Microplastics and Nanoplastics in Aquatic Environments: Aggregation, Deposition, and Enhanced Contaminant Transport.

Plastic litter is widely acknowledged as a global environmental threat, and poor management and disposal lead to increasing levels in the environment. Of recent concern is the degradation of plastics from macro- to micro- and even to nanosized particles smaller than 100 nm in size. At the nanoscale, plastics are difficult to detect and can be transported in air, soil, and water compartments. While the impact of plastic debris on marine and fresh waters and organisms has been studied, the loads, transformations, transport, and fate of plastics in terrestrial and subsurface environments are largely overlooked. In this Critical Review, we first present estimated loads of plastics in different environmental compartments. We also provide a critical review of the current knowledge vis-à-vis nanoplastic (NP) and microplastic (MP) aggregation, deposition, and contaminant cotransport in the environment. Important factors that affect aggregation and deposition in natural subsurface environments are identified and critically analyzed. Factors affecting contaminant sorption onto plastic debris are discussed, and we show how polyethylene generally exhibits a greater sorption capacity than other plastic types. Finally, we highlight key knowledge gaps that need to be addressed to improve our ability to predict the risks associated with these ubiquitous contaminants in the environment by understanding their mobility, aggregation behavior and their potential to enhance the transport of other pollutants.

Effects of weathering on the properties and fate of secondary microplastics from a polystyrene single-use cup.

In this work, we probed the changes to some physicochemical properties of polystyrene microplastics generated from a disposable cup as a result of UV-weathering, using a range of spectroscopy, microscopy, and profilometry techniques. Thereafter, we aimed to understand how these physicochemical changes affect the microplastic transport potential and contaminant sorption ability in model freshwaters. Exposure to UV led to measured changes in microplastic hydrophobicity (20-23 % decrease), density (3% increase), carbonyl index (up to 746 % increase), and microscale roughness (24-86 % increase). The settling velocity of the microplastics increased by 53 % after weathering which suggests that UV aging can increase microplastic deposition to sediments. This impact of aging was greater than the effect of the water temperature. Weathered microplastics exhibited reduced sorption capacity (up to 52 % decrease) to a model hydrophobic contaminant (triclosan) compared to unaged ones. The adsorption of triclosan to both microplastics was slightly reversible with notable desorption hysteresis. These combined effects of weathering could potentially increase the transport potential while decreasing the contaminant transport abilities of microplastics. This work provides new insights on the sorption capacity and mobility of a secondary microplastic, advances our knowledge about their risks in aquatic environments, and the need to use environmentally relevant microplastics.

Fate of microfibres from single-use face masks: Release to the environment and removal during wastewater treatment.

Single-use face masks can release microfibres upon exposure to environmental conditions. This study investigates the number of microfibres released in the presence and absence of UV irradiation and mechanical friction and the removal of the released microfibres in a simulated conventional wastewater treatment process. UV exposure results in a four-fold increase in the number of microfibres released from new masks and used masks resulting in ~2400 microfibres/mask and ~1100 microfibres/mask, respectively. Application of mechanical friction to the UV-exposed new and used masks further increases the number of released microfibres per mask. In a simulated coagulation/flocculation process, the removals of microfibers originating from new masks and used masks are 79% and 91%, respectively. XPS analysis reveals that the silica content of the used masks is 240% higher than that of new masks, which could explain the higher removal efficiency of microfibers from used masks. FTIR analysis of the masks after UV exposure shows carbonyl indices of 0.73 ± 0.70 and 0.27 ± 0.10 for the microfibres from used and new masks, respectively. Based on available data, we estimate that 4-47 million polypropylene microfibres can be released into natural waters per day after wastewater treatment in an urban environment (for a population of 4300 persons/km2).

Weathering pathways and protocols for environmentally relevant microplastics and nanoplastics: What are we missing?

