Next Article in Journal
Compensation of Distributed Generations Outage Using Controlled Switched Capacitors
Next Article in Special Issue
Silicon-Rich Biochar Detoxify Multiple Heavy Metals in Wheat by Regulating Oxidative Stress and Subcellular Distribution of Heavy Metal
Previous Article in Journal
Potential and Complexity of Implementing Financial Instruments in the Framework of Rural Development Policies in Italy—The Friuli Venezia Giulia Revolving Fund
Previous Article in Special Issue
Functionalized Bentonite Clay Composite with NiAl-Layered Double Hydroxide for the Effective Removal of Cd(II) from Contaminated Water
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Mitigating the Toxic Effects of Chromium on Wheat (Triticum aestivum L.) Seed Germination and Seedling Growth by Using Biochar and Polymer-Modified Biochar in Contaminated Soil

Soil Sciences Department, College of Food & Agricultural Sciences, King Saud University, P.O. Box 2460, Riyadh 11451, Saudi Arabia
*
Author to whom correspondence should be addressed.
Sustainability 2022, 14(23), 16093; https://doi.org/10.3390/su142316093
Submission received: 13 November 2022 / Revised: 27 November 2022 / Accepted: 29 November 2022 / Published: 1 December 2022

Abstract

:
The present study was conducted to investigate the potential influences of biochar in mitigating the phytotoxic effects of hexavalent chromium (CrVI) on the germination of wheat (Triticum aestivum L.). Biochar (JBC) was produced from Jujube (Ziziphus jujube L.) wood waste at three different pyrolysis temperatures (300 °C, 500 °C and 700 °C), which was later polymerized (JPBC) via the solution-polymerization method. Phytotoxicity of CrVI was induced to wheat seeds at variable CrVI application rates (5, 10, 20, 40 mg L−1). Applied CrVI concentrations confined the seed germination and seedling growth in order of: 5 < 10 < 20 < 40 mg L−1. The application of JBCs (0.2 g per petri plate) resulted in a 150% increase in shoot length, while dry biomass was increased by 250% with JPBCs application. Uptake of CrVI was significantly lower in JBC-300 (7.74 μg/seedling) and JPBC-300 (1.13 μg/seedling) treatments, as compared to control (13.24 μg/seedling), at the highest stress level (40 mg L−1). Therefore, the findings of the current study showed that JBCs and JPBCs performed excellently in improving seedling growth while JPBCs performed more efficiently than pristine JBCs in mitigating CrVI phytotoxicity and availability.

Graphical Abstract

1. Introduction

Several anthropogenic activities, including industrial waste discharge, mining activities, unplanned municipal waste disposal, use of extensive pesticides, and chemical fertilizers, are responsible for heavy metals accumulation in terrestrial environment and natural water resources. Excessive accumulation of these heavy metals leads to deterioration of fauna and flora in the environment and serious threats to human health [1]. Chromium (Cr) is one of these environmental pollutants, mainly employed in the electroplating, dying, metallurgical, paint, paper, pulp production, and tannery industries. It has complex chemistry, and its solubility, mobility, and bioavailability depend on its oxidation states. Trivalent (CrIII) and hexavalent (CrVI) are the naturally occurring states of Cr. Hexavalent Cr forms chromate and dichromate ions, soluble in water, and more toxic than CrIII. CrVI is carcinogenic for human and toxic for plants and animals [2].
Among several industries responsible for Cr discharge and accumulation in biosphere, tanneries release a higher influx of Cr in the environment, accounting for 40% of the total industrial use [2]. Continuous discharge of huge amount of wastes from these industries, having large number of Cr salt- and Cr ion-containing compounds, cause severe Cr toxicity in soil and ground water. A surplus amount of Cr in soil induces nutrient metal interaction and disturbs plant nutrient uptake [3,4]. Higher Cr concentration in plants causes low protein contents, inhibition of enzyme activity, chlorosis, and necrosis. It also affects several morphological, biochemical, and metabolic parameters in plants such as reduced germination, stunted plant growth, inhibition of early seedlings, and interferes with photosynthesis and low biomass production [5,6]. Cr enters in ground water by natural weathering of Cr-contaminated rocks, direct discharge from industries, and leaching from soil. The maximum discharge limit for Cr in wastewater is 1.0 mg L−1 and maximum permissible limit in drinking water is 0.05 mg L−1 [7]. Use of Cr-contaminated water for irrigation and drinking purposes results in low agricultural production and serious health issues in human beings. Therefore, it is very important to restore such contaminated soil and water resources from Cr toxicity. Previous studies reported that application of organic soil amendments such as bio-solids, manure composites, biochar, and poultry waste in soil reduce CrVI into a less toxic and less mobile state, i.e., CrIII, subsequently decreasing its mobility and bioavailability [8,9,10].
Among these organic soil amendments, biochar (BC) has gained ample attraction of the scientific community owing to its agricultural and environmental benefits. BC, which is a solid by-product of the controlled combustion of organic waste, has a large surface area, rich porous structure, enormous oxygen containing functional groups, alkaline pH, and high cation exchange capacity (CEC) [11,12]. The porous structure of BC can hold heavy metals and several organic and inorganic pollutants. Previous studies reported positive impacts of BC soil application such as improved nitrogen fixation, reduced nutrient loss by leaching, higher crop biomass, controlled diseases, and microbe friendliness [13,14]. The ability of BC to mitigate heavy metal toxicity in water bodies, mobility in soil, and bio-availability largely depends on the source of feedstock and pyrolysis conditions such as temperature and resident time [15,16]. Generally, BC produced at high temperature (600–700 °C) has higher aromaticity and recalcitrant potential, but due to dehydration and deoxygenation, has a smaller number of O- and H-containing functional groups [17,18]. Meanwhile, BC produced at low temperature (300–400 °C) has more O- and H-containing functional groups and variety of organic characteristics [19,20]. Herath et al. [21] reported a 93–97% decrease in Cr, Ni, and Mn bioaccumulation in tomato plants by the application of BC. Application of maize stalk-derived BC to heavily Cr-contaminated soil showed an increase in soil fertility, higher nutrient uptake, and amelioration of Cr-contaminated soil [22].
Modification of BC with foreign materials such as silica, zeolites, polymers, and nutrient enrichment improves its physio chemical properties, and ameliorates its efficiency and environmental influence [23]. Polymers are extensively studied cross-linked macromolecules which are hydrophilic in nature and have carboxylic groups. Ekebafe et al. [24]. reported that polymers enhance soil water holding capacity, promote plant growth and increase plant tolerance in water stress environment. Synthesized polymers have been used extensively with adsorbents for heavy metal removal since the surface properties of the adsorbents can be modified by enhancing available functional groups to improve their adsorption ability for pollutants [25]. One way to decrease heavy metals’ availability to plants is by increasing binding sites for heavy metals in soil through amendments application. It is reported earlier that polymers along with BC induce large number of binding sites to hold cationic contaminants and sequester carbon from environment [24]. Polymers also help to deduce BC pH, and improve its performance in alkaline soils as well. Bai et al. [26]. (2010) found 10.9% to 11.2% decrease in pH in sandy soil using two different kind of polymers. A number of polymers have been used for CrVI removal from water and soil including glycine doped polypyrrole, 1, 2 ethylenediamine-aminated macroporous polystyrene particles [27]. Use of BC amendments along with synthetic (acrylamide, polyurethane, polyvinyl, resins) and natural polymer derivatives of algal polysaccharides has shown promising influence on immobilization of CrVI in soil [28]. However, polymer-modified jujube wood waste-BC has not yet been studied for CrVI immobilization in soil. Therefore, in the current study, BC was produced from Jujube (Ziziphus jujube L.) at different pyrolysis temperature (300 °C, 500 °C, and 700 °C) and subsequently polymerized to synthesize modified-BC. The pristine and modified BCs were thereafter evaluated for their performance to mitigate phytotoxic effects of hexavalent chromium (CrVI) on wheat seed germination and plant growth. This study will focus on application of jujube wood waste derived biochar and its polymer derivatives to mitigate CrVI toxicity in tannery waste contaminated soil and to restore it for agricultural activities. Moreover, it will help to decrease CrVI mobility and bioavailability in soil, and enhance retention and plant availability of essential nutrients, which will ultimately increase plant growth and agriculture production.

