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Titel Chemical compositions of past soluble aerosols reconstructed from NEEM (Greenland) and Dome C (Antarctica) ice cores
VerfasserIn Ikumi Oyabu, Yoshinori Iizuka, Manabu Fukui, Hubertus Fischer, Simon Schüpbach, Gideon Gfeller, Robert Mulvaney, Margareta Hansson
Konferenz EGU General Assembly 2015
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 17 (2015)
Datensatznummer 250101478
Publikation (Nr.) Volltext-Dokument vorhandenEGU/EGU2015-629.pdf
 
Zusammenfassung
Polar ice core preserve past atmospheric aerosols, which is a useful proxy for understanding the interaction between climate changes and atmospheric aerosols. One useful technique for reconstructing past soluble aerosols from ice core is the determination of dissolved ion species. However, since salts and acids melt into ions, chemical compositions of soluble aerosols in the ice cores have not been cleared. To clarify the temporal variations in the chemical compositions of past soluble aerosols, this study investigated chemical compositions of soluble particles preserved in the NEEM (Greenland) and Dome C (Antarctica) ice cores using new method “ice-sublimation method”. The ice-sublimation method can extract soluble salts particles as a solid state without melting. The ice core samples are selected from the sections from the last termination (the Last Glacial Maximum (LGM) to Holocene) of Dome C (inland Antarctica) and NEEM ice cores. Using ice-sublimation method, soluble salts particles were extracted. Chemical components of extracted particles were analysed by scanning electron microscope and energy dispersive spectroscopy, and micro-Raman spectroscopy. The major components of soluble salts particles in the Dome C ice core are CaSO4, Na2SO4 and NaCl. The CaSO4 and NaCl fractions were high in the first half of the last termination, whereas the Na2SO4 fraction is high in the latter half of the last termination. The major components of soluble salts particles in the NEEM ice core are CaCO3, CaSO4, NaCl and Na2SO4. The fractions of CaCO3, CaSO4 and NaCl were high in LGM, whereas those of NaCl and Na2SO4 were high in Holocene. The changes in the salts compositions in Dome C ice core are mainly controlled by concentration of terrestrial material (Ca2+). In the first half of the last termination, most of the terrestrial material (CaCO3) reacted with H2SO4 but some of sea-salt (NaCl) was not reacted with H2SO4 due to high Ca2+ concentration. As a result, the CaSO4 and NaCl fractions were high in this period. In the latter half of the last termination, reaction of NaCl with H2SO4 enhanced due to decreased in the Ca2+ concentration. As a result, Na2SO4 fraction increased. The changes in the salts compositions in NEEM ice core are also mainly controlled by Ca2+ concentration. In the LGM, some of CaCO3 was reacted but some of CaCO3 and most of NaCl were not reacted with H2SO4 due to too high Ca2+ concentration. As a result, CaCO3, CaSO4 and NaCl fractions were high in LGM. In the Holocene, NaCl sulfatization increased due to reduction of Ca2+ concentration. However, some of NaCl was not sulfatized due to different seasonality of NaCl and H2SO4, and increased in the NH4+ inputs originate from vegetation.