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Surface sediments along the Southern Terengganu coast (≤7 km from the coast) were analyzed for polycyclic aromatic hydrocarbons (PAHs). The concentrations of 16 USEPA priority polycyclic aromatic hydrocarbons (ΣPAH 16 ) ranged from 2.59 to 155 ng g -1 and their respective alkylated ranged between 8.80 and 24.90 ng g -1 . Traces of acephenanthrylene, benzo[c]phenanthrene, thiophenic PAH, and benzonaphthofuran were identified. PAH diagnostic ratios and cross-plots revealed that these sedimentary PAH compounds are derived mainly from pyrogenic sources, primarily from biomass burning and petroleum combustion residues with minor petrogenic input. The high correlations between pyrogenic PAHs to total PAHs (r >0.73, p <0.5), and the Bap/Bep ratio to total PAHs (r = 0.88, p <0.5), suggest that atmospheric deposition and urban runoff are the main deposition pathways. The concentrations of the PAHs in the southern South China Sea fall in the moderate contamination range of 100-1000 ng g -1 ., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In an effort to assess the occurrence and sources of polycyclic aromatic hydrocarbons (PAHs) in the ambient air of Riyadh, Saudi Arabia, PM10 samples were collected during December 2010. Diagnostic PAH concentration ratios were used as a tool to identify and characterize the PAH sources. The results reflect high PM10 and PAH concentrations (particulate matter (PM) = 270-1,270 μg/m(3)). The corresponding average PAH concentrations were in the range of 18 ± 8 to 1,003 ± 597 ng/m(3) and the total concentrations (total PAHs (TPAHs) of 17 compounds) varied from 1,383 to 13,470 ng/m(3) with an average of 5,871 ± 2,830 ng/m(3). The detection and quantification limits were 1-3 and 1-10 ng/ml, respectively, with a recovery range of 42-80%. The ratio of the sum of the concentrations of the nine major non-alkylated compounds to the total (CPAHs/TPAHs) was 0.87 ± 0.10, and other ratios were determined to apportion the PM sources. The PAHs found are characteristic for emissions from traffic with diesel being a predominant source.

Despite the increasing agricultural use of biochar as a way of combining the utilization of biomass for energy production with the removal of CO(2) from the atmosphere, it is not known how variations in pyrolysis temperature and feedstock type affect concentration and composition of polycyclic aromatic hydrocarbons (PAHs) that inevitably form and associate with biochar. To close this knowledge gap, we quantified 11 unsubstituted three- to five-ring PAHs as well as alkylated forms of phenanthrene and anthracene in grass and wood chars produced in 100 °C increments across a temperature range (100 to 700 °C). Our results show that solvent-extractable PAH concentrations in biochars produced at heat treatment temperatures (HTTs) of 400 and 500 °C greatly exceed those observed at higher and lower temperature, supporting a low HTT solid-phase formation mechanism operable at temperatures commonly used for industrial biochar production. The maximum extractable yield of 'pyrolytic' unsubstituted PAHs for grass (22 μg g(-1) at HTT = 500 °C) greatly exceeds the value for wood (5.9 μg g(-1)). Moreover, PAH signatures (e.g., total monomethylphenanthrene to phenanthrene ratios, MP/P ~2-3) at intermediate temperatures (400 °C) resemble those of fossil oils rather than that commonly attributed to pyrolytic products. Further research is needed to characterize the PAH evolution in modern pyrolysis reactors and assess the fate of biochar-bound PAHs in soils and sediments. Various commonly applied PAH ratios and indicator compounds show promise as markers for specific feedstock materials and pyrolysis conditions of biochars in environmental systems.

Polycyclic aromatic hydrocarbon (PAH) analyses of surface sediments from the Cross River estuary by gas chromatography-mass spectrometry indicated natural diagenetically derived PAHs in the upper estuary, with minor and variable amounts of petrogenic and combustion-derived PAHs from human activities (lower estuary). The occurrence of significant amounts of perylene (average 23% of all PAHs) with the diagenetic natural PAHs in the middle estuary bordered by mangrove forests supports its origin from terrestrial organic matter. The natural PAHs represent the highest percentage (average 76%) of the total PAHs in this tropical environment. The traditional geochemical parameters, including the petrogenic PAHs, confirmed trace petroleum contamination in the estuary. Specific PAH ratios such as Fl/Py and Fl/(Fl+Py) also support this source contribution.

Source tests were conducted to analyze and characterize diagnostic key tracers for emissions from burning of coals with various ranks. Ambient aerosol particulate matter was also collected in three areas of China and a background area in Corvallis, OR (U.S.) to confirm the presence of tracers specific for coal smoke. The results showed a series of aliphatic and aromatic hydrocarbons and phenolic compounds, including PAHs and hydroxy-PAHs as the major tracers, as well as a significant unresolved complex mixture (UCM) of compounds. The tracers that were found characteristic of coal combustion processes included hydroxy-PAHs and PAHs. Atmospheric ambient samples from Beijing and Taiyuan, cities where coal is burned in northern China, revealed that the hydroxy-PAH tracers were present during the wintertime, but not in cities where coal is not commonly used (e.g., Guangzhou, South China). Thus, the mass of hydroxy-PAHs can be apportioned to coal smoke and the source strength modeled by summing the proportional contents of EC (elemental carbon), PAHs, UCM and alkanes with the hydroxy-PAHs.

