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Gleason, James F.

Publications and source records attributed to Gleason, James F..

Recent Large Reduction in Sulfur Dioxide Emissions from Chinese Power Plants Observed by the Ozone Monitoring Instrument

The Ozone Monitoring Instrument (OMI) aboard NASA's Aura satellite observed substantial increases in total column SO2 and tropospheric column NO2 from 2005 to 2007, over several areas in northern China where large coal-fired power plants were built during this period. The OMI-observed SO2/NO2 ratio is consistent with the SO2/ NO2, emissions estimated from a bottom-up approach. In 2008 over the same areas, OMI detected little change in NO2, suggesting steady electricity output from the power plants. However, dramatic reductions of S0 2 emissions were observed by OMI at the same time. These reductions confirm the effectiveness of the flue-gas desulfurization (FGD) devices in reducing S02 emissions, which likely became operational between 2007 and 2008. This study further demonstrates that the satellite sensors can monitor and characterize anthropogenic emissions from large point sources.

Li, Can

Algorithm for NO2 Vertical Column Retrieval from the Ozone Monitoring Instrument

We describe the operational algorithm for the retrieval of stratospheric, tropospheric, and total column densities of nitrogen dioxide NO2 from earthshine radiances measured by the Ozone Monitoring Instrument (OMI), aboard the EOS-Aura satellite. The algorithm uses the DOAS method for the retrieval of slant column NO densities. Air mass factors (AMFs) calculated from a stratospheric NO2 profile are used to make initial estimates of the vertical column density. Using data collected over a 24-h period, a smooth estimate of the global stratospheric field is constructed. Where the initial vertical column densities exceed the estimated stratospheric field, we infer the presence of tropospheric NO2, and recalculate the vertical column density (VCD) using an AMF calculated from an assumed tropospheric NO2 profile. The parameters that control the operational algorithm were selected with the aid of a set of data assembled from stratospheric and tropospheric chemical transport models. We apply the optimized algorithm to OMI data and present global maps of NO2 VCDs for the first time.

Bucsela, Eric J.

First Global Maps of Stratospheric and Tropospheric NO2 from OMI

The Ozone Monitoring Instrument (OMI) was launched successfully in July 2004, as one of four instruments on the EOS Aura satellite. OMI makes hyperspectral measurements that are used to retrieve column densities of critical trace gases, including formaldehyde, BrO, SO2 and NO2 . We present the first results from the OM1 operational NO2 algorithm and demonstrate its ability to retrieve the tropospheric and stratospheric components of NO2. The DOAS method is used to determine slant column densities, and initial air mass factors (AMFs) are used. to give initial estimates of the vertical column densities (VCDs). VCDs from up to 15 consecutive orbits are collected, and a spatial filtering technique is applied to extract the synoptic-scale features characteristic of the stratospheric, field. features to be evidence of tropospheric excess NO2 , and apply an AMF appropriate to polluted conditions, to obtain an improved retrieval of the NO2 total VCD. We describe the assumptions underlying the algorithm in detail, and show global maps of NO2 VCDs, based on the first operational data from OMI.

Bucsela, Eric J.

Tropospheric Chemistry Studies using Observations from GOME and TOMS

Studies to quantitatively determine trace gas and aerosol amounts from the Global Ozone Monitoring Experiment (GOME) and the Total Ozone Monitoring Experiment (TOMS) and to perform chemical modeling studies which utilize these results are given. This includes: 1. Analysis of measurements from the GOME and TOMS instruments for troposphere distributions of O3 and HCHO; troposphere enhancements of SO2, NO2 and aerosols associated with major sources; and springtime events of elevated BrO in the lower Arctic troposphere. 2. Application of a global 3-dimensional model of troposphere chemistry to interpret the GOME observations in terms of the factors controlling the abundances of troposphere ozone and OH.

Chance, Kelly

Monitoring Air Quality from Space using AURA Data

Measurements from the Earth Observing System (EOS) AURA mission will provide a unique perspective on air quality monitoring. Ozone, nitrogen dioxide, formaldehyde and aerosols from the Ozone Monitoring Instrument (OMI) and carbon monoxide from the Tropospheric Emission Spectrometer (TES) will be simultaneously measured with the spatial resolution and coverage needed for improving our understanding of air quality. AURA data products useful for air quality monitoring will be given.

Gleason, James F.

Workshop on Spanning Regional-to-Global Pollution

Pollution is often considered a localized phenomenon, but it is now clear that it travels from region-to-region, country to country, and even continent to continent. In addition to urban pollution in developed countries, large emissions from developing nations and large-scale biomass fires add to the global pollution burden. Ozone and aerosols are two components of pollution that contribute to radiative forcing of the earth s climate. In turn, as climate changes, rates of chemical and microphysical reactions may be perturbed. Considering the earth as a coupled chemical-microphysical-climate system poses challenges for models and observations alike. These issues were the topic of a Workshop held in May 2002 at NASA GSFC s Laboratory for Atmospheres. Highlights of the Workshop are summarized in this article.

Thompson, Anne M.

