The vegetative growth and remediation potential of Rotala rotundifolia, a novel submerged aquatic plant, for eutrophic waters were investigated on different sediments, and under a range of nitrogen concentrations. Rotala Rotundifolia grew better on silt than on sand and gravel in terms of plant height, tiller number and biomass accumulation. Percent increment of biomass was enhanced at low water nitrogen (ammonium nitrogen concentration ≤10 mg/L). The maximum total nitrogen and total phosphorus removals in the overlying water were between 54% to 66% and 42% to 57%, respectively. Nitrogen contents in the sediments increased with increasing water nitrogen levels, whereas, nitrogen contents in the plant tissues showed no apparent regularity, and the greatest value was obtained at ammonium nitrogen concentration 15 mg/L. Both phosphorus contents in the sediments and tissues of plants were not affected significantly by additional nitrogen supply. Direct nitrogen uptake by plants was in the range of 16% to 39% when total phosphorus concentration was 1.0 mg/L. These results suggested that Rotala Rotundifolia can be used to effectively remove nitrogen and phosphorus in eutrophic waters.
Eutrophication resulted from excessive discharge of nutrients is still the most prevalent water problem in many countries all over the world1. Major nutrient sources include agricultural runoff2, domestic sewage3, industrial effluents4 and atmospheric dry and wet deposition5,6,7. High nutrient loads in water may cause rapid growth of algae, consequently, reduce or eliminate dissolved oxygen (DO) in the water, leading to death of large numbers of fish8,9. Most waters lost its primary functions due to deterioration of water quality and changes in ecological structures. Therefore, reduce and control nutrients in water is still an urgent issue10,11.
Submerged macrophytes are important components of freshwater ecosystem. They inhibit abundant growth of algae12, increase water transparency13, and provide food resources and habitats for aquatic animals14. The stems, leaves and epidermis of submerged macrophytes are capable of assimilating nutrients as roots15. Besides, they can retain sediments and limit the resuspension of nutrients to overlying water16. Thus, the nutrient levels are generally lower in waters dominated by submerged macrophytes17. The re-establishment of submerged vegetation is recognized as an efficient approach for improving water quality and restoring ecological functions of degraded aquatic ecosystem18.
However, many submerged macrophytes grow seasonally, and would die away. For example, Myriophyllum spicatum, Ceratophyllum demersum, and Vallisneria natans could not live through the winter, while Elodea nuttallii and Potamogeton crispus slow down their growth in June and gradually die away19. The decay process of the biomass releases nutrients that have been incorporated into the plant tissues to the overlying water again20. Furthermore, the debris of the plants would settle to the bottom of the water, leading to the pollution of sediments. Therefore, exploring and cultivating new species is of the great significance for ecological restoration and submerged aquatic plant diversity.
Rotala rotundifolia is a perennial aquatic plant with soft stems that branch often to form low, creeping clumps. This species has both submerged and emergent forms, which differs in a number of characteristics. The emergent form has fleshy, bright-green and rounded leaves, while the submerged has darker green or reddish leaves that are thin and lanceolate sword-shaped. It is not considered cold-tolerant, suitable for tropical aquariums with water temperature below 30 °C, but not lower than 21 °C21. However, the submerged Rotala rotundifolia found in the remote valley in Wenzhou city, Zhejiang Province, China, is able to survive across the winter under the temperature as low as 4 °C. Few reports were available on the growth characteristics and nutrient removal potential of this species. Therefore, the present study focused on the growth responses of this novel Rotala rotundifolia on different sediments (gravel, sand and silt), various concentrations of N (3, 5, 7, 10, and 15 mg/L), and the remediation performance for eutrophic waters with the aim of better understanding the characteristics of Rotala rotundifolia and providing data for its further application.
