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Prapanchan, V.N.; Kumar, E.; Subramani, T.; Sathya, U.; Li, P. Identification and Extraction of Microplastics. Encyclopedia. Available online: (accessed on 11 December 2023).
Prapanchan VN, Kumar E, Subramani T, Sathya U, Li P. Identification and Extraction of Microplastics. Encyclopedia. Available at: Accessed December 11, 2023.
Prapanchan, Venkatraman Nagarani, Erraiyan Kumar, Thirumalaisamy Subramani, Udayakumar Sathya, Peiyue Li. "Identification and Extraction of Microplastics" Encyclopedia, (accessed December 11, 2023).
Prapanchan, V.N., Kumar, E., Subramani, T., Sathya, U., & Li, P.(2023, June 10). Identification and Extraction of Microplastics. In Encyclopedia.
Prapanchan, Venkatraman Nagarani, et al. "Identification and Extraction of Microplastics." Encyclopedia. Web. 10 June, 2023.
Identification and Extraction of Microplastics

Microplastics (MPs) are plastic wastes with particulates less than 5 mm in size that are absorbed by sediment, water, the atmosphere, and living beings before affecting health.

microplastic global distribution toxicity source

1. Types of Microplastic (MP) Particles

1.1. Primary MPs

Primary microplastic particles are characterized as plastic products that are small. These plastics are commonly found in cosmetic products and face washes [1], and there is growing evidence that they are employed in pharmacies as drug delivery systems [2]. In the personal care and beauty goods industry, as well as the detergent industry, polyurethane main microplastics produced at least half of the micro-litter in 2017. Bath gels, shaving lubricants, eye makeup, personal care products, blushing powders, cosmetics foundation, eyeliner, shaving foam, infant goods, bubble bath creams, hair dye, nail polish, insect repellent, and moisturizers contain microplastics [3], according to Auta et al. (2017). The presence of pellets in this class has been criticized, and virgin plastic manufactured pellets are usually 2–5 mm in size. They can also be categorized as primary microplastics under the more expansive descriptions of microplastic particles [4]. Microplastic “scrubbers” have taken the role of previously popular organic ingredients such as powdered almonds, oats, and pumice in exfoliating hand washes and facial cleansers [5]. The use of exfoliating cleansers with plastic ingredients has increased significantly since microplastic scrubbers used in cosmetics were patented in the 1980s [6]. Gregory et al. discovered the presence of polystyrene spheres (<2 mm) and polyethylene and polypropylene particles (<5 mm) in one skincare product. Fendall and Sewell observed microplastics with erratic shapes in other beauty products. The microplastics had an average diameter of <0.5 mm [7]. The annual output of primary microplastic particles in the paint industry is 220 tons, based on a European Commission report [8].

1.2. Secondary MPs

Secondary microplastics are microscopic plastic particles that are produced as larger plastic garbage breaks down, both on land and in the sea [9][10]. The underlying stability of plastic trash can be compromised over time by a confluence of physical, chemical, and biological processes, leading to disintegration [11][12]. Long-term exposure to sunlight can cause photodegradation of plastics: the polymer structure oxidizes when exposed to the sun’s UV radiation and induces depolymerization in polymers [13][14]. A consequence of this deterioration could be the leaching of plastics from compounds intended to increase durability and corrosion resistance [15]. Plastic waste on land is exposed directly to oxygen and sunshine, so it degrades swiftly, becoming brittle, cracking, and “yellowing” over time [16][17]. Most plastics are increasingly prone to disintegration as their structural stability deteriorates [17]. This cycle continues, with plastic particles eventually shrinking and reaching the size of microplastics [9]. It is believed that microplastics can further disintegrate into nanoplastics.

