Similarly, the seeds of two Arabidopsis mutants, gl2 and gpat5, were exposed to DBD air plasma, and the seed germination efficiency was assessed under salt stress. Plasma causes structural changes to the mantle layers of the seed coat, which reduces permeability and diminishes the effects of salt stress on seed germination [90]. Upregulation of the drought stress-regulating transcription factor (WRKY) and secondary metabolites in plasma-treated seedlings was reported by Iranbakhsh et al. [106]. More recently, Adhikari et al. [93] demonstrated that cold atmospheric pressure plasma seed priming induces drought stress tolerance in seedlings—improved growth and biochemical alterations were observed in the cold plasma-primed tomato seedlings under 30% PEG-mediated drought stress. Other reports have shown that the plasma-activated water irrigation of barley improves hypoxia and low-temperature stress tolerance [92]. Pollutant soil contamination is a major concern in agriculture; the Air/Ar cold low pressure plasma treatment of wheat seeds reduced the accumulation of Cd during germination. This is because plasma treatment modifies the seed coat and reduces the pH of wheat seeds, resulting in Cd detoxification [91].
Plasma can promote plant tolerance to biotic stressors, such as pathogens and pests. Pathogenic diseases severely damage crop yield and are a major threat to food security. Cold low pressure plasma treatment of tomato seeds reduced bacterial wilt disease (causal agent: Ralstonia solanacearum) at the early vegetative stage [85]. Seed-borne pathogens, such as Fusarium fujikuroi (Bakanae disease) and Burkholderia plantarii (bacterial blight), can also be controlled by cold atmospheric pressure plasma irradiation on rice [107]. Many researchers have reported the inactivation of phytogenic bacteria on seeds and the upregulation of pathogen resistance genes in plants after cold atmospheric pressure plasma exposure [49,87]. Plasma-activated water irrigation induced the tomato plant defense system against Xanthomonas vesicatoria (Xv), although antimicrobial effects of the PAW against X. vesicatoria were not observed [88]. The induced expression of the PAL transcript upon PAW irrigation may be associated with the induced tomato defense system [88].
Harvesting, storage, and processing are crucial steps in the agricultural system. Food processing involves the transportation, cleaning, sorting, blending, and milling of crops to convert them to food. Technological innovations for the post-harvest storage and food processing stages are required to increase the food security index of the current agricultural system. Cold atmospheric or low pressure plasma is a promising technology to decontaminate and improve the shelf life of fresh and processed food products [108]. Several studies have reported plasma effects on post-harvest storage and food processing (Table 3). Microbial contamination during processing, packaging, and storing is a major problem that decreases shelf life, deteriorates taste, and causes food poisoning. Plasma treatment efficiently reduces the microbial contaminants on fruit, vegetables, and other edible products in a time- or dose-dependent manner, as summarized in a recent review [109]. The antimicrobial potential of plasma is well demonstrated by various cold atmospheric or low pressure plasma sources (gliding arc discharge, cold plasma argon jet, helium jet, microwave-generated plasma, and dielectric barrier discharge (DBD) plasma), microbes (Erwinia carotovora, Salmonella anatum, Salmonella enterica serovar Stanley, Salmonella enteritidis, Escherichia coli, Erwinia amylovor, Listeria monocytogenes, Clavibacter michiganensis subsp. Sepedonicus, Dickeya solani, X. campestris pv. Campestris, P. atrosepticum, Pectobacterium carotovorum subsp. Carotovorum, Pseudomonas fluorescens, Pseudomonas marginalis, and P. carotovorum), and fresh products (lettuce, tomatoes, carrots, cherries, figs, black peppers, strawberries, onions, radishes, cress, alfalfa seeds, grapes, bananas, and almonds). Studies have also shown that plasma cannot completely eradicate the microbial load but does prevent the microbes from multiplying [109]. An industrial-based DBD prototype efficiently removed the microflora load of fresh cherry tomatoes and prolonged the shelf life during storage [110]. Plasma-processed air can also reduce the microbial loads of fresh fruits/vegetables and packaged foods [111].
In the food processing industry, conventional techniques such as pasteurization, drying, and freezing, and newer physical strategies, such as ultraviolet (UV) irradiation, X-ray irradiation, ozone washing, and high-pressure processing, have been used to maintain food quality. However, these processing techniques have some drawbacks [112]. In plasma-mediated food processing, cold atmospheric or low pressure plasma can sterilize the food without compromising its flavor, odor, color, and prolonged shelf life. These plasma attributes have attracted the attention of food industry researchers. A comparison of different beverage processing techniques found that the plasma method retained the contents of ascorbic, chlorogenic, sinapic, and gallic acids in a tomato beverage, whereas pasteurization and other non-thermal methods resulted in reduced levels of these same acids [113]. Gas-phase plasma maintained the levels of phenolic compounds and hydroxycinnamic acids and reduced the anthocyanin content (23%), suggesting that anthocyanin is susceptible to the reactive oxygen species produced by cold atmospheric pressure plasma in juice [114]. The color and texture of food are very important to consumers, and studies have shown that plasma treatment has only minor (or no) effects on the color and texture of fruits. Misra et al. [115] used a DBD cold plasma source to process packaged strawberries and observed no changes in the firmness or color, but there was a significant reduction in the microbial load. Similarly, the qualitative attributes of fresh-cut fruit (apple and melon) were not affected by plasma treatment under storage conditions [97,116]. Other food qualities, such as pH, acidity, antioxidants, and the contents of soluble sugar and vitamins, have also been investigated after plasma treatment. About pH, the pH changed due to the reactive oxygen species generated on food after plasma treatment. On the other hand, the pH did not change after plasma treatment because of the buffering capacity of the liquid in living tissue and the physiological activity of removing the acid from the surface [117]. The soluble sugar content is important for the taste of fruit and their juices cold atmospheric pressure plasma reduced the fructose and glucose contents and increased the sucrose content in fruit juices [118,119]. This is because the reactive species generated by plasma promotes ozonolysis reactions, which breaks the glycosidic bond of oligosaccharides and reduces the sugars via oxidation [119,120]. The vitamin contents of fruit and their juices are stable under plasma treatment [116], while the antioxidant activities of fresh food are variably influenced by cold atmospheric pressure plasma treatments, depending on the food products, plasma sources, treatment conditions, and doses [117].

5. Future Prospects and Conclusions

The effects of cold atmospheric or low pressure plasma on plant growth, development, and sustainability have been verified by abundant experimental data. The accumulated data suggest that cold atmospheric or low pressure plasma may provide a reliable method to reduce the risks associated with global climate change and changing agricultural environments. Changes to the traditional agriculture system and practices are inevitable “modern agriculture” has been used to designate this transition. Indoor agriculture, hydroponic culturing, and smart farming associated with ICT (Information and Communication Technology) are frequently used in modern agriculture. Cold atmospheric or low pressure plasma may also contribute to the technological innovations of modern agriculture. For example, plasma applications in indoor and greenhouse cultivation systems are practically possible. Cold atmospheric or low pressure plasma is environmentally and biologically safe and requires little energy compared to other radiation-based technologies. The search for application ways and area to maximize plasma’s advantages should be continued. Recently, plasma-mediated improvements to plant tolerance against abiotic and biotic stresses has drawn great interest because of the influence of climate changes on agriculture. Conventional gene editing strategies are limited by safety concerns and the complexity of gene regulation networks, thus presenting an opportunity for cold atmospheric or low pressure plasma applications.
The efficient application of cold atmospheric or low pressure plasma requires experimental evidence and mechanistic studies. Although enhanced plant vitality and development due to plasma treatments have been well documented, evidence for the applied usage of plasma in agricultural fields and facilities is still lacking. Moreover, available experimental data are biased toward laboratory conditions. Thus, field and facility application studies are required. The underlying mechanisms of the plasma effects are also relatively unexplored compared to phenotypic effects discussed here. More information about the modes of plasma action on plant production and sustainability is necessary to optimize and upgrade the plasma systems and applications.