Materials and Methods
Growth characteristics on different sediments
Rotala rotundifolia (Fig. 1) was collected from the remote valley in Tianzhushan in Wenzhou City, China (Fig. 2), and rinsed to remove invertebrate grazers and cultured in the experimental plot for 45 days. Then the sturdy plants (approximately 45 cm in length) were transplanted to the batch cultures in plastic tanks (upper diameter 30.5 cm, lower diameter 25.5 cm, height 32 cm), containing 15 L of the eutrophic water. A stock solution of NH4Cl and KH2PO4 and 2% N and P free Hoagland solution were used to prepare the eutrophic water. Initial concentrations of ammonium nitrogen (NH4+-N) and total phosphorus (TP) were 5.0 mg/L and 0.3 mg/L, respectively. The composition of the Hoagland solution was based on Epstein22 as follows (in mM): K (KCl) 6, Ca (CaCl2) 4, Mg (MgSO4·7H2O) 1, B (H3BO3) 0.025, Mn (MnSO4·H2O) 0.002, Zn (ZnSO4·7H2O) 0.002, Cu (CuSO4·5H2O) 0.0005, Mo (H2MoO4) 0.0005, Fe (EDTA·FeNa) 0.02. Gravel, sand, and silt were selected in the experiment as they were typical sediments in waters: treatment 1 was gravel (5–8 mm); treatment 2 was sand (0.4–0.9 mm); treatment 3 was silt, each with triplicates. The silt was the dredged silt obtained from the river in November 2015. After being air-dried, silt was sieved through a 0.15 mm sieve to remove coarse debris, and mixed thoroughly. Nitrogen and phosphorus contents of the silt were 2.2 and 0.82 g/kg, respectively. The trial was conducted under natural light from 25 November 2015 to 16 January 2016 in a double-poly greenhouse. During the experiment, losses in water volume due to evaporation of treatment and control plots were compensated by addition of deionized water to the original level every other day. The length and tiller number of the plants, DO of the water were recorded every 10 days. The fresh weight of the plants was analyzed before and at the end of the trial.
Growth and purification performance on different water N levels
The sturdy plants (approximately 45 cm in length) were transplanted to the batch cultures in plastic tanks (upper diameter 30.5 cm, lower diameter 25.5 cm, height 32 cm), containing 15 L of the eutrophic water with various concentrations of NH4+-N. Five N levels (3, 5, 7, 10, and 15 mg/L) were used. Thus, there were five treatments, each with triplicates, while no plant was maintained in the control plots. Silt was adopted as the sediment in the trial. Water samples were collected every 3 days from the control and the treatment plots and analyzed for water quality parameters, including pH, temperature, concentrations of NH4+-N, nitrate nitrogen (NO3−-N), total nitrogen (TN), TP, and DO. Fresh mass of plants, N and P concentrations in the tissues and sediments were analyzed before and after the trial. Percentages removal of N and P shown in the figures were calculated by the values of treatment groups subtract those of control.
Total nitrogen of the water sample was determined by a simultaneous total organic carbon/TN analyser (multi N/C 2100, Analytik Jena, Germany). Nitrate nitrogen was detected by ion chromatography (ICS1500, USA). Ammonium nitrogen was measured according to the Chinese SEPA Standard Methods23. Dissolved oxygen and pH were estimated using a portable DO meter (HI9147-04, Hanna, Italy) and a pH meter (FG2-ELK, Mettler Toledo, USA), respectively. The length of the plant was measured by a ruler. Tiller number was counted. Plants were washed with tap and distilled water, and subsequently oven dried at 65 °C for 48 h. The sediments were oven dried at 85 °C for 24 h. Dried plants and sediments were ground into powders. The subsamples of plants and sediments were digested according to the sulfuric acid-hydrogen peroxide (H2SO4-H2O2) and perchloric-sulfuric acid (HClO4-H2SO4) method24 respectively, and analyzed for TP concentration using colorimetry (λ = 700 nm). As for nitrogen, both subsamples were digested using sulfuric-accelerator, and detected by fully automatic kjeldahl nitrogen analyzer (K370, Buchi, Swiss). The percentage removal efficiency was determined with the following equation: (initial concentration of NH4+-N, TN, or TP−concentration of NH4+-N, TN, or TP after t days) (mg/L)/(initial concentration of NH4+-N, TN, or TP) (mg/L) × 100. The percentage uptake of N or P by plant was calculated as: net uptake content of N or P by plant (mg)/initial TN or TP content in the eutrophic water (mg) × 100.
The results were presented as their mean and standard deviation (SD). All data analyses were conducted using SPSS software (ver.13.0). One-way ANOVA was used to determine significant differences at a significance level of p < 0.05. Post hoc comparisons were done using Turkey HSD test.
