Cloud condensation nuclei (CCN) concentration in the Brazilian northeast semi-arid region: the influence of local circulation

Ground-based aerosol instrumentation covering particle size diameters from 25 nm to 32 µm was deployed to determine aerosol concentration and cloud condensation nuclei (CCN)-activation properties at water vapor supersaturations in the range of S = 0.20–1.50 % in the remote Brazilian northeast semi-arid region (NEB) in coastal (maritime) and continental (inland) regimes. The instruments measured aerosol number concentration and activation spectra for CCN and revealed that aerosol properties are sensitive with respect to the sources as a function of the local wind circulation system. The observations show that coastal aerosol total number concentrations are above 3,000 cm^?3 on average, exhibiting concentration peaks depending on the time of the day in a consistent daily pattern. The variation on aerosol concentration has also influences on the fraction of particles active as CCN. At 1.0 % water vapor supersaturation, the fraction can reach as high as 80 %. Inland aerosol total concentrations were about 1,800–1,900 cm^?3 and did not show much diurnal variation. The fraction of particles active as CCN observed inland depend on the history of the air masses, and was much higher when air masses were originated over the sea. It was found that (NH₄)₂SO₄ and NaCl are the major soluble inorganic fraction of the aerosols at the coast. The major fraction of NaCl was present in the coarse mode, while ammonium sulfate dominates the inorganic fraction at the submicron range, with about 10 % of the total aerosol mass at 0.32 µm. Inorganic compounds are almost absent in particles with sizes around 0.1 μm. The study suggests that the air masses with high concentration of CCN originate at the sea. The feasible explanation lies in the fact that the NEB’s beaches have a particular morphology that produces a wide surf zone and creates a large load of aerosols when combined with strong and permanent winds of the region.     

Spectral investigation of the diffuse-to-direct solar beam irradiances ratio (UV–VIS) in the urban Athens atmosphere

This study explores the influence of air gaseous pollutants–aerosols and solar zenith angle (SZA) on the spectral diffuse-to-direct beam E _dλ/E _bλ irradiances ratio. It does so using ground-based spectroradiometric measurements taken over the Athens atmosphere during May 1995. It was found that the spectral E _dλ/E _bλ ratio decreases rapidly with increasing wavelength and regression curves of the form E _dλ/E _bλ = aλ^?b fitted the experimental data. These curves are strongly modified by aerosols–air pollutants, aerosol optical properties, and SZA. The log–log plot of E _dλ/E _bλ versus λ reveals a significant departure from linearity, which is likely to be associated with aerosol physical properties and SZA effects. The effect of atmospheric turbidity, as expressed through the aerosol optical at 500 nm and SZA on the spectral E _dλ/E _bλ ratio, is investigated in detail for two discernible atmospheric conditions observed in the urban Athens atmosphere. The first case includes different atmospheric turbidity levels under the same SZA, while the second corresponds to different SZA values under the same turbidity levels. It was found that the correlation between E _dλ/E _bλ and spectral aerosol optical depth can be a useful tool in determining the aerosol optical properties and aerosol types composition.     

HAZE-TO-FOG TRANSFORMATION DURING A LONG LASTING, LOW VISIBILITY EPISODE IN NANJING

Haze-to-fog transformation during a long lasting, low visibility episode was examined using the observations from a comprehensive field campaign conducted in Nanjing, China during 4-9 December 2013. In this episode, haze was transformed into fog and the fog lasted for dozens of hours. The impacts of meteorological factors such as wind, temperature (T) and relative humidity (RH) on haze, transition and fog during this episode were investigated. Results revealed significant differences between haze and fog days, due to their different formation mechanisms. Comparison was made for boundary-layer conditions during hazy days, haze-to-fog days and foggy days. Distributions of wind speed and wind direction as well as synoptic weather conditions around Nanjing had determinative impacts on the occurrences and characteristics of haze and fog. Weakened southerly wind in southern Nanjing resulted in high concentration of pollutants, and haze events occurred frequently during the study period. The wind speed was less than 1 m s-1 in the haze event, which resulted in a stable atmospheric condition and weak dispersion of the pollutants. The height of the temperature inversion was about 400 m during the period. The inversion intensity was weak and the temperature-difference was 4°C km-1 or less in haze, while the inversion was stronger, and temperature-difference was about 6°C km-1, approaching the inversion layer intensity in the fog event. Haze event is strongly influenced by ambient RH. RH values increased, which resulted in haze days evidently increased, suggesting that an increasing fraction of haze events be caused by hygroscopic growth of aerosols, rather than simply by high aerosol loading. When RH was above 90%, haze aerosols started to be transformed from haze to fog. This study calls for more efforts to control emissions to prevent haze events in the region.     

