Microplastic particles in river sediments and water of southwestern Nigeria: insights on the occurrence, seasonal distribution, composition, and source apportionment.

Microplastics (MPs) are globally recognized as an emerging environmental threat, particularly in the aquatic environment. This study presents baseline data on the occurrence and distribution of MPs in sediments and surface water of major rivers in southwestern Nigeria. Microplastics were extracted by density separation and polymer identification using Fourier transformed infrared spectroscopy in attenuated total reflectance mode (FTIR-ATR). The abundance of MPs in surface sediment and water samples across all locations ranged from 12.82 to 22.90 particle/kg dw and 6.71 to 17.12 particle/L during the dry season and 5.69 to 14.38 particle/kg dw and 12.41 to 22.73 particle/L during the wet season, respectively. On average, fiber constituted the highest percentage of MP in sediments (71%) and water (67%) while foam accounted for the lowest values of 0.6% and 1.7%, respectively. Polypropylene (PP) and polyethylene (PE) were the main MPs across all locations based on Fourier transform infrared spectroscopy (FTIR). MPs of size < 1 mm were the most abundant (≥ 55%) on average in both water and sediments. The study identified run-off from human activities and industrial wastewater as potential sources of MP exposure based on positive matrix factorization. The study suggests assessing the impact of different land-use activities on MPs occurrence and distribution in addition to quantifying MPs in seafood as a way forward in food safety management systems for further studies. This study confirmed the occurrence and widespread distribution of MPs in surface water and sediments and provides a database on MP pollution in Nigeria.

Occurrence and probabilistic risk assessment of polycyclic aromatic hydrocarbons in blood and urine of auto-mechanics in Akure Metro, Nigeria.

This study provides baseline data on the concentration of polycyclic aromatic hydrocarbons (PAHs) in blood and urine samples of auto-mechanics, using Nigeria as a case study. Eighteen auto-mechanics participated in the study excluding two controls. The concentrations for the ΣPAHs across all participants (excluding control) ranged from 1.67 to 3.30 (2.17 ± 0.58) in blood with a significantly higher (P < 0.05) range of 7.61 to 10.76 (8.69 ± 1.00) in urine. The high molecular weight PAHs (4-6 rings) dominated the PAH profile in both blood (≥ 92%) and urine (≥ 87%) across all locations. Dibenz(a)anthracene was the most distributed PAH, while acenaphthene and indeno(1,2,3-cd)pyrene were the least distributed. The dermal route constituted approximately 99% of the total chronic exposure, followed by ingestion, and the least via inhalation. The hazard index (HI) was below the safe thresholds (HI = 1), suggesting non-carcinogenic PAH effects. However, all the participants including control samples had carcinogenic risk (CR) values above the acceptable level of 10-6 in both blood and urine samples. The carcinogenic and mutagenic potencies were higher in urine than in blood. The results suggest less acute toxicity and more potential chronic effects. The computed elimination ratio (> 1) suggests low excretion in urine and a potentially harmful trend. Molecular diagnostic ratios and principal component analysis suggest mixed PAH sources. The study revealed biomonitoring solely dependent on blood analysis may greatly underestimate health risks due to PAH exposure. To the best of our knowledge, this study is the first to provide levels of PAHs in the blood and urine of Nigerian mechanics. Findings herein will support policymakers at all levels in re-focusing attention to the less prioritized professions that pre-disposes people to PAHs and other emerging pollutants in society.

Nutrient recovery from yellow water to soil-crop systems.

