Characteristics of sub-micron aerosols in the Yellow Sea and its environmental implications.

The Yellow Sea, characterized by an influx of both natural marine and anthropogenic pollutants, coupled with favorable photochemical conditions, serve as key sites for potential interactions between atmospheric gases and aerosols. A recent air monitoring campaign in the Yellow Sea revealed aerosol contributions from four sources, with the highest mass concentrations and dominance of NO3- (38.1 ± 0.37 %) during winds from China. Indications of potential secondary aerosol formation were observed through the presence of hydrolysis and oxidation products of nitrate and volatile organic compounds. Correlations between time series distributions of biomass burning organic aerosols and particle number counts (Dp 100-500 nm, R2 = 0.94) further suggest potential size growth through adsorption and scavenging processes. The results from this study provide observational evidence of a shift in atmospheric compositions from sulfate to nitrate, leading to an increased atmospheric nitrogen deposition in the Yellow Sea.

Emissions from ships' activities in the anchorage zone: A potential source of sub-micron aerosols in port areas.

Busan Port is among the world's top ten most air-polluted ports, but the role of the anchorage zone as a significant contributor to pollution has not been studied. To assess the emission characteristics of sub-micron aerosols, a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was deployed in Busan, South Korea from September 10 to October 6, 2020. The concentration of all AMS-identified species and black carbon were highest when the winds came from the anchorage zone (11.9 µg·m-3) and lowest with winds from the open ocean (6.64 µg·m-3). The positive matrix factorization model identified one hydrocarbon-like organic aerosol (HOA) and two oxygenated organic aerosol (OOA) sources. HOAs were highest with winds from Busan Port, while oxidized OOAs were predominant with winds from the anchorage zone (less oxidized) and the open ocean (more oxidized). We calculated the emissions from the anchorage zone using ship activity data and compared them to the total emissions from Busan Port. Our results suggest that emissions from ship activities in the anchorage zone should be considered a significant source of pollution in the Busan Port area, especially given the substantial contributions of gaseous emissions (NOx: 8.78%; volatile organic compounds: 7.52%) and their oxidized moieties as secondary aerosols.

Mobile measurement of vehicle emission factors in a roadway tunnel: A concentration gradient approach.

Tunnels are the preferred experimental environments for estimating vehicle emission factors (EFs) under real-world driving conditions. In this study, online measurements of traffic-related air pollutants (including CO2, NOX, SO2, O3, particulate matter [PM], and volatile organic compounds [VOCs]) were conducted using a mobile laboratory in the Sujungsan Tunnel in Busan, Korea. Mobile measurements generated concentration profiles of the target exhaust emissions inside the tunnel. These data were used to produce a zonation of the tunnel, i.e., mixing and accumulation zones. There were differences between the CO2, SO2, and NOX profiles, and a starting point that was free from ambient air mixing effects could be set at 600 m from the tunnel entrance. The EFs of vehicle exhaust emissions were calculated using pollutant concentration gradients. The average EFs for CO2, NO, NO2, SO2, PM10, PM2.5, and ∑VOCs were 149,000, 380, 55, 29.2, 9.64, 4.33, and 16.7 mg km-1·veh-1, respectively. Among the VOC groups, alkanes contributed more than 70% of the VOC EF. Mobile measurement-derived EFs were validated using the conventional EFs from stationary measurements. The EF results from the mobile measurements matched those from the stationary measurements, while the absolute concentration differences between them implied complex aerodynamic movements of the target pollutants inside the tunnel. This study demonstrated the usefulness and advantages of applying mobile measurements in a tunnel environment and indicated the potential of the approach for observation-based policymaking.

Chemical characterization of sub-micron aerosols over the East Sea (Sea of Japan).