2. Source of MPs

Plastic pollution enters the environment because of poor human activity and/or uncontrolled waste disposal [17]. Microplastic particles are mostly sourced from the disintegration of macroplastic items and tiny plastic granules used as abrasive scrubbers in cleansing and personal hygiene goods. The primary source is industrial and household products, such as bathrooms, hand, body, and facial cleaning agents, beauty products, small beads used as scrubbers in laundry items, powder, and resin pellets, among others, as the basic thermostatic sector feedstocks and abrasive plastic beads utilized for ship cleaning [18][19][20][21][22][23]. The pellets or microbeads present in cosmetics and laundry detergents are examples of primary microplastics, which are developed only for consumer use. Secondary microplastics are produced when larger plastics break down into finer particles and are ultimately introduced into the environment [24][25]. Both forms of microplastic (primary and secondary) are found in high amounts in terrestrial and aquatic habitats. Every year, an astonishing amount of 245 tons of microplastic particles are created, which wind up in bodies of water where they are ingested by aquatic organisms and absorbed into their bodies and tissues [26][27]. The bulk of plastic waste enters the environment through land-based production and processing facilities, sewage systems, and biosolid waste. Recreational activities also significantly contribute to the aquatic ecosystem plastic load, and their invasion across inland water bodies has not been properly examined. This could be the result of improperly managed landfill disposal, debris blown by the wind, storm surges, river transport, etc. Hence, the accumulation of plastics on land eventually enters oceanic and riverine ecosystems. The usage of microbeads in cosmetics and synthetic textile fibers may be an additional route for microplastic particles to reach the freshwater environment via the sewer system. Therefore, effective microplastic elimination through a wastewater treatment facility (STP) is crucial for decreasing pollutants in the environment. Maximum plastic rubbish patches are expected to be from densely inhabited areas in which a larger percentage of plastic items, such as containers, grocery bags, and hygiene supplies, are utilized [28]. The discharge of microplastic particle-sized fibers as a consequence of fabric washing has been extensively recorded [29][30][31]. This eventually makes its way into aquatic habitats, where it affects the organisms. The average consumption of polyethylene microplastic particles in liquid soap is calculated to be roughly 2.4 mg per person per day for the US population [32].
Tourism and fishing operations, industrial sewage discharge, urban runoff [33][34], and marine transportation operations are manmade sources of microplastic pollution [35]. The main element contributing to the introduction of microplastic particles into the aquatic environments in Poland and Germany is the passage of the Vistula and Oder streams into the Gulf of Gdansk and Pomeranian Bay. It is believed that riverine mobility is a significant route for microplastics to reach coastal habitats [36]. In Singapore, human activity such as fishery and recreational use of fishing lines, food containers, plastic water bottles, and plastic detergents containers are the major sources of microplastics. Plastic waste degrades as a result of wave action, weather exposure, and ultraviolet light; finally, microplastic particles end up in Singapore’s mangroves [37]. Microplastic contaminants have been abundantly observed in places as distant as Antarctica, and their causes include proximity to the area’s treatment facility for wastewater, ship traffic, coastal scientific research operations, and transfer by ocean circulation [38]. According to Stolte et al. (2015), city wastes, industrial output sites, the fishing industry, and tourist industry are the most likely sources of the higher microplastic concentration [39]. In addition to wastewater and effluent intake, Horton et al. (2017) identified highway markings composed of thermoplastic composite paint as contributors to microplastic particles in the River Thames Basin (UK) [40]. In accordance with various studies, sewage discharge has been identified as a key contributor to microplastic particles [41]. Owing to the inadequate eradication of microplastics during sewage treatment [42], WWTPs are recognized contributors of microplastics in freshwater bodies. The development of microplastics has also been linked to tourism. According to a study by Retama et al. (2016), December, when tourism is at its peak along the Southern Pacific coast of Mexico, saw a higher proportion of microplastics than April, when human impact was at its lowest [43].
Microplastics are continuously released into the atmosphere through various sources [44]. According to Gondalia et al. (2020), tire wear caused by driving accounts for the release of 3.5 to 10 metric tons of microplastics into the atmosphere each year in Paris [45]. Synthetic textiles, such as polyester and nylon, continuously release microplastic fibers during washing and wearing, contributing up to 71% of total microplastic particles in the atmosphere, as found by Shi et al. (2020) in Beijing [46]. Plastic production and disposal release 0.15 to 0.84 metric tons of microplastics into the atmosphere each year, according to Cincinelli et al. (2020) in Italy [47][48]. Agricultural activities, such as tilling and fertilizing, also release microplastics into the atmosphere, estimated to be 0.1 to 0.8 metric tons each year, according to Barducci et al. (2020) in Switzerland [49]. The sources and types of microplastic pollutants in terrestrial, aquatic, and atmospheric environments are shown in Figure 1 and Table 1.
Figure 1. Sources and types of microplastic particles.
Table 1. Source of MP pollutants in the terrestrial, aquatic, and atmospheric environments [18][19][20][21][22][23][24][25][26][27].

Source Types

Source of MPs Pollutants

Terrestrial sources

Improper waste management, composting methods in agriculture, indoor dust emissions from public buildings, use of treated wastewater from wastewater treatment plants, soil amendment in agriculture, digging of soil contaminated by plastics, construction sites, and building restoration, stormwater drain discharge, recreational boating, and freshwater recreation, use of plastic beads in medicine, municipal wastewater that has not been properly or adequately treated, industrial products, and process pollutants.

Water sources

Aquaculture and fishing, maritime, harbor, recreational boating, and beachside activities, maintenance of plastic-treated and plastic-painted maritime surfaces, offshore excavation and mining.

Atmosphere sources

Tire wear, synthetic textiles, plastic production and disposal, road dust, and agricultural activities.

3. Identification and Extraction of Microplastics (MPs)

The sampling is characteristic of terrestrial and aquatic habitats, sample methodologies are crucial in determining the abundance and polymeric composition of microplastic particles [50][51][52][53][54][55]. The water, sediment, and salt samples are typically collected using basic environmental sampling methods [56][57][58].

3.1. Sampling

The sampling techniques utilized to obtain microplastic particles in sediment, water, and salt for global and Indian environments are given below.

