Polycyclic Aromatic Hydrocarbons Isomer Ratios Research Articles

Distribution, sources and health risk assessment of polycyclic aromatic hydrocarbons in urban soils under different landform conditions of Taiyuan, China

Public concern about polycyclic aromatic hydrocarbons (PAHs) is rising due to their potential carcinogenic, teratogenic, and mutagenic effects. This study assessed PAHs in Taiyuan City’s plain and mountain soil, investigating concentrations, distribution, sources, and carcinogenic risk. Σ21PAHs concentrations in plain topsoil ranged from 133.2 to 6,410.6 ng/g (mean 1,444.7 ng/g), and in mountain soil from 66.5 to 2,250.2 ng/g (mean 585.5 ng/g). Approximately 55.1% of plain and 19.0% of mountain soil samples had contamination levels exceeding 600 ng/g. In plain soil, 4-ring and 5-ring PAHs dominated, while 2-ring and 3-ring PAHs were prevalent in mountain soil. Polluted areas in Taiyuan were primarily centered in the central-north, with higher content closer to industrial or business districts. PAH isomer ratios and principal component analysis/multiple linear regression (PCA/MLR) indicated coal combustion as the main PAH source, followed by coke production, vehicle emissions, and biomass combustion. Incremental lifetime cancer risks (ILCRs) showed Taiyuan’s PAH-related cancer risks were generally low, though heavily contaminated areas exhibited moderate risks. Plain regions had three times higher cancer risk than mountains, with children facing higher risk than adults. These findings highlight the need to consider PAH pollution while enhancing urban environmental quality.

A multi-criteria approach to investigate spatial distribution, sources, and the potential toxicological effect of polycyclic aromatic hydrocarbons (PAHs) in sediments of urban retention tanks

Bottom sediments deposited in retention tanks (RTs) located on two urban streams (Oliwski and Strzyza) in the central part of Gdansk (Poland) were analysed for polycyclic aromatic hydrocarbons’ (PAHs) content. PAHs were extracted from samples with methylene chloride, then the extracts were subjected to clean-up applying the solid phase extraction (SPE) method. Quantitative and qualitative determination of 16 PAHs was performed with the use of gas chromatography/mass spectrometry technique. A multi-dimensional approach was applied to analyse PAHs’ spatial distribution, source, and contamination status. Potential sources of PAHs were verified using isomer ratios supported by a statistical approach. The Σ16PAHs (in mg/kg d.w.) ranged from 1.95 ± 0.64 to 20.4 ± 6.8 for RTs located on the Oliwski Stream and from 0.50 ± 0.17 to 8.6 ± 2.9 for RTs located on the Strzyza Stream. PAHs detected in bottom sediments were mainly composed of 4- and 5-ring compounds. PAH isomer ratios such as Phen/Anth, Flth/Pyr, B(a)A/B(a)A + Chry, Inpy/Inpy + B(ghi)P, Flth/Flth + Pyr, Anth/Anth + Phen, and Flth/Flth + Pyr suggested delivery pathways for biomass, coal, and petroleum combustion. Petrogenic PAHs related to fuel leaks from cars were not detected. Statistical analyses confirmed traffic and heating system sources, while factor analysis (FA) pointed out the abrasion of wasting parts of vehicles. Based on threshold levels presented in sediment quality guidelines (SQGs), in most cases, PAHs were at low levels with occasional negative biological effects on organisms. Only sediments deposited in two RTs located on the Oliwski Stream presented harmful features for sediment-dwelling organisms. The risk assessment performed accordingly to the Σ16PAHs presented a moderate and high risk for biota. This study not only reflects the direct threat related to PAH content in bottom sediments, but also highlights the overall pollution of an area, considered to be a recreational part of the city (Oliwski Stream catchment). The findings of this study highlight the need to launch preventative methods to protect the area against pollution from heating system emission and traffic.

Spatial and seasonal variation and sources of deposition fluxes of polycyclic aromatic hydrocarbons (PAHs) in Shanghai.

