Next Article in Journal
Impacts of Discretization and Numerical Propagation on the Ability to Follow Challenging Square Wave Commands
Next Article in Special Issue
Oxidative Stress in Far Eastern Mussel Mytilus trossulus (Gould, 1850) Exposed to Combined Polystyrene Microspheres (µPSs) and CuO-Nanoparticles (CuO-NPs)
Previous Article in Journal
Lightweight Structural Concepts in Bearing Quasi-Static Ice Hull Interaction Loads
Previous Article in Special Issue
Depth Profiles of Microplastics in Sediment Cores from Two Mangrove Forests in Northern Vietnam
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Occurrence of Microplastics in Sediment Cores from Two Mangrove Areas in Southern Thailand

1
Coastal Oceanography and Climate Change Research Center, Faculty of Environmental Management, Prince of Songkla University, Songkhla 90110, Thailand
2
Ocean College, Zhejiang University, Zhoushan 316021, China
3
Faculty of Science and Fisheries Technology, Rajamangala University of Technology Srivijaya, Trang 92150, Thailand
4
Institute of Natural Product Chemistry, Vietnam Academy of Science and Technology, Hanoi 11307, Vietnam
5
Faculty of Hydrology and Water Resources Engineering, Institute of Technology of Cambodia, Phnom Penh 12156, Cambodia
6
Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi 43600, Malaysia
7
Institute of Biological Sciences, Universiti Malaya, Kuala Lumpur 50603, Malaysia
8
Department of Geography, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore
9
Soil Science Department, Faculty of Agriculture, Tanjungpura University, Pontianak 78124, West Kalimantan, Indonesia
10
Department of Geological Oceanography, Xiang’an Campus, Xiamen University, Xiamen 361102, China
11
Jiangsu Key Laboratory of Crop Genetics and Physiology, Agricultural College of Yangzhou University, Yangzhou 225009, China
12
Jiangsu Key Laboratory of Crop Cultivation and Physiology, Agricultural College of Yangzhou University, Yangzhou 225009, China
13
Jiangsu Co-Innovation Centre for Modern Production Technology of Grain Crops, Yangzhou University, Yanzhou 225009, China
*
Authors to whom correspondence should be addressed.
J. Mar. Sci. Eng. 2022, 10(3), 418; https://doi.org/10.3390/jmse10030418
Submission received: 22 December 2021 / Revised: 5 March 2022 / Accepted: 10 March 2022 / Published: 13 March 2022

Abstract

:
Mangroves are areas that connect the land and sea, and are important to the ecosystem. They are important places for food sources and the habitat of aquatic fauna in the tidal areas. However, the existence of plastic debris poses a risk to the aquatic environment. This study aimed to investigate the accumulation of microplastics (MPs) in sediment cores from two mangrove areas. The first mangrove area is in the outer section of the Songkhla lagoon (SK), while the second is in the coastal area of Pattani province (PN). Sediment core sampling was performed from SK = 8 stations and PN = 5 stations. Surface enrichment of MP was observed, especially in sediments of 0–4 cm. MPs were found throughout the depth in both areas, while fewer MPs were found in deeper sediment core layers (p < 0.05) at some stations inside the mangrove zone. Simple linear regression of the observed MPs and distance in the horizontal were found to be significant at SK within the mangrove zone with r2 = 0.79 (p < 0.05). MP fibers were the most commonly found MP type in both areas and were less than 1 mm. Blue and black MPs were the most abundant colors found in both areas. The six polymer types reported in this study comprised polyethylene, rayon, rubber, styrene, Poly (vinyl acetate), and paint. The findings of the present study suggest that long-term monitoring of marine debris along coastlines is necessary to help improve national policies and measures related to marine plastic debris.

1. Introduction

Over recent decades, plastic pollution has become a global environmental concern due to increased plastic production and consumption. Global plastic production has increased exponentially from 0.35 million tons in the 1950s [1] to 359 million tons in 2018 [2]. When plastic is released into the ocean, plastic debris will break down continuously through physical, chemical, and biological processes [3,4], which results in the formation of hazardous secondary MPs in the sea. MPs are fragments of any plastic particles less than 5 mm in size [5]. They can be categorized based on their shape, size, color, and raw material. They are generally found in different shapes such as film, fragments, pellets, and fibers [6], which easily disperse into the environment. They are difficult to degrade and pose a long-term threat to marine ecosystems. Plastic contamination in the ocean is a global concern due to its negative effects on marine health and biota. MPs are easily ingestible by marine animals such as zooplankton [7], fish [8], and mollusk [9] due to their small-sized particles, which affect the health of marine biota [10]. Additionally, previous studies indicate that MPs can adsorb persistent organic pollutants (e.g., polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and DDT) and heavy metals (e.g., cadmium, mercury, and chromium), which could be transferred to higher trophic levels [11,12,13].
Previous reports show that only 1% of plastic entering the marine environment remains as floating debris on the water surface [14]. Most MPs sink to deeper layers of the water column [15] and accumulate in sediments [16]. Mangrove forests have been identified as a major sink of marine plastic pollution [17,18], which can effectively trap MPs through their root systems and sediment [19]. Numerous investigations concerning MP pollution in sediments along Thailand’s coastal areas have been conducted, yet few existing studies on MP pollution in mangrove sediment have been conducted. Importantly, mangrove forests are essential food sources and economic resources for coastal fisheries and people in Thailand. Moreover, MP accumulation in mangrove forest areas may influence aquatic animals and people who consume aquatic animals contaminated with MPs.
A mangrove forest is a group of trees and shrubs that are commonly found in coastal areas. A mangrove is a connective place between the land and sea and is important to the ecosystem, especially to the aquatic population. Mangroves are an important food source for aquatic fauna in tidal areas. In addition, the elongated root system makes it possible to trap sediment and pollutants such as trace metals. Mangroves are important carbon reservoirs [20] and regulators of nutrients and pollutants [21]. They provide food, medicine, and fuel; protect coastal zones [22]; and are home to various animal species [23]. Nonetheless, mangroves face threats from deforestation and land use changes [24], as well as erosion [25], farming [26], pollution [27], and climate change [28]. Monitoring the trends of various pollutants within core samples can be used to indicate the degree of human activities in mangroves. Monitoring vegetation cover can further determine whether mangrove areas face deterioration in terms of the reduction of mangrove forest areas. There have been numerous reports on MP ingestion in marine organisms [29]. Some studies of MPs in mangrove sediment have been conducted in Southeast Asia and East Asia, including in Vietnam [30], Indonesia [31], Singapore [32], Malaysia [33], and China [34]. A few studies have emerged in Thailand recently that describe MP ingestion and MP abundance in marine organisms such as sessile invertebrates (oyster, striped barnacle, and periwinkle) collected from eastern Thailand coastal areas [35], fish samples caught in the southern Gulf of Thailand coastal area and from fishery markets [36], and shrimp and fish samples from Songkhla Lagoon, southern Thailand [37]. Yet, few studies of MPs in beach sediment in coastal areas [38,39,40] have been performed until now, while few reports exist considering MPs in mangrove sediment.
This study aimed to investigate the accumulation of MPs in sediment cores in mangrove forests. The study area included Songkhla Lagoon and the coastal area of Pattani province, one of the important mangrove areas in Thailand. The results of this study offer valuable data to develop a conservation policy for mangrove areas in Thailand and other Southeast Asian countries.

