Next Article in Journal
Sustainability Assessment of the Bui Hydropower System
Previous Article in Journal
Indoor Air Quality Assessment and Study of Different VOC Contributions within a School in Taranto City, South of Italy
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Influence of the Ratio of Nitrate to Ammonium Nitrogen on Nitrogen Removal in the Economical Growth of Vegetation in Hybrid Constructed Wetlands

1
School of Energy and Environment, Southeast University, Nanjing 210096, China
2
Department of Environmental Science, Federal Urdu University, Karachi 75000, Pakistan
3
Institute of Forage Crop, 89 “General Vladimir Vazov” Str., Pleven 5800, Bulgaria
*
Author to whom correspondence should be addressed.
Environments 2017, 4(1), 24; https://doi.org/10.3390/environments4010024
Submission received: 14 December 2016 / Revised: 8 March 2017 / Accepted: 15 March 2017 / Published: 17 March 2017

Abstract

:
Growing vegetables economically in the use of constructed wetland for wastewater treatment can play a role in overcoming water and food scarcity. Allium porrum L., Solanum melongena L., Ipomoea aquatica Forsk., and Capsicum annuum L. plants were selected to grow in hybrid constructed wetland (CW) under natural conditions. The impact of the ratio of nitrate to ammonium nitrogen on ammonium and nitrate nitrogen removal and on total nitrogen were studied in wastewater. Constructed wetland planted with Ipomoea aquatica Forsk. and Solanum melongena L. showed higher removal efficiency for ammonium nitrogen under higher ammonium concentration, whereas Allium porrum L.-planted CW showed higher nitrate nitrogen removal when NO3–N concentration was high in wastewater. Capsicum annuum L.-planted CW showed little efficiency for both nitrogen sources compared to other vegetables.

1. Introduction

Wastewater can pollute receiving water bodies and thus need to be treated beforehand [1]. The conventional treatment processes are expensive to build especially for areas of low socioeconomic status [2]. Therefore, cost-effective and environmentally sound methods of treating wastewaters are needed. Constructed wetlands have gained popularity from the last several years and have been used as an alternative to conventional wastewater treatment methods [3] because of their easy maintenance and operation, low energy consumption, and water recyclability [4,5]. Constructed wetlands are successfully used to treat different types of wastewater [6,7,8,9,10,11,12,13]. Currently, the world population is on the edge of scarcity for water and food; therefore, the recycling of water and nutrients (in wastewater) are emerging as integral parts of water and food demand management [14]. Growing vegetation economically in the use of constructed wetlands for wastewater treatment is therefore needed and can help to reduce the gap between supply and demand [15].
Plants take up nitrogen in the form of NO3–N (nitrate) or NH4–N (ammonium); therefore, the total N (nitrogen) absorbed usually consists of a combination of these two forms [16,17]. The ratio of NO3–N to NH4–N is of a great significance and can impact plant growth. The optimum growth of plants species required a different ratio of nitrate to ammonium N. The best ratio to be applied also varies with other factors such as growth stage, temperature, pH, and soil properties [18]. NH4–N in ionic form can compete with other forms (potassium, calcium, magnesium) for uptake by the roots [19]. An unbalanced NO3–N to NH4–N ratio may affect solubility and availability of other nutrients by changing the pH near the roots [20].
Several researchers have reported that NH4–N as a sole source of N is deleterious to the growth of many higher plants [21], and a higher concentration than NO3–N can limit the growth of plants [22,23]. In several crops, combinations of both forms (NH4–N and NO3–N) usually result in elevated growth compared to when either N form is used alone [24,25,26]. However, some plant species showed better growth when NH4–N was the N source [27]. In a controlled environment, some plants absorb NO3–N more rapidly [28], whereas other plants prefer NH4–N [21]. The absorption rates of NO3–N and NH4–N are influenced by the ratio of NO3–N to NH4–N [29]. In several plant species, NH4–N may compete with NO3–N and inhibit NO3–N absorption in the presence of both NO3–N and NH4–N [30]. However, there is no information available on the NO3–N/NH4–N ratio on plants species when grown in a constructed wetland with natural environment. The objective of this study was to improve the constructed wetland system for the economical growth of vegetation by examining the influence of the ratio of nitrate to ammonium N on N removal in wastewater post-treatment.

