Journal of Oceanology and Limnology   2022, Vol. 40 issue(1): 163-172     PDF       
http://dx.doi.org/10.1007/s00343-021-0465-7
Institute of Oceanology, Chinese Academy of Sciences
0

Article Information

ZHANG Kangning, LIANG Junhua, LIU Tao, LI Qingjie, ZHU Mingliang, ZHENG Shan, SUN Xiaoxia
Abundance and characteristics of microplastics in shellfish from Jiaozhou Bay, China
Journal of Oceanology and Limnology, 40(1): 163-172
http://dx.doi.org/10.1007/s00343-021-0465-7

Article History

Received Dec. 4, 2020
accepted in principle Jan. 10, 2021
accepted for publication Feb. 23, 2021
Abundance and characteristics of microplastics in shellfish from Jiaozhou Bay, China
Kangning ZHANG1,4, Junhua LIANG1,2, Tao LIU1,4, Qingjie LI1, Mingliang ZHU1,2, Shan ZHENG1,2, Xiaoxia SUN1,2,3,4     
1 Jiaozhou Bay National Marine Ecosystem Research Station, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China;
2 Laboratory for Marine Ecology and Environmental Science, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao 266237, China;
3 Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China;
4 University of Chinese Academy of Sciences, Beijing 100049, China
Abstract: As an emerging pollutant, the presence of microplastics in marine organisms has been concerned increasingly. Shellfish, which are both economically and ecologically important, are of particular concern. In this study, we investigated the microplastic pollution in wild and farmed oysters (Crassostrea gigas) and clams (Ruditapes philippinarum) in the Jiaozhou Bay, China, for the first time. We found the microplastic pollution in shellfish in Jiaozhou Bay was at a moderate level. The abundance of microplastics in shellfish ranged from 0.16 to 12.09 items/g (wet weight, ww) or 1 to 9 items/ind. The average abundance of the ingested microplastics was 1.21 items/g (or 2.17 items/ind.) in all shellfish, 1.51 items/g (or 2.00 items/ind.) in clams and 0.92 items/g (or 2.34 items/ind.) in oysters. The abundance of microplastics in clams was significantly higher than that in oysters. Most microplastics (92.97%) were fibers, followed by fragments. The predominant color of the microplastics was black (42.97%), followed by blue, transparent, and red. Cellophane and polyethylene terephthalate (PET) dominated the microplastic composition. According to shellfish consumption, it can be inferred that the average microplastic consumption through Chinese diet is 1.27×103 items per capita per year.
Keywords: microplastics    bivalves    Jiaozhou Bay    risk assessment    
1 INTRODUCTION

In recent years, microplastics (plastic debris less than 5 mm in diameter) (Arthur et al., 2009), as emerging pollutants, have become a research hotspot in the fields of ecology and environmental science globally. Microplastics can persist in the ocean due to their stable chemical properties and long degradation times (Cole et al., 2011). They have been found in an increasing number of organisms, such as zooplankton (Desforges et al., 2015), benthos (polychaetes, bivalves, and crustaceans) (Murray and Cowie, 2011; Goldstein and Goodwin, 2013; Lusher, 2015; van Cauwenberghe et al., 2015a), nekton (pelagic and demersal fish) (Lusher et al., 2013), seabirds (Tourinho et al., 2010; Provencher et al., 2014), and large marine mammals (Besseling et al., 2015). There is some evidence to suggest adverse impacts on the ocean ecosystem from microplastics ingested by marine organisms. In addition to physical damage to the intestinal wall caused by microplastics, there are also chemical impacts. Microplastics are not only a source of marine pollutants but also carriers of deleterious pollutants. In addition to the release of plasticizers and other harmful substances (Hirai et al., 2011), microplastics can accumulate organic pollutants, heavy metals or pathogenic microorganisms from the surrounding environment and transfer them along the food chain in the ocean (Mato et al., 2001; Masó et al., 2003). With the expansion of this research area, scholars have discovered that the hazard posed by microplastics to marine ecosystems may be far higher than those posed by visible plastics may. Density microplastics settle naturally in seawater. Adherent biota can alter the microplastic density, causing them to sink into the seafloor (van Cauwenberghe et al., 2015b). Therefore, deposit feeders are particularly vulnerable to plastic debris, but research on deposit feeders is limited.

