Using Urban Streams as Drinking Water: The Potential Risk in Respect to Polycyclic Aromatic Hydrocarbons (PAHs) Content in Sediments

Several polycyclic aromatic hydrocarbons are considered carcinogenic and mutagenic. 16 of these compounds are listed as priority control pollutants by the USEPA. The present study aimed at the evaluation of the presence of PAHs in sediments of an urban stream by GC-MS. The study area was located in Indaiatuba-São Paulo-Brazil, and supplies to approximately 40,000 people of a region with limited availability of water. Therefore, this water body flowing in the urban region represents a case study of the potential risk in using this water for drinking. The results show that, in general, the sampling site near the intake of the water treatment plant for human consumption had the highest concentration of total PAHs (247.7μg kg^?1). This is the site that presents more contact with urban pollution and surface runoff from the streets. The PAHs composition pattern by ring number presented a higher proportion of hydrocarbons of 4- and 5-rings, and showed a tendency, in the majority of the samples, of predominance of the high-molecular-weight PAHs, except for samples collected on June 2011 that had a high concentration of naphthalene (a 2-ring PAH). The application of a principal component analysis helped to identify the sources of hydrocarbons as pyrogenic (PC1) and petrogenic origin (PC2). Through this statistical tool it is postulated that, in some periods, the stream was exposed to point and non-point sources of contamination, showing that this type of water supply option has a high degree of vulnerability mainly during the first rain after of a long dry period, and its consumption can cause long-term problems.     

Distribution and Sources of Polycyclic Aromatic Hydrocarbons (PAHs) in Surface Sediments from the Northern Part of the Persian Gulf (Hormuzgan Province)

Sediments from the intertidal areas of Hormuzgan province in northern part of Persian Gulf (Iran) were investigated for the levels and possible sources of 15 polycyclic aromatic hydrocarbons (PAHs). Samples of sediments were collected from twelve sampling sites and analyzed for PAHs by gas chromatography–mass spectrometry (GC-MS). The results showed that the total concentrations of PAHs ranged from 765 to 1898 ng/g dry weight. Composition pattern in the sediment samples from 12 sampling sites was dominated by 4-ring PAH compounds. Molecular indices based on ratios of PAH concentrations were used to differentiate PAHs from pyrolitic, petrogenic and mixed origins. The results of study suggested that the main sources of PAHs in the sediment were mixed with pyrolitic and petrogenic inputs. According to the US sediments quality guidelines (SQGs) (ERL/ERM) sediments of the mentioned region did not show any ecotoxicological risk for benthic organisms.     

Sources and Health Risk of Organic Compounds in Respirable Particles in Tehran,Iran

Forty-one respirable particle (PM₄) samples were collected from October 2011 through March 2012. This timespan covered the fall and winter seasons in Tehran, Iran. The associated polycyclic aromatic hydrocarbon (PAH) and n-alkane concentrations were analyzed to investigate the sources of these compounds and health risks of the former. The average total PAH and n-alkane concentrations were 16.2 ng/m³ and 758 ng/m³, respectively. The most abundant PAHs were 2- and 3-ring compounds, while the most abundant n-alkanes were nC₁₆ and nC₁₈. The results of source identification by factor analysis (FA) are consistent with and complementary to those from diagnostic ratios (DRs). The PAH DRs indicate a dominant contribution from pyrogenic sources, in particular diesel engines from local traffic sources, while FA reveals a diesel-fuelled vehicle emission related factor, a gasoline engine emission-related factor, an industrial source factor and a wood combustion, incineration and tire tread source factor. The n-alkane DRs indicate dominant contributions from anthropogenic sources or vehicular emissions, while FA reveals a fossil fuel combustion factor and a biogenic source factor. Although the average BaP concentration was below the Iran Department of Environment's annual average standard of 1 ng/m³, the BaP-equivalent concentration of the PAHs (BaP_PEQ) indicates harmful effects cannot be ruled out. The ICR_L and ICR_U data suggests a potential cancer risk incidence of about 1–54 individuals per million in the population from a lifetime of 70 years inhalation of particle associated PAHs in Tehran. These findings highlight the importance of reducing emissions from traffic, in particular emissions from diesel-fuelled vehicles, in Tehran.     

