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Evaluation of ACCMIP ozone simulations and ozonesonde sampling biases using a satellite-based multi-constituent chemical reanalysis

机译:使用基于卫星的多成分化学再分析评估ACCMIP臭氧模拟和臭氧探空仪采样偏差

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The Atmospheric Chemistry Climate Model Intercomparison Project (ACCMIP) ensemble ozone simulations for the present day from the 2000 decade simulation results are evaluated by a state-of-the-art multi-constituent atmospheric chemical reanalysis that ingests multiple satellite data including the Tropospheric Emission Spectrometer (TES), the Microwave Limb Sounder (MLS), the Ozone Monitoring Instrument (OMI), and the Measurement of Pollution in the Troposphere (MOPITT) for 2005–2009. Validation of the chemical reanalysis against global ozonesondes shows good agreement throughout the free troposphere and lower stratosphere for both seasonal and year-to-year variations, with an annual mean bias of less than 0.9?ppb in the middle and upper troposphere at the tropics and mid-latitudes. The reanalysis provides comprehensive spatiotemporal evaluation of chemistry-model performance that compliments direct ozonesonde comparisons, which are shown to suffer from significant sampling bias. The reanalysis reveals that the ACCMIP ensemble mean overestimates ozone in the northern extratropics by 6–11?ppb while underestimating by up to 18?ppb in the southern tropics over the Atlantic in the lower troposphere. Most models underestimate the spatial variability of the annual mean lower tropospheric concentrations in the extratropics of both hemispheres by up to 70?%. The ensemble mean also overestimates the seasonal amplitude by 25–70?% in the northern extratropics and overestimates the inter-hemispheric gradient by about 30?% in the lower and middle troposphere. A part of the discrepancies can be attributed to the 5-year reanalysis data for the decadal model simulations. However, these differences are less evident with the current sonde network. To estimate ozonesonde sampling biases, we computed model bias separately for global coverage and the ozonesonde network. The ozonesonde sampling bias in the evaluated model bias for the seasonal mean concentration relative to global coverage is 40–50?% over the western Pacific and east Indian Ocean and reaches 110?% over the equatorial Americas and up to 80?% for the global tropics. In contrast, the ozonesonde sampling bias is typically smaller than 30?% for the Arctic regions in the lower and middle troposphere. These systematic biases have implications for ozone radiative forcing and the response of chemistry to climate that can be further quantified as the satellite observational record extends to multiple decades.
机译:通过最新的多组分大气化学再分析方法(包括对流层发射光谱仪),利用最新的多组分大气化学再分析方法,对2000年以来的今天的大气化学气候模型比较项目(ACCMIP)整体臭氧模拟进行了评估。 (TES),微波测深仪(MLS),臭氧监测仪(OMI)以及2005-2009年对流层污染测量(MOPITT)。对全球臭氧探空仪进行化学再分析的验证表明,在自由对流层和低平流层中,季节变化和年际变化都具有良好的一致性,热带和中部对流层的年平均偏差小于0.9?ppb。中纬度。重新分析提供了对化学模型性能的综合时空评估,补充了直接进行的臭氧探空仪比较,结果表明臭氧采样仪存在明显的采样偏差。重新分析表明,ACCMIP集合平均值高估了北温带的臭氧6-11ppb,而低估了对流层低层的大西洋南部的热带臭氧,最高达18ppppb。大多数模型都低估了两个半球的外温带年平均对流层低年平均浓度的空间变异性高达70%。在北温带,集合平均还高估了季节幅度25-70%,而在对流层中低层,高估了半球间梯度约30%。部分差异可以归因于十年模型仿真的5年重新分析数据。但是,在当前的主机网络中,这些差异不太明显。为了估算臭氧探空仪的采样偏差,我们分别计算了全球覆盖范围和臭氧探空仪网络的模型偏差。在西太平洋和东印度洋,相对于全球覆盖率的季节性平均浓度评估模型偏差中的臭氧探空仪采样偏差在西太平洋和东印度洋为40–50%,在赤道美洲达到110%,全球最高达到80%。热带。相比之下,对流层中低层北极地区的臭氧探空仪采样偏差通常小于30%。这些系统性偏差对臭氧辐射强迫和化学物质对气候的响应具有影响,随着卫星观测记录延伸到数十年,可以进一步量化。

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