2. Materials and Methods

2.1. Study Area

Sample collection was conducted in two locations with mangrove forests (Figure 1). The first mangrove area is at the outer section of Songkhla Lagoon (SK), Thailand (Figure 1), which is situated in southern Thailand and is connected to the Gulf of Thailand through a narrow strait. The outer section of Songkhla Lake receives pollutants from human activities via drainage from the Songkhla urban area [41]. The lagoon faces problems of environmental degradation due to urban expansion and industrialization. Sources of pollutants to the lake system include municipal waste from the cities of Hat Yai and Songkhla, industrial wastes mainly related to the rubber industry, seafood-processing industry, mining activities, and pollution from boats in Songkhla harbor [42]. The dominant mangrove species in the SK area is Sonneratia caseolaris. The second mangrove area is in the coastal area of Pattani province, adjacent to Pattani Bay (PN), Thailand (Figure 1). PN is a mangrove plantation area in new muddy flats that faces the open sea of the Gulf of Thailand. The main species is Rhizophora apiculata.

2.2. Sediment Sampling

Sediment cores were collected from 13 stations (Figure 1). Eight stations (six inside and two outside the mangrove forest) were sampled in the SK area, while five stations (three inside and two outside the mangrove forest) were sampled in the PN area. The survey was conducted between March and April 2021. Sediment cores were collected by hand pushing using Plexiglas tubes (5 cm diameter and 50 cm length). The collected samples were transported immediately to the laboratory for further sub-sampling.

2.3. Sediment Preparation and Extraction

2.3.1. Experimental Control

To avoid microplastic contamination, distilled water and saturated NaCl were filtered before being used in the experiment. During the separation procedure, extensive measures were applied to avoid any contamination while handling and processing the samples. Cotton lab coats and polymer-free grove were worn to ensure minimal contamination during the experiment [43]. All equipment was rinsed with filtered distilled water before use. Furthermore, all sample processing was performed in a clean fume chamber. Blank was carried out by filtering the distilled water from an 8 cm petri dish filled with distilled water and placed next to the working zone with no observed MP.

2.3.2. Microplastic Extraction from Sediment

Sediment cores were sectioned every 2 cm through the depth and then oven dried at about 50 °C. Due to the agglutination of organic matter, it was necessary for it to be removed from the sediment before analysis [44]. For the typically muddy sediments observed in tidal flats and mangrove forests, MPs were frequently covered or partly covered by clays and organic matter, so a procedure to clean the samples using deionized water was utilized in this study. About 30–50 g of dry sediment was placed in a beaker (1 L). Then, 100 mL of deionized water was added to the sediment, which was stirred vigorously for 5 min using a magnetic stirrer for the purpose of cleaning and separating MPs from the sediment. Thereafter, 400 mL of saturated NaCl (1.2 g/cm2) was added based on the method of Chinfak et al., 2021 [45] and Wang et al., 2020 [46], with some minor changes. The NaCl method has been widely used to separate microplastics from sediments [45,46,47]. A rod was used to mix, after which the mixture was left for 24 h to allow the sediment to settle. Then, 250 mL supernatant was filtered through a glass microfiber GF/B (Whatman, pore size 1 µm) using a vacuum system. Another 250 mL of NaCl was added to the original sample beaker, and the same density separation and filtration was repeated twice for each sediment sample with a new filter paper. Thereafter, all filter paper was oven dried at 50 °C.

