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Review

Nitrous Oxide Emissions from Paddies: Understanding the Role of Rice Plants

by
Arbindra Timilsina
1,2,*,
Fiston Bizimana
1,2,
Bikram Pandey
2,3,
Ram Kailash Prasad Yadav
4,
Wenxu Dong
1 and
Chunsheng Hu
1,*
1
Key Laboratory of Agricultural Water Resources, Hebei Key Laboratory of Soil Ecology, Center for Agricultural Resources Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Shijiazhuang 050021, China
2
University of Chinese Academy of Sciences, Beijing 100049, China
3
Key Laboratory of Mountain Ecological Restoration and Bio-resource Utilization and Ecological Restoration Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, Sichuan, China
4
Central Department of Botany, Tribhuvan University, Kirtipur 44613, Kathmandu, Nepal
*
Authors to whom correspondence should be addressed.
Plants 2020, 9(2), 180; https://doi.org/10.3390/plants9020180
Submission received: 20 December 2019 / Revised: 26 January 2020 / Accepted: 29 January 2020 / Published: 2 February 2020
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Abstract

:
Paddies are a potential source of anthropogenic nitrous oxide (N2O) emission. In paddies, both the soil and the rice plants emit N2O into the atmosphere. The rice plant in the paddy is considered to act as a channel between the soil and the atmosphere for N2O emission. However, recent studies suggest that plants can also produce N2O, while the mechanism of N2O formation in plants is unknown. Consequently, the rice plant is only regarded as a channel for N2O produced by soil microorganisms. The emission of N2O by aseptically grown plants and the distinct dual isotopocule fingerprint of plant-emitted N2O, as reported by various studies, support the production of N2O in plants. Herein, we propose a potential pathway of N2O formation in the rice plant. In rice plants, N2O might be formed in the mitochondria via the nitrate–nitrite–nitric oxide (NO3–NO2–NO) pathway when the cells experience hypoxic or anoxic stress. The pathway is catalyzed by various enzymes, which have been described. So, N2O emitted from paddies might have two origins, namely soil microorganisms and rice plants. So, regarding rice plants only as a medium to transport the microorganism-produced N2O might be misleading in understanding the role of rice plants in the paddy. As rice cultivation is a major agricultural activity worldwide, not understanding the pathway of N2O formation in rice plants would create more uncertainties in the N2O budget.