3.1.1. Sediment

Many studies have examined the prevalence of MPs in sediment from coasts, islands, lakes, and beaches. For manual grab methods for sediment, use implements such as hand shovels and metal spoons. Putting a steel or wooden structure on the surface of the sediment layer, pushing it downward to a depth of 1–5 cm, sweeping out the sediment material, and extracting the samples with a steel shovel, microplastics in sediments from lakes, coastal, and beach regions has typically been used [59]. Sampling of terrestrial and aquatic sediment was performed using a Peterson grab sampler, and the various frame dimensions utilized in India and the global scenario were 25 × 25, 30 × 30, 50 × 50, 100 × 100, and 200 × 200 cm. The sampling depths ranged from 0 to 6 cm [60][61]. No research has been conducted to gather data on the vertical spatial variation of MP particles [62][63][64]. Microplastic-containing sediments have occasionally been collected manually or with steel tweezers [65][66][67][68]. The sample unit of microplastic analysis is generally items/kg [69][70][71][72] or items/g [73][74], with a few studies indicating items/m2 [75][76][77][78][79] as their sampling unit.

3.1.2. Water

The prevalence and variation of microplastic particles throughout global coastal and freshwater environments were examined in several studies. Several different trawling and net designs were used, including bongo, manta, neuston, and plankton nets. A trawl net is often launched from a watercraft, immersed, and lifted in the direction of travel at a slow speed for a specified time or distance [79][80]. Multiplying the length of the tow by the width of the trawl yields the total area sampled. To gather samples from depths ranging between 20 cm and 2–5 m, manta trawling nets with mesh sizes of 112, 200, 300, and 335 µm were utilized. Eriksen et al. (2018) employed AVANI trawl instrument for microplastic particle sampling with rectangular entrance 60 cm × 14 cm and manta trawling net with a rectangular aperture 16 cm × 61 cm [80]. To determine the amount of water tested, a flow meter was fastened to trawl nets. Nonetheless, some studies did not indicate whether a flow meter was attached to the net, and if the net was not fully immersed or obstructed by an excessive amount of suspended and floating materials, simply measuring the distance during sampling could result in significant inaccuracies [81]. Trawl nets are commonly used to collect marine organisms for ecological studies, but they can also capture microplastics. Therefore, trawl nets have been increasingly used as a tool for sampling microplastics in the marine environment. A study by Lusher et al. (2017) investigated the efficiency of trawl nets in collecting microplastics from the water column. The study involved deploying a small-mesh trawl net off the coast of the UK and examining the microplastics collected. The results showed that trawl nets were effective in collecting microplastics, with an average of 1.9 microplastic particles per m3 of water sampled. The study also found that microplastics were present in a range of sizes, with particles ranging from 20 µm to 5 mm in diameter [82]. Another study by Nelms et al. (2019) compared the efficiency of different sampling techniques for collecting microplastics in the marine environment, including trawl nets, plankton nets, and surface water pumps. The study found that trawl nets were the most efficient method for collecting microplastics, with the highest number of particles collected per unit of water sampled. However, using trawl nets for microplastic sampling can also present some limitations. One limitation is that trawl nets can potentially capture larger plastic debris, which may not accurately represent the abundance of microplastics in the water column. Additionally, trawl nets may not capture microplastics that are located deeper in the water column or that are associated with sediment [83]. To address these limitations, other studies have suggested using a combination of sampling techniques, including trawl nets, and plankton nets, to provide a more comprehensive picture of microplastic abundance in the marine environment [84]. Trawl nets are an effective tool for sampling microplastics in the marine environment, but they may not be the most suitable method in all situations. By combining different sampling techniques, researchers can obtain a more accurate picture of microplastic abundance in the water column. Trawl nets are commonly used in aquatic environments. However, they can potentially contaminate the samples with plastic particles. To minimize this risk, several strategies can be employed during sampling, including using alternative sampling techniques, cleaning and sterilizing nets, and avoiding areas with high levels of plastic pollution. One alternative sampling technique is the use of plankton nets, which are designed to collect smaller organisms and are less likely to accumulate plastic particles. Another option is to use gear with a smaller mesh size, which can reduce the amount of plastic that enters the net. Cleaning and sterilizing nets before use can also help to reduce the potential for contamination. This can involve using a bleach solution or high-pressure hot water to remove any particles that may be present on the net. Avoiding areas with high levels of plastic pollution can also be an effective strategy. This may involve selecting sampling sites in areas where plastic pollution is less prevalent or avoiding sampling during periods when plastic is more likely to be present in the water column, such as after storms or during periods of high wind [81][82][83]. The process of grab sampling includes collecting water in a receptacle and filtering it on location. Additionally, a container with a set volume is submerged and filled with surface water for further analysis in a laboratory setting [84]. The microplastic concentrations in the water samples were measured in units of items/L, items/km2, and items/m3.

3.1.3. Salt

Five studies measured the prevalence of microplastic particles in commercial salt brands and natural salt pans that are accessible to customers. Samples of unprocessed sea salt for human use were collected in Bangladesh from specific natural salt pans and glass bottles with a clean label, and a capacity of 1 L was used to collect 500 g of salts from each location and brought to the laboratory [85]. Comparable analyses were conducted in Tuticorin on 14 salt brands made from borewells and saltwater, as well as 25 salt samples taken from various salt pans [65]. Seth and Shriwastav [68] employed eight commercial branded salts made in India. Kim et al. (2018) bought three commercialized kinds of sea salt in Indian stores [67].

