Aerosol indirect effect over Indo-Gangetic plain

Moderate resolution imaging spectroradiometer (MODIS) data are analyzed over the Indo-Gangetic plain (IGP) to study the effect of aerosol optical depth (AOD) on the water (R_eff,w) and ice (R_eff,i) cloud effective radius for the period 2001–2005. The temporal variation of R_eff,w and R_eff,i shows reverse trend as that of AOD for most of the time. The intensity of positive indirect effect (i.e. increase of R_eff,w/i with decrease of AOD and vice versa) is the highest in winter (ΔR_eff,w/ΔAOD∼−9.67 μm and ΔR_eff,i/ΔAOD∼−12.15 μm), when the role of meteorology is the least. The positive indirect effect is significant in 43%, 37%, 68% and 54% of area for water clouds in winter, pre-monsoon, monsoon and post-monsoon seasons, respectively, whereas the corresponding values for ice clouds are 42%, 35%, 53% and 53% for the four seasons, respectively. On the contrast, R_eff,i in some locations shows increment with the increase in AOD (negative indirect effect). The negative indirect effect is significant at 95% confidence level in 7%, 18%, 9% and 6% grids for winter, pre-monsoon, monsoon and post-monsoon seasons, respectively. The restricted spatial distribution of negative indirect effect in IGP shows that the cloud microphysical processes are very complex. Our analyses clearly identify the contrasting indirect effect, which requires further in situ investigations for better understanding of the aerosol–cloud interaction in the region.     

Aerosol radiative forcing for Asian continental outflow

Asian aerosols in elevated layers over the Pacific Ocean were sampled with NASA wire-impactors and a FSSP optical particle spectrometer-probe aboard the NASA DC-8 aircraft in early March 1994. Strong variations in aerosol properties, primarily aerosol concentration, lead to derived mid-visible extinctions between 0.003 and 0.5/km. FSSP data usually identified two size-modes. The larger ‘coarse mode’ (radii of 1–3 μm) was assumed to be dust. The composition of the smaller ‘accumulation mode’ (radii of 0.1–0.3 μm) was based on the analysis of the wire-impactor samples, as significant amounts of soot reduce mid-visible single scattering albedos to the 0.87–0.92 range.Radiative forcing simulations investigated the impact of Asian outflow aerosol on atmospheric radiative fluxes and heating rates. Only events with larger optical depths were important. In those events the solar attenuation of the smaller size mode dominated the net-flux losses at the surface, with values similar those of urban-polluted and/or biomass burning aerosol types (as observed during the TARFOX and INDOEX field experiments). In contrast, changes to net-fluxes at the top of the atmosphere (ToA) for outflow cases are less negative—primarily due to the added greenhouse effect of the dust component. For the climate of the Earth-Atmosphere-System, ToA net-flux losses are considered a cooling, ToA net-flux gains are associated with warming. Weak cooling is determined for the Asian outflow cases under cloud-free conditions. The addition of a reported 50% cloud cover below the aerosol layer causes a switch to slight warming.     

Contribution of anthropogenic aerosols in direct radiative forcing and atmospheric heating rate over Delhi in the Indo-Gangetic Basin

Introduction  

The present work is aimed to understand direct radiation effects due to aerosols over Delhi in the Indo-Gangetic Basin (IGB) region, using detailed chemical analysis of surface measured aerosols during the year 2007.     

Mixing and transformation of Asian dust with pollution in the two dust storms over the northern China in 2006

To study the mixing and transformation of Asian dust with pollution in the two dust storms over the northern China in 2006, both TSP and PM_2.5 samples were collected at three sites of northern China in addition to the dry deposition samples collected in an episode in Beijing. 23 elements, 15 ions, and 16 PAHs in each sample were analyzed. The two dust storms in northern China were observed in April 8–10 (DS1) and April 16–18 (DS2). Compared to DS2, DS1 was weaker and more polluted with stronger mixing between crustal and pollutant aerosols during their long-range transport. The concentrations of pollution species, e.g. pollution elements, ions, and PAHs were higher in DS1 than that in DS2, while the crustal species showed adverse variation. The correlation between chemical species and Al and between PAH(4) and PAH(5,6) further confirmed the stronger chemical transformation and aerosol mixing in DS1 than that in DS2. Back trajectory and chemical analysis revealed that in DS1 the air masses at Beijing were mostly from southern or southwestern direction at lower altitude with much more pollution, while in DS2 the air masses were mostly from the northwestern and northern direction with dust mainly, which explained why there was a stronger mixing of dust with pollution aerosol in DS1 than that in DS2 over Beijing.     