Author Contributions

All authors have written, read, and agreed to the published version of the manuscript.

Funding

This work was supported by the R & D program of the ‘Plasma Advanced Technology for Agriculture and Food (Plasma Farming)’ through the National Fusion Research Institute of Korea (NFRI; funded by governmental funds). This work was partially supported by the National Research Foundation of Korea (NRF) (2016K1A4A3914113, 2020R1F1A107094211).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Arora, N.K. Impact of climate change on agriculture production and its sustainable solutions. Environ. Sustain. 2019, 2, 95–96. [Google Scholar] [CrossRef] [Green Version]
  2. Bebber, D.P.; Ramotowski, M.A.T.; Gurr, S.J. Crop pests and pathogens move polewards in a warming world. Nat. Clim. Chang. 2013, 3, 985–988. [Google Scholar] [CrossRef]
  3. Velásquez, A.C.; Castroverde, C.D.M.; He, S.Y. Plant–pathogen warfare under changing climate conditions. Curr. Biol. 2018, 28, R619–R634. [Google Scholar] [CrossRef]
  4. Pathak, T.; Maskey, M.L.; Dahlberg, J.A.; Kearns, F.; Bali, K.M.; Zaccaria, D. Climate change trends and impacts on California agriculture: A detailed review. Agronomy 2018, 8, 25. [Google Scholar] [CrossRef] [Green Version]
  5. Anderson, R.; Bayer, P.E.; Edwards, D. Climate change and the need for agricultural adaptation. Curr. Opin. Plant Biol. 2019, 13, 1–6. [Google Scholar] [CrossRef] [PubMed]
  6. Ito, M.; Oh, J.-S.; Ohta, T.; Shiratani, M.; Hori, M. Current status and future prospects of agricultural applications using atmospheric-pressure plasma technologies. Plasma Process. Polym. 2017, 2017, e1700073. [Google Scholar] [CrossRef]
  7. Nonogaki, H. Seed dormancy and germination—Emerging mechanisms and new hypotheses. Front. Plant Sci. 2014, 5, 233. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Dubinov, A.; Lazarenko, E.; Selemir, V. Effect of glow discharge air plasma on grain crops seed. IEEE Trans. Plasma Sci. 2000, 28, 180–183. [Google Scholar] [CrossRef]
  9. Volin, J.C.; Denes, F.S.; Young, R.A.; Park, S.M.T. Modification of seed germination performance through cold plasma chemistry technology. Crop Sci. 2000, 40, 1706–1718. [Google Scholar] [CrossRef]
  10. Meiqiang, Y.; Mingjing, H.; Buzhou, M.; Tengcai, M. Stimulating effects of seed treatment by magnetized plasma on tomato growth and yield. Plasma Sci. Technol. 2005, 7, 3143–3147. [Google Scholar] [CrossRef]
  11. Šerá, B.; Stranák, V.; Serý, M.; Tichý, M.; Spatenka, P. Germination of Chenopodium Album in response to microwave plasma treatment. Plasma Sci. Technol. 2008, 10, 506–511. [Google Scholar] [CrossRef]
  12. Šerá, B.; Šerý, M.; Štrañák, V.; Špatenka, P.; Tichý, M. Does cold plasma affect breaking dormancy and seed germination? A study on seeds of Lamb’s quarters (Chenopodium album agg.). Plasma Sci. Technol. 2009, 11, 750–754. [Google Scholar] [CrossRef]
  13. Šerá, B.; Špatenka, P.; Šerý, M.; Vrchotova, N.; Hruskova, I. Influence of plasma treatment on wheat and oat germination and early growth. IEEE Trans. Plasma Sci. 2010, 38, 2963–2967. [Google Scholar] [CrossRef]
  14. Filatova, I.I.; Azharonok, V.V.; Kadyrov, M.A.; Beljavsky, V.; Gvozdov, A.; Shik, A.; Antonuk, A.E.; Belarus, N. The effect of plasma treatment of seeds of some grain and legumes on their sowing quality and productivity. Rom. Rep. Phys. 2011, 56, 139–143. [Google Scholar]
  15. Zhou, Z.; Huang, Y.; Yang, S.; Chen, W. Introduction of a new atmospheric pressure plasma device and application on tomato seeds. Agric. Sci. 2011, 2, 23–27. [Google Scholar] [CrossRef] [Green Version]
  16. Bormashenko, E.; Grynyov, R.; Bormashenko, Y.; Drori, E. Cold radiofrequency plasma treatment modifies wettability and germination speed of plant seeds. Sci. Rep. 2012, 2, 741. [Google Scholar] [CrossRef]
  17. Šerá, B.; Gajdova, I.; Cernak, M.; Gavril, B.; Hnatiuc, E.; Kovacik, D.; Kriha, V.; Slama, J.; Šerý, M.; Špatenka, P. How various plasma sources may affect seed germination and growth. In Proceedings of the 13th International Conference on Optimization of Electrical and Electronic Equipment (OPTIM), Brasov, Romania, 24–26 May 2012; IEEE: Piscataway, NJ, USA, 2012; pp. 1365–1370. [Google Scholar] [CrossRef]
  18. Ling, L.; Jiafeng, J.; Jiangang, L.; Minchong, S.; Xin, H.; Hanliang, S.; Yuanhua, D. Effects of cold plasma treatment on seed germination and seedling growth of soybean. Sci. Rep. 2014, 4, 5859. [Google Scholar] [CrossRef] [Green Version]
  19. Mihai, A.L.; Dobrin, D.; Magureanu, M.; Popa, M.E. Possitive effect of non-thermal plasma treatment on radish seed. Rom. Rep. Phys. 2014, 66, 1110–1117. [Google Scholar]
  20. Tong, J.; He, R.; Zhang, X.; Zhan, R.; Chen, W.; Yang, S. Effects of atmospheric pressure air plasma pretreatment on the seed germination and early growth of Andrographis paniculata. Plasma Sci. Technol. 2014, 16, 260–266. [Google Scholar] [CrossRef] [Green Version]
  21. Bußler, S.; Herppich, W.B.; Neugart, S.; Schreiner, M.; Ehlbeck, J.; Rohn, S.; Schlüter, O. Impact of cold atmospheric pressure plasma on physiology and flavonol glycoside profile of peas (Pisum sativum “Salamanca”). Food Res. Int. 2015, 76, 132–141. [Google Scholar] [CrossRef]
  22. Dobrin, D.; Magureanu, M.; Mandache, N.B.; Ionita, M. The effect of non-thermal plasma treatment on wheat germination and early growth. Innov. Food Sci. Emerg. Technol. 2015, 29, 255–260. [Google Scholar] [CrossRef]
  23. Hayashi, N.; Ono, R.; Shiratani, M.; Yonesu, A. Antioxidative activity and growth regulation of Brassicaceae induced by oxygen radical irradiation. Jpn. J. Appl. Phys. 2015, 54, 6. [Google Scholar] [CrossRef]
  24. Ji, S.H.; Kim, T.; Panngom, K.; Hong, Y.J.; Pengkit, A.; Park, D.H.; Kang, M.H.; Lee, S.H.; Im, J.S.; Kim, J.S.; et al. Assessment of the effects of nitrogen plasma and plasma-generated nitric oxide on early development of Coriandum sativum. Plasma Process. Polym. 2015, 12, 1164–1173. [Google Scholar] [CrossRef]
  25. Ono, R.; Hayashi, N. Variation of antioxidative activity and growth enhancement of Brassicaceae induced by low-pressure oxygen plasma. Jpn. J. Appl. Phys. 2015, 54, 06GD03. [Google Scholar] [CrossRef]