Spatial and temporal variations of polycyclic aromatic hydrocarbons (PAHs) deposition fluxes and sources may significantly facilitate risk evaluation and pollution control of super megacity in China. A study on PAHs of wet and dry deposition in Shanghai was conducted from January to December of 2019. Seventeen sampling sites located in four functional areas were set, including the Baoshan iron and steel industry area (BS), Jinshan petrochemical industry area (JS), city center (CC), and Chongming agricultural area (CM). A total of 15 PAHs were determined by gas chromatography-mass spectrometry (GC-MS, Agilent 7890A/5975C). PAHs atmospheric deposition flux in winter was highest (3.12 ± 1.98μg/(m2·day), mostly attributed to local emissions accumulation under adverse meteorological diffusion conditions, as well as pollutants transport from northern China during heating season. PAHs deposition fluxes in industrial area (BS and JS) were 3.75 ± 4.08μg/(m2·day) and 3.18 ± 3.62μg/(m2·day) respectively, which were greater than those in CC and CM, accounting for 1.91 ± 1.06μg/(m2·day) and 1.41 ± 0.61μg/(m2·day) respectively. Proportional composition and isomer ratios of PAHs indicated that the PAHs deposition in winter and spring samples were more homogeneous, whereas those of summer and autumn seemed to be more variable and dispersed. Positive matrix factorization model were employed to identify the potential sources of PAHs in specific functional areas. A dominance of contribution was attributed to coal combustion (46%) at BS, petroleum volatilization (48%) at JS, biomass burning (55%) at CM, and vehicle emission (49%) at CC. This study highlighted that local urbanization and industrialization have a significant contribution to PAHs deposition to specific functional regions in Shanghai.

Cryoconites as biogeochemical markers of anthropogenic impact in high mountain regions: analysis of polyaromatic pollutants in soil-like bodies

The globalisation and omnidirectional character of anthropogenic processes has challenged scientists around the world to estimate the harmful effects of these processes on ecosystems and human health. Polycyclic aromatic hydrocarbons (PAHs) is one the most infamous group of contaminants, originated both from natural and anthropogenic processes. They could transport to high latitudes and altitudes through atmospheric long-distance transfer and further enter ecosystems of these vulnerable regions by deposition on terrestrial surfaces. An interesting object for tracking transboundary contamination processes in high mountain ecosystems is called cryoconite. Cryoconite, a dark-coloured supraglacial sediment which is abundant in polar and mountain environments, is considered as a storage of various pollutants, including PAHs. Thus, it may pose a risk for local human health and ecosystem through short-distance transfer. Studied cryoconite sediments were collected at the surface of Skhelda and Garabashi glaciers, Central Caucasus high-mountain region, as well as mudflow, moraine material and local soils at the Baksan Gorge in order to examine levels of their contamination. We analysed the content of 15 priority polyaromatic compounds from the US EPA list and used the method of calculation of PAHs isomer ratios with the purpose of identifying their source. To estimate their potential toxicity, Benzo[a]pyrene (BaP) equivalents were calculated. Maximum concentration was defined for NAP (84 ng×g-1), PHE (40 ng×g-1) and PYR (47 ng×g-1), with the minimum concentration for ANT (about 1 ng×g-1). The most polluted material is a cryoconite from Garabashi glacier because of local anthropogenic activities and long-distance transfer. High-molecular weight PAHs are dominated in PAHs composition of almost all samples. The most common sources of PAHs in studied materials are combustion processes and mixed pyrolytic/petrogenic origin. Toxicity levels of separate PAHs did not exceed the maximum permissible threshold concentrations values in most cases. However, the sum of PAHs in BaP equivalents exceed the threshold values in all samples, in some of them more than twice.

