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Geology topics

Laura A. Stern

Publications and source records attributed to Laura A. Stern.

At least 19 recordsLinked to original sources

Summary of the history and research of the U.S. Geological Survey gas hydrate properties laboratory in Menlo Park, California, active from 1993 to 2022

The U.S. Geological Survey (USGS) Clathrate Hydrate Properties Project, active from 1993 to 2022 in Menlo Park, California, stemmed from an earlier project on the properties of planetary ices supported by the National Aeronautics and Space Administration’s (NASA’s) Planetary Geology and Geophysics Program. We took a material science approach in both projects, emphasizing chemical purity of samples, having controlled grain size and grain texture, and having verified crystal structures and phase relations. A foundational contribution from our USGS Gas Hydrate Properties Laboratory (GHPL) was in demonstrating the ability to reproducibly create such pure clathrate hydrate samples for study. Clathrate sample synthesis was achieved by heating sieved and weighed pure granular water ice in the presence of cold clathrate-forming gas or liquid. During heating, the ice melts at the grain scale and reacts with the gas to form clathrate. The resulting material has the desired uniformity and purity, with known intergranular porosity; our subsequent measurements showed that these clathrates exhibited the established clathrate structures and phase relations. This novel synthesis method was successful in creating clathrates of pure methane, ethane, propane, carbon dioxide, and multi-component gases. By mixing sand or silt with granular ice, we were also able to make clathrate-sediment aggregates with controlled grain textures. This simple method, adopted by many others in the community, permitted us to measure the physical and chemical properties of well-characterized and well-crystallized clathrates and clathrate/sediment aggregates. At about the same time, we adapted conventional scanning electron microscopy to cryogenic conditions for analysis of grain-scale characteristics of clathrates made in the GHPL as well as those collected from nature by drill core. The uniformity and reproducibility of our samples also allowed us to investigate how clathrates respond to environmental changes in chemistry, temperature, and pressure: we measured chemical exchange rates with dissolved gas species—such as noble gases and chlorofluorocarbons—as well as rates of clathrate dissolution and decomposition. These advances include the first accurate mapping of the conditions that promote the remarkable process of “anomalous preservation” at room pressure, a metastability that offers potential application for low-cost and safe transportation of natural gas from gas fields far from pipelines. Another advancement stemming from the GHPL was the compaction of as-synthesized porous clathrates to nearly full density by applying external pressure using three different techniques. Compaction allows for high-accuracy measurements of many fundamental physical and chemical properties of these materials, such as elastic wavespeeds and moduli, complete thermal properties, decomposition rates, thermal expansion, and clathrate equations of state. These properties and others, in turn, have helped USGS scientists to interpret geophysical well logs and active geophysical surveys, as well as model the rates of gas production from hydrate deposits in nature. Studying this class of icy minerals that occur in abundance on Earth and in the outer solar system has been a fascinating laboratory journey. Here, we summarize the history and major findings of the USGS GHPL in Menlo Park, including both in-house research as well as findings from the synergistic collaborations with other agencies and institutes that were key to the success of our laboratory. The Menlo Park GHPL was more formally incorporated within the USGS Gas Hydrates Project, a collaboration among multiple USGS Science Centers, in the early 2000s under the leadership of Deborah Hutchinson, and now under the leadership of Carolyn Ruppel and Timothy Collett.

Open-File Report

Monitoring offshore CO2 sequestration using marine CSEM methods; constraints inferred from field- and laboratory-based gas hydrate studies