On the contribution of black carbon to the composite aerosol radiative forcing over an urban environment

This paper discusses the extent of Black Carbon (BC) radiative forcing in the total aerosol atmospheric radiative forcing over Pune, an urban site in India. Collocated measurements of aerosol optical properties, chemical composition and BC were carried out for a period of six months (during October 2004 to May 2005) over the site. Observed aerosol chemical composition in terms of water soluble, insoluble and BC components were used in Optical Properties of Aerosols and Clouds (OPAC) to derive aerosol optical properties of composite aerosols. The BC fraction alone was used in OPAC to derive optical properties of BC aerosols. The aerosol optical properties for composite and BC aerosols were separately used in SBDART model to derive direct aerosol radiative forcing due to composite and BC aerosols. The atmospheric radiative forcing for composite aerosols were found to be +35.5, +32.9 and +47.6 Wm^?2 during post-monsoon, winter and pre-monsoon seasons, respectively. The average BC mass fraction found to be 4.83, 6.33 and 4 μg m^?3 during the above seasons contributing around 2.2 to 5.8% to the total aerosol load. The atmospheric radiative forcing estimated due to BC aerosols was +18.8, +23.4 and +17.2 Wm^?2, respectively during the above seasons. The study suggests that even though BC contributes only 2.2–6% to the total aerosol load; it is contributing an average of around 55% to the total lower atmospheric aerosol forcing due to strong radiative absorption, and thus enhancing greenhouse warming.     

Effects of radiative forcing by black carbon aerosol on spring rainfall decrease over Southeast Asia

The effects of black carbon (BC) aerosol radiative forcing on spring rainfall in Southeast Asia are studied 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).During the boreal spring, March–April–May (MAM), BC from local emissions accumulates over Southeast Asia. The BC aerosol layer, which extends from the surface to higher elevation above planetary boundary layer (PBL), absorbs solar radiation and heats the mid-troposphere through a semi-direct effect over regions of large aerosol optical thickness (AOT) and thereby significantly perturbs large-scale and meridional circulations. Results show that anomalous precipitation patterns and associated large-scale circulations induced by radiative forcing by BC aerosol can explain observed precipitation reductions, especially over Southeast Asia. Therefore, BC aerosol forcing may be one of the important factors affecting the spring rainfall trend over Southeast Asia.     

The evolution of chemical components of aerosols at five monitoring sites of China during dust storms

Daily PM_2.5 and TSP and their chemical composition with two dust events (DS1: 9–10 March and DS2: 27–30 March) were simultaneously observed for the period of 9 March–23 April 2004 from a monitoring network over China. Five monitoring sites were performed along the transport pathway of Asian dust storm, located in Northwest, North, East, and Southeast regions of China. The dust and non-dust days exhibited different characteristics with respect to the composition and the meteorological conditions. In non-dust days, particulate pollution was found to be associated with the city economy, and it primarily consisted of the crustal, the secondary, and the carbonaceous material. In the dust episodes, significant increase in the particle concentration with a large part of the secondary components diluted by the crustal components was observed at all the sites. Particles were getting more and more acidic as the episodic dust progressed eastward. Dust particles were suggested to react with SO₂/NO_X/sulfate/nitrate based on the variations of SO₄²⁻/Ca²⁺ and NO₃⁻/Ca²⁺ along the transport pathway, and the formation mechanism of sulfate and nitrate was proved to be different. Positive matrix factorization analysis showed that the sources from the upstream and the transport pathways could account for 49%, 82%, and 28% of PM mass, crust, and secondary aerosol, respectively, and the contribution decreased, as the dust made its way from source area to the coastal regions. Enrichment factors of the species presented significant correlations among different sites in the dust episodes, suggesting the significant impact of those dust emissions on the local environment.     