To date, most studies of microplastics have been carried out with pristine particles. However, most plastics in the environment will be aged to some extent; hence, understanding the effects of weathering and accurately mimicking weathering processes are crucial. By using microplastics that lack environmental relevance, we are unable to fully assess the risks associated with microplastic pollution in the environment. Emerging studies advocate for harmonization of experimental methods, however, the subject of reliable weathering protocols for realistic assessment has not been addressed. In this work, we critically analysed the current knowledge regarding protocols used for generating environmentally relevant microplastics and leachates for effects studies. We present the expected and overlooked weathering pathways that plastics will undergo throughout their lifecycle. International standard weathering protocols developed for polymers were critically analysed for their appropriateness for use in microplastics research. We show that most studies using weathered microplastics involve sorption experiments followed by toxicity assays. The most frequently reported weathered plastic types in the literature are polystyrene>polyethylene>polypropylene>polyvinyl chloride, which does not reflect the global plastic production and plastic types detected globally. Only ~10% of published effect studies have used aged microplastics and of these, only 12 use aged nanoplastics. This highlights the need to embrace the use of environmentally relevant microplastics and to pay critical attention to the appropriateness of the weathering methods adopted moving forward. We advocate for quality reporting of weathering protocols and characterisation for harmonization and reproducibility across different research efforts.

Exposure of nanoplastics to freeze-thaw leads to aggregation and reduced transport in model groundwater environments.

Despite plastic pollution being a significant environmental concern, the impact of environmental conditions such as temperature cycling on the fate of nanoplastics in cold climates remains unknown. To better understand nanoplastic mobility in subsurface environments following freezing and thawing cycles, the transport of 28 nm polystyrene nanoplastics exposed to either constant (10°C) temperature or freeze-thaw (FT) cycles (-10°C to 10°C) was investigated in saturated quartz sand. The stability and transport of nanoplastic suspensions were examined both in the presence and absence of natural organic matter (NOM) over a range of ionic strengths (3-100 mM NaCl). Exposure to 10 FT cycles consistently led to significant aggregation and reduced mobility compared to nanoplastics held at 10°C, especially at low ionic strengths in the absence of NOM. While NOM increased nanoplastic mobility, it did not prevent the aggregation of nanoplastics exposed to FT. We compare our findings with existing literature and show that nanoplastics will largely aggregate and associate with soils rather than undergo long range transport in groundwater in colder climates following freezing temperatures. In fact, FT exposure leads to the formation of stable aggregates that are not prone to disaggregation. As one of the first studies to examine the coupled effect of cold temperature and NOM, this work highlights the need to account for climate and temperature changes when assessing the risks associated with nanoplastic release in aquatic systems.

Microplastics in African ecosystems: Current knowledge, abundance, associated contaminants, techniques, and research needs.

Despite Africa ranking top in mismanaged plastic waste, there is insufficient data on the extent of microplastics and its interaction with other contaminants in its ecosystems. Microplastics pollution has been documented globally, however, specific data from the continent is crucial for accurate risk assessment and to drive policies. We critically reviewed 56 articles from 1987 to 2020 and provide an overview of the current knowledge of the abundance and distribution of microplastics and associated contaminants in African aquatic systems and organisms. Most of the studies were carried out in the marine environment and there is currently no available data on the abundance of microplastic pollution in the African terrestrial environment. We show that across all studies, 5-100% of all sampled aquatic organisms contained microplastics. Concerning high levels of microplastics were reported in fish from Egypt compared to other parts of Africa and the world. Across all persistent organic pollutants sampled in microplastics, hopanes and phthalates were present at high concentrations while sodium and zinc were high relative to other trace metals reported. The most frequently occurring plastics were polyethylene followed by polypropylene and polystyrene. We found that most of the studies relied on visual inspection (52%) > FTIR (38%) > Raman spectroscopy (5%) > Scanning electron microscopy (3%) > Differential scanning calorimetry (2%) for identifying microplastics. Major gaps in sampling and identification techniques which may have overestimated or underestimated the current levels were identified. We discuss other research priorities and recommend solutions to address these issues associated with microplastic pollution in Africa.