2.3.3. Microplastic Identification

To identify the MPs in the filter paper under a stereomicroscope, visual identification was based on the morphological and physical characteristics of plastic particles. A stereo zoom microscope camera with an attachment (Olympus SZ61, lenses 110AL2X-2 with Canon EOS 600D) was used in this method. As the filters were completely dry, there was no bias in the light reflection from the microscope. The criteria to accept the particles as plastic before being verified by the FTIR spectrophotometer involved the hot needle test [48], which was applied for suspected cases where the researchers were unable to distinguish between plastic and organic matter. In the presence of a hot needle, plastic pieces will melt or curl. We also applied the Hidalgo-Ruz et al. (2012) [49] rules to assist in identifying most MPs that were encountered in this analysis. Rule 1: No cellular or organic structures visible. Rule 2: Fibers should be equally thick throughout their entire length. Rule 3: Particles should exhibit homogenous color throughout the item. We recorded the shape, color, and size of each item.
To ensure an uncontaminated reading by FTIR, the selected MP samples were not covered or were partly covered by clays and organic matter (observed under a stereomicroscope). The MPs were analyzed to identify polymer types using a micro Fourier Transform Infrared(µFTIR) spectrometer, Frontier model coupled with a Spotlight 200i FTIR microscope (PerkinElmer Inc., Waltham, MA, USA). The wavelength used was 4000–600 cm−1 with an attenuated total reflection (ATR) mode using a scanned rate of 16 and resolution of 4 cm−1. To minimize the error from the background during the identification process, the peak of CO2 and H2O was removed from the value. The obtained polymer type was compared with the library, called the Polymer Introductory Library, and 70% matching was accepted.

2.4. Data Analysis

Data analysis of MP abundance, size, color, and shape were performed using MS Excel 2007 (Office Professional Plus 2019) software. A correlation test was performed to find the relationship between the number of MPs found in the sediment and the depth. A significance level of 0.05 was considered for all of the analyses.

3. Results and Discussion

3.1. Vertical Accumulation of MPs

A total of 13 sediment cores were obtained from both areas at various depths, between 18–42 cm for SK and 18–38 cm for PN (Table 1). The range of MPs found in SK was from 71–108 items and 71–155 items for PN. The range of MPs inside the zone for SK and PN were 71–108 items and 71–84 items, respectively. Vertical profiles of the amount of MPs found in the sediment core are given in Figure 2 and Figure 3. Most MPs showed only slight vertical variations, with some exceptions. Surface enrichment of MPs was observed, especially in sediments of 0–4 cm in both areas. Differences were observed between the sediments from inside and outside the mangrove areas. At some stations, the correlation between MP and depth was significant (p < 0.05) in terms of the decrease with depth (SK02, SK05, SK07, and PN03). Generally, a decreasing trend in depth was observed at SK, except for at SK08, which is located outside the mangrove area and resulted in amounts of MPs similar to all depths. The MPs detected at every layer of the sediment samples varied between station and depth. The amount of MPs inside the mangrove area was higher on average in both areas, potentially because mangrove roots could trap marine debris and MPs during high tide. MPs entered during high tide and then attached to the roots or bushes at low tide, then MPs sank onto the surface sediment and mixed into the deeper layers by biological and physical processes in the mangrove. Sediments from the inside zone of SK had a greater abundance of MPs in the mangrove sediment, which could be because of the location of SK in the shelter of the lagoon and near the community, while the PN is far from the community and faces the open sea (GoT). SK provided a lagoon-mouth mangrove forest. However, the selected mangrove forest was dominated by a shore parallel tidal current. When high tide floods into a forest, debris and MPs suspended in water also reach inside the mangrove. While a mangrove forest can reduce the current energy, the suspended MPs settle and become trapped in the sediment. The vertical profiles at PN varied among stations and only PN03 showed a significant (p < 0.05) decrease in MPs with depth.
The cumulative MP abundance between the two study locations (at 10 cm depth) ranged from 106–413 and 108–180 items/kg dry weight, respectively. Table 2 presents a comparison of the data from this study with findings from other areas in the world. Fiber and fragments found were similar in other studies around the world. However, the concentrations of MPs from the present study were higher than those undertaken in Indonesia and Singapore [31,32], and lower than Iran, China, and Brazil [34,50,51,52,53,54,55]. Therefore, mangroves have the potential to act as sinks for MPs and other pollutants [17,18].

3.2. Horizontal Accumulation of MPs

Figure 4a presents the number of MPs observed at 0–10 cm depth and the distance from the shore. The inner zone of SK (SK01 to SK06) tended to show an increase of MPs by distance from landside (SK01) to forest border (SK06: lagoon side). The simple linear regression of observed MP numbers by the distance of the inner zone resulted in r2 = 0.79 with a p-value of 0.011 (p < 0.05). The reduction of MPs numbers at the landside can be explained by the mangrove forest topography. The inside most of the mangrove (landside: SK01 and SK02) forest trended to be at a higher elevation, leading to them expressing a shorter residence time for water. Meanwhile, in the inner zone closest to the mangrove border (lagoon side), the tidal current dropped immediately [56], which resulted in MPs sinking in this area. Moreover, the border of the forest and the highest residence time of the tide resulted in more suspended MPs in the lagoon water. However, the amount of MPs in our results in the PN area had no significant relation to distance (Figure 4b). This was likely because of the lower density and younger mangrove compared to SK, in which the forest was less able to trap MPs compared to SK. Another potential explanation is the topography. From our observations, there was no elevation difference between inside and outside the mangroves. In addition, a further potential reason is that PN is located next to the open sea. MPs are easily transported as suspended loads by the current, waves, tides, and coastal erosion process from other places to the deposit site, thus possessing a dynamic quantity of MPs present in the sediment according to their short residence time in the coastal sediment [57]. Furthermore, plastic debris was found in the study area, which was likely suspended or drifted with the high tide to the mangrove, and could become trapped into the mangrove roots and nearby sediment during low tide (Figure 5).

