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Aquatic particles and organic carbon (OC) regulate the occurrence and transport of hydrophobic organic contaminants such as polycyclic aromatic hydrocarbons (PAHs) in water-suspended particle-sediment interfaces. Conventional studies on the mechanisms regulating the relationships between PAHs and total particles/OC have ignored micro-scale regulatory factors such as particle size and OC composition. Field research in the eutrophic shallow Lake Taihu, China, revealed that the fine particle fractions 2.7-10 μm in diameter had stronger PAH adsorption capacity and significantly regulated PAH particle size distribution and water-particle partitioning. Selective PAH biodegradation by planktonic microorganisms probably significantly weakened the capacity of the coarse fractions to regulate PAHs. OC fragments at different temperature gradients had markedly different influences on the particle size distribution of PAHs. High-temperature pyrogenic OC fractions (part of black carbon) were the principal OC regulatory factors for medium-to high-molecular-weight PAHs. However, the OC fragments did not directly affect the particle distribution of low-molecular-weight PAHs. During particle deposition and burial, microbial PAH utilization and efficiency probably regulated the burial potential of various hydrophobic PAH species. Biodegradation of relatively less hydrophobic PAHs with octanol-water partition coefficients (log K ow ) < 5.8 showed an increasing trend with decreasing PAH hydrophobicity. Biological pump action of the relatively higher hydrophobic PAH species (log K ow > 5.8) showed a decreasing trend with increasing PAH hydrophobicity. The discoveries of the present work further clarified the mechanisms of PAH partitioning and burial in a eutrophic shallow lake and collectively provides a valuable reference for modeling the transport and dispersal mechanisms of hydrophobic, particle-bound organic contaminants in other aquatic ecosystems., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Emerging per-and polyfluoroalkyl substances (PFASs) and traditional organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs) in the marginal seas of China were analyzed to study the occurrence, transport and phase partitioning. The influence of organic carbon (OC) and element carbon (EC) on particulate emerging pollutants in seawater was studied for the first time. The concentrations of PFASs, OCPs and PAHs in the seawater (dissolved phase plus particulate phase) ranged from 1.4 to 8.6, 0.76 to 4.3 and 8.4 to 130 ng L -1 , respectively. Pollutants in the northern East China Sea were generally higher than that in the southern East China Sea and South China Sea, which may be attribute to river discharges and land sources in the Yangtze River Delta. The Yellow Sea Coastal Current and Yangtze River Dilute Water drove the transport of contaminants from north to south marginal seas. Positive correlations between EC and PAHs were found, which can be explained by co-emission of them during combustion. Moreover, positive correlations between OC, EC and Log K d for BkF, BeP, HCB, 6:2 FTSA were found, which demonstrated that OC and EC promoted the partitioning of these high oleophilic compounds to suspended particle., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

As typical chemical indicators of the Anthropocene, polycyclic aromatic hydrocarbons (PAHs) and their environmental behavior in urban estuaries can reveal the influence of anthropogenic activities on coastal zones worldwide. In contrast to conventional approaches based on concentration datasets, we provide a compound-specific radiocarbon ( 14 C) perspective to quantitatively evaluate the sources and land‒sea transport of PAHs in an estuarine‒coastal surficial sedimentary system impacted by anthropogenic activities and coastal currents. Compound-specific 14 C of PAHs and their 14 C end-member mixing models showed that 67-73% of fluoranthene and pyrene and 76-80% of five- and six-ring PAHs in the Jiulong River Estuary (JRE, China) originated from fossil fuels (e.g., coal, oil spill, and petroleum-related emissions). In the adjacent Western Taiwan Strait (WTS), the contributions of fossil fuel to these PAH groups were higher at 74-79% and 84-87%, respectively. Furthermore, as a significant biomarker for source allocation of terrigenous organic matter, perylene, a typical five-ring PAH, and its land‒sea transport from the basin through the JRE and finally to the WTS was quantitatively evaluated based on the 14 C transport models. In the JRE, fluvial erosions and anthropogenic emissions affected the 14 C signature of perylene (Δ 14 C perylene , -535 ± 5‰) with contributions of > 38% and < 62%, respectively. From the JRE to the WTS, the decreased Δ 14 C perylene (-735 ± 4‰) could be attributed to the long‒range transport of "ocean current-driven" perylene (-919 ± 53‰) with a contribution of 53 ± 8%. This compound-specific 14 C approach and PAH transport model help provide a valuable reference for accurately quantifying land‒sea transport and burial of organic pollutants in estuarine‒coastal sedimentary systems., Competing Interests: Declaration of Competing Interest The authors declare no competing financial interest., (Copyright © 2021. Published by Elsevier Ltd.)

