1989年春季阿拉斯加州巴罗地表臭氧破坏的化学和气象影响

W.T Sturges , R.C Schnell , S Landsberger , S.J Oltmans , J.M Harris, S.-M Li
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引用次数: 37

摘要

1989年3月和4月在AK Barrow测量了地表臭氧、微粒溴以及无机和有机气态溴,以检查北极春季地表臭氧破坏的原因。研究人员还研究了同一时期阿拉斯加北极地区的卫星图像,并将其与计算出的气团轨迹结合起来,以调查臭氧消耗空气的可能来源。研究发现,在主要臭氧消耗事件(O3<25 ppbv)期间,颗粒溴和有机溴化气体溴仿和二溴氯甲烷的浓度升高。气团轨迹表明,空气穿过了卫星观测到的北冰洋地区。铅的传输时间通常为一天或更短,这表明臭氧的快速损失机制。用接近日光条件的光化辐射照射室内的夜间空气,也显示出类似的微粒溴的快速产生。这种快速反应与溴仿的气相光解不一致,但进一步的研究表明,颗粒相中有相当一部分有机溴;因此,非均相反应在臭氧破坏中可能是重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemical and meteorological influences on surface ozone destruction at Barrow, Alaska, during Spring 1989

Surface ozone, particulate bromine and inorganic and organic gaseous bromine species were measured at Barrow, AK, during March and April 1989 to examine the causes of surface ozone destruction during the arctic spring. Satellite images of the Alaskan Arctic taken during the same period were also studied in conjunction with calculated air mass trajectories to Barrow to investigate the possible origins of the ozone-depleted air. It was found that during major ozone depletion events (O3<25 ppbv) concentrations of particulate bromine and the organic brominated gases bromoform and dibromochloromethane were elevated. Air mass trajectories indicated that the air had crossed areas of the Arctic Ocean where leads had been observed by satellite. The transport time from the leads was typically a day or less, suggesting a fast loss mechanism for ozone. A similarly fast production of particulate bromine was shown by irradiating ambient nighttime air in a chamber with actinic radiation that approximated daylight conditions. Such rapid reactions are not in keeping with gas-phase photolysis of bromoform, but further studies showed evidence for a substantial fraction of organic bromine in the particulate phase; thus heterogeneous reactions may be important in ozone destruction.

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