scholarly journals STUDY OF AEROSOL OPTICAL PROPERTIES OVER TWO SITES IN THE FOOTHILLS OF THE CENTRAL HIMALAYAS

Author(s):  
D. Rupakheti ◽  
S. Kang ◽  
Z. Cong ◽  
M. Rupakheti ◽  
L. Tripathee ◽  
...  

Atmospheric aerosol possesses impacts on climate system and ecological environments, human health and agricultural productivity. The environment over Himalayas and Tibetan Plateau region are continuously degraded due to the transport of pollution from the foothills of the Himalayas; mostly the Indo-Gangetic Plain (IGP). Thus, analysis of aerosol optical properties over two sites; Lumbini and Kathmandu (the southern slope of central Himalayas) using AERONET’s CIMEL sun photometer were conducted in this study. Aerosol optical depth (AOD at 500 nm), angstrom exponent (α or AE), volume size distribution (VSD), single scattering albedo (SSA) and asymmetry parameter (AP) were studied for 2013–2014 and the average AOD was found to be: 0.64 ± 0.41 (Lumbini) and 0.45 ± 0.30 (Kathmandu). The average AE was found to be: 1.25 ± 0.24 and 1.26 ± 0.18 respectively for two sites. The relation between AOD and AE was used to discriminate the aerosol types over these sites which indicated anthropogenic, mixed and biomass burning origin aerosol constituted the major aerosol types in Lumbini and Kathmandu. A clear bi-modal distribution of aerosol volume size was observed with highest volume concentration during the post-monsoon season in fine mode and pre-monsoon season in coarse mode (Lumbini) and highest value over both modes during pre-monsoon season in Kathmandu. The single scattering albedo (SSA) and asymmetry parameter (AP) analyses suggested aerosols over the Himalayan foothills sites are dominated by absorbing and anthropogenic aerosols from urban and industrial activities and biomass burning. Long-term studies are essential to understand and characterize the nature of aerosol over this research gap zone.

2019 ◽  
Vol 19 (14) ◽  
pp. 9181-9208 ◽  
Author(s):  
Kristina Pistone ◽  
Jens Redemann ◽  
Sarah Doherty ◽  
Paquita Zuidema ◽  
Sharon Burton ◽  
...  

Abstract. The total effect of aerosols, both directly and on cloud properties, remains the biggest source of uncertainty in anthropogenic radiative forcing on the climate. Correct characterization of intensive aerosol optical properties, particularly in conditions where absorbing aerosol is present, is a crucial factor in quantifying these effects. The southeast Atlantic Ocean (SEA), with seasonal biomass burning smoke plumes overlying and mixing with a persistent stratocumulus cloud deck, offers an excellent natural laboratory to make the observations necessary to understand the complexities of aerosol–cloud–radiation interactions. The first field deployment of the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) campaign was conducted in September of 2016 out of Walvis Bay, Namibia. Data collected during ORACLES-2016 are used to derive aerosol properties from an unprecedented number of simultaneous measurement techniques over this region. Here, we present results from six of the eight independent instruments or instrument combinations, all applied to measure or retrieve aerosol absorption and single-scattering albedo. Most but not all of the biomass burning aerosol was located in the free troposphere, in relative humidities typically ranging up to 60 %. We present the single-scattering albedo (SSA), absorbing and total aerosol optical depth (AAOD and AOD), and absorption, scattering, and extinction Ångström exponents (AAE, SAE, and EAE, respectively) for specific case studies looking at near-coincident and near-colocated measurements from multiple instruments, and SSAs for the broader campaign average over the month-long deployment. For the case studies, we find that SSA agrees within the measurement uncertainties between multiple instruments, though, over all cases, there is no strong correlation between values reported by one instrument and another. We also find that agreement between the instruments is more robust at higher aerosol loading (AOD400>0.4). The campaign-wide average and range shows differences in the values measured by each instrument. We find the ORACLES-2016 campaign-average SSA at 500 nm (SSA500) to be between 0.85 and 0.88, depending on the instrument considered (4STAR, AirMSPI, or in situ measurements), with the interquartile ranges for all instruments between 0.83 and 0.89. This is consistent with previous September values reported over the region (between 0.84 and 0.90 for SSA at 550nm). The results suggest that the differences observed in the campaign-average values may be dominated by instrument-specific spatial sampling differences and the natural physical variability in aerosol conditions over the SEA, rather than fundamental methodological differences.