The potentials of the nutrient recovered (NRM), via a facile green and sustainable approach from human urine, as a fertilizer in soil-crop system was studied. Nutrient was recovered using a highly decentralized modular reactor, with packed bed of granular gastropod shell. The cultivations of Zea mays (maize) and Solanum lycopersicum (tomato) were the cases studied. The total nutrient composition, the P-speciation, and the safety-risk assessment of the NRM were determined. Using NPK as the standard fertilizer, and a non-fertilized soil as the control, the fertilizing potential of the NRM was evaluated. The influence of the different fertilizer application regimes on the wet and dry biomass nutrient composition, after-harvest soil nutrient composition, and pH values was studied. The NRM contained 106 mg/g of TN and 374.6 mg/g of TP, and the P species identified were Ca2-P (31.66%), Ca8-P (14.99%), and Ca10-P (53.32%). The growth rate of the NRM crops were lower than that of the NPK crops until the 17th day, when the NRM crops grew faster than that of the NPK and control (p < 0.05). The NRM is beneficial to acidic soils and also acts as a slow nutrient releasing fertilizer.

Concentrations and Toxic Equivalency of Polycyclic Aromatic Hydrocarbons (PAHs) and Polychlorinated Biphenyl (PCB) Congeners in Groundwater Around Waste Dumpsites in South-West Nigeria.

Polyaromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in groundwater and leachate around selected waste dumpsites from two southwestern states of Nigeria were investigated. Samples were Soxhlet-extracted using hexane/methylene chloride mixture and cleaned-up with preconditioned solid-phase extraction cartridges. The ∑PAHs (PCBs) (all in µg/L) in the boreholes, leachate, and hand-dug well across all locations ranged from below detection limit (BDL) to 0.62 (BDL to 0.067), 1.16 to 9.96 (0.003 to 0.041), and BDL to 0.01 (0.001-0.031), respectively. Low molecular weight-PAHs accounted for ≥61% of ∑PAHs detected across all locations. The highly chlorinated hexa-PCBs [2,2',3,4,4',5'-HeCB(#180), 2,2',3,4',5',6-HeCB(#34) and 2,2',4,4',5,5'-HeCB(#153)] dominated the entire congener profiles. Pyrene and 2,3',4,4',5-PeCB(#118) constituted 56% and 58% of the ∑PAHs and ∑PCBs, respectively. Sampled water is not adequately safe for drinking and may pose cancer risk. This study should be sustained for health risk and sustenance of an enduring ecological integrity.

Bioaccumulation and toxic potencies of polycyclic aromatic hydrocarbons in freshwater biota from the Ogbese River, Nigeria.

Samples of fish and shellfish (periwinkles, mussel, and snail) collected from the rapidly contaminated Ogbese River, Ondo State, Nigeria, were analyzed for their polycyclic aromatic hydrocarbon (PAH) levels by gas chromatography-mass spectrometry after cleanup using solid-phase extraction. The rank order of concentration of ΣPAHs in fish follows: gills >> eggs >>> muscle. The dry weight concentrations (µg/g) of total PAHs ranged from < 0.001 to 2.06, 0.01 to 18.67, 0.01 to 9.56, and 0.01 to 8.28 in fish muscle, periwinkle, snail, and mussel respectively. Accumulation levels of PAHs in the biota were used to calculate biota-sediment (or porewater) accumulation factors (BSAF (BPwAF)) and bioaccumulation factor (BAF). The lower molecular weight PAHs constitute major components (≥ 87% in each case) of PAH congener profiles. Bioaccumulation was greatest for PAHs with log Kow values between 5.0 and 5.6. However, the study did not show a good correlation between log Kow of individual PAH and the corresponding BSAFs/BPwAF for the biota. The study indicates that significantly greater (p < 0.05) BSAFs for ΣPAHs were observed in the three bottom dwellers than in fish muscle which suggests that the sediment-feeding behavior largely affected the extent of PAH bioaccumulation in the aquatic organisms. The calculated potency equivalent concentration (PEC) of total PAHs was above the recommended screening value (SV) in US EPA guidelines, suggesting great concern for human consumption. However, estimated excess cancer risk (ECR) induced by dietary exposure only suggests potential cancer risk. The study suggests urgent remediation of the river to safeguard public health.

Influence of electrolyte composition and pH on glyphosate sorption by cow-dung amended soil.

