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Review

Microplastics’ and Nanoplastics’ Interactions with Microorganisms: A Bibliometric Study

by
Carlos David Grande-Tovar
1,
Domingo Cesar Carrascal-Hernández
1,
Jorge Trilleras
2,
Katelediana Mora
3 and
Victoria A. Arana
3,*
1
Grupo de Investigación de Fotoquímica y Fotobiología, Programa de Química, Universidad del Atlántico, Carrera 30 No 8–49, Puerto Colombia 081007, Colombia
2
Grupo de Investigación en Compuestos Heterocíclicos, Programa de Química, Universidad del Atlántico, Carrera 30 No 8–49, Puerto Colombia 081007, Colombia
3
Grupo de Investigación Ciencias, Educación y Tecnología—CETIC, Programa de Maestría en Ciencias Químicas, Universidad del Atlántico, Carrera 30 No 8–49, Puerto Colombia 081007, Colombia
*
Author to whom correspondence should be addressed.
Sustainability 2022, 14(22), 14761; https://doi.org/10.3390/su142214761
Submission received: 6 October 2022 / Revised: 1 November 2022 / Accepted: 2 November 2022 / Published: 9 November 2022

Abstract

:
Microplastics (MPs) and nanoplastics (NPs) are plastic particles of concern worldwide as they negatively affect the environment and human health. The interactions of microorganisms with microplastics and nanoplastics are different. On one hand, microorganisms might biodegrade MPs/NPs through enzymes, but on the other hand, they serve as vehicles to spread diseases or negatively affect their viability. As a result, several studies have reported disturbances in soil balance and negative impacts on geochemical cycles. With an increasing number of investigations into microorganisms and their interactions with MPs and NPs, this study demonstrates a growing interest in biodegradable alternatives. A bibliometric analysis of 719 documents published from 2010 to December 2021 presents the research landscape on the interaction of microplastics and nanoplastics with microorganisms. The study shows that China, the United States, the United Kingdom, and Germany lead the scientific production on this topic. However, in situ studies of large-scale pilot applications in the environment are scarce. More research funding from governments in the form of national action that stimulates national and international cooperation through universities, institutes, and industries is required. There is an urgent need for studies focusing on the degradation mechanisms of various microorganisms through the characterization of enzymes involved in the chemical modification of these emerging contaminants (MPs/NPs) with transparent standard methodologies. Moreover, there is no standardization for MP/NP extraction or characterization methodologies for different environments, especially in atmosphere. The patent need for alternative pathways for MP/NP degradation is evident, using microorganisms such as bacteria, fungi, microalgae, and a consortium (peripheral biofilms) to mitigate the negative impact of the constantly increasing anthropogenic MP/NP pollutants in the world.

1. Introduction

Plastics are materials from petroleum-based polymers widely used due to their easy moldability, low cost, and high mechanical resistance [1,2,3]. According to their moldability, plastics can be used as thermoplastics and thermosets [4]. However, in 2018 there was a large-scale manufacture of thermoplastics with low-cost production (around 360 million tons) [5]. Unfortunately, the enormous plastic output worldwide has led to environmental accumulation, with more than 6 billion tons of plastic waste produced in the last six decades [6,7].
Microplastics (MPs) are tiny plastic particles with sizes smaller than 5 mm, usually produced from the mechanical, chemical, or physical degradation of macroplastics or manufactured with those dimensions for different industrial purposes. Inherent to their tiny size, MPs indiscriminately spread to the environment at the end of their life cycle [8]. Scientifics consider microplastics as plastic particles between 1 µm and 5 mm, whereas plastics smaller than these are considered nanoplastics (NPs) [9,10]. Typically, MPs/NPs comprise polyethylene (PE), polypropylene (PP), polyamide (PA), polyvinyl chloride (PVC), polystyrene (PS), and polyethylene terephthalate (PET) [11].
Microplastics are ubiquitous, with presence in the air [12], land [13], sea [14], rivers [15], and even in the sediment of polar freshwater lakes [16]. One of the most concerning aspects of the uncontrolled spreading of MPs and NPs is that they are vehicles for several pollutants, such as polycyclic hydrocarbons [17], heavy metals [18], and polybrominated ethers [19], and pharmaceutical and cosmetic products worsen global contamination [20,21]. MPs’ recalcitrant capacity relies on their lower density, facilitating accumulation and spreading to different areas. These particles eventually enter the human body by inhalation or ingestion [22]. The physical–chemical characteristics of MPs/NPs facilitate bioretention in several organs and tissues. As a result, microplastic accumulation in the human body leads to diseases due to chronic toxicity [23].
It is well known that MPs can be fragmented into NPs by the action of UV light, the mechanical and shear forces of waves, and wind, which also cause chemical changes in their structure. These reductions in size and chemical changes facilitate their spread and contact with aquatic and terrestrial organisms [24]. At such a small size, these particles move through body barriers [25,26] and internalized cells. For example, the internalization of nanoplastics in vascular plants introduces phytotoxicity, including the adverse effects of photosynthesis and oxidative stress [27]. In addition, these particles can be inhaled, entering the pulmonary tract. Once present in the pulmonary or gastrointestinal tracts, they accumulate and distribute to various organs and tissues, showing teratogenic, carcinogenic, mutagenic, and toxic effects with long-term impacts on the organism [28]. However, despite the rising literature on the effects of MP/NP ingestion, there is a lack of detailed knowledge of the effects of MPs/NPs on marine and human health, mainly due to an underestimation of the effect related to the analytical and sampling methods for MP/NP extraction [29]. MPs/NPs can alter microbial diversity, biogeochemical cycles, and the restoration of healthy soils [22,30,31].
A microorganism is an organism with a large surface-area-to-volume ratio. A microorganism is easy to cultivate and has a high biomass growth capacity [32]. These tiny organisms are vital in restoring the balance of planet life through various biogeochemical cycles. Microorganisms mineralize organic compounds and help distribute nutrients to other life forms, such as plants and higher organisms [33,34,35]. Many microorganisms are essential to superior organisms, as is the case for intestinal microbiota, which facilitate tissue differentiation, stimulate the immune response, and protect the host from pathogens [36,37]. Therefore, the microbiome is fundamental for organisms through the digestion and absorption of nutrients and the prevention of host diseases [36,38].
However, the interaction of microorganisms with MPs (and, even worse, with NPs) is still not well understood. Many studies have focused on analyzing the interaction of MPs with terrestrial and aquatic microorganisms, mainly concerning the ecological effects in those environments, but very little is known about the interaction with atmospheric MPs [39,40,41].
Initially, microbes adsorb on MPs’ surfaces, creating a habitat similar to their living environment [22], as in the case of the “plastisphere” in aquatic environments [42]. Once microbial colonization occurs on the surface, the microorganism secretes enzymes to degrade the constituent polymers through hydrolysis or oxidation–reduction reactions [43,44,45]. Enzyme secretion generates oligomers, dimers, and monomers, which enter microbial cells for energy conservation through metabolic pathways producing CO2, H2O, or CH4 [43].
This study presents the most relevant information about microorganisms’ biodegradation of MPs/NPs as a green approach to mitigate the negative impact on the environment. Due to the relevant information generated through the study, the purpose was to perform a bibliometric analysis of 719 documents published from 2010 to 2021 on the research landscape of MPs’ and NPs’ interactions with microorganisms. The information might be suitable for environmental agencies, research institutes, and the general community as a tool analyzing the most recent literature. This study presents the most relevant information about microorganisms’ biodegradation of MPs/NPs as a green approach to mitigate their negative impact on the environment.

2. Methodology

In the present study, information from the citations and abstracts of scientific journals extracted from the Scopus database of Elsevier, created in 2004, was comprehensively reviewed [46]. Elsevier’s Scopus is one of the most representative databases for scientific information due to the significant content of publishers and journals [47]. According to the information provided by the publisher, the Scopus database contains more than 25,100 titles from more than 5000 international publishers, including broad research production in different areas of science, technology, medicine, arts, and humanities [46]. In addition, Scopus has several analysis functions supporting bibliometric analysis [48]. The analysis functions included by Scopus and extracted here are the journal’s name, the type of document, the year of publication, the authors and their affiliations, the number of citations, and the index h-metrics for papers, imported in this research as a .csv file and a Microsoft Excel file (Supplementary Materials) for further analysis. The journal impact factor (IF) of the extracted articles was extracted from the Journal Citation Report (JCR) 2021, while the Cite Score 2021 retrieval was obtained from Scopus.
The search strategy in this article consisted of using the following search term: (TS) = TITLE-ABS-KEY (((microplastic * OR micro-plastic * OR nanoplastic * OR nano-plastic *) AND (microorganism * OR bacteria * OR fungi * OR algae * OR virus *))). This search retrieved 935 documents (10 March 2022). Subsequently, we performed a refined search by limiting the search to the document types “article”, “review”, and “conference paper,” excluding the year 2022 since it was endless, and limiting the language only to English: (TITLE-ABS-KEY (microplastic * OR micro-plastic * OR nanoplastic * OR nano-plastic *) AND TITLE-ABS-KEY (microorganism * OR bacteria * OR fungi * OR algae * OR virus *)) AND (LIMIT-TO (DOCTYPE, “ar”) OR LIMIT-TO (DOCTYPE, “re”) OR LIMIT-TO (DOCTYPE, “cp”)) AND (EXCLUDE (PUBYEAR, 2022)) AND (LIMIT-TO (LANGUAGE, “English”)). With this search, we retrieved 719 results. However, to obtain an idea of the publication trend, we completed a separate analysis, including the year 2022, even though the year was endless, and 1152 documents were obtained (30 October 2022). This information helped the separate the trend analysis for the 2022 publications, but we did not use them for mapping since the year still is running and several data might change at the end of the year. Despite no restrictions in the period covered for the search, the first publication retrieved was from 2010. The search was carried out on 12 August 2022, and included a bibliography published up to December 2021.
VOSviewer (www.vosviewer.com; Van Eck and Waltman, 2009–2022, version 1.6.18, Leiden University, Leiden, The Netherlands) is a free-access software to create network maps of institutions, countries, keywords, and citations per article [49]. We accessed VOSviewer on 12 August 2022.
Finally, to analyze the most recent published information related to the biodegradation/bioremediation of MPs and NPs by microorganisms, we reviewed the literature and extracted the most relevant information (including the literature of 2022). All the data were analyzed and are discussed in Section 3.6: Review of the interaction of microplastics and nanoplastics with microorganisms to understand MPs’/NPs’ biodegradation with bacteria, fungi, microalgae, biofilms, and periphytic films. Since viruses do not contribute to biodegradation, we discarded them in the final selection of the literature.

3. Results and Discussion

Bibliometric analysis involves obtaining and analyzing data on a topic to map academic literature and quantitatively evaluate and predict the patterns and trends of topics of research [50,51]. The bibliometric analysis (719 documents obtained) shows that MPs/NPs and their interaction with microorganisms is an area of knowledge with high impact and continuous growth. Recently, several investigations have focused on determining the effects of introducing MPs/NPs in terrestrial and marine habitats [22,52,53,54,55].

3.1. How Many Publications Are Produced Per Year on the Topic?

The first publication on microplastics with microorganisms was published in 1972 [56]. Since then, the topic of MPs/NPs and their interaction with microorganisms has been the focus of few literature reports. The 719 documents obtained from Scopus published between the years 2010 and 2021 on the subject investigated are distributed among 584 (81.2%) scientific articles, 124 (17.2%) review articles, and 11 (1.5%) conference articles.
According to our analysis, between 2010 and 2015, only 12 documents were published (2010 (1), 2011 (1), 2012 (1), 2013 (2), 2014 (4), and 2015 (3)). However, since 2016, there has been exponential growth in the number of publications per year (Figure 1A). The publications up to 30 October 2022 were included to analyze the rapid increase in 2022 and the general trend, despite the year not being finished yet. As can be seen in Figure 1B, the number of publications in 2022 (up to 30 October 2022) is 475, demonstrating the rapid increase in publications in the “MPs/NPS and their interaction with microorganisms” topic.
This dramatic increase relates to a primary significant concern about the effects derived from the interaction of MPs/NPs with aquatic, terrestrial, and atmospheric microorganisms, consequently affecting their growth and development [39,57] or causing their degradation [43,44,45]. The high number of documents and the high citation rate reflects these issues’ importance. Other studies of MPs’ interaction with food [28] and marine ecosystems [24,29,58] close to the subject of this study also exhibited this trend.