The impact of natural versus anthropogenic aerosols on atmospheric circulation in the Community Atmosphere Model

The equilibrium response of atmospheric circulation to the direct radiative effects of natural or anthropogenic aerosols is investigated using the Community Atmosphere Model (CAM3) coupled to two different ocean boundary conditions: prescribed climatological sea surface temperatures (SSTs) and a slab ocean model. Anthropogenic and natural aerosols significantly affect the circulation but in nearly opposite ways, because anthropogenic aerosols tend to have a net local warming effect and natural aerosols a net cooling. Aerosol forcings shift the Intertropical Convergence Zone and alter the strength of the Hadley circulation as found in previous studies, but also affect the Hadley cell width. These effects are due to meridional gradients in warming caused by heterogeneous net heating, and are stronger with interactive SST. Aerosols also drive model responses at high latitudes, including polar near-surface warming by anthropogenic aerosols in summer and an Arctic Oscillation (AO)-type responses in winter: anthropogenic aerosols strengthen wintertime zonal wind near 60°N, weaken it near 30°N, warm the troposphere, cool the stratosphere, and reduce Arctic surface pressure, while natural aerosols produce nearly opposite changes. These responses are shown to be due to modulation of stratospheric wave-driving consistent with meridional forcing gradients in midlatitudes. They are more pronounced when SST is fixed, apparently because the contrast in land-ocean heating drives a predominantly wavenumber-2 response in the northern hemisphere which is more efficient in reaching the stratosphere, showing that zonal heating variations also affect this particular response. The results suggest that recent shifts from reflecting to absorbing aerosol types probably contributed to the observed decadal variations in tropical width and AO, although studies with more realistic temporal variations in forcing would be needed to quantify this contribution.     

基于能见度数据分析的气溶胶吸湿增长特征研究

基于相对湿度、能见度等气象数据,分析气溶胶吸湿增长特性,有助于了解气溶胶对大气环境和区域气候的影响。利用南京地区2016年1—12月、2017年2—12月、2018年1—8月和12月相对湿度和能见度等数据,通过非线性拟合研究气溶胶吸湿增长因子(f(RH))与相对湿度(RH)之间的关系。结果表明,吸湿增长因子在RH值较低(<80%)时,增长率较小;当RH值较高(>80%)时,增长率迅速增大。吸湿增长因子随着月RH值变化而表现出较大差异。此外,当南京地区盛行西风时,高能见度出现的时次较多。f(RH)与PM_2.5/PM₁₀成正比,PM_2.5/PM₁₀值越高,对应的气溶胶光学吸湿增长因子往往会越高。     

不同污染条件下气溶胶对短波辐射通量影响的模拟研究

将高光谱分辨率的气溶胶光学参数化方案应用于高精度的辐射传输模式BCC_RAD（974带）中,研究不同污染状况下气溶胶在地表与近地层大气中造成的直接辐射强迫与辐射强迫效率。发现气溶胶在地表产生的直接辐射强迫为负,在近地层大气中产生的直接辐射强迫为正,且随气溶胶浓度的升高变大,说明大气气溶胶的含量越高,单位气溶胶光学厚度产生的直接辐射强迫越大。将短波划分为3个波段:紫外、可见光和近红外,发现在紫外、可见光和近红外波段中,不同污染状况下气溶胶在地表造成的直接辐射强迫范围分别为:-1.36—-13.66、-3.03—-32.41和-2.74—-28.62 W/m2,在近地层大气中产生的直接辐射强迫范围分别为0.44—4.26、0.99—9.80和0.93—8.87 W/m2。通过进一步对比自然和人为气溶胶的影响,发现人为气溶胶在地表和大气层顶产生的负直接辐射强迫以及对整层和近地面大气造成的正直接辐射强迫均大于自然气溶胶的影响,且上述两种排放源的气溶胶对整层大气辐射收支的影响主要集中在800 hPa高度以下的大气中。按照地表直接辐射强迫大小来分析不同种类气溶胶的影响,结果为硫酸盐>有机碳>黑碳>海盐>沙尘;按照近地层大气直接辐射强迫大小排序则为黑碳>有机碳>沙尘>海盐>硫酸盐。最后,通过分析散射型气溶胶与吸收型气溶胶对辐射通量的影响,还探究了大气中散射与吸收过程的异同。      