In order to investigate the impacts of dam-related water impoundment on the spatial-temporal variations and transport of anthropogenic organic pollutants, 15 priority polycyclic aromatic hydrocarbons (PAHs) were analyzed in water samples from the Shuikou Reservoir (SKR) of the Minjiang River. The SKR was formed after the construction of the Shuikou Dam, which is the largest hydropower station in Southeast China. The water samples were collected from the backwater zone of the SKR, in both the wet and dry seasons, corresponding to the drainage and impoundment periods of water flow, respectively. The concentrations of the dissolved PAHs in surface water from the wet season (average of 161 ± 97 ng L -1 ) were significantly higher (ANOVA, p < 0.01) than those from the dry season (average of 43 ± 21 ng L -1 ). PAH concentrations in the SKR decreased from upstream (industrialized cities) to downstream (rural towns or counties), indicating high PAH loads caused by intensive urbanization effects. The high proportions of 3-ring PAHs in the wet season were from local sources via surface runoff; while the elevated proportions of 4- to 6- ring PAHs in the dry season reflected atmospheric deposition emerged of these PAHs and/or volatilization of 3-ring PAHs enhanced. Molecular diagnostic ratios of PAH isomers in multimedium and principal component analysis indicated that PAH presence in the SKR was mainly attributed to pyrogenic origin. The isomeric ratios of fluoranthene to fluoranthene plus pyrene in the wet season were homogeneous, implying that there were continuous new inputs along the riverine runoff. However, these ratios showed spatial downward trend in the dry season, indicating continued degradation of PAHs occurred along the transport path during the impoundment period. The input and output fluxes of PAHs in the SKR were 5330 kg yr -1 and 2991 kg yr -1 , revealing that the reservoir retained contaminants after impoundment of the hydropower dam., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Riverine runoff is one of the most important pathways of pollutants entering the oceans. To study the seasonal variations, spatial transports, sources and mass fluxes of polycyclic aromatic hydrocarbons (PAHs) from the subtropical Jiulong River watershed to estuary, water samples were collected in wet and dry seasons. PAH concentrations showed significant temporal-spatial variations (ANOVA, p < 0.05). In the watershed, PAH concentrations in wet season (48.6 ± 18.2 ng L -1 ) were significantly lower than in dry season (90.3 ± 18.5 ng L -1 ). In contrast, estuarine PAH concentrations in wet season (67.1 ± 24.6 ng L -1 ) were significantly higher than in dry season (27.4 ± 10.6 ng L -1 ) (p < 0.0001). The spatial variations of PAH concentrations in wet and dry seasons reflected positive and restricted transport processes occurred in the river. These findings might be subjected to seasonal changes in precipitation, water discharge, hydrodynamic conditions, and human activities. The compositional patterns of PAHs illustrated that fluorene and phenanthrene were the dominant compounds in the watershed, while phenanthrene was predominant in the estuary. Source analysis by molecular diagnostic ratios and PMF model indicated that fossil fuel and biomass combustion and petroleum both contributed to the presence of PAHs, and the high contributions of pyrogenic PAHs might be related to urban rainstorm runoff in winter and atmospheric inputs in winter. Although the estimated flux of PAHs from watershed to estuary was about 676 kg yr -1 with a low level by comparing the data obtained in the worldwide, continue concern of PAHs in the Jiulong River is recommended due to the intense human activities., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

On July 27, 2003, a spill of approximately 31,000 tons of Iranian light crude oil affected the coast of Karachi, Pakistan. Approximately 11 years after the spill, we analyzed polycyclic aromatic hydrocarbons (PAHs) and their alkylated homologues (alkyl-PAHs) as the indicators to evaluate the residual effect of oil spill to the sediment along the Karachi coast. The total concentrations (dry weight) of parent PAHs and alkyl-PAHs ranged from 121.9 to 735.4 and 42.3-1149.9 ng/g, respectively. The estuary and harbor were the two regions with the highest levels of PAHs in the sediment. Conversely, sedimentary PAHs in the oil spill areas and remote coastal areas showed significantly lower levels. Although the results of the source identification indicated the up to 75.2% of the contribution from petroleum and its derivatives, this could only reflect the direct impact of the Karachi city on the presence of PAHs in the coastal sedimentary environment and did not indicated that the oil spill continues to stay 11 years later. Compared with 11 years ago, the sharply reduced PAH content, great changed composition, and the degradation driven trend of diagnostic ratios all indicated a sharp decrease in the influence of PAHs caused by the oil spill. Finally, the ecological risk caused by the PAH residual in the marine sedimentary ecosystem had disappeared along the Karachi coasts, Pakistan., (Copyright © 2019. Published by Elsevier Ltd.)

