scholarly journals Measurement of scattering and absorption properties of dust aerosol in a Gobi farmland region of northwest China — a potential anthropogenic influence

2017 ◽  
Author(s):  
Jianrong Bi ◽  
Jianping Huang ◽  
Jinsen Shi ◽  
Zhiyuan Hu ◽  
Tian Zhou ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Source Region ◽  
Inversion Layer ◽  
Vertical Mixing ◽  
Northwest China ◽  
Single Scattering ◽  
Dust Aerosol ◽  
Dust Particles ◽  
Valley Wind ◽  
Average Mass

Abstract. We conducted a comprehensive field campaign on exploring the optical characteristics of mineral dust in Dunhuang farmland nearby the Gobi deserts of northwest China during spring of 2012. The day-to-day and diurnal variations of dust aerosol showed prominent features throughout the experiment, primarily attributable to frequent dust events and local anthropogenic emissions. The overall average mass concentration of the particulate matter with an aerodynamic diameter less than 10 μm (PM10), light scattering coefficient (σsp,670), absorption coefficient (σap,670), and single-scattering albedo (SSA670) were 113±169 μgm-3, 53.3 ± 74.8 Mm-1,  3.2± 2.4 Mm-1, and 0.913 ± 0.05, which were comparable to the background levels in southern United States, but smaller than that in the eastern and other northwestern China. The anthropogenic dust produced by agricultural cultivations (e.g., land planning, plowing, and disking) exerted a significant superimposed effect on high dust concentrations in Dunhuang farmland prior to the growing season (i.e., from 1 April to 10 May). Strong south valley wind and vertical mixing in daytime scavenged the pollution and weak northeast mountain wind and stable inversion layer at night favorably accumulated the air pollutants near the surface. In the afternoon (13:00–18:00 LT), mean SSA670 was 0.945 ± 0.04 that was predominant by dust particles, whereas finer particles and lower SSA670 values (~ 0.90–0.92) were measured at night, suggesting the potential influence by the mixed dust-pollutants. During a typical biomass burning event on 4 April 2012, σap,670 changed from ~ 2.0 Mm-1 to 4.75 Mm-1 and SSA670 changed from ~ 0.90 to ~ 0.83, implying remarkable modification of aerosol absorptive properties induced by human activities. The findings of this study would help to advance an in-depth understanding of the interaction among dust aerosol, atmospheric chemistry, and climate change in desert source region.

scholarly journals Measurement of scattering and absorption properties of dust aerosol in a Gobi farmland region of northwestern China – a potential anthropogenic influence

2017 ◽  
Vol 17 (12) ◽  
pp. 7775-7792 ◽  
Author(s):  
Jianrong Bi ◽  
Jianping Huang ◽  
Jinsen Shi ◽  
Zhiyuan Hu ◽  
Tian Zhou ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Source Region ◽  
Inversion Layer ◽  
Vertical Mixing ◽  
Northwest China ◽  
Dust Aerosol ◽  
Dust Particles ◽  
Gobi Desert ◽  
Valley Wind ◽  
Average Mass

Abstract. We conducted a comprehensive field campaign to explore the optical characteristics of mineral dust in Dunhuang farmland near the Gobi Desert of northwest China during spring of 2012. The day-to-day and diurnal variations of dust aerosol showed prominent features throughout the experiment, primarily attributable to frequent dust events and local anthropogenic emissions. The overall average mass concentrations of the particulate matter with an aerodynamic diameter less than 10 µm (PM10), light scattering coefficient (σsp, 670), absorption coefficient (σap, 670), and single-scattering albedo (SSA670) were 113 ± 169 µg m−3, 53.3 ± 74.8 Mm−1, 3.2 ± 2.4 Mm−1, and 0.913 ± 0.05, respectively, which were comparable to the background levels in the southern United States but smaller than those in the eastern and other northwestern Chinese cities. The anthropogenic dust produced by agricultural cultivations (e.g., land planning, plowing, and disking) exerted a significant superimposed effect on high dust concentrations in Dunhuang farmland prior to the growing season (i.e., from 1 April to 10 May). Strong south valley wind and vertical mixing in daytime scavenged the pollution, and the weak northeast mountain wind and stable inversion layer at night favorably accumulated the air pollutants near the surface. In the afternoon (13:00–18:00 LT, local time), mean SSA670 was 0.945 ± 0.04 predominantly from dust particles, whereas finer particles and lower SSA670 values ( ∼  0.90–0.92) were measured at night, suggesting the potential influence by the mixed dust pollutants. During a typical biomass burning event on 4 April 2012, σap, 670 increased from  ∼  2.0 to 4.75 Mm−1 and SSA670 changed from  ∼  0.90 to  ∼  0.83, implying remarkable modification of aerosol absorptive properties induced by human activities. The findings of this study would help to advance an in-depth understanding of the interaction among dust aerosol, atmospheric chemistry, and climate change in a desert source region.

