| Home | E-Submission | Sitemap | Contact Us |  
Environ Eng Res > Volume 30(4); 2025 > Article
Shrivastava, Silori, Verma, Nandan, Kumar, and Giri: Microplastic pollution in the German aquatic environment: Existence, interactions and research needs

Abstract

Plastics, once celebrated for their versatility, have now become a significant environmental threat due to their persistence, with microplastics (MPs) posing serious concerns. This study examines the prevalence of MPs across various environmental domains, focusing on their impact on ecosystems and human health, along with analytical procedures and treatment techniques. It has been found that Fourier Transform Infrared Spectroscopy (FTIR) is the most common analytical procedure for MPs detection. Few policies/steps have been formulated by international organizations/governments to impede the proliferation of MPs, which have been duly included herein. Germany, as Europe’s largest economy and a major contributor to plastic pollution, surprisingly has a dearth of research in this area. So, this study focuses on MP pollution in the German aquatic environment and highlights alarming concentrations of MPs, with up to 11,050 particles/L in rivers and 9,000 particles/m3 in wastewater treatment plants (WWTPs). Fibers dominate in shape, and polyethylene (PE), polypropylene (PP), and polystyrene (PS) are the most common polymers, primarily originating from municipal/industrial wastewater. Based on these findings and identified gaps, the paper provides recommendations for future research and areas of improvement, such as standardized measurement units, more studies, and combined effects of MPs with other emerging contaminants.

Graphical Abstract

/upload/thumbnails/eer-2024-609f7.gif

Introduction

The introduction of synthetic polymer at the beginning of the 20th century is heralded as a revolutionary replacement for natural materials such as wood, natural rubber, metals, etc. [1]. Having some exceptional properties like light weight, strength, durability, light and chemical resistance, ability to work in a varied range of temperatures, and ability to be remolded in different shapes and sizes, these synthetic polymers or plastics have benefitted humans in various sectors and areas such as transportation, food, and beverages, packaging, textiles, household items, etc. [2]. Plastic’s unique properties and its low cost have got it an essential place in everyone’s life, and it is ostensible from its colossal increase in demand, starting with just 25 million tonnes of production in the 1950s to a mammoth 367 million tonnes by 2020 [34].
Global plastic consumption has experienced an unprecedented increase over the past decades. In Europe, plastic waste generation averages approximately 500 kg per capita annually, while in the United States, it exceeds 800 kg per capita per year, highlighting significant disparities in consumption patterns [5]. On a global scale, plastic production has skyrocketed from 2 million tons in 1950 to over 400 million tons in 2021, with a sharp rise observed in the past two decades driven by increasing demand in Asian economies, particularly China, India, and Japan [67]. This exponential growth underscores the urgent need for sustainable management strategies to address the environmental consequences of plastic waste.
However, those that were and are considered revolutionary in the history of human invention are slowly becoming a global cause of concern because of their overuse and ubiquity around us [89]. The degradation of plastic into smaller particles and fragments due to the prevailing environmental conditions, such as ocean currents, solar radiation, abrasions, and interaction with microorganisms, leads to the genesis of microplastics [10]. Initially coined by Thompson et al. [11], microplastics result from such degradation. These are the minute particles whose size is <5 mm [12]. However, the range is still a topic of discussion among the scientific communities. Many authors have reported various size indexes for MPs, such as <1 μm [13], <1 mm [14], or <10 mm [15]. There is still a need to reach a consensus and define standards for these emerging pollutants.
A report by WHO [16] highlighted the gravity of this unintended release of emerging pollutants and immediately called for further research, potential risks to human health, and the scope of this issue. The seriousness of MPs in our environment can also be understood by the increment in their studies by various authors in the scientific world. As shown in Fig. 1, the number of research and studies conducted on microplastics globally grew dramatically in the last 10 years. An astounding increment of 142.40% is observed only between the years 2020 and 2022 in the studies discussing MPs, which shows growing importance in this domain among the scientific community recently. The data presented in the figure originates from the Science Direct website, where the keyword ‘Microplastics’ was employed for retrieval.
Since MPs are the by-product of the degradation of plastic substances by numerous mechanisms, it implies that plastic waste is imprudently scattered in our environment. A number of sources and factors work as the vehicles for MPs for their abundance in soil (sediment and soil), water (wastewater, river, groundwater, seawater etc), and air. Fig. 2 will better represent various sources and pathways taken up by MPs for their intrusion into the environment’s different spheres. These pathways or the source of their occurrence can be either direct or indirect. For instance, irrigation water and plastic mulching were found to be the carriers of MPs in the agricultural soil, further posing a potential risk to groundwater quality [17]. The study identified the presence of MPs up to 50 cm depth of soil. Sewage sludge is rich in potassium and phosphorus and is extensively used in agricultural soil as fertilizer. A study confirmed this sewage sludge as a major vehicle for the introduction of MPs in agricultural soil systems [18]. The author further in that study discovered that the sewage sludge was introducing a concentration of up to 2130 particles/kg of light-density MPs and 3060 particles/kg of heavy-density MPs in farmland soil. Soil is considered to be the biggest exporter of MPs in water bodies. A surprising result in the study by Nizzetto et al. [19] claimed that soil is responsible for 60% of MPs’ pollution in surface water bodies. Phenomena like soil erosion and rainfall events promote the transportation of MPs from the terrestrial environment toward aquatic [20]. The same author conducted a simulated experiment in which fine MPs (10 g m−2) and course MPs (50 g m−2) were added in a simulated plot of 4.5 m × 1.6 m. The result of the experiment showed a substantial enrichment ratio of course and fine MPs in the eroded sediments. It is safer to assume that the eroded sediments can easily travel to any aquatic system in a real-world scenario, leading to their MPs contamination. Lwanga et al. [21] also discussed how soil organisms facilitate the movement of MPs into deeper soil layers. For instance, the author points out that earthworms can carry MPs on their outer skin, potentially enabling these particles to reach deeper soil layers and possibly even migrate into groundwater.
There have been some studies highlighting emerging stealthy sources of MPs polluting our environment. A study by Kole et al. [25] highlighted tires acting as the origin of MPs pollution with an estimated per capita emission ranging from 0.23 to 4.7 kg/year with a global average of 0.81 kg/year. A novel analytical method was employed to quantify polyethylene terephthalate (PET)- and polycarbonate (PC)-based MPs in 286 indoor dust samples collected from 12 countries. PET-based MPs were identified in all samples, with concentrations ranging from 38 to 120,000 μg/g while PC-based MPs were detected at levels between <0.11 and 1700 μg/g [26]. MPs have been found in ocean-bed and a study by Pinheiro et al. [27] attempted to highlight the role of deep-sea mining in that.
In recent years, many studies highlighting the detrimental effects of MPs have started surfacing. One of the studies by UNDP [28] informs the effect of MPs on the human body, such as abnormal weight gain, antibiotic resistance, endocrine disruption, cancer, etc. Likewise, Lee et al. [29] also stress the harmful effects of MPs in the human body, such as oxidative stress, neurotoxicity, reproductive toxicity, carcinogenicity, altered metabolism, etc. Animals, too, have been gravely affected by the presence of MPs within their bodies. Inflammation, cytotoxicity, genotoxicity, and immunotoxicity are a few side effects out of many that have been reported in animals [30]. On plants, it has been found that the MPs adsorbed onto the root hairs, affecting their growth and finally affecting the leaf growth and photosynthesis [3132]. Not only do these pollutants affect living organisms, but they also meddle with environmental services. For example, reducing the nutrient content in microalgae, disrupting the food web, contributing in the decline of biodiversity, biological fouling in the pedosphere, etc [3335].
Another worrying fact emerging out of MPs is their role as carriers for other contaminants, such as persistent organic pollutants (POPs) [33]. The interaction of polyvinyl chloride (PVC) and polyethylene (PE) with several POPs has been declared a threat to our environment [36]. MPs’ hydrophobic nature serves their surface area as a perfect adsorbing spot for heavy metals, and the negative charge on their surface increases their pick-up rate of various airborne pollutants, making the MPs a perfect vehicle or carrier of pollutants in the environment [37]. The biofilm around the MPs surface is becoming a hosting site for antimicrobial-resistant (AMR) bacteria [38]. Although efforts have been put into analyzing and remedying these micro-contaminants using physical, microbial, chemical, and biological techniques, which will be discussed further in this study, these procedures still do not guarantee total elimination. Hence, more research is required in this field. However, there have been regulatory steps taken by governments all across the world barring the use of single-use plastic or putting penalties on the defaulters [3940]. However, a long way is still ahead to achieve the desired results.
This paper will discuss the scenario of MPs globally. Furthermore, the paper aims to document the prevalence of MPs in German surface and groundwater bodies and will attempt to provide any future recommendations to scientific peers working in this field. The idea of taking Germany as the center of the study is that Germany is the biggest polluter and exporter of plastic packaging waste in Europe, along with being the biggest economy in Europe and the 4th largest economy globally. At the same time, Germany is also pushing hard to reduce its plastic waste exports and is seriously working on recycling them. However, the lack of scientific studies on the presence of MPs in the water environment, which is the biggest source of origin and dumping ground for these emerging pollutants, may become a roadblock for Germany’s ambitious drive towards mitigating plastic pollution. The studies included in this review were selected through a targeted literature search using databases such as Web of Science, Scopus, and Google Scholar. Search terms included ‘microplastics in German water bodies,’ ‘German rivers microplastic pollution,’ ‘groundwater microplastics in Germany’, etc. articles published in English or German, with a focus on microplastic pollution in German freshwater systems, were included. The studies were evaluated based on their methodologies, findings, and geographical relevance. This paper comprises all the possible studies from the last 10–15 years, and based on the results, the plausible recommendations have been shared at last.

Distribution in Water Bodies and Sediments

2.1. Occurrence and Abundance in WWTPs

Out of all the places of contamination, WWTPs can be undoubtedly considered as the storehouse for MPs. Domestic waste, pharmaceutical and personal care products, and industrial wastes contribute to MPs colonization in wastewater. According to a study conducted on a Turkish WWTP, a miserable concentration of 2936×106 particles/ day was released in the effluent into the Sea of Marmara [41]. Ngo et al. [42] provided a litany of factors responsible for MPs proliferation in WWTPs. The textile industry is another major contributor of MPs in WWTPs [43]. The author further highlights that the fibers and polymers released from these industries in effluent go to WWTPs. In the same study, the author informed that a WWTP in China had contamination of 4.9 to 12 microplastic fibers per liter. Microbeads, used in tooth-pastes, face, and body wash products, and other cosmetic products, reach WWTP’s influent cycle via domestic discharge [44]. Usually, eroded plastic debris from the construction processes, like admixtures used in concrete and bitumen remnants, abrasion of tires, and packaging of construction machinery and tools, remain suspended in the atmosphere before finally falling and scattering onto the ground. During the time of precipitation, these scattered particles are washed away with the run-off and eventually end up in sewer pipes, taking them straight to WWTPs [45].

2.2. Occurrence and Abundance in River and Groundwater

Microplastics have also been extensively found in water bodies. A study by Ayyamperumal et al. [46] on the Noyyal River in India reported high concentrations of microplastics in both the freshwater and sediments, ranging from 500 to 6,500 items per cubic meter. The cause of such pollution was attributed to the nearby industries and urbanization. Fishing activities are often the major polluter of MPs in the river system. Wang et al. [47] documented that MPs were found in abundance in the water of the Yangtze River, which was a result of the fishing practices of the local fishermen. Usually, nylon nets, fishing lines, and fishing tools degrade and become the source of MPs in the river system. Kiss et al. [48] also stressed that high population density, the spatial distribution of residential and industrial areas, and improper waste management are the root causes of MPs abundance in river water and are ostensible from the study on the Tisza River in Central Europe. Sometimes, flood becomes a major contributor to MPs proliferation in the rivers and other surface water bodies. Previously deposited MPs in any catchment area of an urbanized locality are washed away with flood water and redistributed into the nearby water body [49]. These rivers further become the vectors for MP pollution in seawater. The grim situation of the Black Sea is one primary example of it. 2.6 tons of MPs was discharged to the Black Sea in 2010 by three major transboundary rivers: the Danube, Dnieper, and Don River [50]. The study further added that human activities and mismanagement of the sewage effluent were responsible for the pollution. An unfortunate figure highlighted that 1.15–2.4 million tons of plastic enter oceans globally from the land and out of this, 0.27 million tons of plastic remains in the sea current [5152]. It can be safer to imagine that the remaining concentration gets either submerged and settled on the ocean floor, washed away and left on coastal sediments, or consumed by marine animals.
Talking about another water body upon which not enough studies have been conducted and can be a future potential hotspot for MPs is the groundwater. Nizzetto et al. [19] list various parameters responsible for the MP contamination of the groundwater. The lists include precipitation run-offs, discharge of WWTPs into rivers and lakes, soil erosion, leaching of leachates, infiltration of wastewater from WWTPs, overflowing of sceptic tanks, and repetitive use of reusable irrigation water coming from municipal WWTPs. Generally, soil characteristics, roots, and branches of the plants forming crevices in rocks and sinkholes provide a pathway for MPs to migrate into groundwater [53]. Groundwater monitoring for MPs’ contamination should be of paramount importance because it is one of the major sources of water for human beings. Any contamination in this water can pose direct and indirect effects on human health. A study conducted in India reported that concentrations up to 80 items/L of MPs were found in the groundwater samples of Chennai city [54]. The author also highlighted that landfill dumping sites were close to the sampling sites. This can positively correlate between landfill sites and groundwater contamination with MPs. In Germany, MPs of the size 1 μm, 2 μm, and 5 μm were found to be transported in an alluvial aquifer in Upper Rhine Valley. The worrying fact about this study was that the respective aquifer is a trans-boundary aquifer running between the boundaries of Alsace (France) and Baden-Wuerttemberg (Germany) and caters up to a population of 3 million people [55]. Since there is a dearth of studies encompassing the migration of MPs to the groundwater, scientific communities should pay attention and work on the topic catering to the transportation behavior of MPs in the ground and groundwater. However, it can be stated that the porosity of the soil media must play an important role in the migration of such particles. The greater the porosity and the pore size, the easier the transportation would be. Along with that, soil texture can also affect the migration ability of MPs reaching up to groundwater. Coarser the texture, smoother will be its transition from ground to groundwater level. Finer soil grains will retain the MPs onto its surface, thus retarding its downward progression. Hallaq [56] also supports that the percolation of MPs into the soil media is a function of soil texture. Apart from the leaching around landfill sites and WWTPs, irrigation can significantly increase the concentration of MPs in the groundwater. In a study, an unconfined aquifer was contaminated with MPs, with its maximum concentration reaching up to 55 particles/L [57]. Interestingly, an irrigable horticulture site was in close proximity to the sampling site. This further proves that the irrigation method can work as a carrier for MPs for groundwater.

2.3. Occurrence and Abundance in Sediments

An abundance of MPs has also been identified in the coastal and estuarian sediments. Li et al. [58] specifically mentioned that the factors involved in the proliferation of MPs in coastal and estuarian sediments are anthropogenic activities like tourism and recreational activities, coastal urbanization, ocean currents, and meteorological conditions. Xu [59] describe warm ocean currents as one of the key factors influencing MPs’ presence in coastal and estuarian sediments. The respective author discussed the MP’s pollution in the Changjiang estuary. The author attributed the Taiwan warm currents for circulating these MPs from ocean towards the terrestrial zone. A similar study supported the argument that strong tidal current served as a carrier of these pollutants over coastal sediments. Strong tidal currents were found to be responsible for polluting Hangzhou Bay in Eastern China. The sampling sites on the bay were accumulated with MPs, which were probably the by-products of the degradation of fishing gears, ropes, scuba gear, plastic bottles, and marine plastic littering by cruise and commercial ships. This plastic debris degrades and floats on seawater, which is brought to the shores by ocean currents. Socio-economic development plays a crucial role in the regulation of MPs in coastal sediments and is evident from the study of Li et al. [58]. The study found a maximum concentration of 2250 particles/kg of MPs in Mangroves of Southern coastal areas of China. Sometimes, geography of an area also becomes conducive for trapping MPs loads over its soil. The semi-enclosed area of Bohai Sea was found to be a sinking ground of MPs [60]. The waves enter and then breaks due to semi-enclosed coastal geography and lose its strength. They eventually dump the MPs load on coastal sediments.

Impact of MPs

3.1. Impact on Humans

The rapid proliferation of plastic has raised concern not only for the environment but also for human health. Although there is a lack of trophic transfer of MPs into the human digestive system, the studies on this issue presented some unsettling results. It is well known that human beings are consumers of aquatic animals. Studies have reported that enough MPs fragments have been found in the digestive tracts, circulatory systems, and tissues of marine animals [6162]. It has been forecasted that the European population will have an intake of 11000 particles of MPs per year due to the consumption of shellfish [63]. MPs have also been found to catalyze reactive oxygen species in human epithelial and cerebral cells [64]. Exposure to MPs has also affected the reproductive health of pregnant women. Pregnant women with traces of polycyclic aromatic hydrocarbon (PAH) in their system were found to be giving birth to under-weight with restricted growth babies [65]. Another study recorded the short-term effects of exposure to PAH on human health, in which it was found that frequent exposures to MPs can affect the functioning of the lungs. In some cases, it was even found that exposure to PAH increased the risk of asthma and thrombosis [66]. Goudarzi et al. [67] also covered some short-term effects of PAH’s exposure to humans’ digestive tract. From nausea to vomiting, eye, and skin irritation were common symptoms. The MPs in human intestines show sufficient cytotoxicity in intestinal cell lines and increased in oxidative stress activities [68]. John et al. [69] described certain long-term effects on human health, where it was found that repetitive, prolonged exposure in small doses to PAH could alter the DNA structure. Huang et al. [70] also documented the dire effects of PAH on reproductive health. Abnormal birth weight, side effects in the fetus, lesser testosterone level, the irregular circumference of the head, etc., were some of the comprehensions of the respective study. Can it be posited that it may be a beginning of mutation in humans? Several reports have also discussed the oxidative stress induced due to the exposure of MPs in humans. Sun et al. [65] purported that PAH induces oxidative stress and causes chromosomal damage in women. Although sufficient data is yet to be researched before concluding the impact of MPs on the liver, heart, and kidneys, authors have not ruled out the potential damage that these contaminants can cause [7173]. However, further research is needed to quantify microplastics and correlate their presence with human health impacts. A detailed Fig. 3 diagrammatically represents the effects of MPs on various human body organs.

