Direct and semi-direct radiative effects of anthropogenic aerosols in the Western United States: Seasonal and geographical variations according to regional climate characteristics

The direct and semi-direct radiative effects of anthropogenic aerosols on the radiative transfer and cloud fields in the Western United States (WUS) according to seasonal aerosol optical depth (AOD) and regional climate are examined using a regional climate model (RCM) in conjunction with the aerosol fields from a GEOS-Chem chemical-transport model (CTM) simulation. The two radiative effects cannot be separated within the experimental design in this study, thus the combined direct- and semi-direct effects are called radiative effects hereafter. The CTM shows that the AOD associated with the anthropogenic aerosols is chiefly due to sulfates with minor contributions from black carbon (BC) and that the AOD of the anthropogenic aerosol varies according to local emissions and the seasonal low-level winds. The RCM-simulated anthropogenic aerosol radiative effects vary according to the characteristics of regional climate, in addition to the AOD. The effects on the top of the atmosphere (TOA) outgoing shortwave radiation (OSRT) range from ?0.2?Wm^?2 to ?1?Wm^?2. In Northwestern US (NWUS), the maximum and minimum impact of anthropogenic aerosols on OSRT occurs in summer and winter, respectively, following the seasonal AOD. In Arizona-New Mexico (AZNM), the effect of anthropogenic sulfates on OSRT shows a bimodal distribution with winter/summer minima and spring/fall maxima, while the effect of anthropogenic BC shows a single peak in summer. The anthropogenic aerosols affect surface insolation range from ?0.6?Wm^?2 to ?2.4?Wm^?2, with similar variations found for the effects on OSRT except that the radiative effects of anthropogenic BC over AZNM show a bimodal distribution with spring/fall maxima and summer/winter minima. The radiative effects of anthropogenic sulfates on TOA outgoing longwave radiation (OLR) and the surface downward longwave radiation (DLRS) are notable only in summer and are characterized by strong geographical contrasts; the summer OLR in NWUS (AZNM) is reduced (enhanced) by 0.52?Wm^?2 (1.14?Wm^?2). The anthropogenic sulfates enhance (reduce) summer DLRS by 0.2?Wm^?2 (0.65?Wm^?2) in NWUS (AZNM). The anthropogenic BC affect DLRS noticeably only in AZNM during summer. The anthropogenic aerosols affect the cloud water path (CWP) and the radiative transfer noticeably only in summer when convective clouds are dominant. Primarily shortwave-reflecting anthropogenic sulfates decrease and increase CWP in AZNM and NWUS, respectively, however, the shortwave-absorbing anthropogenic BC reduces CWP in both regions. Due to strong feedback via convective clouds, the radiative effects of anthropogenic aerosols on the summer radiation field are more closely correlated with the changes in CWP than the AOD. The radiative effect of the total anthropogenic aerosols is dominated by the anthropogenic sulfates that contribute more than 80% of the total AOD associated with the anthropogenic aerosols.     

The climatological characteristics of photosynthetically active radiation in arid and semi-arid regions of China

Photosynthetically active radiation (Q _p ) is a key variable in models of net primary productivity and carbon cycle modelling. The relationship between broadband global solar radiation (R _s) and Q _p is investigated using 6?years of radiation data collected at 9 sites in arid and semi-arid regions of China. The dependence of Q _p /R _S on aerosol optical depth (AOD) and water vapour content are also discussed. A simple and efficient all-weather empirically derived model is developed to estimate Q _p from R _s. The annual average daily Q _p in arid and semi-arid areas is 29.9?±?11.7 and 27.3?±?10.1?mol?m^-2 d^-1, respectively. The highest value (31.9?±?11.3?mol?m^-2 d^-1) appears at Linze in the arid area. The lowest value (24.3?±?9.7?mol?m^-2 d^-1) appears at Ansai in the semi-arid area. The results show that the monthly variation of the Q _p /R _s ratio ranges from 1.69?±?0.19?mol?MJ^-1 in Aksu to 1.91?±?0.08?mol?MJ^-1 in Fukang. There is a small decreasing trend of the ratio of Q _p to R _s (PAR fraction) in arid and semi-arid regions because of the recent increase in fine aerosols. A simple and efficient empirically model suit for all-weather condition was developed to estimate Q _p from R _s. The slope a and intercept b of the regression line between estimated and measured values is close to 1 and zero, respectively. The application of the model to data collected from different locations also results in reasonable estimates of Q _p .     