This study investigated the pH-dependent relationship between glyphosate and soils before (NS) and after amendment with cow-dung, CD (SACD). Sorption isotherms were generated using batch equilibration techniques from CaCl2, KCl, CaSO4 and Ca(H2PO4)2 background electrolytes. Linear partition coefficients decreased with increase in pH in the order: CaCl2>KCl > CaSO4>Ca(H2PO4)2, which reflect both the effect of the inorganic anion in terms of competition and the cation in terms of bridging interactions. However, soil amendment with CD minimized the inhibitory effect of pH increase on glyphosate sorption. Variations in glyphosate sorption from CaCl2 and Ca(H2PO4)2 were attributed to fraction of hydrophilic contribution while variations in sorption from CaCl2 and KCl were attributed to Ca-bridging and ranged from 22 to 70% across the two soils. Estimated hydrophobic partitioning ( KOCpH ) systematically decreased with increasing soil solution pH from 36 to 3% and 5 to <1% in NS and SACD, respectively. Greater sorption in NS over SACD was partly attributed to higher phosphate level in SACD which is preferentially sorbed over glyphosate. This study noted CD application as soil amendment for agriculture could impede glyphosate sorption and facilitate its off-site leaching and contamination of surface and groundwater.

Influence of oxic/anoxic condition on sorption behavior of PFOS in sediment.

Sediment components and redox properties change with oxic/anoxic condition, which affect the environmental transport of perfluorooctane sulfonate (PFOS). Herein, the influence of oxic/anoxic condition on the variation of redox and residual components of sediments, where organic matter, iron and manganese oxides are separated from the original sediment collected from Lake Taihu, China, are investigated. Meanwhile, the distinguishing sorption behaviors of PFOS on various residual sediments under oxic and anoxic condition are studied. Sediment after extracting iron and manganese (S-FeMn), which possessed the highest organic carbon (0.99%), had the highest affinity for PFOS under oxic condition. However, anoxic environment resulted in an increase of the pH, dissolving of organic carbon and de-protonation of S-FeMn, which caused the lower sorption capacity of PFOS on S-FeMn. Sediment after extracting manganese (S-Mn) had the higher sorption ability in anoxic environment because the Fe(2+) from S-Mn provided more effective electrostatic sites for anionic PFOS. When the environment changed to oxic condition, the iron existed as trivalent form in S-Mn, which resulted in a block of effective sorption site and reduced the sorption amounts of PFOS. The higher percentage of manganese oxides restrained the sorption of PFOS. Hence, whether or not oxic/anoxic condition promoted the PFOS sorption depended on both the percentage and form of various components in the sediment. The study generated further insight into the environmental transport of PFOS in the sediments with different properties and the wetland system, where oxic/anoxic subsurface flow was constructed.

Influence of organic carbon and metal oxide phases on sorption of 2,4,6-trichlorobenzoic acid under oxic and anoxic conditions.

Chlorobenzoic acids represent crucial recalcitrant metabolites in the environment; thus, the influence of soil components on the sorption of 2,4,6-trichlorobenzoic acid (TCB) under oxic and anoxic conditions was studied. The surficial physiognomies of untreated and isolated soil samples were studied using FTIR, XRD, specific surface area, and PZC determination. The roles of redox potential, dissolved organic carbon (DOC), and pH, particularly under anoxic condition, were appraised. Batch equilibrium adsorption studies on soils of variable Fe/Mn oxides and organic carbon showed that adsorption was low across all components (log Koc = 0.82-3.10 Lg(-1)). The sorption of 2,4,6-TCB was well described by the pseudo second-order kinetic model. The fluctuation of both redox potential and pH during anoxic experiment had a negative impact on the sorption, partitioning, and the oxidation of organic matter. Linear relationships were observed for Kd with both soil total organic carbon (TOC) and surface area (SA). The results showed the existence of DOC-mediated sorption of 2,4,6-TCB which seems to be enhanced at lower pH. The reductive dissolution, particularly of iron compounds, possibly impeded sorption of 2,4,6-TCB under anoxic condition. It could be inferred that habitats dominated by fluctuating oxygen concentrations are best suited for the development of environmental conditions capable of mineralizing 2,4,6-TCB and similar xenobiotics.