Unraveling the nexus: Microplastics, antibiotics, and ARGs interactions, threats and control in aquaculture - A review.

In recent years, aquaculture has expanded rapidly to address food scarcity and provides high-quality aquatic products. However, this growth has led to the release of significant effluents, containing emerging contaminants like antibiotics, microplastics (MPs), and antibiotic resistance genes (ARGs). This study investigated the occurrence and interactions of these pollutants in aquaculture environment. Combined pollutants, such as MPs and coexisting adsorbents, were widespread and could include antibiotics, heavy metals, resistance genes, and pathogens. Elevated levels of chemical pollutants on MPs could lead to the emergence of resistance genes under selective pressure, facilitated by bacterial communities and horizontal gene transfer (HGT). MPs acted as vectors, transferring pollutants into the food web. Various technologies, including membrane technology, coagulation, and advanced oxidation, have been trialed for pollutants removal, each with its benefits and drawbacks. Future research should focus on ecologically friendly treatment technologies for emerging contaminants in aquaculture wastewater. This review provided insights into understanding and addressing newly developing toxins, aiming to develop integrated systems for effective aquaculture wastewater treatment.

Effects of polypropylene microplastics on carbon dioxide dynamics in intertidal mangrove sediments.

Microplastics (MPs) in soil can influence CO2 dynamics by altering organic carbon (OC) and microbial composition. Nevertheless, the fluctuation of CO2 response attributed to MPs in mangrove sediments is unclear. This study explores the impact of micro-sized polypropylene (mPP) particles on the carbon dynamics of intertidal mangrove sediments. In the high-tide level sediment, after 28 days, the cumulative CO2 levels for varying mPP dosages were as follows: 496.86 ± 2.07, 430.38 ± 3.84 and 447.09 ± 1.72 mg kg-1 for 0.1%, 1% and 10% (w/w) mPP, respectively. The CO2 emissions were found to be increased with a 0.1% (w/w) mPP level and decreased with 1% and 10% (w/w) mPP at high-tide level sediment, suggesting a tide level-specific dose dependence of the CO2 emission pattern in mangrove sediments. Overall, results indicated that the presence of mPP in mangrove sediments would potentially affect intertidal total CO2 storage under given experimental conditions.

Go for Economic Transformation and Development in China: Financial Development, Higher Education, and Green Technology Evolution.

Technology innovation is the key driving force in achieving economic transformation and development. Financial development and the expansion of higher education can promote technological progress primarily by easing financing constraints and improving the level of human capital. This study examines the impact of financial development and higher education expansion on green technology innovation. It conducts an empirical analysis by constructing a linear panel model and a nonlinear threshold model. The present study sample is based on the urban panel data of China from 2003-2019. (1) Financial development can significantly promote the expansion of higher education. (2) The expansion of higher education can improve energy and environment-based technological progress. (3) Financial development can both directly and indirectly promote green technology evolution by expanding higher education. The joint financial development and higher education expansion can significantly empower green technology innovation. (4) In the process of promoting green technology innovation, financial development has a non-linear influence on it, with higher education as the threshold. The effect of financial development on green technology innovation varies according to the degree of higher education. Based on these findings, we put forward policy proposals for green technology innovation to promote economic transformation and development in China.

Metformin facilitates anti-PD-L1 efficacy through the regulation of intestinal microbiota.

Metformin is a synthetic biguanide proven to have beneficial effects against various human diseases. Research has confirmed that metformin exerts its effects by regulating the composition of intestinal microbiota. The composition of intestinal microbiota influences the efficacy of anti-PD-L1 immunotherapy. We assume that the regulation of metformin on intestinal microbiota could enhance the therapeutic efficiency of anti-PD-L1 antibodies. In Lewis lung cancer-bearing C57BL/6J mice, we find that metformin enhances PD-L1 antibody efficacy mainly depending on the existence of gut microbiota, and metformin increases the anti-tumor immunity through modulation of intestinal microbiota and affects the integrity of the intestinal mucosa. Antibiotic depletion of gut microbiota abolished the combination efficacy of PD-L1 antibody and metformin, implying the significance of intestinal microbiota in metformin's antitumor action. Combining anti-PD-L1 antibody with metformin provoked tumor necrosis by causing increased CD8 T-cell infiltration and IFN-γ expression. In conclusion, metformin could be employed as a microecological controller to prompt antitumor immunity and increase the efficacy of anti-PD-L1 antibodies. Our study provided reliable evidence that metformin could be synergistically used with anti-PD-L1 antibody to enhance the anti-cancer effect.