3.3. Microplastic Identification

There were 13 colors found in the sediment from SK, consisting of brown, white, yellow, pink silver, purple, red, green, black, dark blue, light blue, transparent, and others (Figure 6a). Black and blue were the most commonly found in SK. At PN, 11 colors were found, including white, yellow, pink, silver, purple, red, green, black, dark blue, light blue, and transparent (Figure 6b). Blue was the most common at PN. The dominant size in both areas was less than 1 mm (Figure 7). Sizes from 1–5 mm were more commonly found inside the mangrove area at SK. Fiber was the most abundant in the area (Figure 8), and was more commonly found outside the mangrove area. An example MPs found in this study is shown in Figure 9. MPs from SK are probably associated with human activity and fishing in the lagoon, while the MP source at PN could be from fishing nets in the coastal area. From the FTIR investigation, the six types of polymers found in this study were polyethylene, rayon, rubber, styrene, Poly (vinyl acetate), and paint. Polyethylene or PE is a common thermoplastic that is widely used in many applications such as food packaging and containers [58]. In polymer context and composition, PE is mainly used for HDPE ropes and the fabrication of fishing nets. This type of rope is used extensively in fishing activities and the docking of ships in marine-related industries [59]. Rayon is a cellulose fiber generated from natural sources of cellulose and synthetic cellulose fibers. Generally, rayon fiber is used to produce artificial silk and other textiles. Paint can come from fragments off fishing boats in the lagoon and coastal areas. Surprisingly, in this study, very common pollutants such as polyvinyl chloride (PVC) and acrylic were not observed, even in areas closest to sources of urban pollution. These results are similar to previous studies, which reported no PVC in marine organisms in southern Thailand [29,37], although they were found on beaches on the eastern coast of Thailand and the Andaman sea [38,57].

4. Conclusions

This study was the first to report on the presence of MPs in mangrove sediment cores from two mangrove areas in southern Thailand. From the study, we found that the accumulation of MPs in mangrove areas in both SK and PN varied according to core depth. This research was undertaken in a single season, so the authors recommend further research to be conducted covering all seasons. In addition, a comparison of the results with the age of sediment would be meaningful. Mangroves are an important wetland currently contaminated with MPs, which can be harmful to benthic fauna and marine organisms. Sediments in coastal and lagoon ecosystems play an important role as a major source for feeding benthic organisms, but they can also accumulate many toxic substances. Anthropogenic pressures can also lead to increased chemical and microbiological pollution of lagoons and coastal areas. Therefore, long-term monitoring of marine debris along coastlines, including apparently pristine and environmentally protected areas, is necessary to help improve national policies and measures related to marine plastic debris.

Author Contributions

Conceptualization, S.P. and P.-S.L.; investigation, P.N.; methodology, S.P., P.N. and T.N.; writing—original draft, S.P. and P.N.; writing—review and editing, S.P., T.N., T.P.Q.L., C.O., C.A.R.M., C.W.L., X.L., G.Z.A., S.K. and J.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Asia-Pacific Network for Global Change Research (APN): grant number CRRP2020-06MY-Loh.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