Studies of the land-sea-air interactions of aerosol are scarce considering their significant role in global environmental changes. Here, we investigated potential sources of sub-micron aerosols over the East Sea (Sea of Japan), which is strongly influenced by continental and marine aerosols. A high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was used to measure the size-resolved chemical compositions of sub-micron aerosols during the period March 10-15, 2020. Concentrations of all AMS species, black carbon (BC), PM10 (particulate matter <10 µm) and PM2.5 (particulate matter <2.5 µm) were higher when cruising in industrialized coastal areas compared to the offshore region. A positive matrix factorization (PMF) model identified five distinct sources, i.e., hydrocarbon-like organic aerosol, semi-volatile and low-volatile oxygenated aerosols, methanesulfonic acid (MSA), and dimethyl sulfide (DMS; C2H6S) oxidation, which accounted for 5.98 %, 21.6 %, 28.3 %, 34.5 %, and 9.64 % of the total organic mass, respectively. The spatiotemporal variation of MSA, as well as the MSA to sulfate ratio (MSA:SO42-) over the East Sea, was determined for the first time. The mass concentrations of MSA displayed a similar time series distribution pattern to those of DMS. The time series distributions of the MSA:SO42- ratio displayed distinct differences, with higher ratios downwind of the ocean (0.216 ± 0.083 µg·m-3) than land (0.089 ± 0.030 µg·m-3). The growth of ultrafine particles (10-35 nm) was observed during two of the elevated MSA:SO42- ratio events, suggesting a potential role of MSA in new particle formation.

Determination of anthropogenic organics in dichlomethane extracts of aerosol particulate matter collected from four different locations in China and Republic of Korea by GC-MS and FTICR-MS.

In this study, the hypothesis that particulate matter in east of Korea peninsula would be significantly influenced by particulate matter originated from east of China was evaluated. To test the hypothesis, water-insoluble compounds in particulate matter samples collected from three different locations in Korea and one in China were characterized by atmospheric pressure photoionization (APPI) coupled with Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS) and gas chromatography mass spectrometry (GC-MS). Each sample was collected twice, in winter and in spring. The GC-MS data revealed the presence of high levels of polycyclic aromatic hydrocarbons (PAHs), such as benzo[a]anthracene in the samples from Tianjin, China. The sample collected in the winter from Baengnyeong Island, which is the location in Korea that is geographically closest to the east coast of China was also rich in aromatic compounds. Meanwhile, the APPI FTICR-MS data showed that polycondensed PAHs and two- to four-ring PAHs with long alkyl chains were abundant in the winter samples from Tianjin and Baengnyeong Island which stems most likely from coal combustion in the eastern China. In contrast, nonaromatic compounds with a biogenic origin were mostly observed in samples collected from islands located in eastern (Ulleung Island) and southern (Jeju Island) Korea. A principal component analysis by FTICR-MS and GC-MS also showed that the samples from Tianjin and those collected from Baengnyeong Island in the winter are strongly associated with coal combustion, whereas the other samples are mainly influenced by vehicle emissions. Therefore, it is concluded that the atmosphere from east of China has significant influence over atmosphere in west of Korea peninsula.

Rapid recovery of coastal environment and ecosystem to the Hebei Spirit oil spill's impact.

The 2007 Hebei Spirit oil spill (HSOS), the largest in the national history, has negatively impacted the entire environment and ecosystem along the west coast of South Korea. Although many studies have reported the damages and impacts from the HSOS, quantitative assessment evaluating the recovery time and status have not been documented. Here, we first address the recovery timeline of the HSOS, by comprehensive analyses of 10-years accumulated data in quantitative manner. Concentrations of residual oils in seawater, sediments, and oysters rapidly dropped to backgrounds in 16, 75, and 33 months, respectively. Also, damaged benthic communities of intertidal and subtidal areas were fully recovered only after ~6 years. The present results collectively indicated unexpectedly fast recovery of the damaged environment and ecosystem from such a huge oil spill. The high tidal mixing (~9 m tidal height) and intensive human cleanup (~1.2 million volunteers) at the initial cleanup period might have contributed to rapid recovery; cf. 4-5 times faster than the Exxon Valdez oil spill. However, potential risk to human health remains unclear. Thus, it is warranted to conduct more in depth epidemiological studies to address chronic health effects associated with the cleanup volunteers as well as the local residents who have been living nearby the oil spill impacted sites.

Environmental significance of lubricant oil: A systematic study of photooxidation and its consequences.