2. Materials and Methods

2.1. Experimental Site and Constructed Wetland

The research was conducted at the Southeast University campus, New District, Wuxi, China. The total area of constructed wetland is 100 m2. The Wuxi has four distinct seasons and exist in a north subtropical humid monsoon climate zone, with rich rainfalls and sunshine. The average perennial temperature over 30 years (1981–2010) is 16.2 °C, and the average precipitation is 1121.7 mm, with 123 days of rain and 1924.3 h of sunshine [31]. Two pilot-scale hybrid constructed wetland systems were established for experimental plants. The hybrid system was a combination of Constructed Floating Treatment Wetlands (CFW) and horizontal flow constructed wetlands (HFCW). Each bed in each unit was 2.5 m × 0.3 m × 0.5 m (length × width × height) made of concrete and lined with epoxy. The first bed was designed for CFW without a substrate, whereas a second bed of each unit was packed with a 10 cm supporting layer of large gravel (30–40 mm), 25 cm of ceramsite (10–20 mm in diameter), and 10 cm of small gravel (10–20 mm). The wastewater entered in the first bed from the distribution channel, that was connected to a wastewater tank, and flow was controlled by value.
Four different types of plants were selected (Table 1) to grow in the constructed wetland, and selections were made keeping in mind the economic value of the vegetables, their easy availability in the local market, their aesthetic worth, and their ability to adapt in existing climatic conditions. Polyethylene foam boards were used for planting as floating mats in the CFW beds, and 2 cm holes were perforated for each plant. The systems were inspected on a daily basis. Special attention was paid to the inlet and outlet flows, as suspended solid-present wastewater can cause obstruction in the pipes.

2.2. Experimental Conditions

The experiment was carried out in the natural environment, and sewage was treated through A2O (anaerobic/anoxic/oxic) system and then artificially stimulated before being introduced into the constructed wetland. Two setups of the hybrid system were established. In the first setup, the CFW beds were planted with A. porum, and the HFCW beds were planted with S. melongena; in the second setup, I. aquatica and C. annum L were planted in the CFW and HFCW beds, respectively. The selection of plants for each setup was random. Potassium nitrate (KNO3) as NO3–N, ammonium bicarbonate (NH4HCO3) as NH4–N, potassium dihydrogen (KH2PO4) as total phosphorus, and glucose (C6H12O6) as a source of chemical oxygen demand were used, whereas micronutrients were added according to Zhang et al. [32]. The pH was adjusted to 6.0 ± 0.2 with dilute NaOH or HCl. These constructed wetlands (CWs) ran for 20 days to achieve stabilization for further experiments, and the NO3–N/NH4–N ratio was adjusted and divided into four experimental runs (ERs) (Table 2). The hydraulic load was 0.2 m·d−1 and the hydraulic retention time was 1.25 d. The average DO in influent and effluent was 1–5 mg·L−1 and 0–2 mg·L−1, respectively. The quality of wastewater was measured at each step on a routine basis.

2.3. Analytical Methods

Standard methods [33] were used to analyze ammonium (NH4–N), nitrate (NO3–N), total nitrogen (TN), total phosphorus (TP), and chemical oxygen demand (COD) parameters in wastewater, whereas DO and pH was measured by DO200 and PH100 probes (YSI), respectively.

2.4. Statistical Method

MS Excel (Office package-16) and SPSS version-18.0 (SPSS incorporation, Chicago, IL, USA) were used for data analysis and presentation.

