Organochlorine pesticide contamination of soils and dust from an urban environment in the Niger Delta of Nigeria.

The concentrations, sources, and risk of twenty organochlorine pesticides (OCPs) in soils and dusts from a typical urban setting in the Niger Delta of Nigeria were examined. The Σ20 OCP concentrations (ng g-1) varied from 4.49 to 150 with an average value of 32.6 for soil, 4.67 to 21.5 with an average of 11.7 for indoor dust, and 1.6 to 96.7 with an average value of 23.5 for outdoor dust. The Σ20 OCP concentrations in these media were in the order: soil > outdoor dust > indoor dust, which was in contrast with the order of the detection frequency, i.e., indoor dust (95 to 100 %) > soil (60 to 90 %) > outdoor dust (30 to 80 %). The concentrations of the different OCP classes in these media followed the order: aldrin + dieldrin + endrin and its isomers (Drins) > chlordanes > dichlorodiphenyltrichloroethane (DDTs) > hexachlorocyclohexane (HCHs) > endosulfans for outdoor dust and soil, while that of the indoor dust followed the order: Drins > chlordanes > endosulfans > DDTs > HCHs. The cancer risk values for human exposure to OCPs in these sites exceeded 10-6 which indicates possible carcinogenic risks. The sources of OCPs in these media reflected both past use and recent inputs.

Safety evaluation of organochlorine pesticides and polybrominated diphenyl ethers in imported canned fish in Nigeria.

Organochlorine pesticide (OCP) and polybrominated diphenyl ether (PBDE) concentrations were measured in thirty popular brands of imported canned fish (mackerel, sardines, and tuna) in Nigeria to ascertain potential threats to humans arising from their consumption. The Σ20 OCP concentrations in mackerel ranged from 0.47 to 7.36 ng g-1, while those of tuna and sardines varied from 1.06 to 2.19 and 0.11 to 12.7 ng g-1, respectively. The Σ39 PBDE concentrations in mackerel varied from 0.06 to 4.21 ng g-1, while those of tuna and sardines ranged from 0.19 to 3.18 and 0.04 to 8.26 ng g-1, respectively. The estimated daily intake (EDI) of OCPs and PBDEs from ingestion of the canned fish by adults and children were in the magnitude of 0.03 to 17.6 ng kg-1 bw day-1 and 9.9 × 10-3 to 11.5 ng kg-1 bw day-1 respectively. The hazard index (HI) and total cancer risk (TCR) values for OCPs and PBDEs from ingestion of the canned fish were less than 1 and 10-6, respectively. The dietary intakes of OCPs and PBDEs from these brands of canned fish by adults and children result in no adverse non-cancer and cancer risks.

Polybrominated diphenyl ether contamination in sediments from rivers in the western Niger Delta of Nigeria.

This study investigated the concentrations of 39 polybrominated diphenyl ether (PBDE) congeners in sediments from three rivers in the western Niger Delta of Nigeria that have been affected by pollution from urbanization and industrial activities. The Σ39 PBDE concentrations in sediments from these rivers ranged from 0.29 to 95.5, 5.15 to 121, and 0.73 to 66.1 ng g-1 for the Afiesere (AR), Edor (ER), and Okpare Rivers (OR), respectively. The homologue distribution patterns indicated the prominence of tetra- and penta-BDE congeners in sediments from these rivers. The ecological risk assessment results showed that the penta-BDEs were the primary source of risk to sediment-dwelling organisms in these rivers. However, the human health risk assessment indicated negligible risks for exposure of both adults and children to PBDEs in these sediments. The source apportionment suggests that the PBDE contamination in these river sediments was derived from long-distance migration, debromination of highly brominated congeners, and commercial penta-BDEs. These results reflect the use of penta-BDE formulations in this region rather than octa- and deca-BDE formulations.

Distribution, sources, and risk of polycyclic aromatic hydrocarbons in soils from rural communities around gas flaring points in the Niger Delta of Nigeria.

