Engineering topics

Weinstock, E. M.

Publications and source records attributed to Weinstock, E. M..

28 records · Page 2

NASA NTRS1996

The Effects of Tropical Cirrus Clouds on the Abundance of Lower Stratospheric Ozone

The distribution of many chemical constituents of the atmosphere (e.g., ozone) is at least partially determined by the distribution of net radiative heating in the atmosphere. In this paper, we demonstrate the significant effect of high cirrus clouds on the net radiative heating of the tropical lower stratosphere. A model of tropical lower stratospheric ozone is then used to demonstrate the sensitivity of calculated ozone to the varying cloud cover used in the model. We conclude that calculated ozone is sensitive to the inclusion of clouds in models and that models of the atmosphere should include a realistic description of tropical cirrus clouds in order to accurately simulate the chemical composition of the atmosphere.

Dessler, A. E.↗

NASA NTRS1994

An examination of the total hydrogen budget of the lower stratosphere

We analyze the hydrogen budget of the lower stratosphere using simultaneous in situ measurements of northern hemispheric water vapor (H2O) and methane (CH4) obtained during the spring Stratospheric Photochemistry, Aerosols, and Dynamics Expedition (SPADE), as well as previously published in situ H2 data. Based on this data, we conclude that approximately two H2O molecules are produced for each CH4 molecule destroyed. This implies that H2 production from CH4 oxidation is balanced by H2 oxidation. The uncertainty in this analysis is greatly reduced by the use of multiple data sets. Additionally, we infer that, on an annual and global average, H2O enters the stratosphere with a mixing ratio of 4.2 +/- 0.5 ppmv, and that the quasi-conserved quantity 2 x CH4 + H2O has a value of 7.6 +/- 0.6 ppmv in these northern hemishere air parcels (where xi denotes the mixing ratio of the constituent xi).

Dessler, A. E.↗

NASA NTRS1993

Balloon-borne measurements of ClO, NO, and O3 in a volcanic cloud: An analysis of heterogeneous chemistry between 20 and 30 km

Balloon profiles of chlorine monoxide (ClO), nitric oxide (NO), and ozone (O3) were measured on March 11, 1992 from 100 to 10 mb over Greenland (67.0 deg N, 50.6 deg W). Measurements from SAGE II indicate that the aerosol surface area in the region was enhanced by sulfur from the eruption of Mt. Pinatubo, reaching 50 times background near 20 km. Concentrations of ClO were enhanced and concentrations of NO were suppressed relative to low aerosol conditions consistent with the effects of hydrolysis of N2O5 on the surface of sulfuric acid aerosols. The data are consistent with a value of 2 x 10(exp -4) for the reaction probability of the heterogeneous hydrolysis of ClONO2, indicating a minor role for this reaction at as temperature of 220 K. At these temperatures, we find no evidence for the catastrophic loss of ozone predicted to occur under conditions of enhanced aerosol surface area.

Dessler, A. E.↗

NASA NTRS1993

Balloon-Borne Measurements of CLO, NO and O3 in a Volcanic Cloud: An Analysis of Heterogeneous Chemistry between 20 and 30 KM

Balloon profiles of chlorine monoxide (ClO), nitric oxide (NO), and ozone (O3) were measured on March 11, 1992 from 100 to 10 mb over Greenland (67.0 deg N, 50.6 deg W). Measurements from SAGE II indicate that the aerosol surface area in the region was enhanced by sulfur from the eruption of Mt. Pinatubo, reaching 50 times background near 20 km. Concentrations of ClO were enhanced and concentrations of NO were suppressed relative to low aerosol conditions consistent with the effects of hydrolysis of N2O5 on the surface of sulfuric acid aerosols. The data are consistent with a value of 2 x 10(exp -4) for the reaction probability of the heterogeneous hydrolysis of ClONO2, indicating a minor role for this reaction at a temperature of 220 K. At these temperatures, we find no evidence for the catastrophic loss of ozone predicted to occur under conditions of enhanced aerosol surface area.