3.2. Impact on Terrestrial and Marine Animals

The toxicological effects of MPs on aquatic and terrestrial animals have been extensively studied and reported and several studies. The MPs can either float on the surface, suspended in water columns at varying depths or settle down and accumulate on bed sediments of any water source. Various authors have verified the presence and adverse effects of MPs in crustaceans, birds, mammals, turtles, fish, bivalves, and so on [62, 7478]. Aquatic animals, especially fishes, feed upon these MPs due to the appearance and size of plankton [79]. Once the MPs are ingested into aquatic fauna’s digestive system, they are not easily emoved by their body as time ensues, and the MPs accrue. The most severe effect of this accumulation is the blocking of the digestive tracts of these animals. Wang et al. [80] argue that once these MPs are retained for a longer duration, they can be transferred to higher trophic predators. In an experimental study by Deng et al. [81] discovered a disturbance in energy and lipid metabolism in mice. In fishes, Danio rerio suffered intestinal damage when introduced to PVC MPs with a size of roughly 70 μm size. The MP’s presence has not only affected the biological metabolism of animals but also interfered with the dynamics of animals’ habitats. MPs accumulation in shore sediments led to an increase in thermal diffusivity, increased heat capacity, and increased permeability of the sand grains, which has affected the hatching cycle of eggs of sea turtles [82]. A positive correlation was also found between the amount of MPs in the fishes of the North Atlantic Sea, chiefly Dicentrarchus labrax, Trachurus trachurus, Scomber colias, and the bisphenol A detected in their cells and tissues [83]. There is no wonder that these toxic fishes can easily find their way into the food chain of humans. Another study highlighted the adverse effect of MPs affecting the reproduction ability and energy balance among black-lip pearl oyster, Pinctada margaritifera, was highlighted by Gardon et al. [84].
In avian species, polybrominated diphenyl ethers were found in the stomach and fatty tissues of birds like Puffinus tenuirostris and was reported at a concentration of 0.3–186 ng/g-lipid weight [75]. This suggests that these birds must have preyed on the fishes which had already accumulated the respective MPs in their digestive system. This can be inferred as a prime example of the transfer of toxic elements climbing up in the food chain. Likewise, other fish species, like Ardea Cinerea, Cygnus olor, and Anas platyrhynchos, were also found to be infested with the fragments of MPs with a concentration of 4.3 ± 2.6 particles per bird in Switzerland [85].
Mammals have also been found to be affected by MP contamination. In the Netherlands, a study conducted on harbor seals provided sufficient evidence for the MPs present in the stomachs and intestines of their corpses [78]. Although it was not clear the actual reason for MPs in the body of seals, it can be hypothesized that either the harbor area is very much polluted with plastic or a lot of anthropogenic activities and recreational activities take place in that area, such as fishing, boating, and cruising. The biggest mammal on this planet, whales, have been found to be highly infested with MPs. Study on Baleen whales revealed the presence of MPs with a size range of 1mm to 17cm of several polymers (polyethylene, polypropylene, polyethylene terephthalate, nylon, etc.) have been recovered from their intestine [86]. Even though, in most cases, the intake of MPs happens accidentally by these animals, but the matter of the fact is their existence and our imprudent attitude in disposing of them. In an experimental study on mice, a worrying result surfaced where it was found that polycyclic aromatic hydrocarbons in mice caused a rapid growth of tumours in the nasal cavity and respiratory tract [65]. MPs in mammals is also a growing cause of concern because it has various associated indirect dangers. The MPs in a mammal biological system can trigger or alter the immune system, oxidative stress, inflammation, reproductive outputs, energy reserves, feeding capacity, etc. [8791].

3.3. Impact on Soil and Crops

The wide application of plastics and their derivatives has led to a huge pollution crisis in our natural environment. Furthermore, the degradation of plastics into MPs has worsened the situation. The presence of MPs in the soil environment has the potential to alter the physical and chemical properties of soil, nutrient content, soil flora and fauna, etc [92]. However, certain soil microorganisms, such as bacteria and fungi, break down MPs using enzymes, improving soil health and promoting crop growth by converting MPs into harmless byproducts like CO2, H2O, and CH4 [93]. Often, continuous use of sewage sludge on the farm fields is considered to be the common source of MPs driving into the soil [94]. Currently, the global production of sewage sludge is estimated to be 45 million Megagrams, out of which the EU’s share is about 13 million Megagrams in 2020 [95]. Due to the colossal generation of sludge, many developed and developing nations are struggling to find ways in order to dispose of this waste, and that is why sewage sludge is not regarded as waste anymore, and focus has been shifted to its utilization, such as composting, landfilling, and agricultural use [9697]. Although, sewage sludge is primarily used as a fertilizer and source of irrigation water in soil because of its high moisture content, richness in organic matter content which is up to 70%, and biogenic matters such as carbon (4%), nitrogen (4%) and phosphorous (2.5%) [95]. But being a carrier of MPs, itself cannot be overlooked easily. Apart from the application of sewage sludge on soil, there are other sources as well responsible for introduction of MPs in soil and sediments environment, such as plastic mulching for water retention and heat preservation, use of plastic pipes, plastic storage tanks, polypropylene woven bags and ropes, refuse from dumping sites, public places like parks and industrial areas, etc [98100]. The introduction of MPs in soil has affected not only the crops but also the animals and organisms living there. The earthworms residing in soil with MPs’ presence weigh relatively much less than those who were living in soil without any MPs’ presence [101]. A similar study on earthworms highlighted that these invertebrates showed recalcitrance in their growth after 60 days of exposure to polyethylene MPs [102]. A similar study also reported a reduction in the germination rate of Lepidium sativum (garden cress), as MPs might be blocking the nutrients and water from being sucked by the pores of seed capsules [101]. A field study conducted on rice crops highlighted the adverse effects of nano polystyrene. In the study, it was found that the given MPs induced oxidative stress, as confirmed by the increased number of antioxidant enzymes in rice roots. This phenomenon caused a reduction in the root length of rice and an increased number of lateral branches of the root [103]. The author also reported several other aftereffects of MPs in the soil system. Some of them are reduced rate of seed germination, genotoxicity in the crops, and bio-accumulation of MPs in the plants transported through vascular tissues of the plants. This reduced the rate of seed germination of the respective plant species. Another invertebrate responsible for sustaining the quality of soil, E. crypticus, was found to be displaying a reduction in its reproduction ability and growth rate when it was exposed to soil with MPs in it [104].

3.4. Impact on Ocean Carbon Sequestration (OCS)

The ocean is a major carbon sink, absorbing approximately 25% of human-made carbon emissions from the 1960s to 2010 [105]. Not just that, oceans also sequester atmospheric carbon, with studies showing the capacities of sequestration up to 20,000 Gt [106]. The presence of plastic in the ocean causes it to absorb more oxygen, reducing the amount available for other marine life. Additionally, the accumulation of organic matter on the ocean’s surface hinders the transfer of oxygen from the ocean to the atmosphere [107]. The study further states that MPs influence marine microorganisms’ ability to absorb carbon dioxide and release oxygen. Additionally, MPs alter the biogenic composition of the sea-surface microlayer, leading to a reduction in dissolved CO2 concentration in the water, thus disrupting the marine carbon cycle [108]. They also hinder algae’s uptake of essential elements like copper, reducing carbon sequestration and affecting the ocean’s role in converting atmospheric carbon into oxygen [109]. Marine microplastics have the potential to impact phytoplankton photosynthesis and growth, induce toxicity in zooplankton, affect their development and reproduction, disrupt the marine biological pump, and alter the ocean’s carbon stock [110]. However, there is still a wide scope and need for further research to understand the impact and interaction of MPs and OCS in a better way.

Interaction of MPs

MPs, due to their small size, do not necessarily affect the environment and living entities alone, but sometimes they interact with other chemical and biological agents and mutate into a different and more toxic substance, which can pose greater threats. For instance, the interaction of MPs with pharmaceutical and personal care products (PPCPs), dissolved organic matter (DOM), antimicrobial-resistant genes (ARGs), heavy metals, surfactants, etc, have been widely discussed and published by the scientific community. Yet, the irony is that even after so many publications, the knowledge about the by-product is still scant and needs further investigation.

4.1. Interaction with PPCPs

Synthetic organic chemicals have emerged as an inseparable part of modern human lives and society in the last few decades, and PPCPs play one such crucial role in it. Polyaromatic hydrocarbons (PAHs), polycarbonate biphenyls (PCBs), perfluorinated alkyl substances (PFAs), etc, are some of those synthesized organic chemicals.
The widespread use of these substances (PPCPs) has made them ubiquitous in every sphere of our surroundings, and their persistence and long residence time are making the scenario worse [111112]. A study revealed that there are more than 160 pharmaceutical chemicals have been found in surface and wastewater [113].
The adsorption of MPs and PPCPs is mainly governed by the adsorption capacity of the MPs, specific surface area, surface texture, shape and size, polymeric properties of MPs, and secondary parameters such as salinity, pH, ionic strength and dissolved organic contents [114].
In several cases, the high ionic strength of the surroundings was found to be a positive catalyst for the interaction between MPs and PPCPs. As reported by Ma et al. [115], the sorption of triclosan upon MPs enhanced by 44% and 74%, with an increase of 35% in the salinity of NaCl. Surface polarity also plays an important role in the interaction of MPs with other entities. MPs that are highly polar and hydrophobic displayed a greater propensity for the hydrophilic PPCPs [114]. Wang et al. [116] state the effect of pH on the interaction where it was reported that when pharmaceutical chemicals, namely estrone, 17β-estradiol, and 17α-ethinylestradiol showed hesitation in their sorption over MPs as the pH of the water raised from 2 up to 12 while perfluorooctanesulfonate (PFOS) and perfluorooctanesulfonamide (PFOSA) improved its sorption over MPs upon the reduction of pH from 7 to 3. Electrostatic interaction between MPs and PPCPs, such as hydrogen bond and van der Waals force, restrict the bond, whereas ionic bond promotes [117]. π-π interaction between aromatic structured compounds and plastic polymer keeps them intact. The strong cohesion between polystyrene and PPCPs is attributed to the strength of the conjugated π cloud of the aromatic structure of PPCPs and polymer [118]. Elizalde-Velázquez et al. [119] state that π-π interaction promotes the interaction between non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen, diclofenac, and naproxen. Interestingly, DOM plays two roles. It can either work for the sorption of PPCPs over MPs, or it may restrict [114]. Tetracycline displayed reticence in interacting with polystyrene, polypropylene, and polyethylene, and the interaction rate dropped by 93%, 95%, and 97%, respectively, upon an increase of fulvic acid by 20 mg/L [120]. Physical characteristics also play a deciding role in aggregating PPCPs over MPs. As the size of polystyrene decreased from micron to submicron to nano-sized particles, phenanthrene, and nitrobenzene were found to be aggregating efficiently on the MPs’ surface [114].

4.2. Interaction with ARGs

ARGs are the genes that have developed resistance to antibiotics and other similar drugs used to treat human infections and diseases [121]. ARGs have been found in almost every zone of our environment, be it water bodies, aquaculture systems, drinking water, STPs, sediments, soil, and air [122128]. Recently, this has been a hot topic of discussion among scientific peers where the interaction of MPs and ARGs has been detected to cause mutation among the microbial communities, thereby providing them resistance against antibiotic medicines [129]. Biofilm around the MPs facilitates the interaction between the polymers and antimicrobialresistant (AMR)bacteria and helps their transmission [130]. MPs hydrophobic surface provides a suitable spot for the aggregation of bacteria and promotes the formation of biofilm [131]. Stenger et al. [132] studied this phenomenon and reported the accumulation of AMR bacteria such as Flavobacteriaceae, Pseudomonas, Desulfovibrio, Morganella morganii, and Acinetobacter beijerinckii on the biofilms of MPs in the Norwegian sea. The interaction between the two contaminants poses serious effects. The retention time of ARGs has increased significantly in the soil ecosystem, with 0.1% polystyrene [133].

4.3. Interaction with Heavy Metals

According to Shrivastava [134], heavy metals are widely used in industries such as medicine, toys, food processing, electronics, chemicals, and household applications.. Vehicle exhaust releases heavy metals like lead (Pb), cadmium (Cd), nickel (Ni), zinc (Zn), and iron (Fe) into the air [135]. These heavy metals, which are persistent pollutants in our environment, have shown greater affinity toward MPs [136].. Heavy metal-laden dust on the ground can also enter surface water bodies through precipitation and runoff, carrying these contaminants into nearby rivers or lakes, the author further added.
There are several factors supporting the adsorption of heavy metals onto MPs surface. The higher the specific surface area, polarity, the polymer’s age, and the surface’s polarity influence the adsorption process [136]. Excessive weathering or aging of these polymers due to adverse environmental conditions like abrasion with other material or UV disintegration increases the surface roughness, thereby increasing its surface area. This makes the surface of MPs as a site for anionic activities and attracts cationic metallic pollutants onto its surface [137]. pH and salinity also affect the interaction process, but there is a certain non-uniformity as the mechanism depends from metal to metal. An experiment conducted by Holmes et al. [138] demonstrated the variation in affinity among the heavy metals for the MPs. The experiment included a mixture of river water and seawater. Upon increasing the salinity gradient, chromium adsorption increased, and that of cadmium, nickel, and cobalt decreased. Wang et al. [139] also manifested a similar kind of experiment to check the effect of pH on the adsorption efficiency. The result showed that higher pH generally leads to more metallic ion adsorption on the polymer surface. A higher specific surface area provides more adsorbing ground for metallic ions and thus promotes the interaction [140]. Zeta potential, or the surface charge on MPs determines the attraction and repulsion trend and is a determining factor for adsorbing the metal ion pollutants over it [141]. Lower zeta potential can trigger the adsorption mechanism of metallic ions due to electrostatic attraction [140]. It was reported that the elevated potential of an aqueous solution of arsenic increased the adsorption affinity over polystyrene and polytetrafluoroethylene [142143].
There are some dire effects of this interaction. Adsorption of heavy metals on MPs is lethal for the growth of the crops. Their combination affects the development of cells and tissues of humans and causes a disruption in enzyme activities in aquatic animals, like zebrafish [144145].

Analysis of MPs

Even though there is an ambiguity about the size range of MPs for all the size ranges, they surely cannot be identified with the naked eye. However, certain analytical methods exist for identifying and quantifying these minute emerging contaminants.

5.1. Identification of MPs

Microscopy is a widely used physical analytical method in which the small size of MPs is magnified. This method is useful for the identification of texture and structural information of MPs. However, this method has its own limitations. MPs with sizes of less than 100 microns, which have amorphous shapes, unlike the other typical shapes of MPs (fiber, film, fragment, etc.), are difficult to identify using microscopy alone. But, another mode of microscopy i.e., scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS) is able to present a highly clear and high-resolution image of MPs. However, the SEM-EDS method is expensive and requires enough amount of time and skilled workers to perform the experiment [146].
Spectroscopy is another technology used to identify MPs, which works on the principle of emission and radiation absorption by any matter. One of the several methods of spectroscopy is Raman spectroscopy. This method involves the knowledge of the vibration of a substance and the scattering of light upon being incident by a light ray [147]. The author further describes the benefits of Raman spectroscopy, which include coverage of a wider spectral range, high-resolution image, higher sensitivity to a non-polar functional group, measurement of particles as small as 1-micron, lower water interference, etc. Furthermore, the sample required for the analysis is also very small. But there are also a few downvotes for this method. For example, the procedure often heats up the sample, which may alter its chemical or physical properties due to using a laser as its light source. The procedure can be affected by fluorescence and has a low signal-to-noise ratio [147]. Although Raman spectroscopy has been extensively used for the identification of MPs, it still has to match the popularity of Fourier-transformation infrared spectroscopy (FT-IR). This state-of-the-art technology is able to analyze the chemical bonds, bond composition, and differentiation between organic and inorganic molecules of MPs and other similar minute particles by generating their unique spectra [148]. Working on the same principles as Raman spectroscopy, FT-IR has its own in-built library, which facilitates the researcher in identifying not only the size of the polymer but also its type [146]. To analyze MPs along with its chemical composition in the environment micro attenuated total reflection FTIR i.e., μ-ATR-FTIR is used [149]. However, this method is not suitable when the size of the MP particle is less than 50 μm [150]. Along with that, sometimes, the pressure produced by the probe tip of ATR may alter and damage the fragile MPs structure [146].
Thermal analysis is another technique that is beneficial in understanding the variation of physical and chemical characteristics of MPs depending upon their thermal stability [146]. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) are two such approaches in this category for the identification of MPs. DSC provides the result of the physical characteristics of a polymer, evaluating its variation in transition, crystallization, dissolution, and its respective entropy and enthalpy [151]. TGA studies the variation in the mass of polymer when it is heated and provides qualitative and quantitative insight into MPs by calculating their dependence on temperature and time [152]. Even though both are modern technologies but they have their own sets of limitations. In a study, it was discovered that a combination of DSC and TGA identified the polyethylene and polypropylene but were unable to detect polyvinyl chloride, polyamide, polyester, and polyurethane due to the overlapping phase transition signal [153]. Pyro gas chromatography mass spectroscopy (PY-GC-MS) is another thermal analysis technique used for the identification of MPs by analyzing the thermally decomposed gas from the polymer. Thermal analysis can be used as an alternative to spectroscopy, but these are destructive methods and entail careful observation and required experience [146]. This method is capable of identifying polyethylene, polypropylene, polyvinyl chloride, polyurethane, polystyrene, polyamide, and polyethylene [154156].
Another novel technology, atomic force microscopy (AFM) coupled with infrared, is a promising analyzing method for identifying MPs. This method uses thermal expansion by absorbing infrared, thereby producing oscillation in the sample. Later, amplitude and frequency are studied based on the oscillation produced [157].
The take-away information from here can be that the identification of MPs depends on various parameters such as their shapes and sizes, their type, composition, polarity, etc. Each technique has its own pros and cons. FT-IR provides detailed chemical composition and polymer type but struggles for particles less than 50 μm. Meanwhile, Raman Spectroscopy gives a detailed resolution for particles as small as 1 μm, but during the identification process, the sample heating can alter the polymer’s properties. On the other hand, PY-GC-MS is excellent with polymer types and their quantification but requires expert intervention to interpret the result. Thus, saying that any single method is superior and the best among all would be incorrect. Rather, to ensure comparability, sampling methods should adhere to standardized protocols, which still need more research, including subsampling and extrapolation techniques, and future work should focus on refining these techniques and standardizing methodologies across studies to enhance the comparability and reliability of MP pollution data globally.

