Multi Path FTIR Agriculture Air Pollution Measurement System

This paper details the design and validation of a Multiple Path OP-FTIR system with elevation and radial scanning ability and demonstrates its capabilities to quantify and monitor gaseous ammonia emitted from agricultural facilities. The OP-FTIR system has a 500 m range (1000 m full path length) and allows 360° radial scan and 45° scan in elevation. To study large scale sources, two or more similar systems may be needed. For comparison purposes, we ran two similar but not identical OP-FTIR systems side-by-side in a controlled lab environment and in a series of field environments. We determined that in a controlled environment, the two systems can attain an NH3 agreement of 1- 3% at concentrations above 500 ppb. Due to the short path length (~10 m) in the lab, 500 ppb was the detection limit of the two systems. Path lengths in a field are much longer, allowing a lower detection limit. Average agreement in the field was 1-6%. This difference in agreement from the laboratory is likely due to the non-homogeneous distribution of the pollutant

Validation of the Measurement of Pollution in the Troposphere (MOPITT) Experiment by Ground-Based Infrared Solar Spectroscopic Measurements of Carbon Monoxide (CO) and Methane (CH4)

The goal of the MOPITT experiment is to enhance our knowledge of the lower atmosphere system and particularly how it interacts with the surface/ocean/biomass systems. The particular focus is the distribution, transport, sources and sinks of carbon monoxide and methane in the troposphere. The MOPITT instrument was launched on EOS TERRA satellite December 18, 1999. After the launch and until March 22, 2000 the MOPITT instrument was in engineering and calibration mode. Beginning March 23, 2000 through May 6, 2001 the instrument was in a science measurement mode with some calibration breaks. On May 7, 2001 a criocooler on a side B died and channels 1 - 4 became inoperational. The MOPITT resumed its scientific measurements on August 25, 2001 with channels 5 - 8. With some calibration breaks the instrument currently provides the data. The project has three elements to it: hardware, data analysis and modeling. The MOPITT instrument, on the NASA EOS Terra satellite, measures the upwelling infrared radiance. Using the technique of correlation spectroscopy, information regarding the distribution of atmospheric CO and CH4 can be extracted. By using appropriate data analysis techniques, concentration profiles of CO are currently obtained on a global basis at a reasonably high horizontal (approximately 22km) and vertical resolution (approximately 3km). Column amounts of methane will be derived over the sunlit side of the orbit. These profiles are assimilated into models to study the chemistry and dynamics of CO, CH4 and other constituents of the lower atmosphere

[Analysis of Multiplatform CO (Carbon Monoxide) Measurements During Trace-P Mission]

Carbon monoxide is considered mission critical (TRACE-P NRA) because it is one of the gases involved in controlling the oxidizing power of the atmosphere and, as a tracer gas, is valuable in interpreting mission data sets. Carbon monoxide exhibits interannual differences, suggesting relatively short-term imbalances in sources and sinks. Sources of CO are dominated by fossil fuel combustion, biomass burning, and the photochemical oxidation of CH4 and nonmethane hydrocarbons while reaction with OH is believed to be the major sink for atmospheric CO, with additional losses due to soil uptake. Uncertainties in the magnitude and distribution of both sources and sinks remain fairly large however, and additional data are required to refine the global budget. Seasonal changes and a northern hemispheric latitudinal gradient have been described for a variety of Pacific basin sites through long-term monitoring of surface background levels. Latitudinal variations have also recently been described at upper tropospheric altitudes over a multi-year period by. TRACE-P will provide an aircraft survey of CO over the northern Pacific in the northern spring when CO concentrations are at their seasonal maximum in the northern hemisphere (NH) and at their seasonal minimum in the southern hemisphere (SH). Previous GTE missions, Le., PEM West-B and PEM Tropics-B, ground-based, and satellite observations (MAPS, April 1994) give us a general picture of the distribution of CO over the northern Pacific during this season. Based on these measurements, background CO levels over remote ocean areas are anticipated to be in the range of 110 - 180 ppbv, while those closer to the Asian continent may rise as high as 600 ppbv. These measurements also reveal high spatial variability (both horizontal and vertical) as well as temporal variations in CO over the area planned for the TRACE-P mission. This variability is a result of multiple CO sources, the meteorological complexity of transport processes, and the photochemical aging of air masses. The influence of biomass burning in the southern Pacific should be relatively small since the mission coincides with the southern tropical wet season when agricultural burning is at its seasonal low. The proposed CO measurements taken during TRACE-P should therefore largely be a function of the impact of various NH sources, primarily Asian and predominantly fossil fuel combustion and biomass burning. These processes are also major sources of many other atmospheric pollutants, consequently making accurate and precise CO measurements is one of the highest TRACE-P priorities [TRACE-P NRA]. The TRACE-P mission emphasizes the dual objectives of assessing the magnitude of the transport of chemically and radiatively important gases such as CO from Asia to the western Pacific, and determining how emissions change and are modified during this transport