Dessler, A. E.↗

NASA NTRS1990

Simultaneous, in situ measurements of OH, HO2, O3, and H2O - A test of modeled stratospheric HO(x) chemistry

Simultaneous, in situ measurements of OH, HO2, H2O, and O3 from 37-23 km are reported. The partitioning between OH and HO2 and the total HO(x) concentration are compared with expected steady-state values. The ratio of HO2 to OH varies from less than 2 at 36 km to more than 3 at 25 km; in the lower stratosphere this ratio is nearly a factor of two less than predicted. The data are used to calculate HO(x) production and loss rates. The measured HO(x) mixing ratio is consistent with production dominated by the reaction of O(1D) with H2O, and loss controlled by NOy below 28 km and HO(x) above 30 km. The steady-state concentration of H2O2 is inferred from the measured HO2 concentration and calculated photolysis rate. The maximum H2O2 mixing ratio (at 33 km) is predicted to be less than 0.2 ppb.

Wennberg, P. O.↗

NASA NTRS1990

In situ measurement of water vapor in the stratosphere with a cryogenically cooled Lyman-alpha hygrometer

In situ measurements of water vapor in the stratosphere with a new instrument are reported. The instrument has been designed to observe daytime water vapor from a multiinstrument balloon gondola that simultaneously measures free radicals such as OH, HO2, and O3 in the stratosphere up to 40 km. Lyman-alpha photofragment fluorescence is used to measure water molecules in a flowing sample of ambient air. A brief description of the instrument is given, followed by the results of the first four balloon flights. The measured mixing ratio for this flight varies from 3.0-5.5 ppmv over the altitude range of 17-34 km. Adjustments in the cooling protocol for the flights of July 6, 1988, July 28, and August 25, 1989, result in a much higher signal-to-noise ratio. Profiles from these three flights are similar to, but somewhat higher, than the 1987 profile. Implications of measurements are discussed, as are the issues of short- and long-term variability of stratospheric water vapor.

Schwab, J. J.↗

NASA NTRS1988

Midlatitude ClO below 22 km altitude - Measurements with a new aircraft-borne instrument

Midlatitude stratospheric ClO at altitudes below 22 km has been measured for the first time. Measurements were made at latitudes between 27 and 48 deg N during three flights from Moffett Field, CA, in June and July of 1987, with a new instrument flown on the NASA ER-2 aircraft. The result from these flights is that the ClO mixing ratio increases from less than 0.5 pptv at 16.8 km to 2.0 pptv at 18.3 km and 10.1 pptv at 21 km. These altitude profiles agree with an extrapolated profile from a May 1986 balloon-borne experiment (Brune and Anderson, 1986).

Brune, Wm. H.↗

NASA NTRS1986

In situ stratospheric ozone measurements by long path UV absorption - Developments and interpretation

A high-sensitivity, in situ UV absorption ozone sensor has been developed for use in the stratosphere. The instrument couples 254-nm radiation from a low-pressure mercury discharge lamp into a 40-pass White cell to attain a high-sensitivity ozone absorption measurement. Preflight/postflight laboratory tests utilizing an ozone source coupled to a laboratory UV ozone photometer in a fast-flow system as well as in-flight diagnostics verify the successful operation of the instrument. Evidence is presented to verify that in situ UV absorption ozone photometers can measure stratospheric ozone with better than 3 percent precision and 5 percent accuracy, provided proper attention is given to both the thermal field surrounding the gondola and the ambient pressure measurements. Ozone data are compared with modeled profiles in the 28- to 40-km region. An assessment of the disagreement between observations and modeled profiles is given along with suggestions for future experiments designed to constrain photochemical models.

Weinstock, E. M.↗

NASA NTRS1985

Stratospheric ClO - In-situ detection with a new approach

Stratospheric chlorine monoxide concentrations were measured in situ using a new and improved observational method in which the detection package is lowered on a tether from a balloon-borne platform floating near 40 km altitude and then reeled back up. Two reel down and reel up sequences covering 38 to 31 km produced (ClO) profiles which agree with each other to + or - 12 percent. The measured (ClO) profile falls within the envelope of nine previous fast parachute drop results, but exhibits a different shape, peaking near 32 km as opposed to approximately 39 km for the average of the previous profiles. These results are lower than but consistent with the profiles derived from remote sensing methods, and indicate the need for simultaneous measurements of relevant species.

Brune, Wm. H.↗

NASA NTRS1985

Free radicals in the stratosphere - A new observational technique

A new approach to in situ observations of trace reactive species in the stratosphere is described. A balloon-borne system, floating 40 kilometers above the earth's surface, successfully lowered and then retracted a cluster of instruments a distance of 12 kilometers on a filament of Kevlar. This instrument cluster is capable of detecting gas-phase free radicals at the part-per-trillion level. The suspended instrument array has excellent stability and has been used to measured atomic oxygen concentrations in the stratosphere.

Anderson, J. G.↗