5.2. Quantification of MPs

When it comes to the quantification of these contaminants, there are a few methods for that, such as the gravimetry method, mass quantification method, sub-sample method [158]. During visual/ microscopy and FTIR analysis, sub-sampling and extrapolation techniques are commonly used. Given the potentially large number of microplastics on the filters, analyzing or counting every particle is labor-intensive and time-consuming. To streamline this, filters are divided into sections, and subsamples are randomly taken from one or more parts. The microplastics counted in these selected areas are then extrapolated to estimate the total microplastic count on the entire filter [159160].
The second method is particle mass quantification, which measures the mass of microplastics using various techniques such as thermos-extraction/desorption-gas chromatography-mass spectrometry (TED-GC/MS), differential scanning calorimetry (DSC), FTIR imaging combined with weighing on an analytical balance, and plane array FTIR imaging [161164].
The third method is gravimetry, which also uses the principle of microplastic mass. However, this method is rarely used since it has been reviewed by only one research study by Sheriff et al. [158]. In this technique, filters are weighed before and after sample filtration and drying. The difference in mass (in 100 mL) is then used to estimate the quantity of microplastics [165].
Another challenge that comes up in front of the research fraternity is the identification of a suitable quantifying unit for MPs. The lack of standardized units for measuring microplastics has been a significant barrier to the comparability of studies. The three commonly used units—items/m3, particles/kg, and mg/kg—each have distinct advantages and limitations. For instance, items/m3 provide particle counts suitable for water-based systems but lack information on mass, which is critical for assessing environmental load. Conversely, mg/kg captures the total mass of microplastics but overlooks the number and morphology of particles, essential for understanding ecological impacts [166]. A few things can be suggested as a first step towards standardizing the measurable unit for MPs. For instance, adopting a dual reporting system by combining mg/kg for mass-based pollution load and particles/m3 or particles/kg for ecological impact assessment. Also, efforts should be made to develop global protocols for sampling and analysis, for example, establishing standardized mesh sizes for particle collection (e.g., 300 μm for initial sieving) and consistent size thresholds for microplastics (e.g., 5 mm upper limit).

Remediation

The accruing of MPs in our surroundings is gradually becoming or already has become a global cause of concern. And the worrying thing is that it significantly impacts humans and animals, as discussed in the previous section. Already stated by Liu et al. [167], the traditional WWTPs are inefficient for the complete removal of MPs from their system, regularly and continuously. However, there are some physical, microbial, chemical, and biological methods discussed further in this section, which appear to be promising for a better removal rate than any traditional WWTP. A detailed Fig. 4 shows some of the many techniques used for the treatment of these emerging contaminants.

6.1. Physical Treatment

Biochar and activated carbon are two extensively used methods to efficiently treat stormwater containing MPs and nanoplastics using their adsorbent surface and porous texture [168171]. Siipola et al. [170] discovered in an experiment that the removal efficiency of biochar-activated carbon effectively impedes the further flow of PE MPs.
Ultrafiltration, microfiltration, reverse osmosis, etc, are some membrane processes that have been widely used in the last five years [172]. The process involves the combination of a porous membrane and a biological process that can improve the removal efficiency of MPs from the effluent by 99.99% [173]. Out of all the membrane processes, ultrafiltration is considered to be the most capable of removing macro molecules and colloidal particles weighing up to a few thousand Dalton suspended in the system and allows the process to perform under a low pressure of 1–10 bar [172]. The author further reports that the ultrafiltration combined with a membrane bioreactor having a pore size of not more than 0.2 μm can remove 100% of MPs from the sample. Meanwhile, reverse osmosis is a promising budding process used to remove MPs from the wastewater working on high pressure to improve efficiency; however, it creates nanoparticles of plastics by fragmenting them during the process [174175]. Dynamic membrane technology is another physical process for the removal of poor-settling and non-biodegradable particles from the effluent by quickly forming a second membrane of microparticles. Less resistance offered by filtrate and easy cleaning make it a suitable option to remove MPs from synthetic wastewater under gravity-driven operation [172, 176]. Traditional WWTPs adjoined with granular activated carbon filtration methods have also proven to be reliable for the removal of such micro contaminants. Yet it is still inefficient relative to the other processes discussed above. Wang et al. [13] reported a removal efficiency of 73.7 to 98.5% in removing MPs with a size range from 1–5 μm. Another process, magnetic separation, suitable only for sediment and water samples and not for the effluent from WWTPs, was found to be efficient for the recovery of these contaminants having a size index of 200μm to 1 mm [171, 177].
Other traditional methods under physical treatment are primary sedimentation tanks with grit chambers. The maximum efficiency for such unit was found to be 79% recently by Ziajahromi et al. [178]. For large-size MPs, this process can remove up to 98% of the contaminants from the WWTPs. Filtration using granular media also offers an option to remove MPs from WWTPs where the porous media of the size range 0.45–1 μm is used [172]. However, using such small-sized porous media frequently clogs the media, which interrupts the flow. Therefore, ferrous salt is used in response to the clogging in which the solid particles form flocculate at one place, which is later skimmed off [179].

6.2. Microbial Treatment

The activated sludge process utilizes the reintroduction of microbes in a treatment unit of a WWTP. The activated sludge process followed by oxidation ditch or anaerobic tanks has been found to remove MPs from the wastewater with an efficiency of 43%, where the reintroduced microbes degrade the MPs by feeding upon them for the source of their nourishment [180182]. Biofilm is another process in which a film is enveloped around the surface of MPs, and then the microbes are adsorbed on it and degrade the particles [172]. Degradation of MPs by fungal and bacterial actions is one of the most eco-friendly methods currently being used for MPs’ removal. Different fungi feed upon MPs since these particles serve as a source of their nutrients, finally degrading them permanently [183]. A study by Anand et al. [184] informs the growing trend of utilizing green algae for the treatment of the MPs (especially LDPE and BPA) infested water. The major advantage of this technique is that this process does not require a rich carbon source to grow and can adapt to diverse types of habitats.

6.3. Biological Treatment

The clarification process and biological treatment after the primary treatment of wastewater in a WWTP constitutes biological treatment. Not very efficient in removing MPs from wastewater, and in fact, many researchers have different opinions on the caliber of this process. Sun et al. [185] report the range of removal efficiency of up to 98% if the preliminary and primary treatment has been provided. Another report suggested a minimal removal efficiency range of 2–55% of wastewater [186]. These variations in the removal can be attributed to changes in physical characteristics (size, shape, surface texture), changes in concentration of microbes, and abiotic components such as pH, temperature, etc. [172]. Constructed wetlands is also a natural treatment unit of wastewater infested with MPs. Macro invertebrates such as snails, bristle worms, beetles, etc, present in these wetlands play a conducive role in stopping the accumulation of sludge [187]. Wang et al. [188] highlighted the role of these invertebrates in removing these contaminants where these wetlands were efficient as high as 90%. Treatment by corals, sea clams, ingestion by marine organisms, and zooplanktons are considered to be highly effective and novel biological approaches for the removal of MPs pollution from the marine environment [189].

6.4. Chemical Treatment

Removal of MPs by oxidising agents like ozone, hydrogen peroxide, photo-catalytic oxidation, electro-Fenton process, etc., comes under oxidation, where the polymers are mineralized into CO2 and water [172]. Although these processes are very efficient, they are uneconomical. Treatment using ozone is one of the oldest oxidant-procedure where degradation of polymers has been found up to 90% at a temperature of 35–45°C [190]. The author further suggests the process to be more effective against polyethylene, polypropylene and polyethylene terephthalate. In this process, the hydrogen peroxide and iron (Fe2+) react and generate free hydroxyl radicles. These hydroxyl radicles consist of heterogeneous catalyst that targets the organic impurities, such as polymers present in the water environment. After the reaction, the organic impurities are converted into either CO2, water, or mineralized [172]. However, very low removal efficiency has been reported by this method in which roughly 26% of MPs were recovered from the sample, after 24 hours at different doses of hydrogen peroxide and Fe2+ [191]. The electro-Fenton process is a modification of its traditional process, which is still a novice technology where the hydrogen peroxide is generated electrochemically for the removal of MPs, especially polyvinyl chloride. However, not enough scientific reports have been published discussing its efficacy for the treatment of this emerging contaminant [172, 192].
Photolysis and photocatalytic are other advanced oxidation processes used to degrade polymers. The photolysis process utilizes ultraviolet rays on samples infested with MPs for a certain period of time, after which the organic impurities eventually convert into water and CO2 [193]. However, Brandon et al. [194] questioned its efficacy where the author found a low degradation rate of MPs (polyethylene and polypropylene) when compared with FT-IR. Coagulation is one of the most widely used processes in which aluminium and ferrous salts are used as flocculating agents, and Murphy et al. [195] found a positive correlation between this salt and the removal of MPs via the flocs formed by these flocculating agents. Ma et al. [196] experimented with a new flocculating agent, polyacrylamide, where the removal efficiency reached up to 90% by varying the dose of the flocculating agent between 3–15 mg/L.
Most of the methods mentioned above are for WWTPs because the wastewater acts as a hub for MPs in them. Although, with new progressing technologies coming forth day by day, we still have a long way to go to develop cost-efficient and bio-inspired materials that should be synthesized to cater to this problem. Moreover, investigation and studies should be conducted on the development of a uniform method for the effective removal of MPs from the environment.

Regulatory Steps

Macro and microplastic corresponding to different polymers like PE (polyethylene), PP (polypropylene), PS (polystyrene), PVC (polyvinyl chloride), etc, have already caused global tension with their ubiquity. From affecting and impacting the environment, flora and fauna and human health, local and state governing bodies have started taking this situation seriously. Several countries and organizations have taken initiatives to mitigate this unfathomable phenomenon.
Republic Act 9003, or the Ecological Solid Waste Management Act 2003 of the Philippines, stipulates the local government unit enforce bans or restrictions on Styrofoam plastic and other single-use plastic. This law also checks the managed disposal, treatment, recovery, and reuse of plastic waste. In India, under the ‘Plastic Waste Management Rules 2016’ the use of plastic bags below 50 μm is banned [197]. However, plastic waste management and formulation of policies catering to the recycling, reusing, and managing plastic is challenging for a big country like India because of the huge plastic production, but some states have taken the initiative to curb this growing issue. A southern state in India (Tamil Nadu), the usage of single-use plastic is banned effectively since January 1, 2019. Another Western State, Maharashtra, has also passed a similar proposal in its assembly. Currently, the government of India has put an all-out ban on the production and sale of the plastic which has no recyclability. Along with that, the use of plastic bags weighing less than 2 grams and thinner than 50 microns is also prohibited for any manufacturer or vendor. Further, the Indian government has also issued a notice to increase the thickness of plastic bags from 50 microns to 120 microns [198]. Jiang [199] states that in France, a law was proposed in the French parliament directing the ban of solid plastic particles in rinse-off cosmetic items and the law came into effect from January first, 2018. This law also urged to the ban on use of plastic cotton buds from January first, 2020. The author also provided information about a Swedish Chemical Industry (KEMI) which proposed a ban on the use of microbeads on every product and their initiative got a positive nod from the Ministry of Environment and Food of Denmark. In the United States of America, ‘Prop 67 bill’ has mandated an all-out ban on shopping bags in the state of the country [200]. Ireland, with its ‘Lowenthal’s Bill’, has imposed a fine of 10 cents fees on plastic shopping bags, and the collected funds will be used for environmental and land conservation projects in the country [201]. In Scotland, the government regulated a policy that prevented 650 million plastic bags from entering into waste streams [201]. South Korea banned the use of MPs and microbeads in rinse-off products and toothpaste in 2016 and 2017, respectively. Other Western countries like Australia, Netherlands, Luxembourg, and Sweden are formulating policies for a ban on the use of microbeads in personal care products. In 2019, more than 180 countries agreed to the Basel Convention on the Control of Transboundary Movement of Hazardous Waste and Their Disposal amendment, which included plastic waste and its trade [202].
Unfortunately, certain countries and international organizations still overlook the threat of MPs in their policy formulations. The Malaysian government is neither yet prudent to include policies preventing or managing plastic waste nor stringent in implementing them. The research institutes also lack proper funding to investigate the MPs’ impact on human health and finding their alternatives [203]. European Directive (EU 86/278/EEC) still does not consider MPs as unwanted pollutant in stabilized sludge or biosolids being used as fertilizers in agricultural fields and link between MPs and sludge is still missing in the policies of the European Union (EU) [204]. Freeman et al. [205] also confirmed that no policy still manages the influx of MPs in wastewater.
But with the growing awareness against the MP’s pollution, there have been some strategies surfaced which partially address the MP pollution. Marine strategy framework directive, proposal for a regulation on preventing pellet losses, and REACH restriction proposal (addressing to the intentionally added MPs in the marine water) are a few initial steps by EU. There are unintentional MPs which come into existence after breaking down from the bigger chunks and this pollution falls outside of the scope. This pollution is monitored by plastic strategy, waste framework directive, marine strategy framework directive, etc. Further, directives have been formulated by EU in response to the release of MPs in the environment either directly or indirectly. Some of them are ecodesign directive, sewage sludge directive, industrial emission directive regulation on tyre labelling directive, etc. [206].
Given the fact that many countries and international organizations are noticing the accruing inimical pattern of MPs upon and around us, there is still a huge faction of the world’s state government bodies and organizations that are still indifferent to the insidious graph of these pollutants. Even when the consequences are published every day in the form of scientific papers, websites, book chapters, etc. This is the time when hard steps need to be taken. It is profoundly expressed that the current pandemic situation has pushed humans more dependent on plastic today than ever before. The scenarios of lockdown home quarantine and social distancing have forced people to rely more on online deliveries for their requirements. The deliveries are carried out in plastic bags, and boxes, and packaging. Mismanagement of PPE kits will also become an issue of accumulating plastic waste sooner or later. Hence, it is imperative to formulate stringent policies solely dedicated to plastic and its waste management.

Insight of Plastic Waste in Europe and Germany

Today, the world produces almost 400 million tons of plastic waste annually, and if this rate of growth continues, then by 2050, the global production of plastic waste per year will rise exponentially up to 1100 tons per annum [207]. As per the report by European Commission [208], European countries produce 26 million tons of plastic waste annually. Fig. 5a demonstrates the share of the top 10 polluters of Europe where in 2019, as per Statista [209], Germany was the leading country for the generation of plastic packaging waste, which was roughly 3250 thousand metric tons, followed by France and Italy with 2390 and 2315 thousand metric tons, respectively. d’Ambrières & Woldemar [210] reported that in 2017, Europe exported 2 billion metric tons of plastic to China. Conversely, Germany is the biggest exporter of recycled plastic (Mainly polyethylene), and the amount varies from 505,616 Mg – 612,738 tons [211]. A trend in Germany’s plastic waste export can be clearly seen in Fig. 5b. International Trade Statistics [212], a wing of the United Nations analysing the Department of Economic and Social Affairs, released a report where it was comprehensively mentioned the amount (in kg) of plastic waste being exported out of Germany to the world and its trade value for the last 5 years. The purpose of choosing the previous five years is to give a better idea about the pre-pandemic, pandemic, and post-pandemic scenario of plastic export and the evaluation (in $). As can be seen for the year 2017, Germany exported a whopping 1,218,351,748 kg of plastic to the world, and its generated revenue touched $433,687,600. For the subsequent year, the plastic export saw a dip of roughly 16%, which was 1,048,687,294 kg with a trade value of $414,690,971. However, in 2019, we witnessed a gentle rise of around 3% in the exported plastic waste relative to that of 2018, with a total amount of 1,091,276,658 kg with a trade value of $382,263,941. The interesting thing here to take is that even though there was a dip in the exports the traded goods generated more revenue for Germany. Thus, so far, the pre-pandemic saw a somewhat similar and constant flow of plastic waste out of Germany. This picture changes during the time of the pandemic year. The year 2020 saw a massive decline in plastic exports, where the quantity of the export fell sharply to 853,860,858 kg, a decline of roughly 27%. The trade value also crashed to $298,616,726. However, the value of the exported quantity of plastic also could not recover post-pandemic to its original value, and instead, it plummeted even more. 2021 saw a dip in the exported quantity once again, where the net weight exported out of Germany was only 820,093,149 kg, with the trade value falling down to $357,511,320. It will be interesting to see whether this data will see or start following an upward trend in 2022. The data has not yet been released by the United Nations. But in the last 4–5 years, China has been shifting its policy towards refraining from importing plastic waste from Europe [213].
Germany, a developed first-world country with the fourth largest economy in the world, is the largest exporter of plastic waste in Europe, which was almost one million tons in 2020 [214]. It can be conjectured that Germany is one of the biggest plastic waste generators. The report further highlights that the domestic plastic waste collection reached up to 38 million tons, which is roughly 457 kg of plastic waste per capita, and out of this, only a third was recycled or incinerated. But to tackle the situation, the German government is taking steps towards sustainable and recyclable options for plastic waste. The policy in Germany has asked the company to pay an extra fee when extra packaging is used. Recycled packaging must be marked, and every household and industry must use five different types of trash bins to facilitate the differentiation process between plastic and other waste [215]. Berry [215] also acknowledged the efforts by Germany as a leader in recycling its plastic waste. Germany recycles almost 70% of its total plastic waste which is, by far, the most in the world. The report also mentioned that by doing this, Germany is reducing its waste by one million tons, every year.
The humongous trading of plastics has significantly shifted the plastic pollution graph upward in Europe, and many studies across the European continent confirm it. Some notable studies have investigated the MPs in several ecological zones in Italy [216218], France [219221], Belgium [222224], Netherlands [225227], England [228230], Spain [231233], etc. These studies re just a speck among the heap of studies conducted, and many more are on their way.

Discussion

9.1. MPs in German Groundwaters

As per the report by BGR [234], groundwater caters to the two-thirds population of Germany as their vital and essential resource. As the population grows, the demand will increase, implying that more groundwater will be used for drinking. According to Umwelt Bundesamt [235], groundwater contributes up to 70% of drinking water in Germany. It is astonishing to see that only a dearth of studies has been conducted on German groundwater to detect and analyze MPs. Mintenig et al. [236] confirmed the presence of MPs in groundwater, which was used for drinking purposes. The detected concentration was very low (7 particles/m3), and the dominant shape was fibre. Another study conducted by Weber et al. [237] on German groundwater could not detect any MPs impurities. Although the concentration of MPs in the two studies discussed (details shown in Table 1) did not pose a threat, more research is needed on groundwater for the presence of MPs.

