論文

The Prede sky radiometer measures direct solar irradiance and the angular distribution of diffuse radiances at the ultraviolet, visible, and near-infrared wavelengths. These data are utilized for the remote sensing of aerosols, water vapor, ozone, and clouds, but the calibration constant, which is the sensor output current of the extraterrestrial solar irradiance at the mean distance between Earth and the Sun, is needed. The aerosol channels, which are the weak gas absorption wavelengths of 340, 380, 400, 500, 675, 870, and 1020 nm, can be calibrated by an on-site self-calibration method, the Improved Langley method. This on-site self-calibration method is useful for the continuous long-term observation of aerosol properties. However, the continuous long-term observation of precipitable water vapor (PWV) by the sky radiometer remains challenging because calibrating the water vapor absorption channel of 940 nm generally relies on the standard Langley (SL) method at limited observation sites (e.g., the Mauna Loa Observatory) and the transfer of the calibration constant by a side-by-side comparison with the reference sky radiometer calibrated by the SL method. In this study, we developed the SKYMAP algorithm, a new on-site method of self-calibrating the water vapor channel of the sky radiometer using diffuse radiances normalized by direct solar irradiance (normalized radiances). Because the sky radiometer measures direct solar irradiance and diffuse radiance using the same sensor, the normalization cancels the calibration constant included in the measurements. The SKYMAP algorithm consists of three steps. First, aerosol optical and microphysical properties are retrieved using direct solar irradiances and normalized radiances at aerosol channels. The aerosol optical properties at the water vapor channel are interpolated from those at aerosol channels. Second, PWV is retrieved using the angular distribution of the normalized radiances at the water vapor channel. Third, the calibration constant at the water vapor channel is estimated from the transmittance of PWV and aerosol optical properties. Intensive sensitivity tests of the SKYMAP algorithm using simulated data of the sky radiometer showed that the calibration constant is retrieved reasonably well for PWV < 2 cm, which indicates that the SKYMAP algorithm can calibrate the water vapor channel on-site in dry conditions. Next, the SKYMAP algorithm was applied to actual measurements under the clear-sky and low-PWV (< 2 cm) conditions at two sites, Tsukuba and Chiba, Japan, and the annual mean calibration constants at the two sites were determined. The SKYMAP-derived calibration constants were 10.1% and 3.2% lower, respectively, than those determined by a side-by-side comparison with the reference sky radiometer. After determining the calibration constant, we obtained PWV from the direct solar irradiances in both the dry and wet seasons. The retrieved PWV values corresponded well to those derived from a global-navigation-satellite-system-global-positioning-system receiver, a microwave radiometer, and an AERONET (Aerosol Robotic Network) sun-sky radiometer at both sites. The correlation coefficients were greater than 0.96. We calculated the bias errors and the root mean square errors by comparing PWV between the DSRAD (direct solar irradiance) algorithm and other instruments. The magnitude of the bias error and the root mean square error were < 0.163 and < 0.251 cm for PWV < 3 cm, respectively.However, our method tended to underestimate PWV in the wet conditions, and the magnitude of the bias error and the root mean square error became large, < 0.594 and < 0.722 cm for PWV > 3 cm, respectively. This problem was mainly due to the overestimation of the aerosol optical thickness before the retrieval of PWV. These results show that the SKYMAP algorithm enables us to observe PWV over the long term, based on its unique on-site self-calibration method.

Knowledge of black carbon (BC) concentrations and size distributions within surface snow in Antarctica is limited. However, these measurements are important to understanding global aerosol transport from combustion sources, and BC contributes to positive radiative forcing. This study analyzed the concentrations and size distributions of BC and inorganic ions in snow samples collected at the Syowa station in Antarctica from April to December 2011 and along a traverse route to an inland (Mizuho) station. The BC size distributions in snow were bimodal with mass median diameters of ~140 and ~690 nm. We also estimated the mass median diameter from unimodal distributions and found smaller diameters than were reported by other studies. The mass concentrations of BC in snow were higher in inland samples than in Syowa samples. Among Syowa samples, the BC concentrations in December (2117.3 ng L−1 on average) were higher than in other periods (288.2 ng L−1 on average). The December samples experienced ambient temperatures above 0 °C, and the atmospheric BC concentrations did not increase simultaneously. Inorganic ions originated from the ocean and decreased with increasing distance from the coastal area. We conclude that the BC concentrations in surface snow increased mainly by postdeposition processes through the loss of water mass due to melting, evaporation, and sublimation. Our study is the first to report detailed BC concentrations and size distributions in eastern Antarctica, and the results will help to evaluate BC global transport, the snow albedo estimations in this region, and the climate impacts of BC.

