Beryllium-7 （^7Be） and lead-210 （^210pb） activities were measured from October 2002 to January 2004 at Waliguan Observatory （WO： 36.287°N, 100.898°E, 3816 m a.s.l （above sea level） in northwest China...Beryllium-7 （^7Be） and lead-210 （^210pb） activities were measured from October 2002 to January 2004 at Waliguan Observatory （WO： 36.287°N, 100.898°E, 3816 m a.s.l （above sea level） in northwest China. ^7Be and ^210pb activities are high with overall averages of 14.74-3.5 mBq m^-3 and 1.8±0.8 mBq m^-3 respectively. For both 7Be and ^210pb, there are significant short-term and seasonal variations with a commonly low value in summer （May-September） and a monthly maximum in April （for ^7Be） and in December （for ^210pb）. The ratio of ^7Be/^210pb showed a broad maximum extending from April to July, coinciding with a seasonal peak in surface ozone （O3）. The seasonal cycles of ^7Be and ^210pb activities were greatly influenced by precipitation and thermal dynamical conditions over the boundary layer, especially for ^210Pb. The vertical mixing process between the boundary layer and the aloft air modulates the variations of ^7Be and ^210pb at WO in summer. It is indicated that air mass had longer residence time and originated from higher altitudes at WO in the spring-summer time and the winter in 2003. During an event with extremely high weeklyaveraged ^7Be concentration （24.8 mBq m^-3） together with high O3 levels and low water mixing ratio, we found that air masses had been convectively transported a long distance to WO from high latitude source regions in central Asia, where significant subsiding motions were observed. In another case with the extreme ^210pb activity of 5.7 mBq m^-3 high CO2 level and specific humidity （in winter）, air masses had come from south China and north Indian regions where 222Rn activities were high. This study, using ^7Be and ^210pb as atmospheric tracers, has revealed that complex interactions of convective mixing from the upper troposphere and long-range transports exist at WO.展开更多
A massive earthquake measuring 9.0 on the Richter scale that occurred on March 11, 2011, on Honshu Island, Japan, caused radioactivity leakage from the Fukushima Nuclear Power Plant, which led to the leakage of artifi...A massive earthquake measuring 9.0 on the Richter scale that occurred on March 11, 2011, on Honshu Island, Japan, caused radioactivity leakage from the Fukushima Nuclear Power Plant, which led to the leakage of artificial nuclides(131I, 137 Cs, and 134Cs) and their global transportation by atmospheric circulation. This paper reports a systematic comparative observation on radioactive concentrations of natural nuclides(7Be and 210Pb) and artificial nuclides(131I, 137 Cs, and 134Cs) at the surface level, measured in weekly continuous aerosol sampling at Mount Guanfeng, Guiyang, China, from March 17, 2011 to April 28, 2011. During this period, the variations in the nuclide concentrations associated with their transport paths were analyzed with 315 hour back-trajectories of air mass initialized 500 m above the surface level at Guiyang. The results show that the pollutants of nuclear leakage from the Fukushima accident were transported to the Guiyang region of China via two significant pathways. In the first pathway the first wave of nuclear pollutants were transported from west to east in air masses at higher altitudes via global atmospheric circulation. The nuclear pollutants encircled the Earth almost once and after about 10 days to two weeks, between March 24 and March 31, 2011, intruded Guiyang from the northwestern region of China. In the second pathway, the nuclear pollutants from the Fukushima region arrived at Guiyang between April 7 and April 14, 2011, via air masses at lower altitudes that moved southwards because of the squeezing of the northeast Asian weather system and then by the influence, in succession, of the northeastern and southeastern air currents in the low-latitude region. The first transport pathway for atmospheric pollutants is on a global scale and based on air masses at higher altitudes, and the second transport pathway is on an eastern Asia regional scale and based on the air masses at lower altitude.展开更多
基金the National Science Foundation of China （Grant Nos. 40175032 , 40575013）.
