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Spatial Distribution and Ecological Risk Assessment of Heavy Metals in Sediments from Pearl River Networks, South China

DOI: 10.4236/oalib.1105709    82 Downloads   182 Views  

ABSTRACT

Sediment samples collected from 21 sites of the Pearl River networks were investigated by the sequential extraction method. Multiple environmental indices were adopted to evaluate the present and potential risks. Results indicated that concentrations of Cu, Zn, As, Cd, and Pb in most of the sedi-ments were substantially higher than their background values, and the primary sources of the contamination coming from municipal, industrial wastewater discharges and upstream mining were inferred by matrix analysis with comparing special distribution characteristics. Cd was the main factor causing the potential ecological risk in Pearl River networks. The potential mobility of heavy metals was shown in the decreasing order: Cd > Mn > Co > Zn > Ni > Cu > Pb > As > Cr.

1. Introduction

Heavy metals have been confirmed to dissolve in aquatic systems easily, and caused realistic and potential serious hazards to organisms and human health. They are typically considered as a high ecological risk chemical pollutant and have attracted increasing attention [1] [2] . The contamination of heavy metals entering aquatic systems could be deposited and co-deposited into sediments by forming a variety of chemical fractions. The chemical stability of sediment-associated heavy metals may be subjected to the aquatic environment, such as the pH value, redox potential, ion strength, and presence of organic chelate. They could exhibit different physical and chemical behaviors, which is a concern in many studies. Once the aquatic environmental condition changed, the contamination of heavy metals may be transferred gradually into the water from sediments and becomes a potential source of biological-availability and toxicity [3] [4] . Heavy metals can be accumulated into aquatic animals from the water environment, and may reach higher levels than the water environment after the migration from sediment to water or to organisms [5] [6] [7] . Evaluating the risk of heavy metals in sediments could offer important information of the overall pollution level, but it was inadequate to perform an assessment on their potential mobility, bioavailability, and environmental risk [8] [9] . The detection and analysis of different chemical forms can facilitate in obtaining more information to determine the degree of mobility, bioavailability, and potential toxicity of heavy metals. The sequential extraction procedure is a widely-applied approach for the qualitative and quantitative analysis of different chemical forms and their binding states in sediments [10] [11] .

The Pearl River networks are located in the Pearl River Delta region of South China, adjacent to the South China Sea, and is the channel connecting land and sea. It is not only one of the most densely populated and economically developed areas in China, but also in the South China primary fishery areas and passage for fish migratory from the South China Sea to the Pearl River. In recent years, along with rapid and extensive industrialization and agricultural growth, a large number of heavy metal contaminants from agriculture, domestic and municipal waters, mining, and processing have directly or indirectly discharged into the Pearl River networks, thus increasing the pollution of heavy metals in the surface sediments [12] [13] [14] . However, information on the distribution and environmental risk assessment of heavy metals in the Pearl River networks is scarce. In the present study, the sediments from 21 sites in the Pearl River networks were collected and analyzed for heavy metals. The primary objectives are: 1) to determine the concentration, chemical forms, and composition ratios of heavy metals in sediments to evaluate the level of contamination and distribution pattern, 2) to evaluate the pollution source, mobile status, bioavailability, and potential risk.

2. Materials and Methods

2.1. Study Area and Sample Collection

Samples were collected from the Pearl River networks with 21 sites from August to December of 2015. All sampling sites were distinguished into three areas: upstream (6 sites), midstream (7 sites), and estuary (8 sites) (Figure 1). The sediments were collected using a standard Van Veen grab sampler of effective area 250 cm2 and were homogenized using a Teflon spoon. The samples were transferred into labeled polyethylene containers under freezing conditions (−4˚C) for safe transportation to the laboratory. The samples were then air-dried for nearly 2 - 3 days under a fume hood, sieved, and subsequently ground with an agate mortar (grain sizes < 63 μm).

2.2. Pretreatment and Analysis of Samples

The determination of heavy metals in sediments were designed to separate metals into four operationally defined fractions modified based on the Tessier sequential extraction method [15] with a few modifications. The fractions were as follows: the exchangeable and carbonates (EX + C), Fe and Mn oxides (Fe/Mn-OX), organics, and residuals [14] [16] [17] [18] .

