Next Article in Journal
Application of Gene Editing Technology in Resistance Breeding of Livestock
Next Article in Special Issue
Elevated CO2 and Increased N Intensify Competition between Two Invasive Annual Plants in China
Previous Article in Journal
Intravenous Thrombolysis for Acute Ischemic Stroke during the COVID-19 Pandemic—Polish Single-Center Retrospective Cohort Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Different Responses of Invasive Weed Alternanthera philoxeroides and Oryza sativa to Plant Growth Regulators

1
School of Agricultural Engineering, Jiangsu University, Zhenjiang 212013, China
2
School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013, China
*
Author to whom correspondence should be addressed.
Life 2022, 12(7), 1069; https://doi.org/10.3390/life12071069
Submission received: 24 June 2022 / Revised: 10 July 2022 / Accepted: 12 July 2022 / Published: 17 July 2022
(This article belongs to the Special Issue Interaction between Invasive and Native Plants)

Abstract

:
Invasive plants cause a global loss of biodiversity, pose a major threat to the environment and economy, and also significantly affect agricultural production and food security. Plant growth regulators (PGRs) are widely used in agricultural production and might also affect invasive weeds distributed around crops in various ways. At present, there are few studies concerning whether there are significant effects of PGRs on invasive weeds. In this study, two widely used PGRs in paddy fields, gibberellic acid (GA) and paclobutrazol (PAC), were applied on Oryza sativa and a noxious weed Alternanthera philoxeroides, which is frequently distributed in paddy fields. The purpose of this study was to investigate if there are different responses of rice and weeds to these two plant regulators and the significant effects of PGRs on invasive weeds. The results showed that GA significantly promotes the total biomass of A. philoxeroides by 52.00%, but does not significantly affect that of O. sativa. GA significantly increases the growth of aboveground and belowground A. philoxeroides, but not that of O. sativa. On the other hand, PAC extremely inhibited the aboveground and belowground biomass of A. philoxeroides by more than 90%, but did not significantly inhibit the belowground biomass of O. sativa. PAC also enhanced the leaf nitrogen content and chlorophyll content of A. philoxeroides, but not the traits of O. sativa. Therefore, the effects of PGRs are significantly different between rice and the invasive weed. The potential promotion effects of PGRs on weeds that are frequently distributed in farmland warrant sufficient attention. This is probably one of the important reasons why invasive weeds can successfully invade the agricultural ecosystem with large human disturbance. This study might sound an alarm for weed control in paddy fields.

1. Introduction

The invasion of alien species leads to the loss of biodiversity, disrupts the stability of ecosystems, and poses a major threat to the environment and economy [1,2,3]. Invasive plant species lead to huge losses in global agriculture and adversely affect food security [4]. Invasive weeds are regarded as a major threat to global agriculture [5], and have many negative effects on crops, including competition with native plants for resources, rapid growth, and they could be host plants for pests and pathogens [6].
Alternanthera philoxeroides (alligator weed), native to South America, is a clonal weed in the family of Amaranthaceae and was introduced into China in the 1930s [7]. This species has become an invasive plant of global proportions, spreading to more than 30 countries [8]. A. philoxeroides has now invaded a variety of different ecosystems, including wetland ecosystems, lake ecosystems, and farmland ecosystems [9,10].
Rice (Oryza sativa) is the main crop and the staple food of an estimated 3.5 billion people all over the world. It is the most cultivated and renowned agricultural crop around the world [11]. More than 80% of rice is produced in Asia, and China is the world’s largest producer of rice [12]. However, it is reported that invasive weeds represent one of the most important factors affecting rice yield [13]. Alligator weed is also considered a harmful weed in China’s rice fields [14,15]. We found that A. philoxeroides is particularly common in rice paddies (Figure 1). Alligator weed has been reported to seriously reduce the yield of rice, maize, and vegetable crops [16,17,18]. Currently, most of the research on A. philoxeroides focuses on its growth characteristics and how to control and reduce its harmful effects on the environment. Ge et al. (2018) found that A. philoxeroides could inhibit the growth of native plants via allelopathic effects on soil enzyme activity and the microbial community [19].
Plant growth regulators (PGRs) are widely used in agricultural ecosystems and play an important role in improving crop yield [20]. Plant growth and development, insect resistance, and disease resistance are regulated by various PGRs [21]. Gibberellin (GA) plays an important role in the process of plant growth and development; it can promote seed germination, vegetative growth, and fruit development [22,23]. GA plays a key role in inhibiting leaf senescence, which can improve tomato yield by inhibiting leaf senescence in a stressful environment [24]. GA is a stimulant for deep-water Oryza sativa, which survives in water by promoting internode elongation [25]. However, for common O. sativa or wheat, GA may lead to excessive internode lodging and reduced yield. Tang et al. (2021) found that wheat with GA-insensitive genes achieved success in increasing yield [26]. Compared with GA, paclobutrazol (PAC), a GA biosynthesis inhibitor [27], has been widely used in rice fields because it can inhibit plant elongation and dwarf plants, thus increasing plant density and resistance to overwhelming, and it improves rice yield and quality [28,29]. When PGRs are applied to rice field crops, they may be directly sprayed on invasive weeds around crops or absorbed by invasive weeds from soil due to rainfall infiltration [30,31]. Therefore, the application of PGRs may also affect the growth of invasive weeds in farmland, which may cause serious harm to agricultural ecosystems. Previous studies have reported that fertilizer applied to crops might affect the invasion of weeds in farmland. Wan et al. (2012) found that long-term fertilization resulted in the growth of invasive weeds in fields and increased the biomass of invasive weeds [32]. However, the effects of PGRs on invasive weeds in farmland are not given enough attention. During the growing season, A. philoxeroides in paddy fields is often exposed to PGRs, such as GA and PAC. However, the effects of these PGRs on A. philoxeroides have not been fully studied. Considering the different effects of GA and PAC on plant growth, we investigated the response of A. philoxeroides and O. sativa to two identical concentrations of PGRs (GA and PAC). We addressed the following questions: (1) Do A. philoxeroides and O. sativa have different response abilities to these two PGRs? (2) Do these two PGRs significantly affect the growth of A. philoxeroides?

