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A test of our understanding of the ozone chemistry in the arctic polar vortex based on in-situ measurements of ClO, BrO, and O3, in the 1994/95 winter

机译:根据1994/95年冬季对ClO,BrO和O3的原位测量,测试我们对北极极涡中臭氧化学的理解

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摘要

We present an analysis of in situ measurements of ClO, BrO, O-3, and long-lived tracers obtained on a balloon flight in the Arctic polar vortex launched from Kiruna, Sweden, 68 degrees N, on February 3, 1995. Using the method of tracer correlations, we deduce that the air masses sampled at an altitude of 21 km (480 K potential temperature), where a layer of enhanced ClO mixing ratios of up to 1150 parts per trillion by volume was observed, experienced a cumulative chemical ozone loss of 1.0+/-0.3 ppmv between late November 1994 and early February 1995, This estimate of chemical ozone loss can be confirmed using independent data sets and independent methods. Calculations using a trajectory box model show that the simulations underestimate the cumulative ozone loss by approximately a factor of 2, although observed ClO and BrO mixing ratios are well reproduced by the model. Employing additional simulations of ozone loss rates for idealized conditions, we conclude that the known chlorine and bromine catalytic cycles destroying odd oxygen with the known rate constants and absorption cross sections do not quantitatively account for the early winter ozone losses infered for air masses observed at 21 km.
机译:我们对1995年2月3日从瑞典基律纳(N°)于北纬68度发射的北极极涡中的气球飞行中获得的ClO,BrO,O-3和长寿命示踪剂进行了现场测量分析。示踪剂相关的方法,我们推论到在21 km(480 K的潜在温度)高度采样的空气质量中,观察到一层增强的ClO混合比高达1150千亿分之一体积的层,经历了累积的化学臭氧在1994年11月下旬至1995年2月初之间的臭氧损失为1.0 +/- 0.3 ppmv,可以使用独立的数据集和独立的方法来确定化学臭氧损失的估算值。使用轨迹盒模型进行的计算表明,尽管该模型很好地再现了观察到的ClO和BrO混合比,但模拟低估了累积臭氧损失约2倍。通过对理想条件下的臭氧损失速率进行其他模拟,我们得出结论,已知的氯和溴催化循环以已知的速率常数和吸收截面破坏了奇数氧,并不能定量地解释21时观测到的空气质量所导致的冬季早期臭氧损失。公里

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