This study investigates the concentrations, sources, and ecological and human health risks resulting from exposure to polycyclic aromatic hydrocarbons (PAHs) in soils of rural communities around gas flaring points in Delta State, Nigeria. PAHs were extracted from these soil samples with hexane/dichloromethane by ultra-sonication and the extracts were cleaned on a silica gel/alumina-packed column. The PAH concentrations in the extracts were quantified by gas chromatography-mass spectrometry (GC-MS). The Σ16 PAH concentrations in soils from these communities varied from 2370-134 000, 461-389 000, and 2130-34 900 µg kg-1 for Emu-Ebendo (EME), Otu-Jeremi (OTJ) and Ebedei (EBD), respectively. The estimated lifetime carcinogenic risk values recorded in this study were above the acceptable limit of 10-6, indicating a high potential carcinogenic risk resulting from human exposure to PAHs in these soils. The isomeric ratio and principal component analysis results suggest that emissions from high-temperature combustion, potentially gas flaring, vehicular emissions, burning of wood/biomass, and fossil fuel combustion are responsible for the high concentrations of PAHs in soils of these rural communities. This study recommends implementing remediation and source control measures to minimise the impact of PAHs in the affected soils on humans and the environment.

Polycyclic aromatic hydrocarbons in dust from rural communities around gas flaring points in the Niger Delta of Nigeria: an exploration of spatial patterns, sources and possible risk.

Indoor and outdoor dust from three rural communities (Emu-Ebendo, EME, Otu-Jeremi, OTJ, and Ebedei, EBD) around gas flaring points, and a rural community (Ugono Abraka, UGA) without gas flare points, in the Niger Delta of Nigeria, was analysed for the concentrations and distribution of polycyclic aromatic hydrocarbons (PAHs), their sources, and possible health risk resulting from human exposure to PAHs in dust from these rural communities. The PAHs were extracted from the dust with a mixture of dichloromethane/n-hexane by ultrasonication, and purified on a silica gel/alumina packed column. Gas chromatography-mass spectrometry was employed to determine the identity and concentrations of PAHs in the cleaned extracts. The Σ16PAH concentrations in the indoor dust ranged from 558 to 167 000, 6580 to 413 000, and 2350-37 500 µg kg-1 for EME, OTJ and EBD respectively, while those of their outdoor counterparts varied from 347 to 19 700, 15 000 to 130 000, and 1780 to 46 300 µg kg-1 for EME, OTJ and EBD respectively. On the other hand, the UGA community without gas flare points had Σ16PAH concentrations in the range of 444-5260 µg kg-1 for indoor dust, and 154-7000 µg kg-1 for outdoor dust. The lifetime cancer risk values for PAHs in these matrices surpassed the acceptable limit of 10-6 suggesting a potential carcinogenic risk resulting from human exposure to PAHs in indoor and outdoor dust from these rural communities. Principal component analysis suggested that PAH contamination of dust from these communities arises principally from gas flaring, combustion of wood/biomass, and vehicular emissions.

Spatial characteristics, sources and exposure risk of polychlorinated biphenyls in dusts and soils from an urban environment in the Niger Delta of Nigeria.

Chlorinated organic compounds, such as polychlorinated biphenyls (PCBs), are a threat to both humans and the environment because of their toxicity, persistence, and capacity for long-range atmospheric transport. The concentrations of 28 PCB congeners, including 12 dioxin-like and seven indicator PCBs, were investigated in soils, and indoor and outdoor dusts from Port Harcourt city, Nigeria, in order to evaluate the characteristic distribution patterns in these media, their sources, and possible risk. The PCB concentrations varied from 4.59 to 116 ng g-1 for soils, and from 1.80 to 23.0 ng g-1 and 2.73 to 57.4 ng g-1 for indoor and outdoor dusts respectively. The sequence of PCB concentrations in these matrices was soil > outdoor dust > indoor dust. The composition of PCBs in these matrices indicated the prevalence of lower chlorinated PCBs in indoor and outdoor dusts, while the higher chlorinated congeners were dominant in soils. Di-PCBs were the predominant homologues in indoor dusts, while deca-PCBs were the most prevalent homologues in outdoor dusts and soils. The TEQ values of dioxin-like PCBs in 60 % of the soils, 100 % of the indoor dust, and 30 % of the outdoor dust were above the indicative value of 4 pg TEQ g-1 established by the Canadian authority. The hazard index (HI) values for exposure of adults and children to PCBs in these media were mostly greater than one, while the total cancer risk (TCR) values exceeded the acceptable risk value of 10-6, which indicate probable non-carcinogenic and carcinogenic risks resulting from exposure to PCBs in these media. Source analysis for PCBs in these matrices shows that they originated from diverse sources.

