Next Article in Journal
Feasibility of Different Weather Data Sources Applied to Building Indoor Temperature Estimation Using LSTM Neural Networks
Next Article in Special Issue
Exploring Potential of Seed Endophytic Bacteria for Enhancing Drought Stress Resilience in Maize (Zea mays L.)
Previous Article in Journal
The Resilience of Urban Retail System in the Face of the COVID-19 Pandemic. The Case Study of Poland
Previous Article in Special Issue
Health Risk Assessment, Pore Water Chemistry, and Assessment of Trace Metals Transfer from Two Untreated Sewage Sludge Types to Tomato Crop (Lycopersicon esculentum) at Different Application Levels
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Trace Metal Accumulation in Rice Variety Kainat Irrigated with Canal Water

1
Department of Botany, University of Sargodha, Sargodha 40100, Pakistan
2
Department of Chemistry, Government College University, Faisalabad 38000, Pakistan
3
College of Plant Science and Technology, Huazhong Agricultural University, Wuhan 430070, China
4
Thathi Pak Farm House, Toba Tek Sigh 36070, Pakistan
5
Department of Botany, Government College University, Lahore 54000, Pakistan
6
Department of Marine Biology, Faculty of Marine Sciences, King Abdualaziz University, P.O. Box 80207, Jeddah 21589, Saudi Arabia
7
Biology Department, Faculty of Science, Tabuk University, Tabuk 71421, Saudi Arabia
8
Department of Environmental Sciences and Engineering, Government College University Allama Iqbal Road, Faisalabad 38000, Pakistan
9
Department of Biological Sciences and Technology, China Medical University, Taichung City 40402, Taiwan
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Sustainability 2021, 13(24), 13739; https://doi.org/10.3390/su132413739
Submission received: 14 October 2021 / Revised: 4 December 2021 / Accepted: 7 December 2021 / Published: 13 December 2021

Abstract

:
Due to the rapid increase in industrial and urban areas, environmental pollution is increasing worldwide, causing unwanted changes in the air, water, and soil at biological, physical, and chemical levels, ultimately causing negative effects for living things. This work was performed in Jhang, Punjab, Pakistan, and examined and measured heavy metal levels in various plant parts of the rice (Oryza sativa) variety Kainat (roots, shoots, and grains) with results been set in relation to the soil around the root area. The samples were taken from five different sites. The mean level of trace metals (mg/kg) in grains was soil-dependent and varied from cadmium (Cd) (2.49–5.52), zinc (Zn) (5.8–10.78), copper (Cu) (4.82–7.85), cobalt (Co) (1.48–6.52), iron (Fe) (8.68–14.73), manganese (Mn) (6.87–13.93), and nickel (Ni) (2.3–8.34). Excluding Cd, the absorption of all metals under inspection was recorded within permissible limits, as recommended by the FAO and WHO. The pollution load index for Cd was highest at all sites. The enrichment coefficient of Co, Cd, and Cu were greater. The bioaccumulation factor at all studied sites was present, in order: Cu ˃ Zn ˃ Fe ˃ Mn ˃ Co ˃ Ni ˃ Cd. The translocation factor was present at five different sites: Mn ˃ Fe ˃ Cu ˃ Zn ˃ Co ˃ Cd ˃ Ni. The health risk index of all inspected metals was lower than 1 and was within safe limits. The higher pollution of Cd suggested maintenance of rice crop is recommended, decreasing health risks in humans.

1. Introduction

In Pakistan, rice is the second staple food after wheat, hence it is a vital crop for the nation’s economy, wealth, and food security. Its contribution to the economy is very significant as its foreign exchange earnings exceed USD 2 billion annually. Pakistan is the fourth largest rice exporter in 2020/2021, accounting for 4 billion metric tons, and rice is a widely distributed cereal crop around the globe [1].
Heavy metals enter the environment both through natural sources and human activities. Recently, heavy metals have attracted worldwide attention, owing to their non-biodegradability, and being accumulated in living things, thus posing considerable threats to humans and the broader ecosystem [2,3,4]. Rice is known to accumulate heavy metals such as cadmium (Cd), lead (Pb), and zinc (Zn); through the roots, it eventually delivers them to the shoots and grains [5,6,7], and consequently, these metals enter the food chain through rice consumption. Even low concentrations accumulated from the soil can cause toxicities in humans [8,9,10]. In short, rice grown on metal contaminated soils is a live challenge to food production, food quality, and food safety [11,12,13,14]; consequently, there are ever-increasing demands by governments, retail, and consumers for metal minimization in rice.
The cultivation of rice crops in polluted soils is a debated subject because of the plant’s capability to uptake and absorb hazardous metals from such contaminated soils. Few micronutrients such as zinc and copper are essential for healthy plant growth, however, others such as cadmium and lead have proven to be hazardous to ecosystems in general and to human health, especially when consumed in higher concentrations. Similarly, their persistence, due to their toxic nature, exposes serious health risks to other living organisms, too [15,16,17]. Contemporary investigations into toxicity and tolerance in metal-stressed plants are prompted by the growing metal pollution of the environment [18,19]. One contributor to this pollution is the intensive application of inorganic and organic fertilizers for intense agriculture [20,21]. Although the levels of heavy metals in agricultural soils are very small at the point of initial application, repeated use of phosphate fertilizers may lead to concerning level accumulation [22,23,24,25].
Many of these heavy metals are carcinogenic, resulting in various diseases, especially kidneys, cardiac, bone, and blood diseases. Heavy metals exert a toxic effect on food crops, animals and humans, and cause various clinical problems in humans [26,27,28,29,30]. Heavy metals are human carcinogens and are the critical basis for various diseases [31,32]. Heavy metal accumulation in soils is of concern in agricultural production because of the adverse effects on food safety and marketability, crop growth due to phytotoxicity, and environmental health of soil organisms [33,34]. The influence of plants and their metabolic activities affects the geological and biological redistribution of heavy metals through pollution of the air, water, and soil.
The translocation factor (TF) and bioaccumulation factor (BAF) are important in screening hyper-accumulators for the phytoremediation of heavy metals. The TF is the capacity of plants to transfer metals from roots to shoots, and BAF expresses the ability of plants to accumulate metals from soils to tissues [35,36].
This study was performed to examine the impact of canal water irrigation on metal uptake in rice through the soil and the potential health risk of this in humans.

2. Materials and Methods

2.1. Experimental Site

The agricultural area of Jhang, a district in central Punjab (Pakistan), was selected as a study site. Most of the land is cultivated except for the land present near the Chenab River. In winters, irregular rainfall occurs, while the annual average rainfall is 100–150 mm per year. The agricultural area of Jhang is about 8809 km2.
At Moza Satiana, Chiniot road, five sites were selected to examine the levels of various metals present in soils of paddies irrigated through canal water.
A detailed description of the experimental sites studied is presented in Figure S1.

2.2. Sample Collection and Preparation

Four samples (using five replicates of each sample) of soil grown over Kainat (a popular variety of rice) from five different sites were selected for analysis. The soil was collected from 150 mm depth, dug up by a stainless augur, and following the method of Sanchez et al. [37]. Before placing the samples in the oven, they were dried in sunlight. The oven temperature was set to 105 °C.
Similarly, four samples of paddy grains, roots, and shoots (five replicas) were taken from the same five study sites, using a sterile apparatus. To remove dust particles, the grains were washed with deionized water, followed by a 0.5 M dilution of HCl. The grains were pre-dried in sunlight, followed by further oven drying at 105 °C for 5 days. The dry samples were taken out from the oven and were ground into a powder with a pestle or mortar.
For rice and soil, 2 g of ground samples were digested using an adoption of the “Wet Digestion Method” [38]. The samples were transferred into a digestion compartment and 10 mL of aqua regia (1:3 v/v) was added. The digestion mix was left overnight and on the next day, the mixture was heated on a hot plate (70 °C) for 4 h and under the addition of 2 mL H2O2. The digestion process was stopped once the solution turned colorless. During cooling, the sample solution was filtered by using a 42 µm filter paper and then diluted with distilled water to 50 mL volume.