2. Materials and Methods

2.1. Experimental Materials

A. philoxeroides fragments were collected from a greenhouse of Jiangsu University, Zhenjiang, China. Seeds of japonica rice were purchased from a local seed company. Stem segments of A. philoxeroides with two nodes and 10 cm height seedlings of O. sativa germinated from seeds were selected for the experiment. The stem segments of A. philoxeroides and O. sativa seedlings were placed in plastic flowerpots (9 × 6 × 7.5 cm), which were filled with washed, sterilized, and dried river sand.
In order to study the effect of PGRs on the growth of A. philoxeroides and O. sativa, 50 mL of 30 μM GA and 30 μM PAC were applied to A. philoxeroides segments and O. sativa seedlings, respectively. The concentrations of GA and PAC were used as they are utilized in rice fields to increase crop yields [33] and prevent lodging [34] in paddy fields. The same volume of distilled water was added as a control treatment (CK). There were six treatments in this experiment: two plant species (A. philoxeroides and O. sativa) with three hormone treatments (CK, GA, PAC), and seven replications for each treatment. There were 21 A. philoxeroides stems and 21 O. sativa seedlings, with one stem or seedling per pot, planted in 42 plastic pots containing 100 g of sand and vermiculite (weight ratio: 2:1). All the plants were randomly arranged in the greenhouse and rotated once per week with natural light. Hoagland’s nutrient solution was added to seedlings every week to meet plant nutritional needs. In this study, PGRs were directly applied to the base of A. philoxeroides to simulate what might happen under natural conditions in which rain erosion and soil infiltration may expose PGRs to the base of plants.

2.2. Growth Trait Measurements

All the plants were harvested after two months of growth. Various growth indicators of the plants were measured, including plant height, root length, leaf nitrogen content, relative chlorophyll content, root area, root volume, aboveground dry mass, and belowground dry mass, and the total dry mass was calculated. The plant height and root length were measured with a ruler, the stem base of the plant was measured with a vernier caliper, and the relative chlorophyll content and leaf nitrogen content were measured with a SPAD-502 chlorophyll content analyzer. Root area and root volume were measured with the WinRHIZO root scanner system. The harvested plant material was dried in a constant temperature drying oven at 80 °C for 72 h, and the dry mass was determined.

2.3. Data Analysis

SPSS software was used for the statistical analysis of the data, and Tukey’s honest significant test (HSD) was used to compare the differences in the growth of A. philoxeroides and O. sativa among PGR treatments.

3. Results

3.1. Responses of Alternanthera philoxeroides and O. sativa to PGR

The results showed that PGRs have significant effects on most growth indicators of A. philoxeroides and O. sativa (Table 1).
Compared with O. sativa, A. philoxeroides is more sensitive to these two PGRs. GA significantly promoted the biomass of A. philoxeroides by 52.00% but had no effects on the biomass of O. sativa (Figure 2). The application of PAC decreased the total biomass of A. philoxeroides by 90.13%, and also significantly decreased that of O. sativa by 51.38% (Figure 2).