LONG TERM MONITORING OF POLYCYCLIC AROMATIC HYDROCARBONS (PAHS) IN BLUE MUSSELS (Mytilus edulis) FROM A REMOTE SCOTTISH LOCATION

Farmed mussels have been collected on a monthly basis since 1999 from a remote site on the west coast of Scotland for polycyclic aromatic hydrocarbon (PAHs) analysis with the aim of establishing background concentrations as a benchmark against which to assess any environmental incident. Total PAH (2- to 6-ring parent and alkylated) concentrations ranged from 12.5 to 151.2 μg kg^?1 wet weight. Seasonal trends were evident with concentrations being significantly higher for samples collected between November and March compared to those collected between April and October. By taking the median of medians for each of these time periods two background concentrations are suggested for the total PAH concentrations (2- to 6-ring PAHs parent and alkylated); for April to October: 31.2 μg kg^?1 wet weight and for November to March: 62.9 μg kg^?1 wet weight. Individual PAH concentrations were mainly below the OSPAR Background Assessment Concentrations (BACs), where they are specified, and were only exceeded for the heavier 4- and 5-ring PAHs (fluoranthene, pyrene, benz[a]anthracene and benzo[a]pyrene) in samples collected between November and March. Differences were also seen in the PAH profiles with season. Mussels collected between November and March had a higher proportion of the heavier PAHs compared to mussels collected in the summer and autumn.     

Characterization of PM2.5-Bound Polycyclic Aromatic Hydrocarbons in the Ambient Air of Győr,Hungary

ABSTRACT

In Hungary, the nationwide monitoring of PM10-bound polycyclic aromatic hydrocarbons (PAHs) in ambient air is great importance for a number of reasons related to human health, the environment and compliance with European Union legislation. However, the measurement of PAH concentrations in PM2.5 aerosol fraction has not been carried out. Therefore, the concentration, distribution and sources of PM2.5-bound PAHs at different urban sites of Gy?r were investigated in a heating season. The total PAH concentrations (sum of 19 individual PAH compounds) ranged from 1.32 to 37.27 ng/m³ with the mean value of 10.54 ng/m³. The high molecular weight PAHs with 5 and 6 aromatic rings were the most abundant PAHs in PM2.5 aerosol samples, which averaged 82% of total PAHs. Using benzo(a)pyrene (BaP) equivalent approach on the concentration data of carcinogenic PAH species, BaP and indeno(1,2,3-cd)pyrene contributed the highest carcinogenic exposure equivalent (1.25 and 0.19 ng/m³ on average). However, the incremental lifetime cancer risk (ILCR) values for resident children and adults indicated low-potential cancer risk (ILCR < 10^?6). The source apportionment results reflected that the major sources of PAH compounds in the Gy?r atmosphere were fossil fuel combustion and vehicle emissions.     

Particle Associated Polycyclic Aromatic Hydrocarbons (PAHS) in Urban Air of Agra

Total Suspended Particulate Matter (TSPM) samples were collected at Nunhai Agra from April to September 2006. The concentrations of 16 PAHs in aerosols were quantified. The dominated predominant PAHs in TSPM include high molecular weight (HMW) congeners BghiP, DbA, IP and BaP. Nap and Acy were not detected in any of the samples. The sum of 14 priority PAHs ranged from 150 to 480 ng m^?3 with a mean value of 269 ± 121 ng m^?3. The Results indicated that PAH concentrations at Nunhai were higher than in other industrial sites, but are comparable to those measured in several urban Chinese cities, however, and less than the industrial locations of China. Higher HMW PAH concentration were attributable to higher rates of emissions as well as or greater scavenging and adsorption of vapor phase PAH on available TSPM. Potential sources of PAHs in aerosols were identified using the diagnostic ratios between PAHs. Vehicular emissions were the main contributors of particulate-associated PAHs, with minor contribution from stationary combustion sources may also contribute to the particulate PAHs. PAHs in aerosols were predominantly from gasoline and diesel engines.     

