| Literature DB >> 35740921 |
Fernanda Cássio1,2, Daniela Batista1,2, Arunava Pradhan1,2.
Abstract
Plastics are a group of synthetic materials made of organic polymers and some additives with special characteristics. Plastics have become part of our daily life due to their many applications and uses. However, inappropriately managed plastic waste has raised concern regarding their ecotoxicological and human health risks in the long term. Due to the non-biodegradable nature of plastics, their waste may take several thousands of years to partially degrade in natural environments. Plastic fragments/particles can be very minute in size and are mistaken easily for prey or food by aquatic organisms (e.g., invertebrates, fishes). The surface properties of plastic particles, including large surface area, functional groups, surface topography, point zero charge, influence the sorption of various contaminants, including heavy metals, oil spills, PAHs, PCBs and DDT. Despite the fact that the number of studies on the biological effects of plastic particles on biota and humans has been increasing in recent years, studies on mixtures of plastics and other chemical contaminants in the aquatic environment are still limited. This review aims to gather information about the main characteristics of plastic particles that allow different types of contaminants to adsorb on their surfaces, the consequences of this adsorption, and the interactions of plastic particles with aquatic biota. Additionally, some missing links and potential solutions are presented to boost more research on this topic and achieve a holistic view on the effects of micro- and nanoplastics to biological systems in aquatic environments. It is urgent to implement measures to deal with plastic pollution that include improving waste management, monitoring key plastic particles, their hotspots, and developing their assessment techniques, using alternative products, determining concentrations of micro- and nanoplastics and the contaminants in freshwater and marine food-species consumed by humans, applying clean-up and remediation strategies, and biodegradation strategies.Entities:
Keywords: adsorption; aquatic ecosystems; interaction; microplastics and nanoplastics; other contaminants
Mesh:
Substances:
Year: 2022 PMID: 35740921 PMCID: PMC9221377 DOI: 10.3390/biom12060798
Source DB: PubMed Journal: Biomolecules ISSN: 2218-273X
Figure 1Schematic representation of the formation of plastic particles, their release into aquatic ecosystems and interactions with other contaminants posing risks to environmental and human health.
Figure 2Number of published articles in different Web of Science categories in last 10 years (2012–2021) found using the search keywords “NANOPLASTICS OR MICROPLASTICS AND TOXICITY AND AQUATIC” in all fields. This analysis was performed on 31 January 2022.
Figure 3Abundance of plastic particles and their size distribution reported in freshwaters (lakes, rivers, reservoirs and drinking waters) (A), and in the marine waters (including coastal areas, estuaries, bays, seas and oceans) (B).
Studies assessing the effects of different types of contaminants combined with nano- and micro-plastics. PS—polystyrene, PE—polyethylene, LDPE—low density polyethylene, HDPE—high density polyethylene, PP—polypropylene, PLA—polyamide, PVC—polyvinyl chloride, PBAT—polybutylene adipate terephthalate, PBDE—polybrominated diphenyl ethers, BPA—bisphenol-A, PAHs—polycyclic aromatic hydrocarbons, PCBs—polychlorinated biphenyls, PBDEs—polybrominated biphenyl ethers, PFOS—perfluorooctane sulfonic acid and DiNP—Diisononylphthalate.
