Distribution and source estimation of polycyclic aromatic hydrocarbons in coastal sediments from Seto Inland Sea, Japan

2020 ◽  
Vol 17 (7) ◽  
pp. 488
Author(s):  
Hiroaki Tsuji ◽  
Waqar Azeem Jadoon ◽  
Yoko Nunome ◽  
Hideo Yamazaki ◽  
Satoshi Asaoka ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Sediment Cores ◽  
Seto Inland Sea ◽  
Emission Sources ◽  
Osaka Bay ◽  
The Seto Inland Sea ◽  
Polycyclic Aromatic ◽  
Mean Concentration ◽  
Total Concentrations

Environmental contextPolycyclic aromatic hydrocarbons are carcinogenic environmental contaminants that tend to migrate into the sediments in oceans and seas. Their vertical distribution in sediments from the Seto Inland Sea matched their emission over time, which in turn reflected changes in energy sources and industrial activities in Japan. This study shows that human activities on land directly and significantly influence the concentration of polycyclic aromatic hydrocarbons in sediments. AbstractSeventeen polycyclic aromatic hydrocarbons (PAHs) were identified in sediment cores collected at several locations in the Seto Inland Sea in 2015 and 2016 to understand their spatial distribution and potential emission sources. PAHs were analysed using gas chromatography–mass spectrometry. The age of the sediment cores was analysed using radioisotopic dating techniques to reconstruct historical PAH emissions. The total concentrations of 17 PAHs in the sediment cores of Osaka Bay in 2015 were in the range of 108–2810ng g−1 dry weight (dw) with a mean concentration of 1050ng g−1 dw. The total concentrations of 17 PAHs in sediment cores from the Seto Inland Sea in 2016 were in the range of 52.6–941ng g−1 dw with a mean concentration of 313ng g−1 dw. The spatial distribution of PAHs showed the highest concentration in Osaka Bay and the lowest in Kii Channel in 2016. The horizontal PAH distribution showed a decreasing trend in concentrations from the estuary offshore to Osaka Bay and Aki-Nada. The vertical PAH distribution revealed that levels were higher before the 1980s–1990s, when oil consumption and industrial activities in the Osaka region reached a maximum in the 20th century. The diagnostic ratios of PAHs and a principal component analysis revealed three main emission sources of PAHs, industry, biomass burning and traffic activities.

scholarly journals A comparison of PM<sub>2.5</sub>-bound polycyclic aromatic hydrocarbons in summer Beijing (China) and Delhi (India)

2020 ◽  
Vol 20 (22) ◽  
pp. 14303-14319
Author(s):  
Atallah Elzein ◽  
Gareth J. Stewart ◽  
Stefan J. Swift ◽  
Beth S. Nelson ◽  
Leigh R. Crilley ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Emission Sources ◽  
Night Time ◽  
Total Pahs ◽  
High Contribution ◽  
Polycyclic Aromatic ◽  
The Mean ◽  
Beijing China ◽  
Mean Concentration

Abstract. Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in air, soil, and water and are known to have harmful effects on human health and the environment. The diurnal and nocturnal variations of 17 PAHs in ambient particle-bound PAHs were measured in urban Beijing (China) and Delhi (India) during the summer season using gas-chromatography–quadrupole time-of-flight mass spectrometry (GC-Q-TOF-MS). The mean concentration of particles less than 2.5 µm (PM2.5) observed in Delhi was 3.6 times higher than in Beijing during the measurement period in both the daytime and night-time. In Beijing, the mean concentration of the sum of the 17 PAHs (∑17 PAHs) was 8.2 ± 5.1 ng m−3 in daytime, with the highest contribution from indeno[1,2,3-cd]pyrene (12 %), while at night-time the total PAHs was 7.2 ± 2.0 ng m−3, with the largest contribution from benzo[b]fluoranthene (14 %). In Delhi, the mean ∑17 PAHs was 13.6 ± 5.9 ng m−3 in daytime and 22.7 ± 9.4 ng m−3 at night-time, with the largest contribution from indeno[1,2,3-cd]pyrene in both the day (17 %) and night (20 %). Elevated mean concentrations of total PAHs in Delhi observed at night were attributed to emissions from vehicles and biomass burning and to meteorological conditions leading to their accumulation from a stable and low atmospheric boundary layer. Local emission sources were typically identified as the major contributors to total measured PAHs in both cities. Major emission sources were characterized based on the contribution from each class of PAHs, with the four-, five- and six-ring PAHs accounting ∼ 95 % of the total PM2.5-bound PAHs mass in both locations. The high contribution of five-ring PAHs to total PAH concentration in summer Beijing and Delhi suggests a high contribution from petroleum combustion. In Delhi, a high contribution from six-ring PAHs was observed at night, suggesting a potential emission source from the combustion of fuel and oil in power generators, widely used in Delhi. The lifetime excess lung cancer risk (LECR) was calculated for Beijing and Delhi, with the highest estimated risk attributed to Delhi (LECR = 155 per million people), which is 2.2 times higher than the Beijing risk assessment value (LECR = 70 per million people). Finally, we have assessed the emission control policies in each city and identified those major sectors that could be subject to mitigation measures.