On-site measured emission factors of polycyclic aromatic hydrocarbons for different types of marine vessels

A portable emission sampling system was used to perform on-site measurements of the emission factors (EFs; quantities of pollutants emitted per unit of energy consumed) of 29 polycyclic aromatic hydrocarbons (PAHs) for five types of marine vessels using light diesel in Hainan Province, China. Both gaseous- and particulate-phase PAHs from vessel emissions were sampled and measured using gas chromatography coupled with mass spectrometry (GC-MS), and the PAH EFs were calculated based on the carbon mass balance method. The average EFs of gaseous- and particulate-phase PAHs were 6.2 ± 7.8 and 17 ± 26 mg/kg, with naphthalene (NAP) and phenanthrene (PHE) dominating the gaseous- and particulate-phase PAH emissions, respectively. Among the five types of vessels, the EFs for small fishing boats were significantly higher than those for other types of vessels, and the lowest EFs were found for tug boats. Composition profiles and typical isomer ratios of PAHs were calculated for five types of vessels. Particulate-phase PAHs accounted for 63 ± 16% of the total emissions of 29 PAH species, and the particulate/gaseous-phase partitioning of PAHs was dominated by organic carbon (OC) absorption rather than black carbon (BC) adsorption. Emission factors of PAHs under different activity conditions were measured and calculated, and relatively higher EFs were found in the maneuvering mode for medium fishing boats and in the operating mode for engineering vessels. No significant differences were found among the PAH composition profiles under different activity conditions.

Spatial distributions and sources of PAHs in soil in chemical industry parks in the Yangtze River Delta, China

The Yangtze River Delta (YRD) is one of the fastest developing areas in eastern China and contains many chemical industry parks. The profiles and sources of polycyclic aromatic hydrocarbons (PAHs) in soil in chemical industry parks and surrounding areas in the YRD were investigated by analyzing soil samples (n = 64) were collected in the YRD and Rudong chemical park (RD), a typical chemical park in the Yangtze River Delta. The total concentrations of 19 PAHs in the YRD soil samples were 16.3–4694 ng g−1 (mean 688 ng g−1), and the total concentrations of PAHs in RD were 21.6–246 ng g−1 (mean 75.4 ng g−1). The PAHs in soil in YRD were dominated by four-ring and five-ring PAHs, and the PAHs in RD were dominated by two-ring and three-ring PAHs. It suggested that PAHs may have been supplied to soil in YRD predominantly through coal combustion and vehicle emissions, PAHs in the soil of RD may be due to the volatilization and leakage of chemical raw material. According to the different distribution characteristics of PAHs, the ratio (1.5) of (2 + 3) rings/4 rings was proposed to identify the chemical source of PAHs. The PAH isomer ratios and principal component analysis/multiple linear regression (PCA/MLRA) results indicated that PAHs concentrations in soil in the YRD and RD are mainly supplied by industrial and traffic emissions. Incremental lifetime cancer risks (ILCRs) indicated that PAHs in soil pose negligible cancer risks to children and adults, but much stronger risks to children than adults.

Distribution and Sources of n-Alkanes and Polycyclic Aromatic Hydrocarbons in Sediments Around Oil Production Facilities in the Escravos River Basin, Niger Delta, Nigeria.

This study provides data on the characteristic levels, spatial patterns, sources, and risk of n-alkanes (AHs) [octane, n-C8, totetracontane, n-C40] and polycyclic aromatic hydrocarbons (PAHs) in surficial sediments from the Escravos River Basin (ERB), Nigeria. The n-alkane and PAH concentrations in sediments were quantified by chromatographic methods. The concentrations of AHs and PAHs in the ERB sediments varied from 95 to 3430µgg-1 and from 0.75 to 213µgg-1, respectively. Both the concentrations of AHs and PAHs in ERB sediments exceeded their respective guideline values. The carbon preference index and other AH markers provide evidence that the AHs in the ERB sediments originated from petroleum sources. Ecological risk assessment indicated that the ecological risk relating to an organism's contact with PAHs in the ERB sediments was high. The possible carcinogenic risk arising from human exposure with PAHs in surface sediments through accidental oral ingestion and skin contact exceeded the safe level of 10-6, indicating a considerable probable cancer risk for fishermen and other inhabitants of the ERB. PAH isomer ratios and multivariate statistics suggested that the PAHs in sediments from the ERB originated from gas flaring inputs, discharges from oil drilling platforms, diesel engines, ships, and speed boats, and combustion of wood and other biomass.

