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. 2023 Sep 28;13:16314. doi: 10.1038/s41598-023-43349-7

Assessment of environmental and carcinogenic health hazards from heavy metal contamination in sediments of wetlands

Bibhu Prasad Panda 1,2, Yugal Kishore Mohanta 3,4, Rakesh Paul 5, B Anjan Kumar Prusty 6, Siba Prasad Parida 7, Abanti Pradhan 2, Muthupandian Saravanan 8, Kaustuvmani Patowary 3, Guangming Jiang 9, Sanket J Joshi 10, Hemen Sarma 11,
PMCID: PMC10539448  PMID: 37770520

Abstract

Sediment contamination jeopardizes wetlands by harming aquatic organisms, disrupting food webs, and reducing biodiversity. Carcinogenic substances like heavy metals bioaccumulate in sediments and expose consumers to a greater risk of cancer. This study reports Pb, Cr, Cu, and Zn levels in sediments from eight wetlands in India. The Pb (51.25 ± 4.46 µg/g) and Cr (266 ± 6.95 µg/g) concentrations were highest in Hirakud, Cu (34.27 ± 2.2 µg/g) in Bhadrak, and Zn (55.45 ± 2.93 µg/g) in Koraput. The mean Pb, Cr, and Cu values in sediments exceeded the toxicity reference value. The contamination factor for Cr was the highest of the four metals studied at Hirakud (CF = 7.60) and Talcher (CF = 6.97). Furthermore, high and moderate positive correlations were observed between Cu and Zn (r = 0.77) and Pb and Cr (r = 0.36), respectively, across all sites. Cancer patients were found to be more concentrated in areas with higher concentrations of Pb and Cr, which are more carcinogenic. The link between heavy metals in wetland sediments and human cancer could be used to make policies that limit people's exposure to heavy metals and protect their health.

Subject terms: Cancer, Ecology, Biogeochemistry, Environmental sciences, Natural hazards, Risk factors

Introduction

Wetlands have had a long and crucial connection to human civilization since ancient times, rendering multiple benefits and services to humans1. The wetland ecosystem supports the hydrological cycle, regulates climate change, and provides many ecosystem services to biodiversity2. In addition, it adds direct and indirect value to human beings by supporting various economic services3. Considering the land area as a unit, the wetland ecosystem can be described as a top ecosystem service that provides 47% of the global ecosystem value4. This fact makes this ecosystem vital and fruitful among all ecosystems2. This ecosystem is also a heavy metal sink due to its importance and role in several physical, chemical, and biological events. In the modern world, anthropogenic activity serves the most to deposit heavy metals in this sink57. The typical heavy metal pollutants produced through urbanization, industrialization, and agricultural practices are lead (Pb), chromium (Cr), cadmium (Cd), copper (Cu), mercury (Hg), nickel (Ni), zinc (Zn), manganese (Mn), and arsenic (As)8.

Heavy metals could be present in soils in various concentrations, indicating either natural lithogenic sources or anthropogenic processes9. Heavy metal concentrations that are too high10 and other necessary and non-essential components in aquatic habitats11 can indicate the inputs from the catchment and surrounding area, and different indices can be employed to measure the contamination level12. Cd, Cr, and Pb are all hazardous to all creatures. Metals like Cu, Zn, and Mn are thought necessary for their function in biochemical functioning in organisms, but they are also known to be harmful beyond the threshold limit1315. The higher tendencies for bioaccumulation make them biologically harmful16,17. These metals are continuously deposited in water and sediment in any given habitat, eventually leading to accumulation in different organisms inhabiting the particular habitat18,19; determining metal concentrations in the habitat is essential10 in evaluating the contamination profiles.

Heavy metal concentrations in bottom sediment have been used to indicate environmental pollution in different ecosystems, viz., rivers20,21, streams22, wetlands2326, forests27, grasslands28, and marine ecosystems29. The heavy metal load in bottom sediments in wetlands can indicate both natural sources and human-caused activities, as industrial waste channelled through streams, rivers, and agricultural runoff23,3032. Because of their tenacity and increased intensity in agriculture7,33,34, heavy metals accumulate in wetland soil over the years, posing threats to the environment and human well-being as they flow through the trophic levels35,36.

The flow of heavy metals from soil to livestock and humans can occur either by directly consuming tainted crops or bioaccumulation through the food chain37,38. Such processes are driven by several factors known to have distinct spatiotemporal variability. Thus, the existing understanding of metal distribution, sources, and contamination risk in wetlands must be supplemented with additional findings from different types of wetlands spread across varied landscapes. The environmental quality of wetlands can be judged using sedimentary heavy metal content as an indicator3941. Analyzing and assessing heavy metal concentrations has become essential to monitoring wetland pollution42,43. Knowledge of the intensity of contamination can be gained by assessing different sediment qualities4446. Only a few studies have investigated the content of heavy metals in the soil in this study area4750. In India, few studies can indicate wetland health from metal contamination and the accompanying human health risk.

Because of these specifics, the current investigation was conducted to: (i) examine the accumulation of Pb, Cr, Cu, and Zn in the soil of wetlands with distinct spatial distribution in Odisha, India; (ii) make an ecological risk assessment of wetlands inside agricultural landscapes; and (iii) evaluate the human health risk potential of Pb and Cr. The expected outcome of this study is to show heavy metal pollution's influence on wetland health and the risk to human health.

Methods

Study area and sampling site

The present study covered eight different wetlands in the Indian state of Odisha, located in distinct landscapes and with distinct sources of contamination (Fig. 1). Of the eight wetlands, Chandaneswar, Chilika, Daringbadi, and Koraput are natural wetlands, and Bhadrak, Hirakud, Talcher, and Titlagarh are constructed wetlands. The details of the location characteristics of the wetlands are presented in Table 1.

Figure 1.

Figure 1

Map of the study region with sampling sites crated using ArcMap 10.2.1.

Table 1.

Details of location characteristics of sampling points of the study area.

Wetland Type Location Land use pattern Sources of pollutants
Bhadrak Constructed Bhadrak Agricultural wetland with seasonal agriculture Insecticide, pesticide from agricultural runoff
Chandaneswar Natural Balasore Agricultural land covered by year-wide crops Agricultural runoff, anthropogenic activity
Chilika Natural Khurda The anthropogenic activity primarily by cattle Agricultural runoff, village runoff, anthropogenic activity
Daringbadi Natural Kandhamal Undisturbed natural water body Natural sources
Hirakud Constructed Bargarh Agricultural activity covering the whole year Natural sources, agricultural runoff
Koraput Natural Koraput Connected to a reservoir in monsoon and separated in other seasons, anthropogenic activity Natural sources, cattle grazing
Talcher Constructed Angul Urban area, anthropogenic activity Urban pollution, industrial pollution, coal mining
Titlagarh Constructed Bolangir Semi-urban area, anthropogenic activity Urban pollution, anthropogenic activity

Sediment sampling

Bed sediment samples (in triplicate) were collected every other month between October 2015 and August 2018 using the grab sampling technique26. In total, 144 samples were collected from the eight identified wetlands. Bed sediment samples, collected from 5 to 10 cm depth, air-dried in the laboratory after being transported in resealable polythene bags, followed by oven-drying at 50–60 °C until constant weight, and homogenized using a mortar and pestle51. Finally, the homogenized samples were sieved using a 2 mm mesh sieve before being placed in clean plastic containers52.

Sample digestion

One gram of powdered sediment sample was transferred to a Teflon digester tube in a microwave digestion system (Milestone, MLS 1200), which was programmed to have the sequential addition of a series of acids, i.e. 10 ml HNO3 for 10 min, 1 ml HClO4 for 5 min, and 5 ml H2O2 for 10 min, at 250W magnetron power settings29. A digestion blank without a sample was also included. By adding deionized water, the digested samples were filtered, made up to 50 ml, and stored in pre-cleaned and acid-treated plastic vials at 4°C53.