Ionic composition of TSP and PM2.5 during dust storms and air pollution episodes at Xi'an,China

TSP and PM_2.5 samples were collected at Xi'an, China during dust storms (DSs) and several types of pollution events, including haze, biomass burning, and firework displays. Aerosol mass concentrations were up to 2 times higher during the particulate matter (PM) events than on normal days (NDs), and all types of PM led to decreased visibility. Water-soluble ions (Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺, F^?, Cl^?, NO₃^?, and SO₄^2?). were major aerosol components during the pollution episodes, but their concentrations were lower during DSs. NH₄⁺, K⁺, F^?, Cl^?, NO₃^?, and SO₄^2? were more abundant in PM_2.5 than TSP but the opposite was true for Mg²⁺ and Ca²⁺. PM collected on hazy days was enriched with secondary species (NH₄⁺, NO₃^?, and SO₄²) while PM from straw combustion showed high K⁺ and Cl^?. Firework displays caused increases in K⁺ and also enrichments of NO₃^? relative to SO₄^2?. During DSs, the concentrations of secondary aerosol components were low, but Ca²⁺ was abundant. Ion balance calculations indicate that PM from haze and straw combustion was acidic while the DSs samples were alkaline and the fireworks' PM was close to neutral. Ion ratios (SO₄^2?/K⁺, NO₃^?/SO₄^2?, and Cl^?/K⁺) proved effective as indicators for different pollution episodes.     

Aerosol organic nitrogen over the remote Atlantic Ocean

Water soluble organic nitrogen (WSON) has been measured in aerosols collected on three research cruises on the Atlantic Ocean from approximately 55°N to 45°S. Results are interpreted using air mass back trajectories and results for other aerosol components. WSON concentrations range from <1 to ～40 (median 5.6) nmol m^?3 with significant WSON concentrations in both fine (<1 μm) and coarse mode (>1 μm) aerosol. Concentrations of WSON were highest in samples containing Saharan dust, suggesting a locally significant source associated with soil dust. More generally WSON concentrations were highest in air which had recently crossed continental areas. In the whole data set, WSON is well correlated to total soluble nitrogen and represents approximately 25% of total nitrogen. This correlation implies a significant anthropogenic contribution to the organic nitrogen.     

Lidar and satellite retrieval of dust aerosols over the Azores during SOFIA/ASTEX

The synergy between active (airborne lidar) and passive (Meteosat) sensors is achieved with the help of a numerical transport model (TM2z) to derive optical properties of Saharan dust during a long range transport over the Azores. Measurements were taken in June 1992 during the surface of the ocean, fluxes and interaction with the atmosphere campaign, which took place during the Atlantic stratocumulus transition experiment. The dust source is identified to be in north Morocco from a TM2z back-trajectory analysis. Lidar observations over the Azores show that the dust is maintained in multiple thin layers (few hundred meters) up to 5 km altitude after a 4-day transport. Horizontal gradients are less marked, with a typical scale of variation of about 5 km. Lidar inversions yield dust optical thicknesses from 0.1 to 0.16 mainly due to two layers centered at 1.3 and 3.7 km. Since the weather was extremely cloudy over this region, the dust plume was not observable on the coincident Meteosat image. We thus processed the image taken two days earlier that clearly shows a dust plume between Azores and Spain. The Meteosat inversion was constrained by using the airborne lidar measurements in the marine boundary layer. The retrieved dust optical thicknesses are in good agreement with that retrieved from the lidar. Coherence of both lidar and radiometry measurements suggests that such a combined analysis is promising for retrieving the optical thickness of elevated dust layers as well as their spatial extent outside the source region even under cloudy conditions.     

Saharan dust incursion over the Tyrrhenian Sea

The Tyrrhenian Sea aerosol was sampled by both mesh and filter techniques. Geostrophic back trajectories were used to identify potential aerosol catchment regions, and it was shown that the atmosphere over the Tyrrhenian Sea received incursions of Saharan dust during the collection period in the autumn of 1979. Mineralogical and chemical parameters were used to characterize this desert-derived material and it was shown that it exerts an important influence on the composition of the local aerosol. On the basis of the present data, it was concluded that the northward movement of Saharan dust across, the Mediterranean can result in the transport of relatively large amounts of crustal material to the southern European coast and so should be included in estimates of Saharan dust production.     

Aerosol indirect effect during successive contrasting monsoon seasons over Indian subcontinent using MODIS data

Aerosol indirect effect (AIE) was estimated over six Indian regions, which have been identified as main source regions of absorbing aerosol emissions, for four successive contrasting monsoon years, 2001 (normal monsoon rainfall year), 2002 (drought year), 2003 (excess monsoon rainfall year) and 2004 (below normal rainfall year). The AIE has been estimated both for fixed cloud liquid water path (CLWP) and for fixed cloud ice path (CIP) bins, ranging from 1 to 350 gm^?2 at 25 gm^?2 intervals obtained from Moderate resolution imaging spectroradiometer (MODIS). In 2002 and 2004, AIE found to be of positive (Twomey effect) in majority of the fixed CLWP and CIP bins, while in 2001 and 2003 majority of the bins were found to be showing negative indirect effect (Anti-Twomey effect). Changes in circulation patterns during contrasting monsoon seasons, bringing up air mass containing aerosols of different source origins may be the main reason for this positive and negative AIE. The study suggests that AIE could be one of the factors in modulating Indian summer monsoon. However, further research on this topic is to be carried out to establish the relationship between AIE and Indian monsoon rainfall and also AIE values may be parameterized in climate models for better prediction of monsoon.     