Growth and morphology on different sediments
Plant height was quite different in five measuring time intervals among three types of sediments (Fig. 3a). The height increment on silt was significantly higher than on gravel and sand. At the end of experiment, average height on silt was 60.58 cm, with an increase of 31%, significantly greater than those on gravel (11%) and sand (10%). There was no apparent trend in the plant height increment on silt, which was slightly higher in the second, fourth and final measuring time intervals. The average height increase rate was 0.28 cm·d−1. On gravel, the plant height increased fast during the first two measuring time intervals, whereas quite slow in the latter period of the experiment. The plant height increment showed no significant difference (p > 0.05) among the first four measuring time intervals on sand, and it was greatest at the last measuring time. Their corresponding height increase rates were 0.09 and 0.10 cm·d−1, respectively.
Tiller emergence was observed on all three types of sediments (Fig. 3b). On silt, the tiller number increased gradually along with time, and was significantly higher than on gravel and sand at day 30 and 40. Tiller production was slow during the initial 40 days on both gravel and sand, however increased markedly in the last 10 days of the experiment. For average, the tiller number per plant was 5.0, 3.5, 3.0 on silt, gravel and sand, respectively at the end of experiment, and the difference was not significant. Biomass accumulation was positively relative to plant height. It was greatest on silt, with an increase of 28%, followed by on sand of 7.1%, and on the gravel of 4.8% (Fig. 4). The biomass of plant grown on silt was significantly higher than on gravel and sand at the end of experiment.
Nutrient removal on silts with different water N supply
Total biomass before and after the experiment was analyzed, and the biomass accumulation ratio was also calculated, the results are shown in Table 1. Total biomass increased gradually with water N supply in the range of 3 to 10 mg/L, but decreased rapidly with further increase of NH4+-N concentration. When NH4+-N concentration was 15 mg/L, the total biomass was 114.2 ± 12.6 g, with the accumulation ratio of 14%, which was slightly lower than the value at NH4+-N concentration of 3 mg/L.
Nitrogen removal in the overlying water
Ammonium nitrogen removal was affected significantly by water N supply, especially at the initial period of the experiment (Fig. 5a). Percent removal of ammonium nitrogen at NH4+-N concentration 3 mg/L was significantly higher than at other concentrations in 8 d. Ammonium nitrogen removal of all treatments increased with time, reached the maxima and decreased thereafter. As shown in the Fig. 5a, it seemed to take a longer time to reach the maxima at higher NH4+-N concentrations. The maximum NH4+-N removal efficiency was more than 80% obtained at day 8 for NH4+-N less than 7 mg/L, and much over 60% at NH4+-N as high as 15 mg/L, indicating plants played an important role in the removal of NH4+-N.
As for TN removal, the removal efficiency showed an increasing trend and reached the maxima of much over 50% at day 12, and then it gradually declined with time and levelled off (Fig. 5b). The difference of removal efficiency among various NH4+-N concentration was relative small. At day 20, there was no significant difference among all N level treatments. The maxima of TN removal was between 54% to 66%, ranked as C4 > C3 > C1 > C2 > C5. Total nitrogen concentration was 2.29 mg/L at the end of the experiment at initial NH4+-N concentration of 15 mg/L, while others were below 0.5 mg/L.
Nitrate nitrogen concentration was much lower during the experiment (Fig. 5c). For initial NH4+-N concentration 3 to 10 mg/L, nitrate nitrogen concentration was less than 0.2 mg/L. However, it was much higher at NH4+-N concentration of 15 mg/L, the maxima reached 0.35 mg/L at day 16.
Phosphorus removal in the overlying water
Total phosphorus removal varied slightly among different NH4+-N treatments, and the difference declined gradually with time (Fig. 5d). At the end of the experiment, there was no significant difference among all treatments. At the first stage of the experiment, TP removal efficiency increased with time, and reached the maximum of 42% to 57% at day 6. Then it decreased slightly and remained constant at day 20. At the end of the experiment, TP concentration of all treatments was lower than 0.1 mg/L, satisfying the Class III standard for surface water environmental quality25.
