面向应用的CBERS-02星高分辨率相机成像数值模拟技术框架

技术框架研究的目标是准确仿真卫星高分辨率相机成像过程中辐射和几何质量的下降情况,从应用方的角度建立评价高分辨率卫星相机在国土资源领域的应用潜力和技术框架,并以CBERS-02B星HR相机在轨成像模拟为例进行了原理验证,同时对今后以国土资源应用评价为目标的高分辨率相机在轨成像模拟改进方案提出了建议。     

云顶以下臭氧对TOMS反演臭氧总量的影响及反演方法的理论研究

目前紫外后向散射反演臭氧总量的所有算法,都将云考虑成不透明的Lambertian反射体,并假定云顶有效反照率不随波长的变化而变化.然而本文通过模拟计算发现,由于云散射、瑞利散射、臭氧吸收三种作用的综合结果,云顶的有效反照率是与波长相关的,即使光学厚度比较大的云,辐射也可由云顶继续向下传输,因而会受到云顶以下臭氧吸收的影响.用V7方法进行反演,模拟计算结果表明：云的出现使得云顶以下,特别是云内光程增强,导致紫外波段的臭氧吸收衰减增大,所以反演出的臭氧总量值比真实值偏大,本文称这种现象为“云吸收效应”,并讨论了该效应的影响因子.最后,在辐射传输模拟的基础上建立一套反演算法,大大减弱了“云吸收效应”的影响.     

华南黑碳气溶胶浓度与南海夏季风关系的年代际突变

利用重建的华南区域黑碳气溶胶(Black Carbon,BC)浓度资料,分析其与南海夏季风在年际尺度上的关系.结果 表明,华南区域BC浓度与南海夏季风的关系在2000年前后有明显的突变,由显著负相关变为显著正相关,即由高BC浓度弱季风变为高BC浓度强季风.通过合成对比分析,发现1988-1999年(第一时间段)的华南B...     

Impacts of Aerosol-Radiation Interactions on the Wintertime Particulate Pollution under Different Synoptic Patterns in the Guanzhong Basin,China

The effects of aerosol–radiation interactions(ARI) are not only important for regional and global climate, but they can also drive particulate matter(PM) pollution. In this study, the ARI contribution to the near-surface fine PM(PM2.5)concentrations in the Guanzhong Basin(GZB) is evaluated under four unfavorable synoptic patterns, including "northlow", "transition", "southeast-trough", and "inland-high", based on WRF-Chem model simulations of a persistent heavy PM pollution episode in January 2019. Simulations show that ARI consistently decreases both solar radiation reaching down to the surface(SWDOWN) and surface temperature(TSFC), which then reduces wind speed, induces sinking motion,and influences cloud formation in the GZB. However, large differences under the four synoptic patterns still exist. The average reductions of SWDOWN and daytime TSFC in the GZB range from 15.2% and 1.04°C in the case of the"transition" pattern to 26.7% and 1.69°C in the case of the "north-low" pattern, respectively. Furthermore, ARI suppresses the development of the planetary boundary layer(PBL), with the decrease of PBL height(PBLH) varying from 18.7% in the case of the "transition" pattern to 32.0% in the case of the "north-low" pattern. The increase of daytime near-surface PM2.5 in the GZB due to ARI is 12.0%, 8.1%, 9.5%, and 9.7% under the four synoptic patterns, respectively. Ensemble analyses also reveal that when near-surface PM2.5 concentrations are low, ARI tends to lower PM2.5 concentrations with decreased PBLH, which is caused by enhanced divergence or a transition from divergence to convergence in an area. ARI contributes 15%–25% toward the near-surface PM2.5 concentrations during the severe PM pollution period under the four synoptic patterns.     

Late Quaternary fluvial aggradation and incision in the monsoon‐dominated Alaknanda valley,Central Himalaya,Uttrakhand, India

The present study aims to explain the spatial and temporal variability in phases of aggradation/incision in response to changes in climate and seismicity during the late Quaternary in the Alaknanda River valley (a major tributary of the river Ganges or Ganga). Geomorphology, stratigraphy and optical dating of the fluvial sediment reveal that the oldest fluvial landforms preserved in the south of the Main Central Thrust are debris flow terraces developed during the early part of pluvial Marine Isotopic Stage 3. Following this, a period of accelerated incision/erosion owing to an increase in uplift rate and more intense rainfall occurred. In the Lesser Himalaya, three phases of valley fill aggradation around 26 ± 3 ka, 18 ± 2 ka and 15 ± 1 ka and 8 ± 1 ka occurred in response to changes in monsoon intensity and sediment flux. The last phase was regionally extensive and corresponds to a strengthening of the early Holocene Indian Summer Monsoon. A gradual decline in the monsoon strength after 8 ± 1 ka resulted in reduced fluvial discharge and lower sediment transport capacity of the Alaknanda River, leading to valley fill incision and the development of terraces. The study suggests that fluvial dynamics in the Alaknanda valley were modulated by monsoon variability and the role of tectonics was subordinate, limited to providing accommodation space and post‐deposition modification of the fluvial landforms. Copyright © 2010 John Wiley & Sons, Ltd.     