  26. Peethambaran, B.; Han, J.; Kermalli, K.; Jiaxing, J.; Fridman, G.; Balsamo, R.; Fridman, A.A.; Miller, V. Nonthermal plasma reduces water consumption while accelerating Arabidopsis thaliana growth and fecundity. Plasma Med. 2015, 5, 87–98. [Google Scholar] [CrossRef]
  27. Stolárik, T.; Henselová, M.; Martinka, M.; Novák, O.; Zahoranová, A.; Černák, M. Effect of low-temperature plasma on the structure of seeds, growth and metabolism of endogenous phytohormones in pea (Pisum sativum L.). Plasma Chem. Plasma Process. 2015, 35, 659–676. [Google Scholar] [CrossRef]
  28. Ji, S.H.; Choi, K.H.; Pengkit, A.; Im, J.S.; Kim, J.S.; Kim, Y.H.; Park, Y.; Hong, E.J.; Jung, S.K.; Choi, E.H.; et al. Effects of high voltage nanosecond pulsed plasma and micro DBD plasma on seed germination, growth development and physiological activities in spinach. Arch. Biochem. Biophys. 2016, 605, 117–128. [Google Scholar] [CrossRef]
  29. Junior, C.A.; de Oliveira Vitoriano, J.O.; da Silva, D.L.S.; de Lima Farias, M.; de Lima Dantas, M.B. Water uptake mechanism and germination of Erythrina velutina seeds treated with atmospheric plasma. Sci. Rep. 2016, 6, 33722. [Google Scholar] [CrossRef]
  30. Park, Y.; Oh, K.S.; Oh, J.; Seok, D.C.; Kim, S.B.; Yoo, S.J.; Lee, M.-J. The biological effects of surface dielectric barrier discharge on seed germination and plant growth with barley. Plasma Process. Polym. 2016, 15, 1600056. [Google Scholar] [CrossRef]
  31. Sarinont, T.; Amano, T.; Attri, P.; Koga, K.; Hayashi, N.; Shiratani, M. Effects of plasma irradiation using various feeding gases on growth of Raphanus sativus L. Arch. Biochem. Biophys. 2016, 605, 129–140. [Google Scholar] [CrossRef] [PubMed]
  32. Zhou, R.; Zhou, R.; Zhang, X.; Zhuang, J.; Yang, S.; Bazaka, K.; Ostrikov, K. Effects of atmospheric-pressure N2, He, Air, and O2 microplasmas on mung bean seed germination and seedling growth. Sci. Rep. 2016, 6, 32603. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Dubinov, A.E.; Kozhayeva, J.P.; Zuimatch, E.A. Changing germination rate of brown mustard seeds after treatment with plasmas of nanosecond electric discharges. IEEE Trans. Plasma Sci. 2017, 45, 294–300. [Google Scholar] [CrossRef]
  34. Gómez-Ramírez, A.; López-Santos, C.; Cantos, M.; García, J.L.; Molina, R.; Cotrino, J.; Espinós, J.P.; González-Elipe, A.R. Surface chemistry and germination improvement of Quinoa seeds subjected to plasma activation. Sci. Rep. 2017, 7, 5924. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Meng, Y.; Qu, G.; Wang, T.; Sun, Q.; Liang, D.; Hu, S. Enhancement of germination and seedling growth of wheat seed using dielectric barrier discharge plasma with various gas sources. Plasma Chem. Plasma Process. 2017, 37, 1105–1119. [Google Scholar] [CrossRef]
  36. Pawlat, J.; Starek, A.; Sujak, A.; Kwiatkowski, M.; Terebun, P.; Budzeń, M. Effects of atmospheric pressure plasma generated in GlidArc reactor on Lavatera thuringiaca L. seeds’ germination. Plasma Process. Polym. 2017, 15, 1700064. [Google Scholar] [CrossRef]
  37. Safari, N.; Iranbakhsh, A.; Oraghi Ardebili, Z. Non-thermal plasma modified growth and differentiation process of Capsicum annuum PP805 Godiva in in vitro conditions. Plasma Sci. Technol. 2017, 19, 055501. [Google Scholar] [CrossRef]
  38. Šerá, B.; Šerý, M.; Gavril, B.; Gajdova, I. Seed germination and early growth responses to seed pre-treatment by non-thermal plasma in hemp cultivars (Cannabis sativa L.). Plasma Chem. Plasma Process. 2017, 37, 207–221. [Google Scholar] [CrossRef]
  39. Da Silva, A.R.M.; Farias, M.L.; da Silva, D.L.S.; Vitoriano, J.O.; de Sousa, R.C.; Alves-Junior, C. Using atmospheric plasma to increase wettability, imbibition and germination of physically dormant seeds of Mimosa caesalpiniafolia. Colloids Surfaces B 2017, 157, 280–285. [Google Scholar] [CrossRef]
  40. Zhang, J.J.; Jo, J.O.; Huynh, D.L.; Mongre, R.K.; Ghosh, M.; Singh, A.K.; Lee, S.B.; Mok, Y.S.; Hyuk, P.; Jeong, D.K. Growth-inducing effects of argon plasma on soybean sprouts via the regulation of demethylation levels of energy metabolism-related genes. Sci. Rep. 2017, 7, 41917. [Google Scholar] [CrossRef]
  41. Matra, K. Atmospheric non-thermal argon–oxygen plasma for sunflower seedling growth improvement. Jpn. J. Appl. Phys. 2018, 57, 01AG03. [Google Scholar] [CrossRef]
  42. Pawlat, J.; Starek, A.; Sujak, A.; Terebun, P.; Kwiatkowski, M.; Budzeń, M.; Andrejko, D. Effects of atmospheric pressure plasma jet operating with DBD on Lavatera thuringiaca L. seeds’ germination. PLoS ONE 2018, 13, e0194349. [Google Scholar] [CrossRef] [Green Version]
  43. Rahman, M.M.; Sajib, S.A.; Rahi, M.S.; Tahura, S.; Roy, N.C.; Parvez, S.; Reza, M.A.; Talukder, M.R.; Kabir, A.H. Mechanisms and signaling associated with LPDBD plasma mediated growth improvement in wheat. Sci. Rep. 2018, 8, 10498. [Google Scholar] [CrossRef] [Green Version]
  44. Ahn, C.; Gill, J.; Ruzic, D.N. Growth of plasma-treated corn seeds under realistic conditions. Sci. Rep. 2019, 9, 4355. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Fadhlalmawla, S.A.; Mohamed, A.-A.H.; Almarashi, J.Q.; Boutraa, T. The impact of cold atmospheric pressure plasma jet on seed germination and seedlings growth of fenugreek (Trigonella foenum-graecum). Plasma Sci. Technol. 2019, 21, 105503. [Google Scholar] [CrossRef]
  46. Holc, M.; Primc, G.; Iskra, J.; Titan, P.; Kovač, J.; Mozetič, M.; Junkar, I. Effect of oxygen plasma on sprout and root growth, surface morphology and yield of garlic. Plants 2019, 8, 462. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Iqbal, T.; Farooq, M.; Afsheen, S.; Abrar, M.; Yousaf, M.; Ijaz, M. Cold plasma treatment and laser irradiation of Triticum spp. seeds for sterilization and germination. J. Laser Appl. 2019, 31, 42013. [Google Scholar] [CrossRef]
  48. Li, L.; Guo, H.; Zong, J.; Chen, J.; Wang, Y.; Li, J.; Li, D.; Shao, H.; Liu, J. Influence of low-vacuum helium cold plasma pre-treatment on the rooting and root growth of zoysiagrass (Zoysia willd.) stolon cuttings. Plasma Sci. Technol. 2019, 21, 55504. [Google Scholar] [CrossRef]