The authors wish to thank Kittiwara Sornplang and Patricia Blair Goh for their support in the field and laboratory work.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Statista. Annual Production of Plastics Worldwide from 1950 to 2020. Available online: https://www.statista.com/statistics/282732/global-production-of-plastics-since-1950 (accessed on 11 November 2020).
  2. Thailand Development Research Institute. Disparity Worsens Ocean Pollution. Available online: https://tdri.or.th/en/2021/06/disparity-worsens-ocean-pollution (accessed on 9 June 2021).
  3. Wang, J.; Zheng, L.; Li, J. A critical review on the sources and instruments of marine microplastics and prospects on the relevant management in China. Waste Manag. Res. 2018, 36, 898–911. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Wayman, C.; Nieman, H. The fate of plastic in the ocean environment—A mini review. Environ. Sci. Processes Impacts 2021, 23, 198–212. [Google Scholar] [CrossRef]
  5. Willis, K.A.; Eriksen, R.; Wilcox, C.; Hardesty, B.D. Microplastic distribution at different sediment depths in an urban estuary. Front. Mar. Sci. 2017, 4, 419. [Google Scholar] [CrossRef] [Green Version]
  6. Suisyo, E.N.; Rahmawati, S.; Putri, R.A.; Arya, N.; Eryan, Y.A. Identification of the existence and type of microplastic in code river fish, special region of Yogyakarta. J. Data Sci. Anal. 2020, 1, 85–91. [Google Scholar]
  7. Kosore, C.; Ojwang, L.; Maghanga, J.; Kamau, J.; Kimei, A.; Omukoto, K.; Ngisiag’e, N.; Mwaluma, J.; Ong’ada, H.; Magori, C.; et al. Occurrence and ingestion of microplastics by zooplankton in Kenya’s marine environment: First documented evidence. Afr. J. Mar. Sci. 2018, 40, 225–234. [Google Scholar] [CrossRef]
  8. Klangnurak, W.; Chunniyom, S. Screening for microplastics in marine fish of Thailand: The accumulation of microplastics in the gastrointestinal tract of different foraging preferences. Environ. Sci. Pollut. Res. 2020, 27, 27161–27168. [Google Scholar] [CrossRef] [PubMed]
  9. Abidli, S.; Lahbib, Y.; El Menif, N.T. Microplastics in commercial molluscs from the lagoon of Bizerte (Northern Tunisia). Mar. Pollut. Bull. 2019, 142, 243–252. [Google Scholar] [CrossRef] [PubMed]
  10. Sharma, S.; Chatterjee, S. Microplastic pollution, a threat to marine ecosystem and human health: A short review. Environ Sci Pollut Res. 2017, 24, 21530–21547. [Google Scholar] [CrossRef] [PubMed]
  11. Frias, J.P.G.L.; Sobral, P.; Ferreira, A.M. Organic pollutants in microplastics from two beaches of the Portuguese coast. Mar. Pollut. Bull. 2010, 60, 1988–1992. [Google Scholar] [CrossRef]
  12. Liu, S.; Shi, J.; Wang, J.; Dai, Y.; Li, H.; Li, J.; Liu, X.; Chen, X.; Wang, Z.; Zhang, P. Interactions between microplastics and heavy metals in aquatic environments: A review. Front. Microbiol. 2021, 12, 652520. [Google Scholar] [CrossRef]
  13. Bayo, J.; Guille’n, M.; Olmos, S.; Jimenez, P.; Sanchez, E.; Roca, M.J. Microplastics as vector for persistent organic pollutants in urban effluents: The role of Polychlorinated biphenyls. Int. J. Sus. Dev. Plan. 2018, 13, 671–682. [Google Scholar] [CrossRef]
  14. Law, K.L. Plastics in the marine environment. Ann. Rev. Mar. Sci. 2017, 9, 205–229. [Google Scholar] [CrossRef] [Green Version]
  15. Choy, C.A.; Robinson, B.H.; Gagne, T.O.; Erwin, B.; Firl, E.; Halden, R.U.; Hamilton, J.A.; Katija, K.; Lisin, S.E.; Rolsky, C.; et al. The vertical distribution and biological transport of marine microplastics across the epipelagic and mesopelagic water column. Sci. Rep. 2019, 9, 7843. [Google Scholar] [CrossRef] [Green Version]
  16. Schröder, K.; Kossel, E.; Lenz, M. Microplastic abundance in beach sediments of the Kiel Fjord, Western Baltic Sea. Environ. Sci. Pollut. Res. 2012, 28, 26515–26528. [Google Scholar] [CrossRef]
  17. Van Emmerik, T.; Mellink, Y.; Hauk, R.; Waldschläger, K.; Schreyers, L. Rivers as Plastic Reservoirs. Front. Water 2022, 3, 1–8. [Google Scholar] [CrossRef]
  18. Martin, C.; Baalkhuyur, F.; Valluzzi, L.; Saderne, V.; Cusack, M.; Almahasheer, H.; Krishnakumar, P.K.; Rabaoui, L.; Qurban, M.; Arias-Ortiz, A.; et al. Exponential increase of plastic burial in mangrove sediments as a major plastic sink. Sci. Adv. 2020, 6, eaaz5593. [Google Scholar] [CrossRef]
  19. Luo, Y.Y.; Not, C.; Cannicci, S. Mangroves as unique but understudied traps for anthropogenic marine debris: A review of present information and the way forward. Environ. Pollut. 2021, 271, 116291. [Google Scholar] [CrossRef] [PubMed]
  20. Perera, K.A.R.S.; Amarasinghe, M.D. Carbon sequestration capacity of mangrove soils in micro tidal estuaries and lagoons: A case study from Sri Lanka. Geoderma 2019, 347, 80–89. [Google Scholar] [CrossRef]
  21. Maiti, S.K.; Chowdhury, A. Effects of Anthropogenic Pollution on Mangrove Biodiversity: A Review. J. Environ. Prot. 2013, 4, 1428–1434. [Google Scholar] [CrossRef] [Green Version]
  22. Veettil, B.K.; Ward, R.D.; Quang, N.X.; Trang, N.T.T.; Giang, T.H. Mangroves of Vietnam: Historical development, current state of research and future threats. Estuar. Coast. Shelf Sci. 2019, 218, 212–236. [Google Scholar] [CrossRef]