Shellfish, typical deposit feeders in the ocean, are ecologically important. They are key players in the food chain, preying on plankton, which are food sources for many large organisms. Therefore, bivalves are often used in experiments as model organisms for studying the ecological hazards of microplastics. Particles ingested by mistake can be transferred to and accumulate in tissues and organs and affect physiological activity. The enzyme activity, growth, development, and reproduction of bivalves have been shown to be impacted by such particles. Sussarellu et al. (2016) indicated that oyster reproduction and feeding behaviors can be affected by exposure to polystyrene microplastics at a concentration of 0.023 mg/L. A strong inflammatory response of blue mussels (Mytilus edulis) after exposure to industrial high-density polyethylene (HDPE) particles was observed by von Moos et al. (2012). Although the concentration of microplastics in those studies was far higher than that in natural habitats and the biomagnification up the food chain and effect on humans from consumption are unclear, cautious consumption is still warranted.

In addition to their ecological value, many shellfish are economically important. With increasing demand and consumption, shellfish has become a major source of food for humans worldwide. However, because of marine pollution, the quality and safety of shellfish products have become serious problems. Walkinshaw et al. (2020) commented that lower-trophic-level organisms may have the highest risk of contamination, and microplastic pollution in shellfish cannot be ignored. Oysters and clams are common filter-feeding shellfish with weak food selectivity and may have different microplastic feeding abilities in different growth environments. Aquaculture, which is heavily influenced by human activity, may have an impact on microplastic ingestion by biota. A few studies comparing microplastic concentrations between cultured and wild shellfish have been carried out (Davidson and Dudas, 2016), most of which focused on clams and mussels, while research on oysters is limited. Many knowledge gaps remain and further research is needed.

Jiaozhou Bay is a typical semi-closed bay located in the south of Shandong Peninsula, China. With high coastal population density along the bank, more than 10 rivers flow into Jiaozhou Bay. As an important area for shellfish cultivation, the shellfish culture area in Jiaozhou Bay accounts for 71.6% of the total aquaculture area, and Ruditapes philippinarum is the main breeding species, accounting for 93.2% of the shellfish culture area (Fan and Liu, 2016).

In this study, we collected two shellfish commonly consumed by humans, oyster (Crassostrea gigas) and clam (Ruditapes philippinarum), from wild and aquaculture settings in Jiaozhou Bay. Our aims were to determine the accumulation abundance and characteristics of microplastics in common shellfish for the first time in Jiaozhou Bay, determine whether there are differences in the microplastics in shellfish between cultured and wild modes of life, and assess preliminarily the microplastic levels in shellfish and potential risks of consumption.

2 MATERIAL AND METHOD 2.1 Sample collection

Two groups of samples were collected of C. gigas and R. philippinarum in wild and farmed conditions respectively in November 2018. Figure 1 shows the sampling stations and the shellfish cultivation area. Samples were taken at random from 3 parallel stations for each species of each growth pattern. Farmed shellfish were cultured through bottom culture (including artificial seed release and sea ranching) technologies. Marine aquaculture in Jiaozhou Bay was restricted, and the aquaculture area was planned by the government. Cultured species were sampled with a grab dredger. As Fig. 1 shows, cultured oysters were sampled at Stations A, B, and C. Farmed clams were collected from the Hongdao aquaculture area (Stations J, K, and L), a highly productive clam culture area. Wild shellfish grow naturally in the sea without human intervention. Wild oysters were collected with small iron shovels on the rocks away from the shore (Stations H, I, and G). Wild clams were sampled with a grab dredger at Stations D, E, and F. The shellfish were wrapped by aluminum foil and stored at -20 ℃ for future analysis.

Fig.1 Map of Jiaozhou Bay showing the sampling stations A–L. symbols with different shapes represent different samples. The orange area represents the oyster cultivation area. The yellow area represents the clam cultivation area. The layout of the cultivation area referred to data from the Qingdao Municipal Marine Development Bureau in China. (http://ocean.qingdao.gov.cn/n12479801/n31588797/index_8.html).
2.2 Microplastic extraction and identification

Thirty-three wild oysters, 33 farmed oysters, 20 wild clams, and 34 farmed clams were analyzed in this study. After complete thawing, the length, height, and width of the shell were measured with a Vernier caliper (0.02 mm), and the wet weight of soft tissue was weighed with a high-precision electronic balance (0.001 g).

The microplastic extraction protocol was adapted from Dehaut et al. (2016). The soft tissue of the mollusks was degraded with 10% KOH solution in flasks placed in a water bath with oscillation at 60 ℃ for 24 h. The conical flasks were spaced evenly in the oscillator as far from one another as possible to ensure sufficient oscillation. The degradation solution was filtered (2.7-μm glass fiber filter, GF/D Whatman), and the equipment was washed with pure water to reduce the loss of microplastics. After filtration, the filters were air-dried and stored in glass petri dishes away from light.