9.2. MPs in German Rivers and Streams

Germany has a vast network of rivers and streams across its land. Danube, Rhine, Ems, Weser, Elbe and Oder are the chief rivers of the country. However, the rivers and their sediments have been gravely infested with MPs, as seen in Table 1.
Roscher et al. [238] report the heavy concentration of MPs in the Weser River water. The contamination was recorded up to 9700 particles/m3. The possible reason was attributed to the estuarian currents that were distributing the MPs at the confluence of the River Weser and the North Sea. Eibes and Gabel [239], in a similar kind of study, reported the presence of MPs in the water of River Ems, where 1.54 ± 1.54 particles/m3 were detected. The weirs present in the downstream impeded the flow of river water which could cause the sedimentation of MPs in the region; the study reported. Another study conducted on the Rhine River by Mani et al. [240] reported the massive MP contamination of 11050 particles/L. The study samples were collected in the vicinity of urban centres and industrial zones having plastic production facilities and air blasting processes along the stretch of the river Rhine. The massive pollution of MPs can be attributed to these locations. Schmidt et al. [241] conducted the analysis of canal water in another megacity of Germany, Berlin, where the author reported maximum contamination of 96 particles/L. The migration of MPs into the canal water could be correlated to the presence of a WWTPs outfall nearby. This is, once again, a strong indication that WWTPs act as the carrier of MPs. In addition to that, the author also stressed the possibility of precipitation to be a chief factor for carrying MPs into the canal water. It can be hypothesized that the stormwater washes off all the MPs of the catchment area and pour it into the canal. 233 ± 36 particles/m3 were also reported in the freshwater river Warnow in north-eastern Germany by Siegel et al. [242]. The sampling site was chosen near a drinking water treatment plant. The author stressed that the flocculants used in the treatment plant were the reason for MPs’ proliferation in the river water. A surprising figure of 30 × 103 particles/kg dry weight was reported in the hyporheic zone of the river [243]. The reason to choose riverbed sediment was because the sedimentation process can lead to the accumulation of MPs at the bottom. The author of the respective study also stressed the fact that river water can easily infiltrate groundwater or a local aquifer, which can be further used as a source of drinking water for the inhabitants. Various authors have already pressed upon the issue to consider the interface between groundwater and river, as this site can be a potential doorway for MPs transportation towards either direction [244246]. Rocío et al. [247] explain that benthic zone organisms can transport MPs or can migrate through the hyporheic zone into the groundwater. Depending upon the situation, water from either the entire river or a specific section can flow into shallow groundwater or vice-versa. This flow of MPs from one zone to another depends on various properties such as the shape of the streambed, material heterogeneities, turbulence in the stream, the flow of porewater, etc. A study in Switzerland revealed that around 33% of microplastics infiltrate groundwater from river water, with concentrations increasing from 8 ± 7 MPs/m3 in groundwater to 36 ± 11 MPs/m3 in nano-filtered water in the three sampling campaigns [248]. Thus, it is important to analyse the riverbed as well, which can also act as a sink and gateway for MPs. The author, once again, focused upon the involvement of WWTPs as a potential carrier of MPs as they are not designed to remove particles of such small size. Dierkes et al. [249] also reported a minuscule trace of 0.028 ± 0.006 mg/g of MPs in Rhine water. A freshwater stream in Varel was investigated by Stolte et al. [250]. The samples were taken and filtered from the site which was close to the vicinity of a paper recycling plant. The author discovered a moderate concentration of 19 fibres/L, which was still higher than the other sampled sites, beach sediments, and seawater. The effluent from the paper recycling plant contributed to the MP’s fiber and flake pollution to the freshwater stream the study comprehended.
Mani et al. [251] studied the 20 km stretch of Rhine between Cologne to Duisburg, where the author discovered a maximum concentration of 9.2 particles/m3. The presence of MPs in the river water was attributed to direct industrial discharge and the three communal WWTPs located along the stretch of the study area.
So far, it can be posited that rivers carry a large fraction of MP pollution with them, acting as a source and sink for these contaminants.
Fig. 6 provides a visual representation of the geographical distribution of microplastic studies conducted across Germany. The map highlights a significant disparity in research coverage, with a concentration of studies in the western regions and a notable scarcity in the central and southern parts of the country. While some research has been carried out in the eastern regions, particularly in major cities like Berlin and Rostock, the western region remains the primary focus, largely due to the presence of significant water bodies such as the Rhine River.
Despite the Elbe River traversing the eastern part of the country and major urban centers being situated along these rivers, the limited number of studies in these areas is concerning. The central region of Germany presents an even starker gap, with minimal research identified, and the southern region, home to major cities like Munich, similarly lacks substantial studies. This distribution underscores the urgent need for expanded research efforts to address microplastic pollution across these underrepresented regions.
The studies depicted in Fig. 6 span various aquatic environments, including groundwater, household tap water, wastewater treatment plants (WWTPs), river sediments, and surface water.

9.3. MPs in Marine Water

Germany has an approximately 3700 km long coastline, with the North and Baltic Seas. Moreover, Europe’s two major rivers, Rhine and Danube, flow through Germany. Rivers have always been considered as a vector for MPs, and European rivers have been detected with MPs traces as small as 0.03 particles/m3 up to 187000 particles/m3 [251252]. Talking about the German coastline, the north and north-west states of Germany contain 1000 companies of plastic alone and, let alone the other industries, several municipal and industrial WWTPs [251]. North Sea and Baltic Sea have also been found to be polluted with MPs. Adding more to it, Germany is the biggest contributor of polyethylene to ocean debris, in terms of absolute mass, in the whole of Europe, and the amount ranged up to 24,461 tons [211]. Mani et al. [251] reported that the Rhine River delivers almost 10 tons of MPs toward the North Sea with it. Dibke et al. [253] corroborate this claim in the study where it was reported that the concentration of MPs in the North Sea, as mentioned in Table 1, reached up to 1396 mg/m3. The author listed several potential reasons that could cause such heavy contamination in the region. Firstly, the area witnesses so many offshore and recreational activities. They can be cruising, fishing, scuba diving, etc. Fishing gears contribute majorly to the MPs’ pollution in marine water. The next reason stated by the author was that the sampled sites were among the busiest shipping routes of the world. The cargo can be a potential proliferator of microcontaminants. The German Bight and the surrounding areas have a number of ports and harbours. The area is also visited by millions of visitors. Thus, anthropogenic activity can lead to spreading of MPs as well. Roscher et al. [238] reported a concentration of 23 particles/m3 in a study conducted at the margin of the North Sea and the estuarian region. However, the same study reported a relatively higher concentration of MPs in the estuarian zones, and the variation decreased towards the sea.
Baltic sea is one of the most studied marine region and many authors have confirmed the presence of MPs [254256]. In a similar way, Stolte et al. [250] confirmed the presence of MPs with a concentration of 3.3 fibres/L which is relatively lower than the concentration obtained from freshwater in that same study. The author corelated this contamination chiefly to municipal WWTPs, industrial discharges, off-shore recreational activities and anthropogenic activities.
It is not a hidden fact that the marine waters are the hot-spot of MPs, yet very few studies have been conducted on German coasts for the identification of MPs. More studies would certainly benefit the researchers and policy maker to assess the situation and respond in an appropriate sense.

9.4. MPs in WWTPs

It is not unknown that WWTPs receive MPs’ load every single day from domestic and industrial outlets abridged the path between domestic and industrial wastes and rivers. So many authors have already reported that the WWTPs act as the biggest source and sink for the MPs [261]. Currently, in Germany, there are roughly 9100 WWTPs, and every year, these WWTPs emanate close to 7.3 × 1012 particles/year, on average, into the river [241]. Table 2 will provide a list of studies conducted on German WWTPs to detect the concentration of MPs emanating from them. Likewise, Dierkes et al. [249] conducted a study in two WWTPs of the Bavaria region catering to a population of 70000 and 170000, respectively. The study revealed that a massive concentration of MPs (3.3 ± 0.3 mg/g) were recovered from the sludge of WWTP catering to a population of 170,000. Clearly, it can be judged that population affects the influent and effluent load of MPs in WWTPs. Mintenig et al. [261] comprehensively examined twelve WWTPs and discovered a large concentration of 9000 particles/ m3 being discharged by a WWTP at Holdorf. The study also revealed that the detected MPs were predominantly composed of polyester and purported that the WWTPs can act as a source and sink for these micro contaminants. An interesting takeaway of this study was about a tertiary WWTP out of all the studied, which was installed with a post-filtration unit. This unit helped to reduce the concentration of MPs’ discharge by 97%. A systematic comparison was observed by Wolff et al. [262], where the average concentration of MPs was compared between dry and wet weather days of a WWTP having an effluent rate of 10,000 m3/d serving a population of 98,500. The concentration of MPs discharged by the WWTP in wet weather days was almost two folds than in dry weather days. While the wet weather days discharge concentration for MPs stood up to 5900 particles/m3, on the other hand, only 3000 particles/m3 were recovered during dry weather days. Residential waste entering into the WWTPs could be the major reason for the recovery of MPs in the effluent. Altmann et al. [263] conducted a study on an urban WWTP, which showed an enormous concentration of 2.2 μg/mg dry weight. Bitter et al. [264] conducted study on four German municipal WWTPs which showed high concentrations of MPs in their effluent. 19.6 μg/L of MPs were recovered from the WWTP, serving a population of 70,000 having an outflow discharge rate of 10,300 m3/d. Out of all the studied WWTPs, WWTP installed with a post-treatment pile cloth media filter unit (PCMF) showed the best removal efficiency of MPs from its system. The removal rate of >94% of MPs was observed at the WWTP. The WWTP, which had a removal unit of continuous up-flow granular activated carbon filter was found to be least efficient for the removal of MPs as its removal rate was only 2%, roughly. This study also mentioned the use of DSC for the analysis of MPs in the sample and thoroughly mentioned its swiftness and user-friendly functions for analysing the samples.
Although Germany has made strides in addressing plastic waste, critical research gaps remain in understanding microplastic pollution in its aquatic environments. For instance, studies on rivers like the Rhine have reported alarming concentrations of up to 11,050 particles/L, predominantly fibers and polymers like polyethylene and polypropylene. However, limited investigations into groundwater contamination, such as a study showing up to 7 particles/m3 in aquifers, highlight the need for broader spatial and temporal coverage. Wagner et al. [267] has already mentioned the wide presence of MPs in the European freshwater system. At the same time, Kye et al. [268] has cited Annex XV restriction report for intentionally added microplastics by the European Chemicals Agency that the granule type of MPs was heavily found in industrial wastewater other than fibers. Meanwhile, limited studies on MPs in the German aquatic system and the associated gaps restrict our ability to fully comprehend the pathways and accumulation mechanisms of microplastics, particularly their transition from surface water to groundwater, which serves as a major drinking water source. Without detailed knowledge of these interactions, devising effective mitigation strategies becomes challenging, leaving ecosystems and human health at continued risk.

Conclusion and Future Prospect

It is not hidden anymore that these invisible pollutants are slowly accruing around us and sooner or later will become a huge problem and responsibility for humans. So far, this paper discusses the state of the knowledge about MPs especially its source, pathway, and impact it casts on humans, aquatic flora and fauna, and crops. It is safer to conclude that WWTPs are the hotspot for MPs and the biggest carrier for carrying them to any other water body or environment. The observable effects on plant and animal life and their implications for human biology prompted a greater emphasis on the seriousness of these contaminants. Not only are these contaminants dangerous on their individual level, but their interaction with other substances and their role as vectors for other contaminants (PPCPs, heavy metals, ARGs, etc) make them even more lethal. Further, this paper highlights several techniques and state-of-the-art technologies to identify and analyze the MPs, with FT-IR being the most favorable analyzing technique. Remediation and removal techniques were also discussed, where it was reported that the traditional WWTPs cannot efficiently remove the MPs.
This paper focuses on the MPs’ abundance in the German aquatic environment. For that, German groundwater, rivers, riverbed sediments, lakes, canals, German marine water, and WWTPs were included in the analysis. It is interesting to notice that the spheres were the dominant shape of these contaminants, followed by spheres, in the considered environment. PE, PP, and PS were the ubiquitous types of polymers discovered in this study in Germany. The data for the German groundwater assures of no heavy contamination of MPs in it with a maximum concentration of 7 particles/m3, and no traces of MPs were found in another study involving the analysis of groundwater. No concrete reasoning could be given for this occurrence, but it was assumed that the remnants of the plastic pipes might have entered during the water purification and transportation process.
The rivers and surface water were relatively very much contaminated with MPs compared to the groundwater. 19000 fibres/m3, 9700 particles/m3 and 30 × 103 particles/kg dry weight corroborate the heavy pollution for the surface water bodies. The major reason for such a high level of contamination was attributed to the industrial and municipal WWTPs and some public littering and recreational activities. These further stresses the fact that the traditional WWTPs are not designed to remove the MPs.
The WWTPs, not just in Germany but globally, are the biggest emanators of MPs. The enormous concentration of MPs in them cements this fact. They are the epicenter of the collected domestic, run-off, and industrial waste from where it diverges to river bodies as effluent with partial removal of MPs. 9000 and 5900 particles/m3 demonstrate the dire situation of WWTPs. Authors from this study and globally reported that the plastic production industries, textiles, and pharmaceutical companies are responsible for this situation.
German sea water’s situation is grave, with 3300 fibres/L and 23000 particles/m3 detected. Not only the rivers and effluent from WTPs are the vehicles for MPs but geography and ocean currents also play an important role in distributing the MPs near German shore. Authors have also confirmed that anthropogenic activities such as fishing and cruising also contribute largely to such pollution.
The data represented in the tables above are sufficient to inform us about the contamination of German water sources. However, Germany has one of the world’s finest infrastructures and study ecosystems with a lot of focus on research. However, the scant number of studies and publications highlights the complacency in certain areas. More research is required to be conducted on MPs occurrence and abundance in German water, especially groundwater since no study has reported substantial traces of MPs to date. Another thing to be noted is that uniformity in the measurement unit is necessary to avoid the misunderstanding. Researchers should come up with a common standard unit, i.e., either particle/ m3, particles/L, micrograms/grams, or grams/L, etc. It is imperative that international organizations define and standardize the spectrum of pollution and clearly delineate the normal, moderate, and severe levels of pollution in every environmental zone. Along with that, currently, there is a lack of information upon the combined effect of MPs with other contaminants and this area needs to be taken seriously. Since the traditional WWTPs are ineffective in removing MPs from their system, a multidisciplinary approach should be devised for the better removal and recovery of MPs.

Acknowledgements

None.

Notes

Conflict-of-Interests Statements

The authors declare that they have no conflict of interest.

Author Contributions

V.S. (Master’s student) contributed to data collection, preparation of the first draft, editing, and revision of the manuscript. R.S. (Professor) conceptualized the work, conducted supervision, and revised the manuscript. S.V. (Master’s student) contributed to illustration, and editing of the manuscript. A.N. (Professor), S.K. (Professor) and B.S.G. (Professor) edited and revised the manuscript.

References

1. la Nasa J, Biale G, Ferriani B, Trevisan R, Colombini MP, Modugno F. Plastics in heritage science: Analytical pyrolysis techniques applied to objects of design. Molecules. 2020;25(7)1–17. https://doi:10.3390/molecules25071705


2. Andrady AL, Neal MA. Applications and societal benefits of plastics. Philos. Trans. R. Soc. B. Biol. Sci. 2009;364(1526)1977. https://doi:10.1098/rstb.2008.0304
crossref pmid pmc pdf

3. Plastics-the Facts 2021 [Internet]. [cited 18 December 2024]. Available from: https://plasticseurope.org/de/knowledge-hub/plastics-the-facts-2021/


4. Chalmin P. The history of plastics: from the Capitol to the Tarpeian Rock. Field Actions Science Reports. 2019. 19:6–11. http://journals.openedition.org/factsreports/5071


5. OECD. Global Plastics Outlook [Internet]. [cited 21 November 2024]. Available from: https://doi:10.1787/aa1edf33-en


6. Plastics Europe. Enabling a sustainable future [Internet]. [cited 16 December 2024]. Available from: https://plasticseurope.org/


7. Geyer R, Jambeck JR, Law KL. Production, use, and fate of all plastics ever made. Sci. Adv. 2017;3(7)e1700782. https://doi:10.1126/sciadv.1700782
crossref pmid pmc

8. Bergmann M, Gutow L, Klages M. Marine anthropogenic litter. 1st edSpringer; Cham: 2015. p. 1–447.


9. Wagner M, Lambert S. Freshwater Microplastics: Emerging Environmental Contaminants? 1st edSpringer; Cham: 2017. p. 1–303.


