Black carbon (BC) aerosols are considered key factors that contribute to rapid climate warming and ice melt in the Arctic region.However,compared with long-term observations from land-based stations,observational data...Black carbon (BC) aerosols are considered key factors that contribute to rapid climate warming and ice melt in the Arctic region.However,compared with long-term observations from land-based stations,observational data over the Arctic Ocean remain relatively scarce.Four Arctic scientific expeditions were conducted in the summer and early autumn of 2010,2012,2016,and 2018 via the Chinese research vessel Xue Long,during which the BC concentrations along the routes were measured via light absorption methods.In this work,the spatiotemporal distribution characteristics of BC over the Arctic Ocean were examined on the basis of these observations.The potential sources of BC along the various routes were analyzed via the weighted potential source contribution function and weighted concentrationweighted trajectory methods of the hybrid single-particle Lagrangian integrated trajectory model in conjunction with Arctic transport potential climate model simulations.The analysis results indicated that wildfires in the western Aleutian Islands,Siberia,and Far East regions were the primary contributors to the BC aerosol concentration observed along the Arctic expedition routes in summer,identifying these regions as major potential source areas.展开更多
Volatile organic compounds(VOCs)are major contributors to air pollution.Based on the emission characteristics of 99 VOCs that daily measured at 10 am in winter from 15 December 2015 to 17 January 2016 and in summer fr...Volatile organic compounds(VOCs)are major contributors to air pollution.Based on the emission characteristics of 99 VOCs that daily measured at 10 am in winter from 15 December 2015 to 17 January 2016 and in summer from 21 July to 25 August 2016 in Beijing,the environmental impact and health risk of VOC were assessed.In the winter polluted days,the secondary organic aerosol formation potential(SOAP)of VOC(199.70±15.05 mg/m^3)was significantly higher than that on other days.And aromatics were the primary contributor(98.03%)to the SOAP during the observation period.Additionally,the result of the ozone formation potential(OFP)showed that ethylene contributed the most to OFP in winter(26.00%and 27.64%on the normal and polluted days).In summer,however,acetaldehyde was the primary contributor to OFP(22.00%and 21.61%on the normal and polluted days).Simultaneously,study showed that hazard ratios and lifetime cancer risk values of acrolein,chloroform,benzene,1,2-dichloroethane,acetaldehyde and 1,3-butadiene exceeded the thresholds established by USEPA,thereby presenting a health risk to the residents.Besides,the ratio of toluene-to-benzene indicated that vehicle exhausts were the main source of VOC pollution in Beijing.The ratio of m-/p-xylene-toethylbenzene demonstrated that there were more prominent atmospheric photochemical reactions in summer than that in winter.Finally,according to the potential source contribution function(PSCF)results,compared with local pollution sources,the spread of pollution from long-distance VOCs had a greater impact on Beijing.展开更多
基金supported by the National Natural Science Foundation of China (No.42201151)the Basic Research Fund of the Chinese Academy of Meteorological Sciences (Nos.2023Z004 and 2024Z007)。
文摘Black carbon (BC) aerosols are considered key factors that contribute to rapid climate warming and ice melt in the Arctic region.However,compared with long-term observations from land-based stations,observational data over the Arctic Ocean remain relatively scarce.Four Arctic scientific expeditions were conducted in the summer and early autumn of 2010,2012,2016,and 2018 via the Chinese research vessel Xue Long,during which the BC concentrations along the routes were measured via light absorption methods.In this work,the spatiotemporal distribution characteristics of BC over the Arctic Ocean were examined on the basis of these observations.The potential sources of BC along the various routes were analyzed via the weighted potential source contribution function and weighted concentrationweighted trajectory methods of the hybrid single-particle Lagrangian integrated trajectory model in conjunction with Arctic transport potential climate model simulations.The analysis results indicated that wildfires in the western Aleutian Islands,Siberia,and Far East regions were the primary contributors to the BC aerosol concentration observed along the Arctic expedition routes in summer,identifying these regions as major potential source areas.
基金supported by the National Key R&D Program of China(No.2016YFC0202500)the National Natural Science Foundation of China(Nos.21677163 and 21876193)+1 种基金the Chengdu Science and Technology Project(No.2018-ZM01-00019-SN)the Youth Innovation Promotion Association CAS。
文摘Volatile organic compounds(VOCs)are major contributors to air pollution.Based on the emission characteristics of 99 VOCs that daily measured at 10 am in winter from 15 December 2015 to 17 January 2016 and in summer from 21 July to 25 August 2016 in Beijing,the environmental impact and health risk of VOC were assessed.In the winter polluted days,the secondary organic aerosol formation potential(SOAP)of VOC(199.70±15.05 mg/m^3)was significantly higher than that on other days.And aromatics were the primary contributor(98.03%)to the SOAP during the observation period.Additionally,the result of the ozone formation potential(OFP)showed that ethylene contributed the most to OFP in winter(26.00%and 27.64%on the normal and polluted days).In summer,however,acetaldehyde was the primary contributor to OFP(22.00%and 21.61%on the normal and polluted days).Simultaneously,study showed that hazard ratios and lifetime cancer risk values of acrolein,chloroform,benzene,1,2-dichloroethane,acetaldehyde and 1,3-butadiene exceeded the thresholds established by USEPA,thereby presenting a health risk to the residents.Besides,the ratio of toluene-to-benzene indicated that vehicle exhausts were the main source of VOC pollution in Beijing.The ratio of m-/p-xylene-toethylbenzene demonstrated that there were more prominent atmospheric photochemical reactions in summer than that in winter.Finally,according to the potential source contribution function(PSCF)results,compared with local pollution sources,the spread of pollution from long-distance VOCs had a greater impact on Beijing.