Phosphorus and nitrogen contents in the sediments
Nitrogen content in the sediment increased with the increase of water N supply, and reached the maxima at NH4+-N concentration 10 mg/L (Fig. 6a). However, the difference between sediment at 3–15 mg/L NH4+-N was not significant (p > 0.05). Nitrogen content ranged from 2.2 to 2.5 g/kg, with an increase of 9.1% to 25%. Phosphorus in the sediments did not vary significantly among the treatments, and it was slightly higher at lower NH4+-N concentration treatments (NH4+-N concentration ≤5 mg/L).
Nitrogen and phosphorus contents in the plants tissues
Nitrogen in the tissues of plants increased slightly with increasing water N supply at lower NH4+-N treatments (NH4+-N concentration ≤10 mg/L) as shown in Fig. 6b. It was noted that nitrogen content was significantly greater at NH4+-N 15 mg/L. The value increased by 23% when the NH4+-N concentration increased from 10 to 15 mg/L. Phosphorus in the tissues was not distinct among all treatments, and did not show significant changes from the initial value.
Growth and morphology on different sediments
Sediment is an important source of nitrogen and phosphorus for submerged plants26,27. It has been reported that in most situations root uptake is the primary pathway for nitrogen and phosphorus28. However, Madsen and Gedergreen15 found that enrichment of sediment had no effect on the relative growth rate of Elodea Canadensis and Callitriche cophocarpa under sufficient nutrient environment. In the present study, the plant height, tiller number, and biomass accumulation were significantly greater on silt than those on gravel and sand. This indicated that Rotala rotundifolia preferred to grow in sediments with high nutrients. Nitrogen and P contents in the silt were 2.0 g/kg and 0.82 g/kg, respectively. The differences in the height and tiller number of plants among silt, gravel and sand sediments at initial period of the experiment were notably smaller than those in the latter period. It may be attributed to the nutrient limitation on gravel and sand sediments in the latter period. The experiment was conducted in relative static mode, and no additional nutrient was provided. Therefore, the plants grown on sand and gravel sediments may not obtain sufficient nutrients as the nutrients in the overlying water gradually reduced with time. However, the plants in the silt treatment could obtain continuous nutrients from the rich sediments during the latter stage. As for similar mineral sediments, the average height increment of plants on sand sediment was 8.4% higher than that on gravel sediment at the end of experiment. The results were consistent with the observations in other freshwater submerged plants29. The reason for this is that the grain size of sediment can be important in determining the rooting depth of species given the different abilities of plants to physically penetrate sediments30.
Nutrient removal on silts with different water N supply
Rotala rotundifolia grew well as the NH4+-N concentration varied from 3 to 15 mg/L. Phenomenon of yellow leaves, stems, rotted roots did not appear in all treatments during the experiment. Total biomass increased with increasing NH4+-N concentration in the range of 3 to 10 mg/L. However, further increase of NH4+-N concentration up to 15 mg/L, total biomass decreased and the value even lower than that at NH4+-N concentration of 3 mg/L. Similar results have previously been observed in other submerged aquatic plants31,32. Higher nutrient availabilities enhanced plant growth and biomass accumulation, but excessive NH4+-N can result in toxicity in plants when cultured on NH4+-N as exclusive N-source33. Wang et al.34 and Su et al.35 observed oxidative stress and inhibition of photosynthesis on plant leaves at NH4+-N concentration more than 10 mg/L.
The effect of NH4+-N concentration in water differs widely among plant species. Sensitive species show chlorosis of leaves and suppression of growth at external NH4+-N concentrations above 0.1–0.5 mM36. However, Salvinia natans grew well at external NH4+-N concentrations up to 5 mM33. Rotala rotundifolia can be tolerant to NH4+-N concentration as high as 10 mg/L. Even at 15 mg/L NH4+-N, it still grew well, although the growth rate slowed down.
Nitrogen removal by plants at the initial period of the experiment was lower at higher NH4+-N, but increased with time, as shown in Fig. 5. At the end of the experiment, differences of nitrogen removal among various NH4+-N concentrations were much smaller. There was no significant difference in TN removal among all treatments at 20 d. This result may be attributed to the adaptation of plant to higher NH4+-N. It also revealed the synergistic effect of plant on nitrification/denitrification note that the removal efficiencies in the figures were calculated by the values of treatment groups minus those of control. The nitrate nitrogen concentration was significantly higher at NH4+-N concentration 15 mg/L than other treatments.
