Polycyclic Aromatic Hydrocarbons In Sediments Research Articles

Sources and distribution of organic matter and polycyclic aromatic hydrocarbons in sediments of the southwestern Portuguese shelf

Total organic carbon (Corg), total nitrogen (Ntot), Corg/Ntot, δ13Corg, δ15N, calcium carbonate (CaCO3), and grain size were analyzed in 70 surface samples and 19 short cores from the southwestern Portuguese shelf. Perylene and USEPA-16 PAHs were quantified in a subset of these samples. The findings suggest that organic matter derives from a mix of terrestrial and marine sources, outlined by Corg, Ntot, and isotopic signatures. Perylene combined with δ13Corg was used to identify the main PAH sources in these environments. Diagnostic perylene ratios revealed contributions from natural sources in the Tagus region and contaminated materials from the Sado Dredged Disposal Site, with additional perylene in Sines linked to atmospheric deposition of pyrogenic sources. A significant correlation between perylene and USEPA-16 PAHs indicates natural and anthropogenic inputs from the Tagus. This multiproxy approach—combining USEPA-16ΣPAHs, perylene, and δ13Corg—offers insights for assessing environmental risks and guiding marine environmental management according to the MSFD.

Identification of dominant natural sources of polycyclic aromatic hydrocarbons in river sediments in Alberta

Sediment collected from the rivers of southern Alberta, Canada, presents patterns of polycyclic aromatic hydrocarbons (PAHs) that demonstrate a varied origin within the Rocky Mountains. An influx of PAHs from sub-bituminous coal sources from erosional processes as the river exit the mountains dominates the pattern of PAHs in the river sediment across the prairies to the Alberta-Saskatchewan border (a distance of 750 km for the Red Deer River and 925 km for the Bow River) continues much further downstream. The concentrations of PAHs are similar to the well-studied Athabasca River in the Alberta Oil Sands Region. Although these results relate to rivers flowing east from the Rocky Mountains in Canada, it is likely that coal-sourced PAHs will contribute to any river where erosion of coal formations is possible within the watershed. A distinctive natural pattern of strongly pyrogenic PAHs from nearby thermal hot springs was also discovered near Banff. Natural pyrogenic PAH sources, aside from wildfires, are uncommon and generally related to hydrothermal vents and igneous intrusions into source rocks. This is the first time the authors are aware of sediment from a thermal spring presenting such PAH patterns.

Distribution and sources of polycyclic aromatic hydrocarbons in cascade reservoir sediments: influence of anthropogenic activities and reservoir hydrology.

The construction of dams has caused disruptions to river connectivity, leading to alterations in the deposition of hydrophobic organic contaminants in reservoir sediments. Further investigation is warranted to explore the impact of cascade reservoirs with differing hydrological characteristics on polycyclic aromatic hydrocarbons (PAHs) distribution in sediment. This study examines the presence of 30PAHs in the sediments collected from six cascade reservoirs situated in the Wujiang River basin during January and July 2017. The results showed that Σ30PAHs ranged from 455-3000ng/g dw (mean 1030ng/g dw). Anthropogenic activities and reservoir hydrology determined the distribution trend of PAHs in sediments, with an overall increase from upstream to midstream and then a decrease downstream. The PAH levels were highly linked to the secondary industry (P < 0.05). This was further supported by the relationship between the PAH emissions from coal combustion and traffic sources analyzed by the positive matrix factorization model and economic parameters in the wet season (P < 0.01). At the same time, reservoir age (RA) showed a positive correlation with PAH concentrations (P < 0.05), while hydraulic retention time (HRT) exhibited a negative correlation with PAH levels (P = 0.03). The relationship between total organic carbon (TOC) and PAHs in stream sediments worldwide was nonlinear (P < 0.01), with PAH concentrations initially rising and then falling as TOC levels increased. Concerns regarding carcinogenic risk were raised due to contributions from coal and vehicular sources, with the risk increasing with RA.