scholarly journals A comparison of PM<sub>2.5</sub>-bound polycyclic aromatic hydrocarbons in summer Beijing (China) and Delhi (India)

2020 ◽  
Author(s):  
Atallah Elzein ◽  
Gareth J. Stewart ◽  
Stefan J. Swift ◽  
Beth S. Nelson ◽  
Leigh R. Crilley ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Emission Sources ◽  
Night Time ◽  
Total Pahs ◽  
High Contribution ◽  
Polycyclic Aromatic ◽  
The Mean ◽  
Beijing China ◽  
Mean Concentration

Abstract. Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in air, soil and water and known to have harmful effects on human health and the environment. The diurnal and nocturnal variation of 17-PAHs in ambient particle-bound PAHs were measured in urban Beijing (China) and Delhi (India) during the summer season using GC-Q-TOF-MS. The mean concentration of particles less than 2.5 microns (PM2.5) observed in Delhi was 3.6 times higher than in Beijing during the measurement period in both the day-time and night-time. In Beijing, the mean concentration of the sum of the 17 PAHs (∑17-PAHs) was 8.2 ± 5.1 ng m−3 in daytime, with the highest contribution from Indeno[1,2,3-cd]pyrene (12 %), while at night-time the total PAHs was 7.2 ± 2.0 ng m−3, with the largest contribution from Benzo[b]fluoranthene (14 %). In Delhi, the mean ∑17-PAHs was 13.6 ± 5.9 ng m−3 in daytime, and 22.7 ± 9.4 ng m−3 at night-time, with the largest contribution from Indeno[1,2,3-cd]pyrene in both the day (17 %) and night (20 %). Elevated mean concentrations of total PAHs in Delhi observed at night were attributed to emissions from vehicles and biomass burning and to meteorological conditions leading to their accumulation from a stable and low atmospheric boundary layer. Local emission sources were typically identified as the major contributors to total measured PAHs, however, in Delhi 25 % of the emissions were attributed to long-range atmospheric transport. Major emission sources were characterized based on the contribution from each class of PAHs, with the 4, 5, and 6 ring PAHs accounting ~ 95 % of the total PM2.5-bound PAHs mass in both locations. The high contribution of 5 ring PAHs to total PAH concentration in summer Beijing and Delhi suggests a high contribution from petroleum combustion. In Delhi, a high contribution from 6 ring PAHs was observed at night, suggesting a potential emission source from the combustion of fuel and oil in power generators, widely used in Delhi. The lifetime excess lung cancer risk (LECR) was calculated for Beijing and Delhi, with the highest estimated risk attributed to Delhi (LECR = 155 per million people), 2.2 times higher than Beijing risk assessment value (LECR = 70 per million people). Finally, we have assessed the emission control policies in each city and identified those major sectors that could be subject to mitigation measures.

scholarly journals Dynamics and Mass Balance of Polycyclic Aromatic Hydrocarbons in and around the Seto Inland Sea, Japan

2021 ◽  
Author(s):  
Hiroaki Tsuji ◽  
Yuta Akiyoshi ◽  
Daichi Asakawa ◽  
Shinya Nakashita ◽  
Yoko Iwamoto ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Polycyclic Aromatic Hydrocarbons ◽  
Mass Balance ◽  
Ecological Risk ◽  
Aromatic Hydrocarbons ◽  
Benthic Communities ◽  
The Yellow Sea ◽  
Seto Inland Sea ◽  
The Seto Inland Sea ◽  
Polycyclic Aromatic

Abstract Polycyclic aromatic hydrocarbons (PAHs) were analyzed to elucidate the distribution, ecological risk, pathways, and fluxes of these pollutants in and around the Seto Inland Sea, Japan. High molecular weight PAHs (5–6 rings) were primarily found in regions close to the bay estuaries, and their proportions decreased at distances further from the estuaries (offshore areas), where low molecular weight PAHs (2–4 rings) were more ubiquitous. Ecological risk assessments revealed that the PAHs found in the sediments should have no adverse effects on benthic communities, with the exception of fluorene, which was detected in high levels in the sediment from Beppu Bay. A mass balance for PAHs in the Seto Inland Sea, calculated based on data collected in the field and published literature findings, showed the PAH flux into the Seto Inland Sea from atmospheric deposition were ca. 5 times higher than that from riverine inflows. Comparison of the amount of the PAH flux between the Seto Inland Sea and other seas suggested that the Seto Inland Sea is less polluted than the Gulf of Lion and the Bohai Sea, and more polluted than the Yellow Sea.

