Chemical Characteristics, Size Distributions, and Aerosol Liquid Water in Size-Resolved Coastal Urban Aerosols Allied with Distinct Air Masses over Tropical Peninsular India

Author(s):  
Suresh Kumar Reddy Boreddy ◽  
Prashant Hegde ◽  
Aravindan Rema Aswini
2016 ◽  
Vol 33 (3) ◽  
pp. 579-595 ◽  
Author(s):  
Christopher R. Williams

AbstractThis study consists of two parts. The first part describes the way in which vertical air motions and raindrop size distributions (DSDs) were retrieved from 449-MHz and 2.835-GHz (UHF and S band) vertically pointing radars (VPRs) deployed side by side during the Midlatitude Continental Convective Clouds Experiment (MC3E) held in northern Oklahoma. The 449-MHz VPR can measure both vertical air motion and raindrop motion. The S-band VPR can measure only raindrop motion. These differences in VPR sensitivities facilitates the identification of two peaks in 449-MHz VPR reflectivity-weighted Doppler velocity spectra and the retrieval of vertical air motion and DSD parameters from near the surface to just below the melting layer.The second part of this study used the retrieved DSD parameters to decompose reflectivity and liquid water content (LWC) into two terms, one representing number concentration and the other representing DSD shape. Reflectivity and LWC vertical decomposition diagrams (Z-VDDs and LWC-VDDs, respectively) are introduced to highlight interactions between raindrop number and DSD shape in the vertical column. Analysis of Z-VDDs provides indirect measure of microphysical processes through radar reflectivity. Analysis of LWC-VDDs provides direct investigation of microphysical processes in the vertical column, including net raindrop evaporation or accretion and net raindrop breakup or coalescence. During a stratiform rain event (20 May 2011), LWC-VDDs exhibited signatures of net evaporation and net raindrop coalescence as the raindrops fell a distance of 2 km under a well-defined radar bright band. The LWC-VDD is a tool to characterize rain microphysics with quantities related to number-controlled and size-controlled processes.


2008 ◽  
Vol 8 (22) ◽  
pp. 6729-6738 ◽  
Author(s):  
N. Kalivitis ◽  
W. Birmili ◽  
M. Stock ◽  
B. Wehner ◽  
A. Massling ◽  
...  

Abstract. Atmospheric particle size distributions were measured on Crete island, Greece in the Eastern Mediterranean during an intensive field campaign between 28 August and 20 October, 2005. Our instrumentation combined a differential mobility particle sizer (DMPS) and an aerodynamic particle sizer (APS) and measured number size distributions in the size range 0.018 μm–10 μm. Four time periods with distinct aerosol characteristics were discriminated, two corresponding to marine and polluted air masses, respectively. In marine air, the sub-μm size distributions showed two particle modes centered at 67 nm and 195 nm having total number concentrations between 900 and 2000 cm−3. In polluted air masses, the size distributions were mainly unimodal with a mode typically centered at 140 nm, with number concentrations varying between 1800 and 2900 cm−3. Super-μm particles showed number concentrations in the range from 0.01 to 2.5 cm−3 without any clear relation to air mass origin. A small number of short-lived particle nucleation events were recorded, where the calculated particle formation rates ranged between 1.1–1.7 cm−3 s−1. However, no particle nucleation and growth events comparable to those typical for the continental boundary layer were observed. Particles concentrations (Diameter <50 nm) were low compared to continental boundary layer conditions with an average concentration of 300 cm−3. The production of sulfuric acid and its subsequently condensation on preexisting particles was examined with the use of a simplistic box model. These calculations suggested that the day-time evolution of the Aitken particle population was governed mainly by coagulation and that particle formation was absent during most days.


2008 ◽  
Vol 8 (2) ◽  
pp. 6571-6601
Author(s):  
N. Kalivitis ◽  
W. Birmili ◽  
M. Stock ◽  
B. Wehner ◽  
A. Massling ◽  
...  

