Engineering topics

Aimedieu, P.

Publications and source records attributed to Aimedieu, P..

14 records

NASA NTRS1996

NO(y) Correlation with N2O and CH4 in the Midlatitude Stratosphere

Total reactive nitrogen (NO(y)), nitrous oxide (NO2), methane (CH4), and ozone (03) were measured on board a balloon launched from Aire sur l'Adour (44 deg N, 0 deg W), France on October 12, 1994. Generally, NO(y) was highly anti-correlated with N2O and CH4 at altitudes between 15 and 32 km. The linear NO(y) - N2O and NO(y) - CH4 relationships obtained by the present observations are very similar to those obtained on board ER-2 and DC-8 aircraft previously at altitude below 20 km in the northern hemisphere. They also agree well with the data obtained by the Atmospheric Trace Molecule Spectroscopy (ATMOS) instrument at 41 deg N in November 1994. Slight departures from linear correlations occurred around 29 km, where N2O and CH4 mixing ratios were larger than typical midlatitude values, suggesting horizontal transport of tropical airmasses to northern midlatitudes in a confined altitude region.

Kondo, Y.↗

NASA NTRS1994

HNO3 profiles obtained during the EASOE campaign

A small cryogenically cooled spectrometer system designed to obtain atmospheric emission spectra in the 7.5 micrometer to 13.0 micrometer region was flown piggyback on 9 balloon flights from ESRANGE (67.9 deg N, 21.2 deg E) during the European Arctic Stratospheric Ozone Experiment (EASOE) campaign. Initial analysis of the spectra obtained has been concentrated on obtaining HNO3 profiles for the various flights. HNO3 profiles for 17 December 1991, 9 January 1992, 22 January 1992, 5 February 1992 and 14 March 1992 are presented.

Murcray, F. J.↗

NASA NTRS1994

In situ measurements of nitric oxide, ozone, and aerosols in the Scandinavian Arctic stratosphere in January 1992

During the European Arctic Stratospheric Ozone Experiment (EASOE) the Arctic stratosphere was investigated with a set of instruments flown on a CNES high altitude balloon from ESRANGE, northern Sweden (67 deg 52 minutes N, 21 deg 4 minutes E) on January 22, 1992. The vertical profiles to an altitude of 30 km are presented for ozone, nitric oxide, aerosols, and the temperature. The ozone mixing ratio was less than 0.1 ppmv below 13 km, and increased significantly only above the 18.5 km level. The aerosol concentration profile shows a large peak between 13 km and 21 km, centered at 18.5 km, reaching as high as about 10 particles/cu cm. Above 24 km the aerosols were absent. Below 22 km, the NO mixing ratio was lower than 50 pptv; however it increased rapidly from 23 km with a sharp peak at 27 km. The rapid increase in NO occurs just at the altitude where the aerosol concentration falls below the detection limit: on this day, NO was present only in the absence of aerosols.

Aimedieu, P.↗

NASA NTRS1994

Systematic stratospheric observations on the Antarctic continent at Dumont d'Urville

Results of different routine measurements performed in Dumont d'Urville (66 deg S, 140 deg E) since 1988 are presented. They include the seasonal variation of total ozone and NO2 as measured by a SAOZ UV-Visible spectrometer, Polar Stratospheric Cloud observations by a backscatter lidar and more recently, vertical ozone profiles by ECC sondes and ozone and aerosols stratospheric profiles by a DIAL lidar. The particular results of 1991 in relation with the volcanic events of Mount Pinatubo and Mount Hudson, and the position of the polar vortex over Dumont d'Urville are discussed.