Field based measurement of multiple pollutant emissions from residential coal burning in rural Shanxi, northern China

It was well recognized that the pollutant emissions from real-world residential coal combustion contributed significantly to air pollution and human health, resulting in an urgent need for a better understanding of the pollutant emission factors (EFs) of residential coal combustion. However, field-based researches on residential coal combustion emissions are still limited at this stage. In this study, based on carbon balance method, emission factors (EFs) of CO2 and a series of pollutants, including gaseous pollutants (CO, NOX, CH4, and SO2), particulate matters (PM2.5 and PM10), elemental carbon (EC), organic carbon (OC), and polycyclic aromatic hydrocarbons (PAHs) from residential honeycomb briquette (HB) and coal chunk (CC) combustions were measured in real-world cooking stoves. As a result, apart from SO2, the burning of HB produced much less pollutants than CC. The median of emission reduction ratios estimated from Monte Carlo simulation ranged from 2.4% (SO2) to 98.8% (EC) by replacing CC with HB in residential combustion in Shanxi province in 2012. EFs of CO, PM2.5 and PAHs derived from the present field measurement were around 1–50 times higher than those from laboratory tests; furthermore, larger variations were found in our field measurement compared to that in the laboratory studies. This result called for more field measurements to reduce uncertainties of emission inventory estimations. As for the PAH emissions, particle phase PAHs dominated in both HB and CC burning and PAH emissions from HB burning had lower toxicity than CC combustion. Hence, HB is an ideal substituted fuel compared with CC. Previous studies suggested that PAH isomer ratios of FLA/(FLA+PYR) and IcdP/(IcdP+BghiP) above 0.5 represented source of coal combustion, which did not fit with our study well, indicating PAH isomer ratios might not be valid enough for source apportionment.

Chemical Characteristics of Atmospheric PM10 and PM2.5 at a Rural Site of Lijiang City, China.

Emissions from biomass burning are very serious in Southeast Asia and South Asia in April. In order to explore the effect of long-range transport of biomass emissions from the Indochina Peninsula in Southwest China during the period of the southeast monsoon season and to find out the main pollution sources in local atmospheric PM2.5, a field campaign was conducted from 6–26 April 2011 in Lijiang, China. Twenty-four-hour PM10 and PM2.5 filter samples were collected, and inorganic ions, elements, and carbonaceous components (including organic carbon (OC) and elemental carbon (EC), polycyclic aromatic hydrocarbons (PAHs) and nitrated PAHs (NPAHs)) were measured. The monthly mean mass concentrations of particulate matter (PM) were 40.4 and 14.4 μg/m3 for PM10 and PM2.5, respectively. The monthly mean concentrations of OC and EC in PM10 were 6.2 and 1.6 μg/m3, respectively. The weekly mean concentrations of ∑PAHs and ∑NPAHs were 11.9 ng/m3 and 289 pg/m3, respectively, in atmospheric PM10 of Lijiang. The diagnostic ratios of PAH and NPAH isomers were used to analyze the sources of PAHs and NPAHs in PM10. The ratios of Benz(a)anthracene/(Chrysene+Benz(a)anthracen), Fluoranthene/(Fluoranthene+Pyrene) and Indeno(1,2,3-cd)pyrene/(Benzo(g,h,i)perylene+Indeno(1,2,3-cd)pyrene) were 0.45 ± 0.04, 0.61 ± 0.01, and 0.53 ± 0.03, respectively, indicating the contribution from coal combustion and biomass burning. The 1-nitropyrene/Pyrene (1-NP/Pyr) ratio was 0.004 ± 0.001, suggesting that the contribution to NPAHs mainly came from coal combustion. Sulfate was the most prominent inorganic ionic species, with monthly mean levels of 2.28 and 1.39 μg/m3 in PM10 and PM2.5, respectively. The monthly mean mass ratios of NO3−/SO42− were 0.40 and 0.23 in PM10 and PM2.5, respectively, indicating that the contribution of atmospheric anions from coal combustion sources was much more important than that from other sources. Based on the relatively high SO42− concentrations and low NO3−/SO42− ratios, combined with the data analysis of isomer ratios of PAHs and NPAHs, we can conclude that coal combustion, traffic, and dust were the major contributors to local atmospheric PM in Lijiang city, while biomass burning may also have contributed to local atmospheric PM in Lijiang city to some degree.