Several studies have indicated that volatilization, plant uptake and nitrification/denitrification are the major mechanisms for nitrogen removal37,38. Since the pH of the water of all treatments was between 6.35–8.0 during the experiment, the shift from NH4+ to NH3 gas was not significant. The contribution of direct uptake by plants and synergistic effect of plants were calculated. Uptake by plants increased at low N levels (NH4+-N concentration ≤7 mg/L), but decreased when NH4+-N concentration increased further. Particularly, uptake by plants decreased sharply from 32% to 16% when NH4+-N concentration increased from 10 mg/L to 15 mg/L. It might have mainly been attributed to the sharp reduction in biomass as shown in Table 1. The contribution of uptake by plants ranged from 16% to 39%, which was similar with Potamogeton crispus reported by Li et al.39. However, direct assimilation by plants varies with considerations of other factors such as density and climate40,41.
Synergistic effect of plants was significant at higher water N levels, and they were 28% and 39% at NH4+-N concentrations of 10 and 15 mg/L respectively. The synergistic effect of plants was much higher than assimilation by plants at NH4+-N concentration 15 mg/L, which was in line with the findings obtained by Jin et al.42. There is a redox micro-interface around the stems and leaves of submerged macrophyte, which provides organic materials for nitrifiers43. Korner44 observed considerable numbers of autotrophic and heterotrophic nitrifying and denitrifying bacteria in the epiphytic communities of different species of submerged macrophytes of a treated sewage channel. It was concluded that epiphytic nitrifiers were important for the total nitrification as nitrifiers in the sediment.
Phosphorus removal in the overlying water was enhanced with increasing water N supply at the initial period of the experiment. However, it did not show significant difference after 12 days. The P contents in the plants tissues were slightly affected by water N supply. Similar results were also reported in previous studies45,46. These results may suggest that abundant external N may not impact both P removal from water and the assimilation capacity of Rotala rotundifolia for P.
Uncertainties of the present study
The present study was indoor experiment under control environment. However, the growth and purification capacity of the plant for eutrophic water are also influenced by many factors, such as sunlight, transparency, temperature, phosphorus concentration, constituents of sediment, etc. Some factors may exert direct mutual influence on each other. Thus, the performance of the plant in the field environment might be a little different. In the future study, the plant will be used in selected region of the river to investigate the long-term performance for nitrogen and phosphorus.
Rotala Rotundifolia grew better on silt than on sand and gravel. Plant height, tiller number and biomass accumulation were significantly greater than grown on other two sediments. It was tolerant to NH4+-N level as high as 15 mg/L. Growth of Rotala rotundifolia was enhanced at N levels in the range of 3 to 10 mg/L, but inhibited by further increase of N concentration. Total nitrogen and TP concentrations in the overlying water at 3–10 mg/L NH4+-N were below 0.5 and 0.1 mg/L respectively at the end of experiment, satisfying the Class II and III standard for surface water environmental quality. Nitrogen contents in the sediments increased with elevated N level. However, N accumulation in the tissue of plants showed no apparent regularity, and the greatest value was obtained at NH4+-N concentration 15 mg/L. Neither P contents in the sediments nor tissues of plants were affected significantly by additional N supply. There was no significant difference in the P content of plants and sediments among all treatments. Direct uptake by plants on N removal accounted for 16% to 39% when P concentration was 1.0 mg/L. Synergistic effect of plants was significant at NH4+-N 15 mg/L. Thus, the study documented that Rotala rotundifolia is a promising candidate for N and P removals from waters.
Haas, M. et al. Roman-driven cultural eutrophication of Lake Murten, Switzerland. Earth. Planet. Sci. Lett. 505, 110–117 (2019).
Fischer, P., Pothig, R., Gucker, B. & Venohr, M. Phosphorus saturation and superficial fertilizer application as key parameters to assess the risk of diffuse phosphorus losses from agricultural soils in Brazil. Sci. Total Environ. 630, 1515–1527 (2018).
Xiao, J., Wang, H., Chu, S. & Wong, M. H. Dynamic remediation test of polluted river water by Eco-tank system. Environ. Technol. 34(4), 553–558 (2013).
Zhang, Y. et al. Temporal and spatial changes of microbial community in an industrial effluent receiving area in Hangzhou Bay. J. Environ. Sci. 44, 57–68 (2016).
