Engineering topics

Schnell, R. C.

Publications and source records attributed to Schnell, R. C..

8 records

NASA NTRS2017

Surface Ozone in the Colorado Northern Front Range and the Influence of Oil and Gas Development During FRAPPE/DISCOVER-AQ in Summer 2014

High mixing ratios of ozone (O3) in the northern Front Range (NFR) of Colorado are not limited to the urban Denver area but were also observed in rural areas where oil and gas activity is the primary source of O3 precursors. On individual days, oil and gas O3 precursors can contribute in excess of 30 ppb to O3 growth and can lead to exceedances of the EPA O3 National Ambient Air Quality Standard. Data used in this study were gathered from continuous surface O3 monitors for June-August 2013-2015 as well as additional flask measurements and mobile laboratories that were part of the FRAPPE/DISCOVER-AQ field campaign of July-August 2014. Overall observed O3 levels during the summer of 2014 were lower than in 2013, likely due to cooler and damper weather than an average summer. This study determined the median hourly surface O3 mixing ratio in the NFR on summer days with limited photochemical production to be approximately 45-55 ppb. Mobile laboratory and flask data collected on three days provide representative case studies of different O3 formation environments in and around Greeley, Colorado. Observations of several gases (including methane, ethane, CO, nitrous oxide) along with O3 are used to identify sources of O3 precursor emissions. A July 23 survey demonstrated low O3 (45-60 ppb) while August 3 and August 13 surveys recorded O3 levels of 75-80 ppb or more. August 3 exemplifies influence of moderate urban and high oil and gas O3 precursor emissions. August 13 demonstrates high oil and gas emissions, low agricultural emissions, and CO measurements that were well correlated with ethane from oil and gas, suggesting an oil and gas related activity as a NOx and O3 precursor source. Low isoprene levels indicated that they were not a significant contributor to O3 precursors measured during the case studies.

Pollution↗

NASA NTRS1993

Bromoalkane production by Antarctic ice algae

Ice microalgae, collected from the underside of annual sea ice in McMurdo Sound, Antarctica, were found to contain and release to seawater a number of brominated hydrocarbons. These included bromoform, dibromomethane, mixed bromochloromethanes, and methyl bromide. Atmospheric measurements in the McMurdo Sound vicinity revealed the presence of bromoform and methyl bromide in the lower atmosphere, with lowest concentrations inland, further indicating that biogenic activity in the Sound is a source of organic bromine gases to the Antarctic atmosphere. This may have important implications for boundary layer chemistry in Antarctica. In the Arctic, the presence of bromoform has been linked to loss of surface ozone in the spring. We report here preliminary evidence for similar surface ozone loss at McMurdo Station.

Sturges, W. T.↗

NASA NTRS1991

Decrease of summer tropospheric ozone concentrations in Antarctica

It is shown here that surface ozone concentrations at the South Pole in the austral summer decreased by 17 percent over the period 1976-90. Over the same period, solar irradiance at the South Pole in January and February decreased by 7 percent as a result of a 25 percent increase in cloudiness. It is suggested that the trend in the summer ozone concentrations is caused by enhanced photochemical destruction of ozone in the lower troposphere caused by the increased penetration of UV radiation associated with stratospheric ozone depletion, coupled with enhanced transport of ozone-poor marine air from lower latitudes to the South Pole.

Schnell, R. C.↗

NASA NTRS1989

NOAA WP-3D instrumentation and flight operations on AGASP-II

One component of the second Arctic Gas and Aerosol Sampling Program conducted in March and April 1986 was supported with an instrumented NOAA WP-3D atmospheric research aircraft, which was used to conduct measurements of wind, temperature, ozone, water vapor, the concentration of condensation nuclei, and aerosol scattering extinction coefficient in order to determine the locations and properties of haze layers. The WP-3D flights consisted of three missions north of Alaska and three in the Canadian Arctic near Alert. This paper describes the NOAA WP-3D aircraft; the meteorological, gas, and aerosol sampling systems utilized; and the flight operations of the six WP-3D flights.

Schnell, R. C.↗

NASA NTRS1989

Lidar detection of leads in Arctic sea ice

REMOTE sensing using an airborne infrared lidar has shown an unexpected capability to detect open leads in Arctic sea ice and their associated meteorology in winter. It is shown here that vertical profiles of backscattered radiation demonstrate strong returns from hydrometeor plumes originating from leads having a surface water temperature near -1.8 C. Recently refrozen leads are also distinguishable by the lidar backscatter from adjacent thicker, older sea ice. Wide leads release enough energy to create buoyant plumes which penetrate the Arctic boundary layer inversion, transporting heat and moisture into the troposphere. These results show that the role of the Arctic as a global heat sink may need to be reevaluated, and that lead plumes have a significant effect on the radiation budget.

Schnell, R. C.↗

NASA NTRS1984

Vertical and horizontal characteristics of Arctic haze during AFASP - Alaskan Arctic

Vertical and horizontal distributions of ozone, extinction due to aerosol light scattering, condensation nucleus concentrations, aerosol spectra, and meteorological parameters were measured with a NOAA WP-3D research aircraft over the Alaskan Arctic in March 1983. Multiple layers of haze, varying in thickness from a few 10's to 100's of meters, were observed throughout the troposphere. A maximum concentration of aerosols was located between 600 and 800 mb. Distribution of the haze layers was associated with distinct meteorological boundaries. The characteristics of the haze changed in response to stages in the progression of a major Arctic haze episode. On March 17, 1983, the Arctic anticyclone was penetrated and its meteorological and aerosol properties determined.

Schnell, R. C.↗

NASA NTRS1984

Aerosol distributions and an arctic aerosol front during AGASP - Norwegian Arctic

Vertical profiles of aerosol characteristics obtained near Svalbard, Norway, during the Arctic Gas and Aerosol Sampling Program indicate that high aerosol concentrations and strong visible haze were distributed throughout the troposphere. Layers of Arctic haze were observed in both dry air and moist air. A research flight on March 31, 1983, crossed a previously undocumented Arctic aerosol front structure. Condensation nucleus concentrations of 450/cu cm within the polluted continental air mass south of the front decreased to 80/cu cm within the clean Arctic air north of the front. Aerosols above the Aitken size range decreased one order of magnitude in both number and mass across this same air mass boundary.

Ratz, W. E.↗

NASA NTRS1984

El Chichon volcanic debris in an Arctic tropopause fold

A research flight with the NOAA WP-3D aircraft revealed evidence for stratospheric-tropospheric exchange within the Arctic through tropopause folding on the flank of the polar vortex. Observations showed descent of the tropopause and of stratospheric ozone to 700 mb along the west coast of Greenland. Measurements of condensation nuclei and analysis of high volume impactor samples documented the presence of volcanic debris probably from the 1982 El Chichon eruption, including H2SO4 droplets, within the polar vortex and associated tropopause fold.

Shapiro, M. A.↗