Sample analysis

The concentration of heavy metals in the digested samples was detected utilizing a double-beam atomic absorption spectrophotometer (Shimadzu, AA 6300) under standard analytical conditions. The detection limits (DL) for Pb, Cr, Cu, and Zn were 0.03 µg/g, 0.02 µg/g, 0.002 µg/g, and 0.02 µg/g, respectively. The standard addition technique was used to reduce the matrix effects in the analyses. As part of the QA/QC process, pre-analyzed soil samples were used as reference material subjected to the same analytical methods for estimating the detection limits of the metals54.

Contamination indices of pollution

Both the Contamination Factor (CF) and Geo-accumulation Index (Igeo) are widely used to assess the contamination level in wetlands, and they provide essential information for comprehending the effects of pollution on these ecosystems. The CF is a measure used to assess the level of contamination in a specific environment, such as wetlands55. It is calculated by comparing the concentration of an element in the sediment to its background value in the environment.

CF=CS/CB. 1

CS = element concentration (µg/g) in the analyzed sediment, and CB = element (µg/g) in the reference background. The background values of the elements used are Pb (20), Cr (35), Cu (25), and Zn (71)8.

The Geo-accumulation index (Igeo) is another used to assess wetland contamination. It measures the accumulation of a specific element in the sediment relative to its background concentration in the environment. The formula can be used to compute it as proposed below56.

Igeo=log2CS/1.5CB. 2

The descriptions for CS and CB have been provided earlier. The Igeo comprises 7 grades in the 5 < Igeo ≤ 0 57–59 range. The grades are Igeo ≤ 0 (soil is not contaminated); 0 < Igeo ≤ 1 (uncontaminated up to moderately contaminated); 1 < Igeo ≤ 2 (moderately contaminated); 2 < Igeo ≤ 3 (moderately up to strongly contaminated); 3 < Igeo ≤ 4 (strongly contaminated); 4 < Igeo ≤ 5 (strongly up to extremely contaminated); and lastly Igeo > 5 (extremely contaminated)57.

Ecological risk assessment

Two indices, the potential ecological risk factor (PERF) and the potential ecological risk index (PERI or RI), were used to conduct the ecological risk assessment. The PERF can describe the contamination due to one element (heavy metal). It can be calculated using the formula.

PERF=CF×TRF. 3

CF represents the contamination factor for each element/heavy metal, and TRF represents the toxicological response factor. The TRF for the detected elements/heavy metals is Pb:5, Cr:2, Cu:5, and Zn:18,45,58. This formula resonates with the hazards to humans and the ecosystem and the ecological vulnerability to heavy metal contamination59. Further, the PERI or RI describes the total potential risk presented by all the components found in the sediment55, which was empirically estimated by summing up all the PREF values obtained for each element using the following equation proposed by58:

RI=PERF. 4

RI represents the potential ecological risk index of all detected elements, and PERF represents the individual elements’ potential ecological risk index.

Human health risk assessment

The relationship between the ecosystem, human health, and contaminants in the environment can be assessed by assessing the human health risk using the guidelines of USEPA60. The present study assesses carcinogenic and non-carcinogenic risks via ingestion pathways. Health risk levels may be site-specific due to exposure to an element (heavy metals). The average daily dose (ADD) can be calculated to identify non-carcinogenic threats. The ADD by ingestion was calculated as follows:

ADD=Cs×IR×EF×ED/BW/AT, 5

where CS is the concentration of heavy metal (µg/g) in analyzed sediment; IR is the ingestion rate of contaminated sediment (0.001 kg/day for children and 0.0035 kg/day for an adult); EF is the exposure frequency (300 days/year, assumed); ED is the exposure duration (6 years for children and 30 years for an adult); BW is the body weight (15 kg for children and 70 kg for an adult), and AT is the average time (2190 days for children and 10,950 days for an adult61.

Using the hazard quotient (HQ), the non-carcinogenic harmful effects of heavy metals were measured62. The HQ value was estimated as follows:

HQ=ADD/RfD. 6

The average daily dose is ADD; RfD is the equivalent reference dose. The RfD values for the detected metals/elements are Pb:0.0035 µg/g; Cr:1.5 µg/g; Cu:0.04 µg/g and Zn:0.3 µg/g8. The hazard index (HI) can determine the full carcinogenic effect, which can be calculated by adding all ‘metals’ HQ to this formula34.

HI=HQ1+HQ2+HQ3++HQn, 7

In addition to the non-carcinogenic effects, humans exposed to contaminated sediment can face carcinogenic risk (CR) their whole lives. The CR can be measured by this formula58:

CR=ADD×SF. 8

ADD is the average daily dose, and SF is the slope factor of the respected element/heavy metal. The SF used in this study for Pb is 0.042, and for Cr is 0.5, according to the US Environmental Protection Agency. However, the other two metals are not listed due to their less carcinogenic effects8.

Spatial distribution of data

In a given geographical framework, interpolating spatial parameters utilizing tools like the Geographic Information System (GIS) integrating field inventory has provided agility in scientific representation63. IDW interpolation method was used in ArcMap 10.2.1's Spatial Analyst Tools to depict the contamination's spatial distribution. No minimum number of points was set, and the output cell size was taken as 0.01 to get a smooth prediction of the values in the unsampled/unmeasured areas and give a detailed account of how each parameter is distributed spatially compared to the others. The neighborhood was taken as 12, the optimal number for eight sampling locations. However, the maximum distance for the search radius was kept as the default because all the parameters are static, and there are no directional influences.

Statistical analysis

The datasets were subjected to an appropriate suite of statistical tests. Descriptive statistics determined the range, median, and average values. First, a two-way Pearson correlation test was conducted to determine the connection between the various metals in the soil. The significant difference in heavy metals and wetlands concerning sediment was tested using a one-way analysis of Variance (ANOVA). Second, hierarchical cluster analysis was conducted to identify the system of organized variables where the same clusters share common data properties. The significance level for the statistical tests was α = 0.05 for all analyses.

Results and discussion

Heavy metal concentration in sediment

The concentrations of Pb, Cr, Cu, and Zn recorded in bed sediments are presented in Table 2. The Pb concentration was the highest at the Hirakud sampling site (51.25 ± 4.46 µg/g), and all sampling sites recorded higher concentrations of Pb than previous studies47,49. The concentration of Pb was found to be significantly different among sites (F = 177.4, P < 0.001). The Cr was the highest at the Hirakud sampling site (266 ± 6.95 µg/g), much higher than previous studies from Odisha4850. The concentration of Cr was found to be significantly different among sites (F = 1911, P < 0.001). The highest Cu concentration was recorded at the Bhadrak site (34.27 ± 2.2 µg/g), and all other sampling sites, except Chandaneswar, also recorded higher concentrations of Cu than previous studies4749. The concentration of Cu was found to be significantly different among sites (F = 226.4, P < 0.001). The mean concentration of Zn was discovered to be the most abundant at Koraput (55.45 ± 2.93 µg/g), which is unlikely to be lower than previous studies in Odisha4749. The concentration of Zn was determined to be distinguishable in a significant manner (F = 245.1, P < 0.001) among all sites (Fig. 2). Comparisons have been made between the concentrations of heavy metals measured at each sampling location and the international standards and threshold levels specified by different agencies (Table 2). A list of metal and sampling locations in decreasing order is presented in Table 3. All the sites recorded higher Cr concentrations than other detected metals. The natural wetlands had Cr, Zn, and Pb in decreasing order, while the constructed wetlands had higher Cr followed by Pb and Zn, respectively (Table 3).

Table 2.