Abstract. Atmospheric particle size distributions were measured on Crete island, Greece in the Eastern Mediterranean during an intensive field campaign between 28 August and 20 October 2005. Our instrumentation combined a differential mobility particle sizer (DMPS) and an aerodynamic particle sizer (APS) and measured number size distributions in the size range 0.018 μm–10 μm. Four time periods with distinct aerosol characteristics were discriminated, two corresponding to marine and polluted air masses, respectively. In marine air, the sub-μm size distributions showed two particle modes centered at 67 nm and 195 nm having total number concentrations between 900 and 2000 cm−3. In polluted air masses, the size distributions were mainly unimodal with a mode typically centered at 140 nm, with number concentrations varying between 1800 and 2900 cm−3. Super-μm particles showed number concentrations in the range from 0.01 to 2.5 cm−3 without any clear relation to air mass origin. A small number of short-lived particle nucleation events were recorded, where the calculated particle formation rates ranged between 1.1–1.7 cm−3 s−1. However, no particle nucleation and growth events comparable to those typical for the continental boundary layer were observed. Particles concentrations (Diameter <50 nm) were low compared to continental boundary layer conditions with an average concentration of 300 cm−3. The production of sulfuric acid and its subsequently condensation on preexisting particles was examined with the use of a simplistic box model. These calculations suggested that the day-time evolution of the Aitken particle population was governed mainly by coagulation and that particle formation was absent during most days.


2004 ◽  
Vol 110 (1-4) ◽  
pp. 851-857 ◽  
Author(s):  
B. Grosswendt ◽  
L. De Nardo ◽  
P. Colautti ◽  
S. Pszona ◽  
V. Conte ◽  
...  

2016 ◽  
Vol 16 (14) ◽  
pp. 9255-9272 ◽  
Author(s):  
Mark Pinsky ◽  
Alexander Khain ◽  
Alexei Korolev ◽  
Leehi Magaritz-Ronen

Abstract. Evolution of monodisperse and polydisperse droplet size distributions (DSD) during homogeneous mixing is analyzed. Time-dependent universal analytical expressions for supersaturation and liquid water content are derived. For an initial monodisperse DSD, these quantities are shown to depend on a sole non-dimensional parameter. The evolution of moments and moment-related functions in the course of homogeneous evaporation of polydisperse DSD is analyzed using a parcel model.It is shown that the classic conceptual scheme, according to which homogeneous mixing leads to a decrease in droplet mass at constant droplet concentration, is valid only in cases of monodisperse or initially very narrow polydisperse DSD. In cases of wide polydisperse DSD, mixing and successive evaporation lead to a decrease of both mass and concentration, so the characteristic droplet sizes remain nearly constant. As this feature is typically associated with inhomogeneous mixing, we conclude that in cases of an initially wide DSD at cloud top, homogeneous mixing is nearly indistinguishable from inhomogeneous mixing.


2008 ◽  
Vol 8 (16) ◽  
pp. 4711-4728 ◽  
Author(s):  
S. R. Zorn ◽  
F. Drewnick ◽  
M. Schott ◽  
T. Hoffmann ◽  
S. Borrmann

Abstract. Measurements of the submicron fraction of the atmospheric aerosol in the marine boundary layer were performed from January to March 2007 (Southern Hemisphere summer) onboard the French research vessel Marion Dufresne in the Southern Atlantic and Indian Ocean (20° S–60° S, 70° W–60° E). We used an Aerodyne High-Resolution-Time-of-Flight AMS to characterize the chemical composition and to measure species-resolved size distributions of non-refractory aerosol components in the submicron range. Within the "standard" AMS compounds (ammonium, chloride, nitrate, sulfate, organics) "sulfate" is the dominant species in the marine boundary layer with concentrations ranging between 50 ng m−3 and 3 μg m−3. Furthermore, what is seen as "sulfate" by the AMS is likely comprised mostly of sulfuric acid. Another sulfur containing species that is produced in marine environments is methanesulfonic acid (MSA). There have been previously measurements of MSA using an Aerodyne AMS. However, due to the use of an instrument equipped with a quadrupole detector with unit mass resolution it was not possible to physically separate MSA from other contributions to the same m/z. In order to identify MSA within the HR-ToF-AMS raw data and to extract mass concentrations for MSA from the field measurements the standard high-resolution MSA fragmentation patterns for the measurement conditions during the ship campaign (e.g. vaporizer temperature) needed to be determined. To identify characteristic air masses and their source regions backwards trajectories were used and averaged concentrations for AMS standard compounds were calculated for each air mass type. Sulfate mass size distributions were measured for these periods showing a distinct difference between oceanic air masses and those from African outflow. While the peak in the mass distribution was roughly at 250 nm (vacuum aerodynamic diameter) in marine air masses, it was shifted to 470 nm in African outflow air. Correlations between the mass concentrations of sulfate, organics and MSA show a narrow correlation for MSA with sulfate/sulfuric acid coming from the ocean, but not with continental sulfate.


2011 ◽  
Vol 11 (12) ◽  
pp. 32921-32964
Author(s):  
S. Mogo ◽  
V. E. Cachorro ◽  
J. F. Lopez ◽  
E. Montilla ◽  
B. Torres ◽  
...  