3.2. Responses of Alternanthera philoxeroides and Oryza sativa to PGRs in Aboveground Growth

The results showed that the application of GA significantly promoted the plant height of A. philoxeroides and O. sativa, while the application of PAC significantly inhibited the plant height of A. philoxeroides and O. sativa (Figure 3a). The same concentration of PAC extremely inhibited the plant height of A. philoxeroides by 96.16%, and inhibited that of O. sativa by 48.60%.
GA significantly increased the aboveground biomass of A. philoxeroides (Figure 3b). However, compared with the control treatment, the aboveground biomass of O. sativa was not significantly affected by GA application (Figure 3b). Meanwhile, PAC significantly inhibited the aboveground biomass of A. philoxeroides and O. sativa. However, PAC extremely inhibited the aboveground biomass of A. philoxeroides by 91.13%, and inhibited the aboveground biomass of O. sativa by 51.38%.

3.3. Responses of Alternanthera philoxeroides and Oryza sativa to PGRs in Belowground Growth

GA slightly, but not significantly, increased the root length of A. philoxeroides, and it slightly inhibited the root length of O. sativa. PAC had a significant inhibitory effect on the root length of both plant species (Figure 4a).
The application of GA significantly promoted the belowground biomass of A. philoxeroides, and the PAC treatment significantly inhibited the belowground biomass of A. philoxeroides. However, both PGRs had no significant effects on the belowground biomass of O. sativa (Figure 4b).
For the morphology traits of roots, GA significantly increased the root area of A. philoxeroides, while GA had no significant effect on O. sativa (Figure 5a,b). PAC significantly reduced the root area of both two plant species (Figure 5a,b). Compared with the control treatment, GA significantly increased the root volume of A. philoxeroides and PAC significantly inhibited the root volume of A. philoxeroides. However, both PGRs had no significant effect on the root volume of O. sativa (Figure 5a,c).

3.4. Response of Alternanthera philoxeroides and Oryza sativa to PGRs in Physiological Traits

In terms of physiological indicators, GA had no significant effect on leaf nitrogen content or relative chlorophyll content of A. philoxeroides, while PAC significantly increased these two physiological traits of A. philoxeroides. However, leaf nitrogen content and relative chlorophyll content of O. sativa were not significantly changed after the application of these two PGRs (Figure 6).

4. Discussion

The results of this study show that the responses of A. philoxeroides and O. sativa are quite different for the two PGRs, GA and PAC. Furthermore, these two PGRs have significant effects on the growth of A. philoxeroides.
PGRs are among the important components of agricultural production. They play important roles in promoting crop development and improving crop yields. They have been widely used in agriculture systems all over the world [35,36]. GA plays an important role in promoting plant growth and shoot elongation [37]. In this study, we found that GA significantly elongated both the invasive weed A. philoxeroides and the crop O. sativa. However, GA significantly enhanced both the biomass and the root morphology of the invasive weed, but not the biomass or root morphology of the rice crop. The growth of A. philoxeroides was more sensitive than rice to the same concentration of GA. Previous studies have found that GA has stronger effects on invasive plants [38], which is consistent with our results. From the physiology traits results, the addition of exogenous GA significantly inhibited leaf nitrogen content and chlorophyll content of O. sativa. It is reported that DELLAs, which negatively regulate gibberellin signaling to repress GA-mediated responses, positively regulate chlorophyll biosynthesis [39]. However, GA did not inhibit the chlorophyll content of A. philoxeroides. These might contribute to the photosynthesis of the invasive weed and promote its growth and development.
Our results showed that the effects of PAC, a synthetic inhibitor of GA, on the growth of A. philoxeroides and O. sativa are completely opposite to GA. PAC significantly inhibited shoot elongation and biomass of both plants. The addition of PAC to A. philoxeroides also significantly inhibited its belowground biomass. Dai et al. (2016) found that PAC inhibited the aboveground and belowground growth of an invasive plant, Sphagneticola trilobata [40], which is consistent with what we found. However, the belowground biomass of O. sativa treated with PAC did not change significantly. The effect of PAC on the growth of belowground also changed due to different species [41,42]. Consistent with this, the belowground growth of A. philoxeroides and O. sativa responds differently to PAC. In this case, although PAC inhibited the biomass of A. philoxeroides, the leaf nitrogen content and chlorophyll content of A. philoxeroides were significantly increased with PAC application. PAC induction in plants leads to the reduction in endogenous GA content [43,44,45]. Endogenous GA is extremely important when encountering biotic or abiotic stress. Endogenous GA reduction might increase flavonoid content in plants [46] and contribute to improving plant ability to resist stress [47]. Therefore, the chlorophyll and leaf nitrogen increasing due to PAC application might affect plant resistance to abiotic or biotic stress. Furthermore, some studies showed that PGRs increased the resistance of invasive weed A. philoxeroides to pathogenic bacteria and promoted its invasion [48]. Meanwhile, as a clonal plant [49], the clonal integration of A. philoxeroides improves its competitiveness [50]. Furthermore, there are other chemicals such as fertilizers applied in paddy fields affecting the growth of invasive weeds [51,52]. These chemicals might not only affect the growth but also the resistance to biotic or abiotic stresses of invasive weeds [53].
In the present study, we found that A. philoxeroides responded stronger to PGRs than O. sativa. According to present results, PGRs significantly affected the weed growth, and this might be one of the important factors contributing to the invasive weed’s rapid growth and spread in paddy fields. The effects of PGRs on invasive weeds should be seriously considered when planning for the prevention and control of invasive clonal species in agricultural and natural ecosystems.