2.3. Sample Analysis

The digested samples were analyzed in an atomic absorption spectrophotometer (AA-6300, Shimadzu, Japan) for the quantitative analysis of heavy metals. Seven metals were selected for investigation in this study, namely cadmium, zinc, copper, cobalt, iron, manganese, and nickel.
To prevent the risk of contamination during laboratory work, the apparatus was washed prior to use. All required chemicals and salts (for digestion and analysis on AAS) used in the experiments were supplied by Merck (Germany).
Concentrations among rice and soil samples were determined on a dry weight basis. All analyses were repeated in triplicate.
The bioaccumulation factor (BAF) was computed according to the equation below [39].
B A F = m e t a l   c o n c e n t r a t i o n   i n   g r a i n ( mg kg ) m e t a l   c o n c e n t r a t i o n   i n   s o i l ( mg kg )  
The translocation factor (TF) was determined as seen in Ref. [40]:
T F = t h e   m e t a l   c o n c e n t r a t i o n   ( mg kg ) i n   p l a n t s s h o o t t h e   m e t a l   c o n c e n t r a t i o n   ( mg kg ) i n   p l a n t s r o o t  
The pollution load index (PLI) calculating the metal quantity in the soil samples was determined by [41]:
P L I = m e t a l   i n   e x a m i n e d   s o i l   ( p p m )   s t a n d a r d   v a l u e   o f   s o i l   m e t a l   ( p p m )
The enrichment factor (EF) describes the amount of metal retained in the soil. EF is reliant on the accessibility of metals according to their chemical form present in the soil, growth rate, and variance in the metal uptake ability of different plant species and has been calculated by [42]:
E F = m e t a l s   ( mg kg ) a t   e d i b l e   p a r t   o f   O r y z a   s a t i v a m e t a l   ( mg kg ) i n   i n v e s t i g a t e d   s o i l s t a n d a r d   c o n c e n t r a t i o n   o f   m e t a l s   ( mg kg ) i n   e d i b l e   p a r t   o f   O r y z a   s a t i v a s t a n d a r d   c o n c e n t r a t i o n   ( mg kg ) o f   m e t a l   i n   s o i l
The daily intake of metals (DIM) in adults was assessed by this formula [43]:
D I M = ( C m e t a l × C d a i l y   f o o d   i n t a k e ) ( B a v e r a g e   w e i g h t )
where Cmetal = metal contents, Cdaily food intake = daily consumption of food crops per person, per day in kg and Baverage weight = average body weight of a person in the exact study area.
The average consumption of rice for this study location equates to 0.345 kg/person and the average body weight is 60 kg/person [44,45].
A calculation has been used to determine the hazard potential of heavy metal exposure involved via ingestion of rice. The so-called health risk index (HRI) was calculated through Ref. [46]:
H R I = D a i l y   i n t a k e   o f   m e t a l O r a l   r e f e r e n c e   d o s e  
HRI < 1 in any food crop denotes that the consumer population is free from serious risks to health, while HRI > 1 designates significant health hazards.

2.4. Statistical Analysis

The results from all the samples were subjected to analysis of variance (ANOVA) according to Duncan’s multiple range test (p < 0.05). Multivariate statistical analysis (MSA) was performed for source apportionment [47]. Minitab 16 and SPSS 21 statistical software were used for the rest of the analysis results. Correlation analysis is considered an effective tool to show relationships between elements within a substance and with other substances. Concentrations of elements show a significant correlation disseminating from a similar or same source.

3. Results and Discussion

3.1. Concentrations of Heavy Metals Involved in Soil

ANOVA highlights the significant (p < 0.05) impact of metal concentrations in soil on Kainat (Table 1, Figure 1). At all sites, the metals were found in the following sequence: Mn ˃ Fe ˃ Zn ˃ Ni ˃ Cd ˃ Cu ˃ Co (Table 1).
In the current study, the levels of Fe, Cu, Mn, Zn, and Ni in irrigation soils (mg/kg) were lower compared to Cd contents and higher as compared to data recorded by Ekmekyapar et al. [48].
A lower amount of Cu content was determined in present soils than outcomes reported by Tariq et al. [1]. Amongst the soil of all sites, the levels of Ni, Zn, and Cu in this study were found within the acceptable range (except for Cd) as set by Awashthi et al. [49]. The concentrations of Mn and Co in soil were within the allowable limit set by the European Union [50] and the ferrous concentration in soil was lower than 21,000 mg/kg as proposed by EPA [51].

3.2. Concentration of Heavy Metals in Roots

Significant (p < 0.05) impact of Cd, Cu, Zn, Co, Mn, Fe, and Ni concentration was seen in roots (Table S1, Figure 1). The concentrations of metals at five sites were in this order: Mn ˃ Fe ˃ Zn ˃ Ni ˃ Cd ˃ Cu ˃ Co (Table 1).
In roots, the levels of Mn, Cu, Zn, Fe, and Ni were lower than levels presented (2.93, 5.37, 1.68, 1.85 and 0.0068 mg/kg, respectively) by Yadav et al. [52]. Co and Cd levels were higher than the concentrations (1.86 and 1.45 mg/kg) observed by Juen et al. [53]. In this study, all metals mean concentrations obtained from root samples were increased compared to Singh et al. [54]. Based on this study’s findings, Kainat rice is a hyper-accumulator plant having a significant potential for absorbing heavy metals from ground soil; this also agrees with the literature [55].

3.3. Concentration of Heavy Metals in Shoot

ANOVA results determined a significant (p < 0.05) influence of Co, Cu, Fe, Cd, Mn, and Ni in the shoot, whereas Zn exhibited a non-significant impact on the plants (Table 1, Figure 1). Following trends were seen for concentrations of metals at all sites: Mn ˃ Fe ˃ Zn ˃ Cu ˃ Cd ˃ Ni ˃ Co (Table 1).
In this study, the levels of Cu, Cd, and Zn were higher than the values (0.24, 0.76, and 0.49 mg/kg) determined by Ogunkunle et al. [56]. Similarly, the values of Cu, Cd, Zn, Mn, and Fe metals were also higher than the findings reported by Yap et al. [15]. However, Yadav et al. [52] presented lower levels of Fe, Mn and Ni compared to current findings.

3.4. Concentration of Heavy Metals in Grains

The result from ANOVA depicted a significant (p < 0.05) impact of Zn, Cd, Fe, Co, Ni, Cu in the sites and Mn in the case of grains (Table 1). The descending order of metals in grains of five sites was: Mn ˃ Fe ˃ Zn ˃ Cu ˃ Ni ˃ Co ˃ Cd (Table 1).
When the mean concentration of heavy metals was compared with SEPA (2005) standards, the Cd concentration noticed in grains was greater, while Ni, Zn, and Cu were lower. Similarly, analyzed Fe, Mn, and Co concentrations in the present study were also below the recommended standards [57]. Metals level ranking in grains of Kainat was Mn ˃ Fe ˃ Zn ˃ Cu ˃ Ni ˃ Co ˃ Cd. Mean levels of Cd, Ni, Co were larger and Zn, Fe, Mn, Cu were found to be lower compared to the findings of Shaar et al. [58]. Comparing metal contents with Jaishree et al. [59], the concentrations of Cd, Cu, and Ni were lower, while Mn, Zn, and Cd were increased.