文摘Beryllium-7 （^7Be） and lead-210 （^210pb） activities were measured from October 2002 to January 2004 at Waliguan Observatory （WO： 36.287°N, 100.898°E, 3816 m a.s.l （above sea level） in northwest China. ^7Be and ^210pb activities are high with overall averages of 14.74-3.5 mBq m^-3 and 1.8±0.8 mBq m^-3 respectively. For both 7Be and ^210pb, there are significant short-term and seasonal variations with a commonly low value in summer （May-September） and a monthly maximum in April （for ^7Be） and in December （for ^210pb）. The ratio of ^7Be/^210pb showed a broad maximum extending from April to July, coinciding with a seasonal peak in surface ozone （O3）. The seasonal cycles of ^7Be and ^210pb activities were greatly influenced by precipitation and thermal dynamical conditions over the boundary layer, especially for ^210Pb. The vertical mixing process between the boundary layer and the aloft air modulates the variations of ^7Be and ^210pb at WO in summer. It is indicated that air mass had longer residence time and originated from higher altitudes at WO in the spring-summer time and the winter in 2003. During an event with extremely high weeklyaveraged ^7Be concentration （24.8 mBq m^-3） together with high O3 levels and low water mixing ratio, we found that air masses had been convectively transported a long distance to WO from high latitude source regions in central Asia, where significant subsiding motions were observed. In another case with the extreme ^210pb activity of 5.7 mBq m^-3 high CO2 level and specific humidity （in winter）, air masses had come from south China and north Indian regions where 222Rn activities were high. This study, using ^7Be and ^210pb as atmospheric tracers, has revealed that complex interactions of convective mixing from the upper troposphere and long-range transports exist at WO.
基金financially supported jointly by National Natural Science Foundation of China(Grant No.41175115)the EML of the United States of America
文摘A massive earthquake measuring 9.0 on the Richter scale that occurred on March 11, 2011, on Honshu Island, Japan, caused radioactivity leakage from the Fukushima Nuclear Power Plant, which led to the leakage of artificial nuclides(131I, 137 Cs, and 134Cs) and their global transportation by atmospheric circulation. This paper reports a systematic comparative observation on radioactive concentrations of natural nuclides(7Be and 210Pb) and artificial nuclides(131I, 137 Cs, and 134Cs) at the surface level, measured in weekly continuous aerosol sampling at Mount Guanfeng, Guiyang, China, from March 17, 2011 to April 28, 2011. During this period, the variations in the nuclide concentrations associated with their transport paths were analyzed with 315 hour back-trajectories of air mass initialized 500 m above the surface level at Guiyang. The results show that the pollutants of nuclear leakage from the Fukushima accident were transported to the Guiyang region of China via two significant pathways. In the first pathway the first wave of nuclear pollutants were transported from west to east in air masses at higher altitudes via global atmospheric circulation. The nuclear pollutants encircled the Earth almost once and after about 10 days to two weeks, between March 24 and March 31, 2011, intruded Guiyang from the northwestern region of China. In the second pathway, the nuclear pollutants from the Fukushima region arrived at Guiyang between April 7 and April 14, 2011, via air masses at lower altitudes that moved southwards because of the squeezing of the northeast Asian weather system and then by the influence, in succession, of the northeastern and southeastern air currents in the low-latitude region. The first transport pathway for atmospheric pollutants is on a global scale and based on air masses at higher altitudes, and the second transport pathway is on an eastern Asia regional scale and based on the air masses at lower altitude.
基金国家自然科学基金面上项目“环境中Pu的地球化学运移”(编号:40873086),“黔中大气核素(Pb-210,Be-7)与气溶胶关系”(编号:40773071),“Pb-210和Be-7大气沉降通量研究”(编号:40373038),“利用7Be和210Pb示踪研究高原大气微量气体成分的输送特征”(编号:40175032)中美国际合作项目“Tracing recent climate and environmental changes by measuring lowlevel radionuclides in the Yunnan-Guizhou plateau,China(2001-2005)”资助
基金国家自然科学基金面上项目“环境中Pu的地球化学运移”(编号:40873086),“黔中大气核素(Pb-210,Be-7)与气溶胶关系”(编号:40773071),“Pb-210和Be-7大气沉降通量研究”(编号:40373038),“利用7Be和210Pb示踪研究高原大气微量气体成分的输送特征”(编号:40175032)中美国际合作项目“Tracing recent climate and environmental changes by measuring lowlevel radionuclides in the Yunnan-Guizhou plateau,China(2001-2005)”资助
