Evidence for the loss of snow-deposited MSA to the interstitial gaseous phase in central Antarctic firn

被引:36
作者
Delmas, RJ
Wagnon, P
Goto-Azuma, K
Kamiyama, K
Watanabe, O
机构
[1] CNRS, Lab Glaciol & Geophys Environm, F-38402 St Martin Dheres, France
[2] Natl Inst Polar Res, Itabashi Ku, Tokyo 1738515, Japan
关键词
D O I
10.1034/j.1600-0889.2003.00032.x
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
We have examined several MSA (methanesulfonic acid) records from the upper 200 m of the Antarctic ice street and in particular the new Dome F profile. At all the four sites studied, concentration profiles exhibit similar patterns as a function of depth. They suggest that snow metamorphism and solid phase migration are responsible for a marked release of gaseous MSA to interstitial firm air as kell as probably to the free atmosphere, in particular at extremely low accumulation sites. Snow acidity can also modify MSA concentration. It is proposed that, belong the upper few metres where the communication with the free atmosphere is possible, gaseous MSA may remain in the firn layers and be entrapped later in air bubbles at pole close-off. i.e. when firn is transformed into ice. Chemical measurements on the firn core do not take into account the MSA released to the gaseous phase. but this fraction is measurable in ice samples. In spite of these alterations occurring in the firn layers, relative charges of the atmospheric MSA concentration in the past are probably still there deep within the Antarctic ice street. However. for glacial periods, different processes have to he considered in relation to modified aerosol properties.
引用
收藏
页码:71 / 79
页数:9
相关论文
共 40 条
[1]  
Ageta Y, 1998, ANN GLACIOL, V27, P333
[2]  
Andreae M.O., 1986, ROLE AIR SEA EXCHANG, P331, DOI [DOI 10.1007/978-94-009-4738-2_14, 10.1007/978-94-009-4738-2_14]
[3]  
Aoki S, 1998, ANN GLACIOL-SER, V27, P338
[4]   CO2-CLIMATE RELATIONSHIP AS DEDUCED FROM THE VOSTOK ICE CORE - A REEXAMINATION BASED ON NEW MEASUREMENTS AND ON A REEVALUATION OF THE AIR DATING [J].
BARNOLA, JM ;
PIMIENTA, P ;
RAYNAUD, D ;
KOROTKEVICH, YS .
TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY, 1991, 43 (02) :83-90
[5]   BIOGENIC SULFUR EMISSIONS FROM THE SUB-ANTARCTIC AND ANTARCTIC OCEANS [J].
BERRESHEIM, H .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1987, 92 (D11) :13245-13262
[6]   Sulfur Chemistry in the Antarctic Troposphere Experiment: An overview of project SCATE [J].
Berresheim, H ;
Eisele, FL .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D1) :1619-1627
[7]  
CHARLSON RJ, 1989, NATURE, V340, P437, DOI 10.1038/340437a0
[8]   OCEANIC PHYTOPLANKTON, ATMOSPHERIC SULFUR, CLOUD ALBEDO AND CLIMATE [J].
CHARLSON, RJ ;
LOVELOCK, JE ;
ANDREAE, MO ;
WARREN, SG .
NATURE, 1987, 326 (6114) :655-661
[9]  
Chenoweth M, 1996, B AM METEOROL SOC, V77, P2077, DOI 10.1175/1520-0477(1996)077<2077:SLAYWA>2.0.CO
[10]  
2