scholarly journals Development of a cavity enhanced aerosol albedometer

2014 ◽  
Vol 7 (3) ◽  
pp. 2981-3019
Author(s):  
W. Zhao ◽  
X. Xu ◽  
M. Dong ◽  
W. Chen ◽  
X. Gu ◽  
...  

Abstract. We report on the development of a cavity enhanced aerosol single scattering albedometer incorporating incoherent broad-band cavity-enhanced spectroscopy (IBBCEAS) approach and an integrating sphere (IS) for simultaneous in situ measurements of aerosol scattering and extinction coefficients in the exact same sample volume. The cavity enhanced albedometer employed a blue light-emitting diode (LED) based IBBCEAS approach for the measurement of wavelength-resolved aerosol optical extinction over the spectral range of 445–480 nm. An integrating sphere nephelometer coupled to the IBBCEAS setup was used for the measurement of aerosol scattering. The scattering signal was measured with a single channel photomultiplier tube (PMT), providing an integrated value over a narrow bandwidth (FWHM ~ 9 nm) in the spectral region of 465–474 nm. A scattering coefficient at a wavelength of 470 nm was deduced as an averaged scattering value and used for data analysis and instrumental performance comparison. Performance evaluation of the albedometer was carried out using laboratory-generated particles and ambient aerosol. The scattering and extinction measurements of monodisperse polystyrene latex (PSL) spheres generated in laboratory proved excellent correlation between two channels of the albedometer. The retrieved refractive index (RI) from the measured scattering and extinction efficiencies agreed well with the values reported in previously published papers. Aerosol light scattering and extinction coefficients, single scattering albedo (SSA) and NO2 concentrations in an ambient sample were directly and simultaneously measured using the developed albedometer. The developed instrument was validated via an intercomparison of the measured aerosol scattering coefficient and NO2 trace concentration against a TSI 3563 integrating nephelometer and a chemiluminescence detector, respectively.

2014 ◽  
Vol 7 (8) ◽  
pp. 2551-2566 ◽  
Author(s):  
W. Zhao ◽  
X. Xu ◽  
M. Dong ◽  
W. Chen ◽  
X. Gu ◽  
...  

Abstract. We report on the development of a cavity-enhanced aerosol single-scattering albedometer based on incoherent broadband cavity-enhanced absorption spectroscopy (IBBCEAS) combined with an integrating sphere (IS) for simultaneous in situ measurements of aerosol scattering and extinction coefficients in an exact same sample volume. The cavity-enhanced albedometer employed a blue light-emitting-diode (LED)-based IBBCEAS approach for the measurement of wavelength-resolved aerosol optical extinction over the spectral range of 445–480 nm and an integrating sphere nephelometer coupled to the IBBCEAS setup for the measurement of aerosol scattering. The scattering signal was measured with a single-channel photomultiplier tube (PMT), providing an averaged value over a narrow bandwidth (full-width at half-maximum, FWHM, ~ 9 nm) in the spectral region of 465–474 nm. A scattering coefficient at a wavelength of 470 nm was deduced as an averaged scattering value over the spectral region of 465–474 nm and used for data analysis and instrumental performance comparison. Performance evaluation of the albedometer was carried out using laboratory-generated particles and ambient aerosol. The scattering and extinction measurements of monodisperse polystyrene latex (PSL) spheres generated in the laboratory proved excellent correlation between two channels of the albedometer. The retrieved refractive index (RI) of the PSL particles from the measured scattering and extinction efficiencies agreed well with the values reported in previously published papers. Aerosol light scattering and extinction coefficients, single-scattering albedo (SSA) and NO2 concentrations in an ambient sample were directly and simultaneously measured using the albedometer developed. The instrument developed was validated via an intercomparison of the measured aerosol scattering coefficients and NO2 trace gas concentrations to a TSI 3563 integrating nephelometer and a chemiluminescence detector, respectively.


2021 ◽  
Vol 14 (2) ◽  
pp. 819-851
Author(s):  
Rob L. Modini ◽  
Joel C. Corbin ◽  
Benjamin T. Brem ◽  
Martin Irwin ◽  
Michele Bertò ◽  
...  