5. Conclusions

In the present study, we confirmed that A. philoxeroides and O. sativa respond differently to PGRs, and PGRs significantly affected the growth of invasive weeds. Thus, the effects of PGRs on plant growth might be species-specific; more research is needed to provide further insights into PGRs, including different responding mechanisms to PGRs between invasive weeds and crops. The impacts of PGRs on invasive weeds have been rarely studied; however, the application of PGRs in farmland may lead to potential harmful effects on the agriculture system, including invasive weeds’ fast growth, which should be seriously considered. Thus, we appeal against the abuse of PGRs in paddy fields. On the other hand, since invasive weeds are more sensitive to PGRs than rice, genetic engineering, such as RNA interference technology, could be used to block plant hormone signaling pathways to control invasive weeds.

Author Contributions

Conceptualization, S.Q. and Z.D.; methodology, J.W.; formal analysis, S.Q. and J.W.; data curation, J.W., D.H. and G.R.; writing—original draft preparation, J.W. and S.Q.; writing—review and editing, J.W., S.Q., Z.D. and D.D.; visualization, J.W., X.S. and J.L.; supervision, S.Q. and Z.D.; project administration, S.Q. and Z.D.; funding acquisition, S.Q., Z.D. and D.D. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Natural Science Foundation of China (32171509, 32071521), Jiangsu Planned Projects for Postdoctoral Research Funds (2021K160B, 2021K384C), the Natural Science Foundation of Jiangsu Province (BK20211321), and the Jiangsu College Student Innovation Training Program (202210299150Y). Part of the funding for this research was supported by Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD) and Youth Talent Cultivation Program of Jiangsu University.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author (e-mail: qishanshan1986120@163.com).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Rockström, J.; Steffen, W.; Noone, K.; Persson, Å.; Chapin, F.S.; Lambin, E.F.; Timothy, M.L.; Marten, S.; Carl, F.; Hans, J.S.; et al. A safe operating space for humanity. Nature 2009, 461, 472–475. [Google Scholar] [CrossRef] [PubMed]
  2. Oliveira, C.M.; Auad, A.M.; Mendes, S.M.; Frizzas, M.R. Crop losses and the economic impact of insect pests on Brazilian agriculture. Crop Prot. 2014, 56, 50–54. [Google Scholar] [CrossRef] [Green Version]
  3. Pimentel, D.; McNair, S.; Janecha, J. Economic and environmental threats of alien plant, animal, and microbe invasion. Agric. Ecosyst. Environ. 2001, 84, 1–20. [Google Scholar] [CrossRef]
  4. Cook, D.C.; Fraser, R.W.; Paini, D.R.; Warden, A.C.; Lonsdale, W.M.; De Barro, P.J. Biosecurity and yield improvement technologies are strategic complements in the fight against food insecurity. PLoS ONE 2011, 6, e26084. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Paini, D.R.; Sheppard, A.W.; Cook, D.C.; De Barro, P.J.; Worner, S.P.; Thomas, M.B. Global threat to agriculture from invasive species. Proc. Natl. Acad. Sci. USA 2016, 113, 7575–7579. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Torres, C.; Mimosa, M.; Ferreira, M.F.; Galetto, L. Reproductive strategies of Datura ferox, an abundant invasive weed in agro-ecosystems from central Argentina. Flora 2013, 208, 253–258.7. [Google Scholar] [CrossRef]
  7. Wu, H.; Zhang, C.; Dai, W.K. Interactive effects of climate warming and species diversity on the invasiveness of the alien weed Alternanthera philoxeroides. Acta Prataculturae Sin. 2020, 29, 38–48. (In Chinese) [Google Scholar]
  8. Geng, Y.P.; Pan, X.Y.; Xu, C.Y.; Zhang, W.J.; Li, B.; Chen, J.K. Phenotypic plasticity of invasive Alternanthera philoxeroides in relation to different water availability, compared to its native congener. Acta Oecol. 2006, 30, 380–385. [Google Scholar] [CrossRef]