1. Introduction

Nitrous oxide (N2O) is a major anthropogenic greenhouse gas and the single most important contributor to stratospheric ozone depletion [1,2]. It accounts for approximately 6% of the enhanced global warming effect [3]. Among the anthropogenic sources of N2O, the agriculture sector represents the largest source [4]. Rice (Oryza sativa) farming plays an important role in the agricultural sector as it is a staple food for one-half of the world’s population [5]. Additionally, rice farming occupies about 158.5 million hectares of the world’s arable land and is one of the most important economic activities that provides a livelihood to millions of people [5]. Paddies are also a contributor of N2O to the atmosphere [5,6]. Moreover, the paddy utilizes one-seventh of the nitrogen (N) fertilizer and one-third of irrigation globally [7], making a more potent zone of N2O formation, as the N fertilizer application [8] and irrigation management practices [9] contribute significantly to N2O emissions. So, global N2O emissions from the paddy might increase considerably [10]. Thus, it is necessary to understand the mechanisms of N2O production in the paddy for necessary steps to be taken towards mitigation strategies for the global warming effect.
N2O in the paddy is emitted by the soil [10,11] and the rice plant [12,13]. The processes involved in the soil are well studied [10,11]. However, processes involving the plant are overlooked and the N2O emitted by the rice plants in paddies is considered to be produced by soil microorganisms, with the rice plant hypothesized to act as a channel to emit it into the atmosphere [12,13]. However, studies hypothesizing rice plants as a channel to emit N2O [12,13] have only measured the flux from the soil and plants and concluded that rice plants are not a source of N2O. Recently, Lenhart et al., (2019) [14] reported the distinct dual isotopocule fingerprint of N2O (δ15N, δ15Nsp and δ18O) emitted from the plant Miscanthus sinensis, and suggested that plants are a natural source of N2O. So, in our opinion, measuring only the N2O fluxes from the soil and the rice plant may not be sufficient to prove that rice plants are not a source of N2O. The results of Smart and Bloom (2000) [15] do not support the hypothesis that N2O emitted by wheat plants is produced by microorganisms and via the transpiration process. To elucidate this, we suggest the use of the 15N natural abundance method by injecting 15N-labelled N2O into the soil zone and, subsequently, measuring the fluxes and the 15N natural abundance of N2O from the soil and plants to reveal whether the N2O emissions are emitted either from soil and plants transport them, or whether N2O emissions can also be produced from plant cells. Furthermore, the rice plants should be aseptically grown in a controlled hydroponic solution with a regulated O2 partial pressure, and NO3 and NH4 concentrations and, subsequently, the N2O fluxes should be measured. Moreover, recent studies have shown that various species of plants can produce N2O and emit it into the atmosphere [14,15,16], however, the mechanism of N2O formation is not clearly understood. Therefore, considering rice plants only as a channel for soil-produced N2O might mislead understanding of the role of rice plants in N2O emission, as it is a conclusion based on studies that just measured the N2O fluxes from rice soil and the rice plant.
There are reports of both higher [17,18] and lower flux rates of N2O from paddies [19,20]. The high or low emissions of N2O from paddies depend on the management practices [18,19,20]. The N fertilizer application rate and water level are major factors controlling the N2O emissions from paddies [8,20]. For example, a meta-analysis by Zou et al. (2007) [19] revealed that under a continuous flooding system, N2O is emitted only after drainage, whereas flooding-midseason drainage-reflooding management triggers a substantial N2O emission. Moreover, flooding-midseason drainage-reflooding moist intermittent irrigation practices without waterlogging trigger a threefold higher N2O emission than the flooding-midseason drainage-reflooding management practice. A recent meta-analysis [9] reported a 105% increase in N2O emission with non-continuous flooding management rather than continuous flooding. Similarly, midseason drainage and N application significantly increased the N2O emissions from the paddy [11]. Another meta-analysis, based on the comparison between flooding irrigation and non-flooding irrigation (reduced irrigation with midseason drainage) and N fertilizer input, showed an increase in N2O emission of 84.4% and 167.3%, respectively [8]. From these observations of the meta-analyses, it can be concluded that water level management and N application significantly affect the N2O fluxes from the paddies. Interestingly, water level management [13] and nitrogen fertilizer application [12] also significantly increased the N2O emission from the rice plants and, in both cases, the emissions of N2O were higher from rice plants than from the soil–water surface [12,13]. These results highlight the role of rice plants in N2O emissions from paddies.
To mitigate the effects of global warming and ozone depletion effectively, a good understanding of all of the sources of N2O and the regulating factors is crucial. There have been numerous studies on paddies regarding their N2O emissions [8,12,13,20,21], however, no study has highlighted the role of the rice plant as a source of N2O. Thus, it is essential to explore the role of the rice plant in paddies—that is, whether it acts as a source of or a medium to channel N2O. The production of N2O in ascetically grown plants [16,22] suggests N2O can be produced by even eukaryotic plant cells. Moreover, based on the distinct dual isotopocule fingerprint of plant-emitted N2O, Lenhart et al. (2019) [14] proposed that plants are a natural source of N2O. So, the rice plant might also be a source of N2O. Now arises the question of what the mechanism of N2O formation in the rice plant cell is, if the rice plant is a source of N2O. Due to the unknown mechanisms of N2O formation in the plant cell, the rice plant might be regarded as just a medium to transport the soil microorganism-produced N2O. Therefore, to elucidate the origin of N2O emitted from paddies, we propose a potential pathway of N2O formation within the rice plant.