3.2. What Is the Collaboration between Countries on This Issue?

The top 10 countries (Table 1) with publications on the topic are led by China, with 288 documents, 40.1% of the total retrieved in the literature review. The following countries are the United States with 94 documents, Germany with 72, and Portugal in 10th place with 18 documents. However, the number of documents and distribution does not reflect the collaboration between countries and institutions. As seen in Figure 2, China, the United States, the United Kingdom, and Germany are the countries with the highest collaboration globally, represented by the proximity and size of the nodes. This result demonstrates the growing concern about the impact of MPs/NPs and their interaction with microorganisms since pathogens spread to environments where they are generally not present and move to other levels of the trophic chain, affecting the health of animals and man. The figure exhibits three clusters. The first cluster is red-colored, led by China, with 299 documents, a total link strength of 118, and 23 links.
The proximity and strength of the link reflect the power of the cooperation between these countries. China’s collaboration with Australia stands out with a link strength of 25, followed by a partnership with the United States with a link strength of 21. The other significant cluster is the United States, which has a total link strength of 83, with 85 documents and 26 links. This country reflects the most effective cooperation worldwide due first to its language, technology, and tradition in many techniques used to analyze microplastics worldwide, despite not having as many documents as China.
The third cluster is Germany, with 77 documents, a total link force of 59, and 24 links, while the United Kingdom presents 48 papers, with a total link force of 70, and 24 links. The United Kingdom, the United States, China, and Germany present cooperation, reflected by their closeness and link strength. It is also important to highlight that European countries, in addition to the United States, Canada, and Australia, cooperate the most with these group leaders. However, there is evidence of the presence of a few African (South Africa, Nigeria), Asian (Japan, Hong Kong, Malaysia, Indonesia, Bangladesh, India, South Korea, and Iran), and American (Brazil, Argentina, Mexico, Canada, and Costa Rica) countries, demonstrating the lack of information and research in these continents due to the lack of resources and technology for that purpose. Therefore, research needs more government and institutional investment programs.

3.3. What Are the Journals That Publish the Most in This Area?

Table 2 shows ten journals with the highest number of published documents (with at least twelve or more publications). The papers published in the ten journals add up to 59.81% of the total publications investigated in Scopus, of which the first three represent 33.52%. According to the Clarivate Journal Citation Report, those ten journals cover at least one of the following areas: environmental sciences; marine and freshwater biology; water resources; environmental engineering; toxicology. In all of these areas, except for the journal Bulletin of Environmental Contamination and Toxicology, journals are Q1 in the topics mentioned above, demonstrating the impact generated with the topic: “interaction of MPs/NPs with microorganisms and viruses.” A relevant aspect to highlight is that all the Journal Impact Factors consulted for 2021 in Clarivate’s Journal Citation Reports increased in the last few years, as did Cite Score 2021 consulted via Scopus for all these journals, confirming a high index of consultation and citation of these journals and a high relevance of the topic globally.
Figure 3, constructed using VOSviewer, exhibits the map of co-citations between the journals. The line thickness that joins two nodes (journals) determines the co-citation between two journals. The node size represents the journal’s total binding strength, while the thickness of the line joining two nodes represents the intensity of co-citation between them. As can be seen, the journal Science of The Total Environment and the journal Environmental Pollution have very strong co-citations, in addition to being very close to each other, indicating that they are closely related to the themes. A similar case is also seen between Marine Pollution Bulletin and Environmental Science and Technology, with a strong collaboration with the two previously described journals. Likewise, the Journal of Hazardous Materials and Chemosphere are heavily co-cited.
Similarly, Chemosphere and Science are very close. The strength of these co-citations is that the journals have topics that affect environmental sciences in their scope and the interaction of MPs/NPs with microorganisms and viruses, affecting the environment’s stability. MPs and NPs are also composed of additives such as flame retardants, antioxidants, plasticizers, and pigments that, after the partial or total degradation of MPs/NPs, can be released into the environment and affect ecosystems drastically [59]. In addition, as stated above, they also affect the quality of the soil, plants, and water, affecting microbial diversity.

3.4. What Are the Most Relevant Keywords to MPs/NPs’ Interactions with Microorganisms and Viruses?

According to the method reported by Salgado-Cruz et al. (2021), we analyzed the importance of keywords with a word cloud as a first qualitative approach to determine the most relevant words of all the articles reviewed in the area of “microplastics and nanoplastics and their interaction with microorganisms and viruses” keywords [60]. We discovered that the essential words in the topic are “marine”, “pollution”, “microplastics”, “microbiota”, “toxicity”, “polyethylene” and “plastics”, among other related words. The importance is related to microorganisms’ (many belonging to the microbiota of marine animals) interactions with MPs/NPs. Figure 4 shows the cloud of the most critical keywords (determined by the size of the words).
VOSviewer software allows a more detailed analysis of the interactions between the keywords and the authors of those works (Figure 5), reflecting the importance of a word with the node’s size and the interaction with other works’ terms by the thickness of the link line.
The keywords network builded from those cited at least ten times, distributed in 467 words grouped in 5 clusters with a total link strength of 189,827. This number of words is the result of eliminating too generic keywords such as “human”, “non-human”, or terms indicating the same thing (microplastic or microplastics). The first cluster (red color) is related to polymers derived from petroleum that cause significant pollution. Terms such as “polypropylene”, “polyethylene”, “elastomers” and “microplastic pollution” stand out as members of this cluster, whose primary term is “plastics” with 466 links, a total bond strength of 9120, and 368 occurrences.
The second cluster (green) is related to contamination in freshwater caused by MPs and NPs, which cause toxicity to microbial species. In this cluster, terms such as “water pollutant” (458 links, a total binding force of 7026 and 277 occurrences) and “toxicity” (449 links, a total binding force of 5031 and 203 occurrences) stand out, highlighting the importance of recognizing these terms within the most co-cited articles around the world, as a growing concern about the effect of MPs/NPs on microorganisms.
The third cluster (blue) is more related to microorganisms that may be using MPs as propagation vectors, including terms such as “antibiotic resistance”, “bacteria” and “microbial community”, which reflect another problem inherent to the recalcitrance of this type of materials serving as vehicles for pathogenic microorganisms. In this cluster, words related to identifying and analyzing the DNA and rRNA of many microorganisms for identification purposes and the effects of their interaction are evident. One of the most prominent terms is “microplastics” present in cluster four (yellow) with 466 links, 10,108 total link strength, and 460 occurrences.
Another interesting word in this cluster is “plastic waste”, with 463 links, 5823 total link strength, and 227 occurrences. In this cluster, many terms are not related to other words due to the recent publication dates. Still, that accounts for the growing concern and interest in research to establish the relationship between microorganisms, marine organisms, and MPs/NPs.
The last cluster (violet) accounts for the concern about the effect of MPs/NPs on soil and terrestrial microorganisms. Words such as “soil pollution”, “soil microbiology”, “microbiota” and “soil property” reflect this aspect.

3.5. What Are the Most Cited Articles?

These studies are interested in the impact of incorporating these particles into the food chain, which considerably affects the stability of ecosystems and represents a threat to human health. Of the total number of articles extracted, 183 (25.4%) contain 50 or more citations. The three most cited articles included in Table 3 correspond to ‘Microplastic Ingestion by Zooplankton’ with 1292 citations [57], ‘The distribution and Importance of Microplastics in the Marine environment: A review of the Sources, Fate, Effects and Potential Solutions’ with 963 citations [61], and ‘Microplastic is an Abundant and Distinct Microbial Habitat in an Urban River’ with 683 citations [62].
Figure 6 shows the map of co-citations of the sources with more than ten citations. This map shows a high relevance of the MP/NP interactions with microorganisms and viruses, with a high rate of co-citation reflected in the thickness of the links and their proximity. The last observation results from a global need for more standardized methodologies and techniques to analyze MPs/NPs and determine their direct effects on the interaction with microorganisms.
From the first cluster (red), Cole et al. [57] publication stands out with 28 links, a total link strength of 205, and 59 citations. The publication by McCormick et al. [62] follows, with 28 links, a total link strength of 211, and 51 citations. This cluster reveals an analysis of microplastics’ impact on marine animals.
In the second cluster (green), the interaction of microorganisms with MPs/NPs stands out more. The study by Besseling et al. [66] stands out which is related to the affectation of microorganism growth by the effect of NPs. This reference has 26 links, with a total link strength of 233 and 54 citations.
Some studies reveal more than ten citations. For example, there is a pioneer study with 27 links, 256 total link strength, and 80 citations, demonstrating that it is a study that many researchers take as a reference due to the impact of MPs in the marine environment and the early stage of publication [79].
Finally, the study by Zettler et al. [42], in which the interaction of MPs with the complex oceanic microbial community that they baptized “plastisphere” [42], made up of autotrophs, heterotrophs, predators, and symbionts, was analyzed. The study is interesting because it has 28 links, a total link strength of 260, and 65 citations [42]. Its high relevance and citation correspond to the fact that they were pioneers in introducing the term “plastisphere”, referring to a very complex community, including opportunistic microorganisms of the genus Vibrio.
Generally, these studies with more than ten citations have a high number of citations because their common shared themes serve as reference studies on the subject.

3.6. Review of the Interaction of Microplastics and Nanoplastics with Microorganisms

Studies show that MPs/NPs in different habitats have a negative impact. MPs/NPs alter the apparent density of the soil due to the different densities present in the MPs’ components [80,81,82]. Introducing MPs/NPs into the soil also affects soil porosity [80,83]. The latter involves a flow of gases, vital in the decomposition of organic matter; in addition, porosity affects the proper introduction and evaporation of water (affecting the nutrition of plants, animals, and microorganisms) [80,84,85], as well as the natural flow of oxygen. These aspects negatively impact the life of anaerobic or aerobic microorganisms in the soil [86].
In this way, changes due to the introduction of MPs/NPs into terrestrial and aquatic ecosystems can alter the pore space of the soil, affecting the water cycle, gas flow, and the associated microorganisms [87].
Other concomitant changes demonstrated by the introduction of MPs/NPs in ecosystems are related to changes in soil nutrients, alterations in pH (due to changes in ion exchange capacity), and the release of toxins (products of adsorption and the release of pesticides, heavy metals, and polycyclic hydrocarbons, among others) [13,22,87,88,89]. Changes in the physicochemical parameters of the soil lead to variations in microbial diversity.
Microplastics alter rhizosphere communities (mycorrhizae and rhizobacteria) due to plants’ altered water and nutrient absorption capacities. In turn, this also changes the ability to break down organic matter and the natural cycle of elements, which ultimately affects plants and all levels of the food chain.
On the other hand, the faunas that ingest MPs/NPs and the adsorbed pollutants alter their intestinal microbiota, with severe consequences for animals’ health [87,89,90,91,92]. For example, the interaction of vascular plants can introduce phytotoxicity and negatively affect growth.