The microplastics were identified, counted, screened, and photographed under a stereoscopic microscope (Stemi SV11, Zeiss, Shanghai, China). To select potential targets, microplastics were analyzed according to shape, color, particle size, and other characteristics. Particle size was determined by measuring the longest length of the microplastics with camera software (Carl Zeiss AxioVision 4.9.1SP2).

All suspected microplastics were identified by a Nicolet iN 10 MX Fourier transform infrared (μFTIR) system (Thermo Fisher, USA). The spectral range was set at 4 000–675 cm-1 in transmittance mode. Spectra were obtained by analysis with OMNIC 8.2 and compared with the spectral library in the software. Finally, the composition of the microplastics was determined from the types of functional groups determined from the spectra and matching degrees to the library spectra.

2.3 Quality control

During the experiment, precautions were taken to prevent airborne plastic contamination by exposure. All the experimental instruments were cleaned with pure water and dried before use. The glass petri dishes used to store the filters were heated in a muffle furnace at 450 ℃ for 4 h, and all reagents, including pure water, were filtered before use. During processing, doors and windows were closed, and the operator moved as little as possible to avoid microplastic interference caused by airflow. In addition, three groups of blank controls were analyzed with each batch of samples for correction.

2.4 Data analysis and statistics

The data were collected and analyzed according to the identification results. For statistical convenience, the particle was assigned to one of several distinct size classes at 500-μm intervals. The abundance of ingested microplastics (items/ind. or items/g) and the proportion of individuals with microplastics were calculated. Data management and statistical analysis were performed using SPSS 23.0. According to the results of the Kolmogorov-Smirnov test, the abundance of microplastics did not follow a normal distribution. Therefore, a nonparametric method (Mann-Whitney test) was used to analyze the differences (α=0.05) between various samples.

3 RESULT 3.1 Biological characteristics of shellfish and ingestion of microplastics

Table 1 lists the biological characteristics, the frequency of individual organisms that ingested microplastics and the ingestion abundance of each sample in detail. Microplastics were observed in both groups of C. gigas and R. philippinarum in Jiaozhou Bay. Combining wild and farmed individuals, the abundance of microplastics in oysters was 2.34± 1.80 items/ind. or 0.92±0.80 items/g (wet weight, ww) and that in clams was 2.00±1.99 items/ind. or 1.51±1.27 items/g (ww). Nonparametric analysis revealed that there were no significant differences in the mean abundance of microplastics (items/g) between the different sources of the same species (P1=0.59 for oyster and P2=0.50 for clam). Overall, the abundance of microplastics in shellfish in Jiaozhou Bay ranged from 0.16 to 12.09 items/g (ww) or 1 to 9 items/ind., with an average of 1.21±1.52 items/g (ww) or 2.17±1.57 items/ind.

Table 1 Biometric characteristics and microplastic ingestion for each group of samples
3.2 Chemical composition of microplastics in shellfish

Among the microplastics ingested by the shellfish of Jiaozhou Bay, cellophane was dominant in the polymer composition (48.48%). Polyethylene terephthalate (PET) (20.71%) and polymerized oxidized organic materials (10.61%) also accounted for considerable proportions, and these three polymers were all found in each sample group. Cellulose (5.56%) and rayon (4.55%) were also common. However, there was a higher frequency of cellulose than cellophane in the wild clams. Armeen was found in the wild clams only. The proportions of microplastics in each sample are shown in Fig. 2.

Fig.2 The polymer types in shellfish from Jiaozhou Bay
3.3 Color of the microplastics

Black (42.97%) microplastics accounted for a large proportion of the microplastics ingested by shellfish in Jiaozhou Bay. In addition, blue (20.31%), transparent (16.41%), and red (14.84%) microplastics were also common. Yellow and white were rare in Jiaozhou Bay. However, it can be clearly observed that some of the original bright colors of the plastics faded. There were some differences in the proportions of different colors among the different groups, and the color proportions in each group are shown in Fig. 3.

Fig.3 Different color proportions of microplastics in shellfish from Jiaozhou Bay
3.4 Microplastic of limited shape in shellfish

The microplastics in the shellfish from Jiaozhou Bay were present only as fibers and fragments (Fig. 4); no other shapes (bead or film) were found. Fibers dominated the shapes in each group and accounted for 92.97% of the total microplastics, while fragments accounted for only 7.03% (see Fig. 5 for the proportions of each shape in each sample group).