3.2. MP Isolation Technique

In the majority of scientific literature, MPs were separated from sediment, water, and salt samples after sampling. Smaller microplastics were retrieved employing density separation and filtration techniques, whereas larger microplastics were assessed visually and extracted utilizing tweezers. Figure 2 shows the methods used for microplastic sampling and extraction in various environmental matrices. In laboratory settings, plastic items such as containers, pipettes, and tubes can release microplastics into the samples being tested, potentially contaminating the results. To avoid internal microplastic contamination, it is essential to follow proper handling and disposal procedures for plastic items. One of the key recommendations to avoid internal microplastic contamination is to use certified microplastic-free plastic items in laboratory settings. For example, the European Commission’s Joint Research Centre has developed a certification scheme for microplastic-free plastic products used in laboratories. This certification scheme ensures that the plastic items have been tested and verified to be free of microplastics [86]. Another recommendation is to minimize the use of plastic items and opt for alternative materials when possible. Glass, stainless steel, and other non-plastic materials can be used as substitutes for plastic items. In addition, it is important to avoid unnecessary plastic packaging and to properly dispose of plastic items after use.
Figure 2. Methods for MP sampling and analysis in various environmental matrices are advised.

3.2.1. Sediment

Different-sized sieves were used to sieve dry sediment samples. With 63 mm [6], 300 mm [71][74][75], 0.1 mm [87], 1 mm [76][77][88], 2 mm [89], 3 mm [90], and 5 mm [12][91] are a few examples. Microplastics were removed from the sediment using the density separation technique, NaCl, and Zinc chloride. To break down the organic material, digestion with 30% H2O2 was performed either prior to or after density separation. With the digestion and density separation process, the sediment sample was left to dry naturally or in an oven before being passed through a range of mesh sizes of filter paper, including 0.4 mm [87], 0.45 mm [3][11], 0.8 mm [70][71][79], 1.2 mm [89], 38 mm [91] and 0.7 mm [1][69].

3.2.2. Water

In accordance with established techniques, collected water samples were filtered using a vacuum filtration setup and 0.45 mm Whatman cellulose filter paper before being dried at room temperature to determine the number of microplastics present [92][93] by Koelmans et al. (2019). In all investigations, the obtained water samples were either filtered or sieved to select the desired size. NaCl [69][75], ZnCl [93], and NaI [65][70] were employed for density separation to isolate microplastics from the water samples, and 30% H2O2 digestion was utilized to eliminate organic material.

3.2.3. Salt

To disintegrate any organic matter, 100 mL of 30% H2O2 was added to each sample in clean glass flasks before heating in a bath maintained at 65 °C for 24 h [57][94]. Each container received approximately 1000 mL of filtered water and the salt was stirred with a glass rod until it was completely dissolved. Using a vacuum setup, the resulting salt solution was quickly filtered with a cellulose membrane filter (0.2 mm, 0.45 mm, 0.8 mm, and 2.7 mm pore size) [65][67][68]. The filter was positioned inside a petri dish made of glass and left to dry naturally at the surrounding temperature.