Distribution, Composition, Sources, and Potential Ecological Risks of PAHs in the Sediments of the Lanzhou Reach of the Yellow River, China.

The distribution, composition, sources, and potential ecological risks of polycyclic aromatic hydrocarbons (PAHs) in the sediments of the Lanzhou Reach of the Yellow River, China were investigated. The total concentration of the 18 individual PAHs (∑18PAHs) in the sediments ranged from 638 to 1620ng/g, with a mean value of 901ng/g. The pollution level of PAHs in the sediments was low to moderate. Spatially, the distribution of PAHs in the sediments showed an increasing trend along the direction of water flow. ∑18PAHs predominantly consisted of low molecular weight PAHs. The principal component analysis and isomer ratios of PAHs suggested the mixed sources of petroleum and those from the combustion of petroleum, coal, and biomass. The results showed that the PAHs in the sediments of the Lanzhou Reach of the Yellow River have a low ecological risk. However, the BaP equivalent exposure values suggested a potential cancer risk.

Appraisal of coal- and coke-derived wastes in soils near a former manufactured gas plant, Jacksonville, Florida

Preliminary site assessments revealed visibly-impacted soils in downtown Jacksonville, Florida (USA) suspected to be associated with a historic (1875–1912) manufactured gas plant (MGP) nearby. In this study, 19 soils from 11 borings within the impacted area were collected and analyzed using GC/FID for quantification of total petroleum hydrocarbons (TPH) and GC/MS for quantification of 87 volatiles and 50 parent and alkylated polycyclic aromatic hydrocarbons (PAHs). The results showed soils (up to 11 m deep and spanning ~90 m) containing elevated concentrations of TPH and PAHs, wherein the total PAHs, which were exclusively pyrogenic in character, comprised (on average) 40 ± 10% of the TPH in most (14 of 19) soils. In accord with visual observations of black-to-maroon, viscous non-aqueous phase liquid (NAPL) in some soils, the chemical results confirm the widespread occurrence of variably-weathered MGP tars throughout the area's subsurface. Multiple PAH isomer ratios indicate all but one of the tars likely were produced from the carbureted water gas (CWG) process; the exceptional tar likely was produced via the coal carbonization process. Both processes were historically used by the nearby former MGP. Three soils contained distinct hydrocarbons and pyrogenic PAHs consistent with particulate coke or coal ash (clinker) or heavy (C10 to C22) gas oil, a feedstock for CWG, the latter of which appeared as a yellowish-green NAPL. When interpreted in light of the typical MGP waste management and decommissioning practices, the results demonstrate the area's soils contain MGP wastes consistent with the discharge and/or disposal of wastes and demolition debris from the former MGP.

Occurrence and Risk Assessment of PAHs in Surface Sediments from Western Arctic and Subarctic Oceans.

In the fourth Chinese National Arctic Research Expedition (from July to September, 2010), 14 surface sediment samples were collected from the Bering Sea, Chukchi Sea, and Canadian Basin to examine the spatial distributions, potential sources, as well as ecological and health risk assessment of polycyclic aromatic hydrocarbons (PAHs). The ∑PAH (refers to the sum of 16 priority PAHs) concentration range from 27.66 ng/g to 167.48 ng/g (dry weight, d.w.). Additionally, the concentrations of ∑PAH were highest in the margin edges of the Canadian Basin, which may originate from coal combustion with an accumulation of Canadian point sources and river runoff due to the surface ocean currents. The lowest levels occurred in the northern of Canadian Basin, and the levels of ∑PAH in the Chukchi Sea were slightly higher than those in the Being Sea. Three isomer ratios of PAHs (Phenanthrene/Anthracene, BaA/(BaA+Chy), and LMW/HMW) were used to investigate the potential sources of PAHs, which showed the main source of combustion combined with weaker petroleum contribution. Compared with four sediment quality guidelines, the concentrations of PAH are much lower, indicating a low potential ecological risk. All TEQPAH also showed a low risk to human health. Our study revealed the important role of the ocean current on the redistribution of PAHs in the Arctic.

