Controlling effects of terrestrial organic matter on metal contamination and toxicity risks in port sediments.

The contents of metals, total carbon, total nitrogen (TN), total organic carbon (TOC), and stable isotope composition (δ13Corg and δ15N) of sediment organic matter (SOM) were investigated to explore the sources and spatial distribution of metals and SOM in the surface sediments (Kaohsiung Port, Taiwan). Results showed that TOC and metals in estuarine sediments are high, gradually decreasing toward the port entrances. The δ13Corg, δ15N, and TOC/TN ratios indicate that SOM comes mainly from terrestrial sources. This study proposes a befitting model between metal pollution and toxicity risk index and SOM sources in port sediments by combining stable isotope composition, correlation matrix, and multiple linear regression analysis. The model indicates that the degree of metal pollution and toxicity risk in sediments are mainly affected by TOCterr content and SOM source. The results help to understand the influence of organic matter sources in port sediments on metal concentration distribution.

Combined toxicity of microplastics and copper on Goniopora columns.

As microplastics (MP) become ubiquitous, their interactions with heavy metals threatens the coral ecosystem. This study aimed to assess the combined toxicity of MP and copper (Cu) in the environment of coral. Goniopora columna was exposed to polyethylene microplastics (PE-MP) combined with Cu2+ at 10, 20, 50, 100, and 300 µg/L for 7 days. Polyp length and adaptability were recorded daily, and coral samples were collected at 1, 3, 5, and 7 days to analyse zooxanthellae density and antioxidant activity. Tissue observations and the analysis of MP and Cu2+ accumulation were conducted on the 7th day. After 1 day of exposure, PE-MP combined with different concentrations of Cu2+ significantly decreased polyp length and adaptability compared with PE-MP alone. Simultaneously, a significant increase in malondialdehyde (MDA) content, lead to coral oxidative stress, which was a combined effect with PE-MP. After 3 days of exposure, PE-MP combined with Cu2+ at >50 µg/L significantly reduced zooxanthellae density, damaging the coral's symbiotic relationship. In antioxidant enzyme activity, superoxide dismutase (SOD) activity decreased significantly after 1 day of exposure. After 3 days of exposure, glutathione peroxidase (GPx) activity significantly increased with Cu2+ at >20 µg/L. After 5 days of exposure, PE-MP combined with different concentrations of Cu2+ significantly reduced catalase (CAT), glutathione (GSH), and glutathione transferase (GST) activity, disrupting the antioxidant enzyme system, and acting antagonistically to PE-MP alone. Tissue observations revealed that the PE-MP combined with Cu2+ at >50 µg/L caused severe mesenteric atrophy, vacuolar, and Cu2+ accumulation in the coral mesenteric compared with PE-MP alone. The results suggest that combined exposure of PE-MP and copper leads to more severe oxidative stress, disruption antioxidant enzyme system, tissue damage, and Cu2+ accumulation, resulting in a significant maladaptation of corals to the environment.

Polycyclic aromatic hydrocarbons in 55-120 µm phytoplankton.

A baseline study was undertaken on polycyclic aromatic hydrocarbons (PAHs) in phytoplankton. Plankton samples from six stations (duplicates) in Kaohsiung Harbor (KH), Taiwan along with a phytoplankton control sample afar from the harbor, were collected. We applied size-fractionation to isolate phytoplankton (55-120 µm), followed by sedimentation and centrifugation to remove abiogenic particulates. The phytoplankton was freeze-dried, extracted with acetone: n-hexane (1:1, v/v), and analyzed using GC-MS. ΣPAHs in phytoplankton ranged between 5204 and 28,903 ng/g dry weight (mean: 12,150 ng/g). The ΣPAHs in KH were >7 times than the control site (C1: 3972 ng/g). Cluster analysis showed spatial gradients (northern < southern KH). Accumulated PAHs in phytoplankton were from petrogenic (fishing ports and ships) and pyrogenic (river outflows), dominated by lower-ring PAHs, likely due to their higher bioavailability in the dissolved phase. We present a practical phytoplankton isolation technique for more accurate phytoplankton PAH concentrations with insights into their distribution and sources.