Optical,Radiative and Chemical Characteristics of Aerosol in Changsha City,Central China

Industrial pollution has a significant effect on aerosol properties in Changsha City, a typical city of central China. Therefore, year-round measurements of aerosol optical, radiative and chemical properties from 2012 to 2014 at an urban site in Changsha were analyzed. During the observation period, the energy structure was continuously optimized, which was characterized by the reduction of coal combustion. The aerosol properties have obvious seasonal variations. The seasonal average aerosol optical depth (AOD) at 500 nm ranged from 0.49 to 1.00, single scattering albedo (SSA) ranged from 0.93 to 0.97, and aerosol radiative forcing at the top of the atmosphere (TOA) ranged from ?24.0 to 3.8 W m^?2. The chemical components also showed seasonal variations. Meanwhile, the scattering aerosol, such as organic carbon, SO₄^2?, NO₃^?, and NH₄⁺ showed a decrease, and elemental carbon increased. Compared with observation in winter 2012, AOD and TOA decreased by 0.14 and ?1.49 W m^?2 in winter 2014. The scattering components, SO₄^2?, NO₃^? and NH₄⁺, decreased by 12.8 μg m^?3 (56.8%), 9.2 μg m^?3 (48.8%) and 6.4 μg m^?3 (45.2%), respectively. The atmospheric visibility and pollution diffusion conditions improved. The extinction and radiative forcing of aerosol were significantly controlled by the scattering aerosol. The results indicate that Changsha is an industrial city with strong scattering aerosol. The energy structure optimization had a marked effect on controlling pollution, especially in winter (strong scattering aerosol).     

Below-cloud rain scavenging of atmospheric aerosols for aerosol deposition models

Below-cloud aerosol scavenging is generally estimated from field measurements using advanced instruments that measure changes in aerosol distributions with respect to rainfall. In this study, we discuss various scavenging mechanisms and scavenging coefficients from past laboratory and field measurements. Scavenging coefficients derived from field measurements (representing natural aerosols scavenging) are two orders higher than that of theoretical ones for smaller particles (D_p < 2 μm). Measured size-resolved scavenging coefficients can be served as a better option to the default scavenging coefficient (e.g. a constant of 10^?4 s^?1 for all size of aerosols, as used in the CALPUFF model) for representing below-cloud aerosol scavenging. We propose scavenging correction parameter (C_R) as an exponential function of size-resolved scavenging coefficients, winds and width in the downwind of the source–receptor system. For a wind speed of 3 m s^?1, C_R decrease with the width in the downwind for particles of diameters D_p < 0.1 μm but C_R does not vary much for particles in the accumulation mode (0.1 < D_p < 2 μm). For a typical urban aerosol distribution, assuming 3 m s^?1 air-flow in the source–receptor system, 10 km downwind width, 2.84 mm h^?1 of rainfall and using aerosol size dependent scavenging coefficients in the C_R, scavenging of aerosols is found to be 16% in number and 24% in volume of total aerosols. Using the default scavenging coefficient (10^?4 s^?1) in the CALPUFF model, it is found to be 64% in both number and volume of total aerosols.     