  23. Vanegas, C.A.; Osorio, A.F.; Urrego, L.E. Wave dissipation across a Rhizophora mangrove patch on a Colombian Caribbean Island: An experimental approach. Ecol. Eng. 2019, 130, 271–281. [Google Scholar] [CrossRef]
  24. Castillo, J.A.A.; Apan, A.A.; Maraseni, T.N.; Salmo, S.G., III. Estimation and mapping of above-ground biomass of mangrove forests and their replacement land uses in the Philippines using Sentinel imagery. ISPRS J. Photogramm. Remote Sens. 2017, 134, 70–85. [Google Scholar] [CrossRef]
  25. Besset, M.; Gratiot, N.; Anthony, E.J.; Bouchette, F.; Goichot, M.; Marchesiello, P. Mangroves and shoreline erosion in the Mekong River delta, Vietnam. Estuar. Coast. Shelf Sci. 2019, 226, 106263. [Google Scholar] [CrossRef]
  26. Ghosh, S.; Bakshi, M.; Bhattacharyya, S.; Nath, B.; Chaudhuri, P. A Review of threats and vulnerabilities to mangrove habitats: With special emphasis on east coast of India. J. Earth Sci. Clim Chang. 2015, 6, 1000270. [Google Scholar] [CrossRef] [Green Version]
  27. Kumar, V.; Parihar, R.D.; Sharma, A.; Bakshi, P.; Sidhu, G.P.S.; Bali, A.S.; Karaouzas, I.; Bhardwaj, R.; Thukral, A.K.; Gyasi-Agyei, Y.; et al. Global evaluation of heavy metal content in surface water bodies: A meta-analysis using heavy metal pollution indices and multivariate statistical analyses. Chemosphere 2019, 236, 124364. [Google Scholar] [CrossRef] [PubMed]
  28. Toosi, N.B.; Soffianian, A.R.; Fakheran, S.; Pourmanafi, S.; Ginzler, C.; Waser, L.T. Comparing different classification algorithms for monitoring mangrove cover changes in southern Iran. Glob. Ecol. Conserv. 2019, 19, e00662. [Google Scholar] [CrossRef]
  29. Goh, P.B.; Pradit, S.; Towatana, P.; Khokkiatiwong, S.; Kongket, B.; Moh, J.H.Z. Microplastics abundance in blood cockles and shrimps from fishery market, Songkhla Province, Southern Thailand. Sains Malays. 2021, 50, 2899–2911. [Google Scholar] [CrossRef]
  30. Viet Dung, L.; Huu Duc, T.; Thi Khanh Linh, L.; Thi Dieu Ly, T.; Anh Duong, H.; Thi My Hao, N. Depth Profiles of Microplastics in sediment cores from two mangrove forests in northern Vietnam. J. Mar. Sci. Eng. 2021, 9, 1381. [Google Scholar] [CrossRef]
  31. Cordova, M.R.; Ulumuddin, Y.I.; Purbonegoro, T.; Shiomoto, A. Characterization of microplastics in mangrove sediment of Muara Angke Wildlife Reserve, Indonesia. Mar. Pollut. Bull. 2021, 163, 112012. [Google Scholar] [CrossRef] [PubMed]
  32. Nor, N.H.M.; Obbard, J.P. Microplastics in Singapore’s coastal mangrove ecosystems. Mar. Pollut. Bull. 2014, 79, 278–283. [Google Scholar] [CrossRef] [PubMed]
  33. Ibrahim, Y.S.; Hamzah, S.R.; Khalik, W.M.A.W.M.; Yusof, K.M.K.K.; Anuar, S.T. Spatiotemporal microplastic occurrence study of Setiu Wetland, South China Sea. Sci. Total Environ. 2021, 788, 147809. [Google Scholar] [CrossRef] [PubMed]
  34. Li, J.; Zhang, H.; Zhang, K.; Yang, R.; Li, R.; Li, Y. Characterization, source, and retention of microplastic in sandy beaches and mangrove wetlands of the Qinzhou Bay, China. Mar. Pollut. Bull. 2018, 136, 401–406. [Google Scholar] [CrossRef] [PubMed]
  35. Thushari, G.G.N.; Chavanich, S.; Yakupitiyage, A. Coastal debris analysis in beaches of Chonburi Province, eastern of Thailand as implications for coastal conservation. Mar. Pollut. Bull. 2017, 116, 121–129. [Google Scholar] [CrossRef] [PubMed]
  36. Azad, S.M.O.; Towatana, P.; Pradit, S.; Goh, P.B.; Hue, H.T.T.; Jualaong, S. First evidence of existence of microplastics in stomach of some commercial fishes in the lower Gulf of Thailand. Appl. Ecol. Environ. Res. 2018, 16, 7345–7360. [Google Scholar] [CrossRef]
  37. Pradit, S.; Noppradit, P.; Goh, B.P.; Sornplang, K.; Ong, M.C.; Towatana, P. Occurrence of microplastics and trace metals in fish and shrimp from Songkhla lake, Thailand during the COVID-19 pandemic. Appl. Ecol. Environ. Res. 2021, 19, 1085–1106. [Google Scholar] [CrossRef]
  38. Pradit, S.; Towatana, P.; Nitiratsuwan, T.; Jualaong, T.; Jirajarus, M.; Sornplang, K.; Noppradit, P.; Darakai, Y.; Weerawong, C. Occurrence of microplastics on beach sediment at Libong, a pristine island in Andaman Sea, Thailand. Sci. Asia 2020, 46, 336–343. [Google Scholar] [CrossRef]
  39. Pradit, S.; Nitiratsuwan, T.; Towatana, P.; Jualaong, T.; Sornplang, K.; Noppradit, P.; Jirajarus, M.; Darakai, Y.; Weerawon, C. Marine debris accumulation on the beach in Libong, a small island in Andaman Sea, Thailand. Appl. Ecol. Environ. Res. 2020, 18, 5461–5474. [Google Scholar] [CrossRef]
  40. Akkajit, P.; Tipmanee, D.; Cherdsukjai, P.; Suteerasak, T.; Thongnonghin, S. Occurrence and distribution of microplastics in beach sediments along Phuket coastline. Mar. Pollut. Bull. 2021, 169, 112496. [Google Scholar] [CrossRef] [PubMed]
  41. Pradit, S.; Wattayakorn, G.; Angsupanich, S.; Baeyens, W.; Leermakers, M. Distribution of trace element in sediment and biota of Songkhla Lake, Southern Thailand. Water Air Soil Pollut. 2010, 206, 155–174. [Google Scholar] [CrossRef]