Effect of biodegradable PBAT microplastics on the C and N accumulation of functional organic pools in tropical latosol.

Microplastics (MPs) pollution is becoming an emerging global stressor for soil ecosystems. However, studies on the impacts of biodegradable MPs on soil C sequestration have been mainly based on bulk C quantity, without considering the storage form of C, its persistency and N demand. To address this issue, the common poly (butylene adipate-co-terephthalate) (PBAT) was used as the model, and its effects on soil functional organic pools, including mineral-associated (MAOM), particulate (POM) and dissolved organic matter (DOM), were investigated from the novel coupled perspective of C and N stocks. After adding PBAT-MPs, the contents of soil POM-C, DOM-C, and MAOM-C were increased by 546.9 %-697.8 %, 54.2 %-90.3 %, and 13.7 %-18.9 %, respectively. Accordingly, the total C increased by 116.0 %-191.1 %. Structural equation modeling showed that soil C pools were regulated by PBAT input and microbial metabolism associated with C and N enzymes. Specifically, PBAT debris could be disguised as soil C to promote POM formation, which was the main pathway for C accumulation. Inversely, the MAOM-C and DOM-C formation was attributed to the PBAT microbial product and the selective consumption in DOM-N. Random forest model confirmed that N-activated (e.g., Nitrospirae) and PBAT-degrading bacteria (e.g., Gemmatinadetes) were important taxa for soil C accumulation, and the key enzymes were rhizopus oryzae lipas, invertase, and ammonia monooxygenase. The soil N accumulation was mainly related to the oligotrophic taxa (e.g., Chloroflexi and Ascomycota) associated with aggregate formation, decreasing the DOM-N by 46.9 %-84.3 %, but did not significantly change the total N storage and other N pools. Collectively, the findings highlight the urgency to control the nutrient imbalance risk of labile N loss and recalcitrant C enrichment in POM to avoid the depressed turnover rate of organic matter in MPs-polluted soil.

Effects of biodegradable and conventional microplastics on the intestine, intestinal community composition, and metabolic levels in tilapia (Oreochromis mossambicus).

Despite growing interest in conventional microplastics (CMPs) and their toxicological effects on aquatic species, little is known about biodegradable microplastics (BMPs) and their corresponding implications for aquatic life. Here, tilapia (Oreochromis mossambicus) were semi-statically exposed for 14 days to the bio-based plastic polylactic acid (PLA, 100 µg/L, 2.52 ± 0.46 µm) and the petroleum-based plastic polyvinyl chloride (PVC, 100 µg/L, 1.58 ± 0.36 µm). The results showed that ingesting the above two types of microplastics (MPs) led to oxidative stress in the fish gut, and damage to gut tissues and organelles, and PLA resulted in more obvious gut tissue edema than PVC. Furthermore, PLA caused increased levels of gut microbiota dysbiosis and a decrease in the abundance of the genus Cetobacterium, which is linked to vitamin B-12 synthesis, whereas an opposite relationship was observed on PVC. Metabolomic analysis indicated that PVC caused a significant down-regulation of orotic acid, co-metabolite of folic acid with vitamin B-12, while PLA did not affect orotic acid, which may lead to the accumulation of folic acid in fish. The joint analysis found that MPs disturbed gut metabolism homeostasis, implying that abnormal gut microbiota metabolites may be a key mechanism for MPs to induce tissue damage and oxidative stress in the gut. Overall, this study systematically illustrates the differential toxic effects of BMPs and CMPs on tilapia through gut microbiota and metabolite interactions, which will contribute to assessing the risks of BMPs to organismal health.

Heterogeneous aggregation between microplastics and microalgae: May provide new insights for microplastics removal.