Vertical distributions of aerosol optical properties during haze and floating dust weather in Shanghai

A comparative study on the vertical distributions of aerosol optical properties during haze and floating dust weather in Shanghai was conducted based on the data obtained from a micro pulse lidar.There was a distinct difference in layer thickness and extinction coefficient under the two types of weather conditions.Aerosols were concentrated below 1 km and the aerosol extinction coefficients ranged from 0.25 to 1.50km^-1 on haze days.In contrast,aerosols with smaller extinction coefficients(0.20 0.35 km^-1) accumulated mainly from the surface to 2 km on floating dust days.The seasonal variations of extinction and aerosol optical depth（AOD） for both haze and floating dust cases were similar greatest in winter,smaller in spring,and smallest in autumn.More than 85%of the aerosols appeared in the atmosphere below 1 km during severe haze and floating dust weather.The diurnal variation of the extinction coefficient of haze exhibited a bimodal shape with two peaks in the morning or at noon,and at nightfall,respectively.The aerosol extinction coefficient gradually increased throughout the day during floating dust weather.Case studies showed that haze aerosols were generated from the surface and then lifted up,but floating dust aerosols were transported vertically from higher altitude to the surface.The AOD during floating dust weather was higher than that during haze.The boundary layer was more stable during haze than during floating dust weather.     

Direct Radiative Forcing of Anthropogenic Aerosols over Oceans from Satellite Observations

Anthropogenic aerosols play an important role in the atmospheric energy balance. Anthropogenic aerosol optical depth (AOD) and its accompanying shortwave radiative forcing (RF) are usually simulated by nu- merical models. Recently, with the development of space-borne instruments and sophisticated retrieval algorithms, it has become possible to estimate aerosol radiative forcing based on satellite observations. In this study, we have estimated shortwave direct radiative forcing due to anthropogenic aerosols over oceans in all-sky conditions by combining clouds and the Single Scanner Footprint data of the Clouds and Earth’s Radiant Energy System (CERES/SSF) experiment, which provide measurements of upward shortwave fluxes at the top of atmosphere, with Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol and cloud products. We found that globally averaged aerosol radiative forcing over oceans in the clear-sky conditions and all-sky conditions were -1.03±0.48 W m-2 and -0.34 ±0.16 W m-2, respectively. Direct radiative forcing by anthropogenic aerosols shows large regional and seasonal variations. In some regions and in particular seasons, the magnitude of direct forcing by anthropogenic aerosols can be comparable to the forcing of greenhouse gases. However, it shows that aerosols caused the cooling effect, rather than warming effect from global scale, which is different from greenhouse gases.     

Simulating Aerosol Optical Depth and Direct Radiative Effects over the Tibetan Plateau with a High-Resolution CAS FGOALS-f3 Model

Current global climate models cannot resolve the complex topography over the Tibetan Plateau (TP) due to their coarse resolution. This study investigates the impacts of horizontal resolution on simulating aerosol and its direct radiative effect (DRE) over the TP by applying two horizontal resolutions of about 100 km and 25 km to the Chinese Academy of Sciences Flexible Global Ocean-Atmosphere Land System (CAS FGOALS-f3) over a 10-year period. Compared to the AErosol RObotic NETwork observations, a high-resolution model (HRM) can better reproduce the spatial distribution and seasonal cycles of aerosol optical depth (AOD) compared to a low-resolution model (LRM). The HRM bias and RMSE of AOD decreased by 0.08 and 0.12, and the correlation coefficient increased by 0.22 compared to the LRM. An LRM is not sufficient to reproduce the aerosol variations associated with fine-scale topographic forcing, such as in the eastern marginal region of the TP. The difference between hydrophilic aerosols in an HRM and LRM is caused by the divergence of the simulated relative humidity (RH). More reasonable distributions and variations of RH are conducive to simulating hydrophilic aerosols. An increase of the 10-m wind speed in winter by an HRM leads to increased dust emissions. The simulated aerosol DREs at the top of the atmosphere (TOA) and at the surface by the HRM are –0.76 W m^–2 and –8.72 W m^–2 over the TP, respectively. Both resolution models can capture the key feature that dust TOA DRE transitions from positive in spring to negative in the other seasons.     