3.5. Correlation

A positive and significant correlation of cadmium, zinc, cobalt, and cuprous was detected in the cases of soil-root and root-shoot and shoot-grain interaction. Fe displayed a positive but non-significant correlation with soil-root, while root-shoot and shoot-grain detected a positive and significant correlation. Similarly, a positive significant correlation was also noticed for soil-root in the case of Mn, but a positive and non-significant correlation was observed for root-shoot and shoot-grain. Nickel exhibited a positive, but non-significant correlation with soil-root and root-shoot’s relationship, whereas a positive and significant correlation from shoot-grain was detected (Table 2).
Again, a positive significant correlation was detected for Cd, Co, Zn and Cu in cases of soil-root, root-shoot, and shoot-grain. Against the present results, Satpathy et al. [60] found a positive significant correlation in soil-grains, in the case of Cd, Cu and Zn, except for Mn. A positive significant correlation was exhibited in root-shoot and shoot-grain for Fe metal while soil-root and root-shoot in the case of Mn. Positive and non-significantly correlated shoot-grain was observed for Mn, while in the case of Fe it is a soil-root correlation. Nickel exhibited a positive and non-significant correlation between soil-root and root-shoot and a positive significant correlation for shoot-grain. Similarly, Woldetsadik et al. [61] assessed during their study the strong positive significant correlation in the case of Ni and Co.

3.6. Bioaccumulation Factor

At Site-I, the BAF for Cu, Mn, Ni, and Zn was recorded to be larger than Cd, Fe, and Co. At Site-II, the BAF of Ni, Fe, and Cd was lesser than Cu, Mn, Zn, and Co. At Site-III, Fe, Zn, and Cu were greater than Ni, Co, Mn, and Cd while BAF at Site-IV was observed to be higher for Cu, Cd, Mn, and Fe than Ni, Co, and Zn. Finally, in the case of Site-V, the BAF for Cu, Zn and Fe were higher than Mn, Ni, Co, and Cd. Amongst all five sites, the maximum BAF was presented by Ni and Mn while Cd and Co showed the lowest BAF index value (Table 3). The BAF order at Site-I was Cu > Zn > Mn > Ni > Fe > Co > Cd, for Site-II was Cu > Mn > Zn > Co > Ni > Fe > Cd, Site-III was Cu > Fe > Zn > Mn > NI > Co > Cd, Site-IV was Cu > Cd > Mn > Fe > Co > Zn > Ni and in Site-V the observed BAF order was Cu > Zn > Fe > Mn > Ni > Co > Cd.
In the current work, the BAF for Co, Cu, Fe, Mn, and Ni was bigger than the ones recorded by Badawy et al. [62]. BAF levels observed for Cd and Zn in present results were lower than those presented in Singh et al. [63]. BAF of all investigated metals, except Cu, was below 1.00 in this study. Among all the sites, the higher BAF for Cu and Zn displayed that these metals were maximally absorbed in the rice grains from the soil [41].

3.7. Translocation Factor (TF)

Site-I and Site-II showed that the TF trend observed for Fe, Ni, Cu, and Mn was greater than Co, Cd and Zn, whereas, in the case of Site-III, Zn, Cd, and Ni was lesser against Mn, Cu, Fe and Co metals. TF trend in Site-IV presented higher concentrations for Mn, Cu, Zn, and Cd metals than Co, Ni, and Fe. Finally, in Site-V TF for Ni, Cu and Cd were lower compared to Co, Mn, Zn, and Fe. Amongst all the sites, maximum TF concentration was given by Fe and Mn, but Co and Cd gave their minimum concentration (Table 3).
The TF sequence studied in Site-I was Fe > Mn > Cu > Ni > Zn > Co > Cd.
The TF trend in Site-II was Mn > Fe > Cu > Co > Zn > Ni > Cd.
The TF in Site-III was Mn> Cd> Cu > Fe > Zn > Co > Ni.
For Site-IV, the TF ranking was Zn> Cu> Cd > Mn > Co > Fe > Ni.
Conversely, the TF trend within Site-V was Mn> Fe> Co> Zn > Cd > Ni > Cu.
TF concentrations recorded for Cd, Zn, Cu, and Fe were bigger, while Mn was lesser than that described in Kumar et al. [64]. Compared to Satpathy et al. [60], a significantly higher TF trend was observed for Zn and Cu, while Mn and Cd were lower in present results. TF values for Ni were higher and the least amount of Co was observed in this study compared to Emurotu et al. [65].
Amongst all sites, the maximum TF value of Fe and Mn revealed that the rice plants have accumulated Mn and Fe concentration from roots to shoots [66]. Minimum TF in the cases of cadmium and cobalt indicate that paddy roots act as barriers to these two metals’ absorption and contamination. The possible reason behind the fact was that the heavy metals under instant investigation had dissimilar properties and in this way, every metal has an explicit absorption, translocation, and accumulation ability [40].

3.8. Pollution Load Index (PLI)

The metal pollution difference level within sites was derived from PLI [67]. PLI pattern at Site-I and Site-II was Cd > Ni > Cu > Co > Mn > Fe > Zn. The sequences of PLI at Site-III was Cd > Ni > Co > Cu > Mn > Zn > Fe, Site-IV was Cd > Ni > Cu > Co > Mn > Zn > Fe and Site-V was Cd > Ni > Cu > Zn > Mn >Fe > Co, respectively. The pollution load index at all five sites for the case of cadmium was recorded as being higher, while that for Fe and Zn was lowest (Table 4).
In this work, Ni, Zn, and Cu contamination was lowered in soils and Cd contaminations were higher than values by Singh et al. [54], which were Ni (9.06 mg/kg), Cu (8.39 mg/kg), Zn (44.19 mg/kg) and Cd (1.49 mg/kg), respectively. Fe contamination in soil was recorded less than 56.9 mg/kg. In the case of present Co and Mn concentrations, PLI was lower than values presented by Dosumu et al. [68] and Singh et al. [54], respectively.
The reason behind the decreased PLI in these selected study areas was the normal canal water irrigation practice, as there is no flow of industrial effluents on agricultural lands. The presented study obtains values of lower PLI for Zn, Cu, Co, Ni, Fe, and Mn when compared to Ahmad et al. [69].

3.9. Enrichment Factor

Tinker et al. [42] stated that EF is a metals binding capability in soil. The enrichment factor is associated with the availability of metals in soil and variances in uptake capability of metals from soil and plant species growth rate. Enrichment factors greater than 1 equate to a hyper-accumulation ability for metal absorption from the soil by the rice crop [55].
In the present study, at five different sites, the EF of Kainat was present and ranked as Co ˃ Cd ˃ Cu ˃ Ni ˃ Zn ˃ Mn ˃ Fe (Table 4).
Among five different sites, EF for examined metals in recent research had ranges as follows: Cd (1.3703–3.5222), Zn (0.1776–0.3007), Cu (0.6026–1.0763), Co (0.7453–5.1452), Mn (0.0428–0.0637), Ni (0.1433–0.5999) and Fe (0.06609–0.0971) mg/kg, respectively. The transfer of metals for Cd and Fe was superior and for Cu, Co Zn and Ni were lower than values reported by Khan et al. [70] findings.

3.10. Daily Intake of Metal

Liu et al. [71] considered that rice intake is a source of heavy metal interaction with human beings. Amongst all the selected sites, the maximum DIM value was observed for ferrous metals, while cobalt metal showed a minimum value for this index.
The DIM sequence found at Site-I was Fe > Mn > Zn > Cu > Ni > Co > Cd, Site-II was Mn > Cu > Fe > Zn > Ni > Co > Cd, Site-III was Cu > Zn > Fe > Mn > Ni > Co > Cd, Site-IV was Mn > Fe > Cu > Cd > Zn > Ni > Co and Site-V was Cu > Zn > Fe > Mn > Ni > Co > Cd (Table 5).
The DIM findings of Cd (0.05 µg/kg/bw/day) in Sun et al. [72] was lower than presented results within this study. Similarly, DIM recorded for Cu was larger, while for Zn was lesser than those given in other studies (i.e., Ref. [56]). Whereas, a higher Ni and Mn (5.2 and 1.6 mg/kg/person/day respectively) intake was proposed by Balkhair et al. [73] than in the present investigation. Daily intake of Cu and Ni was found to be larger, while Zn and Mn were lesser to the recorded results of Singh et al. [52]. The current work cleared the DIM of Ni, Cu, Zn and Fe, which were found to be within the recommended oral reference doses of EPA [46].