Black carbon (BC) particles cause adverse health effects and contribute to the heating of the atmosphere by absorbing visible solar radiation. Efforts have been made to reduce BC emissions, especially in urban areas; however, long-term measurements of BC mass concentration (MBC) are very limited in Japan. We report MBC measurements conducted in Tokyo from 2003 to 2017, showing that MBC decreased by a factor of 3 from 2003 to 2010 and was stable from 2010 to 2017. Fine particulate concentrations (PM2.5) decreased by a much smaller factor during 2003-2010. The diurnal variations of BC size distributions suggest that the BC in Tokyo originates mainly from local sources, even after 2010. Our three-dimensional model calculations show that BC from the Asian continent contributes a small portion (about 20%) of the annual average MBC in the Kanto region of Japan, which includes Tokyo. This indicates that continued reduction of BC emissions inside Japan should be effective in further decreasing MBC.

Black carbon (BC) deposited on snow lowers its albedo, potentially contributing to warming in the Arctic. Atmospheric distributions of BC and inorganic aerosols, which contribute directly and indirectly to radiative forcing, are also greatly influenced by depositions. To quantify these effects, accurate measurement of the spatial distributions of BC and ionic species representative of inorganic aerosols (ionic species hereafter) in snowpack in various regions of the Arctic is needed, but few such measurements are available. We measured mass concentrations of size-resolved BC (CMBC) and ionic species in snowpack by using a single-particle soot photometer and ion chromatography, respectively, over Finland, Alaska, Siberia, Greenland, and Spitsbergen during early spring in 2012–2016. Total BC mass deposited per unit area (DEPMBC) during snow accumulation periods was derived from CMBC and snow water equivalent (SWE). Our analyses showed that the spatial distributions of anthropogenic BC emission flux, total precipitable water, and topography strongly influenced latitudinal variations of CMBC, BC size distributions, SWE, and DEPMBC. The average size distributions of BC in Arctic snowpack shifted to smaller sizes with decreasing CMBC due to an increase in the removal efficiency of larger BC particles during transport from major sources. Our measurements of CMBC were lower by a factor of ~13 than previous measurements made with an Integrating Sphere/Integrating Sandwich spectrophotometer due mainly to interference from coexisting non-BC particles such as mineral dust. The SP2 data presented here will be useful for constraining climate models that estimate the effects of BC on the Arctic climate.

Anthropogenic iron oxide (FeOx) aerosols can affect atmospheric radiation, marine biogeochemistry, and human health. However, due to lack of observational data, their atmospheric abundance and emission flux are not well understood. In this study, we observed size-resolved concentrations of FeOx (170-2100 nm) and black carbon (BC, 70-850 nm) aerosols at a remote site in the East China Sea in March 2016 using a modified single-particle soot photometer (SP2). Light signals measured by the SP2 and particle morphology and compositions analyzed by a transmission electron microscope revealed that most of the observed FeOx aerosols are of anthropogenic origin. Clear correlations were found between mass concentrations of FeOx and BC (R-2 = 0.717) and between FeOx and carbon monoxide (CO) (R-2 = 0.718) in air masses from China, indicating that their emission sources are spatially similar. The correlation slopes of mass concentration (ng/m(3)) are similar to 0.3 and 0.0015, respectively. Based on the correlation slopes and emission inventories of BC and CO in China, we estimated emission flux of anthropogenic FeOx aerosols from China to be 0.21-0.49 FeTg/yr. Based on the observed size distribution and previous studies on mass fraction of FeOx and non-FeOx, we also estimated emission flux of anthropogenic Fe (FeOx + non-FeOx) in PM10 as 0.74-1.7 FeTg/yr. These emission fluxes from China are comparable to global emission fluxes in currently reported inventories of anthropogenic Fe (0.51-1.91 FeTg/yr). Our results suggest that the current emission inventories of anthropogenic Fe are underestimated.

Deposition of black carbon (BC) aerosol in the Arctic lowers snow albedo, thus contributing to warming in the region. However, the processes and impacts associated with BC deposition are poorly understood because of the scarcity and uncertainties of measurements of BC in snow with adequate spatiotemporal resolution. We sampled snowpack at two sites (11 m and 300 m above sea level) at Ny-Ålesund, Spitsbergen, in April 2013. We also collected falling snow near the surface with a windsock from September 2012 to April 2013. The size distribution of BC in snowpack and falling snow was measured using a single-particle soot photometer combined with a characterized nebulizer. The BC size distributions did not show significant variations with depth in the snowpack, suggesting stable size distributions in falling snow. The BC number and mass concentrations (CNBC and CMBC) at the two sites agreed to within 19% and 10%, respectively, despite the sites' different snow water equivalent (SWE) loadings. This indicates the small influence of the amount of SWE (or precipitation) on these quantities. Average CNBC and CMBC in snowpack and falling snow at nearly the same locations agreed to within 5% and 16%, after small corrections for artifacts associated with the sampling of the falling snow. This comparison shows that the dry deposition was a small contributor to the total BC deposition. CMBC were highest (2.4 ± 3.0 μg L−1) in December–February and lowest (1.2 ± 1.2 μg L−1) in September–November.

The lifetime and spatial distributions of accumulation-mode aerosols in a size range of approximately 0.05-1 mu m, and thus their global and regional climate impacts, are primarily constrained by their removal via cloud and precipitation (wet removal). However, the microphysical process that predominantly controls the removal efficiency remains unidentified because of observational difficulties. Here, we demonstrate that the activation of aerosols to cloud droplets (nucleation scavenging) predominantly controls the wet removal efficiency of accumulation-mode aerosols, using water-insoluble black carbon as an observable particle tracer during the removal process. From simultaneous ground-based observations of black carbon in air (prior to removal) and in rainwater (after removal) in Tokyo, Japan, we found that the wet removal efficiency depends strongly on particle size, and the size dependence can be explained quantitatively by the observed size-dependent cloud-nucleating ability. Furthermore, our observational method provides an estimate of the effective supersaturation of water vapour in precipitating cloud clusters, a key parameter controlling nucleation scavenging. These novel data firmly indicate the importance of quantitative numerical simulations of the nucleation scavenging process to improve the model's ability to predict the atmospheric aerosol burden and the resultant climate forcings, and enable a new validation of such simulations.

Mass concentrations of black carbon (BC) in air (M-BC) and rainwater (C-BC) in the East China Sea were measured at Hedo on Okinawa Island, Japan, from April 2010 to March 2013. The monthly averaged M-BC and CBC showed marked seasonal variations, being highest in spring (0.32 +/- 0.13 mu g m(-3) and 92 +/- 76 mu g L-1, respectively) and lowest in summer (0.06 +/- 0.03 mu g m(-3) and 8.0 +/- 4.1 mu g L-1, respectively). The high M-BC and C-BC in spring were associated with transport of airmasses from the Asian continent by northwesterly winds. The BC wet deposition flux (F-BC), estimated as the product of C-BC and precipitation amount, also showed a distinct seasonal variation. The monthly average F-BC during the four spring seasons (16.8 +/- 6.7 mg m(-2) month(-1)) was about 3 times higher than the annual average FBC (5.5 +/- 9.9 mg m(-2) month(-1)) owing to the high C-BC and precipitation amount in spring. As a result, about 76% of the annual BC deposition occurred in spring on average. The F-BC in spring is comparable to the average BC net flux in North China, indicating the importance of precipitation over the East China Sea as a sink of BC transported from North China. In summer, C-BC values were correlated with M-BC for rain events associated with local convective activity, as identified by the convective available potential energy. A one-dimensional thermodynamic model successfully explained the relation between C-BC and M-BC.