Nitrogen and sulfur species in Antarctic aerosols at Mawson,Palmer Station,and Marsh (King George Island)

High volume bulk aerosol samples were collected continuously at three Antarctic sites: Mawson (67.60° S, 62.50° E) from 20 February 1987 to 6 January 1992; Palmer Station (64.77° S, 64.06° W) from 3 April 1990 to 15 June 1991; and Marsh (62.18° S, 58.30° W) from 28 March 1990, to 1 May 1991. All samples were analyzed for Na⁺, SO ₄ ^2– , NO ₃ ^– , methanesulfonate (MSA), NH ₄ ⁺ ,²¹⁰Pb, and⁷Be. At Mawson for which we have a multiple year data set, the annual mean concentration of each species sometimes vary significantly from one year to the next: Na⁺, 68–151 ng m^–3; NO ₃ ^– , 25–30 ng m^–3; nss SO ₄ ^2– , 81–97 ng m^–3; MSA, 19–28 ng m^–3; NH ₄ ⁺ , 16–21 ng m^–3;²¹⁰Pb, 0.75–0.86 fCi m^–3. Results from multiple variable regression of non-sea-salt (nss) SO ₄ ^2– with MSA and NO ₃ ^– as the independent variables indicates that, at Mawson, the nss SO ₄ ^2– /MSA ratio resulting from the oxidation of dimethylsulfide (DMS) is 2.80±0.13, about 13% lower than our earlier estimate (3.22) that was based on 2.5 years of data. A similar analysis indicates that the ratio at Palmer is about 40% lower, 1.71±0.10, and more comparable to previous results over the southern oceans. These results when combined with previously published data suggest that the differences in the ratio may reflect a more rapid loss of MSA relative to nss SO ₄ ^2– during transport over Antarctica from the oceanic source region. The mean²¹⁰Pb concentrations at Palmer and Marsh and the mean NO ₃ ^– concentration at Palmer are about a factor of two lower than those at Mawson. The²¹⁰Pb distributions are consistent with a²¹⁰Pb minimum in the marine boundary layer in the region of 40°–60° S. These features and the similar seasonalities of NO ₃ ^– and²¹⁰Pb at Mawson support the conclusion that the primary source regions for NO ₃ ^– are continental. In contrast, the mean concentrations of MSA, nss SO ₄ ^2– , and NH ₄ ⁺ at Palmer are all higher than those at Mawson: MSA by a factor of 2; nss SO ₄ ^2– by 10%; and NH ₄ ⁺ by more than 50%. However, the factor differences exhibit substantial seasonal variability; the largest differences generally occur during the austral summer when the concentrations of most of the species are highest. NH ₄ ⁺ /(nss SO ₄ ^2– +MSA) equivalent ratios indicate that NH₃ neutralizes about 60% of the sulfur acids during December at both Mawson and Palmer, but only about 30% at Mawson during February and March.     

低Peclet数下剪切流中气溶胶粒子的传质率

本文研究了低Péclet数下剪切流中气溶胶粒子的传质率。Péclet数(Pe)是物质浓度的对流输送项对分子扩散项的比。它等于Reynolds数(Re)与Schmidt数的(Sc)之积。本文应用奇异扰动方法得到了无因次传质率Nu(Nusselt数)在小Péclet数条件下的四项渐近展式，因而?改进了前人的结果。     

BALLOON-BORNE MEASUREMENTS OF AEROSOL VERTICAL DISTRIBUTIONS OVER BEIJING DURING THE SUMMER AND AUTUMN OF 1993

The results of two balloon soundings during the summer and autumn of 1993 from the Xianghe Observation Station are being utilized in a study of the temporal and spatial distribution of the atmospheric aerosols.The balloon,gondola,instrumentation and atmospheric conditions during the observation period are described.The temporal and spatial characteristics of aerosol concentration,size ratio,mixing ratio,and size distribution for both troposphere and strato-sphere are presented and analyzed.     

NOAA WP-3D instrumentation and flight operations on AGASP-II

The second Arctic Gas and Aerosol Sampling Program (AGASP-II) was conducted across the non-Soviet Arctic in March and April 1986, to study the aerosol, gaseous, chemical, and optical properties of Arctic haze. One component of the program was supported with an instrumented NOAA WP-3D atmospheric research aircraft. Measurements of wind, temperature, ozone, water vapor, condensation nucleus concentration, and aerosol scattering extinction coefficient were used to determine the locations and properties of haze layers. The first three NOAA WP-3D research flights were conducted north of Barrow, Alaska, and over the Beaufort Sea northeast of Barter Island, Alaska. The next three sampled conditions in the high Arctic near Alert, Northwest Territories, Canada. All basic meteorological, gas, and aerosol systems are described. The WP-3D flight tracks and operations are presented.