2. Potential Pathway of N2O Formation in Rice Plants

Studies on plants’ N2O emissions, involving the usage of the 15N isotope labeling method, have shown nitrate (NO3) as a precursor to N2O formation, but not ammonium (NH4) [8,14,15,16,22,23,24]. Furthermore, aseptically grown plants and axenic algal cells, when supplied with 15N-NO2, have also been found to produce δ 15N-N2Obulk [16,22,25]. In addition, eukaryotic cells, when supplied with 15N-NO, produce δ 15N-N2Obulk via a reduced form of cytochrome c oxidase [26]. Therefore, NO3, NO2, and nitrous oxide (NO) are the sources of N2O in eukaryotic cells. Thus, N2O formation in the cells of rice plants might occur via the NO3-NO2-NO pathway.
Nitric oxide (NO), being a signaling molecule, is formed at the cellular level in every eukaryotic organism [27]. There are, mainly, two potential pathways of NO formation in cells, namely the oxidative and reductive pathways. The oxidative pathway is L-arginine-dependent and occurs when the oxygen concentration in the cells is sufficient, whereas the reductive pathway is NO3 and NO2-dependent and occurs at a low oxygen concentration in the cells [28,29]. Briefly, the reductive pathway can occur in the hypoxic or anoxic cell environment, via NO3-NO2, and is catalyzed by various enzymes [27,28,30]. For example, NO3 taken by the plant root is reduced to NO2 in the cytoplasm by the cytoplasmic nitrate reductase (NR) [29]. Hypoxia caused by flooding in the root may increase [31], decrease [32], or have no effect [33] on NO3 uptake from the soil. However, flood-tolerant species such as rice might have higher NR activities than flood-sensitive species [34]. During hypoxia and anoxia, the NO2 and NH4 assimilation to amino acids strongly decreases [35]. So, NO2 formed in the cytosol, due to the reduction in NO3 by NR, is transported to the mitochondria by a protein similar to that in the chloroplast [30,36]. Moreover, the mitochondrial inner membrane anion channel may also be responsible for the transport of nitrite to the mitochondria [30].
It is evident that the mitochondrion is a site of NO2 reduction [30,37]. NO2 in the mitochondria is reduced to NO, and the process is pronounced under hypoxic to anoxic stress [30,38,39] and is more favorable at a lower pH [40,41]. Accordingly, Klepper (1987) [42] and Rockel et al. (2002) [43] reported a high emission of NO from plant leaves after the supply of NO3 under anaerobic conditions. The reduction process in the mitochondria is catalyzed by various electron transport chains (ECTs) [39,44]. For example, complex III [45] (Benamar et al., 2008), cytochrome c [44,46], and alternative oxidase (AOX) [47] can catalyze the reduction of NO2 to NO in the mitochondria. The NO subsequently formed is further reduced to N2O by a reduced form of eukaryotic cytochrome c oxidase [26,48]. The conversion of NO into N2O by a reduced form of cytochrome c oxidase is more favorable at low levels of both NO and O2 [48]. Cytochrome c oxidase in aerobic organisms is considered to be evolved from bacterial denitrifying enzymes [49]. Therefore, it is believed that, under the condition of less oxygen in cells, the enzyme exhibits some rudimentary nitrite and nitric oxide reductase activities [26,48,50]. Moreover, quinone in the mitochondria can also catalyze the reduction of NO to N2O [51,52,53].
Therefore, the processes, like the reduction of NO2 to NO and NO to N2O, are favorable under hypoxic and anoxic conditions in the mitochondria of plants. As discussed in the introduction section, the emission of N2O from paddies is very high under non-continuous flooding, midseason drainage, and reduced irrigation with midseason drainage management practices. All of these practices alter the oxygen (O2) level significantly in the root cells of the rice plant [54,55], which may create a favorable zone for N2O formation. Laboratory-based measurements also showed approximately 82–92% of N2O emissions from rice plants under soil flooded conditions, whereas 7–24% were found under unsaturated soil water conditions [13]. Along with O2, NO3 also plays an important role in N2O emission from plants, as NO3 is the precursor to N2O production in plants [14−16]. The role of O2 in the proposed pathway is supported by high NO2 and NO emissions from the soybean plant [56] and N2O [13] from the rice plant under anaerobic conditions. Furthermore, the role of NO3 in the proposed pathway is supported by the emission of 15N-labelled NO and δ 15N-N2Obulk from plants when supplied with 15N-NO3 [23]. Therefore, NO3− concentration in the root zone and cells might affect the N2O emission from rice plants, as NO3− uptake in the plant increases when its concentration in the soil solution is increased [57,58]. It might be the reason that soil fertilization with KNO3 greatly enhances N2O emission from rice plants [12]. Thus, N2O emitted by rice plants might be formed in hypoxic or anoxic mitochondria, as shown in Figure 1. It further suggests the existence of an incomplete denitrification (NO3-NO2-NO-N2O) pathway in the plant cells [16] when the oxygen level in the cells declines. This is further supported by the production of N2O in plants after the supply of NO3 and NO2, but not NH4 [14,15,16,22,23,24]. As there are many reports that the rice plant emits a substantial amount of N2O [12,13], and that within the plant cell there exists evidence of the NO3-NO2-NO-N2O pathway [26,29,30,37,48], this suggests that rice plants are a source of N2O. So, considering rice plants only as a channel for soil-produced N2O might create a gap in understanding N2O emission from paddies.

