<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JEP</journal-id><journal-title-group><journal-title>Journal of Environmental Protection</journal-title></journal-title-group><issn pub-type="epub">2152-2197</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jep.2013.41010</article-id><article-id pub-id-type="publisher-id">JEP-27328</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Earth&amp;Environmental Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Heavy Metal Pollution of Topsoil in the Vicinity of an Industrial Estate Co-Located with a Housing Estate in Southwestern Nigeria
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>ffiong</surname><given-names>Ukorebi Etim</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Percy</surname><given-names>Chuks Onianwa</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Chemistry, University of Ibadan, Ibadan, Nigeria.</addr-line></aff><aff id="aff1"><addr-line>Department of Chemistry, University of Ibadan, Ibadan, Nigeria</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>etim242@yahoo.com(FUE)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>25</day><month>01</month><year>2013</year></pub-date><volume>04</volume><issue>01</issue><fpage>91</fpage><lpage>98</lpage><history><date date-type="received"><day>October</day>	<month>3rd,</month>	<year>2012</year></date><date date-type="rev-recd"><day>November</day>	<month>3rd,</month>	<year>2012</year>	</date><date date-type="accepted"><day>December</day>	<month>2nd,</month>	<year>2012</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   Heavy metals were determined in topsoils around a major industrial estate co-located with a housing estate in the southwestern region of Nigerian. Samples were collected on three-monthly basis for 18 months, from the industrial waste dumpsites, industrial area, residential area, around an effluent channel, outskirts of the estate and control sites. Average levels of Cu (2850 &#177; 3340 mg/kg), Pb (768 &#177; 450 mg/kg) and Ni (105 &#177; 30 mg/kg) at the dumpsites were significantly higher than other locations. At the industrial area and effluent channels, Pb and Cr levels were slightly elevated compared with other metals. Metal levels at the residential area and outskirts of the estate were about the levels in the control. Generally, the degree of contamination within the vicinity of the estate was of the order Cu&gt;Pb&gt;Ni&gt;Cd&gt;Co&gt;Cr. Average total bioavailable (non-residual) fraction of the metals consisted of 52.0% of the metal load, with this fraction for Cd and Pb being 73.9% and 60.7% respectively. Topsoils around the dumpsite were evidently polluted with high levels of copper and lead. Seepage of leachate from the dumpsite has the potential of contaminating ground water reserves. Improper disposal of industrial solid wastes appears to be the likely source of metal pollution in the industrial estate. Heavy metal pollution in the estate can therefore be significantly reduced by prompt and proper disposal of generated solid wastes, and the application of particulate scrubbers in the industries. 
 
</p></abstract><kwd-group><kwd>Heavy Metal; Soil Contamination; Industrial Estate; Industrial Waste Dumpsite</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The mobilization of heavy metals into the biosphere through industrial activities is an important process in the geochemical cycling of metals. This is very evident in urban areas where various industrial sources release large quantities of heavy metals into the atmosphere and soil [1-5]. Some of the pathways of these metals into the soil are via dustfall [6-9], fly ash [<xref ref-type="bibr" rid="scirp.27328-ref10">10</xref>], slag and sludge [<xref ref-type="bibr" rid="scirp.27328-ref11">11</xref>] and solid waste. Several researchers have indicated the need for a better understanding of urban soil pollution [12-14] in relation to industrial activities. Similarly, more research has focused on heavy metals in urban soils around industrial sites [15-17]. Soil contamination by heavy metals has been shown to inhibit soil microbial activities [18,19], in turn reducing soil fertility and inhibiting the germination of certain seed plants [3,20]. Heavy metals contamination may also produce nutrient imbalance in plants with adverse effect on the synthesis and functioning of many biologically active compounds [<xref ref-type="bibr" rid="scirp.27328-ref21">21</xref>]. Subsequent accumulation of the metals in the food chain [3,22] is detrimental to human health.