Abstract. In situ measurements of aerosol optical properties were made in the summer of 2008 at the ALOMAR station facility (69°16 N, 16°00 E), located at a rural site in the north of the island of Andøya (Vesterålen archipelago), approximately 300 km north of the Arctic Circle. The extended three-month campaign was part of the POLARCAT Project (Polar Study using Aircraft, Remote Sensing, Surface Measurements and Models, of Climate, Chemistry, Aerosols, and Transport) of the International Polar Year (IPY-2007-2008). Its goal was to characterize the aerosols of this sub-Arctic area, which are frequently transported to the Arctic region. The ambient light-scattering coefficient, σs (550 nm), at ALOMAR had a measured hourly mean value of 5.41 Mm−1 (StD = 3.55 Mm−1), and the light-absorption coefficient, σa (550 nm), had a measured hourly mean value of 0.40 Mm−1 (StD = 0.27 Mm−1). The scattering/absorption Ångström exponents, αs,a, are used for a detailed analysis of the variations of the spectral shape of σs,a. Whereas αs demonstrates the presence of two particle sizes corresponding to two types of aerosols, the αa demonstrates only one type of absorbing aerosol particles. Values of αa above 1 were not observed. The single-scattering albedo, ω0, ranged from 0.62 to 0.99 (mean = 0.91, StD = 0.05), and the relationships of this property to the absorption/scattering coefficients and the Ångström exponents are presented. The concentration of the particles was monitored using a scanning mobility particle sizer (SMPS), an aerodynamic particle sizer (APS) and an ultrafine condensation particle counter (UCPC). The shape of the median size distribution of the particles in the submicrometer fraction was bimodal, and the submicrometer, micrometer and total concentrations presented hourly mean values of 1277 cm3 (StD = 1563 cm3), 1 cm3 (StD = 1 cm3) and 2463 cm3 (StD = 4251 cm3), respectively. The modal correlations were investigated, and the concentration of particles sized between 30 and 100 nm (Aitken mode) are presented as a function of the concentration of the particles sized between 100 and 390 nm (accumulation mode). The optical and the microphysical parameters are related to each other, and the results are presented. The origins and pathways of air masses were examined by computing the back-trajectories in a trajectory model (HYSPLIT). Six geographical sectors were defined to classify the air masses, and, based on the sector classification, the linkage between the air mass origin and the optical parameters was established. Aerosol size distributions were also evaluated in relation to the air masses. The relationships between the air mass origins and other parameters, especially those related to the single scattering albedo, allow us to describe two characteristic situations: northern and western air masses, which had predominantly marine aerosols, presented lower optical parameter values, indicating predominantly coarser and non-absorbent particles; and eastern and southern air masses, in which continental aerosols were predominant, presented higher values for all optical parameters, indicating the presence of smaller absorbent particles.


2011 ◽  
Vol 11 (8) ◽  
pp. 21677-21711 ◽  
Author(s):  
M. Dall'Osto ◽  
C. Monahan ◽  
R. Greaney ◽  
D. C. S. Beddows ◽  
R. M. Harrison ◽  
...  

Abstract. The Global Atmospheric Watch research station at Mace Head (Ireland) offers the possibility to sample some of the cleanest air masses being imported into Europe as well as some of the most polluted being exported out of Europe. We present a statistical Cluster~analysis of the physical characteristics of aerosol size distributions in air ranging from the cleanest to the most polluted for the year 2008. Data coverage achieved was 75 % throughout the year. By applying the Hartigan-Wong k-Means method, 12 Clusters were identified as systematically occurring and these 12 Clusters could be further combined into 4 categories with similar characteristics, namely: coastal nucleation category (occurring 21.3 % of the time), open ocean nucleation category (occurring 32.6 % of the time), background clean marine category (occurring 26.1 % of the time) and anthropogenic category (occurring 20 % of the time) aerosol size distributions. The coastal nucleation category is characterised by a clear and dominant nucleation mode at sizes less that 10 nm while the open ocean nucleation category is characterised by a dominant Aitken mode between 15 nm and 50 nm. The background clean marine characteristic is a clear bimodality in the size distribution, although it should be noted that either the Aitken mode or the Accumulation mode may dominate the number concentration. By contrast, the continentally-influenced size distributions are generally more mono-modal, albeit with traces of bi-modality. The open ocean category occurs more often during May, June and July, corresponding with the N. E. Atlantic high biological period. Combined with the relatively high percentage frequency of occurrence (32.6 %), this suggests that the marine biota is an important source of new aerosol particles in N. E. Atlantic Air.


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