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Improving a process-based biogeochemistry model using an atmospheric transport chemistry model and in-situ and remotely-sensed terrestrial and atmospheric data.

机译:使用大气传输化学模型以及原位和遥感的陆地和大气数据,改进基于过程的生物地球化学模型。

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摘要

To improve the quantification of methane emissions from natural wetlands, an integrated framework was developed. It includes an improved process-based model and a 4-D VAR inversion algorithm implemented with the adjoint GEOS-Chem model.;The new process-based model was tested comprehensively at two temperate peatlands in Michigan, USA, with historical measurement data for a 3-year period. The results showed that (1) the ebullition can be modeled as a mechanical process that is controlled by the atmospheric pressure, water table level and total pressure of the various dissolved gases; (2) the four-substance structure is the appropriate choice to correctly model the transport pathways to release wetland methane into the atmosphere; and (3) the estimated methane emission is very sensitive to the hydrological forcing used to drive the model and can be seriously biased due to an improper modeling of water tables. The wetland emission from wetland in 45°N north was thence quantified with the one-substance model, and was fed into the GEOS-Chem model for an assessment of forward transport and flux inversion for the year 2004.;The forward simulations were evaluated using observations including low frequency flask measurement, high frequency in-situ time series, atmospheric methane profiles from aircraft campaigns and retrievals from space instruments SCIMACHY and AIRS. It was found that simulations with the anthropogenic emission datasets compiled based on EDGAR4 dataset resulted in better agreement with the high precision surface measurements. The use of GFED2 and GFED3 datasets for methane fluxes from biomass burning lead to small differences in the forward simulations. Overall, the seasonal error characteristics of the model-AIRS misfit, and model-SCIAMACHY misfit, are around 1%-2% in most of the grid cells at the grid resolution for year 2004.;4D-Var inversions were conducted using the adjoint GEOS-Chem to obtain an improved estimation of the surface fluxes. The inversion experiments for year 2004 lead to posterior estimates of net surface methane emissions ranging from 496 Tg CH4 yr-1 to 585 Tg CH4 yr -1. The posterior estimates for the methane emission from vegetation, including wetland, rice paddy and wet tundra, range from 277 Tg CH4 yr-1 to 305 Tg CH4 yr-1.;This study was not possible to obtain a credible estimation for methane emissions from the natural wetland due to the significant uncertainties in the process-based modeling and the flux partition in the atmospheric inverse modeling. Further studies in both of these two regards are needed to improve our understanding of the global wetland methane dynamics.
机译:为了改善自然湿地甲烷排放的量化,开发了一个综合框架。它包括一个改进的基于过程的模型和一个与伴随的GEOS-Chem模型一起实现的4-D VAR反演算法;新的基于过程的模型在美国密歇根州的两个温带泥炭地进行了全面测试,并提供了历史数据3年期限。结果表明:(1)沸腾可以建模为受大气压力,地下水位和各种溶解气体总压力控制的机械过程; (2)四物质结构是正确模拟将湿地甲烷释放到大气中的运输途径的适当选择; (3)估算的甲烷排放量对用于驱动该模型的水文强迫非常敏感,并且由于地下水位建模不当而可能造成严重偏差。然后用一物质模型对北纬45°以北的湿地的湿地排放进行量化,并将其输入到GEOS-Chem模型中,以评估2004年的正向输运和通量反演。观测包括低频烧瓶测量,高频原地时间序列,飞机战役中的大气甲烷剖面以及从空间仪器SCIMACHY和AIRS的检索。发现使用基于EDGAR4数据集编译的人为排放数据集进行的仿真与高精度表面测量结果具有更好的一致性。将GFED2和GFED3数据集用于来自生物质燃烧的甲烷通量导致正演模拟中的微小差异。总体而言,在2004年的网格分辨率下,大多数网格单元中,AIRS模型和SCIAMACHY模型的季节误差特征约为1%-2%。; 4D-Var反演使用了伴随函数GEOS-Chem,以获得对表面通量的改进估计。 2004年的反演实验导致后表面净甲烷排放量的估算值从496 Tg CH4 yr-1到585 Tg CH4 yr -1。包括湿地,稻田和湿地苔原在内的植被的甲烷排放量的后验估计范围为277 Tg CH4 yr-1至305 Tg CH4 yr-1。该研究无法获得可靠的甲烷甲烷排放量估计值自然湿地,这是因为基于过程的建模和大气逆建模中的通量分配存在很大的不确定性。这两个方面都需要进一步研究,以增进我们对全球湿地甲烷动态的了解。

著录项

  • 作者

    Tang, Jinyun.;

  • 作者单位

    Purdue University.;

  • 授予单位 Purdue University.;
  • 学科 Atmospheric Chemistry.;Biogeochemistry.;Atmospheric Sciences.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 214 p.
  • 总页数 214
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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