2. Materials and Methods

2.1. Biochar Production, Polymerization and Characterization

The BC was produced and polymerized by following the procedure already described in our previous research work [10]. Briefly, jujube wood waste was used as a biomass (BM) to produce BC. Raw BM was collected and washed with distilled water to remove dirt particles and other impurities followed by air drying and crushing into small pieces. Afterward, BM was subjected to thermal combustion in controlled supply of oxygen at three different pyrolysis temperatures (300 °C, 500 °C, 700 °C) by using Digital Muffle furnace (Wisetherm FH14, Germany) for 4 h at a heating rate of 10 °C min−1. Produced BCs were collected, cooled in a desiccator, sieved by 0.5 mm mesh, stored in an air tight container and tagged as JBC with numeric numbers to show production temperature, such as JBC-300 (BC produced at 300 °C pyrolysis temperature), JBC-500 (BC produced at 500 °C pyrolysis temperature), and JBC-700 (BC produced at 700 °C pyrolysis temperature). Later on, these freshly produced JBCs were polymerized by following Shigetomi et al. [29] method. Briefly, a specific amount of JBC was added in aqueous solution of N, N1 methylenebisacrylamide (cross-linker) and acrylamide (monomer), mixture was stirred vigorously at 70 °C for 5 h, followed by addition of potassium peroxidisulfate (initiator). Later on, the solution was filtered, and solid material was collected from the filter paper, oven dried, passed through a 0.5 mm size sieve, stored in air-tight containers, and samples were tagged as JPBC-300, JPBC-500, and JPBC-700 with respect to their production pyrolysis temperature. Produced and polymerized JBCs were characterized for physical and chemical characteristics by following standard procedures [30]. Later, all produced materials along with raw BM were subjected to proximate analysis to calculate moisture percentage, volatiles, ash contents, and residual carbon contents by following the ASTM D1762-84 [31] method. Produced and polymerized JBCs were analyzed by scanning electron microscope (SEM, EFI S50 Inspect, Netherlands) for their morphology and structure, while mineral composition and presence of surface functional groups were determined by using X-Ray diffractometer (MAXima X XRD-7000, Shimadzu, Japan), and Fourier transformation infrared (Bruker Alpha-Eco ATR-FTIR, Bruker Optics, Inc), respectively.

2.2. Soil Collection and Characterization

Soil was collected from Derab agriculture research center. Soil was collected in patches and stored in plastic bags. Later, soil was air dried and sieved by a 2 mm size sieve. Soil samples were analyzed for their physio-chemical properties by following standard procedure [30]. Bouyoucos [32] and Walkley and Black [33] methods were followed to determine soil texture and organic matter respectively. Soil samples were digested by Hossner [34] method to determine heavy metal contents by using ICP-OES (Perkin Elmer Optima 4300 DV Inductively coupled plasma-optical emission spectrometry).

2.3. Germination Experiment

A germination experiment was conducted to investigate the potential of produced and polymerized BCs in mitigating CrVI toxic effects on wheat seed germination. One hundred grams of soil was taken in petri plates and plates were irrigated by a CrVI solution of different concentrations (0, 5, 10, 20, and 40 mg L−1) separately. Potassium dichromate (Labogens LG3683 Extra Pure, K2Cr2O7) was used a source compound to prepare CrVI solutions of different concentration. Wheat seeds were provided by Plant Production Department, King Saud University, Riyadh. Subsequently 10 seeds of wheat were added in each petri plate. Amendments (JBCs and JPBCs) were added at 1% (w/w) in each petri plates. The petri plates were covered and placed in growth chamber for 48 h at 25 °C, followed by cycles of 16 h light and 8 h dark for the next 72 h. Afterwards, the number of germinated seeds in each petri plate were counted and germination percentage rate was calculated. Seedlings were harvested after four weeks, fresh weight and root and shoot lengths were recorded followed by oven drying of plant samples. Later, the dry weight of oven-dried seedling samples was measured, and Cr uptake by seedlings was measured by the dry digestion method [35]. Briefly, a specific amount of plant dry biomass was heated in a muffle furnace at 550 °C to obtain ash. Later, these plant biomass ash samples were treated and extracted with diluted HNO3 and collected filtrate was analyzed by ICP-OES to determine Cr concentrations. Then, the uptake of Cr to the seedlings was calculated based on dry biomass of seedlings. All the treatments were triplicated and a control treatment with no added amendments was also included.

2.4. Statistical Analysis

All analyses were performed at least in triplicate. One-way analysis of variance (ANOVA) and Tukey’s honestly significance difference (HSD) studentized range test were applied on mean values of all treatments, using Statistix software [36].

3. Results and Discussion

3.1. Biochar and Polymer MODIFIED Biochar Characteristics

Physiochemical characters of JBCs and JPBCs have already been explained in our previous work [10]. Morphological analysis of feedstock, produced and polymerized materials showed amorphous surface of BM, while more porosity and crystallinity was found in JBC and JPBC, specifically in BCs produced at higher pyrolysis temperature (Figure 1). Amorphous surface of BM could be due to presence of volatiles and clogged impurities while presence of broad channels and more porous surface in JBCs and JPBCs specifically produced at higher thermal treatment (700 °C) indicated more degradation and decomposition of organic compounds and a higher release of moisture and volatiles clogged in the pores [37,38]. Figure 1(i–viii) indicates the penetration of the polymer matrix in the porous structure of JBC, which resultd in the formation of an extended interlocking network between the polymer matrix and the BC particles, leading to enhanced tensile strength and stability in polymerized BC [39].
The difference in the mineralogical composition of raw BM and all BCs is described in Figure 2. In BM, broad peaks indicating calcium oxalate and cellulose were found, which later shifted and diminished in JBCs due to thermal degradation of organic compounds and release of volatiles [40,41]. A similar trend of appearance of organic compounds and calcium oxalate peaks in BM and BC produced at lower thermal treatment was found in study conducted by Al-Wabel et al. [42], which later diminished by increasing pyrolysis temperature from 400 °C to 800 °C. Broad peaks at 3.58–2.93Å range in JBC-500, JBC-700, JPBC-300, JPBC-500, and JPBC-700 indicated a crystal index of carbon which showed higher aromaticity and recalcitrance in the produced BCs [43]. Such peaks appeared again at 2.10–1.92Å in BCs depicting condensed carbonized matrix due to higher degree of thermal treatment of raw BM. Some additional peaks were found in the JPBCs at 1.45–1.23Å values indicating presence of quartz (SiO2) and calcite (CaCO3) [44,45]. FTIR spectra of BM and its derived JBCs showed band of water molecules at 3328.5 cm−1, which later on faded in JBCs produced at higher pyrolysis temperature (Figure 3). C-H group stretching in BM and JBC-300 and JPBC-300 were found indicating the presence of cellulose and hemicellulose compounds. Additionally, the appearance of a band in the range of 1601–1083 cm−1 in JPBCs showed presence of a C=C, C–C, and amine group (C–N) [46].

