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Wan Guojiang Zheng Xiangdong Lee H N Bai Z G Wan Enyuan Wang Shilu Yang Wei 《地球科学进展》2010,25(5):492-504
It′s essential to measure air concentrations and depositional fluxes of environmental radionuclides in different regions for modeling global contamination transfer and validation, tracing deposition process and dating, referencing watershed erosion trace and assessing natural radiation of ecosystem. This study introduces the research background and methods and explains weekly variations of 210Pb and 7Be concentrations in surface air and precipitation at Mt. Guanfeng/Guiyang since 2001. The results indicate that 210Pb and 7Be concentrations in surface air fluctuate periodically at 2~6 week interval because of the meteorological condition changes. The annual trend in 210Pb air concentration is overall influenced by air temperature variation and periodical rainfall. 7Be air concentration varies up and down regualarly. The synchronization of low concentrations for both 210Pb and 7Be in surface air and high ratio (210Pb/7Be ≥ 0.8) indicate oceanic poor 210Pb-7Be air mass invasion. The synchronization of high concentrations of 210Pb and 7Be in surface air and low ratio (210Pb/7Be ≤ 0.7) implies rich 7Be air mass invasion from altostratus atmosphere. Weekly concentrations of 210Pb and 7Be in precipitation and the Kd coefficients are high in late Autumn to Spring, and low in late Spring to Autumn. Although 210Pb and 7Be concentrations vary seasonally, their weekly concentrations in precipitation increase with that of air concentration. The 210Pb and 7Be weekly concentrations for seasonal division is about 0.2 Bq/L and 1 Bq/L, respectively. However, the Kd coefficient decreases when 210Pb and 7Be air concentrations increase. Deposition of 210Pb and 7Be with precipitation mainly take place in Spring and Summer; The weekly fallout of 210Pb and 7Be increases with increasing precipitation; the increase of 7Be is triple of that of 210Pb and 2.5 when precipitation nears to zero. The weekly-high fallout of 210Pb and 7Be with precipitation corresponds with the dramatic decrease of their air concentrations within or vicinal weeks. The ratio of 210Pb to 7Be in rainfall is overall ≤ 0.5 and varies synchronously with the ratio in surface air, indicating that the two radionuclides are cleaned by precipitation from air at close speed. In the extreme freezing disaster in 2008, both 210Pb and 7Be air concentrations were low and coupling with coexist of low concentration of aerosol and high nuclides activities. Weekly concentration of 7Be in surface air at Mt. Guanfeng demonstrates the anticipated concentration level in the low-latitude and high-elevation region; the short-term fluctuations of 7Be concentration indicated the hysteresis was influcenced by the strong air current submersion and the low-elevation air mass rising differently at Mt. Guanfeng and Mt. Waliguan. 相似文献
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利用瓦里关大气本底站甲烷观测数据对美国Aqua卫星的AIRS观测结果进行对比分析,并分析研究了2003~2012年青藏高原对流层大气甲烷的时空分布特征,结果表明:1)AIRS观测结果与近地面观测资料变化趋势一致,存在显著的正相关关系,突变时间比较一致,可以用于青藏高原区域的甲烷浓度特征分析。2)青藏高原对流层甲烷浓度在空间分布上存在显著的西北—东南走向的低值带及其南北侧存在4个固定的高值中心,分别位于阿里、那曲、山南和玉树。3)青藏高原甲烷浓度呈现显著随高度而降低的趋势,年平均甲烷浓度分别为1.810ppm(1 ppm=10-6)、1.797 ppm和1.781 ppm。在对流层中层和中上层,甲烷浓度基本呈现低值带最低、南北侧均高的山谷型分布特征。在对流层层顶,以低值带为分界线,呈现明显的南高北低特征。4)青藏高原甲烷浓度随时间呈缓慢上升趋势,平均速度为0.0018 ppm/a,夏季上升最快,秋季上升最慢。5)青藏高原甲烷存在明显的单峰型季节变化特征,夏秋季高,冬春季低,与东部地区冬、夏双峰型特征不同,随着高度上升季节变化更为明显。 相似文献