Radiative effect of black carbon aerosol on seasonal variation in snow depth in the Northern-Hemisphere

In this research, we studied the effects of black carbon (BC) aerosol radiative forcing on seasonal variation in the Northern Hemisphere (NH) using numerical simulations with the NASA finite-volume General Circulation Model (fvGCM) forced with monthly varying three-dimensional aerosol distributions from the Goddard Ozone Chemistry Aerosol Radiation and Transport Model (GOCART). The results show that atmospheric warming due to black carbon aerosols subsequently warm the atmosphere and land surfaces, especially those over Eurasia. As a result, the snow depth in Eurasia was greatly reduced in late winter and spring, and the reduction in snow cover decreased the surface albedo. Our surface energy balance analysis shows that the surface warming due to aerosol absorption causes early snow melting and further increases surface-atmosphere warming through snow/ice albedo feedback. Therefore, BC aerosol forcing may be an important factor affecting the snow/ice albedo in the NH.     

A GCM study of future climate response to aerosol pollution reductions

We use the global atmospheric GCM aerosol model ECHAM5-HAM to asses possible impacts of future air pollution mitigation strategies on climate. Air quality control strategies focus on the reduction of aerosol emissions. Here we investigate the extreme case of a maximum feasible end-of-pipe abatement of aerosols in the near term future (2030) in combination with increasing greenhouse gas (GHG) concentrations. The temperature response of increasing GHG concentrations and reduced aerosol emissions leads to a global annual mean equilibrium temperature response of 2.18 K. When aerosols are maximally abated only in the Industry and Powerplant sector, while other sectors stay with currently enforced regulations, the temperature response is 1.89 K. A maximum feasible abatement applied in the Domestic and Transport sector, while other sectors remain with the current legislation, leads to a temperature response of 1.39 K. Increasing GHG concentrations alone lead to a temperature response of 1.20 K. We also simulate 2–5% increases in global mean precipitation among all scenarios considered, and the hydrological sensitivity is found to be significantly higher for aerosols than for GHGs. Our study, thus highlights the huge potential impact of future air pollution mitigation strategies on climate and supports the need for urgent GHG emission reductions. GHG and aerosol forcings are not independent as both affect and are influenced by changes in the hydrological cycle. However, within the given range of changes in aerosol emissions and GHG concentrations considered in this study, the climate response towards increasing GHG concentrations and decreasing aerosols emissions is additive.     

Estimation of the Aerosol Radiative Effect over the Tibetan Plateau Based on the Latest CALIPSO Product

Based on the CALIPSO (Cloud–Aerosol Lidar and Infrared Pathfinder Satellite Observation) Version 4.10 products released on 8 November 2016, the Level 2 (L2) aerosol product over the Tibetan Plateau (TP) is evaluated and the aerosol radiative effect is also estimated in this study. As there are still some missing aerosol data points in the daytime CALIPSO Version 4.10 L2 product, this study re-calculated the aerosol extinction coefficient to explore the aerosol radiative effect over the TP based on the CALIPSO Level 1 (L1) and CloudSat 2B-CLDCLASS-LIDAR products. The energy budget estimation obtained by using the AODs (aerosol optical depths) from calculated aerosol extinction coefficient as an input to a radiative transfer model shows better agreement with the Earth’s Radiant Energy System (CERES) and CloudSat 2B-FLXHR-LIDAR observations than that with the input of AODs from aerosol extinction coefficient from CALIPSO Version 4.10 L2 product. The radiative effect and heating rate of aerosols over the TP are further simulated by using the calculated aerosol extinction coefficient. The dust aerosols may heat the atmosphere by retaining the energy in the layer. The instantaneous heating rate can be as high as 5.5 K day^–1 depending on the density of the dust layers. Overall, the dust aerosols significantly affect the radiative energy budget and thermodynamic structure of the air over the TP, mainly by altering the shortwave radiation budget. The significant influence of dust aerosols over the TP on the radiation budget may have important implications for investigating the atmospheric circulation and future regional and global climate.     