Spatial distribution of polycyclic aromatic hydrocarbons in dust and soils from informal trade sites in southern Nigeria: Implications for risk and source analysis.

Polycyclic aromatic hydrocarbons (PAHs) are a group of semi-volatile and persistent organic compounds considered priority pollutants because of their pervasive nature and high toxicity to the ecosystem and humans. Therefore, this study aimed to evaluate the PAH concentrations in dust and soils around informal trade sites (ITS) in Nigeria to determine the level of risk, sources, and significance of these activities to the PAH load of the environment. The 16 US EPA PAHs in dust and soils from ITS were determined by gas chromatography-mass spectrometry (GC-MS). The PAH concentrations in dust from these informal trade sites varied from 120 to 8790, 56 to 4780, and 102-1090 µg kg-1 for automobile mechanic workshops (AMW), car dismantling (CDS), and material recovery sites (MRS), respectively, whereas those of soils ranged from 3000 to 95,500, 554 to 14,700, and 966-25,200 µg kg-1 for AMW, CDS, and MRS respectively. The PAH profiles indicated that 3- to 5-ring PAHs were prominent in dust and soils around the ITS. The concentrations of the US EPA 16 PAHs in dust and soils from these ITS showed no correlation with organic matter, while the concentrations of PAH homologues in soils of these ITS showed no correlation with those of dust. Incremental lifetime cancer risk (ILCR) values in the magnitude of 10-4 to 101 were obtained for adult and childhood exposure to PAHs in dust and soils from these ITS. Exposure to PAHs in dust from these ITS gives rise to less risk than for soils. The results indicated that automobile mechanic workshops contribute more PAHs to the environment than car dismantling and material recovery activities. The source analysis showed that the PAH contamination of these sites arises from burning of biomass, plastic materials, and oils, and emissions from vehicles.

Polychlorinated biphenyls and polychlorinated dibenzo-p-dioxins and furans in imported canned fish in Nigeria and risk assessment.

Concentrations of polychlorinated biphenyls (PCBs) and polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs) were measured in imported canned fish such as mackerel, sardine and tuna to evaluate the risk relating to human consumption of these products. Gas chromatography-mass spectrometry (GC/MS) was used to evaluate the concentrations of PCBs and PCDD/Fs in the samples. The ∑28 PCB concentrations in the canned mackerel, tuna and sardine ranged from 0.33 to 9.48 ng g -1,

Occurrence and spatial characteristics of polychlorinated biphenyls (PCBs) in sediments from rivers in the western Niger delta of Nigeria impacted by urban and industrial activities.

The characteristic concentrations of 28 PCB congeners, their spatial distributions, sources, and associated risks to the ecosystem were investigated in sediments of some rivers around a glass industry and power generating plant in the Niger Delta of Nigeria. Gas chromatography-mass spectrometry (GC-MS) was applied for the identification and quantification of PCBs in sediments from these rivers. The Æ©28 PCB concentrations (dry weight) in sediments ranged from 1520 to 3540 ng g-1 for the Afiesere River, 976-5670 ng g-1 for the Edor River, and from 1440 to 6340 ng g-1 for the Okpare River. The homologue distribution patterns in sediments from these rivers indicated that low-chlorinated (2 Cl to 5 Cl) PCBs were more dominant than high-chlorinated (6 Cl to 10 Cl) PCBs with tri-, penta- and deca-PCBs as the top homologues. The PCB source analyses suggested that the PCB contamination of these river sediments could have originated from Aroclor mixtures, paints, pigments and other inadvertent sources. The risk assessment indicated a high risk to the ecosystem.

Concentrations, sources, and exposure risk of polychlorinated biphenyls in soil profiles of the floodplain of the lower reaches of the River Niger, Nigeria.

The concentrations of 28 polychlorinated biphenyls (PCBs) were determined in soils collected at three depths from thirteen different sites along the floodplain of the lower reaches of the River Niger (LRRN) in Nigeria. The aim of the study was to provide data on the levels of contamination, sources of the contaminants, and risks to the ecosystem and humans. Soil samples were Soxhlet extracted with a solvent mixture of dichloromethane (DCM)/n-hexane and cleaned up on a column packed with Florisil and silica gel. The PCBs in the samples were quantified by gas chromatography-mass spectrometry. The Æ©28 PCB concentrations in the floodplain soils varied between not detected (nd) and 11,151 ng g-1 for different sampling sites and depths. The PCB concentrations and homologue distribution patterns in soil profiles of the floodplain of the LRRN showed remarkable differences with respect to sites and depths. The results obtained were used to evaluate the ecological and human health risks, which indicated that there is a potential risk to organisms and humans from exposure to PCBs in these soil profiles. The source evaluation as determined by principal component analysis suggested that PCBs in these soil profiles came from burnt circuit boards, cable wires, use of paints, discharges from transformers, long-range migration, and deposition.