Microplastics in coastal farmed oyster (Crassostrea angulata) shells: Abundance, characteristics, and diversity.

One of the most concerning emerging pollutants is microplastics (MPs), which can infiltrate soft tissues of organisms by ingestion, adhesion, and fusing and may even become embedded in biominerals. However, very little evidence is available about MPs in biominerals found in the wild. This study detected the abundance and characteristics of MPs in the shells of farmed oysters (Crassostrea angulata) off the coast of Taiwan and discussed the distribution, accumulation, and diversity in the oyster shells. The results showed that MPs were ubiquitous in oyster shells, with an average abundance of 0.70 ± 0.40 MPs/g. MPs abundance was significantly (p < 0.01) higher in small oyster shells (shell length < 6.5 cm, weight 5-10 g) and inorganic (CaCO3) fraction (HCl digestion) than in large oyster shells (>6.5 cm, 10-25 g) and an organic fraction (H2O2 digestion), respectively. However, there was no significant difference in MPs abundance between the top and bottom shells (p > 0.05). MPs with a size <2 mm accounted for 78.5 %, fibrous MPs for 93.7 %, and rayon for 89.5 %. The MPs diversity integrated index (MPDII) in oyster shells was low (0.27), and the small and fibrous MPs seemed more easily embedded in biominerals. The findings confirm the presence of MPs in oyster shells in coastal environments. In addition, oyster shells may contain higher amounts of MPs than soft tissues 4-5 times, which needs to be confirmed. Further revealing the distribution and accumulation of MPs in water/terrestrial biominerals will help to understand the fate of MPs in the environment.

Microplastics in coral reef sediments underestimated? They may hide in biominerals.

Microplastics (MPs) may be underestimated in coral reef sediments. Current pretreatments for determining MPs in the sediments are mainly density separation and organic matter removal, ignoring MPs that may be embedded or encrusted in biominerals. This could lead to discrepancies in assessing the potential risk of MPs contamination. To confirm whether MPs in coral reef sediments are underestimated, a two-step sequential digestion, including organic matter removal (H2O2 digestion) and biomineral removal (HCl digestion), was performed on sediments from the coral reef area of the South Penghu Marine National Park (SPMNP, Taiwan). The MPs abundance and characteristics of the two steps were analyzed separately. The results showed that the average MPs abundance after HCl digestion (78 ± 42 MPs/kg) was significantly higher than that of H2O2 digestion (38 ± 25 MPs/kg). The MPs diversity integrated index (MPDII) in coral reef sediments was low (MPDII = 0.35), and MPs were mainly small (<2.0 mm, 91.3 %), fibrous (93.5 %), colored (60.9 %), and rayon polymers (73.9 %). Correlation analysis showed that MPs in biominerals mainly dominated MPs in the sediments. These results confirm that current assessments of MPs contamination levels in biomineral-rich sediments may be underestimated and uncertain. In addition, the mineralization of organisms in SPMNP reef regions was affected by MPs from moderate to high levels, depending on the proportion of MPs in biominerals.

A novel pollution index to assess the metal bioavailability and ecological risks in sediments.

The chemical forms of metals in sediments of ports around Taiwan were investigated using sequential extraction. Based on the availability of different chemical forms, novel indices such as bioavailability, mobility, availability, and availability risk of metals in sediments were developed. The results showed that Co, Zn, Pb, Mn, and Cu were mainly present in available forms (49-84 %), and the proportion of oxidative or reductive fractionation was the highest. This suggests that the redox potential is a major factor for metal mobility in the sediments. The results from the proposed indexes showed that metals in sediments have low bioavailability but high to very high mobility and availability. Primarily, the proposed index is more appropriate, as the current index for assessing total metal content may overestimate the level of risk. The indexes established can comprehensively evaluate the bioavailability, mobility, availability, and ecological risk of metals in sediments.

Development of alternative disposals for waste rice husk and dredged harbor sediment by sintering as lightweight aggregates.