3. Results

3.1. NH4–N Removal under Different NO3–N/NH4–N Ratios

The impact of the NO3–N/NH4–N ratio on the removal of NH4–N is shown in Figure 1 and Figure 2. For the first setup, the removal efficiency in the first bed was 76.93%, 63.94%, 30.60%, and 40.75%, and in the second bed, the removal efficiency was 90.03%, 87.88%, 73.64%, and 74.74%, whereas for the second setup, removal efficiency was 88.89%, 75.93%, 63.99%, and 58.79% and 89.23%, 82.84%, 69.72%, and 73.65% in Beds 1 and 2, respectively. NH4–N removal efficiency was significant (p > 0.05) (Table 3). There was no significant difference between the two units for NH4–N removal under different NO3–N/NH4–N ratios.

3.2. NO3–N Removal under Different NO3–N/NH4–N Ratios

Figure 3 and Figure 4 show NO3–N removal in Setups 1 and 2 under different NO3–N/NH4–N ratios. In the first setup, the NO3–N removal rate was 18.77%, 29.36%, 30.60%, and 33.01% in the CFW bed and 65.07%, 68.67%, 55.10%, and 53.41% in the HFCW bed. In Setup 2, removal efficiency was 38.04%, 49.68%, 46.31%, and 58.10% for the first bed and 56.55%, 63.47%, 56.48%, and 48.63% for the second bed. In both cases, there was a significant difference (p < 0.05) between the hybrid system beds in both setups.

3.3. Total Nitrogen Removal under Different NO3–N/NH4–N Ratios

Figure 5 reveals that there is no significant difference in the total nitrogen removal between both CW beds in both setups under different NO3–N/NH4–N ratios. The values were as follows: for Setup 1, 32.73%, 26.81%, 34.05%, and 32.65%, and 73.07%, 77.06%, 63.04%, and 61.22% for Beds 1 and 2, respectively; for Setup 2, 34.91%, 37.74%, 47.99%, and 45.18% and 63.59%, 69.17%, 59.05%, and 59.33% for Beds 1 and 2, respectively.

4. Discussion

The NO3–N/NH4–N ratio has great significance in constructed wetland systems by affecting plant growths [34]. For optimum uptake and growth, each plant species requires a different amount of NO3–N/NH4–N ratio [35]. Most of the plants grew well when they were provided by a mixture of NO3–N and NH4–N rather than either of these components alone [36,37]. A. calamus, L. esculentum, and C. sativus grew well and achieved the highest dry weight under a NO3–N/NH4–N ratio of 1:1, and higher amounts of NO3–N suppressed growth [24,25,26]. Nitrogen removal in the constructed wetland system includes adsorption by the substrate, plant uptake, nitrification, and volatilization [38]. Many researchers stated that, in a constructed wetland system, little NH4–N removal occurs through the direct absorption by plants [39] and it is mostly removed through microbial action [40], whereas on higher pH most of the NH4–N is removed by volatilization [41]. The constructed wetland systems can consider a complex bioreactor, various biotic and abiotic factors interact with each other, and a number of physical, chemical and biological processes take place [42].
The effect of NH4–N removal under different NO3–N/NH4–N ratios in hybrid constructed wetland systems was significant, and the removal rate reduces with the decrease in NO3–N/NH4–N ratio. When the ratio of NH4–N/NO3–N was 1:1, there was little impact on NH4–N removal, a possible reason was which being that an insufficient amount of oxygen in the subsurface wetlands limits these processes [43]. For NO3–N removal, there is variation between both experimental setups. In the first setup, the surface wetland removed a high concentration of NO3–N compared to the subsurface constructed wetland, whereas the second setup showed quite the opposite result. The nitrification processes are effected by pH, temperature, inorganic carbon source, alkalinity, dissolve oxygen, and NH4–N concentration [39]. NH4–N uptake consumes more oxygen compared to NO3–N. Ammonium breakdown occurs in roots and reacts with sugar, and this sugar is delivered from leaves to roots, whereas NO3–N is transported to leaves and reduces to ammonium and then reacts with sugar [44]. At higher respiration, plants consumes more sugar, leaving less available for NH4–N metabolism. S. melongena in the HFCW and I. aquatica in the CFW have well developed root systems, and their oxygen transfer ability is strong, rendering a good aerobic environment around the root system, which ultimately favors nitrifying bacteria and increases the removal ability of NH4–N.
The rhizome and roots belowground are critical for the removal of nitrogen from wastewater; in the rhizosphere, they provide nutrients and exudates to fuel the microorganisms [45]. The plant root system is an important parameter to consider when selecting plant species for a constructed wetland, as a bigger root area can take up large amount of nutrients and thus improve N removal.

