Evaluating the quality of sediments in streams draining contrasting land-use areas in Osogbo metropolis, southwestern Nigeria.

The attendant effects of urbanization on the environment and human health are evaluable by measuring the potentially harmful element (PHE) concentrations in environmental media such as stream sediments. To evaluate the effect of urbanization in Osogbo Metropolis, the quality of stream sediments from a densely-populated area with commercial/industrial activities was contrasted with sediments from a sparsely-populated area with minimal anthropogenic input.Forty samples were obtained: 29 from Okoko stream draining a Residential/Commercial Area (RCA, n = 14) and an Industrial Area (IA, n = 15), and 11 from Omu stream draining a sparsely-populated area (SPA). The samples were air-dried, sieved to < 75 micron fraction, and analysed for PHEs using inductively-coupled plasma atomic emission spectrometry (ICP-AES). Index of geoaccumulation (Igeo), pollution index (PI), ecological risk factor (Er) and index (ERI) were used for assessment. Inter-elemental relationships and source identification were done using Pearson's correlation matrix and principal component analysis (PCA).PHE concentrations in the stream sediments were RCA: Zn > Pb > Cu > Cr > Sr > Ni > Co, IA: Zn > Cr > Ni > Co > Pb > Cu > Sr and SPA: Zn > Co > Cr > Cu > Sr > Ni > Pb. Igeo calculations revealed moderate-heavy contamination of Cu, Pb and Zn in parts of RCA, moderate-heavy contamination of Zn in IA while SPA had moderate contamination of Co and Zn. PI values revealed that stream sediments of RCA are extremely polluted, while those of IA and SPA are moderately and slightly polluted, respectively.The pollution of the stream sediments in RCA and IA is adduced to anthropogenic activities like vehicular traffic, automobile repairs/painting, blacksmithing/welding and metal scraping. In SPA however, the contamination resulted from the application of herbicides/fertilizers for agricultural purposes.

Contamination and risk surveillance of potentially toxic elements in different land-use urban soils of Osogbo, Southwestern Nigeria.

The concentrations of potentially toxic elements (PTEs) and their contamination indices were determined in urban soil from five different land-use zones, namely municipal solid waste landfill (MWL), industrial area (INA), heavy traffic area (TRA), residential area with commercial activities (RCA), and farmland (FAL) in Osogbo Metropolis. Ecological and human health risk assessments were also evaluated. Based on the average concentrations, the highest values of As, Cr, Cu, Fe, Mn, Ni, Pb, V, and Zn were found at INA, while the maximum concentrations of Ba, Cd, and Co were observed at MWL. The average enrichment factor (EF) values of Cd, Cu, Pb, and Zn showed very high to extremely high enrichment in the soils of INA, MWL, TRA, and RCA, while the EF values of Ba, Co, Cr, Fe, Ni, and V were significantly to moderately enriched in the aforementioned land-use zones. This trend was consistent with the average contamination factor (Cf) values of Cd, Cu, Pb, and Zn, which indicated considerable to very high contamination at INA, MWL, TRA, and RCA. However, Cf values of Ba, Co, Cr, Fe, Ni, and V had moderate contamination variously at the different land-use zones. Furthermore, the potential ecological risk factor (Eri) values for all the PTEs were < 40, which indicated low Eri, except for Cd and to some extent Pb. The Eri value of Cd was high to very high at MWL, INA, TRA, and RCA, and low at FAL, while Eri of Pb was only moderate at INA. Assessment of health quotient (HQ) of non-carcinogenic health risks was within acceptable limit (< 1) for most of the PTEs in the different zones for adults and children, except the maximum HQ value of Pb at INA (HQ = 1.0), which was beyond the acceptable limit for children. The carcinogenic risk was within the acceptable limit (1.0 × 10-6) in all the zones, except INA. This may pose health challenges to children in the vicinity of the pollution sources. Continuous monitoring of PTEs to reduce exposure to PTE should be considered.

Silver nanoparticles strengthen Zea mays against toxic metal-related phytotoxicity via enhanced metal phytostabilization and improved antioxidant responses.