黄土高原半干旱区典型日吸收性气溶胶综合观测分析

利用兰州大学半干旱气候与环境观测站的太阳光度计、激光雷达、微波辐射计综合观测资料,结合辐射传输模式分析了该地区秋季典型日2012年9月3~4日、21日和28日气溶胶物理特性、垂直分布特征,及其与气象条件的关系。研究时期的气溶胶主要为局地沙尘与人为污染混合气溶胶,吸收性明显,尺度较小。其中,4日西北风增强,远距离传输沙尘气溶胶,气溶胶光学厚度最大,粒子尺度明显增大。尝试利用灰色关联度法确定参考高度,分别为7.41 km、8.47 km、7.13 km和7.66 km,反演气溶胶消光系数,由此积分得到的光学厚度与太阳光度计观测值相关性可达0.975,反演效果较好。研究时期气溶胶的抬升主要受白天热力湍流作用,边界层发展,气溶胶向上传输,每日12时（当地时间,下同）至14时传输至最大高度,气溶胶抬升的高度对应大气加热率的高值区,低层加热率可达1 K d-1。气溶胶在大气层顶和地面造成负辐射强迫,分别为-12.707 W m-2、-25.398 W m-2,大气中表现为正辐射强迫,为12.692 W m-2,大气层顶的辐射强迫对气溶胶的物理特性最为敏感,当气溶胶吸收性明显时,大气层顶的瞬时辐射强迫会出现正值。     

The assessment of aerosol optical properties over Mohal in the northwestern Indian Himalayas using satellite and ground-based measurements and an influence of aerosol transport on aerosol radiative forcing

The present study deals with the aerosol optical properties which are assessed during the period 2007 to 2009 over Mohal (31.9oN, 77.12oE) in the northwestern Indian Himalaya, using ground-based measurements and multi-satellite data. The daily average value of aerosol optical depth (AOD) at 500?nm, ?ngstr?m exponent and turbidity coefficient are 0.24?±?0.08, 1.02?±?0.34 and 0.13?±?0.05, respectively. The comparative study of satellite and ground-based measurements reveals that the percentage retrieval for daily AOD at 550?nm over Mohal within the expected accuracy (???? _p?? ?=?±0.05?±?0.15?? _p?? ) is around 87%, with a significant correlation coefficient of 0.76. The present study suggests that the retrieval of AOD through satellite data is able to characterise the distribution of AOD over Mohal. However, further efforts are needed in order to eliminate systematic errors in the existing Moderate Resolution Imaging Spectroradiometer (MODIS) algorithm. The transport of desert dust and anthropogenic aerosol during high aerosol loading days caused a significant reduction in surface-reaching solar radiation by 149 and 117%, respectively. This large reduction in surface-reaching solar radiation increased the atmospheric heating rate by 0.93 and 0.72?K?day^?1, respectively. This study indicates significant climatic implications due to the transport of aerosols in the northwestern Indian Himalaya.     

Analysis of photosynthetically active radiation and applied parameterization model for estimating of PAR in the North China Plain

As photosynthetically active radiation (PAR) variability and PAR estimating methods play an important role in climate change and ecological process research, PAR variation trends and broadband global solar radiation (R _s ) ratios (PAR/R _s ) in the North China Plain (NCP) are examined using in situ PAR and R _s observed data for 2005 to 2011. The annual average PAR value found in the NCP is 22.9 mol m^?2 d^?1. The highest and lowest values were recorded at Changwu and Luancheng sites, respectively. The highest PAR/R _s value was found in Jiaozhouwan due to large water vapor volumes present in this area. PAR/R _s levels have increased in the NCP due to a decrease in fine aerosols and increase in water vapor concentration. From these analysis results, a parameterization model that can be applied to all sky conditions was checked. Empirical estimation model comparisons for obtaining PAR values indicate that model was least accurate when R _s was used independently. When the model included R _s, the clearness index (K _s) and the solar zenith angle, the model estimated PAR values with acceptable accuracy. A parameterization model was constructed by considering K _s and attenuation factors of PAR under clear weather conditions (ρ _clear). The improved parameterization model more accurately predicts values for local sites and for various observation sites.     