</p><p>Despite growing rates of industrialization, many developing third world countries pay too little attention to environmental issues. This is evident in the location of many industrial facilities near residential areas and the non-availability of adequate regulatory and enforcement measures to guard against pollution. One of such industrial facilities co-located with residential areas is the Ota Industrial/Housing Estate in the southwestern region of Nigeria (<xref ref-type="fig" rid="fig1">Figure 1</xref>). There are thirty nine different factories within the estate dealing with a wide range of products that include chemicals, pharmaceuticals, plastics, paper and pulp, and metals/steel. A third of these industries which represents the primary industrial types are metal-based industries, producing either iron rods, steel or galvanized pipes and sheets. Co-located with these industrial types at very close proximity are low cost residential houses. Emissions of particulates into the atmosphere, and improper disposal of solid wastes are common practices within the estate. This paper investigates the spatial and temporal patterns of heavy metal concentrations in topsoil, and estimates the degree of</p><p>pollution, using the accumulation factor (AF) values.</p></sec><sec id="s2"><title>2. Methodology</title><sec id="s2_1"><title>2.1. Description of Study Locations</title><p>The Ota industrial/housing estate, located on latitude 6˚32'N and longitude 2˚57'E, is sited on a 22.8 km<sup>2</sup> expanse of land in tropical southwestern region of Nigeria (<xref ref-type="fig" rid="fig1">Figure 1</xref>). It is characterized by high humidity with annual rainfall of 128 - 350 cm. The geology within this area is the coastal plain sedimentary formation characterized by sand, clay and silt [<xref ref-type="bibr" rid="scirp.27328-ref23">23</xref>]. The estate consists of two separated co-located segments; the industrial and residential areas. The distance separating the two segments is just about 20 m. The residential area which lies to the east of the estate occupy about one third of the total estate land space. A few thousands inhabitants reside in the residential area of the estate. Waste management in the estate is poor and untreated effluent is often discharge into poorly constructed channels that empty into a local stream. Solid waste piles litter the vicinities of the factories, and most of the factories have no emission control gadgets installed.</p></sec><sec id="s2_2"><title>2.2. Sampling</title><p>Topsoils were sampled from three core industrial areas (SL-IND), three residential areas (SL-RSD), beside two liquid effluent channels (SL-EFL) and two refuse dumpsites (SL-REF). Two other locations were on the outskirt of the estate (SL-OST) where there were no waste dumps. Control samples were obtained from other residential areas located about 1 km from the industrial estate and not affected by industrial activities. Field sampling and analysis were conducted on a quarterly basis for a period of 18 months. Each sample was obtained by compositing surrounding topsoil into a polythene bag with the aid of a plastic scooping trowel.