This study developed the alternative disposals for dredged harbor sediments by co-sintering with waste rice husk into lightweight aggregates (LWA) to benefit resource sustainability and waste valorization. The effects of rice husk addition and sintering temperature on LWA performances such as water absorption, particle density, crushing strength, weight loss, volume shrinkage, and open porosity were investigated. The key parameters (e.g. C/Fe ratio in raw materials) controlling the LWA performances and engineering applications were determined. Results showed that dredged harbor sediments could be made into suitable LWA for engineering applications from the controlled rice husk addition and sintering temperature. The addition of rice husk led to lower LWA particle density, but raised water absorption and reduced crushing strength. The increase of sintering temperature reduced water absorption and improved crushing strength. The aggregates with 10-15% rice husk, sintered at 1150 °C had appropriate particle density (1.60-1.73 g/cm3), water absorption (11.8-16.6%), and crushing strength (6.0-10.6 MPa), which could be suitable for lightweight concrete applications. Low water-soluble chloride and heavy metals leachabilities aligned with Taiwan's regulatory standards for concrete aggregates. Co-treating waste rice husk and dredged harbor sediment into LWA can benefit the waste reduction and circular economy, and reduce the environmental impacts associated with their disposals.

Comparing the applicability of ecological risk indices of metals based on PCA-APCS-MLR receptor models for ports surface sediments.

This study collected surface sediments from seven ports in Taiwan and analyzed their characteristics along with 10 metals. Enrichment factor (EF), relative EF (REF), potential ecological risk index (PERI), and mean effect range median quotient (m-ERM-q) were used to evaluate the levels of metal contamination and ecological risks in sediments. Principal component analysis (PCA) and the absolute principal component score-multiple linear regression (APCS-MLR) model were applied to quantify the main factors affecting the variations in sediment metals. The different normalization techniques that vary between indexes significantly affect the estimates of risk levels for sediment metals. APCS-MLR model confirmed the significant difference among the sediment quality indices in the degree of anthropogenic pollution, ranging in the order of REF (normalized with reference site and Fe, 97.0 %), PERI (normalized with reference site, 85.5 %), EF (normalized with crust and Fe, 79.4 %), and m-ERM-q (not normalized, 56.6 %).

Non-proportional distribution and bioaccumulation of metals between phytoplankton and zooplankton in coastal waters.

Metal concentrations were concurrently quantified in seawater, phytoplankton, and zooplankton from a heavily impacted coast of southern Taiwan. Combined size and density fractionation were used to accurately quantify metal concentrations in phytoplankton. Cr, Co, Ni, Cu, As, and Pb were analyzed using an inductively coupled plasma mass spectrometer (ICP-MS). As expected, metals significantly increased with an order of seawater < phytoplankton < zooplankton (p < 0.05); but did not differ between estuarine, nearshore, and offshore sites (p > 0.05). Metals were higher along Kaohsiung Harbor and marine outfall diffusion sites, highlighting their major impacts on plankton metal contamination. Notably, phytoplankton (Cr BCF > 100; half of the sites) significantly accumulated more metals contrary to zooplankton (BAF < 10). Metal concentrations and bioaccumulation factors between phytoplankton and zooplankton showed significant negative correlations. This demonstrates a non-proportional distribution and bioaccumulation of metals in phytoplankton and zooplankton-corroborating laboratory findings on zooplankton ability to control metals, irrespective of significantly high bioaccumulation in phytoplankton.

Developing ecological risk assessment of metals released from sediment based on sediment quality guidelines linking with the properties: A case study for Kaohsiung Harbor.

This study aimed to introduce sediment properties (total organic carbon (TOC), acid-volatile sulfides (AVS), particle size distribution) into sediment quality guideline-based risk quotients to assess the potential toxicity of metals (Ni, Cu, Zn, Cr, Cd, and Pb) released from sediments. Sediment was collected at three times points in 20 sampling sites in Kaohsiung Harbor. The Microtox® toxicity test was used to assess the sediment toxicity and the relationship between sediment toxicity and risk quotient estimated based on the metal concentration was constructed. To improve the toxicity prediction and modify the risk quotient according to the sediment properties, stepwise multiple linear regression (MLR) models that have been tested over wide ranges of TOC, AVS, and particle size distribution to determine the key sediment properties. Common multimetal indices, including the pollution load index, modified degree of contamination index, Nemerow pollution index, potential ecological risk index, and total toxic risk index, were compared with sediment toxicity to evaluate the degrees of correlation. By modifying the relationship between metal toxicity and the risk quotient by including TOC and AVS, the prediction showed that sediments in Kaohsiung Harbor were generally of slight acute toxicity to acute toxicity to organisms, with sampling sites near an industrial zone showing a higher probability of high acute toxicity. In particular, the acute risk of adverse effects on aquatic organisms from sediments in the Salt River estuary was significantly higher than that at other sites, which was consistent with the results of assessment based on the multimetal indices. This study suggests that the MLR-based approach may facilitate the adoption of updated site-specific metals standards that more accurately account for the parameters affecting metal bioavailability than metal concentration standard alone.