2019 ◽  
Author(s):  
Kristina Pistone ◽  
Jens Redemann ◽  
Sarah Doherty ◽  
Paquita Zuidema ◽  
Sharon Burton ◽  
...  

Abstract. The total effect of aerosols, both directly and on cloud properties, remains the biggest source of uncertainty in anthropogenic radiative forcing on the climate. Correct characterization of intensive aerosol optical properties, particularly in conditions where absorbing aerosol is present, is a crucial factor in quantifying these effects. The Southeast Atlantic Ocean (SEA), with seasonal biomass burning smoke plumes overlying and mixing with a persistent stratocumulus cloud deck, offers an excellent natural laboratory to make the observations necessary to understand the complexities of aerosol-cloud-radiation interactions. The first field deployment of the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) campaign was conducted in September of 2016 out of Walvis Bay, Namibia. Data collected during ORACLES-2016 are used to derive aerosol properties from an unprecedented number of simultaneous measurement techniques over this region. Here we present results from six of the eight independent instruments or instrument combinations, all applied to measure or retrieve aerosol absorption and single scattering albedo. Most but not all of the biomass-burning aerosol was located in the free troposphere, in relative humidities typically ranging up to 60 %. We present the single scattering albedo (SSA), absorbing and total aerosol optical depth (AOD and AAOD), and absorption, scattering, and extinction Ångström exponents (AAE, SAE, EAE) for specific case studies looking at near-coincident and -colocated measurements from multiple instruments, and SSAs for the broader campaign average over the monthlong deployment. For the case studies, we find that SSA agrees within the measurement uncertainties between multiple instruments, though, over all cases, there is no strong correlation between values reported by one instrument and another. We also find that agreement between the instruments is more robust at higher aerosol loading (AOD400 > 0.4). The campaign-wide average and range shows differences in the values measured by each instrument. We find the ORACLES-2016 campaign-average SSA at 500 nm (SSA500) to be between 0.85 and 0.88, depending on the instrument considered (4STAR, AirMSPI, or in situ measurements), with the inter-quartile ranges for all instruments between 0.83 and 0.89. This is consistent with previous September values reported over the region (between 0.84 and 0.90 for SSA at 550 nm). The results suggest that the differences observed in the campaign-average values may be dominated by instrument-specific spatial sampling differences and the natural physical variability in aerosol conditions over the SEA, rather than fundamental methodological differences.


2011 ◽  
Vol 11 (10) ◽  
pp. 29003-29054 ◽  
Author(s):  
A. R. Esteve ◽  
J. A. Ogren ◽  
P. J. Sheridan ◽  
E. Andrews ◽  
B. N. Holben ◽  
...  

Abstract. Aerosol optical properties were measured by NOAA's Airborne Aerosol Observatory over Bondville, Illinois, during more than two years using a light aircraft. Measured properties included total light scattering, backscattering, and absorption, while calculated parameters included aerosol optical depth (AOD), Ångström exponent, single-scattering albedo, hemispheric backscatter fraction, asymmetry parameter, and submicrometer mode fraction of scattering. The in-situ aircraft measurements are compared here with AERONET measurements and retrievals of the aerosol optical properties at the same location. The comparison reveals discrepancies between the aerosol properties retrieved from AERONET and from in-situ aircraft measurements. These discrepancies are smaller for the AOD, while the biggest discrepancies are for the single-scattering albedo, hemispheric backscatter fraction, and asymmetry parameter. Possible sources of discrepancy between the AOD measured by AERONET and the one calculated from the in-situ aircraft measurements are investigated. The largest portion of the AOD discrepancy is likely due to an incorrect adjustment to ambient RH of the scattering coefficient. Another significant part (along with uncertain nephelometer truncation corrections) may come from the possibility that there might be less aerosol below the lowest flight altitude or that the aircraft inlet excludes aerosol particles larger than 5–7 μm diameter.


2008 ◽  
Vol 8 (12) ◽  
pp. 3199-3214 ◽  
Author(s):  
H. Che ◽  
G. Shi ◽  
A. Uchiyama ◽  
A. Yamazaki ◽  
H. Chen ◽  
...  