Aerosol, clouds and rainfall: inter-annual and regional variations over India

Inter-annual and regional variations in aerosol and cloud characteristics, water vapor and rainfall over six homogeneous rainfall zones in India during the core monsoon month of July from 2000 to 2010, and their correlations are analyzed. Aerosol optical depth (AOD) and aerosol absorbing index (AAI) in July 2002, a drought year are higher over India when compared to normal monsoon years. The drier conditions that existed due to deficient rainfall in July 2002 could be responsible for raising more dust and smoke resulting in higher AODs over India. In addition, over India precipitation is not uniform and large-scale interruptions occur during the monsoon season. During these interruptions aerosols can build up over a region and contribute to an increase in AODs. This finding is supported by the occurrence of higher anomalies in AOD, AAI and rainfall over India in July 2002. Aerosol characteristics and rainfall exhibit large regional variations. Cloud effective radius (CER), cloud optical thickness and columnar water vapor over India are the lowest in July 2002. CER decreases as AOD and AAI increase, providing an observational evidence for the indirect effect of aerosols. Eighty percent of CER in northwest India, and 30% of CER over All India in July 2002 are <14 μm, the precipitation threshold critical cloud effective radius. Northeast India shows contrasting features of correlation among aerosols, clouds and rainfall when compared to other regions. These results will be important while examining the inter-annual variation in aerosols, cloud characteristics, rainfall and their trends.     

Spatio-temporal variations of optical properties of aerosols in East Asia measured by MODIS and relation to the ground-based mass concentrations observed in central Korea during 2001∼2010

Long-term variations and trends of atmospheric aerosols in the East Asian region were analyzed by using aerosol optical depth (AOD or τ), and ångström exponent (AE or α) obtained from the Moderate Resolution Imaging Spectroradiometer (MODIS) from 2001 to 2010. The increased emission of anthropogenic fine aerosols in east China resulted in the high AOD in this region during summer. The steady increasing emission of anthropogenic fine aerosols caused an increasing trend of AOD in east China, and the large-scale transport of sandstorms and smoke plume caused by forest fires affected intense inter-annual variations of AOD in the East Asian region. While in the central part of South Korea, located in the lee side of the East Asian continent, AE tended to rise to a level higher than in east China, the ground-based mass concentrations continued to decline. A noticeable decrease of PM10 mass concentration in spring and winter in central Korea is most likely attributable to decreases in sandstorms in the source region of East Asia. However, the ratio of PM2.5 mass concentration to PM10 increases overall with a high level in summer. Aerosol types were classified into dust, smoke plume, and sulphate by using satellite data over Cheongwon in central Korea. The columnar AOD, with different aerosol types, was compared with the ground-based mass concentrations at Cheongwon, and the relatively high level of the correlations presented between PM2.5 and AOD produced in sulphate. Growth and increases of fine hygroscopic aerosols generated as gas-to-particle conversion particularly in summer contribute to increases of columnar AOD in the East Asian region.     

大气气溶胶的卫星遥感及其在气候和环境研究中的应用

卫星遥感可以获得全球范围的大气气溶胶光学特性,目前国内外已有多颗卫星观测能够提供气溶胶特性的资料。本文综述性介绍国内外卫星遥感气溶胶特性方面的研究进展和成果,并讨论了卫星遥感资料在气候和环境研究领域中的应用。主要内容包括:极轨/静止卫星平台搭载的被动遥感传感器及其反演气溶胶特性的方法;星载激光雷达获取气溶胶光学特性的方法;国内外正在研发的新一代卫星主、被动气溶胶遥感探测器;卫星气溶胶产品在气溶胶辐射强迫、气候效应、大尺度污染输送、区域空气质量监测等研究中的应用。     

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.     

