SCITECH - Assessment of Heavy Metal Pollution in a Gold Mining Site in Southwestern Nigeria - Journal of Genetics and Cell Biology (ISSN:2639-3360)

Author Guidelines

Indexing Completed

Research Article

Assessment of Heavy Metal Pollution in a Gold Mining Site in Southwestern Nigeria

Abiya SE, Odiyi BO, Ologundudu FA*, Akinnifesi OJ and Akadiri S

Corresponding Author: Department of Biology, Federal University of Technology, Akure

Received: September 18, 2018; Revised: December 25, 2018; Accepted: October 04, 2018

Citation: Abiya SE, Odiyi BO, Ologundudu FA, Akinnifesi OJ & Akadiri S. (2018) Assessment of Heavy Metal Pollution in a Gold Mining Site in Southwestern Nigeria. J Genet Cell Biol, 1(2): 30-35.

Copyrights: ©2018 Abiya SE, Odiyi BO, Ologundudu FA, Akinnifesi OJ & Akadiri S. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

2843
Views & Citations
1843
Likes & Shares

Abstract
Full Text
References
Tables
Images
PDF
Statistics

The unwanted release of environmental contaminants predisposed by mining activities had reached an alarming proportion that deserves attention. Hence, the purpose of this study was to determine the degree of heavy metal contamination which soil and plants were exposed to in Ijana gold mining site, southwestern Nigeria. To this, Zinc, Arsenic, Cadmium, Lead, Nickel, Chromium and Copper concentrations were measured using Atomic Absorption Spectrometry. Obtained values were used to evaluate the degree of soil pollution and plant contamination using physicochemical analysis, bioaccumulation factor and translocation factor of metals into plant in surrounding mine site. Zinc and Lead show a slightly higher presence than other metals tested. Mean concentrations of Zn (0.70 mg/kg), As (0.09 mg/kg), Cd (0.13 mg/kg), Pb (0.216 kg/mg), Ni (0.08 mg/kg), Cr (0.148 mg/kg), Cu (0.629 mg/kg) in soils around the mining area were considerably the same with the concentration of metal accumulated in plant, respectively. All metal tested showed minimal accumulation in plants. Translocation factor also implicated Zn to be the highest among all the heavy metals analyzed.

Keywords: Bioaccumulation, Translocation, Pollution, Tailings

INTRODUCTION

Amongst many anthropogenic activities, mining has been identified with the potential of impacting negatively on the quality of the environment [1,2]. Mining causes the destruction of natural ecosystems by altering soil, vegetative covers and covering of organisms beneath excavation sites. Aside the physical habitat destruction with accompanying the loss of biodiversity resources, the accumulation of pollutants in different media have been recorded around mining sites [3]. Therefore, mining sites portend great toxicological challenges for the surrounding ecosystems and on human health [4]. Like any exploitative activity, the excavation of mineral resources produces negative impacts upon the hydrospheric, atmospheric and lithospheric components of the environment [5-7].

In gold mining, like many metallurgical extractions, crystallographic bonds are broken in the ore mineral in order to recover the desired element or compound [8]. During gold mining, large quantities of waste are produced. Over 99% of extracted ore in gold mining are released into the surrounding environment as waste [9]. One of the wastes that have been implicated around mining sites is heavy metals. Heavy metals have received global attention of researchers, owing to their deleterious effects on plants, especially those on vegetative and generative plant parts. [10]. Due to variations in the physical and chemical properties of soil, heavy metals in tailings can be translocated and accumulated in plants and animals.

Even in low concentration, heavy metals can persist in soil from and can enter into food chain through plant uptake [1]. Some heavy metals like Lead, Arsenic, Mercury, Canadium, are not essential for plants growth, since they are not known to perform any physiological function in plants. Other metals like, Iron, Copper, Nickel Manganese, Cobalt, Molybdenum, and Zinc are essential elements required for normal plant growth and metabolism, but when they are above desired concentrations, could constitute poisoning to individual plants [11,12]. Among all the heavy metals, cadmium (Cd) is a highly toxic metal for both the plants and animals as well as for human beings. Cadmium enters into soil-plant environment mainly through anthropogenic activities. Elevated Pb in soils may decrease soil productivity and if in very low concentrations, Pb may also inhibit some important plant processes i.e. photosynthesis, mitosis, water absorption and vegetative growth [13]. Studies have also shown the genotoxic effect of chromium on cells. Cr (VI) has been found to 100 times more toxic and 1000 times more mutagenic and carcinogenic compared to Cr (III). Heavy metals also exert toxic effects on soil microorganism hence results in the change of the diversity, population size and overall activity of the soil microbial communities [14].

