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Article

Effects of Domestic Sewage on the Photosynthesis and Chromium Migration of Coix lacryma-jobi L. in Chromium-Contaminated Constructed Wetlands

College of Agriculture, Guangxi University, Nanning 530004, China
*
Authors to whom correspondence should be addressed.
Sustainability 2023, 15(13), 10250; https://0-doi-org.brum.beds.ac.uk/10.3390/su151310250
Submission received: 13 May 2023 / Revised: 19 June 2023 / Accepted: 26 June 2023 / Published: 28 June 2023
(This article belongs to the Special Issue Environmental and Health Risk Assessment of Heavy Metal Pollution)

Abstract

:
To investigate the effects of domestic sewage on the photosynthesis and chromium migration of plants in chromium-contaminated constructed wetlands, small vertical flow constructed wetlands of Coix lacryma-jobi L. were set up. These wetlands were used to treat wastewater containing 0, 20, and 40 mg/L of hexavalent chromium (Cr (VI)), prepared with domestic sewage (DS), 1/2 Hoagland nutrient solution (NS), and 1/2 Hoagland nutrient solution prepared with domestic wastewater (DN), respectively. The aim was to investigate the effects of domestic sewage on indicators, such as plant growth and chromium accumulation. The results were as follows: (1) Plant heights were significantly inhibited under 20 mg/L and 40 mg/L Cr (VI) treatments, and stem diameters were not significantly affected. The use of domestic sewage in treatment alleviated the inhibition of Cr (VI) on the growth of Coix lacryma-jobi L. (2) Indicators such as root activity, photosynthetic gas exchange, and chlorophyll fluorescence properties significantly decreased with the increase in Cr (VI) concentration. The values of these photosynthetic gas exchange parameters under the DN treatment were the greatest, followed by NS and DS. On the 70th day of Cr (VI) treatment, the net photosynthetic rate (Pn) under the DN treatment was significantly higher than that under NS and DS treatments. (3) Glutathione (GSH) content in roots, stems, and leaves of Coix lacryma-jobi L. significantly increased with the increase in Cr concentration, and it increased more significantly under the DN and DS treatments than under the NS treatment. (4) With the same Cr treatment, the Cr content in roots, stems, and leaves of Coix lacryma-jobi L. under the NS treatment was the highest, followed by DS and DN. The total Cr content in the substrate under the DN treatment was the highest, followed by DS and NS. (5) The addition of domestic sewage reduced the Cr (VI) content in the water sample and increased the organic matter content. The Cr (VI) content in the water sample under the NS treatment was the highest, followed by DS and DN. The addition of domestic sewage increased the accumulation of chromium in the substrate, decreased the absorption of chromium by plants, increased GSH content in roots, stems, and leaves, alleviated the damage of Cr (VI) to plants, and thus benefited the growth of Coix lacryma-jobi L. in the constructed wetlands and ensured the sustainable and stable operation of the wetlands.

Graphical Abstract

1. Introduction

Chromium (Cr) exists mainly in the forms of Cr (III) and Cr (VI) in nature. Cr (III) is relatively stable in soil. A small amount of it in the human body can promote carbohydrate metabolism, but an excessively high level can be toxic to the human body [1]. Cr (VI) is highly mobile in soil and easily enriched in crops and may ultimately be absorbed by the human body. Cr (VI) is highly toxic to the human body, with strong mutagenic, carcinogenic, and teratogenic effects [2,3].
Cr is widely used in industries, such as electroplating, printing and dyeing, papermaking, and leathermaking. Both urban and rural industrialization accelerate amid social development, and improper discharge of Cr-containing wastewater can still be seen in China due to supervision, technology, and other reasons. For example, in January 2019, several business owners in Henan Province were reported by Dahebao to have discharged wastewater with an excessive level of Cr during sheepskin dyeing, causing serious environmental pollution [4]. In March 2022, the Wanxiu Court of Wuzhou City reported an incident of illegal discharge of pollutants containing elements, such as nickel and Cr from an electroplating workshop in Wuzhou City [5]. Improper discharge of industrial Cr not only threatens the safety of crop production, but also poses a risk to human health.
Taking technical measures to reduce the Cr content in wastewater is an important way to prevent and control Cr pollution. Constructed wetlands, with the advantages of low construction and operation costs, easy maintenance and management, and high ecological benefits [6], have been widely used in the purification of industrial wastewater and domestic sewage. However, in underdeveloped regions or countries, such as India, Brazil, and South Africa, it is common to find mixed discharge of industrial wastewater and domestic sewage [7,8,9]. Therefore, some researchers have noticed the influence of domestic sewage on the role of constructed wetlands in removing heavy metals from wastewater. For example, a study by Lou suggests that mixing domestic sewage can improve the ability of constructed wetlands to remove Fe, Zn, Cu, Cd, and Ni from acid mine wastewater [10]. A study by Chen et al. shows that adding domestic sewage or straw decomposition products can improve the ability of constructed wetlands to remove heavy metals from wastewater [11]. Wang et al. found that the coexistence of domestic sewage and acid mine wastewater can improve the ability of constructed wetlands to remove heavy metals from wastewater [12]. Constructed wetlands play a good role in purifying Cr in wastewater [13]. Li Kai found that a higher content of domestic sewage in mixed polluted wastewater can better benefit the purification of Cr (VI) and Ni (II) by Leersia hexandra Swartz constructed wetlands [14]. A study by Li Shuai shows that the use of domestic sewage to prepare 1/2 Hoagland nutrient solution can significantly improve the ability of Coix lacryma-jobi L. constructed wetlands to remove Cr from wastewater, which has a better treatment effect and results in better plant growth than irrigation with only domestic sewage or 1/2 Hoagland nutrient solution [15]. Organic matter and microorganisms in domestic sewage may facilitate the transformation of Cr (VI) to Cr (III) in the substrate, increase the adsorption of Cr by the substrate, and reduce the absorption of Cr by plants [16]. Therefore, it is believed that adding domestic sewage may reduce the absorption of Cr by plants, promote the accumulation of Cr in the substrate, and thus alleviate the harm of Cr on plants and benefit the sustainable and efficient operation of constructed wetlands. However, not many studies have been conducted in this field.
Constructed wetlands mainly rely on the absorption of plants and substrates and the effects of microorganisms to remove pollutants from wastewater. How the plants grow is crucial for the continuous and efficient treatment of wastewater by constructed wetlands [17]. Photosynthetic capacity directly reflects the growth of plants, and photosynthetic parameters are extremely sensitive to adversity and stress. Sun et al. [18] found that Cr (VI) stress significantly reduced stomatal conductance (Gs) and the activity of photosystem II (PSII) in wheat leaves, leading to a significant decrease in photosynthetic rate (Pn). Under Cr (VI) stress, plants produce excessive reactive oxygen species (ROS), which can cause serious damage to the photosynthetic system of plants. As a result, the photosynthetic gas exchange and chlorophyll fluorescence properties of plants are inhibited, and the degree of inhibition can reflect the degree of Cr (VI) stress on plants [19]. Glutathione (GSH) generated in plants is a low-molecular-weight antioxidant that can enhance important functions, such as reducing intracellular peroxides, scavenging free radicals, and chelating heavy metals. Fatma et al. [20] found that the toxicity of Cr to the photosynthesis of wheat can be mitigated by the exogenous addition of S and NO, essentially by increasing the level of GSH, and thus mitigating the toxic effects of Cr on photosynthesis and the activity of Calvin cycle enzymes in leaves. Whether the effect of Cr (VI) on the photosynthesis of Coix lacryma-jobi L. is mitigated by regulating the GSH content in leaves under the condition of domestic sewage added needs to be studied in depth.
In this study, miniature Coix lacryma-jobi L. vertical flow constructed wetlands were set up, and wastewater containing different concentrations of Cr (VI) was prepared by adding domestic sewage, 1/2 Hoagland nutrient solution, and 1/2 Hoagland nutrient solution prepared with domestic wastewater. The effects of adding domestic sewage and nutrients on plant growth, photosynthetic system, and GSH content of the plants in chromium-contaminated constructed wetlands were studied to reveal the physiological mechanism of domestic wastewater mitigating the effect of Cr (VI) on plants. The results can provide a theoretical basis and new ideas for the efficient treatment of Cr-polluted wastewater by constructed wetlands.

2. Material and Methods

2.1. Material

Coix lacryma-jobi L., a wild wetland plant in Guangxi, is provided by the Crops Research Institute of Guangxi Academy of Agricultural Sciences.