Distribution, sources and exposure risk of polycyclic aromatic hydrocarbons in soils, and indoor and outdoor dust from Port Harcourt city, Nigeria.

In this study, we evaluated the concentrations, composition, sources, and potential risks of polycyclic aromatic hydrocarbons (PAHs) in soils, and indoor and outdoor dust from Port Harcourt city in Nigeria. Gas chromatography-mass spectrometry (GC-MS) was used for the detection and quantification of PAH species in the samples. The concentrations of the US EPA 16 PAHs plus 2-methyl-naphthalene (∑17 PAHs) in soils, and indoor and outdoor dust from Port Harcourt city ranged from 240 to 38 400, 276 to 9130 and 44 to 13 200 µg kg-1 (dry weight, d.w.) respectively. The PAH concentrations in these matrices followed the sequence: soil > indoor dust > outdoor dust. The composition of PAHs in soils and dust (indoor and outdoor) showed remarkable differences with prominence of 3- and 5-ring PAHs. The estimated carcinogenic risk to the residents arising from exposure to these concentrations of PAHs in soils, and indoor and outdoor dust from Port Harcourt was above the acceptable target cancer risk value of 10-6. We concluded that these sites require clean-up, remedial actions and implementation of stringent pollution control measures with the intention of reducing the undesirable impacts of PAHs on both the ecosystem and humans.

Polycyclic aromatic hydrocarbons (PAHs) in surficial sediments from selected rivers in the western Niger Delta of Nigeria: Spatial distribution, sources, and ecological and human health risks.

This study assessed the concentrations, sources, and risks of polycyclic aromatic hydrocarbons (PAHs) in sediments from the Rivers Niger, Ase and Forcados in the western Niger Delta. The concentrations of PAHs (in µg kg-1 dry weight), as determined by gas chromatography-mass spectrometry, in sediments from these rivers varied from 2400 to 19,000, 2930 to 16,100, and from 1620 to 19,800 for the Niger, Ase and Forcados Rivers respectively. High molecular weight (HMW) PAHs were the most prevalent compounds present in these sediments. An assessment of the possible ecological and human health risks suggested high risks for both organisms and humans. The PAH source analysis suggested that sediments from these river systems were contaminated with PAHs arising from burning of biomass, gasoline/diesel emissions, burning of natural gas, and oil spillages.

Spatial characteristics, sources, and ecological and human health risks of polychlorinated biphenyls in sediments from some river systems in the Niger Delta, Nigeria.

Polychlorinated biphenyls (PCBs) were quantified in sediments from the lower reaches of the Niger, Ase and Forcados Rivers in Nigeria with the aim of elucidating the sources, spatial characteristics and likely ecological and human health risks relating to exposure to PCBs in the sediments. A total of 28 PCB congeners, including 7 indicator PCBs and 12 dioxin-like PCBs, were identified and quantified after Soxhlet extraction with acetone/n-hexane/dichloromethane by gas chromatography-mass spectrometry. The Σ28 PCB concentrations in sediments from the Niger, Ase and Forcados Rivers ranged from 13.5 to 277 ng g-1, not detected to 1633 ng g-1 and 6.9 to 78.6 ng g-1 respectively. The PCB composition in sediments from these three rivers indicate the dominance of lower chlorinated (2-Cl to 5-Cl) congeners over higher chlorinated (6-Cl to 10-Cl) congeners. The ecological and human health risk assessment suggests potential risks for exposure of both organisms and humans to PCBs in sediments from these three river systems.

Risk of human exposure to metals in some household hygienic products in Nigeria.