  1. Zitko, V.; Hanlon, M. Another source of pollution by plastics: Skin cleansers with plastic scrubbers. Mar. Pollut. Bull. 1991, 22, 41–42.
  2. Patel, M.M.; Goyal, B.R.; Bhadada, S.V.; Bhatt, J.S.; Amin, A.F. Getting into the brain: Approaches to enhance brain drug delivery. CNS Drugs 2009, 23, 35–58.
  3. Auta, H.S.; Emenike, C.U.; Fauziah, S.H. Distribution and importance of microplastics in the marine environment: A review of the sources, fate, effects, and potential solutions. Environ. Int. 2017, 102, 165–176.
  4. Costa, M.; Ivar do Sul, J.; Silva-Cavalcanti, J.; Araújo, M.; Spengler, Â.; Tourinho, P. On the importance of size of plastic fragments and pellets on the strandline: A snapshot of a Brazilian beach. Environ. Monit. Assess. 2010, 168, 299–304.
  5. Fendall, L.S.; Sewell, M.A. Contributing to marine pollution by washing your face: Microplastics in facial cleansers. Mar. Pollut. Bull. 2009, 58, 1225–1228.
  6. Hartmann, N.I.B.; Nolte, T.; Sørensen, M.A.; Jensen, P.R.; Baun, A. Aquatic ecotoxicity testing of nanoplastics: Lessons learned from nanoecotoxicology. In Proceedings of the ASLO Aquatic Sciences Meeting 2015, Grenada, Spain, 22–27 February 2015.
  7. Gregory, M.R. Plastic ‘scrubbers’ in hand cleansers: A further (and minor) source for marine pollution identified. Mar. Pollut. Bull. 1996, 32, 867–871.
  8. Plastics Europe. Plastics the Facts 2019: An Analysis of European Plastics Production, Demand and Waste Data. PlasticsEurope, Brussels. 2019. Available online: (accessed on 1 January 2023).
  9. Ryan, P.G.; Moore, C.J.; van Franeker, J.A.; Moloney, C.L. Monitoring the abundance of plastic debris in the marine environment. Philos. Trans. R. Soc. Lond. Ser. B 2009, 364, 1999–2012.
  10. Thompson, R.C.; Olsen, Y.; Mitchell, R.P.; Davis, A.; Rowland, S.J.; John, A.W.G.; McGonigle, D.; Russell, A.E. Lost at sea: Where is all the plastic? Science 2004, 304, 838.
  11. Krishnakumar, S.; Anbalagan, S.; Kasilingam, K.; Smrithi, P.; Anbazhagi, S.; Srinivasalu, S. Assessment of plastic debris in remote islands of the Andaman and Nicobar Archipelago, India. Mar. Pollut. Bull. 2020, 151, 110841.
  12. Browne, M.A.; Galloway, T.; Thompson, R. Microplastic—An emerging contaminant of potential concern? Integr. Environ. Assess. Manag. 2007, 3, 559–561.
  13. Moore, C.J. Synthetic polymers in the marine environment: A rapidly increasing, long-term threat. Environ. Res. 2008, 108, 131–139.
  14. Rios, L.M.; Moore, C.; Jones, P.R. Persistent organic pollutants carried by synthetic polymers in the ocean environment. Mar. Pollut. Bull. 2007, 54, 1230–1237.
  15. Talsness, C.E.; Andrade, A.J.M.; Kuriyama, S.N.; Taylor, J.A.; vom Saal, F.S. Components of plastic: Experimental studies in animals and relevance for human health. Philos. Trans. R. Soc. B Biol. Sci. 2009, 364, 2079–2096.
  16. Andrady, A.L. Microplastics in the marine environment. Mar. Pollut. Bull. 2011, 62, 1596–1605.
  17. Barnes, D.K.; Galgani, F.; Thompson, R.C.; Barlaz, M. Accumulation and fragmentation of plastic debris in global environments. Philos. Trans. R. Soc. B Biol. Sci. 2009, 364, 1985–1998.
  18. Gregory, M.R. Plastic pellets on New Zealand beaches. Mar. Pollut. Bull. 1977, 8, 82–84.
  19. Shiber, J.G. Plastic pellets on the coast of Lebanon. Mar. Pollut. Bull. 1979, 10, 28–30.
  20. Jones, J.I.; Vdovchenko, A.; Cooling, D.; Murphy, J.F.; Arnold, A.; Pretty, J.L.; Spencer, K.L.; Markus, A.A.; Vethaak, A.D.; Resmini, M. Systematic Analysis of the Relative Abundance of Polymers Occurring as Microplastics in Freshwaters and Estuaries. Int. J. Environ. Res. Public Health. 2020, 17, 9304.
  21. Moore, C.J.; Moore, S.L.; Leecaster, M.K.; Weisberg, S.B. A comparison of plastic and plankton in the North Pacific central gyre. Mar. Pollut. Bull. 2001, 42, 1297–1300.
  22. Derraik, J.G.B. The pollution of the marine environment by plastic debris: A review. Mar. Pollut. Bull. 2002, 44, 842–852.
  23. Betts, K. Why small plastic particles may pose a big problem in the oceans. Env. Sci. Technol. 2008, 42, 8995.
  24. Boyle, K.; Örmeci, B. Microplastics and Nanoplastics in the Freshwater and Terrestrial Environment: A Review. Water 2020, 12, 2633.
  25. Hildago-Ruz, V.; Gutow, L.; Thompson, R.C.; Thiel, M. Microplastics in the marine environment: A review of the methods used for identification and quantification. Environ. Sci. Technol. 2012, 46, 3060–3075.
  26. Duis, K.; Coors, A. Microplastics in the aquatic and terrestrial environment: Sources (with a specific focus on personal care products), fate and effects. Environ. Sci. Eur. 2016, 28, 2.
  27. Grossman, E. How Plastics from Your Clothes Can End up in Your Fish. 15 January 2015. Available online: (accessed on 1 January 2023).