Distribution,Sources, and Risk of Polycyclic Aromatic Hydrocarbons in the Core Sediments from Baiyangdian Lake,China

The burial characteristics and risks of 16 polycyclic aromatic hydrocarbons (PAHs) in core sediments from Baiyangdian Lake were investigated through gas-chromato graphy/mass spectrometry. The total concentrations of the 16 PAHs ranged from 39.48–1877.75 ng g^?1. The low-molecular-weight PAHs (two- to three-ring PAHs) were the dominant species, contributing 40.10–92.18% to the total PAHs, with a mean of 71.01%. Based on the observed molecular indices and on principal component analysis, the PAHs inputs were initially dominated by biomass and coal combustion, and atmospheric deposition and surface runoff could be the major transport pathways. The contaminated source characteristics, hydrodynamic condition, and sediment textural composition are the key factors affecting the distribution and source of PAHs. By conducting a risk quotient analysis between specific PAH concentrations and their corresponding sediment quality values, the top layer sediments were found to have a potential biological impact and relatively high toxicity. However, such impact should have no impairment. The toxic potency of PAHs in Baiyangdian Lake could be described by using the toxic equivalent of benzo[a]pyrene.     

Priority Polycyclic Aromatic Hydrocarbons (PAHs): Distribution,Possible Sources and Toxicity Equivalency in Urban Drains

Wastewater from urban areas constitutes one of the major sources of pollutants contributed to aquatic ecosystem. This study was carried out to elucidate the occurrence and possible source of US Environmental Protection Agency identified 16 priority polycyclic aromatic hydrocarbons (PAHs) in water and sediments from the urban wastewater drains in Delhi, India. A total 60 samples (water and sediment) collected during year 2011–2012, and analyzed the following USEPA methods. Water and sediment samples were extracted using liquid-liquid and ultrasonication techniques, respectively. Glass column chromatography with activated silica was used for sample extracts clean-up, followed by quantification on HPLC equipped with diode array detector at 254 nm wavelength using mixture of acetonitrule and water as mobile phase. Concentrations of total 16 PAHs (∑16PAHs) in all drain water samples ranged from 0.29–35.22 μg/L (mean ± SD, 10.83 ± 10.66 μg/L), predominated by two- and three -ring PAHs. The ∑16PAHs concentrations in all collected sediments ranged between 220–19321 μg/kg (mean±SD, 5574 ± 6820 μg/kg) dry weights. High molecular weight PAHs (≥4-ring PAHs) were dominant in sediment samples. Benzo(a)pyrene equivalent (BaPeq), a relative carcinogenic potential to the corresponding PAHs to BaP was estimated and presented. A selected number of concentration ratios of specific PAHs compounds were calculated and used to diagnose the possible sources of PAHs contamination. The diagnostic ratios reflected pyrogenic input from gasoline or diesel powered vehicular emissions as the major source of PAHs. The levels of PAHs observed in water and sediments were compared with similar studies undertaken in other regions of the world.     

Polycyclic aromatic hydrocarbon emissions of non-road diesel engine treated with non-thermal plasma technology

Non-road diesel engines are important polycyclic aromatic hydrocarbon (PAH) sources in the environment due to their high emission concentration compared to on-road diesel engines. Particle- and gas-phase PAH concentrations of a non-road diesel engine were investigated. Non-thermal plasma (NTP) as an effective after-treatment technology was used to reduce PAH emissions. The results showed that particle-phase PAH concentrations were 329.7 µg/m³, 3,206.7 µg/m³, and 1,185.7 µg/m³ without the action of NTP at three different engine loads respectively. Relatively low concentrations were measured for gas-phase PAHs. Excellent linearity was shown for particle-phase with total PAH concentrations both with, and without, NTP. The gas-phase PAH concentrations linearly increased with engine load without NTP. The five most abundant compounds of PAHs were among low molecular weight (LMW) and medium molecular weight (MMW) compounds. Total PAH cleaning efficiency was beyond 50% when treated with NTP at the three different engine loads. We hypothesized that naphthalene (Nap) concentrations increased greatly at 60% and 80% engine loads because it was produced within the plasma zone by decomposition of high molecular weight (HMW) PAHs. The PAHs content of particulate matter (PM) aggregation at 60% load was approximately three times higher than at 40% and 80% loads. High correlation values were observed for MMW PAHs with total PAH concentrations. Correlations of PAH concentration reduction could be important to clarify the PAH reduction mechanism with NTP technology.     

