USGS · 70020158
[No abstract available]
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L.C. Price, R. McNeil. 2007-12-18. Thoughts on the birth, evolution, and current state of petroleum geochemistry. https://doi.org/10.1111/j.1747-5457.1997.tb00763.x
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The present author defends his conclusions. Two errors in his earlier paper (M.A. 84M/1107) are corrected. (Preceding abstract) -P.Br.
Detailed organic geochemistry has been performed on a large number of Lower Mississippian-Upper Devonian Bakken shales from the North Dakota portion of the Williston Basin, and 28 oils mainly from Mississippian Madison Group rocks from different basinal areas. Here we report results of Rock-Eval pyrolysis and vitrinite reflectance ( R o ) analyses. Variable paleoheat flows in the Williston Basin caused the threshold of intense hydrocarbon generation to occur at different depths in different basinal areas. In higher paleogeothermal gradient basinal areas, this event occurred at depths of 7,650-8,000 ft, and at 10,000 ft or deeper in lower paleogeothermal gradient areas of the Basin. Distinct organic metamorphic imprints in Williston Basin sediments were also caused by extreme, but variable, paleoheat flows in the basin, as well as secondary migration of crude oils from deep basinal source areas. The high paleoheat flows are postulated as being due to a Late Cretaceous - Paleocene aborted rift event. Only a small volume of Bakken shales in restricted areas of the Williston Basin was responsible for the oil found reservoired in Mississippian Madison Group rocks. However, this small shale volume has been responsible for a relatively large amount of crude oil. R o profiles in the Tertiary through Middle Jurassic rocks in the Williston Basin had steep, linear R o versus depth gradients, with strong reversals of R o values occurring in the Lower Jurassic rocks. The lower Mesozoic through Paleozoic rocks of the Basin had strongly suppressed R o values compared to the values in the Tertiary through Middle Jurassic rocks. This was especially true of the R o values in the Bakken shales. This R o suppression was due to a change in organic matter (OM) type from oxygen-rich terrestrially derived OM in the younger rocks, to a hydrogen-rich marine derived OM in the deeper, older rocks. The threshold of intense oil generation (TIHG) occurred in the Bakken shales of the Williston Basin at R o values somewhere between 0.9 and 1.7% (best estimate 0.9), as would be read in oxygen-rich OM. Much higher burial temperatures (and consequently R o values) than usually held to be necessary were required for both the TIHG as well as mainstage hydrocarbon generation in the Bakken shales. These results are most likely applicable in general to source rocks with hydrogen-rich OM. The data of this study have major implications to petroleum exploration as well as to petroleum resource assessment.
Oceanic methane hydrates are mineral deposits formed from a crystalline 'ice' of methane and water in sea-floor sediments (buried to less than about 1 km) in water depths greater than about 500 m; economic hydrate deposits are probably restricted to water depths of between 1.5 km and 4 km. Gas hydrates increase a sediment's strength both by 'freezing' the sediment and by filling the pore spaces in a manner similar to water-ice in permafrost. Concentrated hydrate deposits may be underlain by significant volumes of methane gas, and these localities are the most favourable sites for methane gas extraction operations. Seismic reflection records indicate that trapped gas may blow-out naturally, causing large-scale seafloor collapse. In this paper, we consider both the physical properties and the structural integrity of the hydrate stability zone and the associated free gas deposits, with special reference to the Blake Ridge area, SE US offshore, in order to help establish a suitable framework for the safe, efficient, and economic recovery of methane from oceanic gas hydrates. We also consider the potential effects of the extraction of methane from hydrate (such as induced sea-floor faulting, gas venting, and gas-pocket collapse). We assess the ambient pressure effect on the production of methane by hydrate dissociation, and attempt to predict the likelihood of spontaneous gas flow in a production situation.Oceanic methane hydrates are mineral sits formed from a crystalline `ice' of methane and water in sea-floor sediments (buried to less than about 1 km) in water depths greater than about 500 m; economic hydrate deposits are probably restricted to water depths of between 1.5 km and 4 km. Gas hydrates increase a sediment's strength both by `freezing' the sediment and by filling the pore spaces in a manner similar to water-ice in permafrost. Concentrated hydrate deposits may be underlain by significant volumes of methane gas, and these localities are the most favourable sites for methane gas extraction operations. Seismic reflection records indicate that trapped gas may blow-out naturally, causing large-scale seafloor collapse. In this paper, we consider both the physical properties and the structural integrity of the hydrate stability zone and the associated free gas deposits, with special reference to the Blake Ridge area, SE US offshore, in order to help establish a suitable framework for the safe, efficient, and economic recovery of methane from oceanic gas hydrates. We also consider the potential effects of the extraction of methane from hydrate (such as induced sea-floor faulting, gas venting, and gas-pocket collapse). We assess the ambient pressure effect on the production of methane by hydrate dissociation, and attempt to predict the likelihood of spontaneous gas flow in a production situation.