3.2. Germination Experiment

3.2.1. Soil Characterization

Calculated soil parameters are mentioned in Table 1. Soil was found slightly alkaline (pH 7.41) with 1.05 dS m−1 electrical conductivity value. Soil texture was found sandy loam with 2.5% of mean organic matter, and 9.95 cmol kg−1 of average cation exchange capacity. Soil heavy metals were found in permissible range except for Cr which was indicated high toxicity of Cr in soil (160, 270, 129, 119, and 94 mg kg−1 of Cr, Fe, Mn, Zn, and Cu, respectively).

3.2.2. Effect of CrVI Concentration on Germination Percentage

Germination percentage was calculated by using Equation (1). With the increase in the concentration of applied CrVI, there was an obvious decrease in the germination % of seeds (Figure 4). At 0 mg L−1 CrVI concentration, there was 100% germination, and no significant drop in germination was noted up to 10 mg L−1 CrVI concentration. Germination decreased significantly at 20 and 40 mg L−1 of CrVI concentration (Table 1). Germination dropped below 50%, indicating a 40 mg L−1 CrVI concentration as a lethal dose. Toxic effects of CrVI on seed germination were recorded in the following order: 5 > 10 > 20 > 40 mg L−1. These results are in agreement with earlier studies conducted to observe the inhibitory effects of Cr toxicity on seed germination [47,48,49]. Barcelo and Poschenrieder [50] and Panda [49] found that higher application rate of CrVI decreased the germination % by degradation of pigment, higher oxidative stress in the plant, and reducing seeds’ tendency to grow. In separate studies, Rout et al. [51] and Peralta et al. [48] found 75% and 67% decreases in the germination rate of bush bean and lucerne seed by application of CrVI at a rate of 200 µM and 40 mg L−1, respectively. The curtailed ability of seed to germinate under the influence of CrVI stress might be due to the suppressive effects of CrVI on amylases activity and sugar transport to the embryo [52]. Over all, in control treatments with no added amendments, the germination % was decreased significantly as compared to other treatment with JBCs and JPBCs at same CrVI application rates (Table 2).
G e r m i n a t i o n   ( % ) = N o   o f   s e e d s   ( s o w n ) N o   o f   s e e d s   ( g e r m i n a t e d ) × 100

3.2.3. Effect of CrVI Concentration on Fresh and Dry Weight of Seedlings (g)

Seedlings were harvested after 4 weeks of germination and weighed instantly for their respective fresh weight followed by oven drying until constant weight and then dry weight was calculated (Figure 5). A gradual drop in fresh and dry weights of seedlings was found with increasing CrVI concentration, which indicated the toxic effects of CrVI on seedlings growth. Fresh weight was dropped considerably to 0.14, 0.11, 0.07, and 0.03 g at 5, 10, 20, and 40 mg L−1 CrVI concentration, respectively, which was 0.18 g in control condition with no induced CrVI stress. A similar trend of decline in dry weight was found with the highest dry weight (0.13 g). Earlier, Fozia et al. [53] also reported a gradual decrease in fresh and dry weight of Helianthus annus L. under different levels of Cr toxicity. Previous studies reported harmful effects of Cr on plants’ development, including wilted aerial portions, deficient photosynthesis, and scarce mineral and fluid adsorption, resulting in stunted growth of plants and reduced plant BM [54,55,56]. In another study, Kumar [57] reported reduced biomass production and leaf growth in sorghum (sorghum bicolor L.) due to the accumulation of CrVI which generated completion between essential nutrient uptake and oxidative injury to the plant adsorption system.

3.2.4. Effect of CrVI Concentration on Root and Shoot Lengths (cm)

Root and shoot lengths of tested crop were also affected by applied CrVI stress (Figure 6). A similar trend of decreasing lengths was found in both roots and shoots. Maximum root length (7.29 cm) was found at 0 mg L−1 (control) application rate of CrVI, while a gradual decrease in seedlings root length was found at 10 mgL−1 (3.94 cm) and 20 mgL−1 (1.54 cm) application rates (Table 2). Seedlings’ shoot length was also decreased significantly at each application rate of CrVI, which was 7.39 cm at 0 mg L−1, 4.90 cm at 10 mg L−1, 2.66 cm at 20 mg L−1, and 1.37 cm at 40 mg L−1 application rate. Jiang et al. [58] and Liu et al. [59] stated that inhibition of root and shoot elongation under heavy metal stress could be due to the metal intervention with cell division, chromosomal aberration, and asymmetrical mitosis. Samantaray et al. [60] also reported similar findings of decreased root and shoot elongation of mung bean cultivars cultivated in chromite mine-polluted soil. A number of studies have stated the negative impact of excessive Cr accumulation in plants, including decreased efficiency of chloroplast, inhibited photosynthesis, and destructive stem and roots [61,62,63,64].

3.2.5. Effect of Charred Materials on Germination (%)

Significant increase in germination % was found in treatments with JBCs and JPBCs as compared to control treatments with no JBCs (Table 2). JPBC produced at 300 °C pyrolysis temperature (JPBC-300) showed minimum drop in germination % with each increasing rate of CrVI (Figure 7). JPBC-300 showed highest germination % (95%, 80%, 75%, and 65%) at each applied CrVI (5, 10, 20 and 40 mg L−1, respectively) stress followed by JBC-300 (90%, 80%, 70%, and 55%) and JPBC-700 (90%, 75%, 70%, and 55%, respectively). In a study to observe the effects of maize straw-derived BC on germination and growth of wheat in saline soil, Wang and Xu [63] found that wheat seed germination and overall plant growth was enhanced by BC application, while seeds germination and plant growth were found consistently low in control conditions. Addition of JBC as soil amendment immobilized toxic CrVI contents and enhanced bioavailability of essential nutrients in soil and ultimately higher plant uptake [9,10]. Bashir et al. [64] found positive effects of application of sugarcane bagasse derived BC in mitigating germination inhibition of maize cultivars grown in Cr contaminated soil. Chopala et al. [8] found delayed germination of mustard (Brassica juncea L.) seeds in artificially Cr-contaminated soil, while application of chicken manure derived BC avoided delayed germination and improved overall plant growth. Ruqin et al. [38] reported similar result of higher germination of spinach by application of BC with super adsorbent polymer against unmodified BC and no BC (control) treatment.