Abstract. This study compares the aerosol optical and physical properties simultaneously measured by a SKYNET PREDE skyradiometer and AERONET/PHOTONS CIMEL sunphotometer at a location in Beijing, China. Aerosol optical properties (AOP) including the Aerosol Optical Depth (AOD), Angstrom exponent (α), volume size distribution, single scattering albedo (ω) and the complex refractive index were compared. The difference between the two types of instruments was less than 1.3% for the AOD and less than 4% for the single scattering albedo below the wavelength of 670 nm. There is a difference between the volume size distribution patterns derived from two instruments, which is probably due to difference of measurement protocols and inversion algorithms for the respective instruments. AOP under three distinct weather conditions (background, haze, and dust days) over Beijing were compared by using the retrieved skyradiometer and sunphotometer data combined with MODIS satellite results, pyranometer measurements, PM10 measurements, and backtrajectory analysis. The results show that the significant difference of AOP under background, haze, and dust days over Beijing is probably due to different aerosol components under distinct weather conditions.


2005 ◽  
Vol 5 (4) ◽  
pp. 4971-5005 ◽  
Author(s):  
D. Meloni ◽  
A. di Sarra ◽  
G. Pace ◽  
F. Monteleone

Abstract. Aerosol optical properties were retrieved from direct and diffuse spectral irradiance measurements made by a multi-filter rotating shadowband radiometer (MFRSR) at the island of Lampedusa (35.5° N, 12.6° E), in the Central Mediterranean, in the period July 2001–September 2003. In a companion paper (Pace et al., 2005) the aerosol optical depth (AOD) and Ångström exponent were used together with airmass backward trajectories to identify and classify different aerosol types. The MFRSR diffuse-to-direct ratio (DDR) at 415.6 nm and 868.7 nm for aerosol classified as biomass burning-urban/industrial, originating primarily from the European continent, and desert dust, originating from the Sahara, is used in this study to estimate the aerosol single scattering albedo (SSA). A detailed radiative transfer model is initialized with the measured aerosol optical depth; calculations are performed at the two wavelengths varying the SSA values until the modelled DDR matches the MFRSR observations. Sensitivity studies are performed to estimate how uncertainties on AOD, DDR, asymmetry factor (g), and surface albedo influence the retrieved SSA values. The results show that a 3% variation of AOD or DDR produce a change of about 0.02 in the retrieved SSA value at 415.6 and 868.7 nm; a ±0.06 variation of the asymmetry factor g produces a change of the estimated SSA of <0.04 at 415.6 nm, and <0.06 at 868.7 nm; finally, an increase of the assumed surface albedo of 0.05 gives very small changes (0.01–0.02) in the retrieved SSA. The calculations show that the SSA of desert dust (DD) increases with wavelength, from 0.81±0.05 at 415.6 nm to 0.94±0.05 at 868.7 nm; on the contrary, the SSA of urban/industrial (UN) aerosols decreases from 0.96±0.02 at 415.6 nm to 0.87±0.07 at 868.7 nm; the SSA of biomass burning (BB) particles is 0.82±0.04 at 415.6 nm and 0.80±0.05 at 868.7 nm. Episodes of UN aerosols occur usually in June and July; BB aerosol episodes with large AOD and long duration are observed mainly in July and August, the driest months of the year, when the development of fires is favoured.


2007 ◽  
Vol 7 (6) ◽  
pp. 16023-16053 ◽  
Author(s):  
H. Che ◽  
G. Shi ◽  
A. Uchiyama ◽  
A. Yamazaki ◽  
H. Chen ◽  
...  

Abstract. This study compares the aerosol optical and physical properties simultaneously measured by a SKYNET PREDE skyradiometer and AERONET/PHOTONS CIMEL sunphotometer at a location in Beijing, China. Aerosol optical properties (AOP) including the Aerosol Optical Depth (AOD), Angstrom exponent (α), volume size distribution, single scattering albedo (ω) and the complex refractive index were compared. The difference between the two types of instruments was less than 1.3% for the AOD and less than 4% for the single scattering albedo below the wavelength of 670 nm. There is a difference between the volume size distribution patterns derived from two instruments, which is probablely due to difference of measurement protocols and inversion algorithms for the respective instruments. AOP under three distinct weather conditions (background, haze, and dust days) over Beijing were compared by using the retrieved skyradiometer and sunphotometer data combined with MODIS satellite results, pyranometer measurements, PM10 measurements, and backtrajectory analysis. The results show that the significant difference of AOP under background, haze, and dust days over Beijing is probablely due to different aerosol components under distinct weather conditions.


2021 ◽  
Author(s):  
Patrick Weber ◽  
Andreas Petzold ◽  
Oliver Felix Bischof ◽  
Benedikt Fischer ◽  
Marcel Berg ◽  
...  