Sources and Fates of Sedimentary Polycyclic Aromatic Hydrocarbons in the East Siberian Arctic Shelf: Implications for Input Pathways and Black Carbon Constraint

AbstractThe Arctic region is experiencing more rapid climate changes than the other parts of the world and serves as a sink for semi‐volatile persistent organic pollutants, such as polycyclic aromatic hydrocarbons (PAHs), which can be utilized as molecular markers for pyrogenic carbon, such as black carbon (BC). As the sea ice retreats and increased terrestrial inputs with widespread wildfires, the PAH concentrations in the Arctic Ocean are rising. In this study, the sources and fates of PAHs together with BC in surface sediments from the East Siberian Arctic Shelf (ESAS) were analyzed. Positive matrix factorization (PMF) elucidated a mixed petrogenic and pyrogenic sources and distinct PAH fates associated with diverse input pathways including coastal permafrost erosion contribution (∼30%), petrogenic‐related emission (∼34%), fossil fuel combustion (∼26%), and biomass burning (∼10%). Correlation analysis indicated that BC plays a key role in affecting the behavior and fates of PAHs. In the Chukchi Sea, PAHs are closely associated with soot‐BC, whereas in the Laptev Sea (LS) and west East Siberian Sea (W‐ESS), they exhibit a coupling process with char‐BC. The presence of these carbonaceous materials in the sediments of CS is likely influenced by atmospheric deposition and biological activity, whereas the LS and W‐ESS regions are mainly affected by long‐distance river transport and direct deposition from coastal permafrost. As global warming continues, permafrost thawing induces the remobilization and retranslocation of PAHs, thereby becoming a significant PAH contributor and input pathway in the rapidly changing Arctic coastal margin.

Characterization and health risk assessment of n-alkanes and PAHs in sediments from Shalateen (Halayeb Triangle), Egyptian Red Sea Coast

In this paper, the concentrations, origins, and carcinogenic potential of n-alkanes and polycyclic aromatic hydrocarbons (PAHs) collected from Shalateen sediments (Sh), Red Sea, Egypt were discussed. Individual n-alkanes has fluctuated from a minimum of 17.7 μg/g dw recorded for C-9 at Sh-54 to a maximum of 2.02 × 104 μg/g dw recorded for C-12 at Sh-B1. Total n-alkanes have fluctuated from 252–1.41 × 104 μg/g with a mean of 4.84 × 104 μg/g dw. C-12 had the highest average value, and C-19 had the lowest. The total ΣPAH concentrations in sediments from Shalateen as determined by gas chromatography-mass spectrometry/mass spectrometry (GC-MS/MS) ranged from 43.2 to 270 ng/g dw (averaging 95.2 ng/g dw). Carbon preference index (CPI) values were <1, consistent with the prevalence of even-C alkanes vs. the odd-C homologues. High molecular weight (HMW) PAHs were the most abundant substances affecting the collected samples. The cancer risk ranged from 2.25 × 10−5 to 4.78 × 10−2, indicating a moderate cancer risk associated with PAHs. The primary sources of PAHs in sediments included emissions from burning gasoline and diesel, biomass, and natural gas. The current study is considered one of the most important and unique with regard to the amounts and distributions of n-alkanes and PAHs in sediments along the coasts of Shalateen. It is the first baseline data documentation (GC MS/MS approach) of n-alkanes and PAHs in the Shalateen region.

Spatiotemporal variation of polycyclic aromatic hydrocarbons in Tibetan lake sediment cores reveals the influence of forest fires