Lubricant (lube) oil discharge from ships has been widely considered as normal "operational consumption", but is now deemed to be oil pollution. Despite the chronic contamination of the marine environment by lube oil, the number of studies related to its environmental impact, characteristics, and toxicity is limited. This study is the first attempt to investigate the environmental fate of lube oil subjected to photooxidation using in situ mesocosms. A tiered approach using thin-layer chromatography-flame ionization detection (TLC-FID), Fourier-transform infrared spectroscopy (FTIR) and gas chromatography-mass spectrometry (GC-MS) demonstrated compositional changes in lube oil and the water-soluble fraction (WSF). Total polycyclic aromatic hydrocarbons (ΣPAHs) in lube oil after 96 h of photooxidation were measured at 79.8 and 41 µg/g in the control (Con) and exposure (Exp) groups, respectively. Meanwhile, the ΣPAHs concentration in WSF after 96 h was very low, at 0.25 and 0.45 µg/L in Con and Exp, respectively. FTIR and GC-MS helped identify bond changes and photoproducts in WSF. A wide range of photoproducts, including carboxylic acids, esters, anhydrides, aldehydes and ketones, were identified in WSF. Toxic effects of WSF in both the Con and Exp groups obtained after 96 h of photooxidation were evaluated on olive flounder (Paralichthys olivaceus) embryos. Morphological defects, especially tail fin fold defects, were found to be significantly elevated in both the Con and Exp groups, with marginally higher frequency in Exp. The results of this study demonstrate the need for further research on lube oil weathering, including monitoring over prolonged periods of time.

Stability of mechanically and chemically dispersed oil: Effect of particle types on oil dispersion.

Oil spill dispersant (OSD) application is one of the preferred cleanup options to cope with oil spills at sea. OSD, in principle, can enhance biodegradation of oil because of its effectiveness in producing relatively small droplets and dispersing them into the water column. Under turbulent conditions, suspended particulate matter (SPM) which are present naturally in the environment can interact with oil to form aggregates known as oil-SPM aggregates (OSA) which also enhances biodegradation of oil. Despite its high dispersion effectiveness, chemically dispersed oil (CDO) has a tendency to resurface with increasing time which decreases the biodegradation potential. Meanwhile, the presence of SPM prevents recoalescence of dispersed oil which can enhance stability of oil droplets. This study focused on the effects of SPM on the dispersion effectiveness and stability of mechanically dispersed oil (MDO) and CDO. Dispersion tests of MDO and CDO extended to 72 h with and without SPM to see the initial effectiveness and the prolonged stability of dispersed oil. In the presence of SPM, the oil dispersed by MDO increased by 14.8-40.7%, while the resurfacing oil by CDO decreased by 8.7-19.4%. Regardless of SPM type, oil dispersion effectiveness and stability of MDO and CDO were significantly increased. Long-term stability test for 3 months showed that stability of OSA increased as the particle size decreased and particle counts increased.

Molecular level determination of water accommodated fraction with embryonic developmental toxicity generated by photooxidation of spilled oil.

In this study, developmental toxicity was increased as the oil was further degraded under natural sunlight. Detailed chemical composition of the degraded oils was examined by use of gas chromatography (GC) and (-) electrospray ionization ultrahigh resolution mass spectrometry (UHR-MS). Baseline toxicities were estimated based on chemical activities of polycyclic aromatic hydrocarbons, and it was obvious that the predicted chemical activities can not explain increased toxicity alone. However, the ultrahigh resolution mass spectral abundance of polar compounds including O3 and O4 class compounds was significantly increased as the photodegradation proceeded. Further examination of double bond equivalence values of the compounds showed that polar compounds with both non-aromatic and aromatic polar structures were increased. Statistical analysis indicates that the increased toxicity can be well explained by the increased polar compounds. Therefore, the oxygenated compounds identified in this study can play an important role in toxicity of degraded oils.

Suspended particles enhance biodegradation of oil in sea.

Biodegradation patterns of oil in four distinct phases were compared over a 14-day series of exposures. The dispersibility and stability of oil droplets in the water column were important factors affecting oil biodegradation. Due to the stability of oil droplets with particle interactions, oil-suspended particulate matter aggregates (OSA) showed a five-fold enhancement in biodegradation compared to non-dispersed oil. The reduction of total petroleum hydrocarbons was highest in OSA (51.45%), followed by chemically dispersed oil (33.5%), oil film (21.6%), and water-accommodated fractions (WAF, 14.3%). Polycyclic aromatic hydrocarbon (PAH) profiles and percentage weathering plots showed that reductions in PAHs in WAF, oil film, and chemically dispersed oil were mainly due to evaporation (41.5-69.5%) and only partially due to biodegradation (7.4-16.3%). However, the reduction of PAHs in OSA was driven more by biodegradation (36.8%) than evaporation (29.7%). The strong PAH-particle interactions in OSA inhibited evaporation of PAHs and enhanced microorganism biodegradation in the water column.