Xu, W. et al. Quantifying atmospheric nitrogen deposition through a nationwide monitoring network across China, Atmos. Chem. Phys. 15, 12345–12360 (2015).
Xu, W. et al. Spatial–temporal patterns of inorganic nitrogen air concentrations and deposition in eastern China, Atmos. Chem. Phys. 18, 10931–10954 (2018a).
Xu, W. et al. Atmospheric nitrogen deposition in the Yangtze River basin: spatial pattern and source attribution. Environ. Pollut. 232, 546–555 (2018b).
Reddy, V. R. & Beher, B. Impact of water pollution on rural communities: an economic analysis. Ecol. Econ. 58, 520–537 (2006).
Smith, V. H. Eutrophication of freshwater and coastal marine ecosystems: a global problem. Environ. Sci. Pollut. Res. 10(2), 126–39 (2003).
Li, H. et al. Enhanced of nutrient removal from eutrophic water by a plant-microorganisms combined system. Environ. Eng. Sci. 28(8), 543–554 (2011).
Liu, J. et al. Advanced nutrient removal from surface water by a consortium of attached microalgae and bacteria: a review. Bioresour. Technol. 241, 1127–1137 (2017).
Hilt, S. & Gross, E. M. Can allelopathically active submerged macrophytes stabilize clear-water states in shallow lakes? Basic Appl. Ecol. 9, 422–432 (2008).
Watson, A. & Barmuta, L. A. Feeding-preference trials confirm unexpected stable isotope analysis results: freshwater macroinvertebrates do consume macrophytes. Mar. Freshwater Res. 62, 1248–1257 (2011).
Antunes, C. et al. Factors involved in spatiotemporal dynamics of submerged macrophytes in a Portuguese coastal lagoon under Mediterranean climate. Estuar. Coast Shelf. S. 110, 93–100 (2012).
Madsen, T. V. & Cedegreen, N. Sources of nutrients to rooted submerged macrophytes growing in a nutrient-rich river. Freshwater Biol. 47, 283–291 (2002).
Horppila, J. & Nurminen, L. Effects of submerged macrophytes on sediment resuspension and internal phosphorus lading in Lake Hiidenvesi (southern Finland). Water Res. 37(18), 4468–4474 (2003).
Moreno, M. J. Analysis of the relationship between submerged aquatic vegetation (SAV) and water trophic status of lakes clustered in Northwestern Hillsborough County, Florida. Water Air Soil Poll. 214, 539–546 (2011).
Zou, W., Yuan, L. & Zhang, L. Analyzing the spectral response of submerged aquatic vegetation in a eutrophic lake, Shanghai. Ecol. Eng. 57, 65–71 (2013).
Luo, J. et al. Mapping species of submerged aquatic vegetation with multi-seasonal satellite images and considering life history information. Int. J. Appl. Earth Obs 57, 154–165 (2017).
Chu, S. Y., Xiao, J. B., Tian, G. M. & Wong, M. H. Preparation and characterization of activated carbon from aquatic macrophyte debris and its ability to adsorb anthraquinone dyes. J. Ind. Eng. Chem. 8, 283–289 (2014).
Burks, K. C., Hall, D. W., Vandiver, V. V. Jr. & Jacono, C. C. Rotala rotundifolia (Lythraceae) new to Florida. SIDA, Contributions to Botany 20, 1765–1769 (2003).
Epstein, E. Mineral nutrition of plants: principles and perspectives. New York: John Wiley and Sons (1972).
SEPA. Water and Wastewater Monitoring Methods. Fourth ed., Beijing: Chinese Environmental Science Publishing House (2002).
Son, Y. & Gower, S. T. Nitrogen and phosphorus distribution for five plantation species in southwestern Wisconsin. Forest Ecol. Manag. 53, 175–193 (1992).
Ministry of Environmental Protection of the People’s Republic of China, State Administration for Quality Supervision and Inspection and Quarantine of China. Environmental Quality Standards for Surface Water (GB 3838–2002). Beijing: China Environmental Science Press (2002).
Best, M. D. & Mantai, K. E. Growth of Myriophyllum: sediment or lake water as the source of nitrogen and phosphorus. Ecology 59, 1075–1080 (1978).