Offshore geological sequestration of CO 2 offers a viable approach for reducing greenhouse gas emissions into the atmosphere. Strategies include injection of CO 2 into the deep-ocean or ocean-floor sediments, whereby depending on pressure–temperature conditions, CO 2 can be trapped physically, gravitationally, or converted to CO 2 hydrate. Energy-driven research continues to also advance CO 2 -for-CH 4 replacement strategies in the gas hydrate stability zone (GHSZ), producing methane for natural gas needs while sequestering CO 2 . In all cases, safe storage of CO 2 requires reliable monitoring of the targeted CO 2 injection sites and the integrity of the repository over time, including possible leakage. Electromagnetic technologies used for oil and gas exploration, sensitive to electrical conductivity, have long been considered an optimal monitoring method, as CO 2 , similar to hydrocarbons, typically exhibits lower conductivity than the surrounding medium. We apply 3D controlled-source electromagnetic (CSEM) forward modeling code to simulate an evolving CO 2 reservoir in deep-ocean sediments, demonstrating sufficient sensitivity and resolution of CSEM data to detect reservoir changes even before sophisticated inversion of data. Laboratory measurements place further constraints on evaluating certain systems within the GHSZ; notably, CO 2 hydrate is measurably weaker than methane hydrate, and >1 order of magnitude more conductive, properties that may affect site selection, stability, and modeling considerations.

Energies

Diatom influence on the production characteristics of hydrate-bearing sediments: Examples from Ulleung Basin, offshore South Korea

The Ulleung Basin Gas Hydrate field expeditions in 2007 (UBGH1) and 2010 (UBGH2) sought to assess the Basin's gas hydrate resource potential. Coring operations in both expeditions recovered evidence of gas hydrate, primarily as fracture-filling (or vein type) morphologies in mainly silt-sized, fine-grained sediment, but also as pore-occupying hydrate in the coarser-grained layers of interbedded sand and fine-grained systems. A commonality across many of these occurrences is the presence of diatoms in the fine-grained sediment. Here we tested fine-grained sediment (median grain size <12.5 μm) associated with hydrate occurrences at four UBGH2 sites (UBGH2-2-2, UBGH2-3, UBGH2-6 and UBGH2-11) to investigate potential impacts of diatoms on efforts to extract methane from hydrate, or to tap hydrocarbon reservoirs beneath hydrate-bearing sediment. Two key considerations are: the extent to which diatoms control sediment mechanical properties, and the extent to which pore-water freshening, which occurs as gas hydrate breaks down during resource extraction, alters the diatom control on sediment mechanical properties. We conducted experiments to measure sediment index properties, sedimentation behavior and compressibility to address these considerations. We relied on scanning electron microscope (SEM) imagery and X-ray powder diffraction (XRD) to characterize the sediment mineralogy. Our high-level findings are that at the ∼20–45% (by volume) diatom concentrations observed at these UBGH2 sites, sediment compressibility increases with diatom content, but diatoms only appear to increase porosity and permeability at the highest diatom concentration (∼45%). Our measurements suggest in situ compression indices of 0.35–0.55 and permeabilities on the order of 0.01milliDarcies (1 × 10 −17 m 2 ) can be anticipated at these sites. Importantly, these properties are not expected to vary significantly upon pore water freshening that accompanies gas hydrate dissociation during production.

East Sea, Ulleung Basin

Electrical properties of carbon dioxide hydrate: Implications for monitoring CO2 in the gas hydrate stability zone

CO 2 and CH 4 clathrate hydrates are of keen interest for energy and carbon cycle considerations. While both typically form on Earth as cubic structure I (sI), we find that pure CO 2 hydrate exhibits over an order of magnitude higher electrical conductivity ( σ ) than pure CH 4 hydrate at geologically relevant temperatures. The conductivity was obtained from frequency-dependent impedance ( Z ) measurements made on polycrystalline CO 2 hydrate (CO 2 ·6.0 ± 0.2H 2 O by methods here) with 25% gas-filled porosity, compared with CH 4 hydrate (CH 4 ·5.9H 2 O) formed and measured in the same apparatus and exhibiting closely matching grain characteristics. The conductivity of CO 2 hydrate is 6.5 × 10 −4 S/m at 273K with an activation energy ( E a ) of 46.5 kJ/mol at 260–281 K, compared with ∼5 × 10 −5 S/m and 34.8 kJ/m for CH 4 hydrate. Equivalent circuit modeling indicates that different pathways govern conduction in CO 2 versus CH 4 hydrate. Results show promise for use of electromagnetic methods in monitoring CO 2 hydrate formation in certain natural settings or in CO 2 /CH 4 exchange efforts.