Fate of residual oils during remediation activities after the Wu Yi San oil spill.

In this study, the fate of residual oils was investigated during remediation activities for a year after the Wu Yi San oil spill. Microscope observations showed that relatively large amounts of oil-suspended particulate matter aggregate (OSA) were formed. Negatively buoyant OSA was the dominant form (>95%), followed by neutrally (~5%) and positively buoyant (<1%) forms. To elucidate the dominance of negative buoyancy OSA, physicochemical properties of the mineral and residual oils were identified. Chemical analysis showed that the weathering percentage of residual oils was 43.7 ±â€¯2.59%, which was the driving factor for sedimentation of OSA. As the density of oil increased with weathering stages, the density of OSA also increased simultaneously. These results showed that, during mechanical remediation activities, resurfaced residual oils can form negative buoyancy OSA which tends to sink and transfers oil contaminants from intertidal to benthic environments.

A systematic study of the effects of solvents on phenanthrene photooxidation.

A systematic study of the photooxidation of phenanthrene under simulated environmental conditions was conducted in vitro using polar (methanol, acetonitrile) and non-polar (isooctane, hexane) solvents as media. In all solvents, phenanthrene concentration decreased exponentially as exposure time increased. Fourier-transform infrared spectroscopy (FTIR) and gas chromatography-mass spectrometry (GC-MS) analysis were used to investigate the structural changes induced by photooxidation. After 24 h of photooxidation, FTIR showed the formation of characteristic bands of carboxylic acid in all solvents. In non-polar solvents, characteristic phenanthrene peaks were completely depleted after 48 h. In polar solvents, phenanthrene peaks disappeared at a slower rate, with peaks in acetonitrile disappearing at 72 h and methanol persisting at trace levels at 96 h. The reaction rate was higher in non-polar solvents. The obtained half-lives were observed in the following order: isooctane (13.2 h) > hexane (13.5 h) > methanol (18.0 h) > acetonitrile (22.8 h). FTIR and GC-MS results were in good agreement and showed the formation of carboxylic acids, aldehydes, and ketones in polar solvents and carboxylic acids, alkanes, and alkanoic acids in non-polar solvents. Products such as primary amides induced by solvent effects were observed in acetonitrile. Based on the results, the solvents were rated and a solvent selection guide for photooxidation of PAHs was provided.

A preliminary study on the role of suspended particulate matter in the bioavailability of oil-derived polycyclic aromatic hydrocarbons to oysters.

Suspended particulate matter (SPM) refers to fine-grained materials that are suspended in water columns. By providing a surface for the adsorption of non-polar organic compounds, SPM is a carrier for persistent and toxic contaminants. A wide range of organic pollutants, including polycyclic aromatic hydrocarbons (PAHs), can be adsorbed onto SPM. The formation of particle-associated PAHs can sequentially increase the potential for exposure to and bioaccumulation by organisms. Until recently, most oil exposure studies were performed using freely dissolved and dispersed forms, and therefore the role of SPM in influencing the bioavailability and bioaccumulation of PAHs has not been considered. This study found that SPM influences the bioavailability of petrogenic PAHs in the water column and their potential for accumulation in oysters. SPM significantly enhanced the water column entrainment of petrogenic PAHs, thus increasing the potentials for uptake by exposed organisms. PAHs in the water column was highest from mechanically dispersed oil (MDO; 2.27 µg/mL) ≥ oil-SPM aggregate (OSA; 1.96 µg/mL) > water accommodated fraction (WAF; 0.19 µg/mL) but the percentage of PAHs accumulated in oysters were highest from WAF (18.3%) > MDO (14.2%) > OSA (9.62%). Despite the high water column available PAHs, oysters exposed to SPM-associated oil accumulated PAHs at half the accumulation efficiency compared with those exposed to PAHs without SPM.

Estimating degree of degradation of spilled oils based on relative abundance of aromatic compounds observed by paper spray ionization mass spectrometry.