Fig.4 Photographs of microplastics under a stereoscopic microscope
Fig.5 The shapes of microplastics in shellfish from Jiaozhou Bay
3.5 Size characteristics of the microplastics detected

The sizes of the microplastics detected in the shellfish ranged from 15 to 8 201 μm in length. The proportions of microplastics with different lengths are shown in Fig. 6, which reveals that microplastics with lengths < 500 μm accounted for the largest proportion (37.50%), and the proportion decreased as the size increased. Figure 7 shows the size proportions for each sample group.

Fig.6 Total distribution of microplastic sizes in shellfish from Jiaozhou Bay
Fig.7 Distribution of microplastic sizes in shellfish from Jiaozhou Bay
4 DISCUSSION 4.1 The abundance of microplastics in shellfish from Jiaozhou Bay

The abundance of microplastics in wild shellfish was compared with that in farmed shellfish through the Mann-Whitney test. There was no significant difference in the abundance of microplastics (items/g) between groups of the same species with different growth modes (P1=0.50 for clams and P2=0.59 for oysters). That is, the growth patterns of shellfish had no significant effect on their ingestion of microplastics. Most studies on microplastics selected mussels as the object of study, and similar results have been reported by de Witte et al. (2014) and Birnstiel et al. (2019). In contrast, de Witte et al. (2014) and Li et al. (2016) noted significant differences in microplastic abundance between wild and farmed mussels. The long distance between the sampling areas for the mussels with different sources may have been the cause of these differences. However, Davidson and Dudas (2016) and Murphy (2018) studied clams (Venerupis philippinarum) with different growth patterns and found that the amount of microplastics in the body did not differ much. Our findings support these results very well. Research on oysters is limited. Phuong et al. (2018) found no significant differences between the two modes of life of Pacific oyster (C. gigas), which is similar to our result. Therefore, shellfish grown in different conditions contain the same level of microplastic pollution. When evaluating the safety of shellfish products for consumption, from the perspective of microplastics, the influence of the growth pattern can be ignored.

The abundance of microplastics in oysters was 2.34±1.80 items/ind. or 0.92±0.80 items/g (ww) and that in clams was 2.00±1.99 items/ind. or 1.51± 1.27 items/g (ww). Oysters are larger and contain significantly more soft tissue than clams at the individual level. In addition, according to the microplastic distribution, the intake of microplastics by oysters and clams is similar. Therefore, the unit should be items/g when comparing abundances. In this unit, the abundance of microplastics in clams is significantly greater than that in oysters, which has also been reported by Cho et al. (2019). The results show that clams are more likely to ingest microplastic particles. This indicates that different shellfish have different ingestion capacities for microplastics in particle selection. This may be due to their different habitats. Oysters are usually sessile on reefs and remain still, while clams tend to drift with currents and move over a wider range. The limited habitat of oysters may limit their microplastic ingestion ability.

The abundance of microplastics in oysters (C. gigas) in the present study was higher than that in France (Phuong et al., 2018), South Korea (Cho et al., 2019), the USA (Rochman et al., 2015), and other areas in China (Li et al., 2018; Ran et al., 2018) but lower than that in the study by Murphy (2018) in Canada (Table 2). The microplastic abundance in clams (R. philippinarum) was also higher than that in South Korea (Cho et al., 2019) and Canada (Davidson and Dudas, 2016). Regarding both species, the abundance of microplastics in shellfish in Jiaozhou Bay is higher than that in South Korea (Cho et al., 2019) and Iran (Naji et al., 2018) but lower than that in Shanghai, China (Li et al., 2015). This indicates that the microplastic pollution in Jiaozhou Bay is at a moderate level compared with those in other areas where monitoring results are available. The numerous rivers flowing into Jiaozhou Bay, dense residential activities and considerable human activity may have contributed to the pollution in the region. Although the obtained results are not very concerning now, they still need to be taken seriously, and the lack of standardization of the sampling methods in published studies prevents intercomparison of the relative microplastic abundance in organisms worldwide.

Table 2 Comparison of the results of this study with those of other studies
4.2 Characteristics of microplastics in shellfish from Jiaozhou Bay

Cellophane accounted for a large proportion of the detected microplastics. The microplastic composition can be used to trace the microplastic origin. Cellophane is a colorless transparent film often used for packaging, which may explain the presence of transparent microplastics. The content of PET microplastics may be related to the discharge of laundry wastewater (Napper and Thompson, 2016) and packaging (Sobhani et al., 2020) into seawater. Cellulose made up more than half of the microplastics in the bodies of wild clams and was also found extensively in other studies (Scott et al., 2019; Bridson et al., 2020). The frequencies of microplastics composed of polypropylene (PP) and polyethylene (PE) in shellfish were very low, close to zero. It was inferred that this resulted from their low density (0.90–0.91 g/cm3 for PP, 0.92–0.97 g/cm3 for PE, and 1.02 g/cm3 for seawater), causing high buoyancy in seawater. The swimming and feeding capacity of benthic organisms are weak, so the proportion of these two components is low in such organisms. Armeen is an additive in the production of organic pigments and may be leached from coatings at fishery facilities.