The characteristics of ultraviolet radiation in arid and semi-arid regions of China

Measurements of the broadband global solar radiation (R _S) and total ultraviolet radiation (the sum of UV-A and UV-B) were conducted from 2005 to 2010 at 9 sites in arid and semi-arid regions of China. These data were used to determine the temporal variability of UV and UV/R _S and their dependence on the water vapor content and clearness index. The dependence of UV/R _S on aerosol optical depth (AOD) and water vapor content was also investigated. In addition, a simple and efficient empirically model suited for all-weather conditions was developed to estimate UV from R _s. The annual average daily UV level in arid and semi-arid areas is 0.61 and 0.59 MJ m^?2 d^?1, respectively. The highest value (0.66?±?0.25 MJ m^?2 d^?1) was recorded at an arid area at Linze. The lowest value (0.53?±?0.22 MJ m^?2 d^?1) was recorded at a semi-arid area at Ansai. The highest daily value of UV radiation was measured in May, whereas the lowest value was measured in December. The monthly variation of the UV/R _s ratio ranged from 0.41 in Aksu to 0.35 in Qira. The monthly mean value of UV/R _s gradually increased from November and then decreased in August. A small decreasing trend of UV/R _s was observed in the arid and semi-arid regions due to recently increasing amounts of fine aerosol. A simple and efficient empirically model suit for all-weather condition was developed to estimate UV from R _s. The slope a and intercept b of the regression line between the estimated and measured values were close to 1 and zero, respectively. The relative error between the estimated and measured values was less than 11.5%. Application of the model to data collected from different locations in this region also resulted in reasonable estimates of UV.     

Influence of atmospheric relative humidity on ultraviolet flux and aerosol direct radiative forcing: Observation and simulation

The atmospheric aerosols can absorb moisture from the environment due to their hydrophilicity and thus affect atmospheric radiation fluxes. In this article, the ultraviolet radiation and relative humidity (RH) data from ground observations and a radiative transfer model were used to examine the influence of RH on ultraviolet radiation flux and aerosol direct radiative forcing under the clear-sky conditions. The results show that RH has a significant influence on ultraviolet radiation because of aerosol hygroscopicity. The relationship between attenuation rate and RH can be fitted logarithmically and all of the R² of the 4 sets of samples are high, i.e. 0.87, 0.96, 0.9, and 0.9, respectively. When the RH is 60%, 70%, 80% and 90%, the mean aerosol direct radiative forcing in ultraviolet is ?4.22W m^?2, ?4.5W m^?2, ?4.82W m^?2 and ?5.4W m^?2, respectively. For the selected polluted air samples the growth factor for computing aerosol direct radiative forcing in the ultraviolet for the RH of 80% varies from 1.19 to 1.53, with an average of 1.31.     

近十年北京气溶胶光学特性及直接辐射强迫研究

利用SBDART（Santa Barbara DISORT Atmospheric Radiative Transfer）辐射传输模式,结合AERONET（Aerosol Robotic Network）北京站观测的气溶胶光学特性数据,评估北京地区近十年气溶胶以及黑碳气溶胶的辐射强迫,主要研究结果如下:北京近十年气溶胶平均光学厚度（aerosol optical depth, AOD_440nm）为0.61±0.56,?ngstr?m波长指数均值为1.09,单次散射反照率（single scattering albedo, SSA_440nm）的均值为0.888±0.045;AOD呈现下降趋势,SSA呈上升趋势,表明该区域气溶胶污染有所改善。晴空条件下,大气层顶、地面和大气的气溶胶直接辐射强迫多年均值分别为?24.91±19.80 W m?2、?65.52±43.78 W m?2、40.61±28.62 W m?2,即气溶胶对大气层顶和地表为冷却效应,对大气产生加热作用。气溶胶和黑碳气溶胶的直接辐射强迫绝对值的年际变化表现为微弱的下降趋势,季节变化特征为春夏季高,冬季低,这与AOD的变化规律一致。并且黑碳气溶胶的直接辐射强迫下降趋势与SSA的上升趋势呈现较好的反位相关系。     