Descriptive statistics of recorded heavy metal concentrations in different locations (N = 144).

Sampling sites Pb Cr Cu Zn
Bhadrak 27.26–38.74a 172–190 29.46–36.9 40.05–47.37
32.88 ± 3.85b 177 ± 5.19 34.27 ± 2.2 43.18 ± 2.55
0.91c 1.22 0.52 0.6
14.82d 26.94 4.83 6.48
Chandaneswar 21.38–30.91 144–159 11.82–17.6 29.94–35.42
26.44 ± 2.93 152 ± 4.24 13.43 ± 1.49 32.52 ± 1.76
0.69 1 0.35 0.42
8.6 18 2.22 3.11
Chilika 31.46–46.13 74.26–91.3 27.02–34.51 46.11–55.91
40.03 ± 4.14 82.05 ± 5.35 31 ± 2.3 50.99 ± 2.73
0.98 1.26 0.54 0.64
17.17 28.6 5.31 7.44
Daringbadi 18.03–25.98 121–135 18.69–24.59 38.75–47.18
22.32 ± 2.43 127 ± 3.93 21.38 ± 1.78 42.69 ± 2.7
0.57 0.93 0.42 0.64
5.93 15.41 3.18 7.3
Hirakud 43.72–60.3 251–274 18.27–24.74 36.39–43.94
51.25 ± 4.46 266 ± 6.95 20.63 ± 1.74 40.08 ± 2.34
1.05 1.64 0.41 0.55
19.87 48.35 3.03 5.48
Koraput 12.78–18.94 128–153 28.58–37.5 51.42–59.9
15.55 ± 1.9 141 ± 8.18 32.55 ± 2.96 55.45 ± 2.93
0.45 1.93 0.7 0.69
3.62 66.94 8.77 8.59
Talcher 25.43–37.1 219–251 16.15–23.57 26.14–33.21
31.35 ± 3.51 244 ± 8.22 19.18 ± 2.22 29.71 ± 2.26
0.83 1.94 0.52 0.53
12.29 67.53 4.91 5.11
Titlagarh 30.27–42.9 118–132 26.72–34.53 48.33–57.29
36.63 ± 4.14 125 ± 4.65 29.93 ± 2.08 52.87 ± 2.77
0.98 1.1 0.49 0.65
17.14 21.65 4.31 7.67
BVe 20 35 25 71
TVASf 60 110 63 200
TRVg 31 26 16 110
WCTMRLh 10–100 20–190 20–90 50–250

aConcentration ranges (µg/g), bMean ± Standard deviation (SD) (µg/g), cStandard error (SE), dVariance, eBackground value (BV)12, fThreshold values for agricultural soil (TVAS)64, gToxicity reference value (TRV)65, hWorld Common Trace Metal Range in Lake (WCTMRL) sediment66.

Figure 2.

Figure 2

Concentrations of heavy metals (µg/g) in each of the locations in ascending order.

Table 3.

List of metals and sampling locations in decreasing order.

Type Location Metal concentration
Constructed BDRK Cr > Zn > Cu > Pb
Natural CDSR Cr > Zn > Pb > Cu
Natural CHLK Cr > Zn > Pb > Cu
Natural DRBD Cr > Zn > Pb > Cu
Constructed HRKD Cr > Pb > Zn > Cu
Natural KRPT Cr > Zn > Cu > Pb
Constructed TLHR Cr > Pb > Zn > Cu
Constructed TTGH Cr > Zn > Pb > Cu
Metal Locations
Pb HRKD > CHLK > TTGH > BDRK > TLHR > CDSR > DRBD > KRPT
Cr HRKD > TLHR > BDRK > CDSR > KRPT > DRBD > TTGH > CHLK
Cu BDRK > KRPT > CHLK > TTGH > DRBD > HRKD > TLHR > CDSR
Zn KRPT > TTGH > CHLK > BDRK > DRBD > HRKD > CDSR > TLHR

BDRK Bhadrak, CDSR Chandaneswar, CHLK Chilika, DRBD Daringbadi, HRKD Hirakud, KRPT Koraput, TLHR Talcher, TTGH Titlagarh.

Further, when the metal contamination in the wetland soil was examined from the perspective of spatial distribution (Fig. 3), Pb decreased from the northwest to the southeast. The Cr concentration distribution was found to have a decreasing gradient from the west to the east. The distribution of Cu was recorded as increasing from the northwest to the south. The distribution pattern of Zn in soil expressed an increase towards the south from the north (Fig. 3). The threshold values of heavy metals for agricultural soils (TVAS) are given in Table 2. Comparing the detected metals with TVAS, only Cr was determined to exceed the threshold limit at all sites except Chilika64. All other detected metals were under the threshold limit of TVAS (Table 2). Agricultural landscapes surrounded all the sampled wetlands; therefore, comparing the heavy metal concentration with the TVAS value depicts the pollution impact. The mean Pb, Cr, and Cu values in sediment from this study area exceeded the toxicity reference value (TRV)65. The mean concentration of Pb overcomes the TRV at Bhadrak, Chilika, Hirakud, Talcher, and Titlagarh sites. The Cr concentration exceeded the TRV at all sampling sites. Except for Chandaneswar, all other 'sites' Cu concentrations exceeded the limit of TRV. The TRV represented the exceeding limit for heavy metal values in the region. Compared to World Common Trace Metal Range in Lakes (WCTMRL) values, the mean value of Cr was higher at Hirakud and Talcher66. It represented polluted conditions with high Cr concentrations among all the sampled wetlands in the study area.

Figure 3.

Figure 3

Patterns of heavy metals’ spatial distribution throughout the study area crated using ArcMap 10.2.1.

Rapid urbanization, industrialization, and the developmental activity of human habitation have increased the pollutant level in the environment. The application of agrochemicals on agricultural land contributes to the increased concentration of heavy metals in bed sediments64. This increased pollution level ultimately moves sediments through the aquatic ecosystem67. This heavy metal contamination also contaminates sediment-dependent organisms. The level of heavy metals in wetlands can be assessed by detecting their concentrations in water and sediments68, which are found to be low in the water and high in the sediments due to accumulation69. The potentially harmful heavy metal in sediment is always a source of potential bioaccumulation and biomagnification70. Therefore, heavy metals in sediment play an indicator role in gauging environmental conditions71. The presence of heavy metals throughout the sediment is evidence of pollution72. In a given geographical framework, the distribution of spatial parameters utilizing tools like geographic information system (GIS) integrating field inventory has provided agility in scientific representation73. The current study expressed the distribution pattern of contaminants, and this spatial distribution represented the concentration level of heavy metals in the study area (Fig. 3).

Element association and clustering

The association among metals was established by calculating Pearson's correlation analysis. Cu and Zn were highly positively correlated (r = 0.77). A moderately positive correlation was also found between Pb and Cr (r = 0.36). This positive correlation described a similar type of source for their emergence. The negative correlation of Cr with Cu and Zn can be associated with their related geochemical properties. This correlogram supports understanding the presence of heavy metals in the sediment (Fig. 4). Here, the strong association between Cu and Zn may be due to the binding of strong hydrated metals51,74. Having the same chemical characteristics, Cu and Zn show the same behavior and distribution pattern56. Therefore, the association of Pb and Cr may describe the higher affinity between these metals74.

Figure 4.

Figure 4

Correlogram depicting association among the heavy metals.

Cluster analysis was performed among the heavy metal concentrations at all sampling locations (Fig. 5). It indicated the Bhadrak and Chandaneswar sites in one Cluster. These two sampling locations are from coastal regions, and the same lithogenic soil type can be the reason for the clustering into one. This study area region has the fluvisol soil type, representing the genetically younger soil with alluvial deposits. This soil type can be found in coastal lowlands, river fans, and tidal marshes75. Another type of Cluster that was very similar was found at the Hirakud and Talcher sample sites. An exceptionally high Pb and Cr content was found at these two locations.

