09:00 〜 09:15
[ACC37-01] グリーンランドアイスコア中に捕捉された粒子中のカルシウム化学種の同定：炭酸カルシウムの大気中での中和反応と関連して
★招待講演
キーワード：エアロゾル、アイスコア、雲凝結核、中和反応、カルシウム化学種同定、X線吸収微細構造（XAFS)
Aerosol has various influences on the surface environment of the earth, and one of the influences is its global cooling effect including direct and indirect effects. The indirect cooling effect is caused by hygroscopic aerosols which act as cloud condensation nuclei (CCN) and form clouds that can reflect sunlight. However, hygroscopicity of aerosol differs depending on the chemical species that constitute the particles. Therefore, it is important to clarify the chemical species in aerosols to estimate the degree of the indirect cooling effect. Sulfate, one of the major species of aerosols, has high CCN activity, because it is considered that most of sulfate is present as ammonium sulfate ((NH4)2SO4) with high hygroscopicity (Pilinis et al, 1989). On the other hand, it is reported that calcite (CaCO3) in mineral particles reacts with sulfuric acid (H2SO4) during atmospheric transportation and forms gypsum (CaSO4·2H2O) (e.g. Jones and Prospero 1996; Takahashi et al., 2009). In our previous study, sulfate species of aerosol collected in Higashi-Hiroshima, Japan were determined, which suggests that atmospheric neutralization reaction of CaCO3 in mineral dust with H2SO4 causes suppression of forming (NH4)2SO4 decreases hygroscopicity of sulfate aerosols.
Greenlandic ice sheet preserved natural and anthropogenic trace gases and particles transported from continents in the Northern hemisphere (Delmas 1992), which is one of the important samples to reconstruct various factors on climate change of the past, and to contribute to the more accurate prediction of the climate in future. Therefore, determination of amount of CaSO4·2H2O in mineral dust, or identification of the neutralization process of CaCO3, in ice sheet has a potential to reconstruct the variation of sulfate species in aerosols that have information of atmospheric chemical reactions in the past, which will help us to know the CCN activity of sulfate aerosols in the Northern hemisphere. However, there is no study on quantitative determination of CaSO4·2H2O in mineral dust in ice sheet. In this study, calcium speciation experiments of particles trapped in Greenlandic ice sheet were conducted.
Ice core were drilled at southeast Greenland, SE Dome (67.2°N, 36.4°W) in 2015. The parts of the ice dated as 1971, 1978, 1987, 1995, and 2004 were sublimated in low-temperature room (–20℃) to obtain trapped particles using the method in Iizuka et al. (2009, 2012). Calcium-bearing particles in the trapped particles were identified by micro X-ray Fluorescence (μ-XRF) mapping. Subsequently, calcium species of the particles were determined by micro X-ray absorption fine structure (μ-XAFS) spectroscopy.
As a result of the calcium speciation, CaSO4·2H2O fraction to total calcium in 1971, 1978, and 1987 were lower than CaCO3 fraction. In contrast, CaSO4·2H2O fraction in 1995 and 2004 were higher than CaCO3 fraction. It is considered that chemical reaction of CaCO3 in mineral dust with H2SO4 was more active in recent 20 years. On the other hand, sulfate ion (SO42-) concentration in ice core decreased from late 1970s. The trend of SO42- was consistent with emission record of SO2 in industrial countries at the time, however, emission amount of SO2 increased in East Asia in recent 20 years, especially in China (Crippa et al., 2016), which is also an important source of mineral dust in Greenlandic ice sheet. Therefore, it was considered that calcium species in the mineral particles trapped in the ice sheet reflected chemical reactions of calcium with H2SO4 in China. These results suggested that suppression of (NH4)2SO4 formation in the Northern hemisphere was associated with the neutralization reactions of CaCO3 with H2SO4 in East Asia.
Greenlandic ice sheet preserved natural and anthropogenic trace gases and particles transported from continents in the Northern hemisphere (Delmas 1992), which is one of the important samples to reconstruct various factors on climate change of the past, and to contribute to the more accurate prediction of the climate in future. Therefore, determination of amount of CaSO4·2H2O in mineral dust, or identification of the neutralization process of CaCO3, in ice sheet has a potential to reconstruct the variation of sulfate species in aerosols that have information of atmospheric chemical reactions in the past, which will help us to know the CCN activity of sulfate aerosols in the Northern hemisphere. However, there is no study on quantitative determination of CaSO4·2H2O in mineral dust in ice sheet. In this study, calcium speciation experiments of particles trapped in Greenlandic ice sheet were conducted.
Ice core were drilled at southeast Greenland, SE Dome (67.2°N, 36.4°W) in 2015. The parts of the ice dated as 1971, 1978, 1987, 1995, and 2004 were sublimated in low-temperature room (–20℃) to obtain trapped particles using the method in Iizuka et al. (2009, 2012). Calcium-bearing particles in the trapped particles were identified by micro X-ray Fluorescence (μ-XRF) mapping. Subsequently, calcium species of the particles were determined by micro X-ray absorption fine structure (μ-XAFS) spectroscopy.
As a result of the calcium speciation, CaSO4·2H2O fraction to total calcium in 1971, 1978, and 1987 were lower than CaCO3 fraction. In contrast, CaSO4·2H2O fraction in 1995 and 2004 were higher than CaCO3 fraction. It is considered that chemical reaction of CaCO3 in mineral dust with H2SO4 was more active in recent 20 years. On the other hand, sulfate ion (SO42-) concentration in ice core decreased from late 1970s. The trend of SO42- was consistent with emission record of SO2 in industrial countries at the time, however, emission amount of SO2 increased in East Asia in recent 20 years, especially in China (Crippa et al., 2016), which is also an important source of mineral dust in Greenlandic ice sheet. Therefore, it was considered that calcium species in the mineral particles trapped in the ice sheet reflected chemical reactions of calcium with H2SO4 in China. These results suggested that suppression of (NH4)2SO4 formation in the Northern hemisphere was associated with the neutralization reactions of CaCO3 with H2SO4 in East Asia.