Biomass burning is an important primary source of particles containing biomarker compounds, which are introduced into smoke primarily by direct volatilization/steam stripping and by thermal alteration based on combustion conditions. This study presents comprehensive organic compound source profiles for smoke from controlled burning of green vegetation native to the predominant temperate and semiarid forests of the western United States. Smoke particles were extracted with dichloromethane/methanol (2:1, v/v), and the extracts were analyzed as their lMS derivatives by gas chromatography—mass spectrometry. Carbohydrates were by far the major compound class emitted in smoke particles, encompassing 57-77% of the total extractable organic compounds detected here. Lignin derivatives (5-17%) and diterpenoids (up to 16%) from bleed resins were the next most abundant compound groups observed. The major individual compounds encompassed methylinositols (up to 41%, e.g., pinitol) for conifer smokes, deoxyinositols (up to 32%, e.g., quercitol) for samples containing oak vegetation, and the thermally altered product of cellulose combustion levoglucosan (14-21%). The remaining compound classes, i.e., n-alkanoic acids, n-alkanols, n-alkanes, triterpenoids, steroids, and polycyclic aromatic hydrocarbons, were present at lower abundances (mostly <5%). The results showed that burning of green (moist) vegetation imprints high amounts of polar/water-soluble compounds into the smoke probably by volatilization/steam stripping processes, resulting in a different biomarker profile compared to dry/dead vegetation and wood combustion emissions. [ABSTRACT FROM AUTHOR]

Five-stage size-segregated ambient aerosol particles were collected during January 2003 until October 2004 at one urban and one suburban site of Beijing to investigate the seasonal size distributions of aliphatic and polycyclic aromatic hydrocarbons. The concentrations of total n-alkanes ranging from C11 to C35 varied between 2.1 and 2446 ngm3, with higher values at the urban site than suburban site. A seasonal fluctuation was clearly evident, with higher concentrations occurring during the colder period. The carbon preference index (CPI) of the n-alkanes displayed the highest values in the spring and apparently decreased in winter. Furthermore, smaller size airborne particle-bound n-alkanes tend to have lower CPI values. In addition, the presence of pristane, phytane, n-alkylcyclohexanes, hopanes, and steranes, together with the major unresolved complex mixture (UCM) of branched and cyclic compounds, confirmed the contribution from fossil fuel use in ambient aerosol particles of Beijing. The concentrations of 18 unsubstituted PAHs (18-PAH) varied from 0.84883 ngm3, with the content at the urban site 1.16.6 times higher than those for the suburban site. The seasonal variation of 18-PAH concentrations was as follows winter > autumn > spring > summer. About 6788 of the PAHs were associated with particles having an aerodynamic diameter 2.0 m. PAHs concentration diagnostic ratios reflect that the major source of fine particles is from fossil fuel utilization. [ABSTRACT FROM AUTHOR]

In order to evaluate hydrocarbon inputs to Crater Lake from anthropogenic and natural sources, samples of water, aerosol, surface slick and sediment were collected and analyzed by gas chromatography-mass spectrometry (GC-MS) for determination of their aliphatic and aromatic hydrocarbon concentrations and compositions. Results show that hydrocarbons originate from both natural (terrestrial plant waxes and algae) and anthropogenic (petroleum use) sources and are entering the lake through direct input and atmospheric transport. The concentrations of petroleum hydrocarbons range from low to undetectable. The distributions and abundances of n-alkanes, polycyclic aromatic hydrocarbons (PAH) and unresolved complex mixture (UCM) from petroleum are similar for all surface slick sampling sites. The estimated levels of PAH in surface slicks range from 7–9 ng/m2 which are low. Transport of petroleum-derived hydrocarbons from the lake surface has resulted in their presence in some sediments, particularly near the boat operations mooring (total petroleum HC = 1440 µg/kg, dry wt. compared to naturally derived n-alkanes, 240 µg/kg, dry wt.). The presence of biomarkers such as the tricyclic terpanes, hopanes and steranes in shallow sediments further confirms petroleum input from boat traffic. In the deep lake sediments, petroleum hydrocarbon concentrations were very low (16 µg/kg, dry wt.). Very low concentrations of PAH were detected in shallow sediments (17–40 µg/kg at 5 m depth near the boat operations) and deep sediments (3–15 µg/kg at 580 m depth). The individual PAH concentrations in sediments (µg/kg or ppb range) are at least three orders of magnitude less than reported threshold effects levels (mg/kg or ppm range, test amphipod Hyalella azteca). Therefore, no adverse effects are expected to occur in benthic biota exposed to these sediments. Boating activities are leaving a detectable level of petroleum in surface waters and lake sediments but these concentrations are very low. [ABSTRACT FROM AUTHOR]