Study of variation of aerosol optical properties over a high altitude station in Indian Western Himalayan region,palampur using raman lidar system

A Raman lidar system was operated along with the Microtops sunphotometer measurements to carry out the study of the variation of the optical properties of aerosols over Palampur (32.11° N and 76.53° E), India from 17th April to 11th May 2019. The lidar system is furnished with Raman (N₂) channel and depolarization channel allowing independent measurement of Lidar Ratio (LR) and linear depolarization ratio. The study reveals that the majority of the aerosols approximately were restricted within the planetary boundary layer (PBL) and very less loading was present in the free troposphere over the study location. The particle loading over the study period was found to be very less with aerosol backscatter coefficient (at 355 nm) ranging from ～0.13 Mm^?1sr^?1 to ～7.25 Mm^?1sr^?1 with mean value of 2.67?±?0.82 Mm^?1sr^?1 and it is well supplemented by the mean aerosol optical depth (AOD) of 0.37?±?0.13 obtained from Microtops Sunphotometer. The average lidar ratio values for 0-1 km altitude (L1) 72?±?13sr, for 1-2 km (L2) altitude 55?±?8sr, for 2-3 km (L3) 54?±?15sr were observed as suggesting dominance of the biomass burning aerosols and anthropogenic aerosols. The particle depolarization ratio (355 nm) values were found from approximately 4.8?±?2.7% to 11.5?±?1.9% with the mean value of 7?±?1.3% suggesting the presence of non-spherical particles. To trace the sources of the pollution, we derived the HYSPLIT trajectory which shows the majority of the movement was from local sources.

     

Aerosol characteristics during winter fog at Agra,North India

Simultaneous measurements on physical, chemical and optical properties of aerosols over a tropical semi-arid location, Agra in north India, were undertaken during December 2004. The average concentration of total suspended particulates (TSP) increased by about 1.4 times during intense foggy/hazy days. Concentrations of SO₄ ²⁻, NO₃ ⁻, NH₄ ⁺ and Black Carbon (BC) aerosols increased by 4, 2, 3.5 and 1.7 times, respectively during that period. Aerosols were acidic during intense foggy/hazy days but the fog water showed alkaline nature, mainly due to the neutralizing capacity of NH₄ aerosols. Trajectory analyses showed that air masses were predominantly from NW direction, which might be responsible for transport of BC from distant and surrounding local sources. Diurnal variation of BC on all days showed a morning and an evening peak that were related to domestic cooking and vehicular emissions, apart from boundary layer changes. OPAC (Optical properties of aerosols and clouds) model was used to compute the optical properties of aerosols. Both OPAC-derived and observed aerosol optical depth (AOD) values showed spectral variation with high loadings in the short wavelengths (<1 μm). AOD value at 0.5 μm wavelength was significantly high during intense foggy/hazy days (1.22) than during clear sky or less foggy/hazy days (0.63). OPAC-derived Single scattering albedo (SSA) was 0.84 during the observational period, indicating significant contribution of absorbing aerosols. However, the BC mass fraction to TSP increased by only 1% during intense foggy/hazy days and thereby did not show any impact on SSA during that period. A large increase was observed in the shortwave (SW) atmospheric (ATM) forcing during intense foggy/hazy days (+75.8 W/m²) than that during clear sky or less foggy/hazy days (+38 W/m²), mainly due to increase in absorbing aerosols. Whereas SW forcing at surface (SUF) increased from −40 W/m² during clear sky or less foggy/hazy days to −76 W/m² during intense foggy/hazy days, mainly due to the scattering aerosols like SO₄ ^2-.     

