Engineering topics
Publications and source records attributed to Mccormick, M. Patrick.
A method is developed to infer the vertical distribution of the occurrence frequency of clouds that are opaque to the Stratospheric Aerosol and Gas Experiment (SAGE) II instrument. An application of the method to the 1986 SAGE II observations is included in this paper. The 1986 SAGE II results are compared with the 1952-1981 cloud climatology of Warren et al. (1986, 1988)
A global stratospheric aerosol database employed for climate simulations is described. For the period 1883-1990, aerosol optical depths are estimated from optical extinction data, whose quality increases with time over that period. For the period 1850-1882, aerosol optical depths are more crudely estimated from volcanological evidence for the volume of ejecta from major known volcanoes. The data set is available over Internet.
The primary goals of the Lidar In-Space Technology Experiment (LITE) are to demonstrate the maturity of space-based lidar technology, to provide some unique measurements, and to provide a platform for the development of technology for future space-based systems. LITE is currently scheduled to fly on the Shuttle in early 1994. Approval has recently been given for the first of several planned follow-on missions at 2-year intervals. The first mission will be used to develop experience in operating a lidar system in a space environment and to evaluate the sensitivity of the instrument for performing scientific studies. The second mission will focus on scientific studies of clouds, aerosols, and the middle atmosphere. On subsequent follow-on missions, LITE will be used as a test bed for demonstrating more advanced measurement capabilities.
Given here are extended abstracts of papers presented at the 16th International Laser Radar Conference, held in Cambridge, Massachusetts, July 20-24, 1992. Topics discussed include the Mt. Pinatubo volcanic dust laser observations, global change, ozone measurements, Earth mesospheric measurements, wind measurements, imaging, ranging, water vapor measurements, and laser devices and technology.
Satellite measurements of ozone carried out during the Stratospheric Aerosol and Gas Experiment II (SAGE II) are compared with in situ measurements made by the ROCOZ-A and electrochemical concentration cell ozonesondes at Natal (Brazil) during the Southern Hemisphere autumn of 1985. It was found that the SAGE II values were higher than the ROCOZ-A values by 3.4 percent, with an average absolute difference of 3.8 percent. It is suggested that the differences between the ozone density and mixing ratio results are due to the auxiliary temperature and pressure values for the satellite and in situ instruments.
The science objectives of the satellite-borne SAGE III are presented as they pertain to detecting global change. SAGE III is the proposed follow on and improved version of SAM II, SAGE I and SAGE II which have measured stratospheric and, in some cases, tropospheric species since late 1978. Specifically, SAGE III will measure profiles of aerosols, ozone, water vapor, nitrogen dioxide and trioxide, neutral density, temperature, clouds, and chlorine dioxide using the solar and lunar occultation techniques. These techniques are inherently self-calibrating, provide high vertical resolution, and use well-behaved data retrievals making them ideal for trend detection and global change studies. The potential capabilities of SAGE III are illustrated by using data and results from SAM II, SAGE I and SAGE II.
An update of the scientific discussions presented in Chapter 2 of the Intergovernmental Panel on Climate Change (IPCC) report is presented. The update discusses the atmospheric radiative and chemical species of significance for climate change. There are two major objectives of the present update. The first is an extension of the discussion on the Global Warming Potentials (GWP's), including a reevaluation in view of the updates in the lifetimes of the radiatively active species. The second important objective is to underscore major developments in the radiative forcing of climate due to the observed stratospheric ozone losses occurring between 1979 and 1990.
A ground-based, high power, laser remote sensing system for measurements of stratospheric ozone concentration profiles has been in operation at the Jet Propulsion Laboratory Table Mountain Facility located in southern California, since January 1988. The seasonal variations observed in the ozone profiles, during 1988 and as a function of altitude, are described here. These profiles are compared with those from the Stratospheric Aerosol and Gas Experiment satellite instrument made within a radius of 1000 km from the lidar and also with the zonal mean measurements made in the band 34.4 +/- 5 deg. Comparison with the proposed new CIRA ozone reference model has also been carried out. The seasonal variations, between 25 and 50 km, observed by the two instruments and indicated by the reference model are in good agreement.