Geophysical Research Letters

Electrical conductivity of pure CO2 hydrate and CH4 hydrate: Role of the guest molecule

To conclude a series of DOE-sponsored laboratory experiments in which our team measured electrical conductivity of methane hydrate-bearing samples, we investigated electrical conductivity of CO2 hydrate for direct comparison with methane hydrate. Their surprisingly distinct signatures could aid in the monitoring of CO2 in certain deep marine environments. To the best of our knowledge these are the first reported conductivity measurements on pure, polycrystalline CO2 hydrate.

Newsletter

Laboratory electrical conductivity of marine gas hydrate

Methane hydrate was synthesized from pure water ice and flash frozen seawater, with varying amounts of sand or silt added. Electrical conductivity was determined by impedance spectroscopy, using equivalent circuit modeling to separate the effects of electrodes and to gain insight into conduction mechanisms. Silt and sand increase the conductivity of pure hydrate, we infer by contaminant NaCl contributing to conduction in hydrate, to values in agreement with resistivities observed in well logs through hydrate The addition of silt and sand lowers the conductivity of hydrate synthesized from seawater by an amount consistent with Archie's Law. All samples were characterized using cryogenic scanning electron microscopy and energy dispersive spectroscopy, which show good connectivity of salt and brine phases. Electrical conductivity measurements of pure hydrate and hydrate mixed with silt during pressure‐induced dissociation supports previous conclusions that sediment increases dissociation rate.

Geophysical Research Letters

Plastic faulting in ice

Plastic faulting is a brittle‐like failure phenomenon exhibited by water ice and several other rock types under confinement. It is suspected to be the mechanism of deep earthquakes and extreme cases of shear localization in shallow rocks. Unlike ordinary Coulombic failure, plastic faulting is characterized by a pressure‐independent failure strength and fault plane oriented 45° to maximum principal stress. To research the question of how the instability initiates, we conducted over 50 constant‐displacement‐rate experiments on polycrystalline ice (phases Ih and II) near the brittle‐to‐ductile (B‐D) transition, at confining pressures P = 0–300 MPa, applied strain rates = 5 × 10 −5 – 7 × 10 −3 s −1 , temperatures T = 105–233 K, and mean grain sizes d = 0.25–1.18 mm. We find that (1) the width of the B‐D transition in variable space is vanishingly narrow, to the point of appearing as a crossover, (2) a plastic fault plane, once formed, is not a zone of subsequent weakness, (3) distributed ice I→II phase transformation in small amounts (<1 vol%) shows no causal relationship to subsequent failure, and (4) plastic faulting also occurs in ice II. We hypothesize that the elusive nucleating “trigger” parallels that of metals and ceramics undergoing severe plastic deformation, wherein transient local structural rearrangement occurs, in turn causing material strength to drop to a level sufficiently low, in a volume sufficiently large, that adiabatic instability is nucleated. Our results do not require and often are inconsistent with phase transformation. Plastic faulting may therefore be available to all solids undergoing severe deformation, and its appearance in so few is simply the result of insufficiently extreme conditions.

Journal of Geophysical Research- Solid Earth

Potential freshening impacts on fines migration and pore-throat clogging during gas hydrate production: 2-D micromodel study with Diatomaceous UBGH2 sediments

The methane gas hydrate stored in natural sediments is considered a potential gas resource. Countries such as China, India, Japan, and Korea are interested in commercializing this resource, and offshore field pilot tests for gas production have been conducted using depressurization methods to destabilize gas hydrate and facilitate the migration of methane to the production well. However, fine-grained sediments (fines), which are present even in coarse-grained, gas hydrate-bearing sediments, can be resuspended in the production fluid, subsequently clogging pore throats in the formation and reducing the overall production efficiency. We conducted laboratory tests to evaluate the suspension and clogging potential of fines collected from the Ulleung Basin, East Sea, Korea during the 2010 Ulleung Basin Gas Hydrate Expedition 2 (UBGH2). Experimental results reveal that diatoms are prevalent in the sediment and largely control the suspension and clogging behavior. Fluid flow experiments in 2D micromodels show clogging occurs even when injecting the minimum sediment concentration (0.1wt% in the fluid) through micromodels with pore-throat widths at the high end of the anticipated range for UBGH2 gas hydrate-bearing sands (100µm). Mobile gas/fluid interfaces forming during gas hydrate dissociation accentuate clogging by concentrating and mobilizing fines. Sedimentation tests show pore-water freshening during dissociation is not anticipated to change the potential for diatoms to become entrained in the pore water flow, even for the observed gas hydrate saturations of ~80%. Muscovite and illite are also significant components of the tested sediment, however, and pore-water freshening increases their potential for resuspension and clogging. Overall, the resuspension and clogging potential of these fine sediments should increase as gas hydrate dissociation progresses in the thin, gas hydrate-bearing sands investigated in the Ulleung Basin.