3.2.6. Effect of Charred Materials on Fresh and Dry Weight of Seedlings (g)

Application of JBCs and JPBCs showed positive effects on overall seedling growth, and minimum drop in seedling fresh and dry weights was observed under induced CrVI stress (Figure 8). Fresh biomass was increased by 30%, 40%, and 60% in treatments receiving JBC- 500, JBC-700, and JBC-300 application, respectively, while further increases of 48%, 52%, and 79% were recorded in fresh weight as effected by application of JPBC-500, JPBC-700, and JPBC-300, respectively, against control treatments with no added JBCs. Comparatively higher dry weight of seedlings was found in treatment with JPBC-300 (0.07 g) followed by JBC-300, JPBC-700 (0.05 g), and JPBC-500 (0.04 g) at highest applied CrVI stress (40 mg L−1). Rise in fresh and dry weights of seedlings in JBCs and JPBCs treatments against control condition showed potential of applied JBCs in improving overall plant growth. Soil immobilization of CrVI contents by JBCs alleviates competition between Cr contents and essential nutrients, which consequently enhances plant availability of nutrients. In a study, Rafique et al. [9] found 76% increase in plant fresh weight by polymer modified BC at 1.5% and 3% (w/w) application rate. Rajkovich et al. [65] recorded 30–40% increase in corn plant BM by application of different kind of BCs. Similar results have been reported by Wang and Xu [63] and Ruqin et al. [38] by using BC and BC modified with SAPs.

3.2.7. Effect of Charred Materials on Root and Shoot Lengths (cm)

Alike seedling fresh and dry weights, similar trend of gradual decrease in root and shoot lengths was observed as affected CrVI induced stress (Figure 9). In comparison with control conditions, application of JBCs and JPBCs showed minimum drop in seedling root and shoot lengths (Table 3). Minimum drop in seedling growth and rise in seedling root and shoot lengths by application of JBCs and JPBCs under sever CrVI might be attributed to sorption of CrVI on charged surface of applied BCs via electrostatic interaction [22,66]. Likewise, the mineral components of BC might be involved in CrVI precipitation and reduced its bioavailability, which consequently improved essential nutrients supply and better growth of plants [67,68]. Presence of oxygenated and hydrogen functional groups on BCs surface (Figure 3) might have formed complexation with CrVI and reduced its availability [69]. Additionally, BC has ability to reduce CrVI into harmless CrIII, which consequently reduced its toxic effects on plant growth [70,71].

3.2.8. Effect of Charred Materials on Cr Uptake (µg/Seedling)

Effects of JBCs and JPBCs on Cr uptake at applied CrVI concentration are mentioned in Figure 10. All applied charred materials considerably decreased CrVI contents in seedlings, while in control conditions, a gradual increase in CrVI uptake was noted, which was 0.5 µg/seedling at 0 mg L−1 CrVI application and increased to 13.25 μg/seedling at highest application rate of CrVI (40 mg L−1) (Table 1). On the other hand, zero to very low CrVI contents were found in plants grown in JPBCs and JBCs amended treatments. Especially, in presence of JPBCs zero contents of CrVI were found in seedlings, while a minimal increase in CrVI contents was found in seedlings at 40 mg L−1 application rate. Lower CrVI availability and plant accessibility showed excellent sorption ability of JBCs and JPBCs [22]. In a review study about ameliorating effects of BC on physio-chemical properties of weather soil, Glaser et al. [19] found positive effects of BC in immobilizing Cr in soil and lowering plant accessibility. Moreover, lower plant availability of CrVI as affected by applied JPBCs could be due to the presence of more active and binding sites on JPBCs’ surface, which strengthens its ability in fixing heavy metals [24,25].

4. Conclusions

Jujube wood waste derived biochar (JBC) and polymer-modified JBCs (JPBCs) showed characteristic variations in their physio-chemical properties. More porosity and a higher number of functional groups were found in JPBCs, while higher pH and fixed carbon contents were recorded in unmodified JBCs. The findings of this study showed that wheat seed germination and overall seedling growth were adversely affected by induced CrVI stress, while on contrary application of charred materials (JBCs and JPBCs) showed promising effects in lowering CrVI phtotoxicity by restraining its mobility and bioavailability. In comparison to control conditions, the application of unmodified JBCs enhanced shoot length by 150%, while JPBCs increased seedling dry matter by 250%. On the other hand, JBCs and JPBCs decreased CrVI uptake in seedlings, which was 13.24 μg/seedling in the control treatment, and decreased to 7.74 μg/seedling and 1.13 μg/seedling in JBCs and JPBCs, respectively. JPBC application showed higher germination percentages, improved plant growth, and exhibited significantly lower Cr uptake in plants as compared to JBC. In general, the application of JBC and polymer-modified JBC could be a fitting strategy in decreasing phytotoxic effects of CrVI and can potentially improve overall plant growth as well.