As shown independently by two different techniques, nitric acid aerosols and polar stratospheric clouds (PSCs) both form below similar threshold temperatures. This supports the idea that the PSC particles involved in chlorine activation and ozone depletion in the winter polar stratosphere are composed of nitric acid. One technique used to show this is the inertial impaction of nitric acid aerosols using an Er-2 aircraft; the other method is remote sensing of PSCs by the Stratospheric Aerosol Measurement (SAM II) satellite borne optical sensor. Both procedures were in operation during the Arctic Airborne Stratospheric Expedition in 1989, and the Airborne Antarctic Ozone Experiment in 1987. Analysis of Arctic particles gathered in situ indicates the presence of nitric acid below a 'first appearance' temperature Tfa = 202 K. This is the same highest temperature at which PSCs are seen by the SAM II satellite. In comparison, a 'first appearance' temperature Tfa = 198 K as found for the Antarctic samples.
Measurements of N2O and O3 during the Airborne Arctic Stratospheric Expedition have been composited using the potential vorticity and potential temperature of each measurement as coordinates. For ozone, data sources included the ER-2 and balloon ozonesonde in situ measurements, DC-8 DIAL lidar, and Stratospheric Aerosol and Gas Experiment satellite profiles. For N2O, only ER-2 data were used. These chemical composites have been reconstructed onto average meteorological fields for the mission in a latitude-altitude cross section, yielding a picture of the chemical composition of the polar vortex during this period. Tracers inside the vortex show an apparent descent of about 2 km relative to those outside, resulting in an apparent chemical edge on isentropic and isobaric surfaces.
The objectives are: to analyze dual polarization lidar measurements of aerosols and polar stratospheric clouds (PSCs) obtained aboard the NASA Ames DC-8 aircraft during the 1989 Airborne Arctic Stratospheric Expedition (AASE); and to combine lidar, SAM II, and other AASE data with theoretical modeling calculations to study PSC characteristics. A summary of progress and results is given.
Antarctic polar stratospheric cloud (PSC) sightings by the orbiting SAM II sensor during September and October show a pronounced quasi-biennial oscillation (QBO) signal, and October sightings have increased markedly over the past 10 years in years of westerly QBO phase. The QBO in PSC frequency is likely to affect the rate of Antarctic heterogeneous chemical processes and, hence, ozone depletion. Studies of the observed long-term temperature trend suggest that the decadal PSC trend probably results from the ozone decline, through its effect on stratospheric heating rates. A more detailed analysis of data from 1986 to 1987 shows that there were more PSCs in 1987, and that they persisted much later into the spring season as compared to 1986. Qualitatively similar behavior was found for the OClO column abundances and 18-km ozone depletion observed at McMurdo Station during these 2 years. These observations suggest that both the intensity and duration of heterogeneous chemical processes are likely greater during colder OBQ-westerly phase years.
Advances in the development and application of lidar as a tool for the remote sensing of atmospheric aerosols and clouds are reviewed. The lidar sensing technique is described, and various approaches for solving the lidar equation to retrieve aerosol properties are summarized. Examples are presented of lidar applications to aerosol and cloud sensing in both the troposphere and stratosphere. These include environmental monitoring, atmospheric-boundary-layer studies, retrieval of aerosol optical and physical properties, sensing of clouds, and investigation of volcanic effects in the stratosphere. Comments are offered regarding the future outlook for aerosol and cloud sensing by both ground-based and spaceborne lidars.
A theoretical model for the formation and growth of polar stratospheric clouds (PSCs) has been developed. Results for the calculated temperature dependence of optical backscattering are found to agree well with values obtained during two Arctic airborne-lidar experiments. Results for PSC formation in Antarctica show that at the 70-mbar level, about 80 percent of the HNO3 and about 30 percent of the H2O vapor available may be sequestered in relatively large PSC particles at a temperature near 189 K.