In order to evaluate the damages that gold mining activities exert on the environment, especially in areas in which crude methods of mining is still largely used, there lies the need to assess the extents of pollution. These must be based on studies about waste properties, heavy metals content and theirs relation to soil and plant. Hence, the objective of this study is to (i) Determine the physicochemical properties of soil from Ijana goldmine. (ii) Determine the concentration of heavy metals found in soils and plants at the goldmine and (iii) Compare the result of the physicochemical properties of the soil and heavy metal concentration in plants and soils at Ijana goldmine with that of a control site.

MATERIALS AND METHODS

Sampling location

The study was conducted in a gold mining site in Ilesha, Osun state. The site is located at Ijana of Atakunmosa west local government in Osun state. Mining site is on Latitude 7.573°N and longitude 4.678°E and the control site on Latitude 7.578°N and longitude 4.679°E.

Soil and plant samples pre-treatment

Soil and Plant samples were randomly collected at Ijana goldmine site. Control samples were taken at a site a few kilometers away from the mine site. The control sites have no record of mining activities and also have limited human interference. Three soil samples were collected at the surface (0-15 cm) and subsurface (15-30 cm) respectively using a hand trowel and meter rule at both mine and control sites. Plant samples (Chromolena odorata) which was common to both the mine and control sites were carefully uprooted ensuring that the roots remained intact. Both the soil and plant samples were correctly labeled and bagged before taking to the laboratory for analysis. Each soil sample was air-dried for 7 days and sieved to <2 mm prior to analysis. for physico-chemical properties including pH, potassium (K), calcium (Ca), magnesium (Mg), sodium (Na), CaCO₃, organic matter, total organic, heavy metals. Total K, Ca, Na and Mg concentrations were determined using flame emission after digestion of the composite samples with boiling 2 M HNO₃ for 2 h. Porosity and Bulk density, Organic matter contents and other soil and plant analyses were tested using standard methods.

Soil and the plant analyses

The pH and conductivity of soil and plant material were carried out using standard methods as described by Tahar and Keltoum [15]. The porosity and bulk density of soil samples in mining site and control site were tested using the methods of Danielson and Sutherland [16]. Calcium and magnesium (exchangeable bases) content of soil were assayed following standard methods. The organic composition of the soil was tested using the Walkley-Black Wet oxidation method [17]. The cation exchange capacity was determined using the ammonium saturation method.

Bioaccumulation factor of metal concentrations in the receiving plant shoot and were evaluated with concentration in the soil under standard methods of Radulescu et al. [18] and the formula is shown below.

Also the concentrations of metal translocated from root to shoot of the plant around tested site were determined according to the method of Baker and Brooks [19] and the formula is shown below:

Bioaccumualtion Factor (BAF)=metal content in plant shoot (mg/kg) / metal content in soil (mg/kg)

Also the concentrations of metal translocated from root to shoot of the plant around tested site were determined according to the method of Baker and Brooks [19] and the formula is shown below:

TF=concentration of metals (mg/kg) in the receiving level (shoot) / concentration of metals (mg/kg) in the source level (shoot)

METAL ANALYSIS

The metal analyses of samples (Ni, Cd, As, Cu, Zn, Pb and Cr) were carried out by using an Atomic Absorption Spectrophotometer (AAS).

RESULTS AND DISCUSSION

The result of the study carried out on both soil and plants are presented in Table 1.

Soil physico-chemical properties

For the soil physico-chemical properties, the pH of both the mining and control sites for surface (0-15 cm deep) and subsurface (15-30 cm deep) level are approximately neutral and within minimum acceptable limits. However, the pH of the mine site soil at 0-15 cm was found to be slightly acidic (5.91) than the control (6.85). Also soil sample at the subsurface (15-30 cm) level were generally less acidic (Table 1). Effects of such decrease in soil pH is reported to result in an increase in heavy metal absorption by plants due to dissolution of metal carbonate complexes releasing metals into solution during the rainy season [20].

