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Linking uncertainty in simulated Arctic ozone loss to uncertainties in modelled tropical stratospheric water vapour

机译:将模拟北极臭氧损失的不确定性与模型热带地流层水蒸气中的不确定性联系起来

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Stratospheric water vapour influences the chemical ozone loss in the polar stratosphere via control of the polar stratospheric cloud formation. The amount of water vapour entering the stratosphere through the tropical tropopause differs substantially between simulations from chemistry–climate models (CCMs). This is because the present-day models, e.g. CCMs, have difficulties in capturing the whole complexity of processes that control the water transport across the tropopause. As a result there are large differences in the stratospheric water vapour between the models. In this study we investigate the sensitivity of simulated Arctic ozone loss to the simulated amount of water vapour that enters the stratosphere through the tropical tropopause. We used a chemical transport model, FinROSE-CTM, forced by ERA-Interim meteorology. The water vapour concentration in the tropical tropopause was varied between 0.5 and 1.6 times the concentration in ERA-Interim, which is similar to the range seen in chemistry–climate models. The water vapour changes in the tropical tropopause led to about 1.5ppmv less and 2ppmv more water vapour in the Arctic polar vortex compared to the ERA-Interim, respectively. The change induced in the water vapour concentration in the tropical tropopause region was seen as a nearly one-to-one change in the Arctic polar vortex. We found that the impact of water vapour changes on ozone loss in the Arctic polar vortex depends on the meteorological conditions. The strongest effect was in intermediately cold stratospheric winters, such as the winter of 2013/2014, when added water vapour resulted in 2%–7% more ozone loss due to the additional formation of polar stratospheric clouds (PSCs) and associated chlorine activation on their surface, leading to ozone loss. The effect was less pronounced in cold winters such as the 2010/2011 winter because cold conditions persisted long enough for a nearly complete chlorine activation, even in simulations with prescribed stratospheric water vapour amount corresponding to the observed values. In this case addition of water vapour to the stratosphere led to increased areas of ICE PSCs but it did not increase the chlorine activation and ozone destruction significantly. In the warm winter of 2012/2013 the impact of water vapour concentration on ozone loss was small because the ozone loss was mainly NOx-induced. The results show that the simulated water vapour concentration in the tropical tropopause has a significant impact on the Arctic ozone loss and therefore needs to be well simulated in order to improve future projections of the recovery of the ozone layer.
机译:平流层水蒸气通过控制极性平流层云形成,影响极性平流层中的化学臭氧损失。通过热带对象流进入平流层的水蒸气量大幅不同于化学 - 气候模型(CCMS)的模拟之间。这是因为现在的模型,例如, CCMS,难以捕捉控制对流层流量的过程的整体复杂性。结果,模型之间的平坦散水蒸气存在较大的差异。在这项研究中,我们研究模拟北极臭氧损失对通过热带对象流入平流层的模拟量的水蒸气的敏感性。我们使用了化学传输模型,Finrose-CTM,被ERA-INSTIM气象学强制。热带对象流动中的水蒸气浓度在时代浓度的0.5%和1.6倍之间变化,类似于化学 - 气候模型中所见的范围。与ERA-Instim分别相比,热带对象流程中的水蒸气变化导致北极极性涡流中的约1.5ppmV较小和2ppmv更多的水蒸气。热带对象源地区水蒸气浓度中诱导的变化被认为是北极极性涡旋的几乎一对一的变化。我们发现,北极极性涡旋中臭氧损失的水蒸气变化的影响取决于气象条件。最强烈的效果是中间冷的平流层冬天,例如2013/2014年的冬季,当添加的水蒸气导致臭氧损失增加2%-7%,由于极地平流层云(PSC)和相关氯激活的额外形成他们的表面,导致臭氧损失。寒冷的冬季效果不太明显,例如2010/2011冬季,因为冷条件足够长,即使在与观察到的值对应的规定的平坦散水蒸气量的模拟中,仍然足够长的氯激活。在这种情况下,向平流层添加水蒸气导致冰PSC的增加的区域,但它没有显着增加氯激活和臭氧的破坏。在2012/2013年的温暖冬季,水蒸气浓度对臭氧损失的影响很小,因为臭氧损失主要是NOx诱导的。结果表明,热带对象流中的模拟水蒸气浓度对北极臭氧损失产生了重大影响,因此需要良好的模拟,以便改善臭氧层恢复的未来突起。

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