Author Contributions

M.I.R.: Investigation, Conceptualization, Methodology, Writing, Data interpretation, Original draft. M.A.: Statistical analyses, Review and editing. M.I.A.-W.: Project administration, Funding acquisition, Resources, Review and editing, Supervision. J.A.: Formal analyses, Review and editing. A.S.A.-F.: Conceptualization, Methodology, Resources, Supervision, Data interpretation, Review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia for funding this research work through the project number IFKSURG-2-767.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia for funding this research work through the project no. (IFKSURG-2-767).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Karimi, H.; Mahdavi, S.; Asgari Lajayer, B.; Moghiseh, E.; Rajput, V.D.; Minkina, T.; Astatkie, T. Insights on the bioremediation technologies for pesticide-contaminated soils. Environ. Geochem. Health 2022, 44, 1329–1354. [Google Scholar] [CrossRef] [PubMed]
  2. McBride, M.B.; Richards, B.K.; Steenhuis, T. Bioavailability and crop uptake of trace elements in soil columns amended with sewage sludge products. Plant Soil 2004, 262, 71–84. [Google Scholar] [CrossRef]
  3. Surita, C.A.; Gloaguen, T.; Montes, C.R.; Dias, C.T.S. Assessment of soil solution chemicals after tannery effluents disposal. Am. J. Appl. Sci. 2007, 4, 1063–1070. [Google Scholar] [CrossRef]
  4. Famielec, S.; Wieczorek-Ciurowa, K. Waste from leather industry. Threats to the environment. Czasopismo. Techniczne. Chemia. 2011, 108, 43–48. [Google Scholar]
  5. Akter, F.; Tinni, H.H.; Banarjee, P.; Hossain, M.Z. Effects Of heavy metals (Cd, Zn And Cu) on carbon, nitrogen and iron mineralization in soil. Malays. J. Sustain. Agric. 2019, 3, 33–38. [Google Scholar] [CrossRef]
  6. Du, Y.; He, J.H.; Chen, J.J. Effects of heavy metals of Pb, Cd and Cr on the growth of vegetables and their uptake. Acta Hortic. Sin. 2003, 30, 51–55. [Google Scholar]
  7. Gunatilake, S.K. Removal of Cr (III) Ions from Wastewater using Sawdust and Rice Husk Biochar Pyrolyzed at Low Temperature. Int. J. Innov. Educ. Res. 2016, 4, 44–54. [Google Scholar] [CrossRef]
  8. Choppala, G.; Bolan, N.; Kunhikrishnan, A.; Skinner, W.; Seshadri, B. Concomitant reduction and immobilization of chromium in relation to its bioavailability in soils. Environ. Sci. Pollut. 2015, 22, 8969–8978. [Google Scholar] [CrossRef]
  9. Rafique, M.I.; Usman, A.R.; Ahmad, M.; Sallam, A.; Al-Wabel, M.I. In situ immobilization of Cr and its availability to maize plants in tannery waste contaminated soil: Effects of biochar feedstock and pyrolysis temperature. J. Soils. Sediments 2020, 20, 330–339. [Google Scholar] [CrossRef]
  10. Rafique, M.I.; Usman, A.R.; Ahmad, M.; Al-Wabel, M.I. Immobilization and mitigation of chromium toxicity in aqueous solutions and tannery waste-contaminated soil using biochar and polymer-modified biochar. Chemosphere 2021, 266, 129198. [Google Scholar] [CrossRef]
  11. Lehmann, J. Bio-energy in the black. Front. Ecol. Environ. 2007, 5, 381–387. [Google Scholar] [CrossRef] [Green Version]
  12. Al-Wabel, M.I.; Usman, A.R.A.; Al-Farraj, A.S.; Ok, Y.S.; Abduljabbar, A.; Al-Faraj, A.I.; Sallam, A.S. Date palm waste biochars alter a soil respiration, microbial biomass carbon, and heavy metal mobility in contaminated mined soil. Environ. Geochem. Health 2017, 41, 1705–1722. [Google Scholar] [CrossRef]
  13. Lehmann, J.; Rillig, M.C.; Thies, J.; Masiello, C.A.; Hockaday, W.C.; Crowley, D. Biochar effects on soil biota. A review. Soil Biol. Biochem. 2011, 43, 1812–1836. [Google Scholar] [CrossRef]
  14. Paz-Ferreiro, J.; Lu, H.; Fu, S.; Mendez, A.; Gasco, G. Use of phytoremediation and biochar to remediate heavy metal polluted soils. Solid Earth 2014, 5, 65–75. [Google Scholar] [CrossRef] [Green Version]
  15. Luo, L.; Xu, C.; Chen, Z.; Zhang, S. Properties of biomass-derived biochars: Combined effects of operating conditions and biomass types. Bioresour. Technol. 2015, 192, 83–89. [Google Scholar] [CrossRef]
  16. Nobaharan, K.; Bagheri Novair, S.; Asgari Lajayer, B.; van Hullebusch, E.D. Phosphorus removal from wastewater: The potential use of biochar and the key controlling factors. Water 2021, 13, 517. [Google Scholar] [CrossRef]
  17. Ahmad, M.; Lee, S.S.; Lim, J.E.; Lee, S.E.; Cho, J.S.; Moon, D.H.; Hashimoto, Y.; Ok, Y.S. Speciation and phytoavailability of lead and antimony in a small arms range soil amended with mussel shell, cow bone and biochar: EXAF spectroscopy and chemical extractions. Chemosphere 2014, 95, 433–441. [Google Scholar] [CrossRef]
  18. Uchimiya, M.; Chang, S.; Klasson, K.T. Screening biochars for heavy metal retention in soil: Role of oxygen functional groups. J. Hazard. Mater. 2011, 190, 432–441. [Google Scholar] [CrossRef]
  19. Islam, S.N.; Rahman, M.L.; Tareq, M.Z.; Mostofa, B.; Karim, M.M.; Sultana, A.; Sadat, M.A. Nutrient Combination with Biochar: Improving Yield and Quality of Jute Seed. Malays. J. Sustain. Agric. 2021, 5, 43–50. [Google Scholar] [CrossRef]
  20. Novak, J.M.; Lima, I.; Xing, B.; Gaskin, J.W.; Steiner, C.; Das, K.C.; Ahmedna, M.; Rehrah, D.; Watts, D.W.; Busscher, W.J.; et al. Characterization of designer biochar produced at different temperatures and their effects on a loamy sand. Ann. Environ. Sci. 2009, 3, 195–206. [Google Scholar]
  21. Herath, I.; Kumarathilaka, P.; Navaratne, A.; Rajakaruna, N.; Vithanage, M. Immobilization and phytotoxicity reduction of heavy metals in serpentine soil using biochar. J. Soils Sediments 2015, 15, 126–138. [Google Scholar] [CrossRef] [Green Version]
  22. Nigussie, A.; Kissi, E.; Misganaw, M.; Ambaw, G. Effect of biochar application on soil properties and nutrient uptake of lettuces (Lactuca sativa) grown in chromium polluted soils. Am-Eurasian. J. Sustain. Agric. 2012, 12, 369–376. [Google Scholar]
  23. Ok, Y.S.; Chang, S.X.; Gao, B.; Chung, H.J. SMART biochar technology e a shifting paradigm towards advanced materials and healthcare research. Environ. Technol. Innovation. 2015, 4, 206–209. [Google Scholar] [CrossRef]
  24. Ekebafe, L.O.; Ogbeifun, D.E.; Okieimen, F.E. Effect of cassava starch hydrogel on the water requirement of maize (Zea may) seedlings and selected properties of sandy loam soil. Int. J. Basic. Appl. Sci. 2012, 1, 132–139. [Google Scholar]
  25. Wang, K.; Qiu, G.; Cao, H.; Jin, R. Removal of chromium (VI) from aqueous solutions using Fe3O4 magnetic polymer microspheres functionalized with amino groups. Materials 2015, 8, 8378–8391. [Google Scholar] [CrossRef] [PubMed]
  26. Bai, W.; Zhang, H.; Liu, B.; Wu, Y.; Song, J. Effects of superabsorbent polymers on the physical and chemical properties of soil following different wetting and drying cycles. Soil Use Manag. 2010, 26, 253–260. [Google Scholar] [CrossRef]
  27. Ballav, N.; Maity, A.; Mishra, S.B. High efficient removal of chromium (VI) using glycine doped polypyrrole adsorbent from aqueous solution. Chem. Eng. J. 2012, 198, 536–546. [Google Scholar] [CrossRef]
  28. de-Bashan, L.E.; Bashan, Y. Immobilized microalgae for removing pollutants: Review of practical aspects. Bioresour. Technol. 2010, 101, 1611–1627. [Google Scholar] [CrossRef]
  29. Shigetomi, Y.; Hori, Y.O.I.; Kojima, T. The removal of arsenate in waste water with an adsorbent prepared by binding hydrous iron (III) oxide with polyacrylamide. Bull. Chem. Soc. Jpn. 1980, 53, 1475–1476. [Google Scholar] [CrossRef] [Green Version]
  30. Richard, L.A. Diagnosis and Improvement of Saline and Alkali Soils. U.S. Department of Agriculture Handbook: Washington, DC, USA, 1954; Volume 60, p. 160. [Google Scholar]
  31. ASTM D1762-84; Standard Method for Chemical Analysis of Wood Charcoal. American Society for Testing and Materials (ASTM): Philadelphia, PA, USA, 1989.
  32. Bouyoucos, G.J. Hydrometer method improved for making particle size analysis of soils. Agron. J. 1962, 54, 464–465. [Google Scholar] [CrossRef]
  33. Walkley, A.; Black, I.A. An examination of Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Sci. 1934, 37, 29–37. [Google Scholar] [CrossRef]