  49. Pérez-Pizá, M.C.; Prevosto, L.; Grijalba, P.E.; Zilli, C.G.; Cejas, E.; Mancinelli, B.; Balestrasse, K.B. Improvement of growth and yield of soybean plants through the application of non-thermal plasmas to seeds with different health status. Heliyon 2019, 5, e01495. [Google Scholar] [CrossRef] [Green Version]
  50. Volkov, A.G.; Hairston, J.S.; Patel, D.; Gott, R.P.; Xu, K.G. Cold plasma poration and corrugation of pumpkin seed coats. Bioelectrochemistry 2019, 128, 175–185. [Google Scholar] [CrossRef]
  51. Abedi, S.; Iranbakhsh, A.; Oraghi Ardebili, Z.O.; Ebadi, M. Seed priming with cold plasma improved early growth, flowering, and protection of Cichorium intybus against selenium nanoparticle. J. Theor. Appl. Phys. 2020, 14, 113–119. [Google Scholar] [CrossRef]
  52. Ambrico, P.F.; Šimek, M.; Ambrico, M.; Morano, M.; Prukner, V.; Minafra, A.; Allegretta, I.; Porfido, C.; Senesi, G.S.; Terzano, R. On the air atmospheric pressure plasma treatment effect on the physiology, germination and seedlings of basil seeds. J. Phys. D Appl. Phys. 2020, 53, 104001. [Google Scholar] [CrossRef]
  53. Ghasempour, M.; Iranbakhsh, A.; Ebadi, M.; Ardebili, Z.O. Seed priming with cold plasma improved seedling performance, secondary metabolism, and expression of deacetylvindoline O-acetyltransferase gene in Catharanthus roseus. Contrib. Plasma Phys. 2020, 60, e201900159. [Google Scholar] [CrossRef]
  54. Mujahid, Z.; Tounekti, T.; Khemira, H. Cold plasma treatment to release dormancy and improve growth in grape buds: A promising alternative to natural chilling and rest breaking chemicals. Sci. Rep. 2020, 10, 2667. [Google Scholar] [CrossRef] [PubMed]
  55. Park, D.P.; Davis, K.; Gilani, S.; Alonzo, C.-A.; Dobrynin, D.; Friedman, G.; Fridman, A.; Rabinovich, A.; Fridman, G. Reactive nitrogen species produced in water by non-equilibrium plasma increase plant growth rate and nutritional yield. Curr. Appl. Phys. 2013, 13, S19–S29. [Google Scholar] [CrossRef]
  56. Lindsay, A.; Byrns, B.; King, W.; Andhvarapou, A.; Fields, J.; Knappe, D.; Fonteno, W.; Shannon, S. Fertilization of radishes, tomatoes, and marigolds using a large-volume atmospheric glow discharge. Plasma Chem. Plasma Process. 2014, 34, 1271–1290. [Google Scholar] [CrossRef]
  57. Sivachandiran, L.; Khacef, A. Enhanced seed germination and plant growth by atmospheric pressure cold air plasma: Combined effect of seed and water treatment. RSC Adv. 2017, 7, 1822–1832. [Google Scholar] [CrossRef] [Green Version]
  58. Bafoil, M.; Jemmat, A.; Martinez, Y.; Merbahi, N.; Eichwald, O.; Dunand, C.; Yousfi, M. Effects of low temperature plasmas and plasma activated waters on Arabidopsis thaliana germination and growth. PLoS ONE 2018, 13, e0195512. [Google Scholar] [CrossRef]
  59. Judée, F.; Simon, S.; Bailly, C.; Dufour, T. Plasma-activation of tap water using DBD for agronomy applications: Identification and quantification of long lifetime chemical species and production/consumption mechanisms. Water Res. 2018, 133, 47–59. [Google Scholar] [CrossRef] [Green Version]
  60. Lee, E.-J.; Khan, M.S.I.; Shim, J.; Kim, Y.-J. Roles of oxides of nitrogen on quality enhancement of soybean sprout during hydroponic production using plasma discharged water recycling technology. Sci. Rep. 2018, 8, 16872. [Google Scholar] [CrossRef]
  61. Adhikari, B.; Adhikari, M.; Ghimire, B.; Park, G.; Choi, E.H. Cold atmospheric plasma-activated water irrigation induces defense hormone and gene expression in tomato seedlings. Sci. Rep. 2019, 9, 16080. [Google Scholar] [CrossRef] [Green Version]
  62. Gao, X.; Zhang, A.; Héroux, P.; Sand, W.; Sun, Z.; Zhan, J.; Wang, C.; Hao, S.; Li, Z.; Li, Z.; et al. Effect of dielectric barrier discharge cold plasma on pea seed growth. J. Agric. Food Chem. 2019, 67, 10813–10822. [Google Scholar] [CrossRef] [PubMed]
  63. Iwata, N.; Gamaleev, V.; Hashizume, H.; Oh, J.; Ohta, T.; Ishikawa, K.; Hori, M.; Ito, M. Simultaneous achievement of antimicrobial property and plant growth promotion using plasma-activated benzoic compound solution. Plasma Process. Polym. 2019, 16, e1900023. [Google Scholar] [CrossRef]
  64. Kang, M.H.; Jeon, S.S.; Shin, S.M.; Veerana, M.; Ji, S.-H.; Uhm, H.-S.; Choi, E.H.; Shin, J.H.; Park, G. Dynamics of nitric oxide level in liquids treated with microwave plasma-generated gas and their effects on spinach development. Sci. Rep. 2019, 9, 1011. [Google Scholar] [CrossRef]
  65. Liu, B.; Honnorat, B.; Yang, H.; Arancibia, J.; Rajjou, L.; Rousseau, A. Non-thermal DBD plasma array on seed germination of different plant species. J. Phys. D Appl. Phys. 2019, 52, 025401. [Google Scholar] [CrossRef]
  66. Zhou, R.; Li, J.; Zhou, R.; Zhang, X.; Yang, S. Atmospheric-pressure plasma treated water for seed germination and seedling growth of mung bean and its sterilization effect on mung bean sprouts. Innov. Food Sci. Emerg. 2019, 53, 36–44. [Google Scholar] [CrossRef]
  67. Krapivina, S.A.; Filippov, A.K.; Levitskaya, T.N.; Bakhvalov, A. Gas Plasma Treatment of Plant Seeds. U.S. Patent No. US5281315A, 25 January 1994. [Google Scholar]
  68. Mitra, A.; Li, Y.F.; Klämpfl, T.G.; Shimizu, T.; Jeon, J.; Morfill, G.E.; Zimmermann, J.L. Inactivation of surface-borne microorganisms and increased germination of seed specimen by cold atmospheric plasma. Food Bioprocess Technol. 2014, 7, 645–653. [Google Scholar] [CrossRef] [Green Version]
  69. Wang, X.-Q.; Zhou, R.-W.; de Groot, G.; Bazaka, K.; Murphy, A.B.; Ostrikov, K. Spectral characteristics of cotton seeds treated by a dielectric barrier discharge plasma. Sci. Rep. 2017, 7, 5601. [Google Scholar] [CrossRef] [Green Version]
  70. Su, L.; Lan, Q.; Pritchard, H.W.; Xue, H.; Wang, X. Reactive oxygen species induced by cold stratification promote germination of Hedysarum scoparium seeds. Plant Physiol. Bioch. 2016, 109, 406–415. [Google Scholar] [CrossRef]
  71. Mildažienė, V.; Aleknavičiūtė, V.; Žūkienė, R.; Paužaitė, G.; Naučienė, Z.; Filatova, I.; Lyushkevich, V.; Haimi, P.; Tamošiūnė, I.; Baniulis, D. Treatment of common sunflower (Helianthus annus L.) seeds with radio-frequency electromagnetic field and cold plasma induces changes in seed phytohormone balance, seedling development and leaf protein expression. Sci. Rep. 2019, 9, 6437. [Google Scholar] [CrossRef]