2.2. Experiment Design

This study was conducted from March to September 2022 at the teaching and research base of the College of Agriculture, Guangxi University. Miniature vertical flow constructed wetlands were constructed with a study by Li et al. as a reference [21]. Large plastic barrels with a top diameter of 71 cm, a bottom diameter of 45 cm, and a height of 61 cm were used. The barrels were filled with 10 cm of large cobblestones (diameters ranging from 3 to 5 cm) and 40 cm of river sand (particle size ranging from 0.25 to 0.5 mm) from the bottom up, and a tap was installed 10 cm above the bottom for drainage. Twelve uniformly grown Coix lacryma-jobi L. seedlings were planted in each barrel. Within 1 month after planting, the seedlings were irrigated with 1/2 Hoagland nutrient solution. Cr (VI)-containing wastewater treatment was performed after the seedlings grew to 20 cm. Domestic wastewater (DS, main indicators, COD: 200~205 mg/L, TP: 0.78~1.18 mg/L, TN: 8.16~12.33 mg/L, NH3-N: 15.98~22.56 mg/L. Wastewater was collected from sewage pipes on each water inflow day, with its main indicators measured. The wastewater was not pretreated). Thereafter, 1/2 Hoagland nutrient solution (NS) and 1/2 Hoagland nutrient solution prepared with domestic wastewater (DN) were used as mother liquor, respectively. To ensure the stability of Cr (VI) in the incoming water, K2Cr2O7 solution was added to the mother liquor 2 h before each inflow to simulate wastewater containing 0, 20, and 40 mg/L of Cr (VI) (no significant change in Cr (VI) content was detected within 2 h). After entering the constructed wetlands, the wastewater containing Cr (VI) remained for 3 days after the water inflow, followed by a 4-day drying cycle, making a 7-day intermittent cycle. Each treatment was repeated three times, on five wetland pools per repetition. Each wetland tank was filled with 30 L of water by each water inflow.

2.3. Sample Collection

Coix lacryma-jobi L. plant samples and water samples were collected 10, 40, and 70 days after Cr (VI) treatment, and substrate samples were collected 48 days after the treatment. The roots, stems, and leaves of the samples were separated, rinsed with deionized water, and filled into sample bags after the surface was dried. They were kept fresh at 4 °C and brought to the laboratory. The samples were cut into small pieces and stored in sealed bags in a freezer with an ultra-low temperature of −80 °C for further measurement of the total chromium content in various organs of Coix lacryma-jobi L. The root tip was used for root activity measurement. The water samples were collected at the outlet and stored in PE plastic bottles with a capacity of 100 mL, and the bottles were stored in an insulation box with ice packs and sent to the laboratory. After being filtered through a 0.45 μm water filter membrane, the water samples were placed in centrifuge tubes with a capacity of 50 mL at 4 °C for the determination of total Cr content in the water discharged. The surface substrate was randomly sampled to obtain 200 g of fresh sample, which was placed in sealed bags and air-dried in a drying room. The substrate samples were used for the measurement of total Cr and total organic carbon content in the substrate.
Root, stem, and leaf samples were collected 20 and 50 days after the Cr (VI) treatment for GSH content measurement in different organs.

2.4. Experimental Methods

2.4.1. Measurement of Stem Diameters and Plant Heights

Six uniformly grown plants were selected from each repetition 10, 40, and 70 days after Cr (VI) treatment, and plant heights and stem diameters were measured. The plant height is the above-ground length, and the stem diameter is the diameter of the second above-ground node. According to the method developed by Long et al. [22], the inhibition rate of Cr (VI) treatment on plant height and stem diameter was calculated as follows:
Inhibition   rate   of   plant ( % ) = Plant   height   of   CK   Height   of   plants   treated   with   Cr   VI   Plant   height   of   CK   ×   100 %
Inhibition   rate   of   stem   diameter ( % ) =   Stem   diameter   of   CK Stem   diameter   treated   with   Cr   VI   Stem   diameter   of   CK   ×   100

2.4.2. Measurement of Root Activity

The TTC (triphenyl tetrazolium chloride) method was used to measure root activity [23]. Briefly, 0.5 g of Coix lacryma-jobi L. root tip sample was cut into small pieces and added to 5 mL of 0.4% TTC and 5 mL of phosphate buffer (pH = 7.0). The sample was incubated at 37 °C for 3 h and extracted in ethyl acetate for 15 min. The characteristic absorption peak at 458 nm was measured using a spectrophotometer.

2.4.3. Measurement of Photosynthetic Parameters and Chlorophyll Fluorescence Parameters

Photosynthetic parameters were measured using an LI-6400XT portable photosynthesis meter (LI-COR, Lincoln, NE, USA) from 9 to 11 a.m. 10, 40, and 70 days after Cr (VI) treatment, respectively [24]. The chlorophyll fluorescence parameters were measured using an AMP-2100 portable chlorophyll fluorometer (Walz, Effeltrieh, Germany), and the initial fluorescence (Fo), maximum fluorescence (Fm), and maximum photochemical quantum yield of PS II (Fv/Fm) were measured. The same parts of nine effective leaves were selected for each treatment, and one leaf was recorded three times to obtain the mean value for analysis.

2.4.4. Measurement of GSH Content in Different Parts of Coix lacryma-jobi L.

GSH was measured using the colorimetric method developed by Xie et al. [25]. Briefly, 1 g of fresh leaf sample was placed in a mortar, and 3 mL of pre-cooled 5% TCA solution and a small amount of quartz sand were added. The sample was thoroughly ground in an ice bath and then centrifuged at a low temperature (4 °C) for 15 min. Then, 0.25 mL of the supernatant liquid was obtained and mixed with 0.5 mL of Tris-HCl buffer solution (0.25 mol·L−1, pH = 8). Thereafter, 0.25 mL of 3% formaldehyde was added, and the solution was shaken well and stood at room temperature for 20 min. Moreover, 3 mL of the DTNB solution pre-warmed in a constant temperature water bath at 25 °C was added and mixed well. After 5 min of standing, the measurement was obtained at 412 nm using a spectrophotometer, and GSH content was calculated based on its standard curve.

2.4.5. Measurement of Cr Content in Different Parts of Coix lacryma-jobi L., Substrate, and the Water Discharged

Based on the method developed by Wang [26], 0.3 g of the sample was placed into a boiling tube and soaked with 6 mL of HNO3 and 1.5 mL of HClO4 overnight. Thereafter, the sample was boiled and neutralized in a graphite furnace. After cooling, the solution was diluted to 50 mL with 0.2% HNO3 and filtered. The chromium content was measured using an inductively coupled plasma emission spectrometer (model: ICP-5000, manufacturer: Focused Photonics Inc., origin: Beijing, China).
Based on the method developed by Liu [27], the total Cr content in substrate was measured using an inductively coupled plasma emission spectrometer after the samples were boiled and filtered.
Based on the method developed by Ribas [28], the Cr (VI) content in water was measured using diphenylcarbazide spectrophotometry. The colorimetric tubes used were soaked in 10% dilute nitric acid for over 16 h to prevent Cr (VI) adsorption on the inner walls of the tubes. Based on the method developed by Yue [29], the spectrophotometric method was used to measure the total Cr content in the water discharged.

2.4.6. Measurement of Organic Matter Content in Substrate

Based on the method developed by Wang [30], the potassium dichromate oxidation-external heating method was used to measure the total organic carbon content in the soil samples.

2.5. Statistical Analysis

Origin 2021 was used for plotting, Excel 2019 was used to collate data, SPSS Statistics 25 was used for calculation and statistical analysis, and Duncan’s test was used for multiple comparisons of significant differences (p < 0.05).

3. Results and Analysis

3.1. Plant Height and Stem Diameter

As shown in Table 1, the plant heights of CK Coix lacryma-jobi L. ranged from 22.16 to 140.03 cm, and the plant heights under 20 mg/L and 40 mg/L Cr (VI) treatments ranged from 18.67 to 129.4 cm and 16.23 to 109.23 cm, respectively, with all being significantly shorter than CK. The degree of inhibition was greater with a higher Cr (VI) concentration (p < 0.05). The differences between treatments with different Cr (VI) concentrations were significant. With the same Cr concentration, the plant heights of Coix lacryma-jobi L. were greatest under 1/2 Hoagland nutrient solution prepared with domestic wastewater (DN), followed by 1/2 Hoagland nutrient solution (NS) and domestic sewage (DS). The plants under the DN treatment were significantly taller than those under NS and DS treatments (p < 0.05). With 20 mg/L of Cr (VI), the inhibition rates of Coix lacryma-jobi L. plant heights under DN, NS, and DS were 5.33%~75.9%, 15.64%~16.7%, and 13.88%~15.31%, respectively. With 40 mg/L of Cr (VI), the inhibition rates under DN, NS, and, DS were 16.74%~24.45%, 22.81%~28.52%, and 22.39%~26.7%, respectively. The higher the Cr concentration, the more significantly the plant growth is inhibited. The plant heights of Coix lacryma-jobi L. irrigated with domestic sewage were less inhibited than those under NS.
The stem diameters of Coix lacryma-jobi L. ranged from 8.4 to 12.73 mm, and the diameters under DN were the largest, followed by NS and DS, with insignificant differences.