  34. Hossner, L.R. Dissolution for total elemental analysis. In Methods of Soil Analysis: Part 3e Chemical Methods; Sparks, Bigham, J.M., Eds.; SSSA and ASA: Madison, WI, USA, 1996; pp. 49–64. [Google Scholar]
  35. Campbell, C.R.; Plank, C.O. Preparation of plant tissue for laboratory analysis. In Handbook of Reference Methods for Plant Analysis; Kalra, Y.P., Ed.; CRC Press: Boca Raton, FL, USA, 1998; pp. 37–49. [Google Scholar]
  36. Steel, R.G.D.; Torrie, J.H.; Deekey, D.A. Principles and Procedures of Statistics: A Biometrical Approach, 3rd ed.; McGraw Hill Book Co.: New York, NY, USA, 1997. [Google Scholar]
  37. Usman, A.R.A.; Abduljabbar, A.; Vithanage, M.; Ok, Y.S.; Ahmad, M.; Ahmad, M.; Elfaki, J.; Abdulazeem, S.S.; Al-Wabel, M.I. Biochar production from date palm waste: Charring temperature induced changes in composition and surface chemistry. J. Anal. Appl. Pyrolysis 2015, 115, 392–400. [Google Scholar] [CrossRef]
  38. Fan, R.; Luo, J.; Yan, S.; Zhou, Y.; Zhang, Z. Effects of biochar and super absorbent polymer on substrate properties and water spinach growth. Pedosphere 2015, 25, 737–748. [Google Scholar] [CrossRef]
  39. Bartoli, M.; Arrigo, R.; Malucelli, G.; Tagliaferro, A.; Duraccio, D. Recent Advances in Biochar Polymer Composites. Polymers 2022, 14, 2506. [Google Scholar] [CrossRef] [PubMed]
  40. Kim, K.H.; Kim, J.Y.; Cho, T.S.; Choi, J.W. Influence of pyrolysis temperature on physicochemical properties of biochar obtained from the fast pyrolysis of pitch pine (Pinus rigida). Bioresour. Technol. 2012, 118, 158–162. [Google Scholar] [CrossRef]
  41. Mohamed, R.M.; Mkhalid, I.A.; Barakat, M.A. Rice husk ash as a renewable source for the production of zeolite NaY and its characterization. Arab. J. Chem. 2015, 8, 48–53. [Google Scholar] [CrossRef] [Green Version]
  42. Al-Wabel, M.I.; Al-Omran, A.; El-Naggar, A.H.; Nadeem, M.; Usman, A.R.A. Pyrolysis temperature in- duced changes in characteristics and chemical composition of biochar produced from conocarpus wastes. Bioresour. Technol. 2013, 131, 374–379. [Google Scholar] [CrossRef]
  43. Chen, T.; Liu, R.; Scott, N.R. Characterization of energy carriers obtained from the pyrolysis of white ash, switchgrass and corn stover—Biochar, syngas and bio-oil. Fuel Process. Technol. 2016, 142, 124–134. [Google Scholar] [CrossRef]
  44. Ma, X.; Yuan, S.; Yang, L.; Li, L.; Zhang, X.; Su, C.; Wang, K. Fabrication and potential applications of CaCO3–lentinan hybrid materials with hierarchical composite pore structure obtained by self-assembly of nanoparticles. Cryst. Eng. Comm. 2013, 15, 8288–8299. [Google Scholar] [CrossRef]
  45. Xu, X.; Hu, X.; Ding, Z.; Chen, Y. Effects of copyrolysis of sludge with calcium carbonate and calcium hydrogen phosphate on chemical stability of carbon and release of toxic elements in the resultant biochars. Chemosphere 2017, 189, 76–85. [Google Scholar] [CrossRef]
  46. Meri, N.H.; Alias, A.B.; Talib, N.; Rashid, Z.A.; Wan, W.A.; Ghani, A.K. Effect of Chemical Washing Pre-treatment of Empty Fruit Bunch (EFB) biochar on Characterization of Hydrogel Biochar composite as Bioadsorbent. Mater. Sci. Eng. 2018, 358, 012018. [Google Scholar] [CrossRef] [Green Version]
  47. Amin, H.; Arain, B.A.; Amin, F.; Surhio, M.A. Phytotoxicity of Chromium on Germination, Growth and Biochemical Attributes of Hibiscus esculentus L. Am. J. Plant. Sci. 2013, 4, 2431. [Google Scholar] [CrossRef] [Green Version]
  48. Peralta, J.R.; Gardea-Torresdey, J.L.; Tiemann, K.J.; Gomez, E.; Arteaga, S.; Rascon, E.; Parsons, J.G. Uptake and effects of five heavy metals on seed germination and plant growth in alfalfa (Medicago sativa L.). Bull. Environ. Contam. Toxicol. 2001, 66, 727–734. [Google Scholar] [CrossRef] [PubMed]
  49. Panda, S.K. Heavy metal phytotoxicity induces oxidative stress in Taxithalium sp. Curr. Sci. 2003, 84, 631–633. [Google Scholar]
  50. Barcelo, j.; Poschenrieder, C. Chromium in plants. In Chromium Environmental Issue; Carati, S., Tottareli, F., Seqmi, P., Eds.; Francotangati Press: Milan, Italy, 1997; pp. 101–129. [Google Scholar]
  51. Rout, G.R.; Samantaray, S.; Das, P. Differential chromium tolerance among eight mungbean cultivars grown in nutrient culture. J. Plant Nutr. 1997, 20, 473–483. [Google Scholar] [CrossRef]
  52. Zeid, I.M. Responses of Phaseolus vulgaris chromium and cobalt treatments. Biologia. Plantarum. 2001, 44, 111–115. [Google Scholar] [CrossRef]
  53. Fozia, A.; Muhammad, A.Z.; Muhammad, A.; Zafar, M.K. Effect of chromium on growth attributes in sunflower (Helianthus annuus L.). J. Environ. Sci. 2008, 20, 1475–1480. [Google Scholar] [CrossRef]
  54. Chandra, R.; Bharagava, R.N.; Yadav, S.; Mohan, D. Accumulation and distribution of toxic metals in wheat (Triticum aestivum L.) and Indian mustard (Brassica campestris L.) irrigated with distillery and tannery effluents. J. Hazard. Mater. 2009, 15, 1514–1521. [Google Scholar] [CrossRef]
  55. Gill, S.S.; Tuteja, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 2010, 48, 909–930. [Google Scholar] [CrossRef]
  56. Sangwan, P.; Kumar, V.; Joshi, U.N. Chromium (VI) affected nutritive value of forage clusterbean (Cyamopsis tetragonoloba L.). Int. J. Agric. Environ. Biotechnol. 2014, 7, 17. [Google Scholar] [CrossRef]
  57. Kumar, P. Evaluation of toxic effects of hexavalent chromium on the yield and quality of Sorghum. Preprints 2020, 2020110564. [Google Scholar]
  58. Jiang, W.; Liu, D.; Liu, X. Effects of copper on root growth, cell division, and nucleolus of Zea mays. Biol. Plant. 2001, 44, 105–109. [Google Scholar] [CrossRef]
  59. Liu, D.; Jiang, W.; Gao, X. Effects of cadmium on root growth, cell division and nucleoli in root tip cells of garlic. Biol. Plant. 2003, 47, 79–83. [Google Scholar] [CrossRef]
  60. Samantaray, S.; Rout, G.R.; Das, P. Studies on differential tolerance of mungbean cultivars to metalliferous minewastes. Agribiol. Res. 1999, 52, 193–201. [Google Scholar]
  61. Wyszkowski, M.; Radziemska, M. Effects of chromium (III and VI) on spring barley and maize biomass yield and content of nitrogenous compounds. J. Toxicol. Environ. Health Part A 2010, 30, 1274–1282. [Google Scholar] [CrossRef]
  62. Ali, B.; Wang, B.; Ali, S.; Ghani, M.A.; Hayat, M.T.; Yang, C.; Xu, L.; Zhou, W.J. Aminolevulinic acid ameliorates the growth, photosynthetic gas exchange capacity, and ultrastructural changes under cadmium stress in Brassica napus L. J. Plant Growth Regul. 2013, 32, 604–614. [Google Scholar] [CrossRef]
  63. Wang, G.; Xu, Z. The effects of biochar on germination and growth of wheat in different saline-alkali soil. Asian Agric. Res. 2013, 5, 116. [Google Scholar]
  64. Bashir, M.A.; Wang, X.; Naveed, M.; Mustafa, A.; Ashraf, S.; Samreen, T.; Nadeem, S.M.; Jamil, M. Biochar mediated-alleviation of chromium stress and growth improvement of different maize cultivars in tannery polluted soils. Int. J. Environ. Res. Public Health 2021, 18, 4461. [Google Scholar] [CrossRef]
  65. Rajkovich, S.; Enders, A.; Hanley, K.; Hyland, C.; Zimmerman, A.R.; Lehmann, J. Corn growth and nitrogen nutrition after additions of biochars with varying properties to a temperate soil. Biol. Fertil. Soils 2012, 48, 271–284. [Google Scholar] [CrossRef]
  66. Inyang, M.; Gao, B.; Pullammanappallil, P.; Ding, W.; Zimmerman, A.R. Biochar from anaerobically digested sugarcane bagasse. Bioresour. Technol. 2010, 101, 8868–8872. [Google Scholar] [CrossRef]
  67. Ahmad, M.; Rajapaksha, A.U.; Lim, J.E.; Zhang, M.; Bolan, N.; Mohan, D.; Vithanage, M.; Lee, S.S.; Ok, Y.S. Biochar as a sorbent for contaminant management in soil and water: A review. Chemosphere 2013, 99, 19–33. [Google Scholar] [CrossRef]
  68. Cao, X.; Ma, L.; Gao, B.; Harris, W. Dairy-manure derived biochar effectively sorbs lead and atrazine. Environ. Sci. Technol. 2009, 43, 3285–3291. [Google Scholar] [CrossRef] [PubMed]
  69. Beesley, L.; Inneh, O.S.; Norton, G.J.; Moreno-Jimenez, E.; Pardo, T.; Clemente, R.; Dawson, J.J.C. Assessing the influence of compost and biochar amendments of the mobility and toxicity of metals and arsenic in a naturally contaminated mine soil. Environ. Pollut. 2014, 186, 195–202. [Google Scholar] [CrossRef] [PubMed]