  72. Huijser, P.; Schmid, M. The control of developmental phase transitions in plants. Development 2011, 138, 4117–4129. [Google Scholar] [CrossRef] [Green Version]
  73. Kumar, R.; Thakur, A.K.; Vikram, A.; Vaid, A.; Rane, R. Effect of plasma treatment on growth and yield of okra [Abelmoschus esculentus (L.) under field conditions. Int. J. Bio-Resour. Stress Manag. 2017, 8, 659–667. [Google Scholar] [CrossRef]
  74. Li, L.; Li, J.; Shao, H.; Dong, Y. Effects of low-vacuum helium cold plasma treatment on seed germination, plant growth and yield of oilseed rape. Plasma Sci. Technol. 2018, 20, 095502. [Google Scholar] [CrossRef] [Green Version]
  75. Seddighinia, F.S.; Iranbakhsh, A.; Oraghi Ardebili, Z.; Nejad Satari, T.; Soleimanpour, S. Seed priming with cold plasma and multi-walled carbon nanotubes modified growth, tissue differentiation, anatomy, and yield in bitter melon (Momordica charantia). J. Plant Growth Regul. 2019, 39, 87–98. [Google Scholar] [CrossRef]
  76. Mhamdi, A.; Van Breusegem, F. Reactive oxygen species in plant development. Development 2018, 145, 1–12. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Huang, H.; Ullah, F.; Zhou, D.-X.; Yi, M.; Zhao, Y. Mechanisms of ROS regulation of plant development and stress responses. Front. Plant Sci. 2019, 10, 800. [Google Scholar] [CrossRef]
  78. de Simone, A.; Hubbard, R.; de la Torre, N.V.; Velappan, Y.; Wilson, M.; Considine, M.J.; Soppe, W.J.J.; Foyer, C.H. Redox changes during the cell cycle in the embryonic meristem of Arabidopsis thaliana. Antioxid. Redox Signal. 2017, 27, 1505–1519. [Google Scholar] [CrossRef] [Green Version]
  79. Tognetti, V.B.; Bielach, A.; Hrtyan, M. Redox regulation at the site of primary growth: Auxin, cytokinin and ROS crosstalk. Plant Cell Environ. 2017, 40, 2586–2605. [Google Scholar] [CrossRef]
  80. Livanos, P.; Galatis, B.; Quader, H.; Apostolakos, P. Disturbance of reactive oxygen species homeostasis induces atypical tubulin polymer formation and affects mitosis in root-tip cells of Triticum turgidum and Arabidopsis thaliana. Cytoskeleton 2012, 69, 1–21. [Google Scholar] [CrossRef]
  81. Tsukagoshi, H. Control of root growth and development by reactive oxygen species. Curr. Opin. Plant Biol. 2016, 29, 57–63. [Google Scholar] [CrossRef]
  82. Hu, L.; Liang, W.; Yin, C.; Cui, X.; Zong, J.; Wang, X.; Hu, J.; Zhang, D. Rice MADS3 regulates ROS homeostasis during late anther development. Plant Cell 2011, 23, 515–533. [Google Scholar] [CrossRef] [Green Version]
  83. Tian, Y.; Fan, M.; Qin, Z.; Lv, H.; Wang, M.; Zhang, Z.; Zhou, W.; Zhao, N.; Li, X.; Han, C.; et al. Hydrogen peroxide positively regulates brassinosteroid signaling through oxidation of the BRASSINAZOLE-RESISTANT1 transcription factor. Nat. Commun. 2018, 9, 1063. [Google Scholar] [CrossRef] [PubMed]
  84. Ling, L.; Jiangang, L.; Minchong, S.; Chunlei, Z.; Yuanhua, D. Cold plasma treatment enhances oilseed rape seed germination under drought stress. Sci. Rep. 2015, 5, 13033. [Google Scholar] [CrossRef] [PubMed]
  85. Jiang, J.; Lu, Y.; Li, J.; Li, L.; He, X.; Shao, H.; Dong, Y. Effect of seed treatment by cold plasma on the resistance of tomato to Ralstonia solanacearum (Bacterial Wilt). PLoS ONE 2014, 9, e97753. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  86. Buonopane, G.J.; Antonacci, C.; Lopez, J. Effect of cold plasma processing on botanicals and their essential oils. Plasma Med. 2016, 6, 315–324. [Google Scholar] [CrossRef]
  87. Pérez Pizá, M.C.; Prevosto, L.; Zilli, C.; Cejas, E.; Kelly, H.; Balestrasse, K. Effects of non-thermal plasmas on seed-borne Diaporthe/Phomopsis complex and germination parameters of soybean seeds. Innov. Food Sci. Emerg. Technol. 2018, 49, 82–91. [Google Scholar] [CrossRef]
  88. Perez, S.M.; Biondi, E.; Laurita, R.; Proto, M.; Sarti, F.; Gherardi, M.; Bertaccini, A.; Colombo, V. Plasma activated water as resistance inducer against bacterial leaf spot of tomato. PLoS ONE 2019, 14, e0217788. [Google Scholar] [CrossRef]
  89. Kyzek, S.; Holubová, Ľ.; Medvecká, V.; Tomeková, J.; Gálová, E.; Zahoranová, A. Cold atmospheric pressure plasma can induce adaptive response in pea seeds. Plasma Chem. Plasma Process. 2018, 39, 475–486. [Google Scholar] [CrossRef]
  90. Bafoil, M.; Le Ru, A.; Merbahi, N.; Eichwald, O.; Dunand, C.; Yousfi, M. New insights of low-temperature plasma effects on germination of three genotypes of Arabidopsis thaliana seeds under osmotic and saline stresses. Sci. Rep. 2019, 9, 8649. [Google Scholar] [CrossRef] [Green Version]
  91. Kabir, A.H.; Rahman, M.M.; Das, U.; Sarkar, U.; Roy, N.C.; Reza, M.A.; Talukdar, M.R.; Uddin, M.A. Reduction of cadmium toxicity in wheat through plasma technology. PLoS ONE 2019, 14, e0214509. [Google Scholar] [CrossRef] [Green Version]
  92. Gierczik, K.; Vukušić, T.; Kovács, L.; Székely, A.; Szalai, G.; Milošević, S.; Kocsy, G.; Kutasi, K.; Galiba, G. Plasma-activated water to improve the stress tolerance of barley. Plasma Process. Polym. 2020, 17, e1900123. [Google Scholar] [CrossRef]
  93. Adhikari, B.; Adhikari, M.; Ghimire, B.; Chandra Adhikari, B.; Park, G.; Choi, E.H. Cold plasma seed priming modulates growth, redox homeostasis and stress response by inducing reactive species in tomato (Solanum lycopersicum). Free Radic. Biol. Med. 2020, 156, 57–69. [Google Scholar] [CrossRef] [PubMed]
  94. Srey, S.; Park, S.Y.; Jahid, I.K.; Ha, S.-D. Reduction effect of the selected chemical and physical treatments to reduce L. monocytogenes biofilms formed on lettuce and cabbage. Food Res. Int. 2014, 62, 484–491. [Google Scholar] [CrossRef]
  95. Lacombe, A.; Niemira, B.A.; Gurtler, J.B.; Fan, X.; Sites, J.; Boyd, G.; Chen, H. Atmospheric cold plasma inactivation of aerobic microorganisms on blueberries and effects on quality attributes. Food Microbiol. 2015, 46, 479–484. [Google Scholar] [CrossRef] [PubMed]
  96. Ma, R.; Wang, G.; Tian, Y.; Wang, K.; Zhang, J.; Fang, J. Non-thermal plasma-activated water inactivation of food-borne pathogen on fresh produce. J. Hazard. Mater. 2015, 300, 643–651. [Google Scholar] [CrossRef]