5. Conclusions

  • Ipomoea aquatica Forsk. and Solanum melongena L. showed higher removal efficiency for NH4–N under higher ammonium concentrations, whereas Allium porrum L. showed higher NO3–N removal when NO3–N concentrations were high in wastewater. Compared to other vegetables Capsicum annuum L. showed little efficiency for both N sources.
  • The different plants may differ in their capacity to take in N from different nitrogen sources and therefore should select plants economically so that a constructed wetland can obtain optimum removal of nutrients as well as optimum growth.
  • The gap between supply and demand for water and food can be reduced using a constructed wetland for the economical growth of plants, and this approach can broaden the application of a constructed wetland.

Acknowledgments

The authors are thankful to Ministry of Environment, People Republic of China for providing funding for this project. This work was financially supported by the “National 12th Five-Year Major Projects” grant number 2012ZX07101-005.

Author Contributions

Haq Nawaz Abbasi and Xiwu Lu conceived and designed the project, materials, and analysis tools. Haq Nawaz Abbasi performed the experimental works and data analysis. Xiwu Lu supervised the study during all stages. All authors wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Igbinosa, E.; Okoh, A. Impact of discharge wastewater effluents on the physico-chemical qualities of a receiving watershed in a typical rural community. Int. J. Environ. Sci. Technol. 2009, 6, 175–182. [Google Scholar] [CrossRef]
  2. Massoud, M.A.; Tarhini, A.; Nasr, J.A. Decentralized approaches to wastewater treatment and management: Applicability in developing countries. J. Environ. Manag. 2009, 90, 652–659. [Google Scholar] [CrossRef] [PubMed]
  3. Wilkoff, B.L.; Bello, D.; Taborsky, M.; Vymazal, J.; Kanal, E.; Heuer, H.; Hecking, K.; Johnson, W.B.; Young, W.; Ramza, B. Magnetic resonance imaging in patients with a pacemaker system designed for the magnetic resonance environment. Heart Rhythm 2011, 8, 65–73. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Xu, Q.; Chen, S.; Huang, Z.; Cui, L.; Wang, X. Evaluation of organic matter removal efficiency and microbial enzyme activity in vertical-flow constructed wetland systems. Environments 2016, 3, 26. [Google Scholar] [CrossRef]
  5. Abbasi, H.N.; Lu, X.; Xu, F.; Xie, J. Wastewater treatment strategies in china: An overview. Sci. Lett. 2016, 4, 15–25. [Google Scholar]
  6. Jing, S.-R.; Lin, Y.-F.; Lee, D.-Y.; Wang, T.-W. Nutrient removal from polluted river water by using constructed wetlands. Bioresour. Technol. 2001, 76, 131–135. [Google Scholar] [CrossRef]
  7. Kaseva, M. Performance of a sub-surface flow constructed wetland in polishing pre-treated wastewater—A tropical case study. Water Res. 2004, 38, 681–687. [Google Scholar] [CrossRef] [PubMed]
  8. Lee, C.-Y.; Lee, C.-C.; Lee, F.-Y.; Tseng, S.-K.; Liao, C.-J. Performance of subsurface flow constructed wetland taking pretreated swine effluent under heavy loads. Bioresour. Technol. 2004, 92, 173–179. [Google Scholar] [CrossRef] [PubMed]
  9. Wallace, S.; Kadlec, R. Btex degradation in a cold-climate wetland system. Water Sci. Technol. 2005, 51, 165–171. [Google Scholar] [PubMed]
  10. Maine, M.; Sune, N.; Hadad, H.; Sánchez, G. Temporal and spatial variation of phosphate distribution in the sediment of a free water surface constructed wetland. Sci. Total Environ. 2007, 380, 75–83. [Google Scholar] [CrossRef] [PubMed]
  11. Ahmed, S.; Popov, V.; Trevedi, R.C. Constructed wetland as tertiary treatment for municipal wastewater. In Proceedings of the Institution of Civil Engineers-Waste and Resource Management; Thomas Telford Ltd.: London, UK, 2008; pp. 77–84. [Google Scholar]