10. Frias JPGL, Nash R. Microplastics: Finding a consensus on the definition. Mar. Pollut. Bull. 2019;138:145–147. https://doi:10.1016/j.marpolbul.2018.11.022
crossref pmid

11. Thompson RC, Olson Y, Mitchell RP, et al. Lost at Sea: Where Is All the Plastic? Science. 2004;304(5672)838. https://doi:10.1126/science.1094559
crossref pmid

12. Veerasingam S, Ranjani M, Venkatachalapathy R, et al. Microplastics in different environmental compartments in India: Analytical methods, distribution, associated contaminants and research needs. Trends Anal Chem. 2020;133:116071. https://doi:10.1016/j.trac.2020.116071
crossref

13. Wang Z, Lin T, Chen W. Occurrence and removal of microplastics in an advanced drinking water treatment plant (ADWTP). Sci. Total Environ. 2020;700:134520. https://doi.org/10.1016/j.scitotenv.2019.134520
crossref pmid

14. Claessens M, De Meester S, VanLanduyt L, DeClerck K, Janssen CR. Occurrence and distribution of microplastics in marine sediments along the Belgian coast. Mar Pollut Bull. 2011;62(10)2199–2204. https://doi:10.1016/j.marpolbul.2011.06.030
crossref pmid

15. Graham ER, Thompson JT. Deposit- and suspension-feeding sea cucumbers (Echinodermata) ingest plastic fragments. J. Exp. Mar. Bio. Ecol. 2009;368(1)22–29. https://doi:10.1016/j.jembe.2008.09.007
crossref

16. Food Packaging Forum. WHO report on potential human health implications of microplastics. [cited 7 December 2024]. Available from: https://foodpackagingforum.org/news/who-report-onpotential-human-health-implications-of-microplastics


17. Zhao Z, Zhao K, Zhang T, et al. Irrigation-facilitated low-density polyethylene microplastic vertical transport along soil profile: An empirical model developed by column experiment. Ecotoxicol Environ. Saf. 2022;247:114232. https://doi:10.1016/j.ecoenv.2022.114232
crossref pmid

18. Hooge A, Hauggaard-Nielsen H, Heinze WM, et al. Fate of microplastics in sewage sludge and in agricultural soils. TrAC Trends Anal. Chem. 2023;166:117184. https://doi:10.1016/j.trac.2023.117184
crossref

19. Nizzetto L, Bussi G, Futter MN, Butterfield D, Whitehead PG. A theoretical assessment of microplastic transport in river catchments and their retention by soils and river sediments. Environ. Sci. Process Impacts. 2016;18(8)1050–1059. https://doi:10.1039/c6em00206d
crossref pmid

20. Rehm R, Zeyer T, Schmidt A, Fiener P. Soil erosion as transport pathway of microplastic from agriculture soils to aquatic ecosystems. Sci Total Environ. 2021;795. https://doi:10.1016/j.scitotenv.2021.148774
crossref pmid

21. Lwanga EH, Beriot N, Corradini F, et al. Review of microplastic sources, transport pathways and correlations with other soil stressors: a journey from agricultural sites into the environment. Chem. Biol. Technol. Agric. 2022;9(1)1–20. https://doi:10.1186/s40538-021-00278-9
crossref pdf

22. Acarer S. Microplastics in wastewater treatment plants: Sources, properties, removal efficiency, removal mechanisms, and interactions with pollutants. Water Sci. Technol. 2023;87(3)685–710. https://doi:10.2166/wst.2023.022
crossref pmid pdf

23. Liu Y, Wang B, Pileggi V, Chang S. Methods to recover and characterize microplastics in wastewater treatment plants. Case Stud Chem Environ Eng. 2022;5. https://doi:10.1016/j.cscee.2022.100183
crossref

24. Bakaraki Turan N, Sari Erkan H, Onkal Engin G. Microplastics in wastewater treatment plants: Occurrence, fate and identification. Process Saf. Environ. Prot. 2021;146:77–84. https://doi:10.1016/j.psep.2020.08.039
crossref

25. Jan Kole P, Löhr AJ, Van Belleghem FGAJ, Ragas AMJ. Wear and Tear of Tyres: A Stealthy Source of Microplastics in the Environment. Int. J. Environ. Res. Public Health. 2017;14(10)1265. https://doi:10.3390/ijerph14101265
crossref pmid pmc

26. Zhang J, Wang L, Kannan K. Microplastics in house dust from 12 countries and associated human exposure. Environ. Int. 2020;134:105314. https://doi:10.1016/j.envint.2019.105314
crossref pmid

27. Pinheiro M, Martins I, Raimundo J, Caetano M, Neuparth T, Santos MM. Stressors of emerging concern in deep-sea environments: microplastics, pharmaceuticals, personal care products and deep-sea mining. Sci. Total. Environ. 2023;876:162557. https://doi:10.1016/j.scitotenv.2023.162557
crossref pmid

28. United Nations Development Programme. Microplastics on Human Health: How much do they harm us? [Internet]. [cited 5 December 2024]. Available from: https://www.undp.org/kosovo/blog/microplastics-human-health-how-much-do-they-harm-us


29. Lee Y, Cho J, Sohn J, Kim C. Health Effects of Microplastic Exposures: Current Issues and Perspectives in South Korea. Yonsei Med. J. 2023;64(5)301–308. https://doi:10.3349/ymj.2023.0048
crossref pmid pmc pdf

30. Urli S, Corte Pause F, Crociati M, Baufeld A, Monaci M, Stradaioli G. Impact of Microplastics and Nanoplastics on Livestock Health: An Emerging Risk for Reproductive Efficiency. Animals. 2023;13(7)1132. https://doi.org/10.3390/ani13071132
crossref pmid pmc

31. Colzi I, Renna L, Bianchi E, et al. Impact of microplastics on growth, photosynthesis and essential elements in Cucurbita pepo L. J. Hazard. Mater. 2022;423:127238. https://doi:10.1016/j.jhazmat.2021.127238
crossref pmid

32. Bosker T, Bouwman LJ, Brun NR, Behrens P, Vijver MG. Microplastics accumulate on pores in seed capsule and delay germination and root growth of the terrestrial vascular plant Lepidium sativum. Chemosphere. 2019;226:774–781. https://doi:10.1016/j.chemosphere.2019.03.163
crossref pmid

33. Haque F, Fan C. Fate of microplastics under the influence of climate change. iScience. 2023;26(9)107649. https://doi:10.1016/j.isci.2023.107649
crossref pmid pmc

34. Ghosh S, Sinha JK, Ghosh S, Vashisth K, Han S, Bhaskar R. Microplastics as an Emerging Threat to the Global Environment and Human Health. Sustainability. 2023;15(14)10821. https://doi.org/10.3390/su151410821
crossref

35. Li Y, Tao L, Wang Q, Wang F, Li G, Song M. Potential Health Impact of Microplastics: A Review of Environmental Distribution, Human Exposure, and Toxic Effects. Environ. Heal. 2023;1(4)249–257. https://doi:10.1021/envhealth.3C00052
crossref pmid pmc pdf

36. Bakir A, Rowland SJ, Thompson RC. Enhanced desorption of persistent organic pollutants from microplastics under simulated physiological conditions. Environ. Pollut. 2014;185:16–23. https://doi:10.1016/j.envpol.2013.10.007
crossref pmid

37. Verla AW, Enyoh CE, Verla EN, Nwarnorh KO. Microplastic–toxic chemical interaction: a review study on quantified levels, mechanism and implication. SN Appl. Sci. 2019;1(11)1–30. https://doi:10.1007/s42452-019-1352-0
crossref pdf

38. Piergiacomo F, Brusetti L, Pagani L. Understanding the Interplay between Antimicrobial Resistance, Microplastics and Xenobiotic Contaminants: A Leap towards One Health? Int. J. Environ. Res. Public Health. 2023. 201https://doi:10.3390/ijerph20010042
crossref pmid

39. Simantiris N. Single-use plastic or paper products? A dilemma that requires societal change. Clean Waste Syst. 2024;7:100128. https://doi:10.1016/j.clwas.2023.100128
crossref

40. Golmohammadi A, Kraft T, Monemian S. Setting the deadline and the penalty policy for a new environmental standard. Eur. J. Oper. Res. 2024;315(1)88–101. https://doi:10.1016/j.ejor.2023.11.014
crossref

41. Vardar S, Onay TT, Demirel B, Kideys AE. Evaluation of microplastics removal efficiency at a wastewater treatment plant discharging to the Sea of Marmara. Environ. Pollut. 2021;289:117862. https://doi:10.1016/j.envpol.2021.117862
crossref pmid

42. Ngo PL, Pramanik BK, Shah K, Roychand R. Pathway, classification and removal efficiency of microplastics in wastewater treatment plants. Environ. Pollut. 2019;255:113326. https://doi:10.1016/j.envpol.2019.113326
crossref pmid

43. Chan CK-M, Fang JK-H, Fei B, Kan C-W. Microfibres Release from Textile Industry Wastewater Effluents Are Underestimated: Mitigation Actions That Need to Be Prioritised. Fibers. 2023;11(12)105. https://doi.org/10.3390/fib11120105
crossref

44. Reddy AS, Nair AT. The fate of microplastics in wastewater treatment plants: An overview of source and remediation technologies. Environ Technol Innov. 2022;28:102815. https://doi:10.1016/j.eti.2022.102815
crossref

45. Järlskog I, Strömvall AM, Magnusson K, et al. Occurrence of tire and bitumen wear microplastics on urban streets and in sweepsand and washwater. Sci Total Environ. 2020;729:138950. https://doi:10.1016/j.scitotenv.2020.138950
crossref pmid

46. Ayyamperumal R, Huang X, Li F, et al. Investigation of microplastic contamination in the sediments of Noyyal River-Southern India. J. Hazard. Mater. Adv. 2022;8:100198. https://doi:10.1016/j.hazadv.2022.100198
crossref

47. Fting Wang, Bao K, Csheng Huang, et al. Distribution, characteristics, and research status of microplastics in the trunk stream and main lakes of the Yangtze River: A review. China Geol. 2022;5(1)171–184. https://doi:10.31035/cg2022002


48. Kiss T, Fórián S, Szatmári G, Sipos G. Spatial distribution of microplastics in the fluvial sediments of a transboundary river – A case study of the Tisza River in Central Europe. Sci. Total Environ. 2021;785:147306. https://doi:10.1016/j.scitotenv.2021.147306
crossref pmid

49. Hurley R, Woodward J, Rothwell JJ. Microplastic contamination of river beds significantly reduced by catchment-wide flooding. Nat. Geosci. 2018;11(4)251–257. https://doi:10.1038/s41561-018-0080-1
crossref pdf

50. Strokal V, Kuiper EJ, Bak MP, et al. Future microplastics in the Black Sea: River exports and reduction options for zero pollution. Mar. Pollut. Bull. 2022;178:113633. https://doi:10.1016/j.marpolbul.2022.113633
crossref pmid

51. Lebreton LCM, Van Der Zwet J, Damsteeg JW, Slat B, Andrady A, Reisser J. River plastic emissions to the world’s oceans. Nat. Commun. 2017;8(1)1–10. https://doi:10.1038/ncomms15611
crossref pmid pmc pdf

52. Eriksen M, Lebreton LCM, Carson HS, et al. Plastic Pollution in the World’s Oceans: More than 5 Trillion Plastic Pieces Weighing over 250,000 Tons Afloat at Sea. PLoS One. 2014;9(12)e111913. https://doi:10.1371/journal.pone.0111913
crossref pmid pmc

53. Alfonso MB, Arias AH, Ronda AC, Piccolo MC. Continental microplastics: Presence, features, and environmental transport pathways. Sci Total Environ. 2021;799:149447. https://doi:10.1016/j.scitotenv.2021.149447
crossref pmid

54. KMB , Natesan U, RV , RPK , RR , SS . Spatial distribution of microplastic concentration around landfill sites and its potential risk on groundwater. Chemosphere. 2021;277:130263. https://doi:10.1016/j.chemosphere.2021.130263
crossref pmid

55. Goeppert N, Goldscheider N. Experimental field evidence for transport of microplastic tracers over large distances in an alluvial aquifer. J. Hazard. Mater. 2021;408:124844. https://doi:10.1016/J.jhazmat.2020.124844
crossref pmid

56. Hallaq AH. The impact of soil texture on nitrates leaching into groundwater in the North Governorate, Gaza Strip. J.Soc.Sci. 2010;38(2)11–35.


57. Samandra S, Johnston JM, Jaeger JE, et al. Microplastic contamination of an unconfined groundwater aquifer in Victoria, Australia. Sci. Total Environ. 2022;802:149727. https://doi:10.1016/j.scitotenv.2021.149727
crossref pmid

58. Li R, Yu L, Chai M, Wu H, Zhu X. The distribution, characteristics and ecological risks of microplastics in the mangroves of Southern China. Sci Total Environ. 2020;708. https://doi:10.1016/j.scitotenv.2019.135025
crossref pmid

59. Xu P, Peng G, Su L, Gao Y, Gao L, Li D. Microplastic risk assessment in surface waters: A case study in the Changjiang Estuary, China. Mar. Pollut. Bull. 2018;133:647–654. https://doi:10.1016/j.marpolbul.2018.06.020
crossref pmid

60. Yu X, Peng J, Wang J, Wang K, Bao S. Occurrence of microplastics in the beach sand of the Chinese inner sea: the Bohai Sea. Environ. Pollut. 2016;214:722–730. https://doi:10.1016/j.envpol.2016.04.080
crossref pmid

61. Farrell P, Nelson K. Trophic level transfer of microplastic: Mytilus edulis (L.) to Carcinus maenas (L.). Environ. Pollut. 2013;177:1–3. https://doi:10.1016/j.envpol.2013.01.046
crossref pmid

62. Alomar C, Deudero S. Evidence of microplastic ingestion in the shark Galeus melastomus Rafinesque, 1810 in the continental shelf off the western Mediterranean Sea. Environ. Pollut. 2017;223:223–229. https://doi:10.1016/j.envpol.2017.01.015
crossref pmid

63. Van Cauwenberghe L, Janssen CR. Microplastics in bivalves cultured for human consumption. Environ. Pollut. 2014;193:65–70. https://doi:10.1016/j.envpol.2014.06.010
crossref pmid

64. Schirinzi GF, Pérez-Pomeda I, Sanchís J, Rossini C, Farré M, Barceló D. Cytotoxic effects of commonly used nanomaterials and microplastics on cerebral and epithelial human cells. Environ. Res. 2017;159:579–587. https://doi:10.1016/j.envres.2017.08.043
crossref pmid

65. Sun K, Song Y, He F, Jing M, Tang J, Liu R. A review of human and animals exposure to polycyclic aromatic hydrocarbons: Health risk and adverse effects, photo-induced toxicity and regulating effect of microplastics. Sci Total Environ. 2021;773. https://doi:10.1016/j.scitotenv.2021.145403
crossref pmid

66. Kim KH, Jahan SA, Kabir E, Brown RJC. A review of airborne polycyclic aromatic hydrocarbons (PAHs) and their human health effects. Environ. Int. 2013;60:71–80. https://doi:10.1016/j.envint.2013.07.019
crossref pmid

67. Goudarzi G, Geravandi S, Alavi N, et al. Association between cancer risk and polycyclic aromatic hydrocarbons’ exposure in the ambient air of Ahvaz, southwest of Iran. Int. J. Biometeorol. 2018;62(8)1461–1470. https://doi:10.1007/s00484-018-1543-1
crossref pmid pdf

68. Covello C, Di Vincenzo F, Cammarota G, Pizzoferrato M. Micro (nano)plastics and Their Potential Impact on Human Gut Health: A Narrative Review. Curr. Issues Mol. Biol. 2024;46(3)2658–2677. https://doi:10.3390/cimb46030168
crossref pmid pmc

69. John K, Ragavan N, Pratt MM, et al. Quantification of phase I/II metabolizing enzyme gene expression and polycyclic aromatic hydrocarbon–DNA adduct levels in human prostate. The Prostate. 2009;69(5)505–519. https://doi:10.1002/pros.20898
crossref pmid pmc

70. Huang X, Xu X, Dai Y, Cheng Z, Zheng X, Huo X. Association of prenatal exposure to PAHs with anti-Müllerian hormone (AMH) levels and birth outcomes of newborns. Sci. Total Environ. 2020;723:138009. https://doi:10.1016/j.scitotenv.2020.138009
crossref pmid

71. Auguet T, Bertran L, Barrientos-Riosalido A, et al. Are Ingested or Inhaled Microplastics Involved in Nonalcoholic Fatty Liver Disease? Int. J. Environ. Res. Public Health. 2022. 1920https://doi:10.3390/ijerph192013495
crossref pmid

72. LA PORTA E. WCN23-0982 The burden of plastic in human health: presence of microplastics in kidney and their prospective nephrotoxicity. Kidney Int. Reports. 2023;8(3)S254. https://doi:10.1016/j.ekir.2023.02.575
crossref

73. Persiani E, Cecchettini A, Ceccherini E, Gisone I, Morales MA, Vozzi F. Microplastics: A Matter of the Heart (and Vascular System). Biomedicines. 2023. 112https://doi:10.3390/biomedicines11020264
crossref pmid

74. Van Cauwenberghe L, Claessens M, Vandegehuchte MB, Janssen CR. Microplastics are taken up by mussels (Mytilus edulis) and lugworms (Arenicola marina) living in natural habitats. Environ. Pollut. 2015;199:10–17. https://doi:10.1016/j.envpol.2015.01.008
crossref pmid

75. Tanaka K, Takada H, Yamashita R, Mizukawa K, Maki Fukuwaka, Watanuki Y. Accumulation of plastic-derived chemicals in tissues of seabirds ingesting marine plastics. Mar Pollut Bull. 2013;69(1–2)219–222. https://doi:10.1016/j.marpolbul.2012.12.010
crossref pmid

76. Hoarau L, Ainley L, Jean C, Ciccione S. Ingestion and defecation of marine debris by loggerhead sea turtles, Caretta caretta, from by-catches in the South-West Indian Ocean. Mar. Pollut. Bull. 2014;84(1–2)90–96. https://doi:10.1016/j.marpolbul.2014.05.031
crossref pmid

77. Desforges JPW, Galbraith M, Ross PS. Ingestion of Microplastics by Zooplankton in the Northeast Pacific Ocean. Arch. Environ. Contam. Toxicol. 2015;69(3)320–330. https://doi:10.1007/s00244-015-0172-5
crossref pmid pdf

78. Bravo Rebolledo EL, Van Franeker JA, Jansen OE, Brasseur SMJM. Plastic ingestion by harbour seals (Phoca vitulina) in The Netherlands. Mar. Pollut. Bull. 2013;67(1–2)200–202. https://doi:10.1016/j.marpolbul.2012.11.035
crossref pmid

79. Cole M, Lindeque P, Halsband C, Galloway TS. Microplastics as contaminants in the marine environment: A review. Mar. Pollut. Bull. 2011;62(12)2588–2597. https://doi:10.1016/j.marpolbul.2011.09.025
crossref pmid

80. Wang W, Gao H, Jin S, Li R, Na G. The ecotoxicological effects of microplastics on aquatic food web, from primary producer to human: A review. Ecotoxicol Environ. Saf. 2019;173:110–117. https://doi:10.1016/j.ecoenv.2019.01.113
crossref pmid

81. Deng Y, Zhang Y, Lemos B, Ren H. Tissue accumulation of microplastics in mice and biomarker responses suggest widespread health risks of exposure. Sci. Rep. 2017;7(March)1–10. https://doi:10.1038/srep46687
crossref pmid pmc pdf

82. Prata JC, da Costa JP, Lopes I, Andrady AL, Duarte AC, Rocha-Santos T. A One Health perspective of the impacts of microplastics on animal, human and environmental health. Sci. Total Environ. 2021;777:146094. https://doi:10.1016/j.scitotenv.2021.146094
crossref pmid

83. Barboza LGA, Cunha SC, Monteiro C, Fernandes JO, Guilhermino L. Bisphenol A and its analogs in muscle and liver of fish from the North East Atlantic Ocean in relation to microplastic contamination. Exposure and risk to human consumers. J. Hazard. Mater. 2020;393:122419. https://doi:10.1016/j.jhazmat.2020.122419
crossref pmid

84. Gardon T, Reisser C, Soyez C, Quillien V, Le Moullac G. Microplastics Affect Energy Balance and Gametogenesis in the Pearl Oyster Pinctada margaritifera. Environ. Sci. Technol. 2018;52(9)5277–5286. https://doi:10.1021/acs.est.8b00168
crossref pmid