  97. Tappi, S.; Gozzi, G.; Vannini, L.; Berardinelli, A.; Romani, S.; Ragni, L.; Rocculi, P. Cold plasma treatment for fresh-cut melon stabilization. Innov. Food Sci. Emerg. Technol. 2016, 33, 225–233. [Google Scholar] [CrossRef]
  98. Trevisani, M.; Berardinelli, A.; Cevoli, C.; Cecchini, M.; Ragni, L.; Pasquali, F. Effects of sanitizing treatments with atmospheric cold plasma, SDS and lactic acid on verotoxin-producing Escherichia coli and Listeria monocytogenes in red chicory (radicchio). Food Control 2017, 78, 138–143. [Google Scholar] [CrossRef]
  99. Lee, T.; Puligundla, P.; Mok, C. Intermittent corona discharge plasma jet for improving tomato quality. J. Food Eng. 2018, 223, 168–174. [Google Scholar] [CrossRef]
  100. Segura-Ponce, L.; Reyes, J.; Troncoso-Contreras, G.; Valenzuela-Tapia, G. Effect of low-pressure cold plasma (LPCP) on the wettability and the inactivation of Escherichia coli and Listeria innocua on fresh-cut apple (Granny Smith) skin. Food Bioprocess Technol. 2018, 11, 1075–1086. [Google Scholar] [CrossRef]
  101. Ramazzina, I.; Berardinelli, A.; Rizzi, F.; Tappi, S.; Ragni, L.; Sacchetti, G.; Rocculi, P. Effect of cold plasma treatment on physico-chemical parameters and antioxidant activity of minimally processed kiwifruit. Postharvest Biol. Technol. 2015, 107, 55–65. [Google Scholar] [CrossRef]
  102. Xu, Y.; Tian, Y.; Ma, R.; Liu, Q.; Zhang, J. Effect of plasma activated water on the postharvest quality of button mushrooms, Agaricus bisporus. Food Chem. 2016, 197, 436–444. [Google Scholar] [CrossRef]
  103. Oh, Y.J.; Song, A.Y.; Min, S.C. Inhibition of Salmonella typhimurium on radish sprouts using nitrogen-cold plasma. Int. J. Food Microbiol. 2017, 249, 66–71. [Google Scholar] [CrossRef] [PubMed]
  104. Won, M.Y.; Lee, S.J.; Min, S.C. Mandarin preservation by microwave-powered cold plasma treatment. Innov. Food Sci. Emerg. Technol. 2017, 39, 25–32. [Google Scholar] [CrossRef]
  105. Xiang, Q.; Liu, X.; Liu, S.; Ma, Y.; Xu, C.; Bai, Y. Effect of plasma-activated water on microbial quality and physicochemical characteristics of mung bean sprouts. Innov. Food Sci. Emerg. Technol. 2018, 52, 49–56. [Google Scholar] [CrossRef]
  106. Iranbakhsh, A.; Oraghi Ardebili, Z.; Molaei, H.; Oraghi Ardebili, N.; Amini, M. Cold plasma up-regulated expressions of WRKY1 transcription factor and genes involved in biosynthesis of cannabinoids in hemp (Cannabis sativa L.). Plasma Chem. Plasma Process. 2020, 40, 527–537. [Google Scholar] [CrossRef]
  107. Ochi, A.; Konishi, H.; Ando, S.; Sato, K.; Yokoyama, K.; Tsushima, S.; Yoshida, S.; Morikawa, T.; Kaneko, T.; Takahashi, H. Management of bakanae and bacterial seedling blight diseases in nurseries by irradiating rice seeds with atmospheric plasma. Plant Pathol. 2016, 66, 67–76. [Google Scholar] [CrossRef] [Green Version]
  108. Bourke, P.; Ziuzina, D.; Boehm, D.; Cullen, P.J.; Keener, K. The potential of cold plasma for safe and sustainable food production. Trends Biotechnol. 2018, 36, 615–626. [Google Scholar] [CrossRef] [Green Version]
  109. Adhikari, B.; Pangomm, K.; Veerana, M.; Mitra, S.; Park, G. Plant disease control by non-thermal atmospheric-pressure plasma. Front. Plant Sci. 2020, 11, 77. [Google Scholar] [CrossRef]
  110. Ziuzina, D.; Misra, N.; Cullen, P.; Keener, K.; Mosnier, J.; Vilaró, I.; Gaston, E.; Bourke, P. Demonstrating the potential of industrial scale in-package atmospheric cold plasma for decontamination of cherry tomatoes. Plasma Med. 2016, 6, 397–412. [Google Scholar] [CrossRef] [Green Version]
  111. Schnabel, U.; Schmidt, C.; Stachowiak, J.; Bösel, A.; Andrasch, M.; Ehlbeck, J. Plasma processed air for biological decontamination of PET and fresh plant tissue. Plasma Process. Polym. 2018, 15, 1600057. [Google Scholar] [CrossRef]
  112. Pan, Y.; Cheng, J.; Sun, D. Cold plasma-mediated treatments for shelf life extension of fresh produce: A review of recent research developments. Compr. Rev. Food Sci. Food Saf. 2019, 18, 1312–1326. [Google Scholar] [CrossRef]
  113. Mehta, D.; Sharma, N.; Bansal, V.; Sangwan, R.S.; Yadav, S.K. Impact of ultrasonication, ultraviolet and atmospheric cold plasma processing on quality parameters of tomato-based beverage in comparison with thermal processing. Innov. Food Sci. Emerg. Technol. 2019, 52, 343–349. [Google Scholar] [CrossRef]
  114. Kovačević Bursać, D.; Gajdoš Kljusurić, J.; Putnik, P.; Vukušić, T.; Herceg, Z.; Dragović-Uzelac, V. Stability of polyphenols in chokeberry juice treated with gas phase plasma. Food Chem. 2016, 212, 323–331. [Google Scholar] [CrossRef] [PubMed]
  115. Misra, N.; Patil, S.; Moiseev, T.; Bourke, P.; Mosnier, J.; Keener, K.; Cullen, P. In-package atmospheric pressure cold plasma treatment of strawberries. J. Food Eng. 2014, 125, 131–138. [Google Scholar] [CrossRef] [Green Version]
  116. Ramazzina, I.; Tappi, S.; Rocculi, P.; Sacchetti, G.; Berardinelli, A.; Marseglia, A.; Rizzi, F. Effect of cold plasma treatment on the functional properties of fresh-cut apples. J. Agric. Food Chem. 2016, 64, 8010–8018. [Google Scholar] [CrossRef] [PubMed]
  117. Pankaj, S.K.; Wan, Z.; Keener, K.M. Effects of cold plasma on food quality: A review. Foods 2018, 7, 4. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  118. Almeida, F.D.L.; Cavalcante, R.S.; Cullen, P.J.; Frias, J.M.; Bourke, P.; Fernandes, F.A.; Rodrigues, S. Effects of atmospheric cold plasma and ozone on prebiotic orange juice. Innov. Food Sci. Emerg. Technol. 2015, 32, 127–135. [Google Scholar] [CrossRef]
  119. Rodríguez, Ó.; Gomes, W.F.; Rodrigues, S.; Fernandes, F.A. Effect of indirect cold plasma treatment on cashew apple juice (Anacardium occidentale L.). LWT Food Sci. Technol. 2017, 84, 457–463. [Google Scholar] [CrossRef]
  120. Ben’ko, E.M.; Manisova, O.R.; Lunin, V.V. Effect of ozonation on the reactivity of lignocellulose substrates in enzymatic hydrolyses to sugars. Russ. J. Phys. Chem. A 2013, 87, 1108–1113. [Google Scholar] [CrossRef]
Applsci 10 06045 g001 550
