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首页> 外文期刊>Journal of Geophysical Research, D. Atmospheres: JGR >Observation of a fast ozone loss in the marginal ice zone of the Arctic Ocean
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Observation of a fast ozone loss in the marginal ice zone of the Arctic Ocean

机译:在北冰洋边缘冰区观察到快速臭氧流失

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In both polar regions tropospheric ozone regularly decreases during springtime to negligible concentrations in the atmospheric boundary layer. Here we report the observation of a dramatic ozone depletion event in the atmospheric boundary layer in the vicinity of new ice fields in the marginal ice zone (MIZ) of the Arctic Ocean monitored by instrumentation on board the icebreaker RV Polarstern. The ozone mixing ratio decreased from approximately 40 to below 1 ppbV in less than 7 hours. The analyses of backward trajectories and the synoptic conditions indicate that the observed decrease was not caused by the transport of ozone-free air, but that the ozone depletion occurred locally. Accordingly, bromine oxide, which is formed during the photochemical destruction of ozone in the presence of reactive bromine compounds, was significantly enhanced: Bromine oxide concentrations of approximately 1.8 · 109 molecules cm?3 are retrieved around the same location from SCIAMACHY satellite observations assuming a uniform vertical distribution within the boundary layer. The release of bromine in the MIZ where the new ice formation took place appears to be the most likely explanation for the activation of reactive bromine compounds and subsequent depletion of ozone. Since the conditions were favorable for the formation of frost flowers, we suggest that these are the most likely sources of the reactive bromine. However, contributions of heterogeneous reactions on other surfaces like the highly saline brine on the new ice, aerosols generated from frost flowers, and sea salt aerosols deposited on the snowpack on top of the sea ice cannot be ruled out.
机译:在两个极地地区,对流层臭氧在春季有规律地减少到大气边界层中的浓度可以忽略不计。在这里,我们报告了在破冰船RV Polarstern上的仪器监测下,在北冰洋边缘冰区(MIZ)的新冰场附近的大气边界层中,发生了剧烈的臭氧消耗事件,并​​进行了观测。在不到7小时的时间内,臭氧混合比从大约40降至1 ppbV以下。对后退轨迹和天气状况的分析表明,观察到的减少不是由无臭氧空气的运输引起的,而是臭氧消耗在局部发生。因此,在存在反应性溴化合物的情况下臭氧光化学破坏过程中形成的氧化溴得到了显着增强:假设在相同位置附近从SCIAMACHY卫星观测到的相同位置处回收到约1.8·109分子cm?3的氧化溴浓度。边界层内的垂直分布均匀。在发生新冰的MIZ中释放溴似乎是反应性溴化合物活化和随后臭氧消耗的最可能解释。由于条件有利于霜花的形成,我们建议这些是活性溴的最可能来源。但是,不能排除其他表面上异质反应的影响,例如新冰上的高盐盐水,霜花产生的气溶胶以及沉积在海冰顶部雪堆上的海盐气溶胶。

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