Paper spray ionization mass spectrometry (PSI-MS) was applied for the first time to study temporal change of photo-oxidized and weathered oils subjected to degradation. PSI is chosen in this study because it is an optimal ionization technique for the analysis of degraded oils with limited sample quantity and prone to salt and particulate contamination. With PSI-MS, quantitative analysis of oils can be successfully performed with as little as 2 µg of oil sample. In addition, oil solutions containing up to 0.05% sodium chloride were successfully analyzed with PSI-MS. In the PSI-MS spectra of photo-degraded oils, the relative abundance of compounds having double equivalence value (DBE) ≥ 5 increased but those with DBE < 5 decreased in number. The summed abundance ratio of compounds having DBE < 5 and DBE ≥ 5 showed a negative exponential correlation with the duration of UV exposure in laboratory experiments. The same trend was observed from spilled oils obtained from the environment. Therefore, this ratio serves as an effective means to estimate the degree of weathering in spilled oils.

Long-Term Monitoring of PAH Contamination in Sediment and Recovery After the Hebei Spirit Oil Spill.

Approximately 10,900 t of crude oil was released 10 km off the west coast of Korea after the collision between the oil tanker Hebei Spirit and a barge carrying a crane in December 2007. To assess the areal extent and temporal trends of PAH contamination, 428 sediment samples were collected from December 2007 through May 2015 for PAH analysis. Sedimentary PAH concentrations measured immediately after the spill ranged from 3.2 to 71,200 ng g-1, with a mean of 3800 ng g-1. Increases in PAH concentrations were observed at stations 7-23, which were heavily oiled due to tidal currents and northwesterly wind that transported the spilled oil to these locations. Mean and maximum PAH concentrations decreased drastically from 3800 to 88.5 and 71,200 to 1700 ng g-1, respectively, 4 months after the spill. PAH concentrations highly fluctuated until September 2008 and then decreased slowly to background levels. Reduction rate was much faster at the sandy beaches (k = 0.016) than in the muddy sites (k = 0.001). In muddy sediments, low attenuation due to low flushing rate in the mostly anaerobic sediment possibly contributed the persistence of PAHs. By May 2015 (~7.5 years after the spill), mean and maximum PAH concentrations decreased by 54 and 481 times, respectively, compared with the peak concentrations. The sedimentary PAH concentrations in the monitoring area have returned to regional background levels.

Contamination and Human Health Risk Assessment of Polycyclic Aromatic Hydrocarbons (PAHs) in Oysters After the Wu Yi San Oil Spill in Korea.

After the collision of the Singapore-registered oil tanker M/V Wu Yi San into the oil terminal of Yeosu, Korea on January 31, 2014, approximately 900 m3 of oil and oil mixture were released from the ruptured pipelines. The oil affected more than 10 km of coastline along Gwangyang Bay. Emergency oil spill responses recovered bulk oil at sea and cleaned up the stranded oil on shore. As part of an emergency environmental impact assessment, region-wide monitoring of oil contamination in oyster had been conducted for 2 months. Highly elevated concentrations of polycyclic aromatic hydrocarbons (PAHs) were detected at most of the spill affected sites. Four days after the spill, the levels of PAHs in oysters increased dramatically to 627-81,000 ng/g, the average of which was 20 times higher than those found before the spill (321-4040 ng/g). The level of PAHs in these oysters increased until 10 days after the spill and then decreased. Due to the strong tidal current and easterly winter winds, the eastern part of the Bay-the Namhae region-was heavily contaminated compared with other regions. The accumulation and depuration of spilled oil in oyster corresponded with the duration and intensity of the cleanup activities, which is the first field observation in oil spill cases. Human health risk assessments showed that benzo[a]pyrene equivalent concentrations exceeded levels of concern in the highly contaminated sites, even 60 days after the spill.

Developmental toxicity in flounder embryos exposed to crude oils derived from different geographical regions.

Crude oils from distinct geographical regions have distinct chemical compositions, and, as a result, their toxicity may be different. However, developmental toxicity of crude oils derived from different geographical regions has not been extensively characterized. In this study, flounder embryos were separately exposed to effluents contaminated by three crude oils including: Basrah Light (BLO), Pyrenees (PCO), and Sakhalin Vityaz (SVO), in addition to a processed fuel oil (MFO-380), to measure developmental toxicity and for gene expressions. Each oil possessed a distinct chemical composition. Edema defect was highest in embryos exposed to PCO and MFO-380 that both have a greater fraction of three-ring PAHs (33% and 22%, respectively) compared to BLO and SVO. Observed caudal fin defects were higher in embryos exposed to SVO and MFO-380, which are both dominated by naphthalenes (81% and 52%, respectively). CYP1A gene expressions were also highest in embryos exposed to SVO and MFO-380. Higher incidence of cardiotoxicity and lower nkx 2.5 expression were detected in embryos exposed to PCO. Unique gene expression profiles were observed in embryos exposed to crude oils with distinct compositions. This study demonstrates that crude oils of different geographical origins with different compositional characteristics induce developmental toxicity to different degrees.

