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GC
Seismic
Attributes of Gas Hydrate Systems*
By
Diana Sava and Bob Hardage1
Search and Discovery Article #40255 (2007)
Posted August 31, 2007
*Adapted from the Geophysical Corner column, prepared by the authors, in AAPG Explorer, August, 2007, and entitled “Diving Into Gas Hydrate Systems.” Editor of Geophysical Corner is Bob A. Hardage. Managing Editor of AAPG Explorer is Vern Stefanic; Larry Nation is Communications Director.
1Bureau of Economic Geology, The University of Texas at Austin ([email protected])
General Statement
The need to understand deepwater gas hydrate systems is increasing, as several quarters of the geosciences world want answers about:
1) The use of hydrate as an energy resource.
2) The role of hydrate in seafloor stability.
3) Hydrate linkage to shallow-water flow.
4) The nature of hydrate system architecture.
Gas hydrate (Figure 1) is a solid material in which water molecules link together to form a cage, or clathrate, which encloses a single gas molecule. Several of these clathrates then link together to form a basic “unit volume” of crystalline hydrate. Depending on the type of gas molecules that are trapped in these cages, the number of clathrates that are linked to form these unit volumes may be 8 (Structure I), 24 (Structure II) or 6 (Structure H).
Because this ice-like material affects VP and VS
seismic
propagation velocities in deepwater sediment, it appears that accurate
measurements of VP and VS made across deepwater,
near-seafloor strata may allow hydrate concentrations within these strata to be
estimated. However, a major problem that confronts geophysicists who attempt to
use
seismic
attributes to infer hydrate concentration in deepwater systems is
that no one knows with confidence how these small unit-building blocks of
hydrate are distributed within their host sediment.
uGeneral StatementuFigure Captions
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Four Hydrate-Sediment MorphologiesFour possible hydrate-sediment morphologies are illustrated in Figure 2: 1) Model A assumes that the unit volumes of linked clathrates make physical contact with the sediment grains, become a part of the matrix, and bear part of the sediment load. 2) Model B assumes that the unit hydrate volumes float freely in the pore spaces and do not bear any sediment load. 3) In Model C, many unit volumes link together to form thin layers of pure hydrate, and the hydrate system is a series of these pure-hydrate layers alternating with layers of hydrate-free sediment. 4) Model D is similar to “C,” except the layers of pure hydrate are replaced with layers of uniformly dispersed, load-bearing hydrate, the concept described by “A.”
In some areas, hydrate no doubt exists in vertical fractures and dikes, but for brevity, vertically oriented hydrate distributions are not included in this suite of models.
Problems in Determining Concentration
The dilemma
confronting hydrate investigators is that for any given hydrate
concentration,
For a fixed
concentration of hydrate (say a volumetric fraction of 30 percent), VP
can range from 3300 m/s (Model D, fast mode) to 2000 m/s (Model C, slow
mode), and VS can vary from 1600 m/s (Model D, fast mode) to
200 m/s (Model B). As a result,
Laboratory Analyses of Cores
This lack of
understanding about hydrate-sediment morphologies in deepwater strata
exists because there is such a paucity of laboratory analyses of cores
that traverse deepwater hydrate systems. For
1) Must be obtained. 2) Must be maintained in their in situ temperature and pressure environment. 3) Must be subjected to laboratory studies while maintaining these in situ conditions.
These laboratory tests must
be designed so that the spatial distribution of hydrate throughout each
test sample is accurately defined for specific hydrate systems. Only
then can researchers decide whether Model A, B, C, and/or D, or some
other hydrate morphology model, describes the
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