Figure 1. Plausible events of seed germination initiated by plasma seed priming. Plasma treatment causes mechanical damage and facilitates a redox environment for the seed. This redox environment induces different pathways of seed germination. EMW: Electromagnetic wave, GA: Gibberellic acid, MAPK: Mitogen activated protein kinase, OxPPP: Oxidative pentose phosphate pathway, PCB: Protein carbonylation, TRX: Thioredoxin.
Figure 1. Plausible events of seed germination initiated by plasma seed priming. Plasma treatment causes mechanical damage and facilitates a redox environment for the seed. This redox environment induces different pathways of seed germination. EMW: Electromagnetic wave, GA: Gibberellic acid, MAPK: Mitogen activated protein kinase, OxPPP: Oxidative pentose phosphate pathway, PCB: Protein carbonylation, TRX: Thioredoxin.
Applsci 10 06045 g001
Applsci 10 06045 g002 550
Figure 2. Effects of plasma-generated reactive oxygen and nitrogen species (RONS) in different plant organs at different growth stages. Direct and indirect exposure to plasma induces RONS in various plant organs (shoots, roots, leaves, and flowers) and activates different signaling cascades that crosstalk with other small signaling molecules and hormones to affect growth, development, and immunity. BR: Brassinosteroid, ABA: Abscisic acid, SA: Salicylic acid, JA: Jasmonic acid, MAPK: Mitogen activated protein kinase, WUS: WUSCHEL.
Figure 2. Effects of plasma-generated reactive oxygen and nitrogen species (RONS) in different plant organs at different growth stages. Direct and indirect exposure to plasma induces RONS in various plant organs (shoots, roots, leaves, and flowers) and activates different signaling cascades that crosstalk with other small signaling molecules and hormones to affect growth, development, and immunity. BR: Brassinosteroid, ABA: Abscisic acid, SA: Salicylic acid, JA: Jasmonic acid, MAPK: Mitogen activated protein kinase, WUS: WUSCHEL.
Applsci 10 06045 g002
Table
Table 1. Effects of direct plasma on plant germination, growth, and physiology.
Table 1. Effects of direct plasma on plant germination, growth, and physiology.
Plant SpeciesPlasma SourceFeeder GasTreated StageEnhanced EffectsReference
Avena sativa
Hordeum vulgare		Glow discharge air plasmaAirSeedGermination[8]
Hordeum vulgare
Raphanus sativus
Pisum sativum
Glycine max L. Merr.
Zea mays L.
Phaseolus vulgaris L. 		Low-pressure RF (radio frequency) rotating plasmacarbon tetrafluoride (CF4)/octadecafluorodeca -lin (ODFD)SeedGermination[9]
Lycopersicon esculentum L. Mill. cv. Zhongshu No. 6Magnetized plasma SeedlingGrowth and productivity[10]
Chenopodium album agg.Low-pressure microwave plasmaMixture of Argon (Ar), Nitrogen (N2), and Oxygen (O2)SeedGermination[11,12]
Avena sativa
Triticum aestivum		Plasma plant Plasonic AR-550-MAirSeedGermination and early growth[13]
Lupinus angustifolius Galega virginiana Melilotus albusRF air PlasmaAirSeedGermination and productivity[14]
Solanum lycopersicumDBD (dielectric barrier discharge) air plasmaAirSeedGrowth and yield[15]
Lens culinaris
Phaseolus vulgaris
Triticum		Cold radiofrequency Air plasmaAirSeedGermination[16]
Fagopyrum aeseulentumGlidArc plasma
Surface DBD plasma
Downstream microwave plasma
Planar rotating electrode plasma		Air and mixture of air with water vaporsSeedGermination (depending on plasma sources)[17]
Glycine max L. Merr. cv. Zhongdou 40Low-pressure RF helium plasmaVacuumSeed and seedlingGermination and growth[18]
Raphanus sativum var. IcicleSurface discharge plasmaAirSeedEarly growth[19]
Andrographis paniculataDBD air plasmaAirSeedGermination and growth[20]
Pisum sativumSurface DBD plasmaAirSeed, sprout, and seedlingGermination and flavonol glycoside[21]
Triticum aestivumSurface discharge plasmaAirSeed and vegetative stageGermination and growth[22]
Raphanus sativus var. longipinnatusDBD plasmaPure Oxygen (O2)Seed and vegetative stageGermination and growth [23]
Coriander sativumDBD N2 (nitrogen) plasma
Microwave plasma generated gas		Nitrogen (N2)SeedGermination[24]
BrassicaceaeLow-pressure RF O2 (oxygen) plasmaOxygen (O2)SeedAntioxidant activity[25]
Arabidopsis thalianaGliding arc air plasmaAirSeed and reproductive stageGermination and growth[26]
Pisum sativum L. var. ProphetDiffuse coplanar surface DBD plasmaAirSeed and seedlingGermination and growth[27]
Spinacia oleracea L.High voltage nanosecond pulsed plasma
Micro DBD plasma 		Air and nitrogen (N2) gasSeedGermination and growth[28]
Erythrina velutinaDBD He plasmaHelium (He) gasSeedGermination[29]
Hordeum vulgareSurface DBD plasmaNitrogen (N2) with bubble airSeedGermination, growth, and GABA content[30]
Raphanus sativus L.DBD plasma with various feeding gasesAir, oxygen (O2), nitrogen (N2), helium(He), argon (Ar), and NO(10%)+nitrogenSeedGrowth (depending on feeding gas and moisture)[31]
Mung beanDBD plasma generated in water using various gasAir, oxygen (O2), nitrogen (N2), and helium (He)SeedGermination and growth[32]
Brassica juncea L.Nanosecond microspark plasmaAirSeedGermination[33]
Chenopodium quinoaDBD RF air plasma under atmospheric and low pressureAirSeedGermination[34]
WheatDBD plasma with various feeding gasesAir, oxygen (O2), nitrogen (N2), and argon (Ar)SeedGermination and growth[35]
Lavatera thuringiaca L.Gliding arc discharge N2 plasmaNitrogen (N2)SeedGermination[36]
Capsicum annuumDBD Ar (argon) plasmaArgon (Ar)SeedGrowth[37]
Cannabis sativa L.Gliding arc plasma
Microwave plasma		Oxygen (O2) and argon (Ar)Seed and vegetative stageGermination and growth[38]
Mimosa caesalpiniafoliaDBD plasmaAirSeedGermination[39]
Glycine max L. MerrillDBD Ar plasmaArgon (Ar)SeedGermination and growth[40]
SunflowerAr/O2 plasmaOxygen (O2) and argon (Ar)SeedGrowth[41]
Lavatera thuringiaca L.DBD plasma jet with N2/He gasNitrogen (N2), and helium (He)SeedGermination[42]
WheatLow-pressure DBD plasma with Ar/O2 and Ar/air gasesAir, oxygen (O2) and argon (Ar)SeedGermination and growth[43]
CornMicrowave plasma jet
DBD He plasma
Low-pressure RF N2 plasma		Nitrogen (N2), and helium (He)SeedGrowth and yield (field)[44]
Trigonella foenum-graecumAr plasma jetArgon (Ar)SeedGermination and growth[45]
Allium sativum
Ptujski spomladanski		Low-pressure RF O2 plasmaOxygen (O2)Seed and seedlingGermination and growth[46]
Triticum spp.Ar plasma
Q-switched Nd:YAG (Quantel Brilliant) pulsed laser		Argon (Ar)SeedGermination and sterilization[47]
