• Journal of the Korean Geographical Society
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• v.41 no.5 s.116
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• pp.513-526
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• 2006

The timing and extent of glaciations during the Late Quaternary in the South Shetland Islands, West Antarctica were defined using field mapping, geomorphic analysis and radiocarbon dating. Landforms of glacial erosion and deposition, in particular subglacial meltwater channel erosion, suggest that at least three glaciations occurred during the late Quaternary within the study region. During the global LGM, glacial troughs (such as Maxwell Bay and Admiralty Bay) were overdeepened by an ice stream moving south from $an\sim1000m-thick$ ice cap centered on the present-day continental shelf to the north. This ice was responsible for the subglacial meltwater channel erosion, and glacial polished and striated bedrock on the Fildes Peninsula. The recent local glaciations occurred about 2,000 years ago and during Little Ice Age (LIA). During these glaciations, glaciers were less extensive than the previous one and less erosive as a cold-based ice

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.27 no.3
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• pp.144-157
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• 2022

Noble gases, which are chemically inert and behave conservatively in marine environments, have been used as tracers of physical processes such as air-sea gas exchange, mixing of water masses, and distribution of glacial meltwater in the ocean. For precise measurements of Ne, Ar, and Kr, we developed a mass spectrometric system consisting of a quadrupole mass spectrometer (QMS), a high vacuum preparation line, an activated charcoal cryogenic trap (ACC), and a set of isotope standard gases. The high vacuum line consists of three sections: (1) a sample extraction section that extracts the dissolved gases in the sample and mixes them with the standard gases, (2) a gas preparation section that removes reactive gases using getters and separates the noble gases according to their evaporation points with the ACC, and (3) a gas analysis section that measures concentrations of each noble gas. The ACC attached to the gas preparation section markedly lowered the partial pressures of Ar and CO₂ in the QMS, which resulted in a reduced uncertainty of Ne isotope analysis. The isotope standard gases were prepared by mixing ²²Ne, ³⁶Ar, and ⁸⁶Kr. The amounts of each element in the mixed standard gases were determined by the reverse isotope dilution method with repeated measurements of the atmosphere. The analytical system achieved precisions for Ne, Ar, and Kr concentrations of 0.7%, 0.7%, and 0.4%, respectively. The accuracies confirmed by the analyses of air-equilibrated water were 0.5%, 1.0%, and 1.7% for Ne, Ar, and Kr, respectively.