</p></sec><sec id="s2_3"><title>2.3. Sample Processing and Analytical</title><p>The soils were air-dried in a clean room in the laboratory and then passed through a 2 mm mesh sieve. Soil pH was determined by the electrometric method using a 1:1 soilwater mixture [<xref ref-type="bibr" rid="scirp.27328-ref24">24</xref>]. The hydrometer method was used for measuring soil granulometric properties (sand, silt and clay), while the classical redox back-titrimetry procedure was used to determine soil organic matter content. For metal analysis, about 5.0 gram of dried soil was extracted with 50.0 ml of 2 M HNO<sub>3</sub> in a covered glass bottle placed in a boiling water bath for 2 hours with shaking at intervals of 15 minutes, and subsequent filtration for metal analysis. This extraction method has been established to yield results for the ecologically significant fraction of the soil metal content [<xref ref-type="bibr" rid="scirp.27328-ref25">25</xref>]. A blank sample was incorporated for every batch of twenty soil samples processed. The filtrates were analyzed for lead, cadmium, chromium, cobalt, copper and nickel using an atomic absorption spectrophotometer (Buck Scientific, model 200A). Commercial BDH stock standards were used for instrument calibration. Speciation of metal contents was carried out by the sequential extraction scheme of Tessier et al. [<xref ref-type="bibr" rid="scirp.27328-ref26">26</xref>] applied to ten selected samples. The exchangeable fraction was extracted with magnesium chloride solution at pH 7.0, while carbonate fraction was extracted by leaching with 1M sodium acetate which had been adjusted to pH 5.0 with acetic acid. Reducible fraction was extracted with 0.04M NH<sub>2</sub>OH&#215;HCl in 25% (v/v) acetic acid. Oxidizable fraction was determined by treatment of sample with 30% H<sub>2</sub>O<sub>2</sub> adjusted to pH 2.0 with HNO<sub>3, </sub>while residual fraction was digested with a 2:1 mixture of concentrated hydrofluoric and perchloric acids. Reagent blanks were prepared and analysed for each extraction. Extracts were subsequently analysed for metals by atomic absorption spectrophotometry. A recovery study was carried out by spiking portions of five previously analyzed samples with standards of lead, chromium, copper, cobalt and nickel. These were then dried, homogenized and passed through the extraction and analytical steps. Mean percentage recoveries obtained were: Ni: 81.5% &#177; 19.8%, Cr: 100% &#177; 7%, Cu: 96.6% &#177; 7.3%, Pb: 100% &#177; 23% and Co: 96.1% &#177; 9.0%.</p></sec><sec id="s2_4"><title>2.4. Data Treatment</title><p>Accumulation factor (AF) for each metal at each location was calculated to determine the degree of contamination at the sampling locations. This is the ratio of average metal concentration at any one sampling location to the concentration at the control point. The AF is a good index for assessing soil environmental quality [27-31]. In addition, analysis of variance (p = 0.05) was conducted to establish statistical relationships among metal concentrations at different sampling locations.</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><p>Metal concentrations in topsoil of the industrial estate are shown in <xref ref-type="table" rid="table1">Table 1</xref>. Average Cu (2850 &#177; 3340 mg/kg), Pb (768 &#177; 450 mg/kg) and Ni (105 &#177; 30 mg/kg) levels in dumpsite samples were significantly higher than the corresponding values around the industrial area, residential area, outskirt of the estate and beside the effluent channels (Tables 1 and 2, <xref ref-type="fig" rid="fig2">Figure 2</xref>). The industrial area and effluent channels recorded higher levels of Pb and Cr than other metals. Average levels of Pb, Cu, Cd, Cr, Co and Ni in the residential areas and the outskirt of the estate were about the same levels as in the control sites (<xref ref-type="table" rid="table2">Table 2</xref>, <xref ref-type="fig" rid="fig2">Figure 2</xref>). <xref ref-type="table" rid="table3">Table 3</xref> shows results for the soil pH, organic matter and granulometric fractions. These are important for understanding the potential for translocation of contaminants within the soils of the study area. On the average, slightly acidic pH conditions exist in the topsoils, while the textural properties showed the soil to be mostly sandy. The average soil organic carbon is relatively low. These characteristics will enhance metal mobility in the soil with the associated risk of pollutants migrating into ground water reserve, and being bioavailable to plants. Analysis of variance (p = 0.05) showed no significant seasonal variation in metal levels in the topsoil (<xref ref-type="table" rid="table4">Table 4</xref>). However, Cu levels at the dumpsite were slightly higher in the dry season.