Godin, S.↗

NASA NTRS1992

Reactive nitrogen, ozone, and nitrate aerosols observed in the Arctic stratosphere in January 1990

Ozone mixing ratios in the vicinity of the 525-K potential temperature surface in January and early February of 1990 were observed to decrease sharply across the edge of the vortex boundary, where the vortex position was estimated from Ertel's potential vorticity. The changes in NO(y) mixing ratio with respect to altitude measured on January 18 and 31 were quite well correlated with those of ozone between 15 and 24 km, indicating that NO(y) also had a large gradient across the edge of the vortex. This is interpreted as being mainly due to the significant denitrification that occurred inside the vortex. The total amount of gas and particulate phase HNO3 was close to the NO(y) amount at the altitude of the 22- to 23-km region, suggesting that the conversion of non-HNO3 reactive nitrogen to HNO3 had occurred with a PSC.

Kondo, Y.↗

NASA NTRS1990

Diurnal variation of nitric oxide in the upper stratosphere

Two recent measurements of the temporal variation of nitric oxide at constant altitude near 40 km are reported. The observations were made at float altitude with a balloon-borne chemiluminescence detector together with in situ ozone measurements. The first measurement was made at 44 N on September 17, 1987, at an altitude of 40 km from before sunrise until 1000 LT. The second observation was made at the same latitude on June 18, 1988, at 39 km from 0800 to 1230 LT. At an altitude of 40 km, nitric oxide was observed to start increasing very rapidly at sunrise when the solar zenith angle reached about 95 deg. After the rapid initial buildup, the rate of NO increase stabilized for 3 hours at about 1.2 ppbv/hour. Near 1100 LT at 39 km in summer, the NO mixing ratio was observed to become nearly constant. These features of the diurnal variation of NO are in accord with the temporal variation expected from a time-dependent zero-dimensional photochemical model.

Kondo, Y.↗

NASA NTRS1990

Balloon-Borne Measurements of Total Reactive Nitrogen, Nitric Acid, and Aerosol in the Cold Arctic Stratosphere

Total reactive nitrogen (NO(Y)) between 15 and 29 km was measured for the first time on board a balloon within the Arctic cold vortex. Observations of HNO3, aerosol, and ozone were made by instruments on the same balloon gondola which was launched from Esrange, Sweden (68 deg N, 20 deg E) on January 23, 1989. The NO(y) mixing ratio was observed to increase very rapidly from 6 ppbv at 18 km altitude to a maximum of 21 ppbv at 21 km, forming a sharp layer with a thickness of about 2 km. A minimum in the NO(y) mixing ratio of 5 ppbv was found at 27 km. The measured HNO3 profile shows broad similarities to that of NO(y). This observation, together with the observed very low column amount of NO2, shows that NO(x) had been almost totally converted to HNO3, and that NO(y) was composed mainly of HNO3. The enhanced aerosol concentration between 19 and 22 km suggests that the maximum abundance of HNO3 trapped in the form of nitric acid trihydrate (NAT) was about 6 ppbv at 21 km. The sampled air parcels were highly supersaturated with respect to NAT. Although extensive denitrification throughout the stratosphere did not prevail, an indication of denitrification was found at altitudes of 27 and 22 km, and between 18 and 15 km.

Kondo, Y.↗

NASA NTRS1990

A mid-latitude balloon-borne observation of total odd nitrogen

A balloon-borne instrument to measure total odd nitrogen NO(y) has been developed. A converter which enables catalytic conversion of NO(y) into nitric oxide on a heated gold surface is combined with a chemiluminescence detector. The conversion efficiency for NO2 was measured to be close to 100 percent at pressures between 60 and 7 mb. The major source of errors in the balloon-borne measurements are the uncertainties in the estimates of the sample flow rate and the zero level of the instrument. The NO(y) concentration was measured at altitudes between 12 and 28 km with a precision of about 25 percent on a balloon experiment conducted at latitude 44 deg N in June 1989. The NO(y) concentration has been measured to be 1.5 + or - 0.4, 3 + or - 0.7, 10 + or - 3, and 14 + or - 4 ppbv at altitudes of 17, 20, 25, and 28 km, respectively.