3.11. Health Risk Index

HRI value was calculated to quantify the heavy metals risk assessment resulted in by consuming polluted food crops [45,46]. If any food crop specified the HRI value below 1.00, it should be safe for human consumption, while >1.00 is poisonous for public health [46]. The ascendancy sequence for HRI on Site-I was Co > Cd > Cu > Ni > Mn > Fe > Zn, Site-II was Co > Cd > Cu > Ni > Mn > Zn > Fe, Site-III was Co > Cd > Cu > Ni > Zn > Mn > Fe, Site-IV was Co > Cd > Cu > Ni > Mn > Zn > Fe and at Site-V was Co > Cd > Cu > Ni > Zn > Fe > Mn (Table 5).
The health risk index of metals such as Zn, Cu and Ni was lowered compared to Verma et al. [74]. Singh et al. [54], who reported higher values of HRI than the present findings. The HRI value of Mn described in this study was lower compared with the literature (i.e., Ref. [75]). The HRI value for Fe was less than the permitted reference value (1 × 10−1 mg/kg/day) of EPA [51].
In the present analysis, it was also noted that HRI value of Mn (14 × 10−1 mg/kg/day), Zn (3 × 10−1 mg/kg/day) and Cu (4 × 10−2 mg/kg/day) were lowered, while Cd (1 × 10−3 mg/kg/day) and Ni (2 × 10−2 mg/kg/day) values were higher against their permitted EPA [46] findings. EPA [76] also suggested the reference value of cobalt metal to be 43 × 10−2 mg/kg/day, which would seem to be lesser than found in the present investigation.

4. Conclusions

The current research demonstrated that transmission of heavy metals from soils considerably accumulated in grains. Rice grains were watered by water originating from a canal that has increased heavy metal contents due to the water’s accumulation of agri-chemical and industrial wastes. This water was tainted by soils and eventually, this was absorbed by the rice grains, posing a threat to human health.
Comparing grain and soil in respect to the absorption of metals, greater levels of heavy metals were identified to remain in the soil. The level of cadmium was above the allowable range issued by FAO/WHO, while the pollution load index of the canal water irrigated sites was very high and there is a need of attention for environmental cleanup.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/su132413739/s1, Figure S1. Location of the five different sites (red dots) (Google maps extract). Elevation (m a.s.l.): 158. Coordinates: 31.27° N 72.33° E. Location description: Moza Satiana Chiniot road, Jhang 35200, central Punjab, Pakistan. Table S1. Analysis of variance for heavy metals in paddy soil, root, shoot and grains of Kainat.

Author Contributions

Conceptualization, F.T.; data curation, Z.I.K.; formal analysis, K.A., T.A. and M.U.F.A.; funding acquisition, T.A., M.U.F.A. and M.H.A.; investigation, F.T., M.U.F.A. and A.A.; methodology, F.T., K.A., T.A. and M.H.A.; resources, K.A. and A.A.; software, Z.I.K., M.H.S. and K.A.; supervision, S.A. and A.M.; writing—original draft, Z.I.K., A.M., M.H.S., M.H.A. and S.A.; writing—review and editing, M.H.S., A.A., A.M. and S.A. All authors have read and agreed to the published version of the manuscript.

