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首页> 外文期刊>Journal of Geophysical Research, D. Atmospheres: JGR >In situ measurements of trace gases and aerosol optical properties at a rural site in northern China during East Asian Study of Tropospheric Aerosols: An International Regional Experiment 2005
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In situ measurements of trace gases and aerosol optical properties at a rural site in northern China during East Asian Study of Tropospheric Aerosols: An International Regional Experiment 2005

机译:东亚对流层气溶胶研究:2005年国际区域实验期间,对中国北方农村地区的痕量气体和气溶胶光学特性进行的原位测量

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In situ measurements of trace gases and aerosol optical properties were made in March 2005 at Xianghe (39.798°N, 116.958°E, 35 m), a rural site about 70 km southeast, and generally downwind of the Beijing metropolitan area. High pollutant levels were observed during the experiment, with CO (1.09 ± 1.02 ppmv, average ± standard deviation), SO2 (17.8 ± 15.7 ppbv), NOy (26.0 ± 24.0 ppbv), aerosol scattering coefficients (bsp, (468 ± 472) × 10?6 m?1), and aerosol absorption coefficients (bap, (65 ± 75) × 10?6 m?1) all much higher than observed at some rural sites in the United States. O3 (29.1 ± 16.5 ppbv) was relatively low during this study, suggesting inactive photochemical processes. Strong synoptic fluctuations in pollutant levels were detected every 4–5 days during the experiment, as cold fronts passing over the region drastically reduced the ground-level pollution. Very little precipitation was measured during the whole observational period, implying pollutant uplift and transport by rain-free cold fronts and dry convection. The single scattering albedo (SSA) observed (0.81 in the morning and 0.85 in the afternoon) indicates strongly absorbing aerosols near surface. The observed CO/SO2 ratio (35.8) is higher than inventory values, but closer to the updated CO inventory of Streets et al. (2006) than to Streets et al. (2003) or Wang et al. (2005). The observed CO/NOy ratio agrees better with inventories. Further analysis suggests that such comparisons may shed some light on the quality of emission inventories, but quantification of any error requires more extensive measurements over longer period and larger areas, as well as direct characterization of emission sources, especially mobile sources and small boilers. Using black carbon (BC)/CO ratio from the experiment, BC emissions from China are estimated at about 1300 Gg (109 g)/yr, but could be as high as 2600 Gg/yr.
机译:2005年3月,在东南约70公里,北京大都市顺风的农村地区香河(北纬39.798°,北纬116.958°E,35 m)进行了痕量气体和气溶胶光学特性的原位测量。在实验过程中观察到高污染物水平,包括CO(1.09±1.02 ppmv,平均值±标准偏差),SO2(17.8±15.7 ppbv),NOy(26.0±24.0 ppbv),气溶胶散射系数(bsp,(468±472)) ×10?6 m?1)和气溶胶吸收系数(巴,(65±75)×10?6 m?1)都比美国某些农村地区的观测值高得多。在这项研究中,O3(29.1±16.5 ppbv)相对较低,表明光化学过程不活跃。在实验过程中,每4-5天会检测到一道强烈的天气污染物波动,这是因为冷锋经过该地区大大降低了地面污染。在整个观测期内,几乎没有降水量,这意味着通过无雨的冷锋和干燥对流来提升和运输污染物。观测到的单个散射反照率(SSA)(早晨为0.81,下午为0.85)表明在地表附近强烈吸收了气溶胶。观测到的CO / SO2比(35.8)高于清单值,但更接近Streets等人的更新的CO清单。 (2006年)。 (2003)或Wang等。 (2005)。观察到的CO / NOy比与库存更吻合。进一步的分析表明,这样的比较可能对排放清单的质量有所了解,但是要量化任何误差,就需要在更长的时期和更大的范围内进行更广泛的测量,以及对排放源(尤其是移动源和小型锅炉)进行直接表征。使用实验中的黑碳(BC)/ CO比,估计中国的BC排放量约为1300 Gg(109 g)/年,但可能高达2600 Gg /年。

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