2.3. Analysis and Quality Control

Chemical analysis was performed in the Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, China. Quality assurance and quality control (QA/QC) of the examined sediment samples were performed by the analysis of the procedural blank, duplicate samples, and the method of standard addition. All analytical instruments were calibrated daily, and the samples were determined according to the EPA method 3051A and 200.8 by ICP-MS (Agilent 7500-CX). The reference material from the Chinese national standard sediment sample GBW07436 was used to monitor the analysis. The results indicated no contamination during analysis, and the relative standard deviation of all the replicate samples was less than 10%. The ratios of cumulative concentrations of the fractions to the independent total metal concentration ranged from 80% to 120%.

Figure 1. Sampling sites.

The detection limits were calculated by the relevant software in the database of the ICP-MS (ChemStation Software by Agilent). The lowest instrument determination limits of Cr, Mn, Co, Ni, Cu, Zn, As, Mo, Cd, and Pb were 32.60, 20.13, 2.67, 13.43, 83.6, 192.5, 4.04, 39.07, 5.44 and 13.21 μg・L−1 respectively.

2.4. Ecological Risk Assessment

2.4.1. Potential Migration Ability

The risk assessment code (RAC) was used to reflect the heavy metals potential mobility, which has been widely used in the risk analysis of many studies [19] [11] . The RAC values of heavy metals were calculated according to the content of exchangeable and carbonate fractions to the total concentration ratios [20] . The guidelines for interpreting the RAC values are as the following: RAC < 1%, no risk; 1% ≤ RAC < 10%, low risk; 10% ≤ RAC < 30%, medium risk; 30% ≤ RAC < 50%, high risk; RAC ≥ 50%, extremely high risk.

2.4.2. Enrichment Factor (EFc)

The enrichment factor (EFc) was applied to estimate and distinguish the heavy metals sourcing from anthropogenic or natural factor contributions, and to infer the information of dissolution in river sediments. The enrichment factors for each of the elements were calculated with the following formula:

E F c = ( Ms / AIs ) sample / ( Mo / AIo ) standard (1)

where EFc: enrichment factor; Ms: concentration of metal “X” in the sample; AIs: concentration of reference element (AI) in the sample; Mo: background values of metal ‘‘X’’ in surface sediments of Pearl River estuary, is the corresponding background values of China’s continental crust (Cd = 0.055, Pb = 15, Mo = 2, Cr = 63, Mn = 780, Ni = 57, Cu = 38, Zn = 86, As = 1.9, Co = 32, mg/kg). An AIo of 7.8% was elected as the reference element [21] . The criteria for evaluating sediment EFc were as follows: EFc < 1 indicates non-contamination by metal (crustal origin of the metal) and no enrichment; 1 < EFc < 2 indicates low contamination or minor enrichment; 2 < EFc < 10 indicates moderate contamination or moderate enrichment; EFc >10 indicates significant contamination by metals (non-crustal sources) or severe enrichment.

2.4.3. Potential Ecological Risk

The quantitative classification of potential ecological risk was proposed by Hakanson [22] . The potential ecological risk index was adopted to assess the degree of heavy metal pollution in sediments, according to the toxicity of heavy metal elements, the general migration and transformation law in sediments, and the regional sensitivity to heavy metal pollution. The formula for the potential ecological risk of the monomial element is as follows:

E r i = T r i × C s i / C n i (2)

In the formula, E r i is the monomial potential ecological risk index; T r i is a toxicity response parameter of a single contaminated element; C s i is the measured concentration of contaminated elements in the sediments (mg・kg−1); C n i is the background value of heavy metals in the sediments. The biotoxicity coefficient ( T r i ) of Cu, Zn, Ni, Cr, Pb, Cd were 5, 1, 5, 2, 5, 30, respectively. The formula for the comprehensive evaluation method of various pollution elements is shown in formula (3):

RI = E r i (3)

where RI is calculated as the sum of all potential ecological risk indexes of multiple metals. The terminology used to describe the individual potential ecological risk index ( E r i ), integrated potential ecological risk index (RI), and potential ecological risk was suggested by Hakanson [22] , where E r i < 40 indicates a low potential ecological risk; 40 < E r i < 80 indicates a moderate ecological risk; 80 < E r i < 160 indicates a considerable ecological risk; 160 < E r i < 320 indicates a high ecological risk; E r i > 320 indicates an extremely high ecological risk. RI < 95 indicates a low potential ecological risk; 95 < RI < 190 indicates a moderate ecological risk; 190 < RI < 380 indicates a considerable ecological risk, and RI > 380 indicates an extremely high ecological risk.

2.5. Data Statistics

Statistical analyses were conducted using Origin 8.0 (Origin Lab Corp., Northampton, MA, USA) and Excel 2013 (Microsoft Corp., Redmond, WA, USA).