3. Why It Is a Challenge to Understand the Role of Rice Plants with Current Approaches to Methods from Field Studies?

Current methodologies involved in field-based measurements of N2O emissions from paddies include closed static chamber-based methods [18,59] and the micrometerological approach (the eddy covariance method) [10,60,61]. These methods include both soil and rice plants in the same system [10,18,59,60,61], making it difficult to evaluate the role of rice plants. However, for other plants with bigger stems (like trees), recent studies have developed separate chambers that help to capture the fluxes of N2O by avoiding soil N2O emissions [62]. The chamber used for trees cannot be used for crop species, like rice. The studies taken in field conditions [18,59,60,61] have not developed such chambers that could separately quantify the N2O emitted from the rice plant and the rice soil. In this regard, static chambers that could be used for crops like the rice plant should be developed and the N2O fluxes from the rice plant and the rice soil (microbial) should be measured separately. This limitation has made it difficult to evaluate the contribution of the rice plants to the total contribution from the paddy and the N2O budget from rice plants remains unsolved. Although it might be a challenge to prove that all N2O emitted by the plants in field conditions is from either soil microorganisms, plants, or both, injecting δ 15N-N2Obulk into the soil profile and subsequently measuring the N2O fluxes in the soil and the rice plants might help to distinguish the source. Additionally, to understand the role of the rice plants in the paddy, we suggest measuring the isotopocule fingerprint of N2O (δ 15N, δ 15Nsp and δ 18O) emitted from rice plants and rice soil, as isotope analysis methods are a more powerful tool than the flux measurement methods to distinguish the source of the N2O [63].
At the plant’s cellular level, the NO3-NO2-NO-N2O pathway, as represented in Figure 1 operates during limited oxygen in cells and in the presence of NO3, NO2 [26,29,30,37,48]. Similarly, in the rice soil the microbial pathway of denitrification (NO3-NO2-NO-N2O-N2) occurred during limited oxygen conditions and in the presence of NO3 and NO2 [10,64]. So, both in the rice plant and the rice soil, the pathway of N2O formation occurred during the limited oxygen conditions, making the process appear only to occur in the known site, i.e., the soil. As the N2O flux measurement was done with the help of static chambers that captured the N2O fluxes in the soil and the rice plant at bulk [18,59], this masked the role of the rice plant. However, as described in Section 2, the NO3-NO2-NO-N2O pathway existed in the plant cells during hypoxia and anoxia and this pathway in the rice plant cells was overlooked.

4. Role of NO3, NO2 and NO during Hypoxia and Anoxia Tolerance

Rice farming needs frequent irrigation, resulting in hypoxic and anoxic conditions in the root zone. Under such conditions, oxygen concentration in the cells is too low to support aerobic respiration and may cause energy deficit and, ultimately, cell death [65]. Various studies have shown that NO3 fertilization improves tolerance to low oxygen conditions in plants [31,66]. During hypoxia, and in the absence of NO3, the plants’ growth is significantly disturbed [31]. So, for crop species like the rice plant, which is frequently subjected to hypoxia and anoxia, NO3 might play important role in improving tolerance to low oxygen.
Oxygen deprivation affects the plant mitochondria [67,68]. Nitrate and nitrite are shown to have a protective effect on mitochondria under oxygen deprivation [68]. Hypoxia strongly decreases the NO2 reduction to NH4 and the NH4 assimilation to amino acids [35]. As NO2 assimilated to NH4 is reduced during hypoxia [35], it is accumulated in the cytosol [30,65] or released to the external medium [66]. The accumulated NO2 can serve as an alternative electron acceptor at mitochondrial electron transport chain (ETC), with NO as a significant product of the reaction [52]. Moreover, the pathway of NO formation through NO3-NO2 in the mitochondria contributes to the ATP synthesis [33,65,69]. The NO3-NO2-derived ATP production in mitochondria can make an important contribution to hypoxia survival [70]. Although NO is a signaling molecule [27,28,29,30], an excess of NO in the mitochondria can be toxic to the cell and may result in the death of the cell [71]. Although N2O is a potent greenhouse gas, the conversion of NO to N2O by cytochrome c oxidase [26,48] might play an important role in maintaining the integrity of mitochondria during limited oxygen conditions, as an excess of NO can be toxic to the cell [71]. So, the high emissions of N2O from rice plants during limited oxygen conditions, as reported by Yan et al., (2000) [13] might be an efficient mechanism to reduce the toxicity of NO and to maintain the integrity of the mitochondria under hypoxia and anoxia, therefore, this should be a matter of further research.