Existing studies have shown that microplastics (MPs) as artificial surfaces can be colonized by plankton microorganisms. However, systematic research on exploring the aggregation formation process of MPs and microalgae is still lacking and particularly the influencing factors of aggregation remain to be elucidated. Therefore, this study investigated the heterogeneous aggregation process between various microalgal species (i.e., Chlorella vulgaris, Scenedesmus obliquus, Tetraselmis subcordiformis, Chaetoceros müelleri and Streptococcus westermani) and MPs (i.e., mPS and mPLA) with different sizes (i.e., 74 µm and 613 µm), concentrations (i.e., 0.1 g/L, 1 g/L and 2 g/L) and shapes (i.e., the particle and sheet). The results showed that microalgae can first attach to the holes or protrusions of MPs and highly accumulate in the local region, and then multi-layer aggregation can be formed subsequently. The aggregation degree between MPs and microalgae was closely related to the MPs shape and size, and was less related to the MPs concentration. The aggregation speed of small-sized MPs (e.g., 74 µm) was faster than the large-sized ones (e.g., 613 µm). The MPs in a shape of sheet were more obvious than those in particle on their aggregation with microalgae. The density of aggregates was increased compared with pristine MPs, which is related to the cell density and cell number of attached microalgae. For the same type of MPs, the aggregation degree for the tested microalgae was as follows: Scenedesmus obliquus > C. vulgaris > T. subcordiformis > C. müelleri > S. westermani. Meanwhile, MPs inhibited cell growth of microalgae, particularly under the circumstance of their aggregation, by limiting the gas and mass transfer between microalgal cells and the extracellular environment. The heterogeneous aggregation of MPs and microalgae may provide new ideas for treatment and controlling of MPs in the environment.

Microplastics leachate may play a more important role than microplastics in inhibiting microalga Chlorella vulgaris growth at cellular and molecular levels.

The leaching of microplastics (MPs) additives and their negative effects on aquatic organisms remain to be systematically elucidated. In this study, the toxicological effects of MPs leachate (micro-sized polyethylene (mPE) and micro-sized polyvinyl chloride (mPVC) acceleratedly leached by UVA for 15, 90, and 180 days in seawater) on microalga Chlorella vulgaris in terms of cell growth inhibition, oxidative stress, and transcriptomes were investigated. The leachate components of MPs aged for 90 days were further identified to elucidate the corresponding toxicity mechanisms of MPs on microalgal cells. The results revealed that both leachates of mPE and mPVC inhibited cell growth and increased oxidative stress in C. vulgaris, accompanied by a growth inhibition rate to microalgal cells of 4.0%-36.2% and 7.1%-48.2%, respectively. At the same mass concentration, the toxicological effects on C. vulgaris followed the order of mPVC leachate > mPE > mPE leachate > mPVC, whereas MPs leaching time indicated no change in MPs leaching toxicity. Furthermore, the gene functions of "translation, ribosomal structure and biogenesis" were mostly affected by MPs leachate. Compared to mPE leachate and pure MPs, the stronger inhibitory effects of mPVC leachate on microalgal cells may be attributed to the fact that more substances were leached from the polymer of mPVC, including Zn, farnesol isomer a, 2,6-di-tert-butyl-4-methylphenol, and acetyl castor oil methyl ester. In summary, this study provides a better understanding of the ecotoxicological influences of MPs and MPs leachate, and offers a warning on the ecological risk caused by plastic additives.

Recent developments in microplastic contaminated water treatment: Progress and prospects of carbon-based two-dimensional materials for membranes separation.

Micro (nano)plastics pollution is a noxious menace not only for mankind but also for marine life, as removing microplastics (MPs) is challenging due to their physiochemical properties, composition, and response toward salinity and pH. This review provides a detailed assessment of the MPs pollution in different water types, environmental implications, and corresponding treatment strategies. With the advancement in nanotechnology, mitigation strategies for aqueous pollution are seen, especially due to the fabrication of nanosheets/membranes mostly utilized as a filtration process. Two-dimensional (2D) materials are increasingly used for membranes due to their diverse structure, affinity, cost-effectiveness, and, most importantly, removal efficiency. The popular 2D materials used for membrane-based organic and inorganic pollutants from water mainly include graphene and MXenes however their effectiveness for MPs removal is still in its infancy. Albeit, the available literature asserts a 70- 99% success rate in micro/nano plastics removal achieved through membranes fabricated via graphene oxide (GO), reduced graphene oxide (rGO) and MXene membranes. This review examined existing membrane separation strategies for MPs removal, focusing on the structural properties of 2D materials, composite, and how they adsorb pollutants and underlying physicochemical mechanisms. Since MPs and other contaminants commonly coexist in the natural environment, a brief examination of the response of 2D membranes to MPs removal was also conducted. In addition, the influencing factors regulate MPs removal performance of membranes by impacting their two main operating routes (filtration and adsorption). Finally, significant limitations, research gaps, and future prospects of 2D material-based membranes for effectively removing MPs are also proposed. The conclusion is that the success of 2D material is strongly linked to the types, size of MPs, and characteristics of aqueous media. Future perspectives talk about the problems that need to be solved to get 2D material-based membranes out of the lab and onto the market.