Biogenic hydrogen sulphide emissions and non-sea sulfate aerosols over the Indian Sundarban mangrove forest

Temporal variations in atmospheric hydrogen sulphide concentrations and its biosphere-atmosphere exchanges were studied in the World’s largest mangrove ecosystem, Sundarbans, India. The results were used to understand the possible contribution of H₂S fluxes in the formation of atmospheric aerosol of different size classes (e.g. accumulation, nucleation and coarse mode). The mixing ratio of hydrogen sulphide (H₂S) over the Sundarban mangrove atmosphere was found maximum during the post-monsoon season (October to January) with a mean value of 0.59?±?0.02 ppb and the minimum during pre-monsoon (February to May) with a mean value of 0.26?±?0.01 ppb. This forest acted as a perennial source of H₂S and the sediment-air emission flux ranged between 1213?±?276 μg S m^?2 d^?1(December) and 457?±?114 μg S m^?2 d^?1 (August) with an annual mean of 768?±?240 μg S m^?2d^?1. The total annual emissions of H₂S from the Indian Sundarban were estimated to be 1.2?±?0.6 Tg S. The accumulation mode of aerosols was found to be more enriched with non-sea salt sulfate with an average loading of 5.74 μg m^?3 followed by the coarse mode (5.18 μg m^?3) and nucleation mode (1.18 μg m^?3). However, the relative contribution of Non-sea salt sulfate aerosol to total sulfate aerosol was highest in the nucleation mode (83%) followed by the accumulation (73%) and coarse mode (58%). Significant positive relations between H₂S flux and different modes of NSS indicated the likely link between H₂S, a dominant precursor for the non-sea salt sulfate, and non-sea sulfate aerosol particles. An increase in H₂S emissions from the mangrove could result in an increase in enhanced NSS in aerosol and associated cloud albedo, and a decrease in the amount of incoming solar radiation reaching the Sundarban mangrove forest.     

Impact of absorbing aerosol deposition on snow albedo reduction over the southern Tibetan plateau based on satellite observations

We investigate the snow albedo variation in spring over the southern Tibetan Plateau induced by the deposition of light-absorbing aerosols using remote sensing data from moderate resolution imaging spectroradiometer (MODIS) aboard Terra satellite during 2001–2012. We have selected pixels with 100 % snow cover for the entire period in March and April to avoid albedo contamination by other types of land surfaces. A model simulation using GEOS-Chem shows that aerosol optical depth (AOD) is a good indicator for black carbon and dust deposition on snow over the southern Tibetan Plateau. The monthly means of satellite-retrieved land surface temperature (LST) and AOD over 100 % snow-covered pixels during the 12 years are used in multiple linear regression analysis to derive the empirical relationship between snow albedo and these variables. Along with the LST effect, AOD is shown to be an important factor contributing to snow albedo reduction. We illustrate through statistical analysis that a 1-K increase in LST and a 0.1 increase in AOD indicate decreases in snow albedo by 0.75 and 2.1 % in the southern Tibetan Plateau, corresponding to local shortwave radiative forcing of 1.5 and 4.2 W m⁻², respectively.

     

Decadal variation of surface solar radiation in the Tibetan Plateau from observations, reanalysis and model simulations