Barko, J. W. & Smart, R. M. Sediment-based nutrition of submersed macrophytes. Aquat. Bot. 10, 339–352 (1981).
Barko, J. W., Gunnison, D. & Carpenter, S. R. Sediment interactions with submersed macrophyte growth and community dynamics. Aquat. Bot. 41, 41–65 (1991).
Li, Z. Q. et al. Effect of substrate grain size on the growth and morphology of the submersed macrophyte Vallisneria natans L. Limnologica 42, 81–85 (2012).
Denny, P. Solute movement in submerged angiosperms. Biol. Rev. 55, 188–194 (1980).
Litav, M. & Lehrer, Y. The effects of ammonium in water on Potamogeton Iucens. Aquat. Bot. 5, 127–138 (1978).
Yan, C. Z. et al. Physiological effects of ammonia-nitrogen concentrations on Hydrilla verticillata. Acta. Ecol. Sin. 27, 1050–1055 (2007).
Arunothai, J. & Hans, B. Effects of NH4+ concentration on growth, morphology and NH4+ uptake kinetics of Salvinia natans. Ecol. Eng. 35, 695–702 (2009).
Wang, C. et al. Metabolic adaptations to ammonia-induced oxidative stress in leaves of the submerged macrophyte Vallisneria natans (Lour.) Hara. Aquat. Toxicol. 87(2), 88–98 (2008a).
Su, S. Q. et al. Physiological responses of Egeria densa to high ammonium concentration and nitrogen deficiency. Chemosphere 86(5), 538–545 (2012).
Britto, D. T. & Kronzucker, H. J. NH4+ toxicity in higher plants: a critical review. J. Plant Physiol. 159, 567–584 (2002).
Hu, M. H., Ao, Y. S., Yang, X. E. & Li, T. Q. Treating eutrophic water for nutrient reduction using an aquatic macrophyte (Ipomoea aquatic Forsskal) in a deep flow technique system. Agr. Water Manage. 95, 607–615 (2008).
Xiao, J., Chu, S., Tian, G., Thring, R. W. & Cui, L. An Eco-tank system containing microbes and different aquatic plant species for the bioremediation of N,N-dimethylformamide polluted river waters. J. Hazard. Mater. 320, 564–570 (2016).
Li, J., Yang, X., Wang, Z., Shan, Y. & Zheng, Z. Comparison of four aquatic plant treatment systems for nutrient removal from eutrophied water. Bioresour. Technol. 179, 1–7 (2015).
Jiang, J. et al. Sediment type, population density and their combined effect greatly charge the short-time growth of two common submerged macrophytes. Ecol. Eng. 34, 79–90 (2008).
Ye, C. et al. Community collocation of four submerged macrophytes on two kinds of sediments in Lake Taihu, China. Ecol. Eng. 35, 1656‒1663 (2009).
Jin, S. et al. Comparison of nitrogen and phosphorus uptake and water purification ability of five submerged macrophytes. Chin. J. Environ. Sci. 38(1), 156–162 (2017).
Liboriussen, L. & Jeppesen, E. Structure, biomass, production and depth distribution of periphyton on artificial substratum in shallow lakes with contrasting nutrient concentrations. Freshwater Biol. 51(1), 95–109 (2006).
Korner, S. Nitrifying and denitrifying bacteria in epiphytic communities of submerged macrophytes in a treated sewage channel. Acta Hydrochim. Hydrobiol. 27(1), 27–31 (1999).
Jampeetong, A. & Brix, H. Effects of NH4+ concentration on growth, morphology and NH4+ uptake kinetics of Salvinia natans. Ecol. Eng. 35(5), 695–702 (2009).
Saunkaew, P., Wangpakapattanawong, P. & Jampeetong, A. Growth, morphology, ammonium uptake and nutrient allocation of Myriophyllum brasiliense Cambess. Under high NH4+ concentrations. Ecotoxicology 20, 2011–2018 (2011).
This work was financially supported by the Science and Technology Program of Wenzhou, China (No.Z20160011).
The authors declare no competing interests.
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Gu, C., Li, F., Xiao, J. et al. A novel submerged Rotala rotundifolia, its growth characteristics and remediation potential for eutrophic waters. Sci Rep 9, 14855 (2019). https://doi.org/10.1038/s41598-019-51508-y