Recent measurements of ozone, water vapor, and aerosol extinction from the spring of 1987 are presented and compared to 1985 and 1986. The observed changes to variations in meteorological conditions in the vortex for these three years are noted. March ozone data at similar latitudes for these three years will be used to investigate coupling between severity of the springtime depletion and early fall values. Researchers also investigate correlations between the measured species of water vapor, ozone, and aerosols throughout the vortex region.
The persistence of Polar Stratospheric Clouds (PSCs) observed by the Stratospheric Aerosol Measurement (SAM) 2 satellite sensor over a 9-year period is compared and contrasted. Histograms of the SAM 2 1.0 micron extinction ratio data (aerosol extinction normalized by the molecular extinction) at an altitude of 18 km in the Antarctic have been generated for three 10-day periods in the month of September. Statistics for eight different years (1979 to 1982 and 1984 to 1987) are shown in separate panels for each figure. Since the SAM 2 system is a solar occultation experiment, observations are limited to the edge of the polar night and no measurements are made deep within the vortex where temperatures could be colder. For this reason, use is made of the NMC global gridded fields and the known temperature-extinction relationship to infer additional information on the occurrence and areal coverage of PSCs. Calculations of the daily areal coverage of the 195 K isotherm will be presented for this same period of data. This contour level lies in the range of the predicted temperature for onset of the Type 1 particle enhancement mode at 50 mb (Poole and McCormick, 1988b) and should indicate approximately when formation of the binary HNO3-H2O particles begins.
Models indicate that stratospheric aerosols play a major role in the destruction of ozone during the Austral winter. Although many in situ measurements of stratospheric aerosols were made during the Airborne Antarctic Ozone Experiment, changes of aerosol concentration and size distributions across the polar vortex are important to understanding changes of chemical species taking place during this time. Therefore comparing the in situ measurements with measurements made by satellites scanning wider areas will give a clearer picture of the possible role played by aerosols during this period. The wire impactor size distributions are compared to those from the aerosol spectrometers and a best fit size distribution determined. Aerosol extinctions are calculated from the in situ measurements and compared to the extinctions measured by the satellites. Five comparisons are made with SAGE 2 and four with SAM 2. Extinctions agree as close as a factor of two.
A joint field experiment between NASA and NOAA was conducted during August to September 1987 to obtain in situ and remote measurements of key gases and aerosols from aircraft platforms during the formation of the ozone (O3) hole over Antarctica. The ER-2 (advanced U-2) and DC-8 aircraft from the NASA Ames Research Center were used in this field experiment. The NASA Langley Research Center's airborne differential absorption lidar (DIAL) system was operated from the DC-8 to obtain profiles of O3 and polar stratospheric clouds in the lower stratosphere during long-range flights over Antarctica from August 28 to September 29, 1987. The airborne DIAL system was configured to transmit simultaneously four laser wavelengths (301, 311, 622, and 1064 nm) above the DC-8 for DIAL measurements of O3 profiles between 11 to 20 km ASL (geometric altitude above sea level) and multiple wavelength aerosol backscatter measurements between 11 to 24 km ASL. A total of 13 DC-8 flights were made over Antarctica with 2 flights reaching the South Pole. Polar stratospheric clouds (PSC's) were detected in multiple thin layers in the 11 to 21 km ASL altitude range with each layer having a typical thickness of less than 1 km. Two types of PSC's were found based on aerosol backscattering ratios: predominantly water ice clouds (type 2) and clouds with scattering characteristics consistent with binary solid nitric acid/water clouds (type 1). Large-scale cross sections of O3 distributions were obtained. The data provides additional information about a potentially important transport mechanism that may influence the O3 budget inside the vortex. There is also some evidence that strong low pressure systems in the troposphere are associated with regions of lower stratospheric O3. This paper discusses the spatial and temporal variations of O3 inside and outside the polar vortex region during the development of the O3 hole and relates these data to other measurements obtained during this field experiment.