Microplastics smaller than 500 μm were the most common in the tested shellfish, accounting for 37.50% of the total and indicating that shellfish are more prone to ingest smaller microplastics. Filter-feeding shellfish have a low feeding selectivity and often feed on microalgae (diatoms, chrysophytes, and chlorophytes are often used as feed) (Brown et al., 1997), the size of which is between 2–200 μm. Figure 6 shows that the preference of shellfish for microplastics decreases with increasing microplastic size. It can be inferred that a large size can hinder microplastic intake, which may be related to the limitation of cilia functions.

Regarding shape, the majority of microplastics in the shellfish were fibers (92.97%), with fewer fragments. This result is consistent with the research results of many scholars on microplastic shapes in shellfish. Zheng et al. (2019) reported that the proportion of fibrous microplastics in seawater and sediments in Jiaozhou Bay was 93.11%, which is consistent with our experimental results. Most of the microplastics in seawater and sediment were black, followed by blue and red (transparent microplastics were not counted in their study). In this study, the dominant colors of microplastics were as follows: black (42.97%), blue (20.31%), transparent (16.41%), and red (14.84%); this is consistent with the study described above. The shape and color distributions of the microplastics in shellfish from Jiaozhou Bay were similar to those in seawater and sediments. Therefore, we can conclude that the feeding of shellfish on microplastics is greatly influenced by their habitat.

4.3 Risk assessment of shellfish consumption

The production of shellfish in China has been increasing (National Bureau of Statistics, 2018). It is important to determine the level of microplastic contamination of shellfish and the potential risk posed by their consumption to humans. When people eat shellfish, they tend to eat all of the soft tissue. Therefore, diet is generally considered an important source of microplastics for humans (Galloway, 2015; Prata et al., 2020). The average shellfish consumption of a Chinese individual is 2.62 kg/(capita·a) (National Bureau of Statistics, 2018). However, the consumption of coastal residents is even higher; for example, residents of Hainan Province (30.81 kg/(capita·a)) consume far more than the average Chinese population (Gu et al., 2015). One difference to note is that the statistical consumption generally refers to the total weight of shellfish, while the abundance of microplastics in this study represents the weight per unit of soft tissue (Zhang et al., 2020). Because soft tissue weight is typically 40% of the total weight, it can be inferred that the average microplastic consumption through the Chinese diet is 1.27×103 items/(capita·a). In coastal areas with high shellfish intake, the consumption per capita can be greater. A comparison with the results of Cho et al. (2019) (212 items/(capita·a)) revealed that the Chinese dietary intake of microplastics through shellfish is higher than the Korean dietary intake. According to Hantoro et al. (2019), the estimated global intake of microplastics through mollusk consumption varies between (0–1.31)×104 particles/(capita·a). Our results fall at the low level of this range. Wu et al. (2020) concluded that the accumulation of microplastics (~2 items/ind.) in commercial species in Xiangshan Bay in China was negligible. Combining our results with the results of this study indicates that microplastics may pose low health risks via shellfish consumption in China. However, such risks still deserve attention, and more research needs to be conducted.

Zhang et al. (2020) compared human microplastic exposure through different pathways and found that the human body burden resulting from inhalation was estimated to be (0–3)×107 items per person per year. This is significantly higher than the microplastic burden from dietary exposure in this study. Therefore, from a quantitative perspective, the risks posed by dietary microplastic intake are less concerning than those posed by respiratory intake.

5 CONCLUSION

It is common for shellfish with important economic and ecological performance to ingest microplastics. The results of this study provide important insights: microplastic pollution in Jiaozhou Bay is at a moderate level compared with that in other known areas, but actions for controlling plastic pollution in Jiaozhou Bay, China, are needed. Shellfish prefer to eat small microplastics. Moreover, for shellfish, black is the preferred color, and fibers are the preferred shape. Cellophane and PET are the predominant microplastic types in shellfish from Jiaozhou Bay. Clams have a higher ingestion abundance than oysters. Wild and farmed growth modes had no significant effect on the microplastic feeding of shellfish. Dietary intake of microplastics through shellfish consumption poses a low risk to humans. Further studies are required on the risk assessment of microplastics from human seafood consumption.