3.6.1. Enzymatic Degradation of MPs/NPs Mediated by Microorganisms

Studies directed towards different alternatives for the degradation of MPs/NPs are of global interest, given the negative impact they cause both on human health and the environment. There are a high number of studies including relevant aspects such as transport, toxicity, and various chemical additives [93]. Microorganism-mediated enzymatic degradation involves mixed oxidative and biochemical reactions, which vary depending on the species of microorganisms, the morphology of MPs/NPs, and environmental conditions [11]. The stress induced by MPs/NPs causes an enzymatic response in microorganisms, allowing them to adapt to these new conditions by regulating various cellular aspects [94].
The enzymatic response induced by anthropogenic contaminants in microorganisms, in addition to the optimization function in cellular function for their adaptation, plays a critical role in the degradation of these anthropogenic contaminants, such as MPs/NPs.
The enzymes of these pollutants degrade the polymers of the MPs/NPs until they are converted into monomers through biochemical processes or oxidative reactions until they can assimilate and incorporate them into their biochemical cycles for the production of energy as a carbon source [95]. Microorganisms tend to present two types of MP/NP degradation, depending on the enzymes involved in the process. For example, the structural modification of the ester type is catalyzed by Fusarium solani pisi cutinases [96]. Hydrolases are very efficient in the structural transformation of these anthropogenic polymers. These enzymes increase the surface hydrophilicity of MPs/NPs, facilitating their degradation [97]. However, more studies are needed to understand the mechanisms of these enzymes fully and for optimization to increase biodegradation efficiency. A common enzyme-mediated mechanism that alters C-O bonds in polymer backbones to their constituent monomers is shown schematically in Figure 7 [98].
It is known that the degradation of the polymers that constitute MPs/NPs occurs through hydrolyzation reactions, which can act on hydrolyzable polymers and non-hydrolyzable polymers by binding to the MPs’/NPs’ surfaces to catalyze the chemical transformation essential for polymer degradation. The enzymatic degradation processes mediated by microorganisms break the polymeric bonds of the MPs through the action of enzymes such as hydrolases, lipases, and extracellular esterases until oligomers, dimers, or monomers are produced, followed by the assimilation and mineralization to CH4, H2O, and CO2.
PE degradation by Staphylococcus epidermis [99] is an example of enzymatic degradation, as well as in species of the Vibrio genus which colonize MPs/NPs, known as the “plastisphere” [42]. Plastisphere fungi, bacteria, and bryozoans are involved in MP/NP degradation. For example, LDPE is degraded via by Aspergillus sp. [100] and PP and LDPE are degraded by Rhodococcus sp. [101,102]. There are also reports of PE degradation by Zalerion maritimum and PU degradation by Bacillus subtilis [103]. In contrast, some reports are related to PS degradation by Thermus sp., Exiguobacterium sp., Geobacillus sp., and Bacillus sp. [104].

3.6.2. Bacterial Capacity for Biodegradation of MPs/NPs

The adverse effects caused by MP/NP contamination in biota have promoted the study of alternatives for bacterial-mediated degradation, which is of interest given the widespread relevance throughout the world, especially in the oceans, where hundreds of thousands of bacterial species live with degradation potential, evidenced in several reviews of various MP degradation alternatives with several mechanisms [105].
The efficiency of MP degradation varies depending on the type of bacteria, environmental conditions, MP density, functional groups, and chemical additives such as plasticizers [43]. The degradation of MPs mediated by bacteria involves a series of biochemical transformations by extracellular hydrolases that induce polymer backbone deterioration in MPs, reducing their size into monomers that are easy to assimilate. The enzymatic digestion also alters the shape and physicochemical properties, allowing the assimilation as a carbon source incorporated in mineralization processes [106].
The products from bacterial degradation vary depending on the conditions. For example, the enzymatic hydrolysis of polyhydroxy butyrate (PHB) generates 3-hydroxybutyric acid (HBA) as a product. That is, under anaerobic conditions, polyhydroxyalkanoate (PHA) degradation tends to produce methane, unlike aerobic degradations, which generate carbon dioxide and water [107].
Even with the current mechanistic knowledge regarding the biodegradation of MPs/NPs by fungi and bacteria, there is a need for more studies to understand these processes comprehensively. For example, species such as Streptomyces, Pseudomonas, Arthrobacter, Corynebacterium, Rhodococcus, and Micrococcus have good degradation potential [108]. In addition, Polaromonas, Agreia, Subtercola, Cryobacterium, Leifsonia, Flavobacterium, and Cryobacterium with degradation potential due to their production of hydrolases have been isolated [109]. Figure 8 shows the degradation process of plastics due to various synergistic environmental effects, such as biotic and abiotic factors, until sizes less than 5 mm are reached (MPs). Once fragmentation occurs, different bacterial and fungal species interact with these substances, exerting degrading effects on their surface by releasing various bacterial and fungal enzymes such as esterases, cutinases, and lipases. Additionally, oxidative mechanisms in MP degradation involving enzymes such as monooxygenase, dioxygenase, and carboxylesterases have been reported [110,111]. However, many of the studies reported are in silico, which do not entirely cover all the natural conditions that allow the optimization of degradation mechanisms in a short time or with greater efficiency.
Table 4 reports various bacteria with MP degradation activity, such as PP degradation with efficiencies of up to 4.0% and 6.4% mediated by Rhodococcus sp. and Bacillus sp. after 40 days of incubation [101].

3.6.3. Fungal Capacity for the Biodegradation of MPs/NPs

There are also reports on MP biodegradation using fungi. For example, the evaluation of PE biodegradation responses of the marine fungus Z. maritimum through quantifiable mass differences in PE microplastic granules exhibited good biodegrading activity [124]. Given the marine habitat of Z. maritimum and its great capacity for PE degradation, it is a good bioremediation alternative against the increase in MPs/NPs in the oceans. Like bacteria, fungi can also form biofilms on the MP’s surface and cause deformations in their structure, which promotes the formation of functional groups such as carboxyl and carbonyl, reducing properties such as hydrophobicity [125]. Fungi can also use MPs as carbon sources through mineralization processes [126]. Aspergillus niger and Penicillium pinophillum have shown LDPE biodegradation activities through a weight loss of 0.57% and 0.64%, respectively [127]. Table 5 reports the biodegrading activity of some species of fungi, as well as the degradation conditions. However, there is a general requirement for more detailed knowledge of the various degradation mechanisms these fungi use, which could facilitate the use of microorganisms as MP degradation alternatives in the oceans.

3.6.4. Biodegradation Capacity of Microplastics Using Microalgae

The biodegradation of emerging pollutants through microalgae and cyanobacteria has been studied in many fields, given the high efficiency of different processes through the efficient use of sunlight. The microalgae Phaeodactylum trycornutum and Chlamy domonas reinhardtii have shown great potential in environmental and biotechnological research through the energy of photosynthesis [135].
Although there are reports on the various mechanisms and microalgae–MP/NP interaction, more studies are still required to understand the various species of microorganisms and mechanisms for using these microorganisms for biodegradation [136]. A complete understanding of these mechanisms could help accelerate the process or increase the biodegradation efficiency of emerging pollutants such as MPs/NPs, which represent a significant risk for aquatic biota and human health. However, both microalgae and cyanobacteria promise to be exciting alternatives for MP/NP biodegradation and are efficient, sustainable, and environmentally friendly.
Figure 9 schematically shows the three main pathways that microalgae employ during the bioremediation of various emerging contaminants: biouptake, bioadsorption, and biodegradation. Biouptake involves the active transport of emerging contaminants into the cell by binding to intracellular proteins that act on the contaminants. During bioadsorption, emerging contaminant adsorption occurs on the cell wall or extracellular components, and biodegradation involves the transformation of compounds to complex organics (such as MP/NP contaminants) into substances, and into more specific and less toxic compounds through catalytic metabolic degradation processes [137].
Microalgae can colonize synthetic substrates such as PE surfaces, forming biofilms on the MP/NP surfaces and exerting degradative actions [138]. In this context, a microalgae known as Uronema africanum Borge has been reported, which has been identified on surfaces of plastic debris collected in lakes and in domestic waste dumps [139]. U. africanum Borge exerts a degradative action on the LDPE surface after 30 days.
Table 6 reports the biodegradation activities induced by various species of microalgae which have the potential to be exciting biodegradation alternatives to MPs/NPs that respect the environment.

3.6.5. Biofilms and Periphytic Films

The use of periphytic biofilms is a relatively new method for the biodegradation of MPs/NPs such as PP, PE, and PET. Biodegradations ranged between 18.02% for PP, 14.02% for PE, and 19.72% for PET after 60 days of treatment with Deinococcus thermus, Proteobacteria, and Cyanobacteria as the predominant species in the biofilms [147].
While the use of biofilms for MP/NP biodegradation in marine environments promises to be a valuable alternative to mitigate the negative impacts of these pollutants on various marine species, water quality, and human health, synergistic collaborative research efforts to understand the mechanistic process of degradation entirely is not enough. Therefore, more research is required to understand the mechanisms by which these biofilms degrade MPs and the different interactions between MPs/NPs and microorganisms to fully understand the effects of these biofilms’ various biodegradative processes.
In this context, there are reports on biofilms’ biodegrading potential in marine environments. The current research on biodegradation processes through biofilms has been reviewed, along with lagoons and future research prospects [148].
Biofilm formation on the surfaces of MPs, such as PE, usually takes up to a week [149]. After a week, the biofilms begin to be visible on the surfaces of the MPs, which increase in the following weeks, generating morphological and structural changes in the MPs, evidenced by the registration of weight losses of the MPs and structural and morphological alterations. Table 7 exhibits some studies on the degradation effects of MPs/NPs mediated by biofilms and periphytic films.

4. Conclusions

The bibliometric analysis retrieved 719 documents from the 2010 to 2021 timeline, demonstrating MP/NP interactions with microorganisms/viruses, an area of knowledge with high impact and continuous growth. This dramatic increase is related to a more significant concern about the effects derived from the interaction of MPs/NPs with aquatic, terrestrial, and atmospheric microorganisms with consequences on their growth and development, facilitating the biodegradation of MPs/NPs. In addition, there is growing concern about the role that MPs play as vectors since pathogens can spread to environments where they are generally not present and move to other levels of the food chain, affecting the health of animals and humans. From the analysis of the source countries, China (288), the United States (94), and Germany (72) are the leading publishing countries in MP/NP interactions with microorganisms and viruses, accounting for more than 454 documents (65.4%) of the total literature retrieved. However, China, the United States, the United Kingdom, and Germany are the countries with the most significant collaboration at a global level, represented by the proximity and size of the nodes. Nevertheless, there is a need to strengthen synergistic efforts regarding the study of MP/NP degradation in some countries of continents such as Africa (South Africa, Nigeria), Asia (Japan, Hong Kong, Malaysia, Indonesia, Bangladesh, India, South Korea), and America (Brazil, Argentina, Mexico, Canada, and Costa Rica), given their low rate of research reports associated with these issues.
The publications on this research topic have occurred in the most prestigious journals in areas related to environmental sciences, marine and freshwater biology, water resources, environmental engineering, and toxicology. The most relevant keywords related to the topic are “marine”, “pollution”, “microplastics”, “microbiota”, “toxicity”, “polyethylene”, and “plastics”, related to microorganisms’ (many belonging to the microbiota of marine animals) interactions with MPs/NPs. The most cited papers are interested in the effect of these particles’ ingestion and incorporation into the food chain, which considerably affects the stability of ecosystems and represents a threat to human health.
With the analysis of this bibliographic review, there was documentation of the biodegradation of MPs/NPs by bacteria, fungi, microalgae, and biofilms, which promises to mitigate the negative impact generated by the ubiquitous presence of anthropogenic pollutants’ MPs/NPs in various environments, such as terrestrial, aquatic and atmospheric environments. However, the study reveals a need to increase cooperative research on the various interactions between microorganisms and MPs/NPs with pilot-scale analyses that allow the expansion of existing biodegradation methodologies. There is still a lack of detailed knowledge of marine and human health effects, mainly due to an underestimated effect related to the analytical and sampling methods for MP/NP extraction. Finally, in-depth study of the degradation mechanisms and stimulation conditions involved in the periphytic films and microalgae of MPs is necessary.

Supplementary Materials

The following supporting information is available at: https://www.mdpi.com/article/10.3390/su142214761/s1, Imported data (publication and authors) of the selected publications obtained from Scopus.