85. Faure F, Demars C, Wieser O, Kunz M, De Alencastro LF. Plastic pollution in Swiss surface waters: Nature and concentrations, interaction with pollutants. Environ. Chem. 2015;12(5)582–591. https://doi:10.1071/en14218
crossref

86. Besseling E, Foekema EM, Van Franeker JA, et al. Microplastic in a macro filter feeder: Humpback whale Megaptera novaeangliae. Mar. Pollut. Bull. 2015;95(1)248–252. https://doi:10.1016/j.marpolbul.2015.04.007
crossref pmid

87. Hall AJ, Hugunin K, Deaville R, Law RJ, Allchin CR, Jepson PD. The Risk of Infection from Polychlorinated Biphenyl Exposure in the Harbor Porpoise (Phocoena phocoena): A Case–Control Approach. Environ. Health Perspect. 2006;114(5)704–711. https://doi:10.1289/ehp.8222
crossref pmid pmc

88. Kedzierski M, D’Almeida M, Magueresse A, et al. Threat of plastic ageing in marine environment. Adsorption/desorption of micropollutants. Mar. Pollut. Bull. 2018;127:684–694. https://doi:10.1016/j.marpolbul.2017.12.059
crossref pmid

89. Nabi G, Robeck TR, Hao Y, Wang D. Hematologic and Biochemical Reference Interval Development and the Effect of Age, Sex, Season, and Location on Hematologic Analyte Concentrations in Critically Endangered Yangtze Finless Porpoise (Neophocaena asiaeorientalis ssp. asiaeorientalis). Front. Physiol. 2019;10:792. https://doi:10.3389/fphys.2019.00792
crossref pmid pmc

90. Meaza I, Toyoda JH, Wise Sr JP. Microplastics in Sea Turtles, Marine Mammals and Humans: A One Environmental Health Perspective. Front. Environ. Sci. 2021;8:575614. https://doi:10.3389/fenvs.2020.575614
crossref pmid pmc

91. Ugwu K, Herrera A, Gómez M. Microplastics in marine biota: A review. Mar Pollut Bull. 2021;169:112540. https://doi:10.1016/j.marpolbul.2021.112540
crossref pmid

92. Ya H, Jiang B, Xing Y, Zhang T, Lv M, Wang X. Recent advances on ecological effects of microplastics on soil environment. Sci Total Environ. 2021;798:149338. https://doi:10.1016/j.scitotenv.2021.149338
crossref pmid

93. Thapliyal C, Priya A, Singh SB, Bahuguna V, Daverey A. Potential strategies for bioremediation of microplastic contaminated soil. Environ. Chem. Ecotoxicol. 2024;6:117–131. https://doi:10.1016/j.enceco.2024.05.001
crossref

94. Yang J, Li L, Li R, et al. Microplastics in an agricultural soil following repeated application of three types of sewage sludge: A field study. Environ. Pollut. 2021;289:117943. https://doi:10.1016/j.envpol.2021.117943
crossref pmid

95. Buta M, Hubeny J, Zieliński W, Harnisz M, Korzeniewska E. Sewage sludge in agriculture – the effects of selected chemical pollutants and emerging genetic resistance determinants on the quality of soil and crops – a review. Ecotoxicol Environ. Saf. 2021;214:112070. https://doi:10.1016/j.ecoenv.2021.112070
crossref pmid

96. Rorat A, Courtois P, Vandenbulcke F, Lemiere S. Sanitary and environmental aspects of sewage sludge management. Ind Munic Sludge Emerg Concerns Scope Resour Recover. 2019;155–180. https://doi:10.1016/b978-0-12-815907-1.00008-8
crossref

97. Lamastra L, Suciu NA, Trevisan M. Sewage sludge for sustainable agriculture: Contaminants’ contents and potential use as fertilizer. Chem. Biol. Technol. Agric. 2018;5(1)1–6. https://doi:10.1186/s40538-018-0122-3
crossref pdf

98. Corradini F, Casado F, Leiva V, Huerta-Lwanga E, Geissen V. Microplastics occurrence and frequency in soils under different land uses on a regional scale. Sci. Total Environ. 2021;752:141917. https://doi:10.1016/j.scitotenv.2020.141917
crossref pmid

99. Rafique A, Irfan M, Mumtaz M, Qadir A. Spatial distribution of microplastics in soil with context to human activities: a case study from the urban center. Environ. Monit. Assess. 2020;192(11)1–13. https://doi:10.1007/S10661-020-08641-3
crossref pmid pdf

100. Zhang K, Su J, Xiong X, Wu X, Wu C, Liu J. Microplastic pollution of lakeshore sediments from remote lakes in Tibet plateau, China. Environ. Pollut. 2016;219:450–455. https://doi:10.1016/j.envpol.2016.05.048
crossref pmid

101. Boots B, Russell CW, Green DS. Effects of Microplastics in Soil Ecosystems: Above and below Ground. Environ. Sci. Technol. 2019;53(19)11496–11506. https://doi:10.1021/acs.est.9b03304
crossref pmid

102. Huerta Lwanga E, Gertsen H, Gooren H, et al. Microplastics in the Terrestrial Ecosystem: Implications for Lumbricus terrestris (Oligochaeta, Lumbricidae). Environ. Sci. Technol. 2016;50(5)2685–2691. https://doi:10.1021/acs.est.5b05478
crossref pmid

103. Maity S, Guchhait R, Chatterjee A, Pramanick K. Co-occurrence of co-contaminants: Cyanotoxins and microplastics, in soil system and their health impacts on plant – A comprehensive review. Sci. Total Environ. 2021;794:148752. https://doi:10.1016/j.scitotenv.2021.148752
crossref pmid

104. Ding J, Zhu D, Wang HT, et al. Dysbiosis in the Gut Microbiota of Soil Fauna Explains the Toxicity of Tire Tread Particles. Environ. Sci. Technol. 2020;54(12)7450–7460. https://doi:10.1021/acs.est.0c00917
crossref pmid

105. Gruber N, Bakker DCE, DeVries T, et al. Trends and variability in the ocean carbon sink. Nat. Rev. Earth Environ. 2023;4(2)119–134. https://doi:10.1038/s43017-022-00381-x
crossref pdf

106. Rabiu KO, Han L, Bhusan Das D. CO2 Trapping in the Context of Geological Carbon Sequestration. Encycl Sustain Technol. 2017;461–475. https://doi:10.1016/b978-0-12-409548-9.10124-1
crossref

107. Sainger G. Microplastic Pollution in Oceans: A Barrier to Achieve Low Carbon Society. IOP Conf. Ser. Earth Environ. Sci. 2023;1279(1)012021. https://doi:10.1088/1755-1315/1279/1/012021
crossref pdf

108. Galgani L, Tzempelikou E, Kalantzi I, et al. Marine plastics alter the organic matter composition of the air-sea boundary layer, with influences on CO2 exchange: a large-scale analysis method to explore future ocean scenarios. Sci. Total Environ. 2023;857:159624. https://doi:10.1016/j.scitotenv.2022.159624
crossref pmid

109. Du Y, Huang Q, Li S, et al. Carbon sequestration reduced by the interference of nanoplastics on copper bioavailability. J. Hazard. Mater. 2024;468:133841. https://doi:10.1016/j.jhazmat.2024.133841
crossref pmid

110. Shen M, Ye S, Zeng G, et al. Can microplastics pose a threat to ocean carbon sequestration? Mar. Pollut. Bull. 2020. 150:1107–12. https://doi:10.1016/j.marpolbul.2019.110712
crossref pmid

111. Kümmerer K. The presence of pharmaceuticals in the environment due to human use – present knowledge and future challenges. J. Environ. Manage. 2009;90(8)2354–2366. https://doi:10.1016/j.jenvman.2009.01.023
crossref pmid

112. Yin L, Wang B, Yuan H, et al. Pay special attention to the transformation products of PPCPs in environment. Emerg. Contam. 2017;3(2)69–75. https://doi:10.1016/j.emcon.2017.04.001
crossref

113. Oberg G, Leopold A. On the role of review papers in the face of escalating publication rates - a case study of research on contaminants of emerging concern (CECs). Environ. Int. 2019;131:104960. https://doi:10.1016/j.envint.2019.104960
crossref pmid

114. Atugoda T, Vithanage M, Wijesekara H, et al. Interactions between microplastics, pharmaceuticals and personal care products: Implications for vector transport. Environ. Int. 2021;149:106367. https://doi:10.1016/j.envint.2020.106367
crossref pmid

115. Ma J, Zhao J, Zhu Z, Li L, Yu F. Effect of microplastic size on the adsorption behavior and mechanism of triclosan on polyvinyl chloride. Environ. Pollut. 2019;254:113104. https://doi:10.1016/j.envpol.2019.113104
crossref pmid

116. Wang F, Shih KM, Li XY. The partition behavior of perfluorooctanesulfonate (PFOS) and perfluorooctanesulfonamide (FOSA) on microplastics. Chemosphere. 2015;119:841–847. https://doi:10.1016/j.chemosphere.2014.08.047
crossref pmid

117. Wang W, Qi M, Jia X, et al. Differential adsorption of zwitterionic PPCPs by multifunctional resins: The influence of the hydrophobicity and electrostatic potential of PPCPs. Chemosphere. 2020;241:125023. https://doi:10.1016/j.chemosphere.2019.125023
crossref pmid

118. Hüffer T, Hofmann T. Sorption of non-polar organic compounds by micro-sized plastic particles in aqueous solution. Environ. Pollut. 2016;214:194–201. https://doi:10.1016/j.envpol.2016.04.018
crossref pmid

119. Elizalde-Velázquez A, Subbiah S, Anderson TA, Green MJ, Zhao X, Cañas-Carrell JE. Sorption of three common nonsteroidal anti-inflammatory drugs (NSAIDs) to microplastics. Sci. Total. Environ. 2020;715:136974. https://doi:10.1016/j.scitotenv.2020.136974
crossref pmid

120. Xu B, Liu F, Brookes PC, Xu J. Microplastics play a minor role in tetracycline sorption in the presence of dissolved organic matter. Environ. Pollut. 2018;240:87–94. https://doi:10.1016/j.envpol.2018.04.113
crossref pmid

121. Zhang Z, Zhang Q, Wang T, et al. Assessment of global health risk of antibiotic resistance genes. Nat. Commun. 2022;13(1)1–11. https://doi:10.1038/s41467-022-29283-8
crossref pmid pmc pdf

122. Zhou Y, Niu L, Zhu S, Lu H, Liu W. Occurrence, abundance, and distribution of sulfonamide and tetracycline resistance genes in agricultural soils across China. Sci Total Environ. 2017;599–600:1977–1983. https://doi:10.1016/j.scitotenv.2017.05.152
crossref pmid

123. Zhang Y, Niu Z, Zhang Y, Zhang K. Occurrence of intracellular and extracellular antibiotic resistance genes in coastal areas of Bohai Bay (China) and the factors affecting them. Environ. Pollut. 2018;236:126–136. https://doi:10.1016/j.envpol.2018.01.033
crossref pmid

124. Xu Y, Xu J, Mao D, Luo Y. Effect of the selective pressure of sub-lethal level of heavy metals on the fate and distribution of ARGs in the catchment scale. Environ. Pollut. 2017;220:900–908. https://doi:10.1016/j.envpol.2016.10.074
crossref pmid

125. Xie J, Jin L, Luo X, Zhao Z, Li X. Seasonal Disparities in Airborne Bacteria and Associated Antibiotic Resistance Genes in PM2.5 between Urban and Rural Sites. Environ. Sci. Technol. Lett. 2018;5(2)74–79. https://doi:10.1021/acs.estlett.7b00561
crossref

126. Wang JH, Lu J, Zhang YX, Wu J, Luo Y, Liu H. Metagenomic analysis of antibiotic resistance genes in coastal industrial mariculture systems. Bioresour. Technol. 2018;253:235–243. https://doi:10.1016/j.biortech.2018.01.035
crossref pmid

127. Su HC, Liu YS, Pan CG, Chen J, He LY, Ying GG. Persistence of antibiotic resistance genes and bacterial community changes in drinking water treatment system: From drinking water source to tap water. Sci Total Environ. 2018;616–617:453–461. https://doi:10.1016/j.scitotenv.2017.10.318
crossref pmid

128. Niu ZG, Zhang K, Zhang Y. Occurrence and distribution of antibiotic resistance genes in the coastal area of the Bohai Bay, China. Mar. Pollut. Bull. 2016;107(1)245–250. https://doi:10.1016/j.marpolbul.2016.03.064
crossref pmid

129. Laganà P, Caruso G, Corsi I, et al. Do plastics serve as a possible vector for the spread of antibiotic resistance? First insights from bacteria associated to a polystyrene piece from King George Island (Antarctica). Int. J. Hyg. Environ. Health. 2019;222(1)89–100. https://doi:10.1016/j.ijheh.2018.08.009
crossref pmid

130. Kaur K, Reddy S, Barathe P, et al. Microplastic-associated pathogens and antimicrobial resistance in environment. Chemo sphere. 2022;291:133005. https://doi:10.1016/j.chemosphere.2021.133005
crossref pmid

131. Dong H, Chen Y, Wang J, et al. Interactions of microplastics and antibiotic resistance genes and their effects on the aquaculture environments. J. Hazard. Mater. 2021;403:123961. https://doi:10.1016/j.jhazmat.2020.123961
crossref pmid

132. Stenger KS, Wikmark OG, Bezuidenhout CC, Molale-Tom LG. Microplastics pollution in the ocean: Potential carrier of resistant bacteria and resistance genes. Environ. Pollut. 2021;291:118130. https://doi:10.1016/j.envpol.2021.118130
crossref pmid

133. Sun M, Ye M, Jiao W, et al. Changes in tetracycline partitioning and bacteria/phage-comediated ARGs in microplastic-contaminated greenhouse soil facilitated by sophorolipid. J. Hazard. Mater. 2018;345:131–139. https://doi:10.1016/j.jhazmat.2017.11.036
crossref pmid

134. Shrivastava A. Introduction to Plastics Engineering. Introd to Plast Eng. 2018;1–16. https://doi:10.1016/b978-0-323-39500-7.00001-0
crossref

135. Khalid N, Hussain M, Young HS, Boyce B, Aqeel M, Noman A. Effects of road proximity on heavy metal concentrations in soils and common roadside plants in Southern California. Environ. Sci. Pollut. Res. 2018;25(35)35257–35265. https://doi:10.1007/s11356-018-3218-1
crossref pmid pdf

136. Khalid N, Aqeel M, Noman A, Khan SM, Akhter N. Interactions and effects of microplastics with heavy metals in aquatic and terrestrial environments. Environ. Pollut. 2021;290(September)118104. https://doi:10.1016/j.envpol.2021.118104
crossref pmid

137. Vedolin MC, Teophilo CYS, Turra A, Figueira RCL. Spatial variability in the concentrations of metals in beached microplastics. Mar. Pollut. Bull. 2018;129(2)487–493. https://doi:10.1016/j.marpolbul.2017.10.019
crossref pmid

138. Holmes LA, Turner A, Thompson RC. Interactions between trace metals and plastic production pellets under estuarine conditions. Mar. Chem. 2014;167:25–32. https://doi:10.1016/j.marchem.2014.06.001
crossref

139. Wang J, Liu X, Li Y, et al. Microplastics as contaminants in the soil environment: A mini-review. Sci. Total. Environ. 2019;691:848–857. https://doi:10.1016/j.scitotenv.2019.07.209
crossref pmid

140. Gao X, Hassan I, Peng Y, Huo S, Ling L. Behaviors and influencing factors of the heavy metals adsorption onto microplastics: A review. J. Clean. Prod. 2021;319:128777. https://doi:10.1016/j.jclepro.2021.128777
crossref

141. Tang S, Lin L, Wang X, Feng A, Yu A. Pb(II) uptake onto nylon microplastics: Interaction mechanism and adsorption performance. J. Hazard. Mater. 2020;386:121960. https://doi:10.1016/j.jhazmat.2019.121960
crossref pmid

142. Dong Y, Gao M, Song Z, Qiu W. As(III) adsorption onto differentsized polystyrene microplastic particles and its mechanism. Chemosphere. 2020;239:124792. https://doi:10.1016/j.chemosphere.2019.124792
crossref pmid

143. Dong Y, Gao M, Song Z, Qiu W. Adsorption mechanism of As(III) on polytetrafluoroethylene particles of different size. Environ. Pollut. 2019;254:112950. https://doi:10.1016/j.envpol.2019.07.118
crossref pmid

144. Cao Y, Zhao M, Ma X, et al. A critical review on the interactions of microplastics with heavy metals: Mechanism and their combined effect on organisms and humans. Sci. Total Environ. 2021. 788147620. https://doi:10.1016/j.scitotenv.2021.147620
crossref pmid

145. Bhagat J, Nishimura N, Shimada Y. Toxicological interactions of microplastics/nanoplastics and environmental contaminants: Current knowledge and future perspectives. J. Hazard. Mater. 2021;405:123913. https://doi:10.1016/j.jhazmat.2020.123913
crossref pmid

146. Shim WJ, Hong SH, Eo SE. Identification methods in microplastic analysis: A review. Anal. Methods. 2017;9(9)1384–1391. https://doi:10.1039/c6ay02558g
crossref

147. Araujo CF, Nolasco MM, Ribeiro AMP, Ribeiro-Claro PJA. Identification of microplastics using Raman spectroscopy: Latest developments and future prospects. Water Res. 2018;142:426–440. https://doi:10.1016/j.watres.2018.05.060
crossref pmid

148. Löder MGJ, Gerdts G. Methodology used for the detection and identification of microplastics—a critical appraisal Marine anthropogenic litter. 1st edSpringer; Cham: 2015. p. 201–227.