This study investigated the phytostabilization and plant-promoting abilities of silver nanoparticles (AgNPs). Twelve Zea mays seeds were planted in water and AgNPs (10, 15 and 20 mg mL-1) irrigated soil for 21 days on soil containing 0.32 ± 0.01, 3.77 ± 0.03, 3.64 ± 0.02, 69.91 ± 9.44 and 13.17 ± 0.11 mg kg-1 of As, Cr, Pb, Mn and Cu, respectively. In soil treated with AgNPs, the metal contents were reduced by 75%, 69%, 62%, 86%, and 76%. The different AgNPs concentrations significantly reduced accumulation of As, Cr, Pb, Mn, and Cu in Z. mays roots by 80%, 40%, 79%, 57%, and 70%, respectively. There were also reductions in shoots by 100%, 76%, 85%, 64%, and 80%. Translocation factor, bio-extraction factor and bioconcentration factor demonstrated a phytoremediation mechanism based on phytostabilization. Shoots, roots, and vigor index improved by 4%, 16%, and 9%, respectively in Z. mays grown with AgNPs. Also, AgNPs increased antioxidant activity, carotenoids, chlorophyll a and chlorophyll b by 9%, 56%, 64%, and 63%, respectively, while decreasing malondialdehyde contents in Z. mays by 35.67%. This study discovered that AgNPs improved the phytostabilization of toxic metals while also contributing to Z. mays' health-promoting properties.

Enhanced phytoremediation strategies, which use nanoparticles to boost and facilitate the phytoremediation capacity of plants, are being recommended due to the limitations of traditional phytoremediation employing hyperaccumulating plants alone. Nanoparticles enhance phytoremediation potentials by directly reducing phytoavailable pollutants and promoting plant growth. Silver nanoparticles (AgNPs) are recognized as possessing the ability to enhance the phytoremediation of heavy metals HMs by converting them to a less toxic form and immobilizing the remaining phytoavailable HMs. This is in addition to their potential to modify plant biochemical and physiological properties to counteract HM toxicity.

Sources and Level of Rare Earth Element Contamination of Atmospheric Dust in Nigeria.

BACKGROUND: Rare earth element (REE) composition of atmospheric dust has recently been used to trace potential sources of dust pollution. OBJECTIVE: The present study aimed to determine the sources of atmospheric pollution in the study area using REE patterns and determine their level of pollution. METHODS: Twenty-five (25) atmospheric dust samples were collected in the study area, with five samples each from an industrial area, traffic area, dumpsite area, residential area and remote area in Ibadan, southwestern Nigeria. In addition, five (5) topsoil and two (2) rock samples (granite gneiss) were collected for comparison. Concentrations of REE were determined by inductively coupled plasma mass spectrometry (ICP-MS). RESULTS: The ratio of lanthanum/cerium (La/Ce), especially in some locations in industrial area (1.5), traffic area (1.5) and to some extent dumpsite area (1.1) was higher than in soil (0.2), upper continental crust (0.5) and the minimum value of fluid catalytic crackers (1.0). Generally, the respective average values of the ratios of La/praseodymium (Pr), La/neodymium (Nd) and La/samarium (Sm) in industrial area (32.1, 7.8 and 52.6) and traffic area (14.9, 4.4 and 26.8) were higher than their respective averages in soil (4.4, 1.1 and 6.2), rock (5.7, 1.9 and 14.1), upper continental crust (4.4, 1.1 and 6.6) and the minimum value in fluid catalytic crackers (5.8, 3.7 and 37.0). Meanwhile, their corresponding value in the dumpsite area, residential area and remote area were lower or similar to the geological background levels. DISCUSSION: The contamination factors of REEs in the atmospheric dust of the industrial area and traffic area were classified as heavily contaminated, especially with light lanthanoid elements in REE. The degree of contamination of REEs in the atmospheric dust of industrial area (30.9) and traffic area (18.8) fell within the considerable contamination category. The high values of the light lanthanoid ratio and the contamination indices were attributed to their emission from the fired-power plant and vehicular exhaust. CONCLUSIONS: Most of the composition of the atmospheric dust was sourced from the local geology of the study area as observed in the residential area and remote area, while the contamination in the industrial area and traffic area was attributed to human activities. COMPETING INTERESTS: The authors declare no competing financial interests.

Evaluation of Pollution of Soils and Particulate Matter Around Metal Recycling Factories in Southwestern Nigeria.