</p><p><xref ref-type="table" rid="table5">Table 5</xref> shows the accumulation factors of the metals in the topsoil. The dumpsite showed a high degree of contamination with AF values of 322, 66.2 and 17.2 for Cu, Pb and Ni respectively. The degrees of pollution re-</p><p><xref ref-type="table" rid="table1">Table 1</xref>. Metal concentrations (mg/kg) in topsoil of the industrial estate.</p><disp-formula id="scirp.27328-formula18567"><graphic  xlink:href="10-6701672\9884bca5-557c-4b9c-ab08-3e094c8e20df.jpg"  xlink:type="simple"/></disp-formula><p><sup>*</sup>SL-IND—industrial area, SL-RSD—residential area, SL-OST—outskirt of the estate, SL-EFL—beside effluent channels, SL-REF—dumpsite, SL-CTR— control. See <xref ref-type="fig" rid="fig1">Figure 1</xref>. <sup>**</sup>Mean &#177; Standard Deviation (Range).</p><p><xref ref-type="table" rid="table2">Table 2</xref>. Summary of average metal concentrations (mg/kg) in topsoil of the industrial estate.</p><p><img src="10-6701672\f14d6c5b-f4a0-4bd8-ac4d-55603251bdee.jpg" /></p><p><xref ref-type="table" rid="table3">Table 3</xref>. pH, granulometric fractions and organic matter contents of the soils.</p><disp-formula id="scirp.27328-formula18568"><graphic  xlink:href="10-6701672\4c2dbd38-318b-4aed-87e3-aad8eabf0f6c.jpg"  xlink:type="simple"/></disp-formula><p><sup>*</sup>SL-IND—industrial area, SL-RSD—residential area, SL-OST—outskirt of the estate, SL-EFL—beside effluent channels, SL-REF—dumpsite, SL-CTR— control. <sup>**</sup>Mean &#177; Standard Deviation (Range).</p><p><xref ref-type="table" rid="table4">Table 4</xref>. Average seasonal metal concentrations (mg/kg) in topsoil of the industrial estate.</p><disp-formula id="scirp.27328-formula18569"><graphic  xlink:href="10-6701672\eaa9c862-3191-42f9-b129-773636da899e.jpg"  xlink:type="simple"/></disp-formula><p><sup>*</sup>SL-IND—industrial area, SL-RSD—residential area, SL-OST—outskirt of the estate, SL-EFL—beside effluent channels, SL-REF—dumpsite, SL-CTR— control.</p><p>corded here are much higher than previously observed at another industrial estate in the nearby city of Lagos where the corresponding AF values were 15.0, 28.1 and 13.1 [<xref ref-type="bibr" rid="scirp.27328-ref29">29</xref>]. In the vicinity of an auto-battery manufacturing industry in another nearby city of Ibadan, only Pb showed a significant factor of accumulation of 175 [<xref ref-type="bibr" rid="scirp.27328-ref32">32</xref>]. Generally, the degree of contamination within the vicinity of the estate was of the order Cu &gt; Pb &gt; Ni &gt; Cd &gt; Co &gt; Cr (<xref ref-type="table" rid="table5">Table 5</xref>).</p><p><xref ref-type="table" rid="table6">Table 6</xref> shows the results of the speciation study. Average bioavailable (non-residual) fraction was: Pb-60.7%, Cd: 73.9%, Cr: 32.4%, Cu: 47.8%, Co: 50.6% and Ni: 46.8%. The most mobile of the bioavailable phases, the exchangeable phase, was generally less than 8.0% with Cu having the lowest value of 0.02%. A greater proportion of Cr, Cu and Ni (&gt;50%) was in the residual phase. The proportion held in the carbonate-bound, reducible and oxidizable phases were generally higher than in the exchangeable phase. Environmental factors that tend to reduce soil pH will readily mobilize these fractions. Similarly, changes in soil redox potential and soil redox reaction will influence the release and retention of elements in these phases [<xref ref-type="bibr" rid="scirp.27328-ref33">33</xref>]. The low proportion of Cu in the exchangeable and reducible phases will reduce its bioavailability in the soil. The low proportion of residual and exchangeable Pb and Cd in the soil indicates a high affinity of these metals to complexation with organic and inorganic substances in soil Soil quality criteria have not yet been established for Nigeria. Metal levels obtained from this study are therefore compared with soil quality criteria for Canada [<xref ref-type="bibr" rid="scirp.27328-ref34">34</xref>], Norway [<xref ref-type="bibr" rid="scirp.27328-ref35">35</xref>], Netherland and Switzerland [35,36] (<xref ref-type="table" rid="table7">Table 7</xref>). These soil quality criteria address the important areas assessed by this study. The overall average Pb (199</p><p><xref ref-type="table" rid="table5">Table 5</xref>. Accumulation factors of metals in topsoil of the industrial estate.