Marine and Petroleum Geology

Gas hydrate petroleum systems: What constitutes the “seal”?

The gas hydrate petroleum system (GHPS) approach, which has been used to characterize gas hydrates in nature, utilizes three distinct components: a methane source, a methane migration pathway, and a reservoir that not only contains gas hydrate, but also acts as a seal to prevent methane loss. Unlike GHPS, a traditional petroleum system (PS) approach further distinguishes between the reservoir, a unit with generally coarser sediment grains, and a separate overlying seal unit with generally finer sediment grains. Adopting this traditional PS distinction in the GHPS approach facilitates assessments of reservoir growth and production potential. The significance of the seal for the formation of a gas hydrate reservoir as well as for the efficiency in methane extraction from the reservoir as an energy resource is evident in the findings from recent offshore field expeditions, such as India’s second National Gas Hydrate Program expedition (NGHP-02). In regards to gas hydrate-bearing reservoir formation, the NGHP-02 gas chemistry data indicate a primarily microbial methane source. Fine-grained seal sediment in contact with coarser-grained reservoir sediment can facilitate that microbial methane production. Logging-while-drilling and sediment core data also indicate that the overlying fine-grained seal sediment is less permeable than the underlying, highly gas hydrate-saturated reservoir sediment. The overlying seal’s capacity to act as a low-permeability boundary is important not only for preventing methane migration out of the reservoir over time, but for also preventing water invasion into the reservoir during methane extraction from the reservoir. Ultimately, the presence of an overlying, fine-grained, low-permeability “Seal”? influences how gas hydrate initially forms in a coarse-grained reservoir and dictates how efficiently methane can be extracted as an energy resource from the gas hydrate reservoir via depressurization.

Bay of Bengal

The effect of brine on the electrical properties of methane hydrate

Gas hydrates possess lower electrical conductivity (inverse of resistivity) than either seawater or ice, but higher than clastic silts and sands, such that electromagnetic methods can be employed to help identify their natural formation in marine and permafrost environments. Controlled laboratory studies offer a means to isolate and quantify the effects of changing individual components within gas‐hydrate‐bearing systems, in turn yielding insight into the behavior of natural systems. Here we investigate the electrical properties of polycrystalline methane hydrate with ≥25% gas‐filled porosity and in mixture with brine. Initially, pure methane hydrate was synthesized from H 2 O ice and CH 4 gas while undergoing electrical impedance measurement, then partially dissociated to assess the effects of pure pore water accumulation on electrical conductivity. Methane hydrate + brine mixtures were then formed by either adding NaCl (0.25–2.5 wt %) to high‐purity ice or by using frozen seawater as a reactant. Conductivity was obtained from impedance measurements made in situ throughout synthesis while temperature cycled between +15 °C and −25 °C. Several possible conduction mechanisms were subsequently determined using equivalent circuit modeling. Samples with low NaCl concentration show a doping/impurity effect and a log linear conductivity response as a function of temperature. For higher salt content samples, conductivity increases exponentially with temperature and the log linear relationship no longer holds; instead, we observe phase changes within the samples that follow NaCl–H 2 O–CH 4 phase equilibrium predictions. Final samples were quenched in liquid nitrogen and imaged by cryogenic scanning electron microscopy (cryo‐SEM) to assess grain‐scale characteristics.