Despite declining anthropogenic emissions of polycyclic aromatic hydrocarbons (PAHs) due to global control strategies, forest fire emissions have been increasing, significantly affecting PAH dynamics in global sinks. This study investigated the spatiotemporal variations of sedimentary PAHs in three Tibetan lakes—Yiong Tso, Yamdrok Yumtso, and Urru Tso—to determine the influence of forest fires on PAH levels and historical trends. Yiong Tso Lake, located in a fire-affected watershed, exhibited the highest PAH concentrations (average of 43.4 ± 25.7 ng/g) with significant fluctuations since the 1920s, peaking in the 1960s (46.3 ng/g) and 1980s (91.3 ng/g), corresponding to periods of intense forest fires. This pattern aligned with source contribution estimates using the modified Cohen's d (mcd), indicating the dominance of forest fires as a PAH source until the 1990s. PAH concentrations decreased with increasing distance from the southeastern Tibetan Forest, as observed in Yamdrok Yumtso (average of 36.1 ± 19.9 ng/g) and Urru Tso (average of 16.4 ± 6.9 ng/g). Temporal variations in PAH concentrations and mcd values from these lakes also reflected a response to forest fires during the 1960s, suggesting a widespread influence of forest-fire-derived PAHs across the plateau. The impact of forest fires on sedimentary PAHs was expected to persist for decades, with an estimated half-life of approximately 11–12 years. These findings highlight significant emissions of PAHs from forest fires in the Tibetan Plateau, potentially transforming regional PAH dynamics and influencing global cycling.

SOURCE APPORTIONMENT OF ATMOSPHERIC AND SEDIMENTARY PAHS FROM KOLKATA, INDIA USING COMPOUND-CLASS-SPECIFIC RADIOCARBON ANALYSIS (CCSRA)

ABSTRACT Polycyclic aromatic hydrocarbons (PAHs) are major air pollutants that are ubiquitously produced by the combustion of organic materials, and it is extremely important to identify their pollution sources. In this study, molecular fingerprinting and compound class-specific radiocarbon dating (CCSRA) were performed on PAHs from canal sediments and air samples collected in Kolkata, India’s third largest city (population approximately 16 million), where PAHs pollution has been a serious problem. Average PAH (Σ12-parent PAHs) concentrations in air samples were 65.1 ng m–3 in summer and 70.9 ng m–3 in winter and in canal sediments were 32.7 µg g–1, which are classified as “very high-level” pollution. Molecular fingerprinting using methyl-PAH/PAH (MPAHs/PAHs) ratios and isomer pair ratios with molecular weights of 178, 202, 228, and 276 suggested that wood and coal combustion were the dominant sources of PAHs in the sediment, and that atmospheric PAHs were influenced by oil combustion in addition to them. The fraction of contemporary carbon (ƒC) of sedimentary PAHs (0.056–0.100), together with the extremely low MPAHs/PAHs ratio results, lead to the conclusion that the major source of the high concentration of PAHs in the canals is from coal combustion. On the other hand, the ƒC of atmospheric PAHs (0.272–0.369) was close to the share of biomass fuels in India’s domestic fuel consumption in 2011 (about 35%). Furthermore, the observed ƒC-discrepancy between atmospheric and sedimentary PAHs in the same urban environment was interpreted to give an insight into the loading pathway of PAHs to canal sediments in Kolkata.

Chronological evaluation of polycyclic aromatic hydrocarbons in sediments of tangxun lake in central China and impacts of human activities.

This study sheds light on the contamination of polycyclic aromatic hydrocarbons (PAHs) in Tangxun Lake sediments, an urban lake reflecting environmental changes in Central China. By analyzing sediment cores from both the inner and outer areas of the lake, we determined the historical trends and sources of PAHs over the past century. The results reveal a significant increase in PAHs concentrations, particularly since the 1980s, coinciding with China's rapid urbanization and industrialization. Using diagnostic ratios and Absolute principal component score-multivariate linear regression (APCS-MLR) methods, we identified petroleum combustion, coal combustion, and biomass combustion as the primary sources of PAHs in the lake sediments. The spatial analysis indicates higher PAHs levels in the inner lake, likely due to its closer proximity to industrial activities. Moreover, by comparing PAH trends in Tangxun Lake with those in other urban, suburban, and remote lakes across China, based on data from 49 sedimentary cores, we highlight the impact of regional socio-economic dynamics on PAH deposition. These insights are crucial for developing effective pollution mitigation strategies and promoting sustainable development in rapidly urbanizing regions.