  9. Chen, Y.; Zhou, Y.; Yin, T.F.; Liu, C.X.; Luo, F.L. The invasive wetland plant Alternanthera philoxeroides shows a higher tolerance to waterlogging than its native congener Alternanthera sessilis. PLoS ONE 2013, 8, e81456. [Google Scholar] [CrossRef]
  10. Deng, H.; Ye, Z.H.; Wong, M.H. Lead and zinc accumulation and tolerance in populations of six wetland plants. Environ. Pollut. 2006, 141, 69–80. [Google Scholar] [CrossRef]
  11. He, X.Q.; Qiao, Y.H.; Liang, L.; Knudsen, M.T.; Martin, F. Environmental life cycle assessment of long-term organic rice production in subtropical China. J. Clean Prod. 2018, 176, 880–888. [Google Scholar] [CrossRef]
  12. Ahmed, T.; Noman, M.; Luo, J.Y.; Muhammad, S.; Shahid, M.; Ali, M.A.; Zhang, M.C.; Li, B. Bioengineered chitosan-magnesium nanocomposite: A novel agricultural antimicrobial agent against Acidovorax oryzae and Rhizoctonia solani for sustainable rice production. Int. J. Biol. Macromol. 2021, 168, 834–845. [Google Scholar] [CrossRef] [PubMed]
  13. Vigueira, C.C.; Olsen, K.M.; Caicedo, A.L. The red queen in the corn: Agricultural weeds as models of rapid adaptive evolution. Heredity 2013, 110, 303–311. [Google Scholar] [CrossRef]
  14. Mahajan, G.; Timsina, J. Effect of nitrogen rates and weed control methods on weeds abundance and yield of direct-seeded rice. Arch. Agron. Soil Sci. 2011, 57, 239–250. [Google Scholar] [CrossRef]
  15. Zhang, J.X.; Li, C.H.; Lou, Y.L.; Deng, Y.Y.; Qiu, C.Y. Studies on the transplanting rice yield loss caused by weed Alternanthera philoxeroides and its economic threshold. Acta Agric. Shanghai. 2004, 20, 95–98. (In Chinese) [Google Scholar]
  16. Andres, A.; Concenco, G.; Theisen, G.; Vidotto, F.; Ferrero, A. Selectivity and weed control efficacy of pre- and post-emergence applications of clomazone in Southern Brazil. Crop Prot. 2013, 53, 103–108. [Google Scholar] [CrossRef]
  17. Li, L.G. Occurrence and damages of alligator weed in vegetable fields. Weed Sci. 1992, 1, 13–15. [Google Scholar]
  18. Mehmood, A.; Tanveer, A.; Javed, M.M.; Nadeem, M.A.; Naeem, M.; Abbas, T. Estimation of economic threshold level of alligator weed (Alternanthera philoxeroides (Mart.) Griseb.) to tackle grain quality and yield losses in rice. Arch. Agron. Soil Sci. 2018, 64, 208–218. [Google Scholar] [CrossRef]
  19. Ge, Y.Y.; Wang, Q.L.; Wang, L.; Liu, W.X.; Liu, X.Y.; Huang, Y.J.; Christie, P. Response of soil enzymes and microbial communities to root extracts of the alien Alternanthera philoxeroides. Arch. Agron. Soil Sci. 2017, 64, 708–717. [Google Scholar] [CrossRef]
  20. Rademacher, W. Plant growth regulators: Backgrounds and uses in plant production. J. Plant Growth Regul. 2015, 34, 845–872. [Google Scholar] [CrossRef]
  21. Ruth, E.; Luke, R.; Patrick, S. Hormones as go-betweens in plant microbiome assembly. Plant J. 2021, 105, 518–541. [Google Scholar]
  22. Linkies, A.; Leubner-Metzger, G. Beyond gibberellins and abscisic acid: How ethylene and jasmonates control seed germination. Plant Cell Rep. 2012, 31, 253–270. [Google Scholar] [CrossRef] [PubMed]
  23. Ruan, Y.L.; Patrick, J.W.; Bouzayen, M.; Osorio, S.; Fernie, A.R. Molecular regulation of seed and fruit set. Trends Plant Sci. 2012, 17, 656–665. [Google Scholar] [CrossRef] [Green Version]
  24. Mohammad, S.J.; Sheng, S.; Wang, Y.; Hasan, M.M.; El-Yazied, A.A.; Alabdallah, N.M.; Hajjar, D.; Muhammad, A.A.; Sun, J.; Guo, S.R. Melatonin pretreatment confers heat tolerance and repression of heat-induced senescence in tomato through the modulation of ABA-and GA-mediated pathways. Front. Plant Sci. 2021, 381, 650955. [Google Scholar]