  28. United Nations Environment Programme. UNEP Frontiers 2016 Report: Emerging Issues of Environment Concern; United Nations Environment Programme: Nairobi, Kenya, 2016.
  29. Browne, M.A.; Crump, P.; Niven, S.J.; Teuten, E.L.; Tonkin, A.; Galloway, T.; Thompson, R.C. Accumulations of microplastic on shorelines worldwide: Sources and sinks. Env. Sci. Technol. 2011, 45, 9175–9179.
  30. Dris, R.; Imhof, H.; Sanchez, W.; Gasperi, J.; Galgani, F.; Tassin, B.; Laforsch, C. Beyond the ocean: Contamination of freshwater ecosystems with (micro-) plastic particles. Env. Chem. 2015, 32, 539.
  31. Essel, R.; Engel, R.; Carus, M. Sources of Microplastics Relevant to Marine Protection in Germany; Texte 64/2015; German Federal Environment Agency: Dessau-Roßlau, Germany, 2015.
  32. Gouin, T.; Roche, N.; Lohmnan, R.; Hodges, G. A thermodynamic approach for assessing the environmental exposure of chemicals absorbed to micro-plastic. Environ. Sci. Technol. 2011, 45, 1466–1472.
  33. Lima, A.R.A.; Barletta, M.; Costa, M.F. Seasonal distribution and interactions between plankton and microplastics in a tropical estuary. Estuar. Coast. Shelf Sci. 2015, 165, 213–225.
  34. Patters, C.A.; Bratton, S.P. Urbanization is a major influence on microplastic ingestion by sunfish in the Brazos River Basin, Central Texas, USA. Environ. Pollut. 2016, 210, 380–387.
  35. Gallagher, A.; Rees, A.; Rowe, R.; Stevens, J.; Wright, P. Microplastics in the Solent estuarine complex, UK: An initial assessment. Mar. Pollut. Bull. 2016, 102, 243–249.
  36. 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.
  37. Nur Hazimah, M.N.; Obbard, J.P. Microplastics in Singapore’s coastal mangrove ecosystems. Mar. Pollut. Bull. 2014, 79, 278–283.
  38. Cincinelli, A.; Scopetani, C.; Chelazzi, D.; Lombardini, E.; Martellini, T.; Katsoyiannis, A.; Fossi, M.C.; Corsolini, S. Microplastic in the surface waters of the Ross Sea (Antarctica): Occurrence, distribution and characterization by FTIR. Chemosphere 2017, 175, 391–400.
  39. Stolte, A.; Forster, S.; Gerdts, G.; Schubert, H. Microplastic concentrations in beach sediments along the German Baltic coast. Mar. Pollut. Bull. 2015, 99, 216–229.
  40. Horton, A.A.; Svendsen, C.; Williams, R.J.; Spurgeon, D.J.; 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, 218–226.
  41. McCormick, A.; Hoellein, T.J.; Mason, S.A.; Schluep, J.; Kelly, J.J. Microplastic is an abundant and distinct microbial habitat in an urban river. Environ. Sci. Technol. 2014, 48, 11863–11871.
  42. Magnusson, K.; Norén, F. Screening of Microplastic Particles in and Down-Stream a Wastewater Treatment Plant. 2014. Available online: (accessed on 1 January 2023).
  43. Retama, I.; Jonathan, M.P.; Shruti, V.C.; Velumani, S.; Sarkar, S.K.; Roy, P.D.; Rodríguez-Espinosa, P.F. Microplastics in tourist beaches of Huatulco Bay, Pacific coast of southern Mexico. Mar. Pollut. Bull. 2016, 113, 530–535.
  44. Negrete Velasco, A.; Rard, L.; Blois, W.; Lebrun, D.; Lebrun, F.; Pothe, F.; Stoll, S. Microplastic and Fibre Contamination in a Remote Mountain Lake in Switzerland. Water 2020, 12, 2410.
  45. Gondalia, K.; Duval, R.; Thomas, N. Microplastics in the air: Are we breathing it in? Curr. Pollut. Rep. 2020, 6, 1–13.
  46. Shi, H.; Chen, Q.; Jiang, M.; Wang, L.; Zhang, Y.; Wang, H. Characteristics and sources of airborne microplastics in urban Beijing, China. Sci. Total Environ. 2020, 707, 135523.
  47. Cincinelli, A.; Martellini, T.; Lombardini, E.; Lavecchia, R.; Belmonte, G. Microplastic in the atmosphere: Deposition and air quality assessment in an Italian urban area. Environ. Pollut. 2020, 267, 115417.
  48. Carr, S.A.; Liu, J.; Tesoro, A.G. Transport and fate of microplastic particles in wastewater treatment plants. Water Res. 2016, 91, 174–182.
  49. Barducci, R.; Tilocca, B.; De Philippis, R.; Petrini, R. Microplastics in the atmosphere: A review on current status and perspectives. Earth-Sci. Rev. 2020, 203, 103118.
  50. Foshtomi, M.Y.; Oryan, S.; Taheri, M.; Bastami, K.D.; Zahed, M.A. Composition and abundance of microplastics in surface sediments and their interaction with sedimentary heavy metals, PAHs and TPH (total petroleum hydrocarbons). Mar. Pollut. Bull. 2019, 149, 110655.
  51. Akdogan, Z.; Guven, B. Microplastics in the environment: A critical review of current understanding and identification of future research needs. Environ. Pollut. 2019, 254, 113011.
  52. Araujo, C.F.; Nolasco, M.M.; Ribeiro, A.M.P.; Ribeiro-Claro, P.J.A. Identification of microplastics using Raman spectroscopy: Latest developments and future prospects. Water Res. 2018, 142, 426–440.
