Impacts of solid waste management site on some toxic elements contamination of the surrounding soil in Akure, Nigeria.

The distribution of potentially toxic elements (PTEs) such as zinc (Zn), copper (Cu), lead (Pb), nickel (Ni), cadmium (Cd), and chromium (Cr), their potential bioavailability, extent of contamination and potential risk of dumpsite and surrounding soil samples were appraised. Three (3) soil samples were collected randomly from within the dumpsite and three (3) soil samples were also obtained 50 m away from the perimeter fence of the dumpsite. PTEs in the bulk and fractionated portions were determined using inductively coupled plasma - optical emission spectrometry (ICP-OES). The results showed that the concentrations of all the PTEs analysed were higher in the dumpsite soil samples than the surrounding samples, suggesting an impact of the dumpsite activities on the soil. The distribution of PTEs varied significantly within the different fractions of both the surrounding and dumpsite soils and their presence were more of anthropogenic than geogenic. The calculated contamination factor/pollution load index (CF/PLI) revealed that the surrounding soil samples fell within the range of moderate contamination, except for Cu and Cr which showed very high contamination. Cd showed the highest value (60.4) for potential ecological risk index (PERI) at the surrounding area. However, the value of Cd in the surrounding soil samples indicated a low ecological risk. The total concentrations of the PTEs were lower than their corresponding target values for both national and international standards, except for Cd (0.15 mg/kg) and Cu (37.3 mg/kg). The study concluded that the dumping of various wastes at the dumpsite was found to be a contributing factor to PTEs contamination of soil at the study area. Hence, an engineered landfill for Akure metropolis is recommended to replace the existing practice.

Assessment of Microplastics and Potentially Toxic Elements in Surface Sediments of the River Kelvin, Central Scotland, United Kingdom.

Contamination of the environment by microplastics (MPs), polymer particles of <5 mm in diameter, is an emerging concern globally due to their ubiquitous nature, interactions with pollutants, and adverse effects on aquatic organisms. The majority of studies have focused on marine environments, with freshwater systems only recently attracting attention. The current study investigated the presence, abundance, and distribution of MPs and potentially toxic elements (PTEs) in sediments of the River Kelvin, Scotland, UK. Sediment samples were collected from eight sampling points along the river and were extracted by density separation with NaCl solution. Extracted microplastics were characterised for shape and colour, and the polymer types were determined through attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy. Pollution status and ecological risks were assessed for both the microplastics and PTEs. Abundance of MPs generally increased from the most upstream location (Queenzieburn, 50.0 ± 17.3 particles/kg) to the most downstream sampling point (Kelvingrove Museum, 244 ± 19.2 particles/kg). Fibres were most abundant at all sampling locations, with red, blue, and black being the predominant colours found. Larger polymer fragments were identified as polypropylene and polyethylene. Concentrations of Cr, Cu, Ni, Pb and Zn exceeded Scottish background soil values at some locations. Principal component and Pearson's correlation analyses suggest that As, Cr, Pb and Zn emanated from the same anthropogenic sources. Potential ecological risk assessment indicates that Cd presents a moderate risk to organisms at one location. This study constitutes the first co-investigation of MPs and PTEs in a river system in Scotland.

Environmental impacts of covid-19 pandemic: Release of microplastics, organic contaminants and trace metals from face masks under ambient environmental conditions.

The covid-19 pandemic era was characterized by heavy usage and disposal of medical face masks, now estimated at over 1.24 trillion. Few studies had attempted to demonstrate the release of microplastics from face masks using simulated conditions and application of mechanical forces, far different from the effects experienced by face masks dumped in the open environment, in landfills and dumpsites. In the current study, we monitored the release of microplastics, organic contaminants and toxic metals from medical face masks degraded under normal outdoor environmental conditions, over a period of 60 weeks. We showed that face mask's decomposition proceeded via sunlight (UV) - initiated oxidative degradation, leading to the replacement of methylene (CH2-) and alkyl (CH3-) groups in face mask's polypropylene backbone with hydroxyl and ketonic functional groups. Organic compounds released from decaying face masks into the surrounding soil included alkanes, alkenes, carboxylic acids/diesters and phthalate esters. Mean maximum concentration of phthalates in the soil ranged from 3.14 mg/kg (diethyl phthalate) to 11.68 mg/kg di(2-ethylhexyl) phthalate. Heavy metals, including Cu, Pb, Cd, As, Sn and Fe, were released into the soil, leading to contamination factors of 3.11, 2.84, 2.42, 2.26, 1.80 and 0.99, respectively. Together, the metals gave a pollution load index (PLI) of 2.102, indicating that they constitute moderate pollution of the soil surrounding the heap of face masks. This study provides a realistic insight into the fate and impacts of the enormous amounts of face masks, disposed or abandoned in soil environments during the covid-19 pandemic.