Author Contributions

Conceptualization, C.D.G.-T., J.T. and V.A.A.; methodology, C.D.G.-T., D.C.C.-H.; validation C.D.G.-T., D.C.C.-H., J.T. and V.A.A.; investigation, C.D.G.-T., D.C.C.-H. and K.M.; resources, J.T. and V.A.A.; writing—original draft preparation, C.D.G.-T. and D.C.C.-H.; writing—review and editing, C.D.G.-T., D.C.C.-H., J.T., K.M. and V.A.A.; visualization, C.D.G.-T.; supervision, C.D.G.-T., J.T. and V.A.A.; funding acquisition, C.D.G.-T., J.T. and V.A.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by FONDO DE CIENCIA, TECNOLOGÍA E INNOVACIÓN DEL SISTEMA GENERAL DE REGALÍAS de Colombia (FCTeI-SGR), grant BPIN 2020000100065 and the APC was funded by FCTeI-SGR and the Universidad del Atlántico.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Othman, A.R.; Hasan, H.A.; Muhamad, M.H.; Abdullah, S.R.S. Microbial Degradation of Microplastics by Enzymatic Processes: A Review. Environ. Chem. Lett. 2021, 19, 3057–3073. [Google Scholar] [CrossRef]
  2. Worm, B.; Lotze, H.K.; Jubinville, I.; Wilcox, C.; Jambeck, J. Plastic as a Persistent Marine Pollutant. Annu. Rev. Environ. Resour. 2017, 42, 1–26. [Google Scholar] [CrossRef]
  3. Rios, L.M.; Jones, P.R.; Moore, C.; Narayan, U.V. Quantitation of Persistent Organic Pollutants Adsorbed on Plastic Debris from the Northern Pacific Gyre’s “Eastern Garbage Patch”. J. Environ. Monit. 2010, 12, 2226–2236. [Google Scholar] [CrossRef] [PubMed]
  4. Amobonye, A.; Bhagwat, P.; Singh, S.; Pillai, S. Plastic Biodegradation: Frontline Microbes and Their Enzymes. Sci. Total Environ. 2020, 759, 143536. [Google Scholar] [CrossRef] [PubMed]
  5. Europe, P. Plastics—The Facts 2013: An Analysis of European Latest Plastics Production, Demand and Waste Data; Plastics Europe: Bruxelles, Belgium, 2013; p. 40. [Google Scholar]
  6. Liu, P.; Shi, Y.; Wu, X.; Wang, H.; Huang, H.; Guo, X.; Gao, S. Review of the Artificially-Accelerated Aging Technology and Ecological Risk of Microplastics. Sci. Total Environ. 2021, 768, 144969. [Google Scholar] [CrossRef] [PubMed]
  7. Geyer, R.; Jambeck, J.R.; Law, K.L. Production, Use, and Fate of All Plastics Ever Made. Sci. Adv. 2017, 3, e1700782. [Google Scholar] [CrossRef] [Green Version]
  8. Zhang, K.; Shi, H.; Peng, J.; Wang, Y.; Xiong, X.; Wu, C.; Lam, P.K.S. Microplastic Pollution in China’s Inland Water Systems: A Review of Findings, Methods, Characteristics, Effects, and Management. Sci. Total Environ. 2018, 630, 1641–1653. [Google Scholar] [CrossRef]
  9. Bhagat, J.; Zang, L.; Nishimura, N.; Shimada, Y. Zebrafish: An Emerging Model to Study Microplastic and Nanoplastic Toxicity. Sci. Total Environ. 2020, 728, 138707. [Google Scholar] [CrossRef]
  10. Azizi, S.M.M.; Hai, F.I.; Lu, W.; Al-Mamun, A.; Dhar, B.R. A Review of Mechanisms Underlying the Impacts of (Nano) Microplastics on Anaerobic Digestion. Bioresour. Technol. 2021, 329, 124894. [Google Scholar]
  11. Alimi, O.S.; Farner Budarz, J.; Hernandez, L.M.; Tufenkji, N. Microplastics and Nanoplastics in Aquatic Environments: Aggregation, Deposition, and Enhanced Contaminant Transport. Environ. Sci. Technol. 2018, 52, 1704–1724. [Google Scholar] [CrossRef]
  12. Abbasi, S.; Keshavarzi, B.; Moore, F.; Turner, A.; Kelly, F.J.; Dominguez, A.O.; Jaafarzadeh, N. Distribution and Potential Health Impacts of Microplastics and Microrubbers in Air and Street Dusts from Asaluyeh County, Iran. Environ. Pollut. 2019, 244, 153–164. [Google Scholar] [CrossRef] [PubMed]
  13. Guo, J.-J.; Huang, X.-P.; Xiang, L.; Wang, Y.-Z.; Li, Y.-W.; Li, H.; Cai, Q.-Y.; Mo, C.-H.; Wong, M.-H. Source, Migration and Toxicology of Microplastics in Soil. Environ. Int. 2020, 137, 105263. [Google Scholar] [CrossRef] [PubMed]
  14. Wang, S.; Chen, H.; Zhou, X.; Tian, Y.; Lin, C.; Wang, W.; Zhou, K.; Zhang, Y.; Lin, H. Microplastic Abundance, Distribution and Composition in the Mid-West Pacific Ocean. Environ. Pollut. 2020, 264, 114125. [Google Scholar] [CrossRef] [PubMed]
  15. Han, M.; Niu, X.; Tang, M.; Zhang, B.-T.; Wang, G.; Yue, W.; Kong, X.; Zhu, J. Distribution of Microplastics in Surface Water of the Lower Yellow River near Estuary. Sci. Total Environ. 2020, 707, 135601. [Google Scholar] [CrossRef] [PubMed]
  16. González-Pleiter, M.; Velázquez, D.; Edo, C.; Carretero, O.; Gago, J.; Barón-Sola, Á.; Hernández, L.E.; Yousef, I.; Quesada, A.; Leganés, F. Fibers Spreading Worldwide: Microplastics and Other Anthropogenic Litter in an Arctic Freshwater Lake. Sci. Total Environ. 2020, 722, 137904. [Google Scholar] [CrossRef]
  17. Sørensen, L.; Rogers, E.; Altin, D.; Salaberria, I.; Booth, A.M. Sorption of PAHs to Microplastic and Their Bioavailability and Toxicity to Marine Copepods under Co-Exposure Conditions. Environ. Pollut. 2020, 258, 113844. [Google Scholar] [CrossRef]
  18. 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. [Google Scholar] [CrossRef]
  19. Singla, M.; Díaz, J.; Broto-Puig, F.; Borrós, S. Sorption and Release Process of Polybrominated Diphenyl Ethers (PBDEs) from Different Composition Microplastics in Aqueous Medium: Solubility Parameter Approach. Environ. Pollut. 2020, 262, 114377. [Google Scholar] [CrossRef]
  20. Liu, G.; Zhu, Z.; Yang, Y.; Sun, Y.; Yu, F.; Ma, J. Sorption Behavior and Mechanism of Hydrophilic Organic Chemicals to Virgin and Aged Microplastics in Freshwater and Seawater. Environ. Pollut. 2019, 246, 26–33. [Google Scholar] [CrossRef]
  21. 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. [Google Scholar] [CrossRef]
  22. Zhang, X.; Li, Y.; Ouyang, D.; Lei, J.; Tan, Q.; Xie, L.; Li, Z.; Liu, T.; Xiao, Y.; Farooq, T.H.; et al. Systematical Review of Interactions between Microplastics and Microorganisms in the Soil Environment. J. Hazard. Mater. 2021, 418, 126288. [Google Scholar] [CrossRef] [PubMed]
  23. Li, J.; Liu, H.; Chen, J.P. Microplastics in Freshwater Systems: A Review on Occurrence, Environmental Effects, and Methods for Microplastics Detection. Water Res. 2018, 137, 362–374. [Google Scholar] [CrossRef] [PubMed]
  24. García Rellán, A.; Vázquez Ares, D.; Vázquez Brea, C.; Francisco López, A.; Bello Bugallo, P.M. Sources, Sinks and Transformations of Plastics in Our Oceans: Review, Management Strategies and Modelling. Sci. Total Environ. 2023, 854, 158745. [Google Scholar] [CrossRef] [PubMed]
  25. Rubio, L.; Marcos, R.; Hernández, A. Potential Adverse Health Effects of Ingested Micro-and Nanoplastics on Humans. Lessons Learned from in Vivo and in Vitro Mammalian Models. J. Toxicol. Environ. Health Part B 2020, 23, 51–68. [Google Scholar] [CrossRef] [PubMed]
  26. Magrì, D.; Sánchez-Moreno, P.; Caputo, G.; Gatto, F.; Veronesi, M.; Bardi, G.; Catelani, T.; Guarnieri, D.; Athanassiou, A.; Pompa, P.P. Laser Ablation as a Versatile Tool to Mimic Polyethylene Terephthalate Nanoplastic Pollutants: Characterization and Toxicology Assessment. ACS Nano 2018, 12, 7690–7700. [Google Scholar] [CrossRef]
  27. Yin, L.; Wen, X.; Huang, D.; Du, C.; Deng, R.; Zhou, Z.; Tao, J.; Li, R.; Zhou, W.; Wang, Z.; et al. Interactions between Microplastics/Nanoplastics and Vascular Plants. Environ. Pollut. 2021, 290, 117999. [Google Scholar] [CrossRef] [PubMed]
  28. Wong, S.L.; Nyakuma, B.B.; Wong, K.Y.; Lee, C.T.; Lee, T.H.; Lee, C.H. Microplastics and Nanoplastics in Global Food Webs: A Bibliometric Analysis (2009–2019). Mar. Pollut. Bull. 2020, 158, 111432. [Google Scholar] [CrossRef] [PubMed]
  29. Markic, A.; Gaertner, J.-C.; Gaertner-Mazouni, N.; Koelmans, A.A. Plastic Ingestion by Marine Fish in the Wild. Crit. Rev. Environ. Sci. Technol. 2020, 50, 657–697. [Google Scholar] [CrossRef]
  30. Wu, Y.; Cai, P.; Jing, X.; Niu, X.; Ji, D.; Ashry, N.M.; Gao, C.; Huang, Q. Soil Biofilm Formation Enhances Microbial Community Diversity and Metabolic Activity. Environ. Int. 2019, 132, 105116. [Google Scholar] [CrossRef] [PubMed]
  31. De Souza Machado, A.A.; Lau, C.W.; Kloas, W.; Bergmann, J.; Bachelier, J.B.; Faltin, E.; Becker, R.; Görlich, A.S.; Rillig, M.C. Microplastics Can Change Soil Properties and Affect Plant Performance. Environ. Sci. Technol. 2019, 53, 6044–6052. [Google Scholar] [CrossRef] [Green Version]
  32. Huttenhower, C.; Gevers, D.; Knight, R.; Abubucker, S.; Badger, J.H.; Chinwalla, A.T.; Creasy, H.H.; Earl, A.M.; FitzGerald, M.G.; Fulton, R.S. Structure, Function and Diversity of the Healthy Human Microbiome. Nature 2012, 486, 207. [Google Scholar]
  33. Crawford, J.W.; Harris, J.A.; Ritz, K.; Young, I.M. Towards an Evolutionary Ecology of Life in Soil. Trends Ecol. Evol. 2005, 20, 81–87. [Google Scholar] [CrossRef] [PubMed]
  34. Lowery, N.V.; Ursell, T. Structured Environments Fundamentally Alter Dynamics and Stability of Ecological Communities. Proc. Natl. Acad. Sci. USA 2019, 116, 379–388. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Finley, B.K.; Dijkstra, P.; Rasmussen, C.; Schwartz, E.; Mau, R.L.; Liu, X.-J.A.; Van Gestel, N.; Hungate, B.A. Soil Mineral Assemblage and Substrate Quality Effects on Microbial Priming. Geoderma 2018, 322, 38–47. [Google Scholar] [CrossRef]
  36. Thaiss, C.A.; Zmora, N.; Levy, M.; Elinav, E. The Microbiome and Innate Immunity. Nature 2016, 535, 65–74. [Google Scholar] [CrossRef]
  37. Honda, K.; Littman, D.R. The Microbiota in Adaptive Immune Homeostasis and Disease. Nature 2016, 535, 75–84. [Google Scholar] [CrossRef]
  38. Lu, L.; Luo, T.; Zhao, Y.; Cai, C.; Fu, Z.; Jin, Y. Interaction between Microplastics and Microorganism as Well as Gut Microbiota: A Consideration on Environmental Animal and Human Health. Sci. Total Environ. 2019, 667, 94–100. [Google Scholar] [CrossRef]
  39. Tian, H.; Kah, M.; Kariman, K. Are Nanoparticles a Threat to Mycorrhizal and Rhizobial Symbioses? A Critical Review. Front. Microbiol. 2019, 10, 1660. [Google Scholar] [CrossRef] [Green Version]
  40. Rillig, M.C.; de Souza Machado, A.A.; Lehmann, A.; Klümper, U. Evolutionary Implications of Microplastics for Soil Biota. Environ. Chem. 2019, 16, 3–7. [Google Scholar] [CrossRef] [Green Version]
  41. Wang, W.; Ge, J.; Yu, X.; Li, H. Environmental Fate and Impacts of Microplastics in Soil Ecosystems: Progress and Perspective. Sci. Total Environ. 2020, 708, 134841. [Google Scholar] [CrossRef]
  42. Zettler, E.R.; Mincer, T.J.; Amaral-Zettler, L.A. Life in the “Plastisphere”: Microbial Communities on Plastic Marine Debris. Environ. Sci. Technol. 2013, 47, 7137–7146. [Google Scholar] [CrossRef] [PubMed]