6 DATA AVAILABILITY STATEMENT

The data generated or analyzed during the current study are available from the corresponding author on reasonable request.

References
Arthur C, Baker J, Bamford H eds. 2009. Proceedings of the International Research Workshop on the Occurrence, Effects and Fate of Microplastic Marine Debris, Sept 9-11, 2008. NOAA Technical Memorandum NOS-O & R-30. Tacoma, Washington, USA.
Besseling E, Foekema E M, Van Franeker J A, Leopold M F, Kühn S, Rebolledo E L B, Heße E, Mielke L, Ijzer J, Kamminga P, Koelmans A A. 2015. Microplastic in a macro filter feeder: humpback whale Megaptera novaeangliae. Marine Pollution Bulletin, 95(1): 248-252. DOI:10.1016/j.marpolbul.2015.04.007
Birnstiel S, Soares-Gomes A, da Gama B A P. 2019. Depuration reduces microplastic content in wild and farmed mussels. Marine Pollution Bulletin, 140: 241-247. DOI:10.1016/j.marpolbul.2019.01.044
Bridson J H, Patel M, Lewis A, Gaw S, Parker K. 2020. Microplastic contamination in Auckland (New Zealand) beach sediments. Marine Pollution Bulletin, 151: 110867. DOI:10.1016/j.marpolbul.2019.110867
Brown M R, Jeffrey S W, Volkman J K, Dunstan G A. 1997. Nutritional properties of microalgae for mariculture. Aquaculture, 151(1-4): 315-331. DOI:10.1016/s0044-8486(96)01501-3
Cho Y, Shim W J, Jang M, Han G M, Hong S H. 2019. Abundance and characteristics of microplastics in market bivalves from South Korea. Environmental Pollution, 245: 1107-1116. DOI:10.1016/j.envpol.2018.11.091
Cole M, Lindeque P, Halsband C, Galloway T S. 2011. Microplastics as contaminants in the marine environment: a review. Marine Pollution Bulletin, 62(12): 2588-2597. DOI:10.1016/j.marpolbul.2011.09.025
Davidson K, Dudas S E. 2016. Microplastic ingestion by wild and cultured manila clams (Venerupis philippinarum) from Baynes Sound, British Columbia. Archives of Environmental Contamination and Toxicology, 71(2): 147-156. DOI:10.1007/s00244-016-0286-4
de Witte B, Devriese L, Bekaert K, Hoffman S, Vandermeersch G, Cooreman K, Robbens J. 2014. Quality assessment of the blue mussel (Mytilus edulis): comparison between commercial and wild types. Marine Pollution Bulletin, 85(1): 146-155. DOI:10.1016/j.marpolbul.2014.06.006
Dehaut A, Cassone A L, Frère L, Hermabessiere L, Himber C, Rinnert E, Rivière G, Lambert C, Soudant P, Huvet A, Duflos G, Paul-Pont I. 2016. Microplastics in seafood: benchmark protocol for their extraction and characterization. Environmental Pollution, 215: 223-233. DOI:10.1016/j.envpol.2016.05.018
Desforges J P W, Galbraith M, Ross P S. 2015. Ingestion of microplastics by Zooplankton in the Northeast Pacific Ocean. Archives of Environmental Contamination and Toxicology, 69(3): 320-330. DOI:10.1007/s00244-015-0172-5
Fan Y, Liu X S. 2016. Seasonal distribution and resource assessment of manila clam (Ruditapes philippinarum) in Jiaozhou Bay, China. Periodical of Ocean University of China, 46(7): 70-74. (in Chinese with English abstract) DOI:10.16441/j.cnki.hdxb.20150338
Galloway T S. 2015. Micro- and nano-plastics and human health. In: Bergmann M, Gutow L, Klages M eds. Marine Anthropogenic Litter. Springer. Cham, Germany. p. 343-366, https://doi.org/10.1007/978-3-319-16510-3_13.
Goldstein M C, Goodwin D S. 2013. Gooseneck barnacles (Lepas spp. ) ingest microplastic debris in the North Pacific Subtropical Gyre. PeerJ, 1: e184. DOI:10.7717/peerj.184
Gu Y G, Lin Q, Yu Z L, Wang X N, Ke C L, Ning J J. 2015. Speciation and risk of heavy metals in sediments and human health implications of heavy metals in edible nekton in Beibu Gulf, China: a case study of Qinzhou Bay. Marine Pollution Bulletin, 101(2): 852-859. DOI:10.1016/j.marpolbul.2015.11.019