Sediment organic matter predicts polycyclic aromatic hydrocarbon distribution in port sediments

We evaluated the influence of organic matter in polycyclic aromatic hydrocarbons (PAHs) in port sediments using multiple linear regression (MLR) and prediction models. Total sediment PAHs ranged between 45 and 3230 ng/g dw (average: 557 ± 962 ng/g dw), with PAHs primarily originating from river inputs, confined to areas near the estuaries. Coal/biomaterial combustion and petroleum mainly contribute to the presence of PAHs along estuaries, with medium-high to high ecological risks. MLR TPAHs prediction model included variables, namely, the marine-derived total organic carbon (TOCmar), terrestrial fraction of organic matter (Fterr), and carbon-to‑nitrogen ratio (CNR). Results indicate that mainly marine- followed by terrestrially-derived organic matter influenced sediment PAH distribution. Total organic nitrogen and CNR were variables in the toxic equivalent (TEQ) prediction model, demonstrating that terrestrial pollution sources primarily influenced TEQ. The study analyzes and predicts the impact of organic matter and its sources on the fate and transport of PAHs in port sediments.

Data-Driven Insights into the Contamination of Polycyclic Aromatic Hydrocarbons in Marine Bays.

The synthesis of polycyclic aromatic hydrocarbon (PAH) data allows us to quantify and gain insights into the spatiotemporal dynamics of PAH contamination in marine bays. Here, a data synthesis framework was developed to understand data-driven insights into the spatiotemporal levels, compositional profiles, and potential sources of PAHs in water and sediment of marine bays. PAHs were detected in 69 bays worldwide, with contamination hotspots located in Asian bays. PAH concentrations in pre-2000 were significantly lower than those in the 2000s and post-2010, while the dominant species in water and sediment were 2-3 ring and 4-6 ring PAHs, respectively. The composition patterns of PAHs included 2-3 ring, 3-5 ring, and 4-5 ring dominant categories, but no significant distance decay relationship was found in the composition similarity due to international energy trade. Temporal dynamic patterns of concentrations included Descending-, Ascending-, and Inverted V-type, whereas over longer time spans, the pattern is more similar to the Inverted V-type owing to the reductions in emission intensity. PAHs were derived from both petrogenic and pyrolytic sources, with combustion from both coal and petroleum being the dominant source. These data-driven discoveries provide quantitative insights into the spatiotemporal patterns in the concentration and composition of PAHs, contributing to the mitigation of PAH contamination.

Polycyclic aromatic hydrocarbons in ship breaking area and associated ecological risk assessment: evidence from the Sitakund ship-breaking area in Bangladesh.

Ship-breaking yards are recognized for releasing hazardous polycyclic aromatic hydrocarbons (PAHs), leading to severe environmental pollution in the sediment of ship-breaking areas. This study assessed the concentrations of 16 priority PAHs in surface sediments collected from the intertidal zone adjacent to the Sitakund ship-breaking yards. The samples underwent Soxhlet extraction and detection using PerkinElmer GC-Clarus 690 and MS-Clarus SQ8C with an Elite-5MS capillary column (30m × 0.25mm ID × 0.25µm). The study utilized PAH concentrations to reveal spatial distribution patterns, identify point sources, and assess potential toxicity. The total PAH concentration ranged from 1899.2 to 156,800.08ngg-1 dw, while the concentration of 7 carcinogenic PAHs ranged from 822.03 to 1899.15ngg-1 dw. High molecular weight PAHs dominated among the 16 PAHs, whereas low molecular weight PAHs, such as 2-ring PAHs, were negligible. Source characterization based on different molecular ratios suggested that PAHs in the area originated from pyrolytic processes related to ship dismantling, fishing activities, and water transportation for people. The observed PAH concentrations exceeded both national and international standards for sedimentary PAH levels, indicating significant ecological risks. The total TEQcarc values of sediment samples varied from 564.41 to 10,695.12ngg-1, with a mean value of 3091.25ngg-1. The study's findings underscore the immediate biological damage that PAH contamination in the Sitakund ship-breaking area could cause, emphasizing the need for effective control measures to ensure ecological and human safety.