Zoysia willd.Low-vaccum He plasmaHelium (He) and airSeedlingGrowth[48]
Glycine max L. MerrillDBD plasmaOxygen (O2) and nitrogen (N2)Seed and seedlingGermination and growth[49]
Cucurbita pepo L. cv. Cinderella
Cucurbita maxima L. cv.
Jarrahdale
Cucurbita maxima L. cv. Warty Goblin		Cold atmospheric pressure plasmaHelium (He) and argon (Ar)SeedGermination[50]
Cichorium intybusDBD plasma (Model PS200)Argon (Ar)Seed and seedlingGermination, growth, and flowering[51]
Ocimum basilicumVolume barrier discharge plasmaHumid Air (40% RH)SeedGermination[52]
Catharanthus roseusDBD plasmaArgon (Ar)SeedGrowth and physiology[53]
Vitis viniferaDBD Ar plasmaArgon (Ar)Seed and seedlingGermination and growth[54]
Table
Table 2. Effects of plasma treated water/solution on plant germination, growth, and physiology.
Table 2. Effects of plasma treated water/solution on plant germination, growth, and physiology.
Plant SpeciesPlasma SourceFeeder GasTreated StageEnhanced EffectsReference
Citrullus lanatus
Zinnia peruviana
Medicago sativa
Phaseolus cocconeus		Plasma-treated waterAirVegetative stageGrowth[55]
Janie marigold
Better Boy tomato
Early Scarlet radish		Plasma-treated waterAirSeed and seedlingGrowth[56]
Raphanus sativus
Solanum lycopersicum
Capsicum annum		DBD air plasma and
Plasma activated water		AirSeed and vegetative stageGermination and growth[57]
Arabidopsis thalianaDBD air and He (helium) plasma
Plasma-treated water		Air and Helium (He)Seed and seedlingGermination and growth[58]
Coral lentils (Lens culinaris) Plasma-treated tap waterAirSeedGrowth[59]
Glycine max L. MerrillPlasma-treated waterAirSeedGrowth and
quality		[60]
Solanum lycopersicumPlasma-treated waterAirSeedlingGrowth[61]
Pisum sativum L.DBD plasma
Plasma-treated tap water		AirSeed and seedlingGermination, growth, and flowering[62]
Radish sproutPlasma-treated organic solutionsArgon (Ar) and oxygen (O2) mixtureSeedlingGrowth[63]
Spinacia oleracea L.Plasma-treated waterMixture of oxygen (O2) and nitrogen (N2)SeedGrowth[64]
Tomato
Lettuce
Mung bean
Sticky bean
Radish
Dianthus
Mustard
Wheat		DBD plasma
Plasma-treated water		Air, oxygen (O2) and nitrogen (N2)SeedGermination and growth[65]
Mung beanPlasma-treated waterAir, oxygen (O2), nitrogen (N2), and helium (He)SeedGermination and disease tolerance[66]
Table
Table 3. Effects of plasma on pre- and post-harvest plant sustainability.
Table 3. Effects of plasma on pre- and post-harvest plant sustainability.
Plant SpeciesPlasma SourceFeeder GasTreated StageImproved Effects Reference
Pre-harvest tolerance to biotic stresses
Solanum lycopersicumRF helium plasmaHelium (He)SeedBacterial wilt resistance[85]
Glycine maxDBD O2 and N2 plasmaOxygen (O2) and nitrogen (N2)SeedDiaporthe/Phomopsis fungal resistance[87]
Solanum lycopersicum cv. Moneymaker and VF010Plasma-activated waterAmbient airSeedlingBacterial leaf spot resistance[88]
Pre-harvest tolerance to abiotic stresses
Brassica napusHe plasma dischargeHelium (He)SeedDrought stress tolerance [84]
Pisum sativum L.Coplanar DBD plasmaAmbient AirSeedTolerance to zeocinLess DNA damage[89]
Arabidopsis thalianaDBD air plasmaAir and helium (He)SeedSalt stress tolerance[90]
Triticum aestivumLow-pressure DBD plasma with Ar/O2 and Ar/air gasesArgon (Ar)/oxygen (O2) and argon (Ar)/air mixtureSeedTolerance to cadmium (Cd)[91]
Hordeum vulgarePlasma-activated waterNitrogen (N2)SeedTolerance to low temperature and hypoxia[92]
Solanum lycopersicumAir Plasma JetAirSeedTolerance to PEG (polyethlene glycol)-mediated drought stress[93]
Post-harvest sanitation
Lactuca sativaBrassica oleracea sp. CapitataCold oxygen plasma lamp (Photoplasma, Model: Induct ID60)Oxygen (O2)Lettuce and cabbage vegetablesL. monocytogenes biofilm removal[94]
BlueberriesAC plasma jet AirBlueberry fruitsRemoved microbial contamination[95]
StrawberriesPlasma-activated waterArgon (Ar)/oxygen (O2) mixtureStrawberry fruitsRemoved microbial contamination[96]
Cucumis melo L. var. Reticolatus cv. RaptorDBD plasmaAirMelon fruitsRemoved microbial contamination[97]
Red chicoryDBD plasmaAirChicory vegetablesReduced microbial contamination[98]
Lycopersicum esculentum Mill.Intermittent corona discharge plasma jetAirCherry tomato fruitsReduced microbial contamination and increased shelf life[99]
Apple cv. Granny SmithLow-pressure plasma (expanded plasma cleaner PDC-001/002)Argon (Ar), nitrogen (N2), oxygen (O2), and Argon–oxygen (Ar-O2)Apple fruitsRemoved microbial contamination[100]
Post-harvest quality
Actinidia deliciosa cv. HaywardDBD plasmaAirKiwi fruitsImproved visual quality and extended storage life[101]
Agaricus bisporusPlasma jetPlasma-activated waterArgon–oxygen (Ar-O2)Button mushroomsReduced microbial contamination and delayed softening[102]
Radish sproutsMicrowave N2 plasma Nitrogen (N2)Radish sprout vegetablesReduced moisture content during storage without changing antioxidant activity or ascorbic acid concentration.[103]
MandarinsMicrowave N2, He, N2 + O2 plasmaNitrogen (N2), helium (He) and nitrogen (N2)/oxygen (O2) mixtureMandarin fruitsIncreased antioxidant activity and phenolic content[104]
Mung bean sproutsPlasma-activated waterAirMung bean sprout vegetablesReduced microbial contamination without changing polyphenolic and flavonoid contents.[105]

Share and Cite

MDPI and ACS Style

Adhikari, B.; Adhikari, M.; Park, G. The Effects of Plasma on Plant Growth, Development, and Sustainability. Appl. Sci. 2020, 10, 6045. https://doi.org/10.3390/app10176045

AMA Style

Adhikari B, Adhikari M, Park G. The Effects of Plasma on Plant Growth, Development, and Sustainability. Applied Sciences. 2020; 10(17):6045. https://doi.org/10.3390/app10176045

Chicago/Turabian Style

Adhikari, Bhawana, Manish Adhikari, and Gyungsoon Park. 2020. "The Effects of Plasma on Plant Growth, Development, and Sustainability" Applied Sciences 10, no. 17: 6045. https://doi.org/10.3390/app10176045

APA Style

Adhikari, B., Adhikari, M., & Park, G. (2020). The Effects of Plasma on Plant Growth, Development, and Sustainability. Applied Sciences, 10(17), 6045. https://doi.org/10.3390/app10176045

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop