A theoretical study of the effect of relative humidity on light scattering by tropospheric aerosols

1993 ◽  
Vol 98 (D10) ◽  
pp. 18435-18439 ◽  
Author(s):  
Dean Hegg ◽  
Timothy Larson ◽  
Po-Fat Yuen
Keyword(s):  
Light Scattering ◽  
Relative Humidity ◽  
Theoretical Study ◽  
Tropospheric Aerosols

scholarly journals Linking variations in sea spray aerosol particle hygroscopicity to composition during two microcosm experiments

2016 ◽  
Author(s):  
Sara D. Forestieri ◽  
Gavin C. Cornwell ◽  
Taylor M. Helgestad ◽  
Kathryn A. Moore ◽  
Christopher Lee ◽  
...  
Keyword(s):  
Light Scattering ◽  
Relative Humidity ◽  
Salt Content ◽  
Sea Salt ◽  
Sea Spray ◽  
Hygroscopic Growth ◽  
Phytoplankton Blooms ◽  
Aerosol Composition ◽  
Sea Spray Aerosol ◽  
Indoor And Outdoor

Abstract. The extent to which water uptake influences the light scattering ability of marine sea spray aerosol (SSA) particles depends critically on SSA chemical composition. The organic fraction of SSA can increase during phytoplankton blooms, decreasing the salt content and therefore the hygroscopicity of the particles. In this study, subsaturated hygroscopic growth factors at 85 % relative humidity (GF(85 %)) of SSA particles were quantified during two induced phytoplankton blooms in marine aerosol reference tanks (MARTs). One MART was illuminated with fluorescent lights and the other was illuminated with sunlight, referred to as the "indoor" and "outdoor" MARTs, respectively. GF(85 %) values for SSA particles were derived from measurements of light scattering and particle size distributions, concurrently with online single particle and bulk aerosol composition measurements. During both microcosm experiments, the observed bulk average GF(85 %) values were depressed substantially relative to pure, inorganic sea salt, by 10 to 19 %, with a one (indoor MART) and six (outdoor MART) day lag between GF(85 %) depression and the peak chlorophyll-a concentrations. The fraction of organiccontaining SSA particles generally increased after the peak of the phytoplankton blooms. The GF(85 %) values were inversely correlated with the fraction of particles containing organic or other biological markers. This indicates these particles were less hygroscopic than the particles identified as predominately sea salt containing and demonstrates a clear relationship between SSA particle composition and the sensitivity of light scattering to variations in relative humidity. The implications of these observations to the direct climate effects of SSA particles are discussed.

First global assessment of modelled aerosol hygroscopicity in the context of other aerosol optical properties

2021 ◽  
Author(s):  
Maria Ángeles Burgos Simón ◽  
Elisabeth Andrews ◽  
Gloria Titos ◽  
Angela Benedetti ◽  
Huisheng Bian ◽  
...  
Keyword(s):  
Optical Properties ◽  
Light Scattering ◽  
Relative Humidity ◽  
Water Uptake ◽  
Chem Phys ◽  
Earth System ◽  
Aerosol Optical Properties ◽  
System Models ◽  
Earth System Models

<p>The particle hygroscopic growth impacts the optical properties of aerosols and, in turn, affects the aerosol-radiation interaction and calculation of the Earth’s radiative balance. The dependence of particle light scattering on relative humidity (RH) can be described by the scattering enhancement factor f(RH), defined as the ratio between the particle light scattering coefficient at a given RH divided by its dry value.</p><p>The first effort of the AeroCom Phase III – INSITU experiment was to develop an observational dataset of scattering enhancement values at 26 sites to study the uptake of water by atmospheric aerosols, and evaluate f(RH) globally (Burgos et al., 2019). Model outputs from 10 Earth System Models (CAM, CAM-ATRAS, CAM-Oslo, GEOS-Chem, GEOS-GOCART, MERRAero, TM5, OsloCTM3, IFS-AER, and ECMWF) were then evaluated against this in-situ dataset. Building on these results, we investigate f(RH) in the context of other aerosol optical and chemical properties, making use of the same 10 Earth System Models (ESMs) and in-situ measurements as in Burgos et al. (2020) and Titos et al. (2021).</p><p>Given the difficulties of deploying and maintaining instrumentation for long-term, accurate and comprehensive f(RH) observations, it is desirable to find an observational proxy for f(RH). This observation-based proxy would also need to be reproduced in modelling space. Our aim here is to evaluate how ESMs currently represent the relationship between f(RH), scattering Ångström exponent (SAE), and single scattering albedo (SSA). This work helps to identify current challenges in modelling water-uptake by aerosols and their impact on aerosol optical properties within Earth system models.</p><p>We start by analyzing the behavior of SSA with RH, finding the expected increase with RH for all site types and models. Then, we analyze the three variables together (f(RH)-SSA-SAE relationship). Results show that hygroscopic particles tend to be bigger and scatter more than non-hygroscopic small particles, though variability within models is noticeable. This relationship can be further studied by relating SAE to model chemistry, by selecting those grid points dominated by a single chemical component (mass mixing ratios > 90%). Finally, we analyze model performance at three specific sites representing different aerosol types: Arctic, marine and rural. At these sites, the model data can be exactly temporally and spatially collocated with the observations, which should help to identify the models which exhibit better agreement with measurements and for which aerosol type.</p><p> </p><p>Burgos, M.A. et al.: A global view on the effect of water uptake on aerosol particle light scattering. Sci Data 6, 157. https://doi.org/10.1038/s41597-019-0158-7, 2019.</p><p>Burgos, M.A. et al.: A global model–measurement evaluation of particle light scattering coefficients at elevated relative humidity, Atmos. Chem. Phys., 20, 10231–10258, https://doi.org/10.5194/acp-20-10231-2020, 2020.</p><p>Titos, G. et al.: A global study of hygroscopicity-driven light scattering enhancement in the context of other in-situ aerosol optical properties, Atmos. Chem. Phys. Discuss. [preprint], https://doi.org/10.5194/acp-2020-1250, in review, 2020.</p>

Water sorption in wood and modified wood at high values of relative humidity. Part 2: Appendix. Theoretical assessment of the amount of capillary water in wood microvoids

Holzforschung ◽  
2010 ◽  
Vol 64 (3) ◽  
Author(s):  
Emil Tang Engelund ◽  
Lisbeth G. Thygesen ◽  
Preben Hoffmeyer
Keyword(s):  
Relative Humidity ◽  
Theoretical Study ◽  
Capillary Condensation ◽  
Small Contribution ◽  
Structural Elements ◽  
Capillary Water ◽  
Bordered Pits ◽  
Condensed Water ◽  
Theoretical Assessment ◽  
Theoretical Amount

Abstract A theoretical study of the amount of moisture held in wood as capillary condensed water in the relative humidity (RH) range of 90–99.9% is carried out. The study is based on idealized geometries of the softwood structure related to micrographs. It is confined to structural elements such as bordered pits and the pointed ends of tracheids. The theoretical amount of water in these elements is found by employing the Kelvin equation. An equal amount of earlywood and latewood cells with different geometries and with different amounts of pits is assumed. The effect of pit aspiration is considered, and different degrees of pit aspiration are assigned to earlywood and latewood. We suggest based on the results that capillary condensation makes only a very small contribution to the equilibrium moisture content. At 99.9% RH the contribution amounts to less than 0.0035 kg water per kg dry wood. This is in line with the experimental results presented in Part 1 of this study.

Semi-Analytical Study of Aerosol Washout by Rain

2012 ◽  
Author(s):  
Pascal Lemaitre ◽  
Amandine Nuboer ◽  
Arnaud Querel ◽  
Guillaume Depuydt ◽  
Emmanuel Porcheron
Keyword(s):  
Light Scattering ◽  
Relative Humidity ◽  
White Light ◽  
Analytical Approach ◽  
Analytical Study ◽  
Aerosol Particles ◽  
Companion Paper ◽  
Meteorological Conditions ◽  
Internal Diameter ◽  
Special Generator