  43. Yuan, J.; Ma, J.; Sun, Y.; Zhou, T.; Zhao, Y.; Yu, F. Microbial Degradation and Other Environmental Aspects of Microplastics/Plastics. Sci. Total Environ. 2020, 715, 136968. [Google Scholar] [CrossRef] [PubMed]
  44. Sander, M. Biodegradation of Polymeric Mulch Films in Agricultural Soils: Concepts, Knowledge Gaps, and Future Research Directions. Environ. Sci. Technol. 2019, 53, 2304–2315. [Google Scholar] [CrossRef] [PubMed]
  45. Sánchez, C. Fungal Potential for the Degradation of Petroleum-Based Polymers: An Overview of Macro-and Microplastics Biodegradation. Biotechnol. Adv. 2020, 40, 107501. [Google Scholar] [CrossRef]
  46. Elsevier. Scopus Content Coverage Guide; Elsevier: Amsterdam, The Netherlands, 2020. [Google Scholar]
  47. García, J.A.; Rodriguez-Sánchez, R.; Fdez-Valdivia, J. Ranking of the Subject Areas of Scopus. J. Am. Soc. Inf. Sci. Technol. 2011, 62, 2013–2023. [Google Scholar] [CrossRef]
  48. Sweileh, W.M. Research Trends on Human Trafficking: A Bibliometric Analysis Using Scopus Database. Glob. Health 2018, 14, 106. [Google Scholar] [CrossRef] [Green Version]
  49. Van Eck, N.J.; Waltman, L. Software Survey: VOSviewer, a Computer Program for Bibliometric Mapping. Scientometrics 2010, 84, 523–538. [Google Scholar] [CrossRef] [Green Version]
  50. Zhang, Y.; Pu, S.; Lv, X.; Gao, Y.; Ge, L. Global Trends and Prospects in Microplastics Research: A Bibliometric Analysis. J. Hazard. Mater. 2020, 400, 123110. [Google Scholar] [CrossRef]
  51. Jiang, Y.; Xia, W.; Zhao, R.; Wang, M.; Tang, J.; Wei, Y. Insight into the Interaction Between Microplastics and Microorganisms Based on a Bibliometric and Visualized Analysis. Bull. Environ. Contam. Toxicol. 2021, 107, 585–596. [Google Scholar] [CrossRef]
  52. Mbachu, O.; Jenkins, G.; Kaparaju, P.; Pratt, C. The Rise of Artificial Soil Carbon Inputs: Reviewing Microplastic Pollution Effects in the Soil Environment. Sci. Total Environ. 2021, 780, 146569. [Google Scholar] [CrossRef]
  53. Prata, J.C.; Reis, V.; da Costa, J.P.; Mouneyrac, C.; Duarte, A.C.; Rocha-Santos, T. Contamination Issues as a Challenge in Quality Control and Quality Assurance in Microplastics Analytics. J. Hazard. Mater. 2021, 403, 123660. [Google Scholar] [CrossRef] [PubMed]
  54. Büks, F.; Kaupenjohann, M. Global Concentrations of Microplastics in Soils—A Review. Soil 2020, 6, 649–662. [Google Scholar] [CrossRef]
  55. Khalid, N.; Aqeel, M.; Noman, A. Microplastics Could Be a Threat to Plants in Terrestrial Systems Directly or Indirectly. Environ. Pollut. 2020, 267, 115653. [Google Scholar] [CrossRef]
  56. Carpenter, E.J.; Smith, K.L. Plastics on the Sargasso Sea Surface. Science 1972, 175, 1240–1241. [Google Scholar] [CrossRef]
  57. Cole, M.; Lindeque, P.; Fileman, E.; Halsband, C.; Goodhead, R.; Moger, J.; Galloway, T.S. Microplastic Ingestion by Zooplankton. Environ. Sci. Technol. 2013, 47, 6646–6655. [Google Scholar] [CrossRef]
  58. Pauna, V.H.; Buonocore, E.; Renzi, M.; Russo, G.F.; Franzese, P.P. The Issue of Microplastics in Marine Ecosystems: A Bibliometric Network Analysis. Mar. Pollut. Bull. 2019, 149, 110612. [Google Scholar] [CrossRef]
  59. Bardají, D.K.R.; Moretto, J.A.S.; Furlan, J.P.R.; Stehling, E.G. A Mini-Review: Current Advances in Polyethylene Biodegradation. World J. Microbiol. Biotechnol. 2020, 36, 32. [Google Scholar] [CrossRef]
  60. De la Paz Salgado-Cruz, M.; Salgado-Cruz, J.; García-Hernández, A.B.; Calderón-Domínguez, G.; Gómez-Viquez, H.; Oliver-Espinoza, R.; Fernández-Martínez, M.C.; Yáñez-Fernández, J. Chitosan as a Coating for Biocontrol in Postharvest Products: A Bibliometric Review. Membranes 2021, 11, 421. [Google Scholar] [CrossRef]
  61. 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. [Google Scholar] [CrossRef] [PubMed]
  62. 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. [Google Scholar] [CrossRef] [PubMed]
  63. Browne, M.A.; Niven, S.J.; Galloway, T.S.; Rowland, S.J.; Thompson, R.C. Microplastic Moves Pollutants and Additives to Worms, Reducing Functions Linked to Health and Biodiversity. Curr. Biol. 2013, 23, 2388–2392. [Google Scholar] [CrossRef] [Green Version]
  64. Cole, M.; Lindeque, P.; Fileman, E.; Halsband, C.; Galloway, T.S. The Impact of Polystyrene Microplastics on Feeding, Function and Fecundity in the Marine Copepod Calanus Helgolandicus. Environ. Sci. Technol. 2015, 49, 1130–1137. [Google Scholar] [CrossRef] [PubMed]
  65. Steinmetz, Z.; Wollmann, C.; Schaefer, M.; Buchmann, C.; David, J.; Tröger, J.; Muñoz, K.; Frör, O.; Schaumann, G.E. Plastic Mulching in Agriculture. Trading Short-Term Agronomic Benefits for Long-Term Soil Degradation? Sci. Total Environ. 2016, 550, 690–705. [Google Scholar] [CrossRef] [PubMed]
  66. Besseling, E.; Wang, B.; Lürling, M.; Koelmans, A.A. Nanoplastic Affects Growth of S. Obliquus and Reproduction of D. Magna. Environ. Sci. Technol. 2014, 48, 12336–12343. [Google Scholar] [CrossRef] [PubMed]
  67. Rummel, C.D.; Jahnke, A.; Gorokhova, E.; Kühnel, D.; Schmitt-Jansen, M. Impacts of Biofilm Formation on the Fate and Potential Effects of Microplastic in the Aquatic Environment. Environ. Sci. Technol. Lett. 2017, 4, 258–267. [Google Scholar] [CrossRef] [Green Version]
  68. Chae, Y.; An, Y.-J. Current Research Trends on Plastic Pollution and Ecological Impacts on the Soil Ecosystem: A Review. Environ. Pollut. 2018, 240, 387–395. [Google Scholar] [CrossRef]
  69. Bergmann, M.; Wirzberger, V.; Krumpen, T.; Lorenz, C.; Primpke, S.; Tekman, M.B.; Gerdts, G. High Quantities of Microplastic in Arctic Deep-Sea Sediments from the HAUSGARTEN Observatory. Environ. Sci. Technol. 2017, 51, 11000–11010. [Google Scholar] [CrossRef] [Green Version]
  70. Kirstein, I.V.; Kirmizi, S.; Wichels, A.; Garin-Fernandez, A.; Erler, R.; Löder, M.; Gerdts, G. Dangerous Hitchhikers? Evidence for Potentially Pathogenic Vibrio Spp. on Microplastic Particles. Mar. Environ. Res. 2016, 120, 1–8. [Google Scholar] [CrossRef] [Green Version]
  71. De Witte, B.; Devriese, L.; Bekaert, K.; Hoffman, S.; Vandermeersch, G.; Cooreman, K.; Robbens, J. Quality Assessment of the Blue Mussel (Mytilus Edulis): Comparison between Commercial and Wild Types. Mar. Pollut. Bull. 2014, 85, 146–155. [Google Scholar] [CrossRef]
  72. Long, M.; Moriceau, B.; Gallinari, M.; Lambert, C.; Huvet, A.; Raffray, J.; Soudant, P. Interactions between Microplastics and Phytoplankton Aggregates: Impact on Their Respective Fates. Mar. Chem. 2015, 175, 39–46. [Google Scholar] [CrossRef] [Green Version]
  73. Zhang, C.; Chen, X.; Wang, J.; Tan, L. Toxic Effects of Microplastic on Marine Microalgae Skeletonema Costatum: Interactions between Microplastic and Algae. Environ. Pollut. 2017, 220, 1282–1288. [Google Scholar] [CrossRef] [PubMed]
  74. Fadare, O.O.; Okoffo, E.D. COVID-19 Face Masks: A Potential Source of Microplastic Fibers in the Environment. Sci. Total Environ. 2020, 737, 140279. [Google Scholar] [CrossRef] [PubMed]
  75. Wegner, A.; Besseling, E.; Foekema, E.M.; Kamermans, P.; Koelmans, A.A. Effects of Nanopolystyrene on the Feeding Behavior of the Blue Mussel (Mytilus Edulis L.). Environ. Toxicol. Chem. 2012, 31, 2490–2497. [Google Scholar] [CrossRef]
  76. Lu, L.; Wan, Z.; Luo, T.; Fu, Z.; Jin, Y. Polystyrene Microplastics Induce Gut Microbiota Dysbiosis and Hepatic Lipid Metabolism Disorder in Mice. Sci. Total Environ. 2018, 631–632, 449–458. [Google Scholar] [CrossRef]
  77. Jin, Y.; Lu, L.; Tu, W.; Luo, T.; Fu, Z. Impacts of Polystyrene Microplastic on the Gut Barrier, Microbiota and Metabolism of Mice. Sci. Total Environ. 2019, 649, 308–317. [Google Scholar] [CrossRef] [PubMed]
  78. Cole, M.; Lindeque, P.K.; Fileman, E.; Clark, J.; Lewis, C.; Halsband, C.; Galloway, T.S. Microplastics Alter the Properties and Sinking Rates of Zooplankton Faecal Pellets. Environ. Sci. Technol. 2016, 50, 3239–3246. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  79. Andrady, A.L. Microplastics in the Marine Environment. Mar. Pollut. Bull. 2011, 62, 1596–1605. [Google Scholar] [CrossRef] [PubMed]
  80. Jiang, X.J.; Liu, W.; Wang, E.; Zhou, T.; Xin, P. Residual Plastic Mulch Fragments Effects on Soil Physical Properties and Water Flow Behavior in the Minqin Oasis, Northwestern China. Soil Tillage Res. 2017, 166, 100–107. [Google Scholar] [CrossRef]
  81. Qi, R.; Jones, D.L.; Li, Z.; Liu, Q.; Yan, C. Behavior of Microplastics and Plastic Film Residues in the Soil Environment: A Critical Review. Sci. Total Environ. 2020, 703, 134722. [Google Scholar] [CrossRef] [PubMed]
  82. De Souza Machado, A.A.; Lau, C.W.; Till, J.; Kloas, W.; Lehmann, A.; Becker, R.; Rillig, M.C. Impacts of Microplastics on the Soil Biophysical Environment. Environ. Sci. Technol. 2018, 52, 9656–9665. [Google Scholar] [CrossRef] [Green Version]
  83. Kim, S.W.; An, Y.-J. Soil Microplastics Inhibit the Movement of Springtail Species. Environ. Int. 2019, 126, 699–706. [Google Scholar] [CrossRef] [PubMed]
  84. Wan, Y.; Wu, C.; Xue, Q.; Hui, X. Effects of Plastic Contamination on Water Evaporation and Desiccation Cracking in Soil. Sci. Total Environ. 2019, 654, 576–582. [Google Scholar] [CrossRef] [PubMed]
  85. Wang, T.; Xie, T.; Xu, C. Microextractors Applied in Nuclear-Spent Fuel Reprocessing: Micro/Mini Plants and Radiochemical Analysis. Crit. Rev. Environ. Sci. Technol. 2019, 49, 1–31. [Google Scholar] [CrossRef]
  86. Rubol, S.; Manzoni, S.; Bellin, A.; Porporato, A. Modeling Soil Moisture and Oxygen Effects on Soil Biogeochemical Cycles Including Dissimilatory Nitrate Reduction to Ammonium (DNRA). Adv. Water Resour. 2013, 62, 106–124. [Google Scholar] [CrossRef]
  87. Rillig, M.C. Microplastic in Terrestrial Ecosystems and the Soil? Environ. Sci. Technol. 2012, 46, 6453–6454. [Google Scholar] [CrossRef]
  88. Hegan, D.; Tong, L.; Zhiquan, H.; Qinming, S.; Ru, L. Determining Time Limits of Continuous Film Mulching and Examining Residual Effects on Cotton Yield and Soil Properties. J. Environ. Biol. 2015, 36, 677. [Google Scholar]
  89. Awet, T.T.; Kohl, Y.; Meier, F.; Straskraba, S.; Grün, A.-L.; Ruf, T.; Jost, C.; Drexel, R.; Tunc, E.; Emmerling, C. Effects of Polystyrene Nanoparticles on the Microbiota and Functional Diversity of Enzymes in Soil. Environ. Sci. Eur. 2018, 30, 11. [Google Scholar] [CrossRef]