Hantoro I, Löhr A J, Van Belleghem F G A J, Widianarko B, Ragas A M J. 2019. Microplastics in coastal areas and seafood: implications for food safety. Food Additives & Contaminants: Part A, 36(5): 674-711. DOI:10.1080/19440049.2019.1585581
Hirai H, Takada H, Ogata Y, Yamashita R, Mizukawa K, Saha M, Kwan C, Moore C, Gray H, Laursen D, Zettler E R, Farrington J W, Reddy C M, Peacock E E, Ward M W. 2011. Organic micropollutants in marine plastics debris from the open ocean and remote and urban beaches. Marine Pollution Bulletin, 62(8): 1683-1692. DOI:10.1016/j.marpolbul.2011.06.004
Li H X, Ma L S, Lin L, Ni Z X, Xu X R, Shi H H, Yan Y, Zheng G M, Rittschof D. 2018. Microplastics in oysters Saccostrea cucullata along the Pearl River Estuary, China. Environmental Pollution, 236: 619-625. DOI:10.1016/j.envpol.2018.01.083
Li J N, Qu X Y, Su L, Zhang W W, Yang D Q, Kolandhasamy P, Li D J, Shi H H. 2016. Microplastics in mussels along the coastal waters of China. Environmental Pollution, 214: 177-184. DOI:10.1016/j.envpol.2016.04.012
Li J N, Yang D Q, Li L, Jabeen K, Shi H H. 2015. Microplastics in commercial bivalves from China. Environmental Pollution, 207: 190-195. DOI:10.1016/j.envpol.2015.09.018
Lusher A. 2015. Microplastics in the marine environment: distribution, interactions and effects. In: Bergmann M, Gutow L, Klages M eds. Marine Anthropogenic Litter. Springer. Cham, Germany. p. 245-307, https://doi.org/10.1007/978-3-319-16510-3_10.
Lusher A L, McHugh M, Thompson R C. 2013. Occurrence of microplastics in the gastrointestinal tract of pelagic and demersal fish from the English Channel. Marine Pollution Bulletin, 67(1-2): 94-99. DOI:10.1016/j.marpolbul.2012.11.028
Masó M, Garcés E, Pagès F, Camp J. 2003. Drifting plastic debris as a potential vector for dispersing Harmful Algal Bloom (HAB) species. Scientia Marina, 67(1): 107-111. DOI:10.3989/scimar.2003.67n1107
Mato Y, Isobe T, Takada H, Kanehiro H, Ohtake C, Kaminuma T. 2001. Plastic resin pellets as a transport medium for toxic chemicals in the marine environment. Environmental Science & Technology, 35(2): 318-324. DOI:10.1021/es0010498
Murphy C L. 2018. A Comparison of Microplastics in Farmed and Wild Shellfish Near Vancouver Island and Potential Implications for Contaminant Transfer to Humans. Royal Roads University Victoria, British Columbia, Canada.
Murray F, Cowie P R. 2011. Plastic contamination in the decapod crustacean Nephrops norvegicus (Linnaeus, 1758). Marine Pollution Bulletin, 62(6): 1207-1217. DOI:10.1016/j.marpolbul.2011.03.032
Naji A, Nuri M, Vethaak A D. 2018. Microplastics contamination in molluscs from the northern part of the Persian Gulf. Environmental Pollution, 235: 113-120. DOI:10.1016/j.envpol.2017.12.046
Napper I E, Thompson R C. 2016. Release of synthetic microplastic plastic fibres from domestic washing machines: effects of fabric type and washing conditions. Marine Pollution Bulletin, 112(1-2): 39-45. DOI:10.1016/j.marpolbul.2016.09.025
National Bureau of Statistics. 2018. China Statistical Yearbook 2018. China Statistics Press, Beijing. (in Chinese)
Phuong N N, Poirier L, Pham Q T, Lagarde F, Zalouk-Vergnoux A. 2018. Factors influencing the microplastic contamination of bivalves from the French Atlantic coast: location, season and/or mode of life?. Marine Pollution Bulletin, 129(2): 664-674. DOI:10.1016/j.marpolbul.2017.10.054
Prata J C, da Costa J P, Lopes I, Duarte A C, Rocha-Santos T. 2020. Environmental exposure to microplastics: an overview on possible human health effects. Science of the Total Environment, 702: 134455. DOI:10.1016/j.scitotenv.2019.134455