  42. Sompongchaiyakul, P.; Sirinawin, W. Arsenic, Chromium and Mercury in surface sediment of Songkhla Lake system, Thailand. Asian J. Water Environ. Pollut. 2007, 4, 17–24. [Google Scholar]
  43. Jahan, S.; Strezov, V.; Weldekidan, H.; Kumar, R.; Kanm, T.; Sarkodie, S.A.; He, J.; Dastjerdi, B.; Wilson, S.P. Interrelationship of microplastic pollution in sediments and oysters in a seaport environment of the eastern coast of Australia. Sci. Total Environ. 2019, 695, 133924. [Google Scholar] [CrossRef] [PubMed]
  44. Loring, D.H.; Rantala, R.T.T. Manual for the geochemical analyses of marine sediments and suspended particulate matter. Earth Sci. Rev. 1992, 32, 235–283. [Google Scholar] [CrossRef]
  45. Chinfak, N.; Sompongchaiyakul, P.; Charoenpong, C.; Shi, H.; Yeemin, T.; Zhang, J. Abundance, Composition, and Fate of Microplastics in Water, Sediment, and Shellfish in the Tapi-Phumduang River System and Bandon Bay, Thailand. Sci. Total Environ. 2021, 781, 146700. [Google Scholar] [CrossRef] [PubMed]
  46. Wang, Y.; Zou, X.; Peng, C.; Qiao, S.; Wang, T.; Yu, W.; Khokiattiwong, S.; Kornkanitnan, N. Occurrence and Distribution of Microplastics in Surface Sediments from the Gulf of Thailand. Mar. Pollut. Bull. 2020, 152, 110916. [Google Scholar] [CrossRef] [PubMed]
  47. Jiwarungrueangkul, T.; Phaksopa, J.; Sompongchaiyakul, P.; Tipmanee, D. Seasonal Microplastic Variations in Estuarine Sediments from Urban Canal on the West Coast of Thailand: A Case Study in Phuket Province. Mar. Pollut. Bull. 2021, 168, 112452. [Google Scholar] [CrossRef]
  48. 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] [PubMed]
  49. Hidalgo-Ruz, V.; Gutow, L.; Thompson, R.C.; Thiel, M. Microplastics in the marine environment: A Review of the methods used for identification and quantification. Environ. Sci. Technol. 2012, 46, 3060–3075. [Google Scholar] [CrossRef]
  50. Naji, A.; Esmaili, Z.; Khan, F.R. Plastic debris and microplastics along the beaches of the Strait of Hormuz, Persian Gulf. Mar. Pollut. Bull. 2017, 114, 1057–1062. [Google Scholar] [CrossRef]
  51. Li, R.; Zhang, L.; Xue, B.; Wang, Y. Abundance and characteristics of microplastics in the mangrove sediment of the semi-enclosed Maowei Sea of the south China sea: New implications for location, rhizosphere, and sediment compositions. Environ. Pollut. 2019, 244, 685–692. [Google Scholar] [CrossRef] [PubMed]
  52. Zuo, L.; Sun, Y.; Li, H.; Hu, Y.; Lin, L.; Peng, J.; Xu, X. Microplastics in mangrove sediments of the Pearl River Estuary, South China: Correlation with halogenated flame retardants’levels. Sci. Total Environ. 2020, 725, 138344. [Google Scholar] [CrossRef]
  53. Deng, J.; Guo, P.; Zhang, X.; Su, H.; Zhang, Y.; Wu, Y.; Li, Y. Microplastics and accumulated heavy metals in restored mangrove wetland surface sediments at Jinjiang Estuary (Fujian, China). Mar. Pollut. Bull. 2020, 159, 111482. [Google Scholar] [CrossRef] [PubMed]
  54. Huang, Y.; Xiao, X.; Effiong, K.; Xu, C.; Su, Z.; Hu, J.; Jiao, S.; Holmer, M. New Insights into the Microplastic Enrichment in the Blue Carbon Ecosystem: Evidence from Seagrass Meadows and Mangrove Forests in Coastal South China Sea. Environ. Sci. Technol. 2021, 55, 4804–4812. [Google Scholar] [CrossRef]
  55. Zamprogno, G.C.; Caniçali, F.B.; Cozer, C.D.R.; Otegui, M.B.P.; Graceli, J.B.; da Costa, M.B. Spatial distribution of microplastics in the superficial sediment of a mangrove in Southeast Brazil: A comparison between fringe and basin. Sci. Total Environ. 2021, 784, 146963. [Google Scholar] [CrossRef] [PubMed]
  56. Hashim, A.M.; Catherine, S.M.P. A laboratory study on wave reduction by mangrove forest. APCBEE Procedia 2013, 5, 27–32. [Google Scholar] [CrossRef] [Green Version]
  57. Jualaong, S.; Pransilpa, M.; Pradit, S.; Towatana, P. Type and Distribution of microplastics in beach sediment along the coast of the Eastern Gulf of Thailand. J. Mar. Sci. Eng. 2021, 9, 1405. [Google Scholar] [CrossRef]
  58. Li, N. Study on Preparation Process and Properties of Polyethylene Terephthalate (PET). Appl. Mech. Mater. 2013, 312, 406–410. [Google Scholar]
  59. Jang, Y.C.; Lee, J.; Hong, S.; Lee, J.S.; Shim, W.J.; Song, Y.K. Sources of plastic marine debris on beaches of Korea: More from the ocean than the land. Ocean Sci. J. 2014, 49, 151–162. [Google Scholar] [CrossRef]
Figure 1. Study area of the two mangrove sites (in green) in Songkhla (SK) and Pattani (PN) provinces, southern Thailand.
Figure 1. Study area of the two mangrove sites (in green) in Songkhla (SK) and Pattani (PN) provinces, southern Thailand.
Jmse 10 00418 g001
Figure 2. MP vertical distribution in the sediment core at the SK stations.
Figure 2. MP vertical distribution in the sediment core at the SK stations.
Jmse 10 00418 g002
Figure 3. MP vertical distribution in sediment cores at PN stations.
Figure 3. MP vertical distribution in sediment cores at PN stations.
Jmse 10 00418 g003
Figure 4. Number of MPs by distance from the innermost points at SK station (a) and at PN station (b); error bars illustrate the standard error of the mean; blue colors indicate the inner zone; red colors indicate the outer zone. Note that this data correspond with the results from the upper 10 cm depth only.