BACKGROUND: Metal recycling factories (MRFs) have developed rapidly in Nigeria as recycling policies have been increasingly embraced. These MRFs are point sources for introducing potentially toxic elements (PTEs) into environmental media. OBJECTIVES: The aim of this study was to determine the constituents (elemental and mineralogy) of the wastes (slag and particulate matter, (PM)) and soils around the MRFs and to determine the level of pollution within the area. METHODS: Sixty samples (30 slag samples, 15 soil samples and 15 PM samples) were collected for this study. The soils, slag and PM samples were analyzed for elemental constituents using inductively coupled plasma optical emission spectrometry. Mineralogy of the PM was determined using scanning electron microscope-energy dispersive spectroscopy (SEM-EDS), and soil mineralogy was determined by an X-ray diffractometer (XRD). RESULTS: The results of the soil analyses revealed the following concentrations for the selected metals in mg/kg include lead (Pb) (21.0-2399.0), zinc (Zn) (56.0-4188.0), copper (Cu) (10.0-1470.0), nickel (Ni) (6.0-215.0), chromium (Cr) (921.0-1737.0) and cadmium (Cd) (below detectable limit (Bdl)-18.1). For the slags the results were Pb (68.0-.333.0), Zn (1364.0-3062), Cu (119.0-1470.0), Ni (12.0-675.0), Cr (297-1737) and Cd (Bdl-15.8). The results in µg/g for the metal analysis in PM were Pb (4.6-160.0), Zn (18.0-471.0), Cu (2.5-11.0), Ni (0.8-4.2), and Cr (2.5-11.0), while Cd was undetected. The slags are currently utilized for filling the foundations of buildings and roads, providing additional pathways for the introduction of PTEs into the environment from the suspended materials generated from mechanical breakdown of the slags. CONCLUSIONS: The MRFs were found to have impacted the quality of environmental media through the introduction of PTEs, impairing soil quality, in addition to PM, which can have detrimental health consequences. Further studies on the health implications of these pollutants and their impacts on human health are needed. COMPETING INTERESTS: The authors declare no competing financial interests.

Heavy Metal Contamination and Ecological Risk Assessment in Soils and Sediments of an Industrial Area in Southwestern Nigeria.

BACKGROUND: Increased growth of industrial activities, especially in urban centers, is one of the main sources of toxic substances in Nigeria. The level of these impacts is not well known. Soil and sediment samples from one such industrial area were examined for their mineralogical composition and heavy metals contents in order to assess the level of contamination and potential ecological risk status. METHODS: Mineralogical composition of the media and their heavy metals concentrations were determined using X-ray diffractometry and inductively coupled plasma-mass spectrometry methods, respectively. Ecological risk assessment was carried out using single (contamination factor, geo-accumulation index, enrichment factor) and multi-elemental (contamination degree, pollution index and modified pollution index) standard indices. RESULTS: The average heavy metal concentrations in soils and sediments followed the order magnesium (Mn) > chromium (Cr) > lead (Pb) > copper (Cu) > cadmium (Cd) > cobalt (Co) > nickel (Ni), with corresponding values for soils and sediments of 324.3, 79.9, 66.1, 40.7, 14.3, 9.1, 6.8 mg kg-1 and 266.8, 78.6, 40.6, 39.8, 12.9, 8.4, 4.6 mg kg-1, respectively. Principal component (PC) analysis of the results indicated three main sources of metals (industrial, vehicular activities and geogenic input). Evaluated contamination factor (Cf), enrichment factor (Ef) and geo-accumulation index (Igeo) revealed very high contamination for Pb, Cd and Cu in all of the samples, with calculated pollution index (PI) and modified pollution index (MPI) revealing that all the samples were severely polluted. Calculated potential ecological risk factor (ERi) within the industrial area demonstrated a strong potential ecological risk for Cd, Pb and Cu. CONCLUSIONS: Activities in the industrial area have affected the quality of the analyzed environmental media, with possible detrimental health consequences. Regular environmental monitoring of the industrial area and the formulation of appropriate policies that support reduction of contamination are strongly recommended. However, due to the limitations of comparing site samples with a single control sample in this work, further study is recommended to compliment this preliminary study. COMPETING INTERESTS: The authors declare no competing financial interests.