3.2. Root Activity

The root activity of Coix lacryma-jobi L. ranged from 0.475 to 2.418 mg/gFW-h (Figure 1) and decreased with the increase in Cr (VI) concentration. The root activity of the plant showed a trend of increasing and then decreasing as the time of Cr (VI) treatment extended. In each period, the root activity under DN was the highest, followed by NS and DS, and the 40th day of treatment saw the highest root activity. On the 10th day of Cr treatment and with 20 and 40 mg/L of Cr (VI), the differences in root activity under different inflow conditions were not significant. On the 70th day, the root activity under DN was significantly greater than that under NS and DS (p < 0.05). Compared with CK, the root activity of Coix lacryma-jobi L. under DN, NS, and DS with 20 mg/L of Cr (VI) decreased by 18.53%~42.67%, 23.74%~53.62%, and 18.61%~41.08%, respectively, and that with 40 mg/L of Cr (VI) decreased by 39.07%~61.09%, 42.62%~72.27%, and 36.85%~65.76%, respectively. With the same Cr treatment, the root activity under NS dropped to a greater degree than under DN and DS.

3.3. Photosynthetic Gas Exchange Parameters of Coix lacryma-jobi L.

As shown in Table 2, the net photosynthetic rate (Pn) of Coix lacryma-jobi L. leaves ranged from 6.787 to 24.32 μmolCO2/m2·s, stomatal conductance (Gs) ranged from 0.043 to 0.183 mmol/m−2·s−1, intercellular CO2 concentration (Ci) ranged from 115.188 to 273.836 μmol/mol, and transpiration rate (Tr) ranged from 1.32 to 3.69 μmol/m2·s. All these parameters significantly dropped as the Cr (VI) concentration rose, with similar changing trends. The various photosynthetic parameters increased and then decreased as the Cr (VI) treatment time extended, reaching the highest value on the 40th day of Cr (VI) treatment. With the same Cr concentration, the values of these photosynthetic gas exchange parameters under the DN treatment were the greatest, followed by NS and DS. On the 70th day of Cr (VI) treatment, the net photosynthetic rate (Pn) under DN was significantly greater than that under NS and DS. The gas exchange level under the condition of adding domestic sewage increased more significantly than that under NS from 10 to 40 d of Cr (VI) treatment. From 40 to 70 d, the gas exchange level under DN and DS decreased more significantly than that under NS, indicating that the gas exchange of Coix lacryma-jobi L. leaves under the condition of adding domestic sewage maintained a relatively high increase when the plants grew fast, and the rate of gas exchange slightly decreased when the plants grew relatively slow. As the concentration of Cr (VI) increased, the degree to which gas exchange of Coix lacryma-jobi L. leaves irrigated by domestic sewage or the mixture containing domestic sewage was inhibited was smaller than that of leaves irrigated by the pure nutrient solution.

3.4. Chlorophyll Fluorescence Properties of Coix lacryma-jobi L.

Initial Fluorescence (Fo) and Maximum Fluorescence (Fm)

The initial fluorescence (Fo) of leaves reflects the fluorescence yield when the PSII reaction center is fully open, and the Fo of Coix lacryma-jobi L. leaves increased significantly (p < 0.05) with the increase in Cr (VI) concentration and decreased. Then, it increased as the time of Cr (VI) treatment extended (Table 3). The maximum fluorescence (Fm) can show the electron transfer of PSII, and the trend of Fm is opposite to that of Fo. Fv/Fm is the light energy conversion efficiency in the PSII reaction center, which is related to the degree of photoinhibition of Coix lacryma-jobi L. The Fv/Fm of Coix lacryma-jobi L. leaves ranged from 0.65 to 0.888, which decreased significantly (p < 0.05) with the increasing Cr (VI) concentration, indicating a decrease in photosynthetic capacity. Compared with the control, the maximum photochemical quantum yields under DN, NS, and DS under the 20 mg/L Cr (VI) treatment dropped by 4.14%~9.56%, 6.04%~12.6%, and 1.9%~5.2%, respectively, and by 7.21%~15.38%, 9.07%~18.53%, and 5.57%~13.44%, respectively under the 40 mg/L Cr (VI) treatment. With the same Cr concentration, the decrease under NS was the most significant, followed by DN and DS.

3.5. Glutathione (GSH) Content in Different Organs of Coix lacryma-jobi L.

According to Table 4, GSH content in the roots, stems, and leaves of Coix lacryma-jobi L. ranged from 36.56 to 103.14 μg/gFW, 18.64 to 53.13 μg/gFW, and 200.47 to 434.79 μg/gFW, respectively. With the same Cr concentration, the values of GSH content in roots, stems, and leaves of the plant were the highest under NS, followed by DS and DN (except for CK). Specifically, the GSH content in roots and leaves under NS was significantly higher than that under DN and DS (p < 0.05). GSH content in various parts of the plant increased to certain degrees as the time of treatment extended. With the same Cr concentration, the GSH content under NS increased from 5.57% to 18% over time, while that under DS and DN increased from 8.28% to 35.92% (except for CK). With domestic sewage added, the GSH content increased more significantly over time than under NS.
Compared with the control, values of GSH content in roots, stems, and leaves significantly increased after treatment with both 20 mg/L and 40 mg/L of Cr (VI). On the 20th and 50th days of Cr treatment with 40 mg/L of Cr (VI), the values of GSH content in roots, stems, and leaves under DN were 30.27% and 20.56%, 13.96% and 13.58%, and 30.28% and 13.08% higher than those under the treatment with 20 mg/L of Cr (VI); 9.98% and 7.13%, 11.46% and 11.14%, and 5.88% and 6.33% higher than the latter under NS; 29.8% and 27.67%, 19.06% and 15.26%, and 24.63% and 14.29% higher than the latter under DS. With domestic sewage added, the GSH content increased more significantly than under NS.

3.6. Cr Content in Roots, Stems, and Leaves of Coix lacryma-jobi L.

The total Cr content in roots, stems, and leaves of Coix lacryma-jobi L. ranged from 9.16 to 236.16, 1.94 to 80.14, and 3.22 to 91.67 mg/kg, respectively, with the highest Cr content in roots, followed by that in leaves and stems. The Cr content in roots, stems, and leaves increased as the Cr (VI) concentration increased and the treatment time extended. In addition, there were significant differences between treatments with different Cr (VI) concentrations (p < 0.05) (Figure 2).
Under DN, the Cr content in roots, stems, and leaves of Coix lacryma-jobi L. ranged from 9.16 to 144.7, 2.09 to 57.99, and 3.39 to 58.66 mg/kg, respectively. The figures under NS and DS were 9.48~236.16, 1.94~80.14, and 3.22~91.67 mg/kg, and 9.16~166.16, 2.21~63.45, and 3.34~64.7 mg/kg. With the same Cr (VI) concentration, the values of Cr content in roots, stems, and leaves of Coix lacryma-jobi L. under NS were higher than those under DN and DS.

3.7. Organic Matter Content in Substrate

As shown in Table 5, the organic matter content under the three treatments ranged from 18.17 to 34.12 mg/kg (DN), 11.27 to 27.11 mg/kg (NS), and 16.94 to 31.03 mg/kg (DS). Organic matter content decreased as the Cr (VI) concentration increased and increased as the treatment time extended. The organic matter content under both DN and DS was greater than that under NS with the same treatment time and Cr (VI) concentration. The organic matter content was significantly greater (p < 0.05) under DN and DS than under NS on the 10th and 40th days of the Cr (VI) treatment, but on the 70th day, the differences in organic matter content between different conditions were not significant.

3.8. Total Cr Content in Substrate and the Water Discharged

The total Cr content in substrate (Table 6) ranged from 6.74 to 183.44 mg/kg under DN, 3.8 to 174.67 mg/kg under NS, and 7.21 to 189.78 mg/kg under DS, and the total Cr content in substrate increased significantly (p < 0.05) as the concentration of Cr (VI) treatment increased and the treatment time extended. The total Cr content in the discharged water ranged from 0.06 to 0.72 mg/L under DN, 0.03~0.86 mg/L under NS, and 0.07~0.79 mg/L under DS, and the Cr (VI) content in the discharged water under the three treatments was 0.03~0.24 (DN), 0.03~0.38 (NS), and 0.03~0.25 mg/L (DS), respectively (Table 6). NS saw the highest total Cr content in substrate and Cr and Cr (VI) content in the discharged water, followed by DS and DN. Therefore, the DN treatment had the best effect in treating chromium-containing sewage.