This study presents data on the levels and risk of human exposure to Cd, Pb, Cr, Ni, Cu, Co, Mn, Zn and Fe in some popular brands of household hygienic products (HHPs) available in Nigeria. The HHPs were digested with a mixture of HNO3, HCl and HClO4 in a ratio of 1:3:1 and the concentrations of the selected metals were quantified by atomic absorption spectrophotometry. The metal concentrations (in µg g-1) in these products ranged from 0.4 to 5.4, <0.09-47.0, <0.12-43.7, <0.06-7.5, <0.12-9.5, <0.06-15.0, <0.09-24.5, 9.0-675 and 62.4-434 for Cd, Pb, Cr, Cu, Co, Ni, Mn, Zn and Fe respectively. The systemic exposure dosages for the metals, arising from the use of these HPPs, were less than their respective provisional tolerable daily intake/recommended dietary allowance values. The household hygienic products are safe to use by humans based on the margin of safety values that were all above 100. However, the products contained significant levels of toxic (Cd and Pb), allergenic (Ni and Cr) and other low toxicity metals (Mn, Zn and Fe), which could be a potential threat to the environment.

Characterization of metals in indoor dusts from electronic workshops, cybercafés and offices in southern Nigeria: Implications for on-site human exposure.

The levels of Cd, Pb, Cr, Ni, Cu, Co, Ba, Mn, Zn, Al and Fe were evaluated in indoor dusts from electronic workshops, cybercafés and offices in southern Nigeria. The study was aimed at providing information on the distribution patterns, and the associated risks that may arise from exposure of humans to these metals in indoor dusts from the three work environments. The dust samples were digested with aqua-regia and analyzed for the metal concentrations by inductively coupled plasma-atomic emission spectrometry (ICP-AES). The metal concentrations (mg kg-1) in the indoor dusts from these work environments ranged from 0.2 to 20.5 Cd, 0.6-4810 Pb, 8.65-2210 Cr, 1.85-209 Ni, 6.75-2820 Cu, 0.25-19.6 Co, 22.7-597 Mn, 6.65-140 Ba, 43.3-7310 Zn, 1040-16,800 Al and 969-78,300 Fe. The metal distribution patterns in these dust samples followed the order: electronic workshops > cybercafés > offices. The concentrations of Cd, Pb and Cu in significant proportions of the dust samples from the electronic workshops and cybercafés surpassed their respective permissible limits in soils. The health risk assessment suggests considerable non-cancer risks arising from childhood contact with Pb in dust from the electronic workshops while no considerable non-cancer risk is associated with the adult and child exposure to dust from the cybercafés and offices. The results indicated that Cr and Pb are the main elements responsible for the non-carcinogenic risk arising from childhood exposure to electronic workshop dusts. The carcinogenic risk due to exposure of humans to metals in these dust samples were within the range regarded as safe by the USEPA.

Evaluation of human exposure to metals from some commonly used bathing soaps and shower gels in Nigeria.

The concentrations of nine metals (Cd, Pb, Ni, Cr, Co, Cu, Fe, Mn and Zn) were measured in selected brands of medicated, moisturizing and skin-lightening soaps and shower gels with the aim of evaluating the human health risk associated with metal exposure from the use of these products. The concentrations of metals in these products were determined by means of atomic absorption spectrophotometry after sample digestion with a mixture of acids. The concentration ranges of the metals in the bathing soaps and shower gels were found to be: <0.06-3.4 µg g-1 for Cd, <0.09-26.5 µg g-1 for Pb, <0.12-43.0 µg g-1 for Cr, <0.06-32.5 µg g-1 for Ni, <0.06-40.5 µg g-1 for Cu, <0.12-8.0 µg g-1 for Co, 61.8-4000 µg g-1 for Fe, <0.09-29.5 µg g-1 for Mn, and 25.5-1000 µg g-1 for Zn. The systemic exposure dosage values for these metals obtained from the application of these brands of bathing soaps and shower gels were below their respective provisional tolerable daily intake/or recommended daily intake values. The margin of safety values obtained for the metals were greater than 100 which indicated that there was no significant risk to the users of these brands of bathing soaps and shower gels, except in the case of Co.

Lagdo Dam Flood Disaster of 2012: An Assessment of the Concentrations, Sources, and Risks of PAHs in Floodplain Soils of the Lower Reaches of River Niger, Nigeria.