  12. Li, X.; Manman, C.; Anderson, B.C. Design and performance of a water quality treatment wetland in a public park in shanghai, china. Ecol. Eng. 2009, 35, 18–24. [Google Scholar] [CrossRef]
  13. Martín, M.; Oliver, N.; Hernández-Crespo, C.; Gargallo, S.; Regidor, M. The use of free water surface constructed wetland to treat the eutrophicated waters of lake l’albufera de valencia (Spain). Ecol. Eng. 2013, 50, 52–61. [Google Scholar] [CrossRef]
  14. Cordell, D.; Drangert, J.-O.; White, S. The story of phosphorus: Global food security and food for thought. Glob. Environ. Chang. 2009, 19, 292–305. [Google Scholar] [CrossRef]
  15. Qadir, M.; Sharma, B.R.; Bruggeman, A.; Choukr-Allah, R.; Karajeh, F. Non-conventional water resources and opportunities for water augmentation to achieve food security in water scarce countries. Agric. Water Manag. 2007, 87, 2–22. [Google Scholar] [CrossRef]
  16. Briones, A.M., Jr.; Okabe, S.; Umemiya, Y.; Ramsing, N.-B.; Reichardt, W.; Okuyama, H. Ammonia-oxidizing bacteria on root biofilms and their possible contribution to n use efficiency of different rice cultivars. Plant Soil 2003, 250, 335–348. [Google Scholar] [CrossRef]
  17. Vasileva, V.; Ilieva, A. Chemical composition, nitrate reductase activity and plastid pigments content in lucerne under the influence of ammonium and nitrate form mineral nitrogen. Agron. Res. 2011, 9, 357–364. [Google Scholar]
  18. Forde, B.G.; Clarkson, D.T. Nitrate and ammonium nutrition of plants: Physiological and molecular perspectives. Adv. Bot. Res. 1999, 30, 1–90. [Google Scholar]
  19. Rayar, A.J.; Van Hai, T. Effect of ammonium on uptake of phosphorus, potassium, calcium and magnesium by intact soybean plants. Plant Soil 1977, 48, 81–87. [Google Scholar] [CrossRef]
  20. Bindraban, P.S.; Dimkpa, C.; Nagarajan, L.; Roy, A.; Rabbinge, R. Revisiting fertilisers and fertilisation strategies for improved nutrient uptake by plants. Biol. Fertil. Soils 2015, 51, 897–911. [Google Scholar] [CrossRef]
  21. Serna, M.; Borras, R.; Legaz, F.; Primo-Millo, E. The influence of nitrogen concentration and ammonium/nitrate ratio on n-uptake, mineral composition and yield of citrus. Plant Soil 1992, 147, 13–23. [Google Scholar] [CrossRef]
  22. Ali, A.; Tucker, T.; Thompson, T.; Salim, M. Effects of salinity and mixed ammonium and nitrate nutrition on the growth and nitrogen utilization of barley. J. Agron. Crop Sci. 2001, 186, 223–228. [Google Scholar] [CrossRef]
  23. Guo, S.; Brück, H.; Sattelmacher, B. Effects of supplied nitrogen form on growth and water uptake of french bean (phaseolus vulgaris l.) plants. Plant Soil 2002, 239, 267–275. [Google Scholar] [CrossRef]
  24. Vojtíšková, L.; Munzarová, E.; Votrubová, O.; Řihová, A.; Juřicová, B. Growth and biomass allocation of sweet flag (acorus calamus l.) under different nutrient conditions. Hydrobiologia 2004, 518, 9–22. [Google Scholar] [CrossRef]
  25. Kotsiras, A.; Olympios, C.; Passam, H. Effects of nitrogen form and concentration on yield and quality of cucumbers grown on rockwool during spring and winter in southern greece. J. Plant Nutr. 2005, 28, 2027–2035. [Google Scholar] [CrossRef]
  26. Juan, L.; Zhou, J.-M.; Duan, Z.-Q. Effects of elevated CO2 concentration on growth and water usage of tomato seedlings under different ammonium/nitrate ratios. J. Environ. Sci. 2007, 19, 1100–1107. [Google Scholar]
  27. Rosen, C.J.; Allan, D.L.; Luby, J.J. Nitrogen form and solution ph influence growth and nutrition of two vaccinium clones. J. Am. Soc. Hortic. Sci. 1990, 115, 83–89. [Google Scholar]
  28. Below, F.E. Nitrogen metabolism and crop productivity. Handb. Plant Crop Physiol. 2002, 2, 385–406. [Google Scholar]