Distribution, sources and ecological risks of PAHs and n-alkanes in water and sediments of typically polluted estuaries: Insights from the Xiaoqing River

Seasonal water and sediment samples were collected from the Xiaoqing River estuary and the neighboring sea to study the spatial and temporal distributions, sources and ecological risks of polycyclic aromatic hydrocarbons (PAHs) and n-alkanes. The results showed significant spatial and temporal differences in the concentrations of PAHs and n-alkanes under the influence of precipitation, temperature, and human activities. The concentrations of PAHs in water were lower in the wet season than in the dry season, and those in sediments were higher in the wet season than in the dry season. The concentrations of n-alkanes were higher in the rainy season than in the dry season for both water and sediments. The spatial distributions of PAHs and n-alkanes were estuarine > offshore. The concentration ranges of ∑PAHs in water and sediments were 230.66–599.86 ng/L and 84.51–5548.62 ng/g, respectively, in the wet season and 192.46–8649.55 ng/L and 23.39–1208.92 ng/g, respectively, in the dry season. The proportion of three-ring PAHs in water (57.03% and 78.27% in the wet and dry seasons, respectively) was high, followed by two-ring PAHs (27.31% and 13.59% in the wet and dry seasons, respectively). The proportion of four-ring PAHs was higher in sediments (24.79% and 32.20% in the wet and dry seasons, respectively). The ecological risk of PAHs assessed using the toxicity equivalent quotient and risk quotient was at moderate to moderately high risk levels. The high concentration of n-alkane fraction C16 (611.65–75594.58 ng/L) in the water is indicative of petroleum or other fossil fuel inputs. The main peaks of n-alkanes in river sediments were C27, C29 and C31, indicating higher inputs of plant sources. The sediments in the estuary showed dominance of both short-chain C16 and long-chain C25–C31, indicating a combined input of higher plants and petroleum. The diagnostic ratios of PAHs and n-alkanes indicated that their sources were mainly oil/coal/biomass combustion and petroleum spills attributed to frequent vehicular, vessel and mariculture activities. Given the potential ecological risks of PAHs and n-alkanes in water and sediments, future studies should focus on their bioaccumulation and biotoxicity.

Assessing petroleum contamination in parts of the Niger Delta based on a sub-catchment delineated field assessment

The Niger Delta in Nigeria is a complex and heavily contaminated area with over 150,000 interconnected contaminated sites. This intricate issue is compounded by the region’s strong hydrological processes and high-energy environment, necessitating a science-based approach for effective contamination assessment and management. This study introduces the concept of sub-catchment contamination assessment and management, providing an overarching perspective rather than addressing each site individually. A description of the sub-catchment delineation process using the digital elevation model data from an impacted area within the Delta is provided. Additionally, the contamination status from the delineated sub-catchment is reported. Sediment, surface water and groundwater samples from the sub-catchment were analyzed for total petroleum hydrocarbons (TPH) and polycyclic aromatic hydrocarbons (PAHs), respectively. Surface sediment TPH concentrations ranged from 129 to 20,600 mg/kg, with subsurface (2-m depth) concentrations from 15.5 to 729 mg/kg. PAHs in surface and subsurface sediment reached 9.55 mg/kg and 0.46 mg/kg, respectively. Surface water exhibited TPH concentrations from 10 to 620 mg/L, while PAHs ranged from below detection limits to 1 mg/L. Groundwater TPH concentrations spanned 3 to 473 mg/L, with total PAHs varying from below detection limits to 0.28 mg/L. These elevated TPH and PAH levels indicate extensive petroleum contamination in the investigated sediment and water environment. Along with severe impacts on large areas of mangroves and wetlands, comparison of TPH and PAH concentrations with sediment and water quality criteria found 54 to 100% of stations demonstrated exceedances, suggesting adverse biological effects on aquatic and sediment biota are likely occurring.