Potential sources and toxicity risks of polycyclic aromatic hydrocarbons in surface sediments of commercial ports in Taiwan.

The accumulation of pollutants in the semi-enclosed waters of ports has long been a concern. This study assessed the pollution status, sources, and toxicity risks of 16 polycyclic aromatic hydrocarbons (PAHs) in surface sediments of 7 major ports in Taiwan. Total PAHs concentrations in sediments ranged between 8.4 and 572.5 ng/g dw, with an average of 112.4 ± 136.5 ng/g dw. The 3- and 4-ring PAHs (63 %) were the major constituents of PAHs in the sediments. Diagnostic ratios and positive matrix factorization analyses indicated that PAHs in sediments were mainly contributed by biomass combustion (45.0 %), coal combustion (31.5 %), and vehicle emissions and related fossil fuels (23.5 %). The results of ecological risk assessment showed a low-medium risk of PAHs in the sediments outside the port, whereas most of the sediments within the port presented a medium-high risk. An assessment of the possible human health risks indicated that PAHs were present at acceptable levels.

Impacts of microplastics on scleractinian corals nearshore Liuqiu Island southwestern Taiwan.

Seawater, sediments, and three genera of wild scleractinian corals were collected from four coral reef areas nearshore Liuqiu Island, southwestern Taiwan. Abundance, characteristics (sizes, colors, shapes, and polymer types), and enrichment of microplastics (MPs) in the corals, and their impacts on coral cover were determined. The average MPs abundances were 0.95, 0.77, and 0.36 item/g for Galaxea sp, Acropora spp, and Pocillopora sp, respectively. The MPs abundance was relatively higher on the coral surfaces than inside the skeletons, dominated by blue rayon-fibers, correspondingly observed in seawater and sediments. Large-size colorless MPs tended to be mis-ingested by Galaxea sp. (71%) compared with Pocillopora sp. (43%) and Acropora spp. (31%). The low hard coral cover (12.5%) observed at Yufu (L1) on the northeastern coastal zone nearby tourism center of Liuqiu Island where correspondingly associated with high MPs abundance in seawater (10 item/L), sediments (260 item/kg), and corals (0.60 item/g). Tourism induced sewage discharges and sailing activities significantly contributed to the MPs pollution, probably contributing to the loss of coral cover. High MPs enrichment in corals (EFMP = 25-283) shows that the marine MPs pollution can critically threaten coral reef ecosystems. Fibrous MPs present inside the coral skeleton serve as potential indicator of MPs' impact on corals-with the dominance of textile-related rayon and polyester/PET microfibers in the coral reef zones. This study provided valuable information for coral conservation and coastal management.

Impact of polyethylene microplastics on coral Goniopora columna causing oxidative stress and histopathology damages.