Figure 5.

Figure 5

Hierarchical Cluster (a) of all sampling sites according to heavy metals concentration and comparison with soil types (b) of the study area crated using ArcMap 10.2.175.

These regions of the study area were distributed with luvisols of higher clay content. This soil has a higher fertility due to its various mineral parent materials. The Koraput, Daringbadi, and Titlagarh sites comprise the southern portion of the region under investigation. The habitat and the same nitisol soil types might contribute to this clustering (Fig. 5). This soil type is mainly found in the highlands and is formed from the parent rock material. The southern region under investigation was from the Eastern Ghats mountain ranges25,76,77.

Contamination indices of pollution

The contamination factor depicts the pollution and contamination levels of environmental media. Comparing the sediment concentration with the background value describes CF55. This background value comprises the mean international value78 or regional background value79,80. The background values of these metals here were referred to as a nationalized study on sediments8. The present study portrayed the Pb contamination as low at Koraput and moderated at all other sites. The Cr contamination was moderate at Chilika and considerably high at Bhadrak, Chandaneswar, Daringbadi, Koraput, and Titlagarh sites. Sediment samples from Hirakud and Talcher were highly contaminated by Cr pollution, with CF = 7.60 and 6.97, respectively. Contamination due to Cu and Zn was found to be low at all the sites, as CF < 1 (Table 4).

Table 4.

The ecological and human health risk posed by heavy metals at all sampling sites of the study area.

Sampling sites Pb Cr Cu Zn RI
CF Igeo PERF CF Igeo PERF CF Igeo PERF CF Igeo PERF
Bhadrak 1.64 0.33 8.22 5.06 1.01 10.11 0.98 0.28 4.90 0.61 0.12 0.61 23.84
Chandaneswar 1.32 0.27 6.61 4.34 0.87 8.69 0.38 0.11 1.92 0.46 0.09 0.46 17.67
Chilika 2.01 0.40 10.07 2.34 0.47 4.69 0.89 0.25 4.43 0.72 0.14 0.72 19.91
Daringbadi 1.12 0.22 5.58 3.63 0.73 7.26 0.61 0.17 3.05 0.60 0.12 0.60 16.49
Hirakud 2.56 0.51 12.81 7.60 1.53 15.20 0.59 0.17 2.95 0.56 0.11 0.56 31.53
Koraput 0.78 0.16 3.89 4.03 0.81 8.06 0.93 0.26 4.65 0.78 0.16 0.78 17.38
Talcher 1.57 0.31 7.84 6.97 1.40 13.94 0.55 0.15 2.74 0.42 0.08 0.42 24.94
Titlagarh 1.83 0.37 9.16 3.57 0.72 7.14 0.86 0.24 4.28 0.74 0.15 0.74 21.32

CF contamination factor, Igeo Geo-accumulation index, PERF potential ecological risk factor, RI ecological risk index.

The geoaccumulation index (Igeo) calculates the study area's metal accumulation. Considering the Igeo grade depicted previously, Pb, Cu, and Zn accumulations were considered uncontaminated to moderately contaminated sediment. However, the geoaccumulation of Cr at Bhadrak, Hirakud, and Talcher was more significant than 1, so these sampling sites were moderately contaminated (Table 4).

Ecological risk assessment

The current research determined the potential ecological risk factor (PERF) for each type of metal across all locations. The PERF obtained by all detected heavy metals in one region can be added to achieve the ecological risk index (RI)59. The present study depicted a low ecological risk with the highest RI at the Hirakud sampling site (Table 4). As all sampling sites were found to have RI < 150, the region under examination may pose a negligible threat to the environment58. This RI is updated with all detected metals’ limits81,82. The gradient of ecological risk in this study area decreases towards the south from the north (Fig. 6).

Figure 6.

Figure 6

The pattern of ecological risk index, hazard index (adults and children) (a), and carcinogenic risk (b) posed by heavy metals in sediments of the study area crated using ArcMap 10.2.1.

Human risk assessment

The harmful substances from sediment move into the human health system through indirect ingestion83,84. The present study depicted the harmful non-carcinogenic effect on humans due to indirect ingestion, as HQ values for Pb, Cr, Cu, and Zn at all the study sites were more significant than 1. This HQ value indicated a high health risk for adults and children. The only HQ of Cr at the Chilika site had a lower value than the limit for adult ingestion (Table 5). The high-end health risk of heavy metals for humans is also described by the hazard index (HI), which can be calculated from the HQ value85. The HI values were more significant than one, which was always considered a high health risk for adults and children86. The probability of chronic non-carcinogenic effects grows in proportion to the number in HI value58. The HI value in the sediments of the entire sampling site in this investigation showed that it was much greater than the threshold level (HI < 1) (Table 5). It indicates increased danger to human health in the region being studied. The pattern of HI can be seen lower in the southern part of the study area. In contrast, the north-western part depicts the high HI in adults and children (Fig. 6). Oral exposure by ingesting food contaminated with heavy metals from the sediments of this area can have long-term impacts that are not cancer-causing.

Table 5.

Average daily dose (ADD), hazard quotient (HQ), and hazard index (HI) of different heavy metals at different sampling sites of the study area.

Sampling sites Pb Cr Cu Zn HIA HIC
ADDA ADDC HQA HQC ADDA ADDC HQA HQC ADDA ADDC HQA HQC ADDA ADDC HQA HQC
Bhadrak 0.49 0.66 140.91 187.88 2.66 3.54 1.77 2.36 0.51 0.69 12.85 17.13 0.65 0.86 2.16 2.88 157.69 210.26
Chandaneswar 0.40 0.53 113.33 151.10 2.28 3.04 1.52 2.03 0.20 0.27 5.04 6.72 0.49 0.65 1.63 2.17 121.51 162.01
Chilika 0.60 0.81 172.70 230.26 1.23 1.64 0.82 1.09 0.47 0.62 11.63 15.50 0.76 1.02 2.55 3.40 187.69 250.26
Daringbadi 0.33 0.45 95.65 127.54 1.91 2.54 1.27 1.69 0.32 0.43 8.02 10.69 0.64 0.85 2.13 2.85 107.08 142.77
Hirakud 0.77 1.03 219.65 292.87 3.99 5.32 2.66 3.55 0.31 0.41 7.74 10.32 0.60 0.80 2.00 2.67 232.05 309.40
Koraput 0.23 0.31 66.64 88.86 2.12 2.82 1.41 1.88 0.49 0.65 12.21 16.28 0.83 1.11 2.77 3.70 83.03 110.71
Talcher 0.47 0.63 134.34 179.12 3.66 4.88 2.44 3.25 0.29 0.38 7.19 9.59 0.45 0.59 1.49 1.98 145.46 193.94
Titlagarh 0.55 0.73 157.00 209.34 1.88 2.50 1.25 1.67 0.45 0.60 11.22 14.96 0.79 1.06 2.64 3.52 172.12 229.49

ADDA average daily dose for an adult, ADDC average daily dose for children, HQA hazard quotient for adults, HQC hazard quotient for children, HIA hazard index for adults, HIC hazard index for children.

The carcinogenic risk (CR) value < 1 × 10–6 can be considered having no effect, and between 1 × 10–6 and 1 × 10–4 represents the endurable limit for human beings87. This carcinogenic risk calculated in the current investigation was only for the ingestion pathway, which means the accumulation of elements/heavy metals in food from the sediment ultimately leads to cancer in human beings8. All locations where samples were collected from the study area had a carcinogenic risk higher than the threshold limit for Cr. Cu and Zn were not listed due to their non-carcinogenic effects. However, a higher concentration of these two elements can cause endocrine disruption and various chronic diseases in humans88. Previously, one chromite mining location in the study area had explained the carcinogenic effect due to the ingestion of plant parts35. Of all the locations, Hirakud possesses the highest CR in adults and children (Table 6).

