• Journal of Korean Society for Atmospheric Environment
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• v.25 no.3
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• pp.219-236
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• 2009

Particle-phase organic tracers (molecular markers) have been shown to be an effective method to assess and quantify the impact of sources of carbonaceous aerosols. These molecular markers have been used in chemical mass balance (CMB) models to apportion primary sources of organic aerosols in regions where the major organic aerosol source categories have been identified. As in the case of all CMB models, all important sources of the tracer compounds must be included in a Molecular Marker CMB (MM-CMB) model or the MMCMB model can be subject to biases. To this end, the application of the MM-CMB models to locations where reasonably accurate emissions inventory of organic aerosols are not available, should be performed with extreme caution. Of great concern is the potential presence of industrial point sources that emit carbonaceous aerosols and have not been well characterized or inventoried. The current study demonstrates that emissions from industrial point sources in the St. Louis, Missouri area can greatly bias molecular marker CMB models if their emissions are not correctly addressed. At a sampling site in the greater St. Louis Area, carbonaceous aerosols from industrial point sources were found to be important source of carbonaceous aerosols during specific time periods in addition to common urban sources (i.e. mobile sources, wood burning, and road dust). Since source profiles for these industrial sources have not been properly characterized, method to identify time periods when point sources are impacting a sampling site, needs to avoid obtaining biases source apportionment results. The use of real time air pollution measurements, along with molecular marker measurements, as a screening tool to identify when point sources are impacting a receptor site is presented.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 1996.04a
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• pp.18-23
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• 1996

• Proceedings of the KSRS Conference
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• v.1
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• pp.467-470
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• 2006

Geostationary Ocean Color Imager (GOCI) onboard its Communication Ocean and Meteorological Satellite (COMS) is scheduled for launch in 2008. GOCI includes the eight visible-to-near-infrared (NIR) bands, 0.5km pixel resolution, and a coverage region of 2500 ${\times}$ 2500km centered at 36N and 130E. GOCI has had the scope of its objectives broadened to understand the role of the oceans and ocean productivity in the climate system, biogeochemical variables, geological and biological response to physical dynamics and to detect and monitor toxic algal blooms of notable extension through observations of ocean color. To achieve these mission objectives, it is necessary to develop an atmospheric correction technique which is capable of delivering geophysical products, particularly for highly turbid coastal regions that are often dominated by strongly absorbing aerosols from the adjacent continental/desert areas. In this paper, we present a more realistic and cost-effective atmospheric correction method which takes into account the contribution of NIR radiances and include specialized models for strongly absorbing aerosols. This method was tested extensively on SeaWiFS ocean color imagery acquired over the Northwest Pacific waters. While the standard SeaWiFS atmospheric correction algorithm showed a pronounced overcorrection in the violet/blue or a complete failure in the presence of strongly absorbing aerosols (Asian dust or Yellow dust) over these regions, the new method was able to retrieve the water-leaving radiance and chlorophyll concentrations that were consistent with the in-situ observations. Such comparison demonstrated the efficiency of the new method in terms of removing the effects of highly absorbing aerosols and improving the accuracy of water-leaving radiance and chlorophyll retrievals with SeaWiFS imagery.

• Journal of Korean Society for Atmospheric Environment
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• v.16 no.5
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• pp.445-451
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• 2000

To estimate dry deposition flux of 12 elements in aerosols, aerosol particles were sampled by a low-pressure impactor(LPI) and a dust jar. The concentrations of 12 elements in aerosol particle and dry deposition were analyzed by a PIXE analysis using as a 2.0 MeV-proton beam. The mean dry deposition velocities of 12 elements were estimated by ranges of 0.74∼2.62 cm/sec. The results showed that the highest value was 3.26 cm/sec for Ca and the lowest value 0.74 cm/sec for Fe. The dry deposition flux for elements was calculated as a function of particle size by 1-step method and 12-step method. In this work, dry deposition velocities were computed with the two existing models; the coarse-particle fraction(4∼30 mm diameter) using the dry deposition velocity model of the Noll and Fang(1998) and the fine-particle fraction (0.05∼4mm diameter) using the Shemel and Hodgson(1980) model. The ratios of the mean calculated/measured fluxes were 3.59 for 1-step method and 0.60 for 12-step method respectively.

• Journal of Korean Society for Atmospheric Environment
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• v.12 no.4
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• pp.389-398
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• 1996

In order to understand the relative importance of various pathways leading to the production and transformation of aerosols under different atmospheric conditions, the behavior of atmospheric aerosols have been investigated using a high volume tape sample in Seoul for a week period during August 1990. The concentrations of anion $(SO^{2-}_4, NO^-_3, CI^-)$ and cation $(Ca^{2+}, Na^+, NH^+_4)$ species of aerosol samples were analyzed to identify the ionic composition of aerosols and to estimate their relative contributions to aerosol formation. The concentrations of aerosol species were calculated by a multiple regression model. The results of our calculations indicate the existence of various chemical species such as $(NH_4)_2SO_4, Na_2SO_4, CaSO_4, NH_4NO_3, NaNO_3, Ca(NO_3)_2, NH_4Cl$, and NaCl salts. According to our calculations, the most dominant species of aerosol was $(NH_4)_2SO_4$ with the mean concentration of 23.3 $/mu g/m^3$ (66.9%). The proportion of different componts with aerosol (e.g., $NH_4NO_3$ and $NH_4Cl$) was strongly affected by temperature, relative humidity, and partial presure of gases.

• Journal of Korean Society for Atmospheric Environment
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• v.9 no.3
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• pp.230-235
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• 1993

The atmospheric aerosol samples during the Yellow Sand Phenomena in April 1993 were analyzed, and they were compared with those during the normal time. The conclusions are as follows: 1) TSP concentrations in the case of Yellow Sand Phenomena appeared to be 2.2times higher than those of normal conditions. 2) The concentration of aerosols; Inorganic components of soil-originated elements (Ca, Fe, Mn, Mg, K) during the Yellow Sand Phenomena were measured to be 1.9-2.1times higher than those during normal time. 3) During the Yellow Sand Phenomena the EF values of soil-originated metal contents except for elements Cd, Ni, Pb, Zn in the atmospheric aerosol were close to unity. 4) The concentrations of $Ca^{2+}, SO_4^{2-}, F^-$ in water soluble ionic components were higher than those during the normal time. 5) Washout factor by rain fall during the Yellow Sand Phenomena were estimated to 1268. 6) During the Yellow Sand Phenomina average deposition was 37.8ton/$km^2$.

• International Union of Geodesy and Geophysics Korean Journal of Geophysical Research
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• v.21 no.1
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• pp.31-46
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• 1993

A radiative transfer model with two-stream/delta-Eddington approximation has been developed to calculate the vertical distributions of atmospheric heating rates and radiative fluxes. The performance of the model has been evaluated by comparison with the results of ICRCCM (Intercomparison of radiative codes in climate models). It has been demonstrated that the presented model has a capability to calculate the solar radiation not only accurately but also economically. The characteristics of ultraviolet-B radiation (UV-B; 280-320nm) are examined by comparison of relation between the flux at the top of atmosphere and that at the surface. The relation of UV-B is quadratic due to the strong ozone absorption in this band. Also, the dependence of the UV-B radiation on the stratospheric ozone depletion and stratospheric aerosol haze due to volcanic eruption on the stratospheric ozone depletion and stratospheric aerosol haze due to volcanic eruption has been tested with various solar zenith angles. The surface UV-B increases as the solar zenith angle increases. The existence of stratospheric aerosols causes an increase in the planetary albedo due to the aerosols' backscattering. The planetary albedo with aerosol's effect has been increases as the solar zenith angle is not sensitive. It may be caused by the fact that the aerosols' scattering effect becomes saturated with the relatively long path length in a large solar zenith angle. Finally, the regional impact of stratospheric aerosols due to volcanic eruption on the intensity of UV-B radiation at the surface has been estimated. A direct effect is that the flux is diminished at the low latitudes, while it is enhanced in the high latitudes by the aerosols' photon trap or twilight effect. In the high latitudes, both aerosols' scattering and ozone absorption have strong and opposite impacts to the surface UV-B radiation is located at the mid-latitudes during spring season in both hemispheres.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.9 no.5
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• pp.1349-1353
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• 2008

Size-segregated mass and ion concentrations of atmospheric aerosols in Cheonan City were measured using a high volume air sampler equipped with a 5-stage cascade impactor and a ion chromatography between March 2006 and April 2007. The mean values of 24-hr average concentrations of TSP, PM10, PM2.5, and PM1 were 61.7, 55.2, 43.7, $33.2{\mu}g/m^3$, respectively. Mass size distributions of atmospheric aerosols were bimodal distributions with a saddle point in $1.5\;{\sim}\;3.0{\mu}m$ range in diameter separating coarse and fine particle modes. Fine particles, PM2.5 were 70.8% of the total mass of aerosols. Major ion components in aerosols were ${NH_{4}}^+$, $Na^+$, $K^+$, $Ca^{2+}$, $Mg^{2+}$ for cations, and ${SO_{4}}^{2-}$, ${NO_{3}}^-$, $Cl^-$ for anions. ion components occupied 37.4% of coarse particles and 46.2% of fine particles in mass.

• Atmosphere
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• v.18 no.4
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• pp.459-474
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• 2008

Aerosol scattering coefficients for three different wavelengths ($\lambda$=450,550,700 nm) are measured almost continuously by a nephelometer in Seoul for a period of 13 months (February 2007-February 2008), which includes two weeks break in August 2007 for measurements at Daegwallyeong and YoungJongdo. The mean of the daily average scattering coefficients at $\lambda$=550 nm is $194.1{\pm}144.2Mm^{-1}$ and the minimum and maximum are $14.3Mm^{-1}$ and $998.1Mm^{-1}$, respectively. The scattering coefficient shows a general increasing trend with atmospheric relative humidity (RH). When the data are classified according to weather conditions, the days with no major weather events show the smallest scattering coefficient and also the lowest RH. Surprisingly haze/fog days show the largest scattering coefficient and Asian dust days comes in second. Although the variation is large within a season, winter shows the largest and autumn shows the smallest scattering coefficient. The average ${\AA}ngstr{\ddot{o}}m$ exponent is $1.40{\pm}0.32$ for the entire Seoul measurement. As expected, Asian dust days show the smallest ${\AA}ngstr{\ddot{o}}m$ exponent and haze/fog days are the next, suggesting more efficient hygroscopic growth of aerosols for this weather condition. Aerosol scattering coefficient seems to show better correspondence with CCN concentration rather than total aerosol concentration, which may indicate that CCN active aerosols are also good scattering aerosols.

• Journal of Korean Society for Atmospheric Environment
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• v.26 no.5
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• pp.554-566
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• 2010

We present optical and microphysical particle properties of aerosol retrieved by multi-wavelength Raman lidar at Anmyun island ($36.32^{\circ}N$, $126.19^{\circ}E$), Korea. The results present aerosol properties in various height layers of the atmospheric pollution layers observed over the Korean peninsula on eight consecutive days (27, 28, 29, 30 and 31 May, 4, 5 and 7 June) in 2005 at Anmyun island. We found anthropogenic pollution on 27, 28, and 29 May and local haze on other measurement days. The origin of the particle plumes was determined by simulations of FLEXPART. The source regions of the particles resulted in rather clear differences between the optical and microphysical properties of the pollution layers. The single-scattering albedo of anthropogenic aerosols from China ($0.91{\pm}0.01$ at 532 nm) were lower than the single-scattering albedo of local haze aerosols ($0.95{\pm}0.01$ at 532 nm). Local haze aerosols show larger effective radii of $0.24{\pm}0.02\;{\mu}m$ at relative humidity of 55~75%. The effective radii of anthropogenic aerosols are $0.20{\pm}0.2\;{\mu}m$ and $0.27\;{\mu}m$ at relative humidity of 25~50%.