In recent years, the increase of microplastics in the sea exerted a negative impact on coral health. This study has been undertaken to analyze the impact of microplastics on corals. Here, Goniopora columna was exposed to different concentrations of polyethylene microplastics (PE-MP). The daily polyps length and adaptability were recorded. Analysis of the zooxanthellae density and antioxidant activity of coral was done after 1, 3, 5 and 7 days. Further tissue morphology and accumulation of PE-MP were analyzed. The results showed that PE-MP at different concentrations can be adsorbed on the surface of corals and enter inside corals after 7 days. PE-MP at different concentrations reduced polyps length, adaptability and cause the changes in the density of zooxanthellae to be the reason for unbalancing of corals. PE-MP at different concentrations reduced the superoxide dismutase (SOD) activity after exposure to 1 day. PE-MP increased the catalase (CAT) activity at 100 mg/L after exposure; even after reducing the concentration has the same effect. PE-MP at various concentrations increased the glutathione peroxidase (GPx) activity after exposure to 5 and 7 days. It also increased the glutathione transferase (GST) and glutathione (GSH) activity after exposure to 5 and 7 days. PE-MP at different concentrations increased the malondialdehyde (MDA) content after exposure from 1 to 7 days. Analysis of tissue morphology and tissue accumulation shows that different concentrations of PE-MP cause mesenteric atrophy, vacuole, and accumulation in the coral mesenteric. These results indicate that the PE-MP can impact the antioxidant system and hampers the function of enzymes responsible for detoxification of G. columna, increase lipid peroxide content and also cause tissue damage through accumulating in the coral mesenteric.

Comparative trace metal assessment in phytoplankton using size and density fractionation.

Trace metal assessment in marine phytoplankton is challenging due to complex assemblages and variable amounts of abiogenic suspended particulates. Using aliquots, this study were able to compare trace metal concentrations in plankton samples subjected to size and density fractionation. Elements including Cr, Mn, Fe, Ni, Cu, Zn, As, Sr, Hg, and Pb were analyzed by inductively coupled plasma mass spectrometer (ICP-MS). Trace metals were found to be significantly higher in size fractionated than density fractionated plankton for both small (1.2-50 µm) and large (50-120 µm) fractions. Metals from abiogenic sources (61-88%) also significantly contributed to trace metals detected in 1.2-120 µm suspended particulates collected from Kaohsiung Harbor. Results suggest that size fractionation can potentially overestimate trace metals in phytoplankton. It is therefore recommended combining the two methods by first isolating different size fractions followed by density fractionation to separate phytoplankton from zooplankton, and abiogenic particulates from phytoplankton assemblages, respectively.

Evaluation of polycyclic aromatic hydrocarbons in silky sharks Carcharhinus falciformis collected from Western Indian Ocean and human health risk assessment.

The silky shark (Carcharhinus falciformis) is the most abundant and widely distributed shark species in the marine system of tropical regions. However, it appears that there is limited information on USEPA 16 polycyclic aromatic hydrocarbons (PAHs) concentration in silky shark muscle tissue, which has together with the lack of a health risk assessment of human consumption of silky shark filets. The potential toxicity of PAHs in muscles of silky sharks and cancer and non-cancer risk of consumers were assessed. Results showed that the total PAHs (TPAHs) concentration in the muscle tissue of silky sharks was between 62 and 657 ng/g ww, with an average of 234 ± 221 (mean ± standard deviation) ng/g ww, and can be considered as minimally to moderately contaminated level. Naphthalene (NA), phenanthrene (PH), and fluoranthene (FLU) are the most abundant PAHs in silky sharks muscle tissue, accounting for 38.6%, 11.0%, and 19.0% of TPAHs, respectively. The average values of toxic benzo[a]pyrene (BaP) equivalent (TEQcarc) and toxic dioxin equivalent (TEQfish) of PAHs equal to the potency of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in silky shark muscle are 13.5 ± 16.4 ng BaP/g ww and 34.1 ± 77.4 pg TCDD/g ww, respectively, and they showed a good linear relationship (r = 0.928; p < 0.001). The TEQcarc of silky sharks muscle is higher than USEPA's screening value of PAHs of 3.2 ng BaP/g ww for adults, indicating a potential negative impact on public health. The calculated hazard index (HI) of PAHs is less than 1, suggesting that residents eating silky shark muscle will not expect to cause significant non-cancer risk. However, the incremental lifetime cancer risk (ILCR) of BaP as 10.6-26.3% and 8.2-32.4% in males and females, respectively, may pose a significant cancer risk. In general, children and the elderly have relatively higher risks, as well as males have a higher cancer and non-cancer risk than females.

The effect of heavy rainfall on the exposure risks of sedimentary phthalate esters to aquatic organisms.