  25. Kuroha, T.; Nagai, K.; Gamuyao, R.; Wang, D.R.; Furuta, T.; Nakamori, M.; Kitaoka, T.; Adachi, K.; Minami, A.; Mori, Y.; et al. Ethylene-gibberellin signaling underlies adaptation of rice to periodic flooding. Science 2018, 361, 181–186. [Google Scholar] [CrossRef] [Green Version]
  26. Tang, T.; Acuna, T.B.; Spielmeyer, W.; Richards, R.A. Effect of gibberellin-sensitive Rht18 and gibberellin-insensitive Rht-D1b dwarfing genes on vegetative and reproductive growth in bread wheat. J. Exp. Bot. 2021, 72, 445–458. [Google Scholar] [CrossRef] [PubMed]
  27. Hedden, P.; Graebe, J. Inhibition of gibberellin biosynthesis by paclobutrazol in cell-free homogenates of Cucurbita maxima endosperm and Malus pumila embryos. J. Plant Growth Regul. 1985, 4, 111–122. [Google Scholar] [CrossRef]
  28. Peng, D.L.; Chen, X.G.; Yin, Y.P.; Lu, K.L.; Yang, W.B.; Tang, Y.H.; Wang, Z.L. Lodging resistance of winter wheat (Triticum aestivum L.): Lignin accumulation and its related enzymes activities due to the application of paclobutrazol or gibberellin acid. Field Crop Res. 2014, 157, 1–7. [Google Scholar] [CrossRef]
  29. Yeshitela, T.; Robbertse, P.J.; Stassen, P.J.C. Paclobutrazol suppressed vegetative growth and improved yield as well as fruit quality of ‘Tommy Atkins’ mango (Mangifera indica) in Ethiopia. N. Z. J. Crop Hortic. 2004, 32, 281–293. [Google Scholar] [CrossRef]
  30. Wu, C.; Sun, J.Q.; Zhang, A.P.; Liu, W.P. Dissipation and enantioselective degradation of plant growth retardants paclobutrazol and uniconazole in open field, greenhouse, and laboratory soils. Environ. Sci. Technol. 2013, 47, 843–849. [Google Scholar] [CrossRef]
  31. Zhao, M.; Shao, F.B.; Zhou, S.X.; Cui, Y.H. Safety of plant growth regulators to crops and environment. J. Environ. Health 2007, 24, 370–372. [Google Scholar]
  32. Wan, K.Y.; Tao, Y.; Li, R.H.; Pan, J.F.; Tang, L.L.; Chen, F. Influences of long-term different types of fertilization on weed community biodiversity in rice paddy fields. Weed Biol. Manag. 2012, 12, 12–21. [Google Scholar] [CrossRef]
  33. Liu, Y.; Chen, W.P.; Ding, Y.F.; Wang, Q.S.; Li, G.H.; Wang, S.H. Effect of Gibberellic acid (GA3) and α-naphthalene acetic acid (NAA) on the growth of unproductive tillers and the grain yield of rice (Oryza sativa L.). Afr. J. Agric. Res. 2012, 7, 534–539. [Google Scholar]
  34. Du, Y.F.; Fang, X.L.; Zeng, H.L.; Yu, Y.F.; Zhang, L.Q.; Wang, Y. Effects of exogenous paclobutrazol, ABA, 2,4-D, and NAA on growth characteristics of rice seedlings. Mol. Plant Breed. 2020, 18, 2687–2694. (In Chinese) [Google Scholar]
  35. Abdelgadir, H.A.; Johnson, S.D.; Johannes, V.S. Promoting branching of a potential biofuel crop Jatropha curcas L. by foliar application of plant growth regulators. Plant Growth Regul. 2009, 58, 287–295. [Google Scholar] [CrossRef]
  36. Anjum, S.A.; Wang, L.C.; Farooq, M.; Hussain, M.; Xue, L.L.; Zou, C.M. Brassinolide application improves the drought tolerance in Maize through modulation of enzymatic antioxidants and leaf gas exchange. J. Agron. Crop Sci. 2011, 197, 177–185. [Google Scholar] [CrossRef]
  37. Hedden, P.; Thomas, S.G. Gibberellin biosynthesis in higher plants. Ann. Plant Rev. Online 2016, 49, 37–72. [Google Scholar]
  38. Liu, Y.J.; Oduor, A.M.O.; Dai, Z.C.; Gao, F.L.; Li, J.N.; Zhang, X.; Yu, F.H. Suppression of a plant hormone gibberellin reduces growth of invasive plants more than native plants. Oikos 2021, 130, 781–789. [Google Scholar] [CrossRef]
  39. Liu, X.Q.; Li, Y.; Zhong, S.W. Interplay between light and plant hormones in the control of Arabidopsis seedling chlorophyll biosynthesis. Front. Plant Sci. 2017, 8, 1433. [Google Scholar] [CrossRef] [Green Version]
  40. Dai, Z.C.; Fu, W.; Qi, S.S.; Zhai, D.L.; Chen, S.C.; Wan, L.Y.; Huang, P.; Du, D.L. Different responses of an invasive clonal plant Wedelia trilobata and its native congener to gibberellin: Implications for biological invasion. J. Chem. Ecol. 2016, 42, 85–94. [Google Scholar] [CrossRef]