  90. Lwanga, E.H.; Thapa, B.; Yang, X.; Gertsen, H.; Salánki, T.; Geissen, V.; Garbeva, P. Decay of Low-Density Polyethylene by Bacteria Extracted from Earthworm’s Guts: A Potential for Soil Restoration. Sci. Total Environ. 2018, 624, 753–757. [Google Scholar] [CrossRef]
  91. Wang, F.; Zhang, X.; Zhang, S.; Zhang, S.; Sun, Y. Interactions of Microplastics and Cadmium on Plant Growth and Arbuscular Mycorrhizal Fungal Communities in an Agricultural Soil. Chemosphere 2020, 254, 126791. [Google Scholar] [CrossRef]
  92. Yang, X.; Bento, C.P.M.; Chen, H.; Zhang, H.; Xue, S.; Lwanga, E.H.; Zomer, P.; Ritsema, C.J.; Geissen, V. Influence of Microplastic Addition on Glyphosate Decay and Soil Microbial Activities in Chinese Loess Soil. Environ. Pollut. 2018, 242, 338–347. [Google Scholar] [CrossRef]
  93. Padervand, M.; Lichtfouse, E.; Robert, D.; Wang, C. Removal of Microplastics from the Environment. A Review. Environ. Chem. Lett. 2020, 18, 807–828. [Google Scholar] [CrossRef]
  94. Oberbeckmann, S.; Labrenz, M. Marine Microbial Assemblages on Microplastics: Diversity, Adaptation, and Role in Degradation. Ann. Rev. Mar. Sci. 2020, 12, 209–232. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  95. Yoshida, S.; Hiraga, K.; Takehana, T.; Taniguchi, I.; Yamaji, H.; Maeda, Y.; Toyohara, K.; Miyamoto, K.; Kimura, Y.; Oda, K. A Bacterium That Degrades and Assimilates Poly(Ethylene Terephthalate). Science 2016, 351, 1196–1199. [Google Scholar] [CrossRef] [PubMed]
  96. Vertommen, M.A.M.E.; Nierstrasz, V.A.; van der Veer, M.; Warmoeskerken, M.M.C.G. Enzymatic Surface Modification of Poly(Ethylene Terephthalate). J. Biotechnol. 2005, 120, 376–386. [Google Scholar] [CrossRef] [PubMed]
  97. Kawai, F.; Kawabata, T.; Oda, M. Current Knowledge on Enzymatic PET Degradation and Its Possible Application to Waste Stream Management and Other Fields. Appl. Microbiol. Biotechnol. 2019, 103, 4253–4268. [Google Scholar] [CrossRef] [Green Version]
  98. Austin, H.P.; Allen, M.D.; Donohoe, B.S.; Rorrer, N.A.; Kearns, F.L.; Silveira, R.L.; Pollard, B.C.; Dominick, G.; Duman, R.; El Omari, K.; et al. Characterization and Engineering of a Plastic-Degrading Aromatic Polyesterase. Proc. Natl. Acad. Sci. USA 2018, 115, E4350–E4357. [Google Scholar] [CrossRef] [Green Version]
  99. Chatterjee, S.; Roy, B.; Roy, D.; Banerjee, R. Enzyme-Mediated Biodegradation of Heat Treated Commercial Polyethylene by Staphylococcal Species. Polym. Degrad. Stab. 2010, 95, 195–200. [Google Scholar] [CrossRef]
  100. Pramila, R.; Ramesh, K.V. Biodegradation of Low Density Polyethylene (LDPE) by Fungi Isolated from Marine Water—A SEM Analysis. Afr. J. Microbiol. Res. 2011, 5, 5013–5018. [Google Scholar] [CrossRef]
  101. Auta, H.S.; Emenike, C.U.; Jayanthi, B.; Fauziah, S.H. Growth Kinetics and Biodeterioration of Polypropylene Microplastics by Bacillus Sp. and Rhodococcus Sp. Isolated from Mangrove Sediment. Mar. Pollut. Bull. 2018, 127, 15–21. [Google Scholar] [CrossRef]
  102. Sivan, A.; Szanto, M.; Pavlov, V. Biofilm Development of the Polyethylene-Degrading Bacterium Rhodococcus Ruber. Appl. Microbiol. Biotechnol. 2006, 72, 346–352. [Google Scholar] [CrossRef]
  103. Shah, Z.; Krumholz, L.; Aktas, D.F.; Hasan, F.; Khattak, M.; Shah, A.A. Degradation of Polyester Polyurethane by a Newly Isolated Soil Bacterium, Bacillus Subtilis Strain MZA-75. Biodegradation 2013, 24, 865–877. [Google Scholar] [CrossRef] [PubMed]
  104. Chen, Z.; Zhao, W.; Xing, R.; Xie, S.; Yang, X.; Cui, P.; Lü, J.; Liao, H.; Yu, Z.; Wang, S.; et al. Enhanced in Situ Biodegradation of Microplastics in Sewage Sludge Using Hyperthermophilic Composting Technology. J. Hazard. Mater. 2020, 384, 121271. [Google Scholar] [CrossRef] [PubMed]
  105. Du, H.; Xie, Y.; Wang, J. Microplastic Degradation Methods and Corresponding Degradation Mechanism: Research Status and Future Perspectives. J. Hazard. Mater. 2021, 418, 126377. [Google Scholar] [CrossRef] [PubMed]
  106. Tiwari, N.; Santhiya, D.; Sharma, J.G. Microbial Remediation of Micro-Nano Plastics: Current Knowledge and Future Trends. Environ. Pollut. 2020, 265, 115044. [Google Scholar] [CrossRef] [PubMed]
  107. Lear, G.; Kingsbury, J.M.; Franchini, S.; Gambarini, V.; Maday, S.D.M.; Wallbank, J.A.; Weaver, L.; Pantos, O. Plastics and the Microbiome: Impacts and Solutions. Environ. Microbiome 2021, 16, 2. [Google Scholar] [CrossRef]
  108. Pathak, V.M.; Navneet. Review on the Current Status of Polymer Degradation: A Microbial Approach. Bioresour. Bioprocess. 2017, 4, 15. [Google Scholar] [CrossRef] [Green Version]
  109. Singh, P.; Singh, S.M.; Dhakephalkar, P. Diversity, Cold Active Enzymes and Adaptation Strategies of Bacteria Inhabiting Glacier Cryoconite Holes of High Arctic. Extremophiles 2014, 18, 229–242. [Google Scholar] [CrossRef]
  110. Jaiswal, S.; Sharma, B.; Shukla, P. Integrated Approaches in Microbial Degradation of Plastics. Environ. Technol. Innov. 2020, 17, 100567. [Google Scholar] [CrossRef]
  111. Xu, Z.; Xiong, X.; Zhao, Y.; Xiang, W.; Wu, C. Pollutants Delivered Every Day: Phthalates in Plastic Express Packaging Bags and Their Leaching Potential. J. Hazard. Mater. 2020, 384, 121282. [Google Scholar] [CrossRef]
  112. Zhou, Y.; Kumar, M.; Sarsaiya, S.; Sirohi, R.; Awasthi, S.K.; Sindhu, R.; Binod, P.; Pandey, A.; Bolan, N.S.; Zhang, Z.; et al. Challenges and Opportunities in Bioremediation of Micro-Nano Plastics: A Review. Sci. Total Environ. 2022, 802, 149823. [Google Scholar] [CrossRef]
  113. Roy, R.; Mukherjee, G.; Das Gupta, A.; Tribedi, P.; Sil, A.K. Isolation of a Soil Bacterium for Remediation of Polyurethane and Low-Density Polyethylene: A Promising Tool towards Sustainable Cleanup of the Environment. 3 Biotech 2021, 11, 29. [Google Scholar] [CrossRef] [PubMed]
  114. Auta, H.S.; Emenike, C.U.; Fauziah, S.H. Screening of Bacillus Strains Isolated from Mangrove Ecosystems in Peninsular Malaysia for Microplastic Degradation. Environ. Pollut. 2017, 231, 1552–1559. [Google Scholar] [CrossRef] [PubMed]
  115. Girard, E.B.; Kaliwoda, M.; Schmahl, W.W.; Wörheide, G.; Orsi, W.D. Textile Waste and Microplastic Induce Activity and Development of Unique Hydrocarbon-Degrading Marine Bacterial Communities. bioRxiv 2020. [Google Scholar] [CrossRef]
  116. Habib, S.; Iruthayam, A.; Abd Shukor, M.Y.; Alias, S.A.; Smykla, J.; Yasid, N.A. Biodeterioration of Untreated Polypropylene Microplastic Particles by Antarctic Bacteria. Polymers 2020, 12, 2616. [Google Scholar] [CrossRef]
  117. Li, Z.; Wei, R.; Gao, M.; Ren, Y.; Yu, B.; Nie, K.; Xu, H.; Liu, L. Biodegradation of Low-Density Polyethylene by Microbulbifer Hydrolyticus IRE-31. J. Environ. Manag. 2020, 263, 110402. [Google Scholar] [CrossRef]
  118. Li, J.; Kim, H.R.; Lee, H.M.; Yu, H.C.; Jeon, E.; Lee, S.; Kim, D.H. Rapid Biodegradation of Polyphenylene Sulfide Plastic Beads by Pseudomonas Sp. Sci. Total Environ. 2020, 720, 137616. [Google Scholar] [CrossRef] [PubMed]
  119. Dey, A.S.; Bose, H.; Mohapatra, B.; Sar, P. Biodegradation of Unpretreated Low-Density Polyethylene (LDPE) by Stenotrophomonas Sp. and Achromobacter Sp., Isolated From Waste Dumpsite and Drilling Fluid. Front. Microbiol. 2020, 11, 603210. [Google Scholar] [CrossRef]
  120. Gilan, I.; Hadar, Y.; Sivan, A. Colonization, Biofilm Formation and Biodegradation of Polyethylene by a Strain of Rhodococcus Ruber. Appl. Microbiol. Biotechnol. 2004, 65, 97–104. [Google Scholar] [CrossRef]
  121. Sudhakar, M.; Doble, M.; Murthy, P.S.; Venkatesan, R. Marine Microbe-Mediated Biodegradation of Low- and High-Density Polyethylenes. Int. Biodeterior. Biodegrad. 2008, 61, 203–213. [Google Scholar] [CrossRef]
  122. Balasubramanian, V.; Natarajan, K.; Hemambika, B.; Ramesh, N.; Sumathi, C.S.; Kottaimuthu, R.; Rajesh Kannan, V. High-Density Polyethylene (HDPE)-Degrading Potential Bacteria from Marine Ecosystem of Gulf of Mannar, India. Lett. Appl. Microbiol. 2010, 51, 205–211. [Google Scholar] [CrossRef]
  123. Yoon, M.G.; Jeon, H.J.; Kim, M.N. Biodegradation of Polyethylene by a Soil Bacterium and AlkB Cloned Recombinant Cell. J. Bioremediation Biodegrad. 2012, 3, 1–8. [Google Scholar] [CrossRef] [Green Version]
  124. Paço, A.; Duarte, K.; da Costa, J.P.; Santos, P.S.M.; Pereira, R.; Pereira, M.E.; Freitas, A.C.; Duarte, A.C.; Rocha-Santos, T.A.P. Biodegradation of Polyethylene Microplastics by the Marine Fungus Zalerion Maritimum. Sci. Total Environ. 2017, 586, 10–15. [Google Scholar] [CrossRef] [PubMed]
  125. Kettner, M.T.; Rojas-Jimenez, K.; Oberbeckmann, S.; Labrenz, M.; Grossart, H.-P. Microplastics Alter Composition of Fungal Communities in Aquatic Ecosystems. Environ. Microbiol. 2017, 19, 4447–4459. [Google Scholar] [CrossRef] [PubMed]
  126. Spina, F.; Tummino, M.L.; Poli, A.; Prigione, V.; Ilieva, V.; Cocconcelli, P.; Puglisi, E.; Bracco, P.; Zanetti, M.; Varese, G.C. Low Density Polyethylene Degradation by Filamentous Fungi. Environ. Pollut. 2021, 274, 116548. [Google Scholar] [CrossRef] [PubMed]
  127. Volke-Sepúlveda, T.; Saucedo-Castañeda, G.; Gutiérrez-Rojas, M.; Manzur, A.; Favela-Torres, E. Thermally Treated Low Density Polyethylene Biodegradation by Penicillium Pinophilum and Aspergillus Niger. J. Appl. Polym. Sci. 2002, 83, 305–314. [Google Scholar] [CrossRef]
  128. Devi, R.S.; Kannan, V.R.; Nivas, D.; Kannan, K.; Chandru, S.; Antony, A.R. Biodegradation of HDPE by Aspergillus Spp. from Marine Ecosystem of Gulf of Mannar, India. Mar. Pollut. Bull. 2015, 96, 32–40. [Google Scholar] [CrossRef] [PubMed]
  129. Zhang, J.; Gao, D.; Li, Q.; Zhao, Y.Y.; Li, L.; Lin, H.; Bi, Q.; Zhao, Y.Y. Biodegradation of Polyethylene Microplastic Particles by the Fungus Aspergillus Flavus from the Guts of Wax Moth Galleria Mellonella. Sci. Total Environ. 2020, 704, 135931. [Google Scholar] [CrossRef]
  130. Russell, J.R.; Huang, J.; Anand, P.; Kucera, K.; Sandoval, A.G.; Dantzler, K.W.; Hickman, D.S.; Jee, J.; Kimovec, F.M.; Koppstein, D.; et al. Biodegradation of Polyester Polyurethane by Endophytic Fungi. Appl. Environ. Microbiol. 2011, 77, 6076–6084. [Google Scholar] [CrossRef] [Green Version]
  131. Tian, L.; Kolvenbach, B.; Corvini, N.; Wang, S.; Tavanaie, N.; Wang, L.; Ma, Y.; Scheu, S.; Corvini, P.F.-X.; Ji, R. Mineralisation of 14C-Labelled Polystyrene Plastics by Penicillium Variabile after Ozonation Pre-Treatment. New Biotechnol. 2017, 38, 101–105. [Google Scholar] [CrossRef]