Abstract. The CAPS PMssa monitor is a recently commercialized instrument designed to measure aerosol single-scattering albedo (SSA) with high accuracy (Onasch et al., 2015). The underlying extinction and scattering coefficient measurements made by the instrument also allow calculation of aerosol absorption coefficients via the extinction-minus-scattering (EMS) method. Care must be taken with EMS measurements due to the occurrence of large subtractive error amplification, especially for the predominantly scattering aerosols that are typically found in the ambient atmosphere. Practically this means that although the CAPS PMssa can measure scattering and extinction coefficients with high accuracy (errors on the order of 1 %–10 %), the corresponding errors in EMS-derived absorption range from ∼10 % to greater than 100 %. Therefore, we examine the individual error sources in detail with the goal of constraining these as tightly as possible. Our main focus is on the correction of the scattered light truncation effect (i.e., accounting for the near-forward and near-backward scattered light that is undetectable by the instrument), which we show to be the main source of underlying error in atmospheric applications. We introduce a new, modular framework for performing the truncation correction calculation that enables the consideration of additional physical processes such as reflection from the instrument's glass sampling tube, which was neglected in an earlier truncation model. We validate the truncation calculations against comprehensive laboratory measurements. It is demonstrated that the process of glass tube reflection must be considered in the truncation calculation, but that uncertainty still remains regarding the effective length of the optical cavity. Another important source of uncertainty is the cross-calibration constant that quantitatively links the scattering coefficient measured by the instrument to its extinction coefficient. We present measurements of this constant over a period of ∼5 months that demonstrate that the uncertainty in this parameter is very well constrained for some instrument units (2 %–3 %) but higher for others. We then use two example field datasets to demonstrate and summarize the potential and the limitations of using the CAPS PMssa for measuring absorption. The first example uses mobile measurements on a highway road to highlight the excellent responsiveness and sensitivity of the instrument, which enables much higher time resolution measurements of relative absorption than is possible with filter-based instruments. The second example from a stationary field site (Cabauw, the Netherlands) demonstrates how truncation-related uncertainties can lead to large biases in EMS-derived absolute absorption coefficients. Nevertheless, we use a subset of fine-mode-dominated aerosols from the dataset to show that under certain conditions and despite the remaining truncation uncertainties, the CAPS PMssa can still provide consistent EMS-derived absorption measurements, even for atmospheric aerosols with high SSA. Finally, we present a detailed list of recommendations for future studies that use the CAPS PMssa to measure absorption with the EMS method. These recommendations could also be followed to obtain accurate measurements (i.e., errors less than 5 %–10 %) of SSA and scattering and extinction coefficients with the instrument.


2011 ◽  
Vol 11 (7) ◽  
pp. 19213-19222 ◽  
Author(s):  
H. Moosmüller ◽  
R. K. Chakrabarty

Abstract. Ångström coefficients are commonly used to parameterize the slow wavelength dependence of aerosol scattering, absorption, and extinction coefficients and single scattering albedo. Here we introduce simple analytical relationships between these coefficients that establish a framework for intercomparison between theory and experimental results from different instruments and platforms and allow for closure studies and improved physical understanding.


2020 ◽  
Author(s):  
Rob L. Modini ◽  
Joel C. Corbin ◽  
Benjamin T. Brem ◽  
Martin Irwin ◽  
Michele Bertò ◽  
...  

Abstract. The CAPS PMssa monitor is a recently commercialized instrument designed to measure aerosol single scattering albedo (SSA) with high accuracy (Onasch et al., 2015). The underlying extinction and scattering coefficient measurements made by the instrument also allow calculation of aerosol absorption coefficients via the extinction-minus-scattering (EMS) method. Care must be taken with EMS measurements due to the occurrence of large subtractive error amplification, especially for the predominantly scattering aerosols that are typically found in the ambient atmosphere. Practically this means that although the CAPS PMssa can measure scattering and extinction coefficients with high accuracy (errors on the order of 1–10 %), the corresponding errors in EMS-derived absorption range from ~ 10 % to greater than 100 %. Therefore, we examine the individual error sources in detail with the goal of constraining these as tightly as possible. Our main focus is on the correction of the scattered light truncation effect (i.e., accounting for the near-forward and -backward scattered light that is undetectable by the instrument), which we show to be the main source of underlying error in atmospheric applications. We introduce a new, modular framework for performing the truncation correction calculation that enables the consideration of additional physical processes such as reflection from the instrument’s glass sampling tube, which was neglected in an earlier truncation model. We validate the truncation calculations against comprehensive laboratory measurements. It is demonstrated that the process of glass tube reflection must be considered in the truncation calculation, but that uncertainty still remains regarding the effective length of the optical cavity. Another important source of uncertainty is the cross calibration constant that quantitatively links the scattering coefficient measured by the instrument to its extinction coefficient. We present measurements of this constant over a period of ~ 5 months that demonstrate that the uncertainty in this parameter is very well constrained for some instrument units (2–3 %), but higher for others. We then use two example field datasets to demonstrate and summarize the potential and the limitations of using the CAPS PMssa for measuring absorption. The first example uses mobile measurements on a highway road to highlight the excellent responsiveness and sensitivity of the instrument, which enables much higher time resolution measurements of relative absorption than is possible with filter-based instruments. The second example from a stationary field site (Cabauw, the Netherlands) demonstrates how truncation-related uncertainties can lead to large biases in EMS-derived absolute absorption coefficients. Nevertheless, we use a subset of fine-mode dominated aerosols from the dataset to show that under certain conditions and despite the remaining truncation uncertainties, the CAPS PMssa can still provide consistent EMS-derived absorption measurements, even for atmospheric aerosols with high SSA. Finally, we present a detailed list of recommendations for future studies that use the CAPS PMssa to measure absorption with the EMS method. These recommendations could also be followed to obtain accurate measurements (i.e., errors less than 5–10 %) of SSA, and scattering and extinction coefficients with the instrument.