Impacts of microplastic-petroleum pollution on nutrient uptake, growth, and antioxidative activity of Chlorella vulgaris.

As one of the emerging pollutants, microplastics (MPs; <5 mm) can interact with co-contaminants such as petroleum in marine aquatic systems, and their combined toxicity has not been fully investigated. Therefore, this study focused on pollutants such as micro-sized polyethylene (mPE) and petroleum, aiming to explore their single and combined toxicities to microalga Chlorella vulgaris in terms of the cell growth, antioxidative enzymes, and nutrients utilization. The results showed that the MPs alone (particle sizes (i.e., 13, 165, 550 µm), concentrations (i.e., 0.01, 0.1, and 1 g/L), and aging degrees (i.e., aged for 0 d and 90 d under UVA)), and petroleum alone (5% water accommodated fraction, WAF), and their combinations (i.e., 5% WAF + 165 µm-0.1 g/L-aged 0 d mPE, 5% WAF + 165 µm-0.1 g/L-aged 90 d mPE) all posed toxicities risk to C. vulgaris, following an increase in oxidative stress. The cellular utilization of elements such as Fe, Si, Ca, and Mg was inhibited, whereas the uptake of Mn, NO3--N, and PO43--P increased as compared to the control experiments. Furthermore, the relationship between nutrients and growth indicators was analyzed using a structural equation model. The results indicated that Fe and Mn directly affected the indirect NO3--N absorption by C. vulgaris, which indirectly affected the dry cell weight (DCW) of the microalgae. The path coefficient of Fe and Mn affecting nitrate was 0.399 and 0.388, respectively. The absorption of N was the key step for C. vulgaris resist stress. This study provides a novel analysis of the effects of MPs on the growth of microalgae from the perspective of nutrient elements, thereby providing a useful basis for further exploration of the associated mechanisms.

Elucidating the negatively influential and potentially toxic mechanism of single and combined micro-sized polyethylene and petroleum to Chlorella vulgaris at the cellular and molecular levels.

Although microplastics (MPs; <5 mm) may interact with co-contaminants (e.g., petroleum) in marine aquatic systems, little is known about their combined toxicity. Therefore, this study explored the toxicities and their mechanisms of micro-sized polyethylene (mPE) and their combination with petroleum to Chlorella vulgaris. The single MPs at various particle sizes, concentrations, and aging degree, single petroleum, and their combinations, were found to pose toxicities to C. vulgaris. This study also found the microcosm's microbial diversity changed. The microbial communities in the C. vulgaris biotopes were altered under exposure to mPE and petroleum, and were disturbed by external factors such as MPs particle size, concentration, aging time, and the combination with petroleum. Furthermore, as compared with the toxicity of petroleum on microalgal transcriptional function, mPE caused less toxic to C. vulgaris, and only impact the posttranslational modification, protein turnover, and signal transduction processes. Most importantly, mPE reduced petroleum toxicity in C. vulgaris via regulating the ABC transporter, eukaryotic ribosome synthesis, and the citrate cycle metabolic pathways. Overall, our findings could fundamentally provide insights into the joint ecotoxicological effects of MPs and petroleum, and highlight the potential risks of co-exsiting pollutants.

Secondary microplastics formation and colonized microorganisms on the surface of conventional and degradable plastic granules during long-term UV aging in various environmental media.