  132. Jeyakumar, D.; Chirsteen, J.; Doble, M. Synergistic Effects of Pretreatment and Blending on Fungi Mediated Biodegradation of Polypropylenes. Bioresour. Technol. 2013, 148, 78–85. [Google Scholar] [CrossRef]
  133. Darby, R.T.; Kaplan, A.M. Fungal Susceptibility of Polyurethanes. Appl. Microbiol. 1968, 16, 900–905. [Google Scholar] [CrossRef] [PubMed]
  134. Matsumiya, Y.; Murata, N.; Tanabe, E.; Kubota, K.; Kubo, M. Isolation and Characterization of an Ether-Type Polyurethane-Degrading Microorganism and Analysis of Degradation Mechanism by Alternaria Sp. J. Appl. Microbiol. 2010, 108, 1946–1953. [Google Scholar] [CrossRef] [PubMed]
  135. Barone, G.D.; Ferizović, D.; Biundo, A.; Lindblad, P. Hints at the Applicability of Microalgae and Cyanobacteria for the Biodegradation of Plastics. Sustainability 2020, 12, 10449. [Google Scholar] [CrossRef]
  136. Priya, A.K.; Jalil, A.A.; Dutta, K.; Rajendran, S.; Vasseghian, Y.; Karimi-Maleh, H.; Soto-Moscoso, M. Algal Degradation of Microplastic from the Environment: Mechanism, Challenges, and Future Prospects. Algal Res. 2022, 67, 102848. [Google Scholar] [CrossRef]
  137. Sutherland, D.L.; Ralph, P.J. Microalgal Bioremediation of Emerging Contaminants—Opportunities and Challenges. Water Res. 2019, 164, 114921. [Google Scholar] [CrossRef] [PubMed]
  138. Sharma, M.; Dubey, A.; Pareek, A. Algal Flora on Degrading Polythene Waste. CIBTech J. Microbiol. 2014, 3, 43–47. [Google Scholar]
  139. Sanniyasi, E.; Gopal, R.K.; Gunasekar, D.K.; Raj, P.P. Biodegradation of Low-Density Polyethylene (LDPE) Sheet by Microalga, Uronema Africanum Borge; Nature Publishing Group: London, UK, 2021; Volume 11, ISBN 4159802196315. [Google Scholar]
  140. Fu, D.; Zhang, Q.; Fan, Z.; Qi, H.; Wang, Z.; Peng, L. Aged Microplastics Polyvinyl Chloride Interact with Copper and Cause Oxidative Stress towards Microalgae Chlorella Vulgaris. Aquat. Toxicol. 2019, 216, 105319. [Google Scholar] [CrossRef]
  141. Li, Z.; Yi, X.; Zhou, H.; Chi, T.; Li, W.; Yang, K. Combined Effect of Polystyrene Microplastics and Dibutyl Phthalate on the Microalgae Chlorella Pyrenoidosa. Environ. Pollut. 2020, 257, 113604. [Google Scholar] [CrossRef]
  142. Kumar, R.; Kanna, G.R.; Elumalai, S. Biodegradation of Polyethylene by Green Photosynthetic Microalgae. J. Bioremediation Biodegrad. 2017, 8, 1–8. [Google Scholar]
  143. Song, C.; Liu, Z.; Wang, C.; Li, S.; Kitamura, Y. Different Interaction Performance between Microplastics and Microalgae: The Bio-Elimination Potential of Chlorella Sp. L38 and Phaeodactylum Tricornutum MASCC-0025. Sci. Total Environ. 2020, 723, 138146. [Google Scholar] [CrossRef]
  144. Hadiyanto, H.; Khoironi, A.; Dianratri, I.; Huda, K.; Suherman, S.; Muhammad, F. Biodegradation of Oxidized High-Density Polyethylene and Oxo-Degradable Plastic Using Microalgae Dunaliella Salina. Environ. Pollut. Bioavailab. 2022, 34, 469–481. [Google Scholar] [CrossRef]
  145. Cheng, Y.-R.; Wang, H.-Y. Highly Effective Removal of Microplastics by Microalgae Scenedesmus Abundans. Chem. Eng. J. 2022, 435, 135079. [Google Scholar] [CrossRef]
  146. Sarmah, P.; Rout, J. Colonisation of Oscillatoria on Submerged Polythenes in Domestic Sewage Water of Silchar Town, Assam (India). J. Algal Biomass Util. 2017, 8, 135–144. [Google Scholar]
  147. Shabbir, S.; Faheem, M.; Ali, N.; Kerr, P.G.; Wang, L.F.; Kuppusamy, S.; Li, Y. Periphytic Biofilm: An Innovative Approach for Biodegradation of Microplastics. Sci. Total Environ. 2020, 717, 137064. [Google Scholar] [CrossRef] [PubMed]
  148. Debroy, A.; George, N.; Mukherjee, G. Role of Biofilms in the Degradation of Microplastics in Aquatic Environments. J. Chem. Technol. Biotechnol. 2022, 97, 3271–3282. [Google Scholar] [CrossRef]
  149. Lobelle, D.; Cunliffe, M. Early Microbial Biofilm Formation on Marine Plastic Debris. Mar. Pollut. Bull. 2011, 62, 197–200. [Google Scholar] [CrossRef]
  150. Faheem, M.; Shabbir, S.; Zhao, J.; Kerr, P.G.; Ali, S.; Sultana, N.; Jia, Z. Multifunctional Periphytic Biofilms: Polyethylene Degradation and Cd2+ and Pb2+ Bioremediation under High Methane Scenario. Int. J. Mol. Sci. 2020, 21, 5331. [Google Scholar] [CrossRef]
  151. Rosato, A.; Barone, M.; Negroni, A.; Brigidi, P.; Fava, F.; Xu, P.; Candela, M.; Zanaroli, G. Microbial Colonization of Different Microplastic Types and Biotransformation of Sorbed PCBs by a Marine Anaerobic Bacterial Community. Sci. Total Environ. 2020, 705, 135790. [Google Scholar] [CrossRef]
  152. Ogonowski, M.; Motiei, A.; Ininbergs, K.; Hell, E.; Gerdes, Z.; Udekwu, K.I.; Bacsik, Z.; Gorokhova, E. Evidence for Selective Bacterial Community Structuring on Microplastics. Environ. Microbiol. 2018, 20, 2796–2808. [Google Scholar] [CrossRef]
Figure 1. (A) The number of publications per year (2010–2021) related to microplastic–microorganism interactions. (B) Trend analysis of the number of publications per year from 2010, including 2022.
Figure 1. (A) The number of publications per year (2010–2021) related to microplastic–microorganism interactions. (B) Trend analysis of the number of publications per year from 2010, including 2022.
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Figure 2. Co-authorship network of countries working on microplastics–microorganisms and viruses (threshold of 25). The size of the nodes indicates the number of publications produced by the country. The proximity of the two nodes indicates the relatedness of their co-authorship link, while the thickness of the connecting line indicates the strength of the cooperation. Items: 36. Clusters: 3. Links: 198. Total link strength: 423.
Figure 2. Co-authorship network of countries working on microplastics–microorganisms and viruses (threshold of 25). The size of the nodes indicates the number of publications produced by the country. The proximity of the two nodes indicates the relatedness of their co-authorship link, while the thickness of the connecting line indicates the strength of the cooperation. Items: 36. Clusters: 3. Links: 198. Total link strength: 423.
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Figure 3. Co-citation network diagram of journals from articles cited a minimum of 30 times. Items: 190. Clusters: 3. Links: 12,005. Total link strength: 1,017,131.
Figure 3. Co-citation network diagram of journals from articles cited a minimum of 30 times. Items: 190. Clusters: 3. Links: 12,005. Total link strength: 1,017,131.
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Figure 4. Cloud of most essential keywords extracted from https://www.nubedepalabras.es/ (accessed on 10 March 2022).
Figure 4. Cloud of most essential keywords extracted from https://www.nubedepalabras.es/ (accessed on 10 March 2022).
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Figure 5. Map of co-occurrence network visualization based on article weights for the terms related to the first group. Curved lines of varying thickness determined by co-occurrence show term relationships. Their relationship determines the distance between items. The occurrence determines the term size.
Figure 5. Map of co-occurrence network visualization based on article weights for the terms related to the first group. Curved lines of varying thickness determined by co-occurrence show term relationships. Their relationship determines the distance between items. The occurrence determines the term size.
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Figure 6. Map of co-citation network visualization based on the most cited references (cited at least 30 times). The occurrence determines the term size. Their relationship determines the distance between items. Cluster: 2. Links: 283. Total link strength: 2511.
Figure 6. Map of co-citation network visualization based on the most cited references (cited at least 30 times). The occurrence determines the term size. Their relationship determines the distance between items. Cluster: 2. Links: 283. Total link strength: 2511.
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Figure 7. General mechanisms of the enzymatic assimilation of MPs/NPs.
Figure 7. General mechanisms of the enzymatic assimilation of MPs/NPs.
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Figure 8. Different communities of microorganisms degrade MPs/NPs through their enzymes [112].
Figure 8. Different communities of microorganisms degrade MPs/NPs through their enzymes [112].
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Figure 9. Assimilation of MPs/NPs by microalgae in the marine environment.
Figure 9. Assimilation of MPs/NPs by microalgae in the marine environment.
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Table 1. Top 10 countries for scientific production related to MP/NP interactions with microorganisms and viruses.
Table 1. Top 10 countries for scientific production related to MP/NP interactions with microorganisms and viruses.
Country/Territory Documents Distribution
China28840.1
United States9414.3
Germany7211.0
Italy527.9
United Kingdom507.6
France345.2
Australia325.0
Spain304.6
Netherlands253.8
India243.7
Portugal182.7
Table 2. The top 10 publishing sources on MP/NP–microorganism–virus interactions.
Table 2. The top 10 publishing sources on MP/NP–microorganism–virus interactions.
Journal TitleNumber of DocumentsCite Score 2021 Journal’s Impact Factor 2021
Science of the Total Environment11314.110.753
Environmental Pollution7512.7 9.988
Journal of Hazardous Materials5314.714.224
Marine Pollution Bulletin389.27.001
Environmental Science and Technology3314.811.357
Chemosphere3011.78.943
Water Research2318.013.400
Ecotoxicology and Environmental Safety1710.17.129
Environment International1317.113.352
Bulletin of Environmental Contamination and Toxicology123.82.807
Table 3. The top 20 most cited documents (2010–2021).
Table 3. The top 20 most cited documents (2010–2021).
Total CitationsCite Score 2021Journal Impact Factor 2021Reference
133914.811.357[57]
100917.113.352[61]
70714.811.357[62]
66211.610.900[63]
65314.811.357[64]
64214.110.753[65]
61014.110.753[66]
53514.211.558[67]
45812.79.988[68]
42814.110.753[42]
41814.110.753[69]
3825.13.737[70]
3689.27.001[71]
3596.83.994[72]
34412.79.988[73]
33714.110.753[74]
3306.34.218[75]
31514.110.753[76]
30514.110.753[77]