scholarly journals Profiling Dust Mass Concentration in Northwest China Using a Joint Lidar and Sun-photometer Setting

2021 ◽  
Vol 13 (6) ◽  
pp. 1099
Author(s):  
Tianhe Wang ◽  
Ying Han ◽  
Wenli Hua ◽  
Jingyi Tang ◽  
Jianping Huang ◽  
...  
Keyword(s):  
Mass Concentration ◽  
Field Experiments ◽  
Negative Relationship ◽  
Northwest China ◽  
Dust Particles ◽  
Mass Loading ◽  
Average Mass ◽  
Dust Mass ◽  
Dust Loading ◽  
Sun Photometer

The satellite-based estimation of the dust mass concentration (DMC) is essential for accurately evaluating the global biogeochemical cycle of the dust aerosols. As for the uncertainties in estimating DMC caused by mixing dust and pollutants and assuming a fixed value for the mass extinction efficiency (MEE), a classic lidar-photometer method is employed to identify and separate the dust from pollutants, obtain the dust MEE, and evaluate the effect of the above uncertainties, during five dust field experiments in Northwest China. Our results show that this method is effective for continental aerosol mixtures consisting of dust and pollutants. It is also seen that the dust loading mainly occurred in the free troposphere (< 6 km), with the average mass loading of 905 ± 635 µg m−2 trapped in the planetary boundary layer. The dust MEE ranges from 0.30 to 0.60 m2 g−1 and has a significantly negative relationship with the size of dust particles. With the assumption of the dust MEE of 0.37 (0.60) m2 g−1, the DMC is shown to be overestimated (underestimated) by 20–40% (15–30%). In other words, our results suggest that the change of MEE with the size of dust particles should be considered in the estimation of DMC.

scholarly journals A new data set of soil mineralogy for dust-cycle modeling

2014 ◽  
Vol 14 (8) ◽  
pp. 3801-3816 ◽  
Author(s):  
E. Journet ◽  
Y. Balkanski ◽  
S. P. Harrison
Keyword(s):  
Atmospheric Chemistry ◽  
Radiative Forcing ◽  
Single Scattering ◽  
Dust Particles ◽  
Data Set ◽  
Airborne Dust ◽  
Global Soil ◽  
Climate Interactions ◽  
Soil Units ◽  
The Impact

Abstract. The mineralogy of airborne dust affects the impact of dust particles on direct and indirect radiative forcing, on atmospheric chemistry and on biogeochemical cycling. It is determined partly by the mineralogy of the dust-source regions and partly by size-dependent fractionation during erosion and transport. Here we present a data set that characterizes the clay and silt-sized fractions of global soil units in terms of the abundance of 12 minerals that are important for dust–climate interactions: quartz, feldspars, illite, smectite, kaolinite, chlorite, vermiculite, mica, calcite, gypsum, hematite and goethite. The basic mineralogical information is derived from the literature, and is then expanded following explicit rules, in order to characterize as many soil units as possible. We present three alternative realizations of the mineralogical maps, taking the uncertainties in the mineralogical data into account. We examine the implications of the new database for calculations of the single scattering albedo of airborne dust and thus for dust radiative forcing.

scholarly journals Effects of mineral dust on global atmospheric nitrate concentrations

2015 ◽  
Vol 15 (8) ◽  
pp. 11525-11572 ◽  
Author(s):  
V. A. Karydis ◽  
A. P. Tsimpidi ◽  
A. Pozzer ◽  
M. Astitha ◽  
J. Lelieveld
Keyword(s):  
Chemical Composition ◽  
Size Distribution ◽  
Atmospheric Chemistry ◽  
Mineral Dust ◽  
Dust Aerosol ◽  
Dust Particles ◽  
Metallic Ions ◽  
Aerosol Formation ◽  
Atmospheric Nitrate ◽  
Nitrate Aerosol

Abstract. This study provides an assessment of the chemical composition and global aerosol load of the major inorganic aerosol components and determines the effect of mineral dust on their formation, focusing on aerosol nitrate. To account for this effect, the mineral dust aerosol components (i.e., Ca2+, Mg2+, K+, Na+) and their emissions are added to the ECHAM5/MESSy Atmospheric Chemistry model (EMAC). Gas/aerosol partitioning is simulated using the ISORROPIA-II thermodynamic equilibrium model that considers the interactions of K+-Ca2+-Mg2+-NH4+-Na+-SO42−-NO3−-Cl−-H2O aerosol components. Emissions of mineral dust aerosol components (K+-Ca2+-Mg2+-Na+) are calculated online by taking into account the soil particle size distribution and chemical composition of different deserts worldwide. The presence of the metallic ions on the simulated suite of components can substantially affect the nitrate partitioning into the aerosol phase due to thermodynamic interactions. The updated model improved the nitrate predictions over remote areas and found that the fine aerosol nitrate concentration is highest over urban and industrialized areas (1–3 μg m−3), while coarse aerosol nitrate is highest close to deserts (1–4 μg m−3). The contribution of mineral dust components to nitrate formation is large in areas with high dust concentrations with impacts that can extend across southern Europe, western USA and northeastern China. The tropospheric burden of aerosol nitrate increases by 44% by considering the interactions of nitrate with mineral dust cations. The calculated global average nitrate aerosol concentration near the surface increases by 36% while the coarse and fine mode concentrations of nitrate increase by 53 and 21%, respectively. Sensitivity tests show that nitrate aerosol formation is most sensitive to the chemical composition of the emitted mineral dust, followed by the soil size distribution of dust particles, the magnitude of the mineral dust emissions, and the aerosol state assumption.

scholarly journals A new data set of soil mineralogy for dust-cycle modeling

2013 ◽  
Vol 13 (9) ◽  
pp. 23943-23993 ◽  
Author(s):  
E. Journet ◽  
Y. Balkanski ◽  
S. P. Harrison
Keyword(s):  
Atmospheric Chemistry ◽  
Radiative Forcing ◽  
Single Scattering ◽  
Dust Particles ◽  
Data Set ◽  
Airborne Dust ◽  
Global Soil ◽  
Climate Interactions ◽  
Soil Units ◽  
The Impact

Abstract. The mineralogy of airborne dust affects the impact of dust particles on direct and indirect radiative forcing, on atmospheric chemistry and on biogeochemical cycling. It is determined partly by the mineralogy of the dust-source regions and partly by size-dependent fractionation during erosion and transport. Here we present a data set that characterizes the clay and silt sized fractions of global soil units in terms of the abundance of 12 minerals that are important for dust-climate interactions: quartz, feldspars, illite, smectite, kaolinite, chlorite, vermiculite, mica, calcite, gypsum, hematite and goethite. The basic mineralogical information is derived from the literature, and is then expanded following explicit rules, in order to characterize as many soil units as possible. We present three alternative realisations of the mineralogical maps that account for the uncertainties in the mineralogical data. We examine the implications of the new database for calculations of the single scattering albedo of airborne dust and thus for dust radiative forcing.

scholarly journals On realistic size equivalence and shape of spheroidal Saharan mineral dust particles applied in solar and thermal radiative transfer calculations

2011 ◽  
Vol 11 (9) ◽  
pp. 4469-4490 ◽  
Author(s):  
S. Otto ◽  
T. Trautmann ◽  
M. Wendisch
Keyword(s):  
Land Surface ◽  
Mineral Dust ◽  
Single Scattering ◽  
Radiative Heating ◽  
Dust Particles ◽  
Axis Ratio ◽  
Solar Cooling ◽  
Prolate Shape ◽  
Spheroidal Model

Abstract. Realistic size equivalence and shape of Saharan mineral dust particles are derived from in-situ particle, lidar and sun photometer measurements during SAMUM-1 in Morocco (19 May 2006), dealing with measured size- and altitude-resolved axis ratio distributions of assumed spheroidal model particles. The data were applied in optical property, radiative effect, forcing and heating effect simulations to quantify the realistic impact of particle non-sphericity. It turned out that volume-to-surface equivalent spheroids with prolate shape are most realistic: particle non-sphericity only slightly affects single scattering albedo and asymmetry parameter but may enhance extinction coefficient by up to 10 %. At the bottom of the atmosphere (BOA) the Saharan mineral dust always leads to a loss of solar radiation, while the sign of the forcing at the top of the atmosphere (TOA) depends on surface albedo: solar cooling/warming over a mean ocean/land surface. In the thermal spectral range the dust inhibits the emission of radiation to space and warms the BOA. The most realistic case of particle non-sphericity causes changes of total (solar plus thermal) forcing by 55/5 % at the TOA over ocean/land and 15 % at the BOA over both land and ocean and enhances total radiative heating within the dust plume by up to 20 %. Large dust particles significantly contribute to all the radiative effects reported. They strongly enhance the absorbing properties and forward scattering in the solar and increase predominantly, e.g., the total TOA forcing of the dust over land.