Journal of Geophysical Research

Pressure core analysis of geomechanical and fluid flow properties of seals associated with gas hydrate-bearing reservoirs in the Krishna-Godavari Basin, offshore India

Physical properties of the sediment directly overlying a gas hydrate reservoir provide important controls on the effectiveness of depressurizing that reservoir to extract methane from gas hydrate as an energy resource. The permeability of overlying sediment determines if a gas hydrate reservoir’s upper contact will provide an effective seal that enables efficient reservoir depressurization. Compressibility, stiffness and strength indicate how overlying sediment will deform as the in situ stress changes during production, providing engineering data for well designs. Assessing these properties requires minimally-disturbed sediment. India’s National Gas Hydrates Program Expedition 2 (NGHP-02) provided an opportunity to study these seal sediment properties, reducing disturbance from gas exsolution and bubble growth by collecting a pressure core from the seal sediment just above the primary gas hydrate reservoir at Site NGHP-02-08 in Area C of the Krishna-Godavari Basin. The effective stress chamber (ESC) and the direct shear chamber (DSC) devices in the suite of Pressure Core Characterization Tools (PCCTs) were used to measure permeability, compressibility, stiffness and shear strength at the in situ vertical stress. Geotechnical properties of the predominantly fine-grained seal layer at in situ vertical stress are in typical clay sediment ranges, with low measured permeability (0.02 mD), high compressibility (Cc = 0.26 – 0.33) and low shear strength (404 kPa). Though pressure and temperature were maintained throughout the collection and measurement process to stabilize gas hydrate, the lack of effective stress in the pressure core storage chamber and the chamber pressurization with methane-free water caused core expansion and gas hydrate in a thin coarser-grained layer to dissolve. The PCCTs can reapply in situ stress with incremental loading steps during a consolidation test to account for sediment compaction. Gas hydrate dissolution can be limited by storing cores just above freezing temperatures, and by using solid spacers to reduce the storage chamber’s free volume.

Marine and Petroleum Geology

Physical property characteristics of gas hydrate-bearing reservoir and associated seal sediments collected during NGHP-02 in the Krishna-Godavari Basin, in the offshore of India

India’s National Gas Hydrate Program Expedition 02 (NGHP-02), was conducted to better understand geologic controls on gas hydrate occurrence and morphology, targeting potentially coarse-grained sediments near the base of the continental slope offshore eastern India. This study combines seismic, logging-while-drilling data, and a petroleum systems approach to provide a regional geologic context for the core- and grain-scale analyses. This multi-scale approach provides insight on the gas hydrate distribution, morphology and anticipated system response to depressurization-induced methane extraction. The study area, NGHP-02 Area B in the Krishna-Godavari Basin, contains a buried anticline/syncline structure that hosts fracture-filling gas hydrate in fine-grained sediment overlying coarser sediments with pore-occupying gas hydrate. Core- and grain-scale measurements show fine-grained sediment exerts a primary control on the distribution and morphology of gas hydrate in Area B. Diatoms in the fine-grained overburden cause porosity to increase with depth, reaching ~70% at the underlying reservoir contact. High porosity, combined with near-vertical faults, suggests the overlying sediment is an imperfect seal. This allows methane to escape the gas hydrate reservoir sediments and form primarily grain-displacing gas hydrate veins in the fine-grained overburden. Within the reservoir, fine-grained layers are interbedded with coarser-grained gas hydrate reservoir sands. Even in the reservoir sands, however, a soil classification study shows the fines content is high enough to control hydraulic and mechanical properties, such as permeability, compressibility and shear strength. Fluid motion during methane extraction from gas hydrates can mobilize those fines, which can then clog pore throats, limiting production rates. Pore-water freshening during gas hydrate dissociation can increase fines mobilization, particularly given the smectite identified in the fine-grained interbeds. Accounting for fines content and specific fines mineralogy throughout the gas hydrate petroleum system is important for predicting production efficiency from gas hydrate occurrences along the crest of the anticline in NGHP-02 Area B.

Marine and Petroleum Geology

Inhibition of grain boundary sliding creep in fine-grained ice by inter-granular particles: Implications for planetary ice masses

Ice in both terrestrial and planetary settings often contains rock particles. Here we present an experimental investigation of the influence of intergranular particles on the rheological behavior of ice. Experiments were performed on samples fabricated from 10‐μm ice powders +1‐μm graphite or 0.8‐μm alumina particles and subjected to elevated confining pressures. A critical particle fraction, ∼6%, was observed, below which samples behave like pure ice and deform by both grain boundary sliding (GBS) and dislocation creep, and above which GBS creep is impeded. Above this critical fraction, ice grains occur in particle‐free clusters surrounded by bands of particles mixed with fine‐grained ice, resulting in the impedance of GBS in the bands as well as sliding between the ice clusters. Our results imply that South Polar Layered Deposits and midlatitude lobate debris aprons on Mars must contain >94% ice and that the shallow subsurface of Ceres could contain >90% ice.

Geophysical Research Letters

Impact of pore fluid chemistry on fine-grained sediment fabric and compressibility

Fines, defined here as grains or particles, less than 75 μm in diameter, exist nearly ubiquitously in natural sediment, even those classified as coarse. Macroscopic sediment properties, such as compressibility, which relates applied effective stress to the resulting sediment deformation, depend on the fabric of fines. Unlike coarse grains, fines have sizes and masses small enough to be more strongly influenced by electrical interparticle forces than by gravity. These electrical forces acting through pore fluids are influenced by pore fluid chemistry changes. Macroscopic property dependence on pore fluid chemistry must be accounted for in sediment studies involving subsurface flow and sediment stability analyses, as well as in engineered flow situations such as groundwater pollutant remediation, hydrocarbon migration, or other energy resource extraction applications. This study demonstrates how the liquid limit‐based electrical sensitivity index can be used to predict sediment compressibility changes due to pore fluid chemistry changes. Laboratory tests of electrical sensitivity, sedimentation, and compressibility illustrate mechanisms linking microscale and macroscale processes for selected pure, end‐member fines. A specific application considered here is methane extraction via depressurization of gas hydrate‐bearing sediment, which causes a dramatic pore water salinity drop concurrent with sediment being compressed by the imposed effective stress increase.

Journal of Geophysical Research

Electrical properties of methane hydrate + sediment mixtures

Knowledge of the electrical properties of multicomponent systems with gas hydrate, sediments, and pore water is needed to help relate electromagnetic (EM) measurements to specific gas hydrate concentration and distribution patterns in nature. Toward this goal, we built a pressure cell capable of measuring in situ electrical properties of multicomponent systems such that the effects of individual components and mixing relations can be assessed. We first established the temperature-dependent electrical conductivity ( &sigma; ) of pure, single-phase methane hydrate to be ~5 orders of magnitude lower than seawater, a substantial contrast that can help differentiate hydrate deposits from significantly more conductive water-saturated sediments in EM field surveys. Here we report &sigma; measurements of two-component systems in which methane hydrate is mixed with variable amounts of quartz sand or glass beads. Sand by itself has low &sigma; but is found to increase the overall &sigma; of mixtures with well-connected methane hydrate. Alternatively, the overall &sigma; decreases when sand concentrations are high enough to cause gas hydrate to be poorly connected, indicating that hydrate grains provide the primary conduction path. Our measurements suggest that impurities from sand induce chemical interactions and/or doping effects that result in higher electrical conductivity with lower temperature dependence. These results can be used in the modeling of massive or two-phase gas-hydrate-bearing systems devoid of conductive pore water. Further experiments that include a free water phase are the necessary next steps toward developing complex models relevant to most natural systems.

Journal of Geophysical Research

The importance of particulate texture to the flow strength of ice + dust

Preliminary experimental surveys of the flow of dilute mixtures of ice plus hard particulates under planetary conditions indicate a strengthening effect with respect to pure ice, but with dependencies on environmental conditions (temperature, stress, grain size) that vary widely from study to study [1-4]. With the expectation that the textural character of the particulate fraction (size, shape, spatial distribution of particulates; relationship of particulates to ice grain boundaries, etc.) also influences rheological behavior, we have begun a more systematic investigation of the effect of particulates on strength. We rely extensively on cryogenic scanning electron microscopy (CSEM) and to maximize planetary relevance we focus on behavior at low stress and small grain size.