In the mine soils, soil conductivity was found to be higher than the control soils both at the surface and subsurface levels. At 0-15 cm (surface layer), the mining site gives a mean value of 574 as against the control site 142. At the sub-surface layer, the mining site gives a mean value of 1180.33 against the control site 135.33 (Table 1). Conductivity at the control site falls within [21] permissible limit of 16-175, that of mine site far exceeds this limit. Conductivity at the mine site was found to be significantly different when compared to that of the control at the surface level (0-15 cm). This is probably due to the release of ions which ordinarily will be bound to rocks but are broken down and washed off during the gold mining process. These results conform to the findings by Bjuhr [22] in his studies of mine soils.

The mean value for the bulk density of the soil surface level of the mining site was found to be 1.41 and control 1.21 while the bulk density of the soil sub-surface level of the mining site was found to be 1.32 and control 1.21. With respect to physicochemical analyses carried, only bulk density and calcium has significant difference across the two surface levels.

Heavy metals concentration in soil

The highest levels of Zn, Cd, Pb and Cu were found in the soil from mine site (Table 2). The levels of Zn were lower than the range expected in contaminated soils, i.e., 20-300 mg/kg. The levels of Ni found in the soil samples were also below the normal range of 1-110 mg/kg reported for uncontaminated soils. For both surface and subsurface soil in the mine and control sites, arsenic was found to be the element with the least concentration. The concentrations of all metal recorded in the two surfaces are not too different from one another. Soil samples collected top surface (0-15 cm deep) had slightly lower levels of Pb than the normal than the sub-surface (15-30 cm deep). The copper, chromium and arsenic concentrations were, however, lower than the values reported for typical uncontaminated soil. This result conforms to the findings of Tahar and Keltoum [15]. A high contamination of the soil with metal could elicit deleterious effects on microbial activities, Dai et al. [23] provoking a low organic matter mineralization needed for plant growth. The apparent increase of heavy metals concentration in mine site compared to the control site almost certainly confirms the mining waste as the potential source of soil contamination and their accumulation in plants. An increasing level of these metals presents the site as potentially hazardous and could alter food chain and biological life in the environment.

Heavy metal concentrations in plant

In the present study, the results obtained showed that heavy metal (Zn, As, Cd, Pb, Ni, Cr and Cu) concentrations varied in the plants parts. In both the root and shoot, the concentrations of heavy metals were found to be higher in the mine site than the control site (Table 3). Of all the level of heavy metal concentrations, Zinc and Lead shows to be significantly higher in the mine site when compared to the control.

Zinc as a natural soil element play essential functional and structural role in plant growth. It usually occurs in low concentrations and does not pose a toxicity problem for plants, but at higher concentration could pose some risk on plants [24,25]. In Table 3, the values of zinc in both root (1.205 mg/kg) and shoot (1.017 mg/kg), though higher in mine site than the control is much lower compared to environmental quality standard range of 100-400 mg/kg.

Reports from various studies have implicated lead accumulation in vegetative plant part declining with distance from possible contamination sites [26]. This is also noticed in the present study. The rate of deposition of lead on vegetative cover is about four times greater than on bare soil. In the present study the lead concentration recorded in the two plant parts was quite low compared environmental quality standard range of 50 mg/kg. Arsenic tested in plants is below the toxicity threshold for above ground tissues of 3-10 mg/kg.

Nickel play vital metabolic function in higher plants, the value of nickel in study root and shoot: was 0.079 and 0.088 mg/kg, respectively. These values of nickel were quite lower than environmentally acceptable standard of 1-5 mg/kg. [24].

Naturally without pollution, the copper concentration in soil is 20 ppm. In this study, Copper concentrations in plants species were not higher than the toxic values. The little concentration recorded might be due to the presence of copper in minerals which can be released only by very slow disintegration processes [18]. Cadmium is a non-essential nutrient, the value of Cd is recorded in both plant and shoot is equally low. Compared with the other metals cadmium is found to leach more in soil, with increased availability in plant [24]. It has also been found that cadmium pollution without co-contamination by zinc is rare [27]. Although all metals assayed were still within the permissible limit, the presence of metal tends to be higher in the root part than in the shoot. And also higher in the mine site than in the control.