149. Morgado V, Gomes L, Bettencourt da Silva RJN, Palma C. Validated spreadsheet for the identification of PE, PET, PP and PS microplastics by micro-ATR-FTIR spectra with known uncertainty. Talanta. 2021;234:122624. https://doi:10.1016/j.talanta.2021.122624
crossref pmid

150. Woo H, Seo K, Choi Y, et al. Methods of analyzing microsized plastics in the environment. Appl. Sci. 2021. 1122https://doi:10.3390/app112210640
crossref

151. Müsellim E, Tahir MH, Ahmad MS, Ceylan S. Thermokinetic and TG/DSC-FTIR study of pea waste biomass pyrolysis. Appl. Therm. Eng. 2018;137:54–61. https://doi:10.1016/j.applthermaleng.2018.03.050
crossref

152. Ma Z, Wang J, Yang Y, et al. Comparison of the Thermal Degradation Behaviors and Kinetics of Palm Oil Waste under Nitrogen and Air Atmosphere in TGA-FTIR with a Complementary Use of Model-Free and Model-Fitting Approaches. J. Anal. Appli. Pyrol. 2018. 134:p. 12–24. Elsevier B.V; 2018. https://doi:10.1016/j.jaap.2018.04.002
crossref

153. Majewsky M, Bitter H, Eiche E, Horn H. Determination of microplastic polyethylene (PE) and polypropylene (PP) in environmental samples using thermal analysis (TGA-DSC). Sci. Total Environ. 2016;568:507–511. https://doi:10.1016/j.scitotenv.2016.06.017
crossref pmid

154. Nuelle MT, Dekiff JH, Remy D, Fries E. A new analytical approach for monitoring microplastics in marine sediments. Environ. Pollut. 2014;184:161–169. https://doi:10.1016/j.envpol.2013.07.027
crossref pmid

155. Dekiff JH, Remy D, Klasmeier J, Fries E. Occurrence and spatial distribution of microplastics in sediments from Norderney. Environ. Pollut. 2014;186:248–256. https://doi:10.1016/j.envpol.2013.11.019
crossref pmid

156. Fries E, Dekiff JH, Willmeyer J, Nuelle MT, Ebert M, Remy D. Identification of polymer types and additives in marine microplastic particles using pyrolysis-GC/MS and scanning electron microscopy. Environ. Sci. Process Impacts. 2013;15(10)1949–1956. https://doi:10.1039/c3em00214d
crossref pmid

157. Dazzi A, Saunier J, Kjoller K, Yagoubi N. Resonance enhanced AFM-IR: A new powerful way to characterize blooming on polymers used in medical devices. Int. J. Pharm. 2015;484(1–2)109–114. https://doi:10.1016/j.ijpharm.2015.02.046
crossref pmid

158. Sheriff I, Awang NA, Halim HB, Ikechukwu OS, Jusoh AF. Extraction and analytical methods of microplastics in wastewater treatment plants: Isolation patterns, quantification, and size characterization techniques. Desalin. Water Treat. 2024;318:100399. https://doi:10.1016/j.dwt.2024.100399
crossref

159. Jiang J, Wang X, Ren H, et al. Investigation and fate of microplastics in wastewater and sludge filter cake from a wastewater treatment plant in China. Sci. Total. Environ. 2020;746:141378. https://doi:10.1016/j.scitotenv.2020.141378
crossref pmid

160. Long Z, Pan Z, Wang W, et al. Microplastic abundance, characteristics, and removal in wastewater treatment plants in a coastal city of China. Water Res. 2019;155:255–265. https://doi:10.1016/j.watres.2019.02.028
crossref pmid

161. Simon M, van Alst N, Vollertsen J. Quantification of microplastic mass and removal rates at wastewater treatment plants applying Focal Plane Array (FPA)-based Fourier Transform Infrared (FT-IR) imaging. Water Res. 2018;142:1–9. https://doi:10.1016/j.watres.2018.05.019
crossref pmid

162. Rasmussen LA, Iordachescu L, Tumlin S, Vollertsen J. A complete mass balance for plastics in a wastewater treatment plant - Macroplastics contributes more than microplastics. Water Res. 2021;201:117307. https://doi:10.1016/j.watres.2021.117307
crossref pmid

163. Bitter H, Lackner S. First quantification of semi-crystalline microplastics in industrial wastewaters. Chemosphere. 2020;258:127388. https://doi:10.1016/j.chemosphere.2020.127388
crossref pmid

164. Altmann K, Goedecke C, Bannick CG, et al. Identification of microplastic pathways within a typical European urban wastewater system. Appl. Res. 2023;2(5)e202200078. https://doi:10.1002/appl.202200078
crossref pdf

165. Magalhães S, Alves L, Romano A, Medronho B, Rasteiro M, da G. Extraction and Characterization of Microplastics from Portuguese Industrial Effluents. Polymers (Basel). 2022;14(14)2902. https://doi:10.3390/polym14142902
crossref pmid pmc

166. Yadav V, Pal D. Comparative analysis of microplastic measurement units: Concatenating items/m3, particles/kg, and mg/kg. Sustainable Chemistry One World. https://doi:10.1016/j.scowo.2024.100019


167. Liu W, Zhang J, Liu H, et al. A review of the removal of microplastics in global wastewater treatment plants: Characteristics and mechanisms. Environ. Int. 2021;146:106277. https://doi:10.1016/j.envint.2020.106277
crossref pmid

168. Mohan D, Sarswat A, Ok YS, Pittman CU. Organic and inorganic contaminants removal from water with biochar, a renewable, low cost and sustainable adsorbent – A critical review. Bioresour. Technol. 2014;160:191–202. https://doi:10.1016/j.biortech.2014.01.120
crossref pmid

169. Mohanty SK, Valenca R, Berger AW, et al. Plenty of room for carbon on the ground: Potential applications of biochar for stormwater treatment. Sci. Total Environ. 2018;625:1644–1658. https://doi:10.1016/j.scitotenv.2018.01.037
crossref pmid

170. Siipola V, Pflugmacher S, Romar H, Wendling L, Koukkari P. Low-Cost Biochar Adsorbents for Water Purification Including Microplastics Removal. Appl. Sci. 2020;10(3)788. https://doi:10.3390/app10030788
crossref

171. Ahmed MB, Zhou JL, Ngo HH, Guo W, Chen M. Progress in the preparation and application of modified biochar for improved contaminant removal from water and wastewater. Bioresour. Technol. 2016;214:836–851. https://doi:10.1016/j.biortech.2016.05.057
crossref pmid

172. Ahmed MB, Rahman MS, Alom J, et al. Microplastic particles in the aquatic environment: A systematic review. Sci. Total Environ. 2021;775:145793. https://doi:10.1016/j.scitotenv.2021.145793
crossref pmid

173. Talvitie J, Mikola A, Koistinen A, Setälä O. Solutions to microplastic pollution – Removal of microplastics from wastewater effluent with advanced wastewater treatment technologies. Water Res. 2017;123:401–407. https://doi:10.1016/j.watres.2017.07.005
crossref pmid

174. Ibrar I, Altaee A, Zhou JL, Naji O, Khanafer D. Challenges and potentials of forward osmosis process in the treatment of wastewater. Crit. Rev. Env. Sc. Techno. 2019;50(13)1339–1383. https://doi:10.1080/10643389.2019.1657762
crossref

175. Enfrin M, Dumée LF, Lee J. Nano/microplastics in water and wastewater treatment processes – Origin, impact and potential solutions. Water Res. 2019;161:621–638. https://doi:10.1016/j.watres.2019.06.049
crossref pmid

176. Li L, Xu G, Yu H, Xing J. Dynamic membrane for micro-particle removal in wastewater treatment: Performance and influencing factors. Sci. Total Environ. 2018;627:332–340. https://doi:10.1016/j.scitotenv.2018.01.239
crossref pmid

177. Grbic J, Nguyen B, Guo E, You JB, Sinton D, Rochman CM. Magnetic Extraction of Microplastics from Environmental Samples. Environ. Sci. Technol. Lett. 2019;6(2)68–72. https://doi:10.1021/acs.estlett.8b00671
crossref

178. Ziajahromi S, Neale PA, Telles Silveira I, Chua A, Leusch FDL. An audit of microplastic abundance throughout three Australian wastewater treatment plants. Chemosphere. 2021;263:128294. https://doi:10.1016/j.chemosphere.2020.128294
crossref pmid

179. Crawford CB, Quinn B. Microplastic separation techniques. Microplastic Pollut. 2017;203–218. https://doi:10.1016/b978-0-12-809406-8.00009-8
crossref

180. Carson HS, Colbert SL, Kaylor MJ, McDermid KJ. Small plastic debris changes water movement and heat transfer through beach sediments. Mar. Pollut. Bull. 2011;62(8)1708–1713. https://doi:10.1016/j.marpolbul.2011.05.032
crossref pmid

181. Mason SA, Garneau D, Sutton R, et al. Microplastic pollution is widely detected in US municipal wastewater treatment plant effluent. Environ. Pollut. 2016;218:1045–1054. https://doi:10.1016/j.envpol.2016.08.056
crossref pmid

182. Lares M, Ncibi MC, Sillanpää M, Sillanpää M. Occurrence, identification and removal of microplastic particles and fibers in conventional activated sludge process and advanced MBR technology. Water Res. 2018;133:236–246. https://doi:10.1016/j.watres.2018.01.049
crossref pmid

183. Russell JR, Huang J, Anand P, et al. Biodegradation of polyester polyurethane by endophytic fungi. Appl. Environ. Microbiol. 2011;77(17)6076–6084. https://doi:10.1128/aem.00521-11
crossref pmid pmc pdf

184. Anand U, Dey S, Bontempi E, et al. Biotechnological methods to remove microplastics: a review. Environ. Chem. Lett. 2023;21(3)1787. https://doi:10.1007/s10311-022-01552-4
crossref pmid pmc pdf

185. Sun J, Dai X, Wang Q, van Loosdrecht MCM, Ni BJ. Microplastics in wastewater treatment plants: Detection, occurrence and removal. Water. Res. 2019;152:21–37. https://doi:10.1016/j.watres.2018.12.050
crossref pmid

186. Lv X, Dong Q, Zuo Z, Liu Y, Huang X, Wu WM. Microplastics in a municipal wastewater treatment plant: Fate, dynamic distribution, removal efficiencies, and control strategies. J. Clean. Prod. 2019;225:579–586. https://doi:10.1016/j.jclepro.2019.03.321
crossref

187. Ouattara JMP, Coulibaly L, Tiho S, Gourène G. Comparison of macrofauna communities in sediments of the beds of vertical flow constructed wetlands planted with Panicum maximum (Jacq.) treating domestic wastewater. Ecol. Eng. 2009;35(8)1237–1242. https://doi:10.1016/j.ecoleng.2009.05.007
crossref

188. Wang Q, Hernández-Crespo C, Santoni M, Van Hulle S, Rousseau DPL. Horizontal subsurface flow constructed wetlands as tertiary treatment: Can they be an efficient barrier for microplastics pollution? Sci Total Environ. 2020;721. https://doi:10.1016/j.scitotenv.2020.137785
crossref pmid

189. Amjad M, Intisar A, Afzal A, Hussain N. Biological methods for the removal of microplastics from water. Adv. Chem. Pollution. Environ. Manag. Prot. 2023;9:65–78. https://doi:10.1016/bs.apmp.2022.10.003
crossref

190. Chen R, Qi M, Zhang G, Yi C. Comparative experiments on polymer degradation technique of produced water of polymer flooding oilfield. IOP. Conf. Ser. Earth Environ. Sci. 2018;113(1)012208. https://doi:10.1088/1755-1315/113/1/012208
crossref pdf

191. Tagg AS, Harrison JP, Ju-Nam Y, et al. Fenton’s reagent for the rapid and efficient isolation of microplastics from wastewater. Chem. Commun. 2016;53(2)372–375. https://doi:10.1039/c6cc08798a
crossref pmid

192. De Luna MDG, Veciana ML, Su CC, Lu MC. Acetaminophen degradation by electro-Fenton and photoelectro-Fenton using a double cathode electrochemical cell. J Hazard Mater. 2012;217–218:200–207. https://doi:10.1016/j.jhazmat.2012.03.018


193. Tao L, Wang Y, Zou Y, et al. Charge Transfer Modulated Activity of Carbon-Based Electrocatalysts. Adv. Energy Mater. 2020;10(11)1901227. https://doi:10.1002/aenm.201901227
crossref pdf

194. Brandon J, Goldstein M, Ohman MD. Long-term aging and degradation of microplastic particles: Comparing in situ oceanic and experimental weathering patterns. Mar. Pollut. Bull. 2016;110(1)299–308. https://doi:10.1016/j.marpolbul.2016.06.048
crossref pmid

195. Murphy F, Ewins C, Carbonnier F, Quinn B. Wastewater Treatment Works (WwTW) as a Source of Microplastics in the Aquatic Environment. Environ. Sci. Technol. 2016;50(11)5800–5808. https://doi:10.1021/acs.est.5b05416
crossref pmid

196. Ma B, Xue W, Ding Y, Hu C, Liu H, Qu J. Removal characteristics of microplastics by Fe-based coagulants during drinking water treatment. J. Environ. Sci. 2019;78:267–275. https://doi:10.1016/j.jes.2018.10.006
crossref pmid

197. Laskar N, Kumar U. Plastics and microplastics: A threat to environment. Environ. Technol. Innov. 2019;14:100352. https://doi:10.1016/j.eti.2019.100352
crossref

198. Dowarah K, Duarah H, Devipriya SP. A preliminary survey to assess the awareness, attitudes/behaviours, and opinions pertaining to plastic and microplastic pollution among students in India. Mar. Policy. 2022;144:105220. https://doi:10.1016/j.marpol.2022.105220
crossref

199. Jiang JQ. Occurrence of microplastics and its pollution in the environment: A review. Sustain. Prod. Consum. 2018;13:16–23. https://doi:10.1016/j.spc.2017.11.003
crossref

200. Plastic Pollution Coalition. California Introduces National Trash Reduction Act [Internet]. [cited 22 November 2024]. Available from: https://www.plasticpollutioncoalition.org/blog/2015/11/6/california-introduces-national-trash-reduction-act


201. OECD. Preventing single-use plastic waste: Implications of different policy approaches [Internet]. [cited 2 December 2024]. Available from: https://doi.org/10.1787/c62069e7-en


202. Basel Convention. Basel Convention on the Control of Transboundary Movements of Hazardous Wastes and their Disposal [Internet]. [cited 3 December 2024]. Available from:https://www.basel.int/Countries/StatusofRatifications/PartiesSignatories/tabid/4499/default.aspx


203. Usman S, Abdull Razis AF, Shaari K, et al. The Burden of Microplastics Pollution and Contending Policies and Regulations. Int. J. Environ. Res. Public Heal. 2022, Vol 19, Page 6773. 2022;19(11)6773. https://doi:10.3390/ijerph19116773
crossref pmid pmc

204. Milojevic N, Cydzik‐kwiatkowska A. Agricultural use of sewage sludge as a threat of microplastic (Mp) spread in the environment and the role of governance. Energies. 2021;14(19)6293. https://doi:10.3390/en14196293
crossref

205. Freeman S, Booth AM, Sabbah I, et al. Between source and sea: The role of wastewater treatment in reducing marine microplastics. J. Environ. Manage. 2020;266:110642. https://doi:10.1016/j.jenvman.2020.110642
crossref pmid

206. European Commission. Plastics [Internet]. [cited 18 November 2024]. Available from: https://environment.ec.europa.eu/topics/plastics_en


207. Amaral-Zettler LA, Zettler ER, Slikas B, et al. The biogeography of the Plastisphere: Implications for policy. Front. Ecol. Environ. 2015;13(10)541–546. https://doi:10.1890/150017
crossref

208. European Commission. Questions & Answers: A European strategy for plastics [Internet]. [cited 14 November 2024]. Available from: https://ec.europa.eu/commission/presscorner/detail/sk/memo_18_6


209. Statista. EU-27: plastic packaging waste generation [Internet]. [cited 20 November 2024]. Available from: https://www.statista.com/statistics/881996/plastic-packaging-waste-generated-eu/


210. d’Ambrières W. Plastics recycling worldwide: current overview and desirable changes. Field Actions Science Reports. 2019. 1912–21. http://journals.openedition.org/factsreports/5102


211. Bishop G, Styles D, Lens PNL. Recycling of European plastic is a pathway for plastic debris in the ocean. Environ. Int. 2020;142:105893. https://doi:10.1016/j.envint.2020.105893
crossref pmid

212. Comtrade UN. International Trade Statistics [Internet]. [cited 25 November 2024]. Available from: https://comtrade.un.org/data


213. Earth Org. The Consequences of China’s Import Ban On Plastic Waste [Internet]. [cited 11 December 2024]. Available from: https://earth.org/chinas-import-ban/


214. Waste Management World Magazine. Waste exports: Germany’s problems with plastic waste [Internet]. [cited 7 December 2024]. Available from: https://waste-management-world.com/artikel/germany-s-problems-with-plastic-waste/


215. Sustinability Magazine. 10 Countries Tackling Plastic Pollution [Internet]. [cited 8 December 2024]. Available from: https://sustainabilitymag.com/top10/10-countries-tackling-plastic-pollution


216. Rimondi V, Monnanni A, De Beni E, et al. Occurrence and Quantification of Natural and Microplastic Items in Urban Streams: The Case of Mugnone Creek (Florence, Italy). Toxics. 2022;10(4)159. https://doi:10.3390/toxics10040159
crossref pmid pmc

217. Scopetani C, Chelazzi D, Martellini T, et al. Occurrence and characterization of microplastic and mesoplastic pollution in the Migliarino San Rossore, Massaciuccoli Nature Park (Italy). Mar. Pollut. Bull. 2021;171:112712. https://doi:10.1016/j.marpolbul.2021.112712
crossref pmid

218. Vianello A, Boldrin A, Guerriero P, et al. Microplastic particles in sediments of Lagoon of Venice, Italy: First observations on occurrence, spatial patterns and identification. Estuar. Coast. Shelf Sci. 2013;130:54–61. https://doi:10.1016/j.ecss.2013.03.022
crossref

219. Phuong NN, Poirier L, Lagarde F, Kamari A, Zalouk-Vergnoux A. Microplastic abundance and characteristics in French Atlantic coastal sediments using a new extraction method. Environ. Pollut. 2018;243:228–237. https://doi:10.1016/j.envpol.2018.08.032
crossref pmid

220. Dris R, Gasperi J, Rocher V, Saad M, Renault N, Tassin B. Microplastic contamination in an urban area: a case study in Greater Paris. Environ. Chem. 2015;12(5)592–599. https://doi:10.1071/en14167
crossref

221. Frère L, Paul-Pont I, Rinnert E, et al. Influence of environmental and anthropogenic factors on the composition, concentration and spatial distribution of microplastics: A case study of the Bay of Brest (Brittany, France). Environ. Pollut. 2017;225:211–222. https://doi:10.1016/j.envpol.2017.03.023
crossref pmid

222. Semmouri I, Vercauteren M, Van Acker E, Pequeur E, Asselman J, Janssen C. Presence of microplastics in drinking water from different freshwater sources in Flanders (Belgium), an urbanized region in Europe. Int. J. Food Contam. 2022;9(1)1–11. https://doi:10.1186/s40550-022-00091-8
crossref pdf