Funding

Higher Education Commission, Pakistan, research project #2484/13.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The financial support of Higher Education Commission, Pakistan is acknowledged for providing the research project #2484/13 to the first and fifth authors. It should be acknowledged by Zafar Iqbal Khan and Kafeel Ahmad.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Tariq, S.R.; Rashid, N. Multivariate analysis of metal levels in paddy soil, rice plants, and rice grains: A case study from Shakargarh, Pakistan. J. Chem. 2013, 2013, 539251. [Google Scholar] [CrossRef]
  2. Hashem, I.A.; Abbas, A.Y.; Abd El-Hamed, A.E.-N.H.; Salem, H.M.S.; El-hosseiny, O.E.M.; Abdel-Salam, M.A.; Saleem, M.H.; Zhou, W.; Hu, R. Potential of rice straw biochar, sulfur and ryegrass (Lolium perenne L.) in remediating soil contaminated with nickel through irrigation with untreated wastewater. PeerJ 2020, 8, e9267. [Google Scholar] [CrossRef]
  3. Saleem, M.H.; Ali, S.; Rehman, M.; Hasanuzzaman, M.; Rizwan, M.; Irshad, S.; Shafiq, F.; Iqbal, M.; Alharbi, B.M.; Alnusaire, T.S. Jute: A Potential Candidate for Phytoremediation of Metals—A Review. Plants 2020, 9, 258. [Google Scholar] [CrossRef] [Green Version]
  4. Saleem, M.H.; Ali, S.; Hussain, S.; Kamran, M.; Chattha, M.S.; Ahmad, S.; Aqeel, M.; Rizwan, M.; Aljarba, N.H.; Alkahtani, S. Flax (Linum usitatissimum L.): A Potential Candidate for Phytoremediation? Biological and Economical Points of View. Plants 2020, 9, 496. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Afzal, J.; Wang, X.; Saleem, M.-H.; Sun, X.; Hussain, S.; Khan, I.; Rana, M.-S.; Ahmed, S.; Awan, S.-A.; Fiaz, S.; et al. Application of ferrous sulfate alleviates negative impact of cadmium in rice (Oryza sativa L.). Biocell 2021, 45, 1631–1649. [Google Scholar] [CrossRef]
  6. Afzal, J.; Saleem, M.H.; Batool, F.; Elyamine, A.M.; Rana, M.S.; Shaheen, A.; El-Esawi, M.A.; Tariq Javed, M.; Ali, Q.; Arslan Ashraf, M.; et al. Role of Ferrous Sulfate (FeSO4) in Resistance to Cadmium Stress in Two Rice (Oryza sativa L.) Genotypes. Biomolecules 2020, 10, 1693. [Google Scholar] [CrossRef] [PubMed]
  7. Liu, J.; Feng, X.; Qiu, G.; Anderson, C.W.; Yao, H. Prediction of methyl mercury uptake by rice plants (Oryza sativa L.) using the diffusive gradient in thin films technique. Environ. Sci. Technol. 2012, 46, 11013–11020. [Google Scholar] [CrossRef]
  8. Li, Y.; Zhao, J.; Zhang, B.; Liu, Y.; Xu, X.; Li, Y.-F.; Li, B.; Gao, Y.; Chai, Z. The influence of iron plaque on the absorption, translocation and transformation of mercury in rice (Oryza sativa L.) seedlings exposed to different mercury species. Plant Soil 2016, 398, 87–97. [Google Scholar] [CrossRef]
  9. Saleem, M.; Ali, S.; Rehman, M.; Rana, M.; Rizwan, M.; Kamran, M.; Imran, M.; Riaz, M.; Hussein, M.; Elkelish, A.; et al. Influence of phosphorus on copper phytoextraction via modulating cellular organelles in two jute (Corchorus capsularis L.) varieties grown in a copper mining soil of Hubei Province, China. Chemosphere 2020, 248, 126032. [Google Scholar] [CrossRef]
  10. Zhou, J.; Liu, H.; Du, B.; Shang, L.; Yang, J.; Wang, Y. Influence of soil mercury concentration and fraction on bioaccumulation process of inorganic mercury and methylmercury in rice (Oryza sativa L.). Environ. Sci. Pollut. Res. 2015, 22, 6144–6154. [Google Scholar] [CrossRef] [PubMed]
  11. Zhang, C.; Qiu, G.; Anderson, C.W.; Zhang, H.; Meng, B.; Liang, L.; Feng, X. Effect of atmospheric mercury deposition on selenium accumulation in rice (Oryza sativa L.) at a mercury mining region in Southwestern China. Environ. Sci. Technol. 2015, 49, 3540–3547. [Google Scholar] [CrossRef] [PubMed]
  12. Wang, Z.; Sun, T.; Driscoll, C.T.; Yin, Y.; Zhang, X. Mechanism of accumulation of methylmercury in rice (Oryza sativa L.) in a mercury mining area. Environ. Sci. Technol. 2018, 52, 9749–9757. [Google Scholar] [CrossRef] [PubMed]
  13. Imran, M.; Hussain, S.; El-Esawi, M.A.; Rana, M.S.; Saleem, M.H.; Riaz, M.; Ashraf, U.; Potcho, M.P.; Duan, M.; Rajput, I.A. Molybdenum Supply Alleviates the Cadmium Toxicity in Fragrant Rice by Modulating Oxidative Stress and Antioxidant Gene Expression. Biomolecules 2020, 10, 1582. [Google Scholar] [CrossRef]
  14. Tariq, F.; Wang, X.; Saleem, M.H.; Khan, Z.I.; Ahmad, K.; Saleem Malik, I.; Munir, M.; Mahpara, S.; Mehmood, N.; Ahmad, T.; et al. Risk Assessment of Heavy Metals in Basmati Rice: Implications for Public Health. Sustainability 2021, 13, 8513. [Google Scholar] [CrossRef]
  15. Yap, D.; Adezrian, J.; Khairiah, J.; Ismail, B.; Ahmad-Mahir, R.J. The uptake of heavy metals by paddy plants (Oryza sativa) in Kota Marudu, Sabah, Malaysia. Am.-Eurasian J. Agric. Environ. Sci. 2009, 6, 16–19. [Google Scholar]
  16. Durkan, N.; Ugulu, I.; Unver, M.; Dogan, Y.; Baslar, S. Electrolytes, Concentrations of trace elements aluminum, boron, cobalt and tin in various wild edible mushroom species from Buyuk Menderes River Basin of Turkey by ICP-OES. Trace Elem. Electrolytes 2011, 28, 242. [Google Scholar] [CrossRef]
  17. Ozturk, A.; Yarci, C.; Ozyigit, I. Assessment of heavy metal pollution in Istanbul using plant (Celtis australis L.) and soil assays. Biotechnol. Biotechnol. Equip. 2017, 31, 948–954. [Google Scholar] [CrossRef] [Green Version]
  18. Rehman, M.; Liu, L.; Bashir, S.; Saleem, M.H.; Chen, C.; Peng, D.; Siddique, K.H. Influence of rice straw biochar on growth, antioxidant capacity and copper uptake in ramie (Boehmeria nivea L.) grown as forage in aged copper-contaminated soil. Plant Physiol. Biochem. 2019, 138, 121–129. [Google Scholar] [CrossRef]
  19. Rehman, M.; Liu, L.; Wang, Q.; Saleem, M.H.; Bashir, S.; Ullah, S.; Peng, D. Copper environmental toxicology, recent advances, and future outlook: A review. Environ. Sci. Pollut. Res. 2019, 26, 18003–18016. [Google Scholar] [CrossRef] [PubMed]
  20. Rana, M.S.; Hu, C.X.; Shaaban, M.; Imran, M.; Afzal, J.; Moussa, M.G.; Elyamine, A.M.; Bhantana, P.; Saleem, M.H.; Syaifudin, M. Soil phosphorus transformation characteristics in response to molybdenum supply in leguminous crops. J. Environ. Manag. 2020, 268, 110610. [Google Scholar] [CrossRef]
  21. Zaheer, I.E.; Ali, S.; Saleem, M.H.; Ali, M.; Riaz, M.; Javed, S.; Sehar, A.; Abbas, Z.; Rizwan, M.; El-Sheikh, M.A.; et al. Interactive role of zinc and iron lysine on Spinacia oleracea L. growth, photosynthesis and antioxidant capacity irrigated with tannery wastewater. Physiol. Mol. Biol. Plants 2020, 26, 2435–2452. [Google Scholar] [CrossRef] [PubMed]
  22. Marshall, F.; Holden, J.; Ghose, C.; Chisala, B.; Kapungwe, E.; Volk, J.; Agrawal, M.; Agrawal, R.; Sharma, R.; Singh, R. Contaminated Irrigation Water and Food Safety for the Urban and Peri-Urban Poor: Appropriate Measures for Monitoring and Control from Field Research in India and Zambia; Department for International Development: London, UK, 2007; p. 8160. [Google Scholar]