  29. Savvas, D.; Passam, H.; Olympios, C.; Nasi, E.; Moustaka, E.; Mantzos, N.; Barouchas, P. Effects of ammonium nitrogen on lettuce grown on pumice in a closed hydroponic system. HortScience 2006, 41, 1667–1673. [Google Scholar]
  30. Tylova-Munzarova, E.; Lorenzen, B.; Brix, H.; Votrubova, O. The effects of NH4+ and NO3− on growth, resource allocation and nitrogen uptake kinetics of phragmites australis and glyceria maxima. Aquat. Bot. 2005, 81, 326–342. [Google Scholar] [CrossRef]
  31. Zhai, Y.-M.; Hou, M.-M.; Shao, X.-H.; Yang, Q. The comprehensive effects of the subsurface drainage on greenhouse saline soil, tomato yield and quality. Adv. J. Food Sci. Technol. 2016, 10, 691–694. [Google Scholar]
  32. Zhang, Y.; Lin, X.; Zhang, Y.; Zheng, S.J.; Du, S. Effects of nitrogen levels and nitrate/ammonium ratios on oxalate concentrations of different forms in edible parts of spinach. J. Plant Nutr. 2005, 28, 2011–2025. [Google Scholar] [CrossRef]
  33. Federation, W.E.; Association, A.P.H. Standard Methods for the Examination of Water and Wastewater; American Public Health Association (APHA): Washington, DC, USA, 2005. [Google Scholar]
  34. Petrucio, M.; Esteves, F. Uptake rates of nitrogen and phosphorus in the water by eichhornia crassipes and salvinia auriculata. Revista Brasileira de Biologia 2000, 60, 229–236. [Google Scholar] [CrossRef] [PubMed]
  35. Santamaria, P.; Elia, A.; Parente, A.; Serio, F. Fertilization strategies for lowering nitrate content in leafy vegetables: Chicory and rocket salad cases. J. Plant Nutr. 1998, 21, 1791–1803. [Google Scholar] [CrossRef]
  36. Mengel, K.; Kirkby, E.A.; Kosegarten, H.; Appel, T. Nitrogen. In Principles of Plant Nutrition; Springer: Berlin, Germany, 2001; pp. 397–434. [Google Scholar]
  37. Zhang, F.C.; Kang, S.Z.; Li, F.S.; Zhang, J.H. Growth and major nutrient concentrations in brassica campestris supplied with different NH4+/NO3− ratios. J. Integr. Plant Biol. 2007, 49, 455–462. [Google Scholar] [CrossRef]
  38. Vymazal, J. Removal of nutrients in various types of constructed wetlands. Sci. Total Environ. 2007, 380, 48–65. [Google Scholar] [CrossRef] [PubMed]
  39. Lee, C.G.; Fletcher, T.D.; Sun, G. Nitrogen removal in constructed wetland systems. Eng. Life Sci. 2009, 9, 11–22. [Google Scholar] [CrossRef]
  40. Lv, T.; Zhang, Y.; Carvalho, P.N.; Zhang, L.; Button, M.; Arias, C.A.; Weber, K.P.; Brix, H. Microbial community metabolic function in constructed wetland mesocosms treating the pesticides imazalil and tebuconazole. Ecol. Eng. 2017, 98, 378–387. [Google Scholar] [CrossRef]
  41. Picot, B.; El Halouani, H.; Casellas, C.; Moersidik, S.; Bontoux, J. Nutrient removal by high rate pond system in a mediterranean climate (France). Water Sci. Technol. 1991, 23, 1535–1541. [Google Scholar]
  42. Singh, S.; Kaushik, A.; Kaushik, C. Comparing efficacy of down-flow and up-flow vertical constructed wetlands for treatment of simulated dumpsite leachate. Imp. J. Interdiscip. Res. 2016, 2, 942–945. [Google Scholar]
  43. Tang, X.; Huang, S.; Scholz, M. Nutrient removal in wetlands during intermittent artificial aeration. Environ. Eng. Sci. 2008, 25, 1279–1290. [Google Scholar] [CrossRef]
  44. Devaux, C.; Baldet, P.; Joubès, J.; Dieuaide-Noubhani, M.; Just, D.; Chevalier, C.; Raymond, P. Physiological, biochemical and molecular analysis of sugar-starvation responses in tomato roots. J. Exp. Bot. 2003, 54, 1143–1151. [Google Scholar] [CrossRef] [PubMed]
  45. Stottmeister, U.; Wießner, A.; Kuschk, P.; Kappelmeyer, U.; Kästner, M.; Bederski, O.; Müller, R.; Moormann, H. Effects of plants and microorganisms in constructed wetlands for wastewater treatment. Biotechnol. Adv. 2003, 22, 93–117. [Google Scholar] [CrossRef] [PubMed]