An Improved Retrieval of Tropospheric Nitrogen Dioxide from GOME

We present a retrieval of tropospheric nitrogen dioxide (NO2) columns from the Global Ozone Monitoring Experiment (GOME) satellite instrument that improves in several ways over previous retrievals, especially in the accounting of Rayleigh and cloud scattering. Slant columns, which are directly fitted without low-pass filtering or spectral smoothing, are corrected for an artificial offset likely induced by spectral structure on the diffuser plate of the GOME instrument. The stratospheric column is determined from NO2 columns over the remote Pacific Ocean to minimize contamination from tropospheric NO2. The air mass factor (AMF) used to convert slant columns to vertical columns is calculated from the integral of the relative vertical NO2 distribution from a global 3-D model of tropospheric chemistry driven by assimilated meteorological data (Global Earth Observing System (GEOS)-CHEM), weighted by altitude dependent scattering weights computed with a radiative transfer model (Linearized Discrete Ordinate Radiative Transfer), using local surface albedos determined from GOME observations at NO2 wavelengths. The AMF calculation accounts for cloud scattering using cloud fraction, cloud top pressure, and cloud optical thickness from a cloud retrieval algorithm (GOME Cloud Retrieval Algorithm). Over continental regions with high surface emissions, clouds decrease the AMT by 20- 30% relative to clear sky. GOME is almost twice as sensitive to tropospheric NO2 columns over ocean than over land. Comparison of the retrieved tropospheric NO2 columns for July 1996 with GEOS-CHEM values tests both the retrieval and the nitrogen oxide radical (NOx) emissions inventories used in GEOS-CHEM. Retrieved tropospheric NO2 columns over the United States, where NOx emissions are particularly well known, are within 18% of GEOS-CHEM columns and are strongly spatially correlated (r = 0.78, n = 288, p less than 0.005). Retrieved columns show more NO2 than GEOS-CHEM columns over the Transvaal region of South Africa and industrial regions of the northeast United States and Europe. They are lower over Houston, India, eastern Asia, and the biomass burning region of central Africa, possibly because of biases from absorbing aerosols.

Martin, Randall V.

A Comparison of HALOE V19 with SAGE II V6.00 Ozone Observations using Trajectory Mapping

We apply trajectory mapping to an eight-year intercomparison of ozone observations from HALOE (V19) and SAGE II (V6.00) for the months March, May, June, September, October, and December from the period December 1991 - October 1999. Our results, which represent the most extensive such intercomparison of these two data sets to date, suggest a root-mean -square difference between the two data sets of greater than 15% below 22 km and of 4 - 12% throughout most of the rest of the stratosphere. In addition, we find a bias with HALOE ozone low relative to SAGE II by 5 - 20% below 22 km between 40degS and 40degN. Biases throughout most of the rest of the stratosphere are nearly nonexistent. Finally, our analysis suggests almost no drift in the bias between the data sets is observed over the period of study. In the course of our study, we also determine that the employment of the Wang-Cunnold criteria is still recommended with the V6.00 SAGE II ozone data. Results with the new versions of the data sets show significant improvement over previous versions, particularly in the elimination of mid-stratospheric biases and the elimination of the previously observed drifts in the biases between the data sets in the lower stratosphere. Since HALOE V19 and V18 ozone are very similar, these changes can likely be attributed to improvements in the SAGE II retrieval.

Morris, Gary A.

Characterization and analysis of the Nimbus-7 SBUV data in the non-sync period (February 1987 - June 1990)

The SBUV instrument, on Nimbus-7, measures the backscatter ultraviolet radiance at 12 wavelengths. The radiance data from these wavelengths was used to deduce the ozone profile and the total column ozone. In February 1987, there was an instrument malfunction. The purpose of this paper is to describe the malfunction, to determine the effect of the malfunction on the data quality, and if possible, to correct for the effects of the malfunction on the data from the SBUV instrument.

Gleason, James F.

Altitude dependence of stratospheric ozone trends based on Nimbus 7 SBUV data

A multiple regression statistical model is applied to estimate the altitude, latitude, and seasonal dependences of stratospheric ozone trends using 11.5 years of Nimbus 7 SBUV data for the period November 1978 to June 1990. In the upper stratosphere, the derived trends agree in both latitude dependence and approximate amplitude with published predictions from stratospheric models that consider gas-phase chemical processes together with the observed approx. 0.1 ppbV per year increase in tropospheric chlorine. The dominant contribution to column ozone trends occurs in the lower stratosphere where significant negative trends are present at latitudes greater than 20 deg in both hemispheres. The observed latitude dependence is qualitatively consistent with model predictions that include the effects of heterogeneous chemical ozone losses on lower stratospheric aerosols.

Hood, Lon L.

Errors and ozone measurement

It is held that Mimm's (1993) comparison of hand-held TOPS instrument data with the Nimbus 7 satellite's Total Ozone Mapping Spectrometer's (TOMS) ozone data was intrinsically flawed, in that the TOMS data were preliminary and therefore unsuited for quantitative analysis. It is noted that the TOMS calibration was in error.

Mcpeters, Richard D.