Source characterization and the environmental impact of urban street dusts from Egypt based on hydrocarbon distributions

The aliphatic and aromatic fractions of the extracts of ten street dust (SD) samples collected from eight cities covering a wide geographic area of Egypt were analyzed using gas chromatography with flame ionization detector (GC-FID) and GC-MS to compare their hydrocarbon distributions. To identify their sources, the extracts of the possible source materials were also analyzed. The impact of SDs on the marine environment was investigated in a marine sediment collected from the Western Harbor of Alexandria. The GC-FID profiles of the aliphatic fractions showed considerable differences in the n-alkane distribution that permits the classification of the SDs into five groups. This grouping reflects the environments of the cities in which they are collected. The carbon preference index and the unresolved complex mixture relative to the total resolved peaks values revealed that automobile exhaust is the main source of the hydrocarbons in these SDs with a significant contribution from terrestrial higher plant waxes to group 1 (Nile Delta cities). The sterane and hopane profiles supported this conclusion. The total polycyclic aromatic hydrocarbon (PAH) concentrations ranged from 27 to 379 ng/g (dry wt.) and showed clear differences between the SDs. The lowest and highest concentrations were found in samples from Shebeen and Port Said, respectively. The PAH distribution patterns and the ratio of the sum of combustion specific PAHs to total PAHs in samples from Alexandria, Port Said and Cairo were similar, implying similar sources. PAH ratios indicated a mixture of pyrogenic and petrogenic sources of PAHs in all samples where asphalt and automobile fuel exhaust were the major contributors of PAHs in Alexandria, Port Said, Cairo and Sharm El Sheikh cities. These ratios also indicated the predominance of diesel-operated vehicles to the PAHs signatures of Alexandria, Port Said and Cairo while gasoline emissions influence more strongly the PAH distributions in the SDs from Shebeen, Kafr El Sheikh and Sharkea. The PAH fingerprints excluded fresh oil and tire particles as major contributors. Both SDs and petrogenic sources significantly contributed to the hydrocarbon signature of the marine sediment from the Western Harbor of Alexandria.     

Sourcing of Fossil Fuel-Derived PAH in the Environment

To investigate the effects of domestic coal burning on the distribution and isotopic composition of environmental PAH, a series of soil samples were collected in a coal-burning village nearby Glasgow, UK. Analyses showed that, typically, PAHs in the Lochwinnoch village samples were isotopically heavy having δ¹³C values close to ?25‰ that are consistent with the PAHs emanating from coal burning. It was also noted, however, that alkylated PAHs would appear to be more prominent in soot from coal fires than in the samples collected in Lochwinnoch where domestic combustion was determined to be the major source. Therefore, to address the possibility that parent PAHs may survive in soils preferentially, two weathering experiments have commenced using a low temperature coal carbonisation tar from the Coalite process. Initial results have shown that after as little as 80 days weathering period, parent PAHs, particularly fluoranthene and pyrene, become more prominent than alkylated species, suggesting that these compounds may survive oxidation/weathering to a greater extent than their alkylated counterparts.     

Release of PAHs Through Runoff from the Gwangan Bridge to the Coast in Busan,Korea

This study was carried out from the Gwangan Bridge in Busan, Korea in order to examine the characteristics and the amount of PAHs in runoff from Gwangan Bridge, and the consequential PAH burdens in the ocean. The runoff samples were collected in particulate and dissolved phase, and the ambient air samples were collected in particulate and gaseous phase. In this study, 20 samples were collected from 10 different sites. The concentrations of 16 PAHs, in particulate road surface samples, ranged from 76.71 to 170.98 ng/g, and the dissolved road surface runoff samples ranged from 23.31 to 72.9 ng/L. In ambient air, the PAHs concentration in gaseous phase was higher than the samples in particulate phase. From these results, the amount of annual release of PAHs through runoff into the coast was calculated, and the Toxic Potency Equivalency Factors and Dioxin Toxic Equivalency Factors were applied. The annual release of total PAHs and the carcinogenic PAHs via runoff from Gwangan Bridge to the coast were 14.1 g/yr and 3.13 g/yr, respectively. The PAHs-_TPEQ was 0.85 g/yr and the PAH-_{dioxin TEQ} was 0.69 mg/yr.     