Assessment of Polycyclic Aromatic Hydrocarbons in Underground Water around the Viccinity of Balogun-Biiro Dump Site, Oke Bale, Osogbo, Nigeria

2013 ◽  
Vol 2 (1) ◽  
Author(s):  
T A Adedosu
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Water Samples ◽  
Underground Water ◽  
Dump Site ◽  
Diagnostic Indices ◽  
Polycyclic Aromatic ◽  
The Mean ◽  
Mean Concentration ◽  
Significant Concentration

Well-water samples were collected from the vicinity of Balogun–biiro dump site located in Okebaale Osogbo, Osun state, Nigeria. The polycyclic aromatic hydrocarbons were determined qualitatively and quantitatively using GC-FID. The concentration of polycyclic aromatic hydrocarbons in the water samples ranged from 0.01235 µg/kg to 0.05365 µg/kg with mean concentration ranging from 0.00094 µg/kg to 0.00335 µg/kg respectively. The highest concentration of ∑16 𝑃𝐴𝐻𝑠was recorded in S6 and it was observed that there is decline in polycyclic aromatic hydrocarbons concentrations from point of water pollution. There was a significant concentration of both the lower and higher rings polycyclic aromatic hydrocarbons in the samples. These distributions as well as various polycyclic aromatic hydrocarbons diagnostic indices calculated showed that the sources of polycyclic aromatic hydrocarbons in the samples were both petrogenic and pyrogenic. The mean concentrations of polycyclic aromatic hydrocarbons recorded in the water samples showed a little bit enhanced values than the recommended tolerable limits, which indicated some level of pollution in the water samples

scholarly journals Residues of Persistent Organic Pollutants (POPs) in Agricultural Soils Adjacent to Historical Sources of Their Storage and Distribution—The Case Study of Azerbaijan

Molecules ◽  
2020 ◽  
Vol 25 (8) ◽  
pp. 1815 ◽  
Author(s):  
Aleksandra Ukalska-Jaruga ◽  
Karolina Lewińska ◽  
Elton Mammadov ◽  
Anna Karczewska ◽  
Bożena Smreczak ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Environmental Protection Agency ◽  
Agricultural Soils ◽  
The United States ◽  
Natural Soil ◽  
Polycyclic Aromatic ◽  
High Concentrations ◽  
Total Concentrations

The aim of this study was to identify and examine the levels of organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs) in soil collected from the surroundings of historical pesticide storage facilities on former agricultural aerodromes, warehouses, and pesticide distribution sites located in the most important agricultural regions in Azerbaijan. The conducted research included determination of three groups of POPs (occurring together), in the natural soil environment influenced for many years by abiotic and biotic factors that could have caused their transformations or decomposition. In this study, soil samples were collected in 21 georeferenced points located in the administrative area of Bilasuvar, Saatly, Sabirabad, Salyan and Jalilabad districts of Azerbaijan. Soil chemical analysis involved determination of organochlorine compounds (OCP): hexachlorocyclohexanes (HCHs) (three isomers α-HCH, β-HCH and γ-HCH) and dichlorodiphenyltrichloroethanes (DDTs) (six congeners 2,4′DDT; 4,4′DDT; 2,4′DDE; 4,4′DDE; 2,4′DDE; and 4,4′DDE); polycyclic aromatic hydrocarbons (PAHs): 16 compounds from the United States Environmental Protection Agency US EPA list and, PCBs (seven congeners identified with the following IUPAC numbers: 28, 52, 101, 118, 138, 153, and 180). Our research showed that OCPs reached the highest concentration in the studied areas. The total concentrations of OCPs ranged from 0.01 to 21,888 mg∙kg−1 with significantly higher concentrations of Σ6DDTs (0.01 μg kg−1 to 21880 mg kg−1) compared to ΣHCH (0.14 ng kg−1 to 166.72 µg kg−1). The total concentrations of PCBs in the studied soils was varied from 0.02 to 147.30 μg·kg−1 but only PCB138 and PCB180 were detected in all analyzed samples. The concentrations of Σ16 PAHs were also strongly diversified throughout the sampling areas and ranged from 0.15 to 16,026 mg kg−1. The obtained results confirmed that the agricultural soils of Azerbaijan contained much lower (up to by three orders of magnitude) concentrations of PCBs and PAHs than DDT. It is supported by the fact that PCBs and PAHs were not directly used by agriculture sector and their content results from secondary sources, such as combustion and various industrial processes. Moreover, the high concentrations of PAHs in studied soils were associated with their location in direct neighborhood of the airport, as well as with accumulation of contaminants from dispersed sources and long range transport. The high concentrations of pesticides confirm that deposition of parent OCPs have occurred from obsolete pesticide landfills.

Source Apportionment and Identification of Polycyclic Aromatic Hydrocarbons (PAHs) in Sediment Cores of Selected Creeks in Delta State, Nigeria

2015 ◽  
Vol 16 (1) ◽  
pp. 51-75 ◽  
Author(s):  
Peter M. Eguvbe ◽  
Chukwujindu M. A. Iwegbue ◽  
Sunny H. O. Egboh ◽  
Jude E. Ogala ◽  
Godwin E. Nwajei
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Source Apportionment ◽  
Aromatic Hydrocarbons ◽  
Sediment Cores ◽  
Polycyclic Aromatic
Sign in / Sign up

Export Citation Format

Share Document