Aerosol ion characteristics during the Big Bend Regional Aerosol and Visibility Observational study

The ionic compositions of particulate matter with aerodynamic diameter < or = 2.5 microm (PM2.5) and size-resolved aerosol particles were measured in Big Bend National Park, Texas, during the 1999 Big Bend Regional Aerosol and Visibility Observational study. The ionic composition of PM2.5 aerosol was dominated by sulfate (SO4(2-)) and ammonium (NH4+). Daily average SO4(2-) and NH4+ concentrations were strongly correlated (R2 = 0.94). The molar ratio of NH4+ to SO4(2-) averaged 1.54, consistent with concurrent measurements of aerosol acidity. The aerosol was observed to be comprised of a submicron fine mode consisting primarily of ammoniated SO4(2-) and a coarse particle mode containing nitrate (NO3-). The NO3- appears to be primarily associated with sea salt particles where chloride has been replaced by NO3-, although formation of calcium nitrate (Ca(NO3)2) is important, too, on several days. Size-resolved aerosol composition results reveal that a size cut in particulate matter with aerodynamic diameter < or = 1 microm would have provided a much better separation of fine and coarse aerosol modes than the standard PM2.5 size cut utilized for the study. Although considerable nitric acid exists in the gas phase at Big Bend, the aerosol is sufficiently acidic and temperatures sufficiently high that even significant future reductions in PM2.5 SO4(2-) are unlikely to be offset by formation of particulate ammonium nitrate in summer or fall.     

Aerosol optical,chemical and physical properties at Gosan,Korea during Asian dust and pollution episodes in 2001

In order to understand the influence of dust and anthropogenic pollution aerosols on regional climate in East Asia, we analyzed the aerosol optical, chemical and physical properties for two cases with high aerosol loading and assessed the radiative forcing of these cases. The 1st case study is a heavy dust episode (DE) in April (during ACE-Asia) 2001 and the 2nd case is a regional-scale pollution event in November 2001. The Ångström exponent (Å) for DE was 0.38 from sunphotometer measurements. The mean single scattering albedo (550 nm) at the surface reported during the pollution episode (PE, 0.88) was lower than that of DE (0.91). The concentrations of organic (OC) and elemental carbon (EC) measured during the PE were about 90% and 30% higher than DE. The aerosol mass scattering efficiency (α_s) of PE is a factor of about 2 higher than that of the DE. The difference in the mass absorption efficiency (α_a) of EC during DE and PE is small and within the measurement uncertainty. The diurnally averaged aerosol radiative forcing efficiency (ΔDFE, W m⁻² τ⁻¹) during DE is similar to results of other studies at Gosan.     

A contribution of brown carbon aerosol to the aerosol light absorption and its radiative forcing in East Asia

Brown carbon aerosols were recently found to be ubiquitous and effectively absorb solar radiation. We use a 3-D global chemical transport model (GEOS-Chem) together with aircraft and ground based observations from the TRACE-P and the ACE-Asia campaigns to examine the contribution of brown carbon aerosol to the aerosol light absorption and its climatic implication over East Asia in spring 2001. We estimated brown carbon aerosol concentrations in the model using the mass ratio of brown carbon to black carbon (BC) aerosols based on measurements in China and Europe. The comparison of simulated versus observed aerosol light absorption showed that the model accounting for brown carbon aerosol resulted in a better agreement with the observations in East Asian-Pacific outflow. We then used the model results to compute the radiative forcing of brown carbon, which amounts up to ?2.4 W m^?2 and 0.24 W m^?2 at the surface and at the top of the atmosphere (TOA), respectively, over East Asia. Mean radiative forcing of brown carbon aerosol is ?0.43 W m^?2 and 0.05 W m^?2 at the surface and at the TOA, accounting for about 15% of total radiative forcing (?2.2 W m^?2 and 0.33 W m^?2) by absorbing aerosols (BC + brown carbon aerosol), having a significant climatic implication in East Asia.     