30014.811.357[78]
Table 4. Biodegradation of microplastics using bacteria.
Table 4. Biodegradation of microplastics using bacteria.
BacteriaMatrixType of MPTreatment Time (Days)Degradation ConditionsDegradation ResultsRef.
Pseudomonas AKS31 Soil sedimentPUR and LDPE-It was grown on a film containing PU and LDPE.Esterase- and hydroxylase-mediated degradation in LDPE degradation.[113]
Bacillus gottheilii and Bacillus cereusMangrovesPE, PET, PP, and PS40Cultivated in a mineral medium containing MPs. The process followed the loss of weight of the MPs and cultured growth.Weight loss from 1.6% to 7.4%.[114]
Kordiimonas spp and Alcanivorax sppSoil sedimentHDPE and textile fibers4 Evaluation of textile residues degradation capacity of textile residues in the presence of light Higher degradation performance in the presence of light.[115]
Pseudomonas sp. and Rhodococcus sp. Soil sediment PP 40Bushnell haas agar (BH).PP weight loss up to 17.3% with changes in functional groups.[116]
Microbulbifer hydrolyticusMarine biotaLDPE30 Evaluation of potential degradation in the presence of lignin-rich marine cellulose.Surface oxidation and appearance of new functional groups such as hydroxyl.[117]
Pseudomonas sp.Worm intestinePPS10Evaluation of strains’ potential degradation of polystyrene in liquid carbon-free basal medium (LCFBM).6.4% PPS weight loss.[118]
Stenotrophomonas sp. and Achromobacter sp.Municipal waste dumpsLDPE100Air metabolism.Morphological and chemical changes from oxidation followed by dehydrogenation led to LDPE decomposition.[119]
Bacillus sp. and Rhodococcus sp. Soil sedimentPP40 Degradation capacity evaluation through the growth of the strain in samples of marine biota.Weight loss of 6.4% and 4%, respectively, with structural, morphological, and chemical changes.[101]
Rhodococcus ruber C208 Soil sedimentPE film30Report of an 8% degradation under incubation conditions.A 50% increase in biodegradation after adding mineral oil, improving colonization and biodegradation through the degradation of carbonyl groups.[120]
Bacillus sphericus Alt; Bacillus cereus BF20 Marine biotaLDPE film365A biodegradation percentage of 19% under in vitro conditions, pH 7,5, and at 30 °C.The starch treatment increased the biodegrading effect by 25%, observed by the decrease in carbonyl groups through FTIR.[121]
Anthrobacter sp. GMB5; Pseudomonas sp. GMB7 Marine biotaHDPE film30The biodegradation potential was evaluated under incubation conditions, registering a weight loss of HDPE of 12% associated with Arthrobacter sp. and 15% for Pseudomonas sp.The increase in the ester carbonyl bond index, keto carbonyl bond index, and vinyl bond index through FTIR-confirmed biodegradation.[122]
Pseudomonas sp. E4 Marine biotaLMWPE *80Evaluation of the biodegradation potential under incubation conditions at 37 °C.A biodegradation potential that varied between 4.9 and 28.6% was recorded, which mineralized all the LMWPE in CO2.[123]
* LMWPE—low-molecular-weight polyethylene.
Table 5. Biodegradation of microplastics using fungi.
Table 5. Biodegradation of microplastics using fungi.
FungiMP SourceMP TypeTreatment Time (Days)Degradation ConditionsDegradation ResultsRef.
Aspergillus tubingensis VRKPT1 and Aspergillus flavus VRKPT2Commercial HDPE30In vitro conditions based on weight and mass loss of MPs.The highest biodegradation of HDPE occurred with the biofilm formation of both A. flavus VRKPT2 and A. tubingensis VRKPT1. Likewise, there was a change in the morphology of the PE with the appearance of fissures and a rougher surface, suggesting the use of fungal extracellular enzymes. The biodegrading activity of the fungi was viable even 30 days after their inoculation on the PE.[128]
A. flavus PEDX3Intestinal contents of the wax moth Galleria mellonellaHDPE28In vitro conditions.HDPE degradation by FTIR * analysis demonstrated ether and carbonyl groups’ formation. The RT-PCR ** analysis showed the increased expression of two genes, AFLA_006190 and AFLA_053930, indicating the participation of these two enzymes in the degradation.[129]
Zalerion maritimumLaboratory conditionsPE 28In vitro conditions.PE pellets were the carbon source in a controlled growth medium of marine fungus. The biodegradation was evaluated based on the size and mass changes in pellets, as well as the chemical structural changes reflected in the FTIR and NMR *** spectroscopies.[124]
Pestalotiopsis microsporaShrubberyPUR15Anaerobic and aerobic conditions.The fungus degraded the PUR using it as a carbon source under aerobic and anaerobic conditions.[130]
Penicillium pinophilum—A. niger-LDPE940In the presence and absence of ethanol as co-subtraction.Observation of morphological and structural changes with a mineralization rate between 0.64% and 0.34% for P. pinophilum and 0.50% and 0.57% for A. niger.[127]
Penicillium (strainCCF3219)Synthesized in the laboratory with isotope markers (14C)PS112Biodegradation conditions were evaluated at pH 7.5 without external carbon supplies for 16 weeks.The fungus was able to mineralize PS, accelerated by applying a pretreatment with ozone, evidenced by the release of CO2 and by morphological changes, and a decrease in molecular weight.[131]
Phanerochaeté chrysosporium; Engyodontium albumMarine biotaPP film10Biodegradation stimulated with mixed pro-oxidant pretreatment and polypropylenes mixed with starch.The percentage of biodegradation varied between 9.42 and 18.8%, followed by thermogravimetric analysis (TGA).[132]
Chaetomium globosumMarine biotaPE-PUR-The biodegradation consisted of controlled cultures with moderate exposures to PE and PU to evaluate the resistance of the fungus.The degradation occurred by modifying the methyl groups adjacent to the PE and PU polymeric chains.[133]
Alternaria sp. PURDK2Marine biotaPUR film-A report of 27.5% biodegradation under in vitro conditions.The fungus secretes degrading enzymes in the polymer bonds, which generate the mineralization of the polymer.[134]
* FTIR—Fourier transform infrared spectroscopy; ** RT-PCR—real-time polymerase chain reaction; *** NMR—nuclear magnetic resonance.
Table 6. Effects of biodegradation of MPs through microalgae.
Table 6. Effects of biodegradation of MPs through microalgae.
MicroalgaeMP SourceMP TypeTreatment Time (Days)Degradation EffectsDegradation ConditionsDegradation ResultsRef.
Chlorella vulgaris-PVC *-35.26%In vitro conditionsStructural alterations on the aggregation surface, such as wrinkles and deterioration because of the deposition of microalgae.[140]
Chlorella pyrenoidosa-PS—DBP **-20%In vitro conditionsThere was a varied effect at different concentrations which increased the biodegrading effect as the concentration of PS—DBP increased.[141]
Anabaena spiroides—Navicula pupula—Scenedesmus dimorphusUrban water dischargesLDPE45 8.18%–4.4% and 3.74%, respectivelyIn vitro conditionsDegradation potential varies from growth conditions and unique carbon sources.[142]
Phaeodactylum, tricornutum MASCC-0025 and Chlorella sp. L38-PP, PE, and PET421.1%In vitro conditionsThe highest biodegradation activity occurs with P. tricornutum MASCC-0025, with 21.1%.[143]
Dunaliella salina-HDPE15-The degradation potential observed in laboratory bioreactorsChanges in the functional groups of the polymer until its mineralization exhibited biodegradation, followed by FTIR.[144]
Scenedesmus abundans PS-PMMA ***-PLA ****-Higher than 84%In vitro conditionsTotal suspended particles before and after treatment with microalgae determined the biodegradation.[145]
Oscillatoria prínceps, O. subbrevis, O. willei, O. amoena, O. vizagapatensis, O. earlei, O. Formosa, O. geitleriana, O. rubescenssewage waterPE, LDPE--In vitro conditionsThe biodegrading activity was investigated under controlled laboratory conditions, pH, and temperatures, to favor the activity of microalgae.[146]
* PVC—polyvinyl chloride; ** DBP—dibutyl phthalate; *** PMMA—poly(methyl methacrylate); **** PLA—polylactide.
Table 7. Biofilms and periphytic films for MP biodegradation.
Table 7. Biofilms and periphytic films for MP biodegradation.
Biofilm TypeMP TypeTreatment Time (Days)Biodegradation EfficiencyDegradation ConditionsDegradation ResultsRef.
Periphytic biofilmsPP, PE, and PET60Increased biodegradation by periphytic biofilms after adding glucose was recorded, which ranged from 9.52% to 18.02%, 5.95% to 14.02%, and from 13.24 to 19.72% for PP, PE, and PET, respectively.In vitro conditionsThere were pronounced morphological changes on the surfaces of MPs with distinct structures using SEM *, FTIR, and GPC **.[147]
Periphytic biofilmsPE20Biodegradation efficiency increased up to 12% in the presence of methane.In vitro conditionsThe maximum degradation occurs in a methane atmosphere. [150]
Biofilms PE, PET, PS, PP, PVC 70Discoloration of the polymers, followed by a reduction in size, was observed after two weeks of incubation.Laboratory anaerobic conditionsDegradation occurred through reductive dechlorination of the polychlorinated biphenyls adsorbed on MPs’ surfaces and a size reduction from 5.2% to 4.8%[151]
BiofilmsPE and PP15MPs’ morphological and structural changes.In vitro conditionsThe biodegradation activity was observed through the decrease in the hydrophobicity of the MPs, becoming more susceptible.[152]
* SEM—scanning electron microscope; ** GPC—gel permeation chromatography.
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Grande-Tovar, C.D.; Carrascal-Hernández, D.C.; Trilleras, J.; Mora, K.; Arana, V.A. Microplastics’ and Nanoplastics’ Interactions with Microorganisms: A Bibliometric Study. Sustainability 2022, 14, 14761. https://doi.org/10.3390/su142214761

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Grande-Tovar CD, Carrascal-Hernández DC, Trilleras J, Mora K, Arana VA. Microplastics’ and Nanoplastics’ Interactions with Microorganisms: A Bibliometric Study. Sustainability. 2022; 14(22):14761. https://doi.org/10.3390/su142214761

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Grande-Tovar, Carlos David, Domingo Cesar Carrascal-Hernández, Jorge Trilleras, Katelediana Mora, and Victoria A. Arana. 2022. "Microplastics’ and Nanoplastics’ Interactions with Microorganisms: A Bibliometric Study" Sustainability 14, no. 22: 14761. https://doi.org/10.3390/su142214761

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