贡嘎山海螺沟新降雪中多环芳烃的组成差异及来源解析

贡嘎山海螺沟共收集3个新降雪样,利用GC-MS分析了16种优控多环芳烃的含量和组成差异,并解析了它们的来源。结果表明,海螺沟新降雪样中多环芳烃的含量是0.478 2~0.554 2μg/L,主要以2~4环低分子量的化合物为主,以菲的含量最高,通过结合相同分子量和相似结构多环芳烃的比值来分析结果,说明贡嘎山海螺沟地区新降雪中的多环芳烃主要来自煤的不完全燃烧。通过多环芳烃大气传输距离估算模型计算出采样点与排放点的最远距离是455 km。     

Polycyclic Aromatic Hydrocarbons in Residential Soils from an Indian City near Power Plants Area and Assessment of Health Risk for Human Population

This article deals with the distribution, composition profiles, and possible sources of sixteen priority polycyclic aromatic hydrocarbons (PAHs) in residential soils from Korba district in Chhattisgarh State, India. Sixteen priority PAHs in soils were analyzed after ultrasonic extraction, silica gel column chromatographic cleanup, and quantitation was performed using HPLC-DAD. The concentrations of ∑16PAHs were within acceptable limits of soil quality guidelines and the study area got classified as weakly contaminated. The concentration of probable human carcinogenic PAHs in soils accounted for 10% of ∑16PAHs. The concentration of Benzo(a)Pyrene (BaP) accounted 1% to total PAHs. Benzo(a)pyrene Toxicity Equivalency (BaP_TEQ) for 16 PAHs was 30 ± 12 μg BaP_TEQ kg^?1. The composition profiles and molecular ratios of PAHs suggested mixed pyrogenic sources of PAHs from combustion of coal, wood, and vehicular exhaust emissions. Human health risk was assessed by calculating the lifetime average daily dose (LADD) and incremental life time cancer risk (ILCR) for human adults and children. Estimated ILCR was within safe limit (10^?6?10^?5), indicating low risk to human population. Potential risk to contaminated ground water from leaching of carcinogenic PAHs was assessed by estimating the Index of Additive Cancer Risk (IACR).     

Characterization of Gaseous and Particulate Polycyclic Aromatic Hydrocarbons in Ambient Air of Delhi,India

Three seasonal sampling campaigns were undertaken at an urban site of Delhi for collection of PAHs in particulate and gas phase. Sampling was done by using modified Respirable Dust (PM ≤10μm) sampler attached with polyurethane foam (PUF) plugs and compared with conventional Respirable Dust (PM ≤10 μm) sampler. Total 16 EPA PAH (gaseous + particulate) were determined by Gas Chromatograph-Mass Spectrophotometer (GC-MS). The 3-ring PAH constitutes approximately 90% of the gaseous PAHs with phenanthrene, fluoranthene, acenapthylene, and acenaphthene being the most abundant gaseous PAHs. PAHs with 4- to 6- rings accounted for 92%, 87% and 78% in samples collected during winter, summer and monsoon season respectively. Gaseous PAHs, particulate PAHs and total PAHs were higher during winter as compared to summer and monsoon seasons. The contribution of particulate PAHs were 1.4, 2.1, and 2.5 times higher in winter, summer and monsoon, respectively than of gaseous PAHs. Indeno[123-cd]pyrene, benzo[ghi]perylene, dibenzo[ah]anthracene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene and chrysene were found to be the most abundant PAH compounds in the particulate PAHs during all the seasons. The result from application of diagnostic ratio suggests that the higher particulate PAHs emissions were predominantly associated with vehicular emissions along with emissions from biomass burning during winter season.     

Monitoring and Assessment of Polycyclic Aromatic Hydrocarbons (PAHs) in the Atmosphere of Alexandria City,Egypt

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) in the total suspended particulate (TSP) were measured simultaneously between January 30, 2015 and February 11, 2016 at urban, suburb, and rural sites at Alexandria City, Egypt, using pesticide samplers. Samples were extracted and analyzed using chromatography–mass spectrometric (GC–MS). There was a significant difference in concentrations between the three sites, and between particle- and vapor-phases. Mean total PAH concentrations were 502.48, 322.57, and 417.23 ng m^?3 for the urban, the rural, and the suburban sites in particulate-phase and were 723.49, 402.26, and 543.15 for the same sites in vapor-phase, respectively. At the three sites, the most abundant compounds determined were Benzo[k]fluoranthene (BkF), followed by Benzo[a]pyrene (BaP) and Indeno [1,2,3-cd] pyrene (IcdP). These high molecular weight compounds are carcinogenic and known to originate mainly from vehicular emissions. The diagnostic ratios indicated PAHs in urban and suburban sites were predominantly from gasoline and diesel engines, while that in rural site was from biomass burning. Characterization of the emission sources was further substantiated by significant correlation between individual PAH species.     