Impact of dust storm on phytoplankton bloom over the Arabian Sea: a case study during March 2012

Environmental Science and Pollution Research - Dust storms affect the primary productivity of the ocean by providing necessary micronutrients to the surface layer. One such dust storm during March...     

Airborne desert dust and aeromicrobiology over the Turkish Mediterranean coastline

Between 18 March and 27 October 2002, 220 air samples were collected on 209 of 224 calendar days, on top of a coastal atmospheric research tower in Erdemli, Turkey. The volume of air filtered for each sample was 340 liters. Two hundred fifty-seven bacterial and 2598 fungal colony forming units (CFU) were enumerated from the samples using a low-nutrient agar. Ground-based dust measurements demonstrated that the region is routinely impacted by dust generated regionally and from North Africa and that the highest combined percent recovery of total CFU and African dust deposition occurred in the month of April (93.4% of CFU recovery and 91.1% of dust deposition occurred during African dust days versus no African dust present, for that month). A statistically significant correlation was observed (peak regional African dust months of March, April and May; r_s=0.576, P=0.000) between an increase in the prevalence of microorganisms recovered from atmospheric samples on dust days (regional and African as determined by ground-based dust measurements), versus that observed on non-dust days. Given the prevalence of atmospherically suspended desert dust and microorganisms observed in this study, and that culture-based studies typically only recover a small fraction (<1.0%) of the actual microbial population in any given environment, dust-borne microorganisms and other associated constituents (organic detritus, toxins, etc.) may play a significant role in the regional human and ecosystem health.     

Chemical compositions and radiative properties of dust and anthropogenic air masses study in Taipei Basin, Taiwan, during spring of 2004

Asia is one of the major sources of not only mineral dust but also anthropogenic aerosols. Continental air masses associated with the East Asian winter monsoon always contain high contents of mineral dust and anthropogenic species and transported southeastward to Taiwan, which have significant influences on global atmospheric radiation transfer directly by scattering and absorbing solar radiation in each spring. However, few measurements for the long-range transported aerosol and its optical properties were announced in this area, between the Western Pacific and the southeastern coast of Mainland China. The overall objective of this work is to quantify the optical characteristics of different aerosol types in the Eastern Asian. In order to achieve this objective, meteorological parameters, concentrations of PM₁₀ and its soluble species, and optical property of atmospheric scattering coefficients were measured continuously with 1 h time-resolved from 11 February to 7 April 2004 in Taipei Basin (25°00′N, 121°32′E). In this work, the dramatic changes of meteorological parameters such as temperature and winds were used to determine the influenced period of each air mass. Continental, strong continental, marine, and stagnant air masses defined by the back-trajectory analysis and local meteorology were further characterized as long-range transport pollution, dust, clean marine, and local pollution aerosols, respectively, according to the diagnostic ratios. The aerosol mass scattering efficiency of continental pollution, dust, clean marine, and local pollution aerosols were ranged from 1.3 to 1.6, 0.7 to 1.0, 1.4 and 1.4 to 2.3 m² g⁻¹, respectively. Overall, there are two distinct populations of aerosol mass scattering efficiencies, one for an aerosol chemical composition dominated by dust (<1.0 m² g⁻¹) and the other for an aerosol chemical composition dominated by anthropogenic pollutants (1.3–2.3 m² g⁻¹), which were similar to the previous measurements with high degree of temporal resolution.     

Volcanic sulphate and arctic dust plumes over the North Atlantic Ocean

High time resolution aerosol mass spectrometry measurements were conducted during a field campaign at Mace Head Research Station, Ireland, in June 2007. Observations on one particular day of the campaign clearly indicated advection of aerosol from volcanoes and desert plains in Iceland which could be traced with NOAA Hysplit air mass back trajectories and satellite images. In conjunction with this event, elevated levels of sulphate and light absorbing particles were encountered at Mace Head. While sulphate concentration was continuously increasing, nitrate levels remained low indicating no significant contribution from anthropogenic pollutants. Sulphate concentration increased about 3.8 μg m⁻³ in comparison with the background conditions. Corresponding sulphur flux from volcanic emissions was estimated to about 0.3 TgS yr⁻¹, suggesting that a large amount of sulphur released from Icelandic volcanoes may be distributed over distances larger than 1000 km. Overall, our results corroborate that transport of volcanogenic sulphate and dust particles can significantly change the chemical composition, size distribution, and optical properties of aerosol over the North Atlantic Ocean and should be considered accordingly by regional climate models.