Abstract. Aerosol intensive optical properties like the Ångström exponents for aerosol light extinction, scattering and absorption, or the single-scattering albedo are indicators for aerosol size distributions, chemical composition and radiative behaviour and contain also source information. The observation of these parameters requires the measurement of aerosol optical properties at multiple wavelengths which usually implies the use of several instruments. Our study aims to quantify the uncertainties of the determination of multiple-wavelengths intensive properties by an optical closure approach, using different test aerosols. In our laboratory study, we measured the full set of aerosol optical properties for a range of light-absorbing aerosols with different properties, mixed externally with ammonium sulphate to generate aerosols of controlled single-scattering albedo. The investigated aerosol types were: fresh combustion soot emitted by an inverted flame soot generator (SOOT, fractal aggregates), Aquadag (AQ, spherical shape), Cabot industrial soot (BC, compact clusters), and an acrylic paint (Magic Black, MB). One focus was on the validity of the Differential Method (DM: absorption = extinction minus scattering) for the determination of Ångström exponents for different particle loads and mixtures of light-absorbing aerosol with ammonium sulphate, in comparison to data obtained from single instruments. The instruments used in this study were two CAPS PMssa (Cavity Attenuated Phase Shift Single Scattering Albedo, λ = 450, 630 nm) for light extinction and scattering coefficients, one Integrating Nephelometer (λ = 450, 550, 700 nm) for light scattering coefficient and one Tricolour Absorption Photometer (TAP, λ = 467, 528, 652 nm) for filter-based light absorption coefficient measurement. Our key finding is that the coefficients of light absorption σap, scattering σsp and extinction σep from the Differential Method agree with data from single reference instruments, and the slopes of regression lines equal unity within the precision error. We found, however, that the precision error for the DM suppresses 100 % for σap values lower than 10–20 Mm−1 for atmospheric relevant single scattering albedo. This increasing uncertainty with decreasing σap yields an absorption Ångström exponent (AAE) that is too uncertain for measurements in the range of atmospheric aerosol loadings. We recommend using DM only for measuring AAE values for σap > 50 Mm−1. Ångström exponents for scattering and extinction are reliable for extinction coefficients from 20 up to 1000 Mm−1 and stay within 10 % deviation from reference instruments, regardless of the chosen method. Single-scattering albedo (SSA) values for 450 nm and 630 nm wavelengths agree with values from the reference method σsp (NEPH)/σep (CAPS PMSSA) with less than 10 % uncertainty for all instrument combinations and sampled aerosol types which fulfil the proposed goal for measurement uncertainty of 10 % proposed by Laj et al., 2020 for GCOS (Global Climate Observing System) applications.


2018 ◽  
Vol 18 (16) ◽  
pp. 11599-11622 ◽  
Author(s):  
Lauren Schmeisser ◽  
John Backman ◽  
John A. Ogren ◽  
Elisabeth Andrews ◽  
Eija Asmi ◽  
...  

Abstract. Given the sensitivity of the Arctic climate to short-lived climate forcers, long-term in situ surface measurements of aerosol parameters are useful in gaining insight into the magnitude and variability of these climate forcings. Seasonality of aerosol optical properties – including the aerosol light-scattering coefficient, absorption coefficient, single-scattering albedo, scattering Ångström exponent, and asymmetry parameter – are presented for six monitoring sites throughout the Arctic: Alert, Canada; Barrow, USA; Pallas, Finland; Summit, Greenland; Tiksi, Russia; and Zeppelin Mountain, Ny-Ålesund, Svalbard, Norway. Results show annual variability in all parameters, though the seasonality of each aerosol optical property varies from site to site. There is a large diversity in magnitude and variability of scattering coefficient at all sites, reflecting differences in aerosol source, transport, and removal at different locations throughout the Arctic. Of the Arctic sites, the highest annual mean scattering coefficient is measured at Tiksi (12.47 Mm−1), and the lowest annual mean scattering coefficient is measured at Summit (1.74 Mm−1). At most sites, aerosol absorption peaks in the winter and spring, and has a minimum throughout the Arctic in the summer, indicative of the Arctic haze phenomenon; however, nuanced variations in seasonalities suggest that this phenomenon is not identically observed in all regions of the Arctic. The highest annual mean absorption coefficient is measured at Pallas (0.48 Mm−1), and Summit has the lowest annual mean absorption coefficient (0.12 Mm−1). At the Arctic monitoring stations analyzed here, mean annual single-scattering albedo ranges from 0.909 (at Pallas) to 0.960 (at Barrow), the mean annual scattering Ångström exponent ranges from 1.04 (at Barrow) to 1.80 (at Summit), and the mean asymmetry parameter ranges from 0.57 (at Alert) to 0.75 (at Summit). Systematic variability of aerosol optical properties in the Arctic supports the notion that the sites presented here measure a variety of aerosol populations, which also experience different removal mechanisms. A robust conclusion from the seasonal cycles presented is that the Arctic cannot be treated as one common and uniform environment but rather is a region with ample spatiotemporal variability in aerosols. This notion is important in considering the design or aerosol monitoring networks in the region and is important for informing climate models to better represent short-lived aerosol climate forcers in order to yield more accurate climate predictions for the Arctic.