  41. Kamran, M.; Su, W.N.; Ahmad, I.; Meng, X.P.; Cui, W.W.; Zhang, X.D.; Mou, S.W.; Khan, A.; Han, Q.F.; Liu, T.N. Application of paclobutrazol affect maize grain yield by regulating root morphological and physiological characteristics under a semi-arid region. Sci. Rep. 2018, 8, 4818. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Abbas, A.; Huang, P.; Du, Y.; Hussain, S.; Shen, F.; Wang, H.; Du, D. Invasive plant alligator weed (Alternanthera philoxeroides (Mart.) Griseb.) performs better to salinity, drought and abscisic acid stresses than native plant sessile joy weed (Alternanthera sessilis (L.)). Appl. Ecol. Env. Res. 2022, 20, 1173–1187. [Google Scholar] [CrossRef]
  43. Bultynck, L.; Lambers, H. Effects of applied gibberellic acid and paclobutrazol on leaf expansion and biomass allocation in two Aegilops species with contrasting leaf elongation rates. Physiol. Plant 2004, 122, 143–151. [Google Scholar] [CrossRef]
  44. Rademacher, W. Growth retardants: Effects on gibberellin biosynthesis and other metabolic pathways. Annu. Rev. Plant Physiol. Plant Mol. Biol. 2000, 51, 501–531. [Google Scholar] [CrossRef] [Green Version]
  45. Noushina, I.; Khan, N.A.; Antonio, F.; Alice, T.; Alessandra, F.; Khan, M.I.R. Ethylene role in plant growth, development and senescence: Interaction with other phytohormones. Front. Plant Sci. 2017, 08, 475. [Google Scholar]
  46. Sun, H.; Cui, H.; Zhang, J.; Kang, J.; Long, R. Gibberellins inhibit flavonoid biosynthesis and promote nitrogen metabolism in Medicago truncatula. Int. J. Mol. Sci. 2021, 22, 9291. [Google Scholar] [CrossRef] [PubMed]
  47. Gill, U.S.; Uppalapati, S.R.; Gallego-Giraldo, L.; Ishiga, Y.; Dixon, R.A.; Mysore, K.S. Metabolic flux towards the (iso)flavonoid pathway in lignin modified alfalfa lines induces resistance against Fusarium oxysporum f. sp. medicaginis. Plant Cell Environ. 2018, 41, 1997–2007. [Google Scholar]
  48. Manoharan, B.; Qi, S.S.; Dhandapani, V.; Chen, Q.; Rutherford, S.; Wan, J.S.; Jegadeesan, S.; Yang, H.Y.; Li, Q.; Li, J.; et al. Gene expression profiling reveals enhanced defense responses in an invasive weed compared to its native congener during pathogenesis. Int. J. Mol. Sci. 2019, 20, 4916. [Google Scholar] [CrossRef] [Green Version]
  49. Qi, S.S.; Rutherford, S.; He, F.R.; Dong, B.C.; Zhu, B.; Dai, Z.C.; Fu, W.G.; Mao, H.P.; Du, D.L. Opposing effects of plant growth regulators via clonal integration on apical and basal performance in alligator weed. J. Plant Ecol. 2021, 15, 650–662. [Google Scholar] [CrossRef]
  50. Wang, P.; Alpert, P.; Yu, F.H. Physiological integration can increase competitive ability in clonal plants if competition is patchy. Oecologia 2021, 195, 199–212. [Google Scholar] [CrossRef]
  51. Jiang, M.; Liu, T.; Huang, N.; Shen, X.; Shen, M.; Dai, Q. Effect of long-term fertilisation on the weed community of a winter wheat field. Sci. Rep. 2018, 8, 4017. [Google Scholar] [CrossRef] [PubMed]
  52. Sweeney, A.E.; Renner, K.A.; Laboski, C.; Davis, A. Effect of fertilizer nitrogen on weed emergence and growth. Weed Sci. 2008, 56, 714–721. [Google Scholar] [CrossRef]
  53. Powles, S.B.; Yu, Q. Evolution in action: Plants resistant to herbicides. Annu. Rev. Plant Biol. 2010, 61, 317–347. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Alternanthera philoxeroides in a paddy field.
Figure 1. Alternanthera philoxeroides in a paddy field.
Life 12 01069 g001
Figure 2. Effects of plant growth regulators (GA and PAC) on total biomass of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Figure 2. Effects of plant growth regulators (GA and PAC) on total biomass of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Life 12 01069 g002
