Interpretation of Mauna Loa atmospheric transmission relative to aerosols,using photometric precipitable water amouts

Precipitable water measurements made coincident in time and space with direct broadband solar irradiance measurements are used in conjunction with an atmospheric transmission model to derive a parameter whose major dependence is on total aerosol extinction. Irradiance measurements are used to calculate an atmospheric transmission factor (ATF) that is independent of the instrument calibration and the extraterrestrial solar constant. The dependency of the ATF on precipitable water is determined using LOWTRAN5, an atmospheric transmission model with high spectral resolution. Precipitable water measurements are then used to adjust the measured ATF to correspond to an ATF value obtained for a constant precipitable water amount. The remaining variability in the adjusted ATF is due mostly to aerosol extinction. The technique is applied to a 6-year period (1978–1983) for clear-sky mornings at Mauna Loa, Hawaii (MLO). MLO ATF aerosol residuals are compared with independently measured monochromatic aerosol optical depth. Results show that the ATF aerosol residual is nearly equal to the 500 nm aerosol optical depth prior to the eruption of E1 Chichon, at which time a nonlinear time-dependent relationship between the two quantities is evident. ATF aerosol residuals reflect the spectrally integrated aerosol influence on transmission and, therefore, could indicate better than monochromatic optical depth the radiation balance perturbations due to aerosols. The 6-year precipitable water record for MLO, determined from a dual-channel sunphotometer, has a mean value of 0.3 cm. An annual cycle in precipitable water is evident, as is a 4-month 5-standard-deviation drought from December 1982 through March 1983.     

Direct Climatic Effect of Dust Aerosol in the NCAR Community Atmosphere Model Version 3 （CAM3）

Direct climate responses to dust shortwave and longwave radiative forcing (RF) are studied using the NCAR Community Atmosphere Model Version 3 (CAM3). The simulated RF at the top of the atmosphere (TOA) is-0.45 W m-2 in the solar spectrum and +0.09 W m-2 in the thermal spectrum on a global average. The magnitude of surface RF is larger than the TOA forcing, with global mean shortwave forcing of-1.76 W m-2 and longwave forcing of +0.31 W m-2 . As a result, dust aerosol causes the absorption of 1.1 W m-2 in t...     

A Closure Study of Aerosol Hygroscopic Growth Factor during the 2006 Pearl River Delta Campaign

Measurements of aerosol physical, chemical and optical parameterswere carried out in Guangzhou, China from 1 July to 31 July 2006 during thePearl River Delta Campaign. The dry aerosol scattering coefficient was measuredusing an integrating nephelometer and the aerosol scattering coefficient forwet conditions was determined by subtracting the sum of the aerosol absorptioncoefficient, gas scattering coefficient and gas absorption coefficient from theatmospheric extinction coefficient. Following this, the aerosol hygroscopicgrowth factor, f(RH), was calculated as the ratio of wet and dry aerosolscattering coefficients. Measurements of size-resolved chemical composition,relative humidity (RH), and published functional relationships between particlechemical composition and water uptake were likewise used to find the aerosolscattering coefficients in wet and dry conditions using Mie theory forinternally- or externally-mixed particle species [(NH₄)₂SO₄, NH₄NO₃, NaCl, POM, EC and residue]. Closure was obtained by comparingthe measured f(RH) values from the nephelometer and other in situ opticalinstruments with those computed from chemical composition and thermodynamics.Results show that the model can represent the observed f(RH) and isappropriate for use as a component in other higher-order models.     

The Henry's Law Constants of the Haloacetic Acids

Henry's law constants K_H (mol kg^-1 atm^-1) have been measured between 278.15 K and 308.15 K for the following organic acids: CH₂FCOOH (ln(K_H[298.15 K]) = 11.3 ± 0.2), CH₂ClCOOH (11.59 ± 0.14), CH₂BrCOOH (11.94 ± 0.21), CHF₂COOH (10.32 ± 0.10), CHCl₂COOH (11.69 ± 0.11), CHBr₂COOH (12.33 ± 0.29), CBr₃COOH (12.61 ± 0.21), and CClF₂COOH (10.11 ± 0.12). The variation of K_H with temperature was determined for all acids except CH₂FCOOH and CBr₃COOH, with _r H° for the dissolution reaction ranging from –85.2 ± 2.6 to –57.1 ± 2.5 kJ mol^-1, meaning that their solubility is generally more sensitive to temperature than is the case for the simple carboxylic acids. The Henry's law constants show consistent trends with halogen substitution and, together with their high solubility compared to the parent (acetic) acid (ln(K_H[298.15 K]) = 8.61), present a severe test of current predictive models based upon molecular structure. The solubility of haloacetic acids and strong dissociation at normal pH mean that they will partition almost entirely into cloud and fog in the atmosphere (0.05–1.0 g H₂O m^-3), but can reside in both phases for the liquid water contents typical of aerosols (10^-5-10^-4 g H₂O m^-3).     