Water-Particle Distribution of Hydrophobic Micro Pollutants in Storm Water Runoff

Sorptive behaviors of polycyclic aromatic hydrocarbons (PAHs) as well as other classes of hydrophobic pollutants (i.e., n-alkanes and linear alkylbenzenes: LABs) were investigated for street runoff and for particle-size segregated river water samples. PAHs, except for 3-ring aromatics, were mostly transported with particles >1.2μm. In all the environmental samples PAHs were more hydrophobic than expected from their Kow; whereas vigorous mixing of road dust with water for 24 hours resulted in more desorption of PAHs into the aqueous phase. It indicates that although strongly associated with particles, at least some part of the “particle bound” PAHs could be available for active exchange wirh their dissolved counterparts. As opposed to PAHs, n-alkanes and LABs revealed less hydrophobic nature than expected from Kow, although their majorities were in “particulate form”.     

Characteristics of PAHs,PCDD/Fs,PCBs and PBDEs in the Sediment of Lake Baikal,Russia

The levels of PAHs, PCDD/Fs, PCBs, and PBDEs in Lake Baikal were monitored for the first time using deep water sediment. The sediment samples were collected from 15 stations in four regions of Lake Baikal: Ol’khon Island (n = 8), the Angara River estuary (n = 2), the Selenga River delta (n = 2), and the Baikal pulp and paper mill (BPPM) (n = 3). The highest average concentrations of PCDD/Fs (20.24 pg/g d.w.) and PCBs (68.72 ng/g d.w.) were found at Ol’khon Island. The highest total PBDE concentrations were found at BPPM, with a mean concentration of 575.76 pg/g d.w. For PCBs, PCB-52, and PCB-69 were dominant, making up 11% of the total 209 PCB congeners. BDE-209 contributed 60% of PBDEs in Lake Baikal. According to the TPEQ concentration of PAHs, PAHs contributed the most to Lake Baikal contamination. The sources of contamination of PAHs, PCDDs, and PCBs in Lake Baikal are identified as combustion, runoff from the use of the pesticides (PCP) and insulating oil, specifically for PCBs. The source of PBDEs is assumed to be production, use and disposal of products containing PBDEs, in addition to atmospheric long-range transport and deposition.     

Seasonal and Geographical Distribution of PAHs in Mussels,Mytilus Edulis,Collected from an Urban Harbour

Mytilus edulis were collected intertidally from 16–18 sites located around the perimeter of Halifax Harbour, of an island located at the entrance to the harbour and from the Northwest Arm. The concentrations of 31 polycyclic aromatic hydrocarbons (PAHs), lipid and moisture content were determined in pools of this filter feeder sampled over three seasons spanning two years, along with calculating individual condition indices. Contaminants were nearly undetectable in many of the summer mussels and highest in some of the spring samples. At several sites, the sum of PAHs expressed on a dry or lipid weight basis, was either equal or higher in April compared to November. Fluoranthene was the most predominant PAH followed by pyrene and phenanthrene. At most sites, parental PAHs, associated with combustion sources of contamination, were more abundant than alkylated derivatives. A larger petroleum input was noticeable in mussel extracts from sites in close proximity to potential sources.     

Evaluation of Polycyclic Aromatic Hydrocarbons Contamination in the Sediments of the Johor Strait,Peninsular Malaysia

In May 2013, sediment samples were collected from five stations in the Straits of Johor, near the southern tip of Peninsular Malaysia, in order to evaluate the distribution and sources of polycyclic aromatic hydrocarbons (PAHs). The concentrations of 16 United States Environmental Protection Agency PAHs varied from 650.5 to 1441.2 ng g ^?1 dry weight (dw) with a mean value of 985.5 ng g ^?1 dw. PAHs can be classified as moderate level pollution in the collected samples. When comparing PAHs in this study with that of the sediment quality guidelines (SQGs), it was found that the total PAHs, low molecular weight (LMW), and high molecular weight (HMW) PAHs might incur minimal adverse biological effects. The diagnostic ratios of individual PAHs indicated both petrogenic and pyrogenic origins with predominantly pyrogenic sources, the findings of which are further supported by the results from principal component analysis (PCA). The PCA results reveal contributions of 44.44%, 32.3%, and 18.96% for traffic-related, coal combustion, and petroleum-related products, respectively. These findings indicate that the effective monitoring and significant improvement resulting from the implementation of environmental regulations in Malaysia might have caused a shift in the source of petroleum hydrocarbons in the Straits of Johor's aquatic ecosystems from petrogenic to pyrogenic origins.