  23. Başlar, S.; Kula, I.; Doğan, Y.; Yıldız, D.; Ay, G. A study of trace element contents in plants growing at Honaz Dagi-Denizli, Turkey. Ekoloji 2009, 18, 1–7. [Google Scholar] [CrossRef]
  24. Kabata-Pendias, A.; Pendias, H. Trace Elements in Soils and Plants; CRC Press: Boca Raton, FL, USA; London, UK, 2001. [Google Scholar]
  25. Ugulu, I.; Unver, M.; Dogan, Y. Determination and comparison of heavy metal accumulation level of Ficus carica bark and leaf samples in Artvin, Turkey. Oxid. Commun. 2016, 39, 765–775. [Google Scholar]
  26. Ozyigit, I.I.; Yalcin, B.; Turan, S.; Saracoglu, I.A.; Karadeniz, S.; Yalcin, I.E.; Demir, G. Investigation of heavy metal level and mineral nutrient status in widely used medicinal plants’ leaves in Turkey: Insights into health implications. Biol. Trace Elem. Res. 2018, 182, 387–406. [Google Scholar] [CrossRef]
  27. Saleem, M.H.; Ali, S.; Irshad, S.; Hussaan, M.; Rizwan, M.; Rana, M.S.; Hashem, A.; Abd Allah, E.F.; Ahmad, P. Copper Uptake and Accumulation, Ultra-Structural Alteration, and Bast Fibre Yield and Quality of Fibrous Jute (Corchorus capsularis L.) Plants Grown Under Two Different Soils of China. Plants 2020, 9, 404. [Google Scholar] [CrossRef] [Green Version]
  28. Saleem, M.H.; Kamran, M.; Zhou, Y.; Parveen, A.; Rehman, M.; Ahmar, S.; Malik, Z.; Mustafa, A.; Anjum, R.M.A.; Wang, B. Appraising growth, oxidative stress and copper phytoextraction potential of flax (Linum usitatissimum L.) grown in soil differentially spiked with copper. J. Environ. Manag. 2020, 257, 109994. [Google Scholar] [CrossRef] [PubMed]
  29. Kamran, M.; Danish, M.; Saleem, M.H.; Malik, Z.; Parveen, A.; Abbasi, G.H.; Jamil, M.; Ali, S.; Afzal, S.; Riaz, M. Application of abscisic acid and 6-benzylaminopurine modulated morpho-physiological and antioxidative defense responses of tomato (Solanum lycopersicum L.) by minimizing cobalt uptake. Chemosphere 2020, 263, 128169. [Google Scholar] [CrossRef] [PubMed]
  30. Javed, M.T.; Saleem, M.H.; Aslam, S.; Rehman, M.; Iqbal, N.; Begum, R.; Ali, S.; Alsahli, A.A.; Alyemeni, M.N.; Wijaya, L. Elucidating silicon-mediated distinct morpho-physio-biochemical attributes and organic acid exudation patterns of cadmium stressed Ajwain (Trachyspermum ammi L.). Plant Physiol. Biochem. 2020, 157, 23–37. [Google Scholar] [CrossRef]
  31. Zhuang, P.; McBride, M.B.; Xia, H.; Li, N.; Li, Z. Health risk from heavy metals via consumption of food crops in the vicinity of Dabaoshan mine, South China. Sci. Total Environ. 2009, 407, 1551–1561. [Google Scholar] [CrossRef] [PubMed]
  32. Unver, M.C.; Ugulu, I.; Durkan, N.; Baslar, S.; Dogan, Y. Heavy metal contents of Malva sylvestris sold as edible greens in the local markets of Izmir. Ekoloji 2015, 24, 13–25. [Google Scholar] [CrossRef] [Green Version]
  33. Irshad, S.; Xie, Z.; Kamran, M.; Nawaz, A.; Faheem, M.; Mehmood, S.; Gulzar, H.; Saleem, M.H.; Rizwan, M.; Malik, Z.; et al. Biochar composite with microbes enhanced arsenic biosorption and phytoextraction by Typha latifolia in hybrid vertical subsurface flow constructed wetland. Environ. Pollut. 2021, 291, 118269. [Google Scholar] [CrossRef] [PubMed]
  34. Deng, G.; Yang, M.; Saleem, M.H.; Rehman, M.; Fahad, S.; Yang, Y.; Elshikh, M.S.; Alkahtani, J.; Ali, S.; Khan, S.M. Nitrogen fertilizer ameliorate the remedial capacity of industrial hemp (Cannabis sativa L.) grown in lead contaminated soil. J. Plant Nutr. 2021, 44, 1–9. [Google Scholar] [CrossRef]
  35. Rizwan, M.; Ali, S.; Adrees, M.; Rizvi, H.; Zia-ur-Rehman, M.; Hannan, F.; Qayyum, M.F.; Hafeez, F.; Ok, Y.S. Cadmium stress in rice: Toxic effects, tolerance mechanisms, and management: A critical review. Environ. Sci. Pollut. Res. 2016, 23, 17859–17879. [Google Scholar] [CrossRef]
  36. Hussain, A.; Ali, S.; Rizwan, M.; ur Rehman, M.Z.; 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]
  37. Sanchez, P.A.; Logan, T.J. Myths and science about the chemistry and fertility of soils in the tropics. In Myths and Science of Soils of the Tropics; Lal, R., Sanchez, P.A., Eds.; Soil Science Society of America: Madison, WI, USA, 1992; Volume 29, pp. 35–46. [Google Scholar]
  38. Vukadinovic, V.; Bertic, B. Agrochemistry and Plant Nutrition; Faculty of Agriculture: Osijek, Croatia, 1988; p. 56. [Google Scholar]
  39. Cui, Y.-J.; Zhu, Y.-G.; Zhai, R.-H.; Chen, D.-Y.; Huang, Y.-Z.; Qiu, Y.; Liang, J.-Z. Transfer of metals from soil to vegetables in an area near a smelter in Nanning, China. Environ. Int. 2004, 30, 785–791. [Google Scholar] [CrossRef]
  40. Liu, W.-X.; Liu, J.-W.; Wu, M.-Z.; Li, Y.; Zhao, Y.; Li, S.-R. Accumulation and translocation of toxic heavy metals in winter wheat (Triticum aestivum L.) growing in agricultural soil of Zhengzhou, China. Bull. Environ. Contam. Toxicol. 2009, 82, 343–347. [Google Scholar] [CrossRef] [Green Version]
  41. Liu, W.-H.; Zhao, J.-Z.; Ouyang, Z.-Y.; Söderlund, L.; Liu, G.-H. Impacts of sewage irrigation on heavy metal distribution and contamination in Beijing, China. Environ. Int. 2005, 31, 805–812. [Google Scholar] [CrossRef]
  42. Tinker, P. Levels, distribution and chemical forms of trace elements in food plants. Philos. Trans. R. Soc. Lond. B Biol. Sci. 1981, 294, 41–55. [Google Scholar]
  43. Chary, N.S.; Kamala, C.; Raj, D.S.S. Assessing risk of heavy metals from consuming food grown on sewage irrigated soils and food chain transfer. Ecotoxicol. Environ. Saf. 2008, 69, 513–524. [Google Scholar] [CrossRef] [PubMed]
  44. Ge, K.J. The Status of Nutrient and Meal of Chinese in the 1990s; Beijing People’s Hygiene Press: Beijing, China, 1992; pp. 415–434. [Google Scholar]
  45. Wang, X.; Sato, T.; Xing, B.; Tao, S. Health risks of heavy metals to the general public in Tianjin, China via consumption of vegetables and fish. Sci. Total Environ. 2005, 350, 28–37. [Google Scholar] [CrossRef] [PubMed]
  46. Environmental Protection Agency (EPA). National Primary Drinking Water Regulations: Long Term 1 Enhanced Surface Water Treatment Rule. Final rule. Fed. Regist. 2002, 67, 1811–1844. [Google Scholar]
  47. Steel, R.G.; Torrie, J.H. Principles and Procedures of Statistics; McGraw-Hill Book Co.: New York, NY, USA, 1980; p. 481. [Google Scholar]
  48. Ekmekyapar, F.; Sabudak, T.; Seren, G.J. Assessment of heavy metal contamination in soil and wheat (Triticum aestivum L.) plant around the Çorlu–Çerkezkoy highway in Thrace region. Glob. Nest J. 2012, 14, 496–504. [Google Scholar]
  49. Awashthi, S.K. Central and State Rules as Amended for 1999: Prevention of Food Adulteration Act No 37 of 1954; Ashoka House Law: New Delhi, India, 2000. [Google Scholar]
  50. European Union. Commission Regulation (EC) No 1881/2006 of 19 December 2006 Setting Maximum Levels for Certain Contaminants in Foodstuffs; European Union: Brussels, Belgium, 2006; Volume 364, pp. 324–365. [Google Scholar]