Semi-permeable membrane devices (SPMDs) were applied to sample some Organochlorinated Pesticides (OCPs), Polycyclic Aromatic Hydrocarbons (PAHs) and Polychlorinated Biphenyls (PCBs) from the seawater of 14 Chinese coastal areas. The total concentrations of OCPs (∑ 16 OCPs), PAHs (∑ 15 PAHs) and PCBs (∑ 35 PCBs) were in the ranges of 489.2-2174, 589.4-53,160, and 133.2-3658 ng/g lipid, respectively. The ∑ 15 PAHs varied significantly with the sampling locations, which were far higher in north Chinese coastal areas than in south areas, whereas ∑ 16 OCPs and ∑ 35 PCBs only slightly fluctuated along the entire coast line. Comparing SPMD to grab sampler, it was found that the distribution patterns of the PCBs and OCPs in seawater were generally similar. However, the compositional profiles of the PAHs, PCBs, DDTs and HCHs in SPMDs were slightly different to grab samplers and organisms. The SPMDs accumulated less lipotropic compounds, which are inclined to dissolve in water rather than in organisms., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

On the basis of the application of compound-specific radiocarbon analysis (CSRA) and air-water exchange models, the contributions of fossil fuel and biomass burning derived polycyclic aromatic hydrocarbons (PAHs) as well as their air-water transport were elucidated. The results showed that fossil fuel-derived PAHs (an average contribution of 89%) presented the net volatilization process at the air-water interface of the Taiwan Strait in summer. Net volatile fluxes of the dominant fluorene and phenanthrene (>58% of the total PAHs) were 27 ± 2.8 μg m -2 day -1 , significantly higher than the dry deposition fluxes (average 0.43 μg m -2 day -1 ). The Δ 14 C contents of selected PAHs (fluorene, phenanthrene plus anthracene, fluoranthene, and pyrene) determined by CSRA in the dissolved seawater ranged from -997 ± 4‰ to -873 ± 6‰, indicating that 89-100% (95 ± 4%) of PAHs were supplied by fossil fuels. The South China Sea warm current originating from the southwest China in summer (98%) and the Min-Zhe coastal current originating from the north China in winter (97%) input more fossil fuel PAHs than the Jiulong River estuary (90%) and Xiamen harbor water (93%). The more radioactive decayed 14 C of fluoranthene (a 4-ring PAH) than that of phenanthrene and anthracene (3-ring PAHs) represented a greater fossil fuel contribution to the former in dissolved seawater.

Coastal upwelling prevails in the coast of Hainan Island, the northern South China Sea (SCS) during summer. We studied the influences of the upwelling on the horizontal and vertical transport of terrigenous polycyclic aromatic hydrocarbons (PAHs). PAHs in dissolved and suspended particulate phase of water samples were determined in the upper (depth < 1 m) and water column (depth > 10 m). PAH levels decreased sharply from inshore to offshore to open sea. The results showed that terrestrial input was the main source of coastal PAHs. Perylene, an important indicator of land plant-derived PAH, showed the significant correlation with PAHs (p < 0.005). This implied that fluvial transport was the primary pathway of terrigenous PAHs into the coast of northern SCS. Variations of the concentrations, compositions and diagnostic ratios of PAHs, accompanied the partition equilibrium in the water column, could indicate the selective degradation of PAHs by the plankton affected by upwelling. Different from the "traditional" transport pathway of PAHs in the water column (surface enrichment-depth depletion distribution), the upwelling could provide the original driver to elevate the upward diffusion of sediment entrained contaminants towards the intermediate even the upper waters. It could also enhance the outward diffusion of terrigenous PAHs accompanied by the offshore transport of the upper waters. Therefore, the transport pathway of PAHs can be summarized by the coastal upwelling rising PAHs with their subsequent transport offshore and settling in the adjacent open sea., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