Statistical Approach to Validation of Satellite Atmospheric Retrievals

A mathematical model for statistical estimate of the bias and noise in satellite retrievals of atmospheric profiles and a case study are presented. The model allows accurate validation of actual performance of the remote sensing system while in orbit by comparing its measurements to correlative data sets, e. g. radiosonde network. The model accounts for the following factors: (i) The satellite and validating systems sample volumes of the atmosphere at times and locations that are not exactly co-located. (ii) The validated and validating systems have different characteristics, e. g. different vertical resolution and noise level. All the above factors cause apparent difference between the data to be compared. The presented model makes the comparison accurate by allowing for the differences. To demonstrate its practicability we present the case study that involves the radiosonde data from three stations: ARM Tropical Western Pacific (0.5O S, 167O E), ARM Southern Great Planes (37O N, 98O W), and Lindenberg (52O N, 14O E). For each station we considered temperature profile validation scenario and estimated associated errors. The model can be used for interpretation of the validation results when the above mentioned sources of discrepancies are significant, as well as for evaluation of validation data sources, e.g. GRUAN (GCOS Reference Upper-Air Network)

Validation Assessment Model for Atmospheric Retrievals

A linear mathematical error model for the assessment of validation activity of atmospheric retrievals is presented. The purpose of the validation activity is to assess the actual performance of the remote sensing validated system while in orbit by comparing its measurements to some relevant—validating—data sets. The validating system samples volumes of the atmosphere at times and locations that are different from the ones when and where the validated system makes its own observations. The location of the validating system can be either stationary, e.g. a ground ARM site, or movable, e.g. an aircraft or some other satellites. The true states may be correlated or not. The sampled volumes differ from each other by their location, timing, and size. The validated and validating systems have different vertical resolution and grid, absolute accuracy, and noise level. All the above factors cause apparent differences between the data to be compared. The validation assessment model makes the comparison accurate by allowing for the differences. The model can be used for assessment and interpretation of the validation results when the above mentioned sources of discrepancies are significant, as well as for evaluation of a particular validating data source

Northern and southern hemisphere ground-based infrared spectroscopic measurements of tropospheric carbon monoxide and ethane

Time series of CO and C2H6 measurements have been derived from high-resolution infrared solar spectra recorded in Lauder, New Zealand (45.0 degrees S, 169.7 degrees E, altitude 0.37 km), and at the U.S. National Solar Observatory (31.9 degrees N, 111.6 degrees W, altitude 2.09 km) on Kitt Peak. Lauder observations were obtained between July 1993 and November 1997, while the Kitt Peak measurements were recorded between May 1977 and December 1997. Both databases were analyzed with spectroscopic parameters that included significant improvements for C2H6 relative to previous studies. Target CO and C2H6 lines were selected to achieve similar vertical samplings based on averaging kernels. These calculations show that partial columns from layers extending from the surface to the mean tropopause and from the mean tropopause to 100 km are nearly independent. Retrievals based on a semiempirical application of the Rodgers optimal estimation technique are reported for the lower laver, which has a broad maximum in sensitivity in the upper troposphere. The Lauder CO and C2H6 partial columns exhibit highly asymmetrical seasonal cycles with minima in austral autumn and sharp peaks in austral spring. The spring maxima are the result of tropical biomass burning emissions followed by deep convective vertical transport to the upper troposphere and long-range horizontal transport. Significant year-to-year variations are observed for both CO and C2H6, but the measured trends, (+0.37 +/- 0.57)% yr(-1) and (-0.64 +/- 0.79)% yr(-1), 1 sigma, respectively, indicate no significant long-term changes. The Kitt Peak data also exhibit CO and C2H6 seasonal variations in the lower layer with trends equal to (-0.27 +/- 0.17)% yr(-1) and (-1.20 +/- 0.35')% yr(-1), 1 sigma, respectively. Hence a decrease in the Kitt Peak tropospheric C2H6 column has been detected, though the CO trend is not significant. Both measurement sets are compared with previous observations, reported trends, and three-dimensional model calculations