  70. 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]
  71. Wang, X.; Fan, J.; Xing, Y.; Xu, G.; Wang, H.; Deng, J.; Wang, Y.; Zhang, F.; Li, P.; Li, Z. The effects of mulch and nitrogen fertilizer on the soil environment of crop plants. Adv. Agron. 2019, 153, 121–173. [Google Scholar]
Figure 1. SEM images of the biomass (BM), biochars (JBCs) and polymerized biochars (JPBCs). (i): (BM), (iiiv): (JBCS produced at 300, 500 and 700 °C), (vvii): (JPBCs produced at 300, 500 and 700 °C).
Figure 1. SEM images of the biomass (BM), biochars (JBCs) and polymerized biochars (JPBCs). (i): (BM), (iiiv): (JBCS produced at 300, 500 and 700 °C), (vvii): (JPBCs produced at 300, 500 and 700 °C).
Sustainability 14 16093 g001
Figure 2. The X-ray diffraction analyses of the biomass (BM), biochars (JBCs) and polymerized biochars (JPBCs). (a): (BM and JBCs produced at 300, 500 and 700 °C), (b): (BM and JPBCs produced at 300, 500 and 700 °C).
Figure 2. The X-ray diffraction analyses of the biomass (BM), biochars (JBCs) and polymerized biochars (JPBCs). (a): (BM and JBCs produced at 300, 500 and 700 °C), (b): (BM and JPBCs produced at 300, 500 and 700 °C).
Sustainability 14 16093 g002
Figure 3. The FTIR analyses the biomass (BM), biochars (JBCs) and polymerized biochars (JPBCs). (a): (BM and JBCs produced at 300, 500, and 700 °C), (b): (BM and JPBCs produced at 300, 500, and 700 °C).
Figure 3. The FTIR analyses the biomass (BM), biochars (JBCs) and polymerized biochars (JPBCs). (a): (BM and JBCs produced at 300, 500, and 700 °C), (b): (BM and JPBCs produced at 300, 500, and 700 °C).
Sustainability 14 16093 g003
Figure 4. Germination of wheat (Triticum aestivum L.) seeds affected by applied concentrations of CrVI. The bars represent standard deviation.
Figure 4. Germination of wheat (Triticum aestivum L.) seeds affected by applied concentrations of CrVI. The bars represent standard deviation.
Sustainability 14 16093 g004
Figure 5. Fresh (a) and dry weights (b) of wheat (Triticum aestivum L.) seedlings affected by different concentration of CrVI. The bars represent standard deviation.
Figure 5. Fresh (a) and dry weights (b) of wheat (Triticum aestivum L.) seedlings affected by different concentration of CrVI. The bars represent standard deviation.
Sustainability 14 16093 g005
Figure 6. Root (a) and shoot (b) lengths (cm) of wheat (Triticum aestivum L.) seedlings affected by different concentration of CrVI. The bars represent standard deviation.
Figure 6. Root (a) and shoot (b) lengths (cm) of wheat (Triticum aestivum L.) seedlings affected by different concentration of CrVI. The bars represent standard deviation.
Sustainability 14 16093 g006
Figure 7. Effect of the biochars and polymerized biochars on germination of wheat (Triticum aestivum L.) seeds under the influence of applied concentrations of CrVI, JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500, and 700 °C).
Figure 7. Effect of the biochars and polymerized biochars on germination of wheat (Triticum aestivum L.) seeds under the influence of applied concentrations of CrVI, JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500, and 700 °C).
Sustainability 14 16093 g007
Figure 8. Effect of the biochars and polymerized biochars on (a) fresh and (b) dry weights of wheat (Triticum aestivum L.) seedlings under the influence of applied concentrations of CrVI. JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500, and 700 °C).
Figure 8. Effect of the biochars and polymerized biochars on (a) fresh and (b) dry weights of wheat (Triticum aestivum L.) seedlings under the influence of applied concentrations of CrVI. JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500, and 700 °C).
Sustainability 14 16093 g008
Figure 9. Effect of the biochars and polymerized biochars on (a) root and (b) shoot lengths of wheat (Triticum aestivum L.) seedlings under the influence of applied concentrations of CrVI. JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500, and 700 °C).
Figure 9. Effect of the biochars and polymerized biochars on (a) root and (b) shoot lengths of wheat (Triticum aestivum L.) seedlings under the influence of applied concentrations of CrVI. JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500, and 700 °C).
Sustainability 14 16093 g009
Figure 10. Effect of the biochars and polymerized biochars on CrVI uptake of wheat (Triticum aestivum L.) seedlings (µg/seedling) under the influence of applied concentrations of CrVI. JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500 and 700 °C).
Figure 10. Effect of the biochars and polymerized biochars on CrVI uptake of wheat (Triticum aestivum L.) seedlings (µg/seedling) under the influence of applied concentrations of CrVI. JBC-300, JBC-500, and JBC-700, JPBC-300, JPBC-500, and JPBC-700 (Jujube wood waste derived and polymerized biochars produced at 300, 500 and 700 °C).
Sustainability 14 16093 g010
Table 1. Calculated physiochemical characteristics of soil.
Table 1. Calculated physiochemical characteristics of soil.
Electrical Conductivity
(dSm−1)
pH
(1:2.5)
CEC
(cmol kg−1)
Organic Matter
(%)
Total Metal Concentration (mg kg−1)
CrFeMnZnCu
1.05 ± 0.037.41 ± 1.19.95 ± 1.32.5.0 ± 0.15160 ± 16270 ± 14129 ± 30119 ± 1394 ± 11
Table 2. Effects of applied CrVI concentration on germination and seedlings growth of wheat (Triticum aestivum L.).
Table 2. Effects of applied CrVI concentration on germination and seedlings growth of wheat (Triticum aestivum L.).
CrVI
Concentration (mg L−1)
Germination
%
Fresh Weight
(g)
Dry Weight
(g)
Shoot Length (cm)Root Length
(cm)
Cr Uptake (μg/Seedling)
0 100 ± 1.5 A0.18 ± 0.08 A0.13 ± 0.05 A7.39 ± 1.5 A7.29 ± 1.2 A0.5 ± 0.02 C
5 80 ± 2.8 AB0.14 ± 0.07 B0.09 ± 0.02 B6.15 ± 1.4 B5.67 ± 0.9 B7.66 ± 1.1 B
10 65 ± 2.2 BC0.11 ± 0.02 B0.08 ± 0.01 B4.90 ± 0.9 C3.94 ± 0.6 C8.26 ± 1.8 B
20 50 ± 3.8 C0.07 ± 0.01 C0.04 ± 0.01 C2.66 ± 0.4 D1.54 ± 0.8 D9.98 ± 1.5 B
40 40 ± 4.2 C0.03 ± 0.01 D0.02 ± 0.01 C1.37 ± 0.6 E0.84 ± 0.2 D13.24 ± 1.3 A
Tuckey HCD28.3770.03110.03470.82380.89792.6961
Alpha = 0.05. Different letter show significance.
Table 3. Effects of Jujube (Ziziphus jujube L.) wood waste derived biochar (JBC) and polymer modified biochar (JPBC) produced at 300, 500, and 700 °C. on germination, seedling growth and Cr uptake of wheat (Triticum aestivum L) under the influence of cumulative effect of applied concentration of CrVI.
Table 3. Effects of Jujube (Ziziphus jujube L.) wood waste derived biochar (JBC) and polymer modified biochar (JPBC) produced at 300, 500, and 700 °C. on germination, seedling growth and Cr uptake of wheat (Triticum aestivum L) under the influence of cumulative effect of applied concentration of CrVI.
CrVI
Concentration
Germination (%)Fresh Weight
(g)
Dry Weight
(g)
Shoot Length (cm)Root Length
(cm)
Cr Uptake (µg/Seedling)
Control67 ± 3.3 B0.18 ± 0.04 E0.075 ± 0.01 C4.492 ± 0.5 E3.854 ± 0.3 E7.928 ± 1.1 A
JBC-30079 ± 5.9 AB0.164 ± 0.05 B0.123 ± 0.01 AB5.722 ± 0.3 B5.107 ± 0.4 AB4.275 ± 0.8 B
JBC-50076 ± 5.1 AB0.134 ± 0.02 D0.108 ± 0.01 B4.922 ± 0.3 D4.266 ± 0.4 DE5.184 ± 1.1 B
JBC-70074 ± 2.8 AB0.145 ± 0.01 CD0.111 ± 0.01 B5.044 ± 0.4 CD4.502 ± 0.5 CD4.923 ± 0.9 B
JPBC-30083 ± 3.4 A0.179 ± 0.03 A0.139 ± 0.01 A6.226 ± 0.6 A5.442 ± 0.9 A0.226 ± 0.03 C
JPBC-50079 ± 3.6 AB0.148 ± 0.04 CD0.106 ± 0.02 B5.087 ± 0.7 CD4.490 ± 0.7 CD0.396 ± 0.03 C
JPBC-70077 ± 7.8 AB0.152 ± 0.01 BC0.111 ± 0.01 B5.376 ± 0.7 BC4.853 ± 0.8 BC0.328 ± 0.01 C
Tuckey HCD13.2350.01480.01870.36500.56492.4014
Alpha = 0.05, Different alphabetical letters show significance level, JBC-300, JBC-500, and JBC-700 = Biochar produced at 300, 500, and 700 °C temperature, JPBC-300, JPBC-500, and JPBC-700 = Polymer modified biochar produced at 300, 500, and 700 °C temperature.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Rafique, M.I.; Ahmad, M.; Al-Wabel, M.I.; Ahmad, J.; Al-Farraj, A.S. Mitigating the Toxic Effects of Chromium on Wheat (Triticum aestivum L.) Seed Germination and Seedling Growth by Using Biochar and Polymer-Modified Biochar in Contaminated Soil. Sustainability 2022, 14, 16093. https://doi.org/10.3390/su142316093