Spatial variation and sources of polycyclic aromatic hydrocarbons influenced by intensive land use in an urbanized river network of East China

The concentrations and distribution of polycyclic aromatic hydrocarbons (PAHs) in urbanized river networks are strongly influenced by intensive land use, industrial activities and population density. The spatial variations and their influencing factors of 16 priority PAHs were investigated in surface water, suspended particulate matter (SPM) and sediments among areas under different intensive land uses (industrial areas, agricultural areas, inner city, suburban towns and island areas) in the Shanghai river network, East China. Source apportionment was carried out using isomer ratios of PAHs and Positive Matrix Factorization (PMF). Total concentrations of 16 PAHs ranged from 105.2 to 400.5 ng/L, 108.1 to 1058.8 ng/L and 104.4 to 19,480.0 ng/g in water, SPM and sediments, respectively. The concentrations of PAHs in SPM and sediments varied significantly among areas (p < 0.05), with the highest concentrations in inner city characterized by highly intensive land use and high population density. The PAH concentrations in sediments were positively correlated with those in SPM and were more strongly correlated with black carbon than with total organic carbon, indicating a stronger influence of prolonged anthropogenic contamination than the recent surface input in sediments. Biomass and coal combustion contributed strongly to total PAHs, followed by natural gas combustion in water and SPM, and vehicular emissions in sediments. Vehicular emissions were the strongest contributors in SPM and sediments of the inner city, indicating the strong influence of vehicular transportation to PAHs pollution in the urbanized river network.

Sources and chronology of combustion-derived pollution to Shilianghe Reservoir, eastern China: Evidences from PAHs profiles, As, Hg, Pb and Pb isotopes

The sedimentary records of polycyclic aromatic hydrocarbons (PAHs), mercury (Hg), arsenic (As), lead (Pb) and stable Pb isotopic ratios were studied in a sediment core collected from Shilianghe Reservoir in eastern China. Accumulations and distributions of these pollutants were measured in terms of PAHs concentrations, PAHs fluxes, and enrichment factor (EF) of Hg, As, Pb and Pb isotopic ratios. The accumulations showed a synchronous trend throughout the core, due to close correlation with rapid economic and industrial development of the catchment, Linyi City in eastern China. The results from PAH isomer ratios reveal that PAHs in sediments are dominantly from anthropogenic pyrogenic sources, mainly from the combustion of coal and biomass. Furthermore, the Pb isotopic composition clearly indicates that coal combustion dust mainly contributed to the Pb burden in the reservoir sediments. Based on mixing end-member model of Pb isotopic ratios, contributions of coal combustion dust are ranged from 31% to 62%, mainly from anthropogenic Pb sources. The contribution of leaded gasoline was lower than average at 25%. In addition, a steady increase in the contribution from coal combustion sources was found in the sediment core, while the contribution of leaded gasoline showed a decline in recent decades, due to the phase-out of leaded gasoline in China. Capsule abstractPAHs, Hg, As and Pb burden in a reservoir of China were chronicled. Increasing coal combustion dust is responsible for contamination of lake by end-member model of Pb isotopic ratios.

Characteristics, identification, and potential risk of polycyclic aromatic hydrocarbons in road dusts and agricultural soils from industrial sites in Shanghai, China.