Figure 3. Effects of plant growth regulators (GA and PAC) on (a) plant height and (b) aboveground biomass of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Figure 3. Effects of plant growth regulators (GA and PAC) on (a) plant height and (b) aboveground biomass of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Life 12 01069 g003
Figure 4. Effects of plant growth regulators (GA and PAC) on (a) root length and (b) belowground biomass of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Figure 4. Effects of plant growth regulators (GA and PAC) on (a) root length and (b) belowground biomass of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Life 12 01069 g004
Figure 5. Effects of plant growth regulators (GA and PAC) on (a) root morphology (b) root area and (c) root volume of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Figure 5. Effects of plant growth regulators (GA and PAC) on (a) root morphology (b) root area and (c) root volume of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Life 12 01069 g005
Figure 6. Effects of plant growth regulators (GA and PAC) on (a) leaf nitrogen content and (b) chlorophyll content of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Figure 6. Effects of plant growth regulators (GA and PAC) on (a) leaf nitrogen content and (b) chlorophyll content of Alternanthera philoxeroides and Oryza sativa. CK represents the control treatment. Bars show mean ± SE (n = 7). Different letters indicate significant differences (p < 0.05) among the three treatments of PGRs.
Life 12 01069 g006
Table 1. The effects of PGRs on the growth of Alternanthera philoxeroides and Oryza sativa (7 replications).
Table 1. The effects of PGRs on the growth of Alternanthera philoxeroides and Oryza sativa (7 replications).
SpeciesTraitsdfFpMseMstCov
Alternanthera philoxeroidesPlant height274.048<0.00143.7733241.28675.606%
Root length227.774<0.0017.995222.04041.300%
Aboveground biomass293.935<0.0010.0191.82672.317%
Belowground biomass241.677<0.0010.0070.28975.742%
Biomass296.455<0.0010.0373.56372.071%
Chlorophyll content212.450<0.00129.997373.45319.162%
Leaf nitrogen content212.015<0.0010.1561.86916.380%
Proj-area258.984<0.001115.3916806.28067.265%
Root volume231.239<0.0010.40212.55683.137%
Oryza sativaPlant height2161.890<0.0014.079660.33335.277%
Root length25.9770.01020.100120.14731.663%
Aboveground biomass222.586<0.0010.0010.01743.088%
Belowground biomass21.5310.2430.0000.00031.725%
Biomass213.285<0.0010.0020.02036.746%
Chlorophyll content24.0910.03428.028114.65220.768%
Leaf nitrogen content24.2590.0310.1350.57316.278%
Proj-area25.5540.01314.49580.50430.197%
Root volume22.3280.1260.0190.04335.366%
df = degrees of freedom, p = significance, Mse = mean of squares for error, Mst = mean of squares for treatment, Cov = coefficient of variation.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Wang, J.; Hu, D.; Shi, X.; Luo, J.; Ren, G.; Dai, Z.; Qi, S.; Du, D. Different Responses of Invasive Weed Alternanthera philoxeroides and Oryza sativa to Plant Growth Regulators. Life 2022, 12, 1069. https://doi.org/10.3390/life12071069

AMA Style

Wang J, Hu D, Shi X, Luo J, Ren G, Dai Z, Qi S, Du D. Different Responses of Invasive Weed Alternanthera philoxeroides and Oryza sativa to Plant Growth Regulators. Life. 2022; 12(7):1069. https://doi.org/10.3390/life12071069

Chicago/Turabian Style

Wang, Jiahao, Die Hu, Xinning Shi, Jing Luo, Guangqian Ren, Zhicong Dai, Shanshan Qi, and Daolin Du. 2022. "Different Responses of Invasive Weed Alternanthera philoxeroides and Oryza sativa to Plant Growth Regulators" Life 12, no. 7: 1069. https://doi.org/10.3390/life12071069

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