Table 6.

Carcinogenic risks from different sites of the study area.

Sampling sites Pb Cr
CRA CRC CRA CRC
Bhadrak 0.0042 0.0056 1.3275 1.7700
Chandaneswar 0.0034 0.0045 1.1400 1.5200
Chilika 0.0051 0.0069 0.6153 0.8205
Daringbadi 0.0028 0.0038 0.9525 1.2700
Hirakud 0.0065 0.0087 1.9950 2.6600
Koraput 0.0020 0.0026 1.0575 1.4100
Talcher 0.0040 0.0053 1.8300 2.4400
Titlagarh 0.0047 0.0062 0.9375 1.2500

CRA carcinogenic risks by ingestion in adults, CRC carcinogenic risks by ingestion in children.

Since the water from these wetlands is not being drawn directly for human consumption, the only way for people in the surrounding community to indirectly consume it is by consuming various foods from that wetland, such as fish, rice, some vegetables, and spinach. The CR in adults and children caused by indirect ingestion of Pb can be seen decreasing towards the south from the western region. The carcinogenic risk due to Cr ingestion can be depicted as higher in the northern half and lower in the southern portion of the region under investigation (Fig. 6). The districts of western Odisha had been recorded as having the highest number of cancer patients among all the districts89, supporting current research. Bargarh, Sambalpur, and Bolangir districts of the western side of the investigation region have the highest percentage of recorded patients among all the districts (26.34, 24.58, and 10.81, respectively)89. The exposure time to these heavy metals can be a significant factor, as the highest numbers of patients are detected in the 40–60 age group89.

The higher concentration of heavy metals in soils is transferred to edible plants and pesticides that humans ingest and ultimately possess carcinogenic effects90,91. Industrial development in the study area also poses carcinogenic effects due to the addition of heavy metals in soil from the effluents92. The western part of the study area is a hub for rice production93. The contamination of rice grains due to contaminated soils has been documented in previous investigations94,95, and the use of pesticides also increases the carcinogenic risk sometimes91. The local community faces a significant danger to their health if they consume any of this infected rice96 as it has already been recorded in different rice species in previous studies from this region47,49,50. This could be one of the reasons for the increasingly higher number of cancer patients in the particular region of the study area, which is supported by previous studies91,97. Considering the present scenario, this research paper offers some background information on the accumulation of heavy metals in wetland sediments and their carcinogenic effects on human beings. The significance of the current study lies in the fact that it protects the human population and the environmental ecosystem by assessing the potential risks to human health. This study's significance to the region's population stems from the fact that the carcinogenic and non-carcinogenic dangers posed by heavy metal contamination in the environment are considered. Because pollution from heavy metals is a problem affecting the entire developing world, this situation may also represent a worldwide picture. This information could serve as a foundation for formulating successful policies, raising awareness, and creating a future that is both healthy and sustainable.

Conclusions

The levels of metals like Pb, Cr, and Cu found in the investigation region exceeded the toxicity reference value in sediments. The concentration of heavy metals above the threshold limit can be directly linked to the food chain through plant uptake. The natural wetlands had lower Cr, Zn, and Pb, while the constructed wetlands had higher Cr, followed by Pb and Zn. The high contamination of heavy metals poses an ecological risk to the wetlands, leading to human health risks in these regions. The hazard index higher than the threshold for adults and children is the health risk from polluted sediments. Pb and Cr contamination pose a carcinogenic effect on humans and can cause cancer in the study area. Heavy metal contamination in sediments in India's wetlands can have significant environmental and health hazards. The contamination can negatively impact the biodiversity of the wetland ecosystem and potentially harm animals and plants that live in and around the wetland. Heavy metals in sediment can also pose a cancer-causing risk to human health for those who come into contact with the contaminated sediments or consume fish and other aquatic life from the wetland. It is essential for proper monitoring and management of these wetlands to take place to mitigate these hazards.

Acknowledgements

The authors are extending their thanks to all who helped in field works and sample analysis. The authors are also very much thankful to Siksha ‘O’ Anusandhan (Deemed to be University) for providing the necessary facilities to complete this work.

Author contributions

B.P.P. contributed to investigation, methodology, data curation, formal analysis, writing original draft; Y.K.M. contributed in writing—original draft; R.P. contributed in Data curation, Formal analysis; B.A.K.P., M.S., K.P., S.P.P., A.P., G.J., S.J.J. contributed in Writing—review & editing and H.S. contributed in supervision, writing—review & editing and foundation.