2006 ◽  
Vol 6 (3) ◽  
pp. 715-727 ◽  
Author(s):  
D. Meloni ◽  
A. di Sarra ◽  
G. Pace ◽  
F. Monteleone

Abstract. Aerosol optical properties were retrieved from direct and diffuse spectral irradiance measurements made by a multi-filter rotating shadowband radiometer (MFRSR) at the island of Lampedusa (35.5° N, 12.6° E), in the Central Mediterranean, in the period July 2001–September 2003. In a companion paper (Pace et al., 2006) the aerosol optical depth (AOD) and Ångström exponent were used together with airmass backward trajectories to identify and classify different aerosol types. The MFRSR diffuse-to-direct ratio (DDR) at 415.6 nm and 868.7 nm for aerosol classified as "biomass burning-urban/industrial", originating primarily from the European continent, and desert dust, originating from the Sahara, is used in this study to estimate the aerosol single scattering albedo (SSA). A detailed radiative transfer model is initialised with the measured aerosol optical depth; calculations are performed at the two wavelengths varying the SSA values until the modelled DDR matches the MFRSR observations. Sensitivity studies are performed to estimate how uncertainties on AOD, DDR, asymmetry factor (g), and surface albedo influence the retrieved SSA values. The results show that a 3% variation of AOD or DDR produce a change of about 0.02 in the retrieved SSA value at 415.6 and 868.7 nm; a ±0.06 variation of the asymmetry factor g produces a change of the estimated SSA of <0.04 at 415.6 nm, and <0.06 at 868.7 nm; finally, an increase of the assumed surface albedo of 0.05 causes very small changes (0.01–0.02) in the retrieved SSA. The calculations show that the SSA of desert dust (DD) increases with wavelength, from 0.81±0.05 at 415.6 nm to 0.94±0.05 at 868.7 nm; on the contrary, the SSA of urban/industrial (UN) aerosols decreases from 0.96±0.02 at 415.6 nm to 0.87±0.07 at 868.7 nm; the SSA of biomass burning (BB) particles is 0.82±0.04 at 415.6 nm and 0.80±0.05 at 868.7 nm. Episodes of UN aerosols occur usually in June and July; long lasting BB aerosol episodes with large AOD are observed mainly in July and August, the driest months of the year, when the development of fires is frequent.


MAUSAM ◽  
2021 ◽  
Vol 68 (4) ◽  
pp. 673-688
Author(s):  
KANIKA TANEJA ◽  
S. D. ATTRI ◽  
SHAMSHAD AHMAD ◽  
KAFEEL AHMAD ◽  
V. K. SONI ◽  
...  

The present work revolves around the comparative analysis of aerosol optical properties in a mega city, Delhi and in a nearby urban area, Rohtak. It is pertinent to note that despite of the close proximity and similar meteorological conditions, the two study locations show significant differences in aerosol characteristics. The study is conducted using ground based Sky-radiometer measurements for a period of one year. The mean annual Aerosol Optical Depth (AOD) at 500 nm over Delhi and Rohtak is observed to be 1.01 and 0.73 respectively, with correlation coefficient of 0.67 and mean absolute difference of 0.51. The magnitude of AOD in Delhi is higher than in Rohtak throughout the year, except in post-monsoon season. The difference in Angstrom exponent (alpha) between the stations is minimal. However, lower magnitude of alpha is observed in Rohtak, indicating presence of more concentration of coarse-mode particles. Single Scattering Albedo (SSA) also shows seasonal variation with significantly lower values in Delhi throughout the year, indicating contribution of absorbing type of aerosols (like black carbon). The volume concentration in fine-size is found to be higher in Delhi than in Rohtak, indicating combined effect of dust, vehicular, biomass burning and industrial emissions. The aerosol classification via relationship between AOD and alpha shows that urban/biomass burning (U/B) aerosols are dominant in Delhi and mixed type (MT) aerosols in Rohtak during winter and pre-monsoon.


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