Phthalate esters (PAEs) have known widely being used in plastic products leading to being ubiquitous in the environment by easy to release from those products. This study aims to understand the impact of heavy rainfall on the concentration of PAEs in surface sediments of the Salt River in Kaohsiung, Taiwan, and its potential ecological risks on aquatic organisms. The potential ecological risk assessment of sediment PAEs is based on the total risk quotient (TRQ) method. The total concentration of 10 PAEs (∑PAE10) in sediments of the Salt River is 333-13,615 ng/g dw, with an average of 4212 ± 3753 ng/g dw. Before the rainy season, the ∑PAE10 concentration in sediments at the outlets of domestic sewage in upstream was 9768-13,615 ng/g dw, which were relatively higher than other sites (542-3721 ng/g dw). During the rainy season, the ∑PAE10 concentration was 2820-12,041 ng/g dw, which was 1-11 times higher than that determined before the rainy season. After the rainy season, the ∑PAE10 concentration recorded was 530-6652 ng/g dw, which is 1-11 times lower than the value obtained during the rainy season. PAEs in sediments of the Salt River may have low to moderate potential risks to algae, crustaceans, and fish. Bis(2-ethylhexyl) phthalate (DEHP) and diisobutyl phthalate (DiBP) are the main PAE that poses a potential risk to algae and crustaceans, and to fish respectively, whose values of risk quotient accounts for 40-69% of the TRQ value. The distribution of TRQ values for these aquatic organisms show a decreasing trend of PAEs level with respect to the rainy season: during the rainy season > after the rainy season > before the rainy season. Heavy rainfall may cause more serious pollution in sediments and increase the exposure risk of PAEs to aquatic organisms.

Seasonal variation of diversity, weathering, and inventory of microplastics in coast and harbor sediments.

Spatiotemporal variations in the abundance of microplastics (MPs) in surface sediments along the southwestern coast of Taiwan (including harbor and coastal regions) were investigated and the diversity, degree of weathering, and inventory of MPs in the sediments further quantified. The spatiotemporal variations of MP characteristics were used to assess possible transport routes of MPs. Results indicated that the average MP abundance in the partially-enclosed harbor region was 79.3 MPs in 1 kg dry sediment (item/kg dw), which was 3-5 times higher than that in the coastal region. Average MP abundance during the dry season (36.5 ± 52.2 item/kg dw) was relatively higher than that during the wet season (22.3 ± 23.2 item/kg dw). The dominant MPs were small (0.1-1.0 mm, 90%), colored (62.3%), and consisted mainly of fibers (54.1%) and fragments (40.5%). Analysis by µFTIR revealed the presence of ten types of polymers in the MPs, with the most abundant being polypropylene (35.1%), rayon (33.2%), and polystyrene (10.0%). Values of the microplastic diversity integrated index (MPDII) indicated that MP diversity was greater in the harbor region (MPDII = 0.62) than in the coastal region (MPDII = 0.51-0.54), and greater during the wet season (MPDII = 0.60) than during the dry season (MPDII = 0.50). As indicated by values of the MP carbonyl index (CI), the MPs exhibited a high degree of oxidation (CI >0.31) that appeared unrelated to spatiotemporal variations. In the dry season, MP inventory was 12.2 tons and the wet season inventory was 8.1 tons. The hydrodynamic forces may be an influenced force for the spatiotemporal distribution patterns of the MPs in surface sediments. MPs could accumulate in the surface sediments during the dry season and resuspend in the wet season with the higher rainfall and then migrate towards the deep sea following the water flow.

Recycling dredged harbor sediment to construction materials by sintering with steel slag and waste glass: Characteristics, alkali-silica reactivity and metals stability.