Data availability

The datasets generated and analysed during the study are available from Bibhu Prasad Panda (lead author, bibhuprasadpanda14@gmail.com) and Hemen Sarma (corresponding author, hemens02@yahoo.co.in) on reasonable request.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Li L, Su F, Brown MT, Liu H, Wang T. Assessment of ecosystem service value of the Liaohe estuarine wetland. Appl. Sci. 2018;8:2561. [Google Scholar]
  • 2.Hu S, Niu Z, Chen Y, Li L, Zhang H. Global wetlands: Potential distribution, wetland loss, and status. Sci. Total Environ. 2017;586:319–327. doi: 10.1016/j.scitotenv.2017.02.001. [DOI] [PubMed] [Google Scholar]
  • 3.Costanza R, et al. The value of the world’s ecosystem services and natural capital. Nature. 1997;387:253–260. [Google Scholar]
  • 4.Azeez PA, Prusty BAK, Jagadeesh EP. Alkali and alkaline earth metals in decomposing macrophytes in a wetland system. Acta Ecol. Sin. 2009;29:13–19. [Google Scholar]
  • 5.Garg JK. Wetland assessment, monitoring and management in India using geospatial techniques. J. Environ. Manag. 2015;148:112–123. doi: 10.1016/j.jenvman.2013.12.018. [DOI] [PubMed] [Google Scholar]
  • 6.Lu Q, Bai J, Gao Z, Zhao Q, Wang J. Spatial and seasonal distribution and risk assessments for metals in a Tamarix Chinensis wetland China. Wetlands. 2016;36:125–136. [Google Scholar]
  • 7.Oyuela Leguizamo MA, Fernández Gómez WD, Sarmiento MCG. Native herbaceous plant species with potential use in phytoremediation of heavy metals, spotlight on wetlands—A review. Chemosphere. 2017;168:1230–1247. doi: 10.1016/j.chemosphere.2016.10.075. [DOI] [PubMed] [Google Scholar]
  • 8.Kumar V, et al. A review of ecological risk assessment and associated health risks with heavy metals in sediment from India. Int. J. Sediment Res. 2020;35:516–526. [Google Scholar]
  • 9.Iñigo V, Andrades MS, Alonso-Martirena JI, Marín A, Jiménez-Ballesta R. Spatial variability of cadmium and lead in natural soils of a humid mediterranean environment: La Rioja, Spain. Arch. Environ. Contam. Toxicol. 2013;64:594–604. doi: 10.1007/s00244-012-9869-x. [DOI] [PubMed] [Google Scholar]
  • 10.Loska K, Wiechuła D. Speciation of cadmium in the bottom sediment of Rybnik reservoir. Water Air Soil Pollut. 2002;141:73–89. [Google Scholar]
  • 11.Prusty BAK, Azeez PA. Vertical distribution of alkali and alkaline earth metals in the soil profile of a wetland-terrestrial ecosystem complex in India. Aust. J. Soil Res. 2007;45:533–542. [Google Scholar]
  • 12.Kumar V, et al. Assessment of heavy-metal pollution in three different Indian water bodies by combination of multivariate analysis and water pollution indices. Hum. Ecol. Risk Assess. 2020;26:1–16. [Google Scholar]
  • 13.Gale NL, Adams CD, Wixson BG, Loftin KA, Huang YW. Lead, zinc, copper, and cadmium in fish and sediments from the big river and flat river creek of Missouri’s old lead belt. Environ. Geochem. Health. 2004;26:37–49. doi: 10.1023/b:egah.0000020935.89794.57. [DOI] [PubMed] [Google Scholar]
  • 14.Ouyang Y, Higman J, Thompson J, O’Toole T, Campbell D. Characterization and spatial distribution of heavy metals in sediment from Cedar and Ortega rivers subbasin. J. Contam. Hydrol. 2002;54:19–35. doi: 10.1016/s0169-7722(01)00162-0. [DOI] [PubMed] [Google Scholar]
  • 15.Yu Y, et al. Exposure risk of rural residents to copper in the Le’an river basin, Jiangxi province, China. Sci. Total Environ. 2016;548–549:402–407. doi: 10.1016/j.scitotenv.2015.11.107. [DOI] [PubMed] [Google Scholar]
  • 16.Fang H, Huang L, Wang J, He G, Reible D. Environmental assessment of heavy metal transport and transformation in the Hangzhou Bay, China. J. Hazard. Mater. 2016;302:447–457. doi: 10.1016/j.jhazmat.2015.09.060. [DOI] [PubMed] [Google Scholar]
  • 17.Kumar V, et al. Pollution assessment of heavy metals in soils of India and ecological risk assessment: A state-of-the-art. Chemosphere. 2019;216:449–462. doi: 10.1016/j.chemosphere.2018.10.066. [DOI] [PubMed] [Google Scholar]
  • 18.Linnik PM, Zubenko IB. Role of bottom sediments in the secondary pollution of aquatic environments by heavy-metal compounds. Lakes Reserv. Res. Manag. 2000;5:11–21. [Google Scholar]
  • 19.Mishra SR, Chandra R, Prusty BAK. Chelate-assisted phytoaccumulation: Growth of Helianthus annuus L., Vigna radiata (L.) R. Wilczek and Pennisetum glaucum (L.) R. Br. in soil spiked with varied concentrations of copper. Environ. Sci. Pollut. Res. 2020;27:5074–5084. doi: 10.1007/s11356-019-07257-6. [DOI] [PubMed] [Google Scholar]
  • 20.Han L, et al. Lead contamination in sediments in the past 20 years: A challenge for China. Sci. Total Environ. 2018;640–641:746–756. doi: 10.1016/j.scitotenv.2018.05.330. [DOI] [PubMed] [Google Scholar]
  • 21.Kumar KS, Priya SM, Peck AM, Sajwan KS. Mass loadings of triclosan and triclocarbon from four wastewater treatment plants to three rivers and landfill in Savannah, Georgia, USA. Arch. Environ. Contam. Toxicol. 2010;58:275–285. doi: 10.1007/s00244-009-9383-y. [DOI] [PubMed] [Google Scholar]
  • 22.Wojciechowska E, Nawrot N, Walkusz-Miotk J, Matej-Łukowicz K, Pazdro K. Heavy metals in sediments of urban streams: Contamination and health risk assessment of influencing factors. Sustainability. 2019;11:5–10. [Google Scholar]
  • 23.Prusty BAK, Chandra R, Azeez PA. Association of metals with geochemical phases in wetland soils of a Ramsar site in India. Environ. Monit. Assess. 2019 doi: 10.1007/s10661-019-7913-2. [DOI] [PubMed] [Google Scholar]
  • 24.Dash S, Borah SS, Kalamdhad AS. Heavy metal pollution and potential ecological risk assessment for surficial sediments of Deepor Beel India. Ecol. Indic. 2021;122:107265. [Google Scholar]
  • 25.Panda BP, Mahapatra B, Parida SP, Dash AK, Pradhan A. Feathers of Bulbulcus ibis (L.) as a non-destructive biomonitoring tool for assessment of lead pollution: A case study from various severely contaminated wetland habitats. Biointerface Res. Appl. Chem. 2020;10:5085–5090. [Google Scholar]
  • 26.Kalita S, Sarma HP, Devi A. Sediment characterisation and spatial distribution of heavy metals in the sediment of a tropical freshwater wetland of Indo-Burmese province. Environ. Pollut. 2019;250:969–980. doi: 10.1016/j.envpol.2019.04.112. [DOI] [PubMed] [Google Scholar]
  • 27.Prusty BAK, Chandra R, Azeez PA. Chemical partitioning of Cu, Pb and Zn in the soil profile of a semi arid dry woodland. Chem. Speciat. Bioavailab. 2009;21:141–151. [Google Scholar]
  • 28.Prusty BAK, Chandra R, Azeez PA. Cu, Pb and Zn fractionation in a savannah type grassland soil. In: Panagiotaras D, editor. Geochemistry—Earth’s System Processes. InTech; 2012. pp. 413–428. [Google Scholar]
  • 29.Bonanno G, Borg JA, Di Martino V. Levels of heavy metals in wetland and marine vascular plants and their biomonitoring potential: A comparative assessment. Sci. Total Environ. 2017;576:796–806. doi: 10.1016/j.scitotenv.2016.10.171. [DOI] [PubMed] [Google Scholar]
  • 30.Zhang Y, et al. Distribution characteristics, risk assessment, and quantitative source apportionment of typical contaminants (HMs, N, P, and TOC) in river sediment under rapid urbanization: A study case of Shenzhen river, Pearl River Delta, China. Process Saf. Environ. Prot. 2022;162:155–168. [Google Scholar]
  • 31.Hatvani IG, Dokulil MT, Clement A. The role of wetlands in mitigating impacts from diffuse agricultural loads. Encycl. Inl Waters Second Ed. 2022;4:285–299. [Google Scholar]