| Size | Type of Plastic(s) | Contaminant(s) | Organism(s) | Effect(s) | Reference |
|---|---|---|---|---|---|
| Nanoplastics | PS 100 nm | none | Blue mussel | Reduction in filtering activity | [ |
| PS 70 nm | Green algae ( | Reduction of CO2 and increasing production of ROS | [ | ||
| PS 50 and 180 nm | Crustacean | High mortality rates and decrease in fertility | [ | ||
| PS 50 nm | Copepod | Decrease in fertility and reproduction rates | [ | ||
| PS 24 and 28 nm | Crucian carp | Behavioral, physiological and metabolic changes | [ | ||
| PS 100 nm | Aquatic fungal community | Decrease in leaf litter decomposition | [ | ||
| PS 100 and 1000 nm | Aquatic fungal community | Effects on leaf decomposition and fungal community structure | [ | ||
| PS 100 nm | Copper (Cu) | Zebrafish | Synergistic effects (microplastics aggravated Cu toxicity | [ | |
| PS 50 nm | BPA | Zebrafish | Nanoplastics accelerate BPA bioccumulation (head and viscera) | [ | |
| PS 100 nm | Pharmaceutical (Roxithromycin) | Red tilapia | Nanoplastics increase antibiotic bioaccumulation, affect its metabolism and mitigate neurotoxicity and oxidative damage | [ | |
| PS 100 nm | PCBs | Crustacean | Lower concentration of nanoplastics decrease toxicity of PCBs, but higher concentration induce lethal effects | [ | |
| LDPE < 3 nm | PAHs, PCBs and PBDEs | Japonese medaka ( | Nanoplastics trigger an increase in bioaccumulation of the contamination | [ | |
| Microplastics | PS 45 µm | none | Zebrafish larvae | Neurotoxicity in the locomotor activity | [ |
| PE 10–30 μm and | Copepod | Toxic effects on feeding, fecundity, and survival | [ | ||
| PLA 66 μm and HDPE 103 μm | Oysters | High respiration rates, alteration in benthic assemblage structures | [ | ||
| PS 10 μm | Caddisfly larvae ( | Mortality of shredders and decrease in leaf litter decomposition | [ | ||
| Microspheres | Mercury (Hg) | Feshwater bivalve | Antagonistic effects in several biomarkers | [ | |
| PS 20 µm | Copper (Cu) | Zebrafish | Synergistic effects (microplastics aggravated Cu toxicity | [ | |
| PS 32–40 µm | Cadmium (Cd) | Early juvenile discus fish ( | Synergistic effects (increase in protein carboxyl content, catalase, lysozyme and acid & alkaline phosphatase activities) | [ | |
| PE microspheres (19–107 µm) | Silver (Ag) | Zebrafish ( | Microplastics decrease uptake of Ag, but induce localization at intestine | [ | |
| PE 10–106 µm | Silver (Ag) | rainbow trout ( | Ingestion and bioaccumulation of Ag in anterior/mid intestine | [ | |
| PE 1–5 µm | Copper (Cu) | Microalgae ( | Decrease in population growth | [ | |
| PE < 1 mm extracted from personal care product | Nano-silver (Ag-NPs) | Aquatic fungal community | Decrease in fungal biomass, enzyme activities, leaf litter decomposition | [ | |
| PS 10, 50, 100 and 200 µm | PAHs | Copepods ( | Microplastics reduce toxicity of PAHs | [ | |
| PE, PS microspheres | PCBs | Norway lobster ( | No significant bioaccumulation of the contaminants | [ | |
| PE 1–5 µm | PAH (pyrene) | Juvenile common goby ( | Delay in pyrene-induced mortality, reduced acetylcholinesterase and isocitrate dehydrogenase activities | [ | |
| PE (size not mentioned) | Agrochemical (paraquat) | Juvenile common carp ( | Decrease in total | [ | |
| PE 10–700 µm | PBDEs | Rainbow fish ( | Induce bioaccumulation of PBDEs | [ | |
| LDPE 11–13 µm | PAH (benzo[a]pyrene) and PFOS | Peppery furrow shell clam ( | Oxidative damage in digestive gland and gill tissues | [ | |
| PE and PP 0.3–5 mm | PCBs and PBDEs | Zooplankton | Induce bioaccumulation | [ | |
| PP 0.3–5 mm | PCBs | rabbitfish, | Induce bioaccumulation of PCBs in muscle tissues, may harm in long run | [ | |
| PS 400–1300 µm | PCBs | Lugworm ( | Microplastics affect growth and feeding activity and induce bioaccumulation of PCBs | [ | |
| PLA 1–5 µm | BPA | Crustacean | Ingestion of contaminants, decreased immobilization | [ | |
| PVC 1-10 µm | Pharmaceutical (venlafaxine) | Loaches ( | Increase in pharmaceutical bioaccumulation | [ | |
| PVC | DiNP | Crustacean | Inhibition on reproduction and growth | [ |
Figure 4Schematic representation of the affinity between different plastic particles (PP: polypropylene, PE: polyethylene, PS: polystyrene and PVC: polyvinyl chloride) and different contaminants (hydrophilic compounds, hydrophobic compounds and heavy metals) and the impacts of their mixed exposure to aquatic organisms.