5. Conclusions and Future Perspectives

In conclusion, NO3 is reduced to NO2 in the cytosol, and NO2 reduction to NO, along with NO reduction to N2O, occurs in the mitochondria of rice plants. The pathway of N2O formation is formed under hypoxic or anoxic conditions, and the water management practice may often cause hypoxia and anoxia in the rice root, making the rice plant a potent source of N2O. Therefore, we suggest that, while studying N2O emission from paddies, the potential pathway of N2O formation in rice plants should be explored. To date, the rice plant is hypothesized to be a medium to transport the N2O produced in the soil by microorganisms. However, recent studies suggest that plants can produce N2O, which may be during the metabolism of NO to N2O in plant mitochondria [30], as shown in this study. The significant amount of N2O emitted from rice plants suggests the possibility of the existence of the proposed pathway of N2O formation in rice plants. Furthermore, the NO3-NO2-derived NO formation pathway in the hypoxic and anoxic rice plant’s mitochondria helps the ATP synthesis and develop a tolerance to limited oxygen conditions. The rice plant, being an anoxia-tolerant plant, in which NO2 dependent NO production in mitochondria was sustained for almost twice as long as barley [67], suggests that these plants might be a more potent producer of N2O. However, to date, N2O emitted from the paddy is regarded as being produced by various microbes [10,21] and the N2O formation pathway in plants is neglected. Future studies are certainly required to elaborate on the proposed pathway of N2O formation in the rice plant. Furthermore, the transport of soil-produced N2O by plants, as hypothesized by many experiments [12,13], is not supported because there are no emissions of N2O by plants when supplied with NH4 and during a high rate of N2O production in the rhizosphere [15]. So, it would be misleading to understand the N2O emitted by the rice plant to be soil microorganism-produced. Understanding the role of the rice plant is necessary for further strategies to be taken to mitigate N2O emissions from the paddy. Quantifying the dual isotopocule fingerprint of N2O, along with the molecular-based studies, would provide clear insights into the proposed mechanism. Therefore, the extraction of rice mitochondria and the measuring of NO and N2O emissions under different conditions of O2 and NO3 would provide insights into the N2O pathway. Besides, the reduced form of cytochrome c oxidase and quinone are found to catalyze NO reduction to N2O and, therefore, their roles in rice plants should be investigated in detail. Moreover, to differentiate the soil sources from the plant source and quantify the portion of soil and plant contributions to total emissions will be a big challenge with the current approach to the methodology used. The development of static chambers that could capture the fluxes of N2O from the rice plant and separate the soil emissions would help to evaluate the rice plant’s role in the total emissions.

Author Contributions

A.T. and C.H. designed the concept. F.B., B.P., R.K.P.Y. and W.D. commented on the first draft of the manuscript. All the authors confirmed the final version of the manuscript. All authors have read and agreed to the published version of the manuscript

Funding

This study was supported by funding from the Key Program of National Natural Science Foundation of China (Grant No. 41530859) and National Key Research and Development Program of China (2016YFD0800102-4 and 2018YFC0213300-01).

Acknowledgments

Arbindra Timilsina is thankful to CAS-TWAS fellowship for granting the PhD scholarship. We are also grateful to Prof. Oene Oenema for his valuable comments. We are also thankful to the reviewers for their constructive comments and suggestions.

Conflicts of Interest

The authors declare no conflicts of interest.

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Plants 09 00180 g001 550
Figure 1. The potential pathway of N2O formation in rice plants under hypoxic conditions. ?? sign represents the involvement of two or more enzymes [9,23,27,44,48,52].
Figure 1. The potential pathway of N2O formation in rice plants under hypoxic conditions. ?? sign represents the involvement of two or more enzymes [9,23,27,44,48,52].
Plants 09 00180 g001

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Timilsina, A.; Bizimana, F.; Pandey, B.; Yadav, R.K.P.; Dong, W.; Hu, C. Nitrous Oxide Emissions from Paddies: Understanding the Role of Rice Plants. Plants 2020, 9, 180. https://doi.org/10.3390/plants9020180

AMA Style

Timilsina A, Bizimana F, Pandey B, Yadav RKP, Dong W, Hu C. Nitrous Oxide Emissions from Paddies: Understanding the Role of Rice Plants. Plants. 2020; 9(2):180. https://doi.org/10.3390/plants9020180

Chicago/Turabian Style

Timilsina, Arbindra, Fiston Bizimana, Bikram Pandey, Ram Kailash Prasad Yadav, Wenxu Dong, and Chunsheng Hu. 2020. "Nitrous Oxide Emissions from Paddies: Understanding the Role of Rice Plants" Plants 9, no. 2: 180. https://doi.org/10.3390/plants9020180

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