AMA Style

Rafique MI, Ahmad M, Al-Wabel MI, Ahmad J, Al-Farraj AS. Mitigating the Toxic Effects of Chromium on Wheat (Triticum aestivum L.) Seed Germination and Seedling Growth by Using Biochar and Polymer-Modified Biochar in Contaminated Soil. Sustainability. 2022; 14(23):16093. https://doi.org/10.3390/su142316093

Chicago/Turabian Style

Rafique, Muhammad I., Munir Ahmad, Mohammad I. Al-Wabel, Jahangir Ahmad, and Abdullah S. Al-Farraj. 2022. "Mitigating the Toxic Effects of Chromium on Wheat (Triticum aestivum L.) Seed Germination and Seedling Growth by Using Biochar and Polymer-Modified Biochar in Contaminated Soil" Sustainability 14, no. 23: 16093. https://doi.org/10.3390/su142316093

APA Style

Rafique, M. I., Ahmad, M., Al-Wabel, M. I., Ahmad, J., & Al-Farraj, A. S. (2022). Mitigating the Toxic Effects of Chromium on Wheat (Triticum aestivum L.) Seed Germination and Seedling Growth by Using Biochar and Polymer-Modified Biochar in Contaminated Soil. Sustainability, 14(23), 16093. https://doi.org/10.3390/su142316093

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