Engineering topics

Harriss, Robert C.

Publications and source records attributed to Harriss, Robert C..

12 records

NASA NTRS1994

Comment on 'A dramatic decrease in the growth rate of atmospheric methane in the Northern Hemisphere during 1992' by E. J. Dlugokencky et al.

The carefully measured decrease in the growth rate of atmospheric methane (CH4) in 1992 reported by Dlugokencky et al. (1994) is an impressive accomplishment, and testimony for the importance of maintaining high-quality, long-term monitoring of atmospheric composition. The changing growth rate of atmospheric CH4 has important implications for assessing and understanding the potential magnitude and rates of a future greenhouse gas-induced climate change. Furthermore, the CH4 data from the current Climate Monitoring and Diagnostics Laboratory (CMDL) globally-distributed network of cooperative air sampling sites are clearly the best record of global CH4 trends and distribution currently available. However, we argue briefly here that the speculation by Dlugokencky et al. (1994) on possible mechanisms for the decreased growth rate in 1992 is only one scenario of many that could possibly fit with the constraints imposed by the reported data. Our comments are to (1) illustrate the difficulties of deducing small changes in complex, poorly understood, geographically diverse natural and anthropogenic sources of CH4 from measurements at the remotely-located CMDL sampling sites and (2) emphasize that detailed bottoms-up analyses are necessary to really advance the understanding of changes in source strengths; we are not promoting alternative mechanisms to explain the 1992 decrease in atmospheric CH4.

Hogan, Kathleen B.↗

NASA NTRS1992

Carbon monoxide and methane in the North American Arctic and Subarctic troposphere - July-August 1988

Enhanced concentrations of CH4 in the unpolluted atmospheric mixed layer over both Arctic and subarctic tundra landscapes are documented here using data from the NASA Arctic Boundary Layer Expedition (ABLE 3A). The CH4 concentration gradients were determined mainly by interactions of biogenic emission from wet tundra and turbulent mixing proceses. The gradient were most frequently associated with intrusion of upper tropospheric or stratospheric air into the midtroposphere, emissions from forest and tundra fires, and long-range transport of enhanced concentration of these gases from unidentified sources. Summertime haze layers exhibited midtropospheric enhancements of CH4 similar to those measured in winter Arctic events. The observations confirm the importance of Arctic and Subarctic wetland environments as a regional source of global atmospheric CH4.

Harriss, Robert C.↗

NASA NTRS1992

Methane emissions from tundra environments in the Yukon-Kuskokwin Delta, Alaska

This paper reports CH4 flux to the atmosphere from a variety of tundra environments near Bethel, Alaska during the summer months of 1988. Emissions from wet meadow tundra averaged 144 +/- 31 mg/sq m/d and ranged from 15.6 to 426 mg/sq m/d varying with soil moisture and temperature. Flux from the drier upland tundra was about two orders of magnitude lower and averaged 2.3 +/- 1.1 mg/sq m/d. Tundra lakes emit CH4 from the open water surface as well as from fringing aquatic vegetation; the presence of vegetation significantly enhanced flux over open water rates. Calculated diffusive fluxes from open water varied with lake size, the large lakes emitting 3.8 mg/sq m/d and small lakes emitting an average of 77 mg/sq m/d. An updated estimate of global emissions from tundra indicates an annual fluxes of approximately 11 +/- 3 Tg CH4.

Bartlett, Karen B.↗

NASA NTRS1990

Methane flux from the Amazon River floodplain - Emissions during rising water

Methane flux data obtained during a period of high and falling water level in the course of the dry season of 1985 (the Amazon Boundary Layer Experiment, ABLE 2A) and a period of moderate and rising water during the wet season of 1987 (ABLE 2B) were used to characterize the influence of seasonal variations in the vegetation, water column depth, and chemistry, as well as atmospheric dynamics, on the methane flux from the Amazon River floodplain. It was found that the annual estimate of methane from wetlands is identical to the annual estimate made by Matthews and Fung (1987) (both at 111 Tg). However, it was found that peatlands between 50 and 70 N contribute 39 Tg, with the large areas of forested and nonforested bogs making up 37 Tg of this figure, while the figures of Matthews and Fung were 63 and 62 Tg, respectively.

Bartlett, Karen B.↗

NASA NTRS1990

An overview of the NASA Global Tropospheric Experiment

A summary of the results from the field expeditions conducted within the framework of the Global Tropospheric Experiment (GTE) is presented. The missions reviewed include the Chemical Instrumentation Test and Evaluation missions and the Atmospheric Boundary Layer Experiment missions. Future GTE missions are also briefly reviewed.

Hoell, James M., Jr.↗

NASA NTRS1988

Carbon dioxide in the atmosphere over the Amazon Basin

As a part of the NASA's Amazon Boundary Layer Experiment 2A mission, the cycle of atmospheric CO2 over the Amazon Basin was examined using measured vertical profiles of CO2 concentrations in the canopy and aloft, and direct measurements of CO2 emissions from soils. The results provide a detailed picture of daily exchanges of air between the tropical forest (0-30) and the atmospheric boundary layer (30-2000 m). A comparison of atmospheric CO2 distributions over forests, wetlands, and rivers shows that the lower atmosphere over forests functions separately from that over rivers or wetlands during the night and to some extent during the day; the basic diurnal cycle of CO2 over wetlands is much weaker than over forests, and the cycle is almost absent over rivers. This result is consistent with expectations based on the biogeochemistry of organic carbon in these systems.