RegCM3引入气溶胶间接气候效应模拟效果对比

利用2006年区域气候模式RegCM3和Streets气溶胶排放源清单,在原模式中引入间接气候效应模块,改进云降水方案,对硫酸盐气溶胶的时空分布、辐射强迫效应进行了模拟研究。结果表明：硫酸盐气溶胶辐射强迫有明显季节变化;直接效应使地表温度降低,冬春季大值区出现在四川盆地,夏季大值区出现在华北平原。对降水的影响,主要表现在西南—东北水汽输送带上降水减少;其间接气候效应主要表现在使南方地区温度上升、北方地区温度下降;珠江流域和黄河流域降水减少,长江流域和东北地区降水增加。总的来说,直接效应大于间接效应。     

A numerical investigation of the destruction of peroxy radical by Cu ion catalysed reactions on atmospheric particles

To determine if Cu mediated reactions on atmospheric particles are important to HO₂ chemistry in the ambient atmosphere, Cu molalities were calculated from measured Cu aerosol particle concentrations, mass and number size distribution data from a site in central Sweden. A comparison of characteristic times indicates that at low relative humidities the reaction is limited by the mass transport of gas phase HO₂ to the particle surface and not by the chemical kinetics of the aqueous reaction. Comparison of half-lives for particle reactions and the gas phase destruction of HO₂ to form H₂O₂ indicate that heterogeneous reactions on aerosol particles may have important consequences on the chemistry of HO₂ and H₂O₂ in the troposphere.     

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...     

沙尘暴过程中沙尘对流层-平流层输送的数值模拟初步分析

在初步明确东亚沙尘气溶胶对流层-平流层输送监测事实的基础上,利用观测资料、NCEP再分析资料以及基于中尺度天气模式MM5的数值模拟方法,对一次蒙古气旋沙尘暴过程中沙尘对流层-平流层输送问题进行了初步分析.结果表明:斜压不稳定是本次蒙古气旋发展的主要强迫要素,伴随气旋发展成熟,高空切断低涡的形成引导高空急流下落并诱发对流层顶折叠和高空位涡下传.对流层顶折叠区呈漏斗状,底部达500 hPa左右.高空急流产生近似垂直的下落,并在高空切断低涡的南侧和东侧达到最强.在对流层顶折叠区周边的300-500 hPa,上升气流与低涡区偏西、偏南、偏东气流叠加,或水平横穿折叠的对流层顶,或斜升并准垂直地穿过下落的对流层顶到达平流层,且随时间的推移,空气质点能够进一步抵达平流层中部(100 hPa).轨迹分析表明,沙尘天气区对流层低层的空气质点在气旋涡旋上升气流的驱动下呈气旋式盘旋上升,并在对流层高层形成分支,一支穿过对流层顶到达平流层,并在平流层向下游进行反气旋式螺旋运动,另一支则留在对流层高层并向下游进行准水平的气旋式螺旋运动.在高空位涡下传过程中,主要产生平流层到对流层的净输送;高空位涡停止下传之后则出现对流层到平流层的净输送,且强度随时间呈指数型增长.这一特征有利于形成更强的沙尘对流层平流层输送.     

天津城区春节期间大气气溶胶污染特征 和数浓度分布

利用天津城区2009-2014年春节期间大气气溶胶观测资料和相关气象资料,重点分析2013和2014年春节期间气溶胶污染特征,探求燃放烟花爆竹以及气象条件对春节期间大气气溶胶的影响。结果表明,受燃放烟花爆竹影响,春节期间PM_(2.5)质量浓度最高值均发生在除夕夜间;持续雾霾天气条件下燃放烟花爆竹,造成2013年除夕夜间PM_(2.5)质量浓度峰值达到1240μg·m～(-3),是近年来最严重的一次;2014年春节期间烟花爆竹燃放量有所减少,加之空气扩散条件较为有利,PM_(2.5)质量浓度显著低于2013年;不同天气条件下,气溶胶数浓度谱分布特征存在明显差异,燃放烟花爆竹期间气溶胶数浓度水平与严重雾-霾天气相当。     

香河地区亚微米气溶胶粒子尺度谱分布特征

为了解香河地区气溶胶尺度谱的基本特征,自2012年5月起,利用扫描电迁移率粒径谱仪(SMPS)对河北香河地区的亚微米(13.8~723.4 nm)气溶胶尺度谱分布进行了近2 a的测量。基于该数据集,分析了气溶胶尺度谱的季节变化和日变化特征及气象要素对气溶胶浓度的影响。结果发现,观测期间埃根核模态(20.0~100.0 nm)、积聚模态(100.0~723.4 nm),以及总的气溶胶数浓度、表面积浓度和体积浓度均值分别为7.0×103cm~(-3)、7.5×103cm~(-3)、14.9×103cm~(-3)、1125μm2·cm~(-3)和50μm~3·cm~(-3)。香河地区积聚模态的粒子数浓度接近华北地区其他污染测站的结果,但高于发达国家的测值。冬季气溶胶的平均浓度最高(18.1×10~3cm~(-3)),而春季最低(12.3×10~3cm~(-3))。不同季节,气溶胶的数谱分布主要为单峰分布,平均峰值直径约为105 nm。气溶胶浓度的日变化受机动车排放的影响显著,存在早晚两个高值中心,分别出现在早上的06:00—09:00和晚上的19:00—21:00。风速、风向对气溶胶数浓度的影响较大,低风速(2 m/s)和南风条件,尤其是吹西南风时,气溶胶浓度的增加显著。