Recently, biodegradable plastics (BPs) as an alternative of conventional plastics have been widely advocated and applied. However, there is still a large research gap between the formation of secondary microplastics (MPs) and colonized microorganisms on their surface under long-term aging in different environments. In this study, the generation of secondary MPs and the formation of surface biofilms on the micro-sized (3-5 mm) biodegradable plastic poly (butyleneadipate-co-terephthalate) (BP-PBAT) and conventional plastic polyvinyl chloride (CP-PVC) under long-term UV aging was investigated. The results showed that hundreds and even thousands of MPs (185.53 ± 85.73 items/g - 1473.27 ± 143.67 items/g) were generated by BP-PBAT and CP-PVC after aged for 90 days, and the abundance of MPs produced by BP-PBAT was significantly higher than that of CP-PVC. Moreover, the α diversities and detected OTU number of biofilm communities formed on MPs increased with MPs-aging. The genes related to the formation of biofilms was significantly expressed on aged MPs and the genes related to human pathogens and diseases were also detected in enriching on MPs surface. Overall, BPs may lead to greater ecological risks as it releases thousands of secondary MPs after being aged, and their environmental behavior needs to be further explored.

Aging of biodegradable blended plastic generates microplastics and attached bacterial communities in air and aqueous environments.

The use of biodegradable plastics (BPs) has been widely promoted in recent years, but before their complete degradation, the phase of microplastics (MPs) is inevitable. However, little information concerning the production of MPs from blended polymers is available. This study aimed to explore the characteristics of MPs produced from blended plastics and the development of biofilms on plastic surfaces under long-term aging. Here, three blended materials (i.e., PBAT (53%)+PLA (10%)+Starch (20%), PBAT (80%)+Starch (20%), HDPE (60%)+CaCO3 (40%)) were aged for 90 days in air, deionized (DI) water and seawater. The results showed massive production of MPs (9653 ± 3920-20,348 ± 5857 items/g) from blended plastics accompanied by a large quantity of flocculent substances during 90 days aging period. Furthermore, the richness of bacteria communities on hydrophobic plastics (i.e., PBAT (53%)+PLA (10%)+Starch (20%), PBAT (80%)+Starch (20%)) was higher than hydrophilic plastics (i.e., HDPE (60%)+CaCO3 (40%)), and bacterial communities attached to blended plastics exhibited significantly variation with aging times. Overall, promoting the marketable application of blended plastics is risky if their environmental behavior is not effectively addressed.

Polyethylene scaffold net and synthetic grass fragmentation: a source of microplastics in the atmosphere?

Microplastics (MPs) implications in the atmosphere are of current global concern. Currently, there is a growing interest regarding source appointment, fate, level of toxicity, and exposure intensity of ambient air MPs. Recent data suggest that polyethylene (PE) dominates ambient MPs in China's megacities. Albeit understanding of PE sources is limited and restricted to typical sources polluting terrestrial and marine environments. However, the air is a distinct environmental component and may have some separate pollution sources as well as the relative contribution of different sources could also contrast in different environments. Urbanization and fast construction activity resulting from increased economic growth in these places might be a potential source of ambient PE. Recently, the use of scaffold netting on construction sites and synthetic grass as land covering sheets has been on the rise. Generally, these PE items are often inferior and composed of recycled material, making them more prone to degradation. Also, because these items were continually exposed to open air, there is a considerable risk of fragmentation and atmospheric mixing. Therefore, unchecked and excessive usage of these materials can be risky. Here, PE's physical and chemical characteristics, transport and health risks in urban air are discussed here.

Fate of microplastics in deep-sea sediments and its influencing factors: Evidence from the Eastern Indian Ocean.

Although microplastics (MPs) are known to be found in global oceans, their influencing factors and abundance in the deep sea remain largely unknown. Twenty-six surface sediment samples were collected in the deep basin of the Eastern Indian Ocean (EIO). This study showed that MPs abundance ranged from 30.30 particles/kg to 701.7 particles/kg, with an average of 170.5 ± 140.2 particles/kg. The MPs found in the sediment of the EIO mainly contain fragments and fibers, which account for 47.5% and 45.6%. The MPs were measured in a size range of 44-5000 µm, and the most frequently detected MPs in size of 200-500 µm. MPs were in various compositions, but most of them were found in rayon (62.2%) and polyester (25.7%). The spatial distribution of MPs in the sediments shows a decreasing trend from nearshore to the open sea. In the Bay of Bengal (BOB) and the coast of Sri Lanka (COSL), the abundance of MPs was relatively high, indicating that the spatial distribution of MPs is affected by land source input, river input, and anthropogenic activities. Principal component analysis indicated daily commodities and packaging applications/fishing accounted for 36.9% and 12.9% of the MPs occurrence in the EIO, respectively. Average MPs diversity indices for the BOB (0.87 ± 0.38), the COSL (0.64 ± 0.56), and the Eastern Indian Ocean Basin (EIOB) (0.60 ± 0.24) revealed the BOB had the most complicated MPs sources. In addition, we found that the abundance of MPs has no significant effect on organic carbon and sediment grain size. This study is the first report of MPs detection in the deep-sea sediment in the EIO and can provide a baseline of MPs pollution in this area.