4. Discussion

Cr is not an essential element for plants, and excessive accumulation can inhibit plant growth. Cr (VI) can greatly inhibit plant growth due to its strong oxidative properties [31]. A study by Adhikari et al. showed that Cr (VI) stress increases reactive oxygen species (ROS) in maize seedlings and significantly decreases biomass in sand culture [32]. Liu et al. found that the growth of Coix lacryma-jobi L. is significantly inhibited when the Cr (VI) content reaches 20 mg/L [27]. However, studies have also shown that adding domestic sewage to prepare 1/2 Hoagland nutrient solution to constructed wetlands can alleviate the inhibitory effect of Cr (VI) on plant growth [11]. The present study showed that the growth of Coix lacryma-jobi L. was significantly inhibited by treatment with both 20 mg/L and 40 mg/L of Cr (VI) and the degree of inhibition increased significantly with the increase in Cr (VI) concentration. Hussain et al. also found that the growth of rice was severely inhibited under Cr (VI) stress [33]. However, the degree of inhibition of the growth of Coix lacryma-jobi L. was lower under DN and DS conditions than under the NS conditions, indicating that the use of domestic sewage to prepare 1/2 Hoagland nutrient solution can effectively alleviate the inhibitory effect of Cr (VI) on the growth of the plant. Similarly, a study by Saleem et al. found that the use of press mud as an organic amendment can effectively reduce the impact of Cr (VI) on the growth of Helianthus annuus L. [34]. Photosynthesis is an important factor determining how plants grow, and the growth of Coix lacryma-jobi L. is inhibited under Cr stress, which is closely related to the inhibition of photosynthesis [35].
Photosynthesis is highly sensitive to heavy metal stress, and many studies have used changes in the parameters of photosynthetic gas exchange as important indicators of plant response to heavy metal stress [36,37]. When plants are subjected to heavy metal stress, the efficiency of photosynthetic gas exchange is significantly inhibited, leading to a decrease in their photosynthetic capacity [38]. A study by Vernay et al. showed that Cr (VI) stress leads to a significant decrease in photosynthetic gas exchange parameters in Datura innoxia [39]. The present study found that Pn, Gs, Ci, and Tr of Coix lacryma-jobi L. leaves were significantly inhibited under Cr (VI) treatment, which is consistent with the results of previous studies. Chlorophyll fluorescence parameters are important indicators for assessing the effects of adversity and stress on the photosynthetic system of plants. Elevated Fo means reversible inactivation or irreversible damage of PS II reaction centers [40]. Fv/Fm indicates the maximum photochemical efficiency of PS II when all reaction centers are open. When plants are subjected to heavy metal stress, Fv/Fm significantly decreases, and photoinhibition of PS II increases [41]. In this study, Fo of Coix lacryma-jobi L. increased under Cr (VI) stress, indicating that the PSII reaction center was damaged to some extent. Fv/Fm decreased with the increasing intensity of Cr (VI) stress, indicating that the plants were subjected to photoinhibition. The parameters of light energy conversion efficiency of Coix lacryma-jobi L. leaves decreased significantly as the Cr (VI) increased, indicating that Cr stress causes photoinhibition of plants, which is consistent with previous findings. This may be an important reason for the inhibition of photosynthesis in this study. The DN and DS treatments with domestic sewage can reduce the extent to which photosynthetic gas exchange and chlorophyll fluorescence parameters are inhibited under Cr (VI) stress, indicating that domestic sewage may maintain high photosynthetic capacity by alleviating the damage of Cr (VI) to the photosystem, which may be an important reason for normal plant growth. Domestic sewage contains a large amount of organic matter and microorganisms. Previous studies have shown that organic matter and microorganisms can promote the conversion of Cr (VI) to Cr (III). Cr (III) easily binds with anions or organic matter in substrate to generate an insoluble form, which reduces the absorption of Cr by plants [42]. This may be an important reason why plant growth is less inhibited with domestic sewage added.
The root system of plants is an important part that directly contacts and accumulates Cr, which directly affects the growth of the aboveground parts. Root activity reflects the ability of plants to absorb water and nutrients, and is usually inhibited under heavy metal stress [43]. Guo et al. found that under Cd and Pb stress, the root activity of Matricaria chamomilla L. significantly decreased and was positively correlated with the degree of stress [44]. The extent to which the growth of Coix lacryma-jobi L. is inhibited by Cr (VI) can be obtained by studying the effect of Cr (VI) on root activity [45]. In this study, the root activity of Coix lacryma-jobi L. decreased with the increase in Cr (VI) concentration. Compared with CK, the degree of root activity inhibition under DS and DN was lower than that under NS, indicating that the root activity of Coix lacryma-jobi L. was less inhibited with domestic sewage added. The root activity under DN was the highest, and that under NS was higher than under DS. Root activity is closely related to the amount of heavy metals absorbed by plants. A study by Liu et al. suggested that with the increase in Cd accumulation in rice roots, root activity significantly decreased [46]. This study found a similar trend. Root activity under DN and NS was greater than that under DS, indicating that good nutritional conditions facilitate root growth. Under the condition with domestic sewage added, the root activity of Coix lacryma-jobi L. was less inhibited, which may be due to the fact that the plant absorbed less Cr.
In this study, Cr content in different parts of Coix lacryma-jobi L. under DS and DN was lower than that under NS, while Cr content in substrate under DS and DN was higher than that under NS, indicating that adding domestic sewage to chromium-containing wastewater may promote the conversion of Cr into forms in substrate that are difficult for plants to use. Meanwhile, the absorption of Cr by the root system and transfer of Cr from roots to aboveground parts both decrease, which may be an important reason why the growth, photosynthesis, and root activity of Coix lacryma-jobi L. were less inhibited under the condition with domestic sewage added. A study by Yu showed that an increase in organic matter content could promote the chemical form transformation of cadmium and reduce the toxicity of the element in soil [47]. Cr (VI) content in constructed wetlands may be closely related to organic matter content. Xiao found that soluble organic matter is an excellent reducer of Cr (VI), which can promote the conversion of Cr (VI) to Cr (III) [48]. A study by Choppala et al. showed that cattle manure and S can promote the reduction in Cr (VI) and its transformation into forms that are difficult for plants to absorb [49]. Microorganisms play an important role in the chemical form transformation of Cr, which can promote the transformation of Cr (VI) into Cr (III) and reduce its mobility [50]. Domestic sewage contains abundant organic matter and microorganisms, which facilitate the chemical form transformation of Cr. In this study, the organic matter content in the substrate under the treatment with domestic sewage added was significantly higher than when the plants were irrigated with nutrient solution only, which may promote the conversion of Cr (VI) and reduce Cr absorption by plants in the constructed wetlands. Finally, the decrease in the amount of Cr absorbed by Coix lacryma-jobi L. may be an important reason why the plant was less inhibited under the condition with domestic sewage added.
Cr (VI) can produce reactive oxygen species in plants due to its strong oxidative properties, leading to peroxidation of cell membrane lipids and causing chain reactions that lead to cell damage [51]. GSH generated in plants can act as an antioxidant and complex with heavy metals, which is very pivotal for plants to alleviate toxicity [52]. Jan et al. found that Cr (VI) treatment could maintain a high level of GSH content, and GSH content in plants indicates the degree of Cr (VI) stress on plants [53]. The results of this study showed that GSH content in roots, stems, and leaves increased under Cr treatment. The GSH content in various organs of Coix lacryma-jobi L. under DN and DS was lower than that under NS, and the DN treatment saw the lowest values, indicating that plants under NS were subjected to the highest degree of Cr (VI) stress, which is similar to the previous findings. When plants are under adversity or stress, they adapt to or mitigate the damage caused by stress by regulating the generation of GSH [54]. A study by Qiu showed that exogenous GSH can effectively alleviate Cr toxicity in rice [55]. Jan’s study showed that exogenous 24-Epibrassinolide can improve the antioxidative ability and increase the GSH content of plants under Cr stress [56]. The results of this study showed that domestic sewage improved the capability of Coix lacryma-jobi L. leaves to generate GSH, significantly increased GSH content, and improved the antioxidative ability of the plant, which is consistent with previous findings. Additionally, photosynthetic gas exchange parameters and chlorophyll fluorescence parameters of leaves under DN were higher than those under NS, indicating that domestic sewage may mitigate the effect of Cr (VI) on photosynthesis by increasing GSH content. This may be related to the complex composition of domestic sewage. However, further research is needed to investigate how domestic sewage increases GSH content.

5. Conclusions

Adding domestic sewage to chromium-containing wastewater increased the organic matter content in substrate, promoted Cr accumulation in substrate, reduced Cr uptake by plants, increased GSH content in roots, stems, and leaves of Coix lacryma-jobi L., improved indicators, such as photosynthetic gas exchange parameters of leaves, chlorophyll fluorescence parameters, and root activity, and alleviated the inhibition of plant growth by Cr (VI) stress. Under the condition with 1/2 Hoagland nutrient solution, indicators, such as plant growth, photosynthetic parameters, and fluorescence parameters of leaves were better in the constructed wetlands with domestic sewage added than under treatment with the nutrient solution or domestic sewage alone. The capability to remove Cr from wastewater under DN was better than that under NS and DS, indicating that under good nutritional conditions, adding domestic wastewater from external sources can improve the capacity of constructed wetlands to remove Cr (VI) from wastewater and contribute to the sustainable and efficient operation of the wetlands. However, the mechanism of promoting the chemical form transformation of Cr to mitigate the damage of Cr (VI) to plants and improve the effect of Cr (VI) treatment under a condition with domestic wastewater added needs further research.