The spatial–temporal variations in optical properties of atmosphere aerosols derived from AERONET dataset over China

The spatial–temporal properties of aerosol types over China are studied using the radiance measurements and inversions data at four Aerosol Robotic Network (AERONET) stations in China. Based on a cluster analysis, five aerosol classes were identified including a coarse-sized dominated aerosol type (presumably dust) and four fine-sized dominated aerosol types ranging from non-absorbing to highly absorbing fine aerosols. The optical properties and seasonal variations of these aerosol types are investigated. The results of analysis show that: (1) the highly absorbing aerosols usually occur in winter, (2) non-absorbing aerosols are frequently observed in summer; (3) coarse-sized dominated aerosols are frequently occurred in spring.     

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.     

A multifunctional HTDMA system with a robust temperature control

The hygroscopicity of atmospheric aerosols significantly influences their size distribution, cloud condensation nuclei ability, atmospheric residence time, and climate forcing. In order to investigate the hygroscopic behavior of aerosol particles and serious haze in China, a Hygroscopic Tandem Differential Mobility Analyzers (HTDMA) system was designed and constructed at Fudan University. It can function as a scanning mobility particle sizing system to measure particle size distribution in the range of 20--1000 nm in diameter, as well as a hygroscopicity analyzer for aerosol particles with diameters between 20--400 nm in the range of 20%--90% RH (relative humidity). It can also measure the effect of uptake of inorganic acids or semi-VOCs on the hygroscopic behavior of aerosols, such as typical inorganic salts in atmospheric dust or their mixtures. The performance tests show that the system measured particle size of the standard polystyrene latex spheres (PSLs) is 197 nm, which is in excellent agreement with the certified diameter D=199±6 nm, as well as a standard deviation of the repeated runs SD=8.9x10^-4. In addition, the measured hygroscopic growth factors of the model compounds, (NH₄)₂SO₄ and NaNO₃, agree with the Kohler theoretical curves. The results indicate that the HTDMA system is an excellent and powerful tool for studying the hygroscopic behavior of submicron aerosols and meets the demand required for laboratory research and fieldwork on atmospheric aerosols in China.     

Aerosol Optical Properties and Radiative Impacts in the Pearl River Delta Region of China during the Dry Season

Aerosol optical properties and direct radiative effects on surface irradiance were examined using seven years(2006–2012)of Cimel sunphotometer data collected at Panyu—the main atmospheric composition monitoring station in the Pearl River Delta(PRD) region of China. During the dry season(October to February), mean values of the aerosol optical depth(AOD)at 550 nm, the ?ngstr?m exponent, and the single scattering albedo at 440 nm(SSA) were 0.54, 1.33 and 0.87, respectively.About 90% of aerosols were dominated by fine-mode strongly absorbing particles. The size distribution was bimodal, with fine-mode particles dominating. The fine mode showed a peak at a radius of 0.12 μm in February and October(~0.10μm~3μm~(-2)). The mean diurnal shortwave direct radiative forcing at the surface, inside the atmosphere(FATM), and at the top of the atmosphere, was-33.4 ± 7.0, 26.1 ± 5.6 and-7.3 ± 2.7 W m~(-2), respectively. The corresponding mean values of aerosol direct shortwave radiative forcing per AOD were-60.0 ± 7.8, 47.3 ± 8.3 and-12.8 ± 3.1 W m~(-2), respectively. Moreover,during the study period, FATMshowed a significant decreasing trend(p 0.01) and SSA increased from 0.87 in 2006 to 0.91 in 2012, suggesting a decreasing trend of absorbing particles being released into the atmosphere. Optical properties and radiative impacts of the absorbing particles can be used to improve the accuracy of inversion algorithms for satellite-based aerosol retrievals in the PRD region and to better constrain the climate effect of aerosols in climate models.     