To study the spatial distributions and seasonal differences of concentrations, source identification, and phase partitioning of polycyclic aromatic hydrocarbons (PAHs) in surface water, intensive sampling was carried out along the marginal seas of China in four seasons. In the northern South China Sea (SCS), the highest PAH levels occurred in the summer (July to August) and autumn (October to November). In the East China Sea (ECS) and the Yellow Sea, the highest occurred in the summer (August) and winter (December). In all areas, the lowest PAH levels were found in the spring (May to June). The estimated mass inventory of PAHs in the surface water (0-5 m) of the northern SCS and ECS accounted for less than 8% of PAHs outflow into the offshore environment. That showed the consistent seasonal variation with PAHs levels. Land- and ocean-based emissions, surface runoff, and the open seawater dilution were the most important environmental factors influencing the seasonal heterogeneity and the spatial distributions of PAH in the surface water. The decline of observed organic carbon normalized partition coefficients in the four seasons was probably affected by the presence of submicrometer-sized soot particles accompanying the PAH outflow from China.

Historical records of polycyclic aromatic hydrocarbons (PAHs), organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were analyzed in two dated sediment cores (DH05 and DH11) collected from the continental shelf of the East China Sea (ECS) to investigate the influence of anthropogenic activities on marine sediment over the past century. The concentrations and fluxes of 15 PAHs were in the range of 28.6-96.5 ng g -1 and 7.6-35.2 ng cm -2 yr -1 in DH05 (1920s-2009), 18.8-76.4 ng g -1 and 13.9-30.9 ng cm -2 yr -1 in DH11 (1860s-2009). The sedimentary records of PAHs in the two cores generally reflected the economic development and energy consumption change in China. Identification of sources suggested that PAHs in ECS were predominantly from petrogenic origin and various combustion sources. A change of source from low- and moderate-temperature combustion to high-temperature combustion process was observed. Although a production ban of technical HCH and DDT was imposed in China in 1983, their sedimentary fluxes display increasing trends or strong rebounds from 1980s to 1990s as recorded in the core profiles. High proportions of DDD + DDE and γ-HCH suggested those OCPs mainly derived from early residuals. Temporal trends of PCBs presented relative high levels from 1970s to 1980s and high proportions of PCB congeners with 3-6 chlorines atoms indicated industrial sources., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Intensive daytime and nighttime sampling was carried out from 23 Oct to 31 Dec 2008 to investigate the occurrence of nitrated polycyclic aromatic hydrocarbons (NPAHs) in PM10 at a roadside site in Xiamen, China. At the same time, six PM10 samples were collected from a nearby roadway tunnel for comparison. Six NPAHs, namely 9-nitroanthracene, 2- and 3-nitrofluoranthene, 1-nitropyrene, 7-nitrobenz[a]anthracene, and 6-nitrobenzo[a]pyrene, were identified and quantified using GC/MS in negative ion chemical ionization mode. The average total concentration of six NPAHs (sigmaNPAHs) in the cold season (26 Nov-31 Dec) was 2.3 (daytime) and 9.9 (nighttime) times higher than those in the warm season. Significant statistical difference (p < 0.01, 2-tailed) of sigmaNPAHs between daytime and nighttime was found during both the warm and cold seasons. NPAHs were significantly positively correlated with their parent PAHs and nitrogen dioxide but negatively correlated with ambient temperature. The ratio of 2 + 3-nitrofluoranthene to 1-nitropyrene exhibited a similar diurnal pattern as sigmaNPAHs and was generally greater than 5, indicating the importance of secondary atmospheric formation. The diurnal variations of NPAHs were all influenced by the diurnal variations of PAHs, nitrogen dioxide, sunlight, and temperature. The daily inhalable exposure to the six NPAHs in the tunnel was much higher than the roadside values in the warm season but only slightly higher than those in the cold season.

Based on the quantitative and qualitative analysis of sixteen Polycyclic Aromatic Hydrocarbons (PAHs) with GC and GC-MSD, the concentrate distribution and transportation characteristics of PAHs in suspended particulate matter (SPM) and surface sediments (SS) from the Pearl River Estuary were studied. Whether in SPM or in SS, the concentration distribution of PAHs were characterized by acenaphthene (mean 55.5 microg/g in SPM, 226 ng/g in SS) with subordinate amounts of the tri- and tetra-cycle PAHs such as fluorene, fluoranthene, phenaphene and pyrene. However, PAHs had different composition and concentration in SPM and SS. Pentacyclic PAHs appeared in SS and seldom in SPM because of their low solubility and high molecular weight. The concentrations of the tri-, tetracyclic PAHs in SPM were 100-300 times higher than those in SS. The total PAHs varied from 12-281 microg/g (mean 77 microg/g) in SPM and 208-1849 ng/g (mean 537 ng/g) in SS respectively. There were similar correlations between the concentrations of PAHs in SPM and salinity, and between the distance of the stations from the river outlet moving seawards and the concentrations of PAHs. These indicated that PAHs were degraded or transported along with the salinity gradient in SPM and the distance from the river outlet in SS. It was also suggested that the sources of these PAHs are from sewage and shipping discharge-pollutants. Pearl River Estuary had been lightly contaminated by PAHs.