The concentrations of the USEPA 16 priority polycyclic aromatic hydrocarbons (PAHs) in soils of the floodplain of the lower reaches of River Niger, Nigeria, were investigated following the Lagdo Dam flood disaster of 2012. The aim was to provide information on the extent of contamination, sources, and risks of PAHs in these soils. The concentrations of Σ16 PAHs in the floodplain soils ranged from 812 to 10,700 µg kg. The benzo(a)pyrene (BaP) toxic equivalence and incremental lifetime cancer risk (ILCR) factors were used to evaluate the risk of human exposure to PAHs in these soils. The concentrations of benzo(a)pyrene carcinogenic equivalence (BaP) and benzo(a)pyrene mutagenic equivalence (BaP) ranged from not detected to 4090 µg kg and not detected to 4150 µg kg, respectively. The total ILCR for children and adults was calculated as the summation of the individual risks through the three routes of exposure, (ingestion, dermal, and inhalation of vapor or dust). The values obtained indicate that there are 6450 and 4480 chances in one million equally exposed persons to develop the risk of cancer for children and adults, respectively, which were higher than the USEPA acceptable guideline value of one cancer case in one million (10) equally exposed persons. The PAHs source evaluation, using the diagnostic ratios and principal component analysis (PCA), indicated that the major sources of PAHs in these soils were fossil fuel combustion, gas flaring, wood combustion, traffic emissions, and input from petroleum.

Evaluation of human exposure to metals from some commonly used hair care products in Nigeria.

The concentrations of nine metals, namely, cadmium (Cd), lead (Pb), chromium (Cr), copper (Cu), cobalt (Co), nickel (Ni), manganese (Mn), zinc (Zn), and iron (Fe), were determined in 26 brands of hair care products including hair relaxers, conditioners and shampoos. The study was aimed at providing information on the possible risks arising from heavy metals associated with the use of these products. The concentrations of the metals were determined by means of atomic absorption spectrophotometry after digestion of the samples with a mixture of acids. The concentrations of the respective metals in hair relaxers, shampoos and conditioners were found to be 0.8-2.5, 0.6-3.0,

Polycyclic aromatic hydrocarbon concentrations in commercially available infant formulae in Nigeria: estimation of dietary intakes and risk assessment.

The concentrations and profiles of polycyclic aromatic hydrocarbons (PAHs) in commercially available infant formulae and follow-up formulae in Nigeria were determined with a view to providing information on the health risks to children from the consumption of these infant foods. The concentrations of PAHs were measured by means of gas chromatography-mass spectrometry (GC-MS) after extraction by ultrasonication with acetone/dichloromethane and clean-up. The concentrations of the Σ16 PAHs in these infant formulae ranged from 0.102 to 1.98 µg kg(-1), 0.054-1.98 µg kg(-1), 0.081-2.54 µg kg(-1) and 0.51-0.70 µg kg(-1) for infants of ages 0-6 months, 6-12 months, 1-3 years and 0-12 months respectively. The concentrations of benzo(a)pyrene (BaP) in all samples investigated were below the 1 µg kg(-1) European Commission permissible limit for BaP in foods meant for infants. The estimated daily intake of PAHs based on the European Food Safety Authority (EFSA) suggested indicators of occurrence and effects of PAHs in foods were not detected (nd) to 2.67 ng BaP kg(-1) bw day(-1), nd-5.29 ng PAH2 kg(-1) bw day(-1), nd-11.20 ngPAH4 kg(-1) bw day(-1) and nd-34.96 ng PAH8 kg(-1) bw day(-1). The estimated margin of exposure (MOE) values: BaP-MOE, PAH2-MOE, PAH4-MOE and PAH8-MOE values were greater than 10,000 which indicates that there are no health risks from the consumption of these products by infants. The concentrations and dietary exposure to PAHs from these products were similar to values reported in the literature for European Communities.

Trace elements in water, soil, earthworm and fishes from Otokutu end of Warri River, Delta State, Nigeria.

Selected environmental samples such as water, fishes (Tilapia mariae and Clarias gariepinus), earthworm (Libyodrillus violaceous) and soils were obtained from the Otokutu end of Warri River, digested with acid mixtures and analyzed for trace metal concentrations using the atomic absorption spectrophotometry. The trace metals measured include; zinc, lead, copper, arsenic, iron, cadmium and mercury. The results obtained showed variations in the concentrations of metals in the entire samples analyzed. Lowest metal concentrations were recorded in the water samples. Trace metal concentrations in Tilapia mariae, Clarias gariepinus and Libyodrillus violaceous were higher than levels recorded in water and soil samples, respectively. The elevated concentrations of lead, arsenic, iron, cadmium and mercury were traceable to anthropogenic wastes and activities of industries operating in Warri and its environs.