In this study, the annual and seasonal variations of all-sky and clear-sky surface solar radiation (SSR) in the eastern and central Tibetan Plateau (TP) during the period 1960–2009 are investigated, based on surface observational data, reanalyses and ensemble simulations with the global climate model ECHAM5-HAM. The mean annual all-sky SSR series shows a decreasing trend with a rate of ?1.00 Wm^?2 decade^?1, which is mainly seen in autumn and secondly in summer and winter. A stronger decrease of ?2.80 Wm^?2 decade^?1 is found in the mean annual clear-sky SSR series, especially during winter and autumn. Overall, these results confirm a tendency towards a decrease of SSR in the TP during the last five decades. The comparisons with reanalysis show that both NCEP/NCAR and ERA-40 reanalyses do not capture the decadal variations of the all-sky and clear-sky SSR. This is probably due to a missing consideration of aerosols in the reanalysis assimilation model. The SSR simulated with the ECHAM5-HAM global climate model under both all-sky and clear-sky conditions reproduce the decrease seen in the surface observations, especially after 1980. The steadily increasing aerosol optical depth (AOD) at 550 nm over the TP in the ECHAM5-HAM results suggests transient aerosol emissions as a plausible cause.     

Scattering and absorption coefficients of aerosols in a semi-arid area in China: Diurnal cycle, seasonal variability and dust events

The authors investigated variations of aerosol scattering and absorptive properties in a semi-arid climate Observatory in the Inner Mongolia of China and factors affecting the variation. They use integrated nephelometer and aethalometer observations collected in 2005 and 2006 at the Silinhot Observatory. The results are as follows. 1) in autumn and winter, the diurnal cycle of scattering coefficient exhibited a clear bi-modal variation, and the scattering coefficient was indicative of the type of sandy weather. 2) The concentration of black carbon (BC) aerosols was much higher in winter than in the other seasons with an evident bimodal diurnal variation. 3) When the wind speed was lower than 3.5 m s^?1, the dilution effect of air evidently influenced the scattering coefficient and BC mass concentration; for the wind speed above 3.5 m s^?1, there appeared to be little correlation between wind speed and scattering coefficient or BC mass concentration. 4) Atmospheric visibility calculated from the aerosol scattering and absorptive coefficients was in good agreement with the direct observation of visibility. 5) Absorption by aerosols accounted for 25% of the total extinction in December.     

Ionic and elemental composition of PM<Subscript>2.5</Subscript> aerosols over the Caribbean Sea in the Tropical Atlantic

To characterize atmospheric particulate matter equal or less than 2.5 μm in diameter (PM_2.5) over the Tropical Atlantic Ocean, aerosol sampling was carried out in Puerto Rico during August and September, 2006. Aerosols were analyzed by ion chromatography for water-soluble inorganic and organic ions (including Na⁺, NH₄ ⁺, Mg²⁺, Ca²⁺, K⁺, Cl^?, SO₄ ^2?, NH₄ ⁺, F^?, methanesulfonate (MSA), and oxalate), by inductive coupled plasma mass spectrometry (ICPMS) for trace elements (Al, Fe, Zn, Mn, Cu, Ni, V, Pb, Cr, Sb, Co, Sc, Cd), and by scanning electron microscopy for individual aerosol particle composition and morphology. The results show that the dominant cations in aerosols were Na⁺, (mean: 631 ng m^?3), accounting for 63.8 % of the total cation and NH₄ ⁺ (mean: 164 ng m^?3), accounting for 13.8 % of the total cation measured in this study. The main inorganic anions were Cl^? (576 ng m^?3, 54.1 %) and SO₄ ^2? (596 ng m^?3, 38.0 %). The main organic anion was oxalate (18 ng m^?3). Crustal enrichment factor calculations identified 62 % of the trace elements measured (Cu, Ni, V, Co, Al, Mn, Fe, Sc, and Cr) with crustal origin. Single particle analysis demonstrated that 40 % of the aerosol particles examined were Cl^? rich particles as sodium chloride from seawater and 34 % of the total particles were Si-rich particles, mainly in the form of aluminosilicates from dust material. Based on the combination of air-mass trajectories, cluster analysis and principal component analysis, the major sources of these PM_2.5 particles include marine, Saharan dust and biomass burning from West Africa; however, volcanic emissions from the Soufriere Hills in Montserrat had significant impact on aerosol composition in this region at the time of sample collection.