Engineering topics

Yang, Kai

Publications and source records attributed to Yang, Kai.

23 records · Page 2

NASA NTRS2011

Rapid Transpacific Transport in Autumn Observed by the A-Train Satellites

Transpacific transport of dust and pollutants is well documented for spring, but less so for other seasons. Here we investigate rapid transpacific transport in autumn utilizing the A-train satellites. In three episodes studied as examples, SO2 plumes over East Asia were detected by the Ozone Monitoring Instrument aboard the Aura satellite, and found to reach North America in 5-6 days. They were likely derived from anthropogenic sources, given that identical transport patterns of CO, a tracer for incomplete combustion, were simultaneously observed by the Aqua satellite. Trajectory analysis and meteorological data were employed to explore the meteorological circumstances surrounding these events: like many of their counterparts in spring, all three plumes were lifted to the free troposphere in warm conveyor belt associated with mid-latitude wave cyclones, and their migration to downwind region was regulated by the meteorology over the East Pacific. These cases provide further evidence that a fraction of S02 could escape wet scavenging, and be transported at much greater efficiency than NOx (NO + N02). An analysis of the S02 and CO data from September to November during 2005-2008 found 16 S02 long-range transport episodes, out of 62 Asian outflow events. While the counts are sensitive to the choice of criteria, they suggest that the long-range transport of Asian sulfur species occurs quite frequently, and could exert strong impacts on large downstream areas. This study also highlights the importance of transpacific transport in autumn, which has thus far been rarely studied and deserves more attention from the community.

Li. Can↗

NASA NTRS2011

Effect of Tropospheric Aerosols in Satellite-Based Trace Gas Retrieval

Scattering and absorption by tropospheric aerosol particles have an effect on the airmass factor (AMF), a fundamental quantity for trace gas concentration retrieval by inversion of satellite measurements. The interference effect depends on the aerosols micro-physical and optical properties as well as the relative distribution of the tropospheric trace gas and aerosol load. Quantifying the aerosol impact on trace gas retrieval requires a sensitivity study using radiative transfer calculations. In this presentation we will describe a recently initiated effort to characterize the aerosol-related error in trace gas retrievals when the presence of aerosol particles is not accounted in the inversion procedure. A general description of the project will be presented and preliminary results on aerosol effects on SO2 retrieved concentrations will be discussed.

Krotkov, Nickolay↗

NASA NTRS2011

Next-Generation Aura/OMI NO2 and SO2 Products

The measurement of both SO2 and NO2 gases are recognized as an essential component of atmospheric composition missions. We describe current capabilities and limitations of the operational Aura/OMI NO2 and SO2 data that have been used by a large number of researchers. Analyses of the data and validation studies have brought to light a number of areas in which these products can be expanded and improved. Major improvements for new NASA standard (SP) NO2 product include more accurate tropospheric and stratospheric column amounts, along with much improved error estimates and diagnostics. Our approach uses a monthly NO2 climatology based on the NASA Global Modeling Initiative (GMI) chemistry-transport model and takes advantage of OMI data from cloudy scenes to find clean areas where the contribution from the trap NO2 column is relatively small. We then use a new filtering, interpolation and smoothing techniques for separating the stratospheric and tropospheric components of NO2, minimizing the influence of a priori information. The new algorithm greatly improves the structure of stratospheric features relative to the original SP. For the next-generation OMI SO2 product we plan to implement operationally the offline iterative spectral fitting (ISF) algorithm and re-process the OMI Level-2 SO2 dataset using a priori SO2 and aerosol profiles, clouds, and surface reflectivity appropriate for observation conditions. This will improve the ability to detect and quantify weak tropospheric SO2 loadings. The new algorithm is validated using aircraft in-situ data during field campaigns in China (2005 and 2008) and in Maryland (Frostburg, 2010 and DISCOVER-AQ in July 2011). The height of the SO2 plumes will also be estimated for high SO2 loading cases (e.g., volcanic eruptions). The same SO2 algorithm will be applied to the data from OMPS sensor to be launched on NPP satellite later this year. The next-generation NO2 and SO2 products will provide critical information (e.g., averaging kernels) for evaluation of chemistry-transport models, for data assimilation, and to impose top-down constraints on the SO2 and NO2 emission sources.

Krotkov, Nickolay↗

NASA NTRS2008

Validation of SO2 Retrievals from the Ozone Monitoring Instrument over NE China

The Dutch-Finnish Ozone Monitoring Instrument (OMI) launched on the NASA Aura satellite in July 2004 offers unprecedented spatial resolution, coupled with contiguous daily global coverage, for space-based UV measurements of sulfur dioxide (SO2). We present a first validation of the OMI SO2 data with in situ aircraft measurements in NE China in April 2005. The study demonstrates that OMI can distinguish between background SO2 conditions and heavy pollution on a daily basis. The noise (expressed as the standard deviation,sigma) is approximately 1.5 DU (Dobson units; 1 DU = 2.69 10 (exp 16) molecules/cm (exp 2)) for instantaneous field of view boundary layer (PBL) SO2 data. Temporal and spatial averaging can reduce the noise to sigma approximetly 0.3 DU over a remote region of the South Pacific; the long-term average over this remote location was within 0.1 DU of zero. Under polluted conditions collection 2 OMI data are higher than aircraft measurements by a factor of two. Improved calibrations of the radiance and irradiance data (collection 3) result in better agreement with aircraft measurements on polluted days. The air mass corrected collection 3 data still show positive bias and sensitivity to UV absorbing aerosols. The difference between the in situ data and the OMI SO2 measurements within 30 km of the aircraft profiles was about 1 DU, equivalent to approximately 5 ppb from 0 to 3000 m altitude. Quantifying the SO2 and aerosol profiles and spectral dependence of aerosol absorption between 310 and 330 nm are critical for an accurate estimate of SO2 from satellite UV measurements.

Krotkov, Nickolay A.↗

NASA NTRS2004

First Look at the Upper Tropospheric Ozone Mixing Ratio from OMI Estimated using the Cloud Slicing Technique

The Cloud Slicing technique has emerged as a powerful tool for the study of ozone in the upper troposphere. In this technique one looks at the variation with cloud height of the above-cloud column ozone derived from the backscattered ultraviolet instruments, such as TOMS, to determine the ozone mixing ratio. For this technique to work properly one needs an instrument with relatively good horizontal resolution with very good signal to noise in measuring above-cloud column ozone. In addition, one needs the (radiatively) effective cloud pressure rather than the cloud-top pressure, for the ultraviolet photons received by a satellite instrument are scattered from inside the cloud rather than from the top. For this study we use data from the OMI sensor, which was recently launched on the EOS Aura satellite. OMI is a W-Visible backscattering instrument with a nadir pixel size of 13 x 24 km. The effective cloud pressure is derived from a new algorithm based on Rotational Raman Scattering and O2-O2, absorption in the 340-400 nm band of OMI.

Bhartia, Pawan K.↗