Figure 4. Number of MPs by distance from the innermost points at SK station (a) and at PN station (b); error bars illustrate the standard error of the mean; blue colors indicate the inner zone; red colors indicate the outer zone. Note that this data correspond with the results from the upper 10 cm depth only.
Jmse 10 00418 g004
Figure 5. Mangrove area at SK (a) inner zone; (b) outside zone; (c) debris trapped in mangrove root; and at PN (d) inside zone, (e) outside zone, and (f) debris stand on the mudflat.
Figure 5. Mangrove area at SK (a) inner zone; (b) outside zone; (c) debris trapped in mangrove root; and at PN (d) inside zone, (e) outside zone, and (f) debris stand on the mudflat.
Jmse 10 00418 g005
Figure 6. MP colors found in (a) SK and (b) PN stations.
Figure 6. MP colors found in (a) SK and (b) PN stations.
Jmse 10 00418 g006
Figure 7. MP sizes found in (a) SK and (b) PN stations.
Figure 7. MP sizes found in (a) SK and (b) PN stations.
Jmse 10 00418 g007
Figure 8. MP types found in (a) SK and (b) PN stations.
Figure 8. MP types found in (a) SK and (b) PN stations.
Jmse 10 00418 g008
Figure 9. Examples of fibers found in SK and PN mangrove areas.
Figure 9. Examples of fibers found in SK and PN mangrove areas.
Jmse 10 00418 g009
Table 1. Position and sediment sampling information.
Table 1. Position and sediment sampling information.
StationZone Latitude NLongitudeSediment
Depth (cm)
SK1Inside7.1996945100.577329542
SK2Inside7.2006720100.577052238
SK3Inside7.2009051100.577650634
SK4Inside7.2011649100.578348734
SK5Inside7.2002687100.578626230
SK6Inside7.2020615100.577935218
SK7Outside7.2004212100.578998026
SK8Outside7.2018703100.578305834
PN1Inside6.8836973101.231889418
PN2Inside6.8842695101.231295126
PN3Inside6.8845326101.231088326
PN4Outside6.8845442101.230536638
PN5Outside6.8849661101.231180730
Table 2. Abundance and distribution characteristics of microplastics in mangrove sediments.
Table 2. Abundance and distribution characteristics of microplastics in mangrove sediments.
LocationsSize
(mm)
Abundance of MPs
(Items/kg d.w)
Dominate ShapePolymer TypesColorRef.
Singapore’s coastline, Singapore-12.0 ± 8.0–62.7 ± 27.2fiber (72.0%)PP, PVC, Nylontransparent, blue and red[32]
films (23.3%)
Muara Angke
Wildlife Reserve, Indonesia
0.2–4.828.1 ± 10.3foam (13.3%)PS (44.6%)-[31]
PP (29.2%)
fragment (10.1%)PE (15.4%)
Persian Gulf, Iran<5.01258 ± 291fiber (83%)PE, Nylon, PETred, blue and transparent[50]
film (11%)
fragment (6%)
Qinzhou Bay, China0.16–5.015–12,852 fragment (94%)PS (>98%), PP, PEwhite (98%), transparent (1%), yellow, green, red, and blue (<1%)[34]
fiber (0.5%)
sphere (5.2%)
Maowei Sea, China<5.0520 ± 8–2310 ± 29fragmentPP (47.5–79.2%)white (64.6%)[51]
PE (2.5–42.5%)transparent (20.3%)
PS (1.8–12.8%)
Pearl River Estuary, China<5.0100–7900fiber (70%)PP, PE, PET, PS copolymer, LDPE, Cellophanegreen (28.3–47.6%)[52]
fragment (28–29%)black (21.2–43.1%)
Jinjiang Estuary, China0.03–5.0980 ± 254.6–2340 ± 198fiber (68.6%)PET, PE, PPtransparent (47.7%), white (25.3%), blue (15.3%)[53]
film (15.3%)
particle (12.4%)red, black and yellow(11.7%)
fragment (15.3%)
Guangxi, Coastal South China Sea<5.017.7 ± 8.1–611.8 ± 81.5fiber (74.7%)PE, PP, PS
Polyamide
blue (26.7%), black (22.3%)[54]
fragment (14.9%)
the pellet (1.8%)transparent (17.5%), purple (3.4%)
foam (4.2%)
Southeast Brazil<5.03080filament (88.7%)-blue (54%), transparent (21%)[55]
fragment (11.3%)black (10%), red and green (6%), yellow and white (1%)
Thailand: Songkhla lagoon (SK) and Pattani (PN) coastal area<5.0108–180 (PN)
106–413 (SK)
fiber
fragmentttani coastal areap organism. (n the inner lagoon. al rangeurnal tide with a low tidal range of 0.6 m atteh inlet
PE, rayon, rubber, styrene, paint, and poly (vinyl acetate)white, yellow, pink, silver, purple, red, green, black, dark blue, light blue, and transparentThis work
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Pradit, S.; Noppradit, P.; Loh, P.-S.; Nitiratsuwan, T.; Le, T.P.Q.; Oeurng, C.; Mohamed, C.A.R.; Lee, C.W.; Lu, X.; Anshari, G.Z.; et al. The Occurrence of Microplastics in Sediment Cores from Two Mangrove Areas in Southern Thailand. J. Mar. Sci. Eng. 2022, 10, 418. https://doi.org/10.3390/jmse10030418

AMA Style

Pradit S, Noppradit P, Loh P-S, Nitiratsuwan T, Le TPQ, Oeurng C, Mohamed CAR, Lee CW, Lu X, Anshari GZ, et al. The Occurrence of Microplastics in Sediment Cores from Two Mangrove Areas in Southern Thailand. Journal of Marine Science and Engineering. 2022; 10(3):418. https://doi.org/10.3390/jmse10030418

Chicago/Turabian Style

Pradit, Siriporn, Prakrit Noppradit, Pei-Sun Loh, Thongchai Nitiratsuwan, Thi Phuong Quynh Le, Chantha Oeurng, Che Abd Rahim Mohamed, Choon Weng Lee, Xixi Lu, Gusti Z. Anshari, and et al. 2022. "The Occurrence of Microplastics in Sediment Cores from Two Mangrove Areas in Southern Thailand" Journal of Marine Science and Engineering 10, no. 3: 418. https://doi.org/10.3390/jmse10030418

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop