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A Global Assessment of Geologically-Sourced Previous HitMethaneNext Hit Seepage

By

Keith A. KVENVOLDEN , U.S. Geological Survey, Menlo Park, CA 94025 William S. REEBURGH, University of California, Irvine, CA 92717 Thomas D. LORENSON, U.S. Geological Survey, Menlo Park, CA 94025

 

Previous HitMethaneNext Hit is the most abundant organic compound in the Earth's atmosphere, where it acts as a greenhouse gas and thus has implications for global climate change. The total annual net input of Previous HitmethaneNext Hit to the atmosphere has been constrained by others to about 540 Tg (teragrams = 1012 g of Previous HitmethaneNext Hit). Sources of Previous HitmethaneNext Hit to the atmosphere are varied with the Previous HitmethaneNext Hit containing both modern (with 14C) and ancient (without 14C) carbon, but the current atmospheric Previous HitmethaneNext Hit budget does not take into account geologically-sourced Previous HitmethaneNext Hit seepage.

Thus a workshop was organized to address the issue of the missing, geologically-sourced carbon in the current global inventory of sources of atmospheric Previous HitmethaneNext Hit. The eighteen participants addressed the hypothesis that naturally occurring Previous HitmethaneNext Hit seeps contribute a significant amount of Previous HitmethaneNext Hit, containing much geologically-sourced carbon, to the atmosphere. Natural gas seepage rates have previously been ignored in inventories of atmospheric Previous HitmethaneNext Hit sources. However, natural gas seeps, commonly occurring with natural oil seeps, are found in both terrestrial and marine settings. These seeps range from microseepages (often considered in geochemical prospecting for petroleum) to macroseepages (so clearly evident in the Santa Barbara Channel, offshore from southern California). Also ignored have been the natural exhalations of Previous HitmethaneNext Hit from exposed outcrops, particularly petroleum source rocks and coal beds. The workshop, informally named the Gaia's Breath Working Group, addressed issues of natural gas seep occurrence, measurements of rates of Previous HitmethaneNext Hit emission from seeps on local scales, estimates of rates of Previous HitmethaneNext Hit emission from seeps on a global scale, and methods for improved assessment of Previous HitmethaneNext Hit seepage rates.

The Working Group concluded that the contribution of geologically-sourced Previous HitmethaneNext Hit to the atmospheric organic carbon cycle is significant and should be included in any global inventory of atmospheric Previous HitmethaneNext Hit. As a first approximation, the observed global rate of Previous HitmethaneNext Hit emission at the seabed was estimated to be about 50 Tg/yr resulting in an atmospheric emission rate of about 30 Tg/yr. A theoretical estimate, based on the total reservoir of Previous HitmethaneNext Hit available for seepage over geologic time, steady-state conditions, and a half-life of Previous HitmethaneNext Hit in the system of 108 years, resulted in similar rates of Previous HitmethaneNext Hit emission of 30 Tg/yr at the seabed and 10 Tg/yr to the atmosphere. These first approximation rates are strongly influenced by Previous HitmethaneNext Hit oxidation which plays a critical role in limiting the amount of Previous HitmethaneNext Hit available to the ocean-atmosphere system. Knowledge of Previous HitmethaneNext Hit emissions from terrestrial sources (volcanoes, rock outcrops, coal beds) is minimal, but the rate of Previous HitmethaneTop emission from these sources is believed to be less than from the oceans.