Road dusts and agricultural soil samples were collected from eight sites close to steel mills, chemical plants, and municipal solid waste incinerator in suburban Shanghai. Sixteen polycyclic aromatic hydrocarbons (PAHs) in the United States Environmental Protection Agency (US EPA) priority controlled list were analyzed quantitatively using GC-MS. The total PAH concentrations ranged from 0.79 to 6.2μgg-1 in road dust samples with a mean value of 2.38μgg-1 and 0.26 to 0.54μgg-1 in agricultural soils with an average of 0.36μgg-1. The most abundant individual PAHs were phenanthrene, fluoranthene, pyrene, chrysene, and benzo(b)fluoranthene in dust samples and phenanthrene, fluoranthene, chrysene, and benzo(b)fluoranthene, benzo (k) fluoranthene in soil samples. Dominant compounds were four-ring and five- to six-ring PAHs, which accounted for 41.5 and 31.5% in dusts and 33.9 and 41.1% in soils. The spatial distribution of PAHs in dusts and soils was consistent. The wind direction could affect the spatial distribution of PAHs. Organic matter contents were found to be significantly positively correlated with PAH concentrations in both dusts and soils while grain size of particles had no correlation with PAH concentrations and could not significantly influence the distribution of PAH concentrations. PAH isomer ratios showed that combustion of grass, wood, and coal was important sources of PAHs in road dusts and agricultural soils. Toxic equivalent concentrations indicated seven kinds of carcinogenetic PAHs were major toxic equivalent concentration (TEQ) contributors, accounting for 98% of TEQ, in the road dusts and agricultural soils. Incremental lifetime cancer risk (ILCR) estimation results showed that the PAHs in the dusts and soils had potential cancer risk for both children and adults only by direct ingestion exposure. The TEQ and ILCR values of PAHs in road dusts were much higher than those in soils, which suggested that PAHs in road dusts could be an important source of PAHs in soils.

Polycyclic aromatic hydrocarbons (PAHs) and Pb isotopic ratios in a sediment core from Shilianghe Reservoir, eastern China: Implying pollution sources

The history records of polycyclic aromatic hydrocarbons (PAHs), lead and its stable isotope ratios were determined in a sediment core to receive anthropogenic impacts on the Shilianghe Reservoir in eastern China. The historical changes of PAHs concentrations, PAHs fluxes, Pb/Al and Pb isotope ratios showed a synchronous trend throughout the core, suggesting changes in energy usage and correlating closely with the experience of a rapid economic and industrial development of the catchment, Linyi City in eastern China. PAHs isomer ratios results reveal PAHs in sediments are dominantly anthropogenic pyrogenic source, dominated by the combustion of coal and biomass. Furthermore, the Pb isotopic composition also clearly indicates that coal combustion dust mainly contributed to the Pb burden in the reservoir sediments. Based on mix end member model of Pb isotope ratios, coal combustion dust dominated anthropogenic Pb sources over fifty years contributing from 31% to 62% of total Pb in sediment. And the contribution of leaded gasoline was low than average 25%. In addition, a stable increase of coal combustion source was found in sediment core, while the contribution of leaded gasoline had declined in recent decades, with the phase-out of leaded gasoline in China.

Distribution and Source Apportionment of Polycyclic Aromatic Hydrocarbons in Bank Soils and River Sediments From the Middle Reaches of the Huaihe River, China

Bank surface soil and river sediment samples from the middle reaches of the Huaihe River were analyzed by GC‐MS for polycyclic aromatic hydrocarbons (PAHs). The total PAHs concentrations ranged from104 to 947 ng/g in bank soils and from 83 to 2599 ng/g in river sediments. The PAHs levels of the studied samples are relatively higher as compared to those from other world regions, which suggest an enhanced deposition of atmospheric PAHs derived from the emissions of fossil fuel combustion in this area. Possible sources from soil and sediments were diagnosed by the paired PAHs isomer ratios and principal components analysis, and the results indicate that the PAHs in the soils mainly came from coal combustion (74%) followed by combustion of refined petroleum products (26%), and in the sediments mainly from pyrogenic sources (89%) followed by petroleum sources of oil spill emissions (11%). The PAHs exposure risk assessments show that PAHs in majority of the sediments did not pose threats to the ambient ecosystem. However, the calculated total toxic benzo[a]pyrene (BaP) equivalent of PAHs in soil and sediment indicate that BaP is the most potentially carcinogenic individual PAH.

Effect of input pathways and altitudes on spatial distribution of polycyclic aromatic hydrocarbons in background soils, the Tibetan Plateau.