Author Contributions

Validation, X.L.; Formal analysis, L.L.; Resources, X.C., X.W. and Z.L. (Zhengwen Li); Writing—original draft, Y.N.; Writing—review & editing, Y.N., Z.L. (Zhigang Li) and S.L.; Supervision, Z.L. (Zhigang Li); Funding acquisition, Z.P. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China (41867023, 21167002) and the Natural Science Foundation of Guangxi Province (2018GXNSFAA281214).

Data Availability Statement

The data that support the findings of this study are available from the corresponding author, [Li, Z.], upon reasonable request.

Acknowledgments

The authors thank the College of Agriculture of Guangxi University for providing the research platform.

Conflicts of Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

References

  1. Ray, A.; Jankar, J.S. A Comparative Study of Chromium: Therapeutic Uses and Toxicological Effects on Human Health. J. Pharmacol. Pharmacother. 2022, 13, 239–245. [Google Scholar] [CrossRef]
  2. Shahid, M.; Shamshad, S.; Rafiq, M.; Khalid, S.; Bibi, I.; Niazi, N.K.; Dumat, C.; Rashid, M.I. Chromium speciation, bioavailability, uptake, toxicity and detoxification in soil-plant system: A review. Chemosphere 2017, 178, 513–533. [Google Scholar] [CrossRef] [PubMed]
  3. Zhou, X.; Hu, H.; Ying, C.; Zheng, J.; Zhou, F.; Jiang, H.; Ma, Y. Study on Chromium Uptake and Transfer of Different Maize Varieties in Chromium-Polluted Farmland. Sustainability 2022, 14, 14311. [Google Scholar] [CrossRef]
  4. Duan, W. In the “Fur Capital of China” Excessive Chromium Discharge of Sewage? Sentenced and given an industry restraining order! Dahe News, 4 June 2020. [Google Scholar]
  5. Mei, Y. Sentenced for Environmental Pollution by Excessive Discharge of Electroplating Wastewater. 12 March 2022. Available online: https://www.163.com/dy/article/H27UCC7A0514JN6C.html (accessed on 19 June 2023).
  6. Li, Z.; Li, S.; Mei, L.; Wan, X.; Liang, H.; Chen, W.; Chen, H.; Zhou, Z. Purification effect of canna (Canna indica Linn.) and reed (Phragmites australis L.) constructed wetlands on chromium-containing domestic sewage and the physiological and ecological changes of plants. J. Agro-Environ. Sci. 2011, 30, 358–365. [Google Scholar]
  7. Reis, M.M.; Tuffi Santos, L.D.; da Silva, A.J.; de Pinho, G.P.; Montes, W.G. Metal Contamination of Water and Sediments of the Vieira River, Montes Claros, Brazil. Arch. Environ. Contam. Toxicol. 2019, 77, 527–536. [Google Scholar] [CrossRef]
  8. Addo-Bediako, A.; Rasifudi, L. Spatial distribution of heavy metals in the Ga-Selati River of the Olifants River System, South Africa. Chem. Ecol. 2021, 37, 450–463. [Google Scholar] [CrossRef]
  9. Mohanty, B.; Anirban, D. Heavy metals in agricultural cultivated products irrigated with wastewater in India: A review. AQUA-Water Infrastruct. Ecosyst. Soc. 2023, 1, 1–12. [Google Scholar] [CrossRef]
  10. Lou, Y. Research on Pollutant Removal Effect of Joint Treatment of Domestic Sewage and Acidic Mine Wastewater. Master’s Thesis, Guizhou University, Guiyang, China, 16 February 2017. [Google Scholar]
  11. Chen, J.; Deng, S.; Jia, W.; Li, X.; Chang, J. Removal of multiple heavy metals from mining-impacted water by biochar-filled constructed wetlands: Adsorption and biotic removal routes. Bioresour. Technol. 2021, 331, 125061. [Google Scholar] [CrossRef]
  12. Wang, H.; Zhang, M.; Lv, Q.; Xue, J.; Yang, J.; Han, X. Effective co-treatment of synthetic acid mine drainage and domestic sewage using multi-unit passive treatment system supplemented with silage fermentation broth as carbon source. J. Environ. Manag. 2022, 310, 114803. [Google Scholar] [CrossRef]
  13. Peng, Z.; Li, Z.; He, B.; Li, S.; Yang, P.; Li, Z.; Liang, H. Root decomposition and chromium release and chemical form changes of barley constructed wetland. J. Environ. Sci. 2015, 35, 238–244. [Google Scholar]
  14. Li, K.; Gu, C.; Liu, J.; Huang, H.; Gao, Y. Experiment of Li Shihe purifying domestic sewage containing heavy metals. Environ. Sci. Technol. 2014, 37, 151–155. [Google Scholar]
  15. Li, S. Study on the Purification Mechanism of Chromium (VI) Containing Wastewater by Barley Constructed Wetland. Master’s Thesis, Guangxi University, Nanning, China, 16 January 2016. [Google Scholar]
  16. Xu, R.; Wang, Y.-N.; Sun, Y.; Wang, H.; Gao, Y.; Li, S.; Guo, L.; Gao, L. External sodium acetate improved Cr (VI) stabilization in a Cr-spiked soil during chemical-microbial reduction processes: Insights into Cr (VI) reduction performance, microbial community and metabolic functions. Ecotoxicol. Environ. Saf. 2023, 251, 114566. [Google Scholar] [CrossRef]
  17. Li, Y.; Cheng, C.; Li, X. Research progress on water purification efficiency of multiplant combination in constructed wetland. In Proceedings of the IOP Conference Series, Earth and Environmental Science, Philadelphia, PA, USA, 11 October 2020. [Google Scholar]
  18. Sun, C.; Tan, Q.; Liu, X.; Zhang, Z.; Sun, J. Effects of exogenous melatonin on photosynthetic characteristics and nutrient uptake of wheat seedlings under chromium (Cr~(6+)) stress. J. Wheat Crops 2022, 42, 1535–1542. [Google Scholar]
  19. Wu, M.; Jia, Y.; Li, H.; Yang, L.; Wang, G. Effects of chromium stress on chlorophyll fluorescence characteristics and active oxygen metabolism system of tobacco leaves. Jiangsu Agric. Sci. 2014, 42, 92–95. [Google Scholar]
  20. Fatma, M.; Sehar, Z.; Iqbal, N.; Alvi, A.F.; Abdi, G.; Proestos, C.; Khan, N.A. Sulfur supplementation enhances nitric oxide efficacy in reversal of chromium-inhibited Calvin cycle enzymes, photosynthetic activity, and carbohydrate metabolism in wheat. Sci. Rep. 2023, 13, 6858. [Google Scholar] [CrossRef] [PubMed]
  21. Li, Z.; Jiang, Y.; Li, S.; Huang, H.; Chen, W.; Chen, H. Effects of constructed wetland wastewater treatment on photosynthesis and chlorophyll fluorescence characteristics of three plants. Ecol. Environ. 2008, 17, 2187–2191. [Google Scholar]
  22. Long, H.; Zhang, D. Preliminary results of drought resistance identification of 22 Stylophyllum materials at seedling stage. Trop. Agric. Sci. 2015, 35, 26–30. [Google Scholar]
  23. Castañares, J.L.; Bouzo, C.A. Effect of exogenous melatonin on seed germination and seedling growth in melon (Cucumis melo L.) under salt stress. Hortic. Plant J. 2019, 5, 79–87. [Google Scholar] [CrossRef]