3. Results and Discussion

3.1. Concentrations of Heavy Metals in the Sediments

The concentration of heavy metals was shown in the decreasing order: Mn > Zn > Cu > Pb > Cr > Ni > As > Co > Cd (Figure 2). The average values were displayed and compared with the heavy metal target values of the Chinese Government for Marine sediments, the background of sediments of the Pear River estuary, and the average shale value. The sampling sites with concentrations of Cr and Pb exceeded the I Class Standard for Marine Sediment Quality, accounting for 42.8% and 71.4% of the total sampling sites respectively (Table 1). There were 66.7% of sampling sites with the concentrations of Cu, Zn above the II

Figure 2. Distribution of heavy metals in the sediments.

Table 1. Comparison of heavy metals concentration (mg・kg−1 dry wt) in the sediments from Pearl River networks.

na Not available; aGAN H., et al., 2010; bNational Standard of PR China (2002) (GB 18668-2002); CTuredian and Wedepohl (1961).

class, and 91.7% of sampling sites with the concentrations of Cd varying II class and III class. Compared with the background of sediments of the Pear River Estuary, the average concentrations of Zn, As, Cd, and Pb were as high as 4.35, 2.48, 21.95, and 2.49 times, which were higher with respect to their corresponding bench mark values. Cd was the most serious pollution element in this area, and the sampling sites with high concentration occurred in the northern (U5, U6) and middle (N3, N5, and N7) reaches. For other metals, i.e., Cr, Cu, Zn, Cd, and Pb, the distribution characteristics of the middle reaches demonstrated a higher average concentration than in the northern or estuary sites. In particular, Mn, Zn, Cu, As, and Zn demonstrated the highest content at site N7.

The regional distribution characteristics of heavy metals in the sediments are closely related to the upstream input, local population, and industrial distribution. In the upstream Beijiang River Basin, a large number of mining and steel enterprises exist. Historically, illegal emissions from metal processing enterprises have resulted in large-scale Cd pollution. When the upstream pollutants enter the river networks, the flow becomes gentle and easy to precipitate, this may be a major reason for the higher distribution of heavy metals in the northern reaches (U2, U5, and U6). The hydrodynamic conditions became weakened and favored sediment deposition and followed by heavy metal accumulation. Pollution discharges from local metal processing, waste recycling, and the electronics industries are other major factors affecting the distribution of heavy metal pollution in sediments. For example, midstream sites (N3, N5, N7) surrounded by developed manufacturing industries and dense populations exhibited the highest pollution levels.

3.2. Proportion of Various Fractions in the Sediments

The evaluation of chemical fraction and composition of each metal in the sediments can provide useful information regarding the source, mobilization, availability, and transport. The percentage of heavy metals associated with different fractions occurred in the following order (Figure 3):

Cr: residual > Fe/Mn oxide > organic matter/sulfide > exchangeable with carbonate fraction.

Ni: residual > Fe/Mn oxide > exchangeable with carbonate fraction > organic matter/sulfide.

As: residual > Fe/Mn oxide > organic matter/sulfide > exchangeable with carbonate fraction.

Cu: residual > organic matter/sulfide > Fe/Mn oxide > exchangeable with carbonate fraction.

Zn: Fe/Mn oxide > residual > exchangeable with carbonate fraction > organic matter/sulfide.

Pb: Fe/Mn oxide > residual > organic matter/sulfide > exchangeable with carbonate fraction.

Co: Fe/Mn oxide > residual > exchangeable with carbonate fraction > organic matter/sulfide.

Cd: exchangeable with carbonate fraction > Fe/Mn oxide > residual > organic matter/sulfide.

Mn: exchangeable with carbonate fraction > Fe/Mn oxide > residual > organic matter/sulfide.

The results of the distribution patterns of the eight metals indicated that for Cr, Ni, As, and Cu, the residual fraction was dominant in most of the samples, constituting 45.85% - 85.27%, 45.38% - 86.52%, 19.83% - 72.37%, and 66.38% - 75.64% of their total concentrations, respectively. Some studies demonstrated

Figure 3. Proportion of different fractions in the sediments.

that the residual fractions with higher proportions would be generally regarded as relatively stable, difficult to be absorbed, and utilized by organisms [23] [24] [25] . For Zn, Co, and Pb, the Fe/Mn oxide fraction exhibited the largest proportion, constituting 17.00% - 61.08%, 35.94% - 51.27%, and 11.80% - 70.96%, respectively. They could form stable complexes with Fe or Mn oxides [1] . In the Fe/Mn oxide fraction, heavy metals were adsorbed or co-precipitated in the sediments, and could be mobilized or transferred into aquatic organisms in hypoxic environments [26] ; therefore, the fraction of Fe/Mn oxides could be considered as a potential source of heavy metals in the river sediment. The highest proportion with exchangeable and carbonate fractions existed in Cd and Mn, with Cd (16.93% - 65.48%) and Mn (27.74% - 62.69%), respectively. In the exchangeable fraction and carbonate fraction, heavy metals were weakly attached to the sediments by precipitation or co-precipitation. When the ionic composition or pH changed, they could be released easily into water, which was consistent with other studies [17] [27] .