Limited data on the spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in Tibetan soils have been reported. This study measured the concentrations of PAHs in background soils across Tibet including 44 surface soils (0-10 cm) and 14 subsurface soils (10-20 cm) and assessed the effect of input pathways and altitudes on spatial distribution of PAHs. The concentrations of 15 US EPA priority PAHs (∑15-PAHs, naphthalene excluded) in all surface soils ranged from 1.50 to 29.88 ng/g dry weight with a mean concentration of 6.09 ng/g. The levels of PAHs in soils from southeast of Tibet were higher than those from northwest, which might be attributed to both more local emission as a result of relative higher population density and contributions of long-range atmosphere transport (LRAT) processes from Indian subcontinent in the south and Sichuan in the east. For the northwest Tibet, the westerly wind originated from the western boundaries between India and Nepal but not local emission might play an important role in input of PAHs, since there were slight anthropogenic activities. A general decrease of ∑15-PAHs with depth suggested their atmospheric input, while surface runoff might also play an important role in input of PAHs to soils from canyon and valley. The abundances of more volatile three-ring PAHs positively correlated with altitudes while less volatile ones unrelated (four rings) or inversely correlated (five and six rings) with altitudes, indicating cold condensation effect. The results of PAH isomer ratios suggested mixed sources of petroleum evaporation and combustion of petroleum and biomass.

Black carbon in soils from different land use areas of Shanghai, China: Level, sources and relationship with polycyclic aromatic hydrocarbons

Black carbon (BC) in soils plays a key role of carrying hydrophobic pollutants like polycyclic aromatic hydrocarbons (PAHs). However, little is known about the spatial distribution, sources of BC and its relationship with PAHs in urban soils. We studied BC, total organic carbon (TOC) and PAHs concurrently in 77 soils collected from downtown area, suburban and rural area and industrial area of Shanghai, China. BC was determined by both chemical oxidation (dichromate oxidation, BCCr) and chemo-thermal oxidation (CTO-375, BCCTO). BC sources were identified qualitatively by BC/TOC concentration ratios and BC-cogenerated high molecular weight (HMW) PAH isomer ratios and quantitatively by principal component analysis followed by multiple linear regression (PCA-MLR). Results showed that BCCr concentration (4.65g/kg on average) was significantly higher than BCCTO (1.91g/kg on average) in Shanghai soils. BCCr concentrations in industrial area were significantly higher than those in other two. Stronger correlation was found between PAHs and TOC, BCCr than that between PAHs and BCCTO, which indicates the possibility of PAHs being carried by charcoal and other organic matters thus negating its exclusive dependence on soot. Charcoal was therefore suggested to be taken into account in studies of BC and its sorption of PAHs. BC/TOC ratios showed a mixed source of biomass burning and fossil fuel combustion. PCA scores of BC-cogenerated HMW PAHs isomer ratios in potential sources and soil samples clearly demonstrated that sources of BC in urban soils may fall into two categories: coal and biomass combustion, and traffic (oil combustion and tire wear). PCA-MLR of HMW PAHs concentrations in soil samples indicated that coal and oil combustion had the largest contribution to BC in urban soils while tire wear and biomass combustion were important in downtown and rural area, respectively, which indicated they were main sources of HMW PAHs and presumably of BC.

Atmospheric polycyclic aromatic hydrocarbons and isomer ratios as tracers of biomass burning emissions in Northern India

Emission from large-scale post-harvest agricultural-waste burning (paddy-residue burning during October-November and wheat-residue burning in April-May) is a conspicuous feature in northern India. The poor and open burning of agricultural residue result in massive emission of carbonaceous aerosols and organic pollutants to the atmosphere. In this context, concentrations of atmospheric polycyclic aromatic hydrocarbons (PAHs) and their isomer ratios have been studied for a 2-year period from a source region (Patiala: 30.2°N; 76.3°E) of two distinct biomass burning emissions. The concentrations of 4-6 ringPAHs are considerably higher compared to 2-3 ring PAHs in the ambient particulate matter (PM2.5). The crossplots of PAH isomer ratios, fluoranthene / (fluoranthene + pyrene) and indeno[1,2,3-cd]pyrene/(indeno[1,2,3-cd]pyrene + benzo[g,h,i]perylene) for two biomass burning emissions, exhibit distinctly different source characteristics compared to those for fossil-fuel combustion sources in south and south-east Asia. The PAH isomer ratios studied from different geographical locations in northern India also exhibit similar characteristics on the crossplot, suggesting their usefulness as diagnostic tracers of biomass burning emissions.