Conference Paper

Comparison of the physical and geotechnical properties of gas-hydrate-bearing sediments from offshore India and other gas-hydrate-reservoir systems

The sediment characteristics of hydrate-bearing reservoirs profoundly affect the formation, distribution, and morphology of gas hydrate. The presence and type of gas, porewater chemistry, fluid migration, and subbottom temperature may govern the hydrate formation process, but it is the host sediment that commonly dictates final hydrate habit, and whether hydrate may be economically developed. In this paper, the physical properties of hydrate-bearing regions offshore eastern India (Krishna-Godavari and Mahanadi Basins) and the Andaman Islands, determined from Expedition NGHP-01 cores, are compared to each other, well logs, and published results of other hydrate reservoirs. Properties from the hydrate-free Kerala-Konkan basin off the west coast of India are also presented. Coarser-grained reservoirs (permafrost-related and marine) may contain high gas-hydrate-pore saturations, while finer-grained reservoirs may contain low-saturation disseminated or more complex gas-hydrates, including nodules, layers, and high-angle planar and rotational veins. However, even in these fine-grained sediments, gas hydrate preferentially forms in coarser sediment or fractures, when present. The presence of hydrate in conjunction with other geologic processes may be responsible for sediment porosity being nearly uniform for almost 500 m off the Andaman Islands. Properties of individual NGHP-01 wells and regional trends are discussed in detail. However, comparison of marine and permafrost-related Arctic reservoirs provides insight into the inter-relationships and common traits between physical properties and the morphology of gas-hydrate reservoirs regardless of location. Extrapolation of properties from one location to another also enhances our understanding of gas-hydrate reservoir systems. Grain size and porosity effects on permeability are critical, both locally to trap gas and regionally to provide fluid flow to hydrate reservoirs. Index properties corroborate more advanced consolidation and triaxial strength test results and can be used for predicting behavior in other NGHP-01 regions. Pseudo-overconsolidation is present near the seafloor and is underlain by underconsolidation at depth at some NGHP-01 locations.

Journal of Marine and Petroleum Geology

Grain-scale imaging and compositional characterization of cryo-preserved India NGHP 01 gas-hydrate-bearing cores

We report on grain-scale characteristics and gas analyses of gas-hydrate-bearing samples retrieved by NGHP Expedition 01 as part of a large-scale effort to study gas hydrate occurrences off the eastern-Indian Peninsula and along the Andaman convergent margin. Using cryogenic scanning electron microscopy, X-ray spectroscopy, and gas chromatography, we investigated gas hydrate grain morphology and distribution within sediments, gas hydrate composition, and methane isotopic composition of samples from Krishna&ndash;Godavari (KG) basin and Andaman back-arc basin borehole sites from depths ranging 26 to 525 mbsf. Gas hydrate in KG-basin samples commonly occurs as nodules or coarse veins with typical hydrate grain size of 30&ndash;80 &mu;m, as small pods or thin veins 50 to several hundred microns in width, or disseminated in sediment. Nodules contain abundant and commonly isolated macropores, in some places suggesting the original presence of a free gas phase. Gas hydrate also occurs as faceted crystals lining the interiors of cavities. While these vug-like structures constitute a relatively minor mode of gas hydrate occurrence, they were observed in near-seafloor KG-basin samples as well as in those of deeper origin (>100 mbsf) and may be original formation features. Other samples exhibit gas hydrate grains rimmed by NaCl-bearing material, presumably produced by salt exclusion during original hydrate formation. Well-preserved microfossil and other biogenic detritus are also found within several samples, most abundantly in Andaman core material where gas hydrate fills microfossil crevices. The range of gas hydrate modes of occurrence observed in the full suite of samples suggests a range of formation processes were involved, as influenced by local in situ conditions. The hydrate-forming gas is predominantly methane with trace quantities of higher molecular weight hydrocarbons of primarily microbial origin. The composition indicates the gas hydrate is Structure I.

Marine and Petroleum Geology