  24. Bu, Y. Physiological Mechanism of Barley in Response to Different Concentrations of Chromium (VI). Master’s Thesis, Guangxi University, Nanning, China, 16 June 2011. [Google Scholar]
  25. Xie, B.; Jin, T.; Liu, P.; Jin, H.; Kong, L. Changes of phytochelatin and metallothionein in soybean roots and leaves under aluminum stress. Chin. J. Oil Crops 2008, 116, 191–197. [Google Scholar]
  26. Wang, A.; Huang, S.; Zhong, G.; Xu, G.; Liu, Z.; Shen, X. Effects of chromium stress on growth and chromium accumulation of three herbaceous plants. Environ. Sci. 2012, 33, 2028–2037. [Google Scholar]
  27. Liu, X.; Nong, Y.; Huang, J.; Li, S.; Li, L.; Cheng, X.; Wang, X.; Li, Z.; Li, Z. Effects of Cr6+ on Photosynthetic Characteristics and Trace Element Absorption of Coix in Constructed Wetlands. Guangxi Plant 2022, 42, 1959–1970. [Google Scholar]
  28. Ribas, T.C.; Mesquita, R.B.; Machado, A.; Miranda, J.L.; Marshall, G.; Bordalo, A.; Rangel, A.O. A Robust Flow-Based System for the Spectrophotometric Determination of Cr (VI) in Recreational Waters. Molecules 2022, 27, 2073. [Google Scholar] [CrossRef]
  29. Le, H.; Luo, L.; Liu, S. Condition optimization for the simultaneous determination of Cr(VI), Cr(III) and total chromium in water by spectrophotometry. Ind. Water Treat. 2007, 195, 73–75. [Google Scholar]
  30. Wang, M. Discussion on the determination of organic carbon content in soil by potassium dichromate oxidation-external heating method. Xinjiang Nonferrous Met. 2019, 42, 98–99. [Google Scholar]
  31. Stambulska, U.Y.; Bayliak, M.M.; Lushchak, V.I. Chromium (VI) Toxicity in Legume Plants: Modulation Effects of Rhizobial Symbiosis. BioMed Res. Int. 2018, 2018, 8031213. [Google Scholar] [CrossRef]
  32. Adhikari, A.; Adhikari, S.; Ghosh, S.; Azahar, I.; Shaw, A.; Roy, D.; Roy, S.; Saha, S.; Hossain, Z. Imbalance of redox homeostasis and antioxidant defense status in maize under chromium (VI) stress. Environ. Exp. Bot. 2020, 169, 103873. [Google Scholar] [CrossRef]
  33. Hussain, A.; Ali, S.; Rizwan, M.; Zia ur Rehman, M.; Hameed, A.; Hafeez, F.; Alamri, S.A.; Alyemeni, M.N.; Wijaya, L. Role of zinc–lysine on growth and chromium uptake in rice plants under Cr stress. J. Plant Growth Regul. 2018, 37, 1413–1422. [Google Scholar] [CrossRef]
  34. Saleem, M.; Asghar, H.N.; Khan, M.Y.; Zahir, Z.A. Gibberellic acid in combination with pressmud enhances the growth of sunflower and stabilizes chromium (VI)-contaminated soil. Environ. Sci. Pollut. Res. 2015, 14, 10610–10617. [Google Scholar] [CrossRef]
  35. Sharma, A.; Kumar, V.; Shahzad, B.; Ramakrishnan, M.; Singh Sidhu, G.P.; Bali, A.S.; Handa, N.; Kapoor, D.; Yadav, P.; Khanna, K.; et al. Photosynthetic Response of Plants Under Different Abiotic Stresses: A Review. J. Plant Growth Regul. 2020, 39, 509–531. [Google Scholar] [CrossRef]
  36. Zhang, Y. Research progress on the effect of heavy metal chromium on plant photosynthetic system. Mod. Hortic. 2016, 313, 25. [Google Scholar] [CrossRef]
  37. Ali, S.; Rizwan, M.; Bano, R.; Bharwana, S.A.; Rehman, M.Z.U.; Hussain, M.B.; Al-Wabel, M.I. Effects of biochar on growth, photosynthesis, and chromium (Cr) uptake in Brassica rapa L. under Cr stress. Arab. J. Geosci. 2018, 11, 507. [Google Scholar] [CrossRef]
  38. Emamverdian, A.; Ding, Y.; Mokhberdoran, F.; Xie, Y. Growth Responses and Photosynthetic Indices of Bamboo Plant (Indocalamus latifolius) under Heavy Metal Stress. Sci. World J. 2018, 2018, 121936. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Vernay, P.; Gauthier-Moussard, C.; Jean, L.; Bordas, F.; Faure, O.; Ledoigt, G.; Hitmi, A. Effect of chromium species on phytochemical and physiological parameters in Datura innoxia. Chemosphere 2008, 72, 763–771. [Google Scholar] [CrossRef] [PubMed]
  40. Yu, A.; Yang, T.; Gao, X.; Han, W. Effects of high temperature stress on fluorescence parameters of silver leaf tree. Hunan For. Sci. Technol. 2022, 49, 25–30. [Google Scholar]
  41. Luo, J.; Li, Y.; Li, Y.; Zhao, W.; Xu, Y.; Zhao, S.; Zhang, Z.; Gao, H. Effects of six plant growth regulators on photoinhibition of photosystem II and photosystem I in isolated cucumber leaves under light and temperature stress. Acta Plant Physiol. 2021, 57, 178–186. [Google Scholar]
  42. Wang, X.; Lei, L.; Yan, X.; Meng, X.; Chen, Y. Processes of chromium (VI) migration and transformation in chromate production site: A case study from the middle of China. Chemosphere 2020, 257, 127282. [Google Scholar] [CrossRef]
  43. López-Bucio, J.S.; Ravelo-Ortega, G.; López-Bucio, J. Chromium in plant growth and development: Toxicity, tolerance and hormesis. Environ. Pollut. 2022, 312, 120084. [Google Scholar] [CrossRef]
  44. Guo, R.; Fan, M.; Tao, Y.; Wu, H.; Jiang, C. Root activity and heavy metal migration of chamomile chamomile under lead and cadmium stress. Heilongjiang Agric. Sci. 2020, 311, 42–46. [Google Scholar]
  45. Yu, X.-Z.; Lin, Y.-J.; Fan, W.-J.; Lu, M.-R. The role of exogenous proline in amelioration of lipid peroxidation in rice seedlings exposed to Cr (VI). Int. Biodeterior. Biodegrad. 2017, 123, 106–112. [Google Scholar] [CrossRef]
  46. Liu, C.; Liu, Y.; Luo, S.; Cui, L. Effects of different cadmium concentrations on rice root activity and grain quality in cold regions. Anhui Agric. Sci. 2013, 41, 5758–5760. [Google Scholar]
  47. Yu, S.; Gao, S.; Qu, Y.; Chen, Y.; Wang, G. Toxic effects of cadmium on tomato roots under different soil conditions and its toxic critical value. J. Agric. Environ. Sci. 2014, 33, 640–646. [Google Scholar]
  48. Xiao, W. Chromium Migration and Transformation Rules and Pollution Diagnostic Indicators in Typical Soils. Ph.D. Thesis, Zhejiang University, Hangzhou, China, 16 November 2014. [Google Scholar]
  49. Choppala, G.; Kunhikrishnan, A.; Seshadri, B.; Park, J.H.; Bush, R.; Bolan, N. Comparative sorption of chromium species as influenced by pH, surface charge and organic matter content in contaminated soils. J. Geochem. Explor. 2018, 184, 255–260. [Google Scholar] [CrossRef]
  50. Xiao, W.; Ye, X.; Ye, Z.; Zhang, Q.; Zhao, S.; Chen, D.; Gao, N.; Huang, M. Responses of microbial community composition and function to biochar and irrigation management and the linkage to Cr transformation in paddy soil. Environ. Pollut. 2022, 304, 119232. [Google Scholar] [CrossRef] [PubMed]
  51. Zeng, F. Physiological and Molecular Mechanisms of Rice Chromium Toxicity and Tolerance. Ph.D. Thesis, Zhejiang University, Hangzhou, China, 16 July 2010. [Google Scholar]
