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Atmospheric methane

About: Atmospheric methane is a research topic. Over the lifetime, 2034 publications have been published within this topic receiving 119616 citations.


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Journal ArticleDOI
TL;DR: Recent isotopic data appear to finally rule out any major impact of clathrate releases on methane at these time-scales, and the recent EPICA Dome C (Antarctica) record shows that methane tracked climate over the last 650 000 years, with lower methane concentrations in glacials than interglacials, and lower concentrations in cooler interglazials than in warmer ones.
Abstract: Polar ice cores contain, in trapped air bubbles, an archive of the concentrations of stable atmospheric gases. Of the major non-CO2 greenhouse gases, methane is measured quite routinely, while nitrous oxide is more challenging, with some artefacts occurring in the ice and so far limited interpretation. In the recent past, the ice cores provide the only direct measure of the changes that have occurred during the industrial period; they show that the current concentration of methane in the atmosphere is far outside the range experienced in the last 650,000 years; nitrous oxide is also elevated above its natural levels. There is controversy about whether changes in the pre-industrial Holocene are natural or anthropogenic in origin. Changes in wetland emissions are generally cited as the main cause of the large glacial-interglacial change in methane. However, changing sinks must also be considered, and the impact of possible newly described sources evaluated. Recent isotopic data appear to finally rule out any major impact of clathrate releases on methane at these time-scales. Any explanation must take into account that, at the rapid Dansgaard-Oeschger warmings of the last glacial period, methane rose by around half its glacial-interglacial range in only a few decades. The recent EPICA Dome C (Antarctica) record shows that methane tracked climate over the last 650,000 years, with lower methane concentrations in glacials than interglacials, and lower concentrations in cooler interglacials than in warmer ones. Nitrous oxide also shows Dansgaard-Oeschger and glacial-interglacial periodicity, but the pattern is less clear.

49 citations

Journal ArticleDOI
TL;DR: In this paper, the mixing ratio and δ 13 C in methane (δ 13 CH 4 ) are reported from large, clean air samples collected every 2.5° to 5° of latitude on four voyages across the Pacific between New Zealand and the West Coast of the United States in 1996 and 1997.
Abstract: Measurements of the mixing ratio and δ 13 C in methane (δ 13 CH 4 ) are reported from large, clean air samples collected every 2.5° to 5° of latitude on four voyages across the Pacific between New Zealand and the West Coast of the United States in 1996 and 1997. The data show that the interhemispheric gradient for δ 13 CH 4 was highly dependent on season and varied from 0.5‰ in November 1996 with an estimated annual mean of 0.2-0.3‰. The seasonal cycles in δ 13 CH 4 reveal three distinct latitude bands differentiated by phase. Maxima occur in January-February for the extratropical Southern Hemisphere, in September-October for the tropics, and in June-July for the extratropical Northern Hemisphere. The data are compared with results from a three-dimensional transport and atmospheric chemistry model that simulates the observed latitudinal structure of either δ 13 CH 4 or the methane mixing ratio well, but not both simultaneously. The requirement that a methane source-sink budget be consistent with both types of data clearly imposes stricter constraints than arise from either mixing ratio or isotopic data alone. The seasonal δ 13 CH 4 data in the extratropical Southern Hemisphere are used to estimate a value for the net fractionation in the CH 4 sink of 12-15‰, which is larger than can be explained by current laboratory measurements of a kinetic isotope effect for the OH + CH 4 reaction and soil sink processes. The hypothesis that the discrepancy is caused by competitive reaction of active chlorine with methane in the marine boundary layer is discussed.

48 citations

Journal ArticleDOI
TL;DR: In this paper, a study was conducted to investigate methanotrophic activity under practical storage conditions Surface crusts from slurry storages at two pig farms and four dairy farms were sampled in late autumn, and mixed samples were used to determine changes in CH4, O2 and CO2 during incubation.
Abstract: Storages with liquid manure (slurry) may develop a surface crust of particulate organic matter, or an artificial crust can be established Slurry storages are net sources of atmospheric methane (CH4), but a potential for bacterial oxidation of CH4 in surface crusts was recently suggested in a study of experimental storages The present study was conducted to investigate methanotrophic activity under practical storage conditions Surface crusts from slurry storages at two pig farms and four dairy farms were sampled in late autumn Mixed samples (0–4 cm depth) were used to determine changes in CH4, O2 and CO2 during incubation, while intact subsamples were used to characterize CH4 oxidation as a function of CH4 availability and moisture content Methane oxidation was observed in all materials except for an expanded clay product (Leca) sampled from a pig slurry storage Despite significant variation between replicate subsamples, there was a significant increase in methanotrophic activity when CH4 concentrations increased from 500 to 50,000 ppmv Maximum fluxes ranged from −1 to −45 g CH4 m−2 d−1 Surface crust samples were partly dried and then re-wetted in four steps to the original moisture content, each time followed by determination of CH4 fluxes Only one surface crust material showed a relationship between CH4 fluxes and moisture content that would implicate gas diffusivity in the regulation of CH4 oxidation The occurrence of inducible CH4 oxidation activity in slurry storage surface crusts indicates that there is a potential for stimulating the process by manipulation of gas phase composition above the stored slurry

48 citations

Journal ArticleDOI
TL;DR: In this article, the first continental evidence for climate-caused changes in a methane gas hydrate reservoir was presented, which indicated that these emissions were associated with decomposition of sedimentary clathrates, widespread in the Baikal basin.

48 citations

Journal ArticleDOI
TL;DR: In this paper, the authors investigate the response of relict Arctic submarine permafrost and gas hydrate deposits to warming and make predictions of methane gas flux to the water column using a 2-D multiphase fluid flow model.
Abstract: We investigate the response of relict Arctic submarine permafrost and gas hydrate deposits to warming and make predictions of methane gas flux to the water column using a 2-D multiphase fluid flow model. Exposure of the Arctic shelf during the last glacial cycle formed a thick layer of permafrost, protecting hydrate deposits below. However, talik formation below paleo-river channels creates permeable pathways for gas migration from depth. An estimate of the maximum gas flux at the present time for conditions at the East Siberian Arctic Seas is 0.2047 kg yr−1 m−2, which produces a methane concentration of 142 nM in the overlying water column, consistent with several field observations. For conditions at the North American Beaufort Sea, the maximum gas flux at the present time is 0.1885 kg yr−1 m−2, which produces a methane concentration of 78 nM in the overlying water column. Shallow sediments are charged with residual methane gas after venting events. Sustained submergence into the future should increase gas venting rate roughly exponentially as sediments continue to warm. Studying permafrost-associated gas hydrate reservoirs will allow us to better understand the Arctic's contribution to the global methane budget and global warming.

48 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202395
2022153
202175
202077
201974
201872