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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS2022

Estimating Emissions of Methane Consistent with Atmospheric Measurements of Methane and δC-13 of Methane

We have constructed an atmospheric inversion framework based on TM5-4DVAR to jointly assimilate measurements of methane and δC-13 of methane in order to estimate source-specific methane emissions. Here we present global emission estimates from this framework for the period 1999–2016. We assimilate a newly constructed, multi-agency database of CH4 and δC-13 measurements. We find that traditional CH4-only atmospheric inversions are unlikely to estimate emissions consistent with atmospheric δC-13 data and assimilating δC-13 data is necessary to derive emissions consistent with both measurements. Our framework attributes ca. 85% of the post-2007 growth in atmospheric methane to microbial sources, with about half of that coming from the tropics between 23.5° N and 23.5° S. This contradicts the attribution of the recent growth in the methane budget of the Global Carbon Project (GCP). We find that the GCP attribution is only consistent with our top-down estimate in the absence of δC-13 data. We find that at global and continental scales, δC-13 data can separate microbial from fossil methane emissions much better than CH4 data alone, and at smaller scales this ability is limited by the current δC-13 measurement coverage. Finally, we find that the largest uncertainty in using δC-13 data to separate different methane source types comes from our knowledge of atmospheric chemistry, specifically the distribution of tropospheric chlorine and the isotopic discrimination of the methane sink.

Methane↗
NASA NTRS1986

Emission of methane and other trace gases from the Amazon Varzea

Researchers measured the distributions and fluxes of methane and other trace gases from the various Amazon floodplain environments. These were determined during both a large scale, quasi-synoptic survey along a 2000 km reach of the Amazon river and an intensive local study (by J. Melack, R. Harriss et al.) covering a six-week period. The environments studied included the major rivers, connecting channels (paranas), floating macrophyte beds, flooded forests, open lakes and recently wetted soils. The results are summarized. Measured rates of methane emission averaged about 300 mg m-2 d-1, but with considerable variance, and were comparable to or higher than previously reported emissions from similar temperature zone environments. In general, areas covered by floating macrophytes showed the highest emissions. Individual hotspots had among the highest rates ever observed, over 10 g m-2 d-1. The high methane emissions appear to result because about 50% of the organic matter fixed on the floodplain (either terrestrial or aquatic) that is oxidized in the water is decomposed anaerobically via methanogensis. Measured fluxes of methane to the atmosphere appear to be significantly correlated with surface water dissolved methane concentrations.

Richey, Jeffrey E.↗
NASA NTRS1988

Methane emissions to the troposphere from the Amazon floodplain

The magnitudes of CH4 emissions to the troposphere from the Amazon River floodplain and the mechanism of these emissions were investigated using the data of 94 individual flux measurements made along a 1700-km stretch of the river during July/August 1985. The overall average rate of CH4 emission from wetlands was found to be 390 mg CH4/sq m per day, with the highest emissions (590 mg CH4/sq m per day) attributed to the water surfaces covered by aquatic macrophytes. Ebullition was the dominant mechanism of emission, accounting for 85 percent of the total. Surface-water CH4 concentrations were highly supersaturated, averaging 6.4 micromolar. The annual emission of CH4 from the Amazon Basin to the troposphere, estimated from the area and the known emission rate, is about 10 CH4 Tg/yr, indicating the importance of the area in the global atmospheric CH4 cycle.

Devol, Allen H.↗
NASA NTRS1988

Infrared polar brightenings on Jupiter. IV - Spatial properties of methane emission

Different polar 'hot spot' differences are revealed between the northern and southern hemispheres of Jupiter by 7.8-micron observations made with NASA's Mauna Kea IR Telescope Facility. While the northern hot spot is fixed, relative to system III coordinates, at 180 + or - 10 deg longitude and 60 + or - 10 deg latitude, the southern hot spot is fixed with respect to neither the system III longitude and latitude, nor the subpolar point, or even Io's position. Voyager I IRIS data show the north polar hot spot to be more extended in longitude than latitude.

Caldwell, John↗
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 NTRS1992

Methane emissions from Alaska Arctic tundra - An assessment of local spatial variability

The findings of an extensive midsummer survey of CH4 emissions measurements representing the Alaska Arctic tundra are presented. Variability in rates of emissions was similar in magnitude on local and regional scales, ranging from 0 to 286.5 mg/sq m/d overall and often varying across two orders of magnitude within 0.5 m distances. Primary control on rates of emission was determined by the substrate and position of the water table relative to the surface. Emission rates in the Arctic Foothills ranged from 0.2 mg/sq m/d for tussock tundra to 55.53 mg/sq m/d over wet meadows. Plant-mediated release of CH4 to the atmosphere was directly proportional to green leaf area and represented 92-98 percent of the total emission rates over vegetated sites. The results suggest the current published emission rates may have overestimated the contribution of boreal ecosystems to the global CH4 budget by several fold.

Morrissey, L. A.↗
NASA NTRS1993

Primary production control of methane emission from wetlands

Based on simultaneous measurements of CO2 and CH4 exchange in wetlands extending from subarctic peatlands to subtropical marshes, a positive correlation between CH4 emission and net ecosystem production is reported. It is suggested that net ecosystem production is a master variable integrating many factors which control CH4 emission in vegetated wetlands. It is found that about 3 percent of the daily net ecosystem production is emitted back to the atmosphere as CH4. With projected stimulation of primary production and soil microbial activity in wetlands associated with elevated atmospheric CO2 concentration, the potential for increasing CH4 emission from inundated wetlands, further enhancing the greenhouse effect, is examined.

Whiting, G. J.↗