scholarly journals Investigating the role of dust in ice nucleation within clouds and further effects on regional weather system over East Asia – Part I: model development and validation

2017 ◽  
Author(s):  
Lin Su ◽  
Jimmy C.H. Fung
Keyword(s):  
East Asia ◽  
Source Region ◽  
Model Development ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Weather System ◽  
Microphysics Scheme ◽  
Ice Nuclei ◽  
Cloud Ice ◽  
Ice Water

Abstract. The GOCART–Thompson microphysics scheme, which couples the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model and aerosol-aware Thompson microphysics scheme, has been implemented in the Weather Research and Forecast model coupled with Chemistry (WRF-Chem), to quantify and evaluate the effect of dust on the ice nucleation process in the atmosphere by serving as ice nuclei. The performance of the GOCART-Thompson microphysics scheme in simulating the effect of dust in atmospheric ice nucleation is then evaluated over East Asia during spring in 2012, a typical dust-intensive season. Based upon the dust emission reasonably reproduced by WRF-Chem, the effect of dust on atmospheric cloud ice water content is well reproduced. With abundant dust particles serving as ice nuclei, the simulated ice water mixing ratio and ice crystal number concentration increases by one order of magnitude over the dust source region and downwind areas during the investigated period. The comparison with ice water path from satellite observations demonstrated that the simulation of cloud ice profile is substantially improved by applying the GOCART–Thompson microphysics scheme in the simulations. Additional sensitivity experiments are carried out to optimize the parameters in the ice nucleation parameterization in the GOCART–Thompson microphysics scheme, and the results suggest that the calibration factor in the ice nucleation scheme should be set to 3 or 4. Lowering the threshold relative humidity with respect to ice to 100 % for the ice nucleation parameterization leads to further improvement in cloud ice simulation.

scholarly journals Hydroxyl radicals in the tropical troposphere over the Suriname rainforest: comparison of measurements with the box model MECCA

2008 ◽  
Vol 8 (4) ◽  
pp. 15239-15289 ◽  
Author(s):  
D. Kubistin ◽  
H. Harder ◽  
M. Martinez ◽  
M. Rudolf ◽  
R. Sander ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Tropical Rainforest ◽  
Source Region ◽  
Degradation Process ◽  
Reaction Scheme ◽  
Box Model ◽  
Chemical Mechanism ◽  
Similar Amount ◽  
Oxidation Capacity ◽  
Mixing Ratios

Abstract. As a major source region of the hydroxyl radical OH, the Tropics largely control the oxidation capacity of the atmosphere on a global scale. However, emissions of hydrocarbons from the tropical rainforest that react rapidly with OH can potentially deplete the amount of OH and thereby reduce the oxidation capacity. The airborne GABRIEL field campaign in equatorial South America (Suriname) in October 2005 investigated the influence of the tropical rainforest on the HOx budget (HOx=OH+HO2). The first observations of OH and HO2 over a tropical rainforest are compared to steady state concentrations calculated with the atmospheric chemistry box model MECCA. The important precursors and sinks for HOx chemistry, measured during the campaign, are used as constraining parameters for the simulation of OH and HO2. Significant underestimations of HOx are found by the model over land during the afternoon, with mean ratios of observation to model of 12.2±3.5 and 4.1±1.4 for OH and HO2, respectively. The discrepancy between measurements and simulation results is correlated to the abundance of isoprene. While for low isoprene mixing ratios (above ocean or at altitudes >3 km), observation and simulation agree fairly well, for mixing ratios >200 pptV (<3 km over the rainforest) the model tends to underestimate the HOx observations as a function of isoprene. Box model simulations have been performed with the condensed chemical mechanism of MECCA and with the detailed isoprene reaction scheme of MCM, resulting in similar results for HOx concentrations. Simulations with constrained HO2 concentrations show that the conversion from HO2 to OH in the model is too low. However, by neglecting the isoprene chemistry in the model, observations and simulations agree much better. An OH source similar to the strength of the OH sink via isoprene chemistry is needed in the model to resolve the discrepancy. A possible explanation is that the oxidation of isoprene by OH not only dominates the removal of OH but also produces it in a similar amount. Several additional reactions which directly produce OH have been implemented into the box model, suggesting that upper limits in producing OH are still not able to reproduce the observations (improvement by factors of ≈2.4 and ≈2 for OH and HO2, respectively). We determine that OH has to be recycled to 94% instead of the simulated 38% to match the observations, which is most likely to happen in the isoprene degradation process, otherwise additional sources are required.