  • 32.Astatkie H, Ambelu A, Beyene EM. Sources and level of heavy metal contamination in the water of Awetu watershed streams, southwestern Ethiopia. Heliyon. 2021;7:e06385. doi: 10.1016/j.heliyon.2021.e06385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Chen TB, et al. Assessment of heavy metal pollution in surface soils of urban parks in Beijing, China. Chemosphere. 2005;60:542–551. doi: 10.1016/j.chemosphere.2004.12.072. [DOI] [PubMed] [Google Scholar]
  • 34.Xiao R, Wang S, Li R, Wang JJ, Zhang Z. Soil heavy metal contamination and health risks associated with artisanal gold mining in Tongguan, Shaanxi, China. Ecotoxicol. Environ. Saf. 2017;141:17–24. doi: 10.1016/j.ecoenv.2017.03.002. [DOI] [PubMed] [Google Scholar]
  • 35.Naz A, Chowdhury A, Chandra R, Mishra BK. Potential human health hazard due to bioavailable heavy metal exposure via consumption of plants with ethnobotanical usage at the largest chromite mine of India. Environ. Geochem. Health. 2020;42:4213–4231. doi: 10.1007/s10653-020-00603-5. [DOI] [PubMed] [Google Scholar]
  • 36.Ramachandra TV, Sudarshan PB, Mahesh MK, Vinay S. Spatial patterns of heavy metal accumulation in sediments and macrophytes of Bellandur wetland, Bangalore. J. Environ. Manag. 2018;206:1204–1210. doi: 10.1016/j.jenvman.2017.10.014. [DOI] [PubMed] [Google Scholar]
  • 37.Cheng S. Heavy metal pollution in China: Origin, pattern and control. Environ. Sci. Pollut. Res. 2003;10:192–198. doi: 10.1065/espr2002.11.141.1. [DOI] [PubMed] [Google Scholar]
  • 38.Wong SC, Li XD, Zhang G, Qi SH, Min YS. Heavy metals in agricultural soils of the Pearl River Delta, South China. Environ. Pollut. 2002;119:33–44. doi: 10.1016/s0269-7491(01)00325-6. [DOI] [PubMed] [Google Scholar]
  • 39.Akcay H, Oguz A, Karapire C. Study of heavy metal pollution and speciation in Buyak Menderes and Gediz river sediments. Water Res. 2003;37:813–822. doi: 10.1016/s0043-1354(02)00392-5. [DOI] [PubMed] [Google Scholar]
  • 40.Cui L, et al. Spatial distribution of total halogenated organic compounds (TX), adsorbable organic halogens (AOX), and heavy metals in wetland soil irrigated with pulp and paper wastewater. Chem. Speciat. Bioavailab. 2017;29:15–24. [Google Scholar]
  • 41.Gao W, Du Y, Gao S, Ingels J, Wang D. Heavy metal accumulation reflecting natural sedimentary processes and anthropogenic activities in two contrasting coastal wetland ecosystems, eastern China. J. Soils Sediments. 2016;16:1093–1108. [Google Scholar]
  • 42.Das Sharma S. Risk assessment and mitigation measures on the heavy metal polluted water and sediment of the kolleru lake in Andhra Pradesh, India. Pollution. 2019;5:161–178. [Google Scholar]
  • 43.Esmaeilzadeh M, Karbassi A, Moattar F. Assessment of metal pollution in the Anzali wetland sediments using chemical partitioning method and pollution indices. Acta Oceanol. Sin. 2016;35:28–36. [Google Scholar]
  • 44.Brady JP, Ayoko GA, Martens WN, Goonetilleke A. Enrichment, distribution and sources of heavy metals in the sediments of Deception Bay, Queensland, Australia. Mar. Pollut. Bull. 2014;81:248–255. doi: 10.1016/j.marpolbul.2014.01.031. [DOI] [PubMed] [Google Scholar]
  • 45.Duodu GO, Goonetilleke A, Ayoko GA. Comparison of pollution indices for the assessment of heavy metal in Brisbane River sediment. Environ. Pollut. 2016;219:1077–1091. doi: 10.1016/j.envpol.2016.09.008. [DOI] [PubMed] [Google Scholar]
  • 46.Sreenivasulu G, et al. Assessment of heavy metal pollution from the sediment of Tupilipalem Coast, southeast coast of India. Int. J. Sediment Res. 2018;33:294–302. [Google Scholar]
  • 47.Barik SR, Mishra PJ, Nayak AK, Rout S. Assessment of heavy metals in the surrounding soils and their bioconcentrations in few plants near Kathajodi river, Odisha, India. J. Appl. Nat. Sci. 2016;8:790–803. [Google Scholar]
  • 48.Zimik HV, Farooq SH, Prusty P. Source characterization of trace elements and assessment of heavy metal contamination in the soil around Tarabalo geothermal field, Odisha, India. Arab. J. Geosci. 2021 doi: 10.1007/s12517-021-07366-y. [DOI] [Google Scholar]
  • 49.Satpathy D, Reddy MV, Dhal SP. 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;2014:1–11. doi: 10.1155/2014/545473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Panda SS, Dhal NK. Assessment of heavy metal contamination of soils and plants in and around open cast mines of Sukinda India. Asian J. Environ. Sci. 2015;10:76–82. [Google Scholar]
  • 51.Chandra R, Prusty BAK, Azeez PA. Spatial variability and temporal changes in the trace metal content of soils: Implications for mine restoration plan. Environ. Monit. Assess. 2014;186:3661–3671. doi: 10.1007/s10661-014-3648-2. [DOI] [PubMed] [Google Scholar]
  • 52.Panda BP, et al. Relationship among the physico-chemical parameters of soil and water in different wetland ecosystems. Asian J. Chem. 2020;32:1681–1690. [Google Scholar]
  • 53.Panda BP, et al. Heavy metal accumulation in some fishes preferred for consumption by egrets in Odisha, India. Nat. Environ. Pollut. Technol. 2019;18:975–979. [Google Scholar]
  • 54.Naveedullah, et al. Risk assessment of heavy metals pollution in agricultural soils of siling reservoir watershed in Zhejiang province, China. Biomed. Res. Int. 2013;2013:1–10. doi: 10.1155/2013/590306. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Hakanson L. An ecological risk index for aquatic pollution control. A sedimentological approach. Water Res. 1980;14:975–1001. [Google Scholar]
  • 56.Kim BSM, Angeli JLF, Ferreira PAL, de Mahiques MM, Figueira RCL. Critical evaluation of different methods to calculate the geoaccumulation index for environmental studies: A new approach for Baixada Santista—Southeastern Brazil. Mar. Pollut. Bull. 2018;127:548–552. doi: 10.1016/j.marpolbul.2017.12.049. [DOI] [PubMed] [Google Scholar]
  • 57.Huang L, et al. Heavy metals distribution, sources, and ecological risk assessment in Huixian wetland, South China. Water. 2020;12:1–14. [Google Scholar]
  • 58.Alghamdi BA, El Mannoubi I, Zabin SA. Heavy metals' contamination in sediments of Wadi Al-Aqiq water reservoir dam at Al-Baha region, KSA: Their identification and assessment. Hum. Ecol. Risk Assess. 2019;25:793–818. [Google Scholar]
  • 59.Guo W, Liu X, Liu Z, Li G. Pollution and potential ecological risk evaluation of heavy metals in the sediments around Dongjiang Harbor, Tianjin. Procedia Environ. Sci. 2010;2:729–736. [Google Scholar]
  • 60.USEPA. Regional Screening Levels (RSLs) - Generic Tables. Environmental Protection Agency. https://www.epa.gov/risk/regional-screening-levels-rsls-generic-tables (2015).
  • 61.Swarnalatha K, Letha J, Ayoob S, Nair AG. Risk assessment of heavy metal contamination in sediments of a tropical lake. Environ. Monit. Assess. 2015;187:1–14. doi: 10.1007/s10661-015-4558-7. [DOI] [PubMed] [Google Scholar]
  • 62.Genthe B, et al. Health risk implications from simultaneous exposure to multiple environmental contaminants. Ecotoxicol. Environ. Saf. 2013;93:171–179. doi: 10.1016/j.ecoenv.2013.03.032. [DOI] [PubMed] [Google Scholar]
  • 63.Banerjee K, Sahoo CK, Paul R. Assessment and modelling of vegetation biomass in a major bauxite mine of Eastern Ghats, India. Model. Earth Syst. Environ. 2020 doi: 10.1007/s40808-020-01004-4. [DOI] [Google Scholar]
  • 64.Srinivasarao C, et al. Heavy metals concentration in soils under rainfed agro-ecosystems and their relationship with soil properties and management practices. Int. J. Environ. Sci. Technol. 2014;11:1959–1972. [Google Scholar]