  52. Wang, X. Study on the Mechanism of Reduced Glutathione (GSH) Alleviating Cadmium Stress in Wheat Seedlings. Master’s Thesis, Northwest A & F University, Xianyang, China, 15 January 2021. [Google Scholar]
  53. Gupta, P.; Seth, C.S. 24-Epibrassinolide Regulates Functional Components of Nitric Oxide Signalling and Antioxidant Defense Pathways to Alleviate Salinity Stress in Brassica juncea L. cv. Varuna. J. Plant Growth Regul. 2022, 1, 1–16. [Google Scholar] [CrossRef]
  54. Hasanuzzaman, M.; Bhuyan, M.H.M.B.; Anee, T.I.; Parvin, K.; Nahar, K.; Mahmud, J.A.; Fujita, M. Regulation of ascorbate-glutathione pathway in mitigating oxidative damage in plants under abiotic stress. Antioxidants 2019, 8, 384. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Qiu, B. Genetic Analysis of Rice Stress Tolerance to Chromium Stress and Mechanism of Reduced Glutathione Alleviating Chromium Toxicity. Ph.D. Thesis, Zhejiang University, Hangzhou, China, 15 August 2012. [Google Scholar]
  56. Jan, S.; Noman, A.; Kaya, C.; Ashraf, M.; Alyemeni, M.N.; Ahmad, P. 24-Epibrassinolide alleviates the injurious effects of Cr (VI) toxicity in tomato plants: Insights into growth, physio-biochemical attributes, antioxidant activity and regulation of Ascorbate—Glutathione and Glyoxalase cycles. J. Plant Growth Regul. 2020, 39, 1587–1604. [Google Scholar] [CrossRef]
Figure 1. Root activity under different treatments. Note: Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
Figure 1. Root activity under different treatments. Note: Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
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Figure 2. Total Cr content in roots, stems, and leaves of Coix lacryma-jobi L. under irrigation conditions with different Cr concentrations. Note: (A) shows the changes in the total Cr content in the roots of Coix lacryma-jobi L. with different treatments, (B) shows the changes in the stems of the plant, and (C) shows the changes in the leaves of the plant. Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
Figure 2. Total Cr content in roots, stems, and leaves of Coix lacryma-jobi L. under irrigation conditions with different Cr concentrations. Note: (A) shows the changes in the total Cr content in the roots of Coix lacryma-jobi L. with different treatments, (B) shows the changes in the stems of the plant, and (C) shows the changes in the leaves of the plant. Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
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Table 1. Plant heights and stem diameters under different treatments.
Table 1. Plant heights and stem diameters under different treatments.
Treatment Time (d)Irrigation MoistureCr (VI) Concentration (mg/L)Plant Height (cm)Plant Height
Inhibition Rate (%)
Stem Diameter (mm)Stem Diameter
Inhibition Rate (%)
10DNCK22.5 ± 0.72 a 8.77 ± 0.21 a
2021.3 ± 0.72 a5.338.7 ± 0.1 abc0.76
4018.73 ± 0.57 b16.748.47 ± 0.12 cd3.42
NSCK22.17 ± 0.49 a-8.73 ± 0.15 ab
2018.67 ± 0.68 b15.798.5 ± 0.1 bcd2.67
4016.23 ± 0.7 c26.778.4 ± 0.1 d3.82
DSCK22.33 ± 1.07 a-8.67 ± 0.06 abc
2019.23 ± 0.45 b13.888.47 ± 0.15 cd2.31
4017.33 ± 0.55 c22.398.4 ± 0.1 d3.08
40DNCK92.3 ± 1.74 a 11.43 ± 0.25 a
2083.23 ± 1.48 b9.8211.17 ± 0.06 abc2.33
4069.73 ± 1.04 d24.4511.03 ± 0.15 bcd3.5
NSCK91.6 ± 1.73 a-11.33 ± 0.25 ab
2076.3 ± 0.8 c16.7010.93 ± 0.15 cd3.53
4065.47 ± 1.4 e28.5310.83 ± 0.15 cde4.41
DSCK83.37 ± 0.9 b-10.87 ± 0.25 cde
2070.6 ± 1.47 d15.3110.53 ± 0.21 de3.07
4064.53 ± 0.87 e22.5910.7 ± 0.2 e3.68
70DNCK140.03 ± 3.01 a 12.77 ± 0.06 a
20129.4 ± 1.05 b7.5912.3 ± 0.2 b3.66
40109.23 ± 1.29 e21.9912.03 ± 0.06 bcd5.74
NSCK139.7 ± 1.41 a-12.73 ± 0.15 a
20118.43 ± 0.83 d15.6412.17 ± 0.31 bc4.45
40102.4 ± 0.7 f22.8111.93 ± 0.06 cde6.28
DSCK126.57 ± 2.15 c-12.27 ± 0.25 b
20106.77 ± 1.19 e15.2211.73 ± 0.15 de4.35
4098.2 ± 1.47 g22.4111.67 ± 0.06 e4.89
Note: Inhibition rate (%) = Plant   height   of   CK   Height   of   plants   treated   with   Cr   VI   Plant   height   of   CK   × 100%. Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
Table 2. Photosynthetic gas exchange parameters under different treatments.
Table 2. Photosynthetic gas exchange parameters under different treatments.
Photosynthetic Gas Exchange ParametersTreatment Time (d)Water ManagementCKCr 20 mg/LCr 40 mg/L
Net Photosynthetic Rate
(μmol/m2·s)
10DN19.2 ± 0.96 a14.73 ± 0.51 b11.56 ± 0.48 c
NS19 ± 0.98 a12.12 ± 1.05 c9.23 ± 0.73 d
DS13.96 ± 1.54 b9.56 ± 1.52 d6.79 ± 1.09 e
40DN24.32 ± 1.12 a19.52 ± 0.46 bc16.13 ± 0.35 ef
NS24.22 ± 1.1 a18.14 ± 1.25 cd14.34 ± 1.23 fg
DS21.29 ± 1.31 b17.53 ± 0.93 de14.06 ± 1.43 g
70DN18.6 ± 0.54 a14.17 ± 0.9 b11.77 ± 0.75 c
NS18.16 ± 1 a10.17 ± 1.02 d9.38 ± 0.92 d
DS13.94 ± 1.12 b8.71 ± 1.07 d6.9 ± 0.66 e
Stomatal conductivity
(mmol·m−2·s−1)
10DN0.177 ± 0.005 a0.126 ± 0.011 b0.116 ± 0.005 bc
NS0.169 ± 0.013 a0.118 ± 0.014 bc0.098 ± 0.016 cd
DS0.131 ± 0.017 b0.109 ± 0.015 bc0.085 ± 0.008 d
40DN0.183 ± 0.016 a0.143 ± 0.013 bc0.124 ± 0.008 bcd
NS0.182 ± 0.016 a0.138 ± 0.009 bc0.119 ± 0.019 cd
DS0.15 ± 0.013 b0.124 ± 0.012 bcd0.105 ± 0.014 d
70DN0.101 ± 0.007 a0.073 ± 0.004 bc0.064 ± 0.007 c
NS0.097 ± 0.007 a0.064 ± 0.003 c0.049 ± 0.004 d
DS0.081 ± 0.011 b0.053 ± 0.004 d0.043 ± 0.004 d
Intercellular CO2 Concentration (μmol/mol)10DN228.7 ± 15.97 a200.16 ± 17.52 ab163.49 ± 19.5 cde
NS225.49 ± 17.25 a191.74 ± 16.27 bc155.87 ± 17.39 de
DS182.08 ± 16.38 bcd167.51 ± 22.77 bcde147.29 ± 14.94 e
40DN273.84 ± 24.18 a238.79 ± 16.91 ab213.15 ± 26.66 bc
NS272.93 ± 22.5 a231.44 ± 18.14 bc207.63 ± 24.05 bc
DS244 ± 22.26 ab217.99 ± 17.75 bc192.75 ± 20.76 c
70DN176.43 ± 15.26 a150.15 ± 19.67 abc124.49 ± 12.42 cd
NS176.4 ± 16.15 a147.33 ± 19.8 abc120.74 ± 11.32 cd
DS163.66 ± 16.05 ab136.98 ± 16.92 bcd115.19 ± 14.79 d
Transpiration Rate (μmol/m2·s)10DN2.64 ± 0.22 a2.1 ± 0.15 b1.8 ± 0.24 bcd
NS2.61 ± 0.21 a1.97 ± 0.18 bc1.62 ± 0.24 cd
DS2.13 ± 0.21 b1.69 ± 0.23 cd1.46 ± 0.19 d
40DN3.69 ± 0.17 a3.36 ± 0.16 ab2.99 ± 0.19 bcd
NS3.66 ± 0.19 a3.23 ± 0.19 b2.82 ± 0.25 cd
DS3.13 ± 0.19 bc2.98 ± 0.28 bcd2.66 ± 0.23 d
70DN2.42 ± 0.29 a1.99 ± 0.25 b1.66 ± 0.04 bcd
NS2.41 ± 0.3 a1.83 ± 0.19 bc1.52 ± 0.17 cd
DS1.96 ± 0.17 b1.57 ± 0.21 cd1.34 ± 0.11 d
Note: Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
Table 3. Chlorophyll fluorescence parameters under different treatments.