An extensive investigation on human risk associated with PAHs in fish and sediment in Bushehr, Northern of Persian Gulf

Here, a comprehensive study was designed to estimate the human risk assessment attributed to exposure of polycyclic aromatic hydrocarbons (PAHs)in sediment and fish in most polluted shore area in north of Persian Gulf. To this end, a total of 20 sediment and inhabitual Fish, as one of most commercial fish, samples were randomly collected from 20 different stations along Bushehr Province coastline. The 16 different components of PAHs were extracted from sediment and edible parts of inhabitual fish and measured with high-performance liquid chromatography (HPLC) and gas chromatography (GC), respectively. In addition, dietary daily intake (DDI) values of PAHs via ingestion Indian halibut and the incremental lifetime cancer risk (ILCR) attributed to human exposure to sediments PAHs via (a) inhalation, (b) ingestion, and (c) dermal contact for two groups of ages: children (1–11 years) and adults (18–70 years) were estimated. The results indicated that all individual PAHs except for Benzo(b)flouranthene (BbF) and Benzo(ghi) perylene (BgP) were detected in different sediment sample throughout the study area with average concentration between 2.275 ± 4.993 mg.kg–1 dw. Furthermore, Naphthalene (Nap) with highest average concentration of 3.906 ± 3.039 mg.kg–1 dw was measured at the Indian halibut. In addition, the human risk analysis indicated that excess cancer risk (ECR) attributed to PAHs in sediment and fish in Asaluyeh with high industrial activities on oil and derivatives were higher the value recommended by USEPA (10−6). Therefore, a comprehensive analysis on spatial distribution and human risk assessment of PAHs in sediment and fish can improve the awareness on environmental threat in order to aid authorities and decision maker to find a sustainable solution.

Assessment of parent and alkyl -PAHs in surface sediments of Iranian mangroves on the northern coast of the Persian Gulf: Spatial accumulation distribution, influence factors, and ecotoxicological risks

Spatial patterns, potential origins, and ecotoxicological risk of alkylated (APAH) –and parent –(PPAH) polycyclic aromatic hydrocarbons (PAHs) were studied in mangrove surface sediments along the northern coasts of the Persian Gulf, Iran. The mean total concentrations (ngg−1dw) ∑32PAH, ∑PPAHs and ∑APAHs in sediments were 3482 (1689–61228), 2642 (1109–4849), and 840 (478–1273), respectively. The spatial variability was similar among these PAH groups, with the highest levels occurring in Nayband National Marine Park (NNMP). Physicochemical environmental factors, such as sediment grain size, and total organic carbon (TOC) contents, are significant factors of PAH distribution. These findings suggest that PAH pollution level is moderate-to-high, supporting the current view that mangrove ecosystems are under intensive anthropogenic impacts, such as petrochemical, oil and gas loads, port activities, and urbanization. Non-parametric multidimensional scaling (NPMDS) ordination demonstrated that NNMP mangrove is the critical site exhibiting high loading of PAH pollutants. Here, for the first time in this region, Soil quality guidelines (SQGs), Toxic equivalency quotient (TEQ), Mutagenic equivalency quotient (MEQ), and composition indices comprising Mean maximum permissible concentration quotient (m-MPC-Q), and Mean effect range median quotient (m-ERM-Q) methods were used to have a comprehensive risk assessment for PAH compounds and confirmed medium-to-high ecological risks of PAHs in the study area, particularly in the western part of the Gulf, highlighting the industrial impacts on the environment.