Distribution of butyltins and alternative antifouling biocides in sediments from shipping and shipbuilding areas in South Korea.

The occurrence and distribution of tributyltin (TBT) and alternative biocides were investigated in sediment from semi-enclosed bays, fishing ports, and large commercial harbors in Korea. Extremely high concentration of TBT (55,264ngSn/g) was detected near a large shipyard, even after a total ban on its use in Korea. Diuron was the biocide with the highest detection frequency and concentration levels, followed by Irgarol 1051. Sea-Nine 211 was detected at 3 of 32 stations surveyed. Dichlofluanid, zinc and copper pyrithiones levels were below the detection limits at all the stations surveyed. The relatively high levels of Diuron (9-62.3ng/g) and Irgarol 1051 (1.5-11.5ng/g) were detected in harbor and shipyard areas. Diuron and Irgarol 1051 levels including TBT in sediments from hot spots in Korea exceeded global sediment quality guidelines.

A practical review on photooxidation of crude oil: laboratory lamp setup and factors affecting it.

After an oil spill, crude oil in the marine environment is affected by a variety of processes collectively called weathering. Photooxidation induced by ultraviolet (UV) light from the sun is one of the most significant processes of long-term weathering that changes the chemical nature of oil. Experimental studies on photooxidation in the natural environment are generally not practicable due to the variability of factors that are more readily controlled in a laboratory. The emission spectra and irradiance of artificial lamps are critical factors for simulating sunlight, and the process of acceleration should be differentiated from simulation. We present a comprehensive review of the exposure conditions affecting in vitro photooxidation studies, including the types of lamps, their spectra and irradiance levels and maintenance conditions. The importance of xenon arc, metal halide along with mercury­xenon, high-pressure mercury lamps and other lamps with respect to their spectral characteristics is discussed and the selection guide is provided. A brief discussion on other factors affecting photooxidation rates and outcomes, such as photosensitisers, photodegraders, solvents and the synergistic effects of compounds is also given.

Source- and region-specific distribution of polycyclic aromatic hydrocarbons in sediments from Jinhae Bay, Korea.

This study surveyed polycyclic aromatic hydrocarbons (PAHs) at 80 sites in sediment from Jinhae Bay, which consists of Masan Bay (MSB), Haengam Bay (HAB), Bay Proper (JBP), Wonmoon Bay (WMB), and Gohyun Bay (GHB). Levels of the EPA 16 priority PAHs, 5 groups of alkylated PAH homologues and 2 biogenic PAHs were determined. Total PAHs (sum of all target PAHs) ranged from 37.0 ng/g to 3,110 ng/g with a mean of 339 ng/g. WMB had the highest concentration (473 ± 665 ng/g: average ± standard deviation) followed by GHB (214 ± 141 ng/g), MSB (175 ± 358 ng/g), JBP (133 ± 86.0 ng/g) and HAB (118 ± 129 ng/g). A tiered-source identification approach using the pyrogenic index, PAH isomer ratios and alkylated PAH double ratios found that both pyrogenic and petrogenic PAHs were dominant, and identified three different source- and region-specific groups. Input pathway tracers, such as butyltins, nonylphenols and dibenzothiophenes, were used to track the main input pathways. A shipyard and urban runoff were identified as the major input pathways of PAHs into GHB, and urban runoff was identified as a major pathway into MSB and WMB. Used crankcase oil, diesel exhaust, tyre debris and asphalt were considered to be the dominant PAH sources in urban runoff. Several PAH compounds exceeded the interim marine sediment quality guidelines for the protection of aquatic environments, among which dibenz[a,h]anthracene exceeded the guidelines in 16% of surveyed sites. Current PAH levels in MSB indicated an improving situation following the implementation of a total pollutant load management system (TPLMS); this is in accordance with other studies. WMB was recognised as an area of concern within this bay, suggesting the update of the TPLMS in this region.