  • 65.Mohiuddin KM, Ogawa Y, Zakir HM, Otomo K, Shikazono N. Heavy metal pollution in surface water and sediment: A preliminary assessment of an urban river in a developing country. Int. J. Environ. Sci. Technol. 2011;8:723–736. [Google Scholar]
  • 66.Förstner U, Wittmann GTW. Metal Pollution in the Aquatic Environment. Springer Science & Business Media; 1981. [Google Scholar]
  • 67.Ravichandran R, Manickam S. Heavy metal disrtibution in the coastal sediment of Chennai coast. IIOAB J. 2012;3:12–18. [Google Scholar]
  • 68.Malik N, Biswas AK, Qureshi TA, Borana K, Virha R. Bioaccumulation of heavy metals in fish tissues of a freshwater lake of Bhopal. Environ. Monit. Assess. 2010;160:267–276. doi: 10.1007/s10661-008-0693-8. [DOI] [PubMed] [Google Scholar]
  • 69.Sheikh MM, Rezaei MR, Nasseri MA. Heavy metals (Hg, Cr and Pb) concentrations in water and sediment of Kashaf Rood River. Toxicol. Environ. Health Sci. 2013;5:65–70. [Google Scholar]
  • 70.Bastami KD, et al. Distribution and ecological risk assessment of heavy metals in surface sediments along southeast coast of the Caspian Sea. Mar. Pollut. Bull. 2014;81:262–267. doi: 10.1016/j.marpolbul.2014.01.029. [DOI] [PubMed] [Google Scholar]
  • 71.Caccia VG, Millero FJ, Palanques A. The distribution of trace metals in Florida Bay sediments. Mar. Pollut. Bull. 2003;46:1420–1433. doi: 10.1016/S0025-326X(03)00288-1. [DOI] [PubMed] [Google Scholar]
  • 72.Xu G, et al. Surface sediment properties and heavy metal pollution assessment in the near-shore area, north Shandong Peninsula. Mar. Pollut. Bull. 2015;95:395–401. doi: 10.1016/j.marpolbul.2015.03.040. [DOI] [PubMed] [Google Scholar]
  • 73.Paul R, Patra S, Banerjee K. Socio-economic impact on vulnerability of tropical forests of Eastern Ghats using hybrid modelling. Trop. Ecol. 2020 doi: 10.1007/s42965-020-00106-5. [DOI] [Google Scholar]
  • 74.Caporale AG, Violante A. Chemical processes affecting the mobility of heavy metals and metalloids in soil environments. Curr. Pollut. Rep. 2016;2:15–27. [Google Scholar]
  • 75.FAO WRB. World Reference Base for Soil Resources. World Soil Resources Reports No. 106 (2015).
  • 76.Paul R, Banerjee K. Deforestation and forest fragmentation in the highlands of Eastern Ghats, India. J. For. Res. 2021;32:1127–1138. [Google Scholar]
  • 77.Zhang J, et al. Assessment of soil heavy metal pollution in provinces of China based on different soil types: From normalization to soil quality criteria and ecological risk assessment. J. Hazard. Mater. 2023;441:129891. doi: 10.1016/j.jhazmat.2022.129891. [DOI] [PubMed] [Google Scholar]
  • 78.Fukue M, et al. Background values for evaluation of heavy metal contamination in sediments. J. Hazard. Mater. 2006;136:111–119. doi: 10.1016/j.jhazmat.2005.11.020. [DOI] [PubMed] [Google Scholar]
  • 79.Alfaro MR, et al. Background concentrations and reference values for heavy metals in soils of Cuba. Environ. Monit. Assess. 2015 doi: 10.1007/s10661-014-4198-3. [DOI] [PubMed] [Google Scholar]
  • 80.Pan C, Zheng G, Zhang Y. Concentrations of metals in liver, muscle and feathers of tree sparrow: Age, inter-clutch variability, gender, and species differences. Bull. Environ. Contam. Toxicol. 2008;81:558–560. doi: 10.1007/s00128-007-9168-9. [DOI] [PubMed] [Google Scholar]
  • 81.Wang J, Liu W, Yang R, Zhang L, Ma J. Assessment of the potential ecological risk of heavy metals in reclaimed soils at an opencast coal mine. Disaster Adv. 2013;6:366–377. [Google Scholar]
  • 82.Li Y, et al. A combined method for human health risk area identification of heavy metals in urban environments. J. Hazard. Mater. 2023;449:131067. doi: 10.1016/j.jhazmat.2023.131067. [DOI] [PubMed] [Google Scholar]
  • 83.Bashir I, et al. Concerns and threats of xenobiotics on aquatic ecosystems. In: Hakeem K, Bhat R, Qadri H, et al., editors. Bioremediation and Biotechnology. Springer; 2020. pp. 15–23. [Google Scholar]
  • 84.Jaishankar M, Tseten T, Anbalagan N, Mathew BB, Beeregowda KN. Toxicity, mechanism and health effects of some heavy metals. Interdiscip. Toxicol. 2014;7:60–72. doi: 10.2478/intox-2014-0009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Qu C, Sun K, Wang S, Huang L, Bi J. Monte Carlo simulation-based health risk assessment of heavy metal soil pollution: A case study in the Qixia mining area, China. Hum. Ecol. Risk Assess. 2012;18:733–750. [Google Scholar]
  • 86.Qing X, Yutong Z, Shenggao L. Assessment of heavy metal pollution and human health risk in urban soils of steel industrial city (Anshan), Liaoning, Northeast China. Ecotoxicol. Environ. Saf. 2015;120:377–385. doi: 10.1016/j.ecoenv.2015.06.019. [DOI] [PubMed] [Google Scholar]
  • 87.Wu S, et al. Levels and health risk assessments of heavy metals in urban soils in Dongguan, China. J. Geochem. Explor. 2015;148:71–78. [Google Scholar]
  • 88.Briffa J, Sinagra E, Blundell R. Heavy metal pollution in the environment and their toxicological effects on humans. Heliyon. 2020;6:e04691. doi: 10.1016/j.heliyon.2020.e04691. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Majhi KM, Panigrahi AK, Panigrahy A. Prevalence of cancer in an urban cancer centre in Western Odisha—A retrospective. IOSR J. Dent. Med. Sci. 2018;17:57–63. [Google Scholar]
  • 90.Hu B, et al. Assessment of heavy metal pollution and health risks in the soil-plant-human system in the Yangtze river delta, China. Int. J. Environ. Res. Public Health. 2017;14:1042. doi: 10.3390/ijerph14091042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Yadav H, Sankhla MS, Kumar R. Pesticides-induced carcinogenic & neurotoxic effect on human. Forensic Res. Criminol. Int. J. 2019;7:243–245. [Google Scholar]
  • 92.Mohammadi AA, et al. Assessment of heavy metal pollution and human health risks assessment in soils around an industrial zone in Neyshabur, Iran. Biol. Trace Elem. Res. 2020;195:343–352. doi: 10.1007/s12011-019-01816-1. [DOI] [PubMed] [Google Scholar]
  • 93.Sethy PK, Chatterjee A. Rice variety identification of Western Odisha based on geometrical and texture feature. Int. J. Appl. Eng. Res. 2018;13:35–39. [Google Scholar]
  • 94.Bisoi SS, Mishra SS, Barik J, Panda D. Effects of different treatments of fly ash and mining soil on growth and antioxidant protection of Indian wild rice. Int. J. Phytoremediat. 2017;19:446–452. doi: 10.1080/15226514.2016.1244164. [DOI] [PubMed] [Google Scholar]
  • 95.Zhou H, et al. Identification and hazard analysis of heavy metal sources in agricultural soils in ancient mining areas: A quantitative method based on the receptor model and risk assessment. J. Hazard. Mater. 2023;445:130528. doi: 10.1016/j.jhazmat.2022.130528. [DOI] [PubMed] [Google Scholar]
  • 96.Guo B, et al. Health risk assessment of heavy metal pollution in a soil-rice system: A case study in the Jin-Qu Basin of China. Sci. Rep. 2020;10:1–11. doi: 10.1038/s41598-020-68295-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Bhatti SS, et al. Potential carcinogenic and non-carcinogenic health hazards of metal(loid)s in food grains. Environ. Sci. Pollut. Res. 2020;27:17032–17042. doi: 10.1007/s11356-020-08238-w. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets generated and analysed during the study are available from Bibhu Prasad Panda (lead author, bibhuprasadpanda14@gmail.com) and Hemen Sarma (corresponding author, hemens02@yahoo.co.in) on reasonable request.


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