Model analysis of influences of aerosol mixing state upon its optical properties in East Asia

The air quality model system RAMS (Regional Atmospheric Modeling System)-CMAQ (Models-3 Community Multi-scale Air Quality) coupled with an aerosol optical/radiative module was applied to investigate the impact of different aerosol mixing states (i.e., externally mixed, half externally and half internally mixed, and internally mixed) on radiative forcing in East Asia. The simulation results show that the aerosol optical depth (AOD) generally increased when the aerosol mixing state changed from externally mixed to internally mixed, while the single scattering albedo (SSA) decreased. Therefore, the scattering and absorption properties of aerosols can be significantly affected by the change of aerosol mixing states. Comparison of simulated and observed SSAs at five AERONET (Aerosol Robotic Network) sites suggests that SSA could be better estimated by considering aerosol particles to be internally mixed. Model analysis indicates that the impact of aerosol mixing state upon aerosol direct radiative forcing (DRF) is complex. Generally, the cooling effect of aerosols over East Asia are enhanced in the northern part of East Asia (Northern China, Korean peninsula, and the surrounding area of Japan) and are reduced in the southern part of East Asia (Sichuan Basin and Southeast China) by internal mixing process, and the variation range can reach 5 W m－2. The analysis shows that the internal mixing between inorganic salt and dust is likely the main reason that the cooling effect strengthens. Conversely, the internal mixture of anthropogenic aerosols, including sulfate, nitrate, ammonium, black carbon, and organic carbon, could obviously weaken the cooling effect.     

Influence of the Surf Zone on the Marine Aerosol Concentration in a Coastal Area

Sea-salt aerosol concentrations in the coastal zone are assessed with the numerical aerosol-transport model MACMod that applies separate aerosol source functions for open ocean and the surf zone near the sea–land transition. Numerical simulations of the aerosol concentration as a function of offshore distance from the surf zone compare favourably with experimental data obtained during a surf-zone aerosol experiment in Duck, North Carolina in autumn 2007. Based on numerical simulations, the effect of variations in aerosol production (source strength) and transport conditions (wind speed, air–sea temperature difference), we show that the surf-zone aerosols are replaced by aerosols generated over the open ocean as the airmass advects out to sea. The contribution from the surf-generated aerosol is significant during high wind speeds and high wave events, and is significant up to 30 km away from the production zone. At low wind speeds, the oceanic component dominates, except within 1–5 km of the surf zone. Similar results are obtained for onshore flow, where no further sea-salt aerosol production occurs as the airmass advects out over land. The oceanic aerosols that are well-mixed throughout the boundary layer are then more efficiently transported inland than are the surf-generated aerosols, which are confined to the first few tens of metres above the surface, and are therefore also more susceptible to the type of surface (trees or grass) that determines the deposition velocity.     

Evaluation of an automated EA-IRMS method for total carbon analysis of atmospheric aerosol at HEKAL

Comprehensive atmospheric studies have demonstrated that carbonaceous particles are one of the main components of atmospheric aerosols over Europe. The aim of our study was to establish an automated elemental analyser interfaced to a stable isotope mass spectrometer (EA-IRMS) method at the Hertelendi Laboratory of Environmental Studies (HEKAL), as a suitable method of quantification of total carbon mass in individual PM_2.5 aerosol samples. Total carbon (TC) mass and simultaneous stable isotopic ratios were determined for both test standard and genuine aerosol samples. Finally, the results were compared to the ones obtained independently by an alternative sealed tube combustion method developed previously at HEKAL. The TC recovery tests of standard material prepared by the sealed tube method confirmed at least a carbon recovery yield of 92% for a broad range of carbon mass (100–2000 μg). The stable isotopic results confirmed that sealed tube method is reproducible and suitable to be used as a reference to verify our new EA-IRMS method. The EA-IRMS TC measurements of genuine aerosols gave on average 3% higher carbon recovery yield, relative to the uncorrected results of the sealed tube method. The comparison of the stable isotopic results by the two methods for aerosols also showed minimal differences. Consequently, the possibility of simultaneous TC and stable isotopic analyses makes the EA-IRMS method a very attractive alternative for continuous measurement of aerosols, with an accuracy and reliability similar to other commercial devices.