</p><p><img src="10-6701672\50536b05-0451-4a6f-9b49-1f0a85acfe9f.jpg" /></p><p><xref ref-type="table" rid="table6">Table 6</xref>. Average speciation (% in geochemical phases) of the metals.</p><p><img src="10-6701672\04bd4b9e-47c6-440a-ba0d-906d96e3d620.jpg" /></p><p><xref ref-type="table" rid="table7">Table 7</xref>. Soil quality criteria for some countries compared with level (mg/kg) obtained from this study.</p><p><img src="10-6701672\a34b57c9-850b-4d62-a69f-2c5cede6c13f.jpg" /></p><p>mg/kg) and Cu (589 mg/kg) levels in this study exceed the Norwegian and Swiss guide values. Average Pb, Cu, Cd, Cr and Ni in the residential and industrial areas of the study area in <xref ref-type="table" rid="table2">Table 2</xref> were within the Canadian soil limits for residential and industrial areas respectively. However, three sampling locations in the residential area had elevated Cr level and fifteen sampling locations in the industrial area had concentrations of Cr, Cu and Ni exceeding the Canadian soil standards. The dumpsite area recorded average Pb and Cu levels above the Netherlands action level.</p><p>Average metal levels in this study were compared to those obtained in other areas with similar industrial activities. Average Pb level (199 mg/kg) in this study is higher than the 102 mg/kg reported for soils of the Upper Silesia industrial environment in South Poland [<xref ref-type="bibr" rid="scirp.27328-ref37">37</xref>], 172 mg/kg in contaminated soil in Albania [<xref ref-type="bibr" rid="scirp.27328-ref1">1</xref>] and 170 mg/kg in the greater Sofia industrial region of Bulgaria [<xref ref-type="bibr" rid="scirp.27328-ref4">4</xref>]. However, the level was below 552 mg/kg reported for the surrounding of a smelter at Copsa-Mica in central Romania [<xref ref-type="bibr" rid="scirp.27328-ref38">38</xref>], 293 mg/kg in the Pali industrial development area of Rajasthan, India and 2000 mg/kg in the vicinity of a lead-battery factory in Ibadan, Nigeria [<xref ref-type="bibr" rid="scirp.27328-ref32">32</xref>]. Average levels of Cu (589 mg/kg), Cd (3.52 mg/kg), and Co (17.6 mg/kg) in the study are much lower than the corresponding 1107 mg/kg, 3865 mg/kg, and 14 mg/kg obtained in contaminated soil in Albania [<xref ref-type="bibr" rid="scirp.27328-ref1">1</xref>].</p><p>The study reveals that heavy metal pollution of topsoil is significant in the industrial estate. It also points to wastedumping as the most important source of the contamination. The soil characteristics may enhance migration of the metal contaminants into ground water, although the exchangeable fraction is limited. Preventive and remediation actions may be required to reduce present levels of contamination to within safe limits. Such actions must focus on the identified dumpsite point sources, in addition to other measures. This may be managed by prompt and proper disposal of solid wastes, installation of particulate scrubbers, and regular monitoring of soil quality to comply with regulatory standards.</p></sec><sec id="s4"><title>REFERENCES</title></sec><sec id="s5"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.27328-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">S. Shallar, C. Schwartz, A. Hasko and J. L. Morel, “Heavy Metals in Soils and Plants of Serpentine and Industrial Sites of Albania,” Science of the Total Environment, Vol. 209, No. 2-3, 1998, pp. 133-142.</mixed-citation></ref><ref id="scirp.27328-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">C. Bilos, J. C. Colombo, C. 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