Department of Earth, Environmental and Planetary Sciences, Rice University, Houston, TX, USA.
Department of Earth and Environmental Sciences, University of Rochester, Rochester, NY, USA.
Nature. 2019 Jun;570(7760):224-227. doi: 10.1038/s41586-019-1277-1. Epub 2019 Jun 12.
Tropospheric ozone (O) is a key component of air pollution and an important anthropogenic greenhouse gas. During the twentieth century, the proliferation of the internal combustion engine, rapid industrialization and land-use change led to a global-scale increase in O concentrations; however, the magnitude of this increase is uncertain. Atmospheric chemistry models typically predict an increase in the tropospheric O burden of between 25 and 50 per cent since 1900, whereas direct measurements made in the late nineteenth century indicate that surface O mixing ratios increased by up to 300 per cent over that time period. However, the accuracy and diagnostic power of these measurements remains controversial. Here we use a record of the clumped-isotope composition of molecular oxygen (OO in O) trapped in polar firn and ice from 1590 to 2016 AD, as well as atmospheric chemistry model simulations, to constrain changes in tropospheric O concentrations. We find that during the second half of the twentieth century, the proportion of OO in O decreased by 0.03 ± 0.02 parts per thousand (95 per cent confidence interval) below its 1590-1958 AD mean, which implies that tropospheric O increased by less than 40 per cent during that time. These results corroborate model predictions of global-scale increases in surface pollution and vegetative stress caused by increasing anthropogenic emissions of O precursors. We also estimate that the radiative forcing of tropospheric O since 1850 AD is probably less than +0.4 watts per square metre, consistent with results from recent climate modelling studies.
对流层臭氧 (O) 是空气污染的关键组成部分,也是一种重要的人为温室气体。在 20 世纪,内燃机的普及、工业化的快速发展和土地利用的变化导致全球范围内 O 浓度的增加;然而,这种增加的幅度尚不确定。大气化学模型通常预测,自 1900 年以来,对流层 O 负荷增加了 25%至 50%,而在 19 世纪末进行的直接测量表明,在此期间,地表 O 混合比增加了高达 300%。然而,这些测量的准确性和诊断能力仍然存在争议。在这里,我们利用从 1590 年到 2016 年在极地雪和冰中捕获的分子氧(O 中的 OO)的凝聚同位素组成记录,以及大气化学模型模拟,来限制对流层 O 浓度的变化。我们发现,在 20 世纪下半叶,O 中的 OO 比例比 1590-1958 年的平均值低了 0.03 ± 0.02 千分比(95%置信区间),这意味着对流层 O 的浓度在此期间增加不到 40%。这些结果与模型预测一致,即由于人为排放的 O 前体增加,导致地表污染和植被压力的全球范围内增加。我们还估计,自 1850 年以来,对流层 O 的辐射强迫可能小于+0.4 瓦特/平方米,与最近的气候建模研究结果一致。