Figure 1. NH4–N concentration during different experimental runs in the first setup.
Figure 1. NH4–N concentration during different experimental runs in the first setup.
Environments 04 00024 g001
Figure 2. NH4–N concentration during different experimental runs in the second setup.
Figure 2. NH4–N concentration during different experimental runs in the second setup.
Environments 04 00024 g002
Figure 3. NO3–N concentration during different experimental runs in the first setup.
Figure 3. NO3–N concentration during different experimental runs in the first setup.
Environments 04 00024 g003
Figure 4. NO3–N concentration during different experimental runs in the second setup.
Figure 4. NO3–N concentration during different experimental runs in the second setup.
Environments 04 00024 g004
Figure 5. Total nitrogen concentration during different experimental runs in the first and second setups.
Figure 5. Total nitrogen concentration during different experimental runs in the first and second setups.
Environments 04 00024 g005
Table 1. Selected plant species for experiments.
Table 1. Selected plant species for experiments.
NumberCommon NameScientific NameUsed Name
1LeekAllium porrum L.A. porrum
2Egg PlantSolanum melongena L.S. melongena
3Water spinachIpomoea aquatica Forsk.I. aquatica
4Hot pepperCapsicum annuum L.C. annuum L.
Table 2. Average influent stimulated wastewater quality of during experimental runs.
Table 2. Average influent stimulated wastewater quality of during experimental runs.
Experimental Run (ER)NO3–N/NH4–NNO3–NNH4–NTNTPCOD
mg·L−1
15:124.695.0829.513.0589.14
22:120.999.8329.412.9291.25
31:114.2814.9330.102.8688.63
41:29.9019.9429.832.9190.93
Here, TN = total nitrogen, TP = total phosphorus, COD = chemical oxygen demand.
Table 3. Estimated values of effluent during different ERs in Setups 1 and 2.
Table 3. Estimated values of effluent during different ERs in Setups 1 and 2.
Set-upTestERInfluentCFWHFCW
MinMaxMean ± SD **MinMaxMean ± SD **MinMaxMean ± SD **
Mg·L−1
1NH4I4.205.905.061 ± 0.8501.401.601.52 ± 0.1060.400.050.442 ± 0.402
II9.709.909.8104 ± 0.10165.005.605.322 ± 0.3021.581.981.782 ± 0.200
III14.6015.2014.909 ± 0.3008.108.508.325 ± 0.2054.714.914.8133 ± 0.1002
IV19.8919.9919.941 ± 0.05011.7011.9011.806 ± 0.1017.227.287.2521 ± 0.0302
NO3I24.4024.8024.630 ± 0.20719.0021.0020.019 ± 1.0018.428.828.622 ± 0.200
II20.8021.2020.997 ± 0.20014.7014.9014.810 ± 0.1016.476.676.5723 ± 0.1001
III14.0014.6014.295 ± 0.3009.869.969.9110 ± 0.05006.316.516.4112 ± 0.1000
IV9.709.909.8036 ± 0.10026.376.776.571 ± 0.2004.474.674.5703 ± 0.1000
TNI27.0029.0028.002 ± 1.00019.1019.3019.202 ± 0.10010.6410.8410.741 ± 0.100
II29.7029.9029.800 ± 0.10018.1018.5018.304 ± 0.2009.049.089.0623 ± 0.0204
III29.0529.1529.100 ± 0.05015.4815.8815.683 ± 0.20012.1012.5212.315 ± 0.210
IV28.0030.0029.033 ± 1.00216.5816.7816.682 ± 0.10011.0013.2012.118 ± 1.100
2NH4I4.205.905.061 ± 0.8500.300.800.555 ± 0.2500.340.740.543 - 0.200
II9.709.839.8104 ± 0.10162.252.452.3553 ± 0.10041.401.801.629 ± 0.206
III14.6015.2014.909 ± 0.3005.075.675.372 ± 0.3004.304.704.507 ± 0.200
IV19.8919.9919.941 ± 0.0508.108.308.2064 ± 0.10064.206.205.252 ± 1.000
NO3I24.4024.8024.630 ± 0.20714.2916.2915.293 ± 1.0009.7011.7010.709 ± 1.000
II20.8021.2020.997 ± 0.2009.5611.5610.561 ± 1.0006.608.607.623 ± 1.001
III14.0014.6014.295 ± 0.3007.427.827.620 ± 0.2006.006.416.209 ± 0.205
IV9.709.909.8036 ± 0.10023.105.104.103 ± 1.0004.705.305.013 ± 0.301
TNI27.0029.0028.002 ± 1.00017.7521.7519.75 ± 2.007.958.648.276 ± 0.348
II29.7029.9029.800 ± 0.10020.5222.5221.523 ± 1.0006.487.006.743 ± 0.260
III29.0529.1529.100 ± 0.05017.4521.4519.45 ± 2.0010.5011.6211.082 ± 0.561
IV28.0030.0029.033 ± 1.00218.1222.1220.12 ± 2.0010.5612.5611.563 ± 1.000
** probability value > 0.001.