In the sediments of the Pearl River networks, the proportion of Cd associated with exchangeable and carbonate fractions was the highest. The primary reason was attributable to the aquatic environment containing a high concentration of HCO 3 , which originated from the Karst area of the Pearl River upstream basin, and a large amount of calcium lime was used as a flocculant to adsorb and co-precipitate Cd during the cadmium pollution accident that occurred in the Beijiang River, owing to formed CdCO 3 in the neutral pH condition. The exchangeable and carbonate fractions of the sediments are more labile and readily leachable or bio-available, because the adsorbed heavy metal ions can be released into water when the concentration of the hydrogen ion increases in the water, in comparison with other fractions. Therefore, the concentration and accounted proportion of the exchangeable and carbonate fractions in the sediments can be directly related to the bioavailability, mobility, and environmental impact of the heavy metals [28] [29] . Based on the percentage of exchangeable with carbonate fractions to the total concentrations, the mobility of the heavy metals investigated in the sediments of the Pearl River networks were observed in the following order: Cd > Mn > Co > Zn > Ni > Cu > Pb > As > Cr. According to the results, for Cd and Mn, the fractions with the combination of exchangeable and carbonate were found to be predominant in most samples, and could be released gradually from the sediment into the water and organisms.

3.3. Risk Assessment of Heavy Metals in the Sediments

3.3.1. Risk Assessment Code (RAC)

The results indicated that the RAC values for Cr and As mobilization ranged from 0.41 to 6.69 and from 0.33 to 4.68 respectively, corresponding to “no risk” or “low risk” in all sites. The RAC values of Cu, Pb, Co, Zn, and Mn ranged from 2.11 to 22.12, 0.05 to 39.29, 13.54 to 39.56, 6.27 to 21.09, and 27.74 to 62.69, respectively (Figure 4(a), Figure 4(b)). Furthermore, 28.5% of sampling sites (Cu), 71.4% of sampling sites (Zn), and 90% of sampling sites (Mn) exhibited

Figure 4. Ecological risk assessment (RAC values calculated for all sediment samples). (a) Distribution of sampling sites; (b) Comparison with heavy metals; (c) EFc values of sediments from different sampling sites; (d) EFc values by comparing with heavy metals.

“medium risk”. For Pb mobilization, some samples showed “high risk”, but the majority sites were “no risk” or “low risk”. The RAC of Cd varied from 16.93 to 65.4, and over 76.71% of the sampling sites were “extremely high risk”. The results indicated that the toxic metals of Zn and Cd would be more abundant and bio-available than the other metals. The spiking sites were distributed in the midstream reaches, especially in sampling sites N2 to N7 along the river.

3.3.2. Enrichment Factor (EFc)

The contamination of heavy metals in sediments was considered to be derived from human activities and the natural weather; however, it was difficult to obtain the full information to distinguish the pollutant sources by a typical analysis and a comparison to the polluted level. Many studies have highlighted that heavy metals in the sediments coming from natural sources exhibit a higher correlation compared to the background value and reference elements than from anthropogenic sources; therefore, the metal to metal relative ratios were widely used because it could better assess and distinguish their polluted sources [21] [30] . The application of enrichment factors indicated that the ratio ranges of Cr, Co, and Ni were 0.70 - 2.74, 0.32 - 0.81, and 0.26 - 1.91, respectively (Figure 4(c), Figure 4(d)), with mean values 0.93, 0.47, and 0.82, respectively. Most of the samples were classified as “no contamination”, which confirmed that the metals primarily came from natural sources. The ratio ranges of Mn and As were 1.06 - 3.60 and 0.94 - 17.46, with mean values 1.64 and 1.56, respectively, corresponding to the “low contamination or minor enrichment” category for the EFc values, except for Mn in sites of N2 (3.60), N5 (2.62), and N7 (2.99), and As in sites of U1 (2.5), N4 (3.27), N5 (2.45), and N7 (17.43). The EFC values of Cu, Zn and Pb ranged from 1.31 to 7.83 (mean, 2.12), 1.81 to 14.32 (mean, 3.33), and 1.83 to 21.90 (mean, 4.94). For 61.9% of Cu, 90.4% of Zn, and 95.2% of Pb, the category of EFc values was “moderately contaminated or moderate enrichment.” The primary polluted sites are distribution midstream reaches, especially (N2, N4, N5, N6 and N7); thus, it can be concluded that different degrees of anthropogenic contamination occurred. For Cd, “significantly contaminated” was found in most of the sites; the ratios exceeded as high as 17.49 to 351.45 times with the natural background level, indicating the obvious enrichment and anthropogenic sources. The distribution of Cd in the midstream sites was significantly higher, such as N7 (351.45), N6 (87.26), and N5 (78.74), than that of most sites in the estuary and upstream; the results are consistent with those of Cu, Zn, and Pb.

3.3.3. Potential Ecological Risk Assessment

The assessment indexes, including the single potential ecological risk index, comprehensive potential ecological risk index, and grading standard were calculated using the formula with the evaluation of the potential ecological risks of Cr, Ni, Zn, Cu, Pb, and Cd in sediments. The results indicated that the descending order of the single-pollutant ecological risk grade ( E r i , average values) of the heavy metals was as follows: Cd (399.09) > Pb (36.59) > Cu (16.48) > Ni (15.66) > Zn (5.10) > Cr (2.42), and the average contribution rate of each metal to the comprehensive potential ecological risk index (RI) was 84% for Cd, 7.7% for Pd, 3.5% for Cu, 3.3% for Ni, 1.1% for Zn, 1.1% for Zn, and 1.0% for Cr, which revealed that Cd was the primary metal contributing to the sediment toxicity (Table 2).

Table 2. Evaluation of potential risk index of heavy metal in the sediments of Pearl River networks.

Note: “a” E r i < 40, Low risk; “b” 40 ≤ E r i < 80, Moderate risk; “c” 80 ≤ E r i < 160, considerable ecological risk; “d” 160 ≤ E r i < 320, High ecological risk; “e” E r i ≥ 320, Very high ecological risk. “A” RI < 95, Low potential ecological risk; “B” 95 ≤ RI < 190, Moderate potential ecological risk; “C” 190 ≤ RI < 380, Considerable potential ecological risk; “D” RI ≥ 380, Very high potential ecological risk.

The RI value in the sediments ranged from 167.7 to 2481.6, with an average of 475.3, 57% of the sampling sites exhibited “very high ecological risk”. Particularly, N6 (596.2), N7 (2481.6), and S5 (763.4) exhibited the higher potential ecological risk and disperse distribution characteristics. Furthermore, they were all located in the major area of the Pearl River delta around developed processing industries, a highly dense population, and a large number of electronics.

4. Conclusion

The mobility of heavy metals in sediments of the Pearl River networks was indicated as the decreasing order: Cd > Mn > Co > Zn > Ni > Cu > Pb > As > Cr. Cd and Mn showed the higher mobility and bioavailability than the other heavy metals. The enrichment factor demonstrated that most of the samples of Cr, Co, and Ni were classified under “no contamination”, which confirmed that the metal primarily originated from natural sources. The evaluation results indicated that Cu, Zn, Pb, and Cd with peaking sites at N7, owing to the high density of population and industrial distribution. Among the heavy metals, Cd was the primary metal contributing to the sediment toxicity; the average contribution rate to the comprehensive potential ecological risk index constituted 84% in the region, and required more attention.

Acknowledgements

This work was supported by the Special Fund for Agro-scientific Research in the Public Interest (No. 201503108), Science and Technology Planning Project of Guangzhou, China (No. 201604020029, 201804010494), Dedicated Fund for Promoting High-quality Marine Economic Development in Guangdong Province (GDOE-2019-A31), Guangdong Marine and Fishery Bureau Science and Technology Project (No. SDYY-2018-08; A201601B05) and China Innovation & Entrepreneurship Competition for Undergraduate (82619300, 82619225).

NOTES

#First authors; *Corresponding authors.

Conflicts of Interest

The authors declare no conflicts of interest regarding the publication of this paper.

Cite this paper

Zhao, J. , Xie, W. , Zhang, Q. , He, S. , Qin, Y. , Lu, S. , Zhang, S. and Ye, C. (2019) Spatial Distribution and Ecological Risk Assessment of Heavy Metals in Sediments from Pearl River Networks, South China. Open Access Library Journal, 6, 1-5. doi: 10.4236/oalib.1105709.

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