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Particle size distribution of 12–500 nm was measured at Mt. Waliguan, China Global Atmosphere Watch Baseline Observatory, from Aug. in 2005 to May in 2007. 72-hr back-trajectories at 100-m arrival height above ground level for the same period were calculated at 6:00, 12:00, and 21:00 (Beijing Time) for each day using the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT-4) model developed by NOAA/ARL. It was found that air mass sources significantly impact particle number concentration and size distribution at Mt. Waliguan. Cluster analysis of back-trajectories show that higher Aitken mode particle number concentration was observed when air masses came from or passed by the northeastern section of Mt. Waliguan, with short trajectory length. High number concentration of nucleation mode was associated with air masses from clean regions, with long trajectory length 相似文献
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根据Brewer和TOMS资料分析、验证瓦里关地区大气臭氧总量变化特征 总被引：1，自引：0，他引：1
通过对1 9 9 3年9月~2 0 0 3年1 1月瓦里关地区(3 6.1 7°N,1 0 0.5 3°E)Brewer资料和TOMS资料的比较分析,结果表明:1)瓦里关Brewer臭氧光谱仪的观测数据与卫星的TOMS观测数据之间存在一定的差异,两者的差异8 0%以上集中在-2.5%~2.5%之间;2)1 9 9 3~2 0 0 3年瓦里关地区的大气臭氧总量有着明显的下降趋势,这与北半球中纬度地区观测到的平流层臭氧减少的趋势相吻合;3)瓦里关地区大气臭氧总量存在明显的年际变化和季节变化,且每年的2~4月较高,8~1 0月较低,一年中振荡的幅度达到6 0 DU;4)TOMS两个版本的观测数据与地面观测结果呈现出较好的一致性和相关性,相关系数达到0.9以上。 相似文献
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瓦里关山与观风山近地面空气7Be浓度季节性变化对比 总被引：4，自引：0，他引：4
7Be广泛应用于大气物质传输、表土季节性迁移和微粒混合作用的示踪。它在不同地域空气中的浓度分布构成了多领域研究的基础。7Be在对流层空气中的浓度随地表海拔高度而增加。基于瓦里关山和观风山的位置差异和海拔高差,对比观测其近地面空气7Be浓度变化不仅有益于区域尺度的大气和地表环境过程的示踪,而且对全球尺度的研究也将具重要意义。2002-10-09～2004-01-21,利用美国环境测量实验室的低水平核素表层大气采样系统在瓦里关山和观风山同步连续进行每周1个大气气溶胶样品的采集工作。7Be的比活度系用多道能谱仪进行γ谱测定,测量误差小于6%。中美两实验室对逐周样品测量结果表明两实验室的数据具有很好的可比性。两个站点7Be浓度逐周变化趋势总体相似,具有2～6周的短周期波动,波峰与波谷具有良好的对应关系,其高值或低值波动延迟或超前的差异与区域尺度的天气过程传播一致。瓦里关山和观风山7Be的年均浓度分别为(14.7±1.5)mBq/m3和(4.1±0.9)mBq/m3,前者约为后者的3.6倍。近地面空气7Be浓度与同期降水量的比较表明,在周时间尺度上,两者呈现出较好的预期负相关变化;而在月平均尺度上,两地7Be浓度变化比较稳定。位于内陆地区的瓦里关山受低海拔气团上升的影响较小,其空气中7Be浓度变化较真实地反映了中纬度、高海拔地区的背景水平。观风山地区虽然受到低纬度海洋性上升气团的影响,但7Be浓度变化仍然显示出低纬度、较高海拔地区的预期水平。 相似文献
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Beryllium-7(~7Be)and lead-210(~(210)pb)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 ~(210)Pb activities are high with overall averages of 14.7±3.5 mBq m~(3)and 1.8±0.8 mBq m~(-3)respectively. For both ~7Be and ~(210)Pb,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~(210)Pb). The ratio of ~7Be/~(210)pb showed a broad maximum extending from April to July,coinciding with a seasonal peak in surface ozone(O_3).The seasonal cycles of ~7Be and ~(210)Pb activities were greatly influenced by precipitation and thermal dynamical conditions over the boundary layer,especially for ~(210)Pb.The vertical mixing process between the boundary layer and the aloft air modulates the variations of ~7Be and ~(210)pb 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 weekly- averaged ~7Be concentration(24.8 mBq m~(-3))together with high O_3 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 ~(210)pb activity of 5.7 mBq m~(-3)high CO_2 level and specific humidity(in winter),air masses had come from south China and north Indian regions where ~(222)Rn activities were high.This study,using ~7Be and ~(210)Pb as atmospheric tracers,has revealed that complex interactions of convective mixing from the upper troposphere and long-range transports exist at WO. 相似文献
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利用2007—2009年瓦里关本底台降水化学观测资料,分析了瓦里关降水的pH值、电导率及Cl-、NO-3、SO2-4、NH+4、K+、Na+、Ca2+、Mg2+等离子成分的分布特征。结果表明,瓦里关pH值和电导率的年平均值分别为6.60和21.26μs/cm,2007—2009年呈逐年升高趋势。根据pH值,瓦里关降水以中性降水为主,占总降水的65.13%,其次为碱性降水,酸雨最少。离子浓度大小排序依次为Ca2+SO2-4Na+NH+4Cl-Mg2+NO-3K+,且存在明显的季节变化特征,K+、Na+、Ca2+、Mg2+有相似的来源。瓦里关降水中SO2-4/NO3-的范围为0.35~16.48,平均值为3.07;2007—2009年SO2-4/NO-3值呈逐年下降趋势;SO2-4/NO-3全年存在两个峰值,分别在4月和9—10月。 相似文献
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为了研究青海瓦里关和西宁PM10中多环芳烃污染特征及其来源,于2007年5月24日～6月1日在青藏高原东北部的瓦里关大气本底站和青海气象台进行了观测并各采集7组气溶胶样品,分析了PM10质量浓度、粒径分布和多环芳烃谱分布特征。结果表明,瓦里关PM10日均浓度为24.85μg.m-3,粒径分布呈三模态;西宁PM10日均浓度为65.25μg.m-3,呈明显双模态。瓦里关积聚态颗粒物质量百分比大于西宁观测点。瓦里关PM10中多环芳烃含量远低于同季节西宁地区,浓度值为8.38ng.m-3;高分子量的PAHs主要集中在细颗粒上,而粗颗粒上低分子量PAHs相对较多。两地区高分子量多环芳烃均为单峰分布。后向轨迹分析表明,瓦里关PM10中PAHs污染与西宁市以及黄河河谷工业带方向的输送密切相关。 相似文献
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