  51. Environmental Protection Agency (EPA). Exposure Factors Handbook, Volume I-General Factors; EPA/600/P-95/002Fa: 1997; EPA: Washington, DC, USA, 1997. [Google Scholar]
  52. Yadav, A.; Yadav, P.K.; Srivastava, S.; Singh, P.K.; Srivastava, V.; Shukla, D.N. Profitability and health risk estimation of rice cultivation under wastewater irrigation from natural drainage. Int. J. Sci. Res. Publ. 2014, 4, 2250–3153. [Google Scholar]
  53. Juen, L.L.; Aris, A.Z.; Ying, L.W.; Haris, H. Bioconcentration and translocation efficiency of metals in paddy (Oryza sativa): A case study from Alor Setar, Kedah, Malaysia. Sains Malays. 2014, 43, 521–528. [Google Scholar]
  54. Singh, A.; Sharma, R.K.; Agrawal, M.; Marshall, F.M. Health risk assessment of heavy metals via dietary intake of foodstuffs from the wastewater irrigated site of a dry tropical area of India. Food Chem. Toxicol. 2010, 48, 611–619. [Google Scholar] [CrossRef]
  55. Lorestani, B.; Cheraghi, M.; Yousefi, N. Accumulation of Pb, Fe, Mn, Cu and Zn in plants and choice of hyperaccumulator plant in the industrial town of Vian, Iran. Arch. Biol. Sci. 2011, 63, 739–745. [Google Scholar] [CrossRef]
  56. Ogunkunle, C.O.; Varun, M.; Jimoh, M.A.; Olorunmaiye, K.S.; Fatoba, P.O. Evaluating the trace metal pollution of an urban paddy soil and bioaccumulation in rice (Oryza sativa L.) with the associated dietary risks to local population: A case study of Ilorin, north-central Nigeria. Environ. Earth Sci. 2016, 75, 1383. [Google Scholar] [CrossRef]
  57. FAO; WHO. Food Additives and Contaminants. Joint FAO/WHO Food Standards Programme; FAO: Rome, Italy; WHO: Rome, Italy, 2001; Volume 1, pp. 1–289. [Google Scholar]
  58. Shaar, G.Q.; Kazi, T.G.; Jatoi, W.B.; Makhija, P.M.; Sahito, S.B. Determination of heavy metals in eight barley cultivars collected from wheat research station Tandojam, Sindh, Pakistan. Appl. Life Sci. 2013, 14, 47–53. [Google Scholar]
  59. Jaishree, A.; Khan, T. Assessment of heavy metals risk on human health via dietary intake of cereals and vegetables from effluent irrigated land Jaipur district, Rajasthan. Int. J. Innov. Res. Sci. Eng. Technol. 2015, 4, 5142–5148. [Google Scholar]
  60. Satpathy, D.; Reddy, M.V.; Dhal, S.P. Risk assessment of heavy metals contamination in paddy soil, plants, and grains (Oryza sativa L.) at the East Coast of India. BioMed Res. Int. 2014, 2014, 545473. [Google Scholar] [CrossRef] [Green Version]
  61. Woldetsadik, D.; Drechsel, P.; Keraita, B.; Itanna, F.; Gebrekidan, H. Heavy metal accumulation and health risk assessment in wastewater-irrigated urban vegetable farming sites of Addis Ababa, Ethiopia. Int. J. Food Contam. 2017, 4, 1–13. [Google Scholar] [CrossRef]
  62. Badawy, R.; El-Gawad, A.; Osman, H. Health risks assessment of heavy metals and microbial contamination in water, soil and agricultural foodstuff from wastewater irrigation at Sahl El-Hessania area, Egypt. J. Appl. Sci. Res. 2013, 9, 3091–3107. [Google Scholar]
  63. Singh, J.; Upadhyay, S.K.; Pathak, R.K.; Gupta, V. Accumulation of heavy metals in soil and paddy crop (Oryza sativa), irrigated with water of Ramgarh Lake, Gorakhpur, UP, India. Toxicol. Environ. Chem. 2011, 93, 462–473. [Google Scholar] [CrossRef]
  64. Kumar, V.; Chopra, A.K. Heavy metals accumulation in soil and agricultural crops grown in the Province of Asahi India Glass Ltd. Haridwar (Uttarakhand), India. Adv. Crop Sci. Technol. 2015, 4, 1–6. [Google Scholar] [CrossRef]
  65. Emurotu, J.; Onianwa, P. Bioaccumulation of heavy metals in soil and selected food crops cultivated in Kogi State, north central Nigeria. Environ. Syst. Res. 2017, 6, 21. [Google Scholar] [CrossRef] [Green Version]
  66. Rezvani, M.; Zaefarian, F. Bioaccumulation and translocation factors of cadmium and lead in’Aeluropus littoralis’. Aust. J. Agric. Eng. 2011, 2, 114–119. [Google Scholar]
  67. Angulo, E. The Tomlinson Pollution Load Index applied to heavy metal,‘Mussel-Watch’data: A useful index to assess coastal pollution. Sci. Total Environ. 1996, 187, 19–56. [Google Scholar] [CrossRef]
  68. Dosumu, O.; Abdus-Salam, N.; Oguntoye, S.; Afdekale, F. Trace metals bioaccumulation by some Nigerian vegetables. Centrepoint 2005, 13, 23–32. [Google Scholar]
  69. Ahmad, K.; Khan, Z.I.; Ashfaq, A.; Ashraf, M.; Yasmin, S. Assessment of heavy metal and metalloid levels in spinach (Spinacia oleracea L.) grown in wastewater irrigated agricultural soil of Sargodha, Pakistan. Pak. J. Bot. 2014, 46, 1805–1810. [Google Scholar]
  70. Khan, Z.I.; Ahmad, K.; Ashraf, M.; Parveen, R.; Mustafa, I.; Khan, A.; Bibi, Z.; Akram, N.A. Bioaccumulation of heavy metals and metalloids in luffa (Luffa cylindrica L.) irrigated with domestic wastewater in Jhang, Pakistan: A prospect for human nutrition. Pak. J. Bot. 2015, 47, 217–224. [Google Scholar]
  71. Liu, J.; Zhang, X.-H.; Tran, H.; Wang, D.-Q.; Zhu, Y.-N. Heavy metal contamination and risk assessment in water, paddy soil, and rice around an electroplating plant. Environ. Sci. Pollut. Res. Int. 2011, 18, 1623–1632. [Google Scholar] [CrossRef] [PubMed]
  72. Sun, H.-F.; Li, Y.-H.; Ji, Y.-F.; Yang, L.-S.; Wang, W.-Y.; Li, H.-R. Environmental contamination and health hazard of lead and cadmium around Chatian mercury mining deposit in western Hunan Province, China.Trans. Nonferrous Met. Soc. China 2010, 20, 308–314. [Google Scholar] [CrossRef]
  73. Balkhair, K.S.; Ashraf, M. Field accumulation risks of heavy metals in soil and vegetable crop irrigated with sewage water in western region of Saudi Arabia. Saudi J. Biol. Sci. 2016, 23, S32–S44. [Google Scholar] [CrossRef] [Green Version]
  74. Verma, S.; Yadav, S.; Yadav, S.K.; Kadyan, P.S.; Singh, I.; Singh, D. Heavy metals in wheat grains of Haryana (India) and their health implications. J. Pharm. Res. 2015, 7, 342–351. [Google Scholar]
  75. Fan, Y.; Zhu, T.; Li, M.; He, J.; Huang, R. Heavy metal contamination in soil and brown rice and human health risk assessment near three mining areas in central China. J. Health Eng. 2017, 2017, 4124302. [Google Scholar] [CrossRef]
  76. Environmental Protection Agency (EPA). Toxicological Review of Acrylamide (CAS No. 79–06–1) in Support of Summary Information on the Integrated Risk Information System (IRIS); EPA/635/R-07: 2010; EPA: Washington, DC, USA, 2010. [Google Scholar]
Figure 1. Analysis of variance for heavy metals in paddy soil, root, shoot and grains of Kainat. **, ***: Significant at 0.01, and 0.001 levels; ns, non-significant.
Figure 1. Analysis of variance for heavy metals in paddy soil, root, shoot and grains of Kainat. **, ***: Significant at 0.01, and 0.001 levels; ns, non-significant.
Sustainability 13 13739 g001
Table 1. Mean concentration (mg/kg) of heavy metals in soil and grains of Kainat.
