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Publications and source records attributed to Ridley, B. A..
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Results from an intercomparison of techniques to measure tropospheric levels of nitric oxide (NO) are discussed. The intercomparison was part of the National Aeronautics and Space Administration's Global Tropospheric Experiment and was conducted at Wallops Island, VA, in July 1983. Instruments intercompared included a laser-induced fluorescence system and two chemiluminescence instruments. The intercomparisons were performed with ambient air at NO mixing ratios ranging from 10 to 60 pptv and NO-enriched ambient air at mixing ratios from 20 to 170 pptv. All instruments sampled from a common manifold. The techniques exhibited a high degree of correlation among themselves and with changes in the NO mixing ratio. Agreement among the three techniques was placed at approximately + or - 30 percent. Within this level of agreement, no artifacts or species interferences were identified.
In July of 1983, ambient measurements of nitric oxide (NO) were obtained at Wallops Island, VA, during the NASA GTE/CITE ground-based instrument intercomparison field study. The instrument, which was designed for measurements in the remote troposphere from an aircraft platform, is briefly described. Ten days of ambient air observations showed broadly uniform diurnal behavior, although considerable variability was encountered. Two distinct synoptic meteorological conditions resulted in markedly different levels of nitric oxide abundance. When the local winds were from the north to west sectors, which placed the sampling site within 130 to 300 km of large urban centers, the midday mixing ratios were typically in the range of 200-300 pptv. In contrast, when the air mass sustained a 1- or 2-day period over the Atlantic Ocean, the mixing ratios were substantially lower and in the 50-60 pptv range.
The first study is presented in which the mixing ratios of peroxyactyl nitrate (PAN) and nitrogen oxides, as well as those of peroxypropionyl nitrate and O3 and relevant meteorological parameters, were measured concurrently at a location that receives clean, continental air. The results show that, in clean conditions, nitrogen oxides present in the form of PAN can be as much or more abundant than the inorganic form. In addition, PAN can be an important source of peroxyacetyl radicals which may be important to oxidation processes in the gas as well as liquid phases.
Results from an intercomparison of methods to measure carbon monoxide (CO), nitric oxide (NO), and the hydroxyl radical (OH) are discussed. The intercomparison was conducted at Wallops Island, Virginia, in July 1983 and included a laser differential absorption and three grab sample/gas chromatograph methods for CO, a laser-induced fluorescence (LIF) and two chemiluminescence methods for NO, and two LIF methods and a radiocarbon tracer method for OH. The intercomparison was conducted as a field measurement program involving ambient measurements of CO (150-300 ppbv) and NO (10-180 pptv) from a common manifold with controlled injection of CO in incremental steps from 20 to 500 ppbv and NO in steps from 10 to 220 pptv. Only ambient measurements of OH were made. The agreement between the techniques was on the order of 14 percent for CO and 17 percent for NO. Hardware difficulties during the OH tests resulted in a data base with insufficient data and uncertanties too large to permit a meaningful intercomposition.
As part of the instrument evaluation plan for the NASA Global Atmospheric Sampling Program, prototype instruments were tested aboard the NASA Convair 990 during four flights in January and February of 1974. All the data were taken in maritime air between Hawaii and San Francisco and between Hawaii and 155 deg W, 35 deg N. A chemiluminescent instrument was used to measure nitric oxide. Water vapor, which was measured by using an aluminum oxide hygrometer, ranged from 5.2 micro g/g to saturation. Ozone was measured by an instrument using the ultraviolet absorption technique and ranged up to 235 ppbv. Typical temporal plots of the concentrations of the three constituents are presented. All the constituents showed considerable spatial and day-to-day variation in concentration at each altitude flown. Measurements of the three constituents were made simultaneously at various altitudes between 7.6 and 12.5 km.
This paper describes flight tests of prototype instruments for the NASA global atmospheric sampling program (GASP). Three gas sampling instruments were included in the installation: (1) a chemiluminescent nitric oxide monitor; (2) an ultraviolet absorption ozone monitor; and (3) an aluminum oxide water vapor hygrometer. Results indicate the range and kind of variability in NO, H2O, and O3 that can be expected in routine tropospheric air sampling. They have also demonstrated the need for increasing instrument sensitivities, particularly in NO measurement.