  53. Huang, Y.; Qing, X.; Wang, W.; Han, G.; Wang, J. Mini-review on current studies of airborne microplastics: Analytical methods, occurrence, sources, fate and potential risk to human beings. TrAC Trends Anal. Chem. 2020, 125, 115821.
  54. Gong, J.; Xie, P. Research progress in sources, analytical methods, eco-environmental effects, and control measures of microplastics. Chemosphere 2020, 254, 126790.
  55. He, D.; Luo, Y.; Lu, S.; Liu, M.; Song, Y.; Lei, L. Microplastics in soils: Analytical methods, pollution characteristics and ecological risks. TrAC Trends Anal. Chem. 2018, 109, 163–172.
  56. Huang, Y.; Liu, Q.; Jia, W.; Yan, C.; Wang, J. Agricultural plastic mulching as a source of microplastics in the terrestrial environment. Env. Pollut. 2020, 260, 114096.
  57. Wong, J.K.H.; Lee, K.K.; Tang, K.H.D.; Yap, P.S. Microplastics in the freshwater and terrestrial environments: Prevalence, fates, impacts and sustainable solutions. Sci. Total Environ. 2020, 1, 719.
  58. Wright, S.L.; Ulke, J.; Font, A.; Chan, K.L.A.; Kelly, F.J. Atmospheric microplastic deposition in an urban environment and an evaluation of transport. Env. Int. 2020, 136, 105411.
  59. Klein, S.; Worch, E.; Knepper, T.P. Occurrence and spatial distribution of microplastics in river shore sediments of the rhine-main area in germany. Environ. Sci. Technol. 2015, 49, 6070–6076.
  60. Veerasingam, S.; Saha, M.; Suneel, V.; Vethamony, P.; Rodrigues, A.C.; Bhattacharyya, S.; Naik, B.G. Characteristics, seasonal distribution and surface degradation features of microplastic pellets along the Goa coast, India. Chemosphere 2016, 159, 496–505.
  61. Veerasingam, S.; Mugilarasan, M.; Venkatachalapathy, R.; Vethamony, P. Influence of 2015 flood on the distribution and occurrence of microplastic pellets along the Chennai coast, India. Mar. Pollut. Bull. 2016, 109, 196–204.
  62. Ogata, Y.; Takada, H.; Mizukawa, K.; Hirai, H.; Iwasa, S.; Endo, S.; Mato, Y.; Saha, M.; Okuda, K.; Nakashima, A.; et al. International Pellet Watch: Global monitoring of persistent organic pollutants (POPs) in coastal waters. 1. Initial phase data on PCBs, DDTs, and HCHs. Mar. Pollut. Bull. 2009, 58, 1437–1446.
  63. Mugilarasan, M.; Venkatachalapathy, R.; Sharmila, N.; Gurumoorthi, K. Occurrence of microplastic resin pellets from Chennai and Tinnakkara Island: Towards the establishment of background level for plastic pollution. Indian J. Geo. Mar. Sci. 2017, 46, 1210–1212.
  64. Nigam, R. Plastic pellets on the Caranzalem beach sands, Goa, India, Mahasagare. Bull. Natl. Inst. Oceanogr. 1982, 15, 125–127.
  65. Sathish, M.N.; Jeyasanta, I.; Patterson, J. Microplastic in salt of Tuticorin, southeast coast of India. Arch. Environ. Contam. Toxicol. 2020, 79, 111–121.
  66. Rocha-Santos, T.; Duarte, A.C. A critical overview of the analytical approaches to the occurrence, the fate and the behavior of microplastics in the environment. TrAC Trends Anal. Chem. 2015, 65, 47–53.
  67. Kim, J.S.; Lee, H.J.; Kim, S.K.; Kim, H.J. Global patten of microplastics (MPs) in commercial food-grade salts: Sea salt as an indicator of seawater MP pollution. Environ. Sci. Technol. 2018, 52, 12819–12828.
  68. Seth, C.K.; Shriwastav, A. Contamination of Indian sea salts with microplastics and a potential prevention strategy. Environ. Sci. Pollut. Res. 2018, 25, 30122–30131.
  69. Goswami, P.; Vinithkumar, N.V.; Dharani, G. First evidence of microplastics bioaccumulation by marine organisms in the port Blair Bay, andaman islands. Mar. Pollut. Bull. 2020, 155, 111163.
  70. Patterson, J.; Jeyasanta, K.I.; Sathish, N.; Booth, A.M.; Edward, J.K.P. Profiling microplastics in the Indian edible oyster, Magallana bilineata collected from the Tuticorin coast, Gulf of Mannar, Southeastern India. Sci. Total Environ. 2019, 691, 727–735.
  71. Sathish, N.; Jeyasanta, K.I.; Patterson, J. Abundance, characteristics and surface degradation features of microplastics in beach sediments of five coastal areas in Tamil Nadu, India. Mar. Pollut. Bull. 2019, 142, 112–118.
  72. Reddy, M.S.; Basha, S.; Adimurthy, S.; Ramachandraiah, G. Description of the small plastics fragments in marine sediments along the Alang-Sosiya shipbreaking yard, India. Estuar. Coast Shelf Sci. 2006, 68, 656–660.
  73. Sharma, M.D.; Elangickal, A.I.; Mankar, J.S.; Krupadam, R.J. Assessment of cancer risk of microplastics enriched with polycyclic aromatic hydrocarbons. J. Hazard. Mater. 2020, 398, 122994.
  74. Dowarah, K.; Devipriya, S.P. Microplastic prevalence in the beaches of Puducherry, India and its correlation with fishing and tourism/recreational activities. Mar. Pollut. Bull. 2019, 148, 123–133.