This work recovered the dredged sediment around Kaohsiung Harbor, Taiwan, for preparing lightweight aggregates (LWA), of which physicochemical properties as affected by the addition of basic-oxygen-furnace (BOF) slag and waste glass were investigated. LWA properties included water absorption, particle density, compressive strength, shrinkage, and microstructure of sintered pellets were evaluated to ensure feasibility of dredged harbor sediment reutilization technique. Results showed that adding appropriate amount of glass powders (~7%) to the mixtures of sediment and slag significantly reduced the water absorption (as low as 2.2%) of the sintered pellets and increase the compressive strength (as high as 23.1 MPa) of LWA, which were found to be controlled by open porosity and shrinkage. Excessive addition of glass (>10%) led to increase in internal pore sizes of the sintered pellets, and thus reduced the compressive strength. The alkali-silica reactivity (ASR) of the LWA was innocuous according to the ASTM C289 test. Sintering and glass addition improved the stability of heavy metal and environmental compatibility of the LWA. The recycling of waste sediment, slag, and glass for LWA production can provide an alternative for the disposal of dredge harbor sediment and has positive impact on waste reduction, which not only can reduce secondary contamination to the environment, but also can contribute to circular economy.

Microplastics and their affiliated PAHs in the sea surface connected to the southwest coast of Taiwan.

Contamination by microplastics (MPs) and the associated organic pollutants has caused potential threats to the ecological environment of global waters. In this study, MPs were sampled by trawling from the surface waters of the estuary, fishing port entrance and harbor entrance areas connected to the southwestern coast of Taiwan. Moreover, the abundance, morphological characteristics, composition, and associated polycyclic aromatic hydrocarbons (PAHs) of MPs were analyzed. The abundance of MPs was 0.36 ± 0.21 items/m3, which was 6.4 ± 10.7% of the abundance of zooplanktons. The average abundance of MPs was the highest in the estuary area, indicating that river transport was the primary way for MPs to enter the ocean. The most dominant MPs were small (0.33-2 mm; 78.8 ± 8.1%), colored (60.0 ± 12.8%), fragments (66.1 ± 10.6%), comprising PE (52.6 ± 7.6%), and PP (38.7 ± 9.4%). The decomposition of various plastic products and disposable plastic packaging may be the most significant source. The total concentration of PAHs in MPs ranged from 104 to 3595 ng/g dw, with an average of 818 ± 874 ng/g dw. The diagnostic ratios and the results of principal component analysis (PCA) and multiple linear regression of the absolute principal component scores (MLR-APCS) indicated that the PAHs were mainly contributed from sources related to petrogenic (71.4%) and vehicles (28.6%). Most likely due to MPs on the sea surface coming into contact with floating oil spills from ships or floating tar particles.

Distribution, sources, and behavior of PAHs in estuarine water systems exemplified by Salt River, Taiwan.

Water, suspended particulate matter (SPM), and sediment samples were collected from Salt River in Taiwan and analyzed the concentrations of 16 types of polycyclic aromatic hydrocarbons (PAHs). The analysis results were used to examine the distribution, source, partition behavior, and potential ecological risks of PAHs in the estuarine water systems. The mean concentration of total PAHs in water, SPM, and sediment samples was 0.485-10.2 µg/L, 26.7-169 mg/kg dw, and 0.343-29.4 mg/kg dw, respectively. The highest concentration was found at the river mouth and decreased toward the river and sea with the tide. The distribution of the diagnostic ratios of PAHs showed that the combustion of coal and petroleum products are the main sources of PAHs in Salt River. The in site organic carbon normalized partition coefficients for SPM-water (K'oc(SPMW)) and sediment-water (K'oc(SedW)) were 2.8-4.5 and 4.6-6.0 (log units), respectively, increasing with the number of rings in PAHs. The values log K'oc(SedW) and log K'oc(SPM-W) showed a significant linear correlation with their octanol-water partition coefficients (p < 0.01), and their slopes were 0.427 and 0.316, respectively. The fugacity fraction was used to evaluate the exchange of PAHs in water-SPM-sediment systems. Results showed that in SPM, 2-4-ring PAHs tend to be released into water, whereas 5-6-ring PAHs in water tend to be adsorbed onto SPM. The exchange of PAHs between water and sediment occurs in the direction of adsorption onto sediment from water. The assessment of the mean risk quotient, total toxicity equivalence, and mean effect range-median quotient of PAHs showed that the PAHs in the water and SPM of Salt River may have moderate to high ecological risk. In sediment, PAHs in the lower reaches and estuary may pose moderate to high ecological risk, whereas PAHs in the middle and upper reaches show low to moderate ecological risk.