Heavy metals translocation in plant

Translocation factor was calculated as the ratio of heavy-metal concentrations in plant shoot to those in the corresponding root. According to the previous research results [19], TF value should be below 1 (TF>1). This study shows the results of Translocation Factor (TF) of heavy metals from shoot to root.

From the result in Table 4, Zn was found to have the highest translocation factor in C. odorata at the mine site, followed by Cu. For both metals, the translocation factor is less than 1 (0.96 at the mine site against 0.72 at the control site and 0.95 for Cu at the mine site against 0.85 at the control site). This implies that the shoot of this plant hold these metals than others. Therefore, the order of uptake capability from shoot to root is Zn>Cu>Cd>Pb>As>Ni.

Heavy metal bioaccumulation in plant

Bioaccumulation factor (BAF), calculated as the ratio of heavy-metal concentrations in plant shoot to those in the corresponding soil. According to Gautam et al. [28], BAF value should be below 1. In this study only Zinc had a BAF>1, other metals are generally less than 1. This result indicates that the concentration of Zn in the plant shoot is higher than that in soil. Zinc has been confirmed to be easily absorbed by plants [29]. At the control site, none of the heavy metals had a bioaccumulation factor of more than 1. Copper was the highest at 0.67. Zn, As, Cd, Pb, Ni, Cr and Cu had bioaccumulation factor 0.01, 0.01, 0.17, 0.06, 0.14 and 0.67, respectively (Table 5).

CONCLUSION

The concentration levels of heavy of metals (Zn, As, Cd, Pb, Ni, Cr and Cu) in the soil and plants samples from Ijana mining site were generally low and found to be within the World Health Organization (WHO) permissible levels. This could probably be due to the fact that most mining operations in the site are low scale and artisanal in operation unlike other sites where mechanized mining techniques could predispose release of more pollutants and tailings. Therefore, the soils at Ijana at the time of this study doesn’t present significant contaminations, thus the soil environment around the mining field are yet to be impacted negatively by the mining activity. Increased mine expansion would also necessitate continued assessment for possible pollution around the mine site.

1. Donkor AK, Bonzongo JCJ, Nartey VK, Adotey DK (2005) Heavy metals in sediments of the gold mining impacted Pra River basin, Ghana, West Africa. Soil and Sediment Contamination 14: 479-503.

2. Acosta JA, Faz A, Martínez-Martínez S, Zornoza R, Carmona DM, et al. (2011) Multivariate statistical and GIS-based approach to evaluate heavy metals behavior in mine sites for future reclamation. J Geochem Explor 109: 8-17.

3. Getaneh W, Alemayehu T (2006) Metal contamination of the environment by placer and primary gold mining in the Adola region of southern Ethiopia, Environ Geol 50: 339-352.

4. Franco-Hernández MO, Vásquez-Murrieta MS, Patiño-Siciliano A, Dendooven L (2010) Heavy metals concentration in plants growing on mine tailings in Central Mexico. Bioresour Technol 101: 3864-3869.

5. Eisler R (2004) Arsenic hazards to humans, plants and animals from gold mining. Rev Environ Contam Toxicol 180: 133-165.

6. Franco-Hernández González I, Jordán MM, Sanfeliu T, Quiroz M, De La Fuente C (2007) Mineralogy and heavy metal content in sediments from Rio Gato, Carelmapu and Cucao, Southern Chile. Environ Geol 52: 1243-1251.

7. Franco-Hernández MO, Vásquez-Murrieta MS, Patiño-Siciliano A, Dendooven L (2010) Heavy metals concentration in plants growing on mine tailings in Central Mexico. Bioresour Technol 101: 3864-3869.

8. Lottermoser B (2007) Mine wastes: Characterization, treatment and environmental impacts. Springer: New York, NY, USA, pp: 1-290.

9. Adler R, Rascher JA (2007) Strategy for the management of acid mine drainage from gold mines in Gauteng. CSIR: Pretoria, South Africa.