Provencher J F, Bond A L, Hedd A, Montevecchi W A, Muzaffar S B, Courchesne S J, Gilchrist H G, Jamieson S E, Merkel F R, Falk K, Durinck J, Mallory M L. 2014. Prevalence of marine debris in marine birds from the North Atlantic. Marine Pollution Bulletin, 84(1-2): 411-417. DOI:10.1016/j.marpolbul.2014.04.044
Ran W, Teng J, Liu Y L, Wu D, Hou C W, Wang Q, Liu H, Zhao J M. 2018. Microplastic ingestion characteristics in the Pacific oysters collected from the intertidal zone of the Bohai Rim. Marine Science Bulletin, 37(5): 583-590. (in Chinese with English abstract) DOI:10.11840/jissn.1001-6392.2018.05.012
Rochman C M, Tahir A, Williams S L, Baxa D V, Lam R, Miller J T, Teh F C, Werorilangi S, Teh S J. 2015. Anthropogenic debris in seafood: plastic debris and fibers from textiles in fish and bivalves sold for human consumption. Scientific Reports, 5: 14340. DOI:10.1038/srep14340
Scott N, Porter A, Santillo D, Simpson H, Lloyd-Williams S, Lewis C. 2019. Particle characteristics of microplastics contaminating the mussel Mytilus edulis and their surrounding environments. Marine Pollution Bulletin, 146: 125-133. DOI:10.1016/j.marpolbul.2019.05.041
Sobhani Z, Lei Y J, Tang Y H, Wu L W, Zhang X, Naidu R, Megharaj M, Fang C. 2020. Microplastics generated when opening plastic packaging. Scientific Reports, 10(1): 4841. DOI:10.1038/s41598-020-61146-4
Sussarellu R, Suquet M, Thomas Y, Lambert C, Fabioux C, Pernet M E J, Le Goïc N, Quillien V, Mingant C, Epelboin Y, Corporeau C, Guyomarch J, Robbens J, Paul-Pont I, Soudant P, Huvet A. 2016. Oyster reproduction is affected by exposure to polystyrene microplastics. Proceedings of the National Academy of Sciences of the United States of America, 113(9): 2430-2435. DOI:10.1073/pnas.1519019113
Tourinho P S, do Sul J A I, Fillmann G. 2010. Is marine debris ingestion still a problem for the coastal marine biota of southern Brazil?. Marine Pollution Bulletin, 60(3): 396-401. DOI:10.1016/j.marpolbul.2009.10.013
van Cauwenberghe L, Claessens M, Vandegehuchte M B, Janssen C R. 2015a. Microplastics are taken up by mussels (Mytilus edulis) and lugworms (Arenicola marina) living in natural habitats. Environmental Pollution, 199: 10-17. DOI:10.1016/j.envpol.2015.01.008
van Cauwenberghe L, Devriese L, Galgani F, Robbens J, Janssen C R. 2015b. Microplastics in sediments: a review of techniques, occurrence and effects. Marine Environmental Research, 111: 5-17. DOI:10.1016/j.marenvres.2015.06.007
von Moos N, Burkhardt-Holm P, Köhler A. 2012. Uptake and effects of microplastics on cells and tissue of the blue mussel Mytilus edulis L. after an experimental exposure. Environmental Science & Technology, 46(20): 11327-11335. DOI:10.1021/es302332w
Walkinshaw C, Lindeque P K, Thompson R, Tolhurst T, Cole M. 2020. Microplastics and seafood: lower trophic organisms at highest risk of contamination. Ecotoxicology and Environmental Safety, 190: 110066. DOI:10.1016/j.ecoenv.2019.110066
Wu F Z, Wang Y J, Leung J Y S, Huang W, Zeng J N, Tang Y B, Chen J F, Shi A Q, Yu X, Xu X Q, Zhang H G, Cao L. 2020. Accumulation of microplastics in typical commercial aquatic species: a case study at a productive aquaculture site in China. Science of the Total Environment, 708: 135432. DOI:10.1016/j.scitotenv.2019.135432
Zhang Q, Xu E G, Li J N, Chen Q Q, Ma L P, Zeng E Y, Shi H H. 2020. A review of microplastics in table salt, drinking water, and air: direct human exposure. Environmental Science & Technology, 54(7): 3740-3751. DOI:10.1021/acs.est.9b04535
Zheng Y F, Li J X, Cao W, Liu X H, Jiang F H, Ding J F, Yin X F, Sun C J. 2019. Distribution characteristics of microplastics in the seawater and sediment: a case study in Jiaozhou Bay, China. Science of the Total Environment, 674: 27-35. DOI:10.1016/j.scitotenv.2019.04.008