2011 ◽  
Vol 11 (20) ◽  
pp. 10677-10680 ◽  
Author(s):  
H. Moosmüller ◽  
R. K. Chakrabarty

Abstract. Ångström coefficients are commonly used to parameterize the slow wavelength dependence of aerosol scattering, absorption, and extinction coefficients and single scattering albedo. Here we introduce simple analytical relationships between these coefficients that establish a framework for intercomparison between theory and experimental results from different instruments and platforms and allow for closure studies and improved physical understanding.


2012 ◽  
Vol 12 (12) ◽  
pp. 5647-5659 ◽  
Author(s):  
A. Leskinen ◽  
A. Arola ◽  
M. Komppula ◽  
H. Portin ◽  
P. Tiitta ◽  
...  

Abstract. We introduce a four-year (in 2006–2010) continuous data set of aerosol optical properties at Puijo in Kuopio, Finland. We study the annual and diurnal variation of the aerosol scattering and absorption coefficients, hemispheric backscattering fraction, scattering Ångström exponent, and single scattering albedo, whose median values over this period were 7.2 Mm−1 (at 550 nm), 1.0 Mm−1 (at 637 nm), 0.15, 1.93 (between 450 and 550 nm), and 0.85, respectively. The scattering coefficient peaked in the spring and autumn, being 2–4 times those in the summer and winter. An exception was the summer of 2010, when the scattering coefficient was elevated to ~300 Mm−1 by plumes from forest fires in Russia. The absorption coefficient peaked in the winter when soot-containing particles derived from biomass burning were present. The higher relative absorption coefficients resulted in lower single scattering albedo in winter. The optical properties varied also with wind direction and time of the day, indicating the effect of the local pollutant sources and the age of the particles. Peak values in the single scattering albedo were observed when the wind blew from a paper mill and from the sector without local pollutant sources. These observations were linked, respectively, to the sulphate-rich aerosol from the paper mill and the oxygenated organics in the aged aerosol, which both are known to increase the scattering characteristics of aerosols. Decreases in the single scattering albedo in the morning and afternoon, distinct in the summertime, were linked to the increased traffic density at these hours. The scattering and absorption coefficients of residential and long-range transported aerosol (two separate cloud events) were found to be decreased by clouds. The effect was stronger for the scattering than absorption, indicating preferential activation of the more hygroscopic aerosol with higher scattering characteristics.


1988 ◽  
Vol 18 (8) ◽  
pp. 1008-1016 ◽  
Author(s):  
D. G. Leckie ◽  
P. M. Teillet ◽  
G. Fedosejevs ◽  
D. P. Ostaff

Knowledge of the spectral characteristics of trees with varying degrees of needle loss is essential for developing remote sensing techniques for assessing defoliation. Spectra covering the range 400–2400 nm were acquired for single tree crowns suffering varying degrees of cumulative defoliation due to the spruce budworm (Choristoneurafumiferana (Clem.)), using a spectrometer mounted in the bucket of a boom truck. Spectra over the range 360–1100 nm were also obtained for the components of defoliated trees (i.e., needles, bare branches, and lichen), using a separate spectrometer and integrating sphere. Estimates of defoliation symptoms of each tree were made from the ground and above the tree. Changes in reflectance had a close and simple relationship with the defoliation symptoms measured. The spectral differences due to cumulative defoliation that were observed were broad-band features. The best spectral regions for differentiating levels of cumulative defoliation symptoms were the blue, red, shorter near-infrared wavelengths, and middle-infrared. Although currently available satellite and airborne sensors operate in these spectral regions, defoliation assessment may be improved by the use of optimized spectral bands.


2013 ◽  
Vol 13 (10) ◽  
pp. 27811-27854 ◽  
Author(s):  
N. Ma ◽  
W. Birmili ◽  
T. Müller ◽  
T. Tuch ◽  
Y. F. Cheng ◽  
...  

Abstract. This work analyses optical properties of the dry tropospheric aerosol measured at the regional GAW observation site Melpitz in East Germany. For a continuous observation period between 2007 and 2010, we provide representative values of the dry-state scattering coefficient, the hemispheric backscattering coefficient, the absorption coefficient, single scattering albedo, and the Ångström exponent. Besides the direct measurement, the aerosol scattering coefficient was alternatively computed from experimental particle number size distributions using a Mie code. Within pre-defined limits, a closure could be achieved with the direct measurement. The achievement of closure implies that such calculations can be used as a high-level quality control measure for data sets involving multiple instrumentation. All dry optical properties showed significant annual variations, which were attributed to corresponding variations in the regional emission fluxes, the intensity of secondary particle formation, and the mixed layer height. Air mass classification showed that atmospheric stability is a major factor influencing the dry aerosol properties at the GAW station. In the cold season, temperature inversions limit the volume available for atmospheric mixing, so that the aerosol optical properties near the ground proved quite sensitive to the geographical origin of the air mass. In the warm season, when the atmosphere is usually well-mixed during day-time, considerably less variability was observed for the optical properties between different air masses. This work provides, on the basis of quality-checked in-situ measurements, a first step towards a climatological assessment of direct aerosol radiative forcing in the region under study.


2020 ◽  
Vol 13 (12) ◽  
pp. 6755-6769
Author(s):  
Yunxia Huang ◽  
Vijay Natraj ◽  
Zhao-Cheng Zeng ◽  
Pushkar Kopparla ◽  
Yuk L. Yung

Abstract. As a greenhouse gas with strong global warming potential, atmospheric methane (CH4) emissions have attracted a great deal of attention. Although remote sensing measurements can provide information about CH4 sources and emissions, accurate retrieval is challenging due to the influence of atmospheric aerosol scattering. In this study, imaging spectroscopic measurements from the Airborne Visible/Infrared Imaging Spectrometer – Next Generation (AVIRIS-NG) in the shortwave infrared are used to compare two retrieval techniques – the traditional matched filter (MF) method and the optimal estimation (OE) method, which is a popular approach for trace gas retrievals. Using a numerically efficient radiative transfer model with an exact single-scattering component and a two-stream multiple-scattering component, we also simulate AVIRIS-NG measurements for different scenarios and quantify the impact of aerosol scattering in the two retrieval schemes by including aerosols in the simulations but not in the retrievals. The presence of aerosols causes an underestimation of CH4 in both the MF and OE retrievals; the biases increase with increasing surface albedo and aerosol optical depth (AOD). Aerosol types with high single-scattering albedo and low asymmetry parameter (such as water-soluble aerosols) induce large biases in the retrieval. When scattering effects are neglected, the MF method exhibits lower fractional retrieval bias compared to the OE method at high CH4 concentrations (2–5 times typical background values) and is suitable for detecting strong CH4 emissions. For an AOD value of 0.3, the fractional biases of the MF retrievals are between 1.3 % and 4.5 %, while the corresponding values for OE retrievals are in the 2.8 %–5.6 % range. On the other hand, the OE method is an optimal technique for diffuse sources (<1.5 times typical background values), showing up to 5 times smaller fractional retrieval bias (8.6 %) than the MF method (42.6 %) for the same AOD scenario. However, when aerosol scattering is significant, the OE method is superior since it provides a means to reduce biases by simultaneously retrieving AOD, surface albedo, and CH4. The results indicate that, while the MF method is good for plume detection, the OE method should be employed to quantify CH4 concentrations, especially in the presence of aerosol scattering.


2019 ◽  
Author(s):  
Mohanan R. Manoj ◽  
Sreedharan K. Satheesh ◽  
Krishnaswamy K. Moorthy ◽  
Hugh Coe

Abstract. Vertical structures of aerosol single scattering albedo (SSA), from near the surface through the free troposphere, have been estimated for the first time at distinct geographical locations over the Indian mainland and adjoining oceans, using in-situ measurements of aerosol scattering and absorption coefficients aboard the FAAM BAe-146 aircraft during the South West Asian Aerosol Monsoon Interactions (SWAAMI) campaign from June to July 2016. These are used to examine the spatial variation of SSA profiles and also to characterize its transformation from just prior to the onset of Indian Summer Monsoon (June 2016) to its active phase (July 2016). Very strong aerosol absorption, with SSA values as low as 0.7, persisted in the lower altitudes (


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