10. Ekaterina A, Jeliazkova LE (2001) Heavy metals and seed germination in some medicinal and aromatic plants. Department of Plant and Soil Science, University of Massachusetts, Amherst, MA, USA.

11. Garrido S, Campo GMD, Esteller MV, Vaca R, Lugo J (2005) Heavy metals in soil treated with sewage sludge composting, their effect on yield and uptake of broad bean seeds (Vicia faba L.). Water, Air and Soil Pollution 166: 303-319.

12. Rascio N, Izzo FN (2011). Heavy metal hyper accumulating plants: How and why do they do it? And what makes them so interesting? Plant Sci 180: 169-181.

13. Bhattacharyya P, Chakrabarti K, Chakraborty A, Tripathy S, Powell MA (2008) Fractionation and bioavailability of Pb in municipal solid waste compost and Pb uptake by rice straw and grain under submerged condition in amended soil. Geosci J 12: 41-45.

14. Ashraf R, Ali TA (2007) Effect of heavy metals on soil microbial community and mung beans seed germination. Pak J Bot 39: 629-636.

15. Tahar K, Keltoum B (2011) Effects of heavy metals pollution in soil and plant in the industrial area west Algeria. J Korean Chem Soc 55: 1018-1023.

16. Danielson RE, Sutherland PL (1986) Porosity, in methods of soil analysis. Part 1. Physical and Mineralogical Methods, Agronomy Monograph no. 9. Soil Science Society of America, Madison, WI, USA, pp: 443-461.

17. Walkley A, Black IA (1934) An examination of Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Sci 37: 29-38.

18. Radulescu C, Stihi C, Barbes L, Chilian A, Chelarescu ED (2013) Studies concerning heavy metals accumulation of Carduus nutans L. and Taraxacum officinale as potential soil bioindicator species. Revista de Chimie 64: 754-760.

19. Baker AJM, Brooks RR (1989) Terrestrials higher plants which hyper accumulate metallic elements. A review of their distribution, ecology and phytochemistry. Biorecovery 1: 81-126.

20. Mapanda F, Mangwayana EN, Nyamongara JG, Giller KE (2004) The effects of long term irrigation using waste water on heavy metal contents of soil and vegetables in Harare, Zimbabwe. Agric Ecosyst Environ 107: 151-165.

21. WHO (1996) Permissible limits of heavy metals in soil and plants. Geneva: World Health Organization, Switzerland.

22. Bjuhr J (2007) Trace metals in soils irrigated with waste water in a peri-urban area downstream Hanoi city, Vietnam. SLU.

23. Dai J, Becquer T, Rouiller JH, Reversat G, Reversat FB, Lavelle P (2004) Heavy metal accumulation by two earthworm species and its relationship to total and DTPA-extractable metals in soils. Soil Biol Biochem 36: 91-98.

24. Ahmad SS, Erum S (2010) Integrated assessment of heavy metals pollution along motorway M-2. Soil Environ 29: 110-116.

25. Paschke MW, Redente EF, Levy DB (2000) Environmental toxicity and chemistry. SETAC 19: 2751.

26. Little PE (1995) Environmental and medical services division. A. E. R. E., Didcot, Oxford Shire, UK.

27. Clemente R, Paredes C, Bernal MP (2007) A field experiment investigating the effects of olive husk and cow manure on heavy metal availability in a contaminated calcareous soil from Murcia (Spain). Agric Ecosyst Environ 118: 319-326.

28. Gautam P, Blaha U, Appel E (2005) Integration of magnetism and heavy metal chemistry of soils to quantify the environmental pollution in Kathmandu, Nepal. Island Arc 14: 424-435.

29. Mijovilovich A, Leitenmaier B, Meyer-Klaucke W, Kroneck PM, Gotz B, et al. (2009) Complexation and toxicity of copper in higher plants. II. Different mechanisms for copper versus cadmium detoxification in the copper-sensitive cadmium/zinc hyperaccumulator Thlaspi caerulescens (Ganges Ecotype). Plant Physiol 151: 715-731.

Table 1
Table 2
Table 3
Table 4
Table 5

Download PDF View PDF

QUICK LINKS

RELATED JOURNALS

Search

Newsletter signup

Index In

Easy Links

Journal Groups

Find Us