Kondo, Y.↗

NASA NTRS1989

Profiles of nitric oxide in the upper stratosphere

Results are presented from NO measurements obtained with a chemiluminescent NO detector and an in situ ozone instrument aboard high altitude balloons launched at Air sur L'Adour and Gap, France. NO profiles were obtained between 35 and 40 km in the late morning of September 17, 1987 and the early afternoon of June 18, 1988. The average NO concentration was 9 ppbv at 35 km, increasing with altitude to 11.5 ppbv at 40 km. The difference in the temperature profile significantly contributes to the observed change in the NO concentration.

Kondo, Y.↗

NASA NTRS1989

Stratospheric ozone measurements from the 1985 MAP/GLOBUS NO(x) campaign

Nine experiments obtained stratospheric ozone measurements during the fall 1985 Middle Atmosphere Program (MAP) Global Budget of Stratospheric Trace Constituents (GLOBUS) NO(x) campaign. Measurements are grouped into four sets from four air masses and compared. Agreement between individual experiments and weighted mean profiles is generally within 10 percent and within absolute accuracies. Dobson Umkehr values in layer 5 differ by more than absolute accuracies from weighted mean profiles. Brewer sonde values for one data set are outside absolute accuracies near the ozone peak. Solar UV occultation measurements are 30-35 percent less than the weighted mean profile and outside absolute accuracies. Measurements from the Exospheric Satellite backscattered ultraviolet experiment, not previously compared with other techniques, agree within 10-15 percent of weighted mean profiles. Results of the campaign are generally consistent with those of four previous intercomparison campaigns.

Robbins, D.↗

NASA NTRS1989

Measurements of nitric oxide in the stratosphere at 44 N in autumn

Precision of the chemiluminescent instrument for balloon-borne NO measurement was improved by precise determinations of the flow rates of the sample air and the calibration NO in N2 gas. Based on the new calibration of these values, NO mixing ratio in the stratosphere was reanalyzed. The revision of the NO data does not at all alter the form of the diurnal variation. The average of the four NO profiles between 15 and 32 km obtained at 44 N in autumn is given.

Kondo, Y.↗

NASA NTRS1987

Comparison of in situ stratospheric ozone measurements obtained during the MAP/GLOBUS 1983 campaign

Data from five types of in situ ozone sensors flown aboard ballons during the MAP/GLOBUS 1983 campaign were found to agree to within 5 percent uncertainty throughout the middle atmosphere. A description of the individual techniques and the error budget is given in addition to explanations for the discrepancies found at higher and lower altitudes. In comparison to UV photometry values, results from two electrochemical techniques were found to be greater in the lower atmosphere and to be lower in the upper atmosphere. In general, olefin chemiluminescence results were within 8 percent of the UV photometry results. Ozone column contents measured by the indigo colorization technique for two altitude regions of about 6 km height were greater than measurements from other techniques by 52 and 17 percent, respectively.

Aimedieu, P.↗

NASA NTRS1987

General comparison of ozone vertical profiles obtained by various techniques during the 1983 MAP/GLOBUS campaign

As part of the 1983 MAP/GLOBUS campaign, atmospheric ozone profile measurements were made using a large variety of different techniques both from balloon platforms and the ground. It is shown that, for most techniques, the measured height distributions agree to within + or - 5 percent with the exception of the remote visible absorption method. This + or - 5 percent uncertainty is of the order of the individual intersystem accuracy. It is suggested that since the differences with the visible absorption method are in magnitude rather than in form, the absorption cross-section data could be the possible cause for the discrepancy.

Matthews, W. A.↗

NASA NTRS1983

Ozone profile intercomparison based on simultaneous observations between 20 and 40 km

The vertical distribution of stratospheric ozone has been simultaneously measured by means of five different instruments carried on the same balloon payload. The launches were performed from Gap during the intercomparison campaign conducted in June 1981 in southern France. Data obtained between altitudes of 20 and 40 km are compared and discussed. Vertical profiles deduced from Electrochemical Concentration Cell sondes launched from the same location by small balloons and from short Umkehr measurements made at Mt Chiran (France) are also included in this comparison. Systematic differences of the order of 20 percent between ozone profiles deduced from solar u.v. absorption and in situ techniques are found.

Aimedieu, P.↗