Wofsy, Steven C.↗

NASA NTRS1988

Tropospheric methane from an Amazonian floodplain lake

The sources of methane and its flux to the troposphere from the Amazonian floodplain were investigated during the dry season of July and August 1985, using measurements of methane concentration gradients obtained aboard a houseboat laboratory anchored in Lago Calado, a stratified dendritic lake of about 6-sq km area located near the center of the Amazon Basin. Methane concentrations in the mixed layer of the lake were found to vary from 0.0001 to 0.0055 mM, with no consistent temporal trend. The measured methane flux from the surface of the open lake to the atmosphere averaged 27 mg CH4/sq m per day, consistent with the buildup in ambient methane in the nocturnal surface mixed layer of the troposphere. Ebullition contributed 70 percent to the average total flux. The source of methane to the lake and, ultimately, to the troposphere is the benthic sediments.

Crill, Patrick M.↗

NASA NTRS1988

Methane flux from the central Amazonian floodplain

A total of 186 methane measurements from the three primary Amazon floodplain environments of open water lakes, flood forests, and floating grass mats were made over the period 18 July through 2 September 1985. These data indicate that emissions were lowest over open water lakes. Flux from flooded forests and grass mats was significantly higher. At least three transport processes contribute to tropospheric emissions: ebullition from sediments, diffusion along the concentration gradient from sediment to overlaying water to air, and transport through the roots and stems of aquatic plants. Measurements indicate that the first two of these processes are most significant. It was estimated that on the average bubbling makes up 49 percent of the flux from open water, 54 percent of that from flooded forests, and 64 percent of that from floating mats. If the measurements were applied to the entire Amazonian floodplain, it is calculated that the region could supply up to 12 percent of the estimated global natural sources of methane.

Bartlett, Karen B.↗

NASA NTRS1987

Methane flux from the Central Amazonian Floodplain

A total of 186 methane measurements from the three primary Amazon floodplain environments of open water lakes, flood forests, and floating grass mats were made over the period 18 July through 2 September 1985. These data indicate that emissions were lowest over open water lakes. Flux from flooded forests and grass mats was significantly higher. At least three transport processes contribute to tropospheric emissions: ebullition from sediments, diffusion along the concentration gradient from sediment to overlaying water to air, and transport through the roots and stems of aquatic plants. Measurements indicate that the first two of these processes are most significant. It was estimated that on the average bubbling makes up 49% of the flux from open water, 54% of that from flooded forests, and 64% of that from floating mats. If the measurements were applied to the entire Amazonian floodplain, it is calculated that the region could supply up to 12% of the estimated global natural sources of methane.

Bartlett, Karen B.↗

NASA NTRS1987

Remote sensing of the earth's biosphere - A tool for studies of the global atmospheric environment

Recent advances in remote sensing technology and its use for global studies of the biospheric processes are described. Special consideration is given to research related to two issues: (1) quantifying the impacts of natural vegetation and its changing patterns of occurrence on the atmospheric CO2 budget and (2) assessing wetlands (such as the swamps and marshes of Florida's Everglades) as sources of atmospheric CH4. The results include the data from NOAA-AVHRR sensors and from experiments in remote detection of plant growth rate.

Bartlett, David S.↗

NASA NTRS1986

Vertical distributions of molecular hydrogen off the eastern and Gulf coasts of the United States

The vertical distributions of molecular hydrogen (H2) and carbon monoxide (CO) were determined during spiraling maneuvers from aircraft off the eastern coast of the United States and over the Gulf of Mexico. H2 was always at its lowest levels in the boundary layer, averaging about 500 parts per billion by volume (ppbv). H2 mixing ratios determined in the free troposphere were typically higher (600-700 ppbv), and often suggested a small progressive increase with altitude. Several large free-tropospheric H2 plumes (mixing ratios as high as 1-2 parts per million by volume) were implied by the data. These H2 plumes were not always accompanied by corresponding increases in CO mixing ratios. This result is most difficult to explain when it is noted that the primary atmospheric sources for molecular H2 are considered to be combustion and photochemistry, both of which should be strong CO sources also.

Cofer, Wesley R., III↗

NASA NTRS1985

Global tropospheric methane: An indication of atmosphere-biosphere-climate interactions?

Methane is an important atmospheric gas with potentially critical roles in both photochemical and radiation transfer processes. A major natural source of atmospheric methane involves anaerobic fermentation of organic materials in wetland soils and sediments. A data base of field measurements of atmospheric methane was used in the development of a global methane emissions inventory. Calculations support the following hypotheses: (1) Human activities currently produce methane at a rate approximately equal to natural resources (these rapidly increasing anthropogenic sources can explain most of the recent increase observed in tropospheric methane); and (2) Prior to 200 B.P. (before the present), the influence of climate on wetland extent and distribution was probably a dominant factor controlling global biogenic methane emissions to the atmosphere.

Harriss, Robert C.↗