Share and Cite

MDPI and ACS Style

Abbasi, H.N.; Vasileva, V.; Lu, X. The Influence of the Ratio of Nitrate to Ammonium Nitrogen on Nitrogen Removal in the Economical Growth of Vegetation in Hybrid Constructed Wetlands. Environments 2017, 4, 24. https://doi.org/10.3390/environments4010024

AMA Style

Abbasi HN, Vasileva V, Lu X. The Influence of the Ratio of Nitrate to Ammonium Nitrogen on Nitrogen Removal in the Economical Growth of Vegetation in Hybrid Constructed Wetlands. Environments. 2017; 4(1):24. https://doi.org/10.3390/environments4010024

Chicago/Turabian Style

Abbasi, Haq Nawaz, Viliana Vasileva, and Xiwu Lu. 2017. "The Influence of the Ratio of Nitrate to Ammonium Nitrogen on Nitrogen Removal in the Economical Growth of Vegetation in Hybrid Constructed Wetlands" Environments 4, no. 1: 24. https://doi.org/10.3390/environments4010024

APA Style

Abbasi, H. N., Vasileva, V., & Lu, X. (2017). The Influence of the Ratio of Nitrate to Ammonium Nitrogen on Nitrogen Removal in the Economical Growth of Vegetation in Hybrid Constructed Wetlands. Environments, 4(1), 24. https://doi.org/10.3390/environments4010024

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