scholarly journals CUACE/Dust – an integrated system of observation and modeling systems for operational dust forecasting in Asia

2007 ◽  
Vol 7 (4) ◽  
pp. 10323-10342 ◽  
Author(s):  
S. L. Gong ◽  
X. Y. Zhang
Keyword(s):  
East Asia ◽  
Atmospheric Chemistry ◽  
Monitoring Network ◽  
Integrated System ◽  
Dust Aerosol ◽  
China Meteorological Administration ◽  
Source Regions ◽  
Operational Forecasts ◽  
Forecasting System ◽  
Aerosol Module

Abstract. An integrated sand and dust storm (SDS) forecasting system – CUACE/Dust (the Chinese Unified Atmospheric Chemistry Environment for Dust) has been developed, which consists of a comprehensive dust aerosol module with emission, dry/wet depositions and other atmospheric dynamic processes, and a data assimilation system (DAS) using observational data from the CMA (China Meteorological Administration) ground dust monitoring network and retrieved dust information from a Chinese geostationary satellite – FY-2C. This is the first time that a combination of surface network observations and satellite retrievals of the dust aerosol has been successfully used in the real time operational forecasts in East Asia through a DAS. During its application for the operational SDS forecasts in East Asia for spring 2006, this system captured the major 31 SDS episodes observed by both surface and satellite observations. Analysis shows that the seasonal mean threat score (TS) for 0–24 h forecast over the East Asia in spring 2006 increased from 0.22 to 0.31 by using the DAS, a 41% enhancement. The time series of the forecasted dust concentrations for a number of representative stations for the whole spring 2006 were also evaluated against the surface PM10 monitoring data, showing a very good agreement in terms of the SDS timing and magnitudes near source regions where dust aerosols dominate. This is a summary paper for a special issue of ACP featuring the development and results of the forecasting system.

scholarly journals Atmospheric radiative effects of an in-situ measured Saharan dust plume and the role of large particles

2007 ◽  
Vol 7 (3) ◽  
pp. 7767-7817 ◽  
Author(s):  
S. Otto ◽  
M. de Reus ◽  
T. Trautmann ◽  
A. Thomas ◽  
M. Wendisch ◽  
...  
Keyword(s):  
Complex Refractive Index ◽  
Single Scattering ◽  
Single Scattering Albedo ◽  
Saharan Dust ◽  
Dust Particles ◽  
Modal Parameters ◽  
Size Distributions ◽  
Radiative Effects ◽  
Enhanced Absorption ◽  
Large Particles

Abstract. This work will present aerosol size distributions measured in a Saharan dust plume between 0.9 and 12 km altitude during the ACE-2 campaign 1997. The distributions contain a significant fraction of large particles of diameters from 4 to 30 μm. Radiative transfer calculations have been performed using these data as input. Shortwave, longwave as well as total atmospheric radiative effects (AREs) of the dust plume are investigated over ocean and desert within the scope of sensitivity studies considering varied input parameters like solar zenith angle, scaled total dust optical depth, tropospheric standard aerosol profiles and particle complex refractive index. The results indicate that the large particle fraction has a predominant impact on the optical properties of the dust. A single scattering albedo of ωo=0.75–0.96 at 550 nm was simulated in the entire dust column as well as 0.76 within the Saharan dust layer at ~4 km altitude indicating enhanced absorption. The measured dust leads to cooling over the ocean but warming over the desert due to differences in their spectral surface albedo and surface temperature. The large particles absorb strongly and they contribute at least 20% to the ARE in the dusty atmosphere. From the measured size distributions modal parameters of a bimodal lognormal column volume size distribution were deduced, resulting in a coarse median diameter of ~9 μm and a column single scattering albedo of 0.78 at 550 nm. A sensitivity study demonstrates that variabilities in the modal parameters can cause completely different AREs and emphasises the warming effect of the large mineral dust particles.

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