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Detailed Reference Information |
Dickens, G.R., O’Neil, J.R., Rea, D.K. and Owen, R.M. (1995). Dissociation of oceanic methane hydrate as a cause of the carbon isotope excursion at the end of the Paleocene. Paleoceanography 10: doi: 10.1029/95PA02087. issn: 0883-8305. |
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Isotopic records across the ''Latest Paleocene Thermal Maximum'' (LPTM) indicate that bottom water temperature increased by more than 4 ¿C during a brief time interval (<104 years) of the latest Paleocene (~55.6 Ma). There also was a coeval -2 to -3 % excursion in the Δ13C of the ocean/atmosphere inorganic carbon reservoir. Given the large mass of this reservoir, a rapid Δ13C shift of this magnitude is difficult to explain within the context of conventional hypotheses for changing the mean carbon isotope composition of the ocean and atmosphere. However, a direct consequence of warming bottom water temperature from 11 to 15 ¿C over 104 years would be a significant change in sediment thermal gradients and dissociation of oceanic CH4 hydrate at locations with intermediate water depths. In terms of the present-day oceanic CH4 hydrate reservoir, thermal dissociation of oceanic CH4 hydrate during the LPTM could have released greater than 1.1 to 2.1¿1018 g of carbon with a Δ13C of approximately -60 %. The release and subsequent oxidation of this amount of carbon is sufficient to explain a -2 to -3 % excursion in Δ13C across the LPTM. Fate of CH4 in oceanic hydrates must be considered in developing models of the climatic and paleoceanographic regimes that operated during the LPTM. ¿ American Geophysical Union 1995 |
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Abstract |
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Keywords
Oceanography, General, Paleoceanography, Oceanography, Biological and Chemical, Carbon cycling, Information Related to Geologic Time, Cenozoic, Oceanography, Biological and Chemical, Gases |
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Publisher
American Geophysical Union 2000 Florida Avenue N.W. Washington, D.C. 20009-1277 USA 1-202-462-6900 1-202-328-0566 service@agu.org |
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