As unavoidable by-products of the combustion of organic matter, the sources of carcinogenic polycyclic aromatic hydrocarbons (PAHs) are an area of great research interest in environmental monitoring, environmental forensics, and organic geochemistry. Molecular diagnostic ratios, receptor models, and stable isotope analysis are the most widely used methods to identify the sources of PAHs. However, some studies have demonstrated that these conventional methods have several disadvantages including overlapping end-members (or "non-uniqueness"), unexpected "blending," secondary reaction and degradation, which lead to ambiguous PAH source results. At the end of the last century, compound-specific radiocarbon analysis (CSRA) focusing on the molecular level radiocarbon signatures was introduced for PAH source identification, because of its effectiveness in avoiding uncertainties of the conventional methods. CSRA has an excellent ability to distinguish the fractional contributions of fossil fuels and biomass burning. Here, by reviewing the merits and limitations of conventional methods, we point out that their unquestioning application needs to be criticized in PAH source identification, and further highlight the particular advantages of CSRA. Specifically, we summarize the application and prospects of CSRA in PAH source identification. We conclude that CSRA provides a powerful tool to accurately quantify the sources of aromatic pollutants, to reveal their sedimentary radiocarbon records, and to elucidate regional energy structure and fuel consumption. In doing so, we provide a critical resource to expand the application of CSRA in environmental science. To the best of our knowledge, this is the first comprehensive review of the application of CSRA for PAH source identification. [ABSTRACT FROM AUTHOR]

Trace organic pollutants (PAHs, DDTs, HCHs PCBs) in sediments, suspended particulate matter and bivalves were studied during 1994 and 1997 in three estuaries of China: the Jiulong River, the Minjiang River and the Pearl River estuaries. Results indicated that there were somedifferences between the composition characteristics of the trace organic pollutants in the suspended particulate matter and the sediments. Concentrations of trace organic pollutants in the bivalves were 2-300 times higher than those in the sediments. In the three estuaries, the concentrations of PAHs and PCBs were relatively higher in Pearl River estuary, but the concentrations of DDTs were higher in Jiulong River and Minjiang River estuaries. Relatively high values of PAHs appeared at the outlet of river, waterway and harbor. It is suspected that these PAHs mainly came from sewage, shipping discharge and local pollutant sources. Relatively high concentrations of PCBs appeared at the Pearl River estuary that may be related to industrial development. The ratios of DDT to DDTs indicated that DDT may not be newly released into these estuaries. Compared with other estuaries in the world,the sediments of the southeastern estuaries of China had not been polluted. However, the concentrations of trace organic pollutants in organisms were close to the lower limits of food criteria. Thus, the control of trace organic pollutants in these marine environments is very important. [ABSTRACT FROM AUTHOR]

Abstract: PM10 samples from a garden site (site A), an industrial-traffic intersection (site B), a residential site (site C) and an island site (site D) were collected at December 21–29, 2004; March 18–22, 2005; July 4–13, 2005 and October 24–28, 2005 in Xiamen. 15 priority PAHs compounds were analyzed by using a gas chromatograph/mass spectrometer (GC/MS). The abundance and origin of PAHs are discussed to reveal seasonal variations in Xiamen air quality. Average concentrations of Σ15PAHs were 17.5 ng/m3, 3.7 ng/m3, 32.6 ng/m3 and 10.5 ng/m3 from spring to winter with the highest value in autumn. The dominant PAHs components in every season were low and middle molecular weight PAHs including phenanthrene, pyrene, fluoranthene and chrysene. Diagnostic ratios and PCA analysis identified the main sources of particle bound PAHs: mainly from both gasoline and diesel vehicles exhaust, with some contribution from coal combustion, industry emission and cooking sources. [Copyright &y& Elsevier]