COVID-19 face masks attracted Cellulomonas and Acinetobacter bacteria and provided breeding haven for red cotton bug (Dysdercus suturellus) and house cricket (Acheta domesticus).

This study investigated the possibility of COVID-19 medical face masks to affect bacterial and macrofaunal communities in open soil environment. An estimated 1.24 trillion of face masks have been used and discarded as a result of the COVID-19 pandemic, with a significant part of this ending up in the soil environment, where they degrade gradually over time. Because bacteria and macrofauna are sensitive indicators of changes in soil ecosystem, we investigated possible impacts of face masks on population, distribution, and diversity of these soil species. Effect on soil bacterial community was studied by both culture-based and advanced molecular (metagenomics) approach, while impact on macrofauna was investigated by examining monoliths around heap of masks for soil insects. In both cases, control soil experiments without face masks were also set up and monitored over a period of 48 weeks. The study found that the presence of face masks led to a more diverse bacterial community, although no influence on overall bacterial population was evidenced. More importantly, bacteria belonging to the genera Cellulomonas and Acinetobacter were found prominently around face masks and are believed to be involved in biodegradation of the masks. The bacterial community around the masks was dominated by Proteobacteria (29.7-38.7%), but the diversity of species increased gradually with time. Tiny black ants (Monomorium invidium) were attracted to the face masks to take advantage of water retained by the masks during the period of little rainfall. The heaps of face masks also provided shelter and breeding "haven" for soil insects, notably the red cotton bug (Dysdercus suturellus) and house cricket (Acheta domesticus), thereby impacting positively on the population of insect species in the environment. This study provides insights into the actual impacts of face masks on soil organisms under normal outdoor environmental conditions.

Heavy metals research in Nigeria: a review of studies and prioritization of research needs.

Nigeria is experiencing continuous economic and industrial transformations, typical of many developing nations. In addition to its well-established oil industry, which is infamous for exuding various kinds of pollutants, there are increased mining operations, indiscriminate disposal and burning of wastes, illegal oil refinery and terroristic insurgency, all poised to increase the levels of heavy metal contaminants in the Nigerian environment. A recent revelation indicates that about 2 million people in South-western Nigeria alone could potentially be poisoned by lead (Pb) and mercury (Hg), emanating from illegal mining operations. This further underscores the importance of investigations of toxic trace metal levels in the country. The current review of 148 research articles was conducted to provide an understanding of the scope of heavy metals research in Nigeria and to prioritize needed research. The review recognized that the scope of heavy metals studies has been wide, covering matrices such as cosmetics, human blood, hair, medicines, foods, beverages, water, air, soil and crude oil. However, important toxic metals, especially mercury (Hg), arsenic (As) and antimony (Sb), are largely under-investigated. Also, there is a need for more studies to be conducted in the northern part of the country. Furthermore, studies need to focus on marine environments rather than the freshwater ecosystems alone. Techniques such as the inductively coupled plasma-optical emission spectrometry (ICP-OES) and particle-induced X-ray emission (PIXE) analyses are herein recommended to bridge the data gap and to overcome limitations in trace metals analyses in the Nigerian total environment.

Polycarbonate plastic monomer (bisphenol-A) as emerging contaminant in Nigeria: Levels in selected rivers, sediments, well waters and dumpsites.

Despite decades of research into the environmental fate and levels of the endocrine-disrupting polycarbonate Plastic monomer, bisphenol-A (BPA), data remain scarce from many developing countries. Here, occurrence and levels of BPA were investigated in water and sediments of three rivers, selected dumpsites and well waters in Ondo State, Southwestern Nigeria. The study also investigated the influence of matrix physicochemical characteristics on their BPA retention. BPA values ranged from 0.41-5.19 µg/L in river waters, 0.64-10.6 µg/kg in river sediments, 0.63-0.68 µg/L in well waters and 0.72-1.09 µg/kg in waste dumpsites. BPA concentrations in the river waters showed a strong association with chemical oxygen demand (COD) values. High BPA concentrations were also found associated with high chloride contents of drinking well waters. Detection in river and well waters revealed exposure routes of humans, cattle and aquatic species to BPA in the region.