Table 3. Chlorophyll fluorescence parameters under different treatments.
Chlorophyll Fluorescence ParametersTreatment Time (d)Water ManagementCKCr 20 mg/LCr 40 mg/L
Fo10DN0.225 ± 0.016 d0.249 ± 0.006 cd0.276 ± 0.02 bc
NS0.226 ± 0.014 d0.264 ± 0.011 bc0.292 ± 0.019 ab
DS0.264 ± 0.013 bc0.278 ± 0.017 bc0.314 ± 0.021 a
40DN0.189 ± 0.012 e0.229 ± 0.01 d0.258 ± 0.012 abc
NS0.198 ± 0.017 e0.246 ± 0.013 bcd0.271 ± 0.019 ab
DS0.241 ± 0.011 cd0.25 ± 0.015 bcd0.282 ± 0.012 a
70DN0.25 ± 0.014 d0.318 ± 0.01 c0.333 ± 0.009 bc
NS0.251 ± 0.011 d0.331 ± 0.029 bc0.358 ± 0.012 ab
DS0.31 ± 0.016 c0.328 ± 0.025 bc0.37 ± 0.027 a
Fm10DN1.444 ± 0.062 a1.291 ± 0.061 b1.19 ± 0.029 bc
NS1.431 ± 0.065 a1.245 ± 0.074 bc1.121 ± 0.075 cd
DS1.178 ± 0.078 bc1.126 ± 0.068 cd1.014 ± 0.074 d
40DN1.779 ± 0.182 a1.601 ± 0.042 b1.511 ± 0.017 bc
NS1.773 ± 0.163 a1.485 ± 0.059 bc1.41 ± 0.053 c
DS1.476 ± 0.064 bc1.395 ± 0.051 c1.343 ± 0.057 c
70DN1.362 ± 0.067 a1.216 ± 0.055 bc1.078 ± 0.056 cd
NS1.357 ± 0.072 a1.16 ± 0.098 bcd1.071 ± 0.095 d
DS1.245 ± 0.089 ab1.148 ± 0.093 bcd1.06 ± 0.04 d
Fv/Fm10DN0.844 ± 0.017 a0.807 ± 0.006 b0.768 ± 0.018 cd
NS0.841 ± 0.016 a0.788 ± 0.011 bc0.738 ± 0.029 d
DS0.775 ± 0.026 bc0.752 ± 0.03 cd0.69 ± 0.003 e
40DN0.894 ± 0.006 a0.857 ± 0.007 b0.829 ± 0.01 cd
NS0.888 ± 0.013 a0.834 ± 0.015 bc0.807 ± 0.021 de
DS0.837 ± 0.014 bc0.821 ± 0.017 cd0.79 ± 0.013 e
70DN0.816 ± 0.018 a0.738 ± 0.012 bc0.69 ± 0.012 cde
NS0.815 ± 0.017 a0.712 ± 0.043 bcd0.664 ± 0.039 de
DS0.751 ± 0.017 b0.712 ± 0.043 bcd0.65 ± 0.039 e
Note: Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
Table 4. The GSH content (μg/gFW) in different parts of Coix lacryma-jobi L. under different treatments.
Table 4. The GSH content (μg/gFW) in different parts of Coix lacryma-jobi L. under different treatments.
OrgansTreatment Time (d)Water ManagementCKCr 20 mg/LCr 40 mg/L
Root20DN36.915 ± 1.954 e42.296 ± 2.197 de55.099 ± 4.183 c
NS36.563 ± 2.489 e74.323 ± 5.431 b90.784 ± 5.431 a
DS40.959 ± 1.847 de47.022 ± 2.409 d61.037 ± 4.262 c
50DN40.024 ± 6.117 f57.49 ± 4.041 e69.312 ± 2.781 cd
NS41 ± 4.818 f86.561 ± 6.624 b103.137 ± 7.757 a
DS41.532 ± 4.356 f61.265 ± 6.836 de78.218 ± 5.273 bc
Stem20DN36.915 ± 1.954 e42.296 ± 2.197 cd55.099 ± 4.183 bc
NS36.563 ± 2.489 de74.323 ± 5.431 ab90.784 ± 5.431 a
DS40.959 ± 1.847 de47.022 ± 2.409 bc61.037 ± 4.262 a
50DN40.024 ± 6.117 e57.49 ± 4.041 d69.312 ± 2.781 b
NS41 ± 4.818 e86.561 ± 6.624 bc103.137 ± 7.757 a
DS41.532 ± 4.356 e61.265 ± 6.836 c78.218 ± 5.273 a
Leaf20DN36.915 ± 1.954 f42.296 ± 2.197 e55.099 ± 4.183 bc
NS36.563 ± 2.489 f74.323 ± 5.431 c90.784 ± 5.431 a
DS40.959 ± 1.847 f47.022 ± 2.409 d61.037 ± 4.262 b
50DN40.024 ± 6.117 e57.49 ± 4.041 d69.312 ± 2.781 bc
NS41 ± 4.818 e86.561 ± 6.624 b103.137 ± 7.757 a
DS41.532 ± 4.356 e61.265 ± 6.836 cd78.218 ± 5.273 b
Note: Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
Table 5. Organic matter content (mg/kg) under different treatments.
Table 5. Organic matter content (mg/kg) under different treatments.
Treatment Time (d)Water ManagementCKCr 20 mg/LCr 40 mg/L
10DN26.32 ± 2.13 a21.77 ± 2.37 bc18.17 ± 1.87 cde
NS15.17 ± 1.23 ef12.31 ± 2.76 f11.27 ± 1.58 f
DS24.95 ± 2.49 ab19.91 ± 2.58 cd16.94 ± 2.23 de
40DN32.69 ± 1.74 a25.98 ± 2.81 bc23.24 ± 2.01 cd
NS20.15 ± 2.9 de16.16 ± 2.57 ef14.23 ± 3.32 f
DS30.33 ± 1.77 ab24.06 ± 2.6 cd21.66 ± 3.64 cd
70DN34.12 ± 3.62 a27.31 ± 3.29 c24.94 ± 3.58 bcd
NS27.11 ± 4.11 bc21.07 ± 3.65 cd18.78 ± 2.82 d
DS31.03 ± 3.14 ab25.68 ± 4.09 bc22.38 ± 3.62 cd
Note: Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
Table 6. Total Cr content in substrate and total Cr content and Cr (VI) content in the water discharged under different treatments.
Table 6. Total Cr content in substrate and total Cr content and Cr (VI) content in the water discharged under different treatments.
Treatment Time (d)Water ManagementCr Content in the SUBSTRATE (mg/kg)Cr content in the Water Discharged (mg/L)Cr (VI) Content in the Water Discharged (mg/L)
CKCr 20 mg/LCr 40
mg/L
CKCr 20 mg/LCr 40 mg/LCKCr 20 mg/LCr 40 mg/L
10DN6.74 ± 1.57 d42.82 ± 3.16 bc66.55 ± 5.23 a0.06 ± 0.02 d0.24 ± 0.03 c0.43 ± 0.05 b0.03 ± 0.01 d0.08 ± 0.01 c0.15 ± 0.02 b
NS3.8 ± 0.59 d39.79 ± 5.46 c62.78 ± 6.16 a0.03 ± 0.01 d0.3 ± 0.04 c0.56 ± 0.03 a0.03 ± 0.01 d0.16 ± 0.01 b0.19 ± 0.01 a
DS7.21 ± 1.4 d47.89 ± 3.8 b69.23 ± 5.86 a0.07 ± 0.03 d0.27 ± 0.06 c0.5 ± 0.07 ab0.03 ± 0.01 d0.15 ± 0.02 b0.15 ± 0.02 b
40DN8.69 ± 1.48 c76 ± 4.37 b141.87 ± 6.59 a0.08 ± 0.03 e0.36 ± 0.04 d0.65 ± 0.05 b0.04 ± 0.01 d0.14 ± 0.02 c0.19 ± 0.02 b
NS4.79 ± 0.59 c72.88 ± 9.11 b136.16 ± 7.28 a0.04 ± 0.02 e0.45 ± 0.04 c0.77 ± 0.05 a0.04 ± 0.02 d0.22 ± 0.02 b0.31 ± 0.02 a
DS9.95 ± 0.96 c82.27 ± 6.09 b147.45 ± 10.94 a0.1 ± 0.03 e0.41 ± 0.09 cd0.69 ± 0.05 ab0.05 ± 0.01 d0.2 ± 0.02 b0.2 ± 0.02 b
70DN9.7 ± 1.17 d135.27 ± 5.44 c183.44 ± 11.62 ab0.11 ± 0.05 e0.44 ± 0.04 d0.72 ± 0.06 b0.05 ± 0.02 e0.19 ± 0.02 d0.24 ± 0.02 c
NS4.95 ± 0.62 d129.67 ± 8.4 c174.67 ± 7.81 b0.04 ± 0.01 e0.57 ± 0.02 c0.86 ± 0.06 a0.04 ± 0.01 e0.29 ± 0.02 b0.38 ± 0.02 a
DS10.62 ± 0.83 d140.47 ± 8.47 c189.78 ± 10.48 a0.12 ± 0.04 e0.53 ± 0.06 c0.79 ± 0.08 ab0.05 ± 0.01 e0.24 ± 0.02 c0.25 ± 0.02 c
Note: Different lowercase letters indicate significant differences between treatments at the same time (p < 0.05).
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Nong, Y.; Liu, X.; Peng, Z.; Li, L.; Cheng, X.; Wang, X.; Li, Z.; Li, Z.; Li, S. Effects of Domestic Sewage on the Photosynthesis and Chromium Migration of Coix lacryma-jobi L. in Chromium-Contaminated Constructed Wetlands. Sustainability 2023, 15, 10250. https://0-doi-org.brum.beds.ac.uk/10.3390/su151310250

AMA Style

Nong Y, Liu X, Peng Z, Li L, Cheng X, Wang X, Li Z, Li Z, Li S. Effects of Domestic Sewage on the Photosynthesis and Chromium Migration of Coix lacryma-jobi L. in Chromium-Contaminated Constructed Wetlands. Sustainability. 2023; 15(13):10250. https://0-doi-org.brum.beds.ac.uk/10.3390/su151310250

Chicago/Turabian Style

Nong, Yu, Xinyi Liu, Zi Peng, Liangxiang Li, Xiran Cheng, Xueli Wang, Zhengwen Li, Zhigang Li, and Suli Li. 2023. "Effects of Domestic Sewage on the Photosynthesis and Chromium Migration of Coix lacryma-jobi L. in Chromium-Contaminated Constructed Wetlands" Sustainability 15, no. 13: 10250. https://0-doi-org.brum.beds.ac.uk/10.3390/su151310250

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