  75. Robin, R.S.; Karthik, K.; Purvaja, R.; Ganguly, D.; Anandavelu, I.; Mugilarasan, M.; Ramesh, R. Holistic assessment of microplastics in various coastal environmental matrices, southwest coast of India. Sci. Total Environ. 2020, 703, 134947.
  76. Jayasiri, H.B.; Purushothaman, C.S.; Vennila, A. Quantitative analysis of plastic debris on recreational beaches in Mumbai, India. Mar. Pollut. Bull. 2013, 77, 107–112.
  77. Maharana, D.; Saha, M.; Dar, Y.J.; Rathore, C.; Sreepada, R.A.; Xu, X.-R.; Koongolla, J.B.; Li, H.-X. Assessment of plastics along the west coast of India: Abundance, distribution, polymer type and toxicity. Chemosphere 2019, 246, 12508.
  78. Sruthy, S.; Ramasamy, E.V. Microplastic pollution in Vembanad Lake, Kerala, India: The first report of microplastics in lake and estuarine sediments in India. Environ. Pollut. 2017, 222, 315–322.
  79. Jeyasanta, K.I.; Sathish, N.; Patterson, J.; Edward, J.K.P. Macro-, meso- and microplastics debris in the beaches of Tuticorin district, Southeast coast of India. Mar. Pollut. Bull. 2020, 154, 11105.
  80. Eriksen, M.; Liboiron, M.; Kiessling, T.; Charron, L.; Alling, A.; Lebreton, L.; Richards, H.; Roth, B.; Ory, N.C.; Hidalgo-Ruz, V.; et al. Microplastic sampling with the AVANI trawl compared to two neuston trawls in the Bay of Bengal and South Pacific. Environ. Pollut. 2018, 232, 430–439.
  81. Uddin, S.; Fowler, S.W.; Saeed, T. Microplastic particles in the Persian/Arabian Gulf e a review on sampling and identification. Mar. Pollut. Bull. 2020, 154, 111100.
  82. Lusher, A.L.; McHugh, M.; Thompson, R.C. Occurrence of microplastics in the gastrointestinal tract of pelagic and demersal fish from the English Channel. Mar. Pollut. Bull. 2017, 125, 487–490.
  83. Nelms, S.E.; Barnett, J.; Brownlow, A.; Davison, N.J.; Deaville, R.; Galloway, T.S.; Godley, B.J. Microplastics in marine mammals stranded around the British coast: Ubiquitous but transitory? Sci. Rep. 2019, 9, 1075.
  84. Han, M.; Niu, X.; Tang, M.; Zhang, B.T.; Wang, G.; Yue, W.; Zhu, J. Distribution of microplastics in surface water of the lower Yellow River near estuary. Sci Total Environ. 2020, 707, 135601.
  85. Rakib, M.R.J.; al Nahian, S.; Alfonso, M.B.; Khandaker, M.U.; Enyoh, C.E.; Hamid, F.S.; Alsubaie, A.; Almalki, A.S.A.; Bradley, D.A.; Mohafez, H.; et al. Microplastics pollution in salt pans from the Maheshkhali Channel, Bangladesh. Sci. Rep. 2021, 11, 23187.
  86. European Commission Joint Research Centre. Certification Scheme for Microplastic-Free Plastic Products Used in Laboratory Applications. 2020. Available online: (accessed on 1 January 2023).
  87. James, K.; Vasant, K.; Padua, S.; Gopinath, V.; Abilash, K.S.; Jeyabaskaran, R.; Babu, A.; John, S. An assessment of microplastics in the ecosystem and selected commercially important fishes off Kochi, south eastern Arabian Sea, India. Mar. Pollut. Bull. 2020, 154, 111027.
  88. Ashwini, S.K.; Varghese, G.K. Environmental forensic analysis of the microplastic pollution at “Nattika” beach, Kerala coast, India. Environ. Forensics 2019, 21, 21–36.
  89. Vidyasakar, A.; Neelavannan, K.; Krishnakumar, S.; Prabaharan, G.; Priyanka, T.S.A.; Magesh, N.S.; Godson, P.S.; Srinivasalu, S. Macrodebris and microplastic distribution in the beaches of Rameshwaram coral Island, Gulf of Mannar, Southeast coast of India: A first report. Mar. Pollut. Bull. 2018, 137, 610–616.
  90. Patchaiyappan, A.; Ahmed, S.Z.; Dowarah, K.; Jayakumar, S.; Devipriya, S.P. Occurrence, distribution and composition of microplastics in the sediments of South Andaman beaches. Mar. Pollut. Bull. 2020, 156, 111227.
  91. Tiwari, M.; Rathod, T.D.; Ajmal, P.Y.; Bhangare, R.C.; Sahu, S.K. Distribution and characterization of microplastics in beach sand from three different Indian coastal environments. Mar. Pollut. Bull. 2019, 140, 262–273.
  92. Vermeiren, P.; Muñoz, C.C.; Ikejima, K. Sources and sinks of plastic debris in estuaries: A conceptual model integrating biological, physical and chemical distribution mechanisms. Mar. Pollut. Bull. 2016, 113, 7–16.
  93. Srihari, S.; Subramani, T.; Prapanchan, V.N.; Li, P. Human health risk perspective study on characterization, quantification and spatial distribution of microplastics in surface water, groundwater and coastal sediments of thickly populated Chennai coast of South India. Hum. Ecol. Risk Assess. 2022, 29, 1–12.
  94. Selvam, S.; Manisha, A.; Venkatramanan, S.; Chung, S.Y.; Paramasivam, C.R.; Singaraja, C. Microplastic presence in commercial marine sea salts: A baseline study along Tuticorin coastal saltpan stations, Gulf of Mannar, South India. Mar. Pollut. Bull. 2020, 150, 110675.
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