223. Vercauteren M, Semmouri I, Van Acker E, et al. Assessment of road run-off and domestic wastewater contribution to microplastic pollution in a densely populated area (Flanders, Belgium). Envir on. Pollut. 2023;333:122090. https://doi:10.1016/j.envpol.2023.122090
crossref

224. Slootmaekers B, Catarci Carteny C, Belpaire C, et al. Microplastic contamination in gudgeons (Gobio gobio) from Flemish rivers (Belgium). Environ. Pollut. 2019;244:675–684. https://doi:10.1016/j.envpol.2018.09.136
crossref pmid

225. van Wezel A, Caris I, Kools SAE. Release of primary microplastics from consumer products to wastewater in the Netherlands. Environ. Toxicol. Chem. 2016;35(7)1627–1631. https://doi:10.1002/etc.3316
crossref pmid pdf

226. Cohen QM, Glaese M, Meng K, Geissen V, Huerta-Lwanga E. Parks and Recreational Areas as Sinks of Plastic Debris in Urban Sites: The Case of Light-Density Microplastics in the City of Amsterdam, The Netherlands. Environ. 2022;9(1)5. https://doi:10.3390/environments9010005
crossref

227. Mughini-Gras L, van der Plaats RQJ, van der Wielen PWJJ, Bauerlein PS, de Roda Husman AM. Riverine microplastic and microbial community compositions: A field study in the Netherlands. Water Res. 2021;192:116852. https://doi:10.1016/j.watres.2021.116852
crossref pmid

228. Hurley R, Woodward J, Rothwell JJ. Microplastic contamination of river beds significantly reduced by catchment-wide flooding. Nat. Geosci. 2018;11(4)251–257. https://doi:10.1038/s41561-018-0080-1
crossref pdf

229. Horton AA, Svendsen C, Williams RJ, Spurgeon DJ, Lahive E. Large microplastic particles in sediments of tributaries of the River Thames, UK – Abundance, sources and methods for effective quantification. Mar. Pollut. Bull. 2017;114(1)218–226. https://doi:10.1016/j.marpolbul.2016.09.004
crossref pmid

230. Green BC, Johnson CLE. Characterisation of microplastic contamination in sediment of England’s inshore waters. Mar. Pollut. Bull. 2020;151:110788. https://doi:10.1016/j.marpolbul.2019.110788
crossref pmid

231. Álvarez-Hernández C, Cairós C, López-Darias J, et al. Microplastic debris in beaches of Tenerife (Canary Islands, Spain). Mar. Pollut. Bull. 2019;146:26–32. https://doi:10.1016/j.marpolbul.2019.05.064
crossref pmid

232. Bayo J, Rojo D, Olmos S. Abundance, morphology and chemical composition of microplastics in sand and sediments from a protected coastal area: The Mar Menor lagoon (SE Spain). Environ. Pollut. 2019;252:1357–1366. https://doi:10.1016/j.envpol.2019.06.024
crossref pmid

233. Filgueiras AV, Gago J, Campillo JA, León VM. Microplastic distribution in surface sediments along the Spanish Mediterranean continental shelf. Environ. Sci. Pollut. Res. 2019;26(21)21264–21273. https://doi:10.1007/S11356-019-05341-5
crossref pdf

234. Groundwater BGR. Groundwater-resources in Germany [Internet]. [cited 15 December 2024]. Available from: https://www.deutsche-rohstoffagentur.de/EN/Themen/Wasser/grundwasser_deutschland_en.html


235. Umweltbundesamt. Water Body Type of the Year 2022 “Groundwater”. [Internet]. [cited 18 December 2024]. Available from: https://www.umweltbundesamt.de/en/themen/wasser/gewassertyp-des-jahres/water-body-type-of-the-year-2022-groundwater


236. Mintenig SM, Löder MGJ, Primpke S, Gerdts G. Low numbers of microplastics detected in drinking water from ground water sources. Sci. Total Environ. 2019;648:631–635. https://doi:10.1016/j.scitotenv.2018.08.178
crossref pmid

237. Weber F, Kerpen J, Wolff S, Langer R, Eschweiler V. Investigation of microplastics contamination in drinking water of a German city. Sci. Total Environ. 2021;755:143421. https://doi:10.1016/j.scitotenv.2020.143421
crossref pmid

238. Roscher L, Fehres A, Reisel L, et al. Microplastic pollution in the Weser estuary and the German North Sea. Environ. Pollut. 2021;288:117681. https://doi:10.1016/j.envpol.2021.117681
crossref pmid

239. Eibes PM, Gabel F. Floating microplastic debris in a rural river in Germany: Distribution, types and potential sources and sinks. Sci. Total Environ. 2022;816:151641. https://doi:10.1016/j.scitotenv.2021.151641
crossref pmid

240. Mani T, Hauk A, Walter U, Burkhardt-Holm P. Microplastics profile along the Rhine River. Sci. Reports. 2015;5(1)1–7. https://doi:10.1038/srep17988
crossref pdf

241. Schmidt C, Kumar R, Yang S, Büttner O. Microplastic particle emission from wastewater treatment plant effluents into river networks in Germany: Loads, spatial patterns of concentrations and potential toxicity. Sci. Total Environ. 2020;737:139544. https://doi:10.1016/j.scitotenv.2020.139544
crossref pmid

242. Siegel H, Fischer F, Lenz R, Fischer D, Jekel M, Labrenz M. Identification and quantification of microplastic particles in drinking water treatment sludge as an integrative approach to determine microplastic abundance in a freshwater river. Environ. Pollut. 2021;286:117524. https://doi:10.1016/j.envpol.2021.117524
crossref pmid

243. Frei S, Piehl S, Gilfedder BS, et al. Occurence of microplastics in the hyporheic zone of rivers. Sci. Reports. 2019;9(1)1–11. https://doi:10.1038/s41598-019-51741-5
crossref pdf

244. Drummond JD, Nel HA, Packman AI, Krause S. Significance of Hyporheic Exchange for Predicting Microplastic Fate in Rivers. Env. Sci. Techno. Letter. 2020;7(10)727–732. https://doi:10.1021/acs.estlett.0c00595
crossref

245. Frei S, Piehl S, Gilfedder BS, et al. Occurence of microplastics in the hyporheic zone of rivers. Sci. Reports 2019 91. 2019;9(1)1–11. https://doi:10.1038/s41598-019-51741-5
crossref pdf

246. Lee JY, Cha J, Ha K, Viaroli S. Microplastic pollution in groundwater: a systematic review. Environ. Pollut. Bioavailab. 2024. 361https://doi:10.1080/26395940.2023.2299545
crossref

247. Rocío M, Barroso R, Inglezakis VJ, Calero EC, Kovač Viršek M, Mali N. Microplastics in Groundwater: Pathways, Occurrence, and Monitoring Challenges. Water. 2024;16(9)1228. https://doi:10.3390/w16091228
crossref

248. Velasco A, de JN, Rard L, Blois W, et al. Microplastic and fibre contamination in a remote Mountain lake in Switzerland. Water (Switzerland). 2020. 129https://doi:10.3390/w12092410


249. Dierkes G, Lauschke T, Becher S, Schumacher H, Földi C, Ternes T. Quantification of microplastics in environmental samples via pressurized liquid extraction and pyrolysis-gas chromatography. Anal. Bioanal. Chem. 2019;411(26)6959–6968. https://doi:10.1007/s00216-019-02066-9
crossref pmid pdf

250. Stolte A, Forster S, Gerdts G, Schubert H. Microplastic concentrations in beach sediments along the German Baltic coast. Mar. Pollut. Bull. 2015;99(1–2)216–229. https://doi:10.1016/j.marpolbul.2015.07.022
crossref pmid

251. Mani T, Blarer P, Storck FR, Pittroff M, Wernicke T, Burkhardt-Holm P. Repeated detection of polystyrene microbeads in the Lower Rhine River. Environ. Pollut. 2019;245:634–641. https://doi:10.1016/j.envpol.2018.11.036
crossref pmid

252. Leslie HA, Brandsma SH, van Velzen MJM, Vethaak AD. Microplastics en route: Field measurements in the Dutch river delta and Amsterdam canals, wastewater treatment plants, North Sea sediments and biota. Environ. Int. 2017;101:133–142. https://doi:10.1016/j.envint.2017.01.018
crossref pmid

253. Scholz-Böttcher BM, Dibke C, Fischer M. Microplastic mass concentrations and distribution in german bight waters by pyrolysis-gas chromatography-mass spectrometry/ thermochemolysis reveal potential impact of marine coatings: Do ships leave skid marks? Environ. Sci. Technol. 2021;55(4)2285–2295. https://doi:10.1021/acs.est.0c04522/
crossref pmid

254. Aigars J, Barone M, Suhareva N, Putna-Nimane I, Deimantovica -Dimante I. Occurrence and spatial distribution of microplastics in the surface waters of the Baltic Sea and the Gulf of Riga. Mar. Pollut. Bull. 2021;172:112860. https://doi:10.1016/j.marpolbul.2021.112860
crossref pmid

255. Kreitsberg R, Raudna-Kristoffersen M, Heinlaan M, et al. Seagrass beds reveal high abundance of microplastic in sediments: A case study in the Baltic Sea. Mar. Pollut. Bull. 2021;168:112417. https://doi:10.1016/j.marpolbul.2021.112417
crossref pmid

256. Sainio E, Lehtiniemi M, Setälä O. Microplastic ingestion by small coastal fish in the northern Baltic Sea, Finland. Mar. Pollut. Bull. 2021;172:112814. https://doi:10.1016/j.marpolbul.2021.112814
crossref pmid

257. Mintenig SM, Löder MGJ, Primpke S, Gerdts G. Low numbers of microplastics detected in drinking water from ground water sources. Sci. Total Environ. 2019;648:631–635. https://doi:10.1016/j.scitotenv.2018.08.178
crossref pmid

258. Schmidt LK, Bochow M, Imhof HK, Oswald SE. Multi-temporal surveys for microplastic particles enabled by a novel and fast application of SWIR imaging spectroscopy – Study of an urban watercourse traversing the city of Berlin, Germany. Environ. Pollut. 2018;239:579–589. https://doi:10.1016/j.envpol.2018.03.097
crossref pmid

259. Schrank I, Löder MGJ, Imhof HK, et al. Riverine microplastic contamination in southwest Germany: A large-scale survey. Front. Earth Sci. 2022;10:794250. https://doi:10.3389/feart.2022.794250
crossref

260. Lorenz C, Roscher L, Meyer MS, et al. Spatial distribution of microplastics in sediments and surface waters of the southern North Sea. Environ. Pollut. 2019;252:1719–1729. https://doi:10.1016/j.envpol.2019.06.093
crossref pmid

261. Mintenig SM, Int-Veen I, Löder MGJ, Primpke S, Gerdts G. Identification of microplastic in effluents of waste water treatment plants using focal plane array-based micro-Fourier-transform infrared imaging. Water Res. 2017;108:365–372. https://doi:10.1016/j.watres.2016.11.015
crossref pmid

262. Wolff S, Kerpen J, Prediger J, Barkmann L, Müller L. Determination of the microplastics emission in the effluent of a municipal waste water treatment plant using Raman microspectroscopy. Water Res. X. 2019;2:100014. https://doi:10.1016/j.wroa.2018.100014
crossref pmid pmc

263. Altmann K, Goedecke C, Bannick CG, et al. Identification and Quantification of Microplastic in Sewage systems by TED-G C-MS. In : Global NEST International Conference on Environmental Science & Technology; 2019;
crossref

264. Bitter H, Krause L, Kirchen F, Fundneider T, Lackner S. Semi-crystalline microplastics in wastewater plant effluents and removal efficiencies of post-treatment filtration systems. Water Res. X. 2022;17:100156. https://doi:10.1016/j.wroa.2022.100156
crossref pmid pmc

265. Barkmann-Metaj L, Weber F, Bitter H, et al. Quantification of microplastics in wastewater systems of German industrial parks and their wastewater treatment plants. Sci. Total Environ. 2023;881:163349. https://doi:10.1016/j.scitotenv.2023.163349
crossref pmid

266. Roscher L, Halbach M, Nguyen MT, et al. Microplastics in two German wastewater treatment plants: Year-long effluent analysis with FTIR and Py-GC/MS. Sci Total Environ. 2022;817. https://doi:10.1016/j.scitotenv.2021.152619
crossref pmid

267. Wagner M, Scherer C, Alvarez-Muñoz D, et al. Microplastics in freshwater ecosystems: what we know and what we need to know. Environ. Sci. Eur. 2014;26(1)1–9. https://doi:10.1186/s12302-014-0012-7
crossref pmid pmc pdf

268. Kye H, Kim J, Ju S, Lee J, Lim C, Yoon Y. Microplastics in water systems: A review of their impacts on the environment and their potential hazards. Heliyon. 2023;9(3)e14359. https://doi:10.1016/j.heliyon.2023.e14359
crossref pmid pmc

Fig. 1
Trend of studies conducted on microplastics globally from 2011 to 2023. We can observe a jump of almost 69% in the number of publications discussing MPs.
/upload/thumbnails/eer-2024-609f1.gif
Fig. 2
Sources and pathways of MPs. It can be seen that rivers are one of the primary receivers and the emanator of MPs simultaneously. While it has been agreed by several authors that WWTPs are considered to be one of the most preeminent sources of MPs feeding the rivers [2224].
/upload/thumbnails/eer-2024-609f2.gif
Fig. 3
Implication of MPs on the human body. It is visible that these contaminants affect almost all the major organs of the body. However, the number of studies is limited, and further research should be encouraged to understand the profound side effects of these contaminants.
/upload/thumbnails/eer-2024-609f3.gif
Fig. 4
Several remediation techniques, which are used to treat MPs from the environment.
/upload/thumbnails/eer-2024-609f4.gif
Fig. 5
a. Top 10 European Union countries generating plastic packaging waste. The values are given in thousand metric tons. Germany leads the chart with the most plastic packaging waste generation, followed by France and Italy. b. Quantity of plastic waste and scrap (in kg) exported by Germany to the world and its respective trade value (in $) from 2017 until 2021. The percentage decrease in exports from Germany from 2017 to 2021 is approximately 18%; meanwhile, the reduction in the amount dropped by 33% roughly.
/upload/thumbnails/eer-2024-609f5.gif
Fig. 6
Distribution map of microplastic research in various regions of Germany based on the cited literature. The map indicates most of the studies are concentrated in the western part of Germany, with notable gaps in the central and southern parts.
/upload/thumbnails/eer-2024-609f6.gif
Table 1
MPs’ abundance in German groundwater, rivers, lakes, riverbed sediments, and marine water.
Sample Location Analysis Concentration Type Shape Reference
Well Holdorf FT-IR 7 particles/m3 PEST, PE, PVC, PA and epoxy resin Fibre [257]
House installation Rüsselsheim Raman μ-spectroscopy 0 - - [237]
Estuarian water Bremerhaven ATR-FT-IR 9700 particles/m3 PE and PP Sphere, film, pellets, filament and foams [238]
River water North-West Germany (River Ems) FT-IR 1.54 ± 1.54 particles/m3 - - [239]
River water Rees FT-IR 11050 particles/L PS, PE Spherule [240]
Canal water Berlin FT-IR and Raman spectroscopy 96 particles/L LDPE, HDPE, PP, PET, PVC, PS, PA and PC Foam, sphere and pellet [258]
River water Rostock Raman μ-spectroscopy 233 ± 36 particles/m3 PE, PP, PS, PET and PVC Fragments, spheres and fibres [242]
River sediment Bayreuth ATR-FT-IR 30 × 103 particles/kg dry weight PAN, PTFE, PE and PP Fragment and fibre [243]
River sediment Niederwerth Py-GC-MS 0.028 ± 0.006 mg/g PP, PE and PS - [249]
Stream water Varel Stereo microscope 19 fibres/L - Fibre and flake [250]
River water Cologne-Duisburg ATR-FT-IR and Raman spectroscopy 9.2 particles/m3 polystyrene-divi nylbenzene Spherules [251]
River water Thundorf Osterhofen Focal plane array based- μFTIR 150.24 particles/m3 PE, PP, PS, PVA Fiber, fragment [259]
Sea water Baltic sea (Warnemünde) Stereo microscope 3.3 fibres/L - Fibre [250]
Sea water North Sea (German Bight) Py-GC-MS 1.396 mg/m3 PP, PE, PS, PP, PET, PVC - [253]
Sea water North Sea ATR-FT-IR 23 particles/m3 PE and PP Sphere, film, pellets, filament and foams [238]
Sea water North Sea ATR-FTIR 245.4 particles/m3 PE, PP< and, PEST Fibers, spheres, and fragments [260]
Table 2
MPs’ abundance in German WWTPs.
Sample Location Analysis Concentration Type Shape Reference
WWTP effluent Bavaria Py-GC-MS 3.3 ± 0.3 mg/g PP, PE and PS - [249]
WWTP effluent Not disclosed DSC 19.6 μg/L PELD, PEHD, PP, PET and PA6 Fibre [264]
WWTP effluent Holdorf FT-IR 9000 particles/m3 PE, PA, SAN Fibre [261]
WWTP effluent Rüsselsheim Raman μ-spectroscopy 5900 particles/m3 PET, PP, PE and PS Fibre [262]
WWTP influent Kaiserslautern Thermal extraction desorption- GC-MS 2.2 μg/mg dry weight PP and PS - [263]
Downstream WWTP Duisburg Focal plane array based- μFTIR 754.86 particles/m3 PE, PP, PS, PA, PVA Fragment, bead [259]
WWTP effluent Not disclosed μ-Raman spectroscopy and DSC 80000 particles/m3 PE, PET, PS - [265]
WWTP effluent Not disclosed DSC 35.5 μg/L PE, PP, PET, PA - [163]
WWTP effluent - FTIR and pyro GC-MS 3 × 104 items/m3 [266]
TOOLS
PDF Links  PDF Links
PubReader  PubReader
Full text via DOI  Full text via DOI
Download Citation  Download Citation
  Print
Share:      
METRICS
0
Crossref
0
Scopus
450
View
24
Download
Editorial Office
464 Cheongpa-ro, #726, Jung-gu, Seoul 04510, Republic of Korea
FAX : +82-2-383-9654   E-mail : eer@kosenv.or.kr

Copyright© Korean Society of Environmental Engineers.        Developed in M2PI
About |  Browse Articles |  Current Issue |  For Authors and Reviewers