Evaluation of historical data on persistent organic pollutants and heavy metals in Lake Baikal: Implications for accumulation in marine environments

Lake Baikal, the largest freshwater lake by volume, provides drinking water and aquatic food supplies to over 2.5 million people. However, the lake has been contaminated with recalcitrant pollutants released from surrounding industrial complexes, agriculture, and natural lands, thereby increasing the risk of their bioaccumulation in fish and seals. Yet, a collective analysis of historical concentration data and their bioaccumulation potential as well as what factors drive their accumulation in fish or seals remains largely unknown. We analyzed concentration data from 42 studies collected between 1985 and 2019 in water, sediment, fish, and seals of Lake Baikal. Heavy metals had the highest concentrations in water and biota followed closely by polycyclic aromatic hydrocarbons (PAHs) and organochlorines. Among organochlorines, polychlorinated biphenyls (PCBs) showed the highest levels in water, surpassing hexachlorocyclohexane (HCH) concentrations, particularly after normalizing to solubility. While naphthalene and phenanthrene exhibited the highest average concentrations among polycyclic aromatic hydrocarbons (PAHs), their relative concentrations significantly decreased upon solubility normalization. The analysis confirmed that bioconcentration and biomagnification of organochlorine pesticides, PCBs, PAHs, and heavy metals depend primarily on source strength to drive their concentration in water and secondarily on their chemical characteristics as evidenced by the higher concentrations of low-solubility PCBs and high molecular weight PAHs in water and sediment. The differential biomagnification patterns of Cu, Hg, and Zn compared to Pb are attributed to their distinct sources and bioavailability, with Cu, Hg, and Zn showing more pronounced biomagnification due to prolonged industrial release, in contrast to the declining Pb levels. Dibenzo-p-dioxins were detected in sediment and seals, but not in water or fish compartments. These data highlight the importance of addressing even low concentrations of organic and inorganic pollutants and the need for more consistent and frequent monitoring to ensure the future usability of this and other similar essential natural resources.

Risk Assessments of Polycyclic Aromatic Hydrocarbons in the Surface Sediments of Drinking Water Sources in Ifite Ogwari, South-East Nigeria

ABSTRACT Surface water is the main source of drinking water in Ifite Ogwari, Anambra State, South-East Nigeria. In aquatic environments, sediment functions as both a source and a sink of polycyclic aromatic hydrocarbons (PAHs). To determine the level of pollution, health concerns to people and the environment, and potential sources of PAHs in the surface water sediments in Ifite Ogwari, sediment samples were collected from 9 surface water sources used for drinking by Ifite Ogwari people and were analyzed using a Gas Chromatography/Flame Ionization Detector (GC-FID). In all sediment samples, only 11 PAHs out of 16 United States Environmental Protection Agency (USEPA) priority PAHs were detected while 5 were below detectable limits. The concentration of benzo[a]anthracene was high but detected in only 2 sediment samples while fluoranthene has a relatively close concentration across all samples. Benzo[k]fluoranthene has the highest concentration compared to other PAHs in the samples while benzo[a]pyrene has the lowest concentration across all samples. Atammele sediment was analyzed as the most carcinogenic followed by Isiachala with concentrations of 84.23 ng/µL and 51.92 ng/µL respectively. Ube stream sediment has the lowest concentration of PAHs (11.74 ng/µL). Ecological risk of the PAHs revealed a sediment-to-sediment variation in the risk profile. Human health risk assessment depicts that hazard index and total cancer risk for adults and children ranged from 2.3E-07 - 2.57E-05 and 4.85E-07 - 5.43E-05 respectively. Pyrogenic activities are the main source of PAHs in the sediments. The results provide a guide for monitoring PAHs pollution and protecting drinking water sources.

Temporal and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in the Danube River in Hungary