Biodegradable and conventional microplastics posed similar toxicity to marine algae Chlorella vulgaris.

It has been demonstrated that some conventional microplastics (CMPs) have toxicities to organisms, however, whether biodegradable microplastics (BMPs) have similar potential risks to marine ecosystems remains to be elucidated. Therefore, this study aimed to investigate i) the effects of CMPs (i. e., micro-sized polyethylene (mPE) and polyamide (mPA)) on marine algae Chlorella vulgaris; and ii) the potential effects of BMPs (i.e., micro-sized polylactic acid (mPLA) and polybutylene succinate (mPBS)) on C. vulgaris. The results showed that either CMPs or BMPs inhibited the growth of microalgae compared with the control. The maximum inhibition ratio of the four types of MPs on C. vulgaris were 47.24% (mPE, 1 000 mg/L), 40.36% (mPA, 100 mg/L), 47.95% (mPLA, 100 mg/L) and 34.25% (mPBS, 100 mg/L), respectively. Among them, mPLA showed the strongest inhibitory effect on the growth of C. vulgaris. Interestingly, the MPs can stimulate the contents of pigments (e.g., chlorophyll a, chlorophyll b, and carotenoid), which may be acted as cellular defense to the stress induced by MPs. The results also showed that MPs stimulated the production of EPS. Under the investigated condition, the strongest inhibition on C. vulgaris was induced by mPLA, and followed by mPE, mPA, and mPBS. It was found that the factors such as the physicochemical properties of MPs (e.g., shading effect, the roughness of surface, the increase in potential), the chemical changes (i.e., the release of additives, the increase of oxidative stress) contributed to the inhibitory effects of MPs on microalgae, but the deciding factor remains to be further systematically explored.

Occurrence and spatial distribution of microplastics, and their correlation with petroleum in coastal waters of Hainan Island, China.

In this study, the distribution, abundance, morphology, and composition of microplastics (MPs) in surface seawater and sediment of Hainan Island were systematically investigated. Seawater and sediment samples were collected from six functional zones, including harbor, industrial district, sparsely populated area, tourist area, residential area, and aquaculture area. The abundance of MPs in seawater was 0.46-19.32 items/L, with an average of 2.59 ± 0.43 items/L, which were similar to those detected in the South China Sea (e.g., Nansha (1.25-3.20 items/L) and Xisha (2.57 ± 1.78 items/L)). The highest level was detected in Qinglan Bay Estuary, and the lowest was in Sanya West Island. The abundance of MPs in sediment was 41.18-750.63 items/kg, with an average of 372.47 ± 62.10 items/kg; the highest concentration was detected at Tanmen Port, and the lowest was in Lingao sea area. It was detected that the MPs with smaller size exhibited a higher concentration in seawater. MPs were commonly black and white, and predominantly linear and fragmented in shape. Polyethylene terephthalate (PET) was the dominant polymer, which might be derived from laundry wastewater. The petroleum concentration was 0.02-0.21 mg/L in the investigated area, with harbors being the most severely polluted areas. Furthermore, this study also found that MPs pollution was positively correlated with petroleum in seawater, indicating similarities between MPs and petroleum-based sources of pollution. This study identifies the contamination and characteristics of MPs and their correlation with petroleum in Hainan Island, the biggest island in the South China Sea, providing important data for further research on protecting marine ecosystems.

Sorption behaviors of petroleum on micro-sized polyethylene aging for different time in seawater.

