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.

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Geophagy clay has been used in tropical regions as gastrointestinal protector for adsorbing toxins in human body, but it was rarely used in adsorbing heavy metals contaminants in water. This study determines elemental concentration of geophagy clay and evaluates its adsorptive capacity in removing Cd2+ and Pb2+ in water. Fifteen clay samples were randomly collected from three layers in the space of one meter apart from Amawom clay deposit in Ikwuano local government, Southeast Nigeria. Elemental analysis was carried out using the inductively coupled plasma mass spectrophotometer (ICP-MS), and chemical characterization was performed with Fourier transform infrared spectroscopy (FT-IR) and X-ray diffractometer (XRD). The adsorptive capacity of Cd2+ and Pb2+ on the clay samples was evaluated using standard solutions of the metal ions. The result of the elemental analysis in mg/kg (Pb ≤ 12.4, Zn ≤ 2.75, Co ≤ 1.50, Ni ≤ 1.47, Mn ≤ 15.0, Cd = 0.01, Ca ≤ 300, Al ≤ 3466, Na ≤ 13.3, and Hg = 0.02; P≤40.0) revealed that the concentrations of most of the studied metals in the three layers are statistically similar and fall below the permissible recommended safety levels. The presence of functional groups (hydroxyl, amine, and carboxylic/ester) and minerals (kaolinite, goethite, and quartz) provided evidence of the good adsorptive properties of the clay samples. The adsorption of Cd2+ and Pb2+ unto the clay samples increased with increase in pH, concentration, time, and temperature, and the equilibrium data for the adsorption fitted well into Langmuir isotherm. The study, therefore, concluded that geophagy clay possesses the capacity to adsorb Cd2+ and Pb2+ for water treatment.