The Danube is a significant transboundary river on a global scale, with several tributaries. The effluents from industrial operations and wastewater treatment plants have an impact on the river's aquatic ecosystem. These discharges provide a significant threat to aquatic life by deteriorating the quality of water and sediment. Hence, a total of 16 Polycyclic Aromatic Hydrocarbons (PAHs) compounds were analyzed at six locations along the river, covering a period of 12 months. The objective was to explore the temporal and spatial fluctuations of these chemicals in both water and sediment. The study revealed a significant fluctuation in the concentration of PAHs in water throughout the year, with levels ranging from 224.8 ng/L during the summer to 365.8 ng/L during the winter. Similarly, the concentration of PAHs in sediment samples varied from 316.7 ng/g in dry weight during the summer to 422.9 ng/g in dry weight during the winter. According to the Europe Drinking Water Directive, the levels of PAHs exceeded the permitted limit of 100 ng/L, resulting in a 124.8% rise in summer and a 265.8% increase in winter. The results suggest that the potential human-caused sources of PAHs were mostly derived from pyrolytic and pyrogenic processes, with pyrogenic sources being more dominant. Assessment of sediment quality standards (SQGs) showed that the levels of PAHs in sediments were below the Effect Range Low (ERL), except for acenaphthylene (Acy) and fluorene (Fl) concentrations. This suggests that there could be occasional biological consequences. The cumulative Individual Lifetime Cancer Risk (ILCR) exceeds 1/104 for both adults and children in all sites.

Seasonal variation and concentration of PAHs in Lake Balaton sediment: A study on molecular weight distribution and sources of pollution

The temporal and spatial variations of 16 Polycyclic Aromatic Hydrocarbons (PAHs) were examined at multiple sites around Lake Balaton from February 2023 to January 2024. The results indicated that the concentrations of PAHs in sediment were high during the winter months, 448.35 to 619.77 ng/g dry weight, and low during the summer months, 257.21 to 465.49 ng/g dry weight. The concentration of high molecular weight PAHs (HMWPAHs), consisting of 5–6 rings, was greater than that of low molecular weight PAHs (LMWPAHs), which had 2–3 rings. The total incremental lifetime cancer risk (ILCR) for both dermal and ingestion pathways was high for both adults and children during the four seasons, with the highest records as the following: winter > spring > summer > autumn. The ecological effects of the 16 PAHs were negligible except for acenaphthylene (Acy) and fluorene (Fl), which displayed slightly higher concentrations during the autumn and spring, respectively.

Sourcing aliphatic and polycyclic aromatic hydrocarbons (PAHs) in Jinga shrimp (Metapenaeus affinis) muscle tissues and surface sediments (study case: Northwest Persian Gulf).

This study addresses the sources of aliphatic hydrocarbons (AHs) and polycyclic aromatic hydrocarbons (PAHs) in the surface sediments of the northwestern Persian Gulf and the muscle tissues of Jinga shrimp (Metapenaeus affinis), a commercially important aquatic species. In November 2018, 28 Jinga shrimp samples were systematically collected from four key fishing areas in Behrgan and Khormusi: Imam Khomeini Port (S1), Mahshahr Port (S2), Sejafi (S3), and Behrgan Wharf (S4). Additionally, sediment samples were collected from these locations, and AHs and PAHs concentrations were analyzed using gas chromatography-mass spectrometry (GC-MS). The average aliphatic concentration in Jinga shrimp was 4800.32 (μg g-1 DW), exceeding the sediment samples' 2496.69 (μg g-1 DW) estimate. Hydrocarbon component analysis revealed EPA priority list (PAH-16) and measured PAHs (PAH-29) concentrations in Jinga shrimp ranging from 1095.8 to 2698.3 (ng g-1 DW) and in sediments from 653.6 to 1019.5 (ng g-1 DW). Elevated AHs and PAHs in Jinga shrimp, compared to sediments, suggest a petrogenic source, notably at station S4 near Behrgansar and Nowruz oil fields. Low molecular weight (LMW) compounds dominated in both shrimp and sediment PAHs. Aliphatic composition profiles in shrimps closely mirrored sediment profiles, illustrating an even-to-odd carbon dominance gradient. Diagnostic ratio examinations of hydrocarbons indicated pervasive petroleum derivatives in the environment. This study establishes a direct correlation between hydrocarbon concentrations in shrimp and sediment samples and the corresponding aliphatic groups, PAH-16, and PAH-29. The findings underscore the potential of Jinga shrimp as a reliable indicator of hydrocarbon pollution in the northwestern Persian Gulf.