...
首页> 外文期刊>Remote Sensing >Seven Years’ Observation of Mid-Upper Tropospheric Methane from Atmospheric Infrared Sounder
【24h】

Seven Years’ Observation of Mid-Upper Tropospheric Methane from Atmospheric Infrared Sounder

机译:大气红外测深仪对中层对流层甲烷七年观测

获取原文
           

摘要

The Atmospheric Infrared Sounder (AIRS) on EOS/Aqua platform provides a measurement of global methane (CH4) in the mid-upper troposphere since September, 2002. As a thermal infrared sounder, the most sensitivity of AIRS to atmospheric CH4 is in the mid-upper troposphere with the degree of freedom of ~1.0. Validation of AIRS CH4 product versus thousands of aircraft profiles (convolved using the AIRS averaging kernels) demonstrates that its RMS error (RMSE) is mostly less than 1.5%, and its quality is pretty stable from 2003 to 2009. For scientific analysis of the spatial and temporal variation of mid-upper tropospheric CH4 (MUT-CH4) in the High Northern Hemisphere (HNH), it is more valuable to use the AIRS retrieved CH4 in a layer of about 100 hPa below tropopause (“Representative Layer”) than in a fixed pressure layer. Further analysis of deseasonalized time-series of AIRS CH4 in both a fixed pressure layer and the “Representative Layer” of AIRS (only for the HNH) from 2003 to 2009 indicates that, similar to the CH4 in the marine boundary layer (MBL) that was found to increase in 2007–2008, MUT-CH4 was also observed to have a recent increase but the most significant increase occurred in 2008. MUT-CH4 continued to increase in 2009, especially in the HNH. Moreover, the trend of MUT-CH4 from 2006 to 2008 is lower than the trend of CH4 in the MBL by 30–40% in both the southern hemisphere and HNH. This delay for the MUT-CH4 increase of about one year than CH4 in the MBL as well as the smaller increase trend for MUT-CH4 suggest that surface emission is likely a major driver for the recent CH4 increase. It is also found that the seasonal cycle of MUT-CH4 is different from CH4 in the MBL due to the impact of transport, in addition to the surface emission and the photochemical loss.
机译:自2002年9月以来,EOS / Aqua平台上的大气红外测深仪(AIRS)提供了对流层中上层大气中甲烷(CH 4 )的测量。作为热红外测深仪,大气CH 4 的AIRS在对流层中上部,自由度约为1.0。对AIRS CH 4 产品相对于数千架飞机配置文件(使用AIRS平均内核进行卷积)的验证表明,其RMS误差(RMSE)大多小于1.5%,并且从2003年到2007年,其质量相当稳定2009年。为了科学地分析北半球高空对流层中上层CH 4 (MUT-CH 4 )的时空变化,对于在对流层顶以下约100 hPa的层(“代表层”)中使用AIRS检索的CH 4 (比在固定压力层中使用)有价值。进一步分析2003年至2009年AIRS CH 4 在固定压力层和AIRS“代表层”(仅适用于HNH)中的淡季时间序列,表明与CH <发现海洋边界层(MBL)中的sub> 4 在2007–2008年有所增加,还观察到MUT-CH 4 最近有所增加,但最大的增加发生在2008年。MUT-CH 4 在2009年继续增加,特别是在HNH中。此外,从2006年到2008年,MUT-CH 4 的趋势比南北半球和HNH的MBL的CH 4 的趋势低30-40%。 。 MUT-CH 4 的延迟比MBL中的CH 4 延迟约一年,并且MUT-CH 4 的增长趋势较小。 sub>暗示表面排放可能是近期CH 4 增加的主要驱动力。还发现由于运输的影响,MUT-CH 4 的季节周期与MBL中的CH 4 的季节周期不同,除了表面发射和水汽的影响。光化学损失。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号