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Abstract
Chapter from: M
66: Hydrocarbon Migration And Its Near-Surface Expression
Edited By
Dietmar Schumacher and Michael A. AbramsAuthor:
Leigh C. Price Geochemistry, Generation, Migration
Published 1996 as
part of Memoir 66
Copyright © 1996 The American Association of Petroleum
Geologists. All Rights Reserved. |
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Price,
L. C., 1996, Research-derived insights into surface geochemical hydrocarbon
exploration, in D. Schumacher and M. A. Abrams, eds., Hydrocarbon
migration and its near-surface expression: AAPG Memoir 66, p. 285-307.
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Chapter
21
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Research-Derived
Insights into Surface Geochemical Hydrocarbon Exploration |
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| Leigh C.
Price
U.S. Geological Survey
Denver, Colorado, U.S.A.
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Abstract
Research studies
based on foreland basins (mainly in eastern Colorado) examined three surface
geochemical exploration (SGE) methods as possible hydrocarbon (HC) exploration
techniques. The first method, microbial soil surveying, has high potential
as an exploration tool, especially in development and enhanced recovery
operations. Integrative adsorption, the second technique, is not effective
as a quantitative SGE method because water, carbon dioxide, nitrous oxide,
unsaturated hydrocarbons, and organic compounds are collected by the adsorbent
(activated charcoal) much more strongly than covalently bonded microseeping
C1-C5 thermogenic HCs. Qualitative comparisons (pattern
recognition) of C8+ mass spectra cannot gauge HC gas microseepage
that involves only the C1-C5
HCs.
The third method, soil calcite
surveying, also has no potential as an exploration tool. Soil calcite concentrations
had patterns with pronounced areal contrasts, but these patterns had no
geometric relationship to surface traces of established or potential production,
that is, the patterns were random. Microscopic examination of thousands
of soils revealed that soil calcite was an uncrystallized caliche coating
soil particles. During its precipitation, caliche captures or occludes
any gases, elements, or compounds in its immediate vicinity. Thus, increased
signal intensity of some SGE methods should depend on increasing soil calcite
concentrations. Analyses substantiate this hypothesis. Because soil calcite
has no utility as a surface exploration tool, any surface method that depends
on soil calcite has a diminished utility as an SGE tool. Isotopic analyses
of soil calcites revealed carbonate carbon d13C
values of -4.0 to +2.0
(indicating a strong influence of atmospheric CO2) as opposed
to expected values of -45 to -30
if the carbonate carbon had originated from microbial oxidation of microseeping
HC gases. These analyses confirm a surface origin for this soil calcite
(caliche), which is not necessarily related to HC gas microseepage. This
previously unappreciated pivotal role of caliche is hypothesized to contribute
significantly to the poor and inconsistent results of some SGE methods. |
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