Microplastics (MPs; <5 mm) and oil pollution have been receiving global attention. To date, the adsorption mechanism of petroleum by MPs is largely unknown. This study investigated the adsorption of petroleum on micro-sized polyethylene (mPE) undergoing aging (days 0, 15, 30, 90 and 180). The petroleum adsorption capacity of mPE was further assessed at varying pH (2, 5, 7.32, 10 and 12), temperature (4, 15, 25, 45 and 65 °C) and in presence of coexisting pollutants (Cu, bisphenol A (BPA) and petroleum). The results indicated that the adsorption capacity of mPE increased with the prolonged aging time and smaller-sized particles, while the adsorption capacity of the 550 and 165 µm mPE undergoing aging increased by 12.7%-50.9% and 22.1%-63.9%, respectively. The adsorption kinetics and isotherm model of mPE on petroleum were well fitted by pseudo-second order, intraparticle diffusion, Freundlich and Langmuir models, showing the sorption behavior was controlled by the diffusion of pores, liquid film diffusion, and surface adsorption. The petroleum adsorption capacity of mPE was predominant affected by surface roughness, specific surface area, hydrophobicity, oxidation functional groups, adsorption sites, hydrogen bonds, while zeta potential and crystallinity may not be the crucial factors. Likewise, temperature and pH may influence the characteristics of petroleum, and further result in a decreasing adsorption capacity of mPE to petroleum. The highest adsorption capacity of mPE to petroleum was reached at pH 7.32 and 25 °C. The coexisting Cu, BPA and petroleum competed for adsorption sites on the surface of mPE. These findings could fundamentally provide new insights for environmental risk assessment of MPs, particularly for the specific location like harbor which is commonly rich in MPs and petroleum simultaneously.

Addition of biodegradable microplastics alters the quantity and chemodiversity of dissolved organic matter in latosol.

Dissolved organic matter (DOM) chemodiversity plays an important role in regulating nutrient cycles and contaminant behavior in soil. However, how biodegradable microplastic (MPs) affect the DOM chemodiversity is still unknown, although developing biodegradable plastics are regarded as a promising strategy to minimize the risks of MPs residues in soil. Here, with the common poly (butylene adipate-co-terephthalate) (PBAT) as the model, the molecular effect of biodegradable MPs on soil DOM was explored by adding 0%, 5% and 10% (w/w) of PBAT to tropical latosol, respectively. The results showed that PBAT addition increased microbial activity and exoenzyme activity (e.g., rhizopus oryzae lipase, invertase and cellulose). As a result, the quantity and chemodiversity of soil DOM were changed. The multispectroscopic characterization showed that PBAT addition significantly increased the DOC molecules in soil, including condensed aromatic-like substances and carbohydrates. In contrast, the TDN molecules with high bioavailability and low aromaticity, such as amino acids, were decreased. The multivariate statistical analysis indicated that there were three mechanisms that drove the shift in DOM chemodiversity. Firstly, the degradation of PBAT by rhizopus oryzae lipase facilitated the release of exogenous aromatic molecules. Secondly, PBAT decomposition stimulated the selective consumption of native N-rich molecules by soil microbes. Thirdly, PBAT accelerated the enzymatic transformation of native aliphatic CHx and cellulose toward humic substances. In addition, concentration effect was also observed in the study that high-concentration PBAT were more likely to trigger the molecular shift in DOM chemodiversity. These findings provided a new insight into the impact of biodegradable MPs on soil DOM chemodiversity at molecular level, which will be beneficial to understanding the fate and biochemical reactivity of DOM in MPs-polluted soil.

Microplastics aged in various environmental media exhibited strong sorption to heavy metals in seawater.

To date, the degradation of microplastics (MPs; <5 mm) in different environments, particularly their adsorption characteristics for coexisted metal pollutants remains to be elucidated. Thus, this study investigated the effects of aging MPs, including polyamide (mPA), polyethylene terephthalate (mPET), polystyrene (mPS), and polyvinyl chloride (mPVC) for 3 months under UVA irradiation in four environmental media (air, seawater, sand, and soil) and adsorption of heavy metals (Cu, Cd) onto seawater-aged mPS and mPVC. The results showed that surface morphological changes, including cracks, oxidized particles, and wrinkles, appeared on aged MPs. The heavy metal adsorption capacity decreased in the order aged mPVC > aged mPS > unaged mPS > unaged mPVC, and the Cu2+ and Cd2+ ions competed for active adsorption sites on the MPs surfaces. Overall, the aging environment affected the physical and chemical properties of MPs and the aging of MPs enhanced their adsorption of coexisting metals tested.