Table 1. Mean concentration (mg/kg) of heavy metals in soil and grains of Kainat.
SiteMetal
CdZnCuCoFeMnNi
Soil
Site-I11.743 ± 0.005 c14.481 ± 0.004 c10.429 ± 0.006 c11.631 ± 0.004 a24.126 ± 0.005 a22.478 ± 0.006 a13.615 ± 0.005 b
Site-II12.728 ± 0.005 b12.465 ± 0.005 d9.416 ± 0.004 d9.615 ± 0.005 b20.11 ± 0.005 b20.464 ± 0.004 c12.601 ± 0.005 c
Site-III13.714 ± 0.004 a15.452 ± 0.004 b11.402 ± 0.006 b4.6 ± 0.007 c15.09 ± 0.005 d21.448 ± 0.005 b9.585 ± 0.005 e
Site-IV10.702 ± 0.004 d14.438 ± 0.005 c8.385 ± 0.005 e8.583 ± 0.005 b18.077 ± 0.004 c19.433 ± 0.006 d11.573 ± 0.005 d
Site-V9.688 ± 0.005 e18.423 ± 0.005 a12.373 ± 0.005 a12.568 ± 0.005 a19.063 ± 0.005 b18.418 ± 0.005 e14.558 ± 0.005 a
Maximum permissible limit3 a300 a100 a50 a21,000 b2000 a50 a
Root
Site-I9.538 ± 0.288 c10.343 ± 0.420 cd9.65 ± 0.288 b9.09 ± 0.288 a19.342 ± 0.220 a15.596 ± 0.288 a11.698 ± 0.288 b
Site-II10.343 ± 0.388 b9.642 ± 0.520 d8.517 ± 0.220 c7.078 ± 0.288 b10.233 ± 0.220 d16.581 ± 0.363 a9.685 ± 0.480 c
Site-III11.328 ± 0.788 a13.63 ± 0.644 b9.375 ± 0.288 b3.064 ± 0.220 d13.1 ± 0.288 c11.568 ± 0.420 b7.663 ± 0.363 d
Site-IV9.313 ± 0.688 c9.618 ± 0.488 d7.267 ± 0.220 d6.048 ± 0.363 c12.983 ± 0.220 c9.552 ± 0.288 c8.645 ± 0.433 cd
Site-V7.298 ± 0.488 d16.602 ± 0.463 a11.15 ± 0.144 a8.033 ± 0.388 ab15.85 ± 0.288 b12.538 ± 0.320 b12.63 ± 0.344 a
Maximum permissible limit0.1–0.2 c100 c20 c0.01 c425.5 d500 d103 e
Shoot
Site-I7.223 ± 0.541 c10.286 ± 0.720 b8.74 ± 0.288 a7.235 ± 0.288 a18.326 ± 0.220 a15.595 ± 0.288 a10.202 ± 0.288 a
Site-II5.542 ± 0.488 d8.276 ± 0.520 c7.726 ± 0.220 b6.222 ± 0.288 b9.312 ± 0.288 cd16.580 ± 0.363 a8.175 ± 0.388 ab
Site-III10.53 ± 0.344 a10.262 ± 0.488 b8.714 ± 0.220 a2.207 ± 0.288 d11.297 ± 0.288 d11.567 ± 0.420 bc5.170 ± 0.363 cd
Site-IV8.515 ± 0.463 b8.975 ± 0.724 c6.700 ± 0.300 bc5.192 ± 0.288 c10.282 ± 0.288 c9.551 ± 0.288 c4.155 ± 0.220 d
Site-V4.498 ± 0.563 d12.232 ± 0.586 a5.865 ± 0.220 c6.18 ± 0.244 b13.267 ± 0.288 b12.537 ± 0.320 b7.142 ± 0.288 b
Maximum permissible limit0.1–0.2 c100 c20 c0.01 c425.5 d500 d103 e
Grains
Site-I5.552 ± 0.004 b9.855 ± 0.009 b6.881 ± 0.004 b6.521 ± 0.006 a14.735 ± 0.005 a13.933 ± 0.005 a8.343 ± 0.004 a
Site-II3.538 ± 0.005 c7.835 ± 0.006 c5.865 ± 0.005 c5.504 ± 0.006 b8.714 ± 0.004 bc12.916 ± 0.004 b6.331 ± 0.004 b
Site-III2.523 ± 0.005 d9.818 ± 0.005 b7.852 ± 0.004 a1.488 ± 0.005 e9.702 ± 0.004 b8.902 ± 0.006 d3.318 ± 0.005 d
Site-IV6.503 ± 0.006 a5.803 ± 0.005 d5.838 ± 0.005 c3.473 ± 0.005 d8.688 ± 0.005 c9.888 ± 0.005 c2.303 ± 0.005 e
Site-V2.491 ± 0.004 d10.788 ± 0.005 a4.823 ± 0.005 d4.46 ± 0.005 c9.673 ± 0.005 b6.873 ± 0.005 e5.288 ± 0.005 c
Maximum permissible limit0.1–0.2 c100 c20 c0.01 c425.5 d500 d103 e
Sources: a European Union (2006), b USEPA (1997), c FAO/WHO (2011), d FAO/WHO (2001), e SEPA (2005). Different lowercase letter(s) within a column for each parameter are significantly different from each other according to Duncan’s multiple range test (p < 0.05).
Table 2. Metals correlation between (soil-root, root-shoot and shoot-grain) of Kainat.
Table 2. Metals correlation between (soil-root, root-shoot and shoot-grain) of Kainat.
MetalSoil-RootRoot-ShootShoot-Grain
Cd1.00 **0.993 **0.954 *
Zn0.898 *0.997 **0.896 *
Cu0.972 **0.984 **0.965 **
Co0.946 **0.964 **0.922 **
Fe0.9800.907 *0.899 *
Mn0.880 *0.956 *0.863
Ni0.5210.4160.894 *
*, **: Correlation was significant at the 0.05 and 0.01 levels.
Table 3. Bioaccumulation and translocation factors for Kainat.
Table 3. Bioaccumulation and translocation factors for Kainat.
SiteMetal
CdZnCuCoFeMnNi
Bioaccumulation factor
Site-I0.47280.68061.51570.56070.61080.61080.6198
Site-II0.27790.62861.60540.57250.43330.63110.5024
Site-III0.18390.63541.45210.32340.64290.41500.3461
Site-IV0.60770.40191.43640.40460.48060.50880.1989
Site-V0.25710.58562.56560.35490.50740.37320.3632
Translocation factor
Site-I0.77190.81280.90570.79590.94750.91300.8722
Site-II0.53590.85840.90720.87920.91000.91790.8454
Site-III0.92960.75290.94950.72040.86240.96020.6747
Site-IV0.91450.93320.92210.85850.79190.86580.4807
Site-V0.61640.73680.50990.76940.83710.89460.5655
Table 4. Pollution load index and enrichment factor for metals of Kainat.
Table 4. Pollution load index and enrichment factor for metals of Kainat.
SiteMetal
CdZnCuCoFeMnNi
Pollution load index
Site-I7.88090.32770.82010.48450.42400.48081.50278
Site-II8.54190.28210.69900.60470.35340.43771.3908
Site-III9.20410.34970.93580.97670.26520.45881.0579
Site-IV7.18230.32670.69580.59300.31770.41571.2773
Site-V6.50170.41690.57480.26740.33500.39401.6068
Reference value1.49 a 44.19 a 8.39 a 9.1 b56.9 c46.75 d9. 06 a
Enrichment factor
Site-I3.52220.30070.63582.41080.09710.05710.5999
Site-II2.07070.27780.67352.91620.07720.06370.5984
Site-III1.37030.28080.60925.14520.07180.05630.2597
Site-IV4.52730.17760.60260.74530.06090.04280.1433
Site-V1.91550.25881.07631.18810.09710.05020.5999
Sources: a Sing et al. (2010a), b Dutch Standards (2000), c Dosumu et al. (2005), d Singh et al. (2010b).
Table 5. Daily intake of metal and health risk index of Kainat.
Table 5. Daily intake of metal and health risk index of Kainat.
SiteMetal
CdZnCuCoFeMnNi
Daily intake of metal
Site-I0.03190.05670.05100.03750.08470.08010.0479
Site-II0.02030.04510.05410.03160.05010.07430.0364
Site-III0.01450.05650.06560.00860.05580.05120.0191
Site-IV0.03740.03340.04820.01100.04910.05690.0132
Site-V0.01430.06200.07110.02560.05560.03950.0304
Health risk index
Site-I0.02140.00130.00710.87190.00150.00170.0053
Site-II0.01370.00100.00640.73600.00090.00160.0040
Site-III0.00970.00120.00780.19890.000980.00110.0021
Site-IV0.02510.00080.00570.46430.000880.00120.0015
Site-V0.00960.00140.00850.59640.000970.000840.0034
RfD * (mg/kg/day)1 × 10−3 3 × 10−14 × 10−243 × 10−21 × 10−114 × 10−12 × 10−2
Source: * USEPA (2002).
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Khan, Z.I.; Mansha, A.; Saleem, M.H.; Tariq, F.; Ahmad, K.; Ahmad, T.; Farooq Awan, M.U.; Abualreesh, M.H.; Alatawi, A.; Ali, S. Trace Metal Accumulation in Rice Variety Kainat Irrigated with Canal Water. Sustainability 2021, 13, 13739. https://doi.org/10.3390/su132413739

AMA Style

Khan ZI, Mansha A, Saleem MH, Tariq F, Ahmad K, Ahmad T, Farooq Awan MU, Abualreesh MH, Alatawi A, Ali S. Trace Metal Accumulation in Rice Variety Kainat Irrigated with Canal Water. Sustainability. 2021; 13(24):13739. https://doi.org/10.3390/su132413739

Chicago/Turabian Style

Khan, Zafar Iqbal, Asim Mansha, Muhammad Hamzah Saleem, Farah Tariq, Kafeel Ahmad, Tasneem Ahmad, Muhammad Umer Farooq Awan, Muyassar H. Abualreesh, Aishah Alatawi, and Shafaqat Ali. 2021. "Trace Metal Accumulation in Rice Variety Kainat Irrigated with Canal Water" Sustainability 13, no. 24: 13739. https://doi.org/10.3390/su132413739

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