The accidents of Chernobyl and Fukushima have shown the necessity to better understand all the mechanisms implied in the scavenging of aerosol particles released to the atmosphere during a nuclear accident. Among all the phenomena involved in the deposition of aerosol particles, we focus here on the aerosol particles scavenging by the raindrops below the clouds, also called washout (as opposed to the rainout, which concerns scavenging inside the clouds). The strategy of IRSN to enhance the knowledge and the modelling of any mechanism involved in the washout of aerosol particles by rain spans from environmental studies, to analytical ones. The semi-analytical approach chosen here is halfway between these two modes of reasoning. A companion paper is also submitted to the conference to present the microphysical approach chosen at IRSN. In order to perform this study, aerosol particles were dispersed in the TOSQAN chamber, which is a large cylindrical enclosure (4.8 m height with 1.5 m internal diameter). The aerosol particles once dispersed, synthetic rains of different kinds (from stratiform to convective rains) can be activated. Finally, the instantaneous spectral scavenging coefficients are determined from the spectral decrease of aerosol particles concentration in the chamber as a function of time. In order to be able to produce synthetic rains representative of any tropospheric events, a special generator has been designed; it is based on a vibro-rotative disk. This generator is able to produce monodispersed rains at the top of the TOSQAN chamber with rainfall rates from 7 to 15 mm/h and drops diameters from 0.5 to 2.5 mm injected at velocities close to their terminal one. During these tests, the spectral aerosol concentration is measured in line with the help of a Welas granulometer. This instrument is based on white light scattering. The results of these experiments highlight the influence of “meteorological” conditions inside the chamber on the washout of the chamber atmosphere, especially when the relative humidity is reaching saturation.

scholarly journals Effects of relative humidity on aerosol light scattering in the Arctic

2010 ◽  
Vol 10 (8) ◽  
pp. 3875-3890 ◽  
Author(s):  
P. Zieger ◽  
R. Fierz-Schmidhauser ◽  
M. Gysel ◽  
J. Ström ◽  
S. Henne ◽  
...  
Keyword(s):  
Standard Deviation ◽  
Light Scattering ◽  
Relative Humidity ◽  
Aerosol Particles ◽  
Aerosol Size Distribution ◽  
Hygroscopic Growth ◽  
Scattering Coefficients ◽  
Dry Conditions ◽  
Hygroscopic Particles

Abstract. Aerosol particles experience hygroscopic growth in the ambient atmosphere. Their optical properties – especially the aerosol light scattering – are therefore strongly dependent on the ambient relative humidity (RH). In-situ light scattering measurements of long-term observations are usually performed under dry conditions (RH>30–40%). The knowledge of this RH effect is of eminent importance for climate forcing calculations or for the comparison of remote sensing with in-situ measurements. This study combines measurements and model calculations to describe the RH effect on aerosol light scattering for the first time for aerosol particles present in summer and fall in the high Arctic. For this purpose, a field campaign was carried out from July to October 2008 at the Zeppelin station in Ny-Ålesund, Svalbard. The aerosol light scattering coefficient σsp(λ) was measured at three distinct wavelengths (λ=450, 550, and 700 nm) at dry and at various, predefined RH conditions between 20% and 95% with a recently developed humidified nephelometer (WetNeph) and with a second nephelometer measuring at dry conditions with an average RH<10% (DryNeph). In addition, the aerosol size distribution and the aerosol absorption coefficient were measured. The scattering enhancement factor f(RH, λ) is the key parameter to describe the RH effect on σsp(λ) and is defined as the RH dependent σsp(RH, λ) divided by the corresponding dry σsp(RHdry, λ). During our campaign the average f(RH=85%, λ=550 nm) was 3.24±0.63 (mean ± standard deviation), and no clear wavelength dependence of f(RH, λ) was observed. This means that the ambient scattering coefficients at RH=85% were on average about three times higher than the dry measured in-situ scattering coefficients. The RH dependency of the recorded f(RH, λ) can be well described by an empirical one-parameter equation. We used a simplified method to retrieve an apparent hygroscopic growth factor g(RH), defined as the aerosol particle diameter at a certain RH divided by the dry diameter, using the WetNeph, the DryNeph, the aerosol size distribution measurements and Mie theory. With this approach we found, on average, g(RH=85%) values to be 1.61±0.12 (mean±standard deviation). No clear seasonal shift of f(RH, λ) was observed during the 3-month period, while aerosol properties (size and chemical composition) clearly changed with time. While the beginning of the campaign was mainly characterized by smaller and less hygroscopic particles, the end was dominated by larger and more hygroscopic particles. This suggests that compensating effects of hygroscopicity and size determined the temporal stability of f(RH, λ). During sea salt influenced periods, distinct deliquescence transitions were observed. At the end we present a method on how to transfer the dry in-situ measured aerosol scattering coefficients to ambient values for the aerosol measured during summer and fall at this location.

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