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本文引用的文献

1
Boundary layer halogens in coastal Antarctica.南极沿海地区的边界层卤素。
Science. 2007 Jul 20;317(5836):348-51. doi: 10.1126/science.1141408.
2
The role of Br2 and BrCl in surface ozone destruction at polar sunrise.Br2和BrCl在极地日出时对平流层臭氧破坏中的作用。
Science. 2001 Jan 19;291(5503):471-4. doi: 10.1126/science.291.5503.471.

利用主动长程差分光学吸收光谱法观测北极阿蒙森湾的卤素物种。

Observation of halogen species in the Amundsen Gulf, Arctic, by active long-path differential optical absorption spectroscopy.

机构信息

Institute of Environmental Physics, University of Heidelberg, Im Neuenheimer Feld 229, 69120 Heidelberg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2010 Apr 13;107(15):6582-7. doi: 10.1073/pnas.0912231107. Epub 2010 Feb 16.

DOI:10.1073/pnas.0912231107
PMID:20160121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2872394/
Abstract

In the polar tropospheric boundary layer, reactive halogen species (RHS) are responsible for ozone depletion as well as the oxidation of elemental mercury and dimethyl sulphide. After polar sunrise, air masses enriched in reactive bromine cover areas of several million square kilometers. Still, the source and release mechanisms of halogens are not completely understood. We report measurements of halogen oxides performed in the Amundsen Gulf, Arctic, during spring 2008. Active long-path differential optical absorption spectroscopy (LP-DOAS) measurements were set up offshore, several kilometers from the coast, directly on the sea ice, which was never done before. High bromine oxide concentrations were detected frequently during sunlight hours with a characteristic daily cycle showing morning and evening maxima and a minimum at noon. The, so far, highest observed average mixing ratio in the polar boundary layer of 41 pmol/mol (equal to pptv) was detected. Only short sea ice contact is required to release high amounts of bromine. An observed linear decrease of maximum bromine oxide levels with ambient temperature during sunlight, between -24 degrees C and -15 degrees C, provides indications on the conditions required for the emission of RHS. In addition, the data indicate the presence of reactive chlorine in the Arctic boundary layer. In contrast to Antarctica, iodine oxide was not detected above a detection limit of 0.3 pmol/mol.

摘要

在极地对流层边界层中,活性卤素物质(RHS)是臭氧消耗以及元素汞和二甲基硫氧化的原因。极地日出后,富含活性溴的空气团覆盖了数百万平方公里的区域。尽管如此,卤素的来源和释放机制仍不完全清楚。我们报告了在 2008 年春季在南极洲阿蒙森湾进行的卤氧化物测量结果。在距海岸数公里的近海处直接在海冰上进行了主动长程差分光学吸收光谱(LP-DOAS)测量,这是以前从未做过的。在阳光充足的时间里,经常检测到高溴氧化物浓度,其特征的日循环显示出早晨和傍晚的最大值以及中午的最小值。迄今为止,在极地边界层中观察到的最高平均混合比为 41 pmol/mol(相当于 pptv)。只需短暂接触海冰就可以释放大量的溴。在阳光照射下,环境温度从-24°C 到-15°C 之间,溴氧化物的最大值呈线性下降,这表明了 RHS 排放